Foundations: how to think before you act
Every protocol in the next four Parts is an answer to three questions asked here: why do children die, how do you see it coming in sixty seconds, and why does a child's physiology hide the danger until late. Part A is open from the first minute.
▸Unit 1 Why children die, and where this module fits Not attempted
A child who dies in hospital usually does so within the first day, from a short list of physiological end-points, after a period in which someone could have noticed. This module exists because of that sentence.
Learning outcomes
- UG State the leading causes of death in children under five, globally and in India, and explain why most are preventable at first contact.
- UG Describe the deterioration continuum — well, compensated, decompensated, arrest — and name the two final common pathways to paediatric cardiac arrest.
- UG/PG Distinguish recognition failure, diagnostic error and execution failure, and match each to the fix that actually addresses it.
- PG Critique the evidence for structured recognition systems (ETAT, PEWS), including the negative EPOCH trial, and read it across the resource gradient.
1 · The mortality picture Must-know
Under-five mortality has fallen steeply over three decades, but the deaths that remain concentrate into a short list. Beyond the neonatal period the largest contributors are pneumonia, diarrhoea, malaria, injuries and infection in a malnourished child. Within the neonatal period, prematurity, intrapartum-related events and neonatal infection dominate.
Two facts should shape how you read the rest of this module:
- Death clusters early. A large share of in-hospital paediatric deaths happen within 24 hours of arrival — many within the first few hours. The window in which recognition changes the outcome is measured in minutes to hours, not days.
- The pathway is respiratory or circulatory, not primarily cardiac. Children rarely have a primary arrhythmic arrest. Paediatric cardiac arrest is usually the end of progressive respiratory failure or shock. That is good news: there is a long, visible, interruptible runway before arrest.
India lens
India's neonatal period now accounts for the majority of under-five deaths, which is why Unit 17 (the sick young infant) is core, not optional. First contact for a sick child is frequently not a paediatrician: it is an ASHA, an ANM, a PHC medical officer, a general practitioner or a private clinic. IMNCI and F-IMNCI exist precisely to push structured recognition down to that level. A module that teaches only PICU-grade assessment teaches the wrong end of the pathway — recognition at first contact and safe referral save far more lives than any single ICU intervention.
Mortality figures change every year. Quote current Sample Registration System (SRS) bulletins and national cause-of-death estimates, not a number remembered from a lecture.
2 · The deterioration continuum Must-know
WELL
│ insult: infection · dehydration · obstruction · toxin · trauma · metabolic
▼
COMPENSATED tachycardia · tachypnoea · cool peripheries · CRT > 2 s
│ anxious, clingy or quiet · NORMAL blood pressure
│ ▸ this is where you win
▼
DECOMPENSATED hypotension · altered sensorium · mottling
│ weak central pulses · falling respiratory effort
│ ▸ hours of physiological credit already spent
▼
PERI-ARREST bradycardia · gasping · unresponsive
▼
ARREST usually asystole or PEA · survival poor
The clinically decisive point is that a child's blood pressure is a late and treacherous sign. Children hold their blood pressure with vigorous tachycardia and vasoconstriction until compensation fails — abruptly. A normal blood pressure in a tachycardic, cold, unwell child is not reassurance. It is a compensating child, and compensation is a countdown.
The error clinicians actually make
“BP was 96/60, so I wasn't worried.” Hypotension in a child is a pre-terminal sign; in haemorrhage it may not appear until roughly a third of the circulating volume is gone. Treat the heart rate, the capillary refill, the skin temperature and the sensorium — not the number on the cuff.
3 · Three different failures, three different fixes Good-to-know UG/PG
| Failure | What happened | What fixes it |
|---|---|---|
| Recognition failure | The abnormal physiology was present and recordable, but nobody registered it as abnormal — or registered it and did not escalate. | Structured assessment (PAT, ETAT), track-and-trigger charts, mandated escalation, and permission for nurses and parents to escalate. |
| Diagnostic error | The physiology was noticed; the cause was misattributed — DKA called gastroenteritis, myocarditis called bronchiolitis. | Illness scripts, a forced alternative diagnosis, a diagnostic time-out, follow-up loops. |
| Execution failure | Recognised and diagnosed, but the treatment was late, wrongly dosed or unavailable. | Pre-calculated dose charts, checklists, simulation, and oxygen and drug supply chains. |
Parts A and B of this module attack recognition failure. Parts C and D attack diagnostic and execution error for the conditions that kill most often. Part E attacks the systems around them. Deciding which of the three is your own department's real problem is a worthwhile first act of quality improvement.
4 · Does structured recognition work? Read the negative trial too Nice-to-know PG
Evidence note
ETAT in low-resource hospitals. Introducing structured emergency triage, with training and supervision, has been associated with substantial falls in early in-hospital paediatric mortality in several African and Asian hospitals. The mechanism is simple: a queue is replaced by a triage decision.
PEWS in well-resourced hospitals. The EPOCH cluster-randomised trial (Parshuram et al., JAMA 2018; 21 hospitals in 7 countries, over 144,000 admissions) found that the Bedside Paediatric Early Warning System did not reduce all-cause hospital mortality compared with usual care.
How to reconcile them. A track-and-trigger tool adds value in proportion to the surveillance gap it fills. On a tertiary ward with 1:2 nursing and a rapid response team the marginal gain is small. On a 60-bed district ward with two night nurses and no triage, the same tool can be transformative. Do not carry a negative trial's conclusion across a resource gradient — in either direction. It is a habit of appraisal you will need again for FEAST in Unit 8.
A 3-year-old has had fever and poor feeding for three days. Heart rate 168/min, respiratory rate 46/min, BP 98/62 mmHg, capillary refill 4 seconds, cool knees; irritable but consolable. Which statement is most accurate?
Nudge
Which of the findings here does the body sacrifice first, and which does it protect to the very end?
Structured hint
Look at the perfusion findings — capillary refill, skin temperature, behaviour — separately from the blood pressure. If they are abnormal while the pressure is normal, what word describes that state?
Why the answer is what it is
Tachycardia plus delayed capillary refill plus cool peripheries plus altered behaviour is inadequate tissue perfusion, with blood pressure still held up by compensation. That is compensated shock, and it is the stage at which treatment works best.
A registrar reviewing ward deaths finds that in three of five cases the observation charts showed rising heart and respiratory rates for six to ten hours before the arrest call, but no one was called. The correct diagnoses were made at the arrest. What is the principal failure, and the fix most likely to prevent the next one?
Nudge
The physiology was on paper for hours. The diagnosis was right. So where did the chain break?
Structured hint
Sort the failure into one of three bins: not seeing the danger, misnaming it, or acting on it too slowly. Here the numbers were seen and recorded — were they registered as abnormal and escalated?
Why the answer is what it is
The abnormal physiology was recorded and not acted on: that is recognition failure. The fix is to make abnormality impossible to miss and escalation automatic — age-specific thresholds printed on the chart, and a defined response when one is crossed.
▸Unit 2 The sixty-second assessment Not attempted
Before you touch the child, before the thermometer, before the history, you look and listen from the doorway. Done properly it takes under a minute, needs no equipment, and decides the next hour.
Learning outcomes
- UG Perform a Paediatric Assessment Triangle and convert the result into a physiological category and a first move.
- UG Apply WHO ETAT to sort any arriving child into emergency, priority or queue, and name every emergency sign from memory.
- UG Use age-specific normal ranges for heart rate, respiratory rate and systolic blood pressure, and the formula for hypotension in children aged 1–10 years.
- PG Choose and defend a track-and-trigger tool for a given ward, including its escalation response and a carer-concern trigger.
1 · The Paediatric Assessment Triangle Must-know
The PAT is purely observational and hands-off. Its three sides are Appearance, Work of breathing and Circulation to skin. It answers two questions — how sick? and which system? — before any history or investigation.
| Side | What you look for |
|---|---|
| Appearance (TICLS) | Tone — limp or resisting · Interactivity — reaches, plays, tracks · Consolability — settles with the carer · Look/gaze — fixes on you, or stares blankly · Speech/cry — strong, weak, high-pitched or absent |
| Work of breathing | Noises without a stethoscope (stridor, grunting, wheeze) · abnormal position (tripod, sniffing, refusing to lie flat) · recession (subcostal, intercostal, suprasternal) · nasal flaring · head bobbing in infants |
| Circulation to skin | Pallor · mottling · cyanosis |
| Appearance | Breathing | Circulation | Category | First move |
|---|---|---|---|---|
| Normal | Normal | Normal | Stable | History and examination |
| Normal | Abnormal | Normal | Respiratory distress | Oxygen, position of comfort, find the cause |
| Abnormal | Abnormal | Normal | Respiratory failure | Support ventilation now |
| Normal | Normal | Abnormal | Compensated shock | Access, fluid decision, find the cause |
| Abnormal | Normal | Abnormal | Decompensated shock | Resuscitate immediately |
| Abnormal | Normal | Normal | Primary brain or metabolic problem | Glucose, seizures, toxins, infection, raised pressure |
| Abnormal | Abnormal | Abnormal | Cardiopulmonary failure | Full resuscitation; arrest is imminent |
Pearl
The row most often missed on wards is abnormal appearance with normal breathing and normal circulation. That child has a brain or metabolic problem — hypoglycaemia, meningitis or encephalitis, poisoning, non-convulsive seizures, intussusception with lethargy, or an inborn error decompensating. Check a glucose before anything else.
2 · WHO ETAT: emergency, priority, queue Must-know
ETAT is WHO's triage system for facilities where children arrive in numbers and wait. Its strength is that a trained nurse or health worker can perform it at the door, without investigations, in under a minute.
Text version
EMERGENCY SIGNS ▸ treat NOW, do not queue
A Airway obstructed or absent breathing
B Breathing severe respiratory distress · central cyanosis
C Circulation cold hands WITH capillary refill > 3 s
AND a weak, fast pulse
C Coma unconscious (AVPU: responds only to pain, or not at all)
C Convulsing now
D Dehydration severe, in a child with diarrhoea: any two of
lethargy · sunken eyes · very slow skin pinch
(Check for severe malnutrition before giving IV fluid)
PRIORITY SIGNS ("3 TPR MOB") ▸ front of the queue, assess quickly
Tiny baby (under 2 months) · Temperature (very high)
Trauma or urgent surgical condition · Pallor (severe)
Poisoning · Pain (severe) · Respiratory distress
Restless, irritable or lethargic · Referral (urgent)
Malnutrition (visible severe wasting) · Oedema of both feet
Burns (major)
NON-URGENT ▸ queue and see in turnEvidence note
WHO's Paediatric emergency triage, assessment and treatment: care of critically-ill children (2016) updated the ETAT materials and the Pocket Book, with recommendations on oxygen, fluids for shock, and anticonvulsants. Where it has been implemented with training and supervision, ETAT has repeatedly been associated with lower early in-hospital mortality. Note the qualifier: a triage poster on a wall is not a triage system.
3 · Vital signs you must know cold Must-know
Charts are safer than memory, but at 3 a.m. with a crashing child you need approximate ranges instantly. Learn the bands, then check the chart.
| Age | Heart rate, awake (/min) | Respiratory rate (/min) | Hypotension: systolic below |
|---|---|---|---|
| Under 1 month | 100–205 | 30–60 | 60 mmHg |
| 1–12 months | 100–190 | 30–53 | 70 mmHg |
| 1–2 years | 98–140 | 22–37 | 70 + (2 × age in years) mmHg |
| 3–5 years | 80–120 | 20–28 | 70 + (2 × age in years) mmHg |
| 6–10 years | 75–118 | 18–25 | 70 + (2 × age in years) mmHg |
| Over 10 years | 60–100 | 12–20 | 90 mmHg |
Two things to carry without a chart: hypotension in a child aged 1–10 years is a systolic pressure below 70 + (2 × age in years) mmHg, and the IMNCI fast-breathing thresholds: ≥60/min under 2 months, ≥50/min at 2–11 months, ≥40/min at 1–5 years.
The crying child
Counting a screaming toddler's respiratory rate. Count over a full 60 seconds in a calm child — a rate counted for 15 seconds and multiplied by four is unreliable in infants, who breathe periodically. If the child settles on a parent's shoulder, count then.
4 · Track-and-trigger charts: what makes them work Good-to-know UG/PG
Paediatric Early Warning Scores turn repeated observations into an escalation trigger. Whichever tool you use, three design features matter more than the score itself:
- A mandated response, not just a number. A given score must bring a named level of skill within a named time.
- A carer and nurse override. “I am worried about this child” must be a legitimate trigger on its own. Parental concern independently predicts deterioration.
- A feedback loop. Every arrest and unplanned PICU transfer is reviewed against the preceding twelve hours of observations.
Ideal setting
- An electronic PEWS with automatic alerts to a rapid response team
- Continuous monitoring on high-dependency beds; scores recalculated with every observation set
- Audit of trigger-to-review time reported monthly
Resource-constrained setting
- ETAT triage at the door by a trained nurse
- A paper observation chart with age-specific abnormal thresholds printed in colour
- A written escalation ladder at the nursing station, and a standing instruction that any emergency sign means a doctor now
- A “worried” box on the chart that any nurse or parent can tick
India lens
A full electronic PEWS is unrealistic in most district hospitals. The defensible minimum — ETAT at the door, a colour-banded chart and a written escalation ladder — costs almost nothing and attacks the recognition gap directly. Several state programmes and the F-IMNCI facility package already expect triage at the point of entry; a chart makes it continue after admission.
At the door of a busy district-hospital OPD, a 14-month-old with four days of diarrhoea is lethargic, has sunken eyes and a very slow skin pinch. Hands are warm and capillary refill is 2 seconds. There is no visible severe wasting. What is the correct ETAT category?
Nudge
ETAT's “D” is its own emergency sign, separate from “C”. What does it require?
Structured hint
Severe dehydration in a child with diarrhoea needs any two of three signs: lethargy or unconsciousness, sunken eyes, very slow skin pinch. Count how many this child has.
Why the answer is what it is
This child has all three signs of severe dehydration, which is an ETAT emergency sign in its own right. The child is treated now, not queued.
A 4-year-old sits upright on her mother's lap refusing to lie down. She has audible inspiratory stridor and suprasternal recession, is alert and watching you, and her skin colour is normal. What is her PAT category, and your first move?
Nudge
Which side of the triangle tells you the brain is still getting enough oxygen?
Structured hint
Appearance is normal, work of breathing is abnormal, circulation is normal. Match that to the table — then ask what could make an upper-airway problem suddenly worse.
Why the answer is what it is
Normal appearance with increased work of breathing is respiratory distress: she is compensating. With stridor, the priority is not to precipitate complete obstruction — position of comfort, oxygen she will tolerate, and senior airway help before any upsetting intervention.
▸Unit 3 Why children crash late and fast Not attempted
Every difference between adult and paediatric emergency practice traces back to a handful of anatomical and physiological facts. Learn the facts and the protocols stop needing to be memorised.
Learning outcomes
- UG Explain from first principles why airway obstruction, hypoxia, hypoglycaemia and hypothermia develop faster in small children.
- UG Explain why infant cardiac output is rate-dependent and why bradycardia in a sick infant is an emergency.
- UG/PG Recognise the tiring child — the falling respiratory rate that means exhaustion, not recovery.
- PG Apply named forcing strategies against anchoring, premature closure and attribution in a paediatric emergency.
1 · Airway Must-know
- Large occiput. Lying supine flexes an infant's neck and obstructs the airway. Aim for a neutral position in infants (a small roll under the shoulders) and a sniffing position in older children.
- Relatively large tongue, small jaw. The tongue falling back is the commonest cause of airway obstruction in an obtunded child — and a jaw thrust often fixes it completely.
- Narrow airways. Resistance to laminar flow rises with the fourth power of the fall in radius. In a 4 mm infant trachea, 1 mm of circumferential swelling halves the radius and multiplies resistance about sixteen-fold. The same swelling in an adult trachea is trivial. That one relationship explains croup, bronchiolitis and why a crying child with an inflamed airway can decompensate in seconds.
- Nose-breathing in young infants. Nasal blockage alone can cause real distress and feeding failure. Saline drops and gentle suction are genuine therapy.
2 · Breathing Must-know
- High oxygen consumption, small reserve. Infants consume roughly twice as much oxygen per kilogram as adults, with a proportionally smaller functional residual capacity. They desaturate on apnoea dramatically faster; pre-oxygenation buys seconds, not minutes.
- Compliant chest wall, diaphragm-dependent breathing. Recession is prominent and ventilation inefficient. A distended stomach splints the diaphragm — which is why gastric decompression matters during bag-mask ventilation.
- A diaphragm that tires. Sustained high work of breathing ends in exhaustion.
The most dangerous sign in paediatrics
A tiring child looks calmer. Recession lessens, the respiratory rate falls, the child goes quiet and drowsy, and inexperienced observers relax. In a child who was working hard, a falling rate with a falling level of consciousness is pre-arrest. Reassess — do not relax. Get a blood gas and senior help.
3 · Circulation Must-know
- Cardiac output = stroke volume × heart rate. The infant heart has limited ability to raise stroke volume, so output depends largely on rate. Bradycardia in a sick infant is functionally an arrest state, and its commonest cause is hypoxia. Treat it with oxygen and ventilation first; atropine is for vagally mediated bradycardia or primary heart block, not the hypoxic kind.
- Vigorous vasoconstriction. Blood pressure is defended at the expense of the skin and gut: cold peripheries, delayed capillary refill and a narrow pulse pressure appear long before hypotension.
- Small absolute blood volume — about 80 mL/kg in infants and 70 mL/kg in children. A 10 kg child has roughly 800 mL of blood. Modest-looking bleeding or third-spacing is proportionally large; so is repeated blood sampling in a small infant.
4 · Everything else that scales with size Good-to-know
| Property | Paediatric difference | What it means at the bedside |
|---|---|---|
| Surface area to mass | Much higher, especially in neonates | Rapid heat and water loss. Hypothermia during resuscitation and transport is common, and it worsens acidosis and coagulopathy. Cover the head. |
| Glycogen stores | Small, with high glucose demand | Hypoglycaemia within hours of poor intake or any critical illness. Check glucose in every sick child. |
| Renal concentrating ability | Immature in infants | Poor tolerance of both fluid restriction and solute load; dehydration develops fast. |
| Immunity | Immature, especially under 3 months | Serious bacterial infection presents non-specifically; fever may be absent or replaced by a low temperature. |
| Skeleton | Pliable, incompletely ossified | Serious chest or abdominal injury without fractures. Rib fractures in an infant imply major force or abuse. |
| Communication | Pre-verbal or limited | Behaviour is the symptom. A parent saying “he is not himself” carries diagnostic weight. |
5 · How the sick child fools you Nice-to-know PG
Emergency paediatrics runs on fast, pattern-based reasoning — mostly right, and where the errors live. Telling yourself to “be less biased” does not work. Structural forcing strategies do.
| Bias | How it looks in a sick child | Forcing strategy |
|---|---|---|
| Anchoring, premature closure | Referred as “bronchiolitis”: the 4-month-old's wheeze and big liver turn out to be myocarditis or a VSD in failure. | Ask aloud: “If this is not X, what else fits every finding?” Name one alternative before acting. |
| Search satisficing | A fracture found on the trauma series; the splenic injury missed. | Finish the systematic survey even after the first abnormality. |
| Availability | A dengue outbreak: every fever with low platelets becomes dengue, and enteric fever, malaria and rickettsial illness are missed. | “What else is in season, and what is the one I must not miss?” |
| Triage cueing | A “non-urgent” label at the door reduces the effort of every later examination. | Re-triage at every contact; the child at 8 p.m. is not the child at 6 p.m. |
| Attribution | A child with cerebral palsy: new signs attributed to the known condition. | Assume a new symptom has a new cause until proven otherwise. |
Pearl
The diagnostic time-out. Before leaving any sick child, ask: What is my diagnosis? What does not fit? What is the worst thing this could be, and have I excluded it? What must happen if the child worsens, and who will do it? Thirty seconds. It catches more errors than any checklist you will be given.
A 6-month-old with bronchiolitis has had severe recession for six hours. On review the recession is less marked, the respiratory rate has fallen from 70 to 34/min, and the infant is sleepy and not feeding. SpO₂ is 92% on oxygen. What is the most appropriate interpretation?
Nudge
What does a falling respiratory rate mean when the level of consciousness is falling with it?
Structured hint
Put the three changes together: less recession, a much slower rate, and a sleepier infant who will not feed. Does a recovering infant become less interested in feeding?
Why the answer is what it is
In an infant who has been working hard for hours, less effort plus a falling rate plus a falling level of consciousness is exhaustion — decompensation. An SpO₂ of 92% on oxygen is not reassuring: it means the oxygen is barely keeping up. This infant needs respiratory support, a blood gas and senior review now.
A 2-month-old brought in with a week of cough and poor feeding has a heart rate of 54/min, is mottled and barely responsive. SpO₂ does not register. What is the first intervention?
Nudge
In infants, what is the commonest cause of a slow heart?
Structured hint
Infant cardiac output is rate-dependent, and bradycardia in a sick infant is usually hypoxic. Which option treats the cause rather than the number?
Why the answer is what it is
Bradycardia with poor perfusion in an infant is hypoxic until proven otherwise, and because infant output depends on rate it is functionally an arrest state. Oxygenate and ventilate first. If the heart rate stays below 60/min with poor perfusion despite effective ventilation, start chest compressions and give epinephrine (PALS 2025).
The systematic approach: ABCDE
Airway before breathing, breathing before circulation — not because the later letters matter less, but because failure at each step makes the next impossible to fix. Part B builds the spine that every emergency in Parts C and D hangs on.
▸Unit 4 Airway and breathing Not attempted
A child with a patent airway and adequate oxygenation has time. Almost everything else in paediatric resuscitation is buying that time back.
Learning outcomes
- UG Open and maintain a child's airway with positioning, suction and simple adjuncts, and deliver effective bag-mask ventilation.
- UG Classify a breathing problem into one of four patterns and name the first action for each.
- UG Distinguish respiratory distress from respiratory failure, and act on the difference.
- UG/PG Choose an oxygen delivery device and a saturation target, and escalate through high-flow, CPAP and ventilation by mechanism.
- PG Plan a safe paediatric intubation for a shocked or acidotic child, including the physiology that makes induction dangerous.
1 · Four patterns of respiratory illness Must-know
Classify the pattern before you name the disease. The pattern dictates the first action, often before you know the diagnosis.
| Pattern | Hallmarks | Typical causes | First priority |
|---|---|---|---|
| Upper-airway obstruction | Inspiratory stridor, hoarse or muffled voice, drooling, tripod or sniffing posture | Croup, foreign body, retropharyngeal abscess, anaphylaxis, epiglottitis, inhalational burn | Do not upset the child. Position of comfort, oxygen as tolerated, airway help. Nebulised adrenaline for severe croup; IM adrenaline for anaphylaxis. |
| Lower-airway obstruction | Expiratory wheeze, prolonged expiration, hyperinflation | Asthma, bronchiolitis, aspiration, lower foreign body | Oxygen; bronchodilators and steroids for asthma; supportive care for bronchiolitis |
| Lung tissue disease | Grunting, crackles, focal signs, hypoxaemia out of proportion to effort | Pneumonia, paediatric ARDS, pulmonary oedema, drowning | Oxygen, then distending pressure (CPAP/PEEP); treat the cause |
| Disordered control of breathing | Irregular, shallow or apnoeic breathing, or unusually deep breathing, with effort that does not match the physiology | Raised intracranial pressure, poisoning, post-ictal state, metabolic acidosis (deep Kussmaul breathing), neuromuscular disease | Support ventilation and treat the brain or metabolic cause. Oxygen alone is not enough. |
Pearl
Grunting is expiration against a partly closed glottis: the child is making their own PEEP to keep collapsing alveoli open. It means significant lung disease — or, in a young infant, sepsis, pain or acidosis. Never dismiss a grunting child.
2 · Distress or failure Must-know
| Respiratory distress | Respiratory failure | |
|---|---|---|
| Appearance | Alert, anxious, interactive | Agitated, then drowsy, then unresponsive |
| Effort | Increased and sustained | Increased then falling — or inadequate from the start |
| Rate | Fast | Very fast, or slowing, irregular, apnoeic |
| Oxygenation | Maintained on modest oxygen | Hypoxaemia despite oxygen; cyanosis |
| Action | Oxygen, treat the cause, watch closely | Assist ventilation now — bag-mask, then an advanced airway |
The transition from distress to failure is the tiring child of Unit 3. The two signs that mark it are a falling level of consciousness and a falling respiratory rate without clinical improvement.
3 · Opening and supporting the airway Must-know
1. POSITION infant: neutral, small shoulder roll · child: sniffing
trauma: jaw thrust with manual in-line stabilisation
2. CLEAR gentle suction under direct vision · no blind finger sweep
3. ADJUNCT oropharyngeal airway if unconscious with no gag
(size: incisors to angle of jaw; insert the right way up
in young children, with a tongue depressor)
nasopharyngeal airway if a gag is present and no base-of-
skull injury is suspected
4. VENTILATE bag-mask with reservoir and high-flow oxygen
E-C grip · watch the CHEST rise, not the bag
respiratory arrest with a pulse: 1 breath every 2–3 s
5. DECOMPRESS gastric tube · a full stomach splints the diaphragm
6. ESCALATE supraglottic airway or tracheal tube by a competent
operator · confirm with waveform capnography
What current resuscitation guidance says
Current AHA/AAP paediatric guidance: ventilate infants and children in respiratory arrest with a pulse, or during CPR with an advanced airway, at one breath every 2–3 seconds (20–30/min); cuffed tracheal tubes are acceptable in infants and children, with cuff pressure monitored; routine cricoid pressure during intubation is not recommended. Cardiac arrest management itself is covered in the Vikkypaedia PALS module.
4 · Oxygen: how much, how delivered Must-know
| Device | Approximate FiO₂ | Use it for |
|---|---|---|
| Nasal prongs (0.5–1 L/min infant; 1–2 L/min child) | 0.3–0.4 | Mild hypoxaemia in a child who is feeding |
| Simple face mask (≥5 L/min, to prevent rebreathing) | 0.35–0.6 | Moderate distress |
| Non-rebreathing mask with reservoir (10–15 L/min) | 0.6–0.9 | Severe hypoxaemia, shock, resuscitation |
| High-flow nasal cannula (about 1–2 L/kg/min) | Titratable to 1.0 | Bronchiolitis, pneumonia — dead-space washout and modest distending pressure |
| Bubble CPAP or CPAP/NIV | Titratable | Alveolar collapse, severe pneumonia or bronchiolitis in infants |
| Bag-mask, with or without a tracheal tube | Up to 1.0 | Respiratory failure, apnoea, arrest |
When to give oxygen. WHO recommends oxygen for children with emergency signs, and for any child with SpO₂ below 90%. In acutely unwell children most services target SpO₂ of 92–94% or above; aim higher during active resuscitation, and accept lower individualised targets in cyanotic heart disease. Wean deliberately, and never leave a child on high-flow oxygen without monitoring.
India lens
The commonest failure is supply, not prescription: an empty cylinder, no flow-splitter, no paediatric masks or prongs, no working pulse oximeter. WHO's 2016 ETAT update addressed oxygen flow rates and humidification for exactly this reason, and India's post-2021 investment in PSA oxygen plants changed what many district hospitals can deliver. Auditing “was oxygen available and correctly delivered?” is often a higher-yield improvement project than any protocol change.
5 · Supporting the failing airway, across settings Must-know
Ideal setting
- Piped, blended oxygen; continuous pulse oximetry and waveform capnography on every supported child
- Stepwise escalation: prongs, then high-flow, then CPAP or NIV, then intubation and lung-protective ventilation
- A blood gas guides the decision; a video laryngoscope and an anaesthetist are minutes away
- The decision to intubate is made early and electively, before exhaustion
Resource-constrained setting
- Oxygen is the intervention. A concentrator or cylinder, a flow-splitter, a pulse oximeter and correctly sized interfaces — check they exist before the next sick child arrives
- Position of comfort on a parent's lap does much of what equipment does
- Bubble CPAP, run by trained staff, is an evidence-supported option for infants with severe pneumonia or bronchiolitis where ventilation is unavailable
- If you cannot ventilate beyond bag-mask, the decision is when to transfer, not whether to intubate. Make it while the child is still compensating (Unit 20)
- Bag-mask ventilation done well is a legitimate destination, not a failure. Intubating a child you then cannot ventilate or monitor can turn a survivable illness into an arrest
6 · Intubating the sick child safely Good-to-know PG
Choose support by mechanism. High-flow helps where dead-space washout and mild distending pressure are enough. CPAP treats alveolar or upper-airway collapse. NIV helps inadequate tidal ventilation with rising CO₂. Intubation is for airway protection, refractory hypoxaemia or hypercapnia, exhaustion, shock unresponsive to resuscitation, and safe transfer.
Physiological difficulty
A shocked or acidotic child can arrest at induction. Loss of sympathetic drive, positive-pressure ventilation reducing venous return, and apnoea worsening acidosis all arrive at the same moment. Resuscitate before you intubate where you possibly can: correct volume, start a vasoactive if needed, choose a haemodynamically gentler induction agent, have a push-dose vasopressor drawn up, and pre-oxygenate.
- Tube size: cuffed, (age/4) + 3.5 mm; uncuffed, (age/4) + 4 mm. Depth at the lips is roughly three times the internal diameter.
- Confirm with waveform capnography plus chest rise and auscultation; secure; X-ray.
- DOPES for sudden deterioration in a ventilated child: Displacement · Obstruction · Pneumothorax · Equipment failure · Stomach distension.
A 2-year-old starts coughing and has noisy breathing while eating peanuts. She is distressed but coughing forcefully and able to cry and speak. What is the best immediate action?
Nudge
What can a forceful cough do that no manoeuvre you perform can match?
Structured hint
Foreign-body manoeuvres are for an ineffective cough — silent, unable to cry, speak or breathe. Is her cough effective?
Why the answer is what it is
An effective cough generates higher airway pressure than any external manoeuvre. Do not interfere: keep her calm, give oxygen if she tolerates it, and arrange urgent assessment and bronchoscopy with airway help ready in case she deteriorates.
A 9-month-old with pneumonia on nasal prong oxygen at 1 L/min has SpO₂ of 86%, grunting and severe chest indrawing, but is awake and taking a few feeds. The district hospital has no ventilator; the nearest PICU is four hours away by road. What is the most appropriate next step?
Nudge
Grunting tells you what the lungs need. What is the infant trying to generate for himself?
Structured hint
He needs distending pressure, not just more oxygen, and the decision that matters most in a setting without a ventilator is about timing. Which option does both?
Why the answer is what it is
Grunting and hypoxaemia despite oxygen mean alveolar collapse: he needs distending pressure, which bubble CPAP provides and which is evidence-supported for infants with severe pneumonia where ventilation is unavailable. The other decision is transfer while he is still compensating — not after he tires.
▸Unit 5 Circulation: recognising shock and its types Not attempted
Shock is not low blood pressure. Shock is inadequate delivery of oxygen and fuel to tissues relative to demand. A child can be deeply shocked with a textbook blood pressure.
Learning outcomes
- UG Recognise compensated and decompensated shock at the bedside without laboratory support.
- UG Classify shock as hypovolaemic, distributive, cardiogenic or obstructive, and state the treatment that differs for each.
- UG/PG Perform the fifteen-second cardiac check before any bolus, and explain why it prevents a recognisable category of death.
- PG Use lactate and the Phoenix cardiovascular criteria appropriately, knowing what each can and cannot tell you.
1 · Recognising shock from three organs Must-know
Shock is a clinical diagnosis made from the perfusion of three organs you can examine at the bedside: the brain (level of consciousness, interaction), the skin (temperature gradient, capillary refill, mottling) and the kidney (urine output: below 1 mL/kg/h in infants and young children, below 0.5 mL/kg/h in adolescents).
| Sign | Compensated | Decompensated |
|---|---|---|
| Heart rate | Tachycardia | Extreme tachycardia, then bradycardia (pre-terminal) |
| Blood pressure | Normal; narrow pulse pressure | Hypotension |
| Pulses | Weak peripheral pulses (bounding in warm shock) | Absent peripheral, weak central pulses |
| Capillary refill | Over 2–3 s (cold shock) or flash under 1 s (warm shock) | Markedly prolonged; mottling |
| Sensorium | Irritable, anxious, clingy | Lethargic, unresponsive |
| Urine output | Reduced | Anuric |
Know the limits of your best sign
Capillary refill has limits. It varies with room temperature, site, pressure and observer, and performs modestly on its own. Use it as one sign in a cluster and as a trend by the same observer. Standardise: sternum or fingertip at heart level, five seconds of pressure, in a warm room.
2 · Four types of shock — because treatment diverges Must-know
| Type | Mechanism | Paediatric causes | Clues | What changes |
|---|---|---|---|---|
| Hypovolaemic (commonest) | Low preload | Diarrhoea, DKA, burns, haemorrhage, dengue plasma leak | History of losses, dry mucosa, sunken eyes or fontanelle | Volume is the treatment |
| Distributive | Low vascular tone, maldistribution | Sepsis, anaphylaxis, spinal injury | Warm peripheries, flash refill, wide pulse pressure; fever, urticaria or wheeze | Fluid plus early vasoactive; IM adrenaline first in anaphylaxis |
| Cardiogenic | Pump failure or arrhythmia | Myocarditis, cardiomyopathy, congenital heart disease, SVT, duct-dependent lesion in a neonate, scorpion envenomation | Big liver, gallop, crackles, raised JVP; worsens with fluid | Small cautious volume or none; inotrope; treat the rhythm; prostaglandin for a duct-dependent neonate |
| Obstructive | Mechanical block to flow | Tension pneumothorax, tamponade, critical coarctation | Absent breath sounds with tracheal shift; muffled heart sounds with distended neck veins; weak femoral pulses | Fluid will not fix it: needle decompression, pericardiocentesis, prostaglandin |
The habit that saves the most lives in this unit
The fifteen-second cardiac check. Before every bolus in an undifferentiated shocked child: feel for the liver edge, listen for a gallop, listen for crackles, look at the neck veins. A big liver in a shocked child means think cardiogenic — and a 20 mL/kg bolus may kill. This single habit prevents the recognisable death of the “septic” infant with myocarditis or a duct-dependent lesion who arrests after fluid.
3 · Warm and cold shock Good-to-know UG/PG
In septic shock, children more often present cold — high systemic resistance, low cardiac output, prolonged capillary refill and cool, mottled limbs. Adults and adolescents more often present warm — low resistance, flash refill and bounding pulses. The distinction is imperfect and can change within hours, which is why reassessment after every intervention matters more than the initial label. It remains useful for one decision: which vasoactive to start when fluid is not enough (Unit 10).
4 · Lactate and the Phoenix criteria Nice-to-know PG
The 2026 Surviving Sepsis Campaign paediatric guideline makes a strong recommendation to measure lactate as part of the initial evaluation. Use it to support recognition and to track response — never to delay treatment of a child who is clinically shocked.
The Phoenix criteria (JAMA 2024) define paediatric sepsis as suspected infection with a Phoenix Sepsis Score of at least 2, and septic shock as sepsis with at least one cardiovascular point. Cardiovascular points come from vasoactive medication, lactate and age-adjusted mean arterial pressure.
| Cardiovascular component | 1 point | 2 points |
|---|---|---|
| Vasoactive medications | One | Two or more |
| Lactate (mmol/L) | 5–10.9 | 11 or more |
| Mean arterial pressure (mmHg), by age | Below the age threshold (e.g. under 1 month: 17–30; 1–11 months: 25–38; 1–2 years: 31–43) | Below the lower threshold (e.g. under 1 month: <17; 1–11 months: <25; 1–2 years: <31) |
Misusing a definition as a trigger
Using Phoenix to decide whether to treat. Phoenix was built to classify children with established organ dysfunction for research and reporting, largely from data in resourced hospitals. It is not a bedside screening tool, and a child with suspected sepsis who does not yet meet it still needs antibiotics and careful fluid decisions now. The 2026 guideline itself accepts evidence based on either the older 2005 criteria or Phoenix.
A 5-month-old has poor feeding and fast breathing. Heart rate 210/min, cool peripheries, capillary refill 4 seconds. The liver is 4 cm below the costal margin and there is a gallop rhythm. A colleague is drawing up 20 mL/kg of saline. What do you advise?
Nudge
What did the fifteen-second cardiac check find?
Structured hint
A big liver and a gallop in a shocked infant point to one type of shock. And a heart rate of exactly 210 that does not vary — what rhythm should you exclude before anything else?
Why the answer is what it is
Hepatomegaly plus a gallop in a shocked infant means cardiogenic shock — myocarditis, cardiomyopathy, a duct-dependent lesion, or SVT causing failure. A standard 20 mL/kg bolus can precipitate pulmonary oedema and arrest. Get an ECG (an invariant 210 suggests SVT, treated with vagal manoeuvres or adenosine, not fluid), give at most a small, cautious aliquot, and prepare an inotrope.
A 7-year-old with 3 days of fever has heart rate 150/min, capillary refill 5 seconds, cool mottled legs and is drowsy. BP 102/64 mmHg. Point-of-care lactate is not available. Which statement is correct?
Nudge
Which three organs did you examine, and what did each tell you?
Structured hint
Brain (drowsy), skin (5-second refill, mottled, cool) — do these need a laboratory test to be abnormal? And cool mottled legs: warm shock or cold?
Why the answer is what it is
Poor perfusion of brain and skin with a maintained pressure is compensated shock, a clinical diagnosis. Treatment starts now. Lactate is recommended as part of the evaluation and is useful to track the response, but its absence never delays treatment.
▸Unit 6 Disability: the child with altered sensorium Not attempted
A child who is not behaving normally has a brain that is not being perfused, oxygenated or fuelled — or is being poisoned, infected, compressed or is seizing. Those seven words are the differential.
Learning outcomes
- UG Assess and record the level of consciousness with AVPU and the paediatric Glasgow Coma Scale, with pupils and posture.
- UG Perform the first three actions in any child with altered sensorium, beginning with glucose.
- UG/PG Build a structured differential for non-traumatic coma, including the causes that are seasonal and regional in India.
- UG/PG Decide when a lumbar puncture is safe, and give antibiotics without waiting for it when it is not.
1 · The first three actions Must-know
1. ABC FIRST airway at risk if responds only to pain (AVPU "P")
or worse · oxygen · ventilate if breathing is inadequate
2. GLUCOSE bedside capillary glucose in EVERY child with altered
consciousness, seizure or shock ("don't ever forget glucose")
3. LOOK FOR pupils · posture · neck stiffness · fontanelle · rash
THE CAUSE · breath odour · injuries · toxidrome · temperature
If the glucose is low, treat it before anything else (Unit 7). If the child is convulsing, the time-based algorithm in Unit 13 starts now.
2 · Measuring the level of consciousness Must-know
| AVPU | Approximate GCS | Meaning |
|---|---|---|
| Alert | 15 | Normal |
| Responds to Voice | About 13 | Abnormal; find the cause |
| Responds only to Pain | About 8 | ETAT “coma” — an emergency sign. The airway is at risk. |
| Unresponsive | 3 | Airway protection needed now |
AVPU is fast and consistent between observers, which makes it ideal at triage. The paediatric GCS, with modified verbal and motor scales for pre-verbal children, is better for trending, especially after trauma. Record the components as well as the total, and record the trend: a falling score matters more than any single number.
Look also at the pupils (size, symmetry, reaction), posture (decorticate or decerebrate) and breathing pattern. A unilateral fixed dilated pupil, abnormal posturing or a Cushing response (high blood pressure, slow pulse, irregular breathing) means raised intracranial pressure with possible herniation — Unit 13.
3 · The differential for non-traumatic coma Must-know
| Category | Examples | Clues |
|---|---|---|
| Infective | Meningitis, encephalitis (HSV, Japanese encephalitis), cerebral malaria, TB meningitis, scrub typhus, sepsis-associated encephalopathy | Fever, neck stiffness (unreliable under 18 months), bulging fontanelle, rash, eschar, focal seizures, season and region |
| Metabolic | Hypoglycaemia, DKA, sodium disorders, hypocalcaemia, uraemia, liver failure, inborn errors, hyperammonaemia | Deep sighing breathing, ketotic breath, jaundice, big liver, dehydration, consanguinity, decompensation after fasting or illness |
| Toxic | Organophosphates, kerosene, benzodiazepines, opioids, antihistamines, datura, iron, alcohol, traditional preparations | A toxidrome (Unit 12). Ask what is in the house and what was given for this illness. |
| Structural or vascular | Tumour, hydrocephalus or shunt block, haemorrhage, stroke, venous sinus thrombosis | Focal deficit, asymmetric pupils, morning headache and vomiting, a shunt in place |
| Epileptic | Post-ictal state, non-convulsive status | Subtle eye deviation, nystagmus, twitching; obtundation that does not lift |
| Inflammatory | ADEM, autoimmune encephalitis, MIS-C, HLH | Recent infection, movement disorder, behavioural change, multi-organ involvement |
| Hypoxic-ischaemic | After arrest, drowning, severe shock | The event itself |
India lens
A child with fever and altered sensorium meets the Acute Encephalitis Syndrome surveillance definition and must be notified. The likely causes shift with season and region: Japanese encephalitis, dengue, scrub typhus, cerebral malaria, enteroviruses and, in particular districts and seasons, hypoglycaemic encephalopathy linked to litchi consumption in undernourished children. Scrub typhus deserves a low threshold for empirical doxycycline or azithromycin — look for the eschar (Unit 7).
4 · When is a lumbar puncture safe? Must-know UG/PG
Suspected meningitis needs cerebrospinal fluid — but not at the cost of herniation. Defer the LP if any of these are present:
- Reduced or fluctuating consciousness (GCS below 9, or a fall of 3 or more)
- Focal neurological signs, abnormal posture, or unequal or poorly reactive pupils
- Papilloedema, or a slow pulse with high blood pressure
- Shock, respiratory compromise, a recent seizure that has not settled
- Low platelets or a coagulopathy, or infection over the LP site
The rule that matters more than the list
Never let a deferred LP defer the antibiotics. Take blood cultures, give the first dose of an appropriate antibiotic immediately (with antiviral cover where encephalitis is possible), and do the LP later when it is safe. Cultures after antibiotics are less often positive; PCR and CSF cell counts remain informative.
A 4-year-old is brought in drowsy after two days of vomiting. He opens his eyes and groans to a sternal rub but not to his name. His pupils are equal and reactive. Temperature 37.2 °C. What is the single most important immediate test?
Nudge
Which cause of coma can be diagnosed in thirty seconds, treated in two minutes, and kills if missed?
Structured hint
He responds only to pain (AVPU “P”). Before any imaging or laboratory test, what does the first-three-actions rule say?
Why the answer is what it is
In every child with altered consciousness, check the glucose at the bedside immediately. Hypoglycaemia is common after vomiting and poor intake, is instantly treatable, and causes permanent harm if missed while waiting for other tests.
A 6-year-old with fever and headache for a day has GCS 9, a right pupil larger than the left, heart rate 58/min and BP 138/90 mmHg. Which action is contraindicated right now?
Nudge
Put the slow pulse, the high blood pressure and the unequal pupil together. What is happening inside the skull?
Structured hint
This is a Cushing response with pupillary asymmetry. Which of the four options could precipitate herniation?
Why the answer is what it is
Reduced consciousness, an unequal pupil and a Cushing response mean raised intracranial pressure with possible herniation. A lumbar puncture now is contraindicated. Antibiotics are given immediately after blood cultures — they never wait for CSF — with airway protection, head-up positioning and hyperosmolar therapy (Unit 13).
▸Unit 7 Exposure and the metabolic milieu Not attempted
“E” is where the diagnosis often hides: the purpuric rash under the vest, the eschar in the axilla, the cigarette burn, the swollen scrotum, the glucose of 1.8.
Learning outcomes
- UG Perform a complete exposure survey while preventing heat loss, and say what must be looked for.
- UG Recognise and treat hypoglycaemia, and know when to take a critical sample first.
- UG/PG Recognise and begin treatment of the electrolyte disturbances that kill quickly.
- PG Interpret a paediatric blood gas with the anion gap, and name the emergency behind it.
1 · The exposure survey Must-know
Undress fully, look everywhere, then cover and warm. What a hurried examiner misses:
- Rash. A non-blanching purpuric rash is meningococcal sepsis until proven otherwise. Press with a glass. Look at soles, palms, conjunctivae and behind the ears.
- Eschar. Scrub typhus. Axilla, groin, natal cleft, waistband, behind the ear. It is painless, so it is never reported.
- Genitalia and hernial orifices. Torsion and incarcerated hernia. A vomiting, irritable infant needs the nappy off.
- Back and scalp. Log-roll in trauma; look for injuries, a sacral dimple, lice and scabies.
- Bruises in unusual places — torso, ears or neck in a child aged four or under; any bruise in an infant under four months who is not yet mobile; patterned bruises. Consider inflicted injury (Unit 20).
- Temperature. Measure it. In a young infant or a malnourished child, a low temperature is as ominous as fever.
- Weight. A real weight whenever possible — every dose depends on it.
2 · Glucose Must-know
| What to do | |
|---|---|
| Threshold | WHO: treat a blood glucose below 2.5 mmol/L (45 mg/dL), or below 3 mmol/L (54 mg/dL) in a child with severe malnutrition. Many hospital protocols act at 3.0–3.3 mmol/L in a sick child. Neonates follow neonatal thresholds. |
| Treatment | 10% glucose 5 mL/kg IV or IO (0.5 g/kg), then a glucose-containing infusion, and recheck in 15–30 minutes. Never give 50% glucose to a child — dilute it. |
| Unconscious, no access | Sugar solution or expressed breast milk by nasogastric tube, or sugar under the tongue, while access is obtained. Do not let the search for a vein delay glucose. |
| Critical sample | If hypoglycaemia is unexplained or recurrent, take blood before treatment when you safely can: glucose, ketones (β-hydroxybutyrate), lactate, ammonia, insulin, cortisol, growth hormone, acylcarnitines; and the first urine after the event. It can save years of diagnostic uncertainty. |
Pearl
Hypoglycaemia without ketones means hyperinsulinism or a fatty-acid oxidation defect such as MCAD deficiency. Both are dangerous and both are treatable. Ketotic hypoglycaemia after a fast in a small toddler is far commoner and more benign — but only the critical sample tells them apart.
3 · Electrolytes that kill quickly Must-know UG/PG
| Disturbance | Presentation | Immediate action | Trap |
|---|---|---|---|
| Hyponatraemia (symptomatic, or Na <125) | Seizures, lethargy, vomiting, coma | 3% saline 3–5 mL/kg over 10–20 min, repeated until seizures stop | After symptoms settle, limit the rise to about 8–10 mmol/L in 24 h. Hypotonic maintenance fluid is a leading cause: use isotonic maintenance in hospitalised children. |
| Hypernatraemia (Na >150) | Doughy skin, irritability then lethargy, high-pitched cry | Resuscitate shock with isotonic fluid; then correct slowly, no faster than about 0.5 mmol/L per hour | Rapid correction causes cerebral oedema and seizures. |
| Hyperkalaemia (K >6.5 or ECG changes) | Peaked T waves, then wide QRS, then arrest | 10% calcium gluconate 0.5 mL/kg IV (max 20 mL) to protect the heart; then insulin with glucose, nebulised salbutamol; then removal | A haemolysed sample misleads — but never assume haemolysis in an anuric or crushed child. Get an ECG. |
| Hypocalcaemia | Tetany, stridor from laryngospasm, seizures, long QT | 10% calcium gluconate 0.5–1 mL/kg IV slowly, diluted, with ECG monitoring | Extravasation causes necrosis. Check magnesium: low magnesium makes low calcium refractory. |
Verify infusion concentrations and maximum doses against your unit protocol and Appendix E before use.
4 · Reading the blood gas Good-to-know PG
1. pH acidaemia (< 7.35) or alkalaemia (> 7.45)?
2. PRIMARY high PaCO2 with low pH → respiratory acidosis
low HCO3 with low pH → metabolic acidosis
3. COMPENSATED? compensation is never complete. A normal pH with two
abnormal values suggests a MIXED disorder.
4. ANION GAP Na − (Cl + HCO3); normal about 8–12 mmol/L
RAISED gap: Ketones (DKA, starvation) · Uraemia
Lactate (shock, sepsis, seizures, thiamine
deficiency, inborn errors)
Toxins (salicylate, methanol, iron)
NORMAL gap: diarrhoea · renal tubular acidosis ·
large volumes of 0.9% saline
5. OXYGENATION SpO2/FiO2 or PaO2/FiO2 — used in PARDS and Phoenix
A raised-gap metabolic acidosis in a shocked child is usually lactate — but ask whether it is ketones (DKA presenting as “gastroenteritis with fast breathing”) or a toxin. A normal-gap acidosis after several litres of saline is the saline, and a reason the 2026 sepsis guideline prefers balanced crystalloids (Unit 8).
A 2-year-old admitted with gastroenteritis and given 0.18% saline with 5% glucose as maintenance has a generalised seizure on day two. Sodium is 118 mmol/L. What is the best immediate management?
Nudge
Will an antiseizure drug stop a seizure caused by a low sodium?
Structured hint
Symptomatic hyponatraemia needs a small, fast rise in sodium to stop the seizure — then a slow rise after that. Which option does both?
Why the answer is what it is
Symptomatic hyponatraemia is a neurological emergency. 3% saline 3–5 mL/kg produces the small, rapid rise (a few mmol/L) that usually stops the seizure. After that, correct slowly to avoid osmotic demyelination. The deeper lesson: hypotonic maintenance fluid caused this; isotonic maintenance is the standard for hospitalised children.
A 9-year-old with 6 days of fever, headache and myalgia has been treated for typhoid without response. Platelets are 60,000/µL and ALT is 180 U/L. On exposure you find a painless 6 mm black-crusted lesion in the left axilla. What should you do?
Nudge
What painless lesion, hidden in a skin fold, is never mentioned by the patient?
Structured hint
An eschar plus fever, thrombocytopenia and raised transaminases is a classic cluster. Does a definite eschar need a serology result before treatment?
Why the answer is what it is
A painless black eschar in a skin fold with fever, low platelets and transaminitis is scrub typhus until proven otherwise. Start doxycycline (or azithromycin) now; response is usually within 48 hours. Found only because the child was fully exposed.
Resuscitating shock: the core skill
More preventable child deaths pass through shock than through any other door. This Part is built around the 2026 Surviving Sepsis Campaign paediatric guideline, the FEAST trial, and the one skill that separates good from dangerous shock care: knowing when fluid helps and when it kills.
▸Unit 8 Fluids done right Not attempted
Fluid is the most commonly prescribed and least often reassessed drug in paediatric emergency care. Given well it saves the dehydrated child; given reflexively it has killed febrile children in a large randomised trial. This unit is about the difference.
Learning outcomes
- UG Give a fluid bolus correctly: choice of fluid, aliquot size, speed, and the four reassessment questions after every aliquot.
- UG State the 2026 Surviving Sepsis fluid recommendations for settings with and without intensive care.
- UG/PG Identify the children in whom the standard bolus is wrong: cardiogenic shock, severe malnutrition, severe anaemia and dengue.
- PG Read the FEAST trial critically — what it showed, where it was done, and what it does and does not change in an Indian district hospital.
1 · How to give a bolus Must-know
A fluid bolus is a test with a treatment attached. Give a measured aliquot, then ask whether the child got better, and whether the child can take more.
CHOOSE balanced crystalloid (Ringer's lactate, Plasma-Lyte)
0.9% saline if balanced fluid is not available
not albumin as a first choice · never 5% dextrose
MEASURE 10–20 mL/kg, pushed with a syringe or pressure bag
over 5–20 minutes (gravity is too slow in a small cannula)
REASSESS after EVERY aliquot — four questions:
1. Is the heart rate falling?
2. Is perfusion improving? (refill, skin temperature, pulses)
3. Is the child more alert? Is urine coming?
4. STOP SIGNALS: new crackles · liver edge moving down ·
gallop · rising respiratory rate or work of breathing ·
falling SpO2
REPEAT only if 1–3 are "not yet" and 4 is "none"
Pearl
The fourth question is the one people skip. A liver edge that has moved 2 cm down since the last bolus is the child telling you the heart has had enough. Mark it on the skin with a pen before the first bolus.
2 · What the 2026 Surviving Sepsis guideline recommends Must-know
| Setting and child | Recommendation (strength) |
|---|---|
| Intensive care available, septic shock | Up to 40–60 mL/kg of bolus fluid in the first hour, as 10–20 mL/kg per bolus, titrated to perfusion and stopped for signs of overload (conditional) |
| No intensive care, sepsis without hypotension | No fluid bolus (strong recommendation against). Give maintenance fluid and treat the cause. |
| No intensive care, septic shock with hypotension | Up to 40 mL/kg of bolus fluid in the first hour, 10–20 mL/kg per bolus, with reassessment (conditional) |
| Choice of fluid | Crystalloid rather than albumin (conditional); balanced or buffered crystalloid rather than 0.9% saline (conditional), with saline acceptable if balanced fluid is unavailable |
Source
Weiss SL, Peters MJ, et al. Surviving Sepsis Campaign International Guidelines for the Management of Sepsis and Septic Shock in Children 2026. Pediatr Crit Care Med 2026;27(4):379–434 (co-published in Intensive Care Medicine). 61 statements; only three rest on high- or moderate-certainty evidence. The strong recommendation against bolus therapy for non-hypotensive sepsis without intensive care is one of the few firm statements in the whole guideline — and it comes from FEAST.
3 · FEAST: what it showed and where Must-know UG/PG
Read the negative trial carefully
FEAST (Maitland et al., NEJM 2011) randomised 3,141 febrile African children with impaired perfusion to a 20–40 mL/kg bolus of saline or albumin, or to maintenance fluid only. Bolus therapy increased 48-hour mortality (roughly 10.6% vs 7.3%), consistently across subgroups. Later analyses pointed to cardiovascular collapse, rather than simple fluid overload, as the main mode of excess death.
Read the setting. The hospitals had no mechanical ventilation and no inotrope infusions. Many children had malaria and severe anaemia. Children with gastroenteritis, severe malnutrition and non-infectious causes of shock were excluded, and very few were hypotensive.
The defensible reading is not “fluid is bad”. It is: large boluses are dangerous in febrile children without hypotension when you cannot support the airway and heart the bolus may unmask. That is exactly the population the 2026 strong recommendation addresses.
Two errors follow from FEAST, in opposite directions. One is ignoring it and giving 60 mL/kg reflexively to every febrile child with cool hands in a hospital with no ventilator. The other is over-generalising it and withholding fluid from the child with diarrhoeal hypovolaemia or frank hypotension, in whom fluid remains life-saving and who were never in the trial.
4 · Four groups in whom the standard bolus is wrong Must-know
| Group | Why | What to do instead |
|---|---|---|
| Cardiogenic shock | The problem is the pump; volume causes pulmonary oedema and arrest | Small aliquots (5–10 mL/kg) only if clearly under-filled; inotrope; treat arrhythmia (Unit 10) |
| Severe malnutrition | Heart and kidneys handle sodium and water poorly; overload kills | WHO: only for shock with lethargy or unconsciousness, 15 mL/kg over one hour with dextrose, watching pulse and respiratory rate every 5–10 minutes (Unit 16) |
| Severe anaemia | The problem is oxygen-carrying capacity, not volume | Transfuse; do not flood |
| Dengue with plasma leak | Leak is phase-dependent; fluid given in the recovery phase returns as pulmonary oedema | Follow the national dengue guideline: titrated crystalloid by haematocrit and clinical response, with early reduction as the leak stops |
India lens
Dengue is the single commonest reason a paediatric ward in India faces a fluid decision, and it has its own rules. Recognise the critical phase (usually days 3–7, as the fever falls): rising haematocrit with falling platelets, abdominal pain, persistent vomiting, mucosal bleeding, lethargy, a large liver. Fluid is given as titrated infusions guided by haematocrit and perfusion, not repeated large boluses, and is tapered as the leak stops. Most deaths now come from late recognition of shock or from over-infusion — not from lack of fluid alone. Use the current national (NCVBDC) dengue guideline and your state protocol.
5 · Across settings Must-know
Ideal setting
- Balanced crystalloid, 10–20 mL/kg aliquots, up to 40–60 mL/kg in the first hour if the child keeps responding
- Stop signals checked after each aliquot; move to a vasoactive rather than more fluid when they appear
- Point-of-care ultrasound, serial lactate and echocardiography to guide titration
- Ventilation available if fluid unmasks a failing heart
Resource-constrained setting
- Hypotensive shock, or obvious hypovolaemia from diarrhoea or bleeding: fluid is life-saving — give it, 10–20 mL/kg, reassessing each time, up to 40 mL/kg
- Febrile child with poor perfusion but a normal blood pressure: no bolus. Maintenance fluid, antibiotics now, glucose, treat severe anaemia, keep warm, transfer
- Use what you have: Ringer's lactate is on the essential medicines list and usually available; saline is acceptable
- A liver edge marked in pen, a watch and a written reassessment every 15 minutes are the monitoring you can always have
6 · Maintenance fluid Must-know
Holliday–Segar (“4-2-1”), per hour: 4 mL/kg for the first 10 kg, plus 2 mL/kg for the next 10 kg, plus 1 mL/kg for each kg above 20. Per day: 100, 50 and 20 mL/kg respectively.
The lesson paid for in children's lives
Use isotonic maintenance fluid in hospitalised children — 0.9% saline or a balanced solution, with glucose as needed. Hypotonic fluids (0.18% or 0.45% saline) caused a generation of avoidable hospital-acquired hyponatraemic seizures and deaths, because sick children secrete antidiuretic hormone and retain free water. Measure electrolytes if IV fluid continues beyond 24 hours, and reduce volumes in meningitis, pneumonia and after surgery, where water retention is greatest.
At a district hospital with no ventilator or inotrope infusions, a 3-year-old has fever, heart rate 170/min, capillary refill 4 seconds and BP 92/58 mmHg. Glucose is normal and haemoglobin 10 g/dL. The nearest PICU is three hours away. What is the most defensible fluid plan?
Nudge
Is this child hypotensive for his age? And does this hospital have intensive care?
Structured hint
70 + (2 × 3) = 76 mmHg: his pressure is above that. Now find the 2026 recommendation for sepsis without hypotension where intensive care is not available.
Why the answer is what it is
He has sepsis with poor perfusion but no hypotension, in a setting without intensive care: the 2026 guideline strongly recommends against a fluid bolus. What saves him is antibiotics now, maintenance fluid, glucose and anaemia checks, warmth and early transfer while he is still compensating.
In a PICU-backed emergency department, a 6-year-old in septic shock has received two 20 mL/kg boluses of Ringer's lactate. Heart rate has fallen from 165 to 150/min, but crackles have appeared at both bases and the liver edge has moved from 1 cm to 3 cm below the costal margin. Capillary refill is still 4 seconds. What next?
Nudge
Which of the four reassessment questions just returned a stop signal?
Structured hint
“Up to 60 mL/kg” is a ceiling, not a target. When crackles and a descending liver appear, what does the guideline tell you to move to instead of more fluid?
Why the answer is what it is
New crackles and a liver edge moving down are stop signals: the child is no longer fluid-responsive without harm. Shock persists, so move to a vasoactive infusion — which the 2026 guideline suggests starting through a peripheral line rather than waiting for central access — and prepare for respiratory support.
▸Unit 9 Sepsis and septic shock: the first hour Not attempted
Sepsis is the final common pathway for most preventable childhood deaths. It is also where the gap between what guidelines recommend and what a district hospital can deliver is widest — which makes intelligent adaptation, not protocol recitation, the real skill.
Learning outcomes
- UG Recognise sepsis clinically and say the word aloud, so the team starts the clock.
- UG Deliver the first hour: oxygen, access, cultures, antimicrobials within the recommended time, glucose, and a setting-appropriate fluid plan.
- UG/PG Choose empirical antimicrobials for community-acquired sepsis in India, including when to add cover for scrub typhus, malaria and resistant organisms.
- PG Explain what the 2026 guideline changed and why most of it rests on low-certainty evidence.
1 · Recognition comes before definitions Must-know
Screen clinically: an unwell-looking child with fever or a low temperature, tachycardia, poor perfusion, altered behaviour, or a rising early-warning score. Say “this could be sepsis” aloud. Naming it starts the clock for the whole team.
The 2026 guideline found insufficient evidence to recommend any particular systematic screening tool beyond established clinical pathways. What it does strongly recommend is that every hospital has a sepsis performance-improvement programme with standard operating procedures — a local pathway that people actually use.
The error clinicians actually make
Waiting for the Phoenix score, a lactate or a CRP before acting. Phoenix identifies children who already have organ dysfunction; waiting for two points means waiting for organ failure. Treat on suspicion; classify later.
2 · The first hour Must-know
Text version
0 min RECOGNISE · say "sepsis" · call senior help · start the clock
0–15 oxygen · IV or IO access (IO after 2 attempts or 90 s)
blood culture BEFORE antibiotics (never delaying them)
bedside GLUCOSE · LACTATE · gas · Hb · electrolytes
15–60 ANTIMICROBIALS
septic shock ........... within 1 hour (strong)
sepsis without shock ... within 3 hours, after
rapid evaluation
FLUID — depends on setting and blood pressure (Unit 8)
ICU available: 10–20 mL/kg boluses, up to 40–60 mL/kg
no ICU, no hypotension: NO bolus — maintenance only
no ICU, hypotension: 10–20 mL/kg boluses, up to 40 mL/kg
VASOACTIVE if shock persists after fluid (Unit 10)
correct glucose and calcium · treat severe anaemia
ONGOING SOURCE CONTROL · reassess every 15 minutes
transfer early if the setting cannot escalate3 · Antimicrobials: time, choice and source Must-know
Time. For suspected septic shock, the 2026 guideline strongly recommends antimicrobials as soon as possible, ideally within one hour. For probable sepsis without shock, as soon as possible after appropriate evaluation, ideally within three hours. Take a blood culture first when it does not cause delay.
Choice. Empirical cover must match the likely organisms and your local resistance pattern:
| Situation | A common starting point (check your antibiogram) |
|---|---|
| Community-acquired sepsis, previously well child | Third-generation cephalosporin (ceftriaxone or cefotaxime) ± an aminoglycoside |
| Suspected staphylococcal or toxic shock (skin focus, erythroderma) | Add an anti-staphylococcal agent; add clindamycin for toxin suppression |
| Hospital-acquired, recent antibiotics, known ESBL colonisation | Carbapenem or local equivalent; reserve these, do not start with them by habit |
| Fever with eschar, rash, transaminitis, low platelets | Add doxycycline or azithromycin for scrub typhus and other rickettsial illness |
| Malaria-endemic area | Test, and give IV artesunate for severe malaria |
| Young infant under 2 months | See Unit 17 (WHO 2024 regimens) |
Source control — drain the abscess, remove the infected line, operate on the perforation. No antibiotic beats drainage.
India lens
Antimicrobial resistance in Indian community isolates, especially Gram-negative organisms, is high and regionally variable. The ICMR AMR surveillance network publishes annual reports, and ICMR's treatment guidelines for antimicrobial use are a better anchor than any textbook table. Ask your microbiology department for a one-page paediatric antibiogram and put it next to the sepsis pathway.
4 · Adjuncts: what the evidence supports Good-to-know PG
| Intervention | 2026 position and practical reading |
|---|---|
| Hydrocortisone | Suggested against in children whose shock responds to fluid and vasoactives. Insufficient evidence for or against in refractory shock. Give stress-dose steroids where adrenal insufficiency is known or likely (chronic steroid use, congenital adrenal hyperplasia, purpura fulminans). |
| Procalcitonin | Suggested against its routine use to guide stopping antibiotics. |
| Molecular rapid diagnostics | Insufficient evidence for routine use. |
| Blood transfusion | Once stabilised, a restrictive threshold (around 7 g/dL) is appropriate for most critically ill children (TRIPICU); higher in cyanotic heart disease, active bleeding or unstable shock. |
| IV immunoglobulin, blood purification, “metabolic resuscitation” cocktails | Not for routine use. |
| Glucose | Avoid hypoglycaemia and extreme hyperglycaemia; no insulin-driven tight control. |
Evidence note
Of 61 statements in the 2026 guideline, only three rest on high- or moderate-certainty evidence. Almost everything you do for a septic child is a conditional recommendation built on low-certainty evidence. That is a reason to individualise and reassess constantly, and to be sceptical of anyone who presents a sepsis bundle as settled science — not a reason for nihilism.
5 · The first hour across settings Must-know
Ideal setting
- Oxygen; IV or IO within 90 seconds; cultures drawn
- Antimicrobials within 1 hour for septic shock
- Balanced crystalloid in 10–20 mL/kg boluses to 40–60 mL/kg, stopping on overload signs
- Vasoactive infusion if shock persists; serial lactate; source control; ventilation when needed
Resource-constrained setting
- Oxygen; IV or IO; bedside glucose and haemoglobin
- Antibiotics immediately — the intervention with the clearest benefit and the one most often delayed. Add doxycycline where scrub typhus is plausible; test for and treat malaria where endemic
- No bolus in a non-hypotensive child; boluses only for hypotension or obvious hypovolaemia, up to 40 mL/kg
- Correct hypoglycaemia and transfuse severe anaemia — here they change outcome more than fluid volume
- Phone the receiving unit and transfer while the child is still compensating, with weight, drugs and times written down
The divergence is guideline-concordant, not a compromise: the Surviving Sepsis paediatric guidelines have issued setting-specific recommendations since 2020, precisely because of FEAST.
A 20-month-old with fever and a spreading non-blanching rash has heart rate 180/min, capillary refill 5 seconds and is drowsy. IV access failed twice in 90 seconds. What is the correct sequence in the next ten minutes?
Nudge
What is the time target for antimicrobials in suspected septic shock, and what does the access rule say after two attempts or 90 seconds?
Structured hint
A purpuric rash with shock is meningococcal sepsis until proven otherwise. Which option gets antibiotics in within the hour without abandoning the culture?
Why the answer is what it is
This is suspected septic shock with a purpuric rash. After two failed attempts or 90 seconds, go intraosseous. Draw a culture if you can do so without delay, then give antibiotics immediately — within the hour. Fluid follows the setting-specific plan.
A 10-year-old in septic shock has responded to fluid and a low-dose adrenaline infusion: heart rate and perfusion are improving and he is more alert. A colleague suggests adding IV hydrocortisone “to be safe”. He has no history of steroid use. What does the 2026 guideline suggest?
Nudge
Is this child's shock responding, or refractory?
Structured hint
The guideline treats two situations differently: shock that is responding, and shock that remains unstable despite fluid and catecholamines. Which situation is this?
Why the answer is what it is
The 2026 guideline suggests against IV hydrocortisone in children whose shock responds to fluid and vasoactive therapy. Steroids remain appropriate where adrenal insufficiency is known or likely; for truly refractory shock the evidence is insufficient either way.
▸Unit 10 When fluid fails: vasoactives, access and the failing heart Not attempted
When a child is still shocked after appropriate fluid, the next minutes decide the outcome: a vasoactive started early through whatever line you have, an intraosseous needle instead of a fifth venous attempt, and the recognition that some shocked children have a heart problem, not a volume problem.
Learning outcomes
- UG Obtain intraosseous access within the recommended time and use it for every resuscitation drug and fluid.
- UG Recognise anaphylaxis and give intramuscular adrenaline at the correct dose.
- UG/PG Start and titrate a vasoactive infusion through a peripheral or intraosseous line, as the 2026 guideline suggests.
- UG/PG Recognise cardiogenic shock from myocarditis, SVT or a duct-dependent lesion, and change management accordingly.
- PG Describe the options when shock remains refractory to catecholamines, and what the evidence does and does not support.
1 · Access in the shocked child Must-know
PERIPHERAL IV two attempts OR 90 seconds, whichever comes first
│ (in decompensated shock)
▼
INTRAOSSEOUS proximal tibia: 1–2 cm below and medial to the
│ tibial tuberosity · alternatives: distal femur,
│ distal tibia, proximal humerus (older children)
│ anything that goes IV can go IO — fluids, blood,
│ antibiotics, vasoactives
│ flush firmly; push fluid with a syringe or pressure bag
│ avoid: a fractured bone, a bone already punctured,
│ infection over the site
▼
CENTRAL VENOUS once resuscitation is under way, by a competent
operator, ultrasound-guided
Pearl
IO access should be a reflex, not a last resort. It is fast, has a high first-attempt success rate, and every minute spent on a fifth peripheral attempt is a minute without drugs.
2 · Vasoactives: start early, start peripherally Must-know UG/PG
When shock persists after appropriate fluid — or fluid is stopped by overload signs — start a vasoactive infusion.
| 2026 Surviving Sepsis statement | What it means at the bedside |
|---|---|
| Start vasoactives through peripheral venous access rather than delay until central access is obtained (conditional) | Do not wait for a central line. Use a dilute solution in a good peripheral or IO line and watch the site. |
| Insufficient evidence to recommend adrenaline over noradrenaline, or vice versa, as first-line | Choose by physiology and familiarity: adrenaline where the picture is cold, low-output shock; noradrenaline where it is warm, vasodilated shock. Reassess and switch or add as needed. |
| For high-dose requirements, add vasopressin or further titrate catecholamines (conditional) | Refractory shock needs senior and intensive-care input. |
| Agent | Usual starting range | Main effect |
|---|---|---|
| Adrenaline (epinephrine) | 0.05–0.3 microgram/kg/min | Inotropy and heart rate; vasoconstriction at higher doses |
| Noradrenaline (norepinephrine) | 0.05–0.3 microgram/kg/min | Vasoconstriction |
| Dopamine | 5–10 microgram/kg/min | Mixed; where adrenaline or noradrenaline are unavailable |
| Dobutamine | 5–10 microgram/kg/min | Inotropy with vasodilatation — low-output states, myocarditis |
| Milrinone | 0.25–0.75 microgram/kg/min (with or without load) | Inotropy and vasodilatation; specialist use |
Doses and dilutions: verify against Appendix E and your unit protocol. Extravasation of vasoconstrictors causes tissue injury — check the site every 15 minutes.
3 · Anaphylaxis: the distributive shock with a specific drug Must-know
Sudden onset after exposure; skin or mucosal involvement (urticaria, angioedema) with respiratory compromise (stridor, wheeze) or hypotension — or hypotension alone after a known allergen.
ADRENALINE IM, anterolateral thigh, NOW
0.01 mg/kg of 1 mg/mL (1:1000) solution · max 0.5 mg
(practical doses: under 6 years 0.15 mg · 6–12 years 0.3 mg ·
over 12 years 0.5 mg)
repeat after 5 minutes if no improvement
lie flat with legs raised (sit up if breathing is the problem)
oxygen · IV/IO access · crystalloid 10–20 mL/kg if hypotensive
refractory after two IM doses → adrenaline infusion, senior help
antihistamines and steroids are ADJUNCTS — never instead of adrenaline
The error clinicians actually make
Giving chlorpheniramine and hydrocortisone and waiting. Neither treats airway swelling or shock. Delayed adrenaline is the commonest avoidable feature of fatal anaphylaxis. Also: anti-snake venom reactions are anaphylaxis — same drug, same dose (Unit 14).
4 · The failing heart Must-know UG/PG
Suspect a cardiac cause in any shocked child with a big liver, a gallop, crackles, raised neck veins, a heart rate that does not vary, or worsening after fluid.
| Cause | Clues | Key action |
|---|---|---|
| Myocarditis | Recent viral illness; tachycardia out of proportion to fever; gallop; big liver; chest X-ray cardiomegaly; ECG changes | Minimal fluid; inotrope (dobutamine, milrinone or low-dose adrenaline); early PICU. Intubation is high-risk — most experienced operator, cardiovascular support ready. |
| SVT | Heart rate typically over 220/min in infants, over 180/min in children; narrow QRS; no beat-to-beat variation | Vagal manoeuvres (ice to the face in infants); adenosine 0.1 mg/kg rapid push with flush (max 6 mg), then 0.2 mg/kg (max 12 mg); synchronised cardioversion if unstable |
| Duct-dependent lesion in a neonate (days to weeks old) | Shock or cyanosis in the first weeks; weak femoral pulses (coarctation, hypoplastic left heart); pre- and post-ductal saturation difference | Prostaglandin E1 infusion to reopen the duct; watch for apnoea. This is a cardiology emergency. |
| Scorpion envenomation | Sting, sweating, priapism, cold limbs, hypertension then hypotension, pulmonary oedema | Prazosin and scorpion antivenom; dobutamine for low output (Unit 14) |
Danger
Rapid sequence induction in a child with myocarditis or a failing heart is one of the highest-risk procedures in paediatrics. Sympatholytic drugs and positive-pressure ventilation can precipitate arrest. Plan it with the most experienced operator available, with an inotrope running and adrenaline drawn up.
5 · Across settings Good-to-know
Ideal setting
- Infusion pumps, arterial line and echocardiography to guide the choice of vasoactive
- Central access placed once the child is stabilised; vasopressin and ECMO referral for refractory shock
- Paediatric cardiology on call for arrhythmia and duct-dependent lesions
Resource-constrained setting
- IO access is always available: a hollow needle and a syringe are enough in an emergency
- Where there is no infusion pump, a carefully calculated adrenaline or dopamine infusion by a burette with a drop counter, with the site watched constantly, is the pragmatic option
- IM adrenaline for anaphylaxis needs no equipment beyond a syringe — keep a labelled ampoule with every snakebite and vaccination tray
- A child with a suspected cardiac cause of shock should be discussed with the referral centre early; ask about prostaglandin before transfer of a sick neonate
A 7-year-old in septic shock at a teaching hospital has received 40 mL/kg of Ringer's lactate. She has crackles at both bases and her liver is 3 cm below the costal margin. Capillary refill is 4 seconds and BP 78/40 mmHg. A central line is planned but the anaesthetist is 45 minutes away. What now?
Nudge
What did the 2026 guideline say about peripheral access for vasoactives?
Structured hint
She has overload signs, so more fluid is wrong. Is waiting 45 minutes for a central line compatible with ongoing hypotensive shock?
Why the answer is what it is
She is still in shock and has overload signs, so fluid is no longer the answer. The 2026 guideline suggests starting vasoactives through a peripheral line rather than delaying for central access. Choose adrenaline or noradrenaline by physiology; the guideline found insufficient evidence to prefer one.
A 4-year-old develops generalised urticaria, stridor and a BP of 70/40 mmHg five minutes into an anti-snake venom infusion. What is the first drug and dose?
Nudge
What is this reaction, and which drug treats airway swelling and shock at the same time?
Structured hint
An ASV reaction with stridor and hypotension is anaphylaxis. The first-line drug has one route and one dose that you should know without calculation.
Why the answer is what it is
This is anaphylaxis to anti-snake venom. Stop the infusion and give IM adrenaline 0.01 mg/kg of 1 mg/mL (max 0.5 mg) into the thigh; repeat after five minutes if needed. Once the reaction settles, ASV is usually restarted cautiously, because the envenomation still needs treating.
▸Unit 11 Dehydration, diarrhoea and diabetic ketoacidosis Not attempted
Oral rehydration solution is one of the most consequential medical inventions of the twentieth century, and it is still under-used. DKA is the one place in paediatrics where being too enthusiastic with fluid and insulin is more dangerous than being too slow.
Learning outcomes
- UG Classify dehydration with WHO criteria and apply Plans A, B and C correctly.
- UG Recognise DKA in a child presenting with vomiting, abdominal pain or fast breathing, and start a safe first hour.
- UG/PG Manage DKA through the first 24 hours, including potassium, the switch to dextrose, and clinical recognition of cerebral oedema.
- PG Interpret the PECARN FLUID trial and its effect on DKA fluid practice.
1 · Assessing dehydration Must-know
| Sign | No dehydration | Some dehydration | Severe dehydration |
|---|---|---|---|
| Condition | Well, alert | Restless, irritable | Lethargic or unconscious |
| Eyes | Normal | Sunken | Sunken |
| Thirst | Drinks normally | Thirsty, drinks eagerly | Drinks poorly or not able to drink |
| Skin pinch | Goes back quickly | Goes back slowly | Goes back very slowly (over 2 s) |
| WHO plan | Plan A: fluids at home, continue feeding, zinc | Plan B: ORS 75 mL/kg over 4 hours at the facility | Plan C: IV fluid |
Two or more signs in a column place the child in that column. The most useful single signs of significant dehydration in children are prolonged capillary refill, abnormal skin turgor and an abnormal breathing pattern; dry mucosa alone is weak evidence — a mouth-breathing child has a dry mouth.
2 · WHO Plan C Must-know
| Age | First 30 mL/kg | Then 70 mL/kg |
|---|---|---|
| Under 12 months | over 1 hour | over 5 hours |
| 12 months and older | over 30 minutes | over 2½ hours |
Use Ringer's lactate (or 0.9% saline if unavailable). Repeat the first portion once if the radial pulse is still weak. Reassess every 15–30 minutes; start ORS by mouth (about 5 mL/kg/h) as soon as the child can drink; reclassify at the end and switch to Plan A or B. Give zinc for 10–14 days and continue feeding.
Danger
Look for severe malnutrition before starting Plan C. In a child with severe wasting or nutritional oedema, Plan C can kill: rehydration is slower, by mouth or nasogastric tube with ReSoMal where possible, and IV fluid is reserved for shock (Unit 16).
3 · DKA: recognise it Must-know
Diagnosis: hyperglycaemia (blood glucose over 11 mmol/L, about 200 mg/dL) and ketosis (blood β-hydroxybutyrate 3 mmol/L or more, or moderate-to-large urine ketones) and acidosis (venous pH below 7.3 or bicarbonate below 18 mmol/L). Severity: mild pH below 7.3, moderate below 7.2, severe below 7.1.
India lens
A large proportion of Indian children with type 1 diabetes present in DKA at diagnosis, often after being treated for “gastroenteritis”, “acute abdomen” or “pneumonia”. Deep, sighing Kussmaul breathing is repeatedly misread as a chest problem. Check a capillary glucose in every child with unexplained vomiting, abdominal pain, dehydration or fast breathing. It costs a few rupees and prevents deaths.
4 · DKA: the first hours Must-know
WEIGH · assess · but note: clinical assessment OVERESTIMATES the
deficit in DKA. Assume about 5–7% (moderate) or 7–10% (severe).
SHOCK (uncommon — look for another cause too):
0.9% saline or balanced fluid, 20 mL/kg rapidly, reassess
NO SHOCK but volume-depleted:
10–20 mL/kg over 20–30 minutes
THEN deficit + maintenance, replaced evenly over 24–48 h,
isotonic (0.9% saline or balanced) initially
POTASSIUM: add 40 mmol/L once the child passes urine and K is
not high — total body K is ALWAYS depleted
INSULIN: 0.05–0.1 unit/kg/hour by infusion, started at least
1 hour AFTER fluids began · NO insulin bolus
When glucose falls below about 14–17 mmol/L (250–300 mg/dL):
ADD glucose to the fluid — do not stop the insulin, which is
what clears the ketones
NO BICARBONATE except in exceptional, life-threatening
hyperkalaemia or cardiovascular collapse
MONITOR hourly: glucose, neuro obs, fluid balance
2–4 hourly: electrolytes, gas, ketones
Evidence note
PECARN FLUID (Kuppermann et al., NEJM 2018): 1,389 DKA episodes randomised in a factorial design to faster or slower rehydration with 0.9% or 0.45% saline. Neither rate nor sodium content significantly changed rates of clinically apparent cerebral injury or neurocognitive outcome. It relaxed the extreme fluid caution of earlier decades — but ISPAD still advises replacing the deficit over 24–48 hours rather than rushing, and cerebral oedema remains the leading cause of DKA death in children.
5 · Cerebral oedema: diagnose it clinically, treat it immediately Must-know
Usually 4–12 hours into treatment, but it can be present at arrival. Warning signs: headache, recurrent vomiting, slowing heart rate with rising blood pressure, falling or fluctuating consciousness, irritability, incontinence, cranial nerve palsy, abnormal posturing.
Do not wait for the scan
Treat on clinical suspicion, before imaging: mannitol 0.5–1 g/kg over 10–15 minutes, or 3% saline 2.5–5 mL/kg over 10–15 minutes; head up; reduce the fluid rate; call for help. A normal early CT does not exclude cerebral oedema.
6 · Across settings Must-know
Ideal setting
- Insulin by syringe pump, fluids by volumetric pump; hourly glucose and neuro obs; 2–4-hourly gas, electrolytes and ketones
- Hyperosmolar therapy drawn up and labelled at the bedside
- HDU nursing ratio for moderate and severe DKA
Resource-constrained setting
- ORS is the headline act, not the fallback. WHO Plans A and B with zinc and continued feeding resolve the great majority of diarrhoeal dehydration without a cannula
- Without an insulin pump, hourly subcutaneous or intramuscular rapid-acting insulin regimens are a recognised alternative — never a bolus, never large intermittent doses, always with hourly glucometer checks
- Without laboratory potassium, add it only once urine is passed, and watch for arrhythmia
- Cerebral oedema is diagnosed and treated clinically: mannitol or 3% saline at the bedside, without waiting for imaging you may not have
- Transfer moderate and severe DKA to a unit that can monitor hourly — after the first hour of fluid, with insulin plan and flow chart written down
An 11-year-old with new-onset DKA (pH 7.05) had 10 mL/kg saline and an insulin infusion started at hour 2. At hour 6 he complains of headache, vomits twice, and his heart rate falls from 120 to 74/min while his blood pressure rises. What is the next action?
Nudge
What does a falling heart rate with a rising blood pressure mean in a child being treated for DKA?
Structured hint
Headache, vomiting and a Cushing-type response, hours into treatment. Should treatment wait for imaging?
Why the answer is what it is
Headache, vomiting and bradycardia with rising blood pressure during DKA treatment is cerebral oedema until proven otherwise — the leading cause of DKA death in children. Treat immediately on clinical grounds with mannitol 0.5–1 g/kg or 3% saline 2.5–5 mL/kg, head up, reduced fluid rate, senior help.
A 14-month-old weighing 9 kg has severe dehydration from acute watery diarrhoea and no signs of malnutrition. What is the correct initial WHO Plan C regimen?
Nudge
Plan C has two schedules. Which one applies at 14 months?
Structured hint
The slower schedule (1 hour, then 5 hours) is for infants under 12 months. This child is over 12 months.
Why the answer is what it is
For a child 12 months or older in severe dehydration: 30 mL/kg over 30 minutes, then 70 mL/kg over 2½ hours of Ringer's lactate. Start ORS as soon as he can drink, give zinc for 10–14 days and continue feeding.
Specific emergencies
The ABCDE spine keeps a child alive; these four units tell you what to do once you know why the child is sick. They are chosen for India's burden: household poisons, seizures, snake and scorpion envenomation, and injury.
▸Unit 12 Poisoning: toxidromes, decontamination, antidotes and India's common poisons Not attempted
Most poisoned children need good supportive care and nothing else. A few need one specific drug, fast. The skill is knowing which child is which — and knowing the handful of poisons in Indian homes that change the plan.
Learning outcomes
- UG Stabilise a poisoned child with the ABCDE approach, including glucose, before thinking about the poison.
- UG Recognise the four common toxidromes from bedside signs.
- UG/PG Decide when activated charcoal helps and when it is contraindicated; know why emesis and routine lavage are not used.
- UG/PG Manage organophosphate, hydrocarbon (kerosene), paracetamol, iron and button-battery ingestions.
- PG Recognise the poisons with no antidote and a high fatality rate — aluminium phosphide, paraquat, yellow phosphorus — and plan early referral.
1 · Treat the child, then the poison Must-know
1. ABCDE airway and breathing first — most deaths are
from respiratory depression or aspiration
2. GLUCOSE in every child with altered consciousness
3. HISTORY what · how much (worst-case estimate) · when ·
what else is in the house · what was given at home
· bring the container
4. TOXIDROME pupils · skin · secretions · heart rate · BP ·
temperature · bowel sounds · breath odour
5. DECONTAMINATE only if it helps and is safe (section 3)
6. ANTIDOTE for the few that have one (section 4)
7. OBSERVE for the known time course of the poison
8. PREVENT safe storage counselling, before discharge
Take the worst-case amount: the number of tablets missing from the strip, the full volume of the bottle. Children share, siblings hide things, and parents under-estimate.
2 · Toxidromes Must-know
| Toxidrome | Pupils | Skin and secretions | Other signs | Typical agents |
|---|---|---|---|---|
| Cholinergic | Pinpoint | Wet: sweating, salivation, tears, bronchorrhoea | Bradycardia, wheeze, vomiting, diarrhoea, fasciculation, weakness | Organophosphate and carbamate pesticides |
| Anticholinergic | Dilated | Dry, hot, flushed | Delirium, tachycardia, urinary retention, absent bowel sounds | Datura (dhatura) seeds, antihistamines, tricyclics |
| Opioid | Pinpoint | Normal | Slow shallow breathing, coma | Opioids, some antidiarrhoeals, poppy-husk preparations |
| Sympathomimetic | Dilated | Sweaty | Agitation, tachycardia, hypertension, hyperthermia, seizures | Amphetamines, excess salbutamol or theophylline |
Pearl
Cholinergic and anticholinergic both change the pupils and the heart rate — feel the skin. Wet means cholinergic; dry means anticholinergic. The armpit is the quickest place to check.
3 · Decontamination: less than you were taught Must-know
| Method | Current position |
|---|---|
| Activated charcoal 1 g/kg (max 50 g) | Consider within about 1 hour of a potentially serious ingestion of a substance charcoal binds, only if the airway is protected (alert, or intubated). Not for hydrocarbons, corrosives, iron, alcohols or lithium. |
| Induced vomiting | Not used. It delays charcoal, risks aspiration and does not improve outcome. |
| Gastric lavage | Not routine. Rarely considered for a recent, life-threatening ingestion with no good alternative, with the airway protected. Never for hydrocarbons or corrosives. |
| Whole-bowel irrigation | Specialist use: iron, sustained-release preparations, packets. |
| Skin and eye | Remove clothing and wash skin with soap and water for organophosphates; irrigate eyes. Staff wear gloves. |
The error clinicians actually make
Making a child vomit after kerosene or a corrosive. Vomiting turns a stomach problem into a lung problem (hydrocarbon aspiration pneumonitis) or burns the oesophagus a second time. Households are often advised to do this; ask, and counsel against it.
4 · Antidotes worth knowing Must-know UG/PG
| Poison | Antidote | Notes |
|---|---|---|
| Organophosphate, carbamate | Atropine | Titrate to a clear chest and dry secretions (section 5) |
| Opioid | Naloxone 0.1 mg/kg IV/IO/IM (max 2 mg), repeat as needed | Short-acting — watch for re-sedation; infusion may be needed |
| Paracetamol | N-acetylcysteine | Best within 8 hours of ingestion; see section 6 |
| Iron | Desferrioxamine IV | For systemic toxicity or high levels |
| Digoxin, oleander (cardiac glycosides) | Digoxin-specific antibody fragments where available | Otherwise atropine for bradycardia, manage potassium, pacing in specialist units |
| Benzodiazepines | Flumazenil — rarely | Can precipitate seizures; not for undifferentiated coma |
| Methaemoglobinaemia (nitrites, dapsone, some dyes) | Methylene blue | Avoid in G6PD deficiency |
Doses: see Appendix E and verify against your unit protocol. Your state or regional poison information centre can advise in real time — keep the number on the resuscitation trolley.
5 · Organophosphates and carbamates Must-know
India's most important paediatric poisoning: pesticides stored in homes, in soft-drink bottles, or on clothing and skin after field work.
AIRWAY first · suction · oxygen · ventilate if weak
DECONTAMINATE skin and clothing (staff wear gloves)
ATROPINE 0.02–0.05 mg/kg IV, DOUBLE the dose every 5 minutes
until ATROPINISED:
clear chest on auscultation (no crackles, no wheeze)
heart rate adequate for age
adequate blood pressure · dry axillae
pupils no longer pinpoint
then an INFUSION of about 10–20% of the total loading dose per
hour, titrated — watch for toxicity (delirium, fever, ileus,
urinary retention) and for relapse
SEIZURES → benzodiazepine
Evidence note
The endpoint is a clear chest, not pupil size and not heart rate alone: children die of bronchorrhoea and respiratory failure. Doses needed can be far larger than usual. Pralidoxime is used in many Indian units, but its benefit is uncertain — a large randomised trial in Sri Lanka (Eddleston et al., PLoS Med 2009) found no mortality benefit. Follow your local protocol; never let it delay atropine or ventilation. Watch for the intermediate syndrome — neck flexor and proximal weakness with respiratory failure 1–4 days later, after the cholinergic phase has settled.
6 · Kerosene, paracetamol, iron and button batteries Must-know UG/PG
| Poison | Danger | What to do |
|---|---|---|
| Kerosene and other hydrocarbons | Aspiration pneumonitis; fever and chest signs can appear hours later | No emesis, no lavage, no charcoal. Oxygen. Observe at least 6 hours: a child who is symptom-free with normal oxygen saturation and chest examination at 6 hours can usually go home. Chest X-ray if symptomatic. Antibiotics and steroids are not routine. |
| Paracetamol | Liver failure, often after a deceptively well first day | Serious risk is generally considered above about 150 mg/kg in a single acute ingestion (thresholds vary by country). Measure a level at 4 hours or later and use the nomogram; start N-acetylcysteine without waiting for a level if it will not be available within 8 hours of ingestion, or if the ingestion is staggered or unclear. |
| Iron | Vomiting, bloody diarrhoea, then apparent recovery, then shock, acidosis and liver failure | Calculate elemental iron: over about 60 mg/kg is potentially serious. Abdominal X-ray may show tablets. Charcoal does not bind iron. Desferrioxamine for systemic toxicity; discuss with a poison centre. |
| Button battery | Oesophageal burn within 2 hours; late fistula and catastrophic bleeding | X-ray neck, chest and abdomen. A battery in the oesophagus is an emergency: endoscopic removal within hours. While awaiting removal, honey (children over 1 year) is used in some protocols to reduce injury — follow your local ENT or poison centre advice. |
7 · The poisons with no antidote Good-to-know UG/PG
Recognise them, refer them early
Aluminium or zinc phosphide (rodenticide tablets; garlicky odour): refractory shock, arrhythmia, acidosis; very high fatality, no antidote. Paraquat (herbicide): mouth ulcers, then kidney, liver and progressive lung fibrosis; oxygen may worsen the lung injury. Yellow phosphorus (some rat poisons and firecrackers): delayed liver failure after a symptom-free interval. For all three: supportive care, early senior involvement and early referral to a centre with intensive care and, for yellow phosphorus, access to liver-transplant assessment. Take every such history seriously even when the child looks well.
India lens
Paediatric poisoning in India is dominated by household products and farm chemicals: kerosene stored in drink bottles, organophosphate and carbamate pesticides, rodenticides, corrosives, datura, oleander seeds, iron tablets meant for a pregnant mother, and adult medicines. In adolescents, deliberate self-poisoning with pesticides and medicines is common: every adolescent poisoning needs a confidential, non-judgemental psychosocial assessment before discharge. Unregulated traditional preparations can contain lead or other heavy metals. The IAP Standard Treatment Guidelines include a chapter on poisoning in children.
A 4-year-old is drowsy after playing where crops were recently sprayed. He has pinpoint pupils, copious oral secretions, crackles and wheeze, heart rate 64/min and muscle twitching. After airway support and oxygen, what is the priority?
Nudge
Wet skin, wet chest, small pupils, slow heart. Which toxidrome?
Structured hint
In this toxidrome, what do children actually die of — and which drug dries it up? What is its endpoint?
Why the answer is what it is
This is the cholinergic toxidrome from organophosphate or carbamate exposure. Children die of bronchorrhoea and respiratory failure, so the priority is atropine, doubling every five minutes to a clear chest and dry secretions. Decontaminate skin and clothing; staff wear gloves.
A 2-year-old drank “a mouthful” of kerosene from a soft-drink bottle 30 minutes ago. He coughed and gagged at the time but is now playing, with a respiratory rate of 28/min, SpO₂ 98% in air and a clear chest. His mother has already made him vomit once at home. What is the best plan?
Nudge
Where does kerosene do its damage — the stomach or the lungs?
Structured hint
Every option that puts more kerosene near the airway is wrong. Of the rest, which has a time course matched to how aspiration pneumonitis develops?
Why the answer is what it is
Hydrocarbon toxicity is aspiration pneumonitis, which can appear hours later. Do not add risk: no emesis, no lavage, no charcoal. Observe for at least 6 hours; if he remains well with normal oxygen saturation and chest at 6 hours he can usually go home. Counsel the family on storage — and against inducing vomiting.
▸Unit 13 Status epilepticus and raised intracranial pressure Not attempted
Two neurological emergencies where the clock does the damage: a seizure that is not stopped becomes harder to stop with every minute, and a brain under pressure is injured by every minute of low blood pressure or low oxygen.
Learning outcomes
- UG Manage a convulsing child with a time-based algorithm, starting benzodiazepines at five minutes by whatever route is available.
- UG Recognise raised intracranial pressure and impending herniation at the bedside.
- UG/PG Choose a second-line antiseizure medicine and give it at the correct dose, using the ESETT, EcLiPSE and ConSEPT evidence.
- UG/PG Apply the neuroprotective measures that lower intracranial pressure or protect cerebral perfusion, and avoid the ones that harm.
- PG Recognise non-convulsive status and refractory status, and plan escalation.
1 · Status epilepticus: the clock Must-know
Text version
0–5 min ABC · recovery position · oxygen · suction
GLUCOSE · IV/IO access · note the TIME · do not restrain
treat hypoglycaemia: 10% glucose 5 mL/kg
5 min FIRST BENZODIAZEPINE — by the route you have
IV/IO: lorazepam 0.1 mg/kg (max 4 mg)
or diazepam 0.2–0.3 mg/kg (max 10 mg)
No IV: buccal or intranasal midazolam 0.3 mg/kg (max 10 mg)
or rectal diazepam 0.5 mg/kg (max 10–20 mg)
10 min SECOND BENZODIAZEPINE if still seizing — ONE repeat only
~20 min SECOND-LINE MEDICINE — choose ONE
levetiracetam 40–60 mg/kg IV over 5–15 min (max 3–4.5 g)
phenytoin 20 mg/kg IV over 20 min, with ECG monitoring
(or fosphenytoin 20 mg PE/kg)
valproate 40 mg/kg IV (max 3 g) — avoid in liver disease,
suspected metabolic or mitochondrial disease, under 2 y
phenobarbital 20 mg/kg IV — where others are unavailable
~40 min REFRACTORY: senior and anaesthetic help · a second
second-line agent, or anaesthetic induction and a
midazolam infusion with intubation · EEG where availableDanger
Two benzodiazepine doses is the ceiling. A third and fourth dose do not stop the seizure; they stop the breathing. Move to a second-line agent. And nominate one person to call out the elapsed time aloud — without a clock, “20 minutes” becomes an hour.
2 · Choosing the second-line drug Must-know UG/PG
What the trials showed
ESETT (Kapur et al., NEJM 2019; children and adults with benzodiazepine-refractory status): levetiracetam 60 mg/kg, fosphenytoin 20 mg PE/kg and valproate 40 mg/kg each stopped seizures in roughly half of patients, with no meaningful difference between them. EcLiPSE (UK) and ConSEPT (Australia and New Zealand), both Lancet 2019, compared levetiracetam 40 mg/kg with phenytoin 20 mg/kg in children: levetiracetam was not superior, but it is quicker to give, needs no cardiac monitoring and has fewer serious adverse effects. Choose by availability, contraindications and infusion time, not by efficacy.
A seizure that will not stop is a seizure with a cause you have not found. Check glucose, sodium, calcium and magnesium; think of meningitis and encephalitis, cerebral malaria, toxins, raised pressure, and non-accidental head injury in an infant. Hyponatraemic seizures respond to 3% saline, not to antiseizure drugs (Unit 7).
3 · Raised intracranial pressure Must-know
Cerebral perfusion pressure = mean arterial pressure − intracranial pressure. Every intervention either lowers intracranial pressure or protects arterial pressure. Hypotension and hypoxia convert a survivable brain injury into a devastating one.
| Recognise | Do | Avoid |
|---|---|---|
| Headache worse in the morning or lying down; vomiting; falling consciousness; unequal pupils; abnormal posturing; Cushing triad (high BP, slow pulse, irregular breathing — late); bulging fontanelle and “setting sun” eyes in infants | Head up 30°, neck midline · secure airway · normal oxygen (SpO₂ 94% or above) · normal CO₂ (PaCO₂ 35–40 mmHg) · maintain blood pressure · analgesia and sedation · 3% saline 3–5 mL/kg or mannitol 0.5–1 g/kg for signs of herniation · treat fever, seizures and low sodium · urgent imaging and neurosurgery | Lumbar puncture · prolonged hyperventilation (brief only, as a bridge for imminent herniation) · hypotonic fluids · steroids in traumatic brain injury · hypoglycaemia and hyperglycaemia |
Pearl
Steroids have a place for vasogenic oedema around tumours and in TB meningitis — not in traumatic brain injury, where they cause harm.
4 · Across settings Must-know
Ideal setting
- IV lorazepam, then levetiracetam, fosphenytoin or valproate by pump with ECG monitoring
- Refractory status: intubation, midazolam or thiopental infusion, continuous EEG
- ICP monitoring and neurosurgery available; CT or MRI within the hour
Resource-constrained setting
- No IV is not an obstacle: buccal or intranasal midazolam and rectal diazepam need no cannula and can be given by a nurse or trained parent
- The two-dose benzodiazepine ceiling matters more here — you may have no means of supporting respiratory arrest
- Phenobarbital and phenytoin are often the available second-line drugs; give phenytoin slowly, counting the pulse, even without a cardiac monitor
- Without EEG, prolonged unexplained unresponsiveness after a seizure should be assumed to be ongoing seizure activity and discussed with a senior
- Glucose, sodium, calcium, and assessment for meningitis, cerebral malaria and scrub typhus explain more refractory seizures here than imaging would
India lens
Neurocysticercosis is a leading cause of acquired epilepsy and of first seizures in Indian children, and Japanese encephalitis and cerebral malaria remain important in endemic districts. Train families of children with epilepsy to use buccal or intranasal midazolam at home; it shortens seizures before the child reaches hospital.
A 3-year-old has been convulsing for 12 minutes and has had two doses of IV midazolam. The seizure continues. Glucose is 5.4 mmol/L and sodium 138 mmol/L. What next?
Nudge
How many benzodiazepine doses is the ceiling?
Structured hint
He has had two. The glucose and sodium are normal. The trials compared three drugs for exactly this situation — which step is that?
Why the answer is what it is
Two benzodiazepine doses is the ceiling. Move to a second-line medicine. ESETT, EcLiPSE and ConSEPT found levetiracetam, phenytoin (or fosphenytoin) and valproate broadly similar in effect, so choose by availability, contraindications and speed of administration, and prepare for airway support.
A 7-year-old with a head injury from a fall has GCS 7, a dilated left pupil and BP 70/40 mmHg. She is intubated. Which combination best protects her brain in the next 15 minutes?
Nudge
Cerebral perfusion pressure = MAP minus ICP. Which of her numbers is making that worse right now?
Structured hint
She is hypotensive and has signs of herniation. You need to raise one side of the equation and lower the other. Which option does both, without adding harm?
Why the answer is what it is
Her brain is threatened by both low blood pressure and raised pressure. Restore MAP, keep oxygen and CO₂ normal, position head-up with the neck midline, give 3% saline for the herniation signs, and get neurosurgical help. Hypotension and hypoxia are what turn survivable brain injury into devastating injury.
▸Unit 14 Envenomation: snakes and scorpions Not attempted
India carries the world's largest burden of snakebite deaths, most of them rural, many of them children, and many preventable by one decision taken early: give antivenom, and be ready to ventilate.
Learning outcomes
- UG Give correct first aid for snakebite, and name the traditional practices that cause harm.
- UG Recognise neurotoxic and haemotoxic envenomation, including the painless night-time krait bite.
- UG/PG Give polyvalent anti-snake venom at the national-protocol dose, repeat it by the 20-minute whole blood clotting test, and manage reactions.
- UG/PG Recognise the autonomic storm of scorpion envenomation and treat it with prazosin, with or without antivenom.
1 · Snakebite: first aid that works Must-know
- Reassure, keep the child still, and immobilise the bitten limb like a fracture.
- Transport immediately to a facility that has anti-snake venom (ASV) — by the quickest safe means.
- Remove rings, anklets and tight clothing before swelling starts.
Harmful practices
Do not apply a tight tourniquet, cut or suck the wound, apply ice or chemicals, use “snake stones”, or delay transport for a traditional healer. These practices cause limb loss and death, and delayed ASV is the commonest avoidable factor in snakebite deaths.
2 · Recognise the syndrome Must-know
| Syndrome | Species (India's “big four”) | Features |
|---|---|---|
| Neurotoxic | Cobra, common krait | Ptosis (earliest), double vision, difficulty swallowing and speaking, neck weakness, then respiratory paralysis. Krait bites are often painless, happen at night during sleep, and leave no visible mark: a child who wakes with abdominal pain and vomiting and develops ptosis in an endemic area is a krait bite until proven otherwise. |
| Haemotoxic (vasculotoxic) | Russell's viper, saw-scaled viper | Local swelling and blistering, bleeding from gums or bite site, incoagulable blood, acute kidney injury, shock |
Pearl
20-minute whole blood clotting test (20WBCT). Put 2 mL of fresh venous blood in a new, clean, dry glass tube; leave it undisturbed for 20 minutes; tip it once. If the blood has not clotted, it is incoagulable — a haemotoxic bite — and ASV is indicated. Repeat every 6 hours to guide further doses.
3 · Anti-snake venom: national protocol Must-know UG/PG
INDICATIONS: any sign of systemic envenomation
(neurotoxic signs · incoagulable 20WBCT · spontaneous bleeding ·
shock · kidney injury) or rapidly progressive local swelling
CHILDREN RECEIVE THE SAME NUMBER OF VIALS AS ADULTS
(the snake injects the same amount of venom);
only the infusion volume is adjusted — about 5–10 mL/kg
NEUROTOXIC: 10 vials over 30 minutes as an infusion
if no improvement after 1 hour → a second 10 vials
(maximum 20 vials) · then VENTILATE if needed
HAEMOTOXIC: 10 vials over 30 minutes (6 for saw-scaled viper
in the low-dose regimen), then repeat by 20WBCT
every 6 hours until the blood clots, per the
protocol followed in your state
REACTIONS: stop the infusion · IM adrenaline 0.01 mg/kg
(max 0.5 mg) · restart cautiously when settled
NEUROTOXIC ADJUNCT: atropine then neostigmine trial
(national STG: atropine 0.05 mg/kg, then neostigmine
0.04 mg/kg; repeat neostigmine if there is a response)
Source and limits
Source: Ministry of Health and Family Welfare Standard Treatment Guidelines, Management of Snakebite (quick reference guide). Polyvalent ASV in India covers the big four only; bites from other species, such as the hump-nosed pit viper, are not neutralised by it. The neostigmine trial helps mainly in cobra (post-synaptic) envenomation; krait toxins act pre-synaptically and respond poorly — for krait, ventilation is the life-saving treatment and may be needed for days. Check the dose schedule used in your state before quoting it.
4 · Across settings Must-know
Ideal setting
- ASV, adrenaline and a ventilator in the same building
- Laboratory coagulation tests, creatinine and urine output monitoring
- Dialysis for acute kidney injury after viper bites
Resource-constrained setting
- The PHC or CHC with ASV should give it, not refer first: the first dose is the most important one
- 20WBCT needs only a clean glass tube and a clock
- Bag-mask ventilation by relays of staff and family has kept krait-bitten children alive during transfer
- Refer early for ventilation (neurotoxic) and dialysis (haemotoxic with falling urine output) — after the first ASV dose, with adrenaline drawn up for the journey
5 · Scorpion sting Must-know UG/PG
The Indian red scorpion (Mesobuthus tamulus), common in western and southern India, causes an autonomic storm: severe local pain, then sweating, salivation, vomiting, priapism, cold limbs, hypertension and tachycardia, progressing in some children to myocardial dysfunction, pulmonary oedema and shock. Children are more severely affected than adults.
| Treatment | Detail |
|---|---|
| Prazosin (the specific treatment) | 30 microgram/kg by mouth (or nasogastric tube), repeated at intervals according to response — commonly 3–6-hourly — until the peripheries are warm and signs of the storm settle. Watch for first-dose hypotension. |
| Scorpion antivenom | In a randomised trial in Indian children (Pandi et al., 2014), scorpion antivenom plus prazosin produced faster recovery than prazosin alone. Give early where available. |
| Dobutamine | For the low-output, hypotensive phase and pulmonary oedema, with oxygen, CPAP or ventilation |
| Avoid | Atropine for the parasympathetic signs, and nifedipine or other drugs that cause reflex tachycardia |
India lens
The prazosin protocol was developed and popularised by Dr H.S. Bawaskar in rural Maharashtra and cut scorpion-sting mortality dramatically at low cost. It is one of the clearest examples of an Indian clinical innovation designed for resource-constrained care.
A 7-year-old in rural Maharashtra is brought at 3 a.m. having woken with severe abdominal pain and vomiting. There is no visible bite. Over the next hour he develops ptosis and difficulty swallowing. What is the most appropriate action?
Nudge
What kind of snakebite is painless, happens at night and leaves no mark?
Structured hint
Progressive ptosis and swallowing difficulty after night-time abdominal pain in an endemic area. Is the ASV dose for a child smaller than for an adult?
Why the answer is what it is
This is the classic krait presentation. Give ASV at the full dose (10 vials; children receive the same number of vials as adults) and prepare to ventilate — unrecognised respiratory paralysis is the commonest cause of death. A neostigmine trial is reasonable but works less well in krait bites.
A 5-year-old stung by a scorpion two hours ago is sweating profusely, has cold extremities, priapism, heart rate 160/min and BP 140/95 mmHg. Crackles are beginning at both bases. What is the specific treatment?
Nudge
What is driving the cold limbs, high blood pressure and pulmonary oedema — too much of which part of the autonomic system?
Structured hint
The storm is a massive alpha-adrenergic surge. Which drug blocks that receptor without causing reflex tachycardia?
Why the answer is what it is
This is the autonomic storm of Indian red scorpion envenomation, with early pulmonary oedema. Prazosin, an alpha-1 blocker, is the specific treatment; adding scorpion antivenom gives faster recovery. Give oxygen and CPAP or ventilation for the pulmonary oedema, and dobutamine if output falls.
▸Unit 15 Trauma, burns and drowning Not attempted
Injury is now a leading cause of death in Indian children beyond infancy, and it is the area where rehearsed teamwork and a few paediatric-specific facts make the most visible difference.
Learning outcomes
- UG Conduct a paediatric primary survey (<C>ABCDE) and identify immediately life-threatening injuries.
- UG Estimate burn surface area in a child and calculate initial burn fluid, including maintenance.
- UG Give correct first aid for burns and start resuscitation after drowning.
- UG/PG Apply paediatric injury patterns and decision rules to avoid both missed injury and unnecessary CT.
- PG Apply paediatric principles of haemorrhage control and blood-product resuscitation.
1 · The paediatric primary survey Must-know
<C> CATASTROPHIC HAEMORRHAGE — direct pressure, tourniquet,
pelvic binder. Blood volume is only ~70–80 mL/kg.
A airway with manual in-line stabilisation · jaw thrust, not head
tilt · collars fit children badly: manual stabilisation, blocks
and tape are often safer than a struggling child in a collar
B the immediately lethal chest injuries: tension pneumothorax ·
open pneumothorax · massive haemothorax · flail chest ·
tamponade · airway disruption. Compliant ribs mean serious lung
contusion WITHOUT rib fractures.
C two IV or IO lines · cross-match · treat hypotension as major
haemorrhage · blood products EARLY; avoid large crystalloid
volumes (10 mL/kg aliquots while blood is obtained)
D AVPU/GCS · pupils · glucose — head injury is the commonest
cause of paediatric trauma death
E log-roll · full survey · then WARM the child (hypothermia,
acidosis and coagulopathy feed each other)
ADJUNCTS analgesia (children are under-treated) · gastric tube ·
tetanus · and bring the parents in early
| Paediatric difference | Consequence |
|---|---|
| Large head, weak neck | Head injury dominates; high cervical injuries (C1–C3); spinal cord injury without X-ray abnormality occurs |
| Compliant chest | Contusion without fractures; tension pneumothorax develops fast. A rib fracture means major force — or abuse. |
| Relatively large, less protected liver and spleen | Solid-organ injury common; most managed without surgery in a monitored setting. Bicycle handlebars injure duodenum and pancreas. |
| Growth plates | A “sprain” in a child is often a growth-plate fracture |
2 · Head injury: who needs a CT? Good-to-know UG/PG
Validated decision rules (PECARN, CATCH, CHALICE) identify children at very low risk of clinically important brain injury who can be observed rather than scanned. PECARN, the most widely validated, separates children under and over two years; features such as altered mental status, a palpable skull fracture or signs of basal skull fracture put a child in the high-risk group for CT. Use a rule, record which one, and observe children in the intermediate group with a clear plan for re-examination.
Pearl
A decision rule protects children from unnecessary radiation and from a missed bleed. Its value is consistency, not the particular cut-offs — pick one rule for your department and use it every time.
3 · Burns Must-know
- First aid that works: cool running tap water for 20 minutes (useful up to 3 hours after the burn), remove clothing and jewellery, cover with cling film, keep the child warm. Not ice, toothpaste, ink, oil, turmeric or ghee.
- Surface area: the adult “rule of nines” is wrong for children — the head is proportionally larger and the legs smaller. Use a Lund–Browder chart, or the child's own palm with fingers as about 1% for scattered burns. Do not count simple erythema.
- Airway: facial burns, singed nasal hair, soot in the mouth, hoarseness or stridor mean the airway will swell. Involve the most experienced airway operator early; waiting can make intubation impossible.
Children with burns over about 10% TBSA need IV fluid.
RESUSCITATION 3–4 mL × weight (kg) × %TBSA of Ringer's lactate
over 24 hours FROM THE TIME OF THE BURN:
half in the first 8 hours, half over the next 16
PLUS MAINTENANCE with glucose (children, unlike adults, need it —
small glycogen stores)
TITRATE to urine output about 1 mL/kg/h (0.5 mL/kg/h in
adolescents) — the formula is a starting point only
The error clinicians actually make
Two classic arithmetic errors: starting the 8-hour clock at arrival instead of at the time of the burn, and forgetting maintenance fluid in a child. Over-resuscitation (“fluid creep”) is also common: titrate down when urine output is good. Consider inflicted injury when the pattern does not fit the story — sharply demarcated immersion burns, symmetrical burns of both feet or buttocks, cigarette-sized burns (Unit 20).
4 · Drowning Must-know
The primary insult is hypoxia. Start resuscitation with five rescue breaths, then compressions if there are no signs of life. There is no meaningful difference between fresh and salt water for initial management, and abdominal thrusts to “remove water” are harmful. Children rescued from cold water may survive prolonged submersion: continue resuscitation until the child is warmed and senior assessment is made. Every child who needed rescue breaths, or who has cough, breathlessness or low saturation, needs admission and observation for at least several hours — lung injury can worsen late.
India lens
Drowning is one of the leading causes of death in Indian children aged 1–4 years, largely in open wells, ponds, tanks and buckets within metres of home, and in floods. Community measures — well covers, supervised crèches, barriers — prevent more deaths than hospital care can. Road traffic injury (often unhelmeted children on two-wheelers), falls, firecracker and cooking burns, and electrocution complete the picture.
5 · Haemorrhage in children Nice-to-know PG
Hypotension in an injured child suggests the loss of a large fraction of circulating volume. Give blood early — red cells and plasma, with platelets in massive transfusion — rather than repeated crystalloid, which dilutes clotting factors and worsens acidosis. Tranexamic acid is used in significant paediatric trauma haemorrhage in many trauma systems when given early; follow your trauma protocol. Keep the child warm, calcium replaced, and the time to haemorrhage control short.
A 6-year-old weighing 20 kg has 25% TBSA scalds from 1 hour ago. Using 4 mL/kg/%TBSA, how much Ringer's lactate is needed over the rest of the first 8 hours from the burn, and what else must be prescribed?
Nudge
Work out the 24-hour total first. What fraction is due by hour 8, counted from when?
Structured hint
4 × 20 × 25 = 2000 mL in 24 hours. Half is due in the first 8 hours from the time of the burn — and one hour has already passed. Then ask what children need that adults do not.
Why the answer is what it is
The 24-hour total is 4 × 20 × 25 = 2000 mL. Half, 1000 mL, is due within 8 hours of the burn; one hour has passed, so it runs over the remaining 7 hours. Children also need maintenance fluid with glucose because of small glycogen stores. Titrate to urine output of about 1 mL/kg/h.
A 3-year-old is pulled from a village pond after an unknown time underwater. She is not breathing and has no signs of life. What is the correct first action?
Nudge
What is the primary insult in drowning?
Structured hint
Drowning arrest is asphyxial. Which option treats hypoxia first, and which one wastes time or causes harm?
Why the answer is what it is
In drowning the primary insult is hypoxia, so resuscitation begins with five rescue breaths and then compressions if there are no signs of life. Continue CPR, and continue longer if she is cold.
Special populations, systems and future directions
The children most likely to die are the ones in whom the standard rules change: the severely malnourished child, the young infant, the not-quite-well child whose diagnosis is hiding, and the child with a complex chronic condition. Then the systems around them — referral, communication, safeguarding and improvement — and what is coming next.
▸Unit 16 Severe wasting and nutritional oedema: when the rules invert Not attempted
Almost everything you learned in Parts B and C changes in a severely malnourished child. Applying standard emergency protocols to them is one of the commonest and most lethal errors in paediatrics — and it is entirely avoidable.
Learning outcomes
- UG Identify severe wasting and nutritional oedema using WHO anthropometric and clinical criteria.
- UG State how fluids, feeding, antibiotics and transfusion differ in the malnourished child, and the physiology behind each.
- UG/PG Recognise and prevent refeeding syndrome.
- PG Structure an inpatient pathway that links to community management and to India's Nutrition Rehabilitation Centres.
1 · Recognise it Must-know
In children aged 6–59 months, severe wasting and/or nutritional oedema (the 2023 WHO terms for what used to be called severe acute malnutrition) is any one of:
- weight-for-length or weight-for-height below −3 SD of the WHO standards;
- mid-upper arm circumference below 115 mm;
- bilateral pitting oedema of nutritional origin.
Any medical complication, failure of the appetite test, or severe oedema means inpatient care. For infants under six months, the 2023 WHO guideline uses a broader concept — infants at risk of poor growth and development — and emphasises supporting breastfeeding and the mother–infant pair.
Source
WHO guideline on the prevention and management of wasting and nutritional oedema (acute malnutrition) in infants and children under 5 years. Geneva: WHO; 2023. It is the first WHO guideline to cover moderate wasting and infants under six months in detail. Fluid management details in this unit follow the long-standing WHO hospital-care protocol, which the 2023 guideline did not replace.
2 · Why the rules invert Must-know
| Adaptation | Consequence | What changes |
|---|---|---|
| Reductive adaptation: slowed heart, kidney and liver function | The heart cannot handle a fluid load; the kidney cannot excrete sodium | No routine boluses. Slow rehydration, watching pulse, breathing and liver size |
| Low body potassium and magnesium, excess body sodium | Arrhythmia; oedema worsened by sodium | Supplement potassium and magnesium; restrict sodium — hence ReSoMal instead of standard ORS |
| Poor heat regulation | Hypothermia is frequent and lethal | Keep warm: covered head, skin-to-skin, warm room |
| Low glycogen | Hypoglycaemia, especially overnight | Feed every 2–3 hours, day and night |
| Blunted immune response | Infection without fever or raised white count | Antibiotics for every child with complicated malnutrition |
| Low cardiac reserve | Transfusion can cause heart failure | Transfuse only for Hb below 4 g/dL (or below 6 g/dL with respiratory distress): 10 mL/kg slowly over 3 hours |
| Free iron in the absence of binding proteins | Promotes infection and oxidative injury | No iron until rehabilitation, when appetite has returned |
3 · The fluid decision Must-know
DEHYDRATION WITHOUT SHOCK — oral or nasogastric ReSoMal
5 mL/kg every 30 minutes for 2 hours, then
5–10 mL/kg/hour for 4–10 hours, alternating with F-75
STOP if: pulse or breathing rate rises, liver enlarges,
eyelids puff up (signs of over-hydration)
SHOCK (lethargic or unconscious, cold hands, weak fast pulse)
IV 15 mL/kg over 1 hour: Ringer's lactate with 5% glucose
(or half-normal saline with 5% glucose)
check pulse and breathing every 5–10 minutes
improving → repeat 15 mL/kg over 1 hour, then switch to
ReSoMal orally or by NG tube
NOT improving → assume septic shock: maintenance IV fluid,
transfuse 10 mL/kg slowly if severe anaemia,
antibiotics, senior help
NEVER the standard Plan C volumes
Danger
The same child who needed 100 mL/kg in Plan C if well nourished can die of heart failure from it when severely wasted. Before any IV fluid in a child with diarrhoea, look at the arms and feel the feet.
4 · The ten steps Must-know
STABILISATION (days 1–7) 1 treat and prevent HYPOGLYCAEMIA 2 treat and prevent HYPOTHERMIA 3 treat and prevent DEHYDRATION (ReSoMal, section 3) 4 correct ELECTROLYTES (potassium, magnesium; restrict sodium) 5 treat INFECTION (antibiotics for all with complications) 6 correct MICRONUTRIENTS (no iron yet) 7 start cautious FEEDING: F-75, small, frequent, including night REHABILITATION (weeks 2–6) 8 CATCH-UP GROWTH: F-100 or RUTF once appetite returns 9 SENSORY STIMULATION and emotional support 10 PREPARE FOR FOLLOW-UP
The day-three death
Refeeding syndrome. Reintroducing carbohydrate drives phosphate, potassium and magnesium into cells; blood levels crash, causing arrhythmia, heart failure and death, usually on days 2–5 of feeding. It is why WHO starts with low-energy F-75 and increases slowly. Without phosphate measurement, prevent it by protocol: start low, go slow, and suspect it in any child who deteriorates on days 2–5.
5 · Across settings Must-know
Ideal setting
- Daily electrolytes including phosphate and magnesium during refeeding
- Prompt testing for tuberculosis and HIV; echocardiography if heart failure is suspected
- Dietitian and developmental therapy input
Resource-constrained setting
- The WHO ten steps were designed for this setting and need almost no technology: warmth, F-75, feeds every 2–3 hours including night, ReSoMal, potassium and magnesium, antibiotics, no iron
- A MUAC tape and an oedema check are the screening tools — usable by an Anganwadi worker or ASHA with no scales
- Defaulting is the main cause of treatment failure, and it is economic, not clinical. Children without complications who pass the appetite test do well with community-based management using RUTF
- A child not gaining weight on correct feeding has an undiagnosed infection — tuberculosis, HIV, urinary infection — until proven otherwise
India lens
India carries a large share of the world's wasted children. Facility care runs through Nutrition Rehabilitation Centres (NRCs), following the WHO steps, linked to community identification by Anganwadi workers and ASHAs under ICDS and POSHAN Abhiyaan. Know where your nearest NRC is and how to refer to it.
A 14-month-old with visible severe wasting and MUAC 102 mm has had watery diarrhoea for three days. She is irritable, has sunken eyes and drinks eagerly; hands are warm and pulse is normal. What is the correct rehydration plan?
Nudge
What has MUAC 102 mm just changed about every fluid rule you know?
Structured hint
She is dehydrated but not shocked. For a severely wasted child, which solution has less sodium and more potassium — and which volumes are safe for her heart?
Why the answer is what it is
She has severe wasting with dehydration but no shock. Rehydrate slowly with ReSoMal, orally or by nasogastric tube, alternating with F-75, and stop if the pulse or breathing rate rises, the liver enlarges or the eyelids puff up.
On day 3 of treatment with F-75, a severely wasted 2-year-old who had been improving becomes breathless and oedematous, with a heart rate of 170/min. What is the most likely cause?
Nudge
What happens to phosphate, potassium and magnesium when a starved body starts receiving carbohydrate?
Structured hint
Days 2–5 of feeding, cardiac failure, a previously improving child. Which complication has exactly that timing?
Why the answer is what it is
Deterioration with heart failure on days 2–5 of feeding is refeeding syndrome until proven otherwise: insulin drives phosphate, potassium and magnesium into cells and blood levels crash. Reduce the feed volume, check and replace electrolytes including phosphate if possible, and treat the heart failure.
▸Unit 17 The sick young infant (under 2 months) Not attempted
In the first two months of life, serious illness looks like almost nothing: a baby who is not feeding well, who is a little quiet, a little cold. By the time it looks like something, it is late.
Learning outcomes
- UG Use the WHO seven-sign algorithm to identify possible serious bacterial infection in infants aged 0–59 days.
- UG Recognise the young-infant emergencies that are not infection: hypoglycaemia, hypothermia, duct-dependent heart disease, surgical and metabolic crises.
- UG/PG Apply the WHO 2024 recommendations for managing serious bacterial infection, including when referral is not possible.
- PG Recognise the infant presentations of inherited metabolic disease and non-accidental head injury.
1 · The seven signs Must-know
| WHO sign of possible serious bacterial infection (0–59 days) |
|---|
| Not feeding well, or not able to feed at all |
| Movement only when stimulated, or no movement at all |
| Temperature 38 °C or above |
| Temperature below 35.5 °C |
| Severe chest indrawing |
| Convulsions |
| Fast breathing (60/min or more) in an infant aged 0–6 days |
Source
WHO recommendations for management of serious bacterial infections in infants aged 0–59 days (2024) recommend this seven-sign algorithm for identifying infants who need further evaluation (strong recommendation, moderate-certainty evidence). In the source analysis it had a sensitivity of about 0.79 and specificity of about 0.77 — it will miss some infants, which is why follow-up and safety-netting still matter.
2 · What WHO 2024 recommends when referral is not possible Must-know UG/PG
| Group | Recommendation |
|---|---|
| Critical illness (e.g. unable to feed, no movement, convulsions) | Refer. If referral is impossible: IM/IV ampicillin plus gentamicin for at least 10 days |
| Clinical severe infection (any other sign except fast breathing alone) | Refer. If impossible: oral amoxicillin for at least 7 days plus IM gentamicin for at least 7 days (or, if 7 days of injections are not feasible, gentamicin for 2 days) |
| Fast breathing alone, 0–6 days | Refer. If impossible: oral amoxicillin for at least 7 days |
| Fast breathing alone, 7–59 days | Oral amoxicillin for at least 7 days; can be managed outside hospital according to clinical judgement |
Doses (Appendix E): amoxicillin 50 mg/kg twice daily in the first week of life, then three times daily; gentamicin 5 mg/kg daily in the first week, then 7.5 mg/kg daily. In hospital, follow your SNCU or paediatric ward protocol and local resistance patterns.
India lens
India's F-IMNCI, the Home-Based Newborn Care and Home-Based Young Child Care programmes, and the SNCU and NBSU network are the delivery system for exactly these infants. ASHAs visiting at home are often the first to see the seven signs; the quality of what happens next depends on whether the facility they refer to recognises the infant as an emergency.
3 · Young-infant emergencies that are not infection Must-know
| Emergency | Clues | First action |
|---|---|---|
| Hypoglycaemia | Jittery, lethargic, poor feeding, apnoea, seizures | Glucose at the bedside; 10% glucose 2 mL/kg IV then an infusion (neonatal dosing); feed |
| Hypothermia | Cold to touch, lethargic, poor feeding | Skin-to-skin (Kangaroo Mother Care), warm room, cap; look for sepsis |
| Duct-dependent heart disease | Shock or deep cyanosis in the first weeks; weak femoral pulses; big liver | Prostaglandin E1; discuss with cardiology (Unit 10) |
| Surgical emergencies | Bilious (green) vomiting; distension; blood in stool; projectile vomiting at 3–6 weeks | Bilious vomiting is malrotation with volvulus until proven otherwise: nil by mouth, gastric tube, fluids, urgent surgical review |
| Inherited metabolic disease | Well at birth, then poor feeding, vomiting, lethargy, seizures, unusual odour, after feeds start | Glucose, gas, ammonia; stop protein feeds; glucose infusion; metabolic team |
| Non-accidental head injury | Irritability, vomiting, seizures, a bulging fontanelle, unexplained bruises | Treat, then safeguard (Unit 20) |
Pearl
Green vomit in a baby is a surgical emergency until a surgeon says otherwise. Hours matter: a volvulus can infarct the whole midgut.
4 · Across settings Must-know
Ideal setting
- SNCU or NICU care with blood cultures, CSF and inflammatory markers before antibiotics
- Echocardiography, prostaglandin, paediatric surgery and metabolic testing on site
Resource-constrained setting
- The seven signs need no equipment. A thermometer and a watch are enough
- Give the first dose of antibiotics before referral, and keep the baby warm on the journey with skin-to-skin contact
- If referral is refused or impossible, the WHO 2024 outpatient regimens are evidence-based options — not a failure of care
- Keep the mother and baby together; breastfeeding continues unless the infant cannot feed
A 20-day-old is brought by an ASHA because she has been feeding poorly for a day. Temperature 35.2 °C, respiratory rate 52/min, no chest indrawing, moves normally. Which is correct?
Nudge
Count her signs against the seven. Is a low temperature one of them?
Structured hint
Two signs are present: not feeding well, and temperature below 35.5 °C. Which group does that put her in?
Why the answer is what it is
Poor feeding and a temperature below 35.5 °C are both WHO signs of possible serious bacterial infection — clinical severe infection. Warm her (skin-to-skin), give the first antibiotic doses, and refer. If referral is impossible, WHO 2024 gives an outpatient regimen of oral amoxicillin plus gentamicin.
A 10-day-old has vomited green fluid three times this morning. He was well yesterday; his abdomen is soft and he is not distended. What should happen next?
Nudge
What colour of vomit makes a paediatric surgeon come to the emergency room at night?
Structured hint
Bilious vomiting in a neonate is a surgical emergency until proven otherwise — even when the abdomen looks normal. Why does a soft abdomen not reassure you?
Why the answer is what it is
Bilious vomiting in a neonate is malrotation with volvulus until proven otherwise. The abdomen is often soft and undistended early. Stop feeds, pass a gastric tube, start IV fluids and get an urgent surgical review and contrast study; hours of delay can cost the whole midgut.
▸Unit 18 Occult red flags in the not-quite-well child Not attempted
Not every sick child is crashing. Some come to OPD for the fourth time, after three courses of antibiotics, with a parent who keeps saying the same sentence: “He is just not the same child.” That sentence deserves more diagnostic weight than most blood tests.
Learning outcomes
- UG Build a structured differential for prolonged fever, pallor, weight loss and lymphadenopathy.
- UG Recognise the red flags of childhood cancer, tuberculosis and immunodeficiency.
- UG Give a specific, documented safety-net to every family sent home without a diagnosis.
- UG/PG Plan a staged, affordable investigation pathway, and know when to stop giving antibiotics and start investigating.
1 · The parent's concern is a vital sign Must-know
Parental concern independently predicts serious illness and deterioration, which is why it is an escalation trigger in modern early-warning systems. Phrases that should raise your suspicion:
- “He is not himself.” “She is not playing.”
- “He has never been like this before.”
- “I have brought him three times and he is getting worse.”
- “He wakes at night crying with leg pain.”
The reverse matters too: a child who is genuinely playing is rarely about to collapse. Put a toy in front of them and watch.
2 · Prolonged fever Must-know
| Category | Consider | Discriminating step |
|---|---|---|
| Infection (about half) | Tuberculosis, enteric fever, urinary infection, endocarditis, deep abscess, osteomyelitis, malaria, kala-azar, scrub typhus, brucellosis, HIV | Contact, travel, animal and food history; urine; blood culture; chest X-ray |
| Malignancy | Leukaemia, lymphoma, neuroblastoma | Full blood count with a film examined by a person; LDH; imaging |
| Inflammatory | Systemic JIA, Kawasaki disease, SLE, inflammatory bowel disease, HLH | Rash and arthritis pattern, mucocutaneous signs, ferritin |
| Other | Drug fever, thyrotoxicosis, fabricated illness | Medication review; fever documented by staff |
India lens
Tuberculosis is the single most important missed diagnosis in a child with prolonged fever, weight loss or faltering growth. Take a contact history in every such child; a normal chest X-ray does not exclude abdominal, nodal or CNS TB. Use the national programme's diagnostic algorithms and rapid molecular tests (CBNAAT/Truenat) on gastric aspirate, induced sputum or other specimens where available.
3 · Cancer red flags Must-know
| Presentation | Red flags | Think of |
|---|---|---|
| Pallor, bruising, fever | Unexplained pallor, bleeding, bone pain, big liver or spleen, lymphadenopathy | Leukaemia, lymphoma |
| Headache | Morning headache with vomiting, neurological signs, squint, ataxia, head tilt, rising head circumference in an infant | Brain tumour |
| Abdominal mass | Any mass; hypertension; eyes that dart (opsoclonus); bruising around the eyes | Neuroblastoma, Wilms tumour, hepatoblastoma |
| Bone or limb pain | Pain waking the child at night, a limp without injury, a “sprain” that does not settle | Bone tumours, leukaemia |
| Eye | White pupil (leukocoria), new squint, absent red reflex | Retinoblastoma |
| Lymph node | Over 2 cm, hard, matted, painless, growing beyond 2–4 weeks, supraclavicular at any size, with weight loss or night sweats | Lymphoma, tuberculosis |
Pearl
Two four-second habits: check the red reflex in every infant and young child, and feel the abdomen properly in every child with vague symptoms. Retinoblastoma and Wilms tumour are curable when found early.
4 · Safety-netting Must-know
Every child sent home without a diagnosis needs a specific, documented safety-net. “Come back if worse” does not work.
1 WHAT I THINK this is, and how long it should last
2 EXACTLY WHAT should bring you back immediately:
a rash that does not fade under a glass · fast breathing or
sucking in of the ribs · refusing all feeds · floppy or hard
to wake · a fit · cold, mottled hands and feet · no urine for
8–12 hours · fever beyond the day I told you
3 WHERE to go and HOW — the facility, the hours, what to do at
2 a.m. (transport is a clinical variable)
4 A PLANNED REVIEW at a definite time and place
then DOCUMENT the words you used
A 5-year-old has had three weeks of intermittent fever, has become pale, refuses to walk in the mornings because of leg pain, and has a 2.5 cm firm cervical node. What is the most appropriate next step?
Nudge
Fever, pallor, bone pain that stops a child walking, and a node over 2 cm. What cluster is that?
Structured hint
Which single test could show the answer today — and does it need to be read by a machine or a person?
Why the answer is what it is
Prolonged fever, pallor, bone pain limiting walking and a significant node is leukaemia until proven otherwise. A blood count with a film examined by a person can show blasts; LDH and uric acid support the diagnosis and warn of tumour lysis. Refer urgently.
You are discharging a 3-year-old with a viral illness at 11 p.m. Which safety-net advice is most effective?
Nudge
Which answer would still work for a frightened parent at 3 a.m.?
Structured hint
A usable safety-net names what to watch for, where to go, when, and a planned review. Which option contains all four?
Why the answer is what it is
Effective safety-netting names specific signs, where and when to return (including at night), and a planned review. Document the words you used.
▸Unit 19 The child with chronic and complex illness Not attempted
Children with medical complexity are a small fraction of paediatric patients and a large fraction of emergencies, admissions and deaths. They also attract a predictable set of errors.
Learning outcomes
- UG Recognise diagnostic overshadowing and take a structured baseline history from a carer.
- UG Manage the common device emergencies: a blocked tracheostomy, a shunt malfunction, a dislodged gastrostomy, a febrile central line.
- UG/PG Recognise condition-specific crises — adrenal, metabolic, sickle cell, febrile neutropenia, cyanotic spell — and act within the correct time.
- PG Discuss ceilings of treatment and an emergency care plan with a family, within Indian law and practice.
1 · Diagnostic overshadowing Must-know
The central error
A new symptom in a child with cerebral palsy, Down syndrome, autism or a chronic condition is put down to the known diagnosis and not investigated. The child with cerebral palsy who is “irritable because of spasticity” has a fractured femur, a torsion, a corneal abrasion, dental pain or a urinary infection. Assume a new symptom has a new cause.
Ask the carer three questions: What is normal for this child? (tone, alertness, saturations, feeding, seizure frequency) What is different today? What usually works? The carer of a complex child is often the most expert person in the room.
2 · Device emergencies Must-know
| Device | Emergency | Action |
|---|---|---|
| Tracheostomy | Blocked or displaced tube: distress with little air movement | Suction; remove the inner tube if present; if a suction catheter will not pass, change the tube (same size, then smaller). If that fails, ventilate by mask over the face or by the stoma, and call for help. |
| VP shunt | Blockage or infection: headache, vomiting, drowsiness, bulging fontanelle, fever | A raised-pressure emergency (Unit 13): urgent imaging and neurosurgery. Do not send home a drowsy child with a shunt. |
| Gastrostomy | Dislodged tube | The tract closes within hours: replace it, or keep it open with a catheter, then confirm position before use |
| Central line | Fever | Line infection until proven otherwise: cultures from the line and a vein, antibiotics now |
| Home ventilator | Circuit or power failure | Disconnect and ventilate by bag with oxygen. Do not troubleshoot a machine while the child is not breathing. |
3 · Condition-specific crises Must-know UG/PG
| Condition | Crisis | Immediate action |
|---|---|---|
| Adrenal insufficiency, CAH, long-term steroids | Shock, hypoglycaemia, low sodium, high potassium during illness | Hydrocortisone immediately IV or IM (about 25 mg under 1 year, 50 mg 1–5 years, 100 mg over 5 years), with glucose and saline. Never delay for tests. |
| Inherited metabolic disease | Decompensation: vomiting, encephalopathy, high ammonia | Stop protein, high glucose infusion, urgent ammonia, the family's emergency letter, metabolic team |
| Sickle cell disease | Pain crisis, acute chest syndrome, splenic sequestration, stroke | Prompt, adequate analgesia; oxygen; fluids; infection screen; transfusion as indicated. A suddenly enlarging spleen with falling haemoglobin is sequestration — transfuse. |
| Child on chemotherapy | Febrile neutropenia | Broad-spectrum IV antibiotics within one hour of arrival, before the count is back |
| Tetralogy of Fallot | Hypercyanotic spell | Knee-to-chest, oxygen, calm the child, morphine, fluid; then phenylephrine or a beta-blocker. Avoid inotropes that increase contractility. |
Hydrocortisone stress doses vary between national guidelines; use the child's own emergency letter if they have one, and Appendix E.
4 · Ceilings of treatment and emergency care plans Good-to-know PG
For a child with a progressive, life-limiting condition, the most important conversation happens before the crisis, in clinic, unhurried. Frame it around what the family hopes for and fears, not around a list of things to withhold. Record an emergency care plan the family carries with them.
India lens
Indian law on withholding and withdrawing life-sustaining treatment has developed through Supreme Court judgments recognising advance medical directives and passive euthanasia, with procedures simplified in 2023; institutional practice still varies widely and decisions for children are made with extended families. Involve senior colleagues and your institution's ethics committee, document carefully, and prioritise palliative care and symptom relief, which remain under-provided for children.
A 4-year-old with a tracheostomy is in severe respiratory distress. Oxygen to the tracheostomy does not help, the chest barely moves, and a suction catheter will not pass down the tube. What next?
Nudge
If a suction catheter will not pass, where is the obstruction?
Structured hint
The tube itself is blocked or displaced. A blocked tracheostomy is a complete airway obstruction. Which option removes the obstruction?
Why the answer is what it is
A suction catheter that will not pass means the tube is blocked or displaced — complete airway obstruction. Change the tube (same size, then smaller); if that fails, ventilate by mask over the face or the stoma, and call for help.
A 6-year-old on maintenance chemotherapy has a temperature of 38.6 °C and looks reasonably well. The blood count will take two hours. What is the correct action?
Nudge
Does a child with few neutrophils look as sick as their infection is?
Structured hint
Febrile neutropenia has a time target with mortality attached. Is it measured from arrival or from the blood result?
Why the answer is what it is
Treat as febrile neutropenia: cultures, then broad-spectrum IV antibiotics within one hour of arrival, without waiting for the count. Neutropenic children mount little inflammatory response and can deteriorate within hours despite looking well.
▸Unit 20 Referral, transport, safeguarding, quality and future directions Not attempted
In a referral-dependent health system, the quality of the transfer decision often matters more than any single drug. The conversation with the parents is not the soft part of care — it is the part they will remember for the rest of their lives. And nothing in this module helps a child unless a system delivers it reliably at 3 a.m.
Learning outcomes
- UG Decide when to refer, stabilise before transfer, and hand over using ISBAR.
- UG Communicate serious news to a family, and support family presence during resuscitation.
- UG Recognise features of abuse and neglect and know the mandatory reporting duties under POCSO.
- UG/PG Design a small quality-improvement project with outcome, process and balancing measures.
- PG Appraise emerging tools — machine-learning prediction, point-of-care ultrasound, host-response tests — for use in a low-resource setting.
1 · Refer while the child is still compensating Must-know
The commonest transport disaster is the child sent after decompensation, in an unequipped vehicle, without a stable airway, with staff who cannot manage deterioration on the way.
A airway secure; if intubated, position confirmed and taped;
suction in the vehicle
B oxygen for the journey PLUS 50% reserve; saturation monitored
C two working IV or IO lines, secured and visible
D glucose checked; seizures controlled; rescue drugs drawn up
E child WARM — cap, blankets, warm vehicle
+ notes, drugs and times, weight, investigations
+ ACCEPTANCE by a named person at the receiving unit, by phone
+ parent informed and travelling if possible
+ "what is most likely to go wrong in the next hour — and is the
drug and equipment for it in the vehicle?"
ISBAR handover: Identify yourself and the child · Situation · Background · Assessment (with vital signs and weight) · Recommendation (what you need, by when).
Ideal setting
- A paediatric retrieval team stabilises and transports with full monitoring and ventilation
- The referring doctor's job is early referral, stabilisation to the team's advice and complete documentation
Resource-constrained setting
- You are the retrieval team. The checklist is your work, finished before the vehicle leaves
- Phone and secure acceptance from a named person first; an unannounced child may be turned away, and a family may not survive a second journey financially
- Treat cost and transport as clinical variables. Ask whether the family can reach and afford the referral centre, and use 108/102 ambulance services and government scheme coverage (such as PM-JAY) where eligible
- Send oxygen and a trained escort if at all possible, with a written note that includes your phone number
2 · Talking to families Must-know
SPIKES adapts well to paediatrics: Setting (private, seated, both parents if possible, an interpreter — never a sibling) · Perception (“What have you been told so far?”) · Invitation (“How much would you like me to explain?”) · Knowledge (a warning shot, then plain words; say “died”; use the child's name) · Empathy (stop talking; allow silence) · Summary and strategy (what happens next, and when you will speak again).
Family presence
Offering parents the choice to be present during their child's resuscitation is supported by resuscitation guidelines and by evidence on bereavement: parents who were present generally report less anxiety and better-adjusted grief, and they rarely obstruct care. It needs a designated staff member to stay with them and explain.
3 · Safeguarding Must-know
Features that should raise concern:
- A history that is absent, changing, inconsistent between carers, or impossible for the child's development — a 3-month-old who cannot roll did not roll off the bed.
- Unexplained delay in seeking care.
- Any bruise in a non-mobile infant; bruises on the torso, ears or neck under 4 years; patterned bruises.
- Sharply demarcated, glove-and-stocking or cigarette-shaped burns.
- Rib fractures, metaphyseal fractures, fractures of different ages, retinal haemorrhages, unexplained intracranial injury.
- Neglect: faltering growth that recovers in hospital, untreated dental disease, missed immunisations.
- Fabricated or induced illness: symptoms seen only by one carer; findings that never match the reported severity.
India lens
The Protection of Children from Sexual Offences (POCSO) Act, 2012 makes it mandatory for anyone, including doctors, who knows of or suspects a sexual offence against a child to report it to the Special Juvenile Police Unit or local police; failure to report is itself an offence. Medical examination and treatment of a child survivor must not be refused or delayed. Beyond POCSO, report concerns about abuse or neglect to the District Child Protection Unit or Child Welfare Committee under the Juvenile Justice Act, and use Childline 1098. Know who your hospital's designated safeguarding person is before you need them.
4 · Quality improvement: closing the know–do gap Good-to-know UG/PG
| Element | Example |
|---|---|
| Aim | “Increase the proportion of children with suspected sepsis receiving antibiotics within 60 minutes of recognition from 35% to 80% within 6 months.” |
| Outcome measure | Time from recognition to first antibiotic dose |
| Process measures | Documented triage category; recorded weight; time to IV or IO access |
| Balancing measure | Total antibiotic use — to detect over-treatment of children who were not septic |
| Changes to test | A sepsis grab-box; a weight-banded dose card; nurse-initiated antibiotic preparation; a run chart at the nursing station |
Improvements that reliably narrow the gap: pre-calculated weight-banded emergency drug charts; checklists for intubation, transfer and sepsis; in-situ simulation in the real clinical space; structured handover; and no-blame mortality review with documented actions. Report projects using SQUIRE 2.0.
5 · Future directions Nice-to-know PG
| Direction | Where it stands | The honest caveat |
|---|---|---|
| Machine-learning deterioration prediction | Can outperform threshold scores in high-income hospitals with rich electronic records | Mostly built on data that district hospitals do not collect; discrimination in a development set says nothing about whether outcomes improve — the EPOCH lesson again |
| Sepsis sub-phenotypes | Distinct biological endotypes are being identified | The most plausible route out of guidelines built on low-certainty evidence — not yet at the bedside |
| Point-of-care ultrasound | Handheld probes are cheap; useful for lungs, volume and heart function | Operator-dependent; needs training and governance or it produces confident errors |
| Rapid diagnostics and host-response tests | Could distinguish bacterial from viral illness and cut antibiotic use | Cost and supply chain, not the technology, are the constraint |
| Oxygen systems and pulse oximetry | Measurable mortality impact in childhood pneumonia | The highest-yield “technology” here, and the least discussed |
The closing argument
Nothing in this module is hard to understand. Almost all of it is hard to do reliably at three in the morning, on the fortieth child of the shift, when the cylinder is empty and the family cannot afford the referral. That is the real clinical problem — and the reason systems matter as much as knowledge.
A 3-month-old has a bruise on the left cheek. The parents say she rolled off a sofa. On examination she cannot yet roll over. What is the most appropriate action?
Nudge
Can a baby who cannot roll fall off a sofa by rolling?
Structured hint
Any bruise in a non-mobile infant is a red flag, and here the history does not fit the child's development. What does that combination require?
Why the answer is what it is
A bruise in a non-mobile infant with a history that does not fit her development is a safeguarding concern. Examine fully (including skin, fontanelle, eyes and mouth), document exactly, involve senior and safeguarding colleagues, and investigate for hidden injuries according to local protocol.
A CHC is transferring a 2-year-old with septic shock who has responded partly to fluid and antibiotics. The ambulance is ready. Which step is most important before the vehicle leaves?
Nudge
What can a child arriving unannounced at a full tertiary centre face?
Structured hint
The two things that most often cause transfer disasters are an unstable child and an unexpected arrival. Which option prevents both?
Why the answer is what it is
Finish the stabilisation checklist (airway, oxygen plus reserve, secured lines, glucose, warmth, documents) and phone for acceptance by a named person. An unannounced child may be turned away, and a second journey can be dangerous and unaffordable.
Final assessment and certificate
A single score is not a defensible basis for a high-stakes decision about a clinician. This module certifies on three independent criteria, each measuring something the others cannot.
Where you stand
Coverage asks whether you have met every unit. Retention asks whether the learning survived a night's sleep — it counts breadth across units, not raw items, because a raw count can be satisfied entirely from the units you met first, leaving the newest and most fragile learning untested. Applied performance asks whether you can integrate across units under closed-book conditions.
The closed-book integrated assessment
- 50 items sampled from a pool of 70 — your 40 unit checkpoints plus 30 fresh integrative items written for this assessment only.
- Item and option order randomised on every attempt, so two attempts are never the same paper and answer-position memory is worthless.
- 75 minutes, no hints, no rationales, no feedback until you submit. You may move back and forth and change answers.
- Two attempts, with a 24-hour lock between them — deliberately, so that the gap is filled by remediation and sleep rather than by immediate re-guessing.
- Cut score 80%. Shipped labelled provisional — see the note below and the standard-setting worksheets in Appendix C.
- On submission you get a per-unit remediation plan built from your actual misses, and an item-by-item review with full rationales.
—
If you do not reach the cut score
This is designed to be recoverable, not punitive. In order:
- Read the remediation plan printed after your attempt. It names the units your misses clustered in, ranked.
- Re-open those units and re-answer their checkpoints cold. Do not skim the prose first — attempt the questions, fail them if you are going to, and let the rationale teach you. Retrieval before re-reading is worth several passive re-readings.
- Use the hints deliberately. A hinted item stays in the first spaced-retrieval box, so it will come back tomorrow and the day after until you own it.
- Work the key-feature problems in Appendix A. They test the same decisions in an open-response format, which exposes gaps that multiple choice hides.
- Sleep on it. The 24-hour lock is not an obstacle; it is part of the intervention.
If after two attempts you are still short, ask your faculty to reset your attempts from the panel below. There is no limit on learning, only on how many attempts count toward one certificate.
On the cut score — read this before you defend it to anyone
A cut score chosen by preference is the weakest defensible option available. Published comparisons of standard-setting methods applied to the same assessment have produced cut scores ranging from roughly 66% to 86% — which means the method you choose can matter more than the candidates' performance. This module therefore ships its cut score as provisional, and Appendix C provides modified Angoff, Ebel and Hofstee worksheets plus borderline-regression guidance so your institution can set a defensible one for your own cohort before using this for any consequential decision.
Certificate
The certificate becomes available when all three criteria above are met. That is deliberate: it is what lets the certificate say something specific rather than something vague.
Your certificate
All three criteria are met. Enter the name exactly as you want it printed.
The completion record is a small JSON file holding your details, your three criteria and the verification code. Send it to your faculty; they can open it in verify.html alongside this module to read it back and check the figures have not been altered in transit. It is self-attested — generated on your own device — so treat it as a signed statement from you, not as proof issued by a third party.
What this certificate does and does not say
It attests knowledge and clinical reasoning demonstrated by written assessment. It does not attest bedside competence, confers no licence or clinical privilege, and is not a substitute for supervised, hands-on emergency paediatric training. It confers no provider status in ETAT, PALS or any other named course. No CME credit unless separately accredited by your institution. The verification code is a deterministic hash of the displayed figures — it is re-derivable, not tamper-proof, and should be treated as a convenience for checking transcription, not as a security feature.
Faculty settings
Change these before distributing the module, then use Export a configured copy to produce a file with your settings baked in for your learners. These settings live only in this browser until you export.
Scan or photograph your signature on white paper. It is downscaled to 600 px wide, the paper is matted out so only the ink remains, and the result is stored inside the file — so it travels with the exported copy and adds to its size. A PNG that already has a transparent background is used as-is.
Two recurring traps when publishing: uploading the unconfigured file (so the certificate carries no signatory), and embedding a full-resolution photograph (base64 adds about a third to its size — resize to roughly 400 × 400 first).
Appendices A–G
Open from the first minute, whatever your progress. Appendix E (drugs, fluids and equipment) and Appendix F (references) are clinical safety material, and clinical safety material behind a quiz is a patient-safety problem. Every appendix can be printed on its own.
▸A · Assessment bank
A1 · Blueprint against Miller's pyramid
No single instrument samples all four levels. This is what each part of the programme can honestly claim.
| Miller level | What it means | Instrument here | Weight |
|---|---|---|---|
| Knows | Recalls facts, doses, thresholds | Unit checkpoints; final assessment | ~25% |
| Knows how | Applies knowledge to a clinical problem | Case-vignette checkpoints; integrative items; key-feature problems | ~45% |
| Shows how | Demonstrates in simulation | OSCE stations (A3); scenarios (Appendix B); DOPS | ~20% |
| Does | Performs in real practice | Mini-CEX, CBD, MSF, entrustment (A4) | ~10% |
What the written assessment cannot do
The module's certificate covers only the top two rows. Anyone using it for a consequential decision must add the bottom two, with a mannequin, printed vital-sign cards and a faculty observer.
A2 · Key-feature problems
Short answers, no options. They test only the decisions on which the case turns. Use them in remediation clinics and vivas.
KF1 — The febrile toddler at a district hospital
A 2-year-old with fever for three days: heart rate 170/min, capillary refill 4 s, BP 90/60 mmHg, alert. No ventilator, no PICU.
- Is this child hypotensive, and what is your fluid decision?
Model: threshold 74 mmHg, so not hypotensive; no bolus (SSC 2026, strong); maintenance fluid. - Name three actions in the first 30 minutes that do change outcome here.
Model: antibiotics within the hour, glucose check and correction, haemoglobin check and transfusion if severe anaemia, early transfer, warmth.
KF2 — The drowsy child with diabetes
An 11-year-old with DKA, 6 hours into treatment, develops headache and a heart rate falling from 120 to 70/min.
- What is the diagnosis, and what do you give?
Model: cerebral oedema; mannitol 0.5–1 g/kg or 3% saline 2.5–5 mL/kg over 10–15 minutes, head up, reduce fluids. - Does this need a scan first?
Model: no — treat clinically; image after stabilisation.
KF3 — The wasted child with diarrhoea
An 18-month-old, MUAC 105 mm, sunken eyes, drinking eagerly, warm hands.
- Which rehydration solution, how much, how fast?
Model: ReSoMal 5 mL/kg every 30 min for 2 h, then 5–10 mL/kg/h, alternating with F-75. - Name three signs that should make you stop.
Model: rising pulse, rising respiratory rate, enlarging liver, puffy eyelids.
KF4 — Night-time abdominal pain in a farming village
A 7-year-old woke at 3 a.m. with abdominal pain and vomiting; now has ptosis.
- Diagnosis and first treatment?
Model: krait envenomation; 10 vials ASV, adrenaline drawn up. - What is the life-saving supportive treatment?
Model: ventilation — bag-mask if nothing else.
A3 · OSCE stations
Twelve stations, 6–8 minutes each, on a doll with printed vital-sign cards. Score with the six-domain rubric in Appendix C.
| # | Station | Tests | Critical failure |
|---|---|---|---|
| 1 | Paediatric Assessment Triangle from a video or actor | Category and first move | Misses abnormal appearance |
| 2 | ETAT triage of six cards in 6 minutes | Emergency, priority, queue | Queues a child with an emergency sign |
| 3 | Airway opening and bag-mask ventilation | Position, adjunct, E-C grip, rate, chest rise | No chest rise, not corrected |
| 4 | Intraosseous insertion | Site, technique, confirmation, flush | Wrong site or no confirmation |
| 5 | The bolus cycle | Fluid choice, aliquot, four reassessment questions | Misses a stop signal |
| 6 | Sepsis first hour, setting-specific | Time targets, fluid decision by setting | Bolus in a non-hypotensive child without ICU |
| 7 | Status epilepticus to 20 minutes | Drugs, doses, routes, ceiling | Third benzodiazepine |
| 8 | DKA first hour and cerebral oedema recognition | Fluid, insulin timing, warning signs | Insulin bolus or bicarbonate |
| 9 | Severe wasting with shock | 15 mL/kg over an hour; monitoring | Plan C volumes |
| 10 | Snakebite: 20WBCT and ASV | Test, dose, reaction management | Weight-scaled ASV |
| 11 | Anaphylaxis | IM adrenaline dose and site | Antihistamine first |
| 12 | Breaking bad news (SPIKES), with an actor | Setting, language, silence, plan | Euphemism; leaves without a plan |
A4 · Workplace-based assessment
| Tool | Use it for | Frequency | Note |
|---|---|---|---|
| Mini-CEX | An observed triage or first-hour assessment | 2–4 per learner per year | The feedback is the intervention |
| DOPS | IO insertion, bag-mask ventilation, bolus administration | Until entrustment, then annually | Score the procedure, not the person |
| CBD | Reasoning behind a case the learner led | 2–3 per year | Ask “what else did you consider?” |
| MSF | Teamwork and communication, from nurses and peers | Annual | Detects the behaviours that cause harm |
Entrustment scale for the core EPA
EPA: Recognise, triage and lead the first hour of care of a seriously ill child, including a setting-appropriate fluid decision and timely referral.
| Level | Descriptor |
|---|---|
| 1 | Observes only |
| 2 | Performs with direct supervision |
| 3 | Performs with indirect supervision, supervisor reachable within minutes |
| 4 | Performs unsupervised; supervisor available for the unexpected |
| 5 | Supervises and teaches others |
Minimum standard for a doctor covering a paediatric emergency room alone: level 4 for triage, airway support, IO access and the sepsis first hour; level 3 or above for status epilepticus and DKA.
▸B · Simulation library
Four branching scenarios that run on a doll and printed vital-sign cards — no simulator needed. Show the next card only when the team has done, or clearly failed to do, the expected actions.
Scenario 1 — The febrile toddler without a PICU
District hospital, 2 a.m. A 2-year-old, 12 kg, fever 3 days, drowsy. One doctor, two nurses. No ventilator.
| Stage | Vital-sign card | Expected actions | Facilitator trigger |
|---|---|---|---|
| 1 | HR 170, RR 40, CRT 4 s, BP 88/56, SpO₂ 95%, glucose 2.2 | PAT, say “sepsis”, glucose 10% 5 mL/kg, access (IO if needed), antibiotics | If no glucose check after 3 min: “He is now twitching.” |
| 2 | HR 165, BP 90/58, Hb 5 g/dL | No bolus (not hypotensive, no ICU); maintenance; blood transfusion; call referral centre | If a 20 mL/kg bolus is started: next card shows crackles and SpO₂ 88% |
| 3 | Stable or deteriorating per branch | Transfer checklist, ISBAR handover by phone | Receiving unit asks: “What is his weight and what has he had?” |
Debrief points: the 2026 setting-specific fluid recommendation; hypoglycaemia and anaemia as outcome-changing actions; the transfer decision as a treatment.
Scenario 2 — Status epilepticus in a toddler
PHC. An 18-month-old, 10 kg, convulsing on arrival, started 8 minutes ago at home. No IV access yet.
| Stage | Vital-sign card | Expected actions | Facilitator trigger |
|---|---|---|---|
| 1 | Convulsing, SpO₂ 90% | Airway, oxygen, glucose, buccal/intranasal midazolam 0.3 mg/kg, note the time | If no clock: “Mother asks how long it has been.” |
| 2 | Still convulsing at 10 min | Second benzodiazepine; IO/IV access | If a third benzodiazepine is proposed: RR falls to 8 |
| 3 | Still convulsing at 20 min | Second-line drug (phenobarbital/phenytoin/levetiracetam); look for cause; call for help | Sodium card: 121 mmol/L — does the team give 3% saline? |
Debrief points: the two-dose ceiling; route flexibility; searching for a cause.
Scenario 3 — DKA on the ward
Paediatric ward. A 10-year-old, 28 kg, newly diagnosed DKA, pH 7.02, treated for 5 hours.
| Stage | Vital-sign card | Expected actions | Facilitator trigger |
|---|---|---|---|
| 1 | HR 110, BP 110/70, GCS 15, glucose 14 | Add glucose to fluids, continue insulin, check potassium | If insulin is stopped: ketones rise on the next card |
| 2 | Headache, vomiting, HR 68, BP 132/86 | Recognise cerebral oedema; mannitol or 3% saline now; head up; reduce fluid | If CT is requested first: GCS falls to 10 |
| 3 | Improving | Senior review, HDU, imaging once stable | — |
Debrief points: treating cerebral oedema clinically; insulin and glucose together.
Scenario 4 — Snakebite at a CHC
CHC, 9 p.m. A 9-year-old bitten on the ankle while walking in a paddy field, 2 hours ago. Tourniquet applied by family.
| Stage | Vital-sign card | Expected actions | Facilitator trigger |
|---|---|---|---|
| 1 | Swollen leg, gum bleeding | Remove tourniquet carefully, 20WBCT, IV access, adrenaline drawn up | 20WBCT card: unclotted |
| 2 | Unclotted | 10 vials ASV over 30 min | 5 min into infusion: urticaria, stridor, BP 70/40 |
| 3 | Anaphylaxis | Stop infusion, IM adrenaline 0.01 mg/kg, fluid; restart ASV when settled | Urine output falling at 6 h: refer for dialysis with notes |
Debrief points: ASV dose not weight-scaled; reaction management; when to refer.
Debriefing — the PEARLS structure
Debrief for at least as long as the scenario ran. Sit down. Phones away.
| Phase | Time | Say |
|---|---|---|
| Setting the scene | 1 min | “We're here to learn, not to judge. What's said here stays here. I believe everyone did their best with the information they had.” |
| Reactions | 2 min | “In a word or two — how was that?” Let everyone speak. Do not analyse yet. |
| Description | 2 min | “Can someone walk us through what happened, clinically?” Establish shared facts before opinions. |
| Analysis | 10–15 min | The body of the work. Choose 2–3 points, no more. Use the three methods below. |
| Summary | 3 min | “One thing to keep, one thing to change.” From them, not from you. |
Three analysis methods, chosen by what you are addressing:
- Plus–delta — for performance that was broadly good. “What worked? What would you change?” Fast, safe, low yield.
- Advocacy–inquiry — for a specific puzzling action. State your observation and your reasoning, then ask theirs: “I noticed compressions started while the chest wasn't moving. I was concerned because that circulates deoxygenated blood. I'm curious what you were seeing at that moment.” This is the highest-yield technique and the hardest to do well — the inquiry must be genuine.
- Directive feedback with teaching — for a knowledge gap. Do not use inquiry to extract a fact somebody does not have; that is humiliating. Say the fact, explain the mechanism, move on.
Pearl — debrief the system, not only the people
At least one of your two or three analysis points should be about the environment: where the oxygen and the IO needles were, how long help took, whether the clock was visible. Those findings are the ones that improve the next real resuscitation, including the ones this team is not present for.
▸C · Faculty guide
C1 · Three delivery models
| Model | Shape | Best for | Watch out for |
|---|---|---|---|
| Fully self-paced | Learners work through alone; one skills session at the end | Large cohorts, interns, CME | The skills session becoming a demonstration. Cap at 6 learners per doll. |
| Flipped, Part by Part | Learners master a Part before each session; sessions are simulation and discussion | PG residents, nursing cohorts | Verify mastery first, or you end up teaching content |
| Intensive, 2 days | Parts A–C day one with simulation; D–E day two | District outreach, visiting faculty | Retention: schedule the review checks and a 6-week follow-up |
C2 · A worked flipped-classroom session — Part C, shock
90 minutes, 8–12 learners, 2 dolls, 2 facilitators. Prerequisite: Units 8–11 mastered.
| Time | Activity | Purpose |
|---|---|---|
| 0–5 | Learning contract: “Nobody here is being examined.” | Psychological safety |
| 5–15 | Rapid retrieval: the four reassessment questions; the three SSC 2026 fluid recommendations; hypotension formula | Retrieval practice; shows where the cohort is |
| 15–35 | Deliberate practice: IO insertion on a model bone and the push-pull bolus technique | The highest-yield procedural skill in Part C |
| 35–55 | Scenario 1 (Appendix B), run twice — once as a district hospital, once as a PICU-backed ED | The setting-specific decision under time pressure |
| 55–75 | Debrief both runs, PEARLS, two points maximum | Consolidation |
| 75–85 | The fifteen-second cardiac check on each other and on a doll with a “big liver” card | Makes the stop signal a habit |
| 85–90 | “One thing to keep, one thing to change.” | Commitment to change |
C3 · Feedback structures
R2C2 — for longer, formal feedback
- Relationship — establish respect and genuine interest. “How is the rotation going for you?”
- Reaction — explore their response to the data before interpreting it. “What's your reaction to this feedback?”
- Content — confirm shared understanding of what the assessment actually says.
- Coaching — co-create a specific plan with a date. “What would you like to work on before we meet in six weeks?”
Ask–Tell–Ask — for brief, in-the-moment feedback
Ask: “How do you think that went?” · Tell: one specific observation and one specific suggestion · Ask: “What will you do differently next time?” Ninety seconds, at the warmer, immediately afterwards.
C4 · Six-domain performance rubric
Score 1 (needs significant improvement) to 5 (exemplary). Use for OSCE stations and simulation.
| Domain | Level 2 | Level 4 |
|---|---|---|
| Preparation | Glances at the trolley; no device test | Standardised checklist completed; device tested; roles assigned |
| Assessment | Heart rate estimated, not measured; not reported aloud | Six-second count, tapped out, reported with units; oximeter placed pre-ductally |
| Technical skill | Mask leak unaddressed; pressure raised before obstruction excluded | Seal achieved by jaw lift or two hands; MR SOPA in order and announced |
| Decision-making | Escalates on one signal; or delays past 60 seconds | States all signals aloud before acting; escalates only when preconditions met |
| Communication | Instructions to the room; no closed loops | Named individuals, closed loops, drug orders by name-dose-route-concentration |
| Leadership & situation awareness | Absorbed in a procedure; loses the clock | Thinks aloud; delegates; hands over leadership when drawn into a procedure |
C5 · Standard setting — set your own cut score before you use this for anything consequential
Why this matters more than you think
Published comparisons of standard-setting methods applied to the same assessment have produced cut scores ranging from roughly 66% to 86%. That means the method you choose can matter more than how your candidates perform. A cut score chosen by preference — including the 80% this module ships with — is the weakest defensible option available. Do one of the exercises below with three to six judges before the module carries any consequence.
Modified Angoff worksheet
- Define the borderline candidate in writing, as a person: “a first-year resident who would reliably triage, get access and start antibiotics and a setting-appropriate fluid plan within the hour, but would hesitate over a vasoactive dose or a second-line antiseizure drug.” Judges must agree this before seeing any item.
- For each item, each judge independently estimates: out of 100 borderline candidates, how many would answer this correctly? Record as a percentage.
- Discuss items where judges differ by more than 20 points. Do not force consensus; discuss, then re-rate independently.
- The cut score is the mean of the judges' mean estimates.
- Record the standard error and consider whether to adjust for it. Document everything.
Ebel worksheet
Classify each item on two axes, then assign an expected percentage-correct to each cell.
| Easy | Medium | Hard | |
|---|---|---|---|
| Essential | —% | —% | —% |
| Important | —% | —% | —% |
| Acceptable | —% | —% | —% |
Cut score = Σ(items in cell × expected % for that cell) ÷ total items. Ebel is useful here because the module already tiers content as must / good / nice-to-know, which maps onto essential / important / acceptable.
Hofstee — a sanity check on whatever you produce
Judges agree four values: the minimum and maximum acceptable cut score, and the minimum and maximum acceptable failure rate. Plot the cumulative score distribution and find where the line crosses the rectangle those four values define. If your Angoff or Ebel cut falls outside that rectangle, something is wrong — either with the standard or with the assessment. Hofstee will not give you a defensible cut on its own, but it will stop you shipping an indefensible one.
Borderline regression, for the OSCE
For each station, examiners record both a checklist score and a global rating (fail / borderline / pass / good pass). Regress checklist score on global rating; the cut score is the checklist score predicted by a global rating of “borderline”. This is more defensible than a fixed percentage because it is anchored in expert judgement of these candidates on this station, and it generates the data as a by-product of examining.
C6 · Programme evaluation — Kirkpatrick
| Level | Question | How to measure | Realistic? |
|---|---|---|---|
| 1 · Reaction | Did they find it useful? | Five-question post-session survey | Yes — and nearly worthless on its own |
| 2 · Learning | Did knowledge and skill change? | The module's three criteria; OSCE scores; pre/post | Yes. This is what the module measures |
| 3 · Behaviour | Did practice change? | Emergency-room audit: time from arrival to antibiotics, triage-to-treatment time, weight recorded, bolus decisions by setting | Yes, with effort. The most valuable level you can actually reach |
| 4 · Results | Did outcomes change? | Deaths within 24 hours of arrival, unplanned PICU transfers, hospital-acquired hyponatraemia | Rarely attributable to training alone. Report honestly as association |
Most published resuscitation training evaluations stop at level 1 or 2. If you can get to level 3 with an emergency-room audit, you are doing better than most of the literature — and you will have data worth publishing.
▸D · Curriculum mapping
Map each unit to the competency descriptors of the NMC CBME curriculum. The code column is deliberately blank: codes were revised in the September 2024 guidelines, and Volume II is the only authority. Do not invent codes; fill them in from the current document.
| Unit | Competency descriptor (paraphrased) | NMC code (verify) | Domain | Teaching method | Assessment |
|---|---|---|---|---|---|
| 1–3 | Recognise the seriously ill child; explain paediatric physiology relevant to emergencies | K, S | Self-paced module; case discussion | Checkpoints; CBD | |
| 2 | Perform triage using WHO ETAT and the Paediatric Assessment Triangle | S | Simulation with cards | OSCE 1–2 | |
| 4 | Assess and manage the airway and breathing; deliver oxygen and bag-mask ventilation | S | Skills lab | DOPS; OSCE 3 | |
| 5, 8–10 | Recognise and manage shock, including fluid therapy and vascular access | K, S | Flipped session (C2) | OSCE 4–6; Mini-CEX | |
| 6, 13 | Assess the child with altered sensorium; manage status epilepticus and raised ICP | K, S | Simulation | OSCE 7 | |
| 7 | Recognise and treat hypoglycaemia and electrolyte emergencies | K | Case-based | Checkpoints | |
| 11 | Manage dehydration (WHO plans) and DKA | K, S | Case-based; simulation | OSCE 8; KF2 | |
| 12, 14 | Manage common poisonings and envenomations | K, S | Case-based | OSCE 10; KF4 | |
| 15 | Primary survey of the injured child; burns first aid and fluid | K, S | Simulation | Checkpoints | |
| 16 | Manage severe wasting and nutritional oedema | K, S | Ward-based; NRC visit | OSCE 9; KF3 | |
| 17 | Identify and manage serious bacterial infection in young infants | K, S | IMNCI practice | Mini-CEX | |
| 18–19 | Recognise red flags; manage children with complex needs | K, A | Case-based | CBD | |
| 20 | Refer and transport safely; communicate with families; safeguard children | S, A, C | Role play | OSCE 12; MSF |
Why the code column is empty
Invented or outdated competency codes are worse than none — they propagate into curriculum documents and audits. Fill the column from NMC CBME Volume II (2024) at your institution.
▸E · Drug, fluid and equipment annex
Verify before every use
Doses here are drawn from the cited guidelines for learning. Check every dose against your institution's protocol, a current formulary and the child in front of you. Where local protocol differs, follow local protocol. This annex is never locked.
E1 · Resuscitation and emergency drugs
| Drug | Indication | Dose | Notes |
|---|---|---|---|
| Adrenaline 1 mg/mL (1:1000) IM | Anaphylaxis, ASV reaction | 0.01 mg/kg (0.01 mL/kg), max 0.5 mg | Anterolateral thigh; repeat after 5 min |
| Adrenaline 0.1 mg/mL (1:10,000) IV/IO | Cardiac arrest | 0.01 mg/kg (0.1 mL/kg), max 1 mg | Every 3–5 min (see PALS module) |
| Adrenaline infusion | Shock | 0.05–0.3 microgram/kg/min, titrate | Peripheral or IO acceptable; watch the site |
| Noradrenaline infusion | Shock (vasodilated) | 0.05–0.3 microgram/kg/min, titrate | As above |
| Dopamine infusion | Shock where others unavailable | 5–10 microgram/kg/min | |
| Dobutamine infusion | Low output, myocarditis, scorpion | 5–10 microgram/kg/min (up to 20) | |
| Adenosine | SVT | 0.1 mg/kg rapid push (max 6 mg); then 0.2 mg/kg (max 12 mg) | Rapid flush; ECG running |
| Glucose 10% | Hypoglycaemia | 5 mL/kg IV/IO (neonates 2 mL/kg) | Then glucose infusion; recheck in 15–30 min |
| Calcium gluconate 10% | Hyperkalaemia, hypocalcaemia | 0.5 mL/kg IV slowly (max 20 mL) | ECG monitoring; avoid extravasation |
| Naloxone | Opioid toxicity | 0.1 mg/kg (max 2 mg) | Short-acting; watch for re-sedation |
| Hydrocortisone | Adrenal crisis | ~25 mg (<1 y), 50 mg (1–5 y), 100 mg (>5 y) IV/IM | Use the child's emergency letter if available |
| Prostaglandin E1 | Duct-dependent lesion | Per cardiology advice | Apnoea risk; be ready to ventilate |
E2 · Fluids
| Situation | Fluid and volume |
|---|---|
| Septic shock, ICU available | Balanced crystalloid 10–20 mL/kg boluses, up to 40–60 mL/kg in hour 1 |
| Sepsis without hypotension, no ICU | No bolus; maintenance |
| Septic shock with hypotension, no ICU | 10–20 mL/kg boluses, up to 40 mL/kg |
| Severe dehydration (WHO Plan C) | Ringer's lactate 30 mL/kg then 70 mL/kg: under 12 m over 1 h + 5 h; 12 m and over 30 min + 2½ h |
| Severe wasting with shock | 15 mL/kg over 1 h of Ringer's lactate with 5% glucose (or half-normal saline with 5% glucose) |
| DKA | Shock: 20 mL/kg rapidly; otherwise 10–20 mL/kg over 20–30 min; deficit + maintenance over 24–48 h |
| Burns over ~10% TBSA | 3–4 mL/kg/%TBSA Ringer's lactate in 24 h (half in first 8 h from burn) plus maintenance with glucose |
| Maintenance (Holliday–Segar) | 4/2/1 mL/kg/h; isotonic with glucose as needed |
E3 · Neurological and metabolic emergencies
| Drug | Dose | Notes |
|---|---|---|
| Lorazepam IV/IO | 0.1 mg/kg (max 4 mg) | Two benzodiazepine doses maximum |
| Diazepam IV / rectal | 0.2–0.3 mg/kg IV (max 10 mg); 0.5 mg/kg rectal (max 10–20 mg) | |
| Midazolam buccal / intranasal | 0.3 mg/kg (max 10 mg) | No IV needed |
| Levetiracetam IV | 40–60 mg/kg (max 3–4.5 g) over 5–15 min | |
| Phenytoin IV | 20 mg/kg over 20 min | ECG or pulse monitoring |
| Valproate IV | 40 mg/kg (max 3 g) | Avoid in liver or metabolic disease, under 2 years |
| Phenobarbital IV | 20 mg/kg | Respiratory depression |
| 3% saline | Raised ICP: 3–5 mL/kg; DKA cerebral oedema: 2.5–5 mL/kg; hyponatraemic seizure: 3–5 mL/kg | Over 10–20 min |
| Mannitol | 0.5–1 g/kg over 10–15 min | |
| Insulin (DKA) | 0.05–0.1 unit/kg/h, at least 1 h after fluids start | No bolus |
E4 · Poisoning and envenomation
| Agent | Dose | Notes |
|---|---|---|
| Atropine (organophosphate) | 0.02–0.05 mg/kg IV, double every 5 min to a clear chest; then infusion ~10–20% of loading dose/h | Endpoint is secretions, not pupils |
| Activated charcoal | 1 g/kg (max 50 g) | Within ~1 h; airway protected; not for hydrocarbons, iron, corrosives, alcohols |
| N-acetylcysteine | Per national/local regimen | Start within 8 h of paracetamol ingestion |
| Anti-snake venom (polyvalent) | 10 vials over 30 min (same for children); repeat per protocol | Neurotoxic: second 10 vials at 1 h if no improvement (max 20) |
| Neostigmine trial (neurotoxic) | Atropine 0.05 mg/kg then neostigmine 0.04 mg/kg (national STG) | Most useful in cobra bites |
| Prazosin (scorpion) | 30 microgram/kg orally, repeat according to response | Watch for first-dose hypotension |
E5 · Equipment by weight
| Formula or guide | |
|---|---|
| Weight estimate (if no scale) | Use a length-based tape; formula estimates are less accurate |
| Tracheal tube (cuffed) | (age/4) + 3.5 mm; depth ~3 × internal diameter |
| IO needle sites | Proximal tibia (1–2 cm below and medial to tuberosity); distal femur; proximal humerus in older children |
| Systolic hypotension | Under 1 month <60; 1–12 months <70; 1–10 years <70 + 2 × age; over 10 years <90 mmHg |
▸F · References
Primary guidelines — the sources this module is written to
- Weiss SL, Peters MJ, Oczkowski SJW, et al. Surviving Sepsis Campaign International Guidelines for the Management of Sepsis and Septic Shock in Children 2026. Pediatr Crit Care Med 2026;27(4):379–434. PubMed
- Schlapbach LJ, et al. International consensus criteria for pediatric sepsis and septic shock (Phoenix). JAMA 2024.
- Part 8: Pediatric Advanced Life Support. 2025 AHA/AAP Guidelines for CPR and ECC. Pediatrics 2026;157(1):e2025074351.
- World Health Organization. Paediatric emergency triage, assessment and treatment: care of critically-ill children. Geneva: WHO; 2016. WHO
- World Health Organization. Pocket book of hospital care for children, 2nd edition. Geneva: WHO; 2013.
- World Health Organization. WHO guideline on the prevention and management of wasting and nutritional oedema (acute malnutrition) in infants and children under 5 years. Geneva: WHO; 2023.
- World Health Organization. WHO recommendations for management of serious bacterial infections in infants aged 0–59 days. Geneva: WHO; 2024.
- Glaser N, et al. ISPAD Clinical Practice Consensus Guidelines 2022: Diabetic ketoacidosis and hyperglycemic hyperosmolar state. Pediatr Diabetes 2022.
- Emeriaud G, et al. PALICC-2: Second Pediatric Acute Lung Injury Consensus Conference. Pediatr Crit Care Med 2023.
Indian national and professional sources
- Ministry of Health and Family Welfare. Standard Treatment Guidelines: Management of Snakebite (quick reference guide and full document).
- Indian Academy of Pediatrics. Standard Treatment Guidelines, including Poisoning in Children and Snake Envenomation.
- MoHFW. Facility-based IMNCI (F-IMNCI) and Home-Based Newborn / Young Child Care programme guidance.
- National Center for Vector Borne Diseases Control. National guidelines for clinical management of dengue.
- ICMR. Treatment guidelines for antimicrobial use in common syndromes; ICMR AMR surveillance network reports.
- Protection of Children from Sexual Offences Act, 2012; Juvenile Justice (Care and Protection of Children) Act, 2015.
- National Medical Commission. Competency-Based Medical Education curriculum, 2024 guidelines (Volume II for competencies).
Key trials worth reading in full
- Maitland K, et al. Mortality after fluid bolus in African children with severe infection (FEAST). N Engl J Med 2011;364:2483–95.
- Parshuram CS, et al. Effect of a pediatric early warning system on all-cause mortality (EPOCH). JAMA 2018;319:1002–12.
- Kuppermann N, et al. Clinical trial of fluid infusion rates for pediatric diabetic ketoacidosis (PECARN FLUID). N Engl J Med 2018;378:2275–87.
- Kapur J, et al. Randomized trial of three anticonvulsant medications for status epilepticus (ESETT). N Engl J Med 2019;381:2103–13.
- Lyttle MD, et al. Levetiracetam versus phenytoin for second-line treatment of paediatric convulsive status epilepticus (EcLiPSE). Lancet 2019;393:2125–34.
- Dalziel SR, et al. Levetiracetam versus phenytoin (ConSEPT). Lancet 2019;393:2135–45.
- Lacroix J, et al. Transfusion strategies for patients in pediatric intensive care units (TRIPICU). N Engl J Med 2007;356:1609–19.
- Eddleston M, et al. Pralidoxime in acute organophosphorus insecticide poisoning. PLoS Med 2009;6:e1000104.
- Pandi K, et al. Efficacy of scorpion antivenom plus prazosin versus prazosin alone for Mesobuthus tamulus scorpion sting envenomation in children. Arch Dis Child 2014.
Educational evidence base
- Stojan J, et al. BEME Guide No. 69 — technology-enhanced learning in health professions education.
- Regmi K, Jones L (2020) — systematic review of e-learning in health professions education.
- McGee (2024); Taylor (2023); Trumble (2024) — self-directed and asynchronous learning.
- van Gaalen AEJ, et al. (2021) — gamification in health professions education.
- Thompson & Hughes (2023) — spaced retrieval and retention in clinical education.
- Larsen DP, Butler AC, Roediger HL (2009) — test-enhanced learning in medical education. Cepeda NJ, et al. (2006) — distributed practice. Butterfield B, Metcalfe J (2001) — the hypercorrection effect.
- Ottawa 2020 Consensus Statements on programmatic assessment. McKinley RK, Norcini JJ. AMEE Guide No. 85 — standard setting.
Check the edition before you teach from anything
Paediatric emergency guidance changes often: the sepsis guideline changed in 2026, resuscitation in 2025, malnutrition in 2023, young-infant infection in 2024. Before using any figure from this module in teaching or a protocol, confirm it against the current edition of the primary source. If you are reading this more than three years after the build date in the footer, assume something here is out of date and check.
▸G · Evidence-governed design
G1 · Design decisions and the evidence behind them
| Decision | Why |
|---|---|
| Mastery, not completion — no “mark as read” control exists | Completion tracking measures exposure, not learning. A control that lets a learner record progress without demonstrating anything corrupts every downstream figure, including the certificate |
| Two checkpoint items per unit, answered correctly currently | Mastery is a state, not an event. Failing an item later removes the unit's mastered status, which is what makes the coverage criterion meaningful at the moment of certification |
| Sequential Part unlocking | Later content genuinely depends on earlier content — Part C's fluid decisions make no sense without Part B's recognition of shock. Gating also prevents the common self-paced failure of skimming to the topic that looks most interesting |
| Spaced retrieval at 1, 3, 7, 21, 60 days | Retrieval practice at expanding intervals produces substantially better long-term retention than re-reading. Interleaving across units rather than blocking by unit further improves discrimination |
| Confidence rating before each answer; “confident and wrong” flagged | High-confidence errors, once corrected with feedback, are corrected more durably than low-confidence ones (the hypercorrection effect; Butterfield & Metcalfe 2001). Rating confidence also exposes miscalibration, which in clinical work is the profile that harms patients. Confidence-based marking in medical schools (Gardner-Medwin) is the educational precedent. The module reports calibration; it does not score it |
| A review queue with a due count, and a single “next step” | The testing effect is robust in medical education (Larsen, Butler & Roediger 2009) and spacing outperforms massing (Cepeda et al. 2006). A visible due count invites the retrieval that is otherwise the least-performed part of a self-paced course; one named next action reduces the decision cost that stalls self-directed learners |
| Recognition tied to mastery only — no points, badges, leaderboards or streak resets | Short, informative acknowledgement of a mastered unit or an unlocked Part uses the goal-gradient effect without rewarding clicks. Study days are counted but never reset to zero or shamed: learners in Indian postings work rotating nights and irregular duty, and a punitive streak penalises the schedule, not the learning. Gamification reviews in health-professions education report mixed effects, weakest where rewards are decoupled from the learning objective |
| A failed item returns in 10 minutes at box 1 | Immediate re-exposure after an error, followed by expanding intervals, is more effective than either immediate repetition alone or long delay |
| Hinted items stay in box 1 | A hint changes what the item measured. Advancing the interval would record retrieval strength the learner has not demonstrated |
| Rationales explain why wrong options are wrong | Distractor-level feedback corrects the specific misconception that produced the error; “the answer is B” corrects nothing |
| Distractors are errors clinicians actually make | Implausible distractors inflate scores and teach nothing. Several items here are built around a specific documented failure mode |
| Three independent certification criteria | A single score conflates coverage, retention and integration. Separating them lets the certificate state what was actually demonstrated |
| Retention counts breadth across units, not raw items | A raw count can be satisfied entirely from units met earliest, leaving the newest and most fragile learning untested |
| Randomised item and option order; 24-hour lock between attempts | Defeats answer-position memory; the lock forces the gap to be filled with remediation and sleep rather than immediate re-guessing |
| Cut score shipped as provisional with worksheets | Method choice can move a cut score by ~20 points on the same assessment. Shipping a preference-based cut without saying so would be dishonest |
| Dual-track ideal / resource-constrained panels as equals | Guidance written for well-resourced settings is routinely taught unmodified where the equipment does not exist, which teaches learners that correct practice is impossible for them |
| Emergency dosing never gated | Clinical safety material behind a quiz is a patient-safety problem |
| All state local; no account, no telemetry | Collecting nothing is the only fully reliable way to protect learner data, and satisfies the DPDP Act 2023 by construction. It also means the file works offline, which is the difference between usable and unusable in much of India |
| Single self-contained HTML file | No CDN, no framework, no network request. Survives being emailed, copied to a phone, and opened three years from now |
| Learner-controlled priority, level, setting, text size and theme | UDL 3.0: multiple means of representation and engagement, with the learner in control rather than an algorithm |
G2 · Accessibility conformance
- Semantic landmarks, skip link, keyboard-operable accordions with
role="button", Enter/Space activation andaria-expanded. - Scrollable regions given
tabindex="0"androle="region"with labels, so keyboard users can reach wide tables and algorithms. aria-pressedon all toggles; visible:focus-visibleoutlines; minimum 44 px touch targets.- Learner-controlled text scaling;
prefers-reduced-motionrespected; three-state theme (light / dark / system) that works in all three. - No meaning conveyed by colour alone — every status colour is paired with a text label or a symbol.
- Tables receive
data-labelattributes by script and reflow to labelled cards below 560 px. - Mobile-first CSS with desktop enhancement at 900 px; no horizontal page scrolling at 400 px.
- Targets WCAG 2.2 AA. Not independently audited — see limitations.
G3 · Where this design is weaker than it looks
Published honestly, because a module claiming to be evidence-governed must be willing to
- Fixed intervals, not fitted forgetting curves. The Leitner schedule (1-3-7-21-60) is a crude approximation. A genuinely adaptive system would fit each learner's forgetting curve per item. This does not, and cannot, without collecting the data it deliberately does not collect. That is a real trade-off, not a free lunch.
- Thin item sampling per unit. Two checkpoint items cannot reliably sample a unit's content. Mastery of a unit here means “answered these two specific items correctly”, which is a weaker claim than it appears. The final assessment partially compensates; it does not eliminate the problem.
- Rule-based placement, not adaptive testing. The three placement questions set defaults by simple rules. They are not a measurement, and they do not adjust as evidence accumulates about what the learner actually knows.
- Limited form-to-form equivalence. Attempts sample 50 items from a pool of 70 with randomised order, so two attempts are not statistically equated. A score of 88% on one attempt is not strictly the same as 88% on another.
- Unproctored assessment. Nothing prevents a learner opening the module in another tab, or working with a colleague. The module is honest about this: it is a self-assessment with a certificate attached, and any high-stakes use requires proctoring and the skills assessment in Appendices A and B.
- The verification code is not tamper-proof. It is a deterministic hash of the displayed figures, re-derivable by anyone with the same inputs. It helps detect transcription error. It is not a security feature and is described as such on the certificate.
- The cut score is provisional and was chosen by preference. Appendix C exists because this is the weakest defensible option. Until your institution does the standard setting, treat the pass/fail line as an approximation.
- Kirkpatrick levels 3 and 4 are unmeasured. This module has no evidence that it changes emergency-room behaviour or child outcomes. Nor does almost any comparable resource — but the absence should be stated rather than implied away.
- Accessibility is targeted, not audited. WCAG 2.2 AA conformance has not been independently verified, and has not been tested with real screen-reader users. Automated checks and manual keyboard testing are not the same as a user audit.
- Clinical content has not been externally peer reviewed. It is written to the current primary guidelines and cross-checked, but it carries no editorial board and no formal review process. Corrections are welcomed and should be treated as expected rather than exceptional — see CONTRIBUTING.
- India-specific epidemiology moves. The figures quoted are from the most recent sources available at build; verify against the current SRS bulletin and national cause-of-death estimates before quoting them in teaching.
- One author, one perspective. Every choice about what is must-know versus nice-to-know reflects a single clinician's judgement about what matters at a district hospital at 2 a.m. Reasonable educators would tier some of it differently.
G4 · Frameworks this module aligns itself to
WHO ETAT, IMCI and hospital care guidance for children · WFME standards for medical education · NMC CBME (India, 2024 revision) · ICMR and MoHFW national programme guidance · CAST Universal Design for Learning 3.0 · WCAG 2.2 · Digital Personal Data Protection Act 2023 (India) · Ottawa consensus statements on programmatic assessment.