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Paeds Casesgrowth-development-and-behaviour

Paeds Cases · growth-development-and-behaviour

Floppy infant OSCE — localisation, safety and family counselling

OSCE on floppy infant assessment: bedside localisation, red-flag recognition, urgent pathway and closed-loop counselling.

osce short clinical and communication station
On this page & tools

Target exams

RACP General PaediatricsRACP DCEMRCPCH ClinicalRCPSC Pediatrics

Target exams

RACP General PaediatricsRACP DCEMRCPCH ClinicalRCPSC Pediatrics
Prompt
Station A is a 10-minute assessment of a 3-month-old with progressive floppiness. Station B is 8 minutes counselling parents after you identify a peripheral progressive pattern.

Station objectives

  1. Distinguish tone, strength and laxity at the bedside. [1]
  2. Localise central versus peripheral patterns using power, reflexes and posture. [1] [2]
  3. Recognise progressive SMA-pattern red flags and protect airway/feeding. [5] [9]
  4. Counsel concurrent urgent genetics/neuromuscular referral without false reassurance. [9]
  5. Use teach-back and a closed-loop safety-net plan. [5]

Candidate brief

You are the doctor in a paediatric assessment unit. Station A: examine and reason aloud with a parent and infant mannequin/actor. Station B: explain findings and plan. [1]

Station A — Clinical assessment (10 minutes)

Parent script: “She was smiling last month but now her head flops and she tires with feeds. A friend said low tone is common.” [1]

Expected candidate actions: [1]

  1. Observe breathing, posture, spontaneous antigravity movement before handling. [1]
  2. Assess passive tone, traction/suspension manoeuvres, power, deep tendon reflexes, tongue. [1] [2]
  3. Screen suck–swallow, cough and work of breathing; pause oral feeds if unsafe. [5]
  4. State working localisation: progressive peripheral pattern ± SMA concern if areflexia/fasciculations. [9]
  5. List same-day actions: stabilise, SMN1 pathway, neuromuscular referral — not “review next month.” [9]

Station B — Counselling (8 minutes)

Tasks: [5]

  1. Name the problem as a pattern needing urgent work-up, not a casual “floppy baby” label. [1]
  2. Explain that social alertness does not exclude serious neuromuscular disease. [9]
  3. Describe airway/feeding protection in plain language. [5]
  4. Outline tests that change management this week and who owns the referral. [9]
  5. Teach-back return precautions: harder breathing, blue spells with feeds, weaker cry, fewer movements. [5]

Examiner marking grid

DomainFailBorderlinePass
LocalisationCalls everything “tone problem” without power/reflexesMentions central vs peripheral incompletelyClear central vs peripheral with discriminators
SafetyAllows oral feeds despite weak coughMentions feeding vaguelyExplicit airway/feeding plan
UrgencyReassures progressive areflexic phenotypeOrders tests without pathway ownershipTime-critical SMA pathway + named referral
CommunicationJargon, no teach-backPartial planClear, compassionate, closed-loop
[1] [5] [9]

Common candidate errors

  • Equating a social smile with neuromuscular safety. [9]
  • Labelling “benign congenital hypotonia” as a final diagnosis. [2]
  • Waiting for botulism laboratory confirmation before treatment in the descending-paralysis branch. [16]
  • Forgetting to examine the mother when congenital myotonic dystrophy is possible. [17]

References

  1. [1]Peredo DE, Hannibal MC The floppy infant: evaluation of hypotonia. Pediatrics in review, 2009.PMID 19726697
  2. [2]Bodensteiner JB The evaluation of the hypotonic infant. Seminars in pediatric neurology, 2008.PMID 18342256
  3. [5]Laverty CG Hypotonia in the Newborn Infant. Pediatric clinics of North America, 2025.PMID 40619196
  4. [9]Finkel RS, Mercuri E, Darras BT Nusinersen versus Sham Control in Infantile-Onset Spinal Muscular Atrophy. The New England journal of medicine, 2017.PMID 29091570
  5. [16]Sarintra N, Ekdahl R, Sanders SC More Than Just a Floppy Baby: Maintaining High Clinical Suspicion of Infant Botulism. Cureus, 2026.PMID 41728439
  6. [17]Suzui R, Wada I, Matsubara M Undiagnosed Maternal Myotonic Dystrophy Type 1 Revealed by Congenital Myotonic Dystrophy in the Neonate. Cureus, 2026.PMID 42037975