Paeds Vivas · investigations-procedures-and-technology
Intraosseous access — branching viva
A branching viva following one child from septic shock with failed intravenous access, through the decision to place an intraosseous needle, the proximal tibial landmark and weight-based needle, confirmation and the meaning of a failed aspirate, drug and fluid administration at intravenous doses, and the prevention of extravasation, compartment syndrome and infection. The candidate must defend the physiology, the timing rule, and the conscious-child lidocaine regimen.
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Branching viva — intraosseous access
The examiner releases the stem and then branches into four probes. A strong candidate answers the decision first, defends the physiology, demonstrates the technique, and names the complications without prompting. [1] [3]
Opening (examiner)
"A two-year-old arrives cold, mottled, and barely rousable with septic shock. Heart rate 180, capillary refill 6 seconds, blood pressure 60/35. Two peripheral cannulation attempts over 75 seconds have failed. What is your next move?" [1]
Branch 1 — The decision (expected answer)
State the rule and act on it: if intravenous access cannot be secured within 60 to 90 seconds in a child with shock, arrest, status epilepticus, or peri-arrest, place an intraosseous needle now rather than attempting a third cannula. Name the operator, state the decision aloud, and run the clock. Central lines and cut-downs take too long in an unstable child. [1] [3]
Probe. "Why IO and not a central line?" — A central line takes many minutes and interrupts resuscitation; an IO is placed in under a minute, does not interrupt compressions, and delivers drugs to the heart in seconds at intravenous doses. [1] [2]
Branch 2 — Physiology (expected answer)
The medullary cavity holds thin-walled venous sinusoids held open by the rigid cortex, so they do not collapse in shock when peripheral veins have shut down. Fluid and drugs drain through the central venous canal and the nutrient vein into the systemic circulation and reach the heart in seconds, with pharmacokinetics close to a central line. Every drug that can be given intravenously can be given intraosseously at the same dose. [9] [12]
References8ShowHide
- [1]Thim T, Løfgren B, Grove EL Intraosseous catheter placement in children New England Journal of Medicine, 2011.PMID 21631349
- [2]Okubo M, Komukai S, Izawa J, et al Intraosseous vs Intravenous Access for Epinephrine in Pediatric Out-of-Hospital Cardiac Arrest JAMA Network Open, 2025.PMID 40560587
- [3]Pifko EL, Price A, Busch C, et al Observational review of paediatric intraosseous needle placement in the paediatric emergency department Journal of Paediatrics and Child Health, 2018.PMID 29125229
- [5]Ting A, Smith K, Wilson CL, et al Pre-hospital intraosseous use in children: Indications and success rate Emergency Medicine Australasia, 2022.PMID 34704359
- [8]Reades R, Studnek JR, Garrett JS, et al Comparison of first-attempt success between tibial and humeral intraosseous insertions during out-of-hospital cardiac arrest Prehospital Emergency Care, 2011.PMID 21275573
- [9]Neuhaus D Intraosseous infusion in elective and emergency pediatric anesthesia: when should we use it? Current Opinion in Anaesthesiology, 2014.PMID 24651308
- [11]Hasan MY, Kissoon N, Khan TM, et al Intraosseous infusion and pulmonary fat embolism Pediatric Critical Care Medicine, 2001.PMID 12797872
- [12]Orlowski JP, Porembka DT, Gallagher JM, et al The bone marrow as a source of laboratory studies Annals of Emergency Medicine, 1989.PMID 2589704