Chest compression during sustained inflation versus 3:1 chest compression:ventilation ratio during neonatal cardiopulmonary resuscitation: a randomised feasibility trial

Arch Dis Child Fetal Neonatal Ed. 2018 Sep;103(5):F455-F460. doi: 10.1136/archdischild-2017-313037. Epub 2017 Oct 7.


Background: Current neonatal resuscitation guidelines recommend 3:1 compression:ventilation (C:V) ratio. Recently, animal studies reported that continuous chest compressions (CC) during a sustained inflation (SI) significantly improved return of spontaneous circulation (ROSC). The approach of CC during SI (CC+SI) has not been examined in the delivery room during neonatal resuscitation.

Hypothesis: It is a feasibility study to compare CC+SI versus 3:1 C:V ratio during neonatal resuscitation in the delivery room. We hypothesised that during neonatal resuscitation, CC+SI will reduce the time to ROSC. Our aim was to examine if CC+SI reduces ROSC compared with 3:1 C:V CPR in preterm infants <33 weeks of gestation.

Study design: Randomised feasibility trial.

Method: Once CC was indicated all eligible infants were immediately and randomly allocated to either CC+SI group or 3:1 C:V group. A sequentially numbered, brown, sealed envelope contained a folded card box with the treatment allocation was opened by the clinical team at the start of CC.

Study interventions: Infants in the CC+SI group received CC at a rate of 90/min during an SI with a duration of 20 s (CC+SI). After 20 s, the SI was interrupted for 1 s and the next SI was started for another 20 s until ROSC. Infants in the '3:1 group' received CC using 3:1 C:V ratio until ROSC.

Primary outcome: Overall the mean (SD) time to ROSC was significantly shorter in the CC+SI group with 31 (9) s compared with 138 (72) s in the 3:1 C:V group (p=0.011).

Conclusion: CC+SI is feasible in the delivery room.

Trial registration number: NCT02083705, pre-results.

Keywords: chest compression; delivery room; neonatology; newborn; sustained inflation.

Publication types

  • Randomized Controlled Trial

MeSH terms

  • Blood Circulation / physiology
  • Cardiopulmonary Resuscitation / methods*
  • Feasibility Studies
  • Female
  • Gestational Age
  • Heart Arrest* / physiopathology
  • Heart Arrest* / therapy
  • Heart Massage / methods*
  • Humans
  • Infant, Newborn
  • Infant, Premature
  • Insufflation / methods
  • Male
  • Treatment Outcome

Associated data