Resuscitation With Early Adrenaline Infusion for Children With Septic Shock: A Randomized Pilot Trial

Author:

Harley Amanda,George Shane123,Phillips Natalie14,King Megan24,Long Debbie15,Keijzers Gerben236,Lister Paula7,Raman Sainath18,Bellomo Rinaldo,Gibbons Kristen1,Schlapbach Luregn J189,

Affiliation:

1. Child Health Research Centre, The University of Queensland, Brisbane, QLD, Australia.

2. Department of Emergency Medicine, Gold Coast University Hospital, Southport, QLD, Australia.

3. School of Medicine and Menzies Health Institute Queensland, Griffith University, Southport, QLD, Australia.

4. Emergency Department Queensland Children`s Hospital, Brisbane, QLD, Australia.

5. School of Nursing, Centre of Healthcare Transformation, Queensland University of Technology, Brisbane, QLD, Australia.

6. Faculty of Health Sciences and Medicine, Bond University, Gold Coast, QLD, Australia.

7. Children`s Critical Care Unit, Sunshine Coast University Hospital, Birtinya, QLD, Australia.

8. Paediatric Intensive Care Unit, Queensland Children’s Hospital, Children’s Health Queensland, Brisbane, QLD, Australia.

9. Pediatric and Neonatal Intensive Care Unit, and Children`s Research Center, University Children’s Hospital Zurich, Zurich, Switzerland.

Abstract

OBJECTIVES: In children with septic shock, guidelines recommend resuscitation with 40–60 mL/kg of fluid boluses, yet there is a lack of evidence to support this practice. We aimed to determine the feasibility of a randomized trial comparing early adrenaline infusion with standard fluid resuscitation in children with septic shock. DESIGN: Open-label parallel randomized controlled, multicenter pilot study. The primary end point was feasibility; the exploratory clinical endpoint was survival free of organ dysfunction by 28 days. SETTING: Four pediatric Emergency Departments in Queensland, Australia. PATIENTS: Children between 28 days and 18 years old with septic shock. INTERVENTIONS: Patients were assigned 1:1 to receive a continuous adrenaline infusion after 20 mL/kg fluid bolus resuscitation (n = 17), or standard care fluid resuscitation defined as delivery of 40 to 60 mL/kg fluid bolus resuscitation prior to inotrope commencement (n = 23). MEASUREMENTS AND MAIN RESULTS: Forty of 58 eligible patients (69%) were consented with a median age of 3.7 years (interquartile range [IQR], 0.9–12.1 yr). The median time from randomization to inotropes was 16 minutes (IQR, 12–26 min) in the intervention group, and 49 minutes (IQR, 29–63 min) in the standard care group. The median amount of fluid delivered during the first 24 hours was 0 mL/kg (IQR, 0–10.0 mL/kg) in the intervention group, and 20.0 mL/kg (14.6–28.6 mL/kg) in the standard group (difference, –20.0; 95% CI, –28.0 to –12.0). The number of days alive and free of organ dysfunction did not differ between the intervention and standard care groups, with a median of 27 days (IQR, 26–27 d) versus 26 days (IQR, 25–27 d). There were no adverse events reported associated with the intervention. CONCLUSIONS: In children with septic shock, a protocol comparing early administration of adrenaline versus standard care achieved separation between the study arms in relation to inotrope and fluid bolus use.

Publisher

Ovid Technologies (Wolters Kluwer Health)

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