AUTHOR=Schlapbach Luregn J. , Gibbons Kristen , Ridolfi Roberta , Harley Amanda , Cree Michele , Long Debbie , Buckley David , Erickson Simon , Festa Marino , George Shane , King Megan , Singh Puneet , Raman Sainath , Bellomo Rinaldo ,  The RESPOND PICU study investigators and the Australian New Zealand Intensive Care Society Paediatric Study Group (ANZICS PSG) 

TITLE=Resuscitation in Paediatric Sepsis Using Metabolic Resuscitation–A Randomized Controlled Pilot Study in the Paediatric Intensive Care Unit (RESPOND PICU): Study Protocol and Analysis Plan

JOURNAL=Frontiers in Pediatrics

VOLUME=9

YEAR=2021

URL=https://www.frontiersin.org/journals/pediatrics/articles/10.3389/fped.2021.663435

DOI=10.3389/fped.2021.663435

ISSN=2296-2360

ABSTRACT=<p><bold>Introduction:</bold> Septic shock remains amongst the leading causes of childhood mortality. Therapeutic options to support children with septic shock refractory to initial resuscitation with fluids and inotropes are limited. Recently, the combination of intravenous hydrocortisone with high dose ascorbic acid and thiamine (HAT therapy), postulated to reduce sepsis-related organ dysfunction, has been proposed as a safe approach with potential for mortality benefit, but randomized trials in paediatric patients are lacking. We hypothesize that protocolised early use of HAT therapy (“metabolic resuscitation”) in children with septic shock is feasible and will lead to earlier resolution of organ dysfunction. Here, we describe the protocol of the <underline>Res</underline>uscitation in <underline>P</underline>aediatric Sepsis Using Metab<underline>o</underline>lic Resuscitation–A Ra<underline>nd</underline>omized Controlled Pilot Study in the <underline>P</underline>aediatric <underline>I</underline>ntensive <underline>C</underline>are <underline>U</underline>nit (RESPOND PICU).</p><p><bold>Methods and Analysis:</bold> The RESPOND PICU study is an open label randomized-controlled, two-sided multicentre pilot study conducted in paediatric intensive care units (PICUs) in Australia and New Zealand. Sixty children aged between 28 days and 18 years treated with inotropes for presumed septic shock will be randomized in a 1:1 ratio to either metabolic resuscitation (1 mg/kg hydrocortisone q6h, 30 mg/kg ascorbic acid q6h, 4 mg/kg thiamine q12h) or standard septic shock management. Main outcomes include feasibility of the study protocol and survival free of organ dysfunction censored at 28 days. The study cohort will be followed up at 28-days and 6-months post enrolment to assess neurodevelopment, quality of life and functional status. Biobanking will allow ancillary studies on sepsis biomarkers.</p><p><bold>Ethics and Dissemination:</bold> The study received ethical clearance from Children's Health Queensland Human Research Ethics Committee (HREC/18/QCHQ/49168) and commenced enrolment on June 12th, 2019. The primary study findings will be submitted for publication in a peer-reviewed journal.</p><p><bold>Trial Registration:</bold> Australian and New Zealand Clinical Trials Registry (ACTRN12619000829112). <bold>Protocol Version</bold>: V1.8 22/7/20.</p>