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
Child Health Research Centre, The University of Queensland, and Paediatric Intensive Care Unit, Queensland Children's Hospital, Brisbane, QLD, Australia.
Pediatric and Neonatal Intensive Care Unit, and Children's Research Center, University Children's Hospital Zurich, Zurich, Switzerland.
Front Pediatr. 2021 Apr 30;9:663435. doi: 10.3389/fped.2021.663435. eCollection 2021.
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 Resuscitation in Paediatric Sepsis Using Metabolic Resuscitation-A Randomized Controlled Pilot Study in the Paediatric Intensive Care Unit (RESPOND PICU). 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. 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. Australian and New Zealand Clinical Trials Registry (ACTRN12619000829112). : V1.8 22/7/20.
感染性休克仍然是儿童死亡的主要原因之一。对于经液体复苏和使用血管活性药物后仍难治的感染性休克患儿,支持治疗的选择有限。最近,静脉注射氢化可的松联合大剂量维生素C和硫胺素(HAT疗法)被认为可减少脓毒症相关器官功能障碍,已被提议作为一种可能有益降低死亡率的安全方法,但缺乏针对儿科患者的随机试验。我们假设,对感染性休克患儿按方案早期使用HAT疗法(“代谢复苏”)是可行的,并将导致器官功能障碍更早得到缓解。在此,我们描述了在儿科重症监护病房进行的“使用代谢复苏治疗儿科脓毒症——一项随机对照试验性研究”(RESPOND PICU)的方案。RESPOND PICU研究是一项开放标签、随机对照、双侧多中心试验性研究,在澳大利亚和新西兰的儿科重症监护病房开展。60名年龄在28天至18岁之间、因疑似感染性休克而接受血管活性药物治疗的儿童将按1:1比例随机分为代谢复苏组(氢化可的松1mg/kg,每6小时一次;维生素C 30mg/kg,每6小时一次;硫胺素4mg/kg,每12小时一次)或标准感染性休克治疗组。主要结局包括研究方案的可行性以及28天时无器官功能障碍存活。研究队列将在入组后28天和6个月进行随访,以评估神经发育、生活质量和功能状态。生物样本库将用于脓毒症生物标志物的辅助研究。该研究已获得昆士兰儿童健康人类研究伦理委员会(HREC/18/QCHQ/49168)的伦理批准,并于2019年6月12日开始入组。主要研究结果将提交至同行评审期刊发表。澳大利亚和新西兰临床试验注册中心(ACTRN12619000829112)。版本:V1.8 2020年7月22日