Sunthankar Sudeep D, Hill Kevin D, Jacobs Jeffrey P, Baldwin H Scott, Jacobs Marshall L, Li Jennifer S, Graham Eric M, Resheidat Ashraf M, Amula Venugopal, Bleiweis Mark S, Wald Eric L, Eghtesady Pirooz, Scott John P, Anderson Brett R, Swartz Michael F, Benscoter Alexis, Ravekes William, Kannankeril Prince J
Division of Pediatric Cardiology and Center for Pediatric Precision Medicine, Department of Pediatrics, Vanderbilt University Medical Center, 2220 Children's Way; Suite 5230, Nashville, TN, 37232, USA.
Division of Pediatric Cardiology, Duke University Medical Center, Durham, NC, USA.
Pediatr Cardiol. 2025 May 2. doi: 10.1007/s00246-025-03875-9.
Objective Assess the association between intraoperative methylprednisolone and specific postoperative outcomes among subgroups undergoing infant heart surgery.
Subpopulation analyses of The Steroids to Reduce Systemic Inflammation after Infant Heart Surgery trial, a double-blind randomized placebo-controlled trial.
24 congenital heart centers.
Infants (< 1 year old) undergoing heart surgery with cardiopulmonary bypass. Patients stratified by Society of Thoracic Surgeons-European Association for Cardio-Thoracic Surgery Congenital Heart Surgery (STAT) Mortality Category, age, gestational age, and presence of chromosomal or syndromic diagnosis (CSD).
Methylprednisolone (30 mg/kg) versus placebo administered into cardiopulmonary bypass pump-priming fluid.
Outcomes included death, heart transplantation, mechanical circulatory support, reinterventions, and hospital length of stay. Ranked composite outcome (death, transplant, or one of 13 major complications) was compared between placebo and methylprednisolone for each subgroup using the win ratio. Methylprednisolone did not reduce odds of death, transplant, or mechanical circulatory support for any subgroup. Those receiving methylprednisolone had fewer catheterization or surgical reinterventions after STAT Category 1-3 operations [OR 0.50 (0.29-0.86)]; and fewer reoperations for bleeding among patients undergoing STAT Category 1-3 operations [OR 0.28 (0.09-0.87)], term infants [OR 0.30 (0.12-0.76)], and those without CSD [OR 0.22 (0.07-0.68)]. Length of stay was no different between methylprednisolone versus placebo. Those without chromosomal or syndromic diagnosis demonstrated a favorable association for methylprednisolone [win ratio 1.28 (1.01-1.61)] for the composite outcome.
Exploratory subpopulation analyses, although underpowered, suggest that methylprednisolone is not associated with significant harm and may benefit certain subpopulations.
目的评估婴儿心脏手术亚组中术中使用甲泼尼龙与特定术后结局之间的关联。
对“婴儿心脏手术后使用类固醇减少全身炎症”试验进行亚组分析,这是一项双盲随机安慰剂对照试验。
24个先天性心脏病中心。
接受体外循环心脏手术的婴儿(<1岁)。患者按胸外科医师协会 - 欧洲心胸外科学会先天性心脏病手术(STAT)死亡率类别、年龄、胎龄以及是否存在染色体或综合征诊断(CSD)进行分层。
在体外循环泵预充液中给予甲泼尼龙(30mg/kg)与安慰剂。
结局包括死亡、心脏移植、机械循环支持、再次干预以及住院时间。使用获胜比在每个亚组的安慰剂组和甲泼尼龙组之间比较排序后的综合结局(死亡、移植或13种主要并发症之一)。甲泼尼龙对任何亚组均未降低死亡、移植或机械循环支持的几率。接受甲泼尼龙治疗的患者在STAT 1 - 3类手术[比值比0.50(0.29 - 0.86)]后进行导管插入术或手术再次干预的次数较少;在接受STAT 1 - 3类手术的患者[比值比0.28(0.09 - 0.87)]、足月儿[比值比0.30(0.12 - 0.76)]以及无CSD的患者[比值比0.22(0.07 - 0.68)]中因出血进行再次手术的次数较少。甲泼尼龙组与安慰剂组的住院时间无差异。无染色体或综合征诊断的患者在综合结局方面显示出对甲泼尼龙的有利关联[获胜比1.28(1.01 - 1.61)]。
探索性亚组分析虽然效能不足,但表明甲泼尼龙无显著危害,可能对某些亚组有益。