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用于小儿体外循环心脏手术的预防性皮质类固醇

Prophylactic corticosteroids for paediatric heart surgery with cardiopulmonary bypass.

作者信息

Gibbison Ben, Villalobos Lizardi José Carlos, Avilés Martínez Karla Isis, Fudulu Daniel P, Medina Andrade Miguel Angel, Pérez-Gaxiola Giordano, Schadenberg Alvin Wl, Stoica Serban C, Lightman Stafford L, Angelini Gianni D, Reeves Barnaby C

机构信息

Department of Cardiac Anaesthesia and Intensive Care, Bristol Heart Institute/University Hospitals Bristol NHS FT, Bristol, UK.

Emergency Pediatric Department, Hospital Civil de Guadalajara "Fray Antonio Alcalde", Guadalajara, Mexico.

出版信息

Cochrane Database Syst Rev. 2020 Oct 12;10(10):CD013101. doi: 10.1002/14651858.CD013101.pub2.

DOI:10.1002/14651858.CD013101.pub2
PMID:33045104
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8095004/
Abstract

BACKGROUND

Corticosteroids are routinely given to children undergoing cardiac surgery with cardiopulmonary bypass (CPB) in an attempt to ameliorate the inflammatory response. Their use is still controversial and the decision to administer the intervention can vary by centre and/or by individual doctors within that centre.

OBJECTIVES

This review is designed to assess the benefits and harms of prophylactic corticosteroids in children between birth and 18 years of age undergoing cardiac surgery with CPB.

SEARCH METHODS

We searched CENTRAL, MEDLINE, Embase and Conference Proceedings Citation Index-Science in June 2020. We also searched four clinical trials registers and conducted backward and forward citation searching of relevant articles.

SELECTION CRITERIA

We included studies of prophylactic administration of corticosteroids, including single and multiple doses, and all types of corticosteroids administered via any route and at any time-point in the perioperative period. We excluded studies if steroids were administered therapeutically. We included individually randomised controlled trials (RCTs), with two or more groups (e.g. multi-drug or dose comparisons with a control group) but not 'head-to-head' trials without a placebo or a group that did not receive corticosteroids. We included studies in children, from birth up to 18 years of age, including preterm infants, undergoing cardiac surgery with the use of CPB. We also excluded studies in patients undergoing heart or lung transplantation, or both; studies in patients already receiving corticosteroids; in patients with abnormalities of the hypothalamic-pituitary-adrenal axis; and in patients given steroids at the time of cardiac surgery for indications other than cardiac surgery.

DATA COLLECTION AND ANALYSIS

We used the Covidence systematic review manager to extract and manage data for the review. Two review authors independently assessed studies for inclusion, extracted data, and assessed risks of bias. We resolved disagreements by consensus or by consultation with a third review author. We assessed the certainty of evidence with GRADE.

MAIN RESULTS

We found 3748 studies, of which 888 were duplicate records. Two studies had the same clinical trial registration number, but reported different populations and interventions. We therefore included them as separate studies. We screened titles and abstracts of 2868 records and reviewed full text reports for 84 studies to determine eligibility. We extracted data for 13 studies. Pooled analyses are based on eight studies. We reported the remaining five studies narratively due to zero events for both intervention and placebo in the outcomes of interest. Therefore, the final meta-analysis included eight studies with a combined population of 478 participants. There was a low or unclear risk of bias across the domains. There was moderate certainty of evidence that corticosteroids do not change the risk of in-hospital mortality (five RCTs; 313 participants; risk ratio (RR) 0.83, 95% confidence interval (CI) 0.33 to 2.07) for children undergoing cardiac surgery with CPB. There was high certainty of evidence that corticosteroids reduce the duration of mechanical ventilation (six RCTs; 421 participants; mean difference (MD) 11.37 hours lower, 95% CI -20.29 to -2.45) after the surgery. There was high-certainty evidence that the intervention probably made little to no difference to the length of postoperative intensive care unit (ICU) stay (six RCTs; 421 participants; MD 0.28 days lower, 95% CI -0.79 to 0.24) and moderate-certainty evidence that the intervention probably made little to no difference to the length of the postoperative hospital stay (one RCT; 176 participants; mean length of stay 22 days; MD -0.70 days, 95% CI -2.62 to 1.22). There was moderate certainty of evidence for no effect of the intervention on all-cause mortality at the longest follow-up (five RCTs; 313 participants; RR 0.83, 95% CI 0.33 to 2.07) or cardiovascular mortality at the longest follow-up (three RCTs; 109 participants; RR 0.40, 95% CI 0.07 to 2.46). There was low certainty of evidence that corticosteroids probably make little to no difference to children separating from CPB (one RCT; 40 participants; RR 0.20, 95% CI 0.01 to 3.92). We were unable to report information regarding adverse events of the intervention due to the heterogeneity of reporting of outcomes. We downgraded the certainty of evidence for several reasons, including imprecision due to small sample sizes, a single study providing data for an individual outcome, the inclusion of both appreciable benefit and harm in the confidence interval, and publication bias.

AUTHORS' CONCLUSIONS: Corticosteroids  probably do not change the risk of mortality for children having heart surgery using CPB at any time point. They probably reduce the duration of postoperative ventilation in this context, but have little or no effect on the total length of postoperative ICU stay or total postoperative hospital stay. There was inconsistency in the adverse event outcomes reported which, consequently, could not be pooled. It is therefore impossible to provide any implications and policy-makers will be unable to make any recommendations for practice without evidence about adverse effects. The review highlighted the need for well-conducted RCTs powered for clinical outcomes to confirm or refute the effect of corticosteroids versus placebo in children having cardiac surgery with CPB. A core outcome set for adverse event reporting in the paediatric major surgery and intensive care setting is required.

摘要

背景

对于接受体外循环(CPB)心脏手术的儿童,常规会给予皮质类固醇,以减轻炎症反应。其使用仍存在争议,且实施该干预措施的决定可能因中心不同和/或同一中心内的个别医生而异。

目的

本综述旨在评估预防性使用皮质类固醇对18岁及以下接受CPB心脏手术儿童的益处和危害。

检索方法

我们于2020年6月检索了Cochrane系统评价数据库、MEDLINE、Embase和会议论文引文索引 - 科学版。我们还检索了四个临床试验注册库,并对相关文章进行了前后向引文检索。

选择标准

我们纳入了预防性使用皮质类固醇的研究,包括单剂量和多剂量,以及围手术期通过任何途径在任何时间点给予的所有类型皮质类固醇。如果皮质类固醇是用于治疗目的,则排除该研究。我们纳入了个体随机对照试验(RCT),有两个或更多组(例如与对照组进行多药物或剂量比较),但不包括没有安慰剂或未接受皮质类固醇组的“头对头”试验。我们纳入了18岁及以下儿童的研究,包括早产儿,他们接受了使用CPB的心脏手术。我们还排除了接受心脏或肺移植或两者皆有的患者的研究;已经接受皮质类固醇治疗的患者的研究;下丘脑 - 垂体 - 肾上腺轴异常的患者的研究;以及在心脏手术时因心脏手术以外的适应症给予类固醇的患者的研究。

数据收集与分析

我们使用Covidence系统评价管理器提取和管理本综述的数据。两位综述作者独立评估研究是否纳入,提取数据,并评估偏倚风险。我们通过协商一致或与第三位综述作者协商解决分歧。我们使用GRADE评估证据的确定性。

主要结果

我们共找到3748项研究,其中888项为重复记录。两项研究具有相同的临床试验注册号,但报告了不同的人群和干预措施。因此,我们将它们作为单独的研究纳入。我们筛选了2868条记录的标题和摘要,并对84项研究的全文报告进行了审查以确定其是否符合纳入标准。我们提取了13项研究的数据。汇总分析基于8项研究。由于在感兴趣的结局中干预组和安慰剂组的事件数均为零,我们对其余5项研究进行了描述性报告。因此,最终的荟萃分析包括8项研究,合并人群为478名参与者。各领域的偏倚风险较低或不明确。有中等确定性的证据表明,对于接受CPB心脏手术的儿童,皮质类固醇不会改变住院死亡率(5项RCT;313名参与者;风险比(RR)0.83,95%置信区间(CI)为0.33至2.07)。有高确定性的证据表明,皮质类固醇可缩短术后机械通气时间(6项RCT;421名参与者;平均差异(MD)降低11.37小时,95%CI为 -20.29至 -2.45)。有高确定性的证据表明,该干预措施可能对术后重症监护病房(ICU)住院时间影响不大(6项RCT;421名参与者;MD降低0.28天,95%CI为 -0.79至0.24),中等确定性的证据表明,该干预措施可能对术后住院时间影响不大(1项RCT;176名参与者;平均住院时间22天;MD为 -0.70天,95%CI为 -2.62至1.22)。有中等确定性的证据表明,该干预措施在最长随访期对全因死亡率无影响(5项RCT;313名参与者;RR 0.83,95%CI为0.33至2.07),或在最长随访期对心血管死亡率无影响(3项RCT;109名参与者;RR 0.40,95%CI为0.07至2.46)。有低确定性的证据表明,皮质类固醇可能对脱离CPB的儿童影响不大(1项RCT;40名参与者;RR 0.20,95%CI为0.01至3.92)。由于结局报告的异质性,我们无法报告有关该干预措施不良事件的信息。我们因多种原因降低了证据的确定性,包括样本量小导致的不精确性、单个研究为个体结局提供数据、置信区间内既有明显益处又有危害,以及发表偏倚。

作者结论

皮质类固醇可能不会改变任何时间点接受CPB心脏手术儿童的死亡风险。在此情况下,它们可能会缩短术后通气时间,但对术后ICU住院总时长或术后住院总时长影响很小或无影响。报告的不良事件结局存在不一致性,因此无法汇总。因此,无法提供任何启示,并且在没有关于不良反应证据的情况下,政策制定者无法对实践提出任何建议。该综述强调需要开展以临床结局为动力的高质量RCT,以证实或反驳皮质类固醇与安慰剂对接受CPB心脏手术儿童的影响。需要一个儿科大手术和重症监护环境中不良事件报告的核心结局集。

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