Active pharmacotherapy versus expectant management of patent ductus arteriosus in extremely preterm infants: a meta-analysis with trial sequential analysis.

IF 3.5 2区 医学 Q1 PEDIATRICS
Shripada C Rao, Chandra Rath, Sanjay Patole
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引用次数: 0

Abstract

Objectives: To assess the effectiveness and safety of active pharmacotherapy for patent ductus arteriosus (PDA) initiated based on echocardiography-criteria versus expectant management in extremely preterm infants <29 w gestation in the first three weeks of life.

Study design: Systematic review with meta-analysis and trial sequential analysis (TSA). We searched PubMed, Embase, CENTRAL and Emcare for randomised trials published between 2010 and May 2026. We synthesised results using random-effects meta-analysis and conducted a TSA.

Patients: Extremely preterm infants with PDA considered as significant on echocardiography.

Interventions: Pharmacotherapy versus expectant management.

Main outcome measures: Mortality by 36 weeks postconceptional age or before discharge and chronic lung disease (CLD).

Results: We included 12 trials involving 2344 extremely preterm infants. Meta-analysis found increased risk of mortality with active pharmacotherapy (RR 1.34, 95% CI 1.08 to 1.67; p=0.008, I2=0%; 12 randomised controlled trials (RCTs)). Number-needed-to-treat for an additional harmful outcome (i.e. mortality) was 25 (95% CI 17 to 100). On TSA conducted with the stringent alpha error 3.3% and beta 10%, the cumulative Z-score touched the O'Brien-Fleming monitoring boundary at the current sample size, supporting the meta-analysis findings under the specified TSA assumptions.For CLD, meta-analysis showed little or no difference (RR 0.99, 95% CI 0.92 to 1.06, p=0.74, I2=14%, 12 RCTs). The certainty of evidence was high for mortality and moderate for CLD.

Conclusions: In extremely preterm infants, active pharmacotherapy for PDA based on current echocardiographic criteria in the first three weeks of life was associated with increased mortality with a clinically important number needed to harm. These findings should inform treatment decisions and discussions with parents while ongoing research seeks to identify infants who may benefit from treatment.

Prospero registration number: CRD420261303992.

极早产儿动脉导管未闭的积极药物治疗与预期治疗:一项荟萃分析与试验序贯分析。
目的:评估基于超声心动图标准的动脉导管未闭(PDA)积极药物治疗的有效性和安全性,与预期治疗相比。研究设计:采用荟萃分析和试验序贯分析(TSA)进行系统评价。我们检索了PubMed、Embase、CENTRAL和Emcare在2010年至2026年5月间发表的随机试验。我们使用随机效应荟萃分析综合结果并进行TSA。患者:极早产儿,超声心动图认为PDA有显著意义。干预措施:药物治疗与预期治疗。主要结局指标:妊娠后36周或出院前死亡率和慢性肺部疾病(CLD)。结果:我们纳入了12项试验,涉及2344名极早产儿。荟萃分析发现,积极药物治疗增加了死亡风险(RR 1.34, 95% CI 1.08 ~ 1.67; p=0.008, I2=0%; 12项随机对照试验(rct))。额外有害结果(即死亡率)需要治疗的数量为25 (95% CI 17至100)。在严格的alpha误差为3.3%,beta误差为10%的TSA下,累积z分数触及当前样本量下的O'Brien-Fleming监测边界,支持特定TSA假设下的meta分析结果。对于CLD, meta分析显示差异很小或没有差异(RR 0.99, 95% CI 0.92 ~ 1.06, p=0.74, I2=14%, 12个rct)。死亡率的证据确定性高,CLD的证据确定性中等。结论:在极度早产儿中,根据目前的超声心动图标准,在出生后的前三周对PDA进行积极药物治疗与死亡率增加相关,并且需要达到临床重要数字才能造成伤害。这些发现应该为治疗决策和与父母的讨论提供信息,同时正在进行的研究旨在确定可能从治疗中受益的婴儿。普洛斯彼罗注册号:CRD420261303992。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
9.00
自引率
4.50%
发文量
90
审稿时长
6-12 weeks
期刊介绍: Archives of Disease in Childhood is an international peer review journal that aims to keep paediatricians and others up to date with advances in the diagnosis and treatment of childhood diseases as well as advocacy issues such as child protection. It focuses on all aspects of child health and disease from the perinatal period (in the Fetal and Neonatal edition) through to adolescence. ADC includes original research reports, commentaries, reviews of clinical and policy issues, and evidence reports. Areas covered include: community child health, public health, epidemiology, acute paediatrics, advocacy, and ethics.
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