在对窒息新生儿进行心肺复苏时,持续充气和胸外按压与 3:1 的胸外按压和通气比(SURV1VE):分组随机对照试验。

Georg M Schmölzer, Gerhard Pichler, Anne Lee Solevåg, Brenda Hiu Yan Law, Souvik Mitra, Michael Wagner, Daniel Pfurtscheller, Maryna Yaskina, Po-Yin Cheung
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引用次数: 0

摘要

目的:对于需要在产房(DR)进行胸外按压(CC)的新生儿,与按压:通气(3:1 C:V)比例为 3:1 相比,持续按压叠加持续通气(CC+SI)是否会缩短自发性循环(ROSC)恢复时间:国际、多中心、前瞻性、分组交叉随机试验:环境: 加拿大和奥地利四家医院的 DR:干预措施:主要结果测量指标:主要结果为ROSC时间,即CC持续到心脏听诊确定心率上升>60/min并维持60秒的时间。218名婴儿(109名/组)的样本量足以检测到ROSC时间缩短了33%(282秒与420秒CC),这在临床上具有重要意义。分析方法为意向治疗:患者招募时间为 2017 年 10 月 19 日至 2022 年 9 月 22 日,共随机招募了 27 名婴儿(CC+SI(n=12),3:1 C:V(n=15),2 人(每组 1 人)拒绝同意)。CC+SI组的所有11名婴儿和3:1 C:V组的12/14名婴儿在DR中均实现了ROSC。CC+SI和3:1 C:V的ROSC时间中位数(IQR)分别为90(60-270)秒和615(174-780)秒(p=0.0502(对数秩),p=0.16(cox比例危险回归))。CC+SI的死亡率为2/11(18.2%),而3:1 C:V的死亡率为8/14(57.1%)(P=0.10(费雪精确检验),OR(95% CI)为0.17;(0.03至1.07))。由于伦理审批、确保试验保险以及资金等问题,试验被终止:结论:CC+SI和3:1 C:V的ROSC时间和死亡率没有统计学差异:NCT02858583.
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Sustained inflation and chest compression versus 3:1 chest compression to ventilation ratio during cardiopulmonary resuscitation of asphyxiated newborns (SURV1VE): A cluster randomised controlled trial.

Objective: In newborn infants requiring chest compression (CC) in the delivery room (DR) does continuous CC superimposed by a sustained inflation (CC+SI) compared with a 3:1 compression:ventilation (3:1 C:V) ratio decreases time to return of spontaneous circulation (ROSC).

Design: International, multicenter, prospective, cluster cross-over randomised trial.

Setting: DR in four hospitals in Canada and Austria, PARTICIPANTS: Newborn infants >28 weeks' gestation who required CC.

Interventions: Hospitals were randomised to CC+SI or 3:1 C:V then crossed over to the other intervention.

Main outcome measure: The primary outcome was time to ROSC, defined as the duration of CC until an increase in heart rate >60/min determined by auscultation of the heart, which was maintained for 60 s. Sample size of 218 infants (109/group) was sufficient to detect a clinically important 33% reduction (282 vs 420 s of CC) in time to ROSC. Analysis was intention-to-treat.

Results: Patient recruitment occurred between 19 October 2017 and 22 September 2022 and randomised 27 infants (CC+SI (n=12), 3:1 C:V (n=15), two (one per group) declined consent). All 11 infants in the CC+SI group and 12/14 infants in the 3:1 C:V group achieved ROSC in the DR. The median (IQR) time to ROSC was 90 (60-270) s and 615 (174-780) s (p=0.0502 (log rank), p=0.16 (cox proportional hazards regression)) with CC+SI and 3:1 C:V, respectively. Mortality was 2/11 (18.2%) with CC+SI versus 8/14 (57.1%) with 3:1 C:V (p=0.10 (Fisher's exact test), OR (95% CI) 0.17; (0.03 to 1.07)). The trial was stopped due to issues with ethics approval and securing trial insurance as well as funding reasons.

Conclusion: The time to ROSC and mortality was not statistical different between CC+SI and 3:1 C:V.

Trial registration: NCT02858583.

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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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