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Randomized, controlled trial comparing laryngeal mask versus endotracheal intubation during neonatal resuscitation---a secondary publication

机译:随机,受控试验比较喉膜面膜与新生儿复苏期间的气管插管---二次出版物

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This study aimed to study the feasibility, efficacy and safety of using laryngeal mask (LM) ventilation compared with endotracheal intubation (ETI) during neonatal resuscitation. Neonates with a heart rate below 60 beats per minute despite 30?s of face mask ventilation were assigned quasi-randomly (odd/even birth date) to LM (n?=?36) or ETI (n?=?32) ventilation. Differences in first attempt insertion success, insertion time, Apgar score, resuscitation outcome, and adverse effects were compared. There were no significant differences in first attempt at successful insertion (LM, 94.4?% vs. ETI, 90.6?%), insertion time (LM, 7.58?±?1.16?s vs. ETI, 7.89?±?1.52?s), Apgar score at 1 and 5?min, response time, ventilation time, successful resuscitation (LM, 86.1?% vs. ETI,? 96.9?%), and adverse events (LM, n =3 vs. ETI, n =4) between groups. Laryngeal mask ventilation is an effective alternative to endotracheal intubation during resuscitation of depressed newborns who do not respond to face-mask ventilation. During an emergency, laryngeal mask ventilation may be a preferred technique for medical staff who are unable to acquire or maintain endotracheal intubation skills. Current Controlled Trials ChiCTR-IOQ-15006488. Registered on 2 June 2015.
机译:本研究旨在研究与新生儿复苏期间与气管内插管(ETI)相比使用喉面膜(LM)通气的可行性,疗效和安全性。尽管面膜通风30次,但虽然将脸部掩模通风(奇数/偶数出生日期)分配给LM(n?= 36)或ETI(n?= 32)通风,但是每分钟的心率低于60次拍摄的新生儿。比较了第一次尝试成功,插入时间,APGAR评分,复苏结果和不利影响的差异。在成功插入(LM,94.4倍与Eti,90.6Ω4%),插入时间(LM,7.58?±1.16.Δ±Eti,7.89?±1.52?s)中没有显着差异,Apgar得分在1和5?min,响应时间,通风时间,复苏成功(LM,86.1倍,eti ,? 96.9?%)和不良事件(lm,n = 3 vs.eti,n = 4 )组之间。喉部掩模通风是一种有效的替代因子在抑郁的新生​​儿中的内膜插管期间,抑郁的新生​​儿没有响应面部掩模通风。在紧急情况下,喉头掩模通风可能是无法获得或维持气管内插管技能的医务人员的首选技术。目前对照试验CHICTR-IOQ-15006488。 2015年6月2日注册。

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