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静脉注射咪达唑仑用于新生儿气管插管的术前用药:一项双盲随机对照试验。

Premedication with intravenous midazolam for neonatal endotracheal intubation: A double blind randomized controlled trial.

作者信息

Badiee Zohreh, Zandi Hamed, Armanian Amirmohammad, Sadeghnia Alireza, Barekatain Behzad

机构信息

Department of Pediatrics, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran.

出版信息

J Res Med Sci. 2021 Aug 30;26:57. doi: 10.4103/jrms.JRMS_546_19. eCollection 2021.

Abstract

BACKGROUND

Pain during the neonatal period has been associated with immediate and long-term adverse effects. One of the most frequent painful procedures that neonates face in neonatal intensive care unit is the endotracheal intubation. Midazolam has been a candidate for premedication before neonatal intubation. Our aim was to evaluate the effects of midazolam as the premedication on endotracheal intubation of premature infants during surfactant administration.

MATERIALS AND METHODS

In a double-blind clinical trial, 80 preterm infants were undertaken for tracheal intubation following the use of atropine associated to either midazolam or placebo. Patient's vital signs and general conditions were constantly monitored, and pain was assessed using premature infant pain profile (PIPP) score.

RESULTS

The mean ± standard deviation for postnatal age was 95.38 ± 50.04 and 111.63 ± 49.4 min in control and midazolam groups, respectively. The patients in the midazolam group had significantly better outcomes across several intubation outcome measures such as duration of endotracheal intubation (23.5 ± 6.7 vs. 18.8 ± 4.8 s, = 0.001), oxygen saturation level (88.05% ±13.7 vs. 95.1 ± 1.8%, = 0.002), intubation failure (34.2% vs. 2.5%, = 0.0001), awake and resistance during intubation (95% vs. 20%, = 0.0001), and excellent patient condition during intubation (0% vs. 82.5%, = 0.0001). In addition, PIPP score was significantly lower in the midazolam group (5.2 ± 2.06 vs. 12.9 ± 2.9, = 0.0001).

CONCLUSION

Premedication with midazolam in newborns before intubation, can hold promising effects that manifests as better overall outcomes, less complications, better vital signs, more comfortable situation, and lesser pain for these patients.

摘要

背景

新生儿期疼痛与近期及长期的不良影响相关。新生儿重症监护病房中,新生儿面临的最常见的疼痛操作之一是气管插管。咪达唑仑一直是新生儿插管前预处理的候选药物。我们的目的是评估咪达唑仑作为预处理药物在表面活性剂给药期间对早产儿气管插管的影响。

材料与方法

在一项双盲临床试验中,80名早产儿在使用阿托品后接受气管插管,阿托品与咪达唑仑或安慰剂联合使用。持续监测患者的生命体征和一般状况,并使用早产儿疼痛量表(PIPP)评分评估疼痛。

结果

对照组和咪达唑仑组的出生后平均年龄分别为95.38±50.04分钟和111.63±49.4分钟。在多项插管结果指标方面,咪达唑仑组患者的结局明显更好,如气管插管持续时间(23.5±6.7秒对18.8±4.8秒,P=0.001)、血氧饱和度水平(88.05%±13.7对95.1±1.8%,P=0.002)、插管失败率(34.2%对2.5%,P=0.0001)、插管期间清醒和抵抗情况(95%对20%,P=0.0001)以及插管期间患者状况良好率(0%对82.5%,P=0.0001)。此外,咪达唑仑组的PIPP评分显著更低(5.2±2.06对12.9±2.9,P=0.0001)。

结论

新生儿插管前使用咪达唑仑进行预处理可产生良好效果,表现为总体结局更好、并发症更少、生命体征更佳、状况更舒适以及患者疼痛减轻。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/faf1/8506249/737838b029e7/JRMS-26-57-g001.jpg

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