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经鼻给予右美托咪定与口服水合氯醛用于镇静听觉脑干反应检查的回顾性比较

Retrospective Comparison of Intranasal Dexmedetomidine and Oral Chloral Hydrate for Sedated Auditory Brainstem Response Exams.

作者信息

Reynolds Jason, Rogers Amber, Capehart Samantha, Manyang Peter, Watcha Mehernoor F

机构信息

Baylor College of Medicine, Houston, Texas; Children's Hospital of San Antonio, San Antonio, Texas; and

Baylor College of Medicine, Houston, Texas; Texas Children's Hospital, Houston, Texas.

出版信息

Hosp Pediatr. 2016 Mar;6(3):166-71. doi: 10.1542/hpeds.2015-0152.

Abstract

OBJECTIVE

Satisfactory conditions for auditory brainstem responses (ABR) screening tests for pediatric hearing loss are usually achieved with oral chloral hydrate (CH) sedation. When the US manufacture of this drug was discontinued for business reasons, we developed an alternative sedation regimen using intranasal dexmedetomidine (IN DEX) 4 μg/kg. This institutional review board-approved retrospective study compared the efficacy and adverse effect profiles of these 2 sedative regimens.

METHODS

Medical records of children receiving oral CH or IN DEX for ABR were surveyed for demographic data and times from sedative administration to start and completion of the ABR procedure and recovery times. We also noted if the examination was completed with or without interruptions, failed for inadequate sedation, and if predefined cardiorespiratory adverse events occurred.

RESULTS

In the IN DEX cohort, the examination could be completed more frequently with a single dose of medication (P = .002). Satisfactory sedation in these patients permitted an earlier start of both the ABR examination and recovery to the awake status (P < .001 and < .045, respectively). Hypoxia requiring oxygen therapy was more frequent in the CH group.

CONCLUSIONS

This retrospective study found that IN DEX provides effective sedation for ABR examinations, with the benefits of an ability to begin the test sooner and complete the examination with a single dose, in addition to a decreased incidence of hypoxemia. A randomized controlled trial should test the hypothesis that the IN DEX technique is superior to the well-established standard oral CH regimen.

摘要

目的

小儿听力损失的听觉脑干反应(ABR)筛查测试通常采用口服水合氯醛(CH)镇静来达到满意效果。当该药物的美国制造商因商业原因停产时,我们开发了一种替代镇静方案,即使用4μg/kg的鼻内右美托咪定(IN DEX)。这项经机构审查委员会批准的回顾性研究比较了这两种镇静方案的疗效和不良反应情况。

方法

对接受口服CH或IN DEX进行ABR检查的儿童病历进行调查,收集人口统计学数据、从给予镇静剂到ABR检查开始和完成的时间以及恢复时间。我们还记录了检查是否在无中断的情况下完成、因镇静不足而失败的情况,以及是否发生了预先定义的心肺不良事件。

结果

在IN DEX组中,单次给药更频繁地能完成检查(P = 0.002)。这些患者的满意镇静使得ABR检查能更早开始,且恢复到清醒状态也更早(分别为P < 0.001和< 0.045)。CH组中需要吸氧治疗的低氧情况更频繁。

结论

这项回顾性研究发现,IN DEX为ABR检查提供了有效的镇静,除了低氧血症发生率降低外,还具有能更快开始测试并单次给药完成检查的优点。一项随机对照试验应检验IN DEX技术优于已确立的标准口服CH方案这一假设。

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