Efficacy of Rectal Versus Oral Chloral Hydrate in Pediatric Auditory Brainstem Response: Randomized Controlled Trial.

IF 1.8 Q2 OTORHINOLARYNGOLOGY OTO Open Pub Date : 2024-09-29 eCollection Date: 2024-10-01 DOI:10.1002/oto2.70023
Chutaporn Siripermpool, Nalinee Pattrakornkul, Thanitda Thongsattra, Narit Jianbunjongkit
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Abstract

Objective: To compare sedation success rates between rectal (RCH) and oral chloral hydrate (OCH) administration in children undergoing auditory brainstem response (ABR) testing and assess the incidence of adverse effects.

Study design: Randomized controlled trial, performed between May 2023 and August 2023.

Setting: Ear, Nose, and Throat Outpatient Department at tertiary care hospital.

Methods: Pediatric patients aged 1 to 5 years, who were indicated for ABR testing were enrolled and randomly divided into 2 groups. The control group received 10% wt/vol chloral hydrate orally at a dose of 50 mg/kg, while the other group received the same dose through rectal administration. Onset of sedation, duration of sedation, recovery time, vital signs, and adverse effects were recorded and analyzed to assess sedative effectiveness and safety.

Results: Eighty-eight children were randomly assigned to RCH or OCH administration groups, the sedation success rates of RCH and OCH groups were 84.09% and 90.91%, respectively (P = .33). Adverse effects were detected in 11 children (12.5%), with a vomiting rate of 20.45% in the oral group versus 0% in the rectal group (P = .002). The diarrhea rate was 4.55% in the rectal group versus 0% in the oral group (P = .16). In either group, no serious adverse effects were documented.

Conclusion: RCH and OCH are both safe and effective for short-term sedation in pediatric patients during ABR testing. Interestingly, RCH administration offers a high success rate without vomiting or major adverse effects. This study established the effectiveness of RCH for sedation in children under specialized supervision.

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直肠与口服水合氯醛对小儿听性脑干反应的疗效:随机对照试验
目的:比较直肠(RCH)和口服水合氯醛(OCH)对接受听性脑干反应(ABR)测试的儿童的镇静成功率,并评估不良反应发生率:比较直肠(RCH)和口服水合氯醛(OCH)对接受听性脑干反应(ABR)测试的儿童的镇静成功率,并评估不良反应的发生率:随机对照试验,2023年5月至2023年8月期间进行:地点:三级医院耳鼻喉科门诊:入组 1 至 5 岁有 ABR 测试指征的儿科患者,随机分为 2 组。对照组口服 10% wt/vol 水合氯醛,剂量为 50 毫克/千克;另一组通过直肠给药,剂量相同。记录并分析镇静开始时间、镇静持续时间、恢复时间、生命体征和不良反应,以评估镇静的有效性和安全性:结果:88名儿童被随机分配到RCH或OCH给药组,RCH组和OCH组的镇静成功率分别为84.09%和90.91%(P = .33)。11名儿童(12.5%)出现了不良反应,其中口服组的呕吐率为20.45%,而直肠组为0%(P = .002)。直肠组的腹泻率为 4.55%,而口服组为 0%(P = .16)。两组均未发现严重不良反应:结论:RCH 和 OCH 均可安全有效地在 ABR 测试期间对儿科患者进行短期镇静。有趣的是,RCH 给药成功率高,且无呕吐或严重不良反应。这项研究证实了在专门监护下使用 RCH 对儿童镇静的有效性。
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OTO Open
OTO Open Medicine-Surgery
CiteScore
2.70
自引率
0.00%
发文量
115
审稿时长
15 weeks
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