Efficacy and Safety of Intranasal Dexmedetomidine Combined With Oral Chloral Hydrate for Sedation in Neonatal MRI Procedures: A Single-Center Retrospective Study

IF 2.1 4区 医学 Q3 PHARMACOLOGY & PHARMACY
Wenyan Dong, Lingdi Zhu, Linlin Xu, Zhenkun Yang, Shuoxiong Wu
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引用次数: 0

Abstract

Background: Pharmacological sedation during neonatal magnetic resonance imaging (MRI) is crucial for procedure success and minimizing artifacts. Hence, it is vital to evaluate the effectiveness and safety of conventional sedatives in this population. In this study, we aim to evaluate the effectiveness of oral chloral hydrate combined with intranasal dexmedetomidine in neonatal MRI.

Methods: Neonates aged 0 to 28 days undergoing MRI were enrolled and received intranasal dexmedetomidine followed by oral chloral hydrate. Subsequently, sedation scores, onset time, and overall time of sedation, as well as any potential adverse reactions, were recorded.

Results: All neonates completed the MRI without notable adverse reactions. 128 neonates (90.1%) completed the MRI study with a single dose, while 14 neonates (9.9%) required additional medications. In the neonates with a single dose, no statistically significant differences in onset time were observed across postnatal days, gender, and weight. And no statistically significant differences in total time were observed across postnatal days and gender. However, the total time was significantly extended in the neonates with a weight under 3 kg. Furthermore, compared to the neonates with a single dose, the total time was significantly extended in the neonates with additional medications.

Conclusion: Oral chloral hydrate combined with intranasal dexmedetomidine is effective and safe for neonatal MRI, but extra attention is needed for neonates under 3 kg.

Abstract Image

右美托咪定鼻内联合口服水合氯醛用于新生儿MRI镇静的有效性和安全性:一项单中心回顾性研究
背景:新生儿磁共振成像(MRI)期间的药物镇静是手术成功和减少伪影的关键。因此,评估传统镇静剂在这一人群中的有效性和安全性至关重要。在这项研究中,我们的目的是评估口服水合氯醛联合鼻内右美托咪定在新生儿MRI中的有效性。方法:选取0 ~ 28天接受MRI检查的新生儿,经鼻注射右美托咪定后口服水合氯醛。随后,记录镇静评分、起效时间、镇静总时间以及任何潜在的不良反应。结果:所有新生儿均完成MRI检查,无明显不良反应。128名新生儿(90.1%)完成了单剂量的MRI研究,而14名新生儿(9.9%)需要额外的药物治疗。在单剂量的新生儿中,发病时间在出生天数、性别和体重方面没有统计学上的显著差异。在出生后的天数和性别之间,总时间没有统计学上的显著差异。然而,在体重低于3公斤的新生儿中,总时间明显延长。此外,与单一剂量的新生儿相比,使用额外药物的新生儿的总时间显着延长。结论:口服水合氯醛联合鼻内右美托咪定用于新生儿MRI检查是安全有效的,但对于3 kg以下的新生儿需特别注意。
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来源期刊
CiteScore
4.10
自引率
5.00%
发文量
226
审稿时长
6 months
期刊介绍: The Journal of Clinical Pharmacy and Therapeutics provides a forum for clinicians, pharmacists and pharmacologists to explore and report on issues of common interest. Reports and commentaries on current issues in medical and pharmaceutical practice are encouraged. Papers on evidence-based clinical practice and multidisciplinary collaborative work are particularly welcome. Regular sections in the journal include: editorials, commentaries, reviews (including systematic overviews and meta-analyses), original research and reports, and book reviews. Its scope embraces all aspects of clinical drug development and therapeutics, including: Rational therapeutics Evidence-based practice Safety, cost-effectiveness and clinical efficacy of drugs Drug interactions Clinical impact of drug formulations Pharmacogenetics Personalised, stratified and translational medicine Clinical pharmacokinetics.
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