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儿科单纯性急性镰状细胞痛危象的镇痛管理:系统评价和荟萃分析。

Analgesic management of uncomplicated acute sickle-cell pain crisis in pediatrics: a systematic review and meta-analysis.

机构信息

Zhongnan Hospital of Wuhan University, Children's Digital and Health Data Research Center, Department of Pediatrics, Wuhan, China.

Zhongnan Hospital of Wuhan University, Children's Digital and Health Data Research Center, Department of Pediatrics, Wuhan, China.

出版信息

J Pediatr (Rio J). 2020 Mar-Apr;96(2):142-158. doi: 10.1016/j.jped.2019.05.004. Epub 2019 Jul 24.

Abstract

OBJECTIVES

To capture evidence of the efficacy and safety of pharmacological analgesia for uncomplicated acute sickle-cell pain in pediatric patients compared to placebo.

SOURCES OF DATA

Searches for key evidence were performed from March 1 to 31, 2018, for randomized controlled trials of pharmacological analgesia compared to placebo for uncomplicated acute sickle-cell pain in a pediatric sample. The authors searched ten scientific databases including, among others, PubMed, MEDLINE, Embase, and Clinicaltrials.gov for this systematic review and meta-analysis.

SUMMARY OF THE FINDINGS

Four trials (n=227) were selected by the inclusion criteria (intranasal fentanyl, intravenous magnesium, arginine, and inhaled nitric oxide). The quality of evidence ranged from low to moderate for each outcome. Meta-analysis of changes in the ladder of pain score (p=0.72), length-of-stay in hospital (p=0.65), and amount of narcotics used during the study (p=0.10) showed non-statistically significant differences and a lack of amelioration provided by pharmaceutical analgesics in treatment group. The adverse events reported that more participants in the intervention arm underwent pain, with statistically significant differences at the drug delivery site in studies using intranasal fentanyl and intravenous magnesium (p=0.03).

CONCLUSIONS

Pharmacological analgesia appears to be uncertain in improving the intensity and providing relief of acute pain crisis in pediatric patients with sickle-cell anemia. With respect to clinical advantage, no decisive deduction about the clinical efficacy may be made regarding these medications in acute sickle-cell pain management in the pediatric age group.

摘要

目的

与安慰剂相比,评估药物镇痛对儿科单纯性急性镰状细胞疼痛的疗效和安全性。

资料来源

2018 年 3 月 1 日至 31 日,对儿科单纯性急性镰状细胞疼痛的药物镇痛与安慰剂的随机对照试验进行了关键证据的检索。作者在这个系统综述和荟萃分析中,从 10 个科学数据库中进行了搜索,包括 PubMed、MEDLINE、Embase 和 Clinicaltrials.gov 等。

研究结果总结

根据纳入标准(鼻内芬太尼、静脉内镁、精氨酸和吸入一氧化氮),有 4 项试验(n=227)入选。每个结局的证据质量均为低至中度。疼痛评分阶梯变化的荟萃分析(p=0.72)、住院时间(p=0.65)和研究期间使用的麻醉药物量(p=0.10)显示差异无统计学意义,药物镇痛组的治疗也没有改善。报告的不良事件表明,干预组中更多的参与者出现疼痛,使用鼻内芬太尼和静脉内镁的研究在药物输送部位有统计学意义的差异(p=0.03)。

结论

药物镇痛似乎不能改善儿科镰状细胞贫血患者急性疼痛发作的强度和缓解程度。关于临床优势,对于这些药物在儿科急性镰状细胞疼痛管理中的临床疗效,不能做出决定性的推论。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fe72/9432155/490da47e85ad/gr1.jpg

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