Erector spinae plane block versus caudal epidural block in pediatric surgery: a systematic review and meta-analysis of randomized clinical trials

IF 1.9 4区 医学 Q2 ANESTHESIOLOGY
Barbara Bombassaro Masiero , Deivyd Cavalcante , Fatemeh Akbarpoor , Capela António Dicazeco Pascoal , Lubna Al-Sharif , Fellipe Feijó Halfeld , Lucas Cael Azevedo Ramos Bendaham , Patricia Viana , Jesslyn N. Haryianto , Maria Luiza de Souza Rasia , Mariana Copetti de Almeida Cunha , Ana Djulia Tesche , Júlia Caletti Roth de Oliveira , Rafael Arsky Lombardi
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引用次数: 0

Abstract

Background

Caudal Epidural Block (CEB) is a well-established regional anesthesia technique for abdominal and sub-abdominal pediatric surgeries. However, it has a short duration, often leading to additional analgesic administration. Erector Spinae Plane Block (ESPB), for instance, is an emerging technique that, like CEB, provides analgesic effect to a specific dermatome of the body during surgery and in the postoperative period. Therefore, we performed this systematic review with meta-analysis to compare both techniques.

Methods

We searched PubMed, Embase and Cochrane Central for Randomized Controlled Trials (RCTs) comparing ESPB versus CEB in pediatric patients undergoing abdominal and sub-abdominal surgeries. The primary outcome was the time to first analgesic request. Secondary outcomes were I) FLACC score; II) Postoperative nausea and vomiting, and III) Urinary retention.

Results

Nine randomized controlled trials encompassing 507 patients were included in this analysis (1‒9). The patients were predominantly male and under 10 years of age. There was an equal distribution between the two groups regarding the number of patients and patients’ baseline characteristics. The main results were: time to first analgesic request (MD = 3.71; 95% CI: -1.88–9.29; I2 = 99%; p = 0.19); FLACC scores at 2 hours (MD = 0.15; 95% CI: -0.30–0.59; I2 = 0%; p = 0.52); FLACC scores at 24 hours (MD = -0.17; 95% CI: -0.39–0.05; I2 = 41%; I2 = 41%; p = 0.13); urinary retention events (RR = 0.12; 95% CI: 0.02–0.94; I2 = 0%; p = 0.04); and Postoperative Nausea and Vomiting (PONV) which was null in both groups in three studies. However, it is important to clarify that some limitations were identified, such as significant heterogeneity in the following outcomes: time to first analgesic request and FLACC score at 24h, possibly due to different age groups, different types of surgeries, different background analgesia administration, and a relatively small sample size. As for the risk of bias, two studies were found to have some concerns in “bias due to deviations from intended interventions” (8,9).

Conclusion

Our findings suggest that the administration of ESPB did not statistically differ from CEB regarding the time to first analgesic request. FLACC scores also did not show a statistically significant difference between groups. The ESPB group, however, experienced minor urinary retention events compared to the CEB group.

Quality of evidence

According to the GRADE assessment, all outcomes evaluated in this study were classified as high-quality evidence. Quality assessment is detailed in Supplementary Table 1.
竖脊肌平面阻滞与尾侧硬膜外阻滞在儿科手术中的应用:随机临床试验的系统回顾和荟萃分析。
背景:尾侧硬膜外阻滞(CEB)是一种成熟的用于腹部和亚腹部儿科手术的区域麻醉技术。然而,它的持续时间很短,经常导致额外的镇痛药。例如,直立脊柱平面阻滞(ESPB)是一种新兴技术,像CEB一样,在手术期间和术后对身体的特定皮肤区提供镇痛效果。因此,我们采用荟萃分析进行系统评价,比较两种技术。方法:我们检索PubMed、Embase和Cochrane Central的随机对照试验(RCTs),比较ESPB和CEB在接受腹部和亚腹部手术的儿科患者中的作用。主要观察指标为首次请求镇痛的时间。次要结局为:1)FLACC评分;II)术后恶心呕吐,III)尿潴留。结果:9项随机对照试验包括507例患者纳入本分析(1-9)。患者以10岁以下男性为主。两组患者的数量和患者的基线特征分布相等。主要结果为:首次请求镇痛时间(MD = 3.71;95% ci: -1.88-9.29;I2 = 99%; = 0.19页);2小时FLACC评分(MD = 0.15;95% ci: -0.30-0.59;I2 = 0%; = 0.52页);24小时FLACC评分(MD = -0.17;95% ci: -0.39-0.05;I2 = 41%;I2 = 41%; = 0.13页);尿潴留事件(RR = 0.12;95% ci: 0.02-0.94;I2 = 0%; = 0.04页);术后恶心和呕吐(PONV),在三个研究中两组均为零。然而,重要的是要澄清一些局限性,如以下结果的显著异质性:第一次镇痛要求的时间和24小时FLACC评分,可能是由于不同年龄组,不同手术类型,不同背景的镇痛给药,以及相对较小的样本量。在偏倚风险方面,发现有两项研究对“偏离预期干预措施的偏倚”存在一些担忧(8,9)。结论:我们的研究结果表明,ESPB给药与CEB在第一次镇痛要求的时间上没有统计学差异。FLACC评分组间差异无统计学意义。然而,与CEB组相比,ESPB组经历了轻微的尿潴留事件。证据质量:根据GRADE评估,本研究评估的所有结果均被归类为高质量证据。质量评估详见补充表1。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
2.10
自引率
0.00%
发文量
88
审稿时长
68 days
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