A Systematic Review and Meta-Analysis of The Efficacy of Endoscopic Ultrasound Guided Celiac Plexus Blocks for Chronic Pancreatitis Pain.

IF 0.9 Q3 ANESTHESIOLOGY
Luke Kar Man Chan, Tanish Rao, Paolo Masangcay, Samuel Chia Lin Kuo, Tai-Tak Wan
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Abstract

Chronic pancreatitis is a globally prevalent progressive disease, with pain affecting up to 90% of patients, significantly impairing quality of life and leading to high rates of disability, hospitalizations, and opioid dependence. Pain management is crucial in treating chronic pancreatitis, with endoscopic ultrasound-guided celiac plexus block (EUS-CPB) recognized as an interventional option. This systematic review and meta-analysis, following PRISMA guidelines, synthesized data from 12 studies (5 randomized control trials and 7 observational) on the efficacy of EUS-CPB in managing chronic pancreatitis pain. The overall analysis revealed a significant pain relief proportion of 0.64 (n=612) with moderate heterogeneity. Subgroup analyses revealed a proportion of 0.72 in RCTs and 0.59 in observational studies. Common complications included diarrhea and exacerbation of abdominal pain, with no reported mortality. Despite variations in efficacy due to study heterogeneity and patient differences, the findings suggest EUS-CPB as a safe and effective option, with effects lasting weeks to months. Recent studies have demonstrated the applicability of EUS-CPB across ethnically diverse and pediatric populations. However, limitations including small sample sizes and study variability highlight the need for personalized treatment approaches. Future larger randomized sham-controlled trials are recommended to better assess the duration of pain relief and impact on opioid use.

超声内镜引导下腹腔神经丛阻滞治疗慢性胰腺炎疼痛疗效的系统评价和meta分析。
慢性胰腺炎是一种全球普遍存在的进行性疾病,疼痛影响高达90%的患者,严重影响生活质量,导致高致残率、住院率和阿片类药物依赖性。疼痛管理是治疗慢性胰腺炎的关键,内镜下超声引导腹腔丛阻滞(EUS-CPB)被认为是一种介入选择。本系统回顾和荟萃分析,遵循PRISMA指南,综合了12项研究(5项随机对照试验和7项观察性试验)关于EUS-CPB治疗慢性胰腺炎疼痛疗效的数据。总体分析显示疼痛缓解比例为0.64 (n=612),具有中等异质性。亚组分析显示,该比例在随机对照试验中为0.72,在观察性研究中为0.59。常见并发症包括腹泻和腹痛加重,无死亡报告。尽管由于研究的异质性和患者的差异,疗效存在差异,但研究结果表明EUS-CPB是一种安全有效的选择,效果持续数周至数月。最近的研究已经证明了EUS-CPB在不同种族和儿科人群中的适用性。然而,包括小样本量和研究可变性在内的局限性突出了个性化治疗方法的必要性。建议将来进行更大规模的随机假对照试验,以更好地评估疼痛缓解的持续时间和对阿片类药物使用的影响。
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
1.60
自引率
9.10%
发文量
40
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