Evaluating the Therapeutic Effects of Amino Acid Treatment on Vaso-Occlusive Pain in Sickle Cell Disease: A Systematic Review and Meta-Analysis Protocol

Bohan Zhang, Ciaran Bubb, Vivian Dong, Sophie Yao, Priyal Patel, Aanya Shahani, Katie Lobner, Oluwakemi Badaki-Makun
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Abstract

Introduction: Sickle Cell Disease (SCD) affects over 100,000 individuals in the United States and 20 million globally, causing acute and chronic pain. The disease is characterized by misshapen red blood cells caused by mutations in beta-hemoglobin genes. SCD leads to multiorgan damage, chronic anemia, and severe pain crises, with a median life expectancy of 43 years. Current treatments involve opioids, blood transfusions, and hydroxyurea. Amino acids, especially L-Glutamine, have shown promise in managing SCD pain. This systematic review aims to comprehensively analyze the effects of amino acid treatments on vaso-occlusive pain crises in SCD patients. Methods: Following the Cochrane Handbook and PRISMA-P guidelines, this systematic review will include studies comparing amino acid treatment to placebo or standard care for SCD pain crises. Eligible studies of all age ranges, settings, and amino acid types will be considered. A comprehensive search strategy will be employed in PubMed, Embase, and Scopus databases. Studies will be assessed for risk of bias using Cochrane's RoB2 tool. Primary outcomes include a reduction in pain, measured quantitatively through pain scales. Secondary outcomes encompass quality of life, hospital length of stay, and opioid equivalents used. Discussion: Existing literature underscores the therapeutic potential of amino acids, yet there still lacks a systematic review comparing the overall effects of different amino acid treatments for vaso-occlusive crises in patients with SCD. This review aims to serve as a valuable resource for clinicians, offering insights into amino acid interventions as alternatives or supplements to opioid treatments. Additionally, it seeks to encourage further randomized clinical trials, contributing to an informed clinical use of amino acids for pain management in SCD. Ultimately, the findings aim to enhance the understanding of the therapeutic effects of essential amino acids on pediatric patients with SCD, facilitating evidence-based clinical decisions.
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评估氨基酸治疗对镰状细胞病血管闭塞性疼痛的治疗效果:系统回顾和元分析协议
导言:镰状细胞病(Sickle Cell Disease,SCD)在美国影响着 10 万多人,在全球影响着 2 千万人,造成急性和慢性疼痛。这种疾病的特征是由于β-血红蛋白基因突变导致红细胞畸形。SCD 会导致多器官损伤、慢性贫血和严重的疼痛危机,预期寿命中位数为 43 岁。目前的治疗方法包括阿片类药物、输血和羟基脲。氨基酸,尤其是 L-谷氨酰胺,在控制 SCD 疼痛方面显示出了前景。本系统综述旨在全面分析氨基酸治疗对 SCD 患者血管闭塞性疼痛危机的影响:根据 Cochrane 手册和 PRISMA-P 指南,本系统性综述将包括氨基酸治疗与安慰剂或标准护理对 SCD 疼痛危象的比较研究。将考虑所有年龄段、环境和氨基酸类型的合格研究。将在 PubMed、Embase 和 Scopus 数据库中采用综合检索策略。将使用 Cochrane 的 RoB2 工具对研究进行偏倚风险评估。主要结果包括疼痛的减轻,通过疼痛量表进行量化测量。次要结果包括生活质量、住院时间和使用的阿片类药物当量:现有文献强调了氨基酸的治疗潜力,但仍缺乏系统性综述来比较不同氨基酸疗法对 SCD 患者血管闭塞性危象的总体效果。本综述旨在为临床医生提供有价值的资源,让他们深入了解氨基酸干预作为阿片类药物治疗的替代品或补充剂的作用。此外,本综述还旨在鼓励进一步开展随机临床试验,为临床在知情的情况下使用氨基酸治疗 SCD 患者的疼痛做出贡献。最终,研究结果旨在加强人们对必需氨基酸对 SCD 儿童患者治疗效果的了解,从而促进循证临床决策。
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