在血管闭塞性危象患者中使用氯胺酮的安全性和有效性:系统回顾和荟萃分析。

EJHaem Pub Date : 2024-11-25 DOI:10.1002/jha2.1050
Ernesto Calderon Martinez, Stephin Zachariah Saji, Thomas Campos Carmona, Vaidarshi Abbagoni, Mohammad Salman, Mishell Estefanía Llerena Vargas, Suchita Mylavarapu, Druvini Fernando, Lakshmi Sheethal Arvapalli, Nathalia Schettino Samad, Nithin Karnan, Camila Sanchez Cruz
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引用次数: 0

摘要

简介:镰状细胞病(SCD)的特点是急性发作称为血管闭塞危象(VOC)。挥发性有机化合物的特点是由于镰状细胞阻塞血管而引起剧烈疼痛。据报道,氯胺酮在控制SCD患者的VOC方面是有效和安全的。目的/方法:本综述旨在通过临床试验和观察性研究的分析来确定氯胺酮的安全性和有效性。方法:本系统评价和荟萃分析遵循PRISMA指南,于2024年5月20日系统检索了7个数据库,包括随机对照试验(RCT)、队列和病例对照研究。结果:5项研究689名受试者符合纳入标准。数值评定量表(NRS)疼痛评分的两项研究(518项观察)的荟萃分析显示无显著差异,标准化平均差异(MD)为0.23 (95% CI: -0.13至0.59,p = 0.21, i2 = 0%)。对于吗啡毫克当量(MME),两项研究(344项观察)的荟萃分析得出MD为-0.03 (95% CI: -0.09至0.04,p = 0.45, i2 = 97%)。然而,来自4项研究(608项观察)的副作用分析显示,轻微副作用(包括恶心、呕吐和头晕)的相对风险(RR)显著较高,为5.74 (95% CI: 2.80-11.79, p 2 = 0%)。结论:氯胺酮定性合成有可能改善VOC期间SCD患者的疼痛管理,但在减轻疼痛方面无统计学意义。它与轻度副作用增加有关,但没有严重不良事件的报道。需要进一步的研究来增加样本量和分析的能力,以澄清在这种情况下氯胺酮的最佳剂量和给药方案。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Safety and efficacy of ketamine use in patients with vaso-occlusive crisis: A systematic review and meta-analysis

Safety and efficacy of ketamine use in patients with vaso-occlusive crisis: A systematic review and meta-analysis

Introduction

Sickle cell disease (SCD) is characterized by acute episodes called vaso-occlusive crises (VOC). VOC is marked by severe pain due to blocked blood vessels by sickled cells. Ketamine has been reported to be effective and safe in managing VOC in SCD patients.

Objectives/methods

This review aims to determine ketamine's safety and efficacy through analysis of clinical trials and observational studies.

Methods

Adhering to PRISMA guidelines, this systematic review and meta-analysis systematically searched seven databases on May 20, 2024 for randomized control trials (RCT), cohorts, and case–control studies.

Results

Five studies with 689 participants met the inclusion criteria. A meta-analysis of two studies (518 observations) for the Numerical Rating Scale (NRS) pain score showed no significant difference, with a standardized mean difference (MD) of 0.23 (95% CI: −0.13 to 0.59, p = 0.21, I2 = 0%). For morphine milligram equivalent (MME), a meta-analysis of two studies (344 observations) resulted in an MD of −0.03 (95% CI: −0.09 to 0.04, p = 0.45, I2 = 97%). However, the side effects analysis from four studies (608 observations) showed a significantly higher relative risk (RR) of 5.74 (95% CI: 2.80–11.79, p < 0.0001, I2 = 0%) for mild side effects, including nausea, vomiting, and dizziness.

Conclusion

Ketamine qualitative synthesis shows potential for improving pain management in SCD patients during VOC, but without statistically significant differences in pain reduction. It is associated with increased mild side effects, though no severe adverse events were reported. Further research is needed to increase the sample size and power of the analysis to clarify optimal dosing and administration protocols for ketamine in this context.

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