The efficacy and effectiveness of drinking interventions to reduce vasovagal reactions in blood donors: A systematic review and meta-analysis.

IF 1.8 4区 医学 Q3 HEMATOLOGY
Vox Sanguinis Pub Date : 2024-09-05 DOI:10.1111/vox.13724
Hans Van Remoortel, Dieter Van de Sande, Dieter Maes, Jina Khoudary, Veerle Tavernier, Pierre Tiberghien, Emmy De Buck, Veerle Compernolle
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引用次数: 0

Abstract

Background and objectives: Blood establishments strive to ensure the safety and comfort of blood donors while minimizing adverse events. This review aims to assess the efficacy and effectiveness of eating and/or drinking interventions before, during and/or after blood donation in reducing vasovagal reactions (VVRs).

Materials and methods: We analysed randomized and non-randomized controlled trials comparing eating and/or drinking interventions to no intervention, placebo or usual practice on (pre-)syncopal VVRs and related symptoms. The GRADE (Grading of Recommendations, Assessment, Development and Evaluation) approach was used to assess the risk of bias and overall certainty of the evidence.

Results: Pre-donation water ingestion likely results in reduced on-site VVRs, compared to no water (2 fewer per 100 donors, moderate-certainty evidence). A pre-donation isotonic drink likely results in reduced VVRs, compared to usual practice (2 fewer per 100 donors, moderate-certainty evidence). Pre-donation salt-loaded sweetened lemon water may result in fewer off-site VVRs, compared to sweetened lemon water only (1 fewer per 100 donors, low-certainty evidence). Pre-donation water and a gel cap containing sucrose with 250 mg caffeine may result in fewer blood donor reaction ratings, compared to pre-donation water only (low-certainty evidence).

Conclusions: Pre-donation plain water ingestion or isotonic drink probably results in a large reduction in on-site and off-site VVRs. Pre-donation water ingestion with caffeine consumption or salt supplementation may result in a VVR reduction, compared to water ingestion only. Future large trials are required to increase the certainty of the effect of these and other interventions in the prevention of VVRs.

减少献血者血管迷走神经反应的饮酒干预措施的效力和有效性:系统回顾和荟萃分析。
背景和目的:血液机构努力确保献血者的安全和舒适,同时尽量减少不良事件的发生。本综述旨在评估献血前、献血中和/或献血后进食和/或饮水干预对减少血管迷走神经反应(VVRs)的效力和有效性:我们分析了随机和非随机对照试验,这些试验比较了进食和/或饮水干预与无干预、安慰剂或常规做法对(晕厥前)血管迷走神经反应及相关症状的影响。采用GRADE(建议、评估、发展和评价分级)方法评估证据的偏倚风险和总体确定性:结果:与不饮水相比,捐献前饮水可能会减少现场 VVR(每 100 例捐献者中减少 2 例,中度确定性证据)。与通常做法相比,捐献前饮用等渗饮料可能会减少 VVR(每 100 例捐献者中减少 2 例,中度确定性证据)。与只饮用加糖柠檬水相比,捐献前饮用加盐的加糖柠檬水可能会减少站外 VVR(每 100 例捐献者中减少 1 例,低度确定性证据)。与只饮用献血前白开水相比,献血前白开水和含有 250 毫克咖啡因的蔗糖凝胶帽可能会导致较少的献血者反应评级(低确定性证据):结论:献血前饮用白开水或等渗饮料可能会大大减少现场和非现场 VVR。与仅摄入白开水相比,在捐献前摄入白开水并同时摄入咖啡因或补充盐分可能会导致 VVR 下降。未来需要进行大规模试验,以进一步确定这些干预措施和其他干预措施在预防室间静脉回流方面的效果。
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
Vox Sanguinis
Vox Sanguinis 医学-血液学
CiteScore
4.40
自引率
11.10%
发文量
156
审稿时长
6-12 weeks
期刊介绍: Vox Sanguinis reports on important, novel developments in transfusion medicine. Original papers, reviews and international fora are published on all aspects of blood transfusion and tissue transplantation, comprising five main sections: 1) Transfusion - Transmitted Disease and its Prevention: Identification and epidemiology of infectious agents transmissible by blood; Bacterial contamination of blood components; Donor recruitment and selection methods; Pathogen inactivation. 2) Blood Component Collection and Production: Blood collection methods and devices (including apheresis); Plasma fractionation techniques and plasma derivatives; Preparation of labile blood components; Inventory management; Hematopoietic progenitor cell collection and storage; Collection and storage of tissues; Quality management and good manufacturing practice; Automation and information technology. 3) Transfusion Medicine and New Therapies: Transfusion thresholds and audits; Haemovigilance; Clinical trials regarding appropriate haemotherapy; Non-infectious adverse affects of transfusion; Therapeutic apheresis; Support of transplant patients; Gene therapy and immunotherapy. 4) Immunohaematology and Immunogenetics: Autoimmunity in haematology; Alloimmunity of blood; Pre-transfusion testing; Immunodiagnostics; Immunobiology; Complement in immunohaematology; Blood typing reagents; Genetic markers of blood cells and serum proteins: polymorphisms and function; Genetic markers and disease; Parentage testing and forensic immunohaematology. 5) Cellular Therapy: Cell-based therapies; Stem cell sources; Stem cell processing and storage; Stem cell products; Stem cell plasticity; Regenerative medicine with cells; Cellular immunotherapy; Molecular therapy; Gene therapy.
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