关于停用苯二氮卓类药物诱发心房颤动潜在作用机制的叙述性文献综述

Q3 Medicine
Agnė Okulevičiūtė, Gabija Laubner Sakalauskienė
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引用次数: 0

摘要

简介:苯二氮卓类药物是常用处方药,但经常被滥用,导致依赖性和戒断症状。全球处方量的增加引发了不良反应和用药过量的担忧,尤其是对老年人而言。在处方和考虑替代疗法时需要谨慎,以尽量降低风险。目的:对停用苯二氮卓类药物可能诱发心房颤动的作用机制进行叙述性文献综述。材料与方法:使用 "苯二氮卓类药物和心房颤动或外周苯二氮卓受体"、"苯二氮卓类药物的历史"、"苯二氮卓类药物的作用机制"、"苯二氮卓类药物的适应症"、"苯二氮卓类药物的不良反应 "和 "苯二氮卓类药物的戒断效应 "等关键词组合检索数据库PubMed。删除了非全文和非英文科学出版物。共纳入 31 篇出版物。讨论苯二氮卓类药物(BZDs)于 1955 年合成,最初被认为毒性低于巴比妥类药物。它们与 GABA-A 受体相互作用,导致中枢神经系统超极化和抑制作用。BZDs 可用于治疗各种临床疾病,但长期使用会导致不良反应和戒断症状。有证据表明,遗传多样性可通过 GABA 受体影响对 BZDs 的反应。苯二氮卓类药物与外周苯二氮卓受体之间的相互作用可能会影响钙离子通道,从而影响心脏动作电位和收缩力,停用这些药物有可能导致心房颤动。此外,苯二氮卓类药物可能直接影响钙离子通道,导致抗心律失常作用和血管扩张。结论总之,苯二氮卓类药物曾被认为是较安全的镇静剂,但现在却引起了人们对滥用、依赖性和戒断症状的担忧。虽然通过涉及外周苯二氮卓受体和心脏钙通道的机制,停用苯二氮卓类药物与心房颤动之间存在潜在联系,但因果关系仍不确定,且涉及多个方面。需要进一步研究以明确这些机制,医疗保健提供者应谨慎对待苯二氮卓类药物的长期处方,同时探索替代治疗策略以降低风险。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Narrative Literature Review of Potential Atrial Fibrillation Mechanism of Action Induced by Discontinuation of Benzodiazepines
Introduction: Benzodiazepines are commonly prescribed but often misused, leading to dependence and withdrawal symptoms. Increased worldwide prescriptions raise adverse effects and overdose concerns, especially for the elderly. Caution is needed in prescribing and considering alternative treatments to minimize risks. Aim: Narrative literature review of potential atrial fibrillation mechanism of action induced by discontinuation of benzodiazepines. Materials and methods: Database PubMed was searched using the combination of keywords – “Benzodiazepine AND atrial fibrillation OR peripheral benzodiazepine receptors”, “history of benzodiazepines”, “benzodiazepines mechanism of action”, “benzodiazepines indications”, “benzodiazepines adverse effects” and “benzodiazepines withdrawal effects”. Non-full-text and non-English scientific publications were removed. A total of 31 publication was included. Discussion: Benzodiazepines (BZDs) were synthesized in 1955 and initially considered less toxic than barbiturates. They interact with GABA-A receptors, causing hyperpolarization and inhibitory effects in the central nervous system. BZDs are used to treat various clinical disorders, but long-term use can lead to adverse effects and withdrawal symptoms. There is evidence that genetic diversity can influence the response to BZDs through GABA receptors. The interaction between benzodiazepines and peripheral benzodiazepine receptors may influence calcium ion channels, affecting cardiac action potential and contractility, and discontinuation of these medications can potentially contribute to atrial fibrillation. Additionally, benzodiazepines may directly affect calcium channels, causing antiarrhythmic effects and vasodilation. Conclusion: In summary, benzodiazepines, once considered safer sedatives, now raise concerns about misuse, dependence, and withdrawal symptoms. While there is a potential link between discontinuing benzodiazepines and atrial fibrillation through mechanisms involving peripheral benzodiazepine receptors and cardiac calcium channels, causality remains uncertain and multifaceted. Further research is needed to clarify these mechanisms, and healthcare providers should exercise caution in long-term benzodiazepine prescriptions while exploring alternative treatment strategies to mitigate risks.
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来源期刊
Acta Medica Lituanica
Acta Medica Lituanica Medicine-General Medicine
CiteScore
0.70
自引率
0.00%
发文量
33
审稿时长
16 weeks
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