School of Pharmacy and Pharmaceutical Sciences, Trinity College Dublin, Dublin, Ireland.
Department of Psychology, University of Buckingham, Buckingham, UK.
J Psychopharmacol. 2024 Feb;38(2):127-136. doi: 10.1177/02698811231224171.
Medication adherence is a prerequisite to achieving beneficial treatment outcomes. In major depressive disorder, many patients fail to complete medication regimens, raising concern for poor treatment outcomes. It is usual to experience adverse drug reactions (ADRs) while taking antidepressants, and relative discomfort is reported by patients.
The present review focuses on the presence of antidepressant-related side effects and the subsequent relationship with medication non-adherence.
The Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines were followed. Following the preliminary research, the research question and eligibility criteria were created based on the PICO framework. All articles retrieved from the selected databases were exported to Covidence, a Systematic Review managing software tool. Two reviewers assessed the papers to identify the risk of bias using the Joanna Briggs Institute critical appraisal tool for cross-sectional studies. Seven studies with a low-moderate risk of bias fulfilled the eligibility criteria and were conducted from 2013 to 2020 in Europe, Africa and Asia.
The results demonstrated high levels of suboptimal adherence ranging from 46% to 83% amongst the studied population. A variety of side effects were reported by a significant number of participants predominantly with moderate severity. A correlation between the presence of ADRs and suboptimal rates of adherence to antidepressants was found. Somnolence and headaches among other unspecified ADRs were found to increase the dropout rates for selective serotonin reuptake inhibitors.
The present study elucidates the need for effective interventions to facilitate antidepressant adherence and enhance doctor-patient communication, benefiting both the individuals and the healthcare system and leading to better clinical outcomes and reduction of relapse-related costs.
药物依从性是实现有益治疗结果的前提。在重度抑郁症中,许多患者无法完成药物治疗方案,这引起了对治疗结果不佳的担忧。服用抗抑郁药时通常会出现不良反应(ADR),并且患者会报告出现相对不适。
本综述重点关注抗抑郁药相关副作用的存在及其与药物不依从的后续关系。
遵循系统评价和荟萃分析的首选报告项目(PRISMA)指南。在初步研究之后,根据 PICO 框架创建了研究问题和资格标准。从选定的数据库中检索到的所有文章都被导出到 Covidence,这是一种系统综述管理软件工具。两位审查员使用 Joanna Briggs 研究所对横断面研究的批判性评估工具评估论文,以确定偏倚风险。有七项研究具有低中度偏倚风险,符合条件,并于 2013 年至 2020 年在欧洲、非洲和亚洲进行。
结果表明,在所研究的人群中,药物依从性不佳的比例高达 46%至 83%。相当数量的参与者报告了各种副作用,主要为中度严重程度。发现 ADR 的存在与抗抑郁药依从性不佳之间存在相关性。发现 ADR 如嗜睡和头痛等其他未指明的不良反应会增加选择性 5-羟色胺再摄取抑制剂的停药率。
本研究阐明了需要有效的干预措施来促进抗抑郁药的依从性并加强医患沟通,使个人和医疗保健系统受益,并导致更好的临床结果和减少与复发相关的成本。