Johnson Chris F, Maxwell Margaret, Williams Brian, Dougall Nadine, MacGillivray Stephen
Pharmacy Services, NHS Greater Glasgow and Clyde, Glasgow, UK.
Midwifery and AHP Research Unit, University of Stirling, Stirling, UK.
BMJ Med. 2022 Dec 1;1(1):e000017. doi: 10.1136/bmjmed-2021-000017. eCollection 2022.
To assess and clarify the relations between selective serotonin reuptake inhibitor (SSRI) dose efficacy, acceptability (early treatment discontinuation (dropouts)), and tolerability (reported adverse drug effects), and critically evaluate methods previously used to examine SSRI dose-response effects for the treatment of depression in adults.
Systematic review of reviews and meta-narrative synthesis.
Embase, Medline, PsycINFO, Scopus, and the Cochrane Collaboration library, from 1975 to December 2021. Reference lists of national depression treatment guidelines were systemically searched by hand.
Reviews assessing SSRI monotherapy dose-response effects for the treatment of depression in adults (age ≥18 years) reporting efficacy, acceptability, or tolerability. Reviews meeting inclusion criteria had a high degree of heterogeneity, due to methodological diversity; therefore, a meta-narrative synthesis approach was applied. Standard daily doses were defined as 20 mg citalopram, fluoxetine, paroxetine; 50 mg sertraline; and 10 mg escitalopram. Risk of bias was assessed using the Risk of Bias in Systematic Reviews tool, in line with Cochrane recommendations.
The search identified 9138 records; 387 full text reports were assessed for eligibility, 42 of which matched the inclusion criteria. The majority, 83% (n=35), of reviews included data for studies with a duration of ≤12 weeks (ie, the acute phase of depression treatment). Of 39 reviews assessing efficacy, the majority (n=26) indicated that individual SSRIs and SSRI class demonstrated flat dose-response effects; standard doses were optimal for efficacy. Acceptability or tolerability were assessed in 28 reviews. Higher than standard daily doses were associated with higher dropout rates and a greater incidence of adverse drug effects (eg, nausea, sexual dysfunction, fatigue, anxiety). Despite a range of methods being reported, there was an overall consensus regarding SSRI dose related efficacy, dropouts, and adverse drug effects.
Standard daily doses of SSRIs for the treatment of depression in adults provide a favourable balance between efficacy, acceptability, and tolerability. Patients are encouraged to talk to their prescriber or community pharmacist if they experience adverse effects or have any concerns about their drug treatments.
评估并阐明选择性5-羟色胺再摄取抑制剂(SSRI)的剂量疗效、可接受性(早期治疗中断(退出治疗))和耐受性(报告的药物不良反应)之间的关系,并严格评估先前用于研究成人抑郁症治疗中SSRI剂量反应效应的方法。
对综述进行系统评价和元叙事综合分析。
1975年至2021年12月的Embase、Medline、PsycINFO、Scopus和Cochrane协作图书馆。通过手工系统检索国家抑郁症治疗指南的参考文献列表。
评估SSRI单一疗法治疗成人(年龄≥18岁)抑郁症的剂量反应效应并报告疗效、可接受性或耐受性的综述。由于方法的多样性,符合纳入标准的综述具有高度异质性;因此,采用了元叙事综合分析方法。标准日剂量定义为:西酞普兰、氟西汀、帕罗西汀20mg;舍曲林50mg;艾司西酞普兰10mg。根据Cochrane的建议,使用“系统评价中的偏倚风险”工具评估偏倚风险。
检索到9138条记录;评估了387篇全文报告的 eligibility,其中42篇符合纳入标准。大多数综述(83%,n = 35)纳入了持续时间≤12周(即抑郁症治疗急性期)研究的数据。在评估疗效的39篇综述中,大多数(n = 26)表明,个体SSRI和SSRI类别显示出平坦的剂量反应效应;标准剂量对疗效最佳。在28篇综述中评估了可接受性或耐受性。高于标准日剂量与更高的退出率和更高的药物不良反应发生率(如恶心、性功能障碍、疲劳、焦虑)相关。尽管报告了一系列方法,但关于SSRI剂量相关的疗效、退出治疗和药物不良反应存在总体共识。
治疗成人抑郁症的SSRI标准日剂量在疗效、可接受性和耐受性之间提供了良好的平衡。如果患者出现不良反应或对药物治疗有任何担忧,鼓励他们与开处方的医生或社区药剂师交谈。