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Efficacy and safety of second-generation antipsychotic long-acting injections (SGA LAIs) in maintenance treatment of bipolar disorder:protocol for a systematic review and meta-analysis

机译:第二代抗精神病药长效注射液(SGA LAIs)在双相情感障碍维持治疗中的疗效和安全性:用于系统评价和荟萃分析的方案

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摘要

INTRODUCTION: Bipolar disorder requires long-term treatment but non-adherence is a common problem. Antipsychotic long-acting injections (LAIs) have been suggested to improve adherence but none are licensed in the UK for bipolar. However, the use of second-generation antipsychotics (SGA) LAIs in bipolar is not uncommon albeit there is a lack of systematic review in this area. This study aims to systematically review safety and efficacy of SGA LAIs in the maintenance treatment of bipolar disorder. METHODS AND ANALYSIS: The protocol is based on Preferred Reporting Items for Systematic reviews and Meta-Analyses (PRISMA) and will include only randomised controlled trials comparing SGA LAIs in bipolar. PubMed, EMBASE, CINAHL, Cochrane Library (CENTRAL), PsychINFO, LiLACS, http://www.clinicaltrials.gov will be searched, with no language restriction, from 2000 to January 2016 as first SGA LAIs came to the market after 2000. Manufacturers of SGA LAIs will also be contacted. Primary efficacy outcome is relapse rate or delayed time to relapse or reduction in hospitalisation and primary safety outcomes are drop-out rates, all-cause discontinuation and discontinuation due to adverse events. Qualitative reporting of evidence will be based on 21 items listed on standards for reporting qualitative research (SRQR) focusing on study quality (assessed using the Jadad score, allocation concealment and data analysis), risk of bias and effect size. Publication bias will be assessed using funnel plots. If sufficient data are available meta-analysis will be performed with primary effect size as relative risk presented with 95% CI. Sensitivity analysis, conditional on number of studies and sample size, will be carried out on manic versus depressive symptoms and monotherapy versus adjunctive therapy.
机译:简介:躁郁症需要长期治疗,但不坚持治疗是一个普遍的问题。已建议使用抗精神病药长效注射剂(LAIs)改善依从性,但在英国没有双极类药物被许可使用。然而,尽管在这一领域缺乏系统的综述,但在双相情感障碍中使用第二代抗精神病药(SGA)LAI并不少见。本研究旨在系统评价SGA LAI在双相情感障碍维持治疗中的安全性和有效性。方法与分析:该协议基于系统评价和荟萃分析(PRISMA)的首选报告项目,并且仅包括比较双相SGA LAI的随机对照试验。从2000年到2016年1月,将在2000年之后搜索第一个SGA LAI,不受限制地搜索PubMed,EMBASE,CINAHL,Cochrane图书馆(CENTRAL),PsychINFO,LiLACS,http://www.clinicaltrials.gov。也将联系SGA LAI的制造商。主要功效结局是复发率或延迟的复发时间或住院减少,而主要安全结局是辍学率,全因停药和因不良事件而停药。定性证据报告将基于定性研究报告标准(SRQR)中列出的21个项目,这些标准侧重于研究质量(使用Jadad评分,分配隐藏和数据分析进行评估),偏倚风险和效应大小。将使用漏斗图评估出版偏倚。如果有足够的数据可用,将以主要效应量作为95%CI的相对风险进行荟萃分析。敏感性分析将根据躁狂症状与抑郁症状以及单药治疗与辅助治疗的关系,以研究数量和样本量为条件。

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