Department of Medicine, University of Toronto, Suite RFE 3-805, 200 Elizabeth Street, Toronto, Ontario, M5G 2C4, Canada.
Syst Rev. 2013 May 4;2:25. doi: 10.1186/2046-4053-2-25.
Pregabalin is used in the treatment of postherpetic neuralgia, diabetic neuropathic pain, partial seizures, anxiety disorders and fibromyalgia. Recognized adverse effects associated with its use include cognitive impairment, somnolence and dizziness. Heart failure associated with pregabalin has been described, however the strength of this association has not been well characterized. To examine this further, we will conduct a systematic review of the risk of heart failure and edema associated with use of pregabalin.
METHODS/DESIGN: We will include all studies (experimental, quasi-experimental, observational, case series/reports, drug regulatory reports) that examine the use of pregabalin compared to placebo, gabapentin or conventional care. Our primary outcome is heart failure and the secondary outcomes include edema and weight gain. We will search electronic databases (MEDLINE, EMBASE, Cochrane Central Register of Controlled Trials), and grey literature sources (trial registries, conference abstracts) to identify relevant studies. To ensure literature saturation, we will contact drug manufacturers, conduct forward citation searching, and scan the reference lists of key articles and included studies. We will not restrict inclusion by language or publication status.Two reviewers will screen citations (titles and abstracts) and full-text articles, conduct data abstraction, and appraise risk of bias. Random-effects meta-analysis will be conducted if the studies are deemed heterogeneous in terms of clinical, statistical and methodological factors but still suitable for meta-analysis.
The results of this review will assist physicians to better appreciate pregabalin's risk for edema or congestive heart failure and will be pertinent to the thousands of patients worldwide who are administered this medication.Our protocol was registered in the PROSPERO database (CRD42012002948).
普瑞巴林用于治疗疱疹后神经痛、糖尿病性周围神经痛、部分癫痫发作、焦虑症和纤维肌痛。其使用相关的公认不良反应包括认知障碍、镇静和头晕。已描述了与普瑞巴林相关的心力衰竭,但尚未很好地描述这种关联的强度。为了进一步研究这一点,我们将对普瑞巴林使用与心力衰竭和水肿相关的风险进行系统评价。
方法/设计:我们将纳入所有研究(实验性、准实验性、观察性、病例系列/报告、药物监管报告),这些研究比较了普瑞巴林与安慰剂、加巴喷丁或常规护理的使用。我们的主要结局是心力衰竭,次要结局包括水肿和体重增加。我们将搜索电子数据库(MEDLINE、EMBASE、Cochrane 中央对照试验注册库)和灰色文献来源(试验注册处、会议摘要)以确定相关研究。为确保文献饱和,我们将联系药物制造商,进行前瞻性引文搜索,并扫描关键文章和纳入研究的参考文献列表。我们不会因语言或出版状况而限制纳入。两名审查员将筛选引文(标题和摘要)和全文文章,进行数据提取,并评估偏倚风险。如果研究在临床、统计学和方法学因素方面存在异质性,但仍适合进行荟萃分析,则将进行随机效应荟萃分析。
该综述的结果将帮助医生更好地了解普瑞巴林引起水肿或充血性心力衰竭的风险,并与全球数千名接受这种药物治疗的患者有关。我们的方案已在 PROSPERO 数据库(CRD42012002948)中注册。