Rawson Nigel S B
J Popul Ther Clin Pharmacol. 2014;21(2):e214-32. Epub 2014 Jun 2.
Following the publication of a meta-analysis reporting a risk of acute myocardial infarction (AMI) with rosiglitazone that led to severe restrictions being placed on its use, several observational studies of the association were reported. The lifting of restrictions in the United States in 2013 makes a review of these studies pertinent.
To evaluate the quality of population-based observational studies of the rosiglitazone-AMI association.
PubMed and Embase literature databases were searched for observational studies evaluating the association that were published between 2006 and 2010. Publications satisfying the inclusion criteria were reviewed using the Checklist for Retrospective Database Studies.
Nineteen studies satisfied the inclusion criteria. Reasons for the research design and data source were absent or unclear in 18 (95%) and 16 (84%), respectively. Administrative data were used exclusively in 14 (74%). Baseline periods for prior diagnoses and medications varied widely. Reimbursement constraints on rosiglitazone use were reported in only seven studies (37%), although all were likely to have been impacted by them. What was being tested in half of the rosiglitazone treatment comparisons lacked specificity and clarity. All relied on risk ratios and, for 90% of the comparisons, the ratios were between 0.5 and two - a level at which residual confounding can lead to spurious significance.
Important deficiencies existed in the rosiglitazone studies suggesting that standards for methods and reporting of observational safety analyses need improvement. In particular, detailed clinical data should be included when the risk of confounding by indication is likely to be high.
一项荟萃分析报告称罗格列酮有导致急性心肌梗死(AMI)的风险,这使得其使用受到严格限制。随后,有几项关于该关联的观察性研究被报道。2013年美国解除了相关限制,因此对这些研究进行回顾很有必要。
评估基于人群的罗格列酮与AMI关联观察性研究的质量。
检索PubMed和Embase文献数据库,查找2006年至2010年期间发表的评估该关联的观察性研究。使用回顾性数据库研究清单对符合纳入标准的出版物进行审查。
19项研究符合纳入标准。分别有18项(95%)和16项(84%)研究的研究设计和数据来源的相关信息缺失或不明确。14项(74%)研究仅使用了行政数据。先前诊断和用药的基线期差异很大。只有7项研究(37%)报告了罗格列酮使用的报销限制,不过所有研究可能都受到了其影响。在罗格列酮治疗比较中,有一半所测试的内容缺乏特异性和清晰度。所有研究都依赖风险比,并且在90%的比较中,风险比在0.5至2之间——在这个水平上,残余混杂可能导致虚假的显著性。
罗格列酮研究存在重要缺陷,这表明观察性安全性分析的方法和报告标准需要改进。特别是,当因适应证导致混杂的风险可能很高时,应纳入详细的临床数据。