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英国初级保健中罗格列酮安全性警告后噻唑烷二酮处方改变及其影响因素。

Changes and predictors for change to thiazolidinedione prescribing in UK primary care following the rosiglitazone safety warning.

机构信息

Grimsdyke House, London, UK.

出版信息

Int J Clin Pract. 2011 May;65(5):586-91. doi: 10.1111/j.1742-1241.2011.02648.x.

Abstract

OBJECTIVE

To investigate switching from thiazolidinediones, and predictors for switching treatment, after publication of a meta-analysis reporting an increased risk of myocardial infarction associated with rosiglitazone use.

RESEARCH DESIGN AND METHODS

Using the Health Information Network (THIN) UK primary care database, the number of people with type 2 diabetes prescribed either thiazolidinedione, rosiglitazone (n = 10,062) or pioglitazone (n = 4454), and the rate of switching from thiazolidinediones (n = 3301 and 1106, respectively), were computed for each month, May 2006 to January 2008. The probability of switching post-publication, May 2007 to January 2008, was modelled by logistic regression in a forward stepwise model. Variables included demographics, history of ischaemic heart disease (IHD), heart failure (HF) or stroke, risk factors for IHD, glucose-lowering and cardiovascular drug use, HbA(1c) and diabetes duration.

RESULTS

There was a sharp increase in switching from both thiazolidinediones in summer 2007; rosiglitazone prescription numbers then decreased while pioglitazone prescribing increased. Switching from rosiglitazone was associated with IHD [adjusted odds ratio (OR) 1.72; 95% confidence intervals (CI) 1.47-2.00], insulin treatment (OR 5.10; 95% CI 3.21-8.10), HF (OR 2.26; 95% CI 1.62-3.18), a recent sulphonylurea prescription (OR 1.33; 95% CI 1.17-1.51) gender (OR men vs. women 0.79; 95% CI 0.70, 0.90) and duration of therapy. Switching from pioglitazone was associated with HF (OR 3.05; 95% CI 1.77-5.26), duration of therapy, and number of glucose-lowering treatments.

CONCLUSIONS

Prescribing habits for both thiazolidinediones changed immediately following the safety warning. IHD was associated with switching from rosiglitazone; otherwise reasons for change appear to be complex, not directly related to the findings of the meta-analysis.

摘要

目的

在发表荟萃分析报告罗格列酮使用与心肌梗死风险增加后,研究噻唑烷二酮类药物的转换及其转换治疗的预测因素。

研究设计和方法

使用英国健康信息网(THIN)初级保健数据库,计算了 2006 年 5 月至 2008 年 1 月期间,分别接受噻唑烷二酮类、罗格列酮(n = 10062)或吡格列酮(n = 4454)治疗的 2 型糖尿病患者人数(n = 3301 和 1106),以及噻唑烷二酮类药物的转换率(分别为每月和每月)。2007 年 5 月至 2008 年 1 月期间,使用向前逐步模型的逻辑回归对发布后的转换概率进行建模。变量包括人口统计学、缺血性心脏病(IHD)、心力衰竭(HF)或中风病史、IHD 危险因素、降血糖和心血管药物使用、HbA1c 和糖尿病病程。

结果

2007 年夏季,两种噻唑烷二酮类药物的转换率均急剧上升;罗格列酮的处方数量随后下降,而吡格列酮的处方数量增加。与罗格列酮转换相关的因素包括 IHD[调整后的优势比(OR)1.72;95%置信区间(CI)1.47-2.00]、胰岛素治疗(OR 5.10;95%CI 3.21-8.10)、HF(OR 2.26;95%CI 1.62-3.18)、最近使用磺脲类药物(OR 1.33;95%CI 1.17-1.51)、性别(OR 男性与女性 0.79;95%CI 0.70,0.90)和治疗持续时间。与吡格列酮转换相关的因素包括 HF(OR 3.05;95%CI 1.77-5.26)、治疗持续时间和降血糖治疗次数。

结论

安全性警告发布后,两种噻唑烷二酮类药物的处方习惯立即发生变化。IHD 与罗格列酮的转换有关;否则,转换的原因似乎很复杂,与荟萃分析的结果没有直接关系。

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