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磺酰脲类药物作为 2 型糖尿病的初始治疗与严重低血糖风险。

Sulfonylureas as Initial Treatment for Type 2 Diabetes and the Risk of Severe Hypoglycemia.

机构信息

Centre for Clinical Epidemiology, Lady Davis Institute, Jewish General Hospital, Montreal, Canada; Division of Endocrinology, Jewish General Hospital, Montreal, Canada.

Centre for Clinical Epidemiology, Lady Davis Institute, Jewish General Hospital, Montreal, Canada; Department of Epidemiology, Biostatistics, and Occupational Health, McGill University, Montreal, Canada; Gerald Bronfman Department of Oncology, McGill University, Montreal, Canada.

出版信息

Am J Med. 2018 Mar;131(3):317.e11-317.e22. doi: 10.1016/j.amjmed.2017.09.044. Epub 2017 Oct 12.

Abstract

PURPOSE

The magnitude of the risk of severe hypoglycemia associated with sulfonylureas as the initial treatment for type 2 diabetes in the real-world setting is unknown. We assessed the risk of severe hypoglycemia associated with initiating monotherapy with sulfonylurea compared with metformin for the treatment of type 2 diabetes.

METHODS

By using the UK Clinical Practice Research Datalink and Hospital Episode Statistics linked to the Office for National Statistics, we identified a cohort of patients with type 2 diabetes who initiated sulfonylureas or metformin monotherapy between April 1, 1998, and December 31, 2012, with follow-up until December 31, 2013. Sulfonylurea users were matched one-to-one to metformin users by high-dimensional propensity scores. Hazard ratios (HRs) and 95% confidence intervals (CIs) of severe hypoglycemia, defined as requiring hospitalization, were estimated using Cox proportional hazards models comparing sulfonylureas with metformin monotherapy.

RESULTS

The study cohort consisted of 14,012 initiators of sulfonylureas matched to 14,012 initiators of metformin. The mean treated follow-up time was 1.41 (standard deviation, 1.84) years. Use of sulfonylurea was associated with an elevated incidence of severe hypoglycemia compared with metformin as the initiating monotherapy for type 2 diabetes (incidence rate, 2.4/1000 person-years; 95% CI, 1.90-2.90; HR, 4.53; 95% CI, 2.76-7.45).

CONCLUSIONS

Sulfonylureas, when prescribed as the initiating monotherapy for the treatment of type 2 diabetes, is associated with a 4.5-fold increase in the risk of severe hypoglycemia. Given the negative consequences of this outcome, clinicians should consider alternative hypoglycemic agents when metformin is not tolerated or contraindicated.

摘要

目的

在真实环境中,磺酰脲类药物作为 2 型糖尿病初始治疗药物时,严重低血糖相关风险的严重程度尚不清楚。我们评估了与起始使用二甲双胍相比,起始使用磺酰脲类药物单药治疗 2 型糖尿病时严重低血糖的风险。

方法

通过使用英国临床实践研究数据链接和与国家统计局链接的医院入院统计数据,我们确定了一组在 1998 年 4 月 1 日至 2012 年 12 月 31 日期间起始使用磺酰脲类药物或二甲双胍单药治疗的 2 型糖尿病患者队列,并随访至 2013 年 12 月 31 日。通过高维倾向评分对磺酰脲类药物使用者与二甲双胍使用者进行一对一匹配。使用 Cox 比例风险模型比较磺酰脲类药物与二甲双胍单药治疗,估计严重低血糖(定义为需要住院治疗)的风险比(HR)和 95%置信区间(CI)。

结果

研究队列包括 14012 名起始使用磺酰脲类药物的患者和 14012 名起始使用二甲双胍的患者。平均治疗随访时间为 1.41 年(标准差为 1.84 年)。与起始使用二甲双胍作为 2 型糖尿病的单药治疗相比,起始使用磺酰脲类药物与严重低血糖的发生率升高相关(发生率,2.4/1000 人年;95%CI,1.90-2.90;HR,4.53;95%CI,2.76-7.45)。

结论

当磺酰脲类药物被开处方作为 2 型糖尿病的起始单药治疗药物时,严重低血糖的风险增加 4.5 倍。鉴于这种结果的负面影响,当不能耐受或禁忌使用二甲双胍时,临床医生应考虑其他降血糖药物。

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