Kheirbek Raya E, Alemi Farrokh, Zargoush Manaf
District of Columbia Veterans Affairs Medical Center, 50 Irving St., NW, Washington, DC 20422, USA.
J Manag Care Pharm. 2013 Nov-Dec;19(9):740-4. doi: 10.18553/jmcp.2013.19.9.740.
The efficacy of diabetic medications among patients with multiple comorbidities is not tested in randomized clinical studies. It is important to monitor the performance of these medications after marketing approvals.
To investigate the risk of all-cause mortality associated with prescription of hypoglycemic agents.
We retrospectively examined data from 17,773 type 2 diabetic patients seen from March 2, 1998, to December 13, 2010, in 3 Veterans Administration medical centers. Severity was measured using patients' inpatient and outpatient comorbidities during the last year of visits. Severity-adjusted logistic regression was used to measure the odds ratio for mortality within the study period.
Patients' severity of illness correctly classified mortality for 89.8% of the patients (P less than 0.0001). Being younger, married, and white decreased severity adjusted risk of mortality. Exposure to the following medications increased severity adjusted risk of mortality: glyburide (odds ratio [OR] = 1.804, 95% CI from 1.518 to 2.145), glipizide (OR = 1.566, 95% CI from 1.333 to 1.839), rosiglitazone (OR = 1.805, 95% CI from 1.378 to 2.365), chlorpropamide (OR = 3.026, 95% CI from 1.096 to 8.351), insulin (OR = 2.382, 95% CI from 2.112 to 2.686). None of the other medications (metformin, acarbose, glimepiride, pioglitazone, repaglinide, troglitazone, or dipeptidyl peptidase-4) were associated with excess mortality beyond what could be expected from the patients' severity of illness or demographic characteristics. The reported excess mortality could not be explained away by use of other concurrent, nondiabetic classes of medications.
Our findings suggest chlorpropamide, glipizide, glyburide, insulin, and rosiglitazone increased severity-adjusted mortality in veterans with type 2 diabetes. A decision aid that could optimize selection of hypoglycemic medications based on patients' comorbidities might increase patients' survival.
多种合并症患者使用糖尿病药物的疗效尚未在随机临床研究中得到验证。在药物获批上市后监测其性能很重要。
调查与开具降糖药相关的全因死亡风险。
我们回顾性分析了1998年3月2日至2010年12月13日期间在3家退伍军人事务部医疗中心就诊的17773例2型糖尿病患者的数据。使用患者在最后一次就诊年份的住院和门诊合并症来衡量疾病严重程度。采用经严重程度调整的逻辑回归分析来衡量研究期间的死亡比值比。
患者的疾病严重程度正确分类了89.8%患者的死亡情况(P<0.0001)。年轻、已婚和白人可降低经严重程度调整后的死亡风险。使用以下药物会增加经严重程度调整后的死亡风险:格列本脲(比值比[OR]=1.804,95%置信区间为1.518至2.145)、格列吡嗪(OR=1.566,95%置信区间为1.333至1.839)、罗格列酮(OR=1.805,95%置信区间为1.378至2.365)、氯磺丙脲(OR=3.026,95%置信区间为1.096至8.351)、胰岛素(OR=2.382,95%置信区间为2.112至2.686)。其他药物(二甲双胍、阿卡波糖、格列美脲、吡格列酮、瑞格列奈、曲格列酮或二肽基肽酶-4)均未显示出超出患者疾病严重程度或人口统计学特征预期的额外死亡风险。所报告的额外死亡风险无法通过使用其他同时使用的非糖尿病类药物来解释。
我们的研究结果表明,氯磺丙脲、格列吡嗪、格列本脲、胰岛素和罗格列酮会增加2型糖尿病退伍军人经严重程度调整后的死亡率。一种能够根据患者合并症优化降糖药物选择的决策辅助工具可能会提高患者的生存率。