Steno Diabetes Center Copenhagen, Gentofte, Denmark; Department of Endocrinology, Copenhagen University Hospital, Bispebjerg-Frederiksberg Hospital, Copenhagen, Denmark.
Steno Diabetes Center Copenhagen, Gentofte, Denmark.
Lancet Healthy Longev. 2021 Sep;2(9):e561-e570. doi: 10.1016/S2666-7568(21)00170-7. Epub 2021 Aug 13.
Discontinuation of diabetes medication in the last years of life has been suggested to improve quality of life while deemed safe to implement. However, the extent, patterns, and secular changes in discontinuation of glucose-lowering medication in older people with type 2 diabetes have been scarcely described. We therefore aimed to describe the trends in the use of glucose-lowering medication during the last 10 years of life of older people and explore how key clinical and socioeconomic covariates are associated with these patterns.
In this register-based cohort study, all individuals with type 2 diabetes who died aged 80 years or older between Jan 1, 2006, and Dec 31, 2018, were identified through the Danish Diabetes Register and linked to the Danish National Prescription Registry. We followed the population backwards in time from death to date of last medication intake. To estimate the cumulative proportion of people on glucose-lowering medication, a Poisson regression model for the rate of medication as a function of time before death (0 to 10 years before death) and calendar year of death (2006-18) was fitted. Both single-substance and combination glucose-lowering medications were included and categorised as insulins, sulfonylureas, metformin, DPP-4 inhibitors, GLP-1 analogues, SGLT2 inhibitors, acarbose, and thiazolidinediones. Insulin was further subdivided into four groups: fast-acting, intermediate-acting, long-acting, and mixed insulin. To identify which covariates were associated with discontinuation, estimates were adjusted for sex, age at death, diabetes duration at time of death, the total number of diabetes complications at time of death (from no complications to four or more), level of education, immigrant status, and income quartile.
52 523 individuals (28 746 [54·7%] females and 23 777 [45·3%] males) were identified, with a mean age at type 2 diabetes diagnosis of 77 years (SD 8), median age at death of 86 years (IQR 83-90), and median diabetes duration at death of 9 years (IQR 5-14). We found a considerable discontinuation of glucose-lowering medication during the last 10 years of life, with the proportion of people on glucose-lowering medication starting at between 89% (95% CI 87-91) in 2006 and 87% (86-88) in 2018 at 10 years before death and decreasing to between 52% (50-54) in 2006 and 38% (37-39) in 2018 at the time of death. Specifically, we found that the proportion of people on sulfonylureas, at any time before death, decreased substantially from 2006 to 2018, whereas the proportion on metformin and DPP-4 inhibitors increased with calendar year of death. Changes were less pronounced for the remaining medications. The overall discontinuation patterns changed with increasing calendar year of death, such that discontinuation rates increased and occurred earlier (further away from time of death) with increasing calendar year. Discontinuations were generally more pronounced during the last year of life. Proportions of people on medication and patterns of discontinuation, as well as the association with covariates, varied with medication class. Covariates most frequently associated with changes in discontinuation rates were sex, age at death, type 2 diabetes duration at death, and number of complications. For example, females were less likely to receive metformin than males at all years before death (rate ratio 0·91 (95% CI 0·89-0·94, p<0·0001), and there was a negative association between the proportion of individuals on metformin and increasing age at death (rate ratio per year increase 0·96 [0·96-0·96], p<0·0001) and type 2 diabetes duration (0·95 per year increase [0·94-0·95], p<0·0001).
Our results suggest that increased focus on and implementation of discontinuation of glucose-lowering medication in recent years might have had an effect on discontinuation patterns, particularly during the last year of life.
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在生命的最后几年停止使用糖尿病药物已被建议可以提高生活质量,同时被认为实施起来是安全的。然而,老年人中 2 型糖尿病患者停止使用降血糖药物的程度、模式和长期变化很少被描述。因此,我们旨在描述老年人生命最后 10 年期间使用降血糖药物的趋势,并探讨关键的临床和社会经济因素与这些模式的关系。
在这项基于登记的队列研究中,通过丹麦糖尿病登记处和丹麦全国处方登记处,确定了在 2006 年 1 月 1 日至 2018 年 12 月 31 日期间,年龄在 80 岁或以上并死于 80 岁或以上的所有 2 型糖尿病患者。我们从死亡日期向前回溯,按照距末次药物摄入时间的 0 到 10 年和死亡年份(2006-18 年),对人群进行时间追踪。将所有单一药物和联合降糖药物(胰岛素、磺酰脲类、二甲双胍、DPP-4 抑制剂、GLP-1 类似物、SGLT2 抑制剂、阿卡波糖和噻唑烷二酮类)均包括在内,并分为胰岛素、磺酰脲类、二甲双胍、DPP-4 抑制剂、GLP-1 类似物、SGLT2 抑制剂、阿卡波糖和噻唑烷二酮类。胰岛素进一步分为四类:速效、中效、长效和混合胰岛素。为了确定哪些协变量与停药相关,对估计值进行了调整,以调整性别、死亡时的年龄、死亡时的糖尿病病程、死亡时的糖尿病并发症总数(从无并发症到四个或更多)、受教育程度、移民身份和收入四分位数。
共纳入 52523 名患者(28746 名女性[54.7%]和 23777 名男性[45.3%]),2 型糖尿病诊断时的平均年龄为 77 岁(标准差 8),死亡时的中位年龄为 86 岁(IQR 83-90),死亡时的中位糖尿病病程为 9 年(IQR 5-14)。我们发现,在生命的最后 10 年中,降糖药物的使用有相当大的停药率,在死亡前 10 年,2006 年的比例为 89%(95%CI 87-91),2018 年为 87%(86-88),而在死亡时,比例分别为 52%(50-54)和 38%(37-39)。具体而言,我们发现,磺酰脲类药物的使用比例在任何时候都从 2006 年到 2018 年显著下降,而二甲双胍和 DPP-4 抑制剂的使用比例随着死亡年份的增加而增加。其余药物的变化则不太明显。总体停药模式随着日历年份的增加而变化,随着日历年份的增加,停药率增加,且发生得更早(离死亡时间越远)。在生命的最后一年,停药情况更为明显。药物的使用比例和停药模式以及与协变量的关系因药物类别而异。与停药率变化最常相关的协变量是性别、死亡时的年龄、死亡时的 2 型糖尿病病程和并发症的数量。例如,女性在所有死亡前年份接受二甲双胍治疗的可能性均低于男性(率比 0.91(95%CI 0.89-0.94,p<0.0001),而且随着死亡时年龄的增加,接受二甲双胍治疗的个体比例呈负相关(每年增加 0.96[0.96-0.96],p<0.0001),2 型糖尿病病程也呈负相关(每年增加 0.95[0.94-0.95],p<0.0001)。
我们的结果表明,近年来对停止使用降血糖药物的重视和实施可能对停药模式产生了影响,尤其是在生命的最后一年。
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