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血糖管理的悖论:患有糖尿病的成年人的多种合并症、血糖控制和高风险药物使用。

Paradox of glycemic management: multimorbidity, glycemic control, and high-risk medication use among adults with diabetes.

机构信息

Division of Community Internal Medicine, Department of Medicine, Mayo Clinic, Rochester, Minnesota, USA

Division of Health Care Policy & Research, Department of Health Sciences Research, Mayo Clinic, Rochester, Minnesota, USA.

出版信息

BMJ Open Diabetes Res Care. 2020 Feb;8(1). doi: 10.1136/bmjdrc-2019-001007.

Abstract

INTRODUCTION

Glycemic targets and glucose-lowering regimens should be individualized based on multiple factors, including the presence of comorbidities. We examined contemporary patterns of glycemic control and use of medications known to cause hypoglycemia among adults with diabetes across age and multimorbidity.

RESEARCH DESIGN AND METHODS

We retrospectively examined glycosylated hemoglobin (HbA) levels and rates of insulin/sulfonylurea use as a function of age and multimorbidity using administrative claims and laboratory data for adults with type 2 diabetes included in OptumLabs Data Warehouse, 1 January 2014 to 31 December 2016. Comorbidity burden was assessed by counts of any of 16 comorbidities specified by guidelines as warranting relaxation of HbA targets, classified as being diabetes concordant (diabetes complications or risk factors), discordant (unrelated to diabetes), or advanced (life limiting).

RESULTS

Among 194 157 patients with type 2 diabetes included in the study, 45.2% had only concordant comorbidities, 30.6% concordant and discordant, 2.7% only discordant, and 13.0% had ≥1 advanced comorbidity. Mean HbA was 7.7% among 18-44 year-olds versus 6.9% among ≥75 year-olds, and was higher among patients with comorbidities: 7.3% with concordant only, 7.1% with discordant only, 7.1% with concordant and discordant, and 7.0% with advanced comorbidities compared with 7.4% among patients without comorbidities. The odds of insulin use decreased with age (OR 0.51 (95% CI 0.48 to 0.54) for age ≥75 vs 18-44 years) but increased with accumulation of concordant (OR 5.50 (95% CI 5.22 to 5.79) for ≥3 vs none), discordant (OR 1.72 (95% CI 1.60 to 1.86) for ≥3 vs none), and advanced (OR 1.45 (95% CI 1.25 to 1.68) for ≥2 vs none) comorbidities. Conversely, sulfonylurea use increased with age (OR 1.36 (95% CI 1.29 to 1.44) for age ≥75 vs 18-44 years) but decreased with accumulation of concordant (OR 0.76 (95% CI 0.73 to 0.79) for ≥3 vs none), discordant (OR 0.70 (95% CI 0.64 to 0.76) for ≥3 vs none), but not advanced (OR 0.86 (95% CI 0.74 to 1.01) for ≥2 vs none) comorbidities.

CONCLUSIONS

The proportion of patients achieving low HbA levels was highest among older and multimorbid patients. Older patients and patients with higher comorbidity burden were more likely to be treated with insulin to achieve these HbA levels despite potential for hypoglycemia and uncertain long-term benefit.

摘要

简介

血糖目标和降糖方案应根据多种因素进行个体化,包括合并症的存在。我们研究了在年龄和多种合并症的情况下,糖尿病患者的血糖控制和使用已知会导致低血糖的药物的当代模式。

研究设计和方法

我们使用 OptumLabs Data Warehouse 中的行政索赔和实验室数据,回顾性地检查了 2014 年 1 月 1 日至 2016 年 12 月 31 日期间,2 型糖尿病患者的糖化血红蛋白(HbA)水平和胰岛素/磺脲类药物使用率与年龄和多种合并症的关系。通过指南规定的 16 种合并症中任何一种的数量来评估合并症负担,这些合并症被认为需要放宽 HbA 目标,分为与糖尿病一致(糖尿病并发症或危险因素)、不一致(与糖尿病无关)或晚期(危及生命)。

结果

在纳入研究的 194157 名 2 型糖尿病患者中,45.2%仅有与糖尿病一致的合并症,30.6%既有与糖尿病一致的合并症也有不一致的合并症,2.7%仅有与糖尿病不一致的合并症,13.0%有≥1 种晚期合并症。18-44 岁患者的平均 HbA 为 7.7%,≥75 岁患者的平均 HbA 为 6.9%,合并症患者的 HbA 更高:仅有与糖尿病一致的合并症患者为 7.3%,仅有与糖尿病不一致的合并症患者为 7.1%,既有与糖尿病一致的合并症也有与糖尿病不一致的合并症患者为 7.1%,有≥1 种晚期合并症患者为 7.0%,而无合并症患者为 7.4%。胰岛素使用率随年龄增加而降低(年龄≥75 岁与 18-44 岁相比,OR 0.51(95%CI 0.48-0.54)),但随与糖尿病一致(≥3 与无相比,OR 5.50(95%CI 5.22-5.79))、不一致(≥3 与无相比,OR 1.72(95%CI 1.60-1.86))和晚期(≥2 与无相比,OR 1.45(95%CI 1.25-1.68))合并症的积累而增加。相反,磺脲类药物使用率随年龄增加而增加(年龄≥75 岁与 18-44 岁相比,OR 1.36(95%CI 1.29-1.44)),但随与糖尿病一致(≥3 与无相比,OR 0.76(95%CI 0.73-0.79))、不一致(≥3 与无相比,OR 0.70(95%CI 0.64-0.76))合并症的积累而减少,但不随晚期(≥2 与无相比,OR 0.86(95%CI 0.74-1.01))合并症而减少。

结论

在年龄较大和合并症较多的患者中,达到低 HbA 水平的患者比例最高。尽管可能会发生低血糖和不确定的长期获益,但年龄较大的患者和合并症负担较高的患者更有可能使用胰岛素来达到这些 HbA 水平。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cdf9/7039576/0087b77dfe8c/bmjdrc-2019-001007f01.jpg

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