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在临床实践中每日两次使用艾塞那肽或胰岛素:CHOICE 的结果。

Using Exenatide Twice Daily or Insulin in Clinical Practice: Results from CHOICE.

机构信息

Department of Endocrinology, UZ Gasthuisberg, 3000, Leuven, Belgium,

出版信息

Diabetes Ther. 2013 Dec;4(2):285-308. doi: 10.1007/s13300-013-0037-8. Epub 2013 Sep 10.

Abstract

INTRODUCTION

CHOICE (CHanges to treatment and Outcomes in patients with type 2 diabetes initiating InjeCtablE therapy; NCT00635492) assessed, as its primary objective, the time to a 'significant treatment change' (defined within this paper) after patients with type 2 diabetes mellitus initiated their first injectable, glucose-lowering therapy [exenatide twice daily (BID) or insulin] in clinical practice in six European countries and evaluated outcomes during the study.

METHODS

CHOICE was a 24-month, prospective, noninterventional observational study. Patients were invited to participate in CHOICE only after their treating physician had made the clinical decision to initiate first injectable therapy with either exenatide BID or insulin. Clinical data were collected at initiation of first injectable therapy and after approximately 3, 6, 12, 18, and 24 months.

RESULTS

A total of 2,515 patients were recruited; 1,114 patients in the exenatide BID cohort and 1,274 patients in the insulin cohort were eligible for the 24-month analysis. During the study, 42.2% and 36.0% of patients from each cohort, respectively, had a significant treatment change. By 24 months, improved mean glycated hemoglobin (p < 0.001 for both cohorts) and reduced severity of several cardiovascular risk factors were observed in both cohorts; additionally, mean weight was reduced in the exenatide BID cohort (p < 0.001) and increased in the insulin cohort (p < 0.001). Hypoglycemia was reported by 18.4% of the exenatide BID cohort and 36.8% of the insulin cohort; 25.9% of the exenatide BID cohort and 10.0% of the insulin cohort had met the secondary endpoint of glycated hemoglobin <7.0%, no weight gain, and no hypoglycemia.

CONCLUSION

CHOICE provided data on exenatide BID and insulin usage patterns and 24-month outcomes in clinical practice. On average, improved glycemic control and reduced severity of cardiovascular risk factors were observed in both cohorts, and those in the exenatide BID cohort also had mean weight loss.

摘要

简介

CHOICE(治疗选择和 2 型糖尿病患者起始注射治疗的结局变化;NCT00635492)评估了 2 型糖尿病患者起始首次注射降糖治疗(包括每日两次艾塞那肽或胰岛素)后的“治疗显著改变”时间(本文中定义),观察 6 个欧洲国家的临床实践情况,并评估了研究期间的结局。

方法

CHOICE 是一项 24 个月的前瞻性、非干预性观察研究。只有当患者的治疗医生决定起始首次注射用艾塞那肽或胰岛素时,才会邀请患者参加 CHOICE。在起始首次注射治疗时以及大约 3、6、12、18 和 24 个月时收集临床数据。

结果

共招募了 2515 例患者;其中,1114 例患者进入每日两次艾塞那肽组,1274 例患者进入胰岛素组,这两个队列均有 42.2%和 36.0%的患者在 24 个月时有显著的治疗改变。在研究期间,两个队列的患者的平均糖化血红蛋白均得到改善(均 p<0.001),且几种心血管风险因素的严重程度降低;此外,每日两次艾塞那肽组的平均体重降低(p<0.001),胰岛素组的平均体重增加(p<0.001)。每日两次艾塞那肽组有 18.4%的患者和胰岛素组有 36.8%的患者报告低血糖;每日两次艾塞那肽组有 25.9%的患者和胰岛素组有 10.0%的患者达到了次要终点,即糖化血红蛋白<7.0%、无体重增加且无低血糖。

结论

CHOICE 提供了关于每日两次艾塞那肽和胰岛素的使用模式以及 24 个月临床实践结局的数据。平均而言,两个队列的血糖控制均得到改善,心血管风险因素的严重程度降低,每日两次艾塞那肽组的患者平均体重减轻。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/706c/3889314/2b6a90665a0a/13300_2013_37_Fig1_HTML.jpg

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