CC BY-NC-ND 4.0 · Exp Clin Endocrinol Diabetes 2021; 129(09): 666-673
DOI: 10.1055/a-0899-5118
Article

Effectiveness of Insulin Degludec in Thai Patients with Diabetes Mellitus: Real-World Evidence From a Specialized Diabetes Center

Yotsapon Thewjitcharoen
Diabetes and Thyroid Center, Theptarin Hospital, Bangkok, Thailand
,
Nalin Yenseung
Diabetes and Thyroid Center, Theptarin Hospital, Bangkok, Thailand
,
Areeya Malidaeng
Diabetes and Thyroid Center, Theptarin Hospital, Bangkok, Thailand
,
Siriwan Butadej
Diabetes and Thyroid Center, Theptarin Hospital, Bangkok, Thailand
,
Phawinpon Chotwanvirat
Diabetes and Thyroid Center, Theptarin Hospital, Bangkok, Thailand
,
Sirinate Krittiyawong
Diabetes and Thyroid Center, Theptarin Hospital, Bangkok, Thailand
,
Chattip Thammawiwat
Diabetes and Thyroid Center, Theptarin Hospital, Bangkok, Thailand
,
Thep Himathongkam
Diabetes and Thyroid Center, Theptarin Hospital, Bangkok, Thailand
› Author Affiliations
Funding: This work was supported by the grant for promoting research in Theptarin Hospital (Grant No. 1/2560). The funders had no role in the manuscript writing, editing, approval, or decision to publish.

Abstract

Background Insulin degludec, an ultra-long-acting insulin analogue, has been available in Thailand since October 2016. Although clinical trial results revealed less hypoglycemia, data from real-world settings is limited especially in Asian patients. This study aimed to evaluate prospectively the real-world effectiveness, safety, quality of life (QOL) and patient satisfaction with insulin degludec among Thai patients with diabetes mellitus (DM).

Methods From October 2016 to September 2017, all patients who had started insulin degludec for at least 3 months were observed and evaluated at baseline, 3, 6, and 12 months. QOL was assessed using WHOQOL-BREF-THAI and level of satisfaction was measured by 7-point Likert scale. Glycemic fluctuation from paired iPro2 continuous glucose monitoring (CGM) obtained 4–6 weeks apart were also evaluated from a subset of patients with T1DM who switched from insulin glargine to insulin degludec.

Results A total of 55 patients (T2DM 76.4%, females 54.5%, mean age 57.1±16.1 years, duration of diabetes 16.7±8.8 years, BMI 27.3±5.5 kg/m2, baseline A1C 9.3±2.3%, median duration of treatment 8 months) were included in the study. In T1DM patients (n=13), the overall mean A1C reduction at 12 months was 0.5% with minimal weight gain of 0.9 kgs at 12 months. In T2DM patients (n=42), the overall mean A1C reduction at 12 months was 0.8% with minimal weight loss of 0.4 kgs at 12 months. The proportion of T1DM patients who could achieve optimal glycemic control increased slightly from 14.3 to 18.2% but the proportion of T2DM patients who could achieve optimal glycemic control increased from 30.8 to 53.8%. Patient satisfaction showed a sustained improvement throughout the duration of study. In four T1DM patients who had paired CGM data, insulin degludec provided greater reductions in glycemic variability endpoints with increased time-in-range when compared with previous insulin glargine.

Discussion Our data suggested that the effectiveness of insulin degludec was consistent with the results seen in clinical trials with lower risk of patients-reported hypoglycemia, and a significant improvement in glycemic control. Patients also reported higher treatment satisfaction. More long-term and cost-effectiveness data are needed to establish the role of this ultra-long-acting insulin in real-world settings.



Publication History

Received: 02 March 2019
Received: 12 April 2019

Accepted: 24 April 2019

Article published online:
09 October 2019

© 2019. The Author(s). This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonDerivative-NonCommercial-License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commercial purposes, or adapted, remixed, transformed or built upon. (https://creativecommons.org/licenses/by-nc-nd/4.0/).

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