Real-world Safety and Effectiveness of Insulin Glargine 300 U/mL in Participants with Type 2 Diabetes Mellitus During the Period of Ramadan in Four Countries (Egypt, Jordan, Lebanon, and Turkey): A Prospective Observational Study
- 作者: Hassanein M.1, Shaltout I.2, Malek R.3, Assaad Khalil S.4, Ballout H.5, Annabi F.6, Shereen M.7
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隶属关系:
- Dubai Hospital, Dubai Health Authority, Dubai, United Arab Emirates
- Internal Medicine Department, Cairo University, Cairo, Egypt
- Internal Medicine Department, CHU Mohamed Saadna Abdennour, Se´tif, Algeria
- Department of Internal Medicine, Unit of Diabetes, Lipidology & Metabolism, Alexandria Faculty of Medicine, Alexandria, Egypt
- Private Clinic, Al Rassoul Al Aazam Hospital, Beirut, Lebanon
- Private Clinic, Islamic Hospital, Amman, Jordan
- Department of Medical Affairs, Sanofi, Cairo, Egypt
- 期: 卷 20, 编号 5 (2024)
- 栏目: Medicine
- URL: https://snv63.ru/1573-3998/article/view/643003
- DOI: https://doi.org/10.2174/1573399820666230811152520
- ID: 643003
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Aim:This non-interventional observational study aimed to describe the clinical outcomes of patients with T2DM treated with Gla-300 during the period of Ramadan.
Background:Type 2 diabetes mellitus (T2DM) patients who decide to fast during the holy month of Ramadan face several challenges in achieving glycemic control without increasing the risk of hypoglycemia. Insulin glargine-300 (Gla-300) has well-established safety and efficacy in improving glycemic control in multiple randomized clinical trials (RCTs). However, limited evidence is available regarding its safety and effectiveness during fasting.
Objective:The objective of this study was to assess the safety and clinical outcomes of insulin glargine-300 (Gla-300) in T2DM patients before, during, and after Ramadan.
Methods:We conducted a prospective, observational, non-comparative, multicenter study on patients with T2DM currently treated with Gla-300 who planned to fast and continue on Gla-300 during Ramadan in four countries (Egypt, Jordan, Lebanon, and Turkey). The study outcomes included the change in glycemic parameters and incidence of hypoglycemia before, during, and after Ramadan.
Results:One hundred and forty T2DM patients were included. Nearly 61% of the included patients had a duration of diabetes op <00 years. The mean Gla-300 daily doses during the pre-Ramadan, Ramadan, and post-Ramadan periods were 22.2 ±7.4, 20.4 ±7.5, and 22.5 ±4.7 IU, respectively. The mean change values from pre-Ramadan to Ramadan and post-Ramadan were -1.7 ±6.9 IU and 0.5 ±4.7 IU, respectively, among the included patients. The mean HbA1c decreased during the study period initiating from 7.9 ±1.4% pre-Ramadan to 6.9 ±0.4% post-Ramadan. The overall HBA1c target value was 6.9 ±0.4%, while the HbA1c target was achieved by 29 patients (21.9%). The mean fasting blood glucose (FPG) showed a reduction from baseline value in the post-Ramadan period by -0.9 ±2.3mmol/L. Five patients (3.57%) had symptomatic documented hypoglycemia during Ramadan, and none was considered to have severe hypoglycemia.
Conclusion:Our study showed that insulin Gla-300 maintained the glycemic control of T2DM patients who decided to fast during the holy month of Ramadan without increasing the risk of hypoglycemia. Regular self-monitoring of blood glucose levels during Ramadan is highly recommended to avoid possible complications.
作者简介
Mohamed Hassanein
Dubai Hospital, Dubai Health Authority, Dubai, United Arab Emirates
编辑信件的主要联系方式.
Email: info@benthamscience.net
Inass Shaltout
Internal Medicine Department, Cairo University,Cairo, Egypt
Email: info@benthamscience.net
Rachid Malek
Internal Medicine Department, CHU Mohamed Saadna Abdennour, Se´tif, Algeria
Email: info@benthamscience.net
Samir Assaad Khalil
Department ofInternal Medicine, Unit of Diabetes, Lipidology & Metabolism, Alexandria Faculty of Medicine, Alexandria, Egypt
Email: info@benthamscience.net
Hajar Ballout
Private Clinic, Al Rassoul Al Aazam Hospital, Beirut, Lebanon
Email: info@benthamscience.net
Firas Annabi
Private Clinic, Islamic Hospital, Amman, Jordan
Email: info@benthamscience.net
Mark Shereen
Department of Medical Affairs, Sanofi, Cairo, Egypt
Email: info@benthamscience.net
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