Hussin Siti Aisyah, Mohamad Nur Aimi, Othman Mohd Khairi, Wan Mohamed Wan Mohd Izani
Department of Internal Medicine, School of Medical Sciences, Universiti Sains Malaysia, Kelantan, Malaysia.
Department of Pharmacy, Hospital Universiti Sains Malaysia, Kelantan, Malaysia.
Malays J Med Sci. 2024 Apr;31(2):159-169. doi: 10.21315/mjms2024.31.2.14. Epub 2024 Apr 23.
Achieving good glycaemic control is essential to reducing the risk of diabetes complications. Insulin is the most effective therapy for achieving good glycaemic control; however, it is associated with a higher risk of hypoglycaemia, especially with human insulin. This study aimed to evaluate the efficacy of intensification from human to analogue insulin and its added cost.
This retrospective study was conducted at the Hospital Universiti Sains Malaysia (HUSM). Patients with type 2 diabetes mellitus (T2DM) who underwent intensification for at least 3 months from human to analogue insulin were included in this study. The patients' medical records, haemoglobin A1c (Hba1c) and fasting blood sugar (FBS) were retrieved. The total cost pre- and post-intensification of insulin was obtained from the pharmacy database. Differences in HbA1c, FBS and total insulin cost pre- and post-intensification were analysed.
A total of 163 patients with T2DM who had intensification from human to analogue insulin were included in this study. HbA1c and FBS levels were significantly lower in analogue insulin. However, the differences were not clinically significant, as the mean reduction in HbA1c was less than 0.5%. Meanwhile, the total costs of analogue insulin for 3 months were higher.
There were no clinically significant improvements in patients' HbA1c and FBS after the intensification of insulin, despite the extra costs spent. Hence, it is vital to choose the right group of patients to receive an insulin analogue to maximise its benefit but at the most optimal cost.
实现良好的血糖控制对于降低糖尿病并发症风险至关重要。胰岛素是实现良好血糖控制最有效的疗法;然而,它与低血糖风险较高相关,尤其是人胰岛素。本研究旨在评估从人胰岛素强化为类似物胰岛素的疗效及其额外成本。
本回顾性研究在马来西亚理科大学医院(HUSM)进行。纳入了从人胰岛素强化为类似物胰岛素至少3个月的2型糖尿病(T2DM)患者。检索患者的病历、糖化血红蛋白(Hba1c)和空腹血糖(FBS)。从药房数据库获取胰岛素强化前后的总成本。分析强化前后HbA1c、FBS和胰岛素总成本的差异。
本研究共纳入163例从人胰岛素强化为类似物胰岛素的T2DM患者。类似物胰岛素组的HbA1c和FBS水平显著更低。然而,差异无临床意义,因为HbA1c的平均降幅小于0.5%。同时,3个月类似物胰岛素的总成本更高。
尽管增加了成本,但胰岛素强化后患者的HbA1c和FBS并无临床显著改善。因此,选择合适的患者群体接受胰岛素类似物以最大化其益处同时达到最优成本至关重要。