Puspitasari Arina D, Kusuma Hayu, Ratri Dinda M N, Wibisono Cahyo, Suprapti Budi
Universitas Airlangga Hospital Surabaya, Surabaya, Indonesia.
Clinical Pharmacy Department, Faculty of Pharmacy, Universitas Airlangga, Surabaya, Indonesia.
J Basic Clin Physiol Pharmacol. 2020 Jan 11;30(6):/j/jbcpp.2019.30.issue-6/jbcpp-2019-0342/jbcpp-2019-0342.xml. doi: 10.1515/jbcpp-2019-0342.
Background One of the therapies used to treat type 2 diabetes mellitus (T2DM) disease is combination insulin which consists of rapid-acting insulin and intermediate-acting insulin (premixed). This study aimed to examine the profile of premixed insulin related to blood glucose concentration and to identify the drug interactions due to the combination of premixed insulin with other drugs taken by T2DM patients. Methods This study was a prospective observational study with cross-sectional data that were analyzed descriptively. The respondents invited were T2DM patients with or without complication or comorbid disease who received premixed insulin with or without a combination of oral antidiabetic therapy in the Outpatient Unit of Universitas Airlangga Hospital, Surabaya. The research instruments used are data sheet, patient medical record, and fasting and postprandial blood glucose concentration. Results A total of 118 patients received premixed insulin therapy, but only 80 patients were included in the inclusion criteria. Based on types of insulin, the combination of 30% aspart and 70% protamine aspart was used by 91.25% T2DM patients, and a combination of 25% insulin lispro and 75% protamine lispro was used by 8.75% T2DM patients. There were 30.3% of patients who could achieve the target of 80-130 mg/dL in fasting blood glucose concentrations, and 35.1% of patients achieved the target of ≤180 mg/dL in postprandial blood glucose concentration. Drug interactions may occur in patients who use premixed insulin with glimepiride, lisinopril, fenofibrate, candesartan, irbesartan, and gemfibrozil. Conclusions In this study, premixed insulin have not reached the target of fasting and postprandial blood glucose concentrations in most patients.
背景 用于治疗2型糖尿病(T2DM)的疗法之一是复方胰岛素,它由速效胰岛素和中效胰岛素(预混)组成。本研究旨在探讨预混胰岛素与血糖浓度相关的情况,并确定T2DM患者使用预混胰岛素与其他药物联合时的药物相互作用。方法 本研究是一项前瞻性观察性研究,采用横断面数据进行描述性分析。邀请的受访者是在泗水的艾尔朗加大学医院门诊接受预混胰岛素治疗且有或无并发症或合并症的T2DM患者,无论是否联合口服降糖治疗。所使用的研究工具包括数据表、患者病历以及空腹和餐后血糖浓度。结果 共有118名患者接受了预混胰岛素治疗,但只有80名患者符合纳入标准。基于胰岛素类型,91.25%的T2DM患者使用30%门冬胰岛素和70%精蛋白锌门冬胰岛素的组合,8.75%的T2DM患者使用25%赖脯胰岛素和75%精蛋白锌赖脯胰岛素的组合。30.3%的患者空腹血糖浓度能达到80 - 130 mg/dL的目标,35.1%的患者餐后血糖浓度能达到≤180 mg/dL的目标。使用预混胰岛素与格列美脲、赖诺普利、非诺贝特、坎地沙坦、厄贝沙坦和吉非罗齐联合的患者可能会发生药物相互作用。结论 在本研究中,大多数患者使用预混胰岛素未达到空腹和餐后血糖浓度的目标。