Tandon Tanya, Dubey Ashok K, Srivastava Saurabh, Manocha Sachin, Arora Ekta, Hasan Nazer
Department of Pharmacology, SMSR, Sharda University, NCR, Greater Noida, Uttar Pradesh, India.
Department of Medicine, SMSR, Sharda University, NCR, Greater Noida, Uttar Pradesh, India.
J Family Med Prim Care. 2019 Mar;8(3):955-959. doi: 10.4103/jfmpc.jfmpc_22_19.
With the available evidence of early combined oral drug therapies being more effective in lowering blood glucose levels than maximal doses of a single drug, many clinicians are taking the aggressive approach of adding a sulfonylurea or a dipeptidyl peptidase-4 (DPP-4) inhibitor to metformin as the initial therapy in type 2 diabetes mellitus (T2DM). Pharmacotherapy for a chronic disease like diabetes has substantial economic implications for patients especially in a developing country like India. So it is important to scientifically evaluate the cost-effectiveness of these commonly practiced combination therapies in the management of T2DM.
This was a prospective observational randomized comparative study conducted over 8 weeks on patients of T2DM who were prescribed either of the two therapies of metformin (500 mg) plus glimepiride (1 mg) or metformin (500 mg) plus teneligliptin (20 mg). Cost-effectiveness analysis was done by calculating the expense incurred on 0.1% reduction in HbA1 c and 1 mg/dl reduction in fasting plasma glucose (FPG)/post-prandial plasma glucose (PPG) levels after 8 weeks and compared for both the groups. The same was also evaluated for differences in BMI levels.
The cost-effectiveness for per unit reduction in HbA1c and FPG was significant in metformin plus glimepiride group as compared to the metformin plus teneligliptin group though it was comparable for both the groups for per unit PPG reduction. There was no significant change in BMI levels between the groups.
Compared to metformin plus teneligliptin, metformin plus glimepiride is a significantly cost-effective therapy when used as an initial combination therapy in patients of T2DM in lowering HbA1c and FPG.
有证据表明,早期联合口服药物疗法在降低血糖水平方面比单一药物的最大剂量更有效,许多临床医生采取积极的方法,在2型糖尿病(T2DM)的初始治疗中,将磺脲类药物或二肽基肽酶-4(DPP-4)抑制剂添加到二甲双胍中。像糖尿病这样的慢性病的药物治疗对患者有重大的经济影响,尤其是在像印度这样的发展中国家。因此,科学评估这些常用联合疗法在T2DM管理中的成本效益非常重要。
这是一项前瞻性观察性随机对照研究,对T2DM患者进行了为期8周的研究,这些患者被处方了二甲双胍(500毫克)加格列美脲(1毫克)或二甲双胍(500毫克)加替格列汀(20毫克)这两种疗法中的一种。通过计算8周后糖化血红蛋白(HbA1c)降低0.1%以及空腹血糖(FPG)/餐后血糖(PPG)水平降低1毫克/分升所产生的费用,进行成本效益分析,并对两组进行比较。还对两组的体重指数(BMI)水平差异进行了评估。
与二甲双胍加替格列汀组相比,二甲双胍加格列美脲组每降低单位HbA1c和FPG的成本效益显著,尽管两组每降低单位PPG的成本效益相当。两组之间的BMI水平没有显著变化。
与二甲双胍加替格列汀相比,二甲双胍加格列美脲作为T2DM患者的初始联合疗法,在降低HbA1c和FPG方面具有显著的成本效益。