Polavarapu Nareen Krishna, Kale Ravindra, Sethi Bipin, Sahay R K, Phadke Uday, Ramakrishnan Santosh, Mane Amey, Mehta Suyog, Shah Snehal
Dr. Reddy's Laboratories Ltd, 7-1-27, Ameerpet, Hyderabad, Telangana, 500016, India.
CARE Hospitals, Hyderabad, Telangana, India.
Drugs Real World Outcomes. 2020 Dec;7(4):271-279. doi: 10.1007/s40801-020-00206-7.
The efficacy of gliclazide has been reported in clinical trials in India. However, real-world data on the effectiveness of gliclazide in India is unavailable.
To provide real-world evidence regarding the effectiveness of gliclazide or gliclazide + metformin fixed-dose combination or separate medications, used either as monotherapy or as the latest add-on to other antihyperglycemic agents in reducing glycated hemoglobin (HbA1c) levels in Indian patients with type 2 diabetes mellitus (T2DM).
Electronic medical record data of adult patients who were diagnosed with T2DM who were newly initiated on or had been prescribed gliclazide or gliclazide + metformin combination for < 30 days as monotherapy or as add-on therapy to other antihyperglycemic agents, and had HbA1c ≥ 6.5% were retrospectively analyzed. Mean change in HbA1c from baseline was the primary endpoint. Secondary endpoints were assessment of dosages and formulations of gliclazide or gliclazide + metformin prescribed in the HbA1c spectrum and antihyperglycemic agents to which gliclazide or gliclazide + metformin was added as an adjunct. Readings were obtained before initiating gliclazide or gliclazide + metformin and after at least 90 days of treatment with gliclazide or gliclazide + metformin.
Included patients (n = 498) were categorized into gliclazide only (n = 66), gliclazide + metformin only (n = 179), gliclazide add-on (n = 169), and gliclazide + metformin add-on (n = 84) groups. Mean (95% confidence interval [CI]) change in HbA1c among patients with baseline HbA1c > 7% was - 0.8% (- 1.26, - 0.34) in gliclazide only group; - 1.6% (- 1.89, - 1.31; p < 0.001) in gliclazide + metformin group; - 1.2% (- 1.50, - 0.90; p < 0.001) in add-on gliclazide group; and - 1.4% (- 1.75, - 1.05; p < 0.001) in add-on gliclazide + metformin group. Gliclazide once daily was the most prescribed regimen in the gliclazide only group (72.7%), with 60 mg being the most prescribed modified-release dose (62.5%). Gliclazide + metformin twice daily was the most prescribed regimen in the gliclazide + metformin group (69.3%) with 80 mg + 500 mg being the most prescribed immediate-release dose (62.9%). Gliclazide and gliclazide + metformin were most added as an adjunct to existing prescriptions of biguanides (83.4%) or insulin (64.3%), respectively.
Gliclazide or gliclazide + metformin prescribed as mono- or add-on therapy during routine clinical practice effectively reduced HbA1c in Indian patients with T2DM, thus validating the use of gliclazide and gliclazide + metformin for managing T2DM in India.
在印度的临床试验中已报道了格列齐特的疗效。然而,关于格列齐特在印度有效性的真实世界数据尚不可得。
提供关于格列齐特或格列齐特+二甲双胍固定剂量复方制剂或单独用药,作为单药治疗或作为其他降糖药物的最新添加药物,在降低印度2型糖尿病(T2DM)患者糖化血红蛋白(HbA1c)水平方面有效性的真实世界证据。
回顾性分析成年T2DM患者的电子病历数据,这些患者新开始使用或已被处方格列齐特或格列齐特+二甲双胍复方制剂不足30天,作为单药治疗或作为其他降糖药物的添加治疗,且HbA1c≥6.5%。HbA1c相对于基线的平均变化是主要终点。次要终点是评估在HbA1c谱中处方的格列齐特或格列齐特+二甲双胍的剂量和剂型,以及格列齐特或格列齐特+二甲双胍作为辅助添加到的降糖药物。在开始使用格列齐特或格列齐特+二甲双胍之前以及使用格列齐特或格列齐特+二甲双胍治疗至少90天后获取读数。
纳入患者(n = 498)被分为仅使用格列齐特组(n = 66)、仅使用格列齐特+二甲双胍组(n = 179)、格列齐特添加组(n = 169)和格列齐特+二甲双胍添加组(n = 84)。基线HbA1c>7%的患者中,仅使用格列齐特组HbA1c的平均(95%置信区间[CI])变化为-0.8%(-1.26,-0.34);格列齐特+二甲双胍组为-1.6%(-1.89,-1.31;p<0.001);格列齐特添加组为-1.2%(-1.50,-0.90;p<0.001);格列齐特+二甲双胍添加组为-1.4%(-1.75,-1.05;p<0.001)。在仅使用格列齐特组中,每日一次格列齐特是最常处方的方案(72.7%),其中60mg是最常处方的缓释剂量(62.5%)。在格列齐特+二甲双胍组中,每日两次格列齐特+二甲双胍是最常处方的方案(69.3%),其中80mg + 500mg是最常处方的速释剂量(62.9%)。格列齐特和格列齐特+二甲双胍分别最常作为辅助添加到现有双胍类药物(83.4%)或胰岛素(64.3%)的处方中。
在常规临床实践中作为单药或添加治疗处方的格列齐特或格列齐特+二甲双胍有效降低了印度T2DM患者的HbA1c,从而验证了格列齐特和格列齐特+二甲双胍在印度用于管理T2DM的有效性。