仿制药达格列净的真实证据:来自印度多中心回顾性研究的相关性和结果

B. Sethi, S. Kalra, S. Bhattacharya, Anand Kumar, Madhukar Rai, Manoj Srivastava, Srinath A, Ajay Budhwar, Savita Jain, Harish Rastogi, P. Gandhi, G. Vijay Kumar, Joe Georje, M. Abhyankar, A. Prasad, Prashant Sarda
{"title":"仿制药达格列净的真实证据:来自印度多中心回顾性研究的相关性和结果","authors":"B. Sethi, S. Kalra, S. Bhattacharya, Anand Kumar, Madhukar Rai, Manoj Srivastava, Srinath A, Ajay Budhwar, Savita Jain, Harish Rastogi, P. Gandhi, G. Vijay Kumar, Joe Georje, M. Abhyankar, A. Prasad, Prashant Sarda","doi":"10.4103/jod.jod_133_21","DOIUrl":null,"url":null,"abstract":"Objective: The objective was to evaluate the clinical experience and treatment patterns of generic dapagliflozin usage in different patient profiles in Indian settings. Materials and Methods: A retrospective, multicentric, real-world study included patients with type 2 diabetes mellitus (T2DM) (aged >18 years), inadequately controlled by existing antidiabetic therapy and receiving generic dapagliflozin as an add-on to existing oral antidiabetic drug(s) with or without insulin or switch therapy. Baseline characteristics and treatment-related outcomes were retrieved from the medical records and analyzed. Results: A total of 1935 patients were included, of which 1279 (66.1%) were males. The mean age was 57.4 years, and around half of the patients (51.4%) were aged from 45 to 60 years. Hypertension (55.9%) and dyslipidemia (19.8%) were the common comorbidities. The majority (n = 1122; 60%) of patients received dapagliflozin in combination with one or two antihyperglycemic drugs. More than half of the patients received metformin (56.8%) or sulfonylurea (52.3%) in combination with dapagliflozin. A dose of 10 mg (93.4%) was the most commonly used dose of dapagliflozin. The mean levels of glycated hemoglobin, fasting plasma glucose, and postprandial plasma glucose were significantly reduced to 1.1% (1.0–1.1), 30.5 mg/dL (29.2–31.9), and 57.5 mg/dL (55.1–59.9), respectively, after the initiation of dapagliflozin. A total of 1935 patients experienced weight changes during the treatment, of which 90.5% of patients showed weight loss. Hypoglycemic events were reported in 12.5% of patients. Physician global evaluation of efficacy and tolerability showed a majority of patients on a good-to-excellent scale (97.3% and 97.1%). Conclusion: Generic dapagliflozin showed a significant improvement in glycemic parameters and reduced body weight with low hypoglycemic events. The administration of dapagliflozin provided a good-to-excellent efficacy and tolerability profile in patients with T2DM. To the best of our knowledge, this is the first study confirming the efficacy, safety, and usefulness of generic dapagliflozin in patients with T2DM.","PeriodicalId":15627,"journal":{"name":"Journal of Diabetology","volume":"32 1","pages":"242 - 248"},"PeriodicalIF":0.0000,"publicationDate":"2022-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Real-world evidence of generic dapagliflozin: Relevance and results from Indian multicenter retrospective study\",\"authors\":\"B. Sethi, S. Kalra, S. Bhattacharya, Anand Kumar, Madhukar Rai, Manoj Srivastava, Srinath A, Ajay Budhwar, Savita Jain, Harish Rastogi, P. Gandhi, G. Vijay Kumar, Joe Georje, M. Abhyankar, A. Prasad, Prashant Sarda\",\"doi\":\"10.4103/jod.jod_133_21\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Objective: The objective was to evaluate the clinical experience and treatment patterns of generic dapagliflozin usage in different patient profiles in Indian settings. Materials and Methods: A retrospective, multicentric, real-world study included patients with type 2 diabetes mellitus (T2DM) (aged >18 years), inadequately controlled by existing antidiabetic therapy and receiving generic dapagliflozin as an add-on to existing oral antidiabetic drug(s) with or without insulin or switch therapy. Baseline characteristics and treatment-related outcomes were retrieved from the medical records and analyzed. Results: A total of 1935 patients were included, of which 1279 (66.1%) were males. The mean age was 57.4 years, and around half of the patients (51.4%) were aged from 45 to 60 years. Hypertension (55.9%) and dyslipidemia (19.8%) were the common comorbidities. The majority (n = 1122; 60%) of patients received dapagliflozin in combination with one or two antihyperglycemic drugs. More than half of the patients received metformin (56.8%) or sulfonylurea (52.3%) in combination with dapagliflozin. A dose of 10 mg (93.4%) was the most commonly used dose of dapagliflozin. The mean levels of glycated hemoglobin, fasting plasma glucose, and postprandial plasma glucose were significantly reduced to 1.1% (1.0–1.1), 30.5 mg/dL (29.2–31.9), and 57.5 mg/dL (55.1–59.9), respectively, after the initiation of dapagliflozin. A total of 1935 patients experienced weight changes during the treatment, of which 90.5% of patients showed weight loss. Hypoglycemic events were reported in 12.5% of patients. Physician global evaluation of efficacy and tolerability showed a majority of patients on a good-to-excellent scale (97.3% and 97.1%). Conclusion: Generic dapagliflozin showed a significant improvement in glycemic parameters and reduced body weight with low hypoglycemic events. The administration of dapagliflozin provided a good-to-excellent efficacy and tolerability profile in patients with T2DM. To the best of our knowledge, this is the first study confirming the efficacy, safety, and usefulness of generic dapagliflozin in patients with T2DM.\",\"PeriodicalId\":15627,\"journal\":{\"name\":\"Journal of Diabetology\",\"volume\":\"32 1\",\"pages\":\"242 - 248\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2022-07-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Diabetology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.4103/jod.jod_133_21\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Diabetology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.4103/jod.jod_133_21","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

摘要

目的:目的是评估印度不同患者使用通用达格列净的临床经验和治疗模式。材料和方法:一项回顾性、多中心、真实世界的研究纳入了2型糖尿病(T2DM)患者(年龄>18岁),现有降糖药控制不充分,在现有口服降糖药的基础上加用或不加胰岛素或转换治疗的通用达格列清。从医疗记录中检索基线特征和治疗相关结果并进行分析。结果:共纳入1935例患者,其中男性1279例,占66.1%。平均年龄为57.4岁,约一半(51.4%)患者年龄在45 - 60岁之间。高血压(55.9%)和血脂异常(19.8%)是常见的合并症。大多数(n = 1122;60%)的患者使用达格列净联合一种或两种降糖药物。超过一半的患者接受二甲双胍(56.8%)或磺脲类(52.3%)联合达格列净治疗。10 mg(93.4%)是最常用的达格列净剂量。开始服用达格列净后,糖化血红蛋白、空腹血糖和餐后血糖的平均水平分别显著降低至1.1%(1.0-1.1)、30.5 mg/dL(29.2-31.9)和57.5 mg/dL(55.1-59.9)。在治疗过程中,共有1935例患者出现体重变化,其中90.5%的患者出现体重下降。12.5%的患者报告了低血糖事件。医生对疗效和耐受性的整体评估显示,大多数患者的评分为良好至优秀(97.3%和97.1%)。结论:仿制药达格列净能显著改善血糖参数,降低体重并伴有低血糖事件。在T2DM患者中应用达格列净具有良好到极好的疗效和耐受性。据我们所知,这是第一个证实仿制药达格列净对2型糖尿病患者的有效性、安全性和实用性的研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Real-world evidence of generic dapagliflozin: Relevance and results from Indian multicenter retrospective study
Objective: The objective was to evaluate the clinical experience and treatment patterns of generic dapagliflozin usage in different patient profiles in Indian settings. Materials and Methods: A retrospective, multicentric, real-world study included patients with type 2 diabetes mellitus (T2DM) (aged >18 years), inadequately controlled by existing antidiabetic therapy and receiving generic dapagliflozin as an add-on to existing oral antidiabetic drug(s) with or without insulin or switch therapy. Baseline characteristics and treatment-related outcomes were retrieved from the medical records and analyzed. Results: A total of 1935 patients were included, of which 1279 (66.1%) were males. The mean age was 57.4 years, and around half of the patients (51.4%) were aged from 45 to 60 years. Hypertension (55.9%) and dyslipidemia (19.8%) were the common comorbidities. The majority (n = 1122; 60%) of patients received dapagliflozin in combination with one or two antihyperglycemic drugs. More than half of the patients received metformin (56.8%) or sulfonylurea (52.3%) in combination with dapagliflozin. A dose of 10 mg (93.4%) was the most commonly used dose of dapagliflozin. The mean levels of glycated hemoglobin, fasting plasma glucose, and postprandial plasma glucose were significantly reduced to 1.1% (1.0–1.1), 30.5 mg/dL (29.2–31.9), and 57.5 mg/dL (55.1–59.9), respectively, after the initiation of dapagliflozin. A total of 1935 patients experienced weight changes during the treatment, of which 90.5% of patients showed weight loss. Hypoglycemic events were reported in 12.5% of patients. Physician global evaluation of efficacy and tolerability showed a majority of patients on a good-to-excellent scale (97.3% and 97.1%). Conclusion: Generic dapagliflozin showed a significant improvement in glycemic parameters and reduced body weight with low hypoglycemic events. The administration of dapagliflozin provided a good-to-excellent efficacy and tolerability profile in patients with T2DM. To the best of our knowledge, this is the first study confirming the efficacy, safety, and usefulness of generic dapagliflozin in patients with T2DM.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信