Sicras Mainar A, Roldán Suárez C, Font Ramos B, Navarro Artieda R, Ibáñez Nolla J
Dirección de planificación, Badalona Serveis Assistencials SA, Badalona, Barcelona, España.
Rev Clin Esp (Barc). 2013 Nov;213(8):377-84. doi: 10.1016/j.rce.2013.06.003. Epub 2013 Jul 17.
There are different second line glucose lowering drugs whose efficacy, safety and economic profile have not been established in our setting. We have analyzed the clinical (diabetic treatment adherence, metabolic control, hypoglycemia and macrovascular complications) and economic (resource use and costs) consequences of the combination of metformin with dipeptidyl peptidase inhibitors (DPPIV) in patients with type 2 diabetes.
We conducted a multicenter, observational and retrospective study. Patients ≥30 years treated with metformin who initiated a second antidiabetic treatment during 2008-2009 were enrolled in the study. Two groups of patients were established: a) metformin with DPPIV and metformin with other diabetic drugs. The main measurements were comorbidity, compliance/persistence, metabolic control (glycosylated hemoglobin <7%), complications (hypoglycemia, macrovascular) and total costs. Patients were followed-up for 2 years.
A total of 2,067 patients were enrolled (mean age: 66.6 years, 53.1% male). Of these, 519 patients (25.1%) were analyzed in the metformin+DPPIV group and 1,548 patients (74.9%) in the group metformin+other antidiabetic drug. The DPPIV group patients showed better compliance (70.3 vs. 59.6%), persistence (63.4 vs. 51.0%) and metabolic control (64.3 vs. 59.6%), respectively (P<.001) compared to the other group. They also showed a lower proportion of hypoglycemia (13.9 vs. 44.3%), cardiovascular events (3.7 vs. 7.6%) and total costs (2,347 vs. € 2,682), P<.05.
Despite the limitations of the study, patients treated with metformin associated to DPPIV were more likely to show increased adherence, metabolic control and lower rates of hypoglycemia than those treated with metformin associated to other antidiabetics.
有多种二线降糖药物,但其疗效、安全性和经济学特征在我们的研究环境中尚未明确。我们分析了二甲双胍与二肽基肽酶抑制剂(DPPIV)联合使用对2型糖尿病患者的临床(糖尿病治疗依从性、代谢控制、低血糖和大血管并发症)和经济学(资源利用和成本)影响。
我们进行了一项多中心、观察性和回顾性研究。纳入2008 - 2009年期间开始接受二甲双胍治疗且开始第二种抗糖尿病治疗的30岁及以上患者。设立两组患者:a)二甲双胍联合DPPIV组和二甲双胍联合其他糖尿病药物组。主要测量指标为合并症、依从性/持续性、代谢控制(糖化血红蛋白<7%)、并发症(低血糖、大血管)和总成本。对患者进行了2年的随访。
共纳入2067例患者(平均年龄:66.6岁,53.1%为男性)。其中,519例患者(25.1%)在二甲双胍 + DPPIV组进行分析,1548例患者(74.9%)在二甲双胍 + 其他抗糖尿病药物组。与另一组相比,DPPIV组患者分别显示出更好的依从性(70.3%对59.6%)、持续性(63.4%对51.0%)和代谢控制(64.3%对59.6%)(P <.001)。他们还显示出更低的低血糖发生率(13.9%对44.3%)、心血管事件发生率(3.7%对7.6%)和总成本(2347欧元对2682欧元),P <.05。
尽管该研究存在局限性,但与二甲双胍联合其他抗糖尿病药物治疗的患者相比,接受二甲双胍联合DPPIV治疗的患者更有可能表现出依从性增加、代谢控制改善和低血糖发生率降低。