Grup de Recerca Epidemiològica en Diabetis des de l'Atenció Primària (DAP-CAT) Group, Unitat de Suport a la Recerca Barcelona, Fundació Institut Universitari per a la recerca a l'Atenció Primària de Salut Jordi Gol i Gurina (IDIAPJGol), Barcelona, Spain.
Clinical Trials Unit, Germans Trias i Pujol Health Science Research Institute (IGTP), Barcelona, Spain.
Front Endocrinol (Lausanne). 2021 Jul 14;12:708372. doi: 10.3389/fendo.2021.708372. eCollection 2021.
The aims of our study was compare adherence measured by the medical possession ratio (MPR), time until discontinuation and describe adverse events after adding a DPP-4i, SGLT-2i, or sulfonylureas (SU) to metformin in a primary care population with insufficient glycemic control. We used routinely-collected health data from the SIDIAP database. The included subjects were matched by propensity score. The follow-up period was up to 24 months or premature discontinuation. The primary outcomes were the percentage of subjects with good adherence, treatment discontinuation and adverse events among treatment groups. The proportion of patients with good adherence (MPR> 0.8) after the addition of DPP-4i, SGLT-2i or SU was 53.6%, 68.7%, and 43.0%, respectively. SGLT-2i users were 1.7 times more likely to achieve good adherence compared with DPP-4i users (odds ratio [OR]:1.72, 98% confidence interval [CI]:1.51, 1.96), and 2.8 times more likely compared with SU users (OR: 0.35, 98% CI: 0.07, 0.29). The discontinuation hazard ratios were 1.43 (98%CI: 1.26; 1.62) and 1.60 (98%CI: 1.42; 1.81) times higher among SGLT-2i and SU users than DPP-4i users during the follow-up period. No differences were observed for adverse events among the treatment groups. In conclusion, in our real-world setting, the combination of SGLT-2i with metformin was associated with better adherence. The mean time until discontinuation was longer in the SGLT-2i group in comparison with the DPP-4i or SU groups.
我们的研究目的是比较在初级保健人群中,加用二肽基肽酶-4 抑制剂(DPP-4i)、钠-葡萄糖协同转运蛋白 2 抑制剂(SGLT-2i)或磺酰脲类药物(SU)后,通过医疗用药比例(MPR)衡量的药物依从性、停药时间,并描述不良事件。我们使用了来自 SIDIAP 数据库的常规收集的健康数据。通过倾向评分对纳入的研究对象进行匹配。随访期最长为 24 个月或提前停药。主要结局为各组中治疗依从性良好、停药和不良事件的患者比例。加用 DPP-4i、SGLT-2i 或 SU 后,依从性良好(MPR>0.8)的患者比例分别为 53.6%、68.7%和 43.0%。与 DPP-4i 相比,SGLT-2i 使用者更有可能达到良好的依从性(优势比 [OR]:1.72,98%置信区间 [CI]:1.51,1.96),与 SU 相比,更有可能达到良好的依从性(OR:0.35,98%CI:0.07,0.29)。在随访期间,SGLT-2i 和 SU 使用者的停药风险比分别为 1.43(98%CI:1.26;1.62)和 1.60(98%CI:1.42;1.81)倍,高于 DPP-4i 使用者。各组之间不良事件无差异。总之,在我们的真实环境中,与 DPP-4i 相比,SGLT-2i 联合二甲双胍可提高患者的治疗依从性。与 DPP-4i 或 SU 组相比,SGLT-2i 组的平均停药时间更长。