3rd Department of Internal Medicine, 1st Faculty of Medicine, Charles University, Prague, Czech Republic.
Tyumen State Medical University, Tyumen, Russian Federation.
Cardiovasc Diabetol. 2022 Oct 8;21(1):203. doi: 10.1186/s12933-022-01631-4.
Guidelines from 2016 onwards recommend early use of SGLT2i or GLP-1 RA for patients with type 2 diabetes (T2D) and cardiovascular disease (CVD), to reduce CV events and mortality. Many eligible patients are not treated accordingly, although data are lacking for Central and Eastern Europe (CEE).
The CORDIALLY non-interventional study evaluated the real-world characteristics, modern antidiabetic treatment patterns, and the prevalence of CVD and chronic kidney disease (CKD) in adults with T2D at nonhospital-based practices in CEE. Data were retrospectively collated by medical chart review for patients initiating empagliflozin, another SGLT2i, DPP4i, or GLP-1 RA in autumn 2018. All data were analysed cross-sectionally, except for discontinuations assessed 1 year ± 2 months after initiation.
Patients (N = 4055) were enrolled by diabetologists (56.7%), endocrinologists (40.7%), or cardiologists (2.5%). Empagliflozin (48.5%) was the most prescribed medication among SGLT2i, DPP4i, and GLP-1 RA; > 3 times more patients were prescribed empagliflozin than other SGLT2i (10 times more by cardiologists). Overall, 36.6% of patients had diagnosed CVD. Despite guidelines recommending SGLT2i or GLP-1 RA, 26.8% of patients with CVD received DPP4i. Patients initiating DPP4i were older (mean 66.4 years) than with SGLT2i (62.4 years) or GLP-1 RA (58.3 years). CKD prevalence differed by physician assessment (14.5%) or based on eGFR and UACR (27.9%). Many patients with CKD (≥ 41%) received DPP4i, despite guidelines recommending SGLT2is owing to their renal benefits. 1 year ± 2-months after initiation, 10.0% (7.9-12.3%) of patients had discontinued study medication: 23.7-45.0% due to 'financial burden of co-payment', 0-1.9% due to adverse events (no patients discontinued DPP4i due to adverse events). Treatment guidelines were 'highly relevant' for a greater proportion of cardiologists (79.4%) and endocrinologists (72.9%) than diabetologists (56.9%), and ≤ 20% of physicians consulted other physicians when choosing and discontinuing treatments.
In CORDIALLY, significant proportions of patients with T2D and CVD/CKD who initiated modern antidiabetic medication in CEE in autumn 2018 were not treated with cardioprotective T2D medications. Use of DPP4i instead of SGLT2i or GLP-1 RA may be related to lack of affordable access, the perceived safety of these medications, lack of adherence to the latest treatment guidelines, and lack of collaboration between physicians. Thus, many patients with T2D and comorbidities may develop preventable complications or die prematurely. Trial registration NCT03807440.
自 2016 年以来,指南建议将 SGLT2i 或 GLP-1RA 早期用于 2 型糖尿病(T2D)和心血管疾病(CVD)患者,以降低 CV 事件和死亡率。许多符合条件的患者未得到相应治疗,尽管中东欧(CEE)缺乏相关数据。
CORDIALLY 是一项非干预性研究,评估了在 CEE 非医院实践中 T2D 成年患者的真实特征、现代抗糖尿病治疗模式以及 CVD 和慢性肾病(CKD)的流行情况。在 2018 年秋季,通过医疗记录回顾性收集开始使用恩格列净、另一种 SGLT2i、DPP4i 或 GLP-1RA 的患者的数据。除了在起始后 1 年±2 个月评估的停药情况外,所有数据均进行横断面分析。
共纳入 4055 名患者,由糖尿病专家(56.7%)、内分泌专家(40.7%)或心脏病专家(2.5%)进行治疗。在 SGLT2i、DPP4i 和 GLP-1RA 中,恩格列净(48.5%)是最常开的药物;与其他 SGLT2i 相比,开恩格列净的患者多(心脏病专家开恩格列净的患者多 10 倍)。总体而言,36.6%的患者患有 CVD。尽管指南建议使用 SGLT2i 或 GLP-1RA,但 26.8%的 CVD 患者接受了 DPP4i。起始 DPP4i 的患者年龄较大(平均 66.4 岁),高于 SGLT2i(62.4 岁)或 GLP-1RA(58.3 岁)。基于医生评估(14.5%)或 eGFR 和 UACR(27.9%),CKD 的患病率存在差异。尽管指南建议使用 SGLT2i,因为其具有肾脏益处,但仍有许多 CKD(≥41%)患者接受 DPP4i。起始后 1 年±2 个月,有 10.0%(7.9-12.3%)的患者停止使用研究药物:23.7-45.0%因“共付费用的经济负担”,0-1.9%因不良反应(无患者因不良反应而停用 DPP4i)。对于更大比例的心脏病专家(79.4%)和内分泌专家(72.9%),治疗指南“非常相关”,而对于糖尿病专家(56.9%),则比例较低,且只有≤20%的医生在选择和停止治疗时会咨询其他医生。
在 CORDIALLY 中,2018 年秋季在 CEE 开始使用现代抗糖尿病药物的 T2D 和 CVD/CKD 患者中,相当一部分患者未接受心脏保护 T2D 药物治疗。使用 DPP4i 而非 SGLT2i 或 GLP-1RA 可能与缺乏负担得起的药物有关,这些药物的安全性被认为较高,对最新治疗指南的依从性较低,以及医生之间缺乏合作。因此,许多患有 T2D 和合并症的患者可能会出现可预防的并发症或过早死亡。试验注册 NCT03807440。