Department of Cardiology, Toyama Rosai Hospital.
Second Department of Internal Medicine, University of Toyama.
Int Heart J. 2021 Jul 30;62(4):885-890. doi: 10.1536/ihj.21-022. Epub 2021 Jul 17.
Sodium-glucose cotransporter 2 inhibitor (SGLT2i) reduces mortality and morbidity in patients with chronic heart failure (HF). However, the clinical implication of SGLT2i therapy in patients with acute decompensated HF remains uncertain. We prospectively studied 86 type 2 diabetic mellitus (T2DM) patients (71.8 ± 12.1 years, 55 men) who were hospitalized for acute decompensated HF and received SGLT2i during the index hospitalization. Among the patients, 56 continued SGLT2i at discharge and 30 did not. The continued group experienced fewer HF re-hospitalizations than the discontinued group (24% versus 39%, P = 0.008) with a hazard ratio of 0.29 (95% confidence interval 0.10-0.85) adjusted for other significant potential confounders. In conclusion, long-term SGLT2i therapy might prevent unplanned HF re-hospitalization in patients with T2DM and acute decompensated HF.
钠-葡萄糖共转运蛋白 2 抑制剂(SGLT2i)可降低慢性心力衰竭(HF)患者的死亡率和发病率。然而,SGLT2i 治疗在急性失代偿性 HF 患者中的临床意义仍不确定。我们前瞻性研究了 86 例 2 型糖尿病(T2DM)患者(71.8±12.1 岁,55 名男性),这些患者因急性失代偿性 HF 住院,并在住院期间接受了 SGLT2i 治疗。在这些患者中,56 名患者在出院时继续使用 SGLT2i,30 名患者未继续使用。继续组的 HF 再住院率低于停药组(24%比 39%,P=0.008),调整其他重要潜在混杂因素后,风险比为 0.29(95%置信区间 0.10-0.85)。总之,长期 SGLT2i 治疗可能预防 T2DM 合并急性失代偿性 HF 患者的计划外 HF 再住院。