Griffin Matthew, Riello Ralph, Rao Veena S, Ivey-Miranda Juan, Fleming James, Maulion Christopher, McCallum Wendy, Sarnak Mark, Collins Sean, Inzucchi Silvio E, Testani Jeffrey M
Section of Cardiovascular Medicine, Yale University School of Medicine, 135 College Street, Suite 230, New Haven, CT, 06520, USA.
Department of Pharmacy Services, Yale-New Haven Hospital, New Haven, CT, USA.
ESC Heart Fail. 2020 Aug;7(4):1966-1971. doi: 10.1002/ehf2.12759. Epub 2020 May 31.
Diuretic resistance is common in acute decompensated heart failure (ADHF). When loop diuretic monotherapy is ineffective, thiazides are often recommended as adjunctive therapy, but these agents have many side effects and are associated with worsened survival. In contrast, sodium glucose cotransporter 2 inhibitors (SGLT-2i's), initially developed as glucose-lowering medications for type 2 diabetes, improve heart failure outcomes. A candidate contributory mechanism for this benefit is their diuretic effects. We sought to describe the safety and efficacy of SGLT-2i's as loop diuretic adjuvants in ADHF.
We retrospectively analysed patients who received adjuvant SGLT-2i therapy between August 2016 and June 2018 at Yale-New Haven Hospital. Thirty-one patients comprised the cohort, 58% of whom had type 2 diabetes. Compared with the 24 h prior to SGLT-2i initiation, average weight loss improved (1.0 ± 2.2 kg, P = 0.03 at Day 1; 1.7 ± 4.9 kg, P = 0.08 at Day 2; and 2.1 ± 5.6 kg, P = 0.06 at Day 3), as did urine output (3.7 ± 2.0 L, P = 0.002 at Day 1; 3.4 ± 1.7 L, P = 0.02 at Day 2; and 3.1 ± 1.7 L, P = 0.02 at Day 3) while loop diuretic dosing remaining stable. Creatinine remained unchanged during the 3 days after initiation, as did blood pressure and the incidence of hypokalaemia (P = NS for all).
In this cohort of patients with ADHF, SGLT-2i's improved weight loss, urine output, and diuretic efficiency without worsening of creatinine, potassium, or blood pressure. Further study of SGLT-2i's as a loop diuretic adjuvant is warranted.
利尿剂抵抗在急性失代偿性心力衰竭(ADHF)中很常见。当襻利尿剂单药治疗无效时,噻嗪类药物常被推荐作为辅助治疗,但这些药物有许多副作用且与生存率降低有关。相比之下,钠-葡萄糖协同转运蛋白2抑制剂(SGLT-2i)最初是作为2型糖尿病的降糖药物开发的,可改善心力衰竭的预后。这种益处的一个可能的促成机制是它们的利尿作用。我们试图描述SGLT-2i作为ADHF中襻利尿剂辅助药物的安全性和有效性。
我们回顾性分析了2016年8月至2018年6月在耶鲁-纽黑文医院接受SGLT-2i辅助治疗的患者。该队列包括31名患者,其中58%患有2型糖尿病。与开始使用SGLT-2i前的24小时相比,平均体重减轻有所改善(第1天为1.0±2.2kg,P = 0.03;第2天为1.7±4.9kg,P = 0.08;第3天为2.1±5.6kg,P = 0.06),尿量也有所改善(第1天为3.7±2.0L,P = 0.002;第2天为3.4±1.7L,P = 0.02;第3天为3.1±1.7L,P = 0.02),而襻利尿剂的剂量保持稳定。开始使用后的3天内,肌酐、血压和低钾血症的发生率均保持不变(所有P值均无统计学意义)。
在这个ADHF患者队列中,SGLT-2i改善了体重减轻、尿量和利尿效率,而肌酐、血钾或血压并未恶化。有必要进一步研究SGLT-2i作为襻利尿剂辅助药物的作用。