Department of Pharmacy, Affiliated Jinhua Hospital, Zhejiang University School of Medicine, Jinhua, China.
Department of Pharmacy, The Third Hospital of Changsha, Changsha, China.
J Cardiovasc Pharmacol Ther. 2024 Jan-Dec;29:10742484241265337. doi: 10.1177/10742484241265337. Epub 2024 Jul 21.
The efficacy and safety of a lower target dose of sacubitril/valsartan (angiotensin receptor neprilysin inhibitor [ARNI]) for treating heart failure with reduced ejection fraction (HFrEF) in Chinese patients with moderate-to-severe chronic kidney disease (CKD) remain unknown. We performed a retrospective study to compare the efficacy of ARNI with that of angiotensin-converting enzyme inhibitors (ACEIs)/angiotensin receptor blockers (ARBs) in patients with HFrEF and moderate-to-severe CKD. This retrospective study included 129 patients. An inverse probability of treatment weighting (IPTW) analysis was performed to compare the baseline characteristics and outcomes between the 2 groups. The incidence of death due to cardiovascular disease, rehospitalization due to heart failure after treatment, and improvement in cardiac function symptoms (New York Heart Association [NYHA]) were assessed after 12 months. Improvements of ejection fraction (EF), N-terminal pro-brain natriuretic peptide (NT-proBNP) level, left ventricular end-systolic diameter (LVESD), and left ventricular end-diastolic diameter (LVEDD) were compared. Compared with the ACEI/ARB group, the ARNI group, with 90.77% (59/65) in the lower target dose group, showed a lower rate of death due to cardiovascular disease (6.6% vs 0.9% after IPTW) and a lower incidence of rehospitalization (46.5% vs 30.4% after IPTW). NYHA class, estimated glomerular filtration rate, EF, NT-ProBNP levels, LVEDD, and LVESD improved in the ARNI group. None of the patients withdrew from treatment because of adverse drug reactions. Our study showed that ARNI resulted in a greater improvement in heart failure than ACEIs/ARBs in patients with HFrEF and moderate-to-severe CKD.
沙库巴曲缬沙坦(血管紧张素受体脑啡肽酶抑制剂[ARNI])在射血分数降低的心力衰竭(HFrEF)合并中重度慢性肾脏病(CKD)的中国患者中的低目标剂量的疗效和安全性尚不清楚。我们进行了一项回顾性研究,比较了 ARNI 与血管紧张素转换酶抑制剂(ACEI)/血管紧张素受体阻滞剂(ARB)在 HFrEF 合并中重度 CKD 患者中的疗效。
这项回顾性研究纳入了 129 例患者。采用逆概率治疗加权(IPTW)分析比较了两组患者的基线特征和结局。治疗 12 个月后,评估心血管疾病死亡、心力衰竭再住院以及心功能症状(纽约心脏协会[NYHA])改善的发生率。比较射血分数(EF)、N 末端脑钠肽前体(NT-proBNP)水平、左心室收缩末期直径(LVESD)和左心室舒张末期直径(LVEDD)的改善情况。
与 ACEI/ARB 组相比,ARNI 组(低目标剂量组 90.77%,59/65)心血管疾病死亡率较低(IPTW 后分别为 6.6%和 0.9%),再住院率较低(IPTW 后分别为 46.5%和 30.4%)。ARNI 组 NYHA 分级、估算肾小球滤过率、EF、NT-proBNP 水平、LVEDD 和 LVESD 均有所改善。无患者因不良反应而退出治疗。
我们的研究表明,在 HFrEF 合并中重度 CKD 患者中,ARNI 比 ACEI/ARB 更能改善心力衰竭。