Nephrology Department, IIS-La Princesa, Hospital Universitario de la Princesa, Madrid, Spain.
RICORS2040, Madrid, Spain.
Cardiorenal Med. 2024;14(1):202-214. doi: 10.1159/000538030. Epub 2024 Apr 3.
Chronic heart failure (HF) has high rates of mortality and hospitalization in patients with advanced chronic kidney disease (aCKD). However, randomized clinical trials have systematically excluded aCKD population. We have investigated current HF therapy in patients receiving clinical care in specialized aCKD units.
The Heart And Kidney Audit (HAKA) was a cross-sectional and retrospective real-world study including outpatients with aCKD and HF from 29 Spanish centers. The objective was to evaluate how the treatment of HF in patients with aCKD complied with the recommendations of the European Society of Cardiology Guidelines for the diagnosis and treatment of HF, especially regarding the foundational drugs: renin-angiotensin system inhibitors (RASi), angiotensin receptor blocker/neprilysin inhibitors (ARNI), beta-blockers (BBs), mineralocorticoid receptor antagonists (MRAs), and sodium-glucose cotransporter-2 inhibitors (SGLT2i).
Among 5,012 aCKD patients, 532 (13%) had a diagnosis of HF. Of them, 20% had reduced ejection fraction (HFrEF), 13% mildly reduced EF (HFmrEF), and 67% preserved EF (HFpEF). Only 9.3% of patients with HFrEF were receiving quadruple therapy with RASi/ARNI, BB, MRA, and SGLT2i, but the majority were not on the maximum recommended doses. None of the patients with HFrEF and CKD G5 received quadruple therapy. Among HFmrEF patients, approximately half and two-thirds were receiving RASi and/or BB, respectively, while less than 15% received ARNI, MRA, or SGLT2i. Less than 10% of patients with HFpEF were receiving SGLT2i.
Under real-world conditions, HF in aCKD patients is sub-optimally treated. Increased awareness of current guidelines and pragmatic trials specifically enrolling these patients represent unmet medical needs.
慢性心力衰竭(HF)在合并晚期慢性肾脏病(aCKD)的患者中具有较高的死亡率和住院率。然而,随机临床试验系统地排除了 aCKD 人群。我们研究了在专门的 aCKD 单位接受临床治疗的患者中当前 HF 治疗的情况。
Heart And Kidney Audit(HAKA)是一项横断面和回顾性真实世界研究,纳入了来自 29 个西班牙中心的合并 aCKD 和 HF 的门诊患者。目的是评估治疗合并 aCKD 的 HF 患者的治疗方法如何符合欧洲心脏病学会 HF 诊断和治疗指南的建议,特别是关于基础药物:肾素-血管紧张素系统抑制剂(RASi)、血管紧张素受体阻滞剂/脑啡肽酶抑制剂(ARNI)、β受体阻滞剂(BB)、盐皮质激素受体拮抗剂(MRAs)和钠-葡萄糖协同转运蛋白 2 抑制剂(SGLT2i)。
在 5012 例 aCKD 患者中,有 532 例(13%)诊断为 HF。其中,20%为射血分数降低(HFrEF),13%为轻度射血分数降低(HFmrEF),67%为射血分数保留(HFpEF)。仅有 9.3%的 HFrEF 患者接受 RASi/ARNI、BB、MRA 和 SGLT2i 的四联治疗,但大多数患者未接受最大推荐剂量。无合并 CKD G5 的 HFrEF 患者接受四联治疗。在 HFmrEF 患者中,约一半和三分之二分别接受 RASi 和/或 BB,但不到 15%接受 ARNI、MRA 或 SGLT2i。不到 10%的 HFpEF 患者接受 SGLT2i。
在现实环境下,合并 aCKD 的 HF 患者的治疗效果不理想。提高对当前指南的认识和专门纳入这些患者的实用临床试验代表了未满足的医疗需求。