Bánfi-Bacsárdi Fanni, Forrai Zsolt, Kazay Ádám, Füzesi Tamás, Vámos Máté, Gergely Tamás G, Pilecky Dávid, Komáromi Anna, Szőnyi Mihály Dániel, Papp Emese, Solymossi Balázs, Baksa Veronika, Andréka Péter, Piróth Zsolt, Nyolczas Noémi, Muk Balázs
Department of Adult Cardiology, Gottsegen National Cardiovascular Center, Budapest, Hungary.
Doctoral School of Clinical Medicine, University of Szeged, Szeged, Hungary.
Cardiology. 2024 Dec 21:1-11. doi: 10.1159/000543070.
The 2023 Focused Update of the 2021 ESC Heart Failure (HF) Guidelines recommends the rapid up-titration (RT) of guideline-directed medical therapy (GDMT) for all patients hospitalised for HF to improve prognosis in light of the STRONG-HF trial. However, the real-world feasibility of RT and the optimal selection of suitable patients may cause difficulties as the STRONG-HF trial applied strict randomisation criteria. We aimed to assess the proportion of hospitalised HF patients suitable for RT after discharge.
The proportion of patients eligible for RT based on the basic inclusion and exclusion criteria of the STRONG-HF trial (systolic blood pressure [SBP] ≥100 mm Hg, heart rate [HR] ≥60 min-1, serum potassium ≤5 mmol/L, estimated glomerular filtration rate [eGFR] ≥30 mL/min/1.73 m2, discharge N-terminal pro-B type natriuretic peptide [NT-proBNP] >1,500 pg/mL) was assessed in a consecutive patient cohort at a tertiary referral centre between April 01, 2021, and December 31, 2023.
Data from 408 consecutive patients were analysed (male: 71%; age: 62 [51-72] years; left ventricular ejection fraction: 27 [20-35]%; HF with reduced ejection fraction: 82%; hypertension: 67%; diabetes: 36%; atrial fibrillation: 47%). 78% of the patients were suitable for RT based on the SBP criterion, 93% on HR, 89% on serum potassium, and 91% on eGFR values. Thus, 60% were eligible for RT using the combined assessment of these parameters. When including the NT-proBNP value as well (60%), 34% of the cohort were eligible for RT.
Based on our study, the proportion of patients suitable for RT of GDMT ranged from 34% to 60% based on the basic eligibility indicators of the STRONG-HF trial. Our results highlight the strategic importance of careful selection of patients eligible for RT.
2023年对2021年欧洲心脏病学会(ESC)心力衰竭(HF)指南的重点更新建议,鉴于STRONG-HF试验,对所有因HF住院的患者迅速上调指南指导的药物治疗(GDMT)以改善预后。然而,由于STRONG-HF试验采用了严格的随机化标准,上调治疗的现实可行性以及合适患者的最佳选择可能会带来困难。我们旨在评估出院后适合上调治疗的住院HF患者比例。
在一家三级转诊中心,对2021年4月1日至2023年12月31日期间连续的患者队列进行评估,根据STRONG-HF试验的基本纳入和排除标准(收缩压[SBP]≥100 mmHg、心率[HR]≥60次/分钟、血清钾≤5 mmol/L、估算肾小球滤过率[eGFR]≥30 mL/min/1.73 m²、出院时N末端B型利钠肽原[NT-proBNP]>1500 pg/mL)确定适合上调治疗的患者比例。
分析了408例连续患者的数据(男性:71%;年龄:62[51 - 72]岁;左心室射血分数:27[20 - 35]%;射血分数降低的HF:82%;高血压:67%;糖尿病:36%;心房颤动:47%)。基于SBP标准,78%的患者适合上调治疗;基于HR标准,93%适合;基于血清钾标准,89%适合;基于eGFR值,91%适合。因此,综合评估这些参数时,60%的患者适合上调治疗。若同时纳入NT-proBNP值(60%),则该队列中有34%的患者适合上调治疗。
根据我们的研究,基于STRONG-HF试验的基本合格指标,适合GDMT上调治疗的患者比例在34%至60%之间。我们的结果凸显了谨慎选择适合上调治疗患者的战略重要性。