Department of Medicine, Duke University School of Medicine, Durham, North Carolina; Duke Clinical Research Institute, Durham, North Carolina.
Ahmanson-UCLA Cardiomyopathy Center, University of California, Los Angeles, Los Angeles, California.
JACC Heart Fail. 2017 Apr;5(4):305-309. doi: 10.1016/j.jchf.2016.12.018.
The aim of this study was to assess the prevalence and variation in angiotensin receptor/neprilysin inhibitor (ARNI) prescription among a real-world population with heart failure with reduced ejection fraction (HFrEF).
The U.S. Food and Drug Administration approved sacubitril/valsartan for patients with HFrEF in July 2015. Little is known about the early patterns of use of this novel therapy.
The study included patients discharged alive from hospitals in Get With the Guidelines-Heart Failure (GWTG-HF), a registry of hospitalized patients with heart failure, between July 2015 and June 2016 who had documentation of whether ARNIs were prescribed at discharge. Patient and hospital characteristics were compared among patients with HFrEF (ejection fraction ≤40%) with and without ARNI prescription at discharge, excluding those with documented contraindications to ARNIs. To evaluate hospital variation, hospitals with at least 10 eligible hospitalizations during the study period were assessed.
Of 21,078 patients hospitalized with HFrEF during the study period, 495 (2.3%) were prescribed ARNIs at discharge. Patients prescribed ARNIs were younger (median age 65 years vs. 70 years; p < 0.001), had lower ejection fractions (median 23% vs. 25%; p < 0.001), and had higher use of aldosterone antagonists (45% vs. 31%; p < 0.001) at discharge. At the 241 participating hospitals with 10 or more eligible admissions, 125 (52%) reported no discharge prescriptions of ARNIs.
Approximately 2.3% of patients hospitalized for HFrEF in a national registry were prescribed ARNI therapy in the first 12 months following Food and Drug Administration approval. Further study is needed to identify and overcome barriers to implementing new evidence into practice, such as ARNI use among eligible patients with HFrEF.
本研究旨在评估在射血分数降低的心力衰竭(HFrEF)的真实人群中,血管紧张素受体/脑啡肽酶抑制剂(ARNI)的处方率及其变化。
美国食品和药物管理局于 2015 年 7 月批准沙库巴曲缬沙坦用于 HFrEF 患者。对于这种新型治疗方法的早期使用模式知之甚少。
该研究纳入了 2015 年 7 月至 2016 年 6 月期间,在“遵循指南-心力衰竭(GWTG-HF)”注册登记中心出院存活的 HFrEF(射血分数≤40%)患者,这些患者的病历中记录了出院时是否开具了 ARNI。对比了出院时开具或未开具 ARNI 的 HFrEF 患者(排除有 ARNI 禁忌证的患者)的患者和医院特征。为了评估医院间的差异,评估了至少有 10 例符合条件的住院患者的医院。
在研究期间,因 HFrEF 住院的 21078 例患者中,有 495 例(2.3%)出院时开具了 ARNI。开具 ARNI 的患者年龄较小(中位数 65 岁 vs. 70 岁;p<0.001),射血分数较低(中位数 23% vs. 25%;p<0.001),出院时更常使用醛固酮拮抗剂(45% vs. 31%;p<0.001)。在 241 家至少有 10 例符合条件的住院患者的参与医院中,有 125 家(52%)报告出院时未开具 ARNI 处方。
在国家注册登记中,约有 2.3%的因 HFrEF 住院的患者在食品和药物管理局批准后的 12 个月内开具了 ARNI 治疗方案。需要进一步研究以确定并克服将新证据应用于实践的障碍,例如在有资格的 HFrEF 患者中使用 ARNI。