Duke Clinical Research Institute, Durham, North Carolina; Division of Cardiology, Duke University School of Medicine, Durham, NC.
Merck & Co., Inc., Rahway, NJ, US.
Am Heart J. 2022 Sep;251:127-136. doi: 10.1016/j.ahj.2022.05.016. Epub 2022 May 29.
Patients with heart failure with reduced ejection fraction (HFrEF) and worsening HF events (WHFE) represent a distinct subset of patients with a substantial comorbidity burden, greater potential for intolerance to medical therapy, and high risk of subsequent death, hospitalization and excessive healthcare costs. Although multiple therapies have been shown to be efficacious and safe in this high-risk population, there are limited real-world data regarding factors that impact clinical decision-making when initiating or modifying therapy. Likewise, prior analyses of US clinical practice support major gaps in medical therapy for HFrEF and few medication changes during longitudinal follow-up, yet granular data on reasons why clinicians do not initiate or up-titrate guideline-directed medication are lacking.
We designed the CHART-HF study, an observational study of approximately 1,500 patients comparing patients with and without WHFE (WHFE defined as receipt of intravenous diuretics in the inpatient, outpatient, or emergency department setting) who had an index outpatient visit in the US between 2017 and 2019. Patient-level data on clinical characteristics, clinical outcomes, and therapy will be collected from 2 data sources: a single integrated health system, and a national panel of cardiologists. Furthermore, clinician-reported rationale for treatment decisions and the factors prioritized with selection and optimization of therapies in real-world practice will be obtained. To characterize elements of clinician decision-making not documented in the medical record, the panel of cardiologists will review records of patients seen under their care to explicitly note their primary reason for initiating, discontinuing, and titrating medications specific medications, as well as the reason for not making changes to each medication during the outpatient visit.
Results from CHART-HF have the potential to detail real-world US practice patterns regarding care of patients with HFrEF with versus without a recent WHFE, to examine clinician-reported reasons for use and non-use of guideline-directed medical therapy, and to characterize the magnitude and nature of clinical inertia toward evidence-based medication changes for HFrEF.
射血分数降低的心力衰竭(HFrEF)伴心力衰竭恶化事件(WHFE)的患者代表了具有大量合并症负担、对药物治疗不耐受的可能性更大、随后死亡、住院和过度医疗费用风险更高的一个独特亚组。尽管多项治疗方法已被证明在这一高危人群中安全有效,但在启动或调整治疗时影响临床决策的因素方面,实际数据有限。同样,对美国临床实践的先前分析支持 HFrEF 药物治疗存在较大差距,且在纵向随访期间很少改变药物治疗,但缺乏关于临床医生为何不启动或调整指南指导药物治疗的原因的详细数据。
我们设计了 CHART-HF 研究,这是一项大约 1500 名患者的观察性研究,比较了 2017 年至 2019 年期间在美国进行索引门诊就诊的伴有或不伴有 WHFE(WHFE 定义为在住院、门诊或急诊环境中接受静脉利尿剂治疗)的患者。将从两个数据源收集患者的临床特征、临床结局和治疗数据:一个单一的综合医疗系统和一个全国性的心脏病专家小组。此外,还将获得临床医生报告的治疗决策的理由以及在真实实践中选择和优化治疗的优先因素。为了描述病历中未记录的临床医生决策要素,心脏病专家小组将审查其治疗下的患者的记录,明确指出他们启动、停止和调整特定药物的主要原因,以及在门诊就诊期间不改变每种药物的原因。
CHART-HF 的结果有可能详细描述美国真实世界实践中对伴有或不伴有近期 WHFE 的 HFrEF 患者的治疗模式,检查临床医生报告的使用和不使用指南指导的药物治疗的理由,并描述对 HFrEF 的基于证据的药物治疗改变的临床惰性的程度和性质。