Mentz Robert J, Mulder Hillary, Mosterd Arend, Sweitzer Nancy K, Senni Michele, Butler Javed, Ezekowitz Justin A, Lam Carolyn S P, Pieske Burkert, Ponikowski Piotr, Voors Adriaan A, Anstrom Kevin J, Armstrong Paul W, O'connor Christopher M, Hernandez Adrian F
Duke Clinical Research Institute, Duke University, Durham, North Carolina.
Duke Clinical Research Institute, Duke University, Durham, North Carolina.
J Card Fail. 2021 Jun 24. doi: 10.1016/j.cardfail.2021.05.016.
The prediction of outcomes in patients with heart failure (HF) may inform prognosis, clinical decisions regarding treatment selection, and new trial planning. The VerICiguaT Global Study in Subjects With Heart Failure With Reduced Ejection Fraction included high-risk patients with HF with reduced ejection fraction and a recent worsening HF event. The study participants had a high event rate despite the use of contemporary guideline-based therapies. To provide generalizable predictive data for a broad population with a recent worsening HF event, we focused on risk prognostication in the placebo group.
Data from 2524 participants randomized to placebo with chronic HF (New York Heart Association functional class II-IV) and an ejection fraction of less than 45% were studied and backward variable selection was used to create Cox proportional hazards models for clinical end points, selecting from 66 candidate predictors. Final model results were produced, accounting for missing data, and nonlinearities. Optimism-corrected c-indices were calculated using 200 bootstrap samples. Over a median follow-up of 10.4 months, the primary outcome of HF hospitalization or cardiovascular death occurred in 972 patients (38.5%). Independent predictors of increased risk for the primary end point included HF characteristics (longer HF duration and worse New York Heart Association functional class), medical history (prior myocardial infarction), and laboratory values (higher N-terminal pro-hormone B-type natriuretic peptide, bilirubin, urate; lower chloride and albumin). Optimism-corrected c-indices were 0.68 for the HF hospitalization/cardiovascular death model, 0.68 for HF hospitalization/all-cause death, 0.72 for cardiovascular death, and 0.73 for all-cause death.
Predictive models developed in a large diverse clinical trial with comprehensive clinical and laboratory baseline data-including novel measures-performed well in high-risk patients with HF who were receiving excellent guideline-based clinical care.
Clinicaltrials.gov identifier, NCT02861534.Lay Summary: Patients with heart failure may benefit from tools that help clinicians to better understand a patient's risk for future events like hospitalization. Relatively few risk models have been created after the worsening of heart failure in a contemporary cohort. We provide insights on the risk factors for clinical events from a recent, large, global trial of patients with worsening heart failure to help clinicians better understand and communicate prognosis and select treatment options.
心力衰竭(HF)患者预后的预测有助于了解病情、指导治疗方案的临床决策以及新试验的规划。射血分数降低的心力衰竭患者的VerICiguaT全球研究纳入了射血分数降低且近期心力衰竭病情恶化的高危患者。尽管采用了基于当代指南的治疗方法,但研究参与者的事件发生率仍然很高。为了为近期心力衰竭病情恶化的广大人群提供可推广的预测数据,我们重点研究了安慰剂组的风险预后。
对2524名随机分配至安慰剂组的慢性心力衰竭患者(纽约心脏协会心功能II-IV级)且射血分数低于45%的数据进行研究,并采用向后变量选择法建立临床终点的Cox比例风险模型,从66个候选预测因子中进行选择。最终模型结果考虑了缺失数据和非线性因素。使用200个自抽样样本计算乐观校正c指数。在中位随访10.4个月期间,972名患者(38.5%)发生了心力衰竭住院或心血管死亡的主要结局。主要终点风险增加的独立预测因子包括心力衰竭特征(心力衰竭病程较长和纽约心脏协会心功能分级较差)、病史(既往心肌梗死)和实验室检查值(较高的N末端前体B型利钠肽、胆红素、尿酸;较低的氯化物和白蛋白)。心力衰竭住院/心血管死亡模型的乐观校正c指数为0.68,心力衰竭住院/全因死亡为0.68,心血管死亡为0.72,全因死亡为0.73。
在一项包含全面临床和实验室基线数据(包括新指标)的大型多样化临床试验中开发的预测模型,在接受基于指南的优质临床护理的高危心力衰竭患者中表现良好。
Clinicaltrials.gov标识符,NCT02861534。
心力衰竭患者可能会从有助于临床医生更好地了解患者未来住院等事件风险的工具中受益。在当代队列中,心力衰竭病情恶化后建立的风险模型相对较少。我们从最近一项针对心力衰竭病情恶化患者的大型全球试验中提供了临床事件风险因素的见解,以帮助临床医生更好地理解和沟通预后并选择治疗方案。