Raina Amresh, Sketch Margaret R, Wu Benjamin, Broderick Meredith, Shlobin Oksana A
Cardiology-Advanced Heart Failure & Transplant Allegheny General Hospital Pittsburgh Pennsylvania USA.
United Therapeutics Corporation Research Triangle Park North Carolina USA.
Pulm Circ. 2024 Oct 18;14(4):e12455. doi: 10.1002/pul2.12455. eCollection 2024 Oct.
The objective of this analysis was to compare clinician-based and formally calculated risk assessments by REVEAL Lite 2 and COMPERA 2.0 and to characterize parenteral prostacyclin utilization within 90 days of baseline in high-risk patients. A multisite, double-blind, retrospective chart review of patients with pulmonary arterial hypertension (PAH) was conducted with an index period of January 2014-March 2017. Patients were categorized into the "any PAH medication" or "prostacyclin-enriched" cohort based on latest PAH medication initiated within the index period. Clinicians classified the patient's 1-year mortality risk as "low," "intermediate," or "high" based on their clinical assessment. REVEAL Lite 2 and COMPERA 2.0 scores were independently calculated. Risk assessment congruency was evaluated. Parenteral prostacyclin use was evaluated within 90 days of baseline. Thirty-two clinicians participated and abstracted data for 299 patients with PAH. At baseline, mean patient age was 52 years, 6-min walk distance was 226 m, and most patients were WHO functional class II or III. Half of the patients (53%) were classified by clinician assessment as intermediate risk, while most were classified as high risk by REVEAL Lite 2 (59%) and intermediate-high risk by COMPERA 2.0 (52%). Parenteral prostascyclins were underutilized in high-risk patients, and not initiated in a timely fashion. Clinician-assessed risk category was incongruent with tool-based risk assessments in 40%-54% of patients with PAH, suggesting an underestimation of the patient's risk category by clinician gestalt. Additionally, there was a lack of timely prostacyclin initiation for patients with PAH stratified as high-risk by either tool.
本分析的目的是比较基于临床医生的风险评估与REVEAL Lite 2和COMPERA 2.0正式计算的风险评估,并描述高危患者基线后90天内肠外前列环素的使用情况。对2014年1月至2017年3月索引期内的肺动脉高压(PAH)患者进行了多中心、双盲、回顾性病历审查。根据索引期内开始使用的最新PAH药物,将患者分为“任何PAH药物”或“富含前列环素”队列。临床医生根据其临床评估将患者的1年死亡风险分类为“低”、“中”或“高”。独立计算REVEAL Lite 2和COMPERA 2.0评分。评估风险评估的一致性。在基线后90天内评估肠外前列环素的使用情况。三十二名临床医生参与并提取了299例PAH患者的数据。基线时,患者平均年龄为52岁,6分钟步行距离为226米,大多数患者为世界卫生组织功能分级II级或III级。一半的患者(53%)经临床医生评估为中度风险,而大多数患者经REVEAL Lite 2评估为高风险(59%),经COMPERA 2.0评估为中高风险(52%)。高危患者肠外前列环素使用不足,且未及时开始使用。在40%-54%的PAH患者中,临床医生评估的风险类别与基于工具的风险评估不一致,这表明临床医生的整体判断低估了患者的风险类别。此外,对于两种工具均分层为高危的PAH患者,缺乏及时的前列环素起始治疗。