Allegheny General Hospital, Pittsburgh, PA.
George Washington University, Washington, DC.
Chest. 2019 Aug;156(2):323-337. doi: 10.1016/j.chest.2019.02.004. Epub 2019 Feb 14.
Pulmonary arterial hypertension is a progressive, fatal disease. Published treatment guidelines recommend treatment escalation on the basis of regular patient assessment with the goal of achieving or maintaining low-risk status. Various strategies are available to determine risk status. This analysis describes an update of the Registry to Evaluate Early and Long-Term PAH Disease Management (REVEAL) risk calculator (REVEAL 2.0) and compares it with recently published European Society of Cardiology/Respiratory Society guideline-derived risk assessment strategies.
A subpopulation from the US-based registry REVEAL that survived ≥ 1 year postenrollment (baseline for this cohort) was analyzed. For REVEAL 2.0, point values and cutpoints were reassessed, and new variables were evaluated. The Kaplan-Meier method was used to estimate survival at 12 months postbaseline; discrimination was quantified using the c-statistic. Mortality estimates and discrimination were compared between REVEAL 2.0 and Comparative, Prospective Registry of Newly Initiated Therapies for Pulmonary Hypertension (COMPERA) and French Pulmonary Hypertension Registry (FPHR) risk assessment strategies. For this comparison, a three-category REVEAL 2.0 score was computed in which patients were classified as low-, intermediate-, or high-risk.
REVEAL 2.0 demonstrated similar discrimination as the original calculator in this subpopulation (c-statistic = 0.76 vs 0.74), provided excellent separation of risk among the risk categories, and predicted clinical worsening as well as mortality in patients who were followed ≥ 1 year. The REVEAL 2.0 three-category score had greater discrimination (c-statistic = 0.73) than COMPERA (c-statistic = 0.62) or FPHR (c-statistic = 0.64). Compared with REVEAL 2.0, COMPERA and FPHR both underestimated and overestimated risk.
REVEAL 2.0 demonstrates greater risk discrimination than the COMPERA and FPHR risk assessment strategies in patients enrolled in REVEAL. After external validation, the REVEAL 2.0 calculator can assist clinicians and patients in making informed treatment decisions on the basis of individual risk profiles.
ClinicalTrials.gov; No. NCT00370214; URL: www.clinicaltrials.gov.
肺动脉高压是一种进行性、致命性疾病。已公布的治疗指南建议根据定期的患者评估来升级治疗,目标是实现或维持低危状态。有多种策略可用于确定风险状况。本分析描述了评估早期和长期肺动脉高压疾病管理(REVEAL)风险计算器(REVEAL 2.0)的更新,并将其与最近公布的欧洲心脏病学会/呼吸学会指南衍生风险评估策略进行了比较。
对美国登记处 REVEAL 中存活时间超过基线后 1 年(该队列的基线)的亚人群进行分析。对于 REVEAL 2.0,重新评估了点值和切点,并评估了新变量。使用 Kaplan-Meier 方法估计基线后 12 个月的生存率;使用 c 统计量量化区分度。比较了 REVEAL 2.0 与比较性、前瞻性肺动脉高压新疗法登记(COMPERA)和法国肺动脉高压登记(FPHR)风险评估策略之间的死亡率估计值和区分度。对于此比较,计算了 REVEAL 2.0 的三分类评分,其中将患者分为低危、中危或高危。
REVEAL 2.0 在该亚人群中的表现与原始计算器相似(c 统计量=0.76 与 0.74),在风险类别之间提供了出色的风险分层,并预测了至少随访 1 年的患者的临床恶化和死亡率。REVEAL 2.0 的三分类评分(c 统计量=0.73)比 COMPERA(c 统计量=0.62)或 FPHR(c 统计量=0.64)的区分度更高。与 REVEAL 2.0 相比,COMPERA 和 FPHR 都低估和高估了风险。
在纳入 REVEAL 的患者中,REVEAL 2.0 显示出比 COMPERA 和 FPHR 风险评估策略更高的风险区分度。经过外部验证后,REVEAL 2.0 计算器可以根据个体风险概况协助临床医生和患者做出明智的治疗决策。
ClinicalTrials.gov;编号:NCT00370214;网址:www.clinicaltrials.gov。