Núñez Julio, Bayés-Genís Antoni, Revuelta-López Elena, Miñana Gema, Santas Enrique, Ter Maaten Jozine M, de la Espriella Rafael, Carratalá Arturo, Lorenzo Miguel, Palau Patricia, Llàcer Pau, Valle Alfonso, Bodi Vicent, Núñez Eduardo, Lupón Josep, Lang Chim, Ng Leong L, Metra Marco, Sanchis Juan, Voors Adriaan A
Servicio de Cardiología, Hospital Clínico Universitario de Valencia, INCLIVA, Valencia, Spain; Departamento de Medicina, Universitat de Valencia, València, Spain; Centro de Investigación Biomédica en Red Enfermedades Cardiovaculares (CIBERCV), Spain.
Centro de Investigación Biomédica en Red Enfermedades Cardiovaculares (CIBERCV), Spain; Unidad de Insuficiencia Cardiaca, Servicio de Cardiología, Hospital Universitari Germans Trias i Pujol, Badalona, Barcelona, Spain; Departamento de Medicina, Universitat Autònoma de Barcelona, Barcelona, Spain.
Rev Esp Cardiol (Engl Ed). 2022 Apr;75(4):316-324. doi: 10.1016/j.rec.2021.02.002. Epub 2021 Mar 19.
Carbohydrate antigen 125 (CA125) has been shown to be useful for risk stratification in patients admitted with acute heart failure (AHF). We sought to determine a CA125 cutpoint for identifying patients at low risk of 1-month death or the composite of death/HF readmission following admission for AHF.
The derivation cohort included 3231 consecutive patients with AHF. CA125 cutoff values with 90% negative predictive value (NPV) and sensitivity up to 85% were identified. The adequacy of these cutpoints and the risk of 1-month death/HF readmission was then tested using the Royston-Parmar method. The best cutpoint was selected and externally validated in a cohort of patients hospitalized from BIOSTAT-CHF (n=1583).
In the derivation cohort, the median [IQR] CA125 was 57 [25.3-157] U/mL. The optimal cutoff value was <23 U/mL (21.5% of patients), with NPVs of 99.3% and 94.1% for death and the composite endpoint, respectively. On multivariate survival analyses, CA125 <23 U/mL was independently associated with a lower risk of death (HR, 0.20; 95%CI, 0.08-0.50; P <.001), and the combined endpoint (HR, 0.63; 95%CI, 950.45-0.90; P=.009). The ability of this cutpoint to discriminate patients at a low 1-month risk was confirmed in the validation cohort (NPVs of 98.6% and 96.6% for death and the composite endpoint). The predicted ability of this cutoff remained significant at 6 months of follow-up.
In patients admitted with AHF, CA125 <23 U/mL identified a subgroup at low risk of short-term adverse events, a population that may not require intense postdischarge monitoring.
碳水化合物抗原125(CA125)已被证明可用于急性心力衰竭(AHF)患者的风险分层。我们试图确定一个CA125切点,以识别AHF入院患者中1个月死亡或死亡/心力衰竭再入院复合事件风险较低的患者。
推导队列包括3231例连续的AHF患者。确定了具有90%阴性预测值(NPV)且敏感性高达85%的CA125临界值。然后使用Royston-Parmar方法检验这些切点的充分性以及1个月死亡/心力衰竭再入院的风险。选择最佳切点并在BIOSTAT-CHF队列(n = 1583)的住院患者中进行外部验证。
在推导队列中,CA125的中位数[四分位间距]为57[25.3 - 157]U/mL。最佳临界值<23 U/mL(占患者的21.5%),死亡和复合终点的NPV分别为99.3%和94.1%。在多变量生存分析中,CA125<23 U/mL与较低的死亡风险(HR,0.20;95%CI,0.08 - 0.50;P<.001)以及复合终点(HR,0.63;95%CI,0.45 - 0.90;P = .009)独立相关。在验证队列中证实了该切点区分1个月低风险患者的能力(死亡和复合终点的NPV分别为98.6%和96.6%)。该临界值的预测能力在随访6个月时仍然显著。
在AHF入院患者中,CA125<23 U/mL识别出短期不良事件风险较低的亚组,该人群可能不需要出院后强化监测。