Liu Chun-Lin, Wu Qing-Nian, Deng Zhi-Ying, Chen Ping, Guo Shi-Qiang
Department of Laboratory Medicine, The Sixth Affiliated Hospital, School of Medicine, South China University of Technology, Foshan, China.
Department of Clinical Research Laboratory, The Sixth Affiliated Hospital, School of Medicine, South China University of Technology, No.120 Gui Dan Road, Foshan, 528222, China.
Eur J Med Res. 2024 Dec 24;29(1):620. doi: 10.1186/s40001-024-02235-2.
The role of inflammation and hypoproteinemia in influencing outcomes of critically ill patients has been widely recognized. However, there is a paucity of research on the prognostic value of the platelet-to-albumin ratio (PAR) in critically ill patients. Therefore, the aim of this study is to assess the prognostic significance of PAR in this population.
Patients diagnosed with critical illnesses from January 2020 to October 2022 were retrospectively enrolled in our study. Baseline demographic and clinical data were collected for each participant. Platelet counts and albumin levels were measured at baseline, and the PAR was calculated. The area under the receiver operating characteristic curve, Kaplan-Meier survival analysis, and multivariate Cox regression analysis were used to predict 30-day mortality.
Three hundred and seventy-eight patients diagnosed with critical illness were categorized into two groups: survivors (n = 299) and non-survivors (n = 79). Analysis of the 30-day outcome revealed that the area under the curve (AUC) for the PAR (AUC: 0.705; 95% CI 0.639-0.771; p < 0.001) was significantly higher than that for albumin (AUC: 0.673; 95% CI 0.609-0.736; p < 0.001), but slightly lower than that for the APACHE II score (AUC: 0.713; 95% CI 0.650-0.777; p < 0.001). In addition, the Kaplan-Meier survival analysis demonstrated a significantly higher 30-day mortality in the high-PAR group. Furthermore, Cox regression analysis identified albumin (HR: 0.936; 95% CI 0.895-0.978; p = 0.003), APACHE II score (HR: 1.225; 95% CI 1.149-1.305; p < 0.001), and high PAR (HR: 1.237; 95% CI 1.130-1.353; p < 0.001) as independent risk factors for the prognosis of critically ill patients.
The PAR has emerged as a significant prognostic indicator in critically ill patients, with an elevated ratio being associated with poorer clinical outcomes.
炎症和低蛋白血症在影响重症患者预后方面的作用已得到广泛认可。然而,关于血小板与白蛋白比值(PAR)对重症患者的预后价值的研究却很少。因此,本研究的目的是评估PAR在该人群中的预后意义。
回顾性纳入2020年1月至2022年10月诊断为危重病的患者。收集每位参与者的基线人口统计学和临床数据。在基线时测量血小板计数和白蛋白水平,并计算PAR。采用受试者工作特征曲线下面积、Kaplan-Meier生存分析和多因素Cox回归分析来预测30天死亡率。
378例诊断为危重病的患者被分为两组:存活者(n = 299)和非存活者(n = 79)。对30天结局的分析显示,PAR的曲线下面积(AUC:0.705;95%CI 0.639 - 0.771;p < 0.001)显著高于白蛋白(AUC:0.673;95%CI 0.609 - 0.736;p < 0.001),但略低于急性生理学与慢性健康状况评分系统II(APACHE II)评分(AUC:0.713;95%CI 0.650 - 0.777;p < 0.001)。此外,Kaplan-Meier生存分析显示高PAR组的30天死亡率显著更高。此外,Cox回归分析确定白蛋白(HR:0.936;95%CI 0.895 - 0.978;p = 0.003)、APACHE II评分(HR:1.225;95%CI 1.149 - 1.305;p < 0.001)和高PAR(HR:1.237;95%CI 1.130 - 1.353;p < 0.001)是重症患者预后的独立危险因素。
PAR已成为重症患者的一个重要预后指标,比值升高与较差的临床结局相关。