Frontiers in Cellular and Infection Microbiology (Mar 2023)

A multi-subgroup predictive model based on clinical parameters and laboratory biomarkers to predict in-hospital outcomes of plasma exchange-centered artificial liver treatment in patients with hepatitis B virus-related acute-on-chronic liver failure

  • Jie Liu,
  • Jie Liu,
  • Jie Liu,
  • Jie Liu,
  • Xinrong Shi,
  • Xinrong Shi,
  • Xinrong Shi,
  • Xinrong Shi,
  • Hongmin Xu,
  • Hongmin Xu,
  • Hongmin Xu,
  • Hongmin Xu,
  • Yaqiong Tian,
  • Yaqiong Tian,
  • Yaqiong Tian,
  • Yaqiong Tian,
  • Chaoyi Ren,
  • Jianbiao Li,
  • Shigang Shan,
  • Shuye Liu,
  • Shuye Liu,
  • Shuye Liu,
  • Shuye Liu

DOI
https://doi.org/10.3389/fcimb.2023.1107351
Journal volume & issue
Vol. 13

Abstract

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BackgroundPostoperative risk stratification is challenging in patients with hepatitis B virus-related acute-on-chronic liver failure (HBV-ACLF) who undergo artificial liver treatment. This study characterizes patients’ clinical parameters and laboratory biomarkers with different in-hospital outcomes. The purpose was to establish a multi-subgroup combined predictive model and analyze its predictive capability.MethodsWe enrolled HBV-ACLF patients who received plasma exchange (PE)-centered artificial liver support system (ALSS) therapy from May 6, 2017, to April 6, 2022. There were 110 patients who died (the death group) and 110 propensity score-matched patients who achieved satisfactory outcomes (the survivor group). We compared baseline, before ALSS, after ALSS, and change ratios of laboratory biomarkers. Outcome prediction models were established by generalized estimating equations (GEE). The discrimination was assessed using receiver operating characteristic analyses. Calibration plots compared the mean predicted probability and the mean observed outcome.ResultsWe built a multi-subgroup predictive model (at admission; before ALSS; after ALSS; change ratio) to predict in-hospital outcomes of HBV-ACLF patients who received PE-centered ALSS. There were 110 patients with 363 ALSS sessions who survived and 110 who did not, and 363 ALSS sessions were analyzed. The univariate GEE models revealed that several parameters were independent risk factors. Clinical parameters and laboratory biomarkers were entered into the multivariate GEE model. The discriminative power of the multivariate GEE models was excellent, and calibration showed better agreement between the predicted and observed probabilities than the univariate models.ConclusionsThe multi-subgroup combined predictive model generated accurate prognostic information for patients undergoing HBV-ACLF patients who received PE-centered ALSS.

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