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Peer-reviewedCC BY 4.0Journal of Clinical Medicine

Prognosis Prediction in Adult Intensive Care—A Critical Analysis

  1. 1Department of Anesthesiology, Intensive Therapy and Perioperative Medicine, Department of Acute Medicine, Faculty of Medical Sciences in Zabrze, Medical University of Silesia in Katowice, 41-800 Zabrze, Poland

Abstract

Background: Prognosis prediction in adult intensive care units (ICUs) guides clinical decision-making, realistic goal-setting with families, and resource allocation, but is challenged by the marked heterogeneity of critically ill patients in multi-speciality wards. Methods: This narrative review critically analyses commonly used prognostic scoring systems by clinical application timeline. Results: Admission prognostic models, including the Acute Physiology and Chronic Health Evaluation (APACHE II/III/IV), Simplified Acute Physiology Score (SAPS II/SAPS 3) and Mortality Probability Model (MPM), estimate in-hospital mortality from acute physiological derangement and comorbidity; the Clinical Frailty Scale (CFS) adds prognostic value. During the ICU stay, organ dysfunction is tracked with the Sequential Organ Failure Assessment (SOFA/SOFA-2), designed for repeated reassessment, and the Multiple Organ Dysfunction Score (MODS), while the Therapeutic Intervention Scoring System (TISS-28) quantifies nursing workload. At discharge, the Barthel Index, Glasgow Outcome Scale (GOS) and Cerebral Performance Category (CPC) measure functional independence and neurological outcome. Admission-based mortality models use an initial assessment window and may require local recalibration, and discrimination alone does not establish clinical utility. Conclusions: Future directions include trajectory-based models, phenotyping, biomarkers, time-limited trials and machine learning. Prognostic estimates should inform multidisciplinary evaluation and shared decision-making, rather than independently determine treatment intensity or withdrawal.

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BibTeX
@article{liberski2026prognosis,
  title = {{Prognosis Prediction in Adult Intensive Care—A Critical Analysis}},
  author = {Piotr S. Liberski and Szymon Czajka and Krzysztof Żerdziński and Łukasz J. Krzych},
  journal = {Journal of Clinical Medicine},
  year = {2026},
  month = oct,
  doi = {10.3390/jcm15208073},
  url = {https://www.mdpi.com/2077-0383/15/20/8073},
  note = {CC BY 4.0},
}
RIS
TY  - JOUR
TI  - Prognosis Prediction in Adult Intensive Care—A Critical Analysis
AU  - Piotr S. Liberski
AU  - Szymon Czajka
AU  - Krzysztof Żerdziński
AU  - Łukasz J. Krzych
PY  - 2026
DA  - 2026/10/17
JO  - Journal of Clinical Medicine
DO  - 10.3390/jcm15208073
UR  - https://www.mdpi.com/2077-0383/15/20/8073
AB  - Background: Prognosis prediction in adult intensive care units (ICUs) guides clinical decision-making, realistic goal-setting with families, and resource allocation, but is challenged by the marked heterogeneity of critically ill patients in multi-speciality wards. Methods: This narrative review critically analyses commonly used prognostic scoring systems by clinical application timeline. Results: Admission prognostic models, including the Acute Physiology and Chronic Health Evaluation (APACHE II/III/IV), Simplified Acute Physiology Score (SAPS II/SAPS 3) and Mortality Probability Model (MPM), estimate in-hospital mortality from acute physiological derangement and comorbidity; the Clinical Frailty Scale (CFS) adds prognostic value. During the ICU stay, organ dysfunction is tracked with the Sequential Organ Failure Assessment (SOFA/SOFA-2), designed for repeated reassessment, and the Multiple Organ Dysfunction Score (MODS), while the Therapeutic Intervention Scoring System (TISS-28) quantifies nursing workload. At discharge, the Barthel Index, Glasgow Outcome Scale (GOS) and Cerebral Performance Category (CPC) measure functional independence and neurological outcome. Admission-based mortality models use an initial assessment window and may require local recalibration, and discrimination alone does not establish clinical utility. Conclusions: Future directions include trajectory-based models, phenotyping, biomarkers, time-limited trials and machine learning. Prognostic estimates should inform multidisciplinary evaluation and shared decision-making, rather than independently determine treatment intensity or withdrawal.
SN  - 2077-0383
ER  -