A Systematic Review of Predictor Composition, Outcomes, Risk of Bias, and Validation of Coronavirus Disease 2019 (COVID-19) Prognostic Scores

Author:

Appel Katharina S1ORCID,Geisler Ramsia1,Maier Daniel12,Miljukov Olga3,Hopff Sina M4,Vehreschild J Janne156

Affiliation:

1. Department II of Internal Medicine, Hematology/Oncology, Goethe University Frankfurt , Frankfurt am Main , Germany

2. German Cancer Consortium (DKTK), Partner Site Frankfurt/Mainz and German Cancer Research Center (DKFZ) , Heidelberg , Germany

3. Institute of Clinical Epidemiology and Biometry, University of Würzburg , Würzburg , Germany

4. University of Cologne, Faculty of Medicine and University Hospital Cologne, Department I of Internal Medicine, Center for Integrated Oncology Aachen Bonn Cologne Duesseldorf, Cologne, Germany, University of Cologne

5. University of Cologne, Faculty of Medicine and University Hospital Cologne, Department I of Internal Medicine , Cologne , Germany

6. German Centre for Infection Research (DZIF), partner site Bonn-Cologne , Cologne , Germany

Abstract

Abstract Background Numerous prognostic scores have been published to support risk stratification for patients with coronavirus disease 2019 (COVID-19). Methods We performed a systematic review to identify the scores for confirmed or clinically assumed COVID-19 cases. An in-depth assessment and risk of bias (ROB) analysis (Prediction model Risk Of Bias ASsessment Tool [PROBAST]) was conducted for scores fulfilling predefined criteria ([I] area under the curve [AUC)] ≥ 0.75; [II] a separate validation cohort present; [III] training data from a multicenter setting [≥2 centers]; [IV] point-scale scoring system). Results Out of 1522 studies extracted from MEDLINE/Web of Science (20/02/2023), we identified 242 scores for COVID-19 outcome prognosis (mortality 109, severity 116, hospitalization 14, long-term sequelae 3). Most scores were developed using retrospective (75.2%) or single-center (57.1%) cohorts. Predictor analysis revealed the primary use of laboratory data and sociodemographic information in mortality and severity scores. Forty-nine scores were included in the in-depth analysis. The results indicated heterogeneous quality and predictor selection, with only five scores featuring low ROB. Among those, based on the number and heterogeneity of validation studies, only the 4C Mortality Score can be recommended for clinical application so far. Conclusions The application and translation of most existing COVID scores appear unreliable. Guided development and predictor selection would have improved the generalizability of the scores and may enhance pandemic preparedness in the future.

Funder

ORCHESTRA

European Union’s Horizon 2020 research and innovation program

German Federal Ministry of Education and Research

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Microbiology (medical)

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