Evidence map›Paper›PMID 35141170›Full record

ArticleFrontiers in cellular and infection microbiology2021

A Model Predicting Mortality of Hospitalized Covid-19 Patients Four Days After Admission: Development, Internal and Temporal-External Validation.

Stefan Heber, David Pereyra, Waltraud C Schrottmaier, Kerstin Kammerer, Jonas Santol, Benedikt Rumpf, Erich Pawelka, Markus Hanna, Alexander Scholz, Markus Liu and 20 more

Registry-linked trialAbstract readAdaptive Clinical Trial
In one paragraph

Article in Frontiers in cellular and infection microbiology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04351724 (A Multicenter, Randomized, Active Controlled, Open Label, Platform Trial on the Efficacy and Safety of Experimental Therapeutics for Patients With COVID-19), which is not on this map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT04351724 phase2 / phase3unknown statusnot on this map

A Multicenter, Randomized, Active Controlled, Open Label, Platform Trial on the Efficacy and Safety of Experimental Therapeutics for Patients With COVID-19 (Caused by Infection With Severe Acute Respiratory Syndrome Coronavirus-2)

TypeinterventionalSponsorMedical University of ViennaRan2020 to 2022Enrolled500ConditionsCOVID-19ArmsChloroquine or Hydroxychloroquine, Lopinavir/Ritonavir, Best standard of care, Rivaroxaban, Thromboprophylaxis
3 · Its place in the literature

Who cites it

11 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  3. Admission biomarkers and COVID-19 mortality: A retrospective study during Vietnam's pandemic peak.Journal of critical care medicine (Universitatea de Medicina si Farmacie din Targu-Mures) · 2026
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

30 authors.

Stefan HeberInstitute of Physiology, Centre of Physiology and Pharmacology, Medical University of Vienna, Vienna, Austria.
David PereyraDepartment of Vascular Biology and Thrombosis Research, Centre of Physiology and Pharmacology, Medical University of Vienna, Vienna, Austria.
Waltraud C SchrottmaierDepartment of Vascular Biology and Thrombosis Research, Centre of Physiology and Pharmacology, Medical University of Vienna, Vienna, Austria.
Kerstin KammererDepartment of Vascular Biology and Thrombosis Research, Centre of Physiology and Pharmacology, Medical University of Vienna, Vienna, Austria.
Jonas SantolDepartment of Vascular Biology and Thrombosis Research, Centre of Physiology and Pharmacology, Medical University of Vienna, Vienna, Austria.
Benedikt RumpfDepartment of Medicine IV, Kaiser Franz Josef Hospital, Vienna, Austria.
Erich PawelkaDepartment of Medicine IV, Kaiser Franz Josef Hospital, Vienna, Austria.
Markus HannaDepartment of Vascular Biology and Thrombosis Research, Centre of Physiology and Pharmacology, Medical University of Vienna, Vienna, Austria.
Alexander ScholzDepartment of Vascular Biology and Thrombosis Research, Centre of Physiology and Pharmacology, Medical University of Vienna, Vienna, Austria.
Markus LiuDepartment of Vascular Biology and Thrombosis Research, Centre of Physiology and Pharmacology, Medical University of Vienna, Vienna, Austria.
Agnes HellDepartment of Vascular Biology and Thrombosis Research, Centre of Physiology and Pharmacology, Medical University of Vienna, Vienna, Austria.
Klara HeiplikDepartment of Vascular Biology and Thrombosis Research, Centre of Physiology and Pharmacology, Medical University of Vienna, Vienna, Austria.
Benno LickefettDepartment of Vascular Biology and Thrombosis Research, Centre of Physiology and Pharmacology, Medical University of Vienna, Vienna, Austria.
Sebastian HavervallDivision of Internal Medicine, Department of Clinical Sciences, Karolinska Institutet, Danderyd Hospital, Stockholm, Sweden.
Marianna T TraugottDepartment of Medicine IV, Kaiser Franz Josef Hospital, Vienna, Austria.
Matthias J NeuböckDepartment of Pulmonology, Kepler University Hospital and Johannes Kepler University, Linz, Austria.
Christian SchörgenhoferDepartment of Clinical Pharmacology, Medical University of Vienna, General Hospital Vienna, Vienna, Austria.
Tamara SeitzDepartment of Medicine IV, Kaiser Franz Josef Hospital, Vienna, Austria.
Christa FirbasDepartment of Clinical Pharmacology, Medical University of Vienna, General Hospital Vienna, Vienna, Austria.
Mario KarolyiDepartment of Medicine IV, Kaiser Franz Josef Hospital, Vienna, Austria.
Günter WeissDepartment of Internal Medicine II, Medical University of Innsbruck, Innsbruck, Austria.
Bernd JilmaDepartment of Clinical Pharmacology, Medical University of Vienna, General Hospital Vienna, Vienna, Austria.
Charlotte ThålinDivision of Internal Medicine, Department of Clinical Sciences, Karolinska Institutet, Danderyd Hospital, Stockholm, Sweden.
Rosa Bellmann-WeilerDepartment of Internal Medicine II, Medical University of Innsbruck, Innsbruck, Austria.
Helmut J F SalzerDepartment of Pulmonology, Kepler University Hospital and Johannes Kepler University, Linz, Austria.
Gero SzepannekInstitute of Applied Computer Science, Stralsund University of Applied Sciences, Stralsund, Germany.
Michael J M FischerInstitute of Physiology, Centre of Physiology and Pharmacology, Medical University of Vienna, Vienna, Austria.
Alexander ZoufalyDepartment of Medicine IV, Kaiser Franz Josef Hospital, Vienna, Austria.
Andreas GleissSection for Clinical Biometrics, Center for Medical Statistics, Informatics, and Intelligent Systems, Medical University of Vienna, Vienna, Austria.
Alice AssingerDepartment of Vascular Biology and Thrombosis Research, Centre of Physiology and Pharmacology, Medical University of Vienna, Vienna, Austria.

Funding

Austrian Science Fund FWF P 32064Austrian Science Fund FWF P 34783
6 · The paper itself

Abstract

Objective: To develop and validate a prognostic model for in-hospital mortality after four days based on age, fever at admission and five haematological parameters routinely measured in hospitalized Covid-19 patients during the first four days after admission. Methods: Haematological parameters measured during the first 4 days after admission were subjected to a linear mixed model to obtain patient-specific intercepts and slopes for each parameter. A prediction model was built using logistic regression with variable selection and shrinkage factor estimation supported by bootstrapping. Model development was based on 481 survivors and 97 non-survivors, hospitalized before the occurrence of mutations. Internal validation was done by 10-fold cross-validation. The model was temporally-externally validated in 299 survivors and 42 non-survivors hospitalized when the Alpha variant (B.1.1.7) was prevalent. Results: The final model included age, fever on admission as well as the slope or intercept of lactate dehydrogenase, platelet count, C-reactive protein, and creatinine. Tenfold cross validation resulted in a mean area under the receiver operating characteristic curve (AUROC) of 0.92, a mean calibration slope of 1.0023 and a Brier score of 0.076. At temporal-external validation, application of the previously developed model showed an AUROC of 0.88, a calibration slope of 0.95 and a Brier score of 0.073. Regarding the relative importance of the variables, the (apparent) variation in mortality explained by the six variables deduced from the haematological parameters measured during the first four days is higher (explained variation 0.295) than that of age (0.210). Conclusions: The presented model requires only variables routinely acquired in hospitals, which allows immediate and wide-spread use as a decision support for earlier discharge of low-risk patients to reduce the burden on the health care system. Clinical Trial Registration: Austrian Coronavirus Adaptive Clinical Trial (ACOVACT); ClinicalTrials.gov, identifier NCT04351724.

Indexed as

COVID-19SARS-CoV-2HospitalizationHospital MortalityHumansRetrospective Studiesblood parameterCOVID-19hospitalized patientslogistic regressionprediction modelsurvival

Identifiers

PMID35141170
PMCPMC8819729

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Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.