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A Model Predicting Mortality of Hospitalized Covid-19 Patients Four Days After Admission: Development, Internal and Temporal-External Validation.
Heber, Stefan; Pereyra, David; Schrottmaier, Waltraud C; Kammerer, Kerstin; Santol, Jonas; Rumpf, Benedikt; Pawelka, Erich; Hanna, Markus; Scholz, Alexander; Liu, Markus; Hell, Agnes; Heiplik, Klara; Lickefett, Benno; Havervall, Sebastian; Traugott, Marianna T; Neuböck, Matthias J; Schörgenhofer, Christian; Seitz, Tamara; Firbas, Christa; Karolyi, Mario; Weiss, Günter; Jilma, Bernd; Thålin, Charlotte; Bellmann-Weiler, Rosa; Salzer, Helmut J F; Szepannek, Gero; Fischer, Michael J M; Zoufaly, Alexander; Gleiss, Andreas; Assinger, Alice.
  • Heber S; Institute of Physiology, Centre of Physiology and Pharmacology, Medical University of Vienna, Vienna, Austria.
  • Pereyra D; Department of Vascular Biology and Thrombosis Research, Centre of Physiology and Pharmacology, Medical University of Vienna, Vienna, Austria.
  • Schrottmaier WC; Department of General Surgery, Division of Visceral Surgery, Medical University of Vienna, General Hospital Vienna, Vienna, Austria.
  • Kammerer K; Department of Vascular Biology and Thrombosis Research, Centre of Physiology and Pharmacology, Medical University of Vienna, Vienna, Austria.
  • Santol J; Department of Vascular Biology and Thrombosis Research, Centre of Physiology and Pharmacology, Medical University of Vienna, Vienna, Austria.
  • Rumpf B; Department of Vascular Biology and Thrombosis Research, Centre of Physiology and Pharmacology, Medical University of Vienna, Vienna, Austria.
  • Pawelka E; Department of General Surgery, Division of Visceral Surgery, Medical University of Vienna, General Hospital Vienna, Vienna, Austria.
  • Hanna M; Department of Medicine IV, Kaiser Franz Josef Hospital, Vienna, Austria.
  • Scholz A; Department of Medicine IV, Kaiser Franz Josef Hospital, Vienna, Austria.
  • Liu M; Department of Vascular Biology and Thrombosis Research, Centre of Physiology and Pharmacology, Medical University of Vienna, Vienna, Austria.
  • Hell A; Department of Vascular Biology and Thrombosis Research, Centre of Physiology and Pharmacology, Medical University of Vienna, Vienna, Austria.
  • Heiplik K; Department of Vascular Biology and Thrombosis Research, Centre of Physiology and Pharmacology, Medical University of Vienna, Vienna, Austria.
  • Lickefett B; Department of Vascular Biology and Thrombosis Research, Centre of Physiology and Pharmacology, Medical University of Vienna, Vienna, Austria.
  • Havervall S; Department of Vascular Biology and Thrombosis Research, Centre of Physiology and Pharmacology, Medical University of Vienna, Vienna, Austria.
  • Traugott MT; Department of Vascular Biology and Thrombosis Research, Centre of Physiology and Pharmacology, Medical University of Vienna, Vienna, Austria.
  • Neuböck MJ; Division of Internal Medicine, Department of Clinical Sciences, Karolinska Institutet, Danderyd Hospital, Stockholm, Sweden.
  • Schörgenhofer C; Department of Medicine IV, Kaiser Franz Josef Hospital, Vienna, Austria.
  • Seitz T; Department of Pulmonology, Kepler University Hospital and Johannes Kepler University, Linz, Austria.
  • Firbas C; Department of Clinical Pharmacology, Medical University of Vienna, General Hospital Vienna, Vienna, Austria.
  • Karolyi M; Department of Medicine IV, Kaiser Franz Josef Hospital, Vienna, Austria.
  • Weiss G; Department of Clinical Pharmacology, Medical University of Vienna, General Hospital Vienna, Vienna, Austria.
  • Jilma B; Department of Medicine IV, Kaiser Franz Josef Hospital, Vienna, Austria.
  • Thålin C; Department of Internal Medicine II, Medical University of Innsbruck, Innsbruck, Austria.
  • Bellmann-Weiler R; Department of Clinical Pharmacology, Medical University of Vienna, General Hospital Vienna, Vienna, Austria.
  • Salzer HJF; Division of Internal Medicine, Department of Clinical Sciences, Karolinska Institutet, Danderyd Hospital, Stockholm, Sweden.
  • Szepannek G; Department of Internal Medicine II, Medical University of Innsbruck, Innsbruck, Austria.
  • Fischer MJM; Department of Pulmonology, Kepler University Hospital and Johannes Kepler University, Linz, Austria.
  • Zoufaly A; Institute of Applied Computer Science, Stralsund University of Applied Sciences, Stralsund, Germany.
  • Gleiss A; Institute of Physiology, Centre of Physiology and Pharmacology, Medical University of Vienna, Vienna, Austria.
  • Assinger A; Department of Medicine IV, Kaiser Franz Josef Hospital, Vienna, Austria.
Front Cell Infect Microbiol ; 11: 795026, 2021.
Article in English | MEDLINE | ID: covidwho-1686455
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.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: SARS-CoV-2 / COVID-19 Type of study: Observational study / Prognostic study / Randomized controlled trials Topics: Variants Limits: Humans Language: English Journal: Front Cell Infect Microbiol Year: 2021 Document Type: Article Affiliation country: Fcimb.2021.795026

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Full text: Available Collection: International databases Database: MEDLINE Main subject: SARS-CoV-2 / COVID-19 Type of study: Observational study / Prognostic study / Randomized controlled trials Topics: Variants Limits: Humans Language: English Journal: Front Cell Infect Microbiol Year: 2021 Document Type: Article Affiliation country: Fcimb.2021.795026