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Serial cardiac biomarkers for risk stratification of patients with COVID-19.
Tawiah, Kwaku; Jackson, Laurel; Omosule, Catherine; Ballman, Claire; Shahideh, Bobby; Scott, Mitchell G; Murtagh, Gillian; Farnsworth, Christopher W.
  • Tawiah K; Department of Pathology & Immunology, Washington University School of Medicine, St. Louis, MO, United States.
  • Jackson L; Core Diagnostics, Abbott Laboratories, Abbott Park, IL, United States.
  • Omosule C; Department of Pathology & Immunology, Washington University School of Medicine, St. Louis, MO, United States.
  • Ballman C; Department of Pathology & Immunology, Washington University School of Medicine, St. Louis, MO, United States.
  • Shahideh B; Core Diagnostics, Abbott Laboratories, Abbott Park, IL, United States.
  • Scott MG; Department of Pathology & Immunology, Washington University School of Medicine, St. Louis, MO, United States.
  • Murtagh G; Core Diagnostics, Abbott Laboratories, Abbott Park, IL, United States.
  • Farnsworth CW; Department of Pathology & Immunology, Washington University School of Medicine, St. Louis, MO, United States. Electronic address: cwfarnsworth@wustl.edu.
Clin Biochem ; 107: 24-32, 2022 Sep.
Article in English | MEDLINE | ID: covidwho-1881790
ABSTRACT

OBJECTIVES:

Several studies have demonstrated an association between elevated cardiac biomarkers and adverse outcomes in patients with COVID-19. However, the prognostic and predictive capability of a multimarker panel in a prospectively collected, diverse "all-comers" COVID-19 population has not been fully elucidated. DESIGN &

METHODS:

We prospectively assessed high sensitivity cardiac troponin I (hsTnI), NT-pro B-type Natriuretic Peptide (NT-proBNP), Galectin-3 (Gal-3), and procalcitonin (PCT) in 4,282 serial samples from 358 patients admitted with symptomatic, RT-PCR confirmed SARS-CoV-2 infection. Outcomes examined were 30-day in-hospital mortality and requirement for intubation within 10 days.

RESULTS:

Baseline hsTnI had the highest AUC for predicting 30-day mortality (0.81; 95% CI, 0.73-0.88), followed by NT-proBNP (0.80; 0.74-0.86), PCT (0.77; 0.70-0.84), and Gal-3 (0.68; 0.60-0.76). HsTnI < 3.5 ng/L at baseline identified patients at low risk for in-hospital mortality (NPV 95.9%, sensitivity 97.3%) and 10-day intubation (NPV 90.4%, sensitivity 88.5%). Continuous, log-2 increases in troponin concentration were associated with reduced survival (p < 0.001) on Kaplan-Meier curves and increased risk of 30-day mortality HR 1.26 (1.16-1.37) in univariate and 1.19 (1.03-1.4) in multivariate models. Time-varying doubling of concentrations of hsTnI and Gal-3 were associated with increased risk of 30-day mortality (adjusted HR 1.21, 1.06-1.4, and 1.92, 1.40-2.6).

CONCLUSION:

HsTnI, NT-proBNP, Gal-3, and PCT are elevated at baseline in patients that have worse outcomes from COVID-19. HsTnI was the only independent predictor of 30-day mortality and intubation. Time-varying, doubling in hsTnI and Gal-3 further aided in prognostication of adverse outcomes. These results support the use of hsTnI for triaging patients with COVID-19.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: COVID-19 Type of study: Diagnostic study / Prognostic study Limits: Humans Language: English Journal: Clin Biochem Year: 2022 Document Type: Article Affiliation country: J.clinbiochem.2022.06.002

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Full text: Available Collection: International databases Database: MEDLINE Main subject: COVID-19 Type of study: Diagnostic study / Prognostic study Limits: Humans Language: English Journal: Clin Biochem Year: 2022 Document Type: Article Affiliation country: J.clinbiochem.2022.06.002