Predictors of adverse prognosis in COVID-19: A systematic review and meta-analysis

Eur J Clin Invest. 2020 Oct;50(10):e13362. doi: 10.1111/eci.13362. Epub 2020 Aug 27.

Abstract

Background: Identification of reliable outcome predictors in coronavirus disease 2019 (COVID-19) is of paramount importance for improving patient's management.

Methods: A systematic review of literature was conducted until 24 April 2020. From 6843 articles, 49 studies were selected for a pooled assessment; cumulative statistics for age and sex were retrieved in 587 790 and 602 234 cases. Two endpoints were defined: (a) a composite outcome including death, severe presentation, hospitalization in the intensive care unit (ICU) and/or mechanical ventilation; and (b) in-hospital mortality. We extracted numeric data on patients' characteristics and cases with adverse outcomes and employed inverse variance random-effects models to derive pooled estimates.

Results: We identified 18 and 12 factors associated with the composite endpoint and death, respectively. Among those, a history of CVD (odds ratio (OR) = 3.15, 95% confidence intervals (CIs) 2.26-4.41), acute cardiac (OR = 10.58, 5.00-22.40) or kidney (OR = 5.13, 1.78-14.83) injury, increased procalcitonin (OR = 4.8, 2.034-11.31) or D-dimer (OR = 3.7, 1.74-7.89), and thrombocytopenia (OR = 6.23, 1.031-37.67) conveyed the highest odds for the adverse composite endpoint. Advanced age, male sex, cardiovascular comorbidities, acute cardiac or kidney injury, lymphocytopenia and D-dimer conferred an increased risk of in-hospital death. With respect to the treatment of the acute phase, therapy with steroids was associated with the adverse composite endpoint (OR = 3.61, 95% CI 1.934-6.73), but not with mortality.

Conclusions: Advanced age, comorbidities, abnormal inflammatory and organ injury circulating biomarkers captured patients with an adverse clinical outcome. Clinical history and laboratory profile may then help identify patients with a higher risk of in-hospital mortality.

Keywords: COVID-19; meta-analysis; outcomes; predictors.

Publication types

  • Meta-Analysis
  • Systematic Review

MeSH terms

  • Acute Disease
  • Acute Kidney Injury / epidemiology*
  • Adrenal Cortex Hormones / therapeutic use
  • Adult
  • Age Factors
  • Aged
  • Aged, 80 and over
  • Betacoronavirus
  • C-Reactive Protein / metabolism
  • COVID-19
  • Cardiovascular Diseases / epidemiology*
  • Cerebrovascular Disorders / epidemiology
  • Coronavirus Infections / epidemiology
  • Coronavirus Infections / metabolism
  • Coronavirus Infections / mortality
  • Coronavirus Infections / therapy*
  • Diabetes Mellitus / epidemiology
  • Female
  • Ferritins / metabolism
  • Fibrin Fibrinogen Degradation Products / metabolism*
  • Heart Diseases
  • Hospital Mortality
  • Hospitalization
  • Humans
  • Hypertension / epidemiology
  • Intensive Care Units
  • Interleukin-6 / metabolism
  • Liver Diseases / epidemiology
  • Lymphopenia / epidemiology
  • Male
  • Middle Aged
  • Neoplasms / epidemiology
  • Obesity / epidemiology
  • Pandemics
  • Pneumonia, Viral / epidemiology
  • Pneumonia, Viral / metabolism
  • Pneumonia, Viral / mortality
  • Pneumonia, Viral / therapy*
  • Procalcitonin / metabolism*
  • Prognosis
  • Pulmonary Disease, Chronic Obstructive / epidemiology
  • Respiration, Artificial
  • SARS-CoV-2
  • Severity of Illness Index
  • Sex Factors
  • Smoking / epidemiology*
  • Thrombocytopenia / epidemiology*
  • Young Adult

Substances

  • Adrenal Cortex Hormones
  • Fibrin Fibrinogen Degradation Products
  • Interleukin-6
  • Procalcitonin
  • fibrin fragment D
  • C-Reactive Protein
  • Ferritins