Evaluation of Low-Dose Aspirin use among Critically Ill Patients with COVID-19: A Multicenter Propensity Score

Abdullah F Al Harthi1,2,3, Ohoud Aljuhani4,5, Ghazwa B Korayem6

  • 1Pharmaceutical Care Department, 48168King Abdulaziz Medical City, Riyadh, Saudi Arabia.

Insights

Low-dose aspirin use in critically ill COVID-19 patients may reduce mortality, especially when continued from pre-hospitalization. However, this benefit must be weighed against a potential increase in bleeding risk.

Area of Science:

  • Critical Care Medicine
  • Pharmacology
  • Infectious Diseases

Background:

  • Aspirin (acetylsalicylic acid) is a widely recognized cardioprotective agent with antiplatelet and anti-inflammatory effects.
  • Existing research has explored aspirin's role in hospitalized COVID-19 patients, but data for critically ill patients were lacking.
  • This study addresses the knowledge gap concerning aspirin's impact on outcomes in intensive care unit (ICU) patients with severe COVID-19.

Purpose of the Study:

  • To evaluate the effect of low-dose aspirin (81-100 mg) on mortality and other outcomes in critically ill COVID-19 patients.
  • To investigate whether continuing aspirin therapy initiated before ICU admission influences patient outcomes.
  • To assess the safety profile of aspirin use in this patient population, focusing on major bleeding events.

Main Methods:

  • A multicenter, retrospective cohort study included critically ill adult patients with confirmed COVID-19 admitted to ICUs.
  • Patients were divided into two groups: those who received aspirin during their ICU stay and those who did not.
  • Propensity score matching (1:1 ratio) was employed to control for confounding variables, with in-hospital mortality as the primary outcome.

Main Results:

  • After propensity score matching, 352 patients were analyzed. In-hospital mortality was significantly lower in the aspirin group (HR 0.73; p=0.03).
  • Patients receiving aspirin showed a trend towards higher odds of major bleeding (OR 2.92; p=0.07), though this was not statistically significant.
  • Subgroup analysis indicated a potential mortality benefit for patients who continued aspirin from pre-hospitalization (HR 0.72; p=0.05), but not for new aspirin initiations in the ICU (HR 1.22; p=0.50).

Conclusions:

  • Continuation of aspirin therapy in critically ill COVID-19 patients already on the medication prior to ICU admission may be associated with reduced mortality.
  • The potential benefit of aspirin must be carefully considered alongside an observed, albeit not statistically significant, increased risk of major bleeding.
  • Further research is recommended to rigorously evaluate the risk-benefit profile of aspirin use in critically ill COVID-19 patients during their ICU stay.
Abstract

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