Effect of Antiplatelet Therapy on Acute Respiratory Distress Syndrome and Mortality in Critically Ill Patients: A Meta-Analysis

PLoS One. 2016 May 16;11(5):e0154754. doi: 10.1371/journal.pone.0154754. eCollection 2016.

Abstract

Background: Antiplatelet agents are commonly used for cardiovascular diseases, but their pleiotropic effects in critically ill patients are controversial. We therefore performed a meta-analysis of cohort studies to investigate the effect of antiplatelet therapy in the critically ill.

Methods: Nine cohort studies, retrieved from PubMed and Embase before November 2015, involving 14,612 critically ill patients and 4765 cases of antiplatelet users, were meta-analysed. The main outcome was hospital or 30-day mortality. Secondary outcome was acute respiratory distress syndrome (ARDS) or acute lung injury (ALI). Random- or fixed-effect models were taken for quantitative synthesis of the data.

Results: Antiplatelet therapy was associated with decreased mortality (odds ratio (OR) 0.61; 95% confidence interval (CI), 0.52-0.71; I2 = 0%; P <0. 001) and ARDS/ALI (OR 0.64; 95% CI, 0.50-0.82; I2 = 0%; P <0. 001). In every stratum of subgroups, similar findings on mortality reduction were consistently observed in critically ill patients.

Conclusions: Antiplatelet therapy is associated with reduced mortality and lower incidence of ARDS/ALI in critically ill patients, particularly those with predisposing conditions such as high-risk surgery, trauma, pneumonia, and sepsis. However, it remains unclear whether similar findings can be observed in the unselected and broad population with critical illness.

Publication types

  • Meta-Analysis

MeSH terms

  • Cohort Studies
  • Comorbidity
  • Critical Illness / epidemiology
  • Critical Illness / mortality*
  • Humans
  • Incidence
  • Odds Ratio
  • Platelet Aggregation Inhibitors / adverse effects*
  • Publication Bias
  • Respiratory Distress Syndrome / epidemiology
  • Respiratory Distress Syndrome / mortality*

Substances

  • Platelet Aggregation Inhibitors

Grants and funding

The National Natural Science Foundation of China (Grant numbers: 81071588, URLs: https://isisn.nsfc.gov.cn) provided support for this study.