Thromb Haemost 2015; 114(04): 685-694
DOI: 10.1160/TH15-02-0108
Coagulation and Fibrinolysis
Schattauer GmbH

All-cause mortality and use of antithrombotics within 90 days of discharge in acutely ill medical patients

Charles E. Mahan
1   Presbyterian Healthcare Services, University of New Mexico, Albuquerque, New Mexico, USA
,
Larry E. Fields
2   Janssen Scientific Affairs, LLC, Raritan, New Jersey, USA
,
Roger M. Mills
3   Janssen Research and Development, LLC, Raritan-Titusville, New Jersey, USA
,
Judith J. Stephenson
4   HealthCore, Inc., Wilmington, Delaware, USA
,
An-Chen Fu
4   HealthCore, Inc., Wilmington, Delaware, USA
,
Maxine D. Fisher
5   Vector Oncology, Memphis, Tennessee, USA
,
Alex C. Spyropoulos
6   North Shore/LIJ Health System; Hofstra North Shore/LIJ School of Medicine Manhasset, New York, USA
› Author Affiliations
Further Information

Publication History

Received: 10 February 2015

Accepted after major revision: 19 May 2015

Publication Date:
29 November 2017 (online)

Summary

Conflicting evidence exists regarding predictors of and antithrombotic benefit on mortality in hospitalised acutely-ill medical patients. We compared mortality risk within 90 days post-discharge among medically ill patients who did and did not receive antithrombotics. This retrospective claims analysis included patients40 years with nonsurgical hospitalisation2 days between 2005 and 2009 using the HealthCore Integrated Research Database. Antithrombotic use (i.e. anticoagulants and antiplatelets) post-discharge was captured from pharmacy claims. All-cause mortality was determined from Social Security Death Index; cause of death was identified from National Death Index database. Kaplan-Meier survival curves were generated and hazard ratios (HR) for mortality risk were estimated using Cox proportional hazards models. Patients prescribed anticoagulants or antiplatelets post-discharge had lower risk of short-term mortality. For the anticoagulant model, the most significant predictors of mortality were malignant/benign neoplasms (hazard ratio [HR] 1.6, 95 % confidence interval [CI] 1.5–1.7), liver disease (HR 1.6, 95 % CI 1.5–1.7), anticoagulant omission (HR 1.6, 95 % CI 1.4–1.8), gastrointestinal or respiratory tract intubations (HR 1.5, 95 % CI 1.3–1.7), and blood dyscrasias (HR 1.4, 95 % CI 1.4–1.5). For the antiplatelet model, the most significant predictors of mortality were antiplatelet omission (HR 3.7, 95 % CI 3.3–4.1), liver disease (HR 1.6, 95 % CI 1.4–1.7), malignant/benign neoplasms (HR 1.6, 95 % CI 1.5–1.6), gastrointestinal or respiratory tract intubations (HR 1.5, 95 % CI 1.3–1.7), and blood dyscrasias (HR 1.4, 95 % CI 1.4–1.5). These mortality risk factors may guide future studies assessing potential benefits of antithrombotics in specific subsets of patients.

 
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