Association Between Asymptomatic Proximal Deep Vein Thrombosis and Mortality in Acutely Ill Medical Patients

Author:

Raskob Gary E.1ORCID,Spyropoulos Alex C.2ORCID,Cohen Alexander T.3,Weitz Jeffrey I.4,Ageno Walter5,De Sanctis Yoriko6,Lu Wentao7,Xu Jianfeng7,Albanese John8,Sugarmann Chiara8,Weber Traci8ORCID,Lipardi Concetta8,Spiro Theodore E.9,Barnathan Elliot S.8ORCID

Affiliation:

1. Hudson College of Public HealthUniversity of Oklahoma Health Sciences Center Oklahoma City OK

2. The Feinstein Institutes for Medical Research and Zucker School of Medicine at Hofstra/Northwell Anticoagulation and Clinical Thrombosis Services Department of Medicine Northwell Health at Lenox Hill Hospital New York NY

3. Department of Hematological Medicine Guys and St Thomas/NHS Foundation Trust, King's College London London United Kingdom

4. McMaster University, and the Thrombosis and Atherosclerosis Research Institute Hamilton Ontario Canada

5. Department of Medicine and Surgery University of Insubria Varese Italy

6. Statistics and Data Insights Bayer US LLC Whippany NJ

7. Biostatistics Department Janssen Research and Development LLC Raritan NJ

8. Cardiovascular Clinical Development Janssen Research and Development, LLC Raritan NJ

9. Bayer US, LLC Whippany NJ

Abstract

Background Asymptomatic proximal deep vein thrombosis (DVT) is an end point frequently used to evaluate the efficacy of anticoagulant thromboprophylaxis in medical patients. Recently, the clinical relevance of asymptomatic DVT has been challenged. Methods and Results The objective of this study was to evaluate the relationship between asymptomatic proximal DVT and all‐cause mortality (ACM) using a cohort analysis of a randomized trial for the prevention of venous thromboembolism (VTE) in acutely ill medical patients. Patients who received at least 1 dose of study drug and had an adequate compression ultrasound examination of the legs on either day 10 or day 35 were categorized into 1 of 3 cohorts: no VTE, asymptomatic proximal DVT, or symptomatic DVT. Cox proportional hazards model, with adjustment for significant independent predictors of mortality, were used to compare the incidences of ACM. Of the 7036 patients, 6776 had no VTE, 236 had asymptomatic DVT, and 24 had symptomatic VTE. The incidence of ACM was 4.8% in patients without VTE. Both asymptomatic proximal DVT (mortality, 11.4%; hazard ratio [HR], 2.31; 95% CI, 1.52–3.51; P <0.0001) and symptomatic VTE (mortality, 29.2%; HR, 9.42; 95% CI, 4.18–21.20; P <0.0001) were independently associated with significant increases in ACM. The analysis was post hoc, and ultrasound results were not available for all patients. Adjustment for baseline variables significantly associated with ACM may not fully compensate for differences. Conclusions Asymptomatic proximal DVT is associated with higher ACM than no VTE and remains a relevant end point to evaluate the efficacy of anticoagulant thromboprophylaxis in medical patients. Registration URL: https://www.clinicaltrials.gov ; Unique identifier: NCT00571649.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Cardiology and Cardiovascular Medicine

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