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3704 Impact of Hospital-Acquired Venous Thromboembolism on Surviving Medical Admission: Findings from the Medical Inpatient Thrombosis and Hemostasis Study

Program: Oral and Poster Abstracts
Session: 905. Outcomes Research: Non-Malignant Conditions Excluding Hemoglobinopathies: Poster II
Hematology Disease Topics & Pathways:
Research, Bleeding and Clotting, Epidemiology, Clinical Research, Thromboembolism, Diseases, Thrombotic disorders, Adverse Events
Sunday, December 8, 2024, 6:00 PM-8:00 PM

Karlyn A. Martin, MD, MS1, Andrew Sparks, MS2*, Katherine Wilkinson, MS3*, Ryan Packer4*, Deirdra R Terrell, PhD5, Mansour Gergi, MD6, Augusto Ferraris, MD MPH7*, William A. Wood, MD, MPH8, Allen B Repp, MD MSc9*, Nicholas S Roetker, PHD MS10* and Neil Zakai6

1Division of Hematology and Oncology, University of Vermont Larner College of Medicine, Burlington, VT
2Biomedical Statistics Research Core at the University of Vermont, Burlington, VT
3University of Vermont Larner College of Medicine, Burlington, VT
4Biostatistics Core, Laboratory for Clinical Biochemistry Research, University of Vermont Larner College of Medicine, Burlington, VT
5University of Oklahoma Health Sciences Ctr, Oklahoma City, OK
6Larner College of Medicine at the University of Vermont, Burlington, VT
7University of Washington, Ciudad Autonoma De Buenos Aires, BA, ARG
8Division of Hematology/Oncology, Department of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, NC
9University of Vermont, Burlington, VT
10Chronic Disease Research Group, Hennepin Healthcare Research Institute, Minneapolis, MN

Introduction

Approximately 200,000 venous thromboembolism (VTE) events occur each year during or within 3 months after medical (non-surgical) hospitalizations in the U.S. The consequences of hospital-acquired VTE (HA-VTE, VTE occurring while hospitalized), such as likelihood of dying during admission, are unknown. The objective of this study was to examine the association between HA-VTE and risk of in-hospital mortality.

Methods

Adults admitted to medical services for at least 1 midnight at one of 5 hospital systems from 2016-2022 were included. Admissions for primary diagnosis of VTE were excluded. Each admission with HA-VTE was matched with up to 4 admissions without HA-VTE based on day of hospitalization, age (± 5 years), sex, race and ethnicity, hospital system, level of care (medical services versus intensive care unit [ICU]), calendar year, and COVID-19 status at admission. The primary outcome was in-hospital mortality. We used conditional logistic regression to estimate the association of HA-VTE with in-hospital mortality, adjusting for the matching factors, anticoagulation level at admission (therapeutic, prophylactic, or none), and the Elixhauser Comorbidity Index. We tested whether the association varied by COVID-19 status.

Results

The matched cohort included 2,061 medical admissions with HA-VTE and 7,908 medical admissions without HA-VTE. In the matched admissions, the mean age was 58 years (SD 16), 57.1% identified as male, 54.5% as White race, 26.6% as Black race, 24.0% were admitted to an ICU, and 10.8% were admitted with COVID-19. The mean Elixhauser Comorbidity Index score was 14.3 (SD 18.4) and 12.2 (SD 17.3) in admissions with and without HA-VTE, respectively. In-hospital mortality occurred in 12.4% of HA-VTE admissions and 5.1% of non-HA-VTE admissions. Compared to non-HA admissions, the adjusted odds ratio (OR) for in-hospital mortality with HA-VTE was 2.71 (95% confidence interval [CI] 2.23, 3.29). The association of HA-VTE with in-hospital mortality was similar for admissions with COVID-19 (OR 2.93; 95% CI 2.33, 3.70) and admissions without COVID-19 (OR 2.18; 95% CI 1.49, 3.18; pinteraction = 0.12).

Conclusions

HA-VTE was associated with a nearly 3-fold increased odds of death during hospitalization in a diverse patient cohort from 5 hospital systems. While increased illness severity may account for some of the increased mortality risk, HA-VTE itself or interventions to treat HA-VTE (anticoagulation) likely contribute. Efforts should be made to understand whether reducing HA-VTE can translate to decreased mortality.

Disclosures: Martin: Penumbra: Membership on an entity's Board of Directors or advisory committees; Endovascular Engineering: Consultancy. Terrell: Sanofi: Other: advisory board. Wood: Teledoc Health: Consultancy; Koneksa Health: Consultancy, Current equity holder in publicly-traded company; Genetech: Research Funding; Pfizer: Research Funding; ASH Research Collaborative: Consultancy. Roetker: Fresenius Medical Care, Merck & Co., and the National Institutes of Health: Research Funding.

*signifies non-member of ASH