Venous thromboembolism among people with HIV: Design, implementation, and findings of a centralized adjudication system in clinical care sites across the United States.


Journal

Journal of acquired immune deficiency syndromes (1999)
ISSN: 1944-7884
Titre abrégé: J Acquir Immune Defic Syndr
Pays: United States
ID NLM: 100892005

Informations de publication

Date de publication:
21 Nov 2023
Historique:
medline: 21 11 2023
pubmed: 21 11 2023
entrez: 21 11 2023
Statut: aheadofprint

Résumé

People with HIV (PWH) are at increased risk for venous thromboembolism (VTE). We conducted this study to characterize VTE including provoking factors among PWH in the current treatment era. We included PWH with VTE between 2010-2020 at six sites in the CFAR Network of Integrated Clinical Systems (CNICS) cohort. We ascertained for possible VTE using diagnosis, VTE-related imaging, and VTE-related procedure codes, followed by centralized adjudication of primary data by expert physician reviewers. We evaluated sensitivity and positive predictive value of VTE ascertainment approaches. VTEs were classified by type and anatomic location. Reviewers identified provoking factors such as hospitalizations, infections, and other potential predisposing factors such as smoking. We identified 557 PWH with adjudicated VTE: 239 (43%) had pulmonary embolism (PE) with or without deep venous thrombosis (DVT), and 318 (57%) had DVT alone. Ascertainment with clinical diagnoses alone missed 6% of VTEs identified with multiple ascertainment approaches. DVTs not associated with intravenous lines were most often in the proximal lower extremities. Among PWH with VTE, common provoking factors included recent hospitalization (n=134, 42%), infection (n=133, 42%), and immobilization/bed rest (n=78, 25%). Only 57 (10%) PWH had no provoking factor identified. Smoking (46%), HIV viremia (27%) and injection drug use (22%) were also common. We conducted a robust adjudication process that demonstrated the benefits of multiple ascertainment approaches followed by adjudication. Provoked VTEs were more common than unprovoked events. Non-traditional and modifiable potential predisposing factors such as viremia and smoking were common.

Sections du résumé

BACKGROUND BACKGROUND
People with HIV (PWH) are at increased risk for venous thromboembolism (VTE). We conducted this study to characterize VTE including provoking factors among PWH in the current treatment era.
METHODS METHODS
We included PWH with VTE between 2010-2020 at six sites in the CFAR Network of Integrated Clinical Systems (CNICS) cohort. We ascertained for possible VTE using diagnosis, VTE-related imaging, and VTE-related procedure codes, followed by centralized adjudication of primary data by expert physician reviewers. We evaluated sensitivity and positive predictive value of VTE ascertainment approaches. VTEs were classified by type and anatomic location. Reviewers identified provoking factors such as hospitalizations, infections, and other potential predisposing factors such as smoking.
RESULTS RESULTS
We identified 557 PWH with adjudicated VTE: 239 (43%) had pulmonary embolism (PE) with or without deep venous thrombosis (DVT), and 318 (57%) had DVT alone. Ascertainment with clinical diagnoses alone missed 6% of VTEs identified with multiple ascertainment approaches. DVTs not associated with intravenous lines were most often in the proximal lower extremities. Among PWH with VTE, common provoking factors included recent hospitalization (n=134, 42%), infection (n=133, 42%), and immobilization/bed rest (n=78, 25%). Only 57 (10%) PWH had no provoking factor identified. Smoking (46%), HIV viremia (27%) and injection drug use (22%) were also common.
CONCLUSION CONCLUSIONS
We conducted a robust adjudication process that demonstrated the benefits of multiple ascertainment approaches followed by adjudication. Provoked VTEs were more common than unprovoked events. Non-traditional and modifiable potential predisposing factors such as viremia and smoking were common.

Identifiants

pubmed: 37988634
doi: 10.1097/QAI.0000000000003339
pii: 00126334-990000000-00323
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2023 Wolters Kluwer Health, Inc. All rights reserved.

Auteurs

Heidi M Crane (HM)

University of Washington, Seattle, WA, USA.

Robin M Nance (RM)

University of Washington, Seattle, WA, USA.

Stephanie A Ruderman (SA)

University of Washington, Seattle, WA, USA.

Lara Haidar (L)

University of Washington, Seattle, WA, USA.

Mark W Tenforde (MW)

University of Washington, Seattle, WA, USA.

Susan R Heckbert (SR)

University of Washington, Seattle, WA, USA.

Matthew J Budoff (MJ)

University of Manitoba, Manitoba, CA.

Andrew W Hahn (AW)

University of Washington, Seattle, WA, USA.

Lydia N Drumright (LN)

University of Washington, Seattle, WA, USA.

Jimmy Ma (J)

University of Washington, Seattle, WA, USA.

L S Mixson (LS)

University of Washington, Seattle, WA, USA.

William B Lober (WB)

University of Washington, Seattle, WA, USA.

Gregory S Barnes (GS)

University of Washington, Seattle, WA, USA.

Justin McReynolds (J)

University of Washington, Seattle, WA, USA.

Engi F Attia (EF)

University of Washington, Seattle, WA, USA.

Inga Peter (I)

Lundquist Institute at Harbor-UCLA, Torrance, CA USA.

Tesfaye Moges (T)

Mount Sinai University, New York NY, USA.

Laura Bamford (L)

Mount Sinai University, New York NY, USA.

Edward Cachay (E)

Mount Sinai University, New York NY, USA.

William C Mathews (WC)

Mount Sinai University, New York NY, USA.

Katerina Christopolous (K)

University of California, San Diego, CA, USA.

Peter W Hunt (PW)

University of California, San Diego, CA, USA.

Sonia Napravnik (S)

University of California, San Francisco, CA, USA.

Jeanne Keruly (J)

University of North Carolina, Chapel Hill, NC, USA.

Richard D Moore (RD)

University of North Carolina, Chapel Hill, NC, USA.

Greer Burkholder (G)

Johns Hopkins University, Baltimore, Maryland, USA.

Amanda L Willig (AL)

Johns Hopkins University, Baltimore, Maryland, USA.

Sara Lindstrom (S)

University of Washington, Seattle, WA, USA.

Bridget M Whitney (BM)

University of Washington, Seattle, WA, USA.

Michael S Saag (MS)

Johns Hopkins University, Baltimore, Maryland, USA.

Mari M Kitahata (MM)

University of Washington, Seattle, WA, USA.

Kristina A Crothers (KA)

University of Washington, Seattle, WA, USA.

Joseph Ac Delaney (JA)

University of Washington, Seattle, WA, USA.

Classifications MeSH