Apixaban vs Enoxaparin for Post-Surgical Extended-Duration Venous Thromboembolic Event Prophylaxis: A Prospective Quality Improvement Study.


Journal

The Journal of urology
ISSN: 1527-3792
Titre abrégé: J Urol
Pays: United States
ID NLM: 0376374

Informations de publication

Date de publication:
10 2022
Historique:
entrez: 9 9 2022
pubmed: 10 9 2022
medline: 14 9 2022
Statut: ppublish

Résumé

Venous thromboembolic events (VTEs) are a major cause of morbidity following abdominopelvic oncologic surgery. Enoxaparin, a subcutaneous injectable low molecular weight heparin, is commonly used for extended-duration VTE prophylaxis (EP), but has been associated with noncompliance. Newer direct oral anticoagulants have not been prospectively studied in the urologic oncology post-discharge setting. We aimed to improve compliance with EP following abdominopelvic oncologic surgery and secondarily test the hypothesis that apixaban is noninferior to enoxaparin for EP. A single-center prospective quality improvement study measuring patient compliance and safety with EP was conducted between August 10, 2020 and September 21, 2021. Baseline data were continuously collected for 6 months, followed by a uniform departmental change from enoxaparin to apixaban. The duration of data collection was determined A total of 161 patients were discharged with enoxaparin (baseline period) and 154 with apixaban (intervention period). Safety events occurred in 3.1% vs 0% of patients receiving enoxaparin and apixaban, respectively. The absolute risk difference of 3.1% (95% CI: 0.043%-5.8%) met the prespecified noninferiority threshold (p=0.028 for apixaban superiority). Compliance events occurred in 33.5% of enoxaparin patients and 14.3% of apixaban patients (p=0.0001). There were fewer compliance events using apixaban for EP than enoxaparin after urologic oncology surgery. Regarding safety, apixaban is noninferior to enoxaparin and may in fact have fewer associated major complications.

Identifiants

pubmed: 36082549
doi: 10.1097/JU.0000000000002788
doi:

Substances chimiques

Anticoagulants 0
Enoxaparin 0
Pyrazoles 0
Pyridones 0
apixaban 3Z9Y7UWC1J

Types de publication

Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

886-895

Subventions

Organisme : NCATS NIH HHS
ID : KL2 TR003168
Pays : United States

Commentaires et corrections

Type : CommentIn
Type : CommentIn

Auteurs

Mary E Westerman (ME)

Department of Urology, The University of Texas, M.D. Anderson Cancer Center, Houston, Texas.
Department of Urology, Louisiana State University Health Science Center-New Orleans, New Orleans, Louisiana.

Kelly K Bree (KK)

Department of Urology, The University of Texas, M.D. Anderson Cancer Center, Houston, Texas.

Pavlos Msaouel (P)

Department of Genitourinary Medical Oncology, The University of Texas, M.D. Anderson Cancer Center, Houston, Texas.

Janet Baack Kukreja (JB)

Department of Urology, The University of Texas, M.D. Anderson Cancer Center, Houston, Texas.
Division of Urology, University of Colorado, Denver, Colorado.

Cheryl Mantaring (C)

Department of Urology, The University of Texas, M.D. Anderson Cancer Center, Houston, Texas.
Department of Nursing, The University of Texas, M.D. Anderson Cancer Center, Houston, Texas.

Innocent Rukundo (I)

Department of Urology, The University of Texas, M.D. Anderson Cancer Center, Houston, Texas.

Martha Garcia Gonzalez (MG)

Department of Healthcare Systems Engineering, The University of Texas, M.D. Anderson Cancer, Houston, Texas Center.

Justin R Gregg (JR)

Department of Urology, The University of Texas, M.D. Anderson Cancer Center, Houston, Texas.

Kelly N Casteel (KN)

Department of Pulmonology, Division of Internal Medicine, The University of Texas, M.D. Anderson Cancer Center, Houston, Texas.

Surena F Matin (SF)

Department of Urology, The University of Texas, M.D. Anderson Cancer Center, Houston, Texas.

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Classifications MeSH