Extended Anticoagulation after Radical Cystectomy Using Direct Acting Oral Anticoagulants: A Single-Institutional Experience.

anticoagulation reversal cystectomy, quality of health care

Journal

Urology practice
ISSN: 2352-0787
Titre abrégé: Urol Pract
Pays: United States
ID NLM: 101635343

Informations de publication

Date de publication:
Sep 2022
Historique:
medline: 8 5 2023
pubmed: 5 5 2023
entrez: 5 5 2023
Statut: ppublish

Résumé

Extended prophylactic anticoagulation therapy with enoxaparin 40 mg daily is effective in reducing the incidence of venous thromboembolism (VTE) after radical cystectomy. In an effort to improve compliance, we modified our extended anticoagulation options to direct oral anticoagulants (DOAs; eg apixaban 2.5 mg twice daily or rivaroxaban 10 mg daily). This study assesses our experience with extended VTE prophylaxis using DOAs. This is a retrospective review that included all patients who underwent radical cystectomy at our institution between January 2007 and June 2021. Multivariable logistic regression models were constructed to test the hypothesis that use of extended DOAs is similar to enoxaparin in terms of VTE events and risk of gastrointestinal bleeding. In 657 patients, the median age was 71 years. Of the 101 patients who received extended VTE prophylaxis, 46 (45.5%) patients received rivaroxaban/apixaban. At 90 days of followup, 40 patients (7.2%) who did not receive extended prophylaxis on discharge developed a VTE compared to 2 patients (3.6%) in the enoxaparin group and 0 patients in the DOA group (p=0.11). Seven patients (1.3%) who did not receive extended anticoagulation developed gastrointestinal bleeding compared to 0 patients in the enoxaparin group and 1 (2.2%) in the DOA group (p=0.60). On multivariable analysis, both enoxaparin and DOAs were associated with similar reductions in the risk of developing VTE compared to controls (enoxaparin: OR 0.33, p=0.09 and DOAs: OR 0.19, p=0.15). These preliminary data suggest that oral apixaban and rivaroxaban are acceptable alternatives to enoxaparin with similar safety and efficacy profiles.

Identifiants

pubmed: 37145730
doi: 10.1097/UPJ.0000000000000330
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

451-458

Auteurs

Kassem S Faraj (KS)

Department of Urology, Mayo Clinic, Scottsdale, Arizona.

Adri Durant (A)

Department of Urology, Mayo Clinic, Scottsdale, Arizona.

David Mauler (D)

Mayo Clinic, Phoenix, Arizona.

Mouneeb Choudry (M)

Mayo Clinic, Phoenix, Arizona.

Rohan Singh (R)

Department of Urology, Mayo Clinic, Scottsdale, Arizona.

Yu-Hui Chang (YH)

Mayo Clinic, Phoenix, Arizona.

Mark D Tyson (MD)

Department of Urology, Mayo Clinic, Scottsdale, Arizona.

Classifications MeSH