» Articles » PMID: 26010033

Bleeding, Recurrent Venous Thromboembolism, and Mortality Risks During Warfarin Interruption for Invasive Procedures

Overview
Journal JAMA Intern Med
Specialty General Medicine
Date 2015 May 27
PMID 26010033
Citations 25
Authors
Affiliations
Soon will be listed here.
Abstract

Importance: The risk of bleeding and recurrent venous thromboembolism (VTE) among patients receiving long-term warfarin sodium therapy for secondary VTE prevention who require temporary interruption of anticoagulant therapy for surgery or invasive diagnostic procedures has not been adequately described.

Objective: To describe the rates of clinically relevant bleeding and recurrent VTE among patients in whom warfarin therapy is interrupted for invasive procedures and compare these rates among patients who did and did not receive bridge therapy.

Design, Setting, And Participants: A retrospective cohort study was conducted at Kaiser Permanente Colorado, an integrated health care delivery system. Patients in whom warfarin therapy was interrupted for invasive diagnostic or surgical procedures between January 1, 2006, and March 31, 2012, were identified via queries of administrative data sets. A total of 1812 procedures in 1178 patients met inclusion criteria. Data on outcomes and exposures were collected between June 1, 2005, and April 30, 2012.

Exposures: Use of bridge therapy vs no bridge therapy during warfarin interruption.

Main Outcomes And Measures: Thirty-day clinically relevant bleeding, recurrent VTE, and all-cause mortality. Outcomes were verified via manual review of medical records.

Results: Among the 1178 patients, the mean (SD) age was 66.1 (12.7) years, 830 procedures (45.8%) were in men, and the most common indication for warfarin therapy was deep vein thrombosis (56.3%). Most patients were considered to be at low risk for VTE recurrence at the time of warfarin interruption (1431 procedures [79.0%]) according to the consensus guidelines of the American College of Chest Physicians. Clinically relevant bleeding within 30 days after the procedure in the bridge therapy and non-bridge therapy groups occurred in 15 patients (2.7%) and 2 patients (0.2%), respectively (hazard ratio, 17.2; 95% CI, 3.9-75.1). There was no significant difference in the rate of recurrent VTE between the bridge and non-bridge therapy groups (0 vs 3; P = .56). No deaths occurred in either group.

Conclusions And Relevance: Bridge therapy was associated with an increased risk of bleeding during warfarin therapy interruption for invasive procedures in patients receiving treatment for a history of VTE and is likely unnecessary for most of these patients. Further research is needed to identify patient- and procedure-related characteristics associated with a high risk of perioperative VTE recurrence during warfarin therapy interruption.

Citing Articles

Anticoagulation Stewardship to Bridge the Implementation Gap in Perioperative Anticoagulation Management.

Tafur A, Barnes G, Bhagirath V, Douketis J TH Open. 2024; 8(1):e114-e120.

PMID: 38476982 PMC: 10927368. DOI: 10.1055/a-2259-0911.


Platelet Aggregation Inhibitors and Anticoagulants in Gastroenterological and Visceral Surgical Procedures.

Aulinger B, Saner F, Stark K, Mayerle J, Lange C Dtsch Arztebl Int. 2022; 119(49):851-860.

PMID: 36345703 PMC: 9981979. DOI: 10.3238/arztebl.m2022.0342.


Relevance of Non-Bridging Therapy with Heparin during Temporary Interruption of Direct Oral Anticoagulants in Patients with Cancer-Associated Venous Thromboembolism.

Oyakawa T, Fukumitsu M, Ebihara A, Shiga T Ann Vasc Dis. 2022; 15(2):121-125.

PMID: 35860816 PMC: 9257392. DOI: 10.3400/avd.oa.22-00005.


Periprocedural bridging anticoagulation in patients with venous thromboembolism: A registry-based cohort study.

Barnes G, Li Y, Gu X, Haymart B, Kline-Rogers E, Ali M J Thromb Haemost. 2020; 18(8):2025-2030.

PMID: 32428998 PMC: 7415673. DOI: 10.1111/jth.14903.


Ischemic Stroke Symptoms After Warfarin Reversal With 4-Factor Prothrombin Complex Concentrate Case Report.

Carson L, Price 2nd J Hosp Pharm. 2020; 55(1):69-71.

PMID: 31983770 PMC: 6961148. DOI: 10.1177/0018578718823739.