Apixaban Discontinuation Prior to Major Surgery

Thomas Jefferson University130 enrolled

Overview

The ADIOS study is a prospective, observational study will evaluate one hundred and thirty (130) patients with non-valvular atrial fibrillation who are currently receiving treatment with apixaban as indicated to reduce the risk of stroke or systemic embolism, and who require an elective major surgical or invasive procedure will be included in the study. The purpose of the study is to evaluate the efficacy of the recommended pre-procedure washout period of 48 hours.

This study will estimate for what proportion of patients a 48 hour pre-procedure apixaban discontinuation is sufficient to achieve minimal apixaban plasma levels (less than 30 ng/mL) prior to surgery. The investigators hypothesize that this portion will be 80-95%. All patients will have a blood draw at 48 hours prior to procedure and then a second blood draw on the morning of the procedure to test apixaban plasma and anti-Xa levels. Patients will also receive a follow-up phone call at 30 days to collect information on clinical events.

Study Type

OBSERVATIONAL

Enrollment

130

Conditions

Hemorrhage Thromboembolism

Interventions

Lab tests for plasma levels of apixaban and anti-10a factorOTHER

All patients will have a blood draw at 48 hours prior to elective surgical procedure and then a second blood draw on the morning of the procedure to test apixaban plasma and anti-Xa levels.

Eligibility

Sex: ALLMin age: 18 YearsMax age: 99 Years

Medical Language ↔ Plain English

Inclusion Criteria: * At least 18 years of age * On long term anticoagulation with apixaban for treatment of non-valvular atrial fibrillation or venous thromboembolism * Undergoing elective major surgery or invasive procedure Exclusion Criteria: * Inability to obtain informed consent for the blood sample draws * Any condition precluding collection of follow-up information * Participation in another clinical trial * Apixaban Package Insert Recommendations and Cautions * Women of childbearing potential (WOCBP) must have a negative serum or urine pregnancy test (minimum sensitivity 25 IU/L or equivalent units of HCG) within 24 hours prior to the start of study drug. * Women must not be breastfeeding * WOCBP must agree to follow instructions for method(s) of contraception for the duration of treatment with study drug apixaban plus 5 half-lives of study drug apixaban (approximately 3 days) plus 30 days (duration of ovulatory cycle) for a total of 33 days post- treatment completion. * Males who are sexually active with WOCBP must agree to follow instructions for method(s) of contraception for the duration of treatment with study drug apixaban plus 5 half-lives of the study drug (approximately 3 days) plus 90 days (duration of sperm turnover) for a total of 93 days post-treatment completion. * Azoospermic males and WOCBP who are continuously not heterosexually active are exempt from contraceptive requirements. However WOCBP must still undergo pregnancy testing as described. * The safety and efficacy of apixaban have not been studied in patients with prosthetic heart valves. Therefore, use is not recommended in these patients.

Locations (1)

Thomas Jefferson University

Philadelphia, Pennsylvania, United States

Outcomes

Primary Outcomes

Apixaban plasma concentration

Determine whether the recommended 48 hour pre-procedure discontinuation period is sufficient to achieve minimal apixaban plasma concentration of \< 30 ng/ml prior to surgery

Time frame: Prior to elective surgery

Secondary Outcomes

Anti-10a apixaban plasma concentration

Assess changes in anti-Xa apixaban levels following apixaban discontinuation but prior to the procedure

Time frame: Prior to elective surgery

30 day outcomes assessment

Incidence of major events within 30 days including bleeding events, arterial thromboembolic events, and deaths caused by bleeding or thrombosis.

Time frame: Up to 30 days post- procedure

Data from ClinicalTrials.gov

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