The risk vs. benefit calculus of anticoagulation in patients with ibrutinib-related atrial fibrillation.
Ruchi PatelArushi SinghZhiying MengAbigail S BaldridgeDaniel AddisonNausheen AkhterPublished in: Leukemia & lymphoma (2023)
For ibrutinib-related atrial fibrillation (IRAF), guidelines for anticoagulation do not exist. We sought to describe stroke, bleeding, and anticoagulation rates among patients with IRAF. We performed a single-center retrospective review of 168 patients treated with ibrutinib followed from 2013 to 2022. Over a median follow-up of 6.4 years, 44 (26.0%) patients developed IRAF of which 38 (86.4%) had a CHA2DS2-VASc ≥2 and 7 (15.9%) had a HAS-BLED ≥3. Anticoagulation was initiated in 20 (45.5%) without a clear pattern in scores, risk factors, or cumulative dose, besides having another reason for anticoagulation. Few patients with IRAF developed non-hemorrhagic CVA ( n = 3, 6.8%) or significant bleeding ( n = 3, 6.8%). Among those with each adverse outcome, 2 in each group were anticoagulated and all were older than 65 years old. In conclusion, decisions for anticoagulation vary widely and patients who are elderly or with HTN may be most at risk for CVA or significant bleed.
Keyphrases
- atrial fibrillation
- catheter ablation
- oral anticoagulants
- left atrial
- left atrial appendage
- end stage renal disease
- direct oral anticoagulants
- heart failure
- venous thromboembolism
- chronic kidney disease
- risk factors
- ejection fraction
- newly diagnosed
- percutaneous coronary intervention
- peritoneal dialysis
- prognostic factors
- coronary artery disease
- chronic lymphocytic leukemia
- community dwelling
- left ventricular
- subarachnoid hemorrhage
- acute coronary syndrome
- clinical practice
- electronic health record
- blood brain barrier