Risk for serious bleeding complications increased for diltiazem versus metoprolol in patients receiving apixaban or rivaroxaban
WEDNESDAY, March 4, 2026 (HealthDay News) — For patients with atrial fibrillation (AF) receiving apixaban or rivaroxaban, use of diltiazem versus metoprolol is associated with an increased risk for serious bleeding complications, according to a study published online Feb. 24 in the Annals of Internal Medicine.
Ghadeer K. Dawwas, Ph.D., from the Vanderbilt University School of Medicine in Nashville, Tennessee, and colleagues compared the risk for bleeding among AF patients using apixaban or rivaroxaban in combination with diltiazem versus metoprolol. A total of 23,000 users of diltiazem and 23,000 users of metoprolol were included in the matched cohort of AF patients.
The researchers found that diltiazem versus metoprolol was associated with a higher risk for bleeding events after propensity score matching (rate difference, 5.4 per 1,000 person-years). With high- versus low-dose diltiazem, the risk for bleeding increased (risk difference, 9.2 versus 2.6 for high- and low-dose, respectively). The estimated risk differences between diltiazem and metoprolol were 0.48 and 0.31 percentage points, respectively, at 12 and six months.
“Our examination of diltiazem dosages indicated a dose-dependent relationship, with higher doses associated with more bleeding,” the authors write.
Abstract/Full Text (subscription or payment may be required)
Long-Term Medication Adherence Tied to Lower Cardiovascular Event Rate in Type 2 Diabetes
High-Dose Omega-3 Linked to A-Fib Risk in Patients With High CVD Risk
Physical Activity Reduces Stroke, Mortality, Regardless of A-Fib
Once-Weekly Oral Islatravir-Lenacapavir Noninferior to Daily B/F/TAF in HIV
Randomized Trial of Early Vitrectomy Feasible for Postoperative Endophthalmitis
28 Percent of U.S. Adults With HTN Eligible for Treatment Under New Guidelines
Enfortumab Vedotin-Pembrolizumab More Effective for MIBC Than Cisplatin-Gemcitabine
Setmelanotide Beneficial in Acquired Hypothalamic Obesity