Anti-Xa Levels in Morbidly Obese Patients Using Apixaban or Rivaroxaban, Before and After Bariatric Surgery

Background Despite limited evidence about the efficacy and safety of anticoagulation in patients post bariatric surgery, both vitamin K antagonists (VKA) and direct-acting oral anticoagulants (DOACs) are commonly prescribed. Aim To evaluate plasma anti-Xa levels of DOACs in morbidly obese (MO) patie...

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Veröffentlicht in:Obesity surgery 2022-03, Vol.32 (3), p.607-614
Hauptverfasser: Kok, Thom, de Boer, Hans, Witteman, Bart, Hovens, Marcel, van Luin, Matthijs, Monajemi, Houshang
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Sprache:eng
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Zusammenfassung:Background Despite limited evidence about the efficacy and safety of anticoagulation in patients post bariatric surgery, both vitamin K antagonists (VKA) and direct-acting oral anticoagulants (DOACs) are commonly prescribed. Aim To evaluate plasma anti-Xa levels of DOACs in morbidly obese (MO) patients before and after a Roux-en-Y gastric bypass (RYGB) procedure. Patients and Methods Retrospective, cross-sectional, and longitudinal study of anti-Xa activity of apixaban or rivaroxaban in MO patients ( N  = 41). Results Preoperative analysis of plasma anti-Xa levels were within the normal range in patients using apixaban ( n  = 29; body mass index [BMI] 44.5 ± 5.1 kg/m 2 ) as well as those using rivaroxaban ( n  = 12; BMI 42.6 ± 5.9 kg/m 2 ). Postoperative anti-Xa levels of apixaban were all within the therapeutic range, whereas anti-Xa levels of rivaroxaban were subtherapeutic in nine out of 14 (64%) patients. Perioperative longitudinal follow-up in patients using apixaban ( n  = 18) showed no significant change in anti-Xa levels after RYGB. Conclusion Plasma anti-Xa levels of apixaban in MO patients remained within the therapeutic range up to a body weight of 144 kg. In patients using rivaroxaban, no statistically significant relation between anti-Xa levels and bodyweight was found. After RYGB, plasma anti-Xa levels of apixaban were unaffected, whereas plasma anti-Xa levels of rivaroxaban tended to become subtherapeutic.
ISSN:0960-8923
1708-0428
DOI:10.1007/s11695-021-05814-y