Key result
Co-administration of a proton pump inhibitor significantly decreased average trough blood dabigatran concentrations compared to dabigatran alone (55.5 vs. 83 ng/mL; P<0.001).
Why the study?
Does proton pump inhibitor co-administration reduce blood dabigatran concentrations in patients with non-valvular atrial fibrillation?
RCT (n=34)
Open-label
Randomized
Does proton pump inhibitor co-administration reduce blood dabigatran concentrations in patients with non-valvular atrial fibrillation?
Absolute Event Rate: 55.5% vs 83%
p-value: p=< 0.001
Co-administration of proton pump inhibitors significantly decreases trough and peak blood dabigatran concentrations in patients with non-valvular atrial fibrillation, suggesting a potential reduction in bioavailability.
PPI co-administration may reduce dabigatran efficacy in NVAF; confirms pharmacokinetic interaction in RCT.
Background Dabigatran is a direct thrombin inhibitor used to decrease the risk of ischemic stroke in patients with non‐valvular atrial fibrillation (NVAF). Its prodrug, dabigatran etexilate (DE) is often co‐administrated with a proton pump inhibitor (PPI) because of its adverse effects on the gastrointestinal tract. Drug‐drug interactions between DE and PPIs in daily clinical practice have not been fully elucidated. Methods Changes in blood dabigatran concentration (DC) were investigated using the dilute thrombin time test in a randomized, open‐label, two‐period crossover study including 34 Japanese patients with NVAF receiving dabigatran therapy with or without PPI. Results The average trough DC was significantly higher without PPI than with PPI (83 ± 42.3 vs. 55.5 ± 24.6 ng/mL, respectively; P < 0.001). Similarly, the average peak DC was significantly higher without PPI than with PPI (184.1 ± 107.7 vs. 124 ± 59.2 ng/mL, respectively; P = 0.0029). The average ratio of DC change at the trough and peak levels did not differ significantly among the three PPI types. Conclusions PPI administration significantly decreased the trough and peak DCs in patients with NVAF. Therefore, when prescribing PPIs for patients with NVAF in a clinical setting, the possibility that the bioavailability of dabigatran may decrease should be considered.
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Kuwayama et al. (2017) conducted an RCT in Non-valvular atrial fibrillation (NVAF) (n=34). Proton pump inhibitor (PPI) vs. Without PPI was evaluated on Average trough blood dabigatran concentration (ng/mL) (p=< 0.001). Co-administration of a proton pump inhibitor significantly decreased average trough blood dabigatran concentrations compared to dabigatran alone (55.5 vs. 83 ng/mL; P<0.001).
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