Key result
Oral administration of pimobendan at two clinically relevant dosages was not associated with measurable inhibition of platelet function in healthy adult cats.
Why the study?
Concentration-dependent inhibition of feline platelet aggregation by pimobendan has been demonstrated in vitro, but the effect of oral pimobendan administered at therapeutic doses on feline platelet function had not been characterized.
Does orally administered pimobendan inhibit platelet function in healthy adult cats?
Does orally administered pimobendan inhibit platelet function in healthy adult cats?
p-value: p=ns
Oral pimobendan at clinically relevant dosages does not inhibit platelet function in healthy adult cats.
Oral pimobendan unlikely to inhibit feline platelets clinically; leaves open effects in diseased cats or with other PDE inhibitors.
OBJECTIVE: Several phosphodiesterase inhibitors have demonstrable antiplatelet actions when administered to human patients. Concentration-dependent inhibition of feline platelet aggregation by pimobendan has been previously demonstrated in vitro. However, there are no published reports characterizing the effect of oral pimobendan, administered at therapeutic doses, on platelet function in cats. This study aimed to evaluate the effect of orally administered pimobendan on platelet function in healthy adult cats. ANIMALS: 6 healthy purpose-bred adult cats. METHODS: Cats were administered pimobendan orally at a dosage of 0.625 mg/cat (low-dose) twice daily for 1 week, followed by 1.25 mg/cat (high-dose) twice daily for 1 week. Venous blood sampling for platelet testing and plasma drug concentration occurred at baseline, 1 hour postdose on the eighth day of treatment with low-dose pimobendan, 1 hour postdose on the eighth day of treatment with high-dose pimobendan, and after a 1-week washout period. Platelet function was assessed by whole blood aggregometry and by use of a platelet function analyzer (PFA-100®). Friedman tests were used to compare platelet function parameters among the 4 sampling timepoints. RESULTS: After 1 week of treatment, median (range) plasma pimobendan concentrations were 15.1 ng/mL (6.89-20.2 ng/mL) and 32.8 ng/mL (23.3-44.8 ng/mL) in cats receiving low-dose and high-dose pimobendan, respectively. No significant differences in PFA closure time or any aggregometry variable were found among the treatment conditions. CLINICAL RELEVANCE: Pimobendan was not associated with measurable inhibition of platelet function when administered orally to healthy adult cats at 2 clinically relevant dosages.
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Kennerly et al. (2023) studied Healthy (n=6). Pimobendan vs. Baseline was evaluated on Platelet function assessed by whole blood aggregometry and platelet function analyzer (PFA-100) closure time (p=ns). Oral administration of pimobendan at two clinically relevant dosages was not associated with measurable inhibition of platelet function in healthy adult cats.
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