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P2Y12 inhibitors in Staphylococcus aureus bacteraemia: current evidence and clinical implications
Emanuele Rando1, Luis Eduardo López-Cortés1, Jesús Rodríguez-Baño1
1Unidad Clínica de Enfermedades Infecciosas y Microbiología, Hospital Universitario Virgen Macarena, Departamento de Medicina, Facultad de Medicina, Universidad de Sevilla, Instituto de Biomedicina de Sevilla (IBiS)/Consejo Superior de Investigaciones Científicas (CSIC), Seville, Spain; Centro de Investigación Biomédica en Red de Enfermedades Infecciosas (CIBERINFEC), Madrid, Spain.
Abstract:
Staphylococcus aureus bacteraemia presents a substantial clinical burden, with high rates of morbidity and mortality. Despite its severity, therapeutic advancements have been small in the past decade, prompting exploration of adjunctive treatment strategies against S aureus bacteraemia. Among these strategies, P2Y12 inhibitors have gained attention due to their potential antistaphylococcal and platelet-modulating effects. Preclinical studies suggest that ticagrelor enhances platelet-mediated bacterial killing and interferes with S aureus metabolism. Clinical data indicate a potential protective effect of ticagrelor in S aureus bacteraemia, as compared with that of clopidogrel. Nevertheless, clopidogrel itself appears to offer protective effects, when compared with no treatment. However, these findings are based exclusively on non-randomised studies conducted in individuals with cardiovascular disease. Two randomised trials currently in development could provide further evidence on the therapeutic role of P2Y12 inhibitors in S aureus bacteraemia. Future research should also focus on preventive strategies and identifying populations at high risk who could benefit from such interventions.
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