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DOI 10.3390/jcm13154289

Медицинская библиотека · Journal of clinical medicine · 2024

Clinical Significance and Patterns of Potential Drug-Drug Interactions in Cardiovascular Patients: Focus on Low-Dose Aspirin and Angiotensin-Converting Enzyme Inhibitors.

Anfinogenova Nina D, Stepanov Vadim A, Chernyavsky Alexander M, Karpov Rostislav S, Efimova Elena V, Novikova Oksana M, Trubacheva Irina A, Falkovskaya Alla Y, Maksimova Aleksandra S, Ryumshina Nadezhda I, Shelkovnikova Tatiana A, Ussov Wladimir Y, Vaizova Olga E, Popov Sergey V, Repin Alexei N

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Аннотация

Objective

This study assessed the patterns and clinical significance of potential drug-drug interactions (pDDIs) in patients with diseases of the cardiovascular system.

Methods

Electronic health records (EHRs), established in 2018-2023, were selected using the probability serial nested sampling method (n = 1030). Patients were aged 27 to 95 years (65.0% men). Primary diagnosis of COVID-19 was present in 17 EHRs (1.7%). Medscape Drug Interaction Checker was used to characterize pDDIs. The Mann-Whitney U test and chi-square test were used for statistical analysis.

Results

Drug numbers per record ranged from 1 to 23 in T-List and from 1 to 20 in P-List. In T-List, 567 drug combinations resulted in 3781 pDDIs. In P-List, 584 drug combinations resulted in 5185 pDDIs. Polypharmacy was detected in 39.0% of records in T-List versus 65.9% in P-List (p-value < 0.05). The rates of serious and monitor-closely pDDIs due to 'aspirin + captopril' combinations were significantly higher in P-List than in T-List (p-value < 0.05). The rates of serious pDDIs due to 'aspirin + enalapril' and 'aspirin + lisinopril' combinations were significantly lower in P-List compared with the corresponding rates in T-List (p-value < 0.05). Serious pDDIs due to administration of aspirin with fosinopril, perindopril, and ramipril were detected less frequently in T-List (p-value < 0.05).

Conclusions

Obtained data may suggest better patient adherence to 'aspirin + enalapril' and 'aspirin + lisinopril' combinations, which are potentially superior to the combinations of aspirin with fosinopril, perindopril, and ramipril. An abundance of high-order pDDIs in real-world clinical practice warrants the development of a decision support system aimed at reducing pharmacotherapy-associated risks while integrating patient pharmacokinetic, pharmacodynamic, and pharmacogenetic information.

Для цитирования: Anfinogenova Nina D, Stepanov Vadim A, Chernyavsky Alexander M, Karpov Rostislav S, Efimova Elena V, Novikova Oksana M, Trubacheva Irina A, Falkovskaya Alla Y, Maksimova Aleksandra S, Ryumshina Nadezhda I, Shelkovnikova Tatiana A, Ussov Wladimir Y, Vaizova Olga E, Popov Sergey V, Repin Alexei N. Clinical Significance and Patterns of Potential Drug-Drug Interactions in Cardiovascular Patients: Focus on Low-Dose Aspirin and Angiotensin-Converting Enzyme Inhibitors.. Journal of clinical medicine. 2024. DOI: 10.3390/jcm13154289.
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