4.6 Review

Ways to Improve Insights into Clindamycin Pharmacology and Pharmacokinetics Tailored to Practice

Journal

ANTIBIOTICS-BASEL
Volume 11, Issue 5, Pages -

Publisher

MDPI
DOI: 10.3390/antibiotics11050701

Keywords

antibiotic; clindamycin; bacterial infections; pharmacokinetics; special patient populations; CYP450 enzymes; drug-drug interactions

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Given the increase in bacterial resistance and the decrease in the development of new antibiotics, the appropriate use of old antimicrobials has become more important. Clindamycin, a lincosamide antibiotic, is commonly used for the treatment of bacterial infections. However, there is still limited knowledge on the pharmacokinetics and drug interactions in special populations. Further research is needed to provide precise strategies for personalized medicine.
Given the increase in bacterial resistance and the decrease in the development of new antibiotics, the appropriate use of old antimicrobials has become even more compulsory. Clindamycin is a lincosamide antibiotic approved for adults and children as a drug of choice for systemic treatment of staphylococcal, streptococcal, and gram-positive anaerobic bacterial infections. Because of its profile and high bioavailability, it is commonly used as part of an oral multimodal alternative for prolonged parenteral antibiotic regimens, e.g., to treat bone and joint or prosthesis-related infections. Clindamycin is also frequently used for (surgical) prophylaxis in the event of beta-lactam allergy. Special populations (pediatrics, pregnant women) have altered cytochrome P450 (CYP)3A4 activity. As clindamycin is metabolized by the CYP3A4/5 enzymes to bioactive N-demethyl and sulfoxide metabolites, knowledge of the potential relevance of the drug's metabolites and disposition in special populations is of interest. Furthermore, drug-drug interactions derived from CYP3A4 inducers and inhibitors, and the data on the impact of the disease state on the CYP system, are still limited. This narrative review provides a detailed survey of the currently available literature on pharmacology and pharmacokinetics and identifies knowledge gaps (special patient population, drug-drug, and drug-disease interactions) to describe a research strategy for precision medicine.

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