Factors affecting the pharmacokinetics of vancomycin in children admitted to the intensive care unit (icu) of the Red Cross War Memorial Children's Hospital (RCWMCH).

dc.contributor.advisorMugabo, Pierre
dc.contributor.authorAkunne, Onyinye Onyeka
dc.date.accessioned2023-05-09T13:27:04Z
dc.date.accessioned2024-05-15T07:16:47Z
dc.date.available2023-05-09T13:27:04Z
dc.date.available2024-05-15T07:16:47Z
dc.date.issued2023
dc.descriptionDoctor Pharmaceuticae - DPharmen_US
dc.description.abstractVancomycin is a glycopeptide antibiotic that inhibits bacterial cell wall synthesis by binding to the D-alanyl-D-alanine terminal end of cell wall precursor units preventing the elongation and cross-linkage of the peptidoglycan. Vancomycin is used to treat infections with gram-positive bacteria such as methicillin-resistant Staphylococcus aureus (S. aureus), coagulase-negative staphylococci and penicillin-resistant Streptococcus pneumoniae (S. pneumoniae). It is a time-dependent drug, and its efficacy depends on the duration of pathogen exposure to vancomycin. Low plasma concentration may lead to treatment failure and the re-emergence of bacterial resistance. Vancomycin is known to cause adverse effects at high concentrations. Therefore, it is necessary to monitor plasma concentrations to maintain vancomycin concentration within the therapeutic window. Vancomycin is mainly administered as an intravenous (IV) infusion as it is poorly absorbed from the gastrointestinal system.en_US
dc.identifier.urihttps://hdl.handle.net/10566/15039
dc.language.isoenen_US
dc.publisherUniversity of the Western Capeen_US
dc.rights.holderUniversity of the Western Capeen_US
dc.subjectPharmacodynamicsen_US
dc.subjectPaediatricen_US
dc.subjectPharmaceuticalsen_US
dc.subjectPharmacokineticsen_US
dc.subjectCape Townen_US
dc.titleFactors affecting the pharmacokinetics of vancomycin in children admitted to the intensive care unit (icu) of the Red Cross War Memorial Children's Hospital (RCWMCH).en_US

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