Antimicrobial pharmacodynamics: critical interactions of 'bug and drug'
By G. Drusano. Nature Reviews Microbiology, 2004
953 citations recorded by the source corpus.
Subfields: Clinical Biochemistry, Molecular Medicine, Pharmacology
View Paper: https://www.semanticscholar.org/paper/e530a1cbf47f0acf177ef31bf45c83bfc7ff3b23
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In Clinical Biochemistry
In Pharmacology
Citations in the corpus
- Diagnosis and Management of Complicated Intra-Abdominal Infection in Adults and Children: Guidelines by the Surgical Infection Society and the Infectious Diseases Society of America (2010, neutral): “Pharmacokinetic-pharmacodynamic properties of specific antibiotics should be considered in selecting an adequate dosage regimen [144].”
- Infective Endocarditis in Adults: Diagnosis, Antimicrobial Therapy, and Management of Complications: A Scientific Statement for Healthcare Professionals From the American Heart Association (2015, background): “Both β-lactam therapy alone and combination therapy with nafcillin and an aminoglycoside for only 2 weeks have been effective in patients with uncomplicated right-sided IE caused by S aureus91; monotherapy with a β-lactam would be selected for use in cases of uncomplicated IE.92 Of interest, right-s”
- DALI: defining antibiotic levels in intensive care unit patients: are current β-lactam antibiotic doses sufficient for critically ill patients? (2014, background): “Whereas animal in vivo studies have defined an f T>MIC between 40% and 70% of the dosing interval as being necessary [11], retrospective clinical evaluations have suggested that larger drug exposures are required, with β-lactam concentrations up to 4 times the MIC for the entire dosing interval bein”
- Therapeutic monitoring of vancomycin for serious methicillin-resistant Staphylococcus aureus infections: A revised consensus guideline and review by the American Society of Health-System Pharmacists, the Infectious Diseases Society of America, the Pediatric Infectious Diseases Society, and the Socie (2020, methodology): “The early AUC/MIC target ratios derived in animal models were based on the AUC value from 0 to 24 hours.(3,4) More recent clinical assessments that identified a link between AUC/MIC ratio and outcomes also assessed the AUC values achieved early in the course of therapy.”