Abstract |
Retapamulin is a semisynthetic pleuromutilin compound with in vitroactivity against Gram-positive bacteria, no cross-resistance to other classes of antimicrobial agents in current use and a low potential for development of resistance. A 1% ointment formulation has been developed for clinical use, and a placebo-controlled trial of impetigo in 210 patients produced significantly higher rates of clinical and microbiological success compared with placebo - 85.6 versus 52.1% and 91.2 versus 50.9%, respectively. Additional comparative studies in over 1900 patients showed noninferiority to topical fusidic acid and oral cephalexin and a low frequency of adverse events. In 2007, retapamulin was approved in the USA for topical treatment of impetigo caused by Streptococcus pyogenes and methicillin-susceptible Staphylococcus aureus, and in the EU for topical treatment of impetigo and infected wounds caused by S. pyogenes and S. aureus, with approvals including adults and children over 9 months of age.
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Authors | Michael R Jacobs |
Journal | Future microbiology
(Future Microbiol)
Vol. 2
Issue 6
Pg. 591-600
(Dec 2007)
ISSN: 1746-0921 [Electronic] England |
PMID | 18041900
(Publication Type: Clinical Trial, Journal Article)
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Chemical References |
- Anti-Bacterial Agents
- Bridged Bicyclo Compounds, Heterocyclic
- Diterpenes
- Polycyclic Compounds
- pleuromutilin
- retapamulin
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Topics |
- Administration, Topical
- Adult
- Anti-Bacterial Agents
(administration & dosage)
- Bridged Bicyclo Compounds, Heterocyclic
(administration & dosage, chemical synthesis, therapeutic use)
- Child
- Child, Preschool
- Diterpenes
(chemistry)
- Humans
- Impetigo
(drug therapy, microbiology, pathology)
- Infant
- Polycyclic Compounds
- Skin Diseases, Infectious
(drug therapy, etiology)
- Staphylococcal Skin Infections
(drug therapy, etiology)
- Treatment Outcome
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