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DOI 10.1111/j.1742-1241.2008.01988.x

Медицинская библиотека · International journal of clinical practice · 2009

The efficacy and safety of daptomycin vs. vancomycin for the treatment of cellulitis and erysipelas.

Pertel P E, Eisenstein B I, Link A S, Donfrid B, Biermann E J A, Bernardo P, Martone W J

Сравнительное исследованиеСтатьяМногоцентровое исследованиеРандомизированное исследованиеПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

BACKGROUND

Results from previous trials suggest that daptomycin may result in faster clinical improvement than penicillinase-resistant penicillins or vancomycin for patients with complicated skin and skin structure infections.

OBJECTIVE

The objective was to evaluate whether daptomycin treatment of cellulitis or erysipelas would result in faster resolution compared with vancomycin.

DESIGN

The study was a prospective, evaluator-blinded, multi-centre trial. Patients were randomised to receive daptomycin 4 mg/kg once daily or vancomycin according to standard of care for 7-14 days.

PATIENTS: Adults diagnosed with cellulitis or erysipelas requiring hospitalisation and intravenous antibiotic therapy were eligible for enrolment.

RESULTS

The clinical success rates were 94.0% for daptomycin and 90.2% for vancomycin (95% confidence interval for the difference, -6.7%, 14.3%). There were no statistically significant differences between treatment arms in the time to resolution or improvement in any of the predefined clinical end-points. Both daptomycin and vancomycin were well tolerated.

CONCLUSIONS

There was no difference in the rate of resolution of cellulitis or erysipelas among patients treated with daptomycin or vancomycin. Daptomycin 4 mg/kg once daily appeared to be effective and safe for treating cellulitis or erysipelas.

Для цитирования: Pertel P E, Eisenstein B I, Link A S, Donfrid B, Biermann E J A, Bernardo P, Martone W J. The efficacy and safety of daptomycin vs. vancomycin for the treatment of cellulitis and erysipelas.. International journal of clinical practice. 2009. DOI: 10.1111/j.1742-1241.2008.01988.x.

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