Literature DB >> 18212253

Clinical experience with daptomycin for the treatment of patients with documented gram-positive septic arthritis.

Graeme N Forrest1, Brian J Donovan, Kenneth C Lamp, Lawrence V Friedrich.   

Abstract

BACKGROUND: Septic arthritis is considered a rheumatologic emergency that can lead to joint destruction and long-term impairment of joint function. Daptomycin is bactericidal in vitro against Staphylococcus aureus, the primary pathogen associated with septic arthritis.
OBJECTIVE: To describe the use of daptomycin in patients with septic arthritis.
METHODS: Data were collected as part of the Cubicin Outcomes Registry and Experience (CORE) program, a retrospective, observational, multicenter study, to describe the clinical use of daptomycin. Efficacy at the end of daptomycin therapy was determined by each center's investigator(s) as cure, improved, failure, or nonevaluable. Patients who had a diagnosis of septic arthritis, excluding concomitant osteomyelitis, as well as a positive culture by needle aspirate or deep tissue biopsy, were selected from the combined 2005 and 2006 CORE database.
RESULTS: Twenty-two patients were included in this analysis. S. aureus was the most common pathogen isolated, with the majority resistant to methicillin. All patients received an antibiotic prior to daptomycin; in 7 patients, at least one of the prior antibiotics was continued with daptomycin. Almost two-thirds of patients received an antibiotic with daptomycin; rifampin was the most common. The median final dose and duration of daptomycin therapy were 5 mg/kg (range 3-6.3) and 22 days (range 3-52), respectively. Eighty-two percent of patients received daptomycin while admitted to a hospital; however, 68% received at least part of their daptomycin therapy as an outpatient. The outcomes of cure or improved were reported in 41% and 50% of the patients, respectively. Two adverse events were reported; neither was considered to be related to daptomycin.
CONCLUSIONS: Daptomycin appeared to be effective when used as part of a treatment regimen for septic arthritis. These results require verification via a prospective clinical trial.

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Year:  2008        PMID: 18212253     DOI: 10.1345/aph.1K535

Source DB:  PubMed          Journal:  Ann Pharmacother        ISSN: 1060-0280            Impact factor:   3.154


  6 in total

1.  Should daptomycin-rifampin combinations for MSSA/MRSA isolates be avoided because of antagonism?

Authors:  C Stein; O Makarewicz; C Forstner; S Weis; S Hagel; B Löffler; M W Pletz
Journal:  Infection       Date:  2016-01-21       Impact factor: 3.553

2.  Relationship of in vitro synergy and treatment outcome with daptomycin plus rifampin in patients with invasive methicillin-resistant Staphylococcus aureus infections.

Authors:  Warren E Rose; Andrew D Berti; Jacob B Hatch; Dennis G Maki
Journal:  Antimicrob Agents Chemother       Date:  2013-05-06       Impact factor: 5.191

3.  Septic arthritis in the native joint.

Authors:  Meghan B Brennan; Jennifer L Hsu
Journal:  Curr Infect Dis Rep       Date:  2012-10       Impact factor: 3.725

Review 4.  Clinical management of septic arthritis.

Authors:  Katie A Sharff; Eric P Richards; John M Townes
Journal:  Curr Rheumatol Rep       Date:  2013-06       Impact factor: 4.592

5.  Daptomycin versus vancomycin for osteoarticular infections due to methicillin-resistant Staphylococcus aureus (MRSA): a nested case-control study.

Authors:  S Y Liang; H N Khair; J R McDonald; H M Babcock; J Marschall
Journal:  Eur J Clin Microbiol Infect Dis       Date:  2013-11-03       Impact factor: 5.103

6.  Daptomycin to bone and joint infections and prosthesis joint infections: a systematic review.

Authors:  João Paulo Telles; Juliette Cieslinski; Felipe Francisco Tuon
Journal:  Braz J Infect Dis       Date:  2019-06-14       Impact factor: 3.257

  6 in total

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