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Journal of Clinical Microbiology, July 2008, p. 2471-2472, Vol. 46, No. 7
0095-1137/08/$08.00+0 doi:10.1128/JCM.00519-08
Copyright © 2008, American Society for Microbiology. All Rights Reserved.
| LETTER TO THE EDITOR |
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However, what is most striking about the article is the impression that the patient was not managed optimally. Nafcillin/cloxacillin (with/without an aminoglycoside) would be widely accepted as the drug of choice to treat MSSA native valve endocarditis; comparative studies have confirmed cloxacillin/nafcillin to have superior efficacy to vancomycin in patients with MSSA bacteremia (2, 5). Despite confirmation that the offending organism was methicillin sensitive, the patient was first managed on levofloxacin and then switched to vancomycin. Following a poor response to vancomycin, the patient was placed on nafcillin for a very brief period (3 days only), before switching to daptomycin monotherapy. The clinical rationale applied is not explained in the methods section nor taken up in the discussion.
Resistance to daptomycin was documented after 6 to 7 days of treatment. Only after 17 days of antibiotic treatment did the patient receive a prolonged course of nafcillin and gentamicin. Unfortunately, the patient's mitral valve was destroyed by the time infection was brought under control and he underwent successful valve replacement, which remains a suboptimal outcome. It would be interesting to know why first vancomycin and then daptomycin were regarded as the drugs of choice to treat a patient with MSSA bacteremia. According to the clinical trial (3) of daptomycin versus standard therapy of S. aureus bacteremia and right-sided endocarditis referred to in the report by Sakoulas et al., success rates favored daptomycin over vancomycin among patients with methicillin-resistant S. aureus but were higher for MSSA infection treated with an antistaphylococcal penicillin (nafcillin, oxacillin, or flucloxacillin) compared to daptomycin.
Despite the fact that one of the authors is affiliated with the company producing daptomycin, no conflict of interest was declared. We believe it is essential that every publication should include a conflict of interest statement. This article demonstrates the importance of ensuring transparency in order to protect the best interests of our patients.
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Zukile Gqada*
Department of Pathology, Division of Medical Microbiology Faculty of Health Sciences Stellenbosch University and the NHLS Tygerberg Hospital Cape Town, South Africa
Ben Marais
Elizabeth Wasserman
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| * Phone: 27 21 938 4032 Fax: 27 21 938 4005 E-mail: zgqada{at}sun.ac.za |
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In response to the authors' queries, levofloxacin and vancomycin had been administered empirically prior to knowledge of the patient's diagnosis. Nafcillin was indeed used once MSSA bacteria were identified; this was switched to daptomycin in response to persistently positive blood cultures on nafcillin.
We support not only the principle of author transparency, but also the duty, as exemplified by our paper, to report any limitations or other cautionary observations regarding use of antibiotics to treat serious infections. All authors fully declared to the journal any relevant financial relationship when the paper was submitted. These are as follows. G.S. was a consultant for Cubist Pharmaceuticals and Pfizer; had a research grant from Cubist Pharmaceuticals and Pfizer; and was a member of the Speakers Bureau for Cubist Pharmaceuticals, Pfizer, and Wyeth. W.R. had no relevant financial relationships. M.J.R. was a consultant for Cubist Pharmaceuticals, Pfizer, Johnson & Johnson, Astellas, Cerexia/Forrest, and Wyeth; had research grants from Cubist Pharmaceuticals, Pfizer, Johnson & Johnson, Astellas, and Cerexia/Forrest; and was a member of the Speakers Bureau for Cubist Pharmaceuticals, Pfizer, Ortho-McNeil/Johnson & Johnson, and Wyeth. S.P. had no relevant financial relationships. J.A. was employed by Cubist Pharmaceuticals at the time of study and publication. R.C.M. was a consultant to Cubist Pharmaceuticals and Ortho-McNeil/Johnson & Johnson. G.M.E. was a consultant to Cubist Pharmaceuticals and had a research grant from Cubist Pharmaceuticals.
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George Sakoulas*
Department of Medicine Division of Infectious Diseases New York Medical College and Westchester Medical Center Munger Pavilion, Room 245 Valhalla, New York 10595
Warren Rose
Satish Pillai
Jeff Alder
Robert C. Moellering Jr.
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| * Phone: (914) 594-4974 Fax: (845) 361-1156 E-mail: george_sakoulas{at}nymc.edu |
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