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Antimicrobial Agents and Chemotherapy, August 2007, p. 2848-2854, Vol. 51, No. 8
0066-4804/07/$08.00+0     doi:10.1128/AAC.01376-06
Copyright © 2007, American Society for Microbiology. All Rights Reserved.

Dexamethasone as Adjuvant Therapy to Moxifloxacin Attenuates Valve Destruction in Experimental Aortic Valve Endocarditis Due to Staphylococcus aureus{triangledown}

Ioannis Skiadas,1,2* Angelos Pefanis,3 Apostolos Papalois,4 Aspasia Kyroudi,5 Helen Triantafyllidi,6 Thomas Tsaganos,1 and Helen Giamarellou1

Fourth Department of Internal Medicine, University of Athens School of Medicine, University General Hospital Attikon, Athens, Greece,1 Cardiology Department, Hippocration General Hospital, Athens, Greece,2 Third Department of Internal Medicine, University of Athens School of Medicine, Sotiria General Hospital for Chest Diseases, Athens, Greece,3 Experimental Research Department of ELPEN-Pharma, Athens, Greece,4 Department of Histology and Embryology, University of Athens School of Medicine, Athens, Greece,5 Second Department of Cardiology, University of Athens School of Medicine, University General Hospital Attikon, Athens, Greece6

Received 3 November 2006/ Returned for modification 12 March 2007/ Accepted 29 May 2007

Although the beneficial effects of dexamethasone have frequently been investigated in various serious-infection settings, insufficient data on valve histology and cardiac function for infective endocarditis are available. The efficacy of moxifloxacin for the treatment of experimental aortic valve endocarditis due to methicillin-susceptible Staphylococcus aureus and the long-term effects of dexamethasone were evaluated in the current study. Sixty-eight rabbits were randomly assigned to four groups: A, B, C, and D. Group A consisted of 18 animals and functioned as a control group. Groups B and C consisted of 11 and 23 subjects, respectively, which received moxifloxacin for 5 days in a human-like pharmacokinetic simulation. Group D consisted of 16 animals that were administered moxifloxacin plus dexamethasone (0.25 mg/kg of body weight twice a day intravenously). The group B animals were sacrificed a day after the completion of treatment, and group C and D animals were sacrificed after 12 days in order to monitor any possible relapse and allow microbiological, histopathological, and echocardiographic evaluation of the long-term effects of glucocorticoids. No differences in survival, sterilization rates, or inflammatory infiltration and calcification of valve tissue were observed among the treated groups. However, the degrees of valve damage and collagenization were significantly worse, the fibroblast content was higher, and fractional shortening of the left ventricle fluctuated significantly in group C compared to group D (all groups, P < 0.05). We concluded that dexamethasone treatment for experimental S. aureus endocarditis attenuates valve destruction and preserves overall cardiac function without impeding the efficacy of moxifloxacin.


* Corresponding author. Mailing address: Cardiology Department, Hippocration General Hospital, 114 Vas. Sofias Avenue, 11527 Athens, Greece. Phone: 0030-2107483770. Fax: 0030-2107754676. E-mail: iskiadas{at}med.uoa.gr

{triangledown} Published ahead of print on 11 June 2007.


Antimicrobial Agents and Chemotherapy, August 2007, p. 2848-2854, Vol. 51, No. 8
0066-4804/07/$08.00+0     doi:10.1128/AAC.01376-06
Copyright © 2007, American Society for Microbiology. All Rights Reserved.







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