| Literature DB >> 16254727 |
Katsumi Shigemura1, Kazushi Tanaka, Mitsuru Yasuda, Satoshi Ishihara, Tetsuro Muratani, Takashi Deguchi, Tetsuro Matsumoto, Sadao Kamidono, Yuzo Nakano, Soichi Arakawa, Masato Fujisawa.
Abstract
A prospective, randomized trial in which 236 patients received oral levofloxacin, either at 600 mg/day for 1 day (n = 124) or 300 mg/day for 3 days (n = 112). Urinalysis, plasma white blood cell count (WBC) (per mm3), and C reactive protein (CRP) (mg/dl) levels were checked before prostate biopsy (PBX), on the day after PBX, and on the seventh day after PBX. Two patients (1.61%) who received 600 mg for 1 day and 2 patients (1.79%) who received 300 mg for 3 days had febrile infectious complications. There was no statistically significant difference between levofloxacin at 600 mg for 1 day and levofloxacin at 300 mg for 3 days regarding the elevation of WBC and CRP. We can perform PBX safely with levofloxacin at 600 mg for 1 day as prophylaxis and recommend this method from the point of view of the decrease of antibiotic-resistant strains.Entities:
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Year: 2005 PMID: 16254727 DOI: 10.1007/s00345-005-0024-4
Source DB: PubMed Journal: World J Urol ISSN: 0724-4983 Impact factor: 4.226