PMID- 23952463 OWN - NLM STAT- MEDLINE DCOM- 20140121 LR - 20181202 IS - 1742-1241 (Electronic) IS - 1368-5031 (Linking) VI - 67 IP - 9 DP - 2013 Sep TI - Sequential intravenous/oral moxifloxacin monotherapy for complicated skin and skin structure infections: a meta-analysis of randomised controlled trials. PG - 834-42 LID - 10.1111/ijcp.12174 [doi] AB - OBJECTIVES: The presumed superiority of moxifloxacin for the treatment of complicated skin and skin structure infections (cSSSIs) is based on laboratory data, but has not yet been established on clinical grounds. The aim of this meta-analysis was to evaluate the efficacy and safety of sequential intravenous (i.v.)/oral (p.o.) moxifloxacin monotherapy for the treatment of cSSSIs. METHODS: Randomised controlled trials (RCTs) published prior to November 2012 were systematically retrieved from PubMed, MEDLINE, EMBASE, ScienceDirect, ClinicalTrials.gov and the Cochrane Central Register of Controlled Trials. Finally, a meta-analysis of all RCTs eligible for inclusion criteria was performed. RESULTS: Three studies that enrolled 2255 patients were included in the meta-analysis. There were no statistically significant differences between patients given moxifloxacin and those given other antibiotics with regard to clinical success rate [1667 patients, odds ratio (OR) = 0.83, 95% confidence interval (CI) 0.63 to 1.09, p = 0.18], bacteriological success rate (bacteriological success rates: 1502 patients, OR = 0.90, 95% CI 0.68-1.18, p = 0.45) or mortality (2207 patients, OR = 1.96, 95% CI 0.79-4.88, p = 0.15). Significantly, more overall adverse events (AEs) were associated with the use of moxifloxacin than with other antibiotics (2207 patients, OR = 1.21, 95%CI 1.00-1.45, p = 0.04). However, there was no statistically significant difference in the occurrence of drug-related AEs, serious AEs or serious drug-related AEs between patients given moxifloxacin and those given other antibiotics. CONCLUSION: Sequential i.v./p.o. moxifloxacin monotherapy is an effective and relatively safe option for the treatment of cSSSIs. Other benefits of moxifloxacin may make it a more viable option compared with the currently used regimens. CI - (c) 2013 John Wiley & Sons Ltd. FAU - Chen, F AU - Chen F AD - Department of Pharmacy, Zhujiang Hospital, Southern Medical University, Guangzhou, China. FAU - Zheng, N AU - Zheng N FAU - Wang, Y AU - Wang Y FAU - Wen, J L AU - Wen JL FAU - Tu, W F AU - Tu WF FAU - Du, Y Q AU - Du YQ FAU - Lin, J M AU - Lin JM LA - eng PT - Journal Article PT - Meta-Analysis PT - Review PL - India TA - Int J Clin Pract JT - International journal of clinical practice JID - 9712381 RN - 0 (Anti-Bacterial Agents) RN - 0 (Aza Compounds) RN - 0 (Fluoroquinolones) RN - 0 (Quinolines) RN - U188XYD42P (Moxifloxacin) SB - IM CIN - Int J Clin Pract. 2013 Sep;67(9):820-2. PMID: 23952460 MH - Administration, Oral MH - Anti-Bacterial Agents/*administration & dosage/adverse effects MH - Aza Compounds/*administration & dosage/adverse effects MH - Drug Therapy, Combination MH - Fluoroquinolones MH - Humans MH - Infusions, Intravenous MH - Middle Aged MH - Moxifloxacin MH - Quinolines/*administration & dosage/adverse effects MH - Randomized Controlled Trials as Topic MH - Skin Diseases, Bacterial/*drug therapy/mortality MH - Treatment Outcome EDAT- 2013/08/21 06:00 MHDA- 2014/01/22 06:00 CRDT- 2013/08/20 06:00 PHST- 2012/12/28 00:00 [received] PHST- 2013/03/13 00:00 [accepted] PHST- 2013/08/20 06:00 [entrez] PHST- 2013/08/21 06:00 [pubmed] PHST- 2014/01/22 06:00 [medline] AID - 10.1111/ijcp.12174 [doi] PST - ppublish SO - Int J Clin Pract. 2013 Sep;67(9):834-42. doi: 10.1111/ijcp.12174.