In vitro activity of tigecycline against clinical isolates of carbapenem resistant Acinetobacter baumannii complex in Pretoria, South Africa

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dc.contributor.author Ahmed, Nahid H.
dc.contributor.author Baba, Kamaldeen A.
dc.contributor.author Clay, Cornelius G.
dc.contributor.author Lekalakala, M. Ruth
dc.contributor.author Hoosen, Anwar Ahmed
dc.date.accessioned 2012-11-23T10:04:35Z
dc.date.available 2012-11-23T10:04:35Z
dc.date.issued 2012-05-03
dc.description.abstract BACKGROUND: The presence of multi-drug resistant Acinetobacter baumannii raises a big therapeutic challenge in our hospital. Tigecycline, a new glycylcycline with expanded broad spectrum of activity against multi-drug resistant organisms was recently licensed in South Africa. AIM: The aim of this study was to evaluate the in vitro activity of tigecycline against carbapenem resistant A. baumannii complex. METHODS: Consecutive clinical isolates of carbapenem resistant A. baumannii complex were collected between February and July 2010. Species identification and susceptibility testing was performed by Vitek-2 colorimetric compact system with Advanced Expert System (AES). Strains were tested for carbapenemase production by the modified Hodge test, according to the Clinical and Laboratory Standards Institute (CLSI) guidelines. RESULTS: A total of 232 carbapenem resistant clinical isolates of A. baumannii complex were collected over the six months study period; 217 (93.5%) of these were modified Hodge test positive. All isolates were susceptible to colistin and 174 (78%) susceptible to amikacin whilst 20 (9%) were susceptible to ciprofloxacin. For tigecycline 169 (75.8%) were fully susceptible, 37 (16.6%) intermediately resistant and only 17 (7.6%) were fully resistant. None of the carbapenem resistant isolates were susceptible to ampicillin, amoxicillin/clavullanic acid, piperacillin/tazobactam, cefuroxime, cefuroxime axetil, cefoxitin, cefepime or nitrofurantoin. CONCLUSION: All carbapenem resistant isolates were found to be fully susceptible to colistin; amikacin and tigecycline susceptibility was 78% and 76% respectively. Treatment options for infections due to carbapenem and multi-drug resistant A. baumannii organisms are limited and hence tigecycline and amikacin may be considered. The properties of tigecycline i.e. stability, safety, low toxicity, non cross-resistance with other antibiotics and its efficacy against multi-drug resistant A. baumannii isolates make it a good choice. However, ongoing monitoring of A. baumannii susceptibility to tigecycline is needed. en_US
dc.description.uri http://www.biomedcentral.com/1756-0500/5/215 en_US
dc.identifier.citation Ahmed et al.: In vitro activity of tigecycline against clinical isolates of carbapenem resistant Acinetobacter baumannii complex in Pretoria, South Africa. BMC Research Notes 2012 5:215. en_US
dc.identifier.other 10.1186/1756-0500-5-215
dc.identifier.uri http://hdl.handle.net/2263/20471
dc.language.iso en en_US
dc.publisher BioMed Central en_US
dc.rights © 2012 Ahmed et al.; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License. en_US
dc.subject Tigecycline en_US
dc.subject Carbapenems en_US
dc.subject Acinetobacter baumannii complex en_US
dc.subject.lcsh Multidrug-resistant (MDR) en
dc.title In vitro activity of tigecycline against clinical isolates of carbapenem resistant Acinetobacter baumannii complex in Pretoria, South Africa en_US
dc.type Article en_US


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