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

dc.contributor.authorAhmed, Nahid H.
dc.contributor.authorBaba, Kamaldeen A.
dc.contributor.authorClay, Cornelius G.
dc.contributor.authorLekalakala, M. Ruth
dc.contributor.authorHoosen, Anwar Ahmed
dc.date.accessioned2012-11-23T10:04:35Z
dc.date.available2012-11-23T10:04:35Z
dc.date.issued2012-05-03
dc.description.abstractBACKGROUND: 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.urihttp://www.biomedcentral.com/1756-0500/5/215en_US
dc.identifier.citationAhmed 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.other10.1186/1756-0500-5-215
dc.identifier.urihttp://hdl.handle.net/2263/20471
dc.language.isoenen_US
dc.publisherBioMed Centralen_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.subjectTigecyclineen_US
dc.subjectCarbapenemsen_US
dc.subjectAcinetobacter baumannii complexen_US
dc.subject.lcshMultidrug-resistant (MDR)en
dc.titleIn vitro activity of tigecycline against clinical isolates of carbapenem resistant Acinetobacter baumannii complex in Pretoria, South Africaen_US
dc.typeArticleen_US

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