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- Publisher Website: 10.1016/j.jinf.2009.11.011
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- PMID: 19961873
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Article: Vancomycin MIC creep in MRSA isolates from 1997 to 2008 in a healthcare region in Hong Kong
Title | Vancomycin MIC creep in MRSA isolates from 1997 to 2008 in a healthcare region in Hong Kong | ||||||
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Authors | |||||||
Keywords | Methicillin-resistant Staphylococcus aureus Molecular epidemiology Multilocus sequence typing Vancomycin | ||||||
Issue Date | 2010 | ||||||
Publisher | WB Saunders Co Ltd. The Journal's web site is located at http://www.elsevier.com/locate/jinf | ||||||
Citation | Journal Of Infection, 2010, v. 60 n. 2, p. 140-145 How to Cite? | ||||||
Abstract | Objectives: To assess whether vancomycin MIC creeps among blood methicillin-resistant Staphylococcus aureus (MRSA) isolates recovered from 5 hospitals in Hong Kong from 1997 to 2008. Methods: Blood cultures MRSA isolates from 1997 to 1999 (period 1), 2004 (period 2) and 2006-2008 (period 3) were retrieved. Etest method was used to determine their vancomycin MIC. The genotypic features were determined by PCR and sequencing. Results: 247 blood MRSA isolates were studied. The vancomycin MIC were 0.375, 0.5, 0.75 and 1 mg/L for 15 (6.1%), 68 (27.5%), 89 (36%) and 75 (30.4%) isolates, respectively. There was an increase in the percentage of isolates with an MIC=1mg/L from 10.4% (5/48) during period 1 to 21.6% (8/37) during period 2 and 38.3% (62/162) during period 3 (period 1 vs. period 3, P<. 0.001). Molecular typing showed that this was due to increased percentages of clonal cluster (CC) 8/SCC. mec III/IIIA (agr group I), CC45/SCC. mec IV/V (agr group IV) and other minor clones with elevated MIC over time. Conclusion: This study found vancomycin MIC creep among blood MRSA isolates over time. As elevated MIC within the susceptible range may reduce vancomycin efficacy, clinical laboratories should adopt methods with the required precision to accurately determine MICs. © 2009 The British Infection Society. | ||||||
Persistent Identifier | http://hdl.handle.net/10722/151693 | ||||||
ISSN | 2023 Impact Factor: 14.3 2023 SCImago Journal Rankings: 2.669 | ||||||
ISI Accession Number ID |
Funding Information: The work is supported by research grants from the Research Fund for the Control of Infectious Diseases (RFCID) of the Health, Welfare and Food Bureau of the Hong Kong SAR Government and from the UDF Project-Research Centre of Emerging Infectious Diseases. | ||||||
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Ho, PL | en_HK |
dc.contributor.author | Lo, PY | en_HK |
dc.contributor.author | Chow, KH | en_HK |
dc.contributor.author | Lau, EHY | en_HK |
dc.contributor.author | Lai, EL | en_HK |
dc.contributor.author | Cheng, VCC | en_HK |
dc.contributor.author | Kao, RY | en_HK |
dc.date.accessioned | 2012-06-26T06:26:43Z | - |
dc.date.available | 2012-06-26T06:26:43Z | - |
dc.date.issued | 2010 | en_HK |
dc.identifier.citation | Journal Of Infection, 2010, v. 60 n. 2, p. 140-145 | en_HK |
dc.identifier.issn | 0163-4453 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/151693 | - |
dc.description.abstract | Objectives: To assess whether vancomycin MIC creeps among blood methicillin-resistant Staphylococcus aureus (MRSA) isolates recovered from 5 hospitals in Hong Kong from 1997 to 2008. Methods: Blood cultures MRSA isolates from 1997 to 1999 (period 1), 2004 (period 2) and 2006-2008 (period 3) were retrieved. Etest method was used to determine their vancomycin MIC. The genotypic features were determined by PCR and sequencing. Results: 247 blood MRSA isolates were studied. The vancomycin MIC were 0.375, 0.5, 0.75 and 1 mg/L for 15 (6.1%), 68 (27.5%), 89 (36%) and 75 (30.4%) isolates, respectively. There was an increase in the percentage of isolates with an MIC=1mg/L from 10.4% (5/48) during period 1 to 21.6% (8/37) during period 2 and 38.3% (62/162) during period 3 (period 1 vs. period 3, P<. 0.001). Molecular typing showed that this was due to increased percentages of clonal cluster (CC) 8/SCC. mec III/IIIA (agr group I), CC45/SCC. mec IV/V (agr group IV) and other minor clones with elevated MIC over time. Conclusion: This study found vancomycin MIC creep among blood MRSA isolates over time. As elevated MIC within the susceptible range may reduce vancomycin efficacy, clinical laboratories should adopt methods with the required precision to accurately determine MICs. © 2009 The British Infection Society. | en_HK |
dc.language | eng | en_US |
dc.publisher | WB Saunders Co Ltd. The Journal's web site is located at http://www.elsevier.com/locate/jinf | en_HK |
dc.relation.ispartof | Journal of Infection | en_HK |
dc.subject | Methicillin-resistant Staphylococcus aureus | en_HK |
dc.subject | Molecular epidemiology | en_HK |
dc.subject | Multilocus sequence typing | en_HK |
dc.subject | Vancomycin | en_HK |
dc.subject.mesh | Anti-Bacterial Agents - Pharmacology | en_US |
dc.subject.mesh | Bacteremia - Microbiology | en_US |
dc.subject.mesh | Dna, Bacterial - Chemistry - Genetics | en_US |
dc.subject.mesh | Hong Kong | en_US |
dc.subject.mesh | Hospitals | en_US |
dc.subject.mesh | Humans | en_US |
dc.subject.mesh | Methicillin-Resistant Staphylococcus Aureus - Drug Effects - Isolation & Purification | en_US |
dc.subject.mesh | Microbial Sensitivity Tests | en_US |
dc.subject.mesh | Polymerase Chain Reaction | en_US |
dc.subject.mesh | Sequence Analysis, Dna | en_US |
dc.subject.mesh | Staphylococcal Infections - Microbiology | en_US |
dc.subject.mesh | Vancomycin - Pharmacology | en_US |
dc.subject.mesh | Vancomycin Resistance | en_US |
dc.title | Vancomycin MIC creep in MRSA isolates from 1997 to 2008 in a healthcare region in Hong Kong | en_HK |
dc.type | Article | en_HK |
dc.identifier.email | Ho, PL:plho@hkucc.hku.hk | en_HK |
dc.identifier.email | Chow, KH:khchowb@hku.hk | en_HK |
dc.identifier.email | Lau, EHY:ehylau@hku.hk | en_HK |
dc.identifier.email | Kao, RY:rytkao@hkucc.hku.hk | en_HK |
dc.identifier.authority | Ho, PL=rp00406 | en_HK |
dc.identifier.authority | Chow, KH=rp00370 | en_HK |
dc.identifier.authority | Lau, EHY=rp01349 | en_HK |
dc.identifier.authority | Kao, RY=rp00481 | en_HK |
dc.description.nature | link_to_subscribed_fulltext | en_US |
dc.identifier.doi | 10.1016/j.jinf.2009.11.011 | en_HK |
dc.identifier.pmid | 19961873 | - |
dc.identifier.scopus | eid_2-s2.0-75549092161 | en_HK |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-75549092161&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 60 | en_HK |
dc.identifier.issue | 2 | en_HK |
dc.identifier.spage | 140 | en_HK |
dc.identifier.epage | 145 | en_HK |
dc.identifier.isi | WOS:000274282400008 | - |
dc.publisher.place | United Kingdom | en_HK |
dc.identifier.f1000 | 13485030 | - |
dc.identifier.scopusauthorid | Ho, PL=7402211363 | en_HK |
dc.identifier.scopusauthorid | Lo, PY=26423725900 | en_HK |
dc.identifier.scopusauthorid | Chow, KH=7202180736 | en_HK |
dc.identifier.scopusauthorid | Lau, EHY=7103086074 | en_HK |
dc.identifier.scopusauthorid | Lai, EL=8238477100 | en_HK |
dc.identifier.scopusauthorid | Cheng, VCC=23670479400 | en_HK |
dc.identifier.scopusauthorid | Kao, RY=7101675499 | en_HK |
dc.identifier.issnl | 0163-4453 | - |