An outbreak of Burkholderia cepacia complex in the paediatric unit of a tertiary care hospital
Autor: | Sunil Kumar, Jayanthi Shastri, Lona Dash, Swapna Mali, Vikas Gautam |
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Jazyk: | angličtina |
Rok vydání: | 2017 |
Předmět: |
0301 basic medicine
Microbiology (medical) paediatric Burkholderia cenocepacia Isolation (health care) 030106 microbiology Immunology lcsh:QR1-502 India 030501 epidemiology Microbiology lcsh:Microbiology law.invention 03 medical and health sciences Immunology and Microbiology (miscellaneous) law medicine Immunology and Allergy Blood culture Polymerase chain reaction General Immunology and Microbiology medicine.diagnostic_test biology integumentary system outbreak business.industry Outbreak nosocomial biology.organism_classification Burkholderia cepacia complex Infectious Diseases Amikacin Multilocus sequence typing 0305 other medical science business medicine.drug |
Zdroj: | Indian Journal of Medical Microbiology, Vol 35, Iss 2, Pp 216-220 (2017) |
ISSN: | 1998-3646 0255-0857 |
Popis: | Introduction: Burkholderia cepacia complex (Bcc) has emerged as a serious nosocomial pathogen worldwide especially in patients with indwelling catheters and cystic fibrosis. Bcc is a common contaminant of pharmaceutical products. We describe an outbreak of Bcc bacteraemia amongst children admitted in Paediatric Intensive Care Unit (PICU) and paediatric ward at a tertiary care hospital, Mumbai, in Western India. Materials and Methods: Blood culture samples from paediatric patients yielded growth of non-fermenting, oxidase positive, motile, Gram negative bacilli (NFGNB) (76/909) over a period of 8 months. Based on conventional biochemical tests and antimicrobial susceptibility testing, these isolates were provisionally identified as Bcc. The increased, repeated and continued isolation of Bcc alerted the possibility of an outbreak confined to PICU and paediatric ward. Active surveillance was undertaken to trace the source and contain the outbreak. Isolates were subjected to recA polymerase chain reaction (PCR) and Expanded multilocus sequence typing (EMLST). Results: Surveillance revealed the presence of Bcc on the upper surface of rubber stopper of sealed multidose amikacin vials. Isolates from blood culture and rubber stoppers were confirmed as Bcc by recA PCR. EMLST revealed that these isolates shared an identical novel sequence type 824 proving clonality. Timely interventions instituted led to control of the outbreak. Conclusion: This study highlights the importance of identification and molecular characterization of Bcc to establish its role in infection and outbreak. |
Databáze: | OpenAIRE |
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