Open Access具OXA‐72抗藥基因之廣泛耐藥鮑曼不動桿菌群突發的快速控制與分子流行病學研究
Author(s) -
Lin WeiRu,
Lu PoLiang,
Siu LeungKei,
Chen TunChieh,
Lin ChunYu,
Hung ChingTzu,
Chen YenHsu
Publication year - 2011
Publication title -
the kaohsiung journal of medical sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.439
H-Index - 36
eISSN - 2410-8650
pISSN - 1607-551X
DOI - 10.1016/j.kjms.2010.11.004
Subject(s) - outbreak , medicine , acinetobacter baumannii , infection control , intensive care unit , isolation (microbiology) , intensive care , pulsed field gel electrophoresis , microbiology and biotechnology , tigecycline , antibiotics , emergency medicine , genotype , virology , intensive care medicine , pseudomonas aeruginosa , bacteria , biology , biochemistry , gene , genetics
Extensively drug‐resistant Acinetobacter baumannii (XDRAb) emerges as an important pathogen of health care–associated infections and outbreaks worldwide. During January and February 2006, there was a hospital‐wide outbreak of XDRAb at a medical center in Taiwan. Without limiting the usage of carbapenems or the closure of any ward, this outbreak was effectively controlled. We investigated the molecular epidemiology and reported the infection control experiences. XDRAb is defined as A baumannii that is resistant to multiple antibiotics but susceptible to tigecycline and polymyxin B. During the outbreak, the clinical and environmental XDRAb isolates were collected and studied by antimicrobial susceptibility testing, pulsed‐field gel electrophoresis, and polymerase chain reaction for Verona integron‐encoded metallo‐beta‐lactamases, imipenemases, and oxacillinases (OXA). Our measures to control the outbreak included private room isolation of patients until there were three successive negative cultures, reinforcement of contact precautions, daily environmental cleansing with room‐dedicated cleaning tools and sodium hypochlorite, and careful auditing of adherence. During the outbreak, 32 clinical XDRAb isolates came from 13 patients who were hospitalized in four intensive care units and three wards. Most (7 of 13, 53.8%) cases were associated with a surgical intensive care unit. The results from pulsed‐field gel electrophoresis study indicated that all isolates were of one genotype. All 32 isolates harbored IS Aba 1‐ bla OxA‐51‐like and bla OxA‐72 genes. After this outbreak till August 2010, further incidences of XDRAb were sporadic cases of XDRAb with different clones and did not reach the level of outbreak. To our knowledge, this is the first reported hospital‐wide outbreak caused by OXA‐72 carbapenemase–producing A baumannii in the Asia‐Pacific region, with successful and sustained control. Although the source or vehicle of the outbreak was not identified, our results suggest that a hospital‐wide outbreak can be successfully managed with strict infection control measures, and that the limitation of the use of carbapenems and closure of wards may not be necessary.