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Carbapenem‐resistant K lebsiella pneumoniae infections in kidney transplant recipients: a case–control study
Author(s) -
Simkins J.,
Muggia V.,
Cohen H.W.,
Minamoto G.Y.
Publication year - 2014
Publication title -
transplant infectious disease
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.69
H-Index - 67
eISSN - 1399-3062
pISSN - 1398-2273
DOI - 10.1111/tid.12276
Subject(s) - medicine , klebsiella pneumoniae , diabetes mellitus , carbapenem , antibiotics , kidney transplantation , transplantation , intensive care medicine , microbiology and biotechnology , biochemistry , escherichia coli , biology , gene , endocrinology , chemistry
Abstract Introduction Carbapenem‐resistant Klebsiella pneumoniae ( CRKP ) infections have emerged as a significant challenge in solid organ transplantation. CRKP infections in other patient populations have been associated with higher mortality, when compared to infections caused by carbapenem‐sensitive K. pneumoniae ( CSKP ). Aims The aim of this study was to evaluate possible risk factors, clinical characteristics, and outcomes of CRKP infections compared with CSKP infections in kidney transplant recipients ( KTR ). Methods We retrospectively investigated 13 CRKP infections and 39 CSKP infections in KTR (2006–2010). Results CRKP was not significantly associated with age, gender, or comorbidities. CRKP infections were significantly associated with recent exposure to broad‐spectrum antibiotics and were more likely to have been managed on an inpatient basis and to have required source control. CRKP was significantly associated with earlier mortality. Six of 13 (46%) patients with CRKP infection, and none of the patients with CSKP infection, died within 6.5 months of infection onset. Although cases and controls did not differ significantly with respect to diabetes, all patients (100%, n  = 9) who died during the study had diabetes, while 58% of the 43 survivors had diabetes ( P  = 0.02). Conclusion In conclusion, CRKP compared with CSKP is associated with greater risk of mortality. Investigations on ways to better prevent CRKP are urgently needed.

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