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Association between rectal colonisation by Klebsiella pneumoniae carbapenemase-producing K. pneumoniae and mortality: a prospective, observational study

Authors :
Ángela Cano
Belén Gutiérrez-Gutiérrez
Isabel Machuca
Julián Torre-Giménez
Azahara Frutos-Adame
Manuel García-Gutiérrez
Marina Gallo-Marín
Irene Gracia-Ahufinger
María J. Artacho
Alejandra M. Natera
Elena Pérez-Nadales
Juan José Castón
Sabrina Mameli
Francisco Gómez-Delgado
Carmen de la Fuente
Inmaculada Salcedo
Jesús Rodríguez-Baño
Luis Martínez-Martínez
Julián Torre-Cisneros
Source :
Journal of Global Antimicrobial Resistance, Vol 29, Iss , Pp 476-482 (2022)
Publication Year :
2022
Publisher :
Elsevier, 2022.

Abstract

ABSTRACT: Objectives: We evaluated the association of Klebsiella pneumoniae carbapenemase-producing K. pneumoniae (KPC-Kp) rectal colonisation with crude mortality and whether this association is independent of the risk of KPC-Kp infection. Methods: This was a prospective cohort study of patients followed-up 90 days after a study of rectal colonisation. Cox regression was used to study the variables associated with crude mortality. Sensitivity analyses for 90-day crude mortality in different subcohorts were performed. Results: A total of 1244 patients (1078 non-colonised and 166 colonised) were included. None of the non-colonised patients and 78 (47.0%) of the colonised patients developed KPC-Kp infection. The 90-day crude mortality was 18.0% (194/1078) in non-colonised patients and 41.6% (69/166) in colonised patients. Rectal colonisation was not associated with crude mortality [hazard ratio (HR) = 1.03, 95% confidence interval (CI) 0.69–1.54; P = 0.85] when the model was adjusted for severe KPC-Kp infection [INCREMENT-CPE score (ICS) > 7]. KPC-Kp infection with ICS > 7 was associated with an increased risk of all-cause mortality (HR = 2.21, 95% CI 1.35–3.63; P = 0.002). In the sensitivity analyses, KPC-Kp colonisation was not associated with mortality in any of the analysed subcohorts, including patients who did not develop KPC-Kp infection (HR = 0.93, 95% CI 0.60–1.43; P = 0.74). Conclusion: KPC-Kp rectal colonisation was not associated with crude mortality. Mortality increased when colonised patients developed severe KPC-Kp infection (ICS > 7). Rectal colonisation was a necessary although insufficient condition to die from a KPC-Kp infection.

Details

Language :
English
ISSN :
22137165
Volume :
29
Issue :
476-482
Database :
Directory of Open Access Journals
Journal :
Journal of Global Antimicrobial Resistance
Publication Type :
Academic Journal
Accession number :
edsdoj.f6b6530998149fd8a7e7c89840635db
Document Type :
article
Full Text :
https://doi.org/10.1016/j.jgar.2021.10.024