Journal of Global Antimicrobial Resistance (Jun 2022)

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

  • 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

Journal volume & issue
Vol. 29
pp. 476 – 482

Abstract

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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.

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