International Journal of Infectious Diseases (Sep 2014)

Blood stream infections due to OXA-48-like carbapenemase-producing Enterobacteriaceae: treatment and survival

  • Ilker Inanç Balkan,
  • Gökhan Aygün,
  • Selda Aydın,
  • Sibel Islak Mutcalı,
  • Zehra Kara,
  • Mert Kuşkucu,
  • Kenan Midilli,
  • Vicdan Şemen,
  • Şükrü Aras,
  • Mücahit Yemişen,
  • Bilgül Mete,
  • Reşat Özaras,
  • Neşe Saltoğlu,
  • Fehmi Tabak,
  • Recep Öztürk

DOI
https://doi.org/10.1016/j.ijid.2014.05.012
Journal volume & issue
Vol. 26, no. C
pp. 51 – 56

Abstract

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Background: Blood stream infections (BSIs) due to carbapenem-resistant Enterobacteriaceae (CRE) are associated with high hospital mortality rates and present a tremendous challenge to clinicians. The optimal treatment remains undefined. We aimed to investigate the risk factors for mortality and the correlation between different treatment modalities and outcomes. Methods: The clinical characteristics and treatment outcomes of a cohort of 36 patients with BSIs due to CRE were investigated and a retrospective nested case–control study of surviving and non-surviving patients was conducted. Results: Fifty percent of the cases were male and the mean patient age was 54.9 ± 15.8 years. Klebsiella pneumoniae was the etiological agent in 26 cases (72.2%), Escherichia coli in eight (22.2%), and Enterobacter aerogenes in two (5.5%). All strains were phenotypically positive for carbapenemase activity and all except two (one E. coli and one K. pneumoniae) yielded both blaOXA-48 carbapenemases and blaCTX-M-type extended-spectrum beta-lactamases (ESBLs) in PCR products. The 14-day, 28-day, and all-cause in-hospital mortality rates were 41.6%, 50%, and 58.3%, respectively. The median time to death was 8 days (range 2–52 days). No significant differences were observed between survivors and non-survivors in terms of baseline characteristics, comorbid conditions, etiologies, or sources of bacteremia, however hematological malignancies (p = 0.015) and prolonged neutropenia (p = 0.044) were more common in non-survivors. Microbiological eradication and clinical response within 7 days were two major determinants of 28-day attributable mortality (p = 0.001 and p = 0.001, adjusted r2 = 0.845). Colistin-based dual combinations, and preferably triple combinations, were associated with significantly better outcomes when compared to non-colistin-based regimens (p < 0.001). Time to active treatment had a significant effect on the course of infection (p = 0.014). Conclusion: Earlier active treatment with colistin based regimens and microbiological and clinical response wthin 7 days are major predictors of survival in cases of BSIs due to CRE. Rectal screening offers the advantage of earlier recognition and prompt empirical treatment.

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