Empiric Therapy With Carbapenem-Sparing Regimens For Bloodstream Infections Due To Extended-Spectrum Beta-Lactamase-Producing Enterobacteriaceae: Results From The Increment Cohort
Tarih
2017Yazar
Raquel Palacios-Baena, Zaira
Gutierrez-Gutierrez, Belen
Calbo, Esther
Almirante, Benito
Viale, Pierluigi
Oliver, Antonio
Pintado, Vicente
Gasch, Oriol
Martinez-Martinez, Luis
Pitout, Johann
Akova, Murat
Pena, Carmen
Molina Gil-Bermejo, Jose
Hernandez, Alicia
Venditti, Mario
Prim, Nuria
Bou, German
Tacconelli, Evelina
Tumbarello, Mario
Hamprecht, Axel
Giamarellou, Helen
Almela, Manel
Perez, Federico
Schwaber, Mitchell J.
Bermejo, Joaquin
Lowman, Warren
Hsueh, Po-Ren
Ramon Pano-Pardo, Jose
Torre-Cisneros, Julian
Souli, Maria
Bonomo, Robert A.
Carmeli, Yehuda
Paterson, David L.
Pascual, Alvaro
Rodriguez-Bano, Jesus
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Background. There is little information about the efficacy of active alternative drugs to carbapenems except beta-lactam/beta-lactamase inhibitors for the treatment of bloodstream infections (BSIs) due to extended-spectrum beta-lactamase-producing Enterobacteriaceae (ESBL-E). The objective of this study was to assess the outcomes of patients with BSI due to ESBL-E who received empiric therapy with such drugs (other active drugs [OADs]) or carbapenems. Methods. A multinational retrospective cohort study of patients with BSI due to ESBL-E who received empiric treatment with OADs or carbapenems was performed. Cox regression including a propensity score for receiving OADs was performed to analyze 30-day all-cause mortality as main outcome. Clinical failure and length of stay were also analyzed. Results. Overall, 335 patients were included; 249 received empiric carbapenems and 86 OADs. The most frequent OADs were aminoglycosides (43 patients) and fluoroquinolones (20 patients). Empiric therapy with OADs was not associated with mortality (hazard ratio [HR], 0.75; 95% confidence interval [CI],.38-1.48) in the Cox regression analysis. Propensity score-matched pairs, subgroups, and sensitivity analyses did not show different trends; specifically, the adjusted HR for aminoglycosides was 1.05 (95% CI,.51-2.16). OADs were neither associated with 14-day clinical failure (adjusted odds ratio, 0.62; 95% CI,.29-1.36) nor length of hospital stay. Conclusions. We were unable to show that empiric treatment with OAD was associated with a worse outcome compared with carbapenems. This information allows more options to be considered for empiric therapy, at least for some patients, depending on local susceptibility patterns of ESBL-E.