TY - JOUR
T1 - Predictors of outcome in patients with severe sepsis or septic shock due to extended-spectrum β-lactamase-producing Enterobacteriaceae
AU - REIPI/ESGBIS/INCREMENT investigators
AU - Russo, A.
AU - Falcone, M.
AU - Gutiérrez-Gutiérrez, B.
AU - Calbo, E.
AU - Almirante, B.
AU - Viale, P. L.
AU - Oliver, A.
AU - Ruiz-Garbajosa, P.
AU - Gasch, O.
AU - Gozalo, M.
AU - Pitout, J.
AU - Akova, M.
AU - Peña, C.
AU - Cisneros, J. M.
AU - Hernández-Torres, A.
AU - Farcomeni, A.
AU - Prim, N.
AU - Origüen, J.
AU - Bou, G.
AU - Tacconelli, E.
AU - Tumbarello, M.
AU - Hamprecht, A.
AU - Karaiskos, I.
AU - de la Calle, C.
AU - Pérez, F.
AU - Schwaber, M. J.
AU - Bermejo, J.
AU - Lowman, W.
AU - Hsueh, P. R.
AU - Mora-Rillo, M.
AU - Rodriguez-Gomez, J.
AU - Souli, M.
AU - Bonomo, R. A.
AU - Paterson, D. L.
AU - Carmeli, Y.
AU - Pascual, A.
AU - Rodríguez-Baño, J.
AU - Venditti, M.
N1 - Publisher Copyright:
© 2018 Elsevier Ltd
PY - 2018/11
Y1 - 2018/11
N2 - Purpose: There are few data in the literature regarding sepsis or septic shock due to extended-spectrum β-lactamases (ESBL)-producing Enterobacteriaceae (E). The aim of this study was to assess predictors of outcome in septic patients with bloodstream infection (BSI) caused by ESBL-E. Methods: Patients with severe sepsis or septic shock and BSI due to ESBL-E were selected from the INCREMENT database. The primary endpoint of the study was the evaluation of predictors of outcome after 30 days from development of severe sepsis or septic shock due to ESBL-E infection. Three cohorts were created for analysis: global, empirical-therapy and targeted-therapy cohorts. Results: 367 septic patients were analysed. Overall mortality was 43.9% at 30 days. Escherichia coli (62.4%) and Klebsiella pneumoniae (27.2%) were the most frequent isolates. β-lactam/β-lactamase inhibitor (BLBLI) combinations were the most empirically used drug (43.6%), followed by carbapenems (29.4%). Empirical therapy was active in vitro in 249 (67.8%) patients, and escalation of antibiotic therapy was reported in 287 (78.2%) patients. Cox regression analysis showed that age, Charlson Comorbidity Index, McCabe classification, Pitt bacteremia score, abdominal source of infection and escalation of antibiotic therapy were independently associated with 30-day mortality. No differences in survival were reported in patients treated with BLBLI combinations or carbapenems in empirical or definitive therapy. Conclusions: BSI due to ESBL-E in patients who developed severe sepsis or septic shock was associated with high 30-day mortality. Comorbidities, severity scores, source of infection and antibiotic therapy escalation were important determinants of unfavorable outcome.
AB - Purpose: There are few data in the literature regarding sepsis or septic shock due to extended-spectrum β-lactamases (ESBL)-producing Enterobacteriaceae (E). The aim of this study was to assess predictors of outcome in septic patients with bloodstream infection (BSI) caused by ESBL-E. Methods: Patients with severe sepsis or septic shock and BSI due to ESBL-E were selected from the INCREMENT database. The primary endpoint of the study was the evaluation of predictors of outcome after 30 days from development of severe sepsis or septic shock due to ESBL-E infection. Three cohorts were created for analysis: global, empirical-therapy and targeted-therapy cohorts. Results: 367 septic patients were analysed. Overall mortality was 43.9% at 30 days. Escherichia coli (62.4%) and Klebsiella pneumoniae (27.2%) were the most frequent isolates. β-lactam/β-lactamase inhibitor (BLBLI) combinations were the most empirically used drug (43.6%), followed by carbapenems (29.4%). Empirical therapy was active in vitro in 249 (67.8%) patients, and escalation of antibiotic therapy was reported in 287 (78.2%) patients. Cox regression analysis showed that age, Charlson Comorbidity Index, McCabe classification, Pitt bacteremia score, abdominal source of infection and escalation of antibiotic therapy were independently associated with 30-day mortality. No differences in survival were reported in patients treated with BLBLI combinations or carbapenems in empirical or definitive therapy. Conclusions: BSI due to ESBL-E in patients who developed severe sepsis or septic shock was associated with high 30-day mortality. Comorbidities, severity scores, source of infection and antibiotic therapy escalation were important determinants of unfavorable outcome.
KW - carbapenems
KW - extended-spectrum ß-lactamases
KW - sepsis
KW - septic shock
KW - ß-lactam/ß-lactamase inhibitors
UR - http://www.scopus.com/inward/record.url?scp=85054433788&partnerID=8YFLogxK
U2 - 10.1016/j.ijantimicag.2018.06.018
DO - 10.1016/j.ijantimicag.2018.06.018
M3 - ???researchoutput.researchoutputtypes.contributiontojournal.article???
C2 - 29969692
AN - SCOPUS:85054433788
VL - 52
SP - 577
EP - 585
JO - International Journal of Antimicrobial Agents
JF - International Journal of Antimicrobial Agents
SN - 0924-8579
IS - 5
ER -