TY - JOUR
T1 - Propensity score and desirability of outcome ranking analysis of ertapenem for treatment of nonsevere bacteremic urinary tract infections due to extended-spectrum-beta-lactamase-producing enterobacterales in kidney transplant recipients
AU - the REIPI/ESGICH/ESGBIS/INCREMENT-SOT Group
AU - Gutiérrez-Gutiérrez, Belén
AU - Pérez-Nadales, Elena
AU - Pérez-Galera, Salvador
AU - Fernández-Ruiz, Mario
AU - Carratalà, Jordi
AU - Oriol, Isabel
AU - Cordero, Elisa
AU - Lepe, José Antonio
AU - Tan, Ban Hock
AU - Corbella, Laura
AU - Paul, Mical
AU - Natera, Alejandra M.
AU - David, Miruna D.
AU - Montejo, Miguel
AU - Iyer, Ranganathan N.
AU - Pierrotti, Ligia Camera
AU - Merino, Esperanza
AU - Steinke, Seema Mehta
AU - Rana, Meenakshi M.
AU - Muñoz, Patricia
AU - Mularoni, Alessandra
AU - van Delden, Christian
AU - Grossi, Paolo Antonio
AU - Seminari, Elena María
AU - Gunseren, Filiz
AU - Lease, Erika D.
AU - Roilides, Emmanuel
AU - Fortún, Jesús
AU - Arslan, Hande
AU - Coussement, Julien
AU - Tufan, Zeliha Koçak
AU - Pilmis, Benoit
AU - Rizzi, Marco
AU - Loeches, Belén
AU - Eriksson, Britt Marie
AU - Abdala, Edson
AU - Soldani, Fabio
AU - Lowman, Warren
AU - Clemente, Wanessa Trindade
AU - Bodro, Marta
AU - Fariñas, María Carmen
AU - Kazak, Esra
AU - Martínez-Martínez, Luis
AU - Aguado, José María
AU - Torre-Cisneros, Julián
AU - Pascual, Álvaro
AU - Rodríguez-Baño, Jesús
AU - Sabé, Núria
AU - Avery, Robin
AU - Ostrander, Darin
N1 - Funding Information:
This work was supported by Plan Nacional de I1D1i 2013-2016 and Instituto de Salud Carlos III (ISCIII), Subdirección General de Redes y Centros de Investigación Cooperativa, Ministerio de Ciencia, Innovación y Universidades, Spanish Network for Research in Infectious Diseases (REIPI RD16/0016/0001, RD16/0016/0002, RD16/0016/0008; RD16/ 0016/00010) and was cofinanced by the European Development Regional Fund “A way to achieve Europe,” Operative program Intelligent Growth 2014-2020; ESCMID Study Group for Infections in Compromised Hosts (ESGICH grant to J.M.A.); Sociedad Andaluza de Trasplante de Órgano Sólido (SATOT grant to L.M.-M.); ESCMID Study Group for Bloodstream Infections and Sepsis (ESGBIS); and ESCMID Study Group for Antimicrobial Resistance Surveillance (ESGARS). B.G.-G. (PI 18/01849) and E.P.-N. (PI 16/01631) have received research funds from the Spanish Ministry of Science and Innovation, ISCIII; M.F.-R. holds a research contract “Miguel Servet” (CP 18/00073) from the Spanish Ministry of Science and Innovation, ISCIII. The funders had no role in study design, data collection, and interpretation, or the decision to submit the work for publication.
Publisher Copyright:
© 2021 American Society for Microbiology.
PY - 2021/11
Y1 - 2021/11
N2 - There are scarce data on the efficacy of ertapenem in the treatment of bacteremia due to extended-spectrum-beta-lactamase (ESBL)-producing Enterobacterales (ESBL-E) in kidney transplant (KT) recipients. We evaluated the association between treatment with ertapenem or meropenem and clinical cure in KT recipients with nonsevere bacteremic urinary tract infections (B-UTI) caused by ESBL-E. We performed a registered, retrospective, international (29 centers in 14 countries) cohort study (INCREMENT-SOT, NCT02852902). The association between targeted therapy with ertapenem versus meropenem and clinical cure at day 14 (the principal outcome) was studied by logistic regression. Propensity score matching and desirability of outcome ranking (DOOR) analyses were also performed. A total of 201 patients were included; only 1 patient (treated with meropenem) in the cohort died. Clinical cure at day 14 was reached in 45/100 (45%) and 51/101 (50.5%) of patients treated with ertapenem and meropenem, respectively (adjusted OR 1.29; 95% CI 0.51 to 3.22; P = 0.76); the propensity score-matched cohort included 55 pairs (adjusted OR for clinical cure at day 14, 1.18; 95% CI 0.43 to 3.29; P = 0.74). In this cohort, the proportion of cases treated with ertapenem with better DOOR than with meropenem was 49.7% (95% CI, 40.4 to 59.1%) when hospital stay was considered. It ranged from 59 to 67% in different scenarios of a modified (weights-based) DOOR sensitivity analysis when potential ecological advantage or cost was considered in addition to outcome. In conclusion, targeted therapy with ertapenem appears as effective as meropenem to treat nonsevere B-UTI due to ESBL-E in KT recipients and may have some advantages.
AB - There are scarce data on the efficacy of ertapenem in the treatment of bacteremia due to extended-spectrum-beta-lactamase (ESBL)-producing Enterobacterales (ESBL-E) in kidney transplant (KT) recipients. We evaluated the association between treatment with ertapenem or meropenem and clinical cure in KT recipients with nonsevere bacteremic urinary tract infections (B-UTI) caused by ESBL-E. We performed a registered, retrospective, international (29 centers in 14 countries) cohort study (INCREMENT-SOT, NCT02852902). The association between targeted therapy with ertapenem versus meropenem and clinical cure at day 14 (the principal outcome) was studied by logistic regression. Propensity score matching and desirability of outcome ranking (DOOR) analyses were also performed. A total of 201 patients were included; only 1 patient (treated with meropenem) in the cohort died. Clinical cure at day 14 was reached in 45/100 (45%) and 51/101 (50.5%) of patients treated with ertapenem and meropenem, respectively (adjusted OR 1.29; 95% CI 0.51 to 3.22; P = 0.76); the propensity score-matched cohort included 55 pairs (adjusted OR for clinical cure at day 14, 1.18; 95% CI 0.43 to 3.29; P = 0.74). In this cohort, the proportion of cases treated with ertapenem with better DOOR than with meropenem was 49.7% (95% CI, 40.4 to 59.1%) when hospital stay was considered. It ranged from 59 to 67% in different scenarios of a modified (weights-based) DOOR sensitivity analysis when potential ecological advantage or cost was considered in addition to outcome. In conclusion, targeted therapy with ertapenem appears as effective as meropenem to treat nonsevere B-UTI due to ESBL-E in KT recipients and may have some advantages.
KW - BSI
KW - Bloodstream infection
KW - ESBL-E
KW - Ertapenem
KW - Extended-spectrum-b-lactamase-producing Enterobacterales
KW - Kidney transplant
KW - UTI
KW - Urinary tract infection
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U2 - 10.1128/AAC.01102-21
DO - 10.1128/AAC.01102-21
M3 - Article
C2 - 34370578
AN - SCOPUS:85117459450
SN - 0066-4804
VL - 65
JO - Antimicrobial Agents and Chemotherapy
JF - Antimicrobial Agents and Chemotherapy
IS - 11
M1 - e01102-21
ER -