| Literature DB >> 31891235 |
Elena Pérez-Nadales1,2, Belén Gutiérrez-Gutiérrez1,3, Alejandra M Natera1,2, Edson Abdala4, Maira Reina Magalhães4, Alessandra Mularoni5, Francesco Monaco5, Ligia Camera Pierrotti6, Maristela Pinheiro Freire6, Ranganathan N Iyer7, Seema Mehta Steinke8, Elisa Grazia Calvi9, Mario Tumbarello10, Marco Falcone11, Mario Fernández-Ruiz12, José María Costa-Mateo13, Meenakshi M Rana14, Tania Mara Varejão Strabelli15, Mical Paul16, María Carmen Fariñas17, Wanessa Trindade Clemente18, Emmanuel Roilides19, Patricia Muñoz20,21, Laurent Dewispelaere22, Belén Loeches23, Warren Lowman24, Ban Hock Tan25, Rosa Escudero-Sánchez1,26, Marta Bodro27, Paolo Antonio Grossi28, Fabio Soldani29, Filiz Gunseren30, Nina Nestorova31, Álvaro Pascual1,3, Luis Martínez-Martínez1,32, José María Aguado1,12, Jesús Rodríguez-Baño1,3, Julián Torre-Cisneros1,13.
Abstract
Treatment of carbapenemase-producing Enterobacterales bloodstream infections in solid organ transplant recipients is challenging. The objective of this study was to develop a specific score to predict mortality in solid organ transplant recipients with carbapenemase-producing Enterobacterales bloodstream infections. A multinational, retrospective (2004-2016) cohort study (INCREMENT-SOT, ClinicalTrials.gov NCT02852902) was performed. The main outcome variable was 30-day all-cause mortality. The INCREMENT-SOT-CPE score was developed using logistic regression. The global cohort included 216 patients. The final logistic regression model included the following variables: INCREMENT-CPE mortality score ≥8 (8 points), no source control (3 points), inappropriate empirical therapy (2 points), cytomegalovirus disease (7 points), lymphopenia (4 points), and the interaction between INCREMENT-CPE score ≥8 and CMV disease (minus 7 points). This score showed an area under the receiver operating characteristic curve of 0.82 (95% confidence interval [CI] 0.76-0.88) and classified patients into 3 strata: 0-7 (low mortality), 8-11 (high mortality), and 12-17 (very-high mortality). We performed a stratified analysis of the effect of monotherapy vs combination therapy among 165 patients who received appropriate therapy. Monotherapy was associated with higher mortality only in the very-high (adjusted hazard ratio [HR] 2.82, 95% CI 1.13-7.06, P = .03) and high (HR 9.93, 95% CI 2.08-47.40, P = .004) mortality risk strata. A score-based algorithm is provided for therapy guidance.Entities:
Keywords: antibiotic drug resistance; clinical research/practice; infection and infectious agents - bacterial; infectious disease; organ transplantation in general
Year: 2019 PMID: 31891235 DOI: 10.1111/ajt.15769
Source DB: PubMed Journal: Am J Transplant ISSN: 1600-6135 Impact factor: 8.086