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Predictors of mortality in solid organ transplant recipients with bloodstream infections due to carbapenemase-producing Enterobacterales: The impact of cytomegalovirus disease and lymphopenia.

Elena Perez-NadalesBelén Gutiérrez-GutiérrezAlejandra M NateraEdson AbdalaMaira Reina MagalhãesAlessandra MularoniFrancesco MonacoLigia Camera PierrottiMaristela Pinheiro FreireRanganathan N IyerSeema Mehta SteinkeElisa Grazia CalviMario TumbarelloMarco FalconeMario Fernández-RuizJosé María Costa-MateoMeenakshi M RanaTania Mara Varejão StrabelliMical PaulMaría Carmen FariñasWanessa Trindade ClementeEmmanuel RoilidesPatricia MuñozLaurent DewispelaereBelén LoechesWarren LowmanBan Hock TanRosa Escudero-SánchezMarta BodroPaolo Antonio GrossiFabio SoldaniFiliz GunserenNina NestorovaAlvaro PascualLuis Martínez-MartínezJosé María AguadoJesús Rodríguez-BañoJulián Torre-Cisnerosnull null
Published in: American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons (2019)
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.
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