Efficacy of ceftazidime-avibactam in solid organ transplant recipients with bloodstream infections caused by carbapenemase-producing Klebsiella pneumoniae
Copyright © 2023 American Society of Transplantation & American Society of Transplant Surgeons. Published by Elsevier Inc. All rights reserved..
We aimed to compare the efficacy of ceftazidime-avibactam (CAZ-AVI) versus the best available therapy (BAT) in solid organ transplant (SOT) recipients with bloodstream infection caused by carbapenemase-producing Klebsiella pneumoniae (CPKP-BSI). A retrospective (2016-2021) observational cohort study was performed in 14 INCREMENT-SOT centers (ClinicalTrials.gov identifier: NCT02852902; Impact of Specific Antimicrobials and MIC Values on the Outcome of Bloodstream Infections Due to ESBL- or Carbapenemase-producing Enterobacterales in Solid Organ Transplantation: an Observational Multinational Study). Outcomes were 14-day and 30-day clinical success (complete resolution of attributable manifestations, adequate source control, and negative follow-up blood cultures) and 30-day all-cause mortality. Multivariable logistic and Cox regression analyses adjusted for the propensity score to receive CAZ-AVI were constructed. Among 210 SOT recipients with CPKP-BSI, 149 received active primary therapy with CAZ-AVI (66/149) or BAT (83/149). Patients treated with CAZ-AVI had higher 14-day (80.7% vs 60.6%, P = .011) and 30-day (83.1% vs 60.6%, P = .004) clinical success and lower 30-day mortality (13.25% vs 27.3%, P = .053) than those receiving BAT. In the adjusted analysis, CAZ-AVI increased the probability of 14-day (adjusted odds ratio [aOR], 2.65; 95% confidence interval [CI], 1.03-6.84; P = .044) and 30-day clinical success (aOR, 3.14; 95% CI, 1.17-8.40; P = .023). In contrast, CAZ-AVI therapy was not independently associated with 30-day mortality. In the CAZ-AVI group, combination therapy was not associated with better outcomes. In conclusion, CAZ-AVI may be considered a first-line treatment in SOT recipients with CPKP-BSI.
Medienart: |
E-Artikel |
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Erscheinungsjahr: |
2023 |
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Erschienen: |
2023 |
Enthalten in: |
Zur Gesamtaufnahme - volume:23 |
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Enthalten in: |
American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons - 23(2023), 7 vom: 05. Juli, Seite 1022-1034 |
Sprache: |
Englisch |
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Links: |
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Anmerkungen: |
Date Completed 04.07.2023 Date Revised 13.07.2023 published: Print-Electronic ClinicalTrials.gov: NCT02852902 Citation Status MEDLINE |
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doi: |
10.1016/j.ajt.2023.03.011 |
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funding: |
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PPN (Katalog-ID): |
NLM355331721 |
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245 | 1 | 0 | |a Efficacy of ceftazidime-avibactam in solid organ transplant recipients with bloodstream infections caused by carbapenemase-producing Klebsiella pneumoniae |
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500 | |a Citation Status MEDLINE | ||
520 | |a Copyright © 2023 American Society of Transplantation & American Society of Transplant Surgeons. Published by Elsevier Inc. All rights reserved. | ||
520 | |a We aimed to compare the efficacy of ceftazidime-avibactam (CAZ-AVI) versus the best available therapy (BAT) in solid organ transplant (SOT) recipients with bloodstream infection caused by carbapenemase-producing Klebsiella pneumoniae (CPKP-BSI). A retrospective (2016-2021) observational cohort study was performed in 14 INCREMENT-SOT centers (ClinicalTrials.gov identifier: NCT02852902; Impact of Specific Antimicrobials and MIC Values on the Outcome of Bloodstream Infections Due to ESBL- or Carbapenemase-producing Enterobacterales in Solid Organ Transplantation: an Observational Multinational Study). Outcomes were 14-day and 30-day clinical success (complete resolution of attributable manifestations, adequate source control, and negative follow-up blood cultures) and 30-day all-cause mortality. Multivariable logistic and Cox regression analyses adjusted for the propensity score to receive CAZ-AVI were constructed. Among 210 SOT recipients with CPKP-BSI, 149 received active primary therapy with CAZ-AVI (66/149) or BAT (83/149). Patients treated with CAZ-AVI had higher 14-day (80.7% vs 60.6%, P = .011) and 30-day (83.1% vs 60.6%, P = .004) clinical success and lower 30-day mortality (13.25% vs 27.3%, P = .053) than those receiving BAT. In the adjusted analysis, CAZ-AVI increased the probability of 14-day (adjusted odds ratio [aOR], 2.65; 95% confidence interval [CI], 1.03-6.84; P = .044) and 30-day clinical success (aOR, 3.14; 95% CI, 1.17-8.40; P = .023). In contrast, CAZ-AVI therapy was not independently associated with 30-day mortality. In the CAZ-AVI group, combination therapy was not associated with better outcomes. In conclusion, CAZ-AVI may be considered a first-line treatment in SOT recipients with CPKP-BSI | ||
650 | 4 | |a Observational Study | |
650 | 4 | |a Journal Article | |
650 | 4 | |a Research Support, Non-U.S. Gov't | |
650 | 4 | |a INCREMENT-SOT project | |
650 | 4 | |a bloodstream infections | |
650 | 4 | |a carbapenem-resistant Klebsiella pneumoniae | |
650 | 4 | |a ceftazidime-avibactam | |
650 | 4 | |a solid-organ transplantation | |
650 | 7 | |a avibactam, ceftazidime drug combination |2 NLM | |
650 | 7 | |a carbapenemase |2 NLM | |
650 | 7 | |a EC 3.5.2.6 |2 NLM | |
650 | 7 | |a Anti-Bacterial Agents |2 NLM | |
650 | 7 | |a Drug Combinations |2 NLM | |
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700 | 1 | |a Mularoni, Alessandra |e verfasserin |4 aut | |
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700 | 1 | |a Falcone, Marco |e verfasserin |4 aut | |
700 | 1 | |a Tiseo, Giusy |e verfasserin |4 aut | |
700 | 1 | |a Tumbarello, Mario |e verfasserin |4 aut | |
700 | 1 | |a Raffaelli, Francesca |e verfasserin |4 aut | |
700 | 1 | |a Abdala, Edson |e verfasserin |4 aut | |
700 | 1 | |a Bodro, Marta |e verfasserin |4 aut | |
700 | 1 | |a Gervasi, Elena |e verfasserin |4 aut | |
700 | 1 | |a Fariñas, María Carmen |e verfasserin |4 aut | |
700 | 1 | |a Seminari, Elena M |e verfasserin |4 aut | |
700 | 1 | |a Castón, Juan José |e verfasserin |4 aut | |
700 | 1 | |a Marín-Sanz, Juan Antonio |e verfasserin |4 aut | |
700 | 1 | |a Gálvez-Soto, Víctor |e verfasserin |4 aut | |
700 | 1 | |a Rana, Meenakshi M |e verfasserin |4 aut | |
700 | 1 | |a Loeches, Belén |e verfasserin |4 aut | |
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700 | 1 | |a Rodríguez-Álvarez, Regino José |e investigator |4 oth | |
700 | 1 | |a Cordero, Elisa |e investigator |4 oth | |
700 | 1 | |a Lepe, José Antonio |e investigator |4 oth | |
700 | 1 | |a de Lucas, Esperanza Merino |e investigator |4 oth | |
700 | 1 | |a Muñoz, Patricia |e investigator |4 oth | |
700 | 1 | |a Fortún, Jesús |e investigator |4 oth | |
700 | 1 | |a Coussement, Julien |e investigator |4 oth | |
700 | 1 | |a Dewispelaere, Laurent |e investigator |4 oth | |
700 | 1 | |a Eriksson, Britt Marie |e investigator |4 oth | |
700 | 1 | |a van Delden, Christian |e investigator |4 oth | |
700 | 1 | |a Manuel, Oriol |e investigator |4 oth | |
700 | 1 | |a Clemente, Wanessa T |e investigator |4 oth | |
700 | 1 | |a Strabelli, Tania Mara Varejão |e investigator |4 oth | |
700 | 1 | |a Pilmis, Benoit |e investigator |4 oth | |
700 | 1 | |a Roilides, Emmanuel |e investigator |4 oth | |
700 | 1 | |a Ranganathan N, Iyer |e investigator |4 oth | |
700 | 1 | |a Grossi, Paolo A |e investigator |4 oth | |
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