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  1. Article ; Online: Basiliximab induction versus no induction in adult heart transplantation.

    Rudzik, Katelyn N / Rivosecchi, Ryan M / Palmer, Brittany A / Hickey, Gavin W / Huston, Jessica H / Keebler, Mary E / Kaczorowski, David J / Horn, Edward T

    Clinical transplantation

    2023  Volume 37, Issue 5, Page(s) e14937

    Abstract: Background: Induction immunosuppression in heart transplant recipients varies greatly by center. Basiliximab (BAS) is the most commonly used induction immunosuppressant but has not been shown to reduce rejection or improve survival. The objective of ... ...

    Abstract Background: Induction immunosuppression in heart transplant recipients varies greatly by center. Basiliximab (BAS) is the most commonly used induction immunosuppressant but has not been shown to reduce rejection or improve survival. The objective of this retrospective study was to compare rejection, infection, and mortality within the first 12 months following heart transplant in patients who received BAS or no induction.
    Methods: This was a retrospective cohort study of adult heart transplant recipients given BAS or no induction from January 1, 2017 to May 31, 2021. The primary endpoint was incidence of treated acute cellular rejection (ACR) at 12-months post-transplant. Secondary endpoints included ACR at 90 days post-transplant, incidence of antibody-mediated rejection (AMR) at 90 days and 1 year, incidence of infection, and all-cause mortality at 1 year.
    Results: A total of 108 patients received BAS, and 26 patients received no induction within the specified timeframe. There was a lower incidence of ACR within the first year in the BAS group compared to the no induction group (27.7 vs. 68.2%, p < .002). BAS was independently associated with a lower probability of having a rejection event during the first 12-months post-transplant (hazard ratio (HR) .285, 95% confidence interval [CI] .142-.571, p < .001). There was no difference in the rate of infection and in mortality after hospital discharge at 1-year post-transplant (6% vs. 0%, p = .20).
    Conclusion: BAS appears to be associated with greater freedom from rejection without an increase in infections. BAS may be a preferred to a no induction strategy in patients undergoing heart transplantation.
    MeSH term(s) Humans ; Adult ; Basiliximab ; Antibodies, Monoclonal/therapeutic use ; Retrospective Studies ; Immunosuppressive Agents/therapeutic use ; Immunosuppressive Agents/pharmacology ; Graft Rejection/etiology ; Heart Transplantation ; Recombinant Fusion Proteins/therapeutic use
    Chemical Substances Basiliximab (9927MT646M) ; Antibodies, Monoclonal ; Immunosuppressive Agents ; Recombinant Fusion Proteins
    Language English
    Publishing date 2023-02-26
    Publishing country Denmark
    Document type Journal Article
    ZDB-ID 639001-8
    ISSN 1399-0012 ; 0902-0063
    ISSN (online) 1399-0012
    ISSN 0902-0063
    DOI 10.1111/ctr.14937
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Rabbit Antithymocyte Globulin for Treatment of Corticosteroid Refractory Acute Cellular Rejection After Lung Transplantation.

    Rudzik, Katelyn N / Moore, Cody A / Sacha, Lauren M / Rivosecchi, Ryan M / Saul, Melissa / Pilewski, Joseph M / Kilaru, Silpa D / Snyder, Mark E / McDyer, John F / Iasella, Carlo J

    Transplantation

    2023  Volume 107, Issue 8, Page(s) 1828–1834

    Abstract: Background: Chronic lung allograft dysfunction (CLAD) remains a major cause of death after the first year posttransplant, with acute cellular rejection (ACR) being a major risk factor for CLAD. We evaluated the use of rabbit antithymocyte globulin (rATG) ...

    Abstract Background: Chronic lung allograft dysfunction (CLAD) remains a major cause of death after the first year posttransplant, with acute cellular rejection (ACR) being a major risk factor for CLAD. We evaluated the use of rabbit antithymocyte globulin (rATG) for corticosteroid refractory ACR in lung transplant recipients.
    Methods: We retrospectively identified 112 adult lung transplant recipients who received rATG for refractory ACR after lung transplantation. The primary endpoint was the incidence of ACR on follow-up transbronchial biopsy. Secondary endpoints included freedom from ACR within 1 y post-rATG, CLAD progression at 1 y post-rATG, and all-cause mortality at 1 y post-rATG.
    Results: A complete resolution of ACR was observed in 60.2% of patients, an improvement but not complete resolution in 22.1%, and no response on follow-up biopsy in 17.8%. Mean A grade 1 y post-rATG was 0.51 in complete responders, 1.01 in partial responders, and 2.19 in nonresponders ( P  < 0.001). Complete responders had significantly less new or worsening CLAD at 1 y than partial responders (17% versus 40%; P  = 0.02). All-cause mortality rate was 14.9% in complete responders, 40% in partial responders, and 30% in nonresponders ( P  < 0.01).
    Conclusions: rATG appears to be an effective treatment of refractory ACR in lung transplant recipients. Failure to respond to rATG carries an increased risk of early CLAD and death.
    MeSH term(s) Immunosuppressive Agents/adverse effects ; Retrospective Studies ; Antilymphocyte Serum/therapeutic use ; Adrenal Cortex Hormones/therapeutic use ; Lung Transplantation/adverse effects ; Graft Rejection/etiology
    Chemical Substances thymoglobulin (D7RD81HE4W) ; Immunosuppressive Agents ; Antilymphocyte Serum ; Adrenal Cortex Hormones
    Language English
    Publishing date 2023-07-20
    Publishing country United States
    Document type Journal Article
    ZDB-ID 208424-7
    ISSN 1534-6080 ; 0041-1337
    ISSN (online) 1534-6080
    ISSN 0041-1337
    DOI 10.1097/TP.0000000000004617
    Database MEDical Literature Analysis and Retrieval System OnLINE

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