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Efficacy of Equoral in prophylactic immunosuppression after de novo kidney transplantation

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61989592%3A15110%2F07%3A00004300" target="_blank" >RIV/61989592:15110/07:00004300 - isvavai.cz</a>

  • Alternative codes found

    RIV/61988987:17110/07:A1100UBC

  • Result on the web

  • DOI - Digital Object Identifier

Alternative languages

  • Result language

    angličtina

  • Original language name

    Efficacy of Equoral in prophylactic immunosuppression after de novo kidney transplantation

  • Original language description

    Cyclosporin A is a well-known calcineurin ihibitor that has been used for prophylactic immunosuppression after organ transplantation. The aim of this study was to evaluate the efficacy and safety of a new generic cyclosporin formulation, Equoral (Teva Pharmaceuticals), in the treatment of de novo renal transplant. Twenty cadaveric-donor renal transplant recipients between 23 and 71 years of age at the time of transplantation (mean age 52?12,5 years) were followed for 12 months to determine if the graftsfunctioned and if there were rejection attacks and side effects. In addition to cyclosporin, all patients received mycophenolate mofetil (CellCept) and prednisone (Prednison). Mean serum creatinine level decreased significantly after transplantation. In6 of the 20 patients observed, 7 biopsies showed acute rejection episodes (35%). Over the 12 month post-transplant period, all patients showed stable graft function, with a mean serum creatinine level of 202,1?130,9 umol/l. Patient and r

  • Czech name

    Účinnost Equoralu v profylaktické imunosupresi u nemocných po transplantaci ledviny

  • Czech description

    Cyclosporin A je inhibitor kalcineurinu a je dlouhodobě používán k profylaktické immunosupresi po orgánových transplantacích. Cílem studie bylo ověřit účinnost a bezpečnost nového generického cyclosporinu Equoral (TEVA Pharmaceuticals) u nově transplantovaných pacientů. Do studie bylo zařazeno 20 pacientů po transplantaci ledviny, věk 23-71 let (střední věk 52?12,5 let). Pacienti byli sledováni po dobu 12 měsíců. Koncentrace kreatininu v séru po transplantaci signifikantně poklesla, mediální hodnota kreatininu činila 202,1?130,9 umol/l. Bylo pozorováno 7 akutních rejekčních epizod (35%). Přežití pacientů i štěpů bylo 100%. Equoral se jeví jako efektivní a bezpečná alternativa v profylaktické imunosupresi po transplantaci ledviny.

Classification

  • Type

    J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)

  • CEP classification

    FE - Other fields of internal medicine

  • OECD FORD branch

Result continuities

  • Project

  • Continuities

    S - Specificky vyzkum na vysokych skolach

Others

  • Publication year

    2007

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Dialysis and Transplantation

  • ISSN

    0090-2934

  • e-ISSN

  • Volume of the periodical

    36

  • Issue of the periodical within the volume

    11

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    6

  • Pages from-to

    602-607

  • UT code for WoS article

  • EID of the result in the Scopus database