Selection and use of immunosuppressive therapies after liver transplantation current German practice

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Selection and use of immunosuppressive therapies after liver transplantation current German practice. / Herzer, Kerstin; Strassburg, Christian P; Braun, Felix; Engelmann, Cornelius; Guba, Markus; Lehner, Frank; Nadalin, Silvio; Pascher, Andreas; Scherer, Marcus N; Schnitzbauer, Andreas A; Zimmermann, Tim; Nashan, Björn; Sterneck, Martina.

In: CLIN TRANSPLANT, Vol. 30, No. 5, 05.2016, p. 487-501.

Research output: SCORING: Contribution to journalSCORING: Journal articleResearchpeer-review

Harvard

Herzer, K, Strassburg, CP, Braun, F, Engelmann, C, Guba, M, Lehner, F, Nadalin, S, Pascher, A, Scherer, MN, Schnitzbauer, AA, Zimmermann, T, Nashan, B & Sterneck, M 2016, 'Selection and use of immunosuppressive therapies after liver transplantation current German practice', CLIN TRANSPLANT, vol. 30, no. 5, pp. 487-501. https://doi.org/10.1111/ctr.12708

APA

Herzer, K., Strassburg, C. P., Braun, F., Engelmann, C., Guba, M., Lehner, F., Nadalin, S., Pascher, A., Scherer, M. N., Schnitzbauer, A. A., Zimmermann, T., Nashan, B., & Sterneck, M. (2016). Selection and use of immunosuppressive therapies after liver transplantation current German practice. CLIN TRANSPLANT, 30(5), 487-501. https://doi.org/10.1111/ctr.12708

Vancouver

Herzer K, Strassburg CP, Braun F, Engelmann C, Guba M, Lehner F et al. Selection and use of immunosuppressive therapies after liver transplantation current German practice. CLIN TRANSPLANT. 2016 May;30(5):487-501. https://doi.org/10.1111/ctr.12708

Bibtex

@article{03c08164c6ff41679dd16e0c17d6ef41,
title = "Selection and use of immunosuppressive therapies after liver transplantation current German practice",
abstract = "In recent years, immunosuppression (IS) after liver transplantation (LT) has become increasingly diversified as the choice of agents has expanded and clinicians seek to optimize the balance of immunosuppressive potency with the risk of adverse events in individual patients. Calcineurin inhibitors (CNIs) are the primary agents used for patients undergoing liver transplantation. Other therapeutic agents like interleukin-2 receptor antagonists are not universally administered, but can be considered for the delay or reduction in CNI exposure. An early addition of mycophenolate mofetil (MMF) or the mTOR inhibitor everolimus also allows for the reduction in the CNI dose. To reduce the risk of malignancy, in particular of skin tumors, as well as to prevent the deterioration of renal function, everolimus-based therapy may be advantageous. Apart from patients with autoimmune hepatitis, steroids are withdrawn within 3-6 months after transplantation. Overall, immunosuppression can only be standardized in a limited proportion of patients due to specific clinical requirements and risk factors. Future studies should attempt to refine accurate individualization of the immunosuppressive regimen in specific difficult-to-treat patient subpopulations.",
keywords = "Journal Article, Review",
author = "Kerstin Herzer and Strassburg, {Christian P} and Felix Braun and Cornelius Engelmann and Markus Guba and Frank Lehner and Silvio Nadalin and Andreas Pascher and Scherer, {Marcus N} and Schnitzbauer, {Andreas A} and Tim Zimmermann and Bj{\"o}rn Nashan and Martina Sterneck",
note = "{\textcopyright} 2016 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.",
year = "2016",
month = may,
doi = "10.1111/ctr.12708",
language = "English",
volume = "30",
pages = "487--501",
journal = "CLIN TRANSPLANT",
issn = "0902-0063",
publisher = "Wiley-Blackwell",
number = "5",

}

RIS

TY - JOUR

T1 - Selection and use of immunosuppressive therapies after liver transplantation current German practice

AU - Herzer, Kerstin

AU - Strassburg, Christian P

AU - Braun, Felix

AU - Engelmann, Cornelius

AU - Guba, Markus

AU - Lehner, Frank

AU - Nadalin, Silvio

AU - Pascher, Andreas

AU - Scherer, Marcus N

AU - Schnitzbauer, Andreas A

AU - Zimmermann, Tim

AU - Nashan, Björn

AU - Sterneck, Martina

N1 - © 2016 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.

PY - 2016/5

Y1 - 2016/5

N2 - In recent years, immunosuppression (IS) after liver transplantation (LT) has become increasingly diversified as the choice of agents has expanded and clinicians seek to optimize the balance of immunosuppressive potency with the risk of adverse events in individual patients. Calcineurin inhibitors (CNIs) are the primary agents used for patients undergoing liver transplantation. Other therapeutic agents like interleukin-2 receptor antagonists are not universally administered, but can be considered for the delay or reduction in CNI exposure. An early addition of mycophenolate mofetil (MMF) or the mTOR inhibitor everolimus also allows for the reduction in the CNI dose. To reduce the risk of malignancy, in particular of skin tumors, as well as to prevent the deterioration of renal function, everolimus-based therapy may be advantageous. Apart from patients with autoimmune hepatitis, steroids are withdrawn within 3-6 months after transplantation. Overall, immunosuppression can only be standardized in a limited proportion of patients due to specific clinical requirements and risk factors. Future studies should attempt to refine accurate individualization of the immunosuppressive regimen in specific difficult-to-treat patient subpopulations.

AB - In recent years, immunosuppression (IS) after liver transplantation (LT) has become increasingly diversified as the choice of agents has expanded and clinicians seek to optimize the balance of immunosuppressive potency with the risk of adverse events in individual patients. Calcineurin inhibitors (CNIs) are the primary agents used for patients undergoing liver transplantation. Other therapeutic agents like interleukin-2 receptor antagonists are not universally administered, but can be considered for the delay or reduction in CNI exposure. An early addition of mycophenolate mofetil (MMF) or the mTOR inhibitor everolimus also allows for the reduction in the CNI dose. To reduce the risk of malignancy, in particular of skin tumors, as well as to prevent the deterioration of renal function, everolimus-based therapy may be advantageous. Apart from patients with autoimmune hepatitis, steroids are withdrawn within 3-6 months after transplantation. Overall, immunosuppression can only be standardized in a limited proportion of patients due to specific clinical requirements and risk factors. Future studies should attempt to refine accurate individualization of the immunosuppressive regimen in specific difficult-to-treat patient subpopulations.

KW - Journal Article

KW - Review

U2 - 10.1111/ctr.12708

DO - 10.1111/ctr.12708

M3 - SCORING: Journal article

C2 - 26855333

VL - 30

SP - 487

EP - 501

JO - CLIN TRANSPLANT

JF - CLIN TRANSPLANT

SN - 0902-0063

IS - 5

ER -