CMV in kidney transplantation: a single center experience over 22 years.

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CMV in kidney transplantation: a single center experience over 22 years. / Nashan, Björn; Lück, R; Kliem, V; Brunkhorst, R; Schlitt, H J; Klempnauer, J.

In: CLIN TRANSPLANT, 1999, p. 181-188.

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

Harvard

Nashan, B, Lück, R, Kliem, V, Brunkhorst, R, Schlitt, HJ & Klempnauer, J 1999, 'CMV in kidney transplantation: a single center experience over 22 years.', CLIN TRANSPLANT, pp. 181-188. <http://www.ncbi.nlm.nih.gov/pubmed/11038636?dopt=Citation>

APA

Nashan, B., Lück, R., Kliem, V., Brunkhorst, R., Schlitt, H. J., & Klempnauer, J. (1999). CMV in kidney transplantation: a single center experience over 22 years. CLIN TRANSPLANT, 181-188. http://www.ncbi.nlm.nih.gov/pubmed/11038636?dopt=Citation

Vancouver

Nashan B, Lück R, Kliem V, Brunkhorst R, Schlitt HJ, Klempnauer J. CMV in kidney transplantation: a single center experience over 22 years. CLIN TRANSPLANT. 1999;181-188.

Bibtex

@article{18fa53fcd41c4c5189768702340b04ee,
title = "CMV in kidney transplantation: a single center experience over 22 years.",
abstract = "Analysis of a historic renal transplant population for risks of developing CMV disease demonstrated a low mortality (0.2%) and morbidity. In our population of 1,959 patients, 411 (21%) developed subclinical CMV infection and 220 (11%) had CMV disease which was severe in 41 (2%). Important factors for infection were baseline immunosuppression, indicating that triple therapy with the proliferation inhibitors, azathioprine and MMF, had significantly higher infection numbers in comparison to dual, CsA-based immunosuppression. The cumulative dose of steroids correlated strongly with an increased number of CMV infections and disease, as did the addition of ALG/ATG or OKT3 for either steroid-resistant rejections or induction therapy. While CMV serology had an impact on infection in cases of seropositive donors to seronegative recipients, seropositive patients, in general, demonstrated increased infection rates most likely due to reactivation of the virus. Prophylaxis had no impact on the incidence of infection but reduced the severity.",
author = "Bj{\"o}rn Nashan and R L{\"u}ck and V Kliem and R Brunkhorst and Schlitt, {H J} and J Klempnauer",
year = "1999",
language = "Deutsch",
pages = "181--188",
journal = "CLIN TRANSPLANT",
issn = "0902-0063",
publisher = "Wiley-Blackwell",

}

RIS

TY - JOUR

T1 - CMV in kidney transplantation: a single center experience over 22 years.

AU - Nashan, Björn

AU - Lück, R

AU - Kliem, V

AU - Brunkhorst, R

AU - Schlitt, H J

AU - Klempnauer, J

PY - 1999

Y1 - 1999

N2 - Analysis of a historic renal transplant population for risks of developing CMV disease demonstrated a low mortality (0.2%) and morbidity. In our population of 1,959 patients, 411 (21%) developed subclinical CMV infection and 220 (11%) had CMV disease which was severe in 41 (2%). Important factors for infection were baseline immunosuppression, indicating that triple therapy with the proliferation inhibitors, azathioprine and MMF, had significantly higher infection numbers in comparison to dual, CsA-based immunosuppression. The cumulative dose of steroids correlated strongly with an increased number of CMV infections and disease, as did the addition of ALG/ATG or OKT3 for either steroid-resistant rejections or induction therapy. While CMV serology had an impact on infection in cases of seropositive donors to seronegative recipients, seropositive patients, in general, demonstrated increased infection rates most likely due to reactivation of the virus. Prophylaxis had no impact on the incidence of infection but reduced the severity.

AB - Analysis of a historic renal transplant population for risks of developing CMV disease demonstrated a low mortality (0.2%) and morbidity. In our population of 1,959 patients, 411 (21%) developed subclinical CMV infection and 220 (11%) had CMV disease which was severe in 41 (2%). Important factors for infection were baseline immunosuppression, indicating that triple therapy with the proliferation inhibitors, azathioprine and MMF, had significantly higher infection numbers in comparison to dual, CsA-based immunosuppression. The cumulative dose of steroids correlated strongly with an increased number of CMV infections and disease, as did the addition of ALG/ATG or OKT3 for either steroid-resistant rejections or induction therapy. While CMV serology had an impact on infection in cases of seropositive donors to seronegative recipients, seropositive patients, in general, demonstrated increased infection rates most likely due to reactivation of the virus. Prophylaxis had no impact on the incidence of infection but reduced the severity.

M3 - SCORING: Zeitschriftenaufsatz

SP - 181

EP - 188

JO - CLIN TRANSPLANT

JF - CLIN TRANSPLANT

SN - 0902-0063

ER -