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Delay of CMV infection in high-risk CMV mismatch lung transplant recipients due to prophylaxis with oral ganciclovir.

Publication ,  Journal Article
Palmer, SM; Grinnan, DC; Diane Reams, B; Steele, MP; Messier, RH; Duane Davis, R
Published in: Clin Transplant
April 2004

Cytomegalovirus (CMV) is a common opportunistic infection in lung transplant recipients. Despite the use of early post-operative intravenous ganciclovir, most high-risk patients develop CMV infection. We conducted this retrospective study to determine the efficacy of extended CMV prophylaxis with oral ganciclovir in high-risk, donor-positive-recipient-negative, lung recipients. All patients initially received 3 months of intravenous ganciclovir and CMV hyperimmune globulin. Clinical outcomes in all CMV mismatch patients undergoing lung transplant surviving at least 3 months were included (n = 42). Since 1998, 14 patients received no oral ganciclovir prophylaxis (group 1) and 28 patients received indefinite oral ganciclovir after completion of intravenous therapy (group 2). In those patients receiving oral ganciclovir, the prevalence of post-transplant CMV infection was significantly reduced over the first 180 d post-transplant (50% in group 1 vs. 4% in group 2; p < 0.001). Although some CMV events were observed with additional follow-up in group 2, there remained a significantly greater freedom from CMV infection by Kaplan-Meier analysis in group 2 as compared with group 1, with over 30 months follow-up time in each group (log-rank, p = 0.02). A moderate rate of drug discontinuation was observed in group 2, and no severe drug-related events occurred. In high-risk lung transplant recipients, CMV prophylaxis with intravenous ganciclovir, followed by indefinite oral ganciclovir, significantly delays and reduces post-transplant CMV infections. A larger prospective randomized study is needed to confirm the benefits of oral ganciclovir on CMV prevention.

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Published In

Clin Transplant

DOI

ISSN

0902-0063

Publication Date

April 2004

Volume

18

Issue

2

Start / End Page

179 / 185

Location

Denmark

Related Subject Headings

  • Tissue Donors
  • Surgery
  • Risk Factors
  • Retrospective Studies
  • Opportunistic Infections
  • Male
  • Lung Transplantation
  • Injections, Intravenous
  • Immunoglobulins, Intravenous
  • Immunocompromised Host
 

Citation

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Palmer, S. M., Grinnan, D. C., Diane Reams, B., Steele, M. P., Messier, R. H., & Duane Davis, R. (2004). Delay of CMV infection in high-risk CMV mismatch lung transplant recipients due to prophylaxis with oral ganciclovir. Clin Transplant, 18(2), 179–185. https://doi.org/10.1046/j.1399-0012.2003.00152.x
Palmer, Scott M., Dan C. Grinnan, B. Diane Reams, Mark P. Steele, Robert H. Messier, and R. Duane Davis. “Delay of CMV infection in high-risk CMV mismatch lung transplant recipients due to prophylaxis with oral ganciclovir.Clin Transplant 18, no. 2 (April 2004): 179–85. https://doi.org/10.1046/j.1399-0012.2003.00152.x.
Palmer SM, Grinnan DC, Diane Reams B, Steele MP, Messier RH, Duane Davis R. Delay of CMV infection in high-risk CMV mismatch lung transplant recipients due to prophylaxis with oral ganciclovir. Clin Transplant. 2004 Apr;18(2):179–85.
Palmer, Scott M., et al. “Delay of CMV infection in high-risk CMV mismatch lung transplant recipients due to prophylaxis with oral ganciclovir.Clin Transplant, vol. 18, no. 2, Apr. 2004, pp. 179–85. Pubmed, doi:10.1046/j.1399-0012.2003.00152.x.
Palmer SM, Grinnan DC, Diane Reams B, Steele MP, Messier RH, Duane Davis R. Delay of CMV infection in high-risk CMV mismatch lung transplant recipients due to prophylaxis with oral ganciclovir. Clin Transplant. 2004 Apr;18(2):179–185.
Journal cover image

Published In

Clin Transplant

DOI

ISSN

0902-0063

Publication Date

April 2004

Volume

18

Issue

2

Start / End Page

179 / 185

Location

Denmark

Related Subject Headings

  • Tissue Donors
  • Surgery
  • Risk Factors
  • Retrospective Studies
  • Opportunistic Infections
  • Male
  • Lung Transplantation
  • Injections, Intravenous
  • Immunoglobulins, Intravenous
  • Immunocompromised Host