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Evaluation of Two Different CMV-Immunoglobulin Regimens for Combined CMV Prophylaxis in High-Risk Patients following Lung Transplant

Background: The clinical benefits of the common off-label use of cytomegalovirus (CMV)-specific immunoglobulin (CMV-Ig) combined with antivirals in organ transplantation have not been previously assessed. The objective was to compare the risk of CMV infection and other post-transplantation outcomes...

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Autores principales: Mora, Víctor M., Ussetti, Piedad, de Pablo, Alicia, Iturbe, David, Laporta, Rosalía, Alonso, Rodrigo, Aguilar, Myriam, Quezada, Carlos A., Cifrián, José M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9864217/
https://www.ncbi.nlm.nih.gov/pubmed/36677327
http://dx.doi.org/10.3390/microorganisms11010032
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author Mora, Víctor M.
Ussetti, Piedad
de Pablo, Alicia
Iturbe, David
Laporta, Rosalía
Alonso, Rodrigo
Aguilar, Myriam
Quezada, Carlos A.
Cifrián, José M.
author_facet Mora, Víctor M.
Ussetti, Piedad
de Pablo, Alicia
Iturbe, David
Laporta, Rosalía
Alonso, Rodrigo
Aguilar, Myriam
Quezada, Carlos A.
Cifrián, José M.
author_sort Mora, Víctor M.
collection PubMed
description Background: The clinical benefits of the common off-label use of cytomegalovirus (CMV)-specific immunoglobulin (CMV-Ig) combined with antivirals in organ transplantation have not been previously assessed. The objective was to compare the risk of CMV infection and other post-transplantation outcomes between two CMV-Ig prophylaxis regimens in lung transplant recipients; Methods: Retrospective study of 124 donor CMV positive/recipient negative (D+/R–) patients receiving preventive ganciclovir/valganciclovir for 12 months, of whom 62 received adjunctive CMV-Ig as per label indication (short regimen [SR-Ig]; i.e., 7 doses over 2.5 months) and were compared to 62 who received an extended off-label regimen (ER-Ig) consisting of 17 doses over one year after transplantation. Results: The incidence of CMV infection or disease, acute rejection, chronic lung allograft dysfunction, and survival did not differ between the two CMV-Ig schedules. Although the time to the first CMV infection after transplantation was shorter in the ER-Ig than in the SR-Ig adjunctive group (log-rank: p = 0.002), the risk was independently predicted by antiviral cessation (odds ratio = 3.74; 95% confidence interval = 1.04–13.51; p = 0.030), whereas the CMV-Ig schedule had no effect. Conclusions: Extending the adjunctive CMV-Ig prophylaxis beyond the manufacturer’s recommendations up to one year does not confer additional clinical benefits regarding lung post-transplantation outcomes.
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spelling pubmed-98642172023-01-22 Evaluation of Two Different CMV-Immunoglobulin Regimens for Combined CMV Prophylaxis in High-Risk Patients following Lung Transplant Mora, Víctor M. Ussetti, Piedad de Pablo, Alicia Iturbe, David Laporta, Rosalía Alonso, Rodrigo Aguilar, Myriam Quezada, Carlos A. Cifrián, José M. Microorganisms Article Background: The clinical benefits of the common off-label use of cytomegalovirus (CMV)-specific immunoglobulin (CMV-Ig) combined with antivirals in organ transplantation have not been previously assessed. The objective was to compare the risk of CMV infection and other post-transplantation outcomes between two CMV-Ig prophylaxis regimens in lung transplant recipients; Methods: Retrospective study of 124 donor CMV positive/recipient negative (D+/R–) patients receiving preventive ganciclovir/valganciclovir for 12 months, of whom 62 received adjunctive CMV-Ig as per label indication (short regimen [SR-Ig]; i.e., 7 doses over 2.5 months) and were compared to 62 who received an extended off-label regimen (ER-Ig) consisting of 17 doses over one year after transplantation. Results: The incidence of CMV infection or disease, acute rejection, chronic lung allograft dysfunction, and survival did not differ between the two CMV-Ig schedules. Although the time to the first CMV infection after transplantation was shorter in the ER-Ig than in the SR-Ig adjunctive group (log-rank: p = 0.002), the risk was independently predicted by antiviral cessation (odds ratio = 3.74; 95% confidence interval = 1.04–13.51; p = 0.030), whereas the CMV-Ig schedule had no effect. Conclusions: Extending the adjunctive CMV-Ig prophylaxis beyond the manufacturer’s recommendations up to one year does not confer additional clinical benefits regarding lung post-transplantation outcomes. MDPI 2022-12-22 /pmc/articles/PMC9864217/ /pubmed/36677327 http://dx.doi.org/10.3390/microorganisms11010032 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Mora, Víctor M.
Ussetti, Piedad
de Pablo, Alicia
Iturbe, David
Laporta, Rosalía
Alonso, Rodrigo
Aguilar, Myriam
Quezada, Carlos A.
Cifrián, José M.
Evaluation of Two Different CMV-Immunoglobulin Regimens for Combined CMV Prophylaxis in High-Risk Patients following Lung Transplant
title Evaluation of Two Different CMV-Immunoglobulin Regimens for Combined CMV Prophylaxis in High-Risk Patients following Lung Transplant
title_full Evaluation of Two Different CMV-Immunoglobulin Regimens for Combined CMV Prophylaxis in High-Risk Patients following Lung Transplant
title_fullStr Evaluation of Two Different CMV-Immunoglobulin Regimens for Combined CMV Prophylaxis in High-Risk Patients following Lung Transplant
title_full_unstemmed Evaluation of Two Different CMV-Immunoglobulin Regimens for Combined CMV Prophylaxis in High-Risk Patients following Lung Transplant
title_short Evaluation of Two Different CMV-Immunoglobulin Regimens for Combined CMV Prophylaxis in High-Risk Patients following Lung Transplant
title_sort evaluation of two different cmv-immunoglobulin regimens for combined cmv prophylaxis in high-risk patients following lung transplant
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9864217/
https://www.ncbi.nlm.nih.gov/pubmed/36677327
http://dx.doi.org/10.3390/microorganisms11010032
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