dc.contributor.author | Mora Cuesta, Víctor Manuel | es_ES |
dc.contributor.author | Ussetti, Piedad | es_ES |
dc.contributor.author | Pablo, Alicia de | es_ES |
dc.contributor.author | Iturbe Fernández, David | es_ES |
dc.contributor.author | Laporta, Rosalía | es_ES |
dc.contributor.author | Alonso, Rodrigo | es_ES |
dc.contributor.author | Aguilar, Myriam | es_ES |
dc.contributor.author | Quezada, Carlos A. | es_ES |
dc.contributor.author | Cifrián Martínez, José Manuel | es_ES |
dc.contributor.other | Universidad de Cantabria | es_ES |
dc.date.accessioned | 2023-09-12T15:44:10Z | |
dc.date.available | 2023-09-12T15:44:10Z | |
dc.date.issued | 2023 | es_ES |
dc.identifier.issn | 2076-2607 | es_ES |
dc.identifier.uri | https://hdl.handle.net/10902/29874 | |
dc.description.abstract | 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. | es_ES |
dc.description.sponsorship | Funding: This research was funded by Medical SLU (Spanish branch of Biotest AG).
Acknowledgments: We acknowledge Mònica Gratacòs for providing support in the manuscript preparation and editing. | es_ES |
dc.format.extent | 14 p. | es_ES |
dc.language.iso | eng | es_ES |
dc.publisher | MDPI | es_ES |
dc.rights | Attribution 4.0 International | * |
dc.rights | © 2022 by the authors | * |
dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ | * |
dc.source | Microorganisms, 2023, 11, 32 | es_ES |
dc.subject.other | Cytomegalovirus | es_ES |
dc.subject.other | Lung transplantation | es_ES |
dc.subject.other | CMV infection | es_ES |
dc.subject.other | Prophylaxis | es_ES |
dc.subject.other | CMV immunoglobulin | es_ES |
dc.subject.other | Morbidity | es_ES |
dc.subject.other | Survival | es_ES |
dc.title | Evaluation of two different CMV-immunoglobulin regimens for combined CMV prophylaxis in high-risk patients following lung transplant | es_ES |
dc.type | info:eu-repo/semantics/article | es_ES |
dc.relation.publisherVersion | https://doi.org/10.3390/microorganisms11010032 | es_ES |
dc.rights.accessRights | openAccess | es_ES |
dc.identifier.DOI | 10.3390/microorganisms11010032 | es_ES |
dc.type.version | publishedVersion | es_ES |