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dc.date.accessioned2024-01-15T18:05:25Z
dc.date.available2024-01-15T18:05:25Z
dc.date.created2023-07-21T10:16:31Z
dc.date.issued2023
dc.identifier.citationBlom, Kjersti Benedicte Kro, Grete Anette Birkeland Midtvedt, Karsten Jenssen, Trond Reisæter, Anna Varberg Rollag, Halvor Hartmann, Anders Sagedal, Solbjørg Sjaastad, Ivar Tylden, Garth Daryl Njølstad, Gro Nilsen, Einar Christensen, Andreas Åsberg, Anders Birkeland, Jon Arne . Cytomegalovirus High-risk Kidney Transplant Recipients Show No Difference in Long-term Outcomes Following Preemptive Versus Prophylactic Management. Transplantation. 2023, 107(8), 1846-1853
dc.identifier.urihttp://hdl.handle.net/10852/106831
dc.description.abstractBackground. Following kidney transplantation (KT), cytomegalovirus (CMV) infection remains an important challenge. Both prophylactic and preemptive antiviral protocols are used for CMV high-risk kidney recipients (donor seropositive/recipient seronegative; D+/R–). We performed a nationwide comparison of the 2 strategies in de novo D+/R– KT recipients accessing long-term outcomes. Methods. A nationwide retrospective study was conducted from 2007 to 2018, with follow-up until February 1, 2022. All adult D+/R– and R+ KT recipients were included. During the first 4 y, D+/R– recipients were managed preemptively, changing to 6 mo of valganciclovir prophylaxis from 2011. To adjust for the 2 time eras, de novo intermediate-risk (R+) recipients, who received preemptive CMV therapy throughout the study period, served as longitudinal controls for possible confounders. Results. A total of 2198 KT recipients (D+/R–, n = 428; R+, n = 1770) were included with a median follow-up of 9.4 (range, 3.1–15.1) y. As expected, a greater proportion experienced a CMV infection in the preemptive era compared with the prophylactic era and with a shorter time from KT to CMV infection (P < 0.001). However, there were no differences in long-term outcomes such as patient death (47/146 [32%] versus 57/282 [20%]; P = 0.3), graft loss (64/146 [44%] versus 71/282 [25%]; P = 0.5), or death censored graft loss (26/146 [18%] versus 26/282 [9%]; P = 0.9) in the preemptive versus prophylactic era. Long-term outcomes in R+ recipients showed no signs of sequential era–related bias. Conclusions. There were no significant differences in relevant long-term outcomes between preemptive and prophylactic CMV-preventive strategies in D+/R– kidney transplant recipients.
dc.languageEN
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/
dc.titleCytomegalovirus High-risk Kidney Transplant Recipients Show No Difference in Long-term Outcomes Following Preemptive Versus Prophylactic Management
dc.title.alternativeENEngelskEnglishCytomegalovirus High-risk Kidney Transplant Recipients Show No Difference in Long-term Outcomes Following Preemptive Versus Prophylactic Management
dc.typeJournal article
dc.creator.authorBlom, Kjersti Benedicte
dc.creator.authorKro, Grete Anette Birkeland
dc.creator.authorMidtvedt, Karsten
dc.creator.authorJenssen, Trond
dc.creator.authorReisæter, Anna Varberg
dc.creator.authorRollag, Halvor
dc.creator.authorHartmann, Anders
dc.creator.authorSagedal, Solbjørg
dc.creator.authorSjaastad, Ivar
dc.creator.authorTylden, Garth Daryl
dc.creator.authorNjølstad, Gro
dc.creator.authorNilsen, Einar
dc.creator.authorChristensen, Andreas
dc.creator.authorÅsberg, Anders
dc.creator.authorBirkeland, Jon Arne
cristin.unitcode185,53,15,70
cristin.unitnameK.G. Jebsen-senter for hjerteforskning
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1
dc.identifier.cristin2162997
dc.identifier.bibliographiccitationinfo:ofi/fmt:kev:mtx:ctx&ctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Transplantation&rft.volume=107&rft.spage=1846&rft.date=2023
dc.identifier.jtitleTransplantation
dc.identifier.volume107
dc.identifier.issue8
dc.identifier.startpage1846
dc.identifier.endpage1853
dc.identifier.doihttps://doi.org/10.1097/TP.0000000000004615
dc.type.documentTidsskriftartikkel
dc.type.peerreviewedPeer reviewed
dc.source.issn0041-1337
dc.type.versionPublishedVersion


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