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dc.contributor.authorBlom, Kjersti Benedicte
dc.contributor.authorKro, Grete Anette Birkeland
dc.contributor.authorMidtvedt, Karsten
dc.contributor.authorJenssen, Trond
dc.contributor.authorReisæter, Anna Varberg
dc.contributor.authorRollag, Halvor
dc.contributor.authorHartmann, Anders
dc.contributor.authorSagedal, Solbjørg
dc.contributor.authorSjaastad, Ivar
dc.contributor.authorTylden, Garth Daryl
dc.contributor.authorNjølstad, Gro
dc.contributor.authorNilsen, Einar
dc.contributor.authorChristensen, Andreas
dc.contributor.authorÅsberg, Anders
dc.contributor.authorBirkeland, Jon Arne
dc.date.accessioned2024-02-14T15:19:19Z
dc.date.available2024-02-14T15:19:19Z
dc.date.created2023-07-21T10:16:31Z
dc.date.issued2023
dc.identifier.citationTransplantation. 2023, 107 (8), 1846-1853.en_US
dc.identifier.issn0041-1337
dc.identifier.urihttps://hdl.handle.net/11250/3117656
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.en_US
dc.language.isoengen_US
dc.publisherWolters Kluweren_US
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/deed.no*
dc.titleCytomegalovirus High-risk Kidney Transplant Recipients Show No Difference in Long-term Outcomes Following Preemptive Versus Prophylactic Managementen_US
dc.title.alternativeCytomegalovirus High-risk Kidney Transplant Recipients Show No Difference in Long-term Outcomes Following Preemptive Versus Prophylactic Managementen_US
dc.typePeer revieweden_US
dc.typeJournal articleen_US
dc.description.versionpublishedVersionen_US
dc.source.pagenumber1846-1853en_US
dc.source.volume107en_US
dc.source.journalTransplantationen_US
dc.source.issue8en_US
dc.identifier.doi10.1097/TP.0000000000004615
dc.identifier.cristin2162997
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1


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Attribution-NonCommercial-NoDerivatives 4.0 Internasjonal
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