Publication:
Follow-up of human adenovirus viral load in pediatric hematopoietic stem cell transplant recipients

dc.contributor.authorPeker, Bilal Olcay
dc.contributor.authorKıntrup, Gülen Tüysüz
dc.contributor.authorSağlık, İmran
dc.contributor.authorSarinoğlu, Rabia Can
dc.contributor.authorGüler, Elif
dc.contributor.authorMutlu, Derya
dc.contributor.authorKüpesiz, Osman Alphan
dc.contributor.authorÇolak, Dilek
dc.contributor.buuauthorSAĞLIK, İMRAN
dc.contributor.departmentBursa Uludağ Üniversitesi/Tıp Fakültesi/Tıbbi Mikrobiyoloji Anabilim Dalı.
dc.contributor.orcid0000-0003-0864-4989
dc.contributor.researcheridA-4970-2019
dc.contributor.researcheridGCM-3391-2022
dc.date.accessioned2024-06-27T11:03:33Z
dc.date.available2024-06-27T11:03:33Z
dc.date.issued2021-01-16
dc.description.abstractBackground: The spectrum of human adenovirus (HAdV)-related disease is broad, and the virus acts on many organs and systems in hematopoietic stem cell transplantation (HSCT) recipients. We aimed to evaluate the effect of HAdV-DNA positivity with clinical and laboratory findings 4 months after HSCT.Methods and results: We retrospectively investigated HAdV-DNA in 153 HSCT recipients (<= 18 years) by quantitative real-time polymerase chain reaction (RealStar; Altona Diagnostics). The results of samples from January 2014 to December 2017 are included. HAdV-DNA was positive for at least one sample type in 50 (32.67%) patients. HAdV-DNA positivity rate was 8.92% (N: 145/1625), 40.25% (N: 64/159), and 25% (N: 2/8) for plasma, stool, and urine samples, respectively. HAdV-DNA was positive in the plasma of 38 (24.83%) patients at a median 16 (range: 1-58 days) days after HSCT. The mortality rate was 23.68% and 6.95% in plasma HAdV-positive and HAdV-negative patients (p = .014). Moreover, HAdV-DNA positivity had an impact on overall survival for allogeneic-HSCT (p = .013), with the cumulative effect including graft-versus-host disease state in multivariate analysis (p = .014).Conclusions: Plasma HAdV-DNA positivity is a potential influencer that decreases survival in the early post-transplant period. Due to the high mortality rates, close monitoring is required of HAdV infections after HSCT with sensitive methods, especially at the early stage.
dc.identifier.doi10.1111/ctr.14209
dc.identifier.eissn1399-0012
dc.identifier.issn0902-0063
dc.identifier.issue3
dc.identifier.urihttps://doi.org/10.1111/ctr.14209
dc.identifier.urihttps://onlinelibrary.wiley.com/doi/10.1111/ctr.14209
dc.identifier.urihttps://hdl.handle.net/11452/42518
dc.identifier.volume35
dc.identifier.wos000607910900001
dc.indexed.wosWOS.SCI
dc.language.isoen
dc.publisherWiley
dc.relation.journalClinical Transplantation
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectRisk-factors
dc.subjectInfection
dc.subjectDiagnosis
dc.subjectCytomegalovirus
dc.subjectReconstitution
dc.subjectVirus
dc.subjectHematopoietic stem cell transplantation
dc.subjectHuman adenovirus
dc.subjectQuantitative polymerase chain reaction
dc.subjectSurvival
dc.subjectSurgery
dc.subjectTransplantation
dc.titleFollow-up of human adenovirus viral load in pediatric hematopoietic stem cell transplant recipients
dc.typeArticle
dspace.entity.typePublication
relation.isAuthorOfPublicationaab7d5dd-72a4-4f3a-a677-1fdf3e13cadc
relation.isAuthorOfPublication.latestForDiscoveryaab7d5dd-72a4-4f3a-a677-1fdf3e13cadc

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