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Title: | Epidemiology and outcome for viremia in children undergoing bone marrow transplant: A retrospective cohort study | Authors: | Silcock, R. Mitchell, K. Fraser, C. Clark, J. |
Issue Date: | 2021 | Source: | 23, (4), 2021 | Journal: | Transplant Infectious Disease | Abstract: | Introduction: Viral infections pose a serious risk for children undergoing hematopoietic stem cell transplant (HSCT). There are few published case series of prevalence, risk factors, and outcomes examining multiple viruses simultaneously, and no pediatric Australasian data published to date. We describe the real-life experience of viremia in pediatric HSCT in a single tertiary center. Methods: All episodes of viremia in children undergoing HSCT between 2000 and 2018 were identified by matching HSCT patients’ unique identification numbers with positive blood polymerase chain reaction (PCR) results for human adenovirus (HAdV), cytomegalovirus (CMV), Epstein-Barr virus (EBV), and human herpes virus 6 (HHV-6). Paper or electronic charts and electronic pathology results were used to extract the study variables. Results: Viremia was detected in 177/445 (39.8%) HSCT episodes, of which 46% were allogeneic and 19% autologous transplants. Viremia was disseminated in 96 (21.6%) episodes, with 80 (18%) having more than one virus. HAdV was detected in 108 (24.3% of total episodes) and frequently in autologous transplants, CMV in 71 (16.0%), EBV in 60 (13.5%), and HHV-6 in 38 (8.5%). Of 174 children, 19 (10.9%) died of a viral-associated cause, with viral mortality highest in CMV (18.3%), lowest in HHV-6 (2.6%) with HAdV and EBV similar (6.6% and 6.7%). Adenoviral (but not other virus) dissemination was significantly associated with lower lymphocyte count at time of first detection. CMV dissemination and death were significantly associated with initial and highest CMV viral loads (copies/mL). Conclusion: This study presents the first pediatric-specific Australasian data for viremia in HSCT. Findings may help guide clinicians in prophylaxis and treatment decisions.L20105261392021-03-01 | DOI: | 10.1111/tid.13580 | Resources: | https://www.embase.com/search/results?subaction=viewrecord&id=L2010526139&from=exporthttp://dx.doi.org/10.1111/tid.13580 | | Keywords: | clinical outcome;cohort analysis;controlled study;cytomegalovirus infection;cytotoxic T lymphocyte;Epstein Barr virus infection;female;fever;follow up;graft versus host reaction;hematopoietic stem cell transplantation;human;Human adenovirus C;human adenovirus infection;human herpesvirus 6 infection;infant;infection prevention;infection risk;lymphocyte count;major clinical study;male;matched related donor;matched sibling donor;mismatched unrelated donor;mortality;mortality rate;neutrophil count;newborn;pericardial effusion;personal experience;polymerase chain reaction;posttransplant lymphoproliferative disease;preemptive antiviral therapy;prevalence;retrospective study;sibling donor;tertiary care center;treatment duration;unrelated donor;virus detection;virus load;viremia;aciclovirbrincidofovir;cidofovir;Cytomegalovirus antibody;foscarnet;ganciclovir;rituximab;tablecleucel;valganciclovir;virus DNA;adolescent;adult;allogeneic hematopoietic stem cell transplantation;article;bone marrow transplantation;cerebrospinal fluid;child | Type: | Article |
Appears in Sites: | Children's Health Queensland Publications |
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