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About:
INITIAL HIGH VIRAL LOAD IS ASSOCIATED WITH PROLONGED SHEDDING OF HUMAN RHINOVIRUS IN ALLOGENEIC HEMATOPOIETIC CELL TRANSPLANT RECIPIENTS
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An Entity of Type :
schema:ScholarlyArticle
, within Data Space :
covidontheweb.inria.fr
associated with source
document(s)
Type:
Academic Article
research paper
schema:ScholarlyArticle
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type
Academic Article
research paper
schema:ScholarlyArticle
isDefinedBy
Covid-on-the-Web dataset
has title
INITIAL HIGH VIRAL LOAD IS ASSOCIATED WITH PROLONGED SHEDDING OF HUMAN RHINOVIRUS IN ALLOGENEIC HEMATOPOIETIC CELL TRANSPLANT RECIPIENTS
Creator
Campbelld, P
Englundd, A
Jeromed, R
Kuypersd, Xjane
Leisenringd, M
Xalpana, X
Xangela, X
Xchikara Ogimid, X
Xied, Xhu
Xjanet, X
Xkeith, X
Xmichael Boeckhd, X
Xwendy, X
Source
Elsevier; Medline; PMC
abstract
INTRODUCTION: Recent data suggest human rhinovirus (HRV) is associated with lower respiratory tract infection and mortality in hematopoietic cell transplant (HCT) recipients. Examining risk factors for prolonged viral shedding may provide critical insight for the development of novel therapeutics and help inform infection prevention practices. Our objective was to identify risk factors for prolonged shedding of HRV post-HCT. MATERIALS AND METHODS: We prospectively collected weekly nasal samples from allogeneic HCT recipients from day 0 to day 100 post-transplant, and performed realtime RT-PCR (12/2005 to 2/2010). Subjects with symptomatic HRV infection and a negative test within 2 weeks of the last positive were included. Duration of shedding was defined as time between the first positive and first negative samples. Cycle threshold (Ct) values were used as a proxy for viral load. HRV species were identified by sequencing the 5’ non-coding region. Logistic regression analyses were performed to evaluate factors associated with prolonged shedding (≥21 days). RESULTS: We identified 38 HCT recipients with HRV infection fulfilling study criteria (32 adults, 6 children). Median duration of shedding was 9.5 days (2-89 days); 18 patients had prolonged shedding. Among 26 samples sequenced, 69% were species A, and species B and C accounted for 15% each; the median shedding duration of HRV did not differ between species (P = 0.17). Bivariable logistic regression analyses suggest that initial high viral load (low Ct value) is associated with prolonged shedding. CONCLUSIONS: HCT recipients with initial high viral loads are at risk for prolonged HRV viral shedding.
has issue date
2018-10-01
(
xsd:dateTime
)
bibo:doi
10.1016/j.bbmt.2018.07.006
bibo:pmid
30009982
has license
hybrid-oa
sha1sum (hex)
03be1b13bb27c345596bc823c25963ebeb990640
schema:url
https://doi.org/10.1016/j.bbmt.2018.07.006
resource representing a document's title
INITIAL HIGH VIRAL LOAD IS ASSOCIATED WITH PROLONGED SHEDDING OF HUMAN RHINOVIRUS IN ALLOGENEIC HEMATOPOIETIC CELL TRANSPLANT RECIPIENTS
has PubMed Central identifier
PMC6239940
has PubMed identifier
30009982
schema:publication
Biology of Blood and Marrow Transplantation
resource representing a document's body
covid:03be1b13bb27c345596bc823c25963ebeb990640#body_text
is
schema:about
of
named entity 'objective'
named entity 'viral'
named entity 'development'
named entity 'Recent'
named entity 'duration'
named entity 'shedding'
named entity 'shedding'
named entity 'collected'
named entity 'Rhinovirus'
named entity 'Viral'
named entity 'Cell'
covid:arg/03be1b13bb27c345596bc823c25963ebeb990640
named entity 'weeks'
named entity 'species'
named entity 'identified'
named entity 'samples'
named entity 'patients'
named entity '21 days'
named entity 'performed'
named entity 'Median'
named entity 'day'
named entity 'Human'
named entity 'HRV'
named entity 'hematopoietic cell'
named entity 'HRV'
named entity 'Allogeneic'
named entity 'Transplant Recipients'
named entity 'randomized trials'
named entity 'parainfluenza virus'
named entity 'HRV'
named entity 'Fred Hutchinson Cancer Research Center'
named entity 'PCR'
named entity 'HRV'
named entity 'continuous variable'
named entity 'HRV'
named entity 'steroid'
named entity 'Sanger sequencing'
named entity 'RNA'
named entity 'respiratory symptoms'
named entity 'statistical analyses'
named entity 'upper respiratory'
named entity '21 days'
named entity 'lower respiratory tract'
named entity 'conditioning regimen'
named entity 'viral load'
named entity 'viruses'
named entity 'older patients'
named entity 'digital PCR'
named entity '21 days'
named entity 'HRV'
named entity 'Viral shedding'
named entity 'Odds ratios'
named entity 'clinical trials'
named entity 'viral shedding'
named entity 'allogeneic'
named entity 'HRV'
named entity 'RT-PCR'
named entity 'pathogens'
named entity 'transplant recipients'
named entity 'rhinovirus'
named entity 'statistically significant'
named entity 'HRV'
named entity 'dichotomous'
named entity 'upper respiratory tract'
named entity 'viral load'
named entity 'positive test'
named entity 'human coronavirus'
named entity 'coronavirus'
named entity 'viruses'
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