Identificador persistente para citar o vincular este elemento: https://accedacris.ulpgc.es/jspui/handle/10553/156310
Campo DC Valoridioma
dc.contributor.authorSnell, Luke B.en_US
dc.contributor.authorFisher, Chloe L.en_US
dc.contributor.authorTaj, Usmanen_US
dc.contributor.authorStirrup, Oliveren_US
dc.contributor.authorMerrick, Blairen_US
dc.contributor.authorAlcolea-Medina, Adelaen_US
dc.contributor.authorCharalampous, Themoulaen_US
dc.contributor.authorSignell, Adrian W.en_US
dc.contributor.authorWilson, Harry D.en_US
dc.contributor.authorBetancor Quintana, Gilberto Joseen_US
dc.contributor.authorKia Ik, Mark Tanen_US
dc.contributor.authorCunningham, Emmaen_US
dc.contributor.authorCliff, Penelope R.en_US
dc.contributor.authorPickering, Suzanneen_US
dc.contributor.authorGalao, Rui Pedroen_US
dc.contributor.authorBatra, Rahulen_US
dc.contributor.authorNeil, Stuart J.D.en_US
dc.contributor.authorMalim, Michael H.en_US
dc.contributor.authorDoores, Katie J.en_US
dc.contributor.authorDouthwaite, Sam T.en_US
dc.contributor.authorNebbia, Gaiaen_US
dc.contributor.authorEdgeworth, Jonathan D.en_US
dc.contributor.authorAwan, Ali R.en_US
dc.date.accessioned2026-01-28T15:32:43Z-
dc.date.available2026-01-28T15:32:43Z-
dc.date.issued2022en_US
dc.identifier.issn1198-743Xen_US
dc.identifier.urihttps://accedacris.ulpgc.es/jspui/handle/10553/156310-
dc.description.abstractObjectives To analyse nosocomial transmission in the early stages of the coronavirus 2019 (COVID-19) pandemic at a large multisite healthcare institution. Nosocomial incidence is linked with infection control interventions. Methods Viral genome sequence and epidemiological data were analysed for 574 consecutive patients, including 86 nosocomial cases, with a positive PCR test for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) during the first 19 days of the pandemic. Results Forty-four putative transmission clusters were found through epidemiological analysis; these included 234 cases and all 86 nosocomial cases. SARS-CoV-2 genome sequences were obtained from 168/234 (72%) of these cases in epidemiological clusters, including 77/86 nosocomial cases (90%). Only 75/168 (45%) of epidemiologically linked, sequenced cases were not refuted by applying genomic data, creating 14 final clusters accounting for 59/77 sequenced nosocomial cases (77%). Viral haplotypes from these clusters were enriched 1–14x (median 4x) compared to the community. Three factors implicated unidentified cases in transmission: (a) community-onset or indeterminate cases were absent in 7/14 clusters (50%), (b) four clusters (29%) had additional evidence of cryptic transmission, and (c) in three clusters (21%) diagnosis of the earliest case was delayed, which may have facilitated transmission. Nosocomial cases decreased to low levels (0–2 per day) despite continuing high numbers of admissions of community-onset SARS-CoV-2 cases (40–50 per day) and before the impact of introducing universal face masks and banning hospital visitors. Conclusion Genomics was necessary to accurately resolve transmission clusters. Our data support unidentified cases—such as healthcare workers or asymptomatic patients—as important vectors of transmission. Evidence is needed to ascertain whether routine screening increases case ascertainment and limits nosocomial transmission.en_US
dc.languageengen_US
dc.relation.ispartofClinical Microbiology and Infectionen_US
dc.sourceClinical Microbiology and Infection [eISSN 1198-743X], v. 28(1), p. 93-100 (Enero 2022)en_US
dc.subject32 Ciencias médicasen_US
dc.subject320505 Enfermedades infecciosasen_US
dc.subject320103 Microbiología clínicaen_US
dc.subject.otherHealthcare-associated infectionen_US
dc.subject.otherMolecular epidemiologyen_US
dc.subject.otherNosocomial transmissionen_US
dc.subject.otherSARS-CoV-2en_US
dc.subject.otherWhole-genome sequencingen_US
dc.titleCombined epidemiological and genomic analysis of nosocomial SARS-CoV-2 infection early in the pandemic and the role of unidentified cases in transmissionen_US
dc.typeinfo:eu-repo/semantics/Articleen_US
dc.typeArticleen_US
dc.identifier.doi10.1016/j.cmi.2021.07.040en_US
dc.description.lastpage100en_US
dc.identifier.issue1-
dc.description.firstpage93en_US
dc.relation.volume28en_US
dc.investigacionCiencias de la Saluden_US
dc.type2Artículoen_US
dc.description.numberofpages8en_US
dc.utils.revisionen_US
dc.date.coverdateEnero 2022en_US
dc.identifier.ulpgcen_US
dc.contributor.buulpgcBU-MEDen_US
dc.description.sjr3,587
dc.description.jcr14,2
dc.description.sjrqQ1
dc.description.jcrqQ1
dc.description.scieSCIE
dc.description.miaricds10,9
item.grantfulltextnone-
item.fulltextSin texto completo-
crisitem.author.deptGIR IUIBS: Trypanosomosis, Resistencia a Antibióticos, Virología y Medicina Animal-
crisitem.author.deptIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.orcid0000-0003-0548-7690-
crisitem.author.parentorgIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.fullNameBetancor Quintana, Gilberto Jose-
Colección:Artículos
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