Please use this identifier to cite or link to this item: http://hdl.handle.net/1942/33098
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dc.contributor.authorD'ONOFRIO, Valentino-
dc.contributor.authorDonders, Elena-
dc.contributor.authorVanden Abeele, Marie-Elena-
dc.contributor.authorDubois, Jasperina-
dc.contributor.authorCartuyvels, Reinoud-
dc.contributor.authorACHTEN, Ruth-
dc.contributor.authorLammens, Martin-
dc.contributor.authorDendooven, Amelie-
dc.contributor.authorDRIESSEN, Ann-
dc.contributor.authorAugsburg, Lukasz-
dc.contributor.authorVanrusselt, Jan-
dc.contributor.authorCOX, Janneke-
dc.contributor.editorPasin, Laura-
dc.date.accessioned2021-01-15T14:43:01Z-
dc.date.available2021-01-15T14:43:01Z-
dc.date.issued2020-
dc.date.submitted2021-01-12T13:53:44Z-
dc.identifier.citationPLoS One, 15 (11) , (Art N° e0242300)-
dc.identifier.issn1932-6203-
dc.identifier.urihttp://hdl.handle.net/1942/33098-
dc.description.abstractBackground Minimally invasive autopsy (MIA) is a validated and safe method to establish the cause of death (COD), mainly in low-resource settings. However, the additional clinical value of MIA in Coronavirus disease (COVID-19) patients in a high-resource setting is unknown. The objective was to assess if and how MIA changed clinical COD and contributing diagnoses in deceased COVID-19 patients. Methods and findings A prospective observational cohort from April to May 2020 in a 981-bed teaching hospital in the epicenter of the COVID-19 pandemic in Belgium was established. Patients who died with either PCR-confirmed or radiologically confirmed COVID-19 infection were consecutively included. MIA consisted of whole-body CT and CT-guided Tru-Cut (R) biopsies. Diagnostic modalities were clinical chart review, radiology, microbiology, and histopathology which were assessed by two independent experts per modality. MIA COD and contributing diagnoses were established during a multi-disciplinary meeting. Clinical COD (CCOD) and contributing diagnosis were abstracted from the discharge letter. The main outcomes were alterations in CCOD and contributing diagnoses after MIA, and the contribution of each diagnostic modality. We included 18 patients, of which 7 after intensive care unit hospitalization. MIA led to an alteration in 15/18 (83%) patients. The CCOD was altered in 5/18 (28%) patients. MIA found a new COD (1/5), a more specific COD (1/5), a less certain COD (1/5), or a contributing diagnosis to be the COD (2/5). Contributing diagnoses were altered in 14/18 (78%) patients: 9 new diagnoses, 5 diagnoses dismissed, 3 made more specific, and 2 made less certain. Overall, histopathology contributed in 14/15 (93%) patients with alterations, radiology and microbiology each in 6/15 (40%), and clinical review in 3/15 (20%). Histopathology was deemed the most important modality in 10 patients, radiology in two patients, and microbiology in one patient. Conclusion MIA, especially histological examination, can add valuable new clinical information regarding the cause of death in COVID-19 patients, even in a high-resource setting with wide access to premortem diagnostic modalities. MIA may provide important clinical insights and should be applied in the current ongoing pandemic.-
dc.description.sponsorshipThis study/Janneke Cox has received funding from the Research Foundation Flanders (FWO) (G0G2620N). FWO.be. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript. This study is part of the Limburg Clinical Research Center (LCRC) UHasselt-ZOL-Jessa, supported by the foundation Limburg Sterk Merk (LSM), Hasselt University, Ziekenhuis Oost-Limburg and Jessa Hospital.-
dc.language.isoen-
dc.publisherPUBLIC LIBRARY SCIENCE-
dc.rights2020 D’Onofrio et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.-
dc.titleThe clinical value of minimal invasive autopsy in COVID-19 patients-
dc.typeJournal Contribution-
dc.identifier.issue11-
dc.identifier.volume15-
local.format.pages8-
local.bibliographicCitation.jcatA1-
dc.description.notesCox, J (corresponding author), Hasselt Univ, Fac Med & Life Sci, Hasselt, Belgium.; Cox, J (corresponding author), Jessa Hosp, Dept Infect Dis & Immun, Hasselt, Belgium.-
dc.description.notesjanneke.cox@jessazh.be-
dc.description.otherCox, J (corresponding author), Hasselt Univ, Fac Med & Life Sci, Hasselt, Belgium ; Jessa Hosp, Dept Infect Dis & Immun, Hasselt, Belgium janneke.cox@jessazh.be-
local.publisher.place1160 BATTERY STREET, STE 100, SAN FRANCISCO, CA 94111 USA-
local.type.refereedRefereed-
local.type.specifiedArticle-
local.bibliographicCitation.artnre0242300-
dc.identifier.doi10.1371/journal.pone.0242300-
dc.identifier.isiWOS:000593946900026-
local.provider.typewosris-
local.uhasselt.uhpubyes-
local.description.affiliation[D'Onofrio, Valentino; Cox, Janneke] Hasselt Univ, Fac Med & Life Sci, Hasselt, Belgium.-
local.description.affiliation[D'Onofrio, Valentino; Donders, Elena; Cox, Janneke] Jessa Hosp, Dept Infect Dis & Immun, Hasselt, Belgium.-
local.description.affiliation[Vanden Abeele, Marie-Elena] Jessa Hosp, Dept Geriatr, Hasselt, Belgium.-
local.description.affiliation[Dubois, Jasperina] Jessa Hosp, Intens Care & Anesthesiol, Hasselt, Belgium.-
local.description.affiliation[Cartuyvels, Reinoud] Jessa Hosp, Clin Lab, Hasselt, Belgium.-
local.description.affiliation[Achten, Ruth] Jessa Hosp, Dept Pathol, Hasselt, Belgium.-
local.description.affiliation[Achten, Ruth; Lammens, Martin; Dendooven, Amelie; Driessen, Ann] Antwerp Univ Hosp, Dept Pathol, Edegem, Belgium.-
local.description.affiliation[Lammens, Martin; Dendooven, Amelie; Driessen, Ann] Univ Antwerp, CORE, Antwerp, Belgium.-
local.description.affiliation[Dendooven, Amelie] Univ Hosp Ghent, Dept Pathol, Ghent, Belgium.-
local.description.affiliation[Augsburg, Lukasz; Vanrusselt, Jan] Jessa Hosp, Dept Radiol, Hasselt, Belgium.-
local.uhasselt.internationalyes-
item.validationecoom 2021-
item.contributorD'ONOFRIO, Valentino-
item.contributorDonders, Elena-
item.contributorVanden Abeele, Marie-Elena-
item.contributorDubois, Jasperina-
item.contributorCartuyvels, Reinoud-
item.contributorACHTEN, Ruth-
item.contributorLammens, Martin-
item.contributorDendooven, Amelie-
item.contributorDRIESSEN, Ann-
item.contributorAugsburg, Lukasz-
item.contributorVanrusselt, Jan-
item.contributorCOX, Janneke-
item.contributorPasin, Laura-
item.accessRightsOpen Access-
item.fullcitationD'ONOFRIO, Valentino; Donders, Elena; Vanden Abeele, Marie-Elena; Dubois, Jasperina; Cartuyvels, Reinoud; ACHTEN, Ruth; Lammens, Martin; Dendooven, Amelie; DRIESSEN, Ann; Augsburg, Lukasz; Vanrusselt, Jan & COX, Janneke (2020) The clinical value of minimal invasive autopsy in COVID-19 patients. In: PLoS One, 15 (11) , (Art N° e0242300).-
item.fulltextWith Fulltext-
crisitem.journal.issn1932-6203-
crisitem.journal.eissn1932-6203-
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