Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/30138
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dc.contributor.authorKheir, Fayez-
dc.contributor.authorUribe Becerra, Juan Pablo-
dc.contributor.authorBissell, Brittany-
dc.contributor.authorGhazipura, Marya-
dc.contributor.authorHerman, Derrick-
dc.contributor.authorHon, Stephanie M-
dc.contributor.authorHossain, Tanzib-
dc.contributor.authorKhor, Yet H-
dc.contributor.authorKnight, Shandra L-
dc.contributor.authorKreuter, Michael-
dc.contributor.authorMacrea, Madalina-
dc.contributor.authorMammen, Manoj J-
dc.contributor.authorMartinez, Fernando J-
dc.contributor.authorPoletti, Venerino-
dc.contributor.authorTroy, Lauren-
dc.contributor.authorRaghu, Ganesh-
dc.contributor.authorWilson, Kevin C-
dc.date.accessioned2022-06-23T00:23:20Z-
dc.date.available2022-06-23T00:23:20Z-
dc.date.issued2022-05-
dc.identifier.citationAnnals of the American Thoracic Society 2022; 19(5): 827-832en
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/30138-
dc.description.abstractBackground: Usual interstitial pneumonia (UIP) is the histopathologic hallmark of idiopathic pulmonary fibrosis (IPF), the prototypical interstitial lung disease (ILD). Diagnosis of IPF requires that a typical UIP pattern be identified by using high-resolution chest computed tomography or lung sampling. A genomic classifier for UIP has been developed to predict histopathologic UIP by using lung samples obtained through bronchoscopy. Objective: To perform a systematic review to evaluate genomic classifier testing in the detection of histopathologic UIP to inform new American Thoracic Society, European Respiratory Society, Japanese Respiratory Society, and Asociación Latinoamericana del Tórax guidelines. Data Sources: Medline, Embase, and the Cochrane Central Register of Controlled Trials were searched through June 2020. Data Extraction: Data were extracted from studies that enrolled patients with ILD and reported the use of genomic classifier testing. Synthesis: Data were aggregated across studies via meta-analysis. The quality of the evidence was appraised by using the Grading of Recommendations, Assessment, Development, and Evaluation approach. Results: Genomic classifier testing had a sensitivity of 68% (95% confidence interval [CI], 55-73%) and a specificity of 92% (95% CI, 81-95%) in predicting the UIP pattern in ILD. Confidence in an IPF diagnosis increased from 43% to 93% in one cohort and from 59% to 89% in another cohort. Agreement levels in categorical IPF and non-IPF diagnoses measured by using a concordance coefficient were 0.75 and 0.64 in the two cohorts. The quality of evidence was moderate for test characteristics and very low for both confidence and agreement. Conclusions: Genomic classifier testing predicts histopathologic UIP in patients with ILD with a specificity of 92% and improves diagnostic confidence; however, sensitivity is only 68%, and testing is not widely available.en
dc.language.isoeng
dc.subjectgenomic classifieren
dc.subjectidiopathic pulmonary fibrosisen
dc.subjectinterstitial lung diseaseen
dc.subjectusual interstitial pneumoniaen
dc.titleUse of a Genomic Classifier in Patients with Interstitial Lung Disease: A Systematic Review and Meta-Analysis.en
dc.typeJournal Articleen
dc.identifier.journaltitleAnnals of the American Thoracic Societyen
dc.identifier.affiliationRespiratory and Sleep Medicineen
dc.identifier.affiliationDivision of Pulmonary and Critical Care Medicine, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusettsen
dc.identifier.affiliationAcute Care Pharmacy Services, University of Kentucky HealthCare, University of Kentucky, Lexington, Kentuckyen
dc.identifier.affiliationRespiratory Research@Alfred, Central Clinical School, Monash University, Melbourne, Victoria, Australiaen
dc.identifier.affiliationDivision of Thoracic Surgery and Interventional Pulmonology, Beth Israel Deaconess Medical Center and Harvard Medical School, Harvard University, Boston, Massachusettsen
dc.identifier.affiliationPharmacy Practice and Science Department, College of Pharmacy, University of Kentucky, Lexington, Kentuckyen
dc.identifier.affiliationZS Associates, Global Health Economics and Outcomes Research, New York, New Yorken
dc.identifier.affiliationDepartment of Medicine, The Ohio State University, Columbus, Ohioen
dc.identifier.affiliationDepartment of Medicine, School of Medicine, Tufts University, Boston, Massachusettsen
dc.identifier.affiliationDivision of Pulmonary, Critical Care, and Sleep Medicine, Department of Medicine, Grossman School of Medicine, New York University Langone Health, New York, New Yorken
dc.identifier.affiliationLibrary and Knowledge Services, National Jewish Health, Denver, Coloradoen
dc.identifier.affiliationCenter for Interstitial and Rare Lung Diseases, Department of Pneumology, University Hospital Heidelberg and German Center for Lung Research, Heidelberg, Germanyen
dc.identifier.affiliationDepartment of Medicine, Veterans Affairs Medical Center, Salem, Virginiaen
dc.identifier.affiliationDepartment of Medicine, Jacobs School of Medicine and Biomedical Sciences, University at Buffalo, Buffalo, New Yorken
dc.identifier.affiliationJoan and Sanford I. Weill Department of Medicine, New York-Presbyterian Hospital and Weill Cornell Medical Center, Weill Cornell Medical College, Cornell University, New York, New Yorken
dc.identifier.affiliationDepartment of Respiratory Diseases and Allergy, Aarhus University Hospital, Aarhus, Denmarken
dc.identifier.affiliationDepartment of Medicine, School of Medicine, University of Washington, Seattle, Washingtonen
dc.identifier.affiliationDepartment of Medicine, School of Medicine, Boston University, Boston, Massachusettsen
dc.identifier.affiliationDepartment of Respiratory and Sleep Medicine, Royal Prince Alfred Hospital, Camperdown, New South Wales, Australiaen
dc.identifier.affiliationDepartment of Respiratory and Thorax Diseases, GB Morgagni Hospital, Forlì, Italyen
dc.identifier.pubmedurihttps://pubmed.ncbi.nlm.nih.gov/34077697/en
dc.identifier.doi10.1513/AnnalsATS.202102-197OCen
dc.type.contentTexten
dc.identifier.orcid0000-0002-4192-5080en
dc.identifier.orcid0000-0002-7345-9731en
dc.identifier.orcid0000-0003-4328-6822en
dc.identifier.orcid0000-0002-0390-8407en
dc.identifier.orcid0000-0002-1995-7828en
dc.identifier.orcid0000-0002-5434-9342en
dc.identifier.orcid0000-0002-4404-3833en
dc.identifier.orcid0000-0002-5352-9587en
dc.identifier.orcid0000-0003-0343-3234en
dc.identifier.orcid0000-0002-7426-336Xen
dc.identifier.orcid0000-0001-7506-6643en
dc.identifier.orcid0000-0003-4429-2266en
dc.identifier.pubmedid34077697
local.name.researcherKhor, Yet H
item.languageiso639-1en-
item.openairetypeJournal Article-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextNo Fulltext-
item.grantfulltextnone-
item.cerifentitytypePublications-
crisitem.author.deptRespiratory and Sleep Medicine-
crisitem.author.deptInstitute for Breathing and Sleep-
crisitem.author.deptMedicine (University of Melbourne)-
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