{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,6,26]],"date-time":"2026-06-26T10:05:59Z","timestamp":1782468359569,"version":"3.54.5"},"reference-count":38,"publisher":"Elsevier BV","issue":"1","license":[{"start":{"date-parts":[[2022,1,1]],"date-time":"2022-01-01T00:00:00Z","timestamp":1640995200000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2022,1,1]],"date-time":"2022-01-01T00:00:00Z","timestamp":1640995200000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/legal\/tdmrep-license"},{"start":{"date-parts":[[2024,1,1]],"date-time":"2024-01-01T00:00:00Z","timestamp":1704067200000},"content-version":"vor","delay-in-days":730,"URL":"http:\/\/www.elsevier.com\/open-access\/userlicense\/1.0\/"}],"content-domain":{"domain":["clinicalkey.com","clinicalkey.com.au","clinicalkey.es","clinicalkey.fr","clinicalkey.jp","cysticfibrosisjournal.com","elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["Journal of Cystic Fibrosis"],"published-print":{"date-parts":[[2022,1]]},"DOI":"10.1016\/j.jcf.2021.07.008","type":"journal-article","created":{"date-parts":[[2021,7,28]],"date-time":"2021-07-28T23:14:31Z","timestamp":1627514071000},"page":"136-142","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":17,"title":["Clinician variability in the diagnosis and treatment of aspergillus fumigatus-related conditions in cystic fibrosis: An international survey"],"prefix":"10.1016","volume":"21","author":[{"ORCID":"https:\/\/orcid.org\/0000-0001-9321-8399","authenticated-orcid":false,"given":"Gina","family":"Hong","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Sameer","family":"Desai","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Richard B.","family":"Moss","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0003-2059-3352","authenticated-orcid":false,"given":"Patience","family":"Eschenhagen","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Bradley S.","family":"Quon","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0003-3474-2857","authenticated-orcid":false,"given":"Carsten","family":"Schwarz","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"78","reference":[{"issue":"2","key":"10.1016\/j.jcf.2021.07.008_bib0001","doi-asserted-by":"crossref","first-page":"212","DOI":"10.1016\/j.jcf.2018.10.001","article-title":"Prevalence, geographic risk factor, and development of a standardized protocol for fungal isolation in cystic fibrosis: results from the international prospective study \"MFIP\"","volume":"18","author":"Delhaes","year":"2019","journal-title":"J Cyst Fibros"},{"issue":"2","key":"10.1016\/j.jcf.2021.07.008_bib0002","doi-asserted-by":"crossref","first-page":"221","DOI":"10.1016\/j.jcf.2018.11.012","article-title":"Prevalence and diversity of filamentous fungi in the airways of cystic fibrosis patients - a Dutch, multicentre study","volume":"18","author":"Engel","year":"2019","journal-title":"J Cyst Fibros"},{"issue":"4","key":"10.1016\/j.jcf.2021.07.008_bib0003","doi-asserted-by":"crossref","first-page":"1122","DOI":"10.1128\/JCM.02182-16","article-title":"Use of selective fungal culture media increases rates of detection of fungi in the respiratory tract of cystic fibrosis patients","volume":"55","author":"Hong","year":"2017","journal-title":"J Clin Microbiol"},{"issue":"1","key":"10.1016\/j.jcf.2021.07.008_bib0004","doi-asserted-by":"crossref","first-page":"18999","DOI":"10.1038\/s41598-020-75886-w","article-title":"Risk factors for respiratory Aspergillus fumigatus in German Cystic Fibrosis patients and impact on lung function","volume":"10","author":"D\u00fcesberg","year":"2020","journal-title":"Sci Rep"},{"key":"10.1016\/j.jcf.2021.07.008_bib0005","doi-asserted-by":"crossref","first-page":"161","DOI":"10.1016\/j.biocel.2014.03.001","article-title":"Fungi in the cystic fibrosis lung: bystanders or pathogens?","volume":"52","author":"Chotirmall","year":"2014","journal-title":"Int J Biochem Cell Biol"},{"issue":"S3","key":"10.1016\/j.jcf.2021.07.008_bib0006","doi-asserted-by":"crossref","first-page":"S75","DOI":"10.1002\/ppul.24126","article-title":"The myriad challenges of respiratory fungal infection in cystic fibrosis","volume":"53","author":"Tracy","year":"2018","journal-title":"Pediatr Pulmonol"},{"issue":"3","key":"10.1016\/j.jcf.2021.07.008_bib0007","doi-asserted-by":"crossref","first-page":"560","DOI":"10.1016\/j.jaci.2013.04.007","article-title":"Novel immunologic classification of aspergillosis in adult cystic fibrosis","volume":"132","author":"Baxter","year":"2013","journal-title":"J Allergy Clin Immunol"},{"issue":"1","key":"10.1016\/j.jcf.2021.07.008_bib0008","doi-asserted-by":"crossref","first-page":"39","DOI":"10.1097\/MCP.0000000000000129","article-title":"Allergic fungal airway disease: pathophysiologic and diagnostic considerations","volume":"21","author":"Woolnough","year":"2015","journal-title":"Curr Opin Pulm Med"},{"issue":"11","key":"10.1016\/j.jcf.2021.07.008_bib0009","doi-asserted-by":"crossref","first-page":"1211","DOI":"10.1164\/rccm.200603-423OC","article-title":"Effect of allergic bronchopulmonary aspergillosis on lung function in children with cystic fibrosis","volume":"174","author":"Kraemer","year":"2006","journal-title":"Am J Respir Crit Care Med"},{"issue":"1","key":"10.1016\/j.jcf.2021.07.008_bib0010","doi-asserted-by":"crossref","first-page":"171","DOI":"10.1378\/chest.09-1103","article-title":"The effect of chronic infection with Aspergillus fumigatus on lung function and hospitalization in patients with cystic fibrosis","volume":"137","author":"Amin","year":"2010","journal-title":"Chest"},{"issue":"3","key":"10.1016\/j.jcf.2021.07.008_bib0011","doi-asserted-by":"crossref","first-page":"e197","DOI":"10.1016\/j.ejrad.2011.01.114","article-title":"Radiological abnormalities associated with Aspergillus colonization in a cystic fibrosis population","volume":"81","author":"McMahon","year":"2012","journal-title":"Eur J Radiol"},{"issue":"1","key":"10.1016\/j.jcf.2021.07.008_bib0012","doi-asserted-by":"crossref","first-page":"125","DOI":"10.1016\/j.jcf.2019.08.008","article-title":"The presence of Aspergillus fumigatus is associated with worse respiratory quality of life in cystic fibrosis","volume":"19","author":"Hong","year":"2020","journal-title":"J Cyst Fibros"},{"issue":"6","key":"10.1016\/j.jcf.2021.07.008_bib0013","doi-asserted-by":"crossref","first-page":"688","DOI":"10.1164\/rccm.201908-1585OC","article-title":"Aspergillus infections and progression of structural lung disease in children with cystic fibrosis","volume":"201","author":"Breuer","year":"2020","journal-title":"Am J Respir Crit Care Med"},{"issue":"Suppl 3","key":"10.1016\/j.jcf.2021.07.008_bib0014","doi-asserted-by":"crossref","first-page":"S225","DOI":"10.1086\/376525","article-title":"Allergic bronchopulmonary aspergillosis in cystic fibrosis\u2013state of the art: Cystic Fibrosis Foundation Consensus Conference","volume":"37","author":"Stevens","year":"2003","journal-title":"Clin Infect Dis"},{"issue":"3","key":"10.1016\/j.jcf.2021.07.008_bib0015","doi-asserted-by":"crossref","first-page":"656","DOI":"10.1016\/j.chest.2018.01.005","article-title":"A randomized trial of itraconazole vs prednisolone in acute-stage allergic bronchopulmonary aspergillosis complicating asthma","volume":"153","author":"Agarwal","year":"2018","journal-title":"Chest"},{"issue":"3 Suppl","key":"10.1016\/j.jcf.2021.07.008_bib0016","first-page":"S1","article-title":"Infection control recommendations for patients with cystic fibrosis: microbiology, important pathogens, and infection control practices to prevent patient-to-patient transmission","volume":"31","author":"Saiman","year":"2003","journal-title":"Am J Infect Control"},{"issue":"1","key":"10.1016\/j.jcf.2021.07.008_bib0017","doi-asserted-by":"crossref","first-page":"7","DOI":"10.1016\/j.jcf.2004.12.002","article-title":"Standards of care for patients with cystic fibrosis: a European consensus","volume":"4","author":"Kerem","year":"2005","journal-title":"J Cyst Fibros"},{"key":"10.1016\/j.jcf.2021.07.008_bib0018","unstructured":"2019 Annual Data Report. 2020."},{"issue":"Suppl 1","key":"10.1016\/j.jcf.2021.07.008_bib0019","doi-asserted-by":"crossref","first-page":"S88","DOI":"10.3109\/13693786.2010.511287","article-title":"Lack of standardization in the procedures for mycological examination of sputum samples from CF patients: a possible cause for variations in the prevalence of filamentous fungi","volume":"48","author":"Borman","year":"2010","journal-title":"Med Mycol"},{"issue":"2","key":"10.1016\/j.jcf.2021.07.008_bib0020","doi-asserted-by":"crossref","first-page":"155","DOI":"10.1093\/mmy\/myy014","article-title":"The diagnosis and management of respiratory tract fungal infection in cystic fibrosis: a UK survey of current practice","volume":"57","author":"Boyle","year":"2019","journal-title":"Med Mycol"},{"issue":"2","key":"10.1016\/j.jcf.2021.07.008_bib0021","doi-asserted-by":"crossref","first-page":"377","DOI":"10.1016\/j.jbi.2008.08.010","article-title":"Research electronic data capture (REDCap)\u2013a metadata-driven methodology and workflow process for providing translational research informatics support","volume":"42","author":"Harris","year":"2009","journal-title":"J Biomed Inform"},{"key":"10.1016\/j.jcf.2021.07.008_bib0022","series-title":"R: a language and environment for statistical computing","year":"2018"},{"issue":"2","key":"10.1016\/j.jcf.2021.07.008_bib0023","doi-asserted-by":"crossref","first-page":"153","DOI":"10.1016\/j.jcf.2018.02.006","article-title":"ECFS best practice guidelines: the 2018 revision","volume":"17","author":"Castellani","year":"2018","journal-title":"J Cyst Fibros"},{"issue":"8","key":"10.1016\/j.jcf.2021.07.008_bib0024","doi-asserted-by":"crossref","first-page":"781","DOI":"10.1093\/mmy\/myw035","article-title":"Fungal epidemiology and diversity in cystic fibrosis patients over a 5-year period in a national reference center","volume":"54","author":"Ziesing","year":"2016","journal-title":"Med Mycol"},{"issue":"5","key":"10.1016\/j.jcf.2021.07.008_bib0025","doi-asserted-by":"crossref","first-page":"1909","DOI":"10.1016\/j.jaip.2020.12.064","article-title":"Biomarkers for the diagnosis of allergic bronchopulmonary aspergillosis in cystic fibrosis: a systematic review and meta-analysis","volume":"9","author":"Li","year":"2021","journal-title":"J Allergy Clin Immunol Pract"},{"issue":"4","key":"10.1016\/j.jcf.2021.07.008_bib0026","doi-asserted-by":"crossref","first-page":"e31","DOI":"10.1016\/j.jcf.2019.02.002","article-title":"CT evaluation of hyperattenuating mucus to diagnose allergic bronchopulmonary aspergillosis in the special condition of cystic fibrosis","volume":"18","author":"Refait","year":"2019","journal-title":"J Cyst Fibros"},{"issue":"11","key":"10.1016\/j.jcf.2021.07.008_bib0027","doi-asserted-by":"crossref","first-page":"756","DOI":"10.1056\/NEJM200003163421102","article-title":"A randomized trial of itraconazole in allergic bronchopulmonary aspergillosis","volume":"342","author":"Stevens","year":"2000","journal-title":"N Engl J Med"},{"issue":"5","key":"10.1016\/j.jcf.2021.07.008_bib0028","doi-asserted-by":"crossref","first-page":"952","DOI":"10.1067\/mai.2003.1388","article-title":"Anti-inflammatory effect of itraconazole in stable allergic bronchopulmonary aspergillosis: a randomized controlled trial","volume":"111","author":"Wark","year":"2003","journal-title":"J Allergy Clin Immunol"},{"issue":"10","key":"10.1016\/j.jcf.2021.07.008_bib0029","doi-asserted-by":"crossref","first-page":"1210","DOI":"10.1111\/cea.12333","article-title":"Antifungal treatment in allergic bronchopulmonary aspergillosis with and without cystic fibrosis: a systematic review","volume":"44","author":"Moreira","year":"2014","journal-title":"Clin Exp Allergy"},{"issue":"4","key":"10.1016\/j.jcf.2021.07.008_bib0030","doi-asserted-by":"crossref","first-page":"e1","DOI":"10.1093\/cid\/ciw326","article-title":"Practice guidelines for the diagnosis and management of aspergillosis: 2016 update by the Infectious Diseases Society of America","volume":"63","author":"Patterson","year":"2016","journal-title":"Clin Infect Dis"},{"issue":"1","key":"10.1016\/j.jcf.2021.07.008_bib0031","doi-asserted-by":"crossref","first-page":"222","DOI":"10.1378\/chest.130.1.222","article-title":"Aspergillus bronchitis in cystic fibrosis","volume":"130","author":"Shoseyov","year":"2006","journal-title":"Chest"},{"issue":"1","key":"10.1016\/j.jcf.2021.07.008_bib0032","doi-asserted-by":"crossref","first-page":"61","DOI":"10.1007\/s11046-017-0190-0","article-title":"Aspergillus bronchitis in patients with cystic fibrosis","volume":"183","author":"Brandt","year":"2018","journal-title":"Mycopathologia"},{"issue":"4","key":"10.1016\/j.jcf.2021.07.008_bib0033","doi-asserted-by":"crossref","first-page":"E197","DOI":"10.1111\/1469-0691.12133","article-title":"Performance of two Aspergillus IgG EIA assays compared with the precipitin test in chronic and allergic aspergillosis","volume":"19","author":"Baxter","year":"2013","journal-title":"Clin Microbiol Infect"},{"issue":"4","key":"10.1016\/j.jcf.2021.07.008_bib0034","doi-asserted-by":"crossref","first-page":"433","DOI":"10.1093\/cid\/ciw444","article-title":"Executive summary: practice guidelines for the diagnosis and management of aspergillosis: 2016 update by the Infectious Diseases Society of America","volume":"63","author":"Patterson","year":"2016","journal-title":"Clin Infect Dis"},{"issue":"Suppl 1","key":"10.1016\/j.jcf.2021.07.008_bib0035","doi-asserted-by":"crossref","first-page":"e1","DOI":"10.1016\/j.cmi.2018.01.002","article-title":"Diagnosis and management of Aspergillus diseases: executive summary of the 2017 ESCMID-ECMM-ERS guideline","volume":"24","author":"Ullmann","year":"2018","journal-title":"Clin Microbiol Infect"},{"issue":"1","key":"10.1016\/j.jcf.2021.07.008_bib0036","doi-asserted-by":"crossref","first-page":"45","DOI":"10.1183\/13993003.00583-2015","article-title":"Chronic pulmonary aspergillosis: rationale and clinical guidelines for diagnosis and management","volume":"47","author":"Denning","year":"2016","journal-title":"Eur Respir J"},{"issue":"4","key":"10.1016\/j.jcf.2021.07.008_bib0037","doi-asserted-by":"crossref","first-page":"e36077","DOI":"10.1371\/journal.pone.0036077","article-title":"Treatment of Aspergillus fumigatus in patients with cystic fibrosis: a randomized, placebo-controlled pilot study","volume":"7","author":"Aaron","year":"2012","journal-title":"PLoS ONE"},{"issue":"10","key":"10.1016\/j.jcf.2021.07.008_bib0038","doi-asserted-by":"crossref","first-page":"999","DOI":"10.1164\/rccm.201203-0478OC","article-title":"The effect of Aspergillus fumigatus infection on vitamin D receptor expression in cystic fibrosis","volume":"186","author":"Coughlan","year":"2012","journal-title":"Am J Respir Crit Care Med"}],"container-title":["Journal of Cystic Fibrosis"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S1569199321013060?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S1569199321013060?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2025,10,27]],"date-time":"2025-10-27T21:46:08Z","timestamp":1761601568000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S1569199321013060"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2022,1]]},"references-count":38,"journal-issue":{"issue":"1","published-print":{"date-parts":[[2022,1]]}},"alternative-id":["S1569199321013060"],"URL":"https:\/\/doi.org\/10.1016\/j.jcf.2021.07.008","relation":{},"ISSN":["1569-1993"],"issn-type":[{"value":"1569-1993","type":"print"}],"subject":[],"published":{"date-parts":[[2022,1]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"Clinician variability in the diagnosis and treatment of aspergillus fumigatus-related conditions in cystic fibrosis: An international survey","name":"articletitle","label":"Article Title"},{"value":"Journal of Cystic Fibrosis","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.jcf.2021.07.008","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"\u00a9 2021 European Cystic Fibrosis Society. Published by Elsevier B.V.","name":"copyright","label":"Copyright"}]}}