Publication:
Clinical and pathological correlation in pediatric invasive pulmonary aspergillosis

dc.contributor.authorNattachai Anantasiten_US
dc.contributor.authorNoramon Nuntacharruksaen_US
dc.contributor.authorPimpin Incharoenen_US
dc.contributor.authorAroonwan Preutthipanen_US
dc.contributor.otherFaculty of Medicine, Ramathibodi Hospital, Mahidol Universityen_US
dc.date.accessioned2019-08-28T06:23:40Z
dc.date.available2019-08-28T06:23:40Z
dc.date.issued2018-02-21en_US
dc.description.abstract© 2018 Anantasit, Nuntacharruksa, Incharoen and Preutthipan. Introduction: Invasive' pulmonary aspergillosis (IPA) has been one of the major causes of mortality in immunocompromised patients. The gold standard method for a diagnosis of IPA is histopathological examination of the lung tissue; however, post-procedural bleeding limits the feasibility of lung biopsy. The European Organization for Research and Treatment of Cancer/Invasive Fungal Infections Cooperative Group and The National Institute of Allergy and Infectious Disease Mycoses Study Group (EORTC/MSG) defined IPA. The objective of this study was to validate the EORTC/MSG 2008 definition of IPA, compared with histopathology in the pediatric population. Methods: Histopathological examinations of lung tissues of children aged 1 month-18 years with respiratory tract infection at the time of obtaining biopsy were retrieved. Retrospective chart reviews for clinical characteristics were performed. IPA diagnosis was classified according to the EORTC/MSG 2008 definition. Results: During the 10-year period, there were 256 lung tissues, of which 58 specimens were suspected to have pulmonary infection. Fourteen patients (24%) were noted to have IPA. Seven patients (50%) with proven IPA were classified as probable, while the remaining 50% were classified as possible, and none were classified as no IPA, by using EORTC/MSG 2008 definition. Other 44 specimens demonstrated 14 (32%), 14 (32%), and 16 (36%) were classified as probable, possible, and no IPA, respectively. When comparing probable or possible IPA with no IPA, we found that the EORTC/MSG 2008 definition had 100% sensitivity, 36% specificity, 33% positive predictive value, and 100% negative predictive value in diagnosis of IPA. Conclusion: Our study illustrated that the EORTC/MSG 2008 definition provided an excellent sensitivity but low specificity for diagnosing IPA.en_US
dc.identifier.citationFrontiers in Pediatrics. Vol.6, (2018)en_US
dc.identifier.doi10.3389/fped.2018.00031en_US
dc.identifier.issn22962360en_US
dc.identifier.other2-s2.0-85043373870en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/123456789/46940
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85043373870&origin=inwarden_US
dc.subjectMedicineen_US
dc.titleClinical and pathological correlation in pediatric invasive pulmonary aspergillosisen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85043373870&origin=inwarden_US

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