Please use this identifier to cite or link to this item: https://hdl.handle.net/11499/47388
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dc.contributor.authorŞimsek, Fikri Selçuk-
dc.contributor.authorYüksel, Doğangün-
dc.contributor.authorYaylalı, Olga-
dc.contributor.authorAslan, Halil Serdar-
dc.contributor.authorKılıçarslan, Emel-
dc.contributor.authorBir, Ferda-
dc.contributor.authorArslan, Muhammet-
dc.contributor.authorCan, Fatma Ezgi-
dc.contributor.authorUğurlu, Erhan-
dc.date.accessioned2023-01-09T21:24:17Z-
dc.date.available2023-01-09T21:24:17Z-
dc.date.issued2021-
dc.identifier.issn1867-1071-
dc.identifier.urihttps://doi.org/10.1007/s11604-021-01155-z-
dc.identifier.urihttps://hdl.handle.net/11499/47388-
dc.description.abstractPurpose: Sometimes, characterization of pleural effusion (PE) can be challenging especially in patients whom invasive procedures/recurrent invasive procedures cannot be performed. The main purpose of the study is to answer this question, Can 18F-FDG-PET/CT contribute to reduction in the number of invasive procedures or patients undergoing to invasive procedures? Results may increase the effectiveness of patient management by facilitating clinical decision-making, especially in patients who cannot undergo invasive/recurrent invasive procedures. Methods: Sixty-seven patients’ 18F-FDG-PET/CT, pleural fluid cytologies (PFCs) and, if any, pleural biopsies were re-assessed. If patient’s PFC/biopsy was malignant, effusion was considered as malignant. If two consecutive PFCs were negative in patients without biopsy, effusion was considered as benign. Characterization was based on consensus with baseline/follow-up 18F-FDG-PET/CT and clinical parameters in patients with one negative PFC (n = 6). Results: None of the 18F-FDG-PET/CT parameters could characterize PE alone. However, if PE maximum standardized uptake value (SUVmax) > 1.3 or PE SUVmax/mean standardized uptake value of mediastinal blood pool (MBP SUVmean) > 1.2 was combined with at least one of the following, specificity and positive predictive value (PPV) were 100%, accuracy was around 90%. Diffuse-nodular/nodular pleural thickness, post-obstructive atelectasis, nodule/mass with SUVmax > 2.5 in lung, multiple pulmonary nodules. All 29 patients who had SUVmax > 1.3 together with at least one of the mentioned four parameters diagnosed malignant pleural effusion (MPE). However, sensitivity and negative predictive value (NPV) were still insufficient. Conclusion: Patients who have contraindications for invasive diagnostic methods, and meet the aforementioned criteria may be considered as MPE primarily. On the other hand, if PE SUVmax < 1.3 or PE SUVmax/MBP SUVmean < 1.2 with the negativity of the all four parameters mentioned above, it is difficult to say that this can be considered as benign pleural effusion (BPE) according to our results. © 2021, Japan Radiological Society.en_US
dc.language.isoenen_US
dc.publisherSpringer Japanen_US
dc.relation.ispartofJapanese Journal of Radiologyen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subject18F-FDG-PETen_US
dc.subjectCombined approachesen_US
dc.subjectCTen_US
dc.subjectPleural effusionen_US
dc.subjectfluorodeoxyglucose f 18en_US
dc.subjectradiopharmaceutical agenten_US
dc.subjectdiagnostic imagingen_US
dc.subjecthumanen_US
dc.subjectmultiple pulmonary nodulesen_US
dc.subjectpleura effusionen_US
dc.subjectpositron emission tomography-computed tomographyen_US
dc.subjecttumor recurrenceen_US
dc.subjectFluorodeoxyglucose F18en_US
dc.subjectHumansen_US
dc.subjectMultiple Pulmonary Nodulesen_US
dc.subjectNeoplasm Recurrence, Localen_US
dc.subjectPleural Effusionen_US
dc.subjectPositron Emission Tomography Computed Tomographyen_US
dc.subjectRadiopharmaceuticalsen_US
dc.titleCan PET/CT be used more effectively in pleural effusion evaluation?en_US
dc.typeArticleen_US
dc.identifier.volume39en_US
dc.identifier.issue12en_US
dc.identifier.startpage1186en_US
dc.identifier.endpage1194en_US
dc.identifier.doi10.1007/s11604-021-01155-z-
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.authorscopusid56903959400-
dc.authorscopusid6701446280-
dc.authorscopusid23135840600-
dc.authorscopusid57226492427-
dc.authorscopusid57200699270-
dc.authorscopusid8503814800-
dc.authorscopusid35274490400-
dc.identifier.pmid34165683en_US
dc.identifier.scopus2-s2.0-85120397226en_US
dc.identifier.scopusqualityQ2-
item.languageiso639-1en-
item.openairetypeArticle-
item.grantfulltextnone-
item.cerifentitytypePublications-
item.fulltextNo Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
crisitem.author.dept14.02. Internal Medicine-
crisitem.author.dept14.02. Internal Medicine-
crisitem.author.dept14.02. Internal Medicine-
crisitem.author.dept14.02. Internal Medicine-
crisitem.author.dept14.01. Surgical Medicine-
crisitem.author.dept14.01. Surgical Medicine-
crisitem.author.dept14.02. Internal Medicine-
crisitem.author.dept14.02. Internal Medicine-
Appears in Collections:PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection
Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
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