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Am. J. Respir. Crit. Care Med. · Nov 2021
Comparative StudyDiagnostic Accuracy of Endobronchial Optical Coherence Tomography for the Microscopic Diagnosis of Usual Interstitial Pneumonia.
- Sreyankar Nandy, Rebecca A Raphaely, Ashok Muniappan, Angela Shih, Benjamin W Roop, Amita Sharma, Colleen M Keyes, Thomas V Colby, Hugh G Auchincloss, Henning A Gaissert, Michael Lanuti, Christopher R Morse, Harald C Ott, John C Wain, Cameron D Wright, Maria L Garcia-Moliner, Maxwell L Smith, Paul A VanderLaan, Sarita R Berigei, Mari Mino-Kenudson, Nora K Horick, Lloyd L Liang, Diane L Davies, Margit V Szabari, Peter Caravan, Benjamin D Medoff, Andrew M Tager, Melissa J Suter, and Lida P Hariri.
- Division of Pulmonary and Critical Care Medicine.
- Am. J. Respir. Crit. Care Med. 2021 Nov 15; 204 (10): 116411791164-1179.
AbstractRationale: Early, accurate diagnosis of interstitial lung disease (ILD) informs prognosis and therapy, especially in idiopathic pulmonary fibrosis (IPF). Current diagnostic methods are imperfect. High-resolution computed tomography has limited resolution, and surgical lung biopsy (SLB) carries risks of morbidity and mortality. Endobronchial optical coherence tomography (EB-OCT) is a low-risk, bronchoscope-compatible modality that images large lung volumes in vivo with microscopic resolution, including subpleural lung, and has the potential to improve the diagnostic accuracy of bronchoscopy for ILD diagnosis. Objectives: We performed a prospective diagnostic accuracy study of EB-OCT in patients with ILD with a low-confidence diagnosis undergoing SLB. The primary endpoints were EB-OCT sensitivity/specificity for diagnosis of the histopathologic pattern of usual interstitial pneumonia (UIP) and clinical IPF. The secondary endpoint was agreement between EB-OCT and SLB for diagnosis of the ILD fibrosis pattern. Methods: EB-OCT was performed immediately before SLB. The resulting EB-OCT images and histopathology were interpreted by blinded, independent pathologists. Clinical diagnosis was obtained from the treating pulmonologists after SLB, blinded to EB-OCT. Measurements and Main Results: We enrolled 31 patients, and 4 were excluded because of inconclusive histopathology or lack of EB-OCT data. Twenty-seven patients were included in the analysis (16 men, average age: 65.0 yr): 12 were diagnosed with UIP and 15 with non-UIP ILD. Average FVC and DlCO were 75.3% (SD, 18.5) and 53.5% (SD, 16.4), respectively. Sensitivity and specificity of EB-OCT was 100% (95% confidence interval, 75.8-100.0%) and 100% (79.6-100%), respectively, for both histopathologic UIP and clinical diagnosis of IPF. There was high agreement between EB-OCT and histopathology for diagnosis of ILD fibrosis pattern (weighted κ: 0.87 [0.72-1.0]). Conclusions: EB-OCT is a safe, accurate method for microscopic ILD diagnosis, as a complement to high-resolution computed tomography and an alternative to SLB.
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