Underdetection of Interstitial Lung Disease in Juvenile Systemic Sclerosis
Ivan Foeldvari, Jens Klotsche, Bernd Hinrichs, Nicola Helmus, Özgür Kasapçopur, Amra Adroviç, Flávio Sztajnbok, Maria Teresa Terreri, Jordi Antón, Vanessa Smith, María Martha Katsicas, Mikhail M. Kostik, Natalia Vasquez‐Canizares, Tadej Avčin, Brian M. Feldman, Mahesh Janarthanan, María José Santos, Sujata Sawhney, Dieneke Schonenberg‐Meinema, Walter‐Alberto Sifuentes‐Giraldo, Е.I. Alexeeva, Simone Appenzeller, Cristina Battagliotti, Lillemor Berntson, Blanca Bica, Patrícia Costa‐Reis, Despina Eleftheriou, Tilmann Kallinich, Thomas J A Lehman, Edoardo Marrani, Kirsten Minden, Susan Nielsen, Farzana Nuruzzaman, Anjali Patwardhan, Raju Khubchandani, Valda Staņēvicha, Yosef Uziel, Kathryn S. Torok
Abstract
OBJECTIVE: Utilizing data obtained from a prospective, international, juvenile systemic sclerosis (SSc) cohort, the present study was undertaken to determine if pulmonary screening with forced vital capacity (FVC) and diffusing capacity for carbon monoxide (DLco) is sufficient to assess the presence of interstitial lung disease (ILD) in comparison to high-resolution computed tomography (HRCT) in juvenile SSc. METHODS: The juvenile SSc cohort database was queried for patients enrolled from January 2008 to January 2020 with recorded pulmonary function tests (PFTs) parameters and HRCT to determine the discriminatory properties of PFT parameters, FVC, and DLco in detecting ILD. RESULTS: Eighty-six juvenile SSc patients had both computed tomography imaging and FVC values for direct comparison. Using findings on HRCT as the standard measure of ILD presence, the sensitivity of FVC in detecting ILD in juvenile SSc was only 40%, the specificity was 77%, and area under the curve (AUC) was 0.58. Fifty-eight juvenile SSc patients had both CT imaging and DLco values for comparison. The sensitivity of DLco in detecting ILD was 76%, the specificity was 70%, and AUC was 0.73. CONCLUSION: The performance of PFTs in juvenile SSc to detect underlying ILD was quite limited. Specifically, the FVC, which is one of the main clinical parameters in adult SSc to detect and monitor ILD, would miss ~60% of children who had ILD changes on their accompanying HRCT. The DLco was more sensitive in detecting potential abnormalities on HRCT, but with less specificity than the FVC. These results support the use of HRCT in tandem with PFTs for the screening of ILD in juvenile SSc.