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Interstitial Lung Disease in People With Systemic Autoimmune Rheumatic Disease

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6 Screening and Monitoring Figure 1. Recommendations for ILD Screening and Monitoring Conditional recommendation People with SARD of Interest Increased Risk for ILD? * ILD Diagnosed? NO NO YES YES Pulmonary Function Testing (spirometry, lung volumes and diffusion capacity) and High Resolution Computed Tomography (CT) chest Note: Frequency of monitoring in italics are suggestions to assist application of the recommendations. * See Table 2 for risk factors for interstitial lung disease. † Ambulatory desaturation can be done during a routine office visit or as part of 6-minute walk testing. Test in the presence of signs or symptoms of ILD Screening tests Monitoring tests Test if signs or symptoms of ILD develop and consider yearly re-screening in high-risk patients Pulmonary Function Testing (spirometry, lung volumes and diffusion capacity) IIM: every 3–6 months the 1 st year, then less frequently once stable SSc: every 3–6 months the 1 st year, then less frequently once stable RA/SjD/MCTD: every 3–12 months the 1 st year, then less frequently once stable and Ambulatory Desaturation Testing every 3–12 months † and High Resolution CT Chest as needed

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