Diagnosis and monitoring of systemic sclerosis-associated interstitial lung disease using high-resolution computed tomography

Author:

Khanna Dinesh1ORCID,Distler Oliver2,Cottin Vincent3,Brown Kevin K4,Chung Lorinda5,Goldin Jonathan G6,Matteson Eric L7,Kazerooni Ella A89,Walsh Simon LF10,McNitt-Gray Michael1112,Maher Toby M1314

Affiliation:

1. Scleroderma Program, Division of Rheumatology, Department of Internal Medicine, University of Michigan, Ann Arbor, MI, USA

2. Department of Rheumatology, University Hospital Zurich, Zurich, Switzerland

3. Hospices Civils de Lyon, Department of Respiratory Medicine, National Coordinating Reference Center for Rare Pulmonary Diseases, Louis Pradel Hospital, INRAE, UMR754, University Claude Bernard Lyon 1, Lyon, France

4. Department of Medicine, National Jewish Health, Denver, CO, USA

5. Immunology and Rheumatology, Stanford University, Palo Alto, CA, USA

6. David Geffen School of Medicine and UCLA Medical Center, Los Angeles, CA, USA

7. Division of Rheumatology, Mayo Clinic, Rochester, MN, USA

8. Division of Cardiothoracic Radiology, Department of Radiology, Michigan Medicine, Ann Arbor, MI, USA

9. Division of Pulmonary Medicine, Department of Internal Medicine, Michigan Medicine, Ann Arbor, MI, USA

10. National Heart and Lung Institute, Faculty of Medicine, Imperial College London, London, UK

11. Department of Radiology, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA, USA

12. Physics and Biology in Medicine Graduate Program, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA, USA

13. National Heart and Lung Institute, Imperial College London, London, UK

14. Interstitial Lung Disease Unit, Royal Brompton Hospital, London, UK

Abstract

Patients with systemic sclerosis are at high risk of developing systemic sclerosis–associated interstitial lung disease. Symptoms and outcomes of systemic sclerosis–associated interstitial lung disease range from subclinical lung involvement to respiratory failure and death. Early and accurate diagnosis of systemic sclerosis–associated interstitial lung disease is therefore important to enable appropriate intervention. The most sensitive and specific way to diagnose systemic sclerosis–associated interstitial lung disease is by high-resolution computed tomography, and experts recommend that high-resolution computed tomography should be performed in all patients with systemic sclerosis at the time of initial diagnosis. In addition to being an important screening and diagnostic tool, high-resolution computed tomography can be used to evaluate disease extent in systemic sclerosis–associated interstitial lung disease and may be helpful in assessing prognosis in some patients. Currently, there is no consensus with regards to frequency and scanning intervals in patients at risk of interstitial lung disease development and/or progression. However, expert guidance does suggest that frequency of screening using high-resolution computed tomography should be guided by risk of developing interstitial lung disease. Most experienced clinicians would not repeat high-resolution computed tomography more than once a year or every other year for the first few years unless symptoms arose. Several computed tomography techniques have been developed in recent years that are suitable for regular monitoring, including low-radiation protocols, which, together with other technologies, such as lung ultrasound and magnetic resonance imaging, may further assist in the evaluation and monitoring of patients with systemic sclerosis–associated interstitial lung disease. A video abstract to accompany this article is available at: https://www.globalmedcomms.com/respiratory/Khanna/HRCTinSScILD

Funder

boehringer ingelheim

Publisher

SAGE Publications

Subject

Immunology,Rheumatology,Immunology and Allergy

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