Abstract
Systemic sclerosis (SSc) is a heterogenous systemic autoimmune disease of complex multi-organ manifestations with a disease-specific mortality of >50%. The patient journey is fraught with severe, diverse, and diffuse physical impairment, psychological burden, and diminishing health-related quality of life. SSc remains unfamiliar to many clinicians. Delayed/misdiagnosis, inadequate screening, and attention for common complications with potentially preventable disability/death contribute to patients feeling isolated and unsupported. We present actionable standards including screening, anticipatory guidance, and counseling in patient-centered SSc-care emphasizing psycho-social health as the central goal, whereas robust vigilance and efforts to improve biophysical health and survival are imperatives that support this goal.
| Original language | English |
|---|---|
| Pages (from-to) | 211-248 |
| Number of pages | 38 |
| Journal | Rheumatic Disease Clinics of North America |
| Volume | 49 |
| Issue number | 2 |
| Early online date | 5 Apr 2023 |
| DOIs | |
| Publication status | Published - 1 May 2023 |
Bibliographical note
Publisher Copyright:© 2023 Elsevier Inc. All rights reserved.
Keywords
- Humans
- Lung Diseases, Interstitial/complications
- Hypertension, Pulmonary/complications
- Quality of Life
- Scleroderma, Systemic/diagnosis
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