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Clinical burden of digital vasculopathy in limited and diffuse cutaneous systemic sclerosis
S I Nihtyanova1, G M Brough, C M Black
1Centre for Rheumatology, Royal Free Hospital, Pond Street, London NW3 2QG, UK.
Insights
Severe digital vasculopathy (SDV) affects 17.4% of systemic sclerosis (SSc) patients, particularly those with diffuse cutaneous SSc. This complication often requires significant hospital-based treatment, highlighting its clinical burden.
Area of Science:
- Rheumatology
- Vascular Medicine
- Dermatology
Background:
- Vascular damage is a primary pathology in systemic sclerosis (SSc).
- Severe digital vasculopathy (SDV) is a significant complication contributing to morbidity in SSc patients.
- Understanding the clinical burden of SDV is crucial for managing SSc.
Purpose of the Study:
- To assess the clinical burden of severe digital vasculopathy (SDV) in a large systemic sclerosis (SSc) cohort.
- To review hospital-based treatments for SDV complications in SSc patients.
- To identify the frequency and characteristics of SDV in different SSc subsets.
Main Methods:
- Retrospective review of 1168 SSc patients over 18 months.
- Identification of patients with SDV complications (digital ulceration, critical ischemia, gangrene).
- Analysis of hospital admissions for treatments like IV prostacyclin, CGRP, antibiotics, amputation, or sympathectomy.
Main Results:
- 17.4% of the SSc cohort experienced SDV-related complications.
- SDV was significantly more frequent in diffuse cutaneous SSc (27.5%) than limited cutaneous SSc (13%).
- 16.6% had digital ulcers, and 12% required IV prostacyclin/CGRP treatment, totaling 242 admissions (mean 6 days).
Conclusions:
- Severe digital vasculopathy is a serious complication of systemic sclerosis.
- SDV contributes significantly to patient morbidity and frequently necessitates hospital-based management.
- The clinical burden of SDV in SSc warrants further investigation and optimized treatment strategies.
Background:
Vascular damage is a key pathological process in systemic sclerosis (SSc) and accounts for significant disease-related morbidity. To determine the clinical burden of severe digital vasculopathy (SDV), we have reviewed hospital-based treatment for this important complication of SSc in a large single centre cohort.
Methods:
Cases were identified from a cohort of 1168 patients with a diagnosis of SSc who were reviewed during an 18-month period. Patients with recorded episodes of SDV-related complications (digital ulceration, critical digital ischaemia or digital gangrene), requiring surgical amputation, digital sympathectomy or admissions for intravenous prostacyclin or calcitonin gene related peptide (CGRP) and/or intravenous antibiotic treatment were identified.
Results:
From this large SSc cohort, 17.4% had SDV-related complications. Contrary to expectation, their frequency was significantly higher among the patients with the diffuse cutaneous subset of SSc (27.5%) compared with 13% among the patients with limited cutaneous SSc (p<0.0001). 16.6% had at least one recorded episode of digital ulcers, and 12% required at least one hospitalisation during the 18 months for treatment with intravenous prostacyclin/CGRP. Overall, there were 242 admissions with a mean duration of 6 days.
Conclusions:
Digital vasculopathy is a serious complication of SSc contributing significant morbidity and often requiring hospital-based management.
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