Systemic Sclerosis—Recent Advances in Diagnosis and Management

Systemic sclerosis is a multisystem connective tissue disease which can present to a broad range of medical specialities. It carries significant morbidity and mortality, but substantial advances have been made in recent years. Recent advances include autologous haematopoietic stem cell transplantation for early diffuse disease (for highly selected patients), the increasing use of phosphodiesterase type 5 inhibitors and of bosentan for digital ulceration, a better understanding of the use of different immunosuppressant therapies for interstitial lung disease (and which patients are likely to benefit from antifibrotic therapy), and the increasing early use of combination therapies for pulmonary arterial hypertension (PAH). Ongoing clinical trials investigating new therapeutic approaches should lead to further advances in the next 10 years. This review provides a broad overview of the condition with a focus on recent progress in specific areas: early diffuse cutaneous disease, digital vasculopathy, interstitial lung disease, and PAH.

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Publication Details

Journal
British Journal of Hospital Medicine
Published
2025-12-04
DOI
https://doi.org/10.12968/hmed.2024.0940
Primary Topic
Systemic Sclerosis and Related Diseases
Type
article
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article

Systemic Sclerosis—Recent Advances in Diagnosis and Management

Colin Church, Ariane L. Herrick, William Kerrigan
British Journal of Hospital Medicine
Systemic Sclerosis and Related Diseases
article

Systemic Sclerosis—Recent Advances in Diagnosis and Management

Colin Church, Ariane L. Herrick, William Kerrigan
article en

Abstract

Systemic sclerosis is a multisystem connective tissue disease which can present to a broad range of medical specialities. It carries significant morbidity and mortality, but substantial advances have been made in recent years. Recent advances include autologous haematopoietic stem cell transplantation for early diffuse disease (for highly selected patients), the increasing use of phosphodiesterase type 5 inhibitors and of bosentan for digital ulceration, a better understanding of the use of different immunosuppressant therapies for interstitial lung disease (and which patients are likely to benefit from antifibrotic therapy), and the increasing early use of combination therapies for pulmonary arterial hypertension (PAH). Ongoing clinical trials investigating new therapeutic approaches should lead to further advances in the next 10 years. This review provides a broad overview of the condition with a focus on recent progress in specific areas: early diffuse cutaneous disease, digital vasculopathy, interstitial lung disease, and PAH.

British Journal of Hospital MedicineVol. 86(12)
Manchester Academic Health Science Centre (GB), Aberdeen Royal Infirmary (GB), Golden Jubilee National Hospital (GB), University of Manchester (GB), University of Glasgow (GB)
Openalex Percentile: Top 47%
Systemic Sclerosis and Related Diseases
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