Evidence map›Paper›PMID 26116156›Full record

ReviewRheumatology (Oxford, England)2015

Consensus best practice pathway of the UK Scleroderma Study Group: digital vasculopathy in systemic sclerosis.

Michael Hughes, Voon H Ong, Marina E Anderson, Frances Hall, Pia Moinzadeh, Bridget Griffiths, Eileen Baildam, Christopher P Denton, Ariane L Herrick

Abstract readConsensus StatementReview
PubMed Publisher
In one paragraph

Review in Rheumatology (Oxford, England), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed, 3 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

48 citing papers in PubMed, 3 syntheses or guidelines pooled it.

  1. Guideline
  2. Pooled it
  3. Pooled it
  4. Trial
  5. A pilot clinical trial with losartan in Myhre syndrome.American journal of medical genetics. Part A · 2021
    Trial
  6. Trial
  7. Trial
  8. Article
  9. Article
  10. Review
  11. Association Between Risk of Relapse and Type of Surgical Procedure for Raynaud's Disease.Medical science monitor : international medical journal of experimental and clinical research · 2025
    Article
  12. [Systemic sclerosis].Dermatologie (Heidelberg, Germany) · 2024
    Review
  13. Review
  14. Review
  15. Article
  16. Review
  17. Review
  18. Review
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors.

Michael HughesCentre for Musculoskeletal Research, Salford Royal NHS Foundation Trust, University of Manchester, Manchester Academic Health Science Centre, Manchester, michael.hughes-6@postgrad.manchester.ac.uk.
Voon H OngCentre for Rheumatology, Royal Free Hospital, London.
Marina E AndersonInstitute of Ageing and Chronic Disease, Faculty of Health & Life Sciences, University of Liverpool.
Frances HallDepartment of Rheumatology, Cambridge University Hospitals NHS Foundation Trust, Cambridge, UK.
Pia MoinzadehDepartment for Dermatology and Venereology, University of Cologne, Cologne, Germany.
Bridget GriffithsDepartment of Rheumatology, Freeman Hospital, Newcastle upon Tyne and.
Eileen BaildamDepartment of Paediatric Rheumatology, Alder Hey Children's Foundation NHS Trust, Liverpool, UK.
Christopher P DentonCentre for Rheumatology, Royal Free Hospital, London.
Ariane L HerrickCentre for Musculoskeletal Research, Salford Royal NHS Foundation Trust, University of Manchester, Manchester Academic Health Science Centre, Manchester.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveDigital vasculopathy (comprising RP, digital ulceration and critical digital ischaemia) is responsible for much of the pain and disability experienced by patients with SSc. However, there is a limited evidence base to guide clinicians in the management of SSc-related digital vasculopathy. Our aim was to produce recommendations that would be helpful for clinicians, especially for those managing patients outside specialist centres.

methodsThe UK Scleroderma Study Group set up several working groups to develop a number of consensus best practice pathways for the management of SSc-specific complications, including digital vasculopathy.

resultsThis overview presents the background and best practice consensus pathways for SSc-related RP, digital ulceration and critical ischaemia. Examples of drug therapies, including doses, are suggested in order to inform prescribing practice.

conclusionA number of treatment algorithms are provided that are intended to provide the clinician with accessible reference tools for use in daily management.

Indexed as

Practice Patterns, Physicians'AlgorithmsDisease ManagementFingersHumansIschemiaRaynaud DiseaseScleroderma, SystemicUlcerUnited KingdomVascular Diseasescritical digital ischaemiadigital ulcerdigital vasculopathyRaynaud’s phenomenonsclerodermasystemic sclerosis

Identifiers

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.