Systemic sclerosis & Raynaud's

Longitudinal trajectories of the Scleroderma Health Assessment Questionnaire (Scleroderma HAQ (SHAQ)) visual analogue scales: a retrospective cohort study

Rheumatology (Oxford)Published Retrospective cohort study

Authors' conclusion

Longitudinal assessment of the six SHAQ VAS, and associations of baseline characteristics with the individual VAS time courses, provide insights into disease trajectory and overall disability.

Study context

Population
Patients with SSc attending a single tertiary centre, 2005–2022, with at least two time-pointsmean follow-up 6.8 (SD 4.2) years
Participants
537 patients
Outcome
Trajectories over time of the six SHAQ VAS (pain, intestinal, breathing, RP, digital ulcers, overall)
Methodological detailssingle tertiary centre, data collected prospectively, linear mixed-effects models
  • Single tertiary centre
  • Data collected prospectively
  • Linear mixed-effects models

Main finding

As reported in the abstract

Change in SHAQ VAS scores per year

Visual analogue scales (VAS) intestinal increased (worsened) per year, points

0.085

95% CI 0.041–0.130P < 0.001

VAS breathing increased per year, points

0.056

95% CI 0.016–0.096P = 0.006

VAS overall increased per year, points

0.073

95% CI 0.032–0.114P = 0.001

Observational data: associations, not effects.

Further findings

Associations of baseline factors with VAS trajectories

Longer duration between RP onset and SSc diagnosis associated with lower VAS pain and VAS intestinal scores
Odds of at least one digital ulcer reduced with disease duration, diffuse cutaneous subtype and anti-Scl70 positivity

Correlation of VAS gradients with HAQ Disability Index (HAQ-DI) and scleroderma functional index (FI) gradients

Average gradients for all six VAS correlated (albeit variably/weakly) with HAQ-DI and scleroderma FI gradients

Original publication

Longitudinal trajectories of the Scleroderma Health Assessment Questionnaire (SHAQ) visual analogue scales: a retrospective cohort study. Rheumatology (Oxford). Published 6 December 2024. doi:10.1093/rheumatology/keae667

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