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. Author manuscript; available in PMC: 2019 Sep 1.
Published in final edited form as: Arthritis Care Res (Hoboken). 2018 Aug 16;70(9):1373–1384. doi: 10.1002/acr.23475

Table 1.

Demographics and clinical phenotype of enrolled participants according to purposive sampling framework

Demographics and clinical feature of
enrolled patients presented according to
purposive sampling framework
Bath Pittsburgh New
Orleans
Overall

Number of participants, n (n per focus group held) 17 (8,9) 6 (6) 17 (7,7,3) 40

Mean age, years (SD) 62.5 (11.5) 50.8 (17.7) 52.7 (12) 56.6 (13.4)

Mean disease duration*, years (SD) 13.8 (11.3) 8.8 (6.6) 7.7 (6.3) 10.5 (9.1)

Disease subtype, n (%):
  Limited cutaneous SSc 15 (88) 5 (83) 4 (24) 24 (60)
  Diffuse cutaneous SSc 2 (12) 1 (17) 13 (76) 16 (40)

Disease duration*, n (%):
  ≤3 years 2 (12) 2 (33) 5 (29) 9 (23)
  >3 years 15 (88) 4 (67) 12 (71) 31 (77)

Gender, n (%):
  Female 16 (94) 5 (83) 13 (76) 34 (85)
  Male 1 (6) 1 (17) 4 (24) 6 (15)

Ethnicity, n (%):
  White/Caucasian 17 (100) 6 (100) 3 (18) 26 (65)
  Black/African-American 0 (0) 0 (0) 12 (71) 12 (30)
  Hispanic 0 (0) 0 (0) 2 (12) 2 (5)

Vasodilator medication use, n (%):
  Nil 3 (18) 2 (33) 2 (12) 7 (18)
  Calcium channel blocker 9 (54) 2 (33) 14 (82) 25 (63)
  Phosphodiesterase inhibitor 5 (29) 4 (67) 3 (18) 12 (30)
  Prostanoids 0 (0) 0 (0) 1 (6) 1 (3)
  Angiotensin II antagonists 4 (24) 1 (17) 0 (0) 5 (13)
  Selective serotonin reuptake inhibitor 2 (12) 0 (0) 0 (0) 2 (5)
  Endothelin receptor antagonist 1 (6) 1 (17) 2 (12) 4 (10)
  Combination therapy 3 (18) 3 (50) 3 (18) 9 (23)

History of digital ulcer disease, n (%):
  Yes 7 (41) 4 (33) 12 (71) 23 (58)
  No 10 (59) 2 (67) 5 (29) 17 (42)

Indication not specified and includes SSc-RP, SSc-DU, SSc-PAH and/or systemic hypertension/cardiovascular risk

*

Since first non-Raynaud’s symptom

SSc, systemic sclerosis; DU, digital ulcer; PAH, pulmonary arterial hypertension