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Table 1 Baseline demographics and clinical characteristics (randomized set, observed cases)

From: Discriminant validity, responsiveness and reliability of the arthritis-specific Work Productivity Survey assessing workplace and household productivity in patients with psoriatic arthritis

 

All randomized patients (n = 409)

Demographic characteristics

  Age (years)

47.6 ± 11.4

  Sex (% female)

55.3

  Race (% white)

97.8

  Weight (kg)

84.4 ± 18.8

  Body mass index (kg/m2)

29.8 ± 6.5

Arthritis characteristics

  Time from psoriatic arthritis diagnosisa (years)

8.6 ± 8.2

  C-reactive proteinb (mg/l)

8.0 (0.1 to 238.0)

  Mean tender joint count (0 to 68 joints)

20.3 ± 14.9

  Mean swollen joint count (0 to 66 joints)

10.7 ± 8.0

  Physician’s Assessment of Disease Activity, by VAS (mm)

57.9 ± 18.6

  Patient’s Assessment of Disease Activity

59.1 ± 20.7

  Patient’s Assessment of Arthritis Pain, by VAS (mm)

60.3 ± 20.4

  DAS28 (CRP)

5.0 ± 1.0

  Mean HAQ-DI (range 0 to 3)

1.31 ± 0.64

Psoriasis characteristics

  Psoriasis BSA ≥3% (%)

61.6

  PASIc

11.7 ± 11.9

  Prior use of synthetic DMARDs (%)

50.6

  1

47.2

  ≥2

 

  Prior TNF inhibitor exposure (%)

19.6

Health-related quality of life

  Mean SF-36 MCS

41.7 ± 12.1

  Mean SF-36 PCS

33.4 ± 7.7

  Mean PsAQoL

11.1 ± 5.6

  Mean DLQI

8.5 ± 7.2

  Mean EQ-5D VAS

49.9 ± 20.4

  1. Data presented as mean ± SD, percentage or median (minimum to maximum). BSA, body surface area; DAS28(CRP), Disease Activity Score – 28-joint count based on C-reactive protein; DLQI, Dermatology Life Quality Index; DMARD, disease-modifying antirheumatic drug; EQ-5D, EuroQoL-5 dimensions; HAQ-DI, Health Assessment Questionnaire – Disability Index; MCS, mental component summary; PASI, Psoriasis Area and Severity Index; PCS, physical component summary; PsAQoL, Psoriatic Arthritis Quality of Life; SF-36, Short Form-36 items; TNF, tumor necrosis factor; VAS, visual analogue scale. aFrom the start date of the primary disease. bNormal range < 8.0 mg/l. cPASI scores are presented for patients with psoriasis body surface area ≥ 3% at baseline.