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. Author manuscript; available in PMC: 2018 Apr 9.
Published in final edited form as: J Patient Rep Outcomes. 2018 Jan 4;2:16. doi: 10.1186/s41687-017-0025-2

Table 3.

Prevalence and demographic correlates of disease burden and treatment burden

Disease burden
Treatment burden
Pain interference T-scorea Morning stiffness Serious medication side effect Intolerance to methotrexateb
Mean (SD) % >15 mins % Yes % Intolerant
Total (N = 180) 50.1 (11.1) 17.8% 26.7% 42.2%
Disease duration
  > 8 years 50.3 (11.8) 24.0% 32.0% 41.9%
  ≤ 8 years 49.9 (10.6) 13.3% 22.9% 42.4%
  p-value 0.8676 0.0650 0.1715 0.9682
Age group
  ≥ 13 years 51.3 (11.7) 25.3% 39.2% 40.0%
  < 13 years 49.1 (10.5) 11.9% 16.8% 43.6%
  p-value 0.1481 0.0193 0.0007 0.7335
Sex
  Female 50.3 (11.1) 18.1% 26.1% 48.5%
  Male 49.3 (11.1) 16.7% 28.6% 22.7%
  p-value 0.5835 0.8297 0.7499 0.0332
Race/Ethnicity
  White non-Hispanic 49.2 (10.7) 19.2% 26.7% 40.6%
  Other 53.8 (12.0) 11.8% 26.5% 47.6%
  p-value 0.0266 0.3086 0.9771 0.5674
Highest parental education
  ≤ High school graduate 50.2 (10.6) 22.9% 27.1% 42.9%
  Any college 50.0 (11.3) 15.9% 26.5% 42.0%
  p-value 0.7779 0.2768 0.9392 0.9464

Data are presented as mean and standard deviation (SD) for pain interference and as row percentages for other outcomes

P-values derived from the chi-squared (χ2) or Wilcoxon tests

Disease duration was dichotomized using the sample mean rounded to the nearest integer as the cut point

a

Raw pain interference scores were transformed into a ‘T-score’ for each participant. The T-score rescales the raw score into a standardized score with a mean of 50, standard deviation of 10, and possible range of 38–78

b

Intolerance to methotrexate was assessed only among those who were on methotrexate (N= 90)