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Abstract Number: 315

Long Term Outcomes In Psoriatic Arthritis 2; A Prospective Multicentre Observational Study Of Work Disability In Psoriatic Arthritis: First Report Of The Clinical and Socioeconomic Associations Of Work Disability In Psoriatic Arthritis

William Tillett1, Gavin Shaddick2, Ayman Askari3, Annie Cooper4, Paul Creamer5, Gavin Clunie6, Philip S. Helliwell7, Lesley Kay8, Eleanor Korendowych1, Suzanne Lane9, Jonathon Packham10, Ragai Shaban11, Lyn Williamson12, Corinne deVries13 and Neil McHugh14, 1Rheumatology, Royal National Hospital for Rheumatic Diseases, Bath, United Kingdom, 2Department of Mathematics, University of Bath, Bath, United Kingdom, 3Robert Jones and Agnes Hunt Hospital, Shrophire, United Kingdom, 4Rheumatology, Royal Hampshire County Hospital, Winchester, United Kingdom, 5Rheumatology, North Bristol NHS foundation trust, Bristol, United Kingdom, 6Rheumatology, Cambridge University Hospitals NHS Foundation Trust, Cambridge, United Kingdom, 7PsAID taskforce, EULAR, Zurich, Switzerland, 8Department of Rheumatology, Newcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle upon Tyne, United Kingdom, 9Rheumatology, Ipswich Hospital NHS Trust, Ipswich, United Kingdom, 10Rheumatology, Haywood Rheumatology Centre, Stoke-on-Trent, United Kingdom, 11Rheumatology, Queen Alexandra Hospital, Portsmouth, United Kingdom, 12Rheumatology, Great Western Hospitals NHS Foundation Trust, Swindon, United Kingdom, 13Pharmacy and Pharmacology, University of Bath, Bath, United Kingdom, 14Department of Rheumatology, Royal National Hospital for Rheumatic Diseases, Bath, United Kingdom

Meeting: 2013 ACR/ARHP Annual Meeting

Keywords: Employment, Work Disability and psoriatic arthritis

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Session Information

Title: Spondylarthropathies and Psoriatic Arthritis: Clinical Aspects and Treatment: Psoriatic Arthritis: Clinical Aspects and Treatment I

Session Type: Abstract Submissions (ACR)

Background/Purpose:

Psoriatic arthritis (PsA) is a chronic inflammatory arthritis that is associated with joint damage, impaired quality of life and high levels of work disability (WD). However, data on the associations of WD in PsA is limited. Long Term Outcomes in Psoriatic Arthritis II is a prospective UK multicentre observational study of the impact of PsA on WD and the effect of treatment intervention. In this first analysis we set out to determine to what extent structural damage, clinical disease activity, demographic and social factors are associated with WD.

Methods:

Four hundred patients fulfilling CASPAR criteria for PsA were recruited from 23 hospitals across the UK at initiation of DMARD or anti-TNF therapy. Physician assessments (DAPSA score), radiographs (PsA Ratingen score) and patient reported outcomes (HAQ, EQ5D, FACIT, DLQI, global, joint and skin specific activity VAS scores, comorbidities, demographic details, education, location, employer awareness/helpfulness) and work type were collected. WD was assessed with the WPAI which reports work disability as percentage of absenteeism (work time missed), presenteeism (impairment at work/reduced effectiveness) and work productivity loss (overall work impairment/absenteeism plus presenteeism). All variables were considered for inclusion. Logistic and linear regressions were conducted to investigate independent associations with WD. Age demonstrated a non-linear relationship with WD and was therefore included as a quadratic term.

Results:

Of the 400 participants three hundred and fifty three were of UK working age (18-65 years), mean age 46.8 years (sd 11.02), mean disease duration 5.8 years (sd 8.00), 49.9% female. Two hundred and twenty six (64%) were in work with a further 10 over retirement age, but still working. Unemployed participants were older than those in employment, 55 years (sd 14.7) versus 47 years (sd 10.9), had longer disease duration, 8 years (sd 9.8) versus 6 years (sd 7.8), had worse physical function, HAQ 1.3 (sd 0.78) versus 1.0 (sd 0.68), had worse quality of life, EQ5D 0.4 (sd 0.36) versus 0.5 (sd 0.54) and had more radiographic damage, Ratingen score 19 (sd 31.9) versus 8 (sd 16.5). Of the 236 participants in work the mean absenteeism, presenteeism and productivity loss was 14% (sd 29.0), 39% (sd 27.2) and 46% (sd 30.4) respectively. Independent associations with WD are reported in table 1.

Conclusion:

Greater global, joint specific disease activity and worse physical function exerted a negative influence on presenteeism and productivity loss suggesting disease activity is important amongst those who are in work. Greater age, recent disease onset and worse physical function exert a negative influence on remaining in employment. Patient reported employer awareness and helpfulness exerts a strongly positive influence on remaining in employment, even if patients perceive no help is required.


Table 1: Regression models for work disability associations

Variable

Model 1- logistic

Employed

Odds Ratio (CI)

Model 2- Logistic

Absenteeism (0-1)

Odds Ratio (CI)

Model 3- Linear

Presenteeism (0-1)

Estimate (CI)

Model 4- Linear

Productivity loss (0-1)

Estimate (CI)

Intercept

0.01 (0.000 to 1.622) p=0.07

0.04 (0.010 to 0.127) p<0.01

-0.02 (-0.114 to 0.074) p=0.67

-0.05 (-0.143 to 0.040) p=0.27

Age years

1.31 (1.029 to 1.672) p=0.03

Age (quadratic) years

0.99 (0.994 to 0.999) p=0.02

Disease duration 2-5 years

0.41 (0.180 to 0.953) p=0.03

0.02 (-0.066 to 0.112) p=0.61

Disease duration >5 years

1.36 (0.557 to 3.319) p=0.49

-0.09 (-0.167 to -0.021) p=0.01

Global activity VAS 0-10

0.02 (0.001 to 0.053) p=0.01

0.03 (0.001 to 0.06) p<0.01

Joint activity VAS 0-10

1.04 (1.018 to 1.055) p<0.01

0.03 (0.006 to 0.055) p=0.01

0.02 (0.000 to 0.049) p=0.05

HAQ 0-3

0.56 (0.343 to 0.926) p=0.02

0.63 (0.005 to 1.200) p=0.03

0.12 (0.066 to 0.182) p<0.01

Employer very helpful

15.10 (4.658 to 48.753) p<0.01

Employer helpful

17.46 (4.395 to 69.355) p<0.01

No help required

3.22 (1.264 to 8.229) p<0.01

Employer unhelpful

1.29 (0.325 to 5.155) p=0.72

Employer very unhelpful

0.39 (0.039 to 3.942) p=0.42


Disclosure:

W. Tillett,
None;

G. Shaddick,
None;

A. Askari,
None;

A. Cooper,
None;

P. Creamer,
None;

G. Clunie,
None;

P. S. Helliwell,
None;

L. Kay,

Roche-Chugai,

5,

Abbott Laboratories,

8,

Pfizer Inc,

8;

E. Korendowych,
None;

S. Lane,
None;

J. Packham,
None;

R. Shaban,
None;

L. Williamson,
None;

C. deVries,
None;

N. McHugh,
None.

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