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Abstract Number: 2003

Validation of the ASAS Health Index: Results of a Multicenter International Study in 23 Countries

Uta Kiltz1, Désirée van der Heijde2, Annelies Boonen3, Jürgen Braun1 and ASAS HI international validation study, 1Rheumazentrum Ruhrgebiet, Herne, Germany, 2Rheumatology, Leiden University Medical Center, Leiden, Netherlands, 3Department of Internal Medicine, Division of Rheumatology, Maastricht University Medical Center, Maastricht, Netherlands

Meeting: 2016 ACR/ARHP Annual Meeting

Date of first publication: September 28, 2016

Keywords: Ankylosing spondylitis (AS), functional status, patient outcomes, questionnaires and spondylarthritis

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Session Information

Date: Monday, November 14, 2016

Title: Spondylarthropathies and Psoriatic Arthritis – Clinical Aspects and Treatment III: Axial Spondyloarthritis – Clinical

Session Type: ACR Concurrent Abstract Session

Session Time: 2:30PM-4:00PM

Background/Purpose:  The ASAS Health Index (ASAS HI) was developed to measure functioning and health in patients with spondyloarthritis (SpA) aiming to better define the impact of disease in these patients. The 17 questions of the questionnaire (range 0-17, with a lower score indicating a better health status) have now been translated into 18 languages worldwide. Face validity and feasibility (time of completion) have already been assessed in a field test. The objective of the present study was test construct validity, discrimination across relevant health states, reliability and responsiveness of the original English version and the 16 translations of the ASAS HI in 23 countries

Methods:  A convenient sample of SpA patients fullfilling the ASAS classification criteria for either axial (axSpA) or peripheral SpA (pSpA) were included into the study from 33 centers of 22 countries worldwide. Data were collected by the local rheumatologist. Construct validity against other health outcomes was evaluated by Spearman correlation. Discrimination across patient reported health states was decribed. Test-retest reliability was assessed by intraclass correlation coefficient (ICC) in patients without treatment changes (stable disease state, interval 4-7 days). In those patients who required a therapeutic change because of high disease activity, responsiveness was tested (standardized response mean (SRM)) after 2-24 weeks depending on the type of medication.

Results:  1548 patients were included: 64.9% male, mean (SD) age 42.0 (13.4) years, mean (SD) BASDAI 4.1 (2.5). There were 1299 patients with axSpA (375 nr-axSpA and 924 AS patients) and 256 patients with pSpA. The total score of the ASAS HI was 6.7 ± 4.3 (mean ± SD). Floor or ceiling effects were limited (0.8 and 6.9%, respectively). Convergent validity ranged as hypothesized with Spearman correlations from low (age: 0.10) to good (BASDAI: 0.70). ASAS HI scores showed<span” roman”=”Roman”” new=”New”> a high internal consistency with a Cronbachs-α of 0.93. The ASAS HI discriminated well between patients with different stages of disease activity and function irrespective of the tool applied (ASDAS, BASDAI and BASFI) (table). The groups with greater disease activity and more impaired functioning had higher mean ASAS HI scores (indicating impaired functioning) than those with lower disease activity. Reliability (tested in 578 patients) was good (ICC: 0.87 (95%CI 0.84 to 0.89), p<0.01) and comparable across all disease subtypes. Sensitivity to change (tested in 246 patients) showed a moderate SRM of -0.44 for NSAIDs (n= 75 patients), 0.69 for DMARDs (n=41) and -0.85 for TNFi (n=127). The smallest detectable change in this cohort was 3.0.

Conclusion: The ASAS HI is a valid, reliable and responsive measure of disease severity in people affected by SpA. It should be used in clinical trials to evaluate the impact of SpA and its treatment on overall functioning and health. Table: Discriminative ability of the ASAS HI stratified by disease activity

ASDAS status groups
inactive (n=245) moderate (n=283) high (n=500) very high (n=289
ASAS HI 2.9 ± 3.1 5.1 ± 3.5 7.3 ± 3.6 10.4 ± 35
BASFI 0.9 ± 1.4 2.1 ± 1.9 3.7 ± 2.5 5.9 ± 2.5
BASDAI 1.2 ± 0.9 2.7 ± 1.3 4.7 ± 1.7 7.0 ± 1.6

Disclosure: U. Kiltz, None; D. van der Heijde, None; A. Boonen, None; J. Braun, None.

To cite this abstract in AMA style:

Kiltz U, van der Heijde D, Boonen A, Braun J. Validation of the ASAS Health Index: Results of a Multicenter International Study in 23 Countries [abstract]. Arthritis Rheumatol. 2016; 68 (suppl 10). https://acrabstracts.org/abstract/validation-of-the-asas-health-index-results-of-a-multicenter-international-study-in-23-countries/. Accessed .
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