A systematic review of measurement properties of patient reported outcome measures in psoriatic arthritis

A GRAPPA-OMERACT initiative

Pil Højgaard, Louise Klokker, Ana-Maria Orbai, Kim Holmsted, Else M Bartels, Ying Ying Leung, Niti Goel, Maarten de Wit, Dafna D Gladman, Philip J Mease, Lene Dreyer, Lars E Kristensen, Oliver Fitzgerald, William Tillett, Laure Gossec, Philip Helliwell, Vibeke Strand, Alexis Ogdie, Caroline B Terwee, Robin Christensen

Research output: Contribution to journalReview article

9 Citations (Scopus)
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Abstract

BACKGROUND: An updated psoriatic arthritis (PsA) core outcome set (COS) for randomized controlled trials (RCTs) was endorsed at the Outcome Measures in Rheumatology (OMERACT) meeting in 2016.

OBJECTIVES: To synthesize the evidence on measurement properties of patient reported outcome measures (PROMs) for PsA and thereby contribute to development of a PsA core outcome measurement set (COMS) as described by the OMERACT Filter 2.0.

METHODS: A systematic literature search was performed in EMBASE, MEDLINE and PsycINFO on Jan 1, 2017 to identify full-text articles with an aim of assessing the measurement properties of PROMs in PsA. Two independent reviewers rated the quality of studies using the COnsensus based standards for the Selection of health Measurement INstruments (COSMIN) checklist, and performed a qualitative evidence synthesis.

RESULTS: Fifty-five studies were included in the systematic review. Forty-four instruments and a total of 89 scales were analyzed. PROMs measuring COS domains with at least fair quality evidence for good validity and reliability (and no evidence for poor properties) included the Stockerau Activity Score for PsA (German), Psoriasis Symptom Inventory, visual analogue scale for Patient Global, 36 Item Short Form Health Survey Physical Function subscale, Health Assessment Questionnaire Disability Index, Bath Ankylosing Spondylitis Functional Index, PsA Impact of Disease questionnaire, PsA Quality of Life questionnaire, VITACORA-19, Functional Assessment of Chronic Illness Therapy Fatigue scale and Social Role Participation Questionnaire.

CONCLUSIONS: At least one PROM with some evidence for aspects of validity and reliability was available for six of the eight mandatory domains of the PsA COS.

Original languageEnglish
Pages (from-to)654-665
Number of pages12
JournalSeminars in Arthritis and Rheumatism
Volume47
Issue number5
Early online date9 Sep 2017
DOIs
Publication statusPublished - 1 Apr 2018

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Psoriatic Arthritis
Reproducibility of Results
Social Participation
Patient Reported Outcome Measures
Ankylosing Spondylitis
Health
Rheumatology
Health Surveys
Checklist
Visual Analog Scale
Baths
Psoriasis
MEDLINE
Fatigue
Chronic Disease
Randomized Controlled Trials
Quality of Life
Outcome Assessment (Health Care)
Equipment and Supplies
Surveys and Questionnaires

Keywords

  • Antirheumatic Agents/therapeutic use
  • Arthritis, Psoriatic/diagnosis
  • Humans
  • Patient Reported Outcome Measures
  • Quality of Life
  • Severity of Illness Index

Cite this

A systematic review of measurement properties of patient reported outcome measures in psoriatic arthritis : A GRAPPA-OMERACT initiative. / Højgaard, Pil; Klokker, Louise; Orbai, Ana-Maria; Holmsted, Kim; Bartels, Else M; Leung, Ying Ying; Goel, Niti; de Wit, Maarten; Gladman, Dafna D; Mease, Philip J; Dreyer, Lene; Kristensen, Lars E; Fitzgerald, Oliver; Tillett, William; Gossec, Laure; Helliwell, Philip; Strand, Vibeke; Ogdie, Alexis; Terwee, Caroline B; Christensen, Robin.

In: Seminars in Arthritis and Rheumatism, Vol. 47, No. 5, 01.04.2018, p. 654-665.

Research output: Contribution to journalReview article

Højgaard, P, Klokker, L, Orbai, A-M, Holmsted, K, Bartels, EM, Leung, YY, Goel, N, de Wit, M, Gladman, DD, Mease, PJ, Dreyer, L, Kristensen, LE, Fitzgerald, O, Tillett, W, Gossec, L, Helliwell, P, Strand, V, Ogdie, A, Terwee, CB & Christensen, R 2018, 'A systematic review of measurement properties of patient reported outcome measures in psoriatic arthritis: A GRAPPA-OMERACT initiative', Seminars in Arthritis and Rheumatism, vol. 47, no. 5, pp. 654-665. https://doi.org/10.1016/j.semarthrit.2017.09.002, https://doi.org/10.1016/j.semarthrit.2017.09.002
Højgaard, Pil ; Klokker, Louise ; Orbai, Ana-Maria ; Holmsted, Kim ; Bartels, Else M ; Leung, Ying Ying ; Goel, Niti ; de Wit, Maarten ; Gladman, Dafna D ; Mease, Philip J ; Dreyer, Lene ; Kristensen, Lars E ; Fitzgerald, Oliver ; Tillett, William ; Gossec, Laure ; Helliwell, Philip ; Strand, Vibeke ; Ogdie, Alexis ; Terwee, Caroline B ; Christensen, Robin. / A systematic review of measurement properties of patient reported outcome measures in psoriatic arthritis : A GRAPPA-OMERACT initiative. In: Seminars in Arthritis and Rheumatism. 2018 ; Vol. 47, No. 5. pp. 654-665.
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abstract = "BACKGROUND: An updated psoriatic arthritis (PsA) core outcome set (COS) for randomized controlled trials (RCTs) was endorsed at the Outcome Measures in Rheumatology (OMERACT) meeting in 2016.OBJECTIVES: To synthesize the evidence on measurement properties of patient reported outcome measures (PROMs) for PsA and thereby contribute to development of a PsA core outcome measurement set (COMS) as described by the OMERACT Filter 2.0.METHODS: A systematic literature search was performed in EMBASE, MEDLINE and PsycINFO on Jan 1, 2017 to identify full-text articles with an aim of assessing the measurement properties of PROMs in PsA. Two independent reviewers rated the quality of studies using the COnsensus based standards for the Selection of health Measurement INstruments (COSMIN) checklist, and performed a qualitative evidence synthesis.RESULTS: Fifty-five studies were included in the systematic review. Forty-four instruments and a total of 89 scales were analyzed. PROMs measuring COS domains with at least fair quality evidence for good validity and reliability (and no evidence for poor properties) included the Stockerau Activity Score for PsA (German), Psoriasis Symptom Inventory, visual analogue scale for Patient Global, 36 Item Short Form Health Survey Physical Function subscale, Health Assessment Questionnaire Disability Index, Bath Ankylosing Spondylitis Functional Index, PsA Impact of Disease questionnaire, PsA Quality of Life questionnaire, VITACORA-19, Functional Assessment of Chronic Illness Therapy Fatigue scale and Social Role Participation Questionnaire.CONCLUSIONS: At least one PROM with some evidence for aspects of validity and reliability was available for six of the eight mandatory domains of the PsA COS.",
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T1 - A systematic review of measurement properties of patient reported outcome measures in psoriatic arthritis

T2 - A GRAPPA-OMERACT initiative

AU - Højgaard, Pil

AU - Klokker, Louise

AU - Orbai, Ana-Maria

AU - Holmsted, Kim

AU - Bartels, Else M

AU - Leung, Ying Ying

AU - Goel, Niti

AU - de Wit, Maarten

AU - Gladman, Dafna D

AU - Mease, Philip J

AU - Dreyer, Lene

AU - Kristensen, Lars E

AU - Fitzgerald, Oliver

AU - Tillett, William

AU - Gossec, Laure

AU - Helliwell, Philip

AU - Strand, Vibeke

AU - Ogdie, Alexis

AU - Terwee, Caroline B

AU - Christensen, Robin

N1 - Copyright © 2018 Elsevier Inc. All rights reserved.

PY - 2018/4/1

Y1 - 2018/4/1

N2 - BACKGROUND: An updated psoriatic arthritis (PsA) core outcome set (COS) for randomized controlled trials (RCTs) was endorsed at the Outcome Measures in Rheumatology (OMERACT) meeting in 2016.OBJECTIVES: To synthesize the evidence on measurement properties of patient reported outcome measures (PROMs) for PsA and thereby contribute to development of a PsA core outcome measurement set (COMS) as described by the OMERACT Filter 2.0.METHODS: A systematic literature search was performed in EMBASE, MEDLINE and PsycINFO on Jan 1, 2017 to identify full-text articles with an aim of assessing the measurement properties of PROMs in PsA. Two independent reviewers rated the quality of studies using the COnsensus based standards for the Selection of health Measurement INstruments (COSMIN) checklist, and performed a qualitative evidence synthesis.RESULTS: Fifty-five studies were included in the systematic review. Forty-four instruments and a total of 89 scales were analyzed. PROMs measuring COS domains with at least fair quality evidence for good validity and reliability (and no evidence for poor properties) included the Stockerau Activity Score for PsA (German), Psoriasis Symptom Inventory, visual analogue scale for Patient Global, 36 Item Short Form Health Survey Physical Function subscale, Health Assessment Questionnaire Disability Index, Bath Ankylosing Spondylitis Functional Index, PsA Impact of Disease questionnaire, PsA Quality of Life questionnaire, VITACORA-19, Functional Assessment of Chronic Illness Therapy Fatigue scale and Social Role Participation Questionnaire.CONCLUSIONS: At least one PROM with some evidence for aspects of validity and reliability was available for six of the eight mandatory domains of the PsA COS.

AB - BACKGROUND: An updated psoriatic arthritis (PsA) core outcome set (COS) for randomized controlled trials (RCTs) was endorsed at the Outcome Measures in Rheumatology (OMERACT) meeting in 2016.OBJECTIVES: To synthesize the evidence on measurement properties of patient reported outcome measures (PROMs) for PsA and thereby contribute to development of a PsA core outcome measurement set (COMS) as described by the OMERACT Filter 2.0.METHODS: A systematic literature search was performed in EMBASE, MEDLINE and PsycINFO on Jan 1, 2017 to identify full-text articles with an aim of assessing the measurement properties of PROMs in PsA. Two independent reviewers rated the quality of studies using the COnsensus based standards for the Selection of health Measurement INstruments (COSMIN) checklist, and performed a qualitative evidence synthesis.RESULTS: Fifty-five studies were included in the systematic review. Forty-four instruments and a total of 89 scales were analyzed. PROMs measuring COS domains with at least fair quality evidence for good validity and reliability (and no evidence for poor properties) included the Stockerau Activity Score for PsA (German), Psoriasis Symptom Inventory, visual analogue scale for Patient Global, 36 Item Short Form Health Survey Physical Function subscale, Health Assessment Questionnaire Disability Index, Bath Ankylosing Spondylitis Functional Index, PsA Impact of Disease questionnaire, PsA Quality of Life questionnaire, VITACORA-19, Functional Assessment of Chronic Illness Therapy Fatigue scale and Social Role Participation Questionnaire.CONCLUSIONS: At least one PROM with some evidence for aspects of validity and reliability was available for six of the eight mandatory domains of the PsA COS.

KW - Antirheumatic Agents/therapeutic use

KW - Arthritis, Psoriatic/diagnosis

KW - Humans

KW - Patient Reported Outcome Measures

KW - Quality of Life

KW - Severity of Illness Index

U2 - 10.1016/j.semarthrit.2017.09.002

DO - 10.1016/j.semarthrit.2017.09.002

M3 - Review article

VL - 47

SP - 654

EP - 665

JO - Seminars in Arthritis and Rheumatism

JF - Seminars in Arthritis and Rheumatism

SN - 0049-0172

IS - 5

ER -