Literature DB >> 18021510

Quantitative measurement of patient status in the regular care of patients with rheumatic diseases over 25 years as a continuous quality improvement activity, rather than traditional research.

T Pincus1, R Maclean, Y Yazici, J T Harrington.   

Abstract

Patient assessment in rheumatology is characterized by an important paradox: many extensively-characterized quantitative measures and indices have been developed for rheumatoid arthritis (RA), psoriatic arthritis, systemic lupus erythematosus (SLE), ankylosing spondylitis, vasculitis, osteoarthritis, fibromyalgia, and other rheumatic diseases. However, most regular rheumatology care is guided largely by qualitative clinical impressions, without such measures or indices or any quantitative data other than laboratory tests to assess patient status and/or quality of care. This paradox may be explained in part by regarding the development of measures primarily as clinical research activities, while viewing the application of measurements in regular clinical care as continuous quality improvement (CQI) activities. The development of measures has emphasized validity and reliability, but generally ignored feasibility and acceptability to patients and health professionals, both of which are needed for application in regular clinical care. A summary of the application of clinical measurement in patients with RA over 25 years between 1982 and 2007 at a weekly academic rheumatology clinic conducted by the senior author is presented as 20 often contemporaneous CQI cycles. These cycles include development of a user-friendly modified health assessment questionnaire (MHAQ); assessment of psychological status; monitoring of mortality outcomes; comparisons of joint counts, radiographic scores, and laboratory tests to the MHAQ; a 28-joint count; prospective study of the MHAQ to predict mortality when joint counts, radiographic scores, and laboratory tests are available; development of a multidimensional HAQ (MDHAQ) with complex activities; a fatigue scale; a self-report joint count; scoring templates; a computerized data management system; flow sheets to monitor MDHAQ status; visual analog scales as 21 circles rather than 10 cm lines; composite RAPID3 (rheumatology assessment patient index data) scores for 3 patient measures; and defining RAPID categories for high, moderate and low severity, and near remission. The latter cycles remain under study as ongoing CQI activities.

Entities:  

Mesh:

Year:  2007        PMID: 18021510

Source DB:  PubMed          Journal:  Clin Exp Rheumatol        ISSN: 0392-856X            Impact factor:   4.473


  8 in total

Review 1.  Quality measurement and improvement in rheumatology: rheumatoid arthritis as a case study.

Authors:  Sonali P Desai; Jinoos Yazdany
Journal:  Arthritis Rheum       Date:  2011-12

Review 2.  Lupus community panel proposals for optimising clinical trials: 2018.

Authors:  Joan T Merrill; Susan Manzi; Cynthia Aranow; Anca Askanase; Ian Bruce; Eliza Chakravarty; Ben Chong; Karen Costenbader; Maria Dall'Era; Ellen Ginzler; Leslie Hanrahan; Ken Kalunian; Joseph Merola; Sandra Raymond; Brad Rovin; Amit Saxena; Victoria P Werth
Journal:  Lupus Sci Med       Date:  2018-03-23

3.  Fibromyalgia Assessment Screening Tools (FAST) Based on Only Multidimensional Health Assessment Questionnaire (MDHAQ) Scores as Clues to Fibromyalgia.

Authors:  Juan Schmukler; Shakeel Jamal; Isabel Castrejon; Joel A Block; Theodore Pincus
Journal:  ACR Open Rheumatol       Date:  2019-08-22

4.  Development and validation of the self-administered Fibromyalgia Assessment Status: a disease-specific composite measure for evaluating treatment effect.

Authors:  Fausto Salaffi; Piercarlo Sarzi-Puttini; Rita Girolimetti; Stefania Gasparini; Fabiola Atzeni; Walter Grassi
Journal:  Arthritis Res Ther       Date:  2009-08-18       Impact factor: 5.156

5.  Usefulness of patients-reported outcomes in rheumatoid arthritis focus group.

Authors:  Jenny Amaya-Amaya; Diana Botello-Corzo; Omar-Javier Calixto; Rolando Calderón-Rojas; Aura-Maria Domínguez; Paola Cruz-Tapias; Gladis Montoya-Ortiz; Ruben-Dario Mantilla; Juan-Manuel Anaya; Adriana Rojas-Villarraga
Journal:  Arthritis       Date:  2012-09-28

6.  Routine Assessment of Patient Index Data (RAPID3) and Bath Ankylosing Spondylitis Disease Activity Index (BASDAI) Scores Yield Similar Information in 85 Korean Patients With Ankylosing Spondylitis Seen in Usual Clinical Care.

Authors:  Sung-Hoon Park; Jung-Yoon Choe; Seong-Kyu Kim; Hwajeong Lee; Isabel Castrejón; Theodore Pincus
Journal:  J Clin Rheumatol       Date:  2015-09       Impact factor: 3.517

7.  Pragmatic assessment of exercise in routine care using an MDHAQ: associations with changes in RAPID3 and other clinical variables.

Authors:  Isabel Castrejón; Yusuf Yazici; Selda Celik; Theodore Pincus
Journal:  Arthritis Res Ther       Date:  2016-09-06       Impact factor: 5.156

8.  Implementation of a community-based, physiotherapy-led, multidisciplinary model of care for the management of knee osteoarthritis: protocol for a feasibility study.

Authors:  Rebecca Livings; Justine M Naylor; Kathryn Gibson; Sarah Dennis; Jeanette Thom; Kathryn Mills; Siobhan M Schabrun
Journal:  BMJ Open       Date:  2020-07-30       Impact factor: 2.692

  8 in total

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