Literature DB >> 28966205

Development of a Canadian Core Clinical Dataset to Support High-quality Care for Canadian Patients with Rheumatoid Arthritis.

Claire E H Barber1,2, Dianne P Mosher3,4, Vandana Ahluwalia3,4, Michel Zummer3,4, Deborah A Marshall3,4, Denis Choquette3,4, Diane Lacaille3,4, Claire Bombardier3,4, Anne Lyddiatt3,4, Vinod Chandran3,4, Dmitry Khodyakov3,4, Emily Dao3,4, Cheryl Barnabe.   

Abstract

OBJECTIVE: To develop a Canadian Rheumatoid Arthritis Core Clinical Dataset (CAN-RACCD) to standardize documentation encouraging high-quality care.
METHODS: A set of candidate elements was drafted through meetings with 27 rheumatologists, researchers, and patients, and supplemented with focused literature reviews. A 3-round online-modified Delphi consensus process was held with rheumatologists (n = 26), allied health professionals (n = 7), and patients (n = 4); for the remainder there was no demographic information. Participants rated both the importance and feasibility of documenting candidate elements on a Likert scale of 1-9, contributed to an online moderated discussion, and re-rated the elements for inclusion in the CAN-RACCD. Elements were included in the final set if importance and feasibility ratings had a median score of ≥ 6.5 and there was no disagreement among participants.
RESULTS: Fifty-five individual elements in 10 subgroups were proposed to the Delphi participants: measures of RA disease activity; dates to calculate waiting times, disease duration, and disease-modifying antirheumatic drug start; comorbidities; smoking status; patient-reported pain and fatigue; physical function; laboratory and radiographic investigations; medications; clinical characteristics; and vaccines. All groups were included in the final set, with the exception of vaccination status. Additionally, 3 individual elements from the smoking subgroup were eliminated with a recommendation to record smoking status as never/ever/current, and 2 elements relating to coping and effect of fatigue were eliminated due to low feasibility and importance ratings.
CONCLUSION: The CAN-RACCD stands as a national recommendation on which data elements should be routinely collected in clinical practice to monitor and support high-quality RA care.

Entities:  

Keywords:  PHYSICIAN PRACTICE PATTERNS; QUALITY OF CARE; RHEUMATOID ARTHRITIS

Mesh:

Substances:

Year:  2017        PMID: 28966205     DOI: 10.3899/jrheum.170421

Source DB:  PubMed          Journal:  J Rheumatol        ISSN: 0315-162X            Impact factor:   4.666


  3 in total

1.  European Network of Pregnancy Registers in Rheumatology (EuNeP)-an overview of procedures and data collection.

Authors:  Yvette Meissner; Anja Strangfeld; Nathalie Costedoat-Chalumeau; Frauke Förger; Doreen Goll; Anna Molto; Rebecca Özdemir; Marianne Wallenius; Rebecca Fischer-Betz
Journal:  Arthritis Res Ther       Date:  2019-11-14       Impact factor: 5.156

2.  Validity and reliability of the EULAR instrument RAID.7 as a tool to assess individual domains of impact of disease in rheumatoid arthritis: a cross-sectional study of 671 patients.

Authors:  Jose Antonio Pereira da Silva; Laure Gossec; Catia Duarte; Eduardo José Ferreira Santos; Ricardo J O Ferreira; Tore K Kvien; Maxime Dougados; Maarten de Wit
Journal:  RMD Open       Date:  2021-02

Review 3.  Planning and Reporting Effective Web-Based RAND/UCLA Appropriateness Method Panels: Literature Review and Preliminary Recommendations.

Authors:  Jordan B Sparks; Mandi L Klamerus; Tanner J Caverly; Sarah E Skurla; Timothy P Hofer; Eve A Kerr; Steven J Bernstein; Laura J Damschroder
Journal:  J Med Internet Res       Date:  2022-08-26       Impact factor: 7.076

  3 in total

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