Quality indicators in rheumatoid arthritis: results from the METEOR database

被引:25
作者
Navarro-Compan, Victoria [1 ]
Smolen, Josef S. [2 ,3 ]
Huizinga, Tom W. J. [1 ]
Landewe, Robert [4 ,5 ]
Ferraccioli, Gianfranco [6 ]
da Silva, Jose A. P. [7 ]
Moots, Robert J. [8 ]
Kay, Jonathan [9 ,10 ]
van der Heijde, Desiree [1 ]
机构
[1] Leiden Univ, Med Ctr, Dept Rheumatol, NL-2300 RC Leiden, Netherlands
[2] Med Univ Vienna, Dept Internal Med 3, Vienna, Austria
[3] Hietzing Hosp, Ctr Rheumat Dis, Dept Med 2, Vienna, Austria
[4] Amsterdam Rheumatol Ctr, Amsterdam, Netherlands
[5] Atrium Med Ctr Heerlen, Dept Rheumatol, Heerlen, Netherlands
[6] Univ Cattolica Sacro Cuore, Sch Med, Inst Rheumatol & Affine Sci, Div Rheumatol, I-00168 Rome, Italy
[7] Univ Coimbra, Hosp & Fac Med, Dept Rheumatol, P-3000 Coimbra, Portugal
[8] Univ Liverpool, Inst Chron Dis & Ageing, Liverpool L69 3BX, Merseyside, England
[9] UMass Mem Med Ctr, Div Rheumatol, Dept Med, Worcester, MA USA
[10] Univ Massachusetts, Sch Med, Worcester, MA USA
关键词
rheumatoid arthritis; quality indicator; care; AMERICAN-COLLEGE; OF-CARE; PERFORMANCE; REMISSION; CRITERIA; OUTCOMES; EUROPE;
D O I
10.1093/rheumatology/kev108
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective. To test the feasibility of collecting, storing, retrieving and analysing necessary information to fulfil a preliminary set of quality indicators (QIs) that have been proposed by an international task force in a large multinational clinical practice database of patients with RA. Methods. Data from all 12 487 patients with 46 005 visits in the Measurement of Efficacy of Treatment in the Era of Outcome in Rheumatology database from January 2008 until January 2012 were analysed to test the feasibility of collecting information on 10 QIs: time to diagnosis; frequency of visits; assessment of autoantibodies and radiographs, disease activity and function; disease remission, low disease activity, normal function; time to first DMARD and type of first DMARD. For each QI, two aspects were assessed: information availability and target achievement. Results. Information was available for <50% of patients regarding the following QIs: time to diagnosis, assessment of ACPAs or radiographs, time to first DMARD and type of first DMARD. Information was available for function assessment in 49% of visits and 67% of patients and for disease activity assessment in 85% of visits and 86% of patients. Information relevant to the QI frequency of visits was available for all patients. Relevant information to calculate the proportion of patients who achieved a defined target could be obtained for all QIs. Conclusion. Collecting storing, retrieving and analysing the core data necessary to meaningfully assess quality of care is feasible in a multinational, practice-based electronic database.
引用
收藏
页码:1630 / 1639
页数:10
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