An Italian Multicenter Study for Application of a Diagnostic Algorithm in Autoantibody Testing

被引:14
作者
Bonaguri, Chiara [1 ]
Melegari, Alessandra [4 ]
Dall'Aglio, PierPaolo [2 ]
Ballabio, Andrea [5 ]
Terenziani, Paolo [6 ]
Russo, Annalisa [1 ]
Battistelli, Luisita [1 ]
Aloe, Rosalia [1 ]
Camisa, Roberta [1 ]
Campaniello, Giovanna [3 ]
Sartori, Elisabetta [3 ]
Monica, Cesare [1 ]
机构
[1] Parma Hosp, Diagnost Lab Dept, Parma, Italy
[2] Parma Hosp, Dept Immunol, Parma, Italy
[3] Parma Hosp, Dept Adm, Parma, Italy
[4] Modena Hosp, Diagnost Lab Dept, Modena, Italy
[5] Piacenza Hosp, Diagnost Lab Dept, Piacenza, Italy
[6] Reggio Emilia Hosp, Diagnost Lab Dept, Reggio Emilia, Italy
来源
CONTEMPORARY CHALLENGES IN AUTOIMMUNITY | 2009年 / 1173卷
关键词
diagnostic algorithm; autoimmune rheumatic disease; antinuclear antibodies; anti-extractable nuclear antigens; anti-double-stranded DNA; AUTOIMMUNE; GUIDELINES; REQUEST;
D O I
10.1111/j.1749-6632.2009.04635.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The presence in the serum of specific autoantibodies, such as antinuclear antibodies (ANA), anti-double-stranded DNA (anti-dsDNA), and antiextractable nuclear antigens (anti-ENA), is one of the diagnostic criteria for autoimmune rheumatic disease, and the requests for these tests in the last few years have grown remarkably. A guideline for reducing clinically inappropriate requests in autoantibody testing (ANA, anti-dsDNA, anti-ENA) has been applied in the Parma Hospital since 2007. The results for the period January-December 2007 were compared to those of the previous period January-December 2006, and a significant reduction in the number of anti-dsDNA (23.9%) and anti-ENA (20.7%) was found. The aim of this study was to assess the applicability of a similar guideline in a wide area (Parma, Modena, Piacenza, Reggio-Emilia) with reference to the diagnosis of autoimmune rheumatic disease. This project, supported by a regional grant for innovative research projects, was started in January 2008 and consists of three different steps: (1) a study group of clinicians and laboratory physicians to evaluate the diagnostic criteria, the analytical procedures, and the number of tests performed in different hospitals; (2) developing common guidelines for autoantibody testing that takes into account the different clinical needs with the aim of improving efficiency and clinical effectiveness of diagnosis and monitoring; and (3) assessing compliance with the guidelines in the different hospitals that are evaluating the second-level test (anti-dsDNA, anti-ENA) decrease. We think that the validation of guidelines for the laboratory diagnosis of autoimmune rheumatic disease can represent a tool for improving patients' outcomes and economic efficiency.
引用
收藏
页码:124 / 129
页数:6
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