2007
DOI: 10.1136/ard.2006.062711
|View full text |Cite
|
Sign up to set email alerts
|

EULAR recommendations for conducting clinical studies and/or clinical trials in systemic vasculitis: focus on anti-neutrophil cytoplasm antibody-associated vasculitis

Abstract: Objectives: To develop the European League Against Rheumatism (EULAR) recommendations for conducting clinical studies and/or clinical trials in systemic vasculitis. Methods: An expert consensus group was formed consisting of rheumatologists, nephrologists and specialists in internal medicine representing five European countries and the USA, a clinical epidemiologist and representatives from regulatory agencies. Using an evidence-based and expert opinion-based approach in accordance with the standardised EULAR … Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
4
1

Citation Types

3
369
0
40

Year Published

2007
2007
2022
2022

Publication Types

Select...
9

Relationship

0
9

Authors

Journals

citations
Cited by 572 publications
(427 citation statements)
references
References 74 publications
3
369
0
40
Order By: Relevance
“…It was not a requirement that ANCA be present at initiation of rituximab. All patients received rituximab as off-label therapy for refractory disease, encompassing those whose disease had failed to remit or had relapsed despite standard immunosuppression, as well as patients in whom standard therapies were contraindicated (22). Patients treated with rituximab as first-line therapy were excluded, as were those with fewer than 6 months of followup after a first rituximab course.…”
Section: Methodsmentioning
confidence: 99%
See 1 more Smart Citation
“…It was not a requirement that ANCA be present at initiation of rituximab. All patients received rituximab as off-label therapy for refractory disease, encompassing those whose disease had failed to remit or had relapsed despite standard immunosuppression, as well as patients in whom standard therapies were contraindicated (22). Patients treated with rituximab as first-line therapy were excluded, as were those with fewer than 6 months of followup after a first rituximab course.…”
Section: Methodsmentioning
confidence: 99%
“…Complete remission was defined as the absence of disease symptoms and signs with a reduction in the steroid dosage (22). Partial remission was defined as a Ͼ50% reduction in disease activity, as assessed by the Disease Extent Index (DEI) (23).…”
Section: Methodsmentioning
confidence: 99%
“…Disease activity was assessed by the BVAS index (5,15,16). A BVAS score of 0 corresponded to remitted disease.…”
Section: Methodsmentioning
confidence: 99%
“…Characteristics at the initiation of IVIG therapy are referred to as the baseline characteristics. Response to therapy was defined according to the recommendations of the European League Against Rheumatism (19). Remission was defined as the absence of signs and symptoms attributable to active disease (i.e., BVAS score of 0), and response was defined as a .50% reduction in disease activity as assessed by the BVAS in the absence of new manifestations.…”
Section: Methodsmentioning
confidence: 99%