THU0297 Prevalence and Clinical Significance of Severe Flares in a Cohort of Systemic Lupus Erythematosus. (23rd January 2014)
- Record Type:
- Journal Article
- Title:
- THU0297 Prevalence and Clinical Significance of Severe Flares in a Cohort of Systemic Lupus Erythematosus. (23rd January 2014)
- Main Title:
- THU0297 Prevalence and Clinical Significance of Severe Flares in a Cohort of Systemic Lupus Erythematosus
- Authors:
- López, R.
Erausquin, C.
Rodríguez-Lozano, C.
Naranjo, A.
Ojeda, S.
Francisco, F.
Quevedo, J. C.
Cáceres, L.
García-Bello, M.
Rúa-Figueroa, I. - Abstract:
- Abstract : Background: Systemic Lupus Erythematosus (SLE) is a systemic autoinmune disorder of relapsing-remitting nature. However, we don´t have enough knowing about severe flare´s relevance on damage, severity or death in SLE patients. Objectives: To analyze the cumulative incidence and clinical significance of severe flares (SF) in a monocentric, well characterized SLE cohort. Methods: Cumulative clinical data were retrospectively collected at the moment of the last assessment. SF was defined using Selena-Sledai Flare Index (SFI) tool. Persistently active disease was not considered. SLICC/ACR/DI (SDI) was used to assess damage. Fisher exact test was used for qualitative variables and Kruskal-Wallis for quantitative ones. We compared patients with SF with patients without SF antecedents using bivariate analysis, and also analyzed the impact of SF on SLE-related mortality. Results: We studied 286 SLE patients (1997 ACR criteria); 3 patients were excluded by insufficient data about flare; 283 were finally included. Female: 91%; caucasian 94.5 %; mean age 48.5 (±13.3); mean SLE duration: 17.1 (±8.8) years; mean follow-up 14.3 (±10.2) years. Median SLE criteria: 6.0 (5.0-7.0); major organ involvement 49 %; class III or IV (OMS) lupus nephritis : 30%; hospitalization by SLE:64 %; median SLICC/ACR/DI 1.0 (0.0 2.0): 7.8 % of the patients had died at the study moment. Severe infection (SInf): 32% hospitalization by SInf : 30%. Cumulative treatment: 84% had received antimalarialsAbstract : Background: Systemic Lupus Erythematosus (SLE) is a systemic autoinmune disorder of relapsing-remitting nature. However, we don´t have enough knowing about severe flare´s relevance on damage, severity or death in SLE patients. Objectives: To analyze the cumulative incidence and clinical significance of severe flares (SF) in a monocentric, well characterized SLE cohort. Methods: Cumulative clinical data were retrospectively collected at the moment of the last assessment. SF was defined using Selena-Sledai Flare Index (SFI) tool. Persistently active disease was not considered. SLICC/ACR/DI (SDI) was used to assess damage. Fisher exact test was used for qualitative variables and Kruskal-Wallis for quantitative ones. We compared patients with SF with patients without SF antecedents using bivariate analysis, and also analyzed the impact of SF on SLE-related mortality. Results: We studied 286 SLE patients (1997 ACR criteria); 3 patients were excluded by insufficient data about flare; 283 were finally included. Female: 91%; caucasian 94.5 %; mean age 48.5 (±13.3); mean SLE duration: 17.1 (±8.8) years; mean follow-up 14.3 (±10.2) years. Median SLE criteria: 6.0 (5.0-7.0); major organ involvement 49 %; class III or IV (OMS) lupus nephritis : 30%; hospitalization by SLE:64 %; median SLICC/ACR/DI 1.0 (0.0 2.0): 7.8 % of the patients had died at the study moment. Severe infection (SInf): 32% hospitalization by SInf : 30%. Cumulative treatment: 84% had received antimalarials at any time, 81%, corticosteroids (≥ 60mg/day: 45 %) and 54 % inmunosupressants; 272 (96.4%) patients had ≥1 flare, median 2 (IQR:1-3). Median SF:1.00 (IQI:0-2), (range: 0-13), mean: 1.4. Median SF per year:0.073 (IQR:0.00-0.17). SF was associated to more damage, Sinf, hospitalization by SInf, more number of hospitalization by infectionand number of SLE criteria (table1). Conclusions: In our SLE cohort, a history of severe flare was associated to dead, more damage and severe infection. Disclosure of Interest: None Declared … (more)
- Is Part Of:
- Annals of the rheumatic diseases. Volume 72:Supplement 3(2013)
- Journal:
- Annals of the rheumatic diseases
- Issue:
- Volume 72:Supplement 3(2013)
- Issue Display:
- Volume 72, Issue 3 (2013)
- Year:
- 2013
- Volume:
- 72
- Issue:
- 3
- Issue Sort Value:
- 2013-0072-0003-0000
- Page Start:
- A266
- Page End:
- A266
- Publication Date:
- 2014-01-23
- Subjects:
- Rheumatism -- Periodicals
616.723005 - Journal URLs:
- http://ard.bmjjournals.com/ ↗
http://www.pubmedcentral.nih.gov/tocrender.fcgi?journal=149&action=archive ↗
http://www.bmj.com/archive ↗
http://gateway.ovid.com/server3/ovidweb.cgi?T=JS&MODE=ovid&D=ovft&PAGE=titles&SEARCH=annals+of+the+rheumatic+diseases.tj&NEWS=N ↗ - DOI:
- 10.1136/annrheumdis-2013-eular.825 ↗
- Languages:
- English
- ISSNs:
- 0003-4967
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 23134.xml