Skip Navigation

This Article
Right arrow Full Text Freely available
Right arrow FREE Full Text (PDF) Freely available
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (30)
Right arrowRequest Permissions
Right arrow Disclaimer
Google Scholar
Right arrow Articles by Simeón, C. P.
Right arrow Articles by Vilardell, M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Simeón, C. P.
Right arrow Articles by Vilardell, M.
Related Collections
Right arrow Systemic Sclerosis
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Rheumatology 2003; 42: 71-75
© 2003 British Society for Rheumatology

Mortality and prognostic factors in Spanish patients with systemic sclerosis

C. P. Simeón, L. Armadans1, V. Fonollosa, R. Solans, A. Selva, M. Villar, J. Lima, J. Vaqué1 and M. Vilardell

Department of Internal Medicine and
1 Department of Preventive Medicine and Epidemiology, Hospital Vall d'Hebron, Barcelona, Spain

Objective. To determine survival and mortality in a cohort of Spanish patients with scleroderma (systemic sclerosis, SSc) and to analyse whether survival is influenced by demographic, clinical or immunological variables or the extent of skin involvement.

Methods. The study included 79 patients diagnosed with SSc and taking part in a study to determine the extent of sclerosis, visceral involvement and immunological alterations. We studied the number of observed and expected deaths (the expected number being based on age- and sex-specific rates in the background population) and derived standardized mortality ratios with their 95% confidence intervals (CI). Cumulative survival after onset of the first symptom was estimated according to the Kaplan–Meier method. The Cox method was used to identify the prognostic factors.

Results. The mortality rate was 0.0249 deaths per person-year. Survival at 15 yr was 0.62 (95% CI 0.410–0.778). The standardized mortality ratio was 429.4% (95% CI 222–750). On crude analysis, lung involvement [forced vital capacity (FVC) <70%, pulmonary hypertension], SSc renal crisis, an active capillaroscopic pattern, pericardial effusion and age over 60 yr at diagnosis were associated with shorter survival. On multivariate analysis, only age at diagnosis over 60 yr, FVC <70% and SSc renal crisis were independent prognostic factors.

Conclusions. The mortality rate associated with SSc showed a four-fold increase compared with the background population. Lung involvement and sclerodermal renal crisis were found to be independently associated with reduced survival.

KEY WORDS: Scleroderma, Survival, Standardized mortality ratio, Prognostic factors.

Correspondence to: C.-P. Simeón, Servicio de Medicina Interna (3a planta), Hospital General Vall d'Hebron, Paseo Vall d'Hebron 119, 08035 Barcelona, Spain. E-mail: cpsimeon{at}hg.vhebron.es


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
Eur Respir JHome page
K. M. Antoniou, G. Margaritopoulos, F. Economidou, and N. M. Siafakas
Pivotal clinical dilemmas in collagen vascular diseases associated with interstitial lung involvement
Eur. Respir. J., April 1, 2009; 33(4): 882 - 896.
[Abstract] [Full Text] [PDF]


Home page
Rheumatology (Oxford)Home page
E. Hachulla, P. Carpentier, V. Gressin, E. Diot, Y. Allanore, J. Sibilia, D. Launay, L. Mouthon, P. Jego, J. Cabane, et al.
Risk factors for death and the 3-year survival of patients with systemic sclerosis: the French ItinerAIR-Sclerodermie study
Rheumatology, March 1, 2009; 48(3): 304 - 308.
[Abstract] [Full Text] [PDF]


Home page
Ann Rheum DisHome page
M C Vonk, C E van Die, M M Snoeren, K J Bhansing, P L C M van Riel, J Fransen, and F H J van den Hoogen
Oesophageal dilatation on high-resolution computed tomography scan of the lungs as a sign of scleroderma
Ann Rheum Dis, September 1, 2008; 67(9): 1317 - 1321.
[Abstract] [Full Text] [PDF]


Home page
Ann Rheum DisHome page
M C Vonk, Z Marjanovic, F H J van den Hoogen, S Zohar, A V M B Schattenberg, W E Fibbe, J Larghero, E Gluckman, F W M B Preijers, A P J van Dijk, et al.
Long-term follow-up results after autologous haematopoietic stem cell transplantation for severe systemic sclerosis
Ann Rheum Dis, January 1, 2008; 67(1): 98 - 104.
[Abstract] [Full Text] [PDF]


Home page
Rheumatology (Oxford)Home page
L. Chung, E. Krishnan, and E. F. Chakravarty
Hospitalizations and mortality in systemic sclerosis: results from the Nationwide Inpatient Sample
Rheumatology, December 1, 2007; 46(12): 1808 - 1813.
[Abstract] [Full Text] [PDF]


Home page
Rheumatology (Oxford)Home page
P. Caramaschi, S. Canestrini, N. Martinelli, A. Volpe, S. Pieropan, M. Ferrari, L. M. Bambara, A. Carletto, and D. Biasi
Scleroderma patients nailfold videocapillaroscopic patterns are associated with disease subset and disease severity
Rheumatology, October 1, 2007; 46(10): 1566 - 1569.
[Abstract] [Full Text] [PDF]



Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.