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Annals of the Rheumatic Diseases 1997;56:723-728; doi:10.1136/ard.56.12.723
Copyright © 1997 BMJ Publishing Group Ltd & European League Against Rheumatism.
Ann Rheum Dis 1997;56:723-728 ( December )

Extended reports

Survival prognostic factors and markers of morbidity in Spanish patients with systemic sclerosis Carmen-Pilar Simeon,a Luis Armadans,b Vicent Fonollosa,a Miquel Vilardell,a Jaume Candell,c Carles Tolosa,a Fermín Mearin,d María José Rodrigo,e Roser Solans,a Joan Lima,a Gabriel Sampolf

a Department of Internal Medicine, b Service of Preventive Medicine and Epidemiology, c Service of Cardiology, d Service of Gastroenterology, e Department of Biochemistry and Immunology, f Service of Pneumology, g Hospital General Universitari Vall D'Hebron, Barcelona, Spain

Correspondence to: Dr C P Simeon, C/ Provenza 473 sat 2a, 08025 Barcelona, Spain.

Accepted for publication 10 September 1997

OBJECTIVE---To identify survival prognostic factors and markers of morbidity among patients with systemic sclerosis (SSc).
PATIENTS AND METHODS---The study included 72 patients diagnosed with SSc. According to the extent of skin involvement, three groups of patients were established: group 1, without sclerosis and with sclerosis of fingers and neck; group 2, with sclerosis of face and distal to elbows and knees; group 3, with generalised sclerosis including the trunk. All patients were included in a study protocol to determine visceral involvement. Cumulative survival after first symptom has been estimated according to the Kaplan-Meier method. The association between a hypothetical prognostic factor and cumulative survival after first symptom was assessed by log rank test. The association between a hypothetical risk factor and the prevalence of severe morbity was assessed by the odds ratio. Multiple logistic regression models were used to identify the main predictors of severe morbidity.
RESULTS---Survival was estimated to be 85% 10 years after first SSc symptom. Survival was higher among SSc patients with skin involvement distal to elbows and knees than among the rest of patients; a forced vital capacity (FVC) on spirometry lower than 70% of expected value was associated with a shorter survival, even after adjustment for diffuse SSc. Skin involvement proximal to elbows or knees was associated with a higher prevalence of severe morbidity (OR = 46.57; p<0.001). According to a multiple logistic regression, severe morbidity was higher among patients with skin involvement proximal to knees or elbows (OR = 40.92; p<0.001) or among patients with pulmonary hypertension detected by Doppler echocardiography (OR = 23.66 p<0.001).
CONCLUSIONS---In patients with SSc the extent of skin sclerosis was found to be a determining factor on the prognosis. According to skin sclerosis extent two main subsets of SSc patients with different survival incidence and degree of morbidity could be clearly established: limited SSc, formed by patients with no skin sclerosis or with sclerosis distal to elbows and knees and diffuse SSc, formed by patients with skin sclerosis distal and proximal to elbows and knees. Moreover, lung involvement (FVC<70% on survival study and pulmonary hypertension on morbidity study) was an important and independent prognostic factor.


© 1997 by Annals of the Rheumatic Diseases

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