Mortality in systemic sclerosis (scleroderma)

P. Lee, P. Langevitz, C. A. Alderdice, M. Aubrey, P. A. Baer, M. Baron, D. Buskila, J. P. Dutz, I. Khostanteen, S. Piper, M. Ramsden, T. O. Rosenbach, S. Sukenik, S. Wilkinson, E. C. Keystone

Research output: Contribution to journalArticlepeer-review

172 Scopus citations

Abstract

Two hundred and thirty-seven patients with systemic sclerosis were followed prospectively in a scleroderma clinic. The overall 3, 6, and 9-year survival rates were 86, 76 and 61 per cent respectively. Renal, cardiac and pulmonary disease, and older age at enrolment were adverse prognostic factors associated with reduced survival. There were no significant differences in survival between males and females or in patients with restricted compared to those with diffuse skin thickening. Death from systemic sclerosis was most frequently due to pulmonary hypertension, with fewer than expected deaths from renal or cardiac causes. Twenty-eight per cent of deaths were due to causes unrelated to systemic sclerosis, most commonly cancer and ischaemic heart disease, and in older patients.

Original languageEnglish
Pages (from-to)139-148
Number of pages10
JournalQJM: An International Journal of Medicine
Volume82
Issue number2
DOIs
StatePublished - 1 Jan 1992
Externally publishedYes

ASJC Scopus subject areas

  • General Medicine

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