Literature DB >> 21784727

Clinical prediction of 5-year survival in systemic sclerosis: validation of a simple prognostic model in EUSTAR centres.

J Fransen1, D Popa-Diaconu, R Hesselstrand, P Carreira, G Valentini, L Beretta, P Airo, M Inanc, S Ullman, A Balbir-Gurman, S Sierakowski, Y Allanore, L Czirjak, V Riccieri, R Giacomelli, A Gabrielli, G Riemekasten, M Matucci-Cerinic, D Farge, N Hunzelmann, F H J Van den Hoogen, M C Vonk.   

Abstract

OBJECTIVE: Systemic sclerosis (SSc) is associated with a significant reduction in life expectancy. A simple prognostic model to predict 5-year survival in SSc was developed in 1999 in 280 patients, but it has not been validated in other patients. The predictions of a prognostic model are usually less accurate in other patients, especially from other centres or countries. A study was undertaken to validate the prognostic model to predict 5-year survival in SSc in other centres throughout Europe.
METHODS: A European multicentre cohort of patients with SSc diagnosed before 2002 was established. Patients with SSc according to the preliminary American College of Rheumatology classification criteria were eligible for the study when they were followed for at least 5 years or shorter if they died. The primary outcome was 5-year survival after diagnosis of SSc. The predefined prognostic model uses the following baseline variables: age, gender, presence of urine protein, erythrocyte sedimentation rate (ESR) and carbon monoxide diffusing capacity (DLCO).
RESULTS: Data were available for 1049 patients, 119 (11%) of whom died within 5 years after diagnosis. Of the patients, 85% were female, the mean (SD) age at diagnosis was 50 (14) years and 30% were classified as having diffuse cutaneous SSc. The prognostic model with age (OR 1.03), male gender (OR 1.93), urine protein (OR 2.29), elevated ESR (1.89) and low DLCO (OR 1.94) had an area under the receiver operating characteristic curve of 0.78. Death occurred in 12 (2.2%) of 509 patients with no risk factors, 45 (13%) of 349 patients with one risk factor, 55 (33%) of 168 patients with two risk factors and 7 (30%) of 23 patients with three risk factors.
CONCLUSION: A simple prognostic model using three disease factors to predict 5-year survival at diagnosis in SSc showed reasonable performance upon validation in a European multicentre study.

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Year:  2011        PMID: 21784727     DOI: 10.1136/ard.2010.144360

Source DB:  PubMed          Journal:  Ann Rheum Dis        ISSN: 0003-4967            Impact factor:   19.103


  29 in total

Review 1.  [Autologous stem cell transplantation in systemic sclerosis].

Authors:  J C Henes; S Wirths; I Kötter
Journal:  Z Rheumatol       Date:  2016-10       Impact factor: 1.372

Review 2.  Moving towards a molecular taxonomy of autoimmune rheumatic diseases.

Authors:  Guillermo Barturen; Lorenzo Beretta; Ricard Cervera; Ronald Van Vollenhoven; Marta E Alarcón-Riquelme
Journal:  Nat Rev Rheumatol       Date:  2018-01-24       Impact factor: 20.543

3.  Connective tissue diseases: Predicting death in SSc: planning and cooperation are needed.

Authors:  Robyn T Domsic; Thomas A Medsger
Journal:  Nat Rev Rheumatol       Date:  2011-10-04       Impact factor: 20.543

Review 4.  [The German network for systemic sclerosis (DNSS): current data on diagnostics and therapy].

Authors:  N Hunzelmann; T Krieg
Journal:  Hautarzt       Date:  2012-04       Impact factor: 0.751

5.  Are diffuse and limited juvenile systemic sclerosis different in clinical presentation? Clinical characteristics of a juvenile systemic sclerosis cohort.

Authors:  Ivan Foeldvari; Jens Klotsche; Kathryn S Torok; Ozgur Kasapcopur; Amra Adrovic; Valda Stanevicha; Maria Teresa Terreri; Ekaterina Alexeeva; Maria Katsicas; Rolando Cimaz; Mikhail Kostik; Thomas Lehman; Walter-Alberto Sifuentes-Giraldo; Vanessa Smith; Flavio Sztajnbok; Tadej Avcin; Maria Jose Santos; Monika Moll; Dana Nemcova; Cristina Battagliotti; Despina Eleftheriou; Mahesh Janarthanan; Tilmann Kallinich; Jordi Anton; Kirsten Minden; Susan Nielsen; Yosef Uziel; Nicola Helmus
Journal:  J Scleroderma Relat Disord       Date:  2018-08-07

6.  Prediction of organ involvement and survival in systemic sclerosis patients in the first 5 years from diagnosis.

Authors:  Wieneke Mt van den Hombergh; Hanneke Ka Knaapen-Hans; Frank Hj van den Hoogen; Patricia Carreira; Oliver Distler; Roger Hesselstrand; Nicolas Hunzelmann; Serena Vettori; Jaap Fransen; Madelon C Vonk
Journal:  J Scleroderma Relat Disord       Date:  2019-09-06

7.  Survival and causes of death in systemic sclerosis patients: a single center registry report from Iran.

Authors:  Hadi Poormoghim; Elham Andalib; Arash Jalali; Afshin Ghaderi; Ali Ghorbannia; Nazanin Mojtabavi
Journal:  Rheumatol Int       Date:  2016-04-09       Impact factor: 2.631

8.  Does ex vivo CD34+ positive selection influence outcome after autologous hematopoietic stem cell transplantation in systemic sclerosis patients?

Authors:  M C Oliveira; M Labopin; J Henes; J Moore; N Del Papa; A Cras; I Sakellari; R Schroers; H U Scherer; A Cuneo; S Kyrcz-Krzemien; T Daikeler; T Alexander; J Finke; M Badoglio; B Simões; J A Snowden; D Farge
Journal:  Bone Marrow Transplant       Date:  2015-12-07       Impact factor: 5.483

9.  Derivation and validation of a prediction rule for two-year mortality in early diffuse cutaneous systemic sclerosis.

Authors:  Robyn T Domsic; Svetlana I Nihtyanova; Stephen R Wisniewski; Michael J Fine; Mary Lucas; C Kent Kwoh; Christopher P Denton; Thomas A Medsger
Journal:  Arthritis Rheumatol       Date:  2014-06       Impact factor: 10.995

10.  Causes of death, survival and risk factors of mortality in Thai patients with early systemic sclerosis: inception cohort study.

Authors:  Suparaporn Wangkaew; Narawudt Prasertwitayakij; Arintaya Phrommintikul; Saowanee Puntana; Juntima Euathrongchit
Journal:  Rheumatol Int       Date:  2017-10-12       Impact factor: 2.631

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