Morbidity and mortality in systemic lupus erythematosus during a 5-year period. A multicenter prospective study of 1,000 patients. European Working Party on Systemic Lupus Erythematosus
In the present study we assessed the frequency and characteristics of the main causes of morbidity and mortality in SLE during a 5-year period and analyzed the prognostic significance for morbidity and mortality of the main immunologic parameters used in clinical practice. We started in 1990 a multi...
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Veröffentlicht in: | Medicine (Baltimore) 1999-05, Vol.78 (3), p.167-175 |
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creator | Cervera, R Khamashta, M A Font, J Sebastiani, G D Gil, A Lavilla, P Aydintug, A O Jedryka-Góral, A de Ramón, E Fernández-Nebro, A Galeazzi, M Haga, H J Mathieu, A Houssiau, F Ruiz-Irastorza, G Ingelmo, M Hughes, G R |
description | In the present study we assessed the frequency and characteristics of the main causes of morbidity and mortality in SLE during a 5-year period and analyzed the prognostic significance for morbidity and mortality of the main immunologic parameters used in clinical practice. We started in 1990 a multicenter study of 1,000 patients from 7 European countries. All had medical histories documented and underwent medical interview and routine general physical examination when entered in the study, and all were followed prospectively by the same physicians during the ensuing 5 years (1990-1995). Four hundred thirteen patients (41.3%) presented 1 or more episodes of arthritis, 264 (26.4%) had malar rash, 222 (22.2%) active nephropathy, 139 (13.9%) fever, 136 (13.6%) neurologic involvement, 132 (13.2%) Raynaud phenomenon, 129 (12.9%) serositis (pleuritis and/or pericarditis), 95 (9.5%) thrombocytopenia, and 72 (7.2%) thrombosis. Two hundred seventy patients (27%) presented infections, 113 (11.3%) hypertension, 75 (7.5%) osteoporosis, and 59 (5.9%) cytopenia due to immunosuppressive agents. Sixteen patients (1.6%) developed malignancies, with the most frequent primary localizations the uterus and the breast. Several immunologic parameters (anti-dsDNA or antiphospholipid antibodies) were found to have a predictive value for the development of SLE manifestations during the period of the study. Forty-five patients (4.5%) died; the most frequent causes of death were divided similarly among active SLE (28.9%), infections (28.9%), and thromboses (26.7%). A survival probability of 95% at 5 years was found. A lower survival probability (92%) was detected in those patients who presented at the beginning of the study with nephropathy. |
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A multicenter prospective study of 1,000 patients. European Working Party on Systemic Lupus Erythematosus</title><source>MEDLINE</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>Journals@Ovid Complete</source><source>Wolters Kluwer Open Health</source><creator>Cervera, R ; Khamashta, M A ; Font, J ; Sebastiani, G D ; Gil, A ; Lavilla, P ; Aydintug, A O ; Jedryka-Góral, A ; de Ramón, E ; Fernández-Nebro, A ; Galeazzi, M ; Haga, H J ; Mathieu, A ; Houssiau, F ; Ruiz-Irastorza, G ; Ingelmo, M ; Hughes, G R</creator><creatorcontrib>Cervera, R ; Khamashta, M A ; Font, J ; Sebastiani, G D ; Gil, A ; Lavilla, P ; Aydintug, A O ; Jedryka-Góral, A ; de Ramón, E ; Fernández-Nebro, A ; Galeazzi, M ; Haga, H J ; Mathieu, A ; Houssiau, F ; Ruiz-Irastorza, G ; Ingelmo, M ; Hughes, G R</creatorcontrib><description>In the present study we assessed the frequency and characteristics of the main causes of morbidity and mortality in SLE during a 5-year period and analyzed the prognostic significance for morbidity and mortality of the main immunologic parameters used in clinical practice. We started in 1990 a multicenter study of 1,000 patients from 7 European countries. All had medical histories documented and underwent medical interview and routine general physical examination when entered in the study, and all were followed prospectively by the same physicians during the ensuing 5 years (1990-1995). Four hundred thirteen patients (41.3%) presented 1 or more episodes of arthritis, 264 (26.4%) had malar rash, 222 (22.2%) active nephropathy, 139 (13.9%) fever, 136 (13.6%) neurologic involvement, 132 (13.2%) Raynaud phenomenon, 129 (12.9%) serositis (pleuritis and/or pericarditis), 95 (9.5%) thrombocytopenia, and 72 (7.2%) thrombosis. Two hundred seventy patients (27%) presented infections, 113 (11.3%) hypertension, 75 (7.5%) osteoporosis, and 59 (5.9%) cytopenia due to immunosuppressive agents. Sixteen patients (1.6%) developed malignancies, with the most frequent primary localizations the uterus and the breast. Several immunologic parameters (anti-dsDNA or antiphospholipid antibodies) were found to have a predictive value for the development of SLE manifestations during the period of the study. Forty-five patients (4.5%) died; the most frequent causes of death were divided similarly among active SLE (28.9%), infections (28.9%), and thromboses (26.7%). A survival probability of 95% at 5 years was found. A lower survival probability (92%) was detected in those patients who presented at the beginning of the study with nephropathy.</description><identifier>ISSN: 0025-7974</identifier><identifier>PMID: 10352648</identifier><language>eng</language><publisher>United States</publisher><subject>Adolescent ; Adult ; Aged ; Aged, 80 and over ; Cause of Death ; Chi-Square Distribution ; Child ; Child, Preschool ; Enzyme-Linked Immunosorbent Assay ; Europe - epidemiology ; Female ; Fluorescent Antibody Technique, Direct ; Humans ; Logistic Models ; Lupus Erythematosus, Systemic - complications ; Lupus Erythematosus, Systemic - immunology ; Lupus Erythematosus, Systemic - mortality ; Male ; Middle Aged ; Predictive Value of Tests ; Prospective Studies ; Survival Analysis</subject><ispartof>Medicine (Baltimore), 1999-05, Vol.78 (3), p.167-175</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10352648$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Cervera, R</creatorcontrib><creatorcontrib>Khamashta, M A</creatorcontrib><creatorcontrib>Font, J</creatorcontrib><creatorcontrib>Sebastiani, G D</creatorcontrib><creatorcontrib>Gil, A</creatorcontrib><creatorcontrib>Lavilla, P</creatorcontrib><creatorcontrib>Aydintug, A O</creatorcontrib><creatorcontrib>Jedryka-Góral, A</creatorcontrib><creatorcontrib>de Ramón, E</creatorcontrib><creatorcontrib>Fernández-Nebro, A</creatorcontrib><creatorcontrib>Galeazzi, M</creatorcontrib><creatorcontrib>Haga, H J</creatorcontrib><creatorcontrib>Mathieu, A</creatorcontrib><creatorcontrib>Houssiau, F</creatorcontrib><creatorcontrib>Ruiz-Irastorza, G</creatorcontrib><creatorcontrib>Ingelmo, M</creatorcontrib><creatorcontrib>Hughes, G R</creatorcontrib><title>Morbidity and mortality in systemic lupus erythematosus during a 5-year period. A multicenter prospective study of 1,000 patients. European Working Party on Systemic Lupus Erythematosus</title><title>Medicine (Baltimore)</title><addtitle>Medicine (Baltimore)</addtitle><description>In the present study we assessed the frequency and characteristics of the main causes of morbidity and mortality in SLE during a 5-year period and analyzed the prognostic significance for morbidity and mortality of the main immunologic parameters used in clinical practice. We started in 1990 a multicenter study of 1,000 patients from 7 European countries. All had medical histories documented and underwent medical interview and routine general physical examination when entered in the study, and all were followed prospectively by the same physicians during the ensuing 5 years (1990-1995). Four hundred thirteen patients (41.3%) presented 1 or more episodes of arthritis, 264 (26.4%) had malar rash, 222 (22.2%) active nephropathy, 139 (13.9%) fever, 136 (13.6%) neurologic involvement, 132 (13.2%) Raynaud phenomenon, 129 (12.9%) serositis (pleuritis and/or pericarditis), 95 (9.5%) thrombocytopenia, and 72 (7.2%) thrombosis. Two hundred seventy patients (27%) presented infections, 113 (11.3%) hypertension, 75 (7.5%) osteoporosis, and 59 (5.9%) cytopenia due to immunosuppressive agents. Sixteen patients (1.6%) developed malignancies, with the most frequent primary localizations the uterus and the breast. Several immunologic parameters (anti-dsDNA or antiphospholipid antibodies) were found to have a predictive value for the development of SLE manifestations during the period of the study. Forty-five patients (4.5%) died; the most frequent causes of death were divided similarly among active SLE (28.9%), infections (28.9%), and thromboses (26.7%). A survival probability of 95% at 5 years was found. A lower survival probability (92%) was detected in those patients who presented at the beginning of the study with nephropathy.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Cause of Death</subject><subject>Chi-Square Distribution</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Enzyme-Linked Immunosorbent Assay</subject><subject>Europe - epidemiology</subject><subject>Female</subject><subject>Fluorescent Antibody Technique, Direct</subject><subject>Humans</subject><subject>Logistic Models</subject><subject>Lupus Erythematosus, Systemic - complications</subject><subject>Lupus Erythematosus, Systemic - immunology</subject><subject>Lupus Erythematosus, Systemic - mortality</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Predictive Value of Tests</subject><subject>Prospective Studies</subject><subject>Survival Analysis</subject><issn>0025-7974</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpNkNtKw0AQhnOh2Fp9BZkrr0zZTbI5XJZSD1BRsOBl2MNEV5Ns3IOQR_PtTLWCV8M_fPx8M0fRnJCExUVVZLPo1Lk3QmhaJNlJNKMkZUmelfPo695YoZX2I_BeQWes5-0-6R7c6Dx2WkIbhuAA7ehfsePeuCmpYHX_AhxYPCK3MKDVRi1hBV1ovZbYe5y21rgBpdefCM4HNYJpgF4RQmDgXk-QW8ImWDMg7-HZ2Pd96SO3k4Hp4enPYPtjsPlvcBYdN7x1eH6Yi2h3vdmtb-Ptw83derWNB5aVMRMkT9KEslTmaSXLUjBJOCNKKa4UFWlGcyoFK5ho8iZjNFe0FDLnmFeFQEwX0eVv7XTKR0Dn6047iW3LezTB1RNW0YxkE3hxAIPoUNWD1R23Y_336_Qb7A5-kA</recordid><startdate>199905</startdate><enddate>199905</enddate><creator>Cervera, R</creator><creator>Khamashta, M A</creator><creator>Font, J</creator><creator>Sebastiani, G D</creator><creator>Gil, A</creator><creator>Lavilla, P</creator><creator>Aydintug, A O</creator><creator>Jedryka-Góral, A</creator><creator>de Ramón, E</creator><creator>Fernández-Nebro, A</creator><creator>Galeazzi, M</creator><creator>Haga, H J</creator><creator>Mathieu, A</creator><creator>Houssiau, F</creator><creator>Ruiz-Irastorza, G</creator><creator>Ingelmo, M</creator><creator>Hughes, G R</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>199905</creationdate><title>Morbidity and mortality in systemic lupus erythematosus during a 5-year period. 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European Working Party on Systemic Lupus Erythematosus</title><author>Cervera, R ; Khamashta, M A ; Font, J ; Sebastiani, G D ; Gil, A ; Lavilla, P ; Aydintug, A O ; Jedryka-Góral, A ; de Ramón, E ; Fernández-Nebro, A ; Galeazzi, M ; Haga, H J ; Mathieu, A ; Houssiau, F ; Ruiz-Irastorza, G ; Ingelmo, M ; Hughes, G R</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p548-5b06232153c639c88b5c0a50dddadd1b34161cb575bf6f4516d18bc6ae697bee3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1999</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Cause of Death</topic><topic>Chi-Square Distribution</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>Enzyme-Linked Immunosorbent Assay</topic><topic>Europe - epidemiology</topic><topic>Female</topic><topic>Fluorescent Antibody Technique, Direct</topic><topic>Humans</topic><topic>Logistic Models</topic><topic>Lupus Erythematosus, Systemic - complications</topic><topic>Lupus Erythematosus, Systemic - immunology</topic><topic>Lupus Erythematosus, Systemic - mortality</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Predictive Value of Tests</topic><topic>Prospective Studies</topic><topic>Survival Analysis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Cervera, R</creatorcontrib><creatorcontrib>Khamashta, M A</creatorcontrib><creatorcontrib>Font, J</creatorcontrib><creatorcontrib>Sebastiani, G D</creatorcontrib><creatorcontrib>Gil, A</creatorcontrib><creatorcontrib>Lavilla, P</creatorcontrib><creatorcontrib>Aydintug, A O</creatorcontrib><creatorcontrib>Jedryka-Góral, A</creatorcontrib><creatorcontrib>de Ramón, E</creatorcontrib><creatorcontrib>Fernández-Nebro, A</creatorcontrib><creatorcontrib>Galeazzi, M</creatorcontrib><creatorcontrib>Haga, H J</creatorcontrib><creatorcontrib>Mathieu, A</creatorcontrib><creatorcontrib>Houssiau, F</creatorcontrib><creatorcontrib>Ruiz-Irastorza, G</creatorcontrib><creatorcontrib>Ingelmo, M</creatorcontrib><creatorcontrib>Hughes, G R</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>Medicine (Baltimore)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Cervera, R</au><au>Khamashta, M A</au><au>Font, J</au><au>Sebastiani, G D</au><au>Gil, A</au><au>Lavilla, P</au><au>Aydintug, A O</au><au>Jedryka-Góral, A</au><au>de Ramón, E</au><au>Fernández-Nebro, A</au><au>Galeazzi, M</au><au>Haga, H J</au><au>Mathieu, A</au><au>Houssiau, F</au><au>Ruiz-Irastorza, G</au><au>Ingelmo, M</au><au>Hughes, G R</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Morbidity and mortality in systemic lupus erythematosus during a 5-year period. A multicenter prospective study of 1,000 patients. European Working Party on Systemic Lupus Erythematosus</atitle><jtitle>Medicine (Baltimore)</jtitle><addtitle>Medicine (Baltimore)</addtitle><date>1999-05</date><risdate>1999</risdate><volume>78</volume><issue>3</issue><spage>167</spage><epage>175</epage><pages>167-175</pages><issn>0025-7974</issn><abstract>In the present study we assessed the frequency and characteristics of the main causes of morbidity and mortality in SLE during a 5-year period and analyzed the prognostic significance for morbidity and mortality of the main immunologic parameters used in clinical practice. We started in 1990 a multicenter study of 1,000 patients from 7 European countries. All had medical histories documented and underwent medical interview and routine general physical examination when entered in the study, and all were followed prospectively by the same physicians during the ensuing 5 years (1990-1995). Four hundred thirteen patients (41.3%) presented 1 or more episodes of arthritis, 264 (26.4%) had malar rash, 222 (22.2%) active nephropathy, 139 (13.9%) fever, 136 (13.6%) neurologic involvement, 132 (13.2%) Raynaud phenomenon, 129 (12.9%) serositis (pleuritis and/or pericarditis), 95 (9.5%) thrombocytopenia, and 72 (7.2%) thrombosis. Two hundred seventy patients (27%) presented infections, 113 (11.3%) hypertension, 75 (7.5%) osteoporosis, and 59 (5.9%) cytopenia due to immunosuppressive agents. Sixteen patients (1.6%) developed malignancies, with the most frequent primary localizations the uterus and the breast. Several immunologic parameters (anti-dsDNA or antiphospholipid antibodies) were found to have a predictive value for the development of SLE manifestations during the period of the study. Forty-five patients (4.5%) died; the most frequent causes of death were divided similarly among active SLE (28.9%), infections (28.9%), and thromboses (26.7%). A survival probability of 95% at 5 years was found. A lower survival probability (92%) was detected in those patients who presented at the beginning of the study with nephropathy.</abstract><cop>United States</cop><pmid>10352648</pmid><tpages>9</tpages></addata></record> |
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subjects | Adolescent Adult Aged Aged, 80 and over Cause of Death Chi-Square Distribution Child Child, Preschool Enzyme-Linked Immunosorbent Assay Europe - epidemiology Female Fluorescent Antibody Technique, Direct Humans Logistic Models Lupus Erythematosus, Systemic - complications Lupus Erythematosus, Systemic - immunology Lupus Erythematosus, Systemic - mortality Male Middle Aged Predictive Value of Tests Prospective Studies Survival Analysis |
title | Morbidity and mortality in systemic lupus erythematosus during a 5-year period. A multicenter prospective study of 1,000 patients. European Working Party on Systemic Lupus Erythematosus |
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