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本文引用的文献

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CLINICAL MANIFESTATIONS OF SYSTEMIC LUPUS ERYTHEMATOSUS. COMPUTER ANALYSIS OF 520 CASES.系统性红斑狼疮的临床表现。520例病例的计算机分析。
JAMA. 1964 Oct 12;190:104-11. doi: 10.1001/jama.1964.03070150014003.
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OBSERVATIONS ON THE NATURAL COURSE OF DISSEMINATED LUPUS ERYTHEMATOSUS.播散性红斑狼疮自然病程的观察
Medicine (Baltimore). 1964 May;43:387-91. doi: 10.1097/00005792-196405000-00016.
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SYSTEMIC LUPUS ERYTHEMATOSUS. A STATISTICAL EVALUATION OF MORTALITY BASED ON A CONSECUTIVE SERIES OF 299 PATIENTS.系统性红斑狼疮。基于299例连续病例的死亡率统计评估。
Arch Intern Med. 1964 Feb;113:200-7. doi: 10.1001/archinte.1964.00280080036008.
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Factors influencing the course and prognosis of systemic lupus erythematosus.
N Engl J Med. 1959 Jun 11;260(24):1195-204. doi: 10.1056/NEJM195906112602401.
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The effect of the L. E. cell test on the clinical picture of systemic lupus erythematosus.红斑狼疮细胞检查对系统性红斑狼疮临床表现的影响。
Ann Intern Med. 1953 Jun;38(6):1265-94. doi: 10.7326/0003-4819-38-6-1265.
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Systemic lupus erythematosus--survival patterns. Experience with 609 patients.系统性红斑狼疮——生存模式。609例患者的经验。
JAMA. 1981 Mar 6;245(9):934-8. doi: 10.1001/jama.245.9.934.
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The 1982 revised criteria for the classification of systemic lupus erythematosus.1982年系统性红斑狼疮分类的修订标准。
Arthritis Rheum. 1982 Nov;25(11):1271-7. doi: 10.1002/art.1780251101.
8
A multicenter study of outcome in systemic lupus erythematosus. I. Entry variables as predictors of prognosis.一项系统性红斑狼疮结局的多中心研究。I. 作为预后预测指标的入组变量。
Arthritis Rheum. 1982 Jun;25(6):601-11. doi: 10.1002/art.1780250601.
9
Detection of anti-dsDNA as diagnostic tool.将抗双链DNA作为诊断工具进行检测。
Ann Rheum Dis. 1981 Feb;40(1):45-9. doi: 10.1136/ard.40.1.45.
10
Prognostic value of anti-dsDNA in SLE.抗双链DNA在系统性红斑狼疮中的预后价值。
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系统性红斑狼疮。I. 结局与生存情况:荷兰对110例患者进行前瞻性研究的经验

Systemic lupus erythematosus. I. Outcome and survival: Dutch experience with 110 patients studied prospectively.

作者信息

Swaak A J, Nossent J C, Bronsveld W, Van Rooyen A, Nieuwenhuys E J, Theuns L, Smeenk R J

机构信息

Department of Rheumatology, Daniel den Hoed Clinic, Rotterdam, The Netherlands.

出版信息

Ann Rheum Dis. 1989 Jun;48(6):447-54. doi: 10.1136/ard.48.6.447.

DOI:10.1136/ard.48.6.447
PMID:2742399
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1003786/
Abstract

This report presents an analysis of the cumulative survival in 110 well defined patients with systemic lupus erythematosus (SLE) who were followed up over a prolonged period of time. Special attention was paid to possible differences between patients who died and those who were still alive at the end of the study. Of the 110 patients with SLE, 96 (87%) were still alive after 10 years; the cumulative survival for men was 69% (11/16) and for women 90% (85/94). Patients who never developed a new exacerbation after the diagnosis for SLE had been established had a 10 year survival of 100%; for patients with one, two, or three exacerbations the 10 year survival was 91%, 69%, and 33% respectively. From these prospective studies it was found that the exacerbation frequency is most closely related to survival. Disease symptoms of renal involvement or neurological involvement, or both, present at the onset or at the moment the SLE diagnosis was established, were predominantly seen in patients who died during the follow up.

摘要

本报告对110例确诊的系统性红斑狼疮(SLE)患者进行了长期随访,并分析了其累积生存率。特别关注了研究结束时死亡患者与仍存活患者之间可能存在的差异。110例SLE患者中,96例(87%)在10年后仍存活;男性的累积生存率为69%(11/16),女性为90%(85/94)。在确诊SLE后从未出现新的病情加重的患者10年生存率为100%;有一次、两次或三次病情加重的患者10年生存率分别为91%、69%和33%。从这些前瞻性研究中发现,病情加重频率与生存率最为密切相关。在随访期间死亡的患者中,主要出现了发病时或确诊SLE时存在的肾脏受累或神经受累或两者皆有的疾病症状。