Gladman D D, Goldsmith C H, Urowitz M B, Bacon P, Fortin P, Ginzler E, Gordon C, Hanly J G, Isenberg D A, Petri M, Nived O, Snaith M, Sturfelt G
Centre for Prognosis Studies in the Rheumatic Diseases, University Health Network, Toronto Western Hospital, Canada.
J Rheumatol. 2000 Feb;27(2):373-6.
To compare patients with systemic lupus erythematosus (SLE) from different centers with respect to demographics and Systemic Lupus International Collaborating Clinics/American College of Rheumatology Damage Index (SLICC/ACR DI) scores, and to assess whether the SLICC/ACR DI changed over time, and whether initial DI scores were related to outcome.
Members of SLICC completed DI scores and patient demographics on patients followed in their centers. Information was provided at 2, 5-10, and > 10 years of followup. Data were entered on computer and analyzed on SPSS/PC+ and SAS using descriptive statistics and analysis of variance.
Information for 1297 patients within 2 years of first clinic visit was submitted from 8 centers. There were 1187 women and 110 men with a mean age at diagnosis of SLE of 32 years. Seven hundred sixty-two were Caucasian, 423 were black, and the remainder were of other races. There were more blacks in the American centers than in Canadian or European centers. Five centers provided information for the 3 time periods. The DI increased over time. Ninety-nine patients had died. Higher SLICC/ACR DI scores were documented in patients who went on to die.
The SLICC/ACR DI is a valid measure for damage in SLE.
比较来自不同中心的系统性红斑狼疮(SLE)患者在人口统计学和系统性红斑狼疮国际协作临床/美国风湿病学会损伤指数(SLICC/ACR DI)评分方面的情况,并评估SLICC/ACR DI是否随时间变化,以及初始DI评分是否与预后相关。
SLICC成员完成了其所在中心随访患者的DI评分和患者人口统计学信息。在随访2年、5 - 10年以及超过10年时提供相关信息。数据录入计算机,并使用描述性统计和方差分析在SPSS/PC +和SAS上进行分析。
8个中心提交了1297例患者首次就诊后2年内的信息。有1187名女性和110名男性,SLE诊断时的平均年龄为32岁。762人为白种人,423人为黑人,其余为其他种族。美国中心的黑人比加拿大或欧洲中心的多。5个中心提供了3个时间段的信息。DI随时间增加。99例患者死亡。死亡患者的SLICC/ACR DI评分更高。
SLICC/ACR DI是SLE损伤的有效测量指标。