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首页> 外文期刊>Pharmacoepidemiology and drug safety >Systemic lupus erythematosus prevalence in the UK: methodological issues when using the General Practice Research Database to estimate frequency of chronic relapsing-remitting disease.
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Systemic lupus erythematosus prevalence in the UK: methodological issues when using the General Practice Research Database to estimate frequency of chronic relapsing-remitting disease.

机译:英国的系统性红斑狼疮患病率:使用“全科医学研究数据库”估算慢性复发-传播性疾病的频率时的方法论问题。

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PURPOSE: The purpose of this study was to calculate the prevalence of systemic lupus erythematosus (SLE) between 1992 and 1998 using the General Practice Research Database (GPRD) METHODS: We identified all individuals who had contributed at least 3 years of data to the GPRD and who had a diagnosis of SLE with supporting evidence of their diagnosis. We calculated the annual age- and sex-specific prevalence of SLE. Additionally, we stratified the prevalence by years of data contributed to the GRPD. RESULTS: In males the point estimate of the prevalence of SLE increased from 7.5/100,000 (CI(95) 6.3, 8.8) to 10.1/100,000 (CI(95) 7.8, 12.2) but this rise was not statistically significant. However, prevalence appeared to increase significantly amongst females from 42.6/100,000 (CI(95) 39.6, 45.6) in 1992 to 70.8/100,000 (CI(95) 65.1, 76.6) in 1998. This increase was mainly amongst women aged 50-79 and in those contributing more than 5 years of data and could not be explained by increasing incidence of SLE ordecreasing mortality during the study period. CONCLUSIONS: We found an increasing prevalence of SLE that could not be explained by increasing incidence or decreasing mortality. This is almost certainly an artefact caused by the increased likelihood of detecting or confirming cases of chronic relapsing-remitting diseases with increasing time contributed to the GPRD.
机译:目的:本研究的目的是使用全科医学研究数据库(GPRD)计算1992年至1998年系统性红斑狼疮(SLE)的患病率。方法:我们确定了对GPRD贡献了至少3年数据的所有个体并已被诊断为SLE并有确诊证据。我们计算了SLE的年度年龄和性别特异性患病率。此外,我们根据对GRPD贡献的多年数据对患病率进行了分层。结果:在男性中,SLE患病率的点估计值从7.5 / 100,000(CI(95)6.3,8.8)增加到10.1 / 100,000(CI(95)7.8,12.2),但这种上升没有统计学意义。但是,女性的患病率似乎从1992年的42.6 / 100,000(CI(95)39.6,45.6)显着增加到1998年的70.8 / 100,000(CI(95)65.1,76.6)。这一增加主要是在50-79岁的女性中在那些提供超过5年数据的研究中,无法用研究期间SLE的发生率增加或死亡率降低来解释。结论:我们发现SLE的患病率增加,这不能通过增加发病率或降低死亡率来解释。几乎可以肯定,这是一种伪影,是由于随着GPRD的增加,随着时间的增加,发现或确认慢性复发性疾病病例的可能性增加。

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