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Epidemiology of systemic sclerosis in a district of northern Italy

机译:意大利北部某地区系统性硬化的流行病学

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OBJECTIVES: To estimate, using both the American College of Rheumatology-ACR 1980 classification criteria and revised LeRoy and Medsger 2001 criteria, the incidence and prevalence of systemic sclerosis (SSc) in an area in north-eastern Italy with a referral base population of about 346,000 inhabitants. METHODS: Retrospective examination of all patients 16 years and older of native Italian origin and resident in the Ferrara district who had either been admitted to hospital or referred to our outpatient clinic with a diagnosis of SSc between 1st January 1999 and 31st December 2007. SSc subjects were identified both by a search of hospital discharge code 710.1, as per the international classification of disease-9 codes, and using a computerised search for this pathology code in the national health care system. The subjects referred to our outpatient clinic were identified from a dedicated data base. Incidence and prevalence rates were calculated as the number of cases per 100,000 inhabitants (population data based on the October 2001 national census). The medical records of each potential case were accurately examined and reviewed by the same physician who determined whether those patients identified as having a diagnosis of SSc did indeed meet the ACR 1980 classification criteria for SSc and/or the LeRoy and Medsger 2001 criteria. RESULTS: After reviewing all cases, of the 118 patients meeting the LeRoy-Medsger 2001 criteria, only 88 patients had a definitive diagnosis of SSc according to the ACR 1980 criteria. Considering the ACR criteria, the prevalence rate was 25.4 cases per 100,000 (95% CI: 22.2a€“28.6), and the annual incidence rate over the study period was 3.2 per 100,000 (95% CI: 2.0a€“4.4). Considering the LeRoy and Medsger criteria epidemiological data were respectively 34.1 cases per 100,000 (95% CI: 30.4a€“37.8) and 4.3 cases per 100,000 (95% CI: 3.0a€“5.6). According to the LeRoy and Medsger criteria, the SSc subsets were broken down as follows: 20 limited-SSc (19.2%), 76 limited cutaneous-SSc (62.1%), 22 diffuse cutaneous-SSc (18.7%). The female/male ratio was 9.7:1. CONCLUSIONS: Incidence and prevalence of SSc observed in an area in north-eastern Italy were found to be higher than reported in the various geographical area (UK, US, Australia, etc.) but similar to another Italian study adopting, as here, the LeRoy-Medsger criteria. The different diagnostic criteria adopted may explain some of the differences found in comparison to the studies based only on the ACR criteria, however, regional discrepancies in disease occurrence cannot easily be dismissed only on the basis of methodological approaches to case definition or ascertainment; genetic, ethnic and environmental factors should also be considered. Currently the main challenge remains to determine the scientific basis for the observed differences, distinguishing between changes deriving from geographic/ethnic features and from the analytic methods.
机译:目的:使用1980年美国风湿病学会ACR分类标准和经修订的LeRoy和Medsger 2001标准估算意大利东北部某地区系统性硬化症(SSc)的发病率和患病率34.6万居民。方法:回顾性检查所有1999年1月1日至2007年12月31日之间住院并转诊到我们门诊且诊断为SSc的16岁及以上意大利原住民且居住在费拉拉地区的患者。根据国际9类疾病分类标准,通过搜索医院出院代码710.1进行识别,并在国家卫生保健系统中通过计算机搜索此病理代码来进行识别。从专门的数据库中识别出转诊至我们门诊的受试者。发病率和患病率以每10万居民的病例数计算(根据2001年10月的全国人口普查得出的人口数据)。同一位医师对每个潜在病例的病历进行了准确的检查和检查,该医师确定被诊断为SSc的那些患者的确符合ACR 1980分类标准和/或LeRoy和Medsger 2001的标准。结果:在回顾所有病例后,在118例符合LeRoy-Medsger 2001标准的患者中,只有88例根据ACR 1980标准明确诊断为SSc。考虑到ACR标准,患病率为每100,000例25.4例(95%CI:22.2aa28.6),研究期间的年发病率为每100,000例3.2(95%CI:2.0a€4.4)。考虑到LeRoy和Medsger标准,流行病学数据分别为每100,000例34.1例(95%CI:30.4a-37.8)和每100,000例4.3例(95%CI:3.0a-5.6%)。根据LeRoy和Medsger的标准,将SSc子集细分为:20个有限SSc(19.2%),76个有限皮肤SSc(62.1%),22个弥散性皮肤SSc(18.7%)。男女比例为9.7:1。结论:发现在意大利东北部地区观察到的SSc的发生率和患病率高于各个地理区域(英国,美国,澳大利亚等)的报道,但与意大利另一项采用类似研究的研究相似。 LeRoy-Medsger标准。与仅基于ACR标准的研究相比,采用的不同诊断标准可以解释与研究相比发现的某些差异,但是,仅根据病例定义或确定的方法学方法,无法轻易消除疾病发生的区域差异;还应考虑遗传,种族和环境因素。当前,主要的挑战仍然是确定所观察到的差异的科学依据,区分由地理/种族特征和分析方法引起的变化。

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