Assistance Publique - Hôpitaux de Paris, Service de Pneumologie, Hôpital Avicenne, Bobigny, France.
Université Paris 13, Sorbonne Paris Cité, EA2363 'hypoxie et poumon', Paris, France.
Eur Respir J. 2017 Aug 3;50(2). doi: 10.1183/13993003.02419-2016. Print 2017 Aug.
The objective of the study was to estimate the prevalence and incidence of interstitial lung diseases (ILDs) in Seine-Saint-Denis, a multi-ethnic county of Greater Paris, France.Patients with ILDs were identified between January and December 2012 by using several sources; all potentially involved medical specialists from public and private hospitals, community-based pulmonologists and general practitioners, and the Social Security system. Diagnoses were validated centrally by an expert multidisciplinary discussion.1170 ILD cases were reported (crude overall prevalence: 97.9/10 and incidence: 19.4/10/year). In the 848 reviewed cases, the most prevalent diagnoses were sarcoidosis (42.6%), connective tissue diseases associated ILDs (CTDs-ILDs) (16%), idiopathic pulmonary fibrosis (IPF) (11.6%), and occupational ILDs (5.0%), which corresponded to a crude prevalence of 30.2/10 for sarcoidosis, 12.1/10 for CTDs-ILDs and 8.2/10 for IPF. The prevalence of fibrotic idiopathic interstitial pneumonias, merging IPF, nonspecific interstitial pneumonia and cases registered with code J84.1 was 16.34/10 An adjusted multinomial model demonstrated an increased risk of sarcoidosis in North Africans and Afro-Caribbeans and of CTDs-ILDs in Afro-Caribbeans, compared to that in Europeans.This study, with a comprehensive recruitment and stringent diagnostic criteria, emphasises the importance of secondary ILDs, particularly CTDs-ILDs and the relatively low prevalence of IPF, and confirms that sarcoidosis is a rare disease in France.
这项研究的目的是估计法国大巴黎塞纳-圣但尼( Seine-Saint-Denis )地区间质性肺病(ILDs)的流行率和发病率。ILDs 患者是通过多种来源在 2012 年 1 月至 12 月期间确定的;所有可能涉及公共和私立医院、社区肺病专家和全科医生以及社会保障系统的潜在相关医学专家。诊断结果由专家多学科讨论进行中心验证。报告了 1170 例 ILD 病例(粗总体患病率:97.9/10,发病率:19.4/10/年)。在 848 例审查病例中,最常见的诊断为结节病(42.6%)、结缔组织病相关ILDs(CTD-ILDs)(16%)、特发性肺纤维化(IPF)(11.6%)和职业性ILDs(5.0%),这对应于结节病的粗患病率为 30.2/10,CTD-ILDs 为 12.1/10,IPF 为 8.2/10。纤维化特发性间质性肺炎,合并 IPF、非特异性间质性肺炎和以 J84.1 代码登记的病例的患病率为 16.34/10。调整后的多项式模型表明,与欧洲人相比,北非人和加勒比黑人和 CTD-ILDs 的患结节病风险增加,而加勒比黑人和 CTD-ILDs 的患 CTD-ILDs 风险增加。这项研究采用全面的招募和严格的诊断标准,强调了继发性 ILDs 的重要性,特别是 CTD-ILDs 和相对较低的 IPF 患病率,并证实结节病在法国是一种罕见疾病。