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全国性儿童间质性肺疾病互联网数据库:法国网络。

A national internet-linked based database for pediatric interstitial lung diseases: the French network.

机构信息

AP-HP, Hôpital Trousseau, Pediatric Pulmonary Department, Paris, France.

出版信息

Orphanet J Rare Dis. 2012 Jun 15;7:40. doi: 10.1186/1750-1172-7-40.

Abstract

BACKGROUND

Interstitial lung diseases (ILDs) in children represent a heterogeneous group of rare respiratory disorders that affect the lung parenchyma. After the launch of the French Reference Centre for Rare Lung Diseases (RespiRare®), we created a national network and a web-linked database to collect data on pediatric ILD.

METHODS

Since 2008, the database has been set up in all RespiRare® centres. After patient's parents' oral consent is obtained, physicians enter the data of children with ILD: identity, social data and environmental data; specific aetiological diagnosis of the ILD if known, genetics, patient visits to the centre, and all medical examinations and tests done for the diagnosis and/or during follow up. Each participating centre has a free access to his own patients' data only, and cross-centre studies require mutual agreement. Physicians may use the system as a daily aid for patient care through a web-linked medical file, backed on this database.

RESULTS

Data was collected for 205 cases of ILD. The M/F sex ratio was 0.9. Median age at diagnosis was 1.5 years old [0-16.9]. A specific aetiology was identified in 149 (72.7%) patients while 56 (27.3%) cases remain undiagnosed. Surfactant deficiencies and alveolar proteinosis, haemosiderosis, and sarcoidosis represent almost half of the diagnoses. Median length of follow-up is 2.9 years [0-17.2].

CONCLUSIONS

We introduce here the French network and the largest national database in pediatric ILDs. The diagnosis spectrum and the estimated incidence are consistent with other European databases. An important challenge will be to reduce the proportion of unclassified ILDs by a standardized diagnosis work-up. This database is a great opportunity to improve patient care and disease pathogenesis knowledge. A European network including physicians and European foundations is now emerging with the initial aim of devising a simplified European database/register as a first step to larger European studies.

摘要

背景

儿童间质性肺疾病(ILDs)是一组影响肺实质的罕见呼吸系统疾病。在法国罕见肺病参考中心(RespiRare®)成立后,我们创建了一个全国性网络和一个网络链接数据库,以收集儿科ILD 数据。

方法

自 2008 年以来,该数据库已在所有 RespiRare®中心建立。在获得患儿父母的口头同意后,医生会输入ILD 患儿的数据:身份、社会数据和环境数据;ILD 的特定病因诊断(如果已知)、遗传学、患者就诊中心、以及为诊断和/或随访而进行的所有医学检查和测试。每个参与中心只能自由访问自己的患者数据,跨中心研究需要相互同意。医生可以通过网络链接的医疗档案系统将该系统作为日常患者护理的辅助工具。

结果

共收集了 205 例ILD 数据。男女比例为 0.9。诊断时的中位年龄为 1.5 岁[0-16.9]。在 149 名(72.7%)患者中确定了特定病因,而 56 名(27.3%)患者仍未确诊。表面活性剂缺乏症和肺泡蛋白沉积症、血铁沉着症和结节病几乎占所有诊断的一半。中位随访时间为 2.9 年[0-17.2]。

结论

我们在此介绍法国网络和最大的儿科ILD 国家数据库。诊断谱和估计发病率与其他欧洲数据库一致。一个重要的挑战将是通过标准化诊断工作流程减少未分类ILD 的比例。该数据库为改善患者护理和疾病发病机制知识提供了绝佳机会。一个包括医生和欧洲基金会的欧洲网络正在出现,其最初目标是设计一个简化的欧洲数据库/登记册,作为进行更大规模欧洲研究的第一步。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4443/3458912/fbfe3506b4e0/1750-1172-7-40-1.jpg

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