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基于索赔数据库分析的日本特发性肺纤维化患病率。

Prevalence of idiopathic pulmonary fibrosis in Japan based on a claims database analysis.

机构信息

Department of Respiratory Medicine and Allergy, Tosei General Hospital, Aichi, Japan.

The Second Division, Department of Internal Medicine, Hamamatsu University School of Medicine, Shizuoka, Japan.

出版信息

Respir Res. 2022 Feb 8;23(1):24. doi: 10.1186/s12931-022-01938-6.

Abstract

BACKGROUND

Idiopathic pulmonary fibrosis (IPF) is a cryptogenic chronic interstitial pneumonia with progressive fibrosis and a poor prognosis. A substantial number of epidemiological studies have been conducted in Europe and the United States (US). In contrast, in Japan, only one study reported the prevalence of IPF (10.0 per 100,000 population) using clinical data (2003-2007) from one prefecture; thus, the nationwide prevalence of IPF remains unknown. This study aimed to estimate the nationwide prevalence of IPF in Japan using a nationwide claims database.

METHODS

We extracted data from a Japanese claims database provided by Medical Data Vision (MDV database, April 2008-March 2019) containing data from approximately 28 million patients from 385 acute-care hospitals. Patients with IPF (those diagnosed with IPF at least once) from April 2017 to March 2018 were identified in the MDV database. The number of patients in the MDV database was extrapolated nationwide using the fourth NDB Open Data (April 2017-March 2018), and the prevalence was estimated using demographic data as denominators. The prevalence in the US, considering the same definition of IPF, was also calculated and compared with that in Japan.

RESULT

The number of patients with IPF in the MDV database was 4278. The estimated nationwide number of patients in Japan was estimated to be 34,040 (mean age: 73 years, percentage of men: 73%), and the prevalence was 27 per 100,000 population. In comparison with that in the US, the prevalence was similar in men and relatively lower in women until the age of 75-79 years, and it was notably lower in both sexes aged ≥ 80 years.

CONCLUSIONS

We report the nationwide IPF prevalence in Japan using data from claims databases for the first time. The prevalence estimated in this study was higher than that reported in a previous study. The difference might be due to differences in study settings and definitions of IPF. Further research should be performed to determine the prevalence more accurately and compare it with those in other countries.

摘要

背景

特发性肺纤维化(IPF)是一种特发性慢性间质性肺炎,具有进行性纤维化和预后不良的特点。欧洲和美国(美国)已经进行了大量的流行病学研究。相比之下,在日本,只有一项研究报告了使用一个县的临床数据(2003-2007 年)得出的 IPF 患病率(每 10 万人中有 10.0 人);因此,IPF 的全国患病率仍不清楚。本研究旨在使用全国性的索赔数据库估计日本的 IPF 全国患病率。

方法

我们从 Medical Data Vision(MDV 数据库)中提取了数据,该数据库由一个日本索赔数据库提供,包含了来自 385 家急症医院的大约 2800 万患者的数据。从 MDV 数据库中确定了 2017 年 4 月至 2018 年 3 月间至少确诊过一次 IPF 的患者。使用第四个 NDB Open Data(2017 年 4 月至 2018 年 3 月)对 MDV 数据库中的患者数量进行全国范围的推断,并使用人口统计数据作为分母来估计患病率。还计算了考虑到相同的 IPF 定义的美国患病率,并与日本进行了比较。

结果

MDV 数据库中 IPF 患者的数量为 4278 人。据估计,日本全国的患者人数为 34040 人(平均年龄:73 岁,男性比例:73%),患病率为 27/100000。与美国相比,男性的患病率相似,75-79 岁年龄段的女性患病率相对较低,而≥80 岁的男女患病率则明显较低。

结论

我们首次使用索赔数据库报告了日本全国性的 IPF 患病率。本研究估计的患病率高于之前的研究报告。这种差异可能是由于研究环境和 IPF 定义的不同所致。应进一步开展研究以更准确地确定患病率,并与其他国家进行比较。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/44a7/8822670/e28190614e79/12931_2022_1938_Fig1_HTML.jpg

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