Servizio Di Fisiopatologia Respiratoria Ed Emodinamica Polmonare, Unità Operativa Di Pneumologia E Terapia Semi-Intensiva Respiratoria, San Giuseppe-Multimedica IRCCS Hospital, Via San Vittore, 12, 20123, Milan, MI, Italy.
Roche S.P.A, Monza, Italy.
Intern Emerg Med. 2020 Apr;15(3):437-445. doi: 10.1007/s11739-019-02195-0. Epub 2019 Sep 20.
Idiopathic pulmonary fibrosis (IPF) is a chronic disease with unknown etiology and poor prognosis. Little is known about the epidemiology of this disease; most of the studies are limited by small and restricted cohort studies. We aim to investigate the epidemiology of IPF in the Italian primary care setting using the Health Search Database (HSD) between January 2002 and June 2017. In an attempt to define cases of IPF we adopted iterative combinations of International Classification of Diseases Ninth Revision (ICD-9-CM) and other clinical investigations according to three different operational Algorithms. Incidence and prevalence rate, according to the three Algorithms defining IPF, were calculated and the association with candidate determinants [sex, age, gastro-esophageal reflux (GERD) and smoking status] was evaluated. We identified 1,104,307 eligible patients. The prevalence rate of IPF varies between 2.6 to 24.3 per 100.000 person-year, using algorithm 1 and from 0.8 to 7 using algorithm 3. The incidence rate of IPF varies between 1.25 and 3.77 per 100.000 person-years, using algorithm 1 and from 0.10 to 1.61 using algorithm 3. The mean adjusted incidence rate ratio of IPF, using algorithm 1, is 2.33 (95% CI 2.11-2.57) per 100.000 person-years. Over the study years, the trend of prevalence was statistically significantly increasing while the incidence rate started to increase in the last 3 years. The analyses on candidate determinants showed that patients aged 61 years or older, those suffering from GERD, and former smokers were statistically significantly at greater risk of incurring IPF. To our knowledge, this is one of the first European IPF epidemiological studies conducted in primary care. The increase of the incidence rates is likely due to a growing awareness for IPF among General Practitioners, while the increase of prevalence rates may be due to an increase of survival, a result of recent advances in the diagnosis, management and therapies for the disease.
特发性肺纤维化(IPF)是一种病因不明且预后较差的慢性疾病。对于这种疾病的流行病学了解甚少;大多数研究都受到小样本和有限队列研究的限制。我们旨在使用健康搜索数据库(HSD),从 2002 年 1 月至 2017 年 6 月,调查意大利初级保健环境中的 IPF 流行病学。为了尝试定义 IPF 病例,我们根据三种不同的操作算法,采用国际疾病分类第九修订版(ICD-9-CM)和其他临床研究的迭代组合。根据三种定义 IPF 的算法计算了发病率和患病率,并评估了与候选决定因素(性别、年龄、胃食管反流病(GERD)和吸烟状况)的关联。我们共确定了 1,104,307 名合格患者。使用算法 1,IPF 的患病率在每 100,000 人年 2.6 至 24.3 之间变化,而使用算法 3 则在每 100,000 人年 0.8 至 7 之间变化。使用算法 1,IPF 的发病率在每 100,000 人年 1.25 至 3.77 之间变化,而使用算法 3 则在每 100,000 人年 0.10 至 1.61 之间变化。使用算法 1,调整后的平均发病率比为每 100,000 人年 2.33(95%CI 2.11-2.57)。在研究期间,患病率的趋势呈统计学显著增加,而发病率在过去 3 年开始增加。候选决定因素的分析表明,年龄在 61 岁或以上的患者、患有 GERD 的患者和曾经吸烟的患者发生 IPF 的风险显著增加。据我们所知,这是在初级保健中进行的首批欧洲 IPF 流行病学研究之一。发病率的增加可能是由于全科医生对 IPF 的认识不断提高,而患病率的增加可能是由于疾病诊断、管理和治疗的最新进展导致生存率的提高所致。