Literature DB >> 31541394

Epidemiology of idiopathic pulmonary fibrosis: a population-based study in primary care.

Sergio Harari1, Michele Davì2, Alice Biffi3, Antonella Caminati1, Alessandra Ghirardini2, Valeria Lovato2, Claudio Cricelli4, Francesco Lapi5.   

Abstract

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.

Entities:  

Keywords:  Algorithms; Fibrotic lung disease; Gastro-esophageal reflux; General practitioners; Idiopathic interstitial pneumonia; Outpatient; Risk factors

Mesh:

Year:  2019        PMID: 31541394     DOI: 10.1007/s11739-019-02195-0

Source DB:  PubMed          Journal:  Intern Emerg Med        ISSN: 1828-0447            Impact factor:   3.397


  33 in total

1.  IPF: New insight in diagnosis and prognosis.

Authors:  Antonella Caminati; Sergio Harari
Journal:  Respir Med       Date:  2010-06-08       Impact factor: 3.415

2.  An official ATS/ERS/JRS/ALAT statement: idiopathic pulmonary fibrosis: evidence-based guidelines for diagnosis and management.

Authors:  Ganesh Raghu; Harold R Collard; Jim J Egan; Fernando J Martinez; Juergen Behr; Kevin K Brown; Thomas V Colby; Jean-François Cordier; Kevin R Flaherty; Joseph A Lasky; David A Lynch; Jay H Ryu; Jeffrey J Swigris; Athol U Wells; Julio Ancochea; Demosthenes Bouros; Carlos Carvalho; Ulrich Costabel; Masahito Ebina; David M Hansell; Takeshi Johkoh; Dong Soon Kim; Talmadge E King; Yasuhiro Kondoh; Jeffrey Myers; Nestor L Müller; Andrew G Nicholson; Luca Richeldi; Moisés Selman; Rosalind F Dudden; Barbara S Griss; Shandra L Protzko; Holger J Schünemann
Journal:  Am J Respir Crit Care Med       Date:  2011-03-15       Impact factor: 21.405

Review 3.  Antacid therapy in idiopathic pulmonary fibrosis: more questions than answers?

Authors:  Kerri A Johannson; Irina Strâmbu; Claudia Ravaglia; Jan C Grutters; Claudia Valenzuela; Nesrin Mogulkoc; Fabrizio Luppi; Luca Richeldi; Athol U Wells; Carlo Vancheri; Michael Kreuter
Journal:  Lancet Respir Med       Date:  2017-07       Impact factor: 30.700

4.  Incidence and mortality of idiopathic pulmonary fibrosis and sarcoidosis in the UK.

Authors:  J Gribbin; R B Hubbard; I Le Jeune; C J P Smith; J West; L J Tata
Journal:  Thorax       Date:  2006-07-14       Impact factor: 9.139

5.  The association between air pollution and the incidence of idiopathic pulmonary fibrosis in Northern Italy.

Authors:  Sara Conti; Sergio Harari; Antonella Caminati; Antonella Zanobetti; Joel D Schwartz; Pietro A Bertazzi; Giancarlo Cesana; Fabiana Madotto
Journal:  Eur Respir J       Date:  2018-01-25       Impact factor: 16.671

6.  Prevalence estimates for chronic diseases in Italy: exploring the differences between self-report and primary care databases.

Authors:  Claudio Cricelli; Giampiero Mazzaglia; Fabio Samani; Marco Marchi; Andrea Sabatini; Roberto Nardi; Giuseppe Ventriglia; Achille P Caputi
Journal:  J Public Health Med       Date:  2003-09

7.  Idiopathic pulmonary fibrosis in US Medicare beneficiaries aged 65 years and older: incidence, prevalence, and survival, 2001-11.

Authors:  Ganesh Raghu; Shih-Yin Chen; Wei-Shi Yeh; Brad Maroni; Qian Li; Yuan-Chi Lee; Harold R Collard
Journal:  Lancet Respir Med       Date:  2014-05-27       Impact factor: 30.700

8.  The rising incidence of idiopathic pulmonary fibrosis in the U.K.

Authors:  V Navaratnam; K M Fleming; J West; C J P Smith; R G Jenkins; A Fogarty; R B Hubbard
Journal:  Thorax       Date:  2011-04-27       Impact factor: 9.139

9.  Epidemiology of Pulmonary Fibrosis: A Cohort Study Using Healthcare Data in Sweden.

Authors:  Giovanni Ferrara; Lisen Arnheim-Dahlström; Karen Bartley; Christer Janson; Klaus-Uwe Kirchgässler; Aaron Levine; C Magnus Sköld
Journal:  Pulm Ther       Date:  2019-03-05

10.  Incidence, Prevalence, and Survival of Patients with Idiopathic Pulmonary Fibrosis in the UK.

Authors:  Helen Strongman; Imran Kausar; Toby M Maher
Journal:  Adv Ther       Date:  2018-04-11       Impact factor: 3.845

View more
  6 in total

Review 1.  Involvement of 4-hydroxy-2-nonenal in the pathogenesis of pulmonary fibrosis.

Authors:  Edilburga Reyes-Jiménez; Alma Aurora Ramírez-Hernández; Jovito Cesar Santos-Álvarez; Juan Manuel Velázquez-Enríquez; Socorro Pina-Canseco; Rafael Baltiérrez-Hoyos; Verónica Rocío Vásquez-Garzón
Journal:  Mol Cell Biochem       Date:  2021-08-31       Impact factor: 3.396

2.  Inflammatory bowel disease and risk of idiopathic pulmonary fibrosis: A protocol for systematic review and meta-analysis.

Authors:  Jiali Wang; Fushun Kou; Xiao Han; Lei Shi; Rui Shi; Zhibin Wang; Tangyou Mao; Junxiang Li
Journal:  PLoS One       Date:  2022-06-24       Impact factor: 3.752

3.  Effect of Total Flavonoids of Oxytropis falcata Bunge on the Expression of p-JAK1-and p-STAT1-Related Proteins in Idiopathic Pulmonary Fibrosis.

Authors:  Yan-Jun Wang; Yang Li; Xue-Lin Wang; Xin-Ze Li; Yan-Wen Chen; Ling-Ling Yang; Hai-Xia Ming
Journal:  Evid Based Complement Alternat Med       Date:  2020-08-28       Impact factor: 2.629

4.  Incremental prognostic value of arterial elastance in mild-to-moderate idiopathic pulmonary fibrosis.

Authors:  Andrea Sonaglioni; Antonella Caminati; Gian Luigi Nicolosi; Michele Lombardo; Sergio Harari
Journal:  Int J Cardiovasc Imaging       Date:  2022-02-01       Impact factor: 2.357

Review 5.  Progress of Statin Therapy in the Treatment of Idiopathic Pulmonary Fibrosis.

Authors:  Leiya Kou; Pei Kou; Guangwei Luo; Shuang Wei
Journal:  Oxid Med Cell Longev       Date:  2022-03-19       Impact factor: 6.543

6.  Occurrence of Idiopathic Pulmonary Fibrosis in Italy: Latest Evidence from Real-World Data.

Authors:  Marica Iommi; Martina Bonifazi; Andrea Faragalli; Lara Letizia Latini; Federico Mei; Liana Spazzafumo; Edlira Skrami; Luigi Ferrante; Flavia Carle; Rosaria Gesuita
Journal:  Int J Environ Res Public Health       Date:  2022-02-22       Impact factor: 3.390

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.