Current approaches to the diagnosis and treatment of idiopathic pulmonary fibrosis in Europe: the AIR survey

被引：20

作者：

Cottin, Vincent ^{[1
,2
]}

机构：

[1] Hosp Civils Lyon, Hop Louis Pradel, Serv Pneumol, Ctr Ref Natl Malad Pulm Rares, Lyon, France

[2] Univ Claude Bernard Lyon 1, Univ Lyon, INRA, IFR 128 UMR754, Lyon, France

来源：

EUROPEAN RESPIRATORY REVIEW | 2014年 / 23卷 / 132期

关键词：

D O I：

10.1183/09059180.00001914

中图分类号：

R56 [呼吸系及胸部疾病];

学科分类号：

摘要：

This review presents the results of the 2013 Advancing IPF Research (AIR) survey, which assessed current approaches to the diagnosis and treatment of idiopathic pulmonary fibrosis (IPF) by experienced physicians. A total of 149 physicians, predominantly from European countries, replied to the 28-question survey. The results of the AIR survey were compared with a similar survey of 509 French pulmonologists conducted by the French National Reference Centre and the Network of Regional Competence Centres for Rare Lung Diseases. A number of positive findings emerged from the AIR survey, including the high level of multidisciplinary team involvement in both diagnosis and management. This survey, when taken together with the French survey, suggests that there is still a need to improve earlier diagnosis of IPF.

引用

页码：225 / 230

页数：6

共 14 条

[1]

Zolak J.S., de Andrade J.A., Idiopathic pulmonary fibrosis, Immunol Allergy Clin North Am, 32, pp. 473-485, (2012)

[2]

Raghu G., Collard H.R., Egan J.J., Et al., An official ATS/ERS/JRS/ALAT statement: Idiopathic pulmonary fibrosis: Evidence-based guidelines for diagnosis and management, Am J Respir Crit Care Med, 183, pp. 788-824, (2011)

[3]

Ley B., Collard H.R., King Jr. T.E., Clinical course and prediction of survival in idiopathic pulmonary fibrosis, Am J Respir Crit Care Med, 183, pp. 431-440, (2011)

[4]

Wolters P.J., Collard H.R., Jones K.D., Pathogenesis of idiopathic pulmonary fibrosis, Annu Rev Pathol, 9, pp. 157-179, (2014)

[5]

Richeldi L., Collard H.R., du Bois R.M., Et al., Mapping the future for pulmonary fibrosis: Report from the 17<sup>th</sup> International Colloquium on Lung and Airway Fibrosis, Eur Respir J, 42, pp. 230-238, (2013)

[6]

American Thoracic Society/European Respiratory Society international multidisciplinary consensus classification of the idiopathic interstitial pneumonias, Am J Respir Crit Care Med, 165, pp. 277-304, (2002)

[7]

(2014)

[8]

Cottin V., Cadranel J., Crestani B., Et al., Management of idiopathic pulmonary fibrosis in France: A survey of 1244 pulmonologists, Respir Med, 108, pp. 195-202, (2014)

[9]

Raghu G., Anstrom J.A., King Jr. T.E., Et al., Prednisone, azathioprine, and N-acetylcysteine for pulmonary fibrosis, N Engl J Med, 366, pp. 1968-1977, (2012)

[10]

Cottin V., Cordier J.F., Velcro crackles: The key for early diagnosis of idiopathic pulmonary fibrosis?, Eur Respir J, 40, pp. 519-521, (2012)

← 1 2 →