Incidence and prevalence of idiopathic pulmonary fibrosis: review of the literature, European Respiratory Review, vol.21, issue.126, pp.355-61, 2012. ,
DOI : 10.1183/09059180.00002512
Epidemiology and survival of idiopathic pulmonary fibrosis from national data in Canada, European Respiratory Journal, vol.48, issue.1, 2016. ,
DOI : 10.1183/13993003.01504-2015
An Official ATS/ERS/JRS/ALAT Statement: Idiopathic Pulmonary Fibrosis: Evidence-based Guidelines for Diagnosis and Management, American Journal of Respiratory and Critical Care Medicine, vol.183, issue.6, pp.788-824, 2011. ,
DOI : 10.1378/chest.07-2488
Recommandations pratiques pour le diagnostic et la prise en charge de la fibrose pulmonaire idiopathique. ??labor??es par le centre national de r??f??rence et les centres de comp??tence pour les maladies pulmonaires rares sous l?????gide de la Soci??t?? de pneumologie de langue fran??aise, Revue des Maladies Respiratoires, vol.30, issue.10, pp.879-902, 2013. ,
DOI : 10.1016/j.rmr.2013.09.007
URL : https://hal.archives-ouvertes.fr/hal-01655039
Méthode « Recommandations pour la pratique clinique ». Saint-Denis: HAS, 2010. ,
Incidence and mortality of idiopathic pulmonary fibrosis and sarcoidosis in the UK, Thorax, vol.61, issue.11, pp.980-985, 2006. ,
DOI : 10.1136/thx.2006.062836
What causes cryptogenic fibrosing alveolitis? A case-control study of environmental exposure to dust., BMJ, vol.301, issue.6759, pp.1015-1022, 1990. ,
DOI : 10.1136/bmj.301.6759.1015
Pulmonary fibrosis deaths in the United States, 1979-1991. An analysis of multiple-cause mortality data., American Journal of Respiratory and Critical Care Medicine, vol.153, issue.5, pp.1548-52, 1996. ,
DOI : 10.1164/ajrccm.153.5.8630600
High prevalence of abnormal acid gastro-oesophageal reflux in idiopathic pulmonary fibrosis, European Respiratory Journal, vol.27, issue.1, pp.136-178, 2006. ,
DOI : 10.1183/09031936.06.00037005
Idiopathic Pulmonary Fibrosis, American Journal of Respiratory and Critical Care Medicine, vol.157, issue.4, pp.1172-1180, 2000. ,
DOI : 10.1164/ajrccm.150.4.7921471
Predicting survival in idiopathic pulmonary fibrosis: scoring system and survival model, Am J Respir Crit Care Med, vol.164, pp.1171-81, 2001. ,
Velcro crackles: the key for early diagnosis of idiopathic pulmonary fibrosis?, European Respiratory Journal, vol.40, issue.3, pp.519-540, 2012. ,
DOI : 10.1183/09031936.00001612
Auscultation of Velcro Crackles is Associated With Usual Interstitial Pneumonia, Medicine, vol.95, issue.5, p.2573, 2016. ,
DOI : 10.1097/MD.0000000000002573
Interobserver Variability in the CT Assessment of Honeycombing in the Lungs, Radiology, vol.266, issue.3, pp.936-980, 2013. ,
DOI : 10.1148/radiol.12112516
Interobserver agreement for the ATS/ERS/JRS/ALAT criteria for a UIP pattern on CT, Thorax, vol.71, issue.1, pp.45-51, 2016. ,
DOI : 10.1136/thoraxjnl-2015-207252
Diagnosis of idiopathic pulmonary fibrosis with high-resolution CT in patients with little or no radiological evidence of honeycombing: secondary analysis of a randomised, controlled trial, The Lancet Respiratory Medicine, vol.2, issue.4, pp.277-84, 2014. ,
DOI : 10.1016/S2213-2600(14)70011-6
Effect of Nintedanib in Subgroups of Idiopathic Pulmonary Fibrosis by Diagnostic Criteria, American Journal of Respiratory and Critical Care Medicine, vol.46, issue.1, 2016. ,
DOI : 10.1183/13993003.02316-2014
Pneumopathies interstitielles diffuses idiopathiques, Revue des Maladies Respiratoires, vol.21, issue.2, pp.299-318, 2004. ,
DOI : 10.1016/S0761-8425(04)71288-7
CT Scan Findings of Probable Usual Interstitial Pneumonitis Have a High Predictive Value for Histologic Usual Interstitial Pneumonitis, Chest, vol.147, issue.2, pp.450-459, 2015. ,
DOI : 10.1378/chest.14-0976
CT in Idiopathic Pulmonary Fibrosis: Diagnosis and Beyond, American Journal of Roentgenology, vol.206, issue.3, pp.495-507, 2016. ,
DOI : 10.2214/AJR.15.15674
In-Hospital Mortality after Surgical Lung Biopsy for Interstitial Lung Disease in the United States. 2000 to 2011, American Journal of Respiratory and Critical Care Medicine, vol.30, issue.10, pp.1161-1168, 2000. ,
DOI : 10.1016/S2213-2600(14)70101-8
Surgical lung biopsy for the diagnosis of interstitial lung disease in England, Eur Respir J, pp.1997-2008, 2016. ,
Transbronchial Cryobiopsy: A New Tool for Lung Biopsies, Respiration, vol.78, issue.2, pp.203-211, 2009. ,
DOI : 10.1159/000203987
Diagnostic Yield and Complications of Transbronchial Lung Cryobiopsy for Interstitial Lung Disease: A Systematic Review and Meta-analysis, Annals of the American Thoracic Society, 2016. ,
DOI : 10.1513/AnnalsATS.201606-461SR
Efficacy and safety of cryobiopsy versus forceps biopsy for interstitial lung diseases and lung tumours: A systematic review and meta-analysis, Respirology, vol.88, issue.Suppl 1, 2016. ,
DOI : 10.1155/2013/730574
Transbronchial cryobiopsy in diffuse parenchymal lung disease. A new star in the horizon, Sarcoidosis Vasc Diffuse Lung Dis, vol.31, pp.178-81, 2014. ,
Safety of Cryo-Transbronchial Biopsy in Diffuse Lung Diseases: Analysis of Three Hundred Cases, Respiration, vol.90, issue.1, pp.40-46, 2015. ,
DOI : 10.1159/000381921
Lung cryobiopsies: A paradigm shift in diagnostic bronchoscopy?, Respirology, vol.162, issue.5, pp.645-54, 2014. ,
DOI : 10.1016/j.trsl.2013.06.004
Bronchoscopic Lung Cryobiopsy Increases Diagnostic Confidence in the Multidisciplinary Diagnosis of Idiopathic Pulmonary Fibrosis, American Journal of Respiratory and Critical Care Medicine, vol.31, issue.7, 2015. ,
DOI : 10.1164/rccm.200606-833OC
European respiratory society American thoracic societyEuropean respiratory society international multidisciplinary consensus classification of the idiopathic interstitial pneumonias This joint statement of the American thoracic society (ATS), and the European respiratory society (ERS) was adopted by the ATS board of directors, Am J Respir Crit Care Med, vol.165, pp.277-304, 2001. ,
Chronic hypersensitivity pneumonitis in patients diagnosed with idiopathic pulmonary fibrosis: a prospective case-cohort study, The Lancet Respiratory Medicine, vol.1, issue.9, pp.685-94, 2013. ,
DOI : 10.1016/S2213-2600(13)70191-7
Chronic Hypersensitivity Pneumonitis and Pulmonary Sarcoidosis: Differentiation From Usual Interstitial Pneumonia Using High-Resolution Computed Tomography, Seminars in Ultrasound, CT and MRI, vol.35, issue.1, pp.47-58, 2014. ,
DOI : 10.1053/j.sult.2013.10.006
Differential diagnosis of usual interstitial pneumonia: when is it truly idiopathic?, European Respiratory Review, vol.23, issue.133, pp.308-327, 2014. ,
DOI : 10.1183/09059180.00004914
Prognosis of Fibrotic Interstitial Pneumonia, American Journal of Respiratory and Critical Care Medicine, vol.175, issue.7, pp.705-716, 2007. ,
DOI : 10.1002/art.21322
Interstitial lung disease: are we missing formes frustes of connective tissue disease?, European Respiratory Journal, vol.28, issue.5, pp.893-899, 2006. ,
DOI : 10.1183/09031936.00101506
Idiopathic inflammatory myopathies and the lung, European Respiratory Review, vol.24, issue.136, pp.216-254, 2015. ,
DOI : 10.1183/16000617.00002015
URL : https://hal.archives-ouvertes.fr/hal-01594100
ANCA-associated lung fibrosis: Analysis of 17 patients, Respiratory Medicine, vol.102, issue.10, pp.1392-1400, 2008. ,
DOI : 10.1016/j.rmed.2008.04.023
URL : https://hal.archives-ouvertes.fr/hal-00673305
Clinical Significance of Serum Autoantibodies in Idiopathic Interstitial Pneumonia, Journal of Korean Medical Science, vol.28, issue.5, pp.731-738, 2013. ,
DOI : 10.3346/jkms.2013.28.5.731
Usual Interstitial Pneumonia Preceding Collagen Vascular Disease: A Retrospective Case Control Study of Patients Initially Diagnosed with Idiopathic Pulmonary Fibrosis, PLoS ONE, vol.106, issue.4, p.94775, 2014. ,
DOI : 10.1371/journal.pone.0094775.t006
Biomarkers in Connective Tissue Disease-Associated Interstitial Lung Disease, Seminars in Respiratory and Critical Care Medicine, vol.35, issue.02, pp.181-200, 2014. ,
DOI : 10.1055/s-0034-1371527
Molecular biomarkers in idiopathic pulmonary fibrosis, AJP: Lung Cellular and Molecular Physiology, vol.307, issue.9, pp.681-91, 2014. ,
DOI : 10.1152/ajplung.00014.2014
Longitudinal change in collagen degradation biomarkers in idiopathic pulmonary fibrosis: an analysis from the prospective, multicentre PROFILE study, The Lancet Respiratory Medicine, vol.3, issue.6, pp.462-72, 2015. ,
DOI : 10.1016/S2213-2600(15)00048-X
An Official American Thoracic Society Clinical Practice Guideline: The Clinical Utility of Bronchoalveolar Lavage Cellular Analysis in Interstitial Lung Disease, American Journal of Respiratory and Critical Care Medicine, vol.145, issue.9, pp.1004-1018, 2012. ,
DOI : 10.1136/thx.54.8.697
Significance of Bronchoalveolar Lavage for the Diagnosis of Idiopathic Pulmonary Fibrosis, American Journal of Respiratory and Critical Care Medicine, vol.179, issue.11, pp.1043-1050, 2009. ,
DOI : 10.1183/09031936.03.00105202
Familial pulmonary fibrosis, Revue des Maladies Respiratoires, vol.32, issue.4, pp.413-447, 2015. ,
DOI : 10.1016/j.rmr.2014.07.017
URL : https://hal.archives-ouvertes.fr/hal-01595463
Clinical and Pathologic Features of Familial Interstitial Pneumonia, American Journal of Respiratory and Critical Care Medicine, vol.172, issue.9, pp.1146-52, 2005. ,
DOI : 10.1164/ajrccm.164.9.2103074
High-Resolution CT Scan Findings in Familial Interstitial Pneumonia Do Not Conform to Those of Idiopathic Interstitial Pneumonia, Chest, vol.142, issue.6, pp.1577-83, 2012. ,
DOI : 10.1378/chest.11-2812
Familial Idiopathic Pulmonary Fibrosis, Chest, vol.127, issue.6, pp.2034-2075, 2005. ,
DOI : 10.1378/chest.127.6.2034
Telomere-related lung fibrosis is diagnostically heterogeneous but uniformly progressive, European Respiratory Journal, vol.48, issue.6, pp.1710-1730, 2016. ,
DOI : 10.1183/13993003.00308-2016
mutations in suspected genetic pulmonary fibrosis, European Respiratory Journal, vol.48, issue.6, pp.1721-1752, 2016. ,
DOI : 10.1183/13993003.02115-2015
URL : https://hal.archives-ouvertes.fr/hal-01467555
Telomere Lengths, Pulmonary Fibrosis and Telomerase (TERT) Mutations, PLoS ONE, vol.123, issue.5, p.10680, 2010. ,
DOI : 10.1371/journal.pone.0010680.s003
Telomere Shortening in Familial and Sporadic Pulmonary Fibrosis, American Journal of Respiratory and Critical Care Medicine, vol.178, issue.7, pp.729-766, 2008. ,
DOI : 10.1086/500052
Severe hematologic complications after lung transplantation in patients with telomerase complex mutations, The Journal of Heart and Lung Transplantation, vol.34, issue.4, pp.538-584, 2015. ,
DOI : 10.1016/j.healun.2014.11.010
URL : https://hal.archives-ouvertes.fr/hal-01146848
Surfactant Protein C Mutations Are the Basis of a Significant Portion of Adult Familial Pulmonary Fibrosis in a Dutch Cohort, American Journal of Respiratory and Critical Care Medicine, vol.182, issue.11, pp.1419-1444, 2010. ,
DOI : 10.1136/thx.2004.026336
Subclinical Lung Disease, Macrocytosis, and Premature Graying in Kindreds With Telomerase ( TERT ) Mutations, Chest, vol.140, issue.3, pp.753-63, 2011. ,
DOI : 10.1378/chest.10-2865
Effect of telomere length on survival in patients with idiopathic pulmonary fibrosis: an observational cohort study with independent validation, The Lancet Respiratory Medicine, vol.2, issue.7, pp.557-65, 2014. ,
DOI : 10.1016/S2213-2600(14)70124-9
Running Short on Time, Chest, vol.147, issue.6, pp.1450-1452, 2015. ,
DOI : 10.1378/chest.15-0077
Multicentre evaluation of multidisciplinary team meeting agreement on diagnosis in diffuse parenchymal lung disease: a case-cohort study, The Lancet Respiratory Medicine, vol.4, issue.7, 2016. ,
DOI : 10.1016/S2213-2600(16)30033-9
Delayed Access and Survival in Idiopathic Pulmonary Fibrosis, American Journal of Respiratory and Critical Care Medicine, vol.127, issue.7, pp.842-849, 2011. ,
DOI : 10.1164/rccm.200210-1245OC
???Any fool can make a rule and any fool will mind it???, BMC Medicine, vol.348, issue.2, p.23, 2016. ,
DOI : 10.1136/bmj.g3725
An Official American Thoracic Society/European Respiratory Society Statement: Update of the International Multidisciplinary Classification of the Idiopathic Interstitial Pneumonias, American Journal of Respiratory and Critical Care Medicine, vol.39, issue.1, pp.733-781, 2013. ,
DOI : 10.1136/thx.2008.102814
Unclassifiable interstitial lung disease: A review, Respirology, vol.366, issue.Suppl. 5, pp.51-57, 2016. ,
DOI : 10.1056/NEJMoa1113354
Clinical Course and Prediction of Survival in Idiopathic Pulmonary Fibrosis, American Journal of Respiratory and Critical Care Medicine, vol.183, issue.4, pp.431-471, 2011. ,
DOI : 10.1056/NEJMoa1002110
Forced Vital Capacity in Patients with Idiopathic Pulmonary Fibrosis, American Journal of Respiratory and Critical Care Medicine, vol.184, issue.12, pp.1382-1391, 2011. ,
DOI : 10.1164/rccm.201007-1179OC
Six-Minute-Walk Test in Idiopathic Pulmonary Fibrosis, American Journal of Respiratory and Critical Care Medicine, vol.183, issue.9, pp.1231-1238, 2011. ,
DOI : 10.1183/09031936.00140507
Ascertainment of Individual Risk of Mortality for Patients with Idiopathic Pulmonary Fibrosis, American Journal of Respiratory and Critical Care Medicine, vol.181, issue.4, pp.459-66, 2011. ,
DOI : 10.1164/rccm.200412-1756OC
A Multidimensional Index and Staging System for Idiopathic Pulmonary Fibrosis, Annals of Internal Medicine, vol.156, issue.10, pp.684-91, 2012. ,
DOI : 10.7326/0003-4819-156-10-201205150-00004
Unified baseline and longitudinal mortality prediction in idiopathic pulmonary fibrosis, European Respiratory Journal, vol.45, issue.5, pp.1374-81, 2015. ,
DOI : 10.1183/09031936.00146314
Idiopathic Pulmonary Fibrosis, Chest, vol.149, issue.2, 2015. ,
DOI : 10.1378/chest.15-0530
Idiopathic Pulmonary Fibrosis: CT and Risk of Death, Radiology, vol.273, issue.2, pp.570-579, 2014. ,
DOI : 10.1148/radiol.14130216
Idiopathic Pulmonary Fibrosis, American Journal of Respiratory and Critical Care Medicine, vol.167, issue.7, pp.962-971, 2003. ,
DOI : 10.1148/radiology.217.3.r00nv31701
URL : https://hal.archives-ouvertes.fr/hal-00499159
Predicting Pulmonary Fibrosis Disease Course From Past Trends in Pulmonary Function, Chest, vol.145, issue.3, pp.579-85, 2014. ,
DOI : 10.1378/chest.13-0844
Marginal decline in forced vital capacity is associated with a poor outcome in idiopathic pulmonary fibrosis, European Respiratory Journal, vol.35, issue.4, pp.830-836, 2010. ,
DOI : 10.1183/09031936.00155108
Relative versus absolute change in forced vital capacity in idiopathic pulmonary fibrosis, Thorax, vol.67, issue.5, pp.407-418, 2012. ,
DOI : 10.1136/thoraxjnl-2011-201184
Forced vital capacity as a primary end point in idiopathic pulmonary fibrosis treatment trials: making a silk purse from a sow's ear, Thorax, vol.68, issue.4, 2012. ,
DOI : 10.1136/thoraxjnl-2012-202640
EFX et pneumopathies interstitielles diffuses : qu'en attendre et quelle place dans la prise en charge ?, Lett Pneumol, vol.19, pp.17-20, 2016. ,
Review series: Aspects of interstitial lung disease: Exercise limitation in interstitial lung disease - mechanisms, significance and therapeutic options, Chronic Respiratory Disease, vol.40, issue.135, pp.101-112, 2010. ,
DOI : 10.1111/j.1475-6773.2005.0k375.x
Pirfenidone, Drugs, vol.183, issue.4, pp.1721-1753, 2011. ,
DOI : 10.1164/rccm.201006-0894CI
Treatment of Idiopathic Pulmonary Fibrosis with a New Antifibrotic Agent, Pirfenidone, American Journal of Respiratory and Critical Care Medicine, vol.33, issue.4, pp.1061-1070, 1999. ,
DOI : 10.1097/00000478-199402000-00003
Double-blind, Placebo-controlled Trial of Pirfenidone in Patients with Idiopathic Pulmonary Fibrosis, American Journal of Respiratory and Critical Care Medicine, vol.171, issue.9, pp.1040-1047, 2005. ,
DOI : 10.1056/NEJMcpc020028
Pirfenidone in idiopathic pulmonary fibrosis, European Respiratory Journal, vol.35, issue.4, pp.821-830, 2010. ,
DOI : 10.1183/09031936.00005209
Pirfenidone in patients with idiopathic pulmonary fibrosis (CAPACITY): two randomised trials, The Lancet, vol.377, issue.9779, pp.1760-1769, 2011. ,
DOI : 10.1016/S0140-6736(11)60405-4
URL : https://hal.archives-ouvertes.fr/hal-00873255
A phase 3 trial of pirfenidone in patients with idiopathic pulmonary fibrosis, N Engl J Med, vol.370, pp.2083-92, 2014. ,
A progression-free end-point for idiopathic pulmonary fibrosis trials: lessons from cancer, European Respiratory Journal, vol.41, issue.2, pp.262-271, 2013. ,
DOI : 10.1183/09031936.00115112
Non-steroid agents for idiopathic pulmonary fibrosis, Cochrane Database Syst Rev, vol.99, issue.3, p.3134, 2010. ,
DOI : 10.1002/14651858.CD003134
Sensitivity Analyses of the Change in FVC in a Phase 3 Trial of Pirfenidone for Idiopathic Pulmonary Fibrosis, Chest, vol.148, issue.1, pp.196-201, 2015. ,
DOI : 10.1378/chest.14-2817
Pirfenidone for idiopathic pulmonary fibrosis: analysis of pooled data from three multinational phase 3 trials, European Respiratory Journal, vol.47, issue.1, pp.243-53, 2016. ,
DOI : 10.1183/13993003.00026-2015
Comparison of clinical characteristics and prognostic factors of combined pulmonary fibrosis and emphysema versus idiopathic pulmonary fibrosis alone, Respirology, vol.38, issue.2, pp.239-284, 2014. ,
DOI : 10.1183/09031936.00114010
CT analysis of the effect of pirfenidone in patients with idiopathic pulmonary fibrosis, European Journal of Radiology, vol.83, issue.1, pp.32-40, 2014. ,
DOI : 10.1016/j.ejrad.2012.02.014
Intraindividual Response to Treatment with Pirfenidone in Idiopathic Pulmonary Fibrosis, American Journal of Respiratory and Critical Care Medicine, vol.191, issue.1, pp.110-113, 2015. ,
DOI : 10.1371/journal.pone.0073279
Efficacy of pirfenidone for idiopathic pulmonary fibrosis: An Italian real life study, Respiratory Medicine, vol.109, issue.7, pp.904-917, 2015. ,
DOI : 10.1016/j.rmed.2015.04.010
Pirfenidone in Idiopathic Pulmonary Fibrosis: Real-Life Experience from a German Tertiary Referral Center for Interstitial Lung Diseases, Respiration, vol.88, issue.3, 2014. ,
DOI : 10.1159/000363064
Pirfenidone: an update on clinical trial data and insights from everyday practice, European Respiratory Review, vol.23, issue.131, pp.111-118, 2014. ,
DOI : 10.1183/09059180.00008513
Analysis of lung function and survival in RECAP: An open-label extension study of pirfenidone in patients with idiopathic pulmonary fibrosis, Sarcoid Vasc Diffuse Lung Dis, vol.31, pp.198-205, 2014. ,
Comprehensive assessment of the long-term safety of pirfenidone in patients with idiopathic pulmonary fibrosis, Respirology, vol.15, issue.9, pp.740-747, 2014. ,
DOI : 10.1002/pds.1211
Adverse Events of Pirfenidone for the Treatment of Pulmonary Fibrosis: A Meta-Analysis of Randomized Controlled Trials, PLoS ONE, vol.7, issue.10, p.47024, 2012. ,
DOI : 10.1371/journal.pone.0047024.s001
Management of patients with idiopathic pulmonary fibrosis in clinical practice: the INSIGHTS-IPF registry, European Respiratory Journal, vol.46, issue.1, pp.186-96, 2015. ,
DOI : 10.1183/09031936.00217614
Pirfenidone in Idiopathic Pulmonary Fibrosis: Expert Panel Discussion on the Management of Drug-Related Adverse Events, Advances in Therapy, vol.184, issue.4, pp.375-91, 2014. ,
DOI : 10.1164/rccm.201101-0138OC
The role of tyrosine kinases in the pathogenesis of idiopathic pulmonary fibrosis, European Respiratory Journal, vol.45, issue.5, pp.1426-1459, 2015. ,
DOI : 10.1183/09031936.00149614
Antifibrotic and Anti-inflammatory Activity of the Tyrosine Kinase Inhibitor Nintedanib in Experimental Models of Lung Fibrosis, Journal of Pharmacology and Experimental Therapeutics, vol.349, issue.2, pp.209-229, 2014. ,
DOI : 10.1124/jpet.113.208223
Mode of action of nintedanib in the treatment of idiopathic pulmonary fibrosis, European Respiratory Journal, vol.45, issue.5, pp.1434-1479, 2015. ,
DOI : 10.1183/09031936.00174914
Anti-fibrotic effects of nintedanib in lung fibroblasts derived from patients with idiopathic pulmonary fibrosis, Respiratory Research, vol.25, issue.3, p.157, 2014. ,
DOI : 10.1016/j.cytogfr.2014.03.003
Novel Mechanisms for the Antifibrotic Action of Nintedanib, American Journal of Respiratory Cell and Molecular Biology, vol.2, issue.1, pp.51-60, 2016. ,
DOI : 10.4161/auto.7.11.17652
Efficacy of a Tyrosine Kinase Inhibitor in Idiopathic Pulmonary Fibrosis, New England Journal of Medicine, vol.365, issue.12, pp.1079-87, 2011. ,
DOI : 10.1056/NEJMoa1103690
Design of the INPULSIS??? trials: Two phase 3 trials of nintedanib in patients with idiopathic pulmonary fibrosis, Respiratory Medicine, vol.108, issue.7, pp.1023-1053, 2014. ,
DOI : 10.1016/j.rmed.2014.04.011
Efficacy and Safety of Nintedanib in Idiopathic Pulmonary Fibrosis, New England Journal of Medicine, vol.370, issue.22, pp.2071-82, 2014. ,
DOI : 10.1056/NEJMoa1402584
Efficacy of Nintedanib in Idiopathic Pulmonary Fibrosis across Prespecified Subgroups in INPULSIS, American Journal of Respiratory and Critical Care Medicine, vol.191, issue.2, pp.178-85, 2016. ,
DOI : 10.1164/rccm.201411-2044ED
Nintedanib in patients with idiopathic pulmonary fibrosis and preserved lung volume, Thorax, vol.48, issue.Suppl 60, 2016. ,
DOI : 10.1136/thoraxjnl-2016-208710
Nintedanib: a new treatment for idiopathic pulmonary fibrosis, Clinical Investigation, vol.5, issue.7, pp.621-653, 2015. ,
DOI : 10.4155/cli.15.27
First Data on Efficacy and Safety of Nintedanib in Patients with Idiopathic Pulmonary Fibrosis and Forced Vital Capacity of?????50??% of Predicted Value, Lung, vol.191, issue.Suppl 59, pp.739-782, 2016. ,
DOI : 10.1183/13993003.congress-2015.OA4499
Nintedanib in patients with idiopathic pulmonary fibrosis: Combined evidence from the TOMORROW and INPULSIS?? trials, Respiratory Medicine, vol.113, 2016. ,
DOI : 10.1016/j.rmed.2016.02.001
Safety and efficacy of bridging to lung transplantation with antifibrotic drugs in idiopathic pulmonary fibrosis: a case series, BMC Pulmonary Medicine, vol.35, issue.4, p.156, 2016. ,
DOI : 10.1016/j.healun.2016.01.010
Efficacy of pirfenidone in patients with idiopathic pulmonary fibrosis with more preserved lung function, European Respiratory Journal, vol.48, issue.3, pp.843-51, 2016. ,
DOI : 10.1183/13993003.01966-2015
High-Dose Acetylcysteine in Idiopathic Pulmonary Fibrosis, New England Journal of Medicine, vol.353, issue.21, pp.2229-2271, 2005. ,
DOI : 10.1056/NEJMoa042976
Prednisone, azathioprine , and N-acetylcysteine for pulmonary fibrosis, N Engl J Med, vol.366, 2012. ,
-Acetylcysteine among Individuals with Idiopathic Pulmonary Fibrosis, American Journal of Respiratory and Critical Care Medicine, vol.124, issue.12, pp.1475-82, 2015. ,
DOI : 10.1056/NEJMc1013504
Safety and tolerability of acetylcysteine and pirfenidone combination therapy in idiopathic pulmonary fibrosis: a randomised, double-blind, placebo-controlled, phase 2 trial, The Lancet Respiratory Medicine, vol.4, issue.6, pp.445-53, 2016. ,
DOI : 10.1016/S2213-2600(16)30044-3
Hospital-based historical cohort study of 234 histologically proven Japanese patients with IPF, Sarcoid Vasc Diffuse Lung Dis, vol.16, pp.209-223, 1999. ,
Idiopathic Pulmonary Fibrosis, American Journal of Respiratory and Critical Care Medicine, vol.162, issue.4, pp.1063-72, 1998. ,
DOI : 10.1164/ajrccm.149.6.8004317
Diffuse interstitial pneumonitis, The American Journal of Medicine, vol.65, issue.4, pp.661-72, 1978. ,
DOI : 10.1016/0002-9343(78)90855-0
Azathioprine Combined with Prednisone in the Treatment of Idiopathic Pulmonary Fibrosis: A Prospective Double-blind, Randomized, Placebo-controlled Clinical Trial, American Review of Respiratory Disease, vol.102, issue.1, pp.291-297, 1991. ,
DOI : 10.1136/thx.44.4.280
Randomised controlled trial comparing prednisolone alone with cyclophosphamide and low dose prednisolone in combination in cryptogenic fibrosing alveolitis., Thorax, vol.44, issue.4, pp.280-288, 1989. ,
DOI : 10.1136/thx.44.4.280
Combined Corticosteroid and Cyclophosphamide Therapy Does Not Alter Survival in Idiopathic Pulmonary Fibrosis, Chest, vol.125, issue.6, pp.2169-74, 2004. ,
DOI : 10.1378/chest.125.6.2169
Survival in idiopathic pulmonary fibrosis???cytotoxic agents compared to corticosteroids, Respiratory Medicine, vol.100, issue.2, pp.340-347, 2006. ,
DOI : 10.1016/j.rmed.2005.05.008
A Study of the Cough Reflex in Idiopathic Pulmonary Fibrosis, American Journal of Respiratory and Critical Care Medicine, vol.168, issue.8, pp.995-1002, 2003. ,
DOI : 10.1164/ajrccm/145.5.1191
Anticoagulant Therapy for Idiopathic Pulmonary Fibrosis, Chest, vol.128, issue.3, pp.1475-82, 2005. ,
DOI : 10.1378/chest.128.3.1475
A Placebo-Controlled Randomized Trial of Warfarin in Idiopathic Pulmonary Fibrosis, American Journal of Respiratory and Critical Care Medicine, vol.111, issue.1 ,
DOI : 10.1186/1465-9921-10-101
Unfavourable effects of medically indicated oral anticoagulants on survival in idiopathic pulmonary fibrosis, European Respiratory Journal, vol.47, issue.6, pp.1776-84, 2016. ,
DOI : 10.1183/13993003.02087-2015
Colchicine, cyclophosphamide and prednisone in the treatment of mild-moderate idiopathic pulmonary fibrosis: comparison of three currently available therapeutic regimens, Eur Rev Med Pharmacol Sci, vol.12, pp.105-116, 2008. ,
Long-term clinical effects of interferon gamma-1b and colchicine in idiopathic pulmonary fibrosis, European Respiratory Journal, vol.28, issue.3, pp.496-504, 2006. ,
DOI : 10.1183/09031936.06.00032605
Colchicine versus Prednisone in the Treatment of Idiopathic Pulmonary Fibrosis, American Journal of Respiratory and Critical Care Medicine, vol.187, issue.1, pp.220-225, 1998. ,
DOI : 10.1378/chest.110.2.378
Progression of Fibrosis in Usual Interstitial Pneumonia: Serial Evaluation of the Native Lung after Single Lung Transplantation, Respiration, vol.68, issue.2, pp.139-184, 2008. ,
DOI : 10.1159/000064006
Progression of Idiopathic Pulmonary Fibrosis in Native Lungs After Single Lung Transplantation, Chest, vol.121, issue.6, pp.2072-2078, 2002. ,
DOI : 10.1378/chest.121.6.2072
A Placebo-Controlled Trial of Interferon Gamma-1b in Patients with Idiopathic Pulmonary Fibrosis, New England Journal of Medicine, vol.350, issue.2, pp.125-158, 2004. ,
DOI : 10.1056/NEJMoa030511
Effect of interferon gamma-1b on survival in patients with idiopathic pulmonary fibrosis (INSPIRE): a multicentre, randomised, placebo-controlled trial, Lancet, vol.374, pp.222-230, 2009. ,
BUILD-1: a randomized placebo-controlled trial of bosentan in idiopathic pulmonary fibrosis, Am J Respir Crit Care Med, vol.177, pp.75-81, 2008. ,
BUILD-3: a randomized, controlled trial of bosentan in idiopathic pulmonary fibrosis ,
Efficacy And Safety Of Macitentan In Idiopathic Pulmonary Fibrosis: Results Of A Prospective, Randomized, Double-Blind, Placebo-Controlled Trial, B93. CLINICAL TRIALS IN IDIOPATHIC PULMONARY FIBROSIS AND SARCOIDOSIS, p.3631, 2012. ,
DOI : 10.1164/ajrccm-conference.2012.185.1_MeetingAbstracts.A3631
ARTEMIS-IPF: A Placebo-Controlled Trial Of Ambrisentan In Idiopathic Pulmonary Fibrosis, B93. CLINICAL TRIALS IN IDIOPATHIC PULMONARY FIBROSIS AND SARCOIDOSIS, p.3632, 2012. ,
DOI : 10.1164/ajrccm-conference.2012.185.1_MeetingAbstracts.A3632
Treatment of Idiopathic Pulmonary Fibrosis with Etanercept, American Journal of Respiratory and Critical Care Medicine, vol.178, issue.9, pp.948-55, 2008. ,
DOI : 10.1056/NEJMoa030511
CC-chemokine ligand 2 inhibition in idiopathic pulmonary fibrosis: a phase 2 trial of carlumab, European Respiratory Journal, vol.46, issue.6, pp.1740-50, 2015. ,
DOI : 10.1183/13993003.01558-2014
Efficacy of simtuzumab versus placebo in patients with idiopathic pulmonary fibrosis: a randomised, double-blind, controlled, phase 2 trial, The Lancet Respiratory Medicine, vol.5, issue.1, pp.22-32, 2017. ,
DOI : 10.1016/S2213-2600(16)30421-0
Lung Transplantation for Idiopathic Pulmonary Fibrosis, The Annals of Thoracic Surgery, vol.84, issue.4, pp.1121-1129, 2007. ,
DOI : 10.1016/j.athoracsur.2007.04.096
Lung Transplantation in Pulmonary Fibrosis: Challenging Early Outcomes Counterbalanced by Surprisingly Good Outcomes Beyond 15 Years, Transplantation Proceedings, vol.41, issue.1, pp.289-91, 2009. ,
DOI : 10.1016/j.transproceed.2008.10.042
Survival benefit of lung transplantation for patients with idiopathic pulmonary fibrosis, The Journal of Thoracic and Cardiovascular Surgery, vol.126, issue.2, pp.469-75, 2003. ,
DOI : 10.1016/S0022-5223(03)00600-7
A consensus document for the selection of lung transplant candidates: 2014???An update from the Pulmonary Transplantation Council of the International Society for Heart and Lung Transplantation, The Journal of Heart and Lung Transplantation, vol.34, issue.1, pp.1-15, 2015. ,
DOI : 10.1016/j.healun.2014.06.014
Survival After Bilateral Versus Single-Lung Transplantation for Idiopathic Pulmonary Fibrosis, Annals of Internal Medicine, vol.151, issue.11, pp.767-74, 2009. ,
DOI : 10.7326/0003-4819-151-11-200912010-00004
Post-transplant survival in idiopathic pulmonary fibrosis patients concurrently listed for single and double lung transplantation, The Journal of Heart and Lung Transplantation, vol.35, issue.5, pp.657-60, 2016. ,
DOI : 10.1016/j.healun.2015.12.030
Thalidomide inhibits the intractable cough of idiopathic pulmonary fibrosis, Thorax, vol.63, issue.8, p.749, 2008. ,
DOI : 10.1136/thx.2008.098699
Thalidomide for the Treatment of Cough in Idiopathic Pulmonary Fibrosis, Annals of Internal Medicine, vol.157, issue.6, pp.398-406, 2012. ,
DOI : 10.7326/0003-4819-157-6-201209180-00003
Effect of acid suppression therapy on gastroesophageal reflux and cough in idiopathic pulmonary fibrosis: an intervention study, Cough, vol.10, issue.1, p.4, 2014. ,
DOI : 10.1378/chest.10-0438
Long-Term Effects of a 12-Week Exercise Training Program on Clinical Outcomes in Idiopathic Pulmonary Fibrosis, Lung, vol.17, issue.3, pp.345-54, 2015. ,
DOI : 10.1111/j.1365-2281.1997.tb00008.x
Exercise Training-Based Pulmonary Rehabilitation Program Is Clinically Beneficial for Idiopathic Pulmonary Fibrosis, Respiration, vol.88, issue.5, pp.378-88, 2014. ,
DOI : 10.1159/000367899
Pulmonary Rehabilitation in Patients with Idiopathic Pulmonary Fibrosis - A Review, Respiration, vol.86, issue.2, pp.89-99, 2013. ,
DOI : 10.1159/000354112
Pulmonary rehabilitation for interstitial lung disease, Cochrane Database Syst Rev, vol.63, issue.4, p.6322, 2014. ,
DOI : 10.1002/14651858.CD006322.pub2
Increased Exercise Capacity in Hypoxemic Patients after Long-term Oxygen Therapy, Chest, vol.102, issue.2, pp.542-50, 1992. ,
DOI : 10.1378/chest.102.2.542
Ambulatory oxygen in interstitial lung disease, European Respiratory Journal, vol.38, issue.4, pp.987-90, 2011. ,
DOI : 10.1183/09031936.00190710
Ambulatory oxygen in idiopathic pulmonary fibrosis: of what benefit?: Table 1???, European Respiratory Journal, vol.40, issue.1, pp.269-70, 2012. ,
DOI : 10.1183/09031936.00007712
Effect of ambulatory oxygen on exertional dyspnea in IPF patients without resting hypoxemia, Respiratory Medicine, vol.107, issue.8, pp.1241-1247, 2013. ,
DOI : 10.1016/j.rmed.2013.05.015
A systematic review of the use of opioids in the management of dyspnoea, Thorax, vol.57, issue.11, pp.939-983, 2002. ,
DOI : 10.1136/thorax.57.11.939
Opioids: an unexplored option for treatment of dyspnea in IPF, European Clinical Respiratory Journal, vol.4, issue.1, p.30629, 2016. ,
DOI : 10.1183/09031936.05.00021005
Low dose diamorphine reduces breathlessness without causing a fall in oxygen saturation in elderly patients with end-stage idiopathic pulmonary fibrosis, Palliative Medicine, vol.4, issue.2, pp.128-158, 2005. ,
DOI : 10.1136/bmj.327.7414.523
Short term improvement in exercise capacity and symptoms following exercise training in interstitial lung disease, Thorax, vol.63, issue.6, pp.549-54, 2008. ,
DOI : 10.1136/thx.2007.088070
Effects of pulmonary rehabilitation in patients with idiopathic pulmonary fibrosis Pulmonary rehabilitation in interstitial lung disease: benefits and predictors of response, Respirology Chest, vol.13168135, pp.442-449, 2008. ,
Predictors of benefit following pulmonary rehabilitation for interstitial lung disease, Respiratory Medicine, vol.106, issue.3, pp.429-464, 2012. ,
DOI : 10.1016/j.rmed.2011.11.014
Pulmonary rehabilitation improves long-term outcomes in interstitial lung disease: A prospective cohort study, Respiratory Medicine, vol.108, issue.1, pp.203-213, 2014. ,
DOI : 10.1016/j.rmed.2013.11.016
Differences in Response to Pulmonary Rehabilitation in Idiopathic Pulmonary Fibrosis and Chronic Obstructive Pulmonary Disease, Respiration, vol.71, issue.3, pp.196-205, 2011. ,
DOI : 10.1159/000077422
Effects of inpatient pulmonary rehabilitation in patients with interstitial lung disease, European Respiratory Journal, vol.42, issue.2, 2012. ,
DOI : 10.1183/09031936.00081512
Home-based pulmonary rehabilitation in idiopathic pulmonary fibrosis, Revue des Maladies Respiratoires, vol.28, issue.7, pp.275-82, 2009. ,
DOI : 10.1016/j.rmr.2011.06.006
Où meurent les patients atteints de fibrose pulmonaire idiopathique ? Info Respir, 2015. ,
End-of-life care in oxygen-dependent ILD compared with lung cancer: a national population-based study, Thorax, vol.11, issue.6, pp.510-516, 2016. ,
DOI : 10.6004/jnccn.2013.0029
Palliative care for patients with advanced fibrotic lung disease: a randomised controlled phase II and feasibility trial of a community case conference intervention, Thorax, vol.63, issue.(Suppl 5), pp.830-839, 2015. ,
DOI : 10.3111/13696998.2012.680553
Effect of palliative oxygen versus room air in relief of breathlessness in patients with refractory dyspnoea: a double-blind, randomised controlled trial, The Lancet, vol.376, issue.9743, pp.784-93, 2010. ,
DOI : 10.1016/S0140-6736(10)61115-4
Acute Exacerbations of Idiopathic Pulmonary Fibrosis, American Journal of Respiratory and Critical Care Medicine, vol.176, issue.7, pp.265-75, 2016. ,
DOI : 10.1378/chest.120.1.213
Outcomes After Hospitalization in Idiopathic Pulmonary Fibrosis, Chest, vol.147, issue.1, pp.173-182, 2015. ,
DOI : 10.1378/chest.13-2424
Acute exacerbation of idiopathic pulmonary fibrosis: a clinical review, Internal and Emergency Medicine, vol.20, issue.4, pp.401-412, 2015. ,
DOI : 10.1097/MCP.0000000000000073
Acute exacerbation of idiopathic pulmonary fibrosis associated with air pollution exposure, European Respiratory Journal, vol.43, issue.4, pp.1124-1155, 2014. ,
DOI : 10.1183/09031936.00122213
Acute Exacerbations of Idiopathic Pulmonary Fibrosis, American Journal of Respiratory and Critical Care Medicine, vol.176, issue.7, pp.636-679, 2007. ,
DOI : 10.1378/chest.120.1.213
Idiopathic Pulmonary Fibrosis: Increased Survival with ???Gastroesophageal Reflux Therapy???, American Journal of Respiratory and Critical Care Medicine, vol.184, issue.12, pp.1330-1332, 2011. ,
DOI : 10.1164/rccm.201101-0138OC
Exacerbations of idiopathic pulmonary fibrosis treated with corticosteroids and cyclophosphamide pulses, European Respiratory Journal, vol.38, issue.6, pp.1487-1496, 2011. ,
DOI : 10.1183/09031936.00127311
Cyclophosphamide for acute exacerbation of idiopathic pulmonary fibrosis (EXAFIP); 2016 Available from: https://clinicaltrials. gov/ct2/show, p.1 ,
Time for prevention of idiopathic pulmonary fibrosis exacerbation, Ann Am Thorac Soc, vol.12, pp.181-186, 2015. ,
Outcome of Patients with Interstitial Lung Disease Treated with Extracorporeal Membrane Oxygenation for Acute Respiratory Failure, American Journal of Respiratory and Critical Care Medicine, vol.8, issue.5 ,
DOI : 10.1164/rccm.200611-1739OC
Outcome of Patients With Idiopathic Pulmonary Fibrosis Admitted to the ICU for Respiratory Failure, Chest, vol.120, issue.1, pp.209-221, 2001. ,
DOI : 10.1378/chest.120.1.209
Acute exacerbation of idiopathic pulmonary fibrosis: frequency and clinical features, European Respiratory Journal, vol.27, issue.1, pp.143-50, 2006. ,
DOI : 10.1183/09031936.06.00114004
Caracter??sticas cl??nicas y pron??stico de los pacientes con fibrosis pulmonar que ingresan en cuidados intensivos por insuficiencia respiratoria. An??lisis de 20 casos, Medicina Cl??nica, vol.121, issue.2, pp.63-70, 2003. ,
DOI : 10.1016/S0025-7753(03)73856-1
Outcome of Patients with Idiopathic Pulmonary Fibrosis Admitted to the Intensive Care Unit, American Journal of Respiratory and Critical Care Medicine, vol.166, issue.6, pp.839-881, 2002. ,
DOI : 10.1136/thx.54.5.390
Lung and chest wall mechanics in ventilated patients with end stage idiopathic pulmonary fibrosis, Thorax, vol.54, issue.5, pp.390-395, 1999. ,
DOI : 10.1136/thx.54.5.390
Prognosis of Patients With Advanced Idiopathic Pulmonary Fibrosis Requiring Mechanical Ventilation for Acute Respiratory Failure, Chest, vol.120, issue.1, pp.213-222, 2001. ,
DOI : 10.1378/chest.120.1.213
Outcome of Patients Admitted to Intensive Care Unit for Acute Exacerbation of Idiopathic Pulmonary Fibrosis, Canadian Respiratory Journal, vol.11, issue.2, pp.117-139, 2004. ,
DOI : 10.1155/2004/379723
Outcome of mechanical ventilation for acute respiratory failure in patients with pulmonary fibrosis, Intensive Care Medicine, vol.27, issue.12, pp.1868-74, 2001. ,
DOI : 10.1007/s00134-001-1150-0
Mechanical Ventilation in Patients with End-Stage Idiopathic Pulmonary Fibrosis, Respiration, vol.79, issue.3, pp.209-224, 2010. ,
DOI : 10.1159/000225932
Outcomes of patients admitted to the intensive care unit with idiopathic pulmonary fibrosis, Crit Care Resusc, vol.11, pp.102-111, 2009. ,
Outcome of patients with idiopathic pulmonary fibrosis (IPF) ventilated in intensive care unit, Respiratory Medicine, vol.102, issue.10, pp.1355-1364, 2008. ,
DOI : 10.1016/j.rmed.2008.06.003
The use of mechanical ventilation in patients with idiopathic pulmonary fibrosis in the United States: A nationwide retrospective cohort analysis, Respiratory Medicine, vol.111, pp.72-78, 2016. ,
DOI : 10.1016/j.rmed.2015.12.005
Invasive mechanical ventilation in patients with fibrosing interstitial pneumonia, The Journal of Thoracic and Cardiovascular Surgery, vol.147, issue.1, pp.47-53, 2014. ,
DOI : 10.1016/j.jtcvs.2013.06.039
Noninvasive Ventilation in Acute Exacerbation of Idiopathic Pulmonary Fibrosis, Internal Medicine, vol.49, issue.15, pp.1509-1523, 2010. ,
DOI : 10.2169/internalmedicine.49.3222
Fibrose pulmonaire : dans quels cas et sur quels critères envisager une admission en réanimation ? Reanimation 2013, pp.45-53 ,
Pulmonary hypertension in patients with idiopathic pulmonary fibrosis, Eur Respir Mon, vol.57, pp.148-60, 2012. ,
DOI : 10.1183/1025448x.10019511
Pulmonary hypertension in patients with pulmonary fibrosis awaiting lung transplant, European Respiratory Journal, vol.30, issue.4, pp.715-736, 2007. ,
DOI : 10.1183/09031936.00107206
Prevalence and Outcomes of Pulmonary Arterial Hypertension in Advanced Idiopathic Pulmonary Fibrosis, Chest, vol.129, issue.3, pp.746-52, 2006. ,
DOI : 10.1378/chest.129.3.746
Acute exacerbations and pulmonary hypertension in advanced idiopathic pulmonary fibrosis, European Respiratory Journal, vol.40, issue.1, pp.93-100, 2012. ,
DOI : 10.1183/09031936.00115511
Right ventricular systolic pressure by echocardiography as a predictor of pulmonary hypertension in idiopathic pulmonary fibrosis, Respiratory Medicine, vol.102, issue.9, pp.1305-1315, 2008. ,
DOI : 10.1016/j.rmed.2008.03.022
Doppler echocardiographyright heart catheterization relationships in patients with idiopathic pulmonary fibrosis and suspected pulmonary hypertension, Med Sci Monit, vol.14, pp.177-82, 2008. ,
Echocardiographic Assessment of Pulmonary Hypertension in Patients with Advanced Lung Disease, American Journal of Respiratory and Critical Care Medicine, vol.167, issue.5, pp.735-775, 2003. ,
DOI : 10.1164/rccm.2107027
The Effect of Diffuse Pulmonary Fibrosis on the Reliability of CT Signs of Pulmonary Hypertension, Radiology, vol.249, issue.3, pp.1042-1051, 2008. ,
DOI : 10.1148/radiol.2492080269
Brain Natriuretic Peptide Is a Prognostic Parameter in Chronic Lung Disease, American Journal of Respiratory and Critical Care Medicine, vol.173, issue.7, pp.744-50, 2006. ,
DOI : 10.1164/rccm.200401-006OC
Validation of a Method To Screen for Pulmonary Hypertension in Advanced Idiopathic Pulmonary Fibrosis, Chest, vol.133, issue.3, pp.640-645, 2008. ,
DOI : 10.1378/chest.07-2488
2015 ESC/ERS Guidelines for the diagnosis and treatment of pulmonary hypertension, European Respiratory Journal, vol.46, issue.4, pp.903-75, 2015. ,
DOI : 10.1183/13993003.01032-2015
Pulmonary Hypertension in Chronic Lung Diseases, Journal of the American College of Cardiology, vol.62, issue.25, pp.109-125, 2013. ,
DOI : 10.1016/j.jacc.2013.10.036
Treatment of pulmonary hypertension in idiopathic pulmonary fibrosis: shortfall in efficacy or trial design?, Drug Design, Development and Therapy, vol.8, pp.875-85, 2014. ,
DOI : 10.2147/DDDT.S64907
Vaso-active therapy can improve 6-min walk distance in patients with pulmonary hypertension and fibrotic interstitial lung disease, Respiratory Medicine, vol.102, issue.7, pp.1015-1035, 2008. ,
DOI : 10.1016/j.rmed.2008.02.002
Bosentan in Pulmonary Hypertension Associated with Fibrotic Idiopathic Interstitial Pneumonia, American Journal of Respiratory and Critical Care Medicine, vol.145, issue.2, pp.208-225, 2014. ,
DOI : 10.1183/09031936.00011308
Pulmonary hypertension in idiopathic pulmonary fibrosis with mild-to-moderate restriction, European Respiratory Journal, vol.46, issue.5, pp.1370-1377, 2015. ,
DOI : 10.1183/13993003.01537-2014
Sildenafil for treatment of lung fibrosis and pulmonary hypertension: a randomised controlled trial, The Lancet, vol.360, issue.9337, pp.895-900, 2002. ,
DOI : 10.1016/S0140-6736(02)11024-5
A potential role for sildenafil in the management of pulmonary hypertension in patients with parenchymal lung disease, Vascular Pharmacology, vol.44, issue.5, pp.372-378, 2006. ,
DOI : 10.1016/j.vph.2006.01.013
Sildenafil Improves Walk Distance in Idiopathic Pulmonary Fibrosis, Chest, vol.131, issue.3, pp.897-906, 2007. ,
DOI : 10.1378/chest.06-2101
A controlled trial of sildenafil in advanced idiopathic pulmonary fibrosis, N Engl J Med, vol.363, pp.620-628, 2010. ,
Sildenafil Preserves Exercise Capacity in Patients With Idiopathic Pulmonary Fibrosis and Right-sided Ventricular Dysfunction, Chest, vol.143, issue.6, pp.1699-708, 2013. ,
DOI : 10.1378/chest.12-1594
Pulmonary Hypertension in Patients with Chronic Fibrosing Idiopathic Interstitial Pneumonias, PLOS ONE, vol.42, issue.6, p.141911, 2015. ,
DOI : 10.1371/journal.pone.0141911.t004
Riociguat for interstitial lung disease and pulmonary hypertension: a pilot trial, European Respiratory Journal, vol.41, issue.4, pp.853-60, 2013. ,
DOI : 10.1183/09031936.00213911
Gastro-oesophageal reflux and gastric aspiration in idiopathic pulmonary fibrosis patients, European Respiratory Journal, vol.42, issue.5, pp.1322-1353, 2013. ,
DOI : 10.1183/09031936.00101212
Prevalence of hiatal hernia by blinded multidetector CT in patients with idiopathic pulmonary fibrosis, European Respiratory Journal, vol.39, issue.2, pp.344-51, 2012. ,
DOI : 10.1183/09031936.00099910
Hiatal hernia on thoracic computed tomography in pulmonary fibrosis, European Respiratory Journal, vol.48, issue.3, pp.833-875, 2016. ,
DOI : 10.1183/13993003.01796-2015
Increased Prevalence of Gastroesophageal Reflux in Patients with Idiopathic Pulmonary Fibrosis, American Journal of Respiratory and Critical Care Medicine, vol.91, issue.6, pp.1804-1812, 1998. ,
DOI : 10.1378/chest.99.6.1330
Gastroesophageal reflux in patients with idiopathic pulmonary fibrosis referred for lung transplantation, The Journal of Thoracic and Cardiovascular Surgery, vol.133, issue.4, pp.1078-84, 2007. ,
DOI : 10.1016/j.jtcvs.2006.09.085
Progression of idiopathic pulmonary fibrosis: lessons from asymmetrical disease, Thorax, vol.66, issue.3, pp.226-257, 2011. ,
DOI : 10.1136/thx.2010.137190
Does Chronic Microaspiration Cause Idiopathic Pulmonary Fibrosis?, The American Journal of Medicine, vol.123, issue.4, pp.304-315, 2010. ,
DOI : 10.1016/j.amjmed.2009.07.033
Laparoscopic fundoplication in patients with end-stage lung disease awaiting transplantation, The Journal of Thoracic and Cardiovascular Surgery, vol.131, issue.2, pp.438-484, 2006. ,
DOI : 10.1016/j.jtcvs.2005.10.014
Gastroesophageal Reflux Therapy Is Associated with Longer Survival in Patients with Idiopathic Pulmonary Fibrosis, American Journal of Respiratory and Critical Care Medicine, vol.184, issue.12, pp.1390-1394, 2011. ,
DOI : 10.1164/rccm.200808-1359OC
Silent gastro-oesophageal reflux and microaspiration in IPF: mounting evidence for anti-reflux therapy?, European Respiratory Journal, vol.39, issue.2, pp.242-247, 2012. ,
DOI : 10.1183/09031936.00211311
Anti-acid treatment and disease progression in idiopathic pulmonary fibrosis: an analysis of data from three randomised controlled trials, The Lancet Respiratory Medicine, vol.1, issue.5, pp.369-76, 2013. ,
DOI : 10.1016/S2213-2600(13)70105-X
Antacid therapy and disease outcomes in idiopathic pulmonary fibrosis: a pooled analysis, The Lancet Respiratory Medicine, vol.4, issue.5, 2016. ,
DOI : 10.1016/S2213-2600(16)00067-9
Updated Guidelines for the Diagnosis and Treatment of Gastroesophageal Reflux Disease, The American Journal of Gastroenterology, vol.59, issue.1, pp.190-200, 2005. ,
DOI : 10.1111/j.1572-0241.2003.08109.x
Predictors of the clinical effects of pirfenidone on idiopathic pulmonary fibrosis, Respiratory Investigation, vol.52, issue.2, pp.136-179, 2014. ,
DOI : 10.1016/j.resinv.2013.09.002
Idiopathic Pulmonary Fibrosis and Emphysema, Chest, vol.136, issue.1, pp.10-15, 2009. ,
DOI : 10.1378/chest.08-2306
Combined pulmonary fibrosis and emphysema: a distinct underrecognised entity, European Respiratory Journal, vol.26, issue.4, pp.586-93, 2005. ,
DOI : 10.1183/09031936.05.00021005
Pulmonary hypertension in patients with combined pulmonary fibrosis and emphysema syndrome, European Respiratory Journal, vol.35, issue.1, pp.105-116, 2010. ,
DOI : 10.1183/09031936.00038709
URL : https://hal.archives-ouvertes.fr/hal-01608607
Combined Pulmonary Fibrosis and Emphysema: An Experimental and Clinically Relevant Phenotype, American Journal of Respiratory and Critical Care Medicine, vol.172, issue.12, p.1605, 2005. ,
DOI : 10.1164/ajrccm.150.3.8087340
Coexistent emphysema delays the decrease of vital capacity in idiopathic pulmonary fibrosis, Respiratory Medicine, vol.103, issue.8, pp.1209-1224, 2009. ,
DOI : 10.1016/j.rmed.2009.02.001
Pulmonary function measures predict mortality differently in IPF versus combined pulmonary fibrosis and emphysema, European Respiratory Journal, vol.38, issue.1, pp.176-83, 2011. ,
DOI : 10.1183/09031936.00114010
Effect of baseline emphysema on reduction in FVC decline with nintedanib in the Inpulsis(trials. In: 18th International colloquium on lung and airway fibrosis, 2014. ,
A survey of nocturnal hypoxaemia and health related quality of life in patients with cryptogenic fibrosing alveolitis, Thorax, vol.56, issue.6, pp.482-488, 2001. ,
DOI : 10.1136/thorax.56.6.482
Assessment of sleep with polysomnography in patients with interstitial lung disease] Sleep-related breathing disorders in patients with idiopathic pulmonary fibrosis, Tuberk Toraks Lung, vol.54185, pp.173-181, 2006. ,
Obstructive Sleep Apnea Is Common in Idiopathic Pulmonary Fibrosis, Chest, vol.136, issue.3, pp.772-780, 2009. ,
DOI : 10.1378/chest.08-2776
Obstructive sleep apnea should be treated in patients with idiopathic pulmonary fibrosis, Sleep and Breathing, vol.61, issue.1, pp.385-91, 2015. ,
DOI : 10.1111/j.1742-1241.2006.01213.x
Increasing the functional residual capacity may reverse obstructive sleep apnea, Sleep, vol.11, pp.349-53, 1988. ,
Lung Volume and Continuous Positive Airway Pressure Requirements in Obstructive Sleep Apnea, American Journal of Respiratory and Critical Care Medicine, vol.172, issue.1, pp.114-121, 2005. ,
DOI : 10.1164/ajrccm.150.2.8049832
Société française d'anesthésie réanimation, Société française de cardiologie SFdMdT, Société française d'ORL, Société de physiologie , Société française de recherche et de médecine du sommeil. Recommandations pour la pratique clinique. Syndrome d'apnées hypopnées obstructives du sommeil de l'adulte, Rev Mal Respir, vol.27, pp.806-839, 2010. ,
Lung Cancer and Cryptogenic Fibrosing Alveolitis, American Journal of Respiratory and Critical Care Medicine, vol.161, issue.1, pp.5-8, 2000. ,
DOI : 10.1164/ajrccm.154.2.8756825
Cryptogenic fibrosing alveolitis: clinical features and their influence on survival, Thorax, vol.35, issue.3, pp.171-80, 1980. ,
DOI : 10.1136/thx.35.3.171
Cryptogenic fibrosing alveolitis and lung cancer: the BTS study, Thorax, vol.65, issue.1, pp.70-76, 2010. ,
DOI : 10.1136/thx.2009.121962
Cumulative incidence of and predictive factors for lung cancer in IPF, Respirology, vol.164, issue.5, pp.723-731, 2009. ,
DOI : 10.1164/ajrccm.164.7.2003140
The Impact of Lung Cancer on Survival of Idiopathic Pulmonary Fibrosis, Chest, vol.147, issue.1, pp.157-64, 2015. ,
DOI : 10.1378/chest.14-0359
Impact of Comorbidities on Mortality in Patients with Idiopathic Pulmonary Fibrosis, PLOS ONE, vol.161, issue.2, p.151425, 2016. ,
DOI : 10.1371/journal.pone.0151425.s002
Lung Cancer in Combined Pulmonary Fibrosis and Emphysema: A Series of 47 Western Patients, Journal of Thoracic Oncology, vol.9, issue.8, pp.1162-70, 2014. ,
DOI : 10.1097/JTO.0000000000000209
URL : https://hal.archives-ouvertes.fr/hal-01063912
Evolving Early Lung Cancers Detected During Follow-Up of Idiopathic Interstitial Pneumonia: Serial CT Features, American Journal of Roentgenology, vol.204, issue.6, pp.1190-1196, 2015. ,
DOI : 10.2214/AJR.14.13587
Idiopathic Pulmonary Fibrosis: Phenotypes and Comorbidities, Clinics in Chest Medicine, vol.33, issue.1, pp.51-58, 2012. ,
DOI : 10.1016/j.ccm.2011.12.005
Impact and predictors of acute exacerbation of interstitial lung diseases after pulmonary resection for lung cancer, The Journal of Thoracic and Cardiovascular Surgery, vol.147, issue.5, pp.1604-1615, 2014. ,
DOI : 10.1016/j.jtcvs.2013.09.050
Experience with perioperative pirfenidone for lung cancer surgery in patients with idiopathic pulmonary fibrosis, Surgery Today, vol.158, issue.10, pp.1263-70, 2015. ,
DOI : 10.1164/ajrccm.158.5.9803115
Impact of Pretreatment Interstitial Lung Disease on Radiation Pneumonitis and Survival after Stereotactic Body Radiation Therapy for Lung Cancer, Journal of Thoracic Oncology, vol.10, issue.1, pp.116-141, 2015. ,
DOI : 10.1097/JTO.0000000000000359
Stereotactic body radiotherapy for lung tumors in patients with subclinical interstitial lung disease: The potential risk of extensive radiation pneumonitis, Lung Cancer, vol.82, issue.2, pp.260-265, 2013. ,
DOI : 10.1016/j.lungcan.2013.08.024
Prevalence of underlying lung disease in smokers with epidermal growth factor receptor-mutant lung cancer, Oncology Reports, vol.29, issue.5, 2013. ,
DOI : 10.3892/or.2013.2320
The frequency of epidermal growth factor receptor mutation of non small cell lung cancer according to the underlying pulmonary diseases, Pulm Med, p.290132, 2011. ,
Preexisting interstitial lung disease is inversely correlated to tumor epidermal growth factor receptor mutation in patients with lung adenocarcinoma, Lung Cancer, vol.80, issue.2, pp.159-64, 2013. ,
DOI : 10.1016/j.lungcan.2013.01.017
Pulmonary adenocarcinoma mutation profile in smokers with smokingrelated interstitial fibrosis, Int J Chron Obstruct Pulmon Dis, vol.9, pp.525-556, 2014. ,
Risk of interstitial lung disease associated with EGFR-TKIs in advanced non-small-cell lung cancer: a meta-analysis of 24 phase III clinical trials, Journal of Chemotherapy, vol.4, issue.3, pp.40-51, 2015. ,
DOI : 10.1200/JCO.2007.15.6695
Gefitinib and Erlotinib in Metastatic Non-Small Cell Lung Cancer: A Meta-Analysis of Toxicity and Efficacy of Randomized Clinical Trials, The Oncologist, vol.20, issue.4, pp.400-410, 2015. ,
DOI : 10.1634/theoncologist.2014-0154
Carboplatin plus weekly paclitaxel treatment in non-small cell lung cancer patients with interstitial lung disease, Anticancer Res, vol.30, pp.4357-61, 2010. ,
The safety and efficacy of weekly paclitaxel in combination with carboplatin for advanced non-small cell lung cancer with idiopathic interstitial pneumonias, Lung Cancer, vol.71, issue.1, pp.70-74, 2011. ,
DOI : 10.1016/j.lungcan.2010.04.014
Evaluation of the safety and efficacy of combination chemotherapy with vinorelbine and platinum agents for patients with non-small cell lung cancer with interstitial lung disease, Anticancer Res, vol.32, pp.5475-80, 2012. ,
Efficacy of Chemotherapy for Advanced Non-Small Cell Lung Cancer with Idiopathic Pulmonary Fibrosis, Respiration, vol.85, issue.4, pp.326-357, 2013. ,
DOI : 10.1159/000342046
The safety and efficacy of paclitaxel and carboplatin with or without bevacizumab for treating patients with advanced nonsquamous non-small cell lung cancer with interstitial lung disease, Cancer Chemotherapy and Pharmacology, vol.211, issue.2, pp.1159-66, 2014. ,
DOI : 10.1148/radiology.211.2.r99ma01555
Safety and efficacy of gemcitabine or pemetrexed in combination with a platinum in patients with non-small-cell lung cancer and prior interstitial lung disease, Cancer Chemotherapy and Pharmacology, vol.183, issue.Suppl 2, pp.1217-1242, 2014. ,
DOI : 10.1164/rccm.2009-040GL
The Risk of Cytotoxic Chemotherapy-Related Exacerbation of Interstitial Lung Disease with Lung Cancer, Journal of Thoracic Oncology, vol.6, issue.7, pp.1242-1248, 2011. ,
DOI : 10.1097/JTO.0b013e318216ee6b
The Feasibility Study of Carboplatin Plus Etoposide for Advanced Small Cell Lung Cancer with Idiopathic Interstitial Pneumonias, Journal of Thoracic Oncology, vol.6, issue.4, pp.801-808, 2011. ,
DOI : 10.1097/JTO.0b013e3182103d3c
Safety and efficacy of platinum agents plus etoposide for patients with small cell lung cancer with interstitial lung disease, Anticancer Res, vol.33, pp.1175-1184, 2013. ,
Chemotherapy for extensive-stage small-cell lung cancer with idiopathic pulmonary fibrosis, International Journal of Clinical Oncology, vol.177, issue.2, pp.260-265, 2014. ,
DOI : 10.1164/ajrccm.177.12.1397a
Interstitial lung disease in patients with small cell lung cancer, Medical Oncology, vol.19, issue.3 Suppl, pp.763-770, 2010. ,
DOI : 10.1016/j.clon.2007.01.112
Prognostic Significance of Preexisting Interstitial Lung Disease in Japanese Patients With Small-Cell Lung Cancer, Clinical Lung Cancer, vol.13, issue.4, pp.304-315, 2012. ,
DOI : 10.1016/j.cllc.2011.11.001
Comorbidities in idiopathic pulmonary fibrosis patients: a systematic literature review, European Respiratory Journal, vol.46, issue.4, pp.1113-1143, 2015. ,
DOI : 10.1183/13993003.02316-2014
IPF, comorbidities and management implications, Sarcoidosis Vasc Diffuse Lung Dis, vol.32, pp.17-23, 2015. ,
How does comorbidity influence survival in idiopathic pulmonary fibrosis?, Respiratory Medicine, vol.108, issue.4, pp.647-53, 2014. ,
DOI : 10.1016/j.rmed.2014.01.008
Presence of a prothrombotic state in people with idiopathic pulmonary fibrosis: a population-based case???control study, Thorax, vol.168, issue.(Pt 1), pp.207-222, 2014. ,
DOI : 10.1164/rccm.2201082
Burden of illness in idiopathic pulmonary fibrosis, Journal of Medical Economics, vol.15, issue.5, pp.829-864, 2012. ,
DOI : 10.3111/13696998.2012.680553
Telomeres and disease: An overview, Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis, vol.730, issue.1-2, pp.1-2, 2012. ,
DOI : 10.1016/j.mrfmmm.2011.11.005
Loss-of-function mutations in the RNA biogenesis factor NAF1 predispose to pulmonary fibrosis-emphysema, Science Translational Medicine, vol.7, issue.suppl_1, pp.351-107, 2016. ,
DOI : 10.1093/nar/gkj002
Exome sequencing links mutations in PARN and RTEL1 with familial pulmonary fibrosis and telomere shortening, Nature Genetics, vol.47, issue.5, pp.512-519, 2015. ,
DOI : 10.1086/302662
mutations are associated with familial pulmonary fibrosis, European Respiratory Journal, vol.46, issue.2, pp.474-85, 2015. ,
DOI : 10.1183/09031936.00040115
URL : https://hal.archives-ouvertes.fr/hal-01214563
ELMOD2 Is a Candidate Gene for Familial Idiopathic Pulmonary Fibrosis, The American Journal of Human Genetics, vol.79, issue.1, pp.149-54, 2006. ,
DOI : 10.1086/504639
Neurofibromatosis-associated lung disease: a case series and literature review, European Respiratory Journal, vol.29, issue.1, pp.210-214, 2007. ,
DOI : 10.1183/09031936.06.00044006
Heterogeneous Pulmonary Phenotypes Associated With Mutations in the Thyroid Transcription Factor Gene NKX2-1, Chest, vol.144, issue.3, pp.794-804, 2013. ,
DOI : 10.1378/chest.12-2502
Altered Trafficking of Lysosomal Proteins in Hermansky-Pudlak Syndrome Due to Mutations in the ??3A Subunit of the AP-3 Adaptor, Molecular Cell, vol.3, issue.1, pp.11-21, 1999. ,
DOI : 10.1016/S1097-2765(00)80170-7
Mutations in FAM111B Cause Hereditary Fibrosing Poikiloderma with Tendon Contracture, Myopathy, and Pulmonary Fibrosis, The American Journal of Human Genetics, vol.93, issue.6, pp.1100-1107, 2013. ,
DOI : 10.1016/j.ajhg.2013.10.013