Predicting Outcomes in Idiopathic Pulmonary Fibrosis Using Automated Computed Tomographic Analysis

scientific article published on 01 September 2018

Predicting Outcomes in Idiopathic Pulmonary Fibrosis Using Automated Computed Tomographic Analysis is …
instance of (P31):
scholarly articleQ13442814

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P356DOI10.1164/RCCM.201711-2174OC
P932PMC publication ID6222463
P698PubMed publication ID29684284

P50authorAndré AltmannQ42941113
Sujal R DesaiQ59981461
Ryoko EgashiraQ76390576
Joseph JacobQ87998624
Sebastien OurselinQ88381761
Toby MaherQ42886895
P2093author name stringAthol U Wells
Brian J Bartholmai
Srinivasan Rajagopalan
Coline H M van Moorsel
Joseph Barnett
Hendrik W van Es
Arjun Nair
Anne Laure Brun
Maria Kokosi
Ronald Karwoski
Simon L F Walsh
Eoin P Judge
Gary Cross
Frouke T van Beek
Elisabetta Renzoni
Angelo de Lauretis
Marjolijn H L Struik
P2860cites workRelative versus absolute change in forced vital capacity in idiopathic pulmonary fibrosisQ45373404
Fibrotic idiopathic interstitial pneumonias: HRCT findings that predict mortalityQ46719418
Changes in clinical and physiologic variables predict survival in idiopathic pulmonary fibrosisQ47878148
Mortality prediction in idiopathic pulmonary fibrosis: evaluation of computer-based CT analysis with conventional severity measures.Q50553825
Comparison of the quantitative CT imaging biomarkers of idiopathic pulmonary fibrosis at baseline and early change with an interval of 7 months.Q51032061
A clinical study of idiopathic pulmonary fibrosis based on autopsy studies in elderly patients.Q51663744
Fibrotic idiopathic interstitial pneumonia: the prognostic value of longitudinal functional trends.Q51669678
CT analysis of the effect of pirfenidone in patients with idiopathic pulmonary fibrosis.Q53168264
Texture-Based Automated Quantitative Assessment of Regional Patterns on Initial CT in Patients With Idiopathic Pulmonary Fibrosis: Relationship to Decline in Forced Vital Capacity.Q53926010
Forced Vital Capacity in Patients with Idiopathic Pulmonary FibrosisQ56751555
Marginal decline in forced vital capacity is associated with a poor outcome in idiopathic pulmonary fibrosisQ56905474
Adjusting multiple testing in multilocus analyses using the eigenvalues of a correlation matrixQ57121444
Improving Survival in Idiopathic Pulmonary Fibrosis: The Race Has Just BegunQ89455552
Determinants of survival in idiopathic pulmonary fibrosisQ23911353
Prognostic implications of physiologic and radiographic changes in idiopathic interstitial pneumoniaQ28207419
The rising incidence of idiopathic pulmonary fibrosis in the U.KQ28236424
Efficacy and safety of nintedanib in idiopathic pulmonary fibrosisQ28240230
A phase 3 trial of pirfenidone in patients with idiopathic pulmonary fibrosisQ28240241
Computed tomography findings in pathological usual interstitial pneumonia: relationship to survivalQ28255594
Interpretative strategies for lung function testsQ28279970
An official ATS/ERS/JRS/ALAT statement: idiopathic pulmonary fibrosis: evidence-based guidelines for diagnosis and managementQ28308246
Incidence, prevalence, and clinical course of idiopathic pulmonary fibrosis: a population-based studyQ33577359
Incidence and prevalence of idiopathic pulmonary fibrosisQ33997249
Efficacy of a tyrosine kinase inhibitor in idiopathic pulmonary fibrosisQ34223462
Radiological versus histological diagnosis in UIP and NSIP: survival implications.Q35535697
Epidemiology of Idiopathic Pulmonary Fibrosis in Northern ItalyQ35913543
Evaluation of computer-based computer tomography stratification against outcome models in connective tissue disease-related interstitial lung disease: a patient outcome studyQ36201461
Idiopathic Pulmonary Fibrosis: Gender-Age-Physiology Index Stage for Predicting Future Lung Function DeclineQ37094687
Quantitative computed tomography imaging of interstitial lung diseasesQ37363128
Future directions in idiopathic pulmonary fibrosis research. An NHLBI workshop reportQ37698325
Clinical Course and Prediction of Survival in Idiopathic Pulmonary FibrosisQ37799183
Long-term course and prognosis of idiopathic pulmonary fibrosis in the new millenniumQ37897776
Idiopathic pulmonary fibrosis: early detection and referralQ38205617
Global incidence and mortality of idiopathic pulmonary fibrosis: a systematic review.Q38481710
Idiopathic Pulmonary Fibrosis: The Association between the Adaptive Multiple Features Method and Fibrosis OutcomesQ39262934
Automated Quantitative Computed Tomography Versus Visual Computed Tomography Scoring in Idiopathic Pulmonary Fibrosis: Validation Against Pulmonary FunctionQ39709865
Analyses of efficacy end points in a controlled trial of interferon-gamma1b for idiopathic pulmonary fibrosis.Q40454070
Physiology is a stronger predictor of survival than pathology in fibrotic interstitial pneumonia.Q40455979
P433issue6
P407language of work or nameEnglishQ1860
P921main subjectpulmonary fibrosisQ32446
automationQ184199
idiopathic pulmonary fibrosisQ2290446
P304page(s)767-776
P577publication date2018-09-01
P1433published inAmerican Journal of Respiratory and Critical Care MedicineQ4744267
P1476titlePredicting Outcomes in Idiopathic Pulmonary Fibrosis Using Automated Computed Tomographic Analysis
P478volume198

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cites work (P2860)
Q92041717Automated Parenchymal Pattern Analysis of Treatment Responses in Pulmonary Alveolar Proteinosis
Q92931424Bacterial burden in the lower airways predicts disease progression in idiopathic pulmonary fibrosis and is independent of radiological disease extent
Q93099100Computer-Aided Diagnosis of Pulmonary Fibrosis Using Deep Learning and CT Images
Q92459477Experimental and quantitative imaging techniques in interstitial lung disease
Q90193612High-Resolution CT Change over Time in Patients with Idiopathic Pulmonary Fibrosis on Antifibrotic Treatment
Q64062461High-Resolution Computed Tomography (HRCT) Reflects Disease Progression in Patients with Idiopathic Pulmonary Fibrosis (IPF): Relationship with Lung Pathology
Q91923174Idiopathic Pulmonary Fibrosis: Best Practice in Monitoring and Managing a Relentless Fibrotic Disease
Q58735224Investigating the effects of nintedanib on biomarkers of extracellular matrix turnover in patients with IPF: design of the randomised placebo-controlled INMARK®trial
Q92732127Longitudinal prediction of outcome in idiopathic pulmonary fibrosis using automated CT analysis
Q91436674Lung transplantation for idiopathic pulmonary fibrosis
Q58592165Mediastinal Lymphadenopathy in Interstitial Lung Disease: Time to Be Counted
Q91882642New Developments in Imaging Idiopathic Pulmonary Fibrosis With Hyperpolarized Xenon Magnetic Resonance Imaging
Q60921512Predicting outcomes in rheumatoid arthritis related interstitial lung disease
Q58608704Quantitative CT analysis using functional imaging is superior in describing disease progression in idiopathic pulmonary fibrosis compared to forced vital capacity
Q64257982Quantitative CT-derived vessel metrics in idiopathic pulmonary fibrosis: A structure-function study
Q58797780Statin as a novel pharmacotherapy of pulmonary alveolar proteinosis
Q89476441Stratification of long-term outcome in stable idiopathic pulmonary fibrosis by combining longitudinal computed tomography and forced vital capacity

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