interstitial lung disease - an approach to diagnosis and ... · approach to diagnosis and...
TRANSCRIPT
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Approach to Diagnosis and Management of Interstitial Lung Disease : Changing Landscape
Girish B. Nair MD, FACP, FCCP
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No Conflicts Of Interest
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Objectives
1. Review the diagnostic approach to a patient with ILD
2. Identify the indications for surgical lung biopsy
3. Recognize the newer treatment options available for Idiopathic Pulmonary Fibrosis
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Murray & Nadel’s Textbook of Respiratory Medicine- 6th Edition
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Exposures• Drugs
• Hypersensitivity pneumonitis – bird, molds
• Radiation
• Infections
Connective tissue Diseases
• Rheumatoid arthritis
• Lupus
• Scleroderma
• Sjogren’s syndrome
• Mixed connective tissue disease
Idiopathic• Sarcoidosis
• IIP
Genetic
• FPF
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Interstitial Lung Diseases
ILD of Known Cause or Association
Medications
Radiation
Connective Tissue Disease
Vasculitis & DAH
Hypersensitivity Pneumonitis
Pneumoconioses
Idiopathic Interstitial
Pneumonias
Sarcoidosis & Other
Granulomatous Diseases
Other
LAM
Pulmonary LCH
Eosinophilic Pneumonias
Alveolar Proteinosis
Genetic Syndromes
ATS/ERS Guidelines for IIP. AJRCCM. 2002;165:277-304.
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Major idiopathic interstitial pneumonias
Idiopathic pulmonary fibrosisIdiopathic nonspecific interstitial pneumoniaRespiratory bronchiolitis–interstitial lung diseaseDesquamative interstitial pneumoniaCryptogenic organizing pneumoniaAcute interstitial pneumonia
Rare idiopathic interstitial pneumonias
Idiopathic lymphoid interstitial pneumoniaIdiopathic pleuroparenchymal fibroelastosis
Unclassifiable idiopathic interstitial pneumonias*
REVISED ATS/ERS CLASSIFICATION OF IDIOPATHIC INTERSTITIAL PNEUMONIAS: MULTIDISCIPLINARY DIAGNOSES
W Travis . AJRCCM 2013;188,733–748
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Disease Mechanisms
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S. Puglisi. Semin Respir Crit Care Med 2016;37,358–367.
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Genetics
Fingerlin et al Nat Genet. 2013; 45, 613–620
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Influences of Innate Immunity
D. O’Dwyer. Am J Physiol Lung Cell Mol Physiol (July 29, 2016)
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Molyneaux. AJRCCM 2014; 190, 906–913
Role of Bacteria in the Pathogenesis and Progression of IPF
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M. Han, F. Martinez. Lancet Respir Med 2014; 2, 548–556
Lung Microbiome
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Diagnosis
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Fibrotic lung disease
Hypersensitivity pneumonia Interstitial
pneumonia with Auto immune features
Connective tissue disease related ILD
Granulomatous
FamilialLAM, PLCH
Idiopathic Interstitial pneumonias
Drug induced ILD
Radiation related ILD
Infections
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King TE. Lancet 2011; 378, 1949–61
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Delayed Access to subspecialty and Survival in IPF
Lamas. AJRCCM 2011; 184, 842–847
• Prospective cohort study of 129 adults
• Onset of dyspnea to be seen at tertiary care center
• A longer delay was associated with an increased risk of deathindependent of age, sex, forced vital capacity, third-party payer, and educational attainment
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Jay Ryu. Mayo Clin Proc 2002;77,1221-27
Interstitial Lung Disease
• Clinical context
• Tempo or evolution of the disease
• Radiographic pattern
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Clinical presentation
• ‘I am feeling tired than usual’• ‘I used to walk several blocks – but can’t anymore’• ‘Have this dry cough’• Examination may show clubbing and inspiratory bibasilar “velcro-like”
crackles on auscultation
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Physical Examination
Fusiform SwellingSymmetry
Ulnar DeviationSwan Neck Deformity
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Mixed Connective Tissue Disease Puffy hands (polyarthritis)Raynaud’s phenomenonLow blood countsMyositis- muscle disease
Sjogren’s SyndromeDry Eyes Dry Mouthsalivary/parotid swelling
SclerodermaSkin thickening Joint and tendon contracturesRaynaud’sDistal skin thickeningCalcinosisTelangiectasia
Polymyositis/DermatomyositisSymmetric, proximal muscle weaknessDermatologic findings
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Serological Evaluation
• Performed before surgical biopsy• 1 step: ANA, RF, CCP, ESR, CRP, Hypersensitivity pneumonitis panel• Based on history & physical exam: Extractable nuclear antigen (ENA) autoantibody panel Anti-centromere antibodyMPO/PR3 (ANCA) antibodies Anti-cardiolipin antibodies, lupus anticoagulant Creatine kinase, aldolase
Pulmonary Function studySix minute walk testEchocardiogram
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All Four Features
• Sub pleural, basal predominance
• Reticular abnormality
• Honeycombing with or without traction bronchiectasis
• Absence of features listed as inconsistent with UIP pattern
AJRCM. 2011; 183,788–824
UIP Pattern
Inconsistent with UIP Pattern – Any of the 7 featuresUpper or mid-lung predominancePeribronchovascular predominanceExtensive ground glass abnormality (extent > reticular abnormality)Profuse micronodules (bilateral, predominantly upper lobes)Discrete cysts (multiple, bilateral, away from areas of honeycombingDiffuse mosaic attenuation/air-trapping (bilateral, in three or more lobes)Consolidation in bronchopulmonary segment(s)/lobe(s)
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UIP Pattern
AJRCM. 2011; 183.788–824
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AJRCM. 2011; 183,788–824
NSIP Pattern
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Honeycombing in UIP
• Present in 70-80% of cases of UIP
Strongest indicator of UIP on CT
• Median survival
UIP with honeycombing: 2.1 years UIP without honeycombing: 5.8 years
Hunninghake GW, et al. Chest 2003;124:1215-1223. Elliot TL. J Comput Assist Tomogr 2005;29:339-345. Flaherty KR, et al. Thorax 2003;58:143-148.
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Mortality HRCT diagnosis compared to surgical lung biopsy diagnosis of UIP
5-year survival in monthshistological vs. radiological diagnosis
45.4 vs. 34.6%; p = 0.799
Quadrelli Respiration 2010;79,32–37
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Surgical biopsy – it is important to sample multiple lobes
• SLBs from 168 patients
• 109 patients multiple lobes biopsied
• Reviewed by three pathologists
• Significant intrapatient heterogeneity
• Prognosis in patients with at least one lobe positive for UIP worse compared to non-UIP pattern
Flaherty AJRCCM 2001;164, 1722–27
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Diagnosis of idiopathic pulmonary fibrosis with high-resolution CT in patients with little or no radiological evidence of honeycombing
G Raghu. Lancet Respir Med 2014; 2, 277–84
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Multidisciplinary approach To IIP Diagnosis
• 58 suspected IIP
• 3 clinicians, 2 radiologists, 2 pathologists
• Information in sequential manner
• Clinicians identified 75% and radiologists 48% of IPF prior to histopathologicinformation was provided
• Dynamic interactions between specialists improve inter-observer agreement and diagnostic confidence
Flaherty, King, Raghu. AJRCCM 2004;170,904–910
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Ryerson. Eur Respir J 2013; 42, 750–757
Unclassifiable Idiopathic Interstitial Pneumonia
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IPAF Interstitial Pneumonitis with Autoimmune Features
1) ILD by HRCT or Lung Bx2) Other etiologies for ILD excluded3) Does not meet criteria for AI Dz4) 1 feature from @ least 2/3 Domains
– Clinical– Serologic– Morphologic (HRCT or Lung Bx)
Fischer A, Antoniou KM, Brown KK, et al. Eur Respir J 2015
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Walsh S. Lancet Respir Med 2016; 4, 557-65
Multicenter Evaluation of Multidisciplinary Meeting
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History + Exam + Labs + PFT + CXR
Confident Diagnosis
CT chest
NoSarcoid, Pneumoconiosis, Infection
Yes
IPF, HP, LAM
Does CT pattern suggest BAL +TBLB will be useful?Yes
Sarcoidosis, COP, HP, PAP, Malignancy
Can patient have surgical lung biopsy?
Confident Diagnosis
Confident Diagnosis
Confident Diagnosis Diagnosis of highest probability
Yes
Multi – Disciplinary Discussion
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Newer Modalities of Diagnosis
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Casoni. PloS one 2014;9:e86716
Trans-bronchial Lung Cryobiopsy
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Differentiating UIP based on Transcriptional Data
Kim. Lancet Respir Med 2015, 3(6):473-82
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SPECT/CT Imaging using Integrins
John. AE J Nucl Med 2013; 54,2146–2152
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Noninvasive Imaging of Experimental Lung Fibrosis
• Micro-CT• Proton MRI • Hyperpolarized Gas–Enhanced MRI • Respiratory-Gated and Self-Gated MRI • PET and PET/CT Imaging of Proline Uptake • PET/CT and SPECT/CT Imaging of Receptors on the Cell Surface
Zhou Y. Am J Respir Cell Mol Biol 2015; 53,8–13
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Early Diagnosis
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HIGH ATTENUATION ON CT – SMOKING & RESTRICTION ON SPIROMETRY
Lederer. AJRCCM 2009 ;180, 407–414.
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Putman, Rosas, Hunninghake. Am J Respir Crit Care Med 2014;189,770–78
Subclinical Interstitial Lung Disease
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Early Diagnosis• CT scan of 884
smokers lung cancer screening
• ILA 9.7%- 2.1% fibrotic,5.9% non fibrotic
• 2 years non-fibrotic ILA improved 48.9%, while fibrotic did not improved in anyone and progressed in 36.8%.
Gong Yong Jin. Radiology 268: August 2013
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Interstitial Lung Abnormalities and MUC5B Genotype in the Framingham Heart Study
Hunninghake. N Engl J Med 2013;368,2192-200
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Putman. JAMA 2016;315,672-681
Association Between ILA
and All-Cause Mortality
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Doyle, Rosas, Hunninghake. Am J Respir Crit Care Med 2012(185)1147–1153Putman, Rosas, Hunninghake. Am J Respir Crit Care Med 2014 (189)770–78
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Disease Predictors
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Raghu. AJRCCM 2011,183,431–440
IPF – Predictors of Survival
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GAP Index
Ley. Ann Intern Med 2012;156,684–91Ryerson CJ. Chest 2014 Apr;145,723-8
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Ley B. AJRCCM Mar 2016
Predictors of Mortality are Poor Predictors of Disease Progression
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Personalized Medicine
Biomarker– Identify patients at risk of progression– More accurate and less invasive diagnostic tool– Response to treatment– Prediction of disease outcome
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Am J Physiol Lung Cell Mol Physiol 2014 ;307(9)
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Alveolar Epithelial Cell DysfunctionSurfactant ProteinsKrebs Von Den Lungen-6/Mucin 1MUC5BTelomeresCaspase-Cleaved Cytokeratin-18
Immune DysregulationInnate Immunity
Toll-like Receptor 3Toll-Interacting Protein
Alveolar Macrophage ActivationCC Chemokine Ligand 18S100A12
Adaptive ImmunityAnti-HSP70 AntibodiesC-X-C Motif Chemokine 13Costimulatory Signal During T Cell ActivationSemaphorin 7a
Microbiome
Extracellular Matrix Remodeling and Fibroproliferation
Matrix MetalloproteinasesMatrix Metalloproteinase-Degraded Extracellular Matrix ProteinsLysyl Oxidase-like Protein-2
Epigenetic Markers
Metabolomics
Spagnolo. Curr Opin Pulm Med 2015;21,470-478
BIOMARKERS FOR OUTCOME IN BLOOD AND BRONCHOALVEOLAR LAVAGE -HIGHER LEVELS PREDICTING POOR SURVIVAL
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Song CHEST 2013; 143(5):1422–1429
MMP-7, KL-6 and SP-A as Predictors of Outcome
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Treatment Targets
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Maher TM. Clin Chest Med 2012,33,69-83.
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NEGATIVE TRIALS IN IPF
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King TE Jr et al. N Engl J Med 2014;370:2083-2092
ASCEND Study
King TE, et al. N Engl J Med 2014;370,2083-92.
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King TE, et al. N Engl J Med 2014;370, 2083-2092.
Patie
nts w
ith ≥
10%
FVC
De
clin
e or
Dea
th (%
)
Week
Primary Endpoint
48% Relative
Reduction
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Richeldi L et al. N Engl J Med 2014;370:2071-2082
INPULSIS Trials
Richeldi L, et al. N Engl J Med 2014;370,2071-2082.
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Annual Rate of Change of FVC
Richeldi L, et al. N Engl J Med 2014;370, 2071-2082.
INPULSIS-1 INPULSIS-2
45% RelativeReduction
Nintedanib Placebo
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Treatment of IPF: Systematic Review and Network Meta-Analysis
W. Canestaro, G. Raghu CHEST 2016
Decrease in Percent Predicted FVC by =10%
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N. Ahluwalia. AJRCCM, 2014, 190, 867–878
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Agent Potential mechanism
of action
Clinical trial
registry number
Study design Endpoints Outcomes
GC1008 Anti-TGFβ antibodyNCT00125385 Phase I study ,non-
randomized , open
label, single group
assignment (n=25)
Primary end point : Safety and
tolerability
Completed.
Awaiting results.
BG00011 (formerly known as STX-100)
Anti-αvβ6 integrin NCT01371305
Phase II study, randomized, placebo-controlled
Primary end point: Safety and tolerability
Trial ongoing.
FG-3019 Connective tissue growth factor inhibitor
NCT01890265 Phase II, randomized, placebo-controlled study
Primary end point: Change from baseline in FVC (percent of predicted value) at Week 48
Trial ongoing.
PBI-4050 Connective tissue growth factor and collagen I mRNA expression inhibitor NCT02538536 Phase II, open-label,
Single-arm studyPrimary end point: Safety and tolerability
Trial ongoing.
CNTO 888 (Carlumab) Anti-CCL2 antibody NCT00786201 Phase II randomized, placebo-controlled study
Primary end points: Safety and efficacy Trial completed. No benefit on IPF.
QAX576 Anti-IL-13 antibody NCT00532233 Phase II ,open label study (n=50)
Primary end point: IL-13 serum levels Secondary end point: change in designated serum biomarkers
Completed. Awaiting results.
NCT01266135 Phase II, randomized, Double-blind, Placebo-controlled study.
Primary end point: Safety, tolerability, and effect on lung function.Change in forced vital capacity (FVC)
Trial terminated.
Nair GB, Expert Rev Respir Med 2016;10, 699-711
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Tralokinumab Anti-IL-13 antibody NCT01629667 Phase II study, prospective, double-blinded, randomized placebo-controlled; (n=186)
Primary end point: Absolute change from baseline in percent predicted forced vital capacity ( FVC) Trial ongoing
Lebrikizumab Anti-IL-13 antibody NCT01872689 Phase II, randomized, multicenter, double-blind, placebo-controlled, parallel-group study
Primary end point: Absolute change from baseline in percent predicted forced vital capacity (FVC) Trial ongoing.
SAR156597 Anti-IL-13 and IL-4 antibody
NCT01529853 Phase II study, prospective, double-blinded, randomized placebo-controlled study
Primary end point: Safety and tolerability Secondary end point: change in FVC, DlCO and dyspnea score from baseline
Completed.
Awaiting results.
NCT02345070 Phase II, randomized, double-blind, placebo-controlled study
Primary end point: Efficacy and Safety Absolute change from baseline in percent predicted FVC at 52 weeks
Secondary end points:-Proportion of patients with disease progression.-Number of deaths ( All causes)
Trial ongoing.
BMS-986020 Lysophosphatidic Acid receptor antagonist
NCT01766817Phase II, randomized, placebo-controlled study
Primary end point: safety and efficacy Rate of change in forced vital capacity
Trial ongoing
Simtuzumab (GS-
6624)Anti-LOXL2 antibody NCT01362231 Part A: Phase I,
randomized, placebo-controlled.Part B: Phase I randomized, open label.
Primary end point: Safety, tolerability and pharmacokinetics.
Sponsor aborted trial after interval Data monitoring Committee report
NCT01769196 Phase 2 randomized, placebo-controlled, multicenter study.
Primary end point: progression free survival defined as all –cause mortality or decrease in percent predicted in FVC
Secondary end point: All-cause mortality.
Trial ongoing.
Nair GB, Expert Rev Respir Med 2016;10, 699-711
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PRM-151 An anti-fibrotic
and
immunomodulator
NCT02550873 Phase 2, randomized, double-
blind, placebo controlled, pilot
study .
Primary end point: Safety and efficacy.
Forced vital capacity (FVC) percent predicted change from
baseline.
Trial ongoing.
GSK2126458(Omipalisib)
PI3Kα and mTOR
inhibitor
NCT01725139
Phase I randomized, placebo-
controlled study.
Primary end point: pharmacodynamics measured by inhibition of
pAKT/AKT in platelet-rich plasma and BAL cells and inhibition of
glucose uptake measured by thoracic PET/CT
Trial ongoing.
Sirolimus mTOR inhibitor NCT01462006 Randomized, double-blind,
placebo-controlled pilot study
Primary end point:
- Fibrocytes change in peripheral blood concentration of CXCR4+
fibrocytes
-Number of subjects with drug side-effects
Nair GB, Expert Rev Respir Med 2016;10, 699-711
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Disease Specific TreatmentScleroderma – MMF vs. Cytoxan
Rheumatoid ArthritisTreatment with anti-inflammatory and/or immunosuppressive agents is recommended regardless of the pattern of fibrosis
Corticosteroids Cyclophosphamide AzathioprineMycophenalate
Tashkin. N Engl J Med 354:2655–2666, 2006Clements 2015 ACR/ARHP Annual MeetingAnn Rheum Dis 2015 Jun;74(6):1188-94
Fischer A, J Rheumatol 2013; 40: 640–646.Assayag D Respirology 2014; 19: 493–500
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Non-Pharmacological Treatment
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Non – Pharmacological Therapies
• Long term oxygen therapy
• Mechanical ventilation
• Palliative care
Am J Respir Crit Care Med 183. 788–824, 2011
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Pulmonary rehabilitation
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Non – Pharmacological Therapies
• Altered respiratory mechanics• Impaired gas exchange• Circulatory limitation• Peripheral muscle dysfunction
Pulmonary rehabilitation• Improves 6 minute walk
distance• Decreased dyspnea score• Improved health – related
quality of life
Holland Thorax 2008;63:549–554Nishiyama Respirology 2008; 1: 394–399Am J Respir Crit Care Med 188, e13–e64, Oct 15, 2013
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Vainshelboim B. Exercise training in idiopathic pulmonary fibrosis: is it of benefit? Breathe 2016; 12: 130–138
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Treatment of GERD
Lee. AJRCCM 2011 184. 1390–1394
• Role of chronic microaspiration
• 204 patients with IPF
• Symptoms of GER (34%), a history of GER disease (45%), reported use of GER medications (47%)
• Anti-reflux therapy associated with increased survival and decreased radiological fibrosis score
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Pulmonary Fibrosis Support Group
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Summary