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DIAGNOSIS & TREATMENT OF
COPD
Presented by
Dr.J A DEVA (PG-1)
SPIROMETRY
• Spirometry measurements are evaluated by comparison of results with appropriate reference
values based on age ,height,sex and race.
• The presence of post bronchodilator FEV1/FVC < 0.7 confirms the presence of non - fully
reversible airflow obstruction .
• Patients already on bronchodilator treatment in whom spirometry is requested for monitoring
purposes do not need to stop their regular treatment .
• 400mcg SABA or 160mcg short acting anticholinergic or a combination of both can be used.
• Spirometry is done 10-15 mins after administration of SABA or 30-45 mins after anticholinergics.
• Category E - has two more
sub-categories
- C (Moderate to severe
exacerbation history with
mMRC 0-1 or CAT < 10 )
- D (Moderate to severe
exacerbation history with
mMRC >2 or CAT >= 10 )
• The combined COPD assesment allows patients with same FEV1 to be
diffrentiated based on symptomatology
• For eg,
- A subject with FEV1 < 30 % with an mMRC of 2 & 3 exacerbations
in the past year would be labled GOLD GRADE 4 , group D
- Wheras a subject with FEV1 < 30% with an mMRC of 1 & 0
exacerbations in the past year would be labled GOLD GRADE 4 ,
group A
• Non specific xray findings.
• Tubular heart.
• Increased rib spaces.
• Saber sheath trachea &
B/L Hyperinflated lungs
HRCT CHEST
• In chronic bronchitis, bronchial wall thickening may
be seen in addition to enlarged vessels. Repeated
inflammation can lead to scarring with
bronchovascular irregularity and fibrosis.
• Emphysema is diagnosed by alveolar septal
destruction and airspace enlargement, which may
occur in a variety of distributions.
• for COPD patients with persistent exacerbations,
symptoms out of proportion to disease severity on lung
function testing, FEV1 less than 45% predicted with
significant hyperinflation or for those who meet
criteria for lung cancer screening, chest CT imaging
should be considered.
• Also helps to rule out any infective causes for the
symptoms.
Alpha1 antitrypsin levels.
• WHO recommends screening for alpha 1 antitrypsin for all COPD
patients especially in endemic areas.
• Normal ranges b/w 75 - 150 mg/dl
• Alpha-1 antitrypsin deficiency is associated with the development of
COPD , where as increased levels of serum alpha-1 antitrypsin occur
in response to inflammation.
• so in Non-COPD patients , it is a risk factor, whereas in lung diseases
it is a marker of extend of lung damage.
SEVERITY OF COPD
• The early stages of COPD, based on the severity of airflow obstruction it is primarily
associated with medium and small airway disease .
• It is indicated by the majority of Global Initiative for Chronic Obstructive Lung Disease
(GOLD) spirometric airflow obstruction stage 1 and stage 2 subjects demonstrating little
or no emphysema.
• The early development of chronic airflow obstruction is driven by small airway disease.
• Advanced stages of COPD (GOLD stages 3 and 4) are typically characterized by
extensive emphysema.
• The subjects at greatest risk of progression in COPD are those with both aggressive
airway disease and emphysema.
• Thus, finding emphysema (by CT) either early or late in the disease process suggests
enhanced risk for disease progression.
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DIAGNOSIS AND TREATMENT OF COPD.pptx

  • 1. DIAGNOSIS & TREATMENT OF COPD Presented by Dr.J A DEVA (PG-1)
  • 2.
  • 3. SPIROMETRY • Spirometry measurements are evaluated by comparison of results with appropriate reference values based on age ,height,sex and race. • The presence of post bronchodilator FEV1/FVC < 0.7 confirms the presence of non - fully reversible airflow obstruction . • Patients already on bronchodilator treatment in whom spirometry is requested for monitoring purposes do not need to stop their regular treatment . • 400mcg SABA or 160mcg short acting anticholinergic or a combination of both can be used. • Spirometry is done 10-15 mins after administration of SABA or 30-45 mins after anticholinergics.
  • 4.
  • 5.
  • 6.
  • 7.
  • 8.
  • 9. • Category E - has two more sub-categories - C (Moderate to severe exacerbation history with mMRC 0-1 or CAT < 10 ) - D (Moderate to severe exacerbation history with mMRC >2 or CAT >= 10 )
  • 10. • The combined COPD assesment allows patients with same FEV1 to be diffrentiated based on symptomatology • For eg, - A subject with FEV1 < 30 % with an mMRC of 2 & 3 exacerbations in the past year would be labled GOLD GRADE 4 , group D - Wheras a subject with FEV1 < 30% with an mMRC of 1 & 0 exacerbations in the past year would be labled GOLD GRADE 4 , group A
  • 11. • Non specific xray findings. • Tubular heart. • Increased rib spaces. • Saber sheath trachea & B/L Hyperinflated lungs
  • 12. HRCT CHEST • In chronic bronchitis, bronchial wall thickening may be seen in addition to enlarged vessels. Repeated inflammation can lead to scarring with bronchovascular irregularity and fibrosis. • Emphysema is diagnosed by alveolar septal destruction and airspace enlargement, which may occur in a variety of distributions. • for COPD patients with persistent exacerbations, symptoms out of proportion to disease severity on lung function testing, FEV1 less than 45% predicted with significant hyperinflation or for those who meet criteria for lung cancer screening, chest CT imaging should be considered. • Also helps to rule out any infective causes for the symptoms.
  • 13. Alpha1 antitrypsin levels. • WHO recommends screening for alpha 1 antitrypsin for all COPD patients especially in endemic areas. • Normal ranges b/w 75 - 150 mg/dl • Alpha-1 antitrypsin deficiency is associated with the development of COPD , where as increased levels of serum alpha-1 antitrypsin occur in response to inflammation. • so in Non-COPD patients , it is a risk factor, whereas in lung diseases it is a marker of extend of lung damage.
  • 14. SEVERITY OF COPD • The early stages of COPD, based on the severity of airflow obstruction it is primarily associated with medium and small airway disease . • It is indicated by the majority of Global Initiative for Chronic Obstructive Lung Disease (GOLD) spirometric airflow obstruction stage 1 and stage 2 subjects demonstrating little or no emphysema. • The early development of chronic airflow obstruction is driven by small airway disease. • Advanced stages of COPD (GOLD stages 3 and 4) are typically characterized by extensive emphysema. • The subjects at greatest risk of progression in COPD are those with both aggressive airway disease and emphysema. • Thus, finding emphysema (by CT) either early or late in the disease process suggests enhanced risk for disease progression.
  • 15.
  • 16.
  • 17.
  • 18.
  • 19.
  • 20.
  • 21.
  • 22.
  • 23.
  • 24.
  • 25.
  • 26.
  • 27.
  • 28.
  • 29.