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Guides : Dr. Jitendra Bhargava 
Dr. Sanjay Bharty 
Dr. Brahma Prakash 
By-DR ANKUR KAUSHIK
 COPD, a common preventable and treatable disease, 
is characterized by persistent airflow limitation that 
is usually progressive and associated with an 
enhanced chronic inflammatory response in the 
airways and the lung to noxious particles or gases. 
 Exacerbations and comorbidities contribute to the 
overall severity in individual patients. 
Definition from GOLD 2014
 COPD is a leading cause of morbidity and mortality worldwide. COPD 
also accounts for more than 3 million deaths per year globally making it the 
third leading cause of death worldwide. According to World Health 
Organization estimates, 400 million people worldwide suffers from COPD. 
The estimated burden of COPD in India is about 15 million cases (males 
and females contributing to 9.02 and 5.75 million, respectively). 
 In India, according to INSEARCH I and II trials, prevalence of COPD 
is 3.67% (4.46 and 2.86% among males and females, respectively).The 
prevalence was found to be increasing with an increase in age. 
 The burden of COPD is projected to increase in coming decades due to 
continued exposure to COPD risk factors and the aging of the world’s 
population. it is estimated to be the third leading cause of death by 2030. 
Data from Guidelines for diagnosis and management of chronic obstructive pulmonary disease: Joint 
ICS/NCCP (I) recommendations 2013
AIRFLOW 
LIMITATION 
Small Airways Disease 
• Airway inflammation 
• Airway fibrosis, 
luminal plugs 
• Increased airway 
resistance 
Parenchymal 
Destruction 
• Loss of alveolar 
attachments 
• Decrease of elastic 
recoil
Picture from Gold 2014 updates 
Professor Peter J. Barnes, MD 
National Heart and Lung Institute, London UK
• Genes 
• Exposure to particles 
 Tobacco smoke 
 Occupational dusts, organic 
and inorganic 
 Indoor air pollution from 
heating and cooking with 
biomass in poorly ventilated 
dwellings 
 Outdoor air pollution 
• Lung growth and development 
• Gender 
• Age 
• Respiratory infections 
• Socioeconomic status 
• Asthma/Bronchial hyperactivity 
• Chronic Bronchitis
The goals of COPD assessment are to 
determine 
 the severity of the disease, 
including the severity of airflow limitation. 
 The impact on the patient’s 
health status, and the risk of future 
events. 
 Comorbidities that occur frequently in COPD 
patients, and should be actively looked 
for and treated appropriately if present.
Chronic cough Present intermittently or every day, often 
present throughout 
the day 
Chronic sputum 
production 
Any pattern of sputum production may 
indicate COPD 
Acute bronchitis Repeated episodes 
Dyspnea that is Progressive, persistent, worse on exercise, 
worse during 
respiratory infections 
History of exposure 
to risk factors 
Smoke, biomass fuel, occupational dusts 
The diagnosis should be 
confirmed by Spirometry
Diagnosis of COPD 
SYMPTOMS 
• shortness of breath 
• chronic cough 
• sputum 
EXPOSURE 
TO RISK 
FACTORS 
• Tobacco 
• Occupation 
• indoor/outdoor 
pollution 
SPIROMETRY: Required 
to establish diagnosis
ASSESSMENT OF COPD 
Assess symptoms 
Assess risk of exacerbations 
Assess degree of airflow limitation using 
spirometry
 COPD Assessment Test (CAT) 
 Clinical COPD Questionnaire (CCQ) 
 mMRC Breathlessness scale
 COPD Assessment Test (CAT): An 8-item measure of 
health status impairment in COPD 
(http://catestonline.org). 
 Clinical COPD Questionnaire (CCQ): Self-administered 
questionnaire developed to measure clinical 
control in patients with COPD (http://www.ccq.nl). 
 Breathlessness Measurement using the Modified 
British Medical Research Council (mMRC) 
Questionnaire: relates well to other measures of health 
status and predicts future mortality risk
CAT SCORE
 Spirometry should be performed after the 
administration of an adequate dose of a short acting 
inhaled bronchodilator to minimize variability. 
 A post-bronchodilator FEV1/FVC < 0.70 confirms the 
presence of airflow limitation. 
 Where possible, values should be compared to age-related 
normal values to avoid over diagnosis of COPD 
in the elderly.
We use spirometry for grading severity according to spirometry, using four 
grades split at 80%, 50% and 30% of predicted value 
Classification of Severity of Airflow Limitation in COPD* 
In patients with FEV1/FVC < 0.70: 
 GOLD 1: Mild FEV1 > 80% predicted 
 GOLD 2: Moderate 50% < FEV1 < 80% predicted 
 GOLD 3: Severe 30% < FEV1 < 50% predicted 
 GOLD 4: Very Severe FEV1 < 30% predicted 
*Based on Post-Bronchodilator FEV1
To assess risk of exacerbations use history of 
exacerbations and spirometry: 
• Two or more exacerbations within the last year or an 
FEV1 < 50 % of predicted value are indicators of high 
risk. 
• One or more hospitalizations for COPD exacerbation 
should be considered high risk.
Patient Characteristic Spirometry 
Classification 
Exacerbations per 
year 
CAT mMRC 
A Low Risk 
Less Symptoms 
GOLD 1-2 ≤ 1 < 10 0-1 
B Low Risk 
More Symptoms 
GOLD 1-2 ≤ 1 > 10 > 2 
C High Risk 
Less Symptoms 
GOLD 3-4 > 2 < 10 0-1 
D High Risk 
More Symptoms 
GOLD 3-4 > 2 > 10 > 2
COPD patients are at increased risk for: 
 Cardiovascular diseases 
 Osteoporosis 
 Respiratory infections 
 Anxiety and Depression 
 Diabetes 
 Lung cancer 
 Bronchiectasis
Chest X-ray: Valuable to exclude alternative diagnoses and 
establish presence of significant comorbidities. 
Lung Volumes and Diffusing Capacity: Help to 
characterize severity. 
Oximetry and Arterial Blood Gases: Pulse oximetry can be 
used to evaluate a patient’s oxygen saturation and need for 
supplemental oxygen therapy. 
Alpha-1 Antitrypsin Deficiency Screening: Perform when 
COPD develops in patients of Caucasian descent under 45 
years or with a strong family history of COPD.
Exercise Testing: Objectively measured exercise 
impairment, assessed by a reduction in self-paced 
walking distance (such as the 6 min walking test) or 
during incremental exercise testing in a laboratory, is a 
powerful indicator of health status impairment and 
predictor of prognosis.
• Smoking cessation has the greatest capacity to influence the natural 
history of COPD. Health care providers should encourage all 
patients who smoke to quit. 
• Pharmacotherapy and nicotine replacement reliably increase long-term 
smoking abstinence rates. 
• All COPD patients benefit from regular physical activity and 
should repeatedly be encouraged to remain active. 
• Appropriate pharmacologic therapy can reduce COPD symptoms, 
reduce the frequency and severity of exacerbations, and improve 
health status and exercise tolerance. 
• Influenza and pneumococcal vaccination should be offered 
depending on local guidelines.
Beta2-agonists 
Short-acting beta2-agonists 
Long-acting beta2-agonists 
Anticholinergic 
Short-acting anticholinergic 
Long-acting anticholinergic 
Combination short-acting beta2-agonists + anticholinergic in one inhaler 
Combination long-acting beta2-agonists + anticholinergic in one inhaler 
Methylxanthines 
Inhaled corticosteroids 
Combination long-acting beta2-agonists + corticosteroids in one inhaler 
Systemic corticosteroids 
Phosphodiesterase-4 inhibitors
 Bronchodilator medications are central to the 
symptomatic management of COPD. 
 The principal bronchodilator treatments are beta2 
agonists, anticholinergic, theophylline or 
combination therapy. 
 The choice of treatment depends on the availability 
of medications and each patient’s individual response 
in terms of symptom relief and side effects.
 Regular treatment with inhaled corticosteroids improves 
symptoms, lung function and quality of life and reduces 
frequency of exacerbations for COPD patients with an FEV1 
< 60% predicted.
 An inhaled corticosteroid combined with a long-acting 
beta2-agonist is more effective than the 
individual components in improving lung function 
and health status and reducing exacerbations in 
moderate to very severe COPD. 
 Addition of a long-acting beta2-agonist/inhaled 
glucorticosteroid combination to an anticholinergic 
(tiotropium) appears to provide additional benefits.
 Theophylline is less effective and less well tolerated than 
inhaled long-acting bronchodilators and is not 
recommended if those drugs are available and affordable. 
 There is evidence for a modest bronchodilator effect and 
some symptomatic benefit compared with placebo in stable 
COPD. Addition of theophylline to salmeterol produces a 
greater increase in FEV1 and breathlessness than 
salmeterol alone. 
 Low dose theophylline reduces exacerbations but does not 
improve post-bronchodilator lung function.
 Chronic treatment with systemic corticosteroids 
should be avoided because of an unfavorable benefit-to- 
risk ratio.
 First novel therapy for COPD in nearly 20 years. 
 In patients with severe and very severe COPD 
(GOLD 3 and 4) and a history of exacerbations and 
chronic bronchitis, it’s a selective phospodiesterase-4 
inhibitor, roflumilast, reduces exacerbations treated 
with oral glucocorticosteroids. 
 This medication is not a bronchodilator, and it is not 
indicated for the treatment of acute bronchospasm.
 Influenza vaccines can reduce serious illness. Pneumococcal 
polysaccharide vaccine is recommended for COPD patients 65 
years and older and for COPD patients younger than age 65 
with an FEV1 < 40% predicted. 
 The use of antibiotics, other than for treating infectious 
exacerbations of COPD and other bacterial infections, is 
currently not indicated.
 Alpha-1 antitrypsin augmentation therapy: not recommended 
for patients with COPD that is unrelated to the genetic deficiency. 
 Mucolytics: Patients with viscous sputum may benefit from 
mucolytics; overall benefits are very small. Example, n-acetyl 
cystiene. 
 Antitussives: Not recommended. 
 Vasodilators: Nitric oxide is contraindicated in stable COPD. 
The use of endothelium-modulating agents for the treatment of 
pulmonary hypertension associated with COPD is not 
recommended.
 All COPD patients benefit from exercise training programs 
with improvements in exercise tolerance and symptoms of 
dyspnea and fatigue. 
 Although an effective pulmonary rehabilitation program is 6 
weeks, the longer the program continues, the more effective 
the results. 
 If exercise training is maintained at home, the patient's health 
status remains above pre-rehabilitation levels.
 Oxygen Therapy: The long-term administration of oxygen (> 
15 hours per day) to patients with chronic respiratory failure 
has been shown to increase survival in patients with severe, 
resting hypoxemia. 
 Ventilatory Support: Combination of noninvasive 
ventilation (NIV) with long-term oxygen therapy may be of 
some use in a selected subset of patients, particularly in those 
with pronounced daytime hypercapnia.
 Lung volume reduction surgery (LVRS) is more 
efficacious than medical therapy among patients with 
upper-lobe predominant emphysema and low exercise 
capacity. 
 LVRS is costly relative to health-care programs not 
including surgery. 
 In appropriately selected patients with very severe 
COPD, lung transplantation has been shown to 
improve quality of life and functional capacity
• Relieve symptoms 
• Improve exercise tolerance 
• Improve health status 
• Prevent disease progression 
• Prevent and treat exacerbations 
• Reduce mortality
Avoidance of risk factors 
- smoking cessation 
- reduction of indoor pollution 
- reduction of occupational exposure 
Influenza vaccination
 Long-acting formulations of beta2-agonists and 
anticholinergics are preferred over short-acting 
formulations. Based on efficacy and side effects, inhaled 
bronchodilators are preferred over oral bronchodilators. 
 Long-term treatment with inhaled corticosteroids added 
to long-acting bronchodilators is recommended for 
patients with high risk of exacerbations. 
 The phospodiesterase-4 inhibitor roflumilast may be 
useful to reduce exacerbations for patients with FEV1 < 
50% of predicted, chronic bronchitis, and frequent 
exacerbations.
Patient 
Group 
Essential Recommended Depending on local 
guidelines 
A 
Smoking cessation (can 
include pharmacologic 
treatment) 
Physical activity 
Flu vaccination 
Pneumococcal 
vaccination 
B, C, D 
Smoking cessation (can 
include pharmacologic 
treatment) 
Pulmonary rehabilitation 
Physical activity 
Flu vaccination 
Pneumococcal 
vaccination
Patient Recommended 
First choice 
Alternative choice Other Possible 
Treatments 
A 
SAMA prn 
or 
SABA prn 
LAMA 
or 
LABA 
or 
SABA and SAMA 
Theophylline 
B 
LAMA 
or 
LABA 
LAMA and LABA 
SABA and/or SAMA 
Theophylline 
C 
ICS + LABA 
or 
LAMA 
LAMA and LABA or 
LAMA and PDE4- 
inh. or 
LABA and PDE4- 
inh. 
SABA and/or SAMA 
Theophylline 
D 
ICS + LABA 
and/or 
LAMA 
ICS + LABA and 
LAMA or 
ICS+LABA and 
PDE4-inh. or 
LAMA and LABA or 
LAMA and PDE4- 
inh. 
Carbocysteine 
SABA and/or SAMA 
Theophylline
 Osteoporosis and anxiety/depression: often under-diagnosed 
and associated with poor health status 
and prognosis. 
 Lung cancer: frequent in patients with COPD; the 
most frequent cause of death in patients with mild 
COPD. 
 Serious infections: respiratory infections are 
especially frequent. 
 Metabolic syndrome and manifest diabetes: more 
frequent in COPD and the latter is likely to impact 
on prognosis.
COPD VS ASTHMA 
Feature: if present suggest ASTHMA COPD 
Age of Onset Before 20 After 40 
Pattern of Symptoms • Variation of minutes, hours, days 
• Worst during night or early morning 
• Triggered by exercise, emotions, 
including laughter dust or emotions 
• Persistent besides treatment 
• Good and bad days but always daily 
symptoms and exertional dyspnea 
• Chronic cough and sputum 
precedes onset of dyspnea unrelated 
to trigger. 
Lung Functions Record of variable airflow limitation 
(spirometry or peak flow 
Records persistent airflow limitation 
FEV1/FVC < 0.70 post BD 
Lung functions between symptoms Normal Abnormal 
Past history or family history • Previous doctor diagnosis of asthma 
• Family history of asthma, or other 
allergic condition (allergic rhinitis or 
eczema) 
• Previous doctor diagnosis of COPD, 
chronic bronchitis or emphysema 
• Heavy exposure to risk factors-tobacco 
smoke or biomass fuel 
Time course • No worsening of symptoms over time. 
Variation in symptoms either seasonally 
or from year to year. 
• May improve spontaneously or have an 
immediate response to bronchodilators 
or ICS over weeks 
• Symptoms slowly worsen over time 
(progressive course over years 
• Rapid acting bronchodilator 
treatment only provide limited relief 
Chest xray Normal Severe hyperinflation
Professor Peter J. Barnes, MD 
National Heart and Lung Institute, London UK
THANK YOU………………….

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COPD 2014

  • 1. Guides : Dr. Jitendra Bhargava Dr. Sanjay Bharty Dr. Brahma Prakash By-DR ANKUR KAUSHIK
  • 2.  COPD, a common preventable and treatable disease, is characterized by persistent airflow limitation that is usually progressive and associated with an enhanced chronic inflammatory response in the airways and the lung to noxious particles or gases.  Exacerbations and comorbidities contribute to the overall severity in individual patients. Definition from GOLD 2014
  • 3.  COPD is a leading cause of morbidity and mortality worldwide. COPD also accounts for more than 3 million deaths per year globally making it the third leading cause of death worldwide. According to World Health Organization estimates, 400 million people worldwide suffers from COPD. The estimated burden of COPD in India is about 15 million cases (males and females contributing to 9.02 and 5.75 million, respectively).  In India, according to INSEARCH I and II trials, prevalence of COPD is 3.67% (4.46 and 2.86% among males and females, respectively).The prevalence was found to be increasing with an increase in age.  The burden of COPD is projected to increase in coming decades due to continued exposure to COPD risk factors and the aging of the world’s population. it is estimated to be the third leading cause of death by 2030. Data from Guidelines for diagnosis and management of chronic obstructive pulmonary disease: Joint ICS/NCCP (I) recommendations 2013
  • 4. AIRFLOW LIMITATION Small Airways Disease • Airway inflammation • Airway fibrosis, luminal plugs • Increased airway resistance Parenchymal Destruction • Loss of alveolar attachments • Decrease of elastic recoil
  • 5. Picture from Gold 2014 updates Professor Peter J. Barnes, MD National Heart and Lung Institute, London UK
  • 6. • Genes • Exposure to particles  Tobacco smoke  Occupational dusts, organic and inorganic  Indoor air pollution from heating and cooking with biomass in poorly ventilated dwellings  Outdoor air pollution • Lung growth and development • Gender • Age • Respiratory infections • Socioeconomic status • Asthma/Bronchial hyperactivity • Chronic Bronchitis
  • 7. The goals of COPD assessment are to determine  the severity of the disease, including the severity of airflow limitation.  The impact on the patient’s health status, and the risk of future events.  Comorbidities that occur frequently in COPD patients, and should be actively looked for and treated appropriately if present.
  • 8. Chronic cough Present intermittently or every day, often present throughout the day Chronic sputum production Any pattern of sputum production may indicate COPD Acute bronchitis Repeated episodes Dyspnea that is Progressive, persistent, worse on exercise, worse during respiratory infections History of exposure to risk factors Smoke, biomass fuel, occupational dusts The diagnosis should be confirmed by Spirometry
  • 9. Diagnosis of COPD SYMPTOMS • shortness of breath • chronic cough • sputum EXPOSURE TO RISK FACTORS • Tobacco • Occupation • indoor/outdoor pollution SPIROMETRY: Required to establish diagnosis
  • 10. ASSESSMENT OF COPD Assess symptoms Assess risk of exacerbations Assess degree of airflow limitation using spirometry
  • 11.  COPD Assessment Test (CAT)  Clinical COPD Questionnaire (CCQ)  mMRC Breathlessness scale
  • 12.  COPD Assessment Test (CAT): An 8-item measure of health status impairment in COPD (http://catestonline.org).  Clinical COPD Questionnaire (CCQ): Self-administered questionnaire developed to measure clinical control in patients with COPD (http://www.ccq.nl).  Breathlessness Measurement using the Modified British Medical Research Council (mMRC) Questionnaire: relates well to other measures of health status and predicts future mortality risk
  • 14.
  • 15.
  • 16.  Spirometry should be performed after the administration of an adequate dose of a short acting inhaled bronchodilator to minimize variability.  A post-bronchodilator FEV1/FVC < 0.70 confirms the presence of airflow limitation.  Where possible, values should be compared to age-related normal values to avoid over diagnosis of COPD in the elderly.
  • 17.
  • 18. We use spirometry for grading severity according to spirometry, using four grades split at 80%, 50% and 30% of predicted value Classification of Severity of Airflow Limitation in COPD* In patients with FEV1/FVC < 0.70:  GOLD 1: Mild FEV1 > 80% predicted  GOLD 2: Moderate 50% < FEV1 < 80% predicted  GOLD 3: Severe 30% < FEV1 < 50% predicted  GOLD 4: Very Severe FEV1 < 30% predicted *Based on Post-Bronchodilator FEV1
  • 19. To assess risk of exacerbations use history of exacerbations and spirometry: • Two or more exacerbations within the last year or an FEV1 < 50 % of predicted value are indicators of high risk. • One or more hospitalizations for COPD exacerbation should be considered high risk.
  • 20.
  • 21.
  • 22. Patient Characteristic Spirometry Classification Exacerbations per year CAT mMRC A Low Risk Less Symptoms GOLD 1-2 ≤ 1 < 10 0-1 B Low Risk More Symptoms GOLD 1-2 ≤ 1 > 10 > 2 C High Risk Less Symptoms GOLD 3-4 > 2 < 10 0-1 D High Risk More Symptoms GOLD 3-4 > 2 > 10 > 2
  • 23. COPD patients are at increased risk for:  Cardiovascular diseases  Osteoporosis  Respiratory infections  Anxiety and Depression  Diabetes  Lung cancer  Bronchiectasis
  • 24. Chest X-ray: Valuable to exclude alternative diagnoses and establish presence of significant comorbidities. Lung Volumes and Diffusing Capacity: Help to characterize severity. Oximetry and Arterial Blood Gases: Pulse oximetry can be used to evaluate a patient’s oxygen saturation and need for supplemental oxygen therapy. Alpha-1 Antitrypsin Deficiency Screening: Perform when COPD develops in patients of Caucasian descent under 45 years or with a strong family history of COPD.
  • 25. Exercise Testing: Objectively measured exercise impairment, assessed by a reduction in self-paced walking distance (such as the 6 min walking test) or during incremental exercise testing in a laboratory, is a powerful indicator of health status impairment and predictor of prognosis.
  • 26. • Smoking cessation has the greatest capacity to influence the natural history of COPD. Health care providers should encourage all patients who smoke to quit. • Pharmacotherapy and nicotine replacement reliably increase long-term smoking abstinence rates. • All COPD patients benefit from regular physical activity and should repeatedly be encouraged to remain active. • Appropriate pharmacologic therapy can reduce COPD symptoms, reduce the frequency and severity of exacerbations, and improve health status and exercise tolerance. • Influenza and pneumococcal vaccination should be offered depending on local guidelines.
  • 27. Beta2-agonists Short-acting beta2-agonists Long-acting beta2-agonists Anticholinergic Short-acting anticholinergic Long-acting anticholinergic Combination short-acting beta2-agonists + anticholinergic in one inhaler Combination long-acting beta2-agonists + anticholinergic in one inhaler Methylxanthines Inhaled corticosteroids Combination long-acting beta2-agonists + corticosteroids in one inhaler Systemic corticosteroids Phosphodiesterase-4 inhibitors
  • 28.  Bronchodilator medications are central to the symptomatic management of COPD.  The principal bronchodilator treatments are beta2 agonists, anticholinergic, theophylline or combination therapy.  The choice of treatment depends on the availability of medications and each patient’s individual response in terms of symptom relief and side effects.
  • 29.  Regular treatment with inhaled corticosteroids improves symptoms, lung function and quality of life and reduces frequency of exacerbations for COPD patients with an FEV1 < 60% predicted.
  • 30.  An inhaled corticosteroid combined with a long-acting beta2-agonist is more effective than the individual components in improving lung function and health status and reducing exacerbations in moderate to very severe COPD.  Addition of a long-acting beta2-agonist/inhaled glucorticosteroid combination to an anticholinergic (tiotropium) appears to provide additional benefits.
  • 31.  Theophylline is less effective and less well tolerated than inhaled long-acting bronchodilators and is not recommended if those drugs are available and affordable.  There is evidence for a modest bronchodilator effect and some symptomatic benefit compared with placebo in stable COPD. Addition of theophylline to salmeterol produces a greater increase in FEV1 and breathlessness than salmeterol alone.  Low dose theophylline reduces exacerbations but does not improve post-bronchodilator lung function.
  • 32.  Chronic treatment with systemic corticosteroids should be avoided because of an unfavorable benefit-to- risk ratio.
  • 33.  First novel therapy for COPD in nearly 20 years.  In patients with severe and very severe COPD (GOLD 3 and 4) and a history of exacerbations and chronic bronchitis, it’s a selective phospodiesterase-4 inhibitor, roflumilast, reduces exacerbations treated with oral glucocorticosteroids.  This medication is not a bronchodilator, and it is not indicated for the treatment of acute bronchospasm.
  • 34.
  • 35.  Influenza vaccines can reduce serious illness. Pneumococcal polysaccharide vaccine is recommended for COPD patients 65 years and older and for COPD patients younger than age 65 with an FEV1 < 40% predicted.  The use of antibiotics, other than for treating infectious exacerbations of COPD and other bacterial infections, is currently not indicated.
  • 36.  Alpha-1 antitrypsin augmentation therapy: not recommended for patients with COPD that is unrelated to the genetic deficiency.  Mucolytics: Patients with viscous sputum may benefit from mucolytics; overall benefits are very small. Example, n-acetyl cystiene.  Antitussives: Not recommended.  Vasodilators: Nitric oxide is contraindicated in stable COPD. The use of endothelium-modulating agents for the treatment of pulmonary hypertension associated with COPD is not recommended.
  • 37.  All COPD patients benefit from exercise training programs with improvements in exercise tolerance and symptoms of dyspnea and fatigue.  Although an effective pulmonary rehabilitation program is 6 weeks, the longer the program continues, the more effective the results.  If exercise training is maintained at home, the patient's health status remains above pre-rehabilitation levels.
  • 38.  Oxygen Therapy: The long-term administration of oxygen (> 15 hours per day) to patients with chronic respiratory failure has been shown to increase survival in patients with severe, resting hypoxemia.  Ventilatory Support: Combination of noninvasive ventilation (NIV) with long-term oxygen therapy may be of some use in a selected subset of patients, particularly in those with pronounced daytime hypercapnia.
  • 39.  Lung volume reduction surgery (LVRS) is more efficacious than medical therapy among patients with upper-lobe predominant emphysema and low exercise capacity.  LVRS is costly relative to health-care programs not including surgery.  In appropriately selected patients with very severe COPD, lung transplantation has been shown to improve quality of life and functional capacity
  • 40. • Relieve symptoms • Improve exercise tolerance • Improve health status • Prevent disease progression • Prevent and treat exacerbations • Reduce mortality
  • 41. Avoidance of risk factors - smoking cessation - reduction of indoor pollution - reduction of occupational exposure Influenza vaccination
  • 42.  Long-acting formulations of beta2-agonists and anticholinergics are preferred over short-acting formulations. Based on efficacy and side effects, inhaled bronchodilators are preferred over oral bronchodilators.  Long-term treatment with inhaled corticosteroids added to long-acting bronchodilators is recommended for patients with high risk of exacerbations.  The phospodiesterase-4 inhibitor roflumilast may be useful to reduce exacerbations for patients with FEV1 < 50% of predicted, chronic bronchitis, and frequent exacerbations.
  • 43. Patient Group Essential Recommended Depending on local guidelines A Smoking cessation (can include pharmacologic treatment) Physical activity Flu vaccination Pneumococcal vaccination B, C, D Smoking cessation (can include pharmacologic treatment) Pulmonary rehabilitation Physical activity Flu vaccination Pneumococcal vaccination
  • 44. Patient Recommended First choice Alternative choice Other Possible Treatments A SAMA prn or SABA prn LAMA or LABA or SABA and SAMA Theophylline B LAMA or LABA LAMA and LABA SABA and/or SAMA Theophylline C ICS + LABA or LAMA LAMA and LABA or LAMA and PDE4- inh. or LABA and PDE4- inh. SABA and/or SAMA Theophylline D ICS + LABA and/or LAMA ICS + LABA and LAMA or ICS+LABA and PDE4-inh. or LAMA and LABA or LAMA and PDE4- inh. Carbocysteine SABA and/or SAMA Theophylline
  • 45.
  • 46.
  • 47.  Osteoporosis and anxiety/depression: often under-diagnosed and associated with poor health status and prognosis.  Lung cancer: frequent in patients with COPD; the most frequent cause of death in patients with mild COPD.  Serious infections: respiratory infections are especially frequent.  Metabolic syndrome and manifest diabetes: more frequent in COPD and the latter is likely to impact on prognosis.
  • 48. COPD VS ASTHMA Feature: if present suggest ASTHMA COPD Age of Onset Before 20 After 40 Pattern of Symptoms • Variation of minutes, hours, days • Worst during night or early morning • Triggered by exercise, emotions, including laughter dust or emotions • Persistent besides treatment • Good and bad days but always daily symptoms and exertional dyspnea • Chronic cough and sputum precedes onset of dyspnea unrelated to trigger. Lung Functions Record of variable airflow limitation (spirometry or peak flow Records persistent airflow limitation FEV1/FVC < 0.70 post BD Lung functions between symptoms Normal Abnormal Past history or family history • Previous doctor diagnosis of asthma • Family history of asthma, or other allergic condition (allergic rhinitis or eczema) • Previous doctor diagnosis of COPD, chronic bronchitis or emphysema • Heavy exposure to risk factors-tobacco smoke or biomass fuel Time course • No worsening of symptoms over time. Variation in symptoms either seasonally or from year to year. • May improve spontaneously or have an immediate response to bronchodilators or ICS over weeks • Symptoms slowly worsen over time (progressive course over years • Rapid acting bronchodilator treatment only provide limited relief Chest xray Normal Severe hyperinflation
  • 49. Professor Peter J. Barnes, MD National Heart and Lung Institute, London UK