SlideShare a Scribd company logo
1 of 90
C O P D
CHRONIC OBSTRUCTIVE LUNG
DISEASE
PRESENTED BY DR KD DELE
DEPARTMENT OF FAMILY MEDICINE; DORA NGINZA HOSPITAL
CONTENT
• Definition and Overview
• Diagnosis and Assessment
• Therapeutic Options
• Management of Exacerbations
• Management of Stable COPD
• Management of Comorbidities
• Slides On Pathophysiology Of COPD
DEFINITION AND
OVERVIEW
Definition of COPD
• 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.
Mechanisms Underlying Airflow
Limitation in COPD
Burden of COPD
• COPD is a leading cause of morbidity and mortality worldwide.
• 30% of smokers develop COPD
• 20% of adult males have COPD
• 15% of COPD patients are severely symptomatic
• 4th leading cause of death (USA)
• Mortality rate still rising
• High prevalence in low birth weight and low socioeconomic status
• Tuberculosis in smokers predisposes to COPD
• COPD is associated with significant economic burden.
Risk Factors for COPD
• 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
Risk Factors for COPD cont.
• Lung growth and development
• Gender
• Age
• Respiratory infections
• Socioeconomic status
• Asthma/Bronchial hyperreactivity
• Chronic Bronchitis
Risk Factors for COPD cont.
Aging Populations
Genes
Infections
Socio-economic
status
DIAGNOSIS AND
ASSESSMENT
Diagnosis and Assessment
• A clinical diagnosis of COPD:
• any patient who has dyspnoea, chronic cough or sputum production,
• and a history of exposure to risk factors for the disease.
• to make the diagnosis;
• Spirometry is required
• the presence of a post-bronchodilator FEV1/FVC < 0.70 confirms the
presence of persistent airflow limitation and thus of COPD.
Diagnosis and Assessment, cont.
• The goals of COPD assessment
• to determine
• the severity of the disease,
• the severity of airflow limitation,
• the impact on the patient’s health status,
• and the risk of future events.
• Comorbidities
• They occur frequently in COPD patients
• They should be actively looked for and treated appropriately if present.
© 2015 Global Initiative for Chronic Obstructive Lung Disease
Diagnosis of COPD
Spirometry:
Assessment of Airflow Limitation
• 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.
Spirometry
Pulmonary Function Tests
© 2015 Global Initiative for Chronic Obstructive Lung Disease
Spirometry:
Normal Trace Showing FEV1 and FVC
© 2015 Global Initiative for Chronic Obstructive Lung Disease
Spirometry: Obstructive Disease
Diagnosis of COPD – Pulmonary
Function Tests
•  Forced Expiratory Volume for 1 second (FEV1)
• FEV1/FVC (Forced Vital Capacity) ratio
Other Suggestive Criteria
•  Total Lung Capacity (TLC)
•  Forced Residual Capacity (FRC)
•  Residual Volume (RV)
•  Vital Capacity (VC)
Pulmonary Function Tests
ASSESSMENT OF
COPD
Assessment of COPD: Goals
• Determine the severity of the disease, its impact on the patient’s health
status and the risk of future events (for example exacerbations) to guide
therapy.
• Consider the following aspects of the disease separately:
• current level of patient’s symptoms
• severity of the spirometric abnormality
• frequency of exacerbations
• presence of comorbidities.
ASSESSMENT OF COPD
• Assess symptoms
• Assess degree of airflow limitation using spirometry
• Assess risk of exacerbations
• Assess comorbidities
• Combine these assessments (first three) for the purpose of improving
management of COPD
1. Assess Symptoms of COPD
• The characteristic symptoms of COPD are chronic and progressive
dyspnoea, cough, and sputum production that can be variable from
day-to-day.
• Dyspnoea: Progressive, persistent and characteristically worse with
exercise.
• Chronic cough: May be intermittent and may be unproductive.
• Chronic sputum production: COPD patients commonly cough up
sputum.
• Others include:Wheezing; Cyanosis; Right heart failure; Weight loss,
anorexia
Need For Simple Tools
• Significant numbers of patients have COPD that is under-recognised,
untreated and sub-optimally managed, despite widening use of spirometry
• Patients underestimate their condition: in a study1 (n=3265),
• 36% of those too breathless to leave the house described their condition as mild or
moderate; and
• 60% of those who were short of breath after walking for a few minutes on the flat
described their condition as mild or moderate
• Studies also confirm that patients and physicians require a tool to
• facilitate fact-based dialogue
• to help achieve a mutual understanding of disease status and impact; and
• to help to optimise disease management
Assess Symptoms of COPD, cont.
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.
Assess Symptoms of COPD, cont.
• The CAT has been designed to overcome the shortfalls of earlier
questionnaires measuring disability in COPD.
• The CAT is a simple, short, easy to use self-administered, paper-based
questionnaire for use in clinical practice.
• The MRC dyspnoea questionnaire measures dyspnoea only whereas
CAT is a holistic measure of the impact of COPD on the patient
COPD Assessment Test (CAT)
CCQ: COPD Clinical questionnaire
Modified MRC (mMRC)Questionnaire
Differences between COPD questionnaires
SGRQ MRC Dyspnoea
Questionnaire
CCQ CAT
• Measures impaired
health and wellbeing
• Measures dyspnoea
only
• Measures clinical
disease control
• Measures holistic
impact of COPD on
patients
• Used largely in clinical
trials
– • Used in clinical
practice
• Used in clinical
practice
• Long (76-items) • Short (5-items) • Short (10-items) • Short (8 items)
• Patient completed • Patient completed • Patient completed • Patient completed
• Computer required • Paper based • Paper based • Paper based
• Complex to administer • Simple to administer • Simple to administer • Simple to administer
2. Assess degree of airflow limitation
• 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*
*Based on Post-Bronchodilator FEV1
© 2015 Global Initiative for Chronic Obstructive Lung Disease
3. Assess Risk of Exacerbations
• To assess risk of exacerbations:
• Use history of exacerbations and spirometry.
• Two exacerbations or more within the last year or
• an FEV1 < 50 % of predicted value
are indicators of high risk.
• Hospitalization for a COPD exacerbation associated with
increased risk of death.
Combined Assessment Of COPD
• Assess symptoms
• Assess degree of airflow limitation using spirometry
• Assess risk of exacerbations
• Combine these assessments for the purpose of improving management
of COPD
Combined Assessment Of COPD, cont
Assess symptoms first
Assess risk of exacerbations next
Patient Characteristics Spirometric
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
Combined Assessment of COPD
• When assessing risk, choose the highest risk according to GOLD grade or exacerbation history.
• One or more hospitalizations for COPD exacerbations should be considered high risk.
© 2015 Global Initiative for Chronic Obstructive Lung Disease
4. Assess COPD Comorbidities
• COPD patients are at increased risk for:
• Cardiovascular diseases
• Osteoporosis
• Respiratory infections
• Anxiety and Depression
• Diabetes
• Lung cancer
• Bronchiectasis
• These comorbid conditions may influence mortality and hospitalizations and
should be looked for routinely, and treated appropriately
DIFFERENTIAL DIAGNOSIS
Differential Diagnoses - Pulmonary
• Asthma
• Bronchogenic carcinoma
• Bronchiectasis
• Tuberculosis
• Cystic fibrosis
• Interstitial lung disease
• Bronchiolitis obliterans
• Pleural effusion
• Pulmonary oedema
• Recurrent aspiration
• Recurrent pulmonary emboli
• Foreign body
• Alpha-1 antitrypsin deficiency
• Tracheobronchomalacia
Differential Diagnoses - Non-Pulmonary
• Congestive Heart Failure
• Hyperventilation syndrome/panic attacks
• Vocal cord dysfunction
• Obstructive sleep apnoea – undiagnosed
• Aspergillosis
• Chronic Fatigue Syndrome
COPD and Asthma
COPD
• Onset in mid-life
• Symptoms slowly progressive
• Long smoking history
Asthma
• Onset early in life (often childhood)
• Symptoms vary from day to day
• Symptoms worse at night/early morning
• Allergy, rhinitis, and/or eczema also
present
• Family history of asthma
ADDITIONAL
INVESTIGATIONS
Physical Examination
• Vitals:  RR,  HR,  O2 saturation
• General: Barrel-chest, accessory muscle use
• Cardiovascular: Quiet heart sounds
• Respiratory: Decreased breath sounds, wheezing, rhonchi, crackles
• Full Blood Count:  Haemoglobin/Haematocrit
• ABG:  pH; /N pCO2 (>5kPa);  pO2 (<8kPa);  HCO3 (chronic
respiratory acidosis)
Additional Investigations
Chest X-ray:
• Seldom diagnostic but valuable to exclude alternative diagnoses and establish
presence of significant comorbidities.
Lung Volumes and Diffusing Capacity:
• Help to characterize severity, but not essential to patient management.
Oximetry and Arterial Blood Gases:
• Pulse oximetry can be used to evaluate a patient’s oxygen saturation and need for
supplemental oxygen therapy.
Additional Investigations
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.
Composite Scores:
• Several variables (FEV1, exercise tolerance assessed by walking distance or peak oxygen
consumption, weight loss and reduction in the arterial oxygen tension) identify patients at
increased risk for mortality.
THERAPEUTIC
OPTIONS
Therapeutic Options
• Smoking cessation has the greatest capacity to influence the natural history of COPD.
Encourage all patients who smoke to quit.
• Pharmacotherapy and nicotine replacement increase long-term smoking abstinence rates.
• All COPD patients benefit from regular physical activity – 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.
• None of the existing medications for COPD has been shown conclusively to modify the
long-term decline in lung function.
• Influenza and pneumococcal vaccination should be offered per local guidelines.
Quit Smoking: Strategies
• ASK Systematically identify all tobacco users at every visit
• ADVISE Strongly urge all tobacco users to quit
• ASSESS Determine willingness to make a quit attempt
• ASSIST Aid the patient in quitting eg nicotine replacement
• ARRANGE Schedule follow-up
Therapeutic Options: Risk Reduction
Tobacco-control:
• clear, consistent, and repeated non-smoking messages.
Primary prevention:
• elimination or reduction of exposures in the workplace.
Secondary prevention:
• surveillance and early detection.
Others
• Reduce or avoid indoor air pollution from biomass fuel, burned for cooking and
heating in poorly ventilated dwellings.
• monitor public announcements of air quality and, depending on the severity of
their disease, avoid vigorous exercise outdoors or stay indoors during pollution
episodes.
THERAPEUTIC OPTIONS:
COPD MEDICATIONS
Therapeutic Options: COPD Medications
1. Beta2-agonists
• Short-acting beta2-agonists:
e.g. Salbutamol (Asthavent/Ventolin); Fenoterol (Berotec); Terbutaline (Bricanyl)}
• Long-acting beta2-agonists:
e.g. Salmeterol (Serevent); Formoterol (Foradil / Oxis)
2. Anticholinergics, e.g. Ipratropium bromide (Atrovent)
• Short-acting anticholinergics
• Long-acting anticholinergics
3. Combination short-acting beta2-agonists + anticholinergic in one inhaler
• e.g. Atrovent beta (Ipratropium bromide 0.5mg + fenoterol hydrobromide 1.25mg/4ml
4. Combination long-acting beta2-agonist + anticholinergic in one inhaler
Therapeutic Options: COPD Medications
• 5. Methylxanthines
Sustained release theophylline preparations e.g. Neulin
• 6. Inhaled corticosteroids
e.g. Beclomethasone; Beclate; Budesonide; Fluticasone propionate; Ciclesonide; Budeflam/
Inflammide; Flixotide
• 7. Combination long-acting beta2-agonists + corticosteroids in one inhaler
e.g. budesonide plus formoterol; fluticasone plus salmeterol (Seretide)
• 8. Systemic corticosteroids
• 9. Phosphodiesterase-4 inhibitors – roflumilast
COPD Medications: Summary
Therapeutic Options: Bronchodilators
• Bronchodilator medications are central to the symptomatic management of
COPD.
• Bronchodilators are prescribed on an as-needed or on a regular basis to
prevent or reduce symptoms.
• The principal bronchodilator treatments are
• beta2-agonists
• anticholinergics
• theophylline or
• combination therapy.
Therapeutic Options: Bronchodilators cont.
• The choice of treatment depends on: availability of medications and each
patient’s response in terms of symptom relief and side effects.
Long-acting inhaled bronchodilators:
• are convenient and more effective for symptom relief than short-acting
bronchodilators.
• reduce exacerbations and related hospitalizations and improve symptoms
and health status.
Combining bronchodilators of different pharmacological classes:
• may improve efficacy and decrease the risk of side effects compared to
increasing the dose of a single bronchodilator.
Therapeutic Options: Inhaled Corticosteroids
• 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.
• Inhaled corticosteroid therapy is associated with an increased risk of
pneumonia.
• Withdrawal from treatment with inhaled corticosteroids may lead to
exacerbations in some patients.
Therapeutic Options: Combination Therapy
• 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.
• Combination therapy is associated with an increased risk of pneumonia.
Therapeutic Options cont.
Phosphodiesterase-4 Inhibitors
• In patients with severe and very severe COPD (GOLD 3 and 4) and a history
of exacerbations and chronic bronchitis, the phospodiesterase-4 inhibitor,
roflumilast, reduces exacerbations treated with oral glucocorticosteroids.
Systemic Corticosteroids
• Chronic treatment with systemic corticosteroids should be AVOIDED because
of an unfavourable benefit-to-risk ratio.
Therapeutic Options: Theophylline
• Low dose theophylline reduces exacerbations but does not improve post-
bronchodilator lung function.
• Theophylline is less effective and less well tolerated than inhaled long-acting
bronchodilators (not recommended if those drugs are available and
affordable).
• Theophylline has a modest bronchodilator effect and some symptomatic
benefit in stable COPD.
• Addition of theophylline to salmeterol (laba) produces a greater increase in
FEV1 and breathlessness than salmeterol alone.
Therapeutic Options: Other Pharmacologic
Treatments
Influenza vaccines:
• it 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.
Antibiotics:
• 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.
Therapeutic Options: Other Pharmacologic
Treatments cont.
Mucolytics:
• Patients with viscous sputum may benefit from mucolytics; overall benefits are very small.
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
Therapeutic Options: Surgical Treatments
Bullectomy
• Resection of large bullae compressing normal lung
Lung volume reduction surgery (LVRS)
• 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.
Double lung transplantation
• For patients with very severe COPD,
• It improves quality of life and functional capacity.
• It is costly, can be lack of donor availability and requires lifelong immunosuppression.
Therapeutic Options: Other Treatments
Pulmonary Rehabilitation:
• Aimed at keeping patient conditioned with exercise, perception of dyspnea, quality
of life and self-efficacy.
Oxygen Therapy:
• The long-term administration of oxygen (> 15 hours per day) to patients with chronic respiratory
failure increases survival in patients with severe, resting hypoxemia.
Ventilatory Support:
• Combination of non-invasive ventilation (NIV) with long-term oxygen therapy may be of some
use in patients with pronounced daytime hypercapnia.
Palliative Care, End-of-life Care, Hospice Care:
• Communication with advanced COPD patients about end-of-life care and advance care planning
gives patients and their families the opportunity to make informed decisions.
MANAGE
EXACERBATIONS
COPD EXACERBATION
• An exacerbation of COPD is:
• “an acute event characterized by a worsening of the patient’s
respiratory symptoms that is beyond normal day-to-day variations and
leads to a change in medication.”
• The goal of treatment is to minimize the impact of the current
exacerbation and to prevent the development of subsequent
exacerbations.
COPD EXACERBATION cont.
The most common causes of COPD exacerbations:
• viral upper respiratory tract infections and
• infection of the tracheobronchial tree.
Diagnosis
• relies exclusively on the clinical presentation of the patient complaining of an acute change of
symptoms that is beyond normal day-to-day variation.
• COPD exacerbations can often be prevented.
Immediate management.
• Assess severity of attack.
• Start treatment prior to investigations.
• Sit up and give oxygen e.g. 60%.
• Salbutamol 5mg in saline nebulization.
• Hydrocortisone 200mg IV or 30mg predisone per os.
• If life threatening add ipratropium 0.5mg to beta 2 stimulant as
nebulization
• MgSO4 2g in 200ml N saline over 20 minutes
• Intubate and Ventilate
• If still not improving consider ICU.
Manage Exacerbations: Assessments
• Arterial blood gas measurements (in hospital):
• PaO2 < 8.0 kPa with or without PaCO2 > 6.7 kPa when breathing room air
indicates respiratory failure.
• Chest radiographs:
• useful to exclude alternative diagnoses.
• ECG:
• may aid in the diagnosis of coexisting cardiac problems.
• Whole blood count:
• identify polycythaemia, anaemia or bleeding.
Manage Exacerbations: Assessments
• Purulent sputum during an exacerbation:
• indication to begin empirical antibiotic treatment.
• Biochemical tests:
• detect electrolyte disturbances, diabetes, and poor nutrition.
• Spirometric tests:
• not recommended during an exacerbation.
Manage Exacerbations: Treatment
options
Oxygen:
• titrate to improve the patient’s hypoxemia with a target saturation of 88-92%.
Bronchodilators:
• short-acting inhaled beta2-agonists with or without short-acting anticholinergics are
usually the preferred bronchodilators for treatment of an exacerbation.
Systemic Corticosteroids:
• shortens recovery time,
• improves lung function (FEV1) and arterial hypoxemia (PaO2),
• reduce the risk of early relapse, treatment failure, and length of hospital stay.
• dose of 40 mg prednisone per day for 5 days.
Manage Exacerbations: Treatment
Options cont.
Antibiotics:
• should be given to
• patients with three cardinal symptoms: increased dyspnoea, increased sputum volume, and
increased sputum purulence.
• Patients who require mechanical ventilation.
• It reduces the risk of early relapse, treatment failure, and length of hospital stay
Non-invasive ventilation (NIV):
• For patients hospitalized for acute exacerbations of COPD:
• Improves respiratory acidosis, decreases respiratory rate, severity of dyspnoea,
complications and length of hospital stay.
• Decreases mortality and needs for intubation.
Indications for hospital admission
• Marked increase in intensity of symptoms
• Severe underlying COPD
• Onset of new physical signs
• Failure of an exacerbation to respond to initial medical management
• Presence of serious comorbidities
• Frequent exacerbations
• Older age
• Insufficient home support
Consequences Of COPD Exacerbations
MANAGE STABLE
COPD
Manage Stable COPD: Overview
• Identification and reduction of exposure to risk factors
• Individualized assessment of symptoms, airflow limitation, and future
risk of exacerbations
• All COPD patients benefit from rehabilitation and maintenance of
physical activity.
• Pharmacologic therapy is used to
• reduce symptoms,
• reduce frequency and severity of exacerbations, and
• improve health status and exercise tolerance.
• Influenza vaccination
Goals of Therapy
Manage Stable COPD: Non-
Pharmacologic
Manage Stable COPD: Pharmacologic
Manage Stable COPD: Pharmacologic
Recommended First Choice
Manage Stable COPD: Pharmacologic
Alternative Choice
Manage Stable COPD: Pharmacologic
Other Possible Treatments
MANAGE
COMORBIDITIES
Manage Comorbidities
• COPD often coexists with other diseases (comorbidities) that may have
a significant impact on prognosis. In general, presence of comorbidities
should not alter COPD treatment and comorbidities should be treated
as if the patient did not have COPD.
Manage Comorbidities cont.
• 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.
• Cardiovascular disease (ischemic heart disease, heart failure, atrial fibrillation &
hypertension)
• most frequent and most important disease coexisting with COPD.
• Benefits of cardioselective beta-blocker treatment in heart failure may outweigh potential risk.
THANK YOU
References
• Global Initiative For Chronic Obstructive Lung Disease (GOLD):
Teaching Slide Set; January 2015.
• http://www.goldcopd.org

More Related Content

What's hot

Massive hemoptysis / Nahid Sherbini
Massive hemoptysis / Nahid SherbiniMassive hemoptysis / Nahid Sherbini
Massive hemoptysis / Nahid Sherbini
Nahid Sherbini
 
Diffuse Parenchymal Lung Diseases
Diffuse Parenchymal Lung DiseasesDiffuse Parenchymal Lung Diseases
Diffuse Parenchymal Lung Diseases
Ashraf ElAdawy
 

What's hot (20)

Interstitial Lung Disease
Interstitial Lung DiseaseInterstitial Lung Disease
Interstitial Lung Disease
 
Complications of pulmonary tb
Complications of pulmonary tbComplications of pulmonary tb
Complications of pulmonary tb
 
Copd seminar
Copd seminarCopd seminar
Copd seminar
 
Introduction to Interstitial Lung Disease(ILD) or Diffuse Parenchymal Lung ...
Introduction to Interstitial Lung Disease(ILD)  or  Diffuse Parenchymal Lung ...Introduction to Interstitial Lung Disease(ILD)  or  Diffuse Parenchymal Lung ...
Introduction to Interstitial Lung Disease(ILD) or Diffuse Parenchymal Lung ...
 
COPD(chronic obstructive pulmonary disease) ppt slideshare
COPD(chronic obstructive pulmonary disease) ppt slideshareCOPD(chronic obstructive pulmonary disease) ppt slideshare
COPD(chronic obstructive pulmonary disease) ppt slideshare
 
Post covid pulmonary fibrosis , atypical covid19 sequele
Post covid pulmonary fibrosis , atypical covid19 sequelePost covid pulmonary fibrosis , atypical covid19 sequele
Post covid pulmonary fibrosis , atypical covid19 sequele
 
Bronchectasis
BronchectasisBronchectasis
Bronchectasis
 
Mahu copd
Mahu copdMahu copd
Mahu copd
 
Acute eosinophilic pneumonia
Acute eosinophilic pneumoniaAcute eosinophilic pneumonia
Acute eosinophilic pneumonia
 
Copd
CopdCopd
Copd
 
Approach to a patient with Haemoptysis
Approach to a patient with HaemoptysisApproach to a patient with Haemoptysis
Approach to a patient with Haemoptysis
 
COPD
COPDCOPD
COPD
 
Massive hemoptysis / Nahid Sherbini
Massive hemoptysis / Nahid SherbiniMassive hemoptysis / Nahid Sherbini
Massive hemoptysis / Nahid Sherbini
 
Bronchiectasis
BronchiectasisBronchiectasis
Bronchiectasis
 
Interstitial Lung Disease ( ILD)
Interstitial Lung Disease ( ILD)Interstitial Lung Disease ( ILD)
Interstitial Lung Disease ( ILD)
 
Diffuse Parenchymal Lung Diseases
Diffuse Parenchymal Lung DiseasesDiffuse Parenchymal Lung Diseases
Diffuse Parenchymal Lung Diseases
 
Copd
Copd Copd
Copd
 
Interstitial lung disease; Basic Understanding and approach
Interstitial lung disease; Basic Understanding and approachInterstitial lung disease; Basic Understanding and approach
Interstitial lung disease; Basic Understanding and approach
 
COPD - Chronic obstructive pulmonary disease - Aby
COPD - Chronic obstructive pulmonary disease - Aby COPD - Chronic obstructive pulmonary disease - Aby
COPD - Chronic obstructive pulmonary disease - Aby
 
COPD ppt
COPD pptCOPD ppt
COPD ppt
 

Similar to Chronic Obstructive Pulmonary Disease (COPD) by Dr Kemi Dele

COPD AND ICU MANAGEMENT : DR DEVAWRAT BUCHE
COPD AND ICU MANAGEMENT : DR DEVAWRAT BUCHECOPD AND ICU MANAGEMENT : DR DEVAWRAT BUCHE
COPD AND ICU MANAGEMENT : DR DEVAWRAT BUCHE
Devawrat Buche
 
CHRONIC OBSTRUCTIVE PULMONARY.pptx
CHRONIC OBSTRUCTIVE PULMONARY.pptxCHRONIC OBSTRUCTIVE PULMONARY.pptx
CHRONIC OBSTRUCTIVE PULMONARY.pptx
ImanuIliyas
 
Dual bronchodilatation in copd dr vijay
Dual bronchodilatation in copd   dr vijayDual bronchodilatation in copd   dr vijay
Dual bronchodilatation in copd dr vijay
vkatbcd
 

Similar to Chronic Obstructive Pulmonary Disease (COPD) by Dr Kemi Dele (20)

COPD AND ICU MANAGEMENT : DR DEVAWRAT BUCHE
COPD AND ICU MANAGEMENT : DR DEVAWRAT BUCHECOPD AND ICU MANAGEMENT : DR DEVAWRAT BUCHE
COPD AND ICU MANAGEMENT : DR DEVAWRAT BUCHE
 
Indian guidelines for copd
Indian guidelines for copd Indian guidelines for copd
Indian guidelines for copd
 
YUVA THANJAVUR COPD DAY.pptx
YUVA THANJAVUR COPD DAY.pptxYUVA THANJAVUR COPD DAY.pptx
YUVA THANJAVUR COPD DAY.pptx
 
COPD - Ldh Jan 2010.ppt
COPD - Ldh Jan 2010.pptCOPD - Ldh Jan 2010.ppt
COPD - Ldh Jan 2010.ppt
 
Indian guidelines for COPD
Indian guidelines for COPDIndian guidelines for COPD
Indian guidelines for COPD
 
COPD 2014
COPD 2014COPD 2014
COPD 2014
 
COPD
COPD COPD
COPD
 
COPD:CLINICAL REVIEW AND ANESTHESIA CONSIDERATION
COPD:CLINICAL REVIEW AND ANESTHESIA CONSIDERATIONCOPD:CLINICAL REVIEW AND ANESTHESIA CONSIDERATION
COPD:CLINICAL REVIEW AND ANESTHESIA CONSIDERATION
 
Gold pocket 2015_feb18
Gold pocket 2015_feb18Gold pocket 2015_feb18
Gold pocket 2015_feb18
 
Gold pocket 2015_feb18
Gold pocket 2015_feb18Gold pocket 2015_feb18
Gold pocket 2015_feb18
 
Copd
CopdCopd
Copd
 
CHRONIC OBSTRUCTIVE PULMONARY.pptx
CHRONIC OBSTRUCTIVE PULMONARY.pptxCHRONIC OBSTRUCTIVE PULMONARY.pptx
CHRONIC OBSTRUCTIVE PULMONARY.pptx
 
COPD.pptx
COPD.pptxCOPD.pptx
COPD.pptx
 
Gold COPD guideline 2024 . A review on change in guideline by GOLD .
Gold COPD guideline 2024 . A review on change in guideline by GOLD .Gold COPD guideline 2024 . A review on change in guideline by GOLD .
Gold COPD guideline 2024 . A review on change in guideline by GOLD .
 
End Stage Pulmonary Disease | VITAS Healthcare
End Stage Pulmonary Disease | VITAS HealthcareEnd Stage Pulmonary Disease | VITAS Healthcare
End Stage Pulmonary Disease | VITAS Healthcare
 
COPD chronic obstructive pulmonary disease
COPD chronic obstructive pulmonary diseaseCOPD chronic obstructive pulmonary disease
COPD chronic obstructive pulmonary disease
 
Dual bronchodilatation in copd dr vijay
Dual bronchodilatation in copd   dr vijayDual bronchodilatation in copd   dr vijay
Dual bronchodilatation in copd dr vijay
 
COPD.pptx
COPD.pptxCOPD.pptx
COPD.pptx
 
EMS Respiratory Emergencies.pdf
EMS Respiratory Emergencies.pdfEMS Respiratory Emergencies.pdf
EMS Respiratory Emergencies.pdf
 
Covid 19 a cardiologists perspective
Covid 19   a cardiologists perspectiveCovid 19   a cardiologists perspective
Covid 19 a cardiologists perspective
 

More from Kemi Dele-Ijagbulu

More from Kemi Dele-Ijagbulu (20)

Patient Safety Incidents & Reporting by Dr. KD Dele
Patient Safety Incidents & Reporting by Dr. KD DelePatient Safety Incidents & Reporting by Dr. KD Dele
Patient Safety Incidents & Reporting by Dr. KD Dele
 
Post Exposure Prophylaxis by Dr Dele
Post Exposure Prophylaxis by Dr DelePost Exposure Prophylaxis by Dr Dele
Post Exposure Prophylaxis by Dr Dele
 
U=U for HIV Prevention by Dr Dele.pptx
U=U for HIV Prevention by Dr Dele.pptxU=U for HIV Prevention by Dr Dele.pptx
U=U for HIV Prevention by Dr Dele.pptx
 
TB IRIS Presentation by KD Dele
TB IRIS Presentation by KD DeleTB IRIS Presentation by KD Dele
TB IRIS Presentation by KD Dele
 
Lower GI Bleed by Dr Dele 13.10.2023.pdf
Lower GI Bleed by Dr Dele 13.10.2023.pdfLower GI Bleed by Dr Dele 13.10.2023.pdf
Lower GI Bleed by Dr Dele 13.10.2023.pdf
 
Approach to Headaches in Prmary Care
Approach to Headaches in Prmary CareApproach to Headaches in Prmary Care
Approach to Headaches in Prmary Care
 
EBM - Evidence Based Medicine by Dr KD DELE
EBM - Evidence Based Medicine by Dr KD DELEEBM - Evidence Based Medicine by Dr KD DELE
EBM - Evidence Based Medicine by Dr KD DELE
 
Infection Prevention and Control in Hospitals by Dr Dele
Infection Prevention and Control in Hospitals by Dr DeleInfection Prevention and Control in Hospitals by Dr Dele
Infection Prevention and Control in Hospitals by Dr Dele
 
Disorders of Kidney Function by Dr Kemi DELE
Disorders of Kidney Function by Dr Kemi DELEDisorders of Kidney Function by Dr Kemi DELE
Disorders of Kidney Function by Dr Kemi DELE
 
TUBERCULOSIS. Presented by Dr KD DELE
TUBERCULOSIS. Presented by Dr KD DELETUBERCULOSIS. Presented by Dr KD DELE
TUBERCULOSIS. Presented by Dr KD DELE
 
WORLD TB DAY (March 2020) by Dr KD DELE
WORLD TB DAY (March 2020) by Dr KD DELEWORLD TB DAY (March 2020) by Dr KD DELE
WORLD TB DAY (March 2020) by Dr KD DELE
 
VAGINAL DISCHARGES by DR KD DELE
VAGINAL DISCHARGES by DR KD DELEVAGINAL DISCHARGES by DR KD DELE
VAGINAL DISCHARGES by DR KD DELE
 
TERMINATION OF PREGNANCY by DR KD DELE
TERMINATION OF PREGNANCY by DR KD DELETERMINATION OF PREGNANCY by DR KD DELE
TERMINATION OF PREGNANCY by DR KD DELE
 
CHILD MALNUTRITION by DR KD DELE
CHILD MALNUTRITION by DR KD DELECHILD MALNUTRITION by DR KD DELE
CHILD MALNUTRITION by DR KD DELE
 
Pyrexia (Fever) of Unknown Origin by DR KD DELE
Pyrexia (Fever) of Unknown Origin by DR KD DELEPyrexia (Fever) of Unknown Origin by DR KD DELE
Pyrexia (Fever) of Unknown Origin by DR KD DELE
 
Obstetrics Emergencies by Dr KD DELE
Obstetrics Emergencies by Dr KD DELEObstetrics Emergencies by Dr KD DELE
Obstetrics Emergencies by Dr KD DELE
 
Respiratory Emergencies by DR KD DELE
Respiratory Emergencies by DR KD DELERespiratory Emergencies by DR KD DELE
Respiratory Emergencies by DR KD DELE
 
Evidence Based Medicine by DR KD DELE
Evidence Based Medicine by DR KD DELEEvidence Based Medicine by DR KD DELE
Evidence Based Medicine by DR KD DELE
 
Multiple Myeloma, by Dr KD DELE
Multiple Myeloma, by Dr KD DELEMultiple Myeloma, by Dr KD DELE
Multiple Myeloma, by Dr KD DELE
 
Spinal Cord Injuries - presented by Dr KD DELE
Spinal Cord Injuries - presented  by Dr KD DELESpinal Cord Injuries - presented  by Dr KD DELE
Spinal Cord Injuries - presented by Dr KD DELE
 

Recently uploaded

Jual Obat Aborsi Di Dubai UAE Wa 0838-4800-7379 Obat Penggugur Kandungan Cytotec
Jual Obat Aborsi Di Dubai UAE Wa 0838-4800-7379 Obat Penggugur Kandungan CytotecJual Obat Aborsi Di Dubai UAE Wa 0838-4800-7379 Obat Penggugur Kandungan Cytotec
Jual Obat Aborsi Di Dubai UAE Wa 0838-4800-7379 Obat Penggugur Kandungan Cytotec
jualobat34
 
Difference Between Skeletal Smooth and Cardiac Muscles
Difference Between Skeletal Smooth and Cardiac MusclesDifference Between Skeletal Smooth and Cardiac Muscles
Difference Between Skeletal Smooth and Cardiac Muscles
MedicoseAcademics
 
Cara Menggugurkan Kandungan Dengan Cepat Selesai Dalam 24 Jam Secara Alami Bu...
Cara Menggugurkan Kandungan Dengan Cepat Selesai Dalam 24 Jam Secara Alami Bu...Cara Menggugurkan Kandungan Dengan Cepat Selesai Dalam 24 Jam Secara Alami Bu...
Cara Menggugurkan Kandungan Dengan Cepat Selesai Dalam 24 Jam Secara Alami Bu...
Cara Menggugurkan Kandungan 087776558899
 
Physiologic Anatomy of Heart_AntiCopy.pdf
Physiologic Anatomy of Heart_AntiCopy.pdfPhysiologic Anatomy of Heart_AntiCopy.pdf
Physiologic Anatomy of Heart_AntiCopy.pdf
MedicoseAcademics
 

Recently uploaded (20)

Jual Obat Aborsi Di Dubai UAE Wa 0838-4800-7379 Obat Penggugur Kandungan Cytotec
Jual Obat Aborsi Di Dubai UAE Wa 0838-4800-7379 Obat Penggugur Kandungan CytotecJual Obat Aborsi Di Dubai UAE Wa 0838-4800-7379 Obat Penggugur Kandungan Cytotec
Jual Obat Aborsi Di Dubai UAE Wa 0838-4800-7379 Obat Penggugur Kandungan Cytotec
 
Shazia Iqbal 2024 - Bioorganic Chemistry.pdf
Shazia Iqbal 2024 - Bioorganic Chemistry.pdfShazia Iqbal 2024 - Bioorganic Chemistry.pdf
Shazia Iqbal 2024 - Bioorganic Chemistry.pdf
 
HISTORY, CONCEPT AND ITS IMPORTANCE IN DRUG DEVELOPMENT.pptx
HISTORY, CONCEPT AND ITS IMPORTANCE IN DRUG DEVELOPMENT.pptxHISTORY, CONCEPT AND ITS IMPORTANCE IN DRUG DEVELOPMENT.pptx
HISTORY, CONCEPT AND ITS IMPORTANCE IN DRUG DEVELOPMENT.pptx
 
Drug development life cycle indepth overview.pptx
Drug development life cycle indepth overview.pptxDrug development life cycle indepth overview.pptx
Drug development life cycle indepth overview.pptx
 
MOTION MANAGEMANT IN LUNG SBRT BY DR KANHU CHARAN PATRO
MOTION MANAGEMANT IN LUNG SBRT BY DR KANHU CHARAN PATROMOTION MANAGEMANT IN LUNG SBRT BY DR KANHU CHARAN PATRO
MOTION MANAGEMANT IN LUNG SBRT BY DR KANHU CHARAN PATRO
 
Intro to disinformation and public health
Intro to disinformation and public healthIntro to disinformation and public health
Intro to disinformation and public health
 
Difference Between Skeletal Smooth and Cardiac Muscles
Difference Between Skeletal Smooth and Cardiac MusclesDifference Between Skeletal Smooth and Cardiac Muscles
Difference Between Skeletal Smooth and Cardiac Muscles
 
ANATOMY AND PHYSIOLOGY OF REPRODUCTIVE SYSTEM.pptx
ANATOMY AND PHYSIOLOGY OF REPRODUCTIVE SYSTEM.pptxANATOMY AND PHYSIOLOGY OF REPRODUCTIVE SYSTEM.pptx
ANATOMY AND PHYSIOLOGY OF REPRODUCTIVE SYSTEM.pptx
 
Part I - Anticipatory Grief: Experiencing grief before the loss has happened
Part I - Anticipatory Grief: Experiencing grief before the loss has happenedPart I - Anticipatory Grief: Experiencing grief before the loss has happened
Part I - Anticipatory Grief: Experiencing grief before the loss has happened
 
Top 10 Most Beautiful Russian Pornstars List 2024
Top 10 Most Beautiful Russian Pornstars List 2024Top 10 Most Beautiful Russian Pornstars List 2024
Top 10 Most Beautiful Russian Pornstars List 2024
 
See it and Catch it! Recognizing the Thought Traps that Negatively Impact How...
See it and Catch it! Recognizing the Thought Traps that Negatively Impact How...See it and Catch it! Recognizing the Thought Traps that Negatively Impact How...
See it and Catch it! Recognizing the Thought Traps that Negatively Impact How...
 
TEST BANK For Porth's Essentials of Pathophysiology, 5th Edition by Tommie L ...
TEST BANK For Porth's Essentials of Pathophysiology, 5th Edition by Tommie L ...TEST BANK For Porth's Essentials of Pathophysiology, 5th Edition by Tommie L ...
TEST BANK For Porth's Essentials of Pathophysiology, 5th Edition by Tommie L ...
 
TEST BANK For Guyton and Hall Textbook of Medical Physiology, 14th Edition by...
TEST BANK For Guyton and Hall Textbook of Medical Physiology, 14th Edition by...TEST BANK For Guyton and Hall Textbook of Medical Physiology, 14th Edition by...
TEST BANK For Guyton and Hall Textbook of Medical Physiology, 14th Edition by...
 
Cardiac Output, Venous Return, and Their Regulation
Cardiac Output, Venous Return, and Their RegulationCardiac Output, Venous Return, and Their Regulation
Cardiac Output, Venous Return, and Their Regulation
 
Creeping Stroke - Venous thrombosis presenting with pc-stroke.pptx
Creeping Stroke - Venous thrombosis presenting with pc-stroke.pptxCreeping Stroke - Venous thrombosis presenting with pc-stroke.pptx
Creeping Stroke - Venous thrombosis presenting with pc-stroke.pptx
 
Top 10 Most Beautiful Chinese Pornstars List 2024
Top 10 Most Beautiful Chinese Pornstars List 2024Top 10 Most Beautiful Chinese Pornstars List 2024
Top 10 Most Beautiful Chinese Pornstars List 2024
 
Cara Menggugurkan Kandungan Dengan Cepat Selesai Dalam 24 Jam Secara Alami Bu...
Cara Menggugurkan Kandungan Dengan Cepat Selesai Dalam 24 Jam Secara Alami Bu...Cara Menggugurkan Kandungan Dengan Cepat Selesai Dalam 24 Jam Secara Alami Bu...
Cara Menggugurkan Kandungan Dengan Cepat Selesai Dalam 24 Jam Secara Alami Bu...
 
Physiologic Anatomy of Heart_AntiCopy.pdf
Physiologic Anatomy of Heart_AntiCopy.pdfPhysiologic Anatomy of Heart_AntiCopy.pdf
Physiologic Anatomy of Heart_AntiCopy.pdf
 
Face and Muscles of facial expression.pptx
Face and Muscles of facial expression.pptxFace and Muscles of facial expression.pptx
Face and Muscles of facial expression.pptx
 
ANATOMY AND PHYSIOLOGY OF RESPIRATORY SYSTEM.pptx
ANATOMY AND PHYSIOLOGY OF RESPIRATORY SYSTEM.pptxANATOMY AND PHYSIOLOGY OF RESPIRATORY SYSTEM.pptx
ANATOMY AND PHYSIOLOGY OF RESPIRATORY SYSTEM.pptx
 

Chronic Obstructive Pulmonary Disease (COPD) by Dr Kemi Dele

  • 1. C O P D CHRONIC OBSTRUCTIVE LUNG DISEASE PRESENTED BY DR KD DELE DEPARTMENT OF FAMILY MEDICINE; DORA NGINZA HOSPITAL
  • 2. CONTENT • Definition and Overview • Diagnosis and Assessment • Therapeutic Options • Management of Exacerbations • Management of Stable COPD • Management of Comorbidities • Slides On Pathophysiology Of COPD
  • 4. Definition of COPD • 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.
  • 6. Burden of COPD • COPD is a leading cause of morbidity and mortality worldwide. • 30% of smokers develop COPD • 20% of adult males have COPD • 15% of COPD patients are severely symptomatic • 4th leading cause of death (USA) • Mortality rate still rising • High prevalence in low birth weight and low socioeconomic status • Tuberculosis in smokers predisposes to COPD • COPD is associated with significant economic burden.
  • 7. Risk Factors for COPD • 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
  • 8. Risk Factors for COPD cont. • Lung growth and development • Gender • Age • Respiratory infections • Socioeconomic status • Asthma/Bronchial hyperreactivity • Chronic Bronchitis
  • 9. Risk Factors for COPD cont. Aging Populations Genes Infections Socio-economic status
  • 11. Diagnosis and Assessment • A clinical diagnosis of COPD: • any patient who has dyspnoea, chronic cough or sputum production, • and a history of exposure to risk factors for the disease. • to make the diagnosis; • Spirometry is required • the presence of a post-bronchodilator FEV1/FVC < 0.70 confirms the presence of persistent airflow limitation and thus of COPD.
  • 12. Diagnosis and Assessment, cont. • The goals of COPD assessment • to determine • the severity of the disease, • the severity of airflow limitation, • the impact on the patient’s health status, • and the risk of future events. • Comorbidities • They occur frequently in COPD patients • They should be actively looked for and treated appropriately if present.
  • 13. © 2015 Global Initiative for Chronic Obstructive Lung Disease Diagnosis of COPD
  • 14. Spirometry: Assessment of Airflow Limitation • 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. © 2015 Global Initiative for Chronic Obstructive Lung Disease Spirometry: Normal Trace Showing FEV1 and FVC
  • 18. © 2015 Global Initiative for Chronic Obstructive Lung Disease Spirometry: Obstructive Disease
  • 19. Diagnosis of COPD – Pulmonary Function Tests •  Forced Expiratory Volume for 1 second (FEV1) • FEV1/FVC (Forced Vital Capacity) ratio Other Suggestive Criteria •  Total Lung Capacity (TLC) •  Forced Residual Capacity (FRC) •  Residual Volume (RV) •  Vital Capacity (VC)
  • 22. Assessment of COPD: Goals • Determine the severity of the disease, its impact on the patient’s health status and the risk of future events (for example exacerbations) to guide therapy. • Consider the following aspects of the disease separately: • current level of patient’s symptoms • severity of the spirometric abnormality • frequency of exacerbations • presence of comorbidities.
  • 23. ASSESSMENT OF COPD • Assess symptoms • Assess degree of airflow limitation using spirometry • Assess risk of exacerbations • Assess comorbidities • Combine these assessments (first three) for the purpose of improving management of COPD
  • 24. 1. Assess Symptoms of COPD • The characteristic symptoms of COPD are chronic and progressive dyspnoea, cough, and sputum production that can be variable from day-to-day. • Dyspnoea: Progressive, persistent and characteristically worse with exercise. • Chronic cough: May be intermittent and may be unproductive. • Chronic sputum production: COPD patients commonly cough up sputum. • Others include:Wheezing; Cyanosis; Right heart failure; Weight loss, anorexia
  • 25. Need For Simple Tools • Significant numbers of patients have COPD that is under-recognised, untreated and sub-optimally managed, despite widening use of spirometry • Patients underestimate their condition: in a study1 (n=3265), • 36% of those too breathless to leave the house described their condition as mild or moderate; and • 60% of those who were short of breath after walking for a few minutes on the flat described their condition as mild or moderate • Studies also confirm that patients and physicians require a tool to • facilitate fact-based dialogue • to help achieve a mutual understanding of disease status and impact; and • to help to optimise disease management
  • 26. Assess Symptoms of COPD, cont. 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.
  • 27. Assess Symptoms of COPD, cont. • The CAT has been designed to overcome the shortfalls of earlier questionnaires measuring disability in COPD. • The CAT is a simple, short, easy to use self-administered, paper-based questionnaire for use in clinical practice. • The MRC dyspnoea questionnaire measures dyspnoea only whereas CAT is a holistic measure of the impact of COPD on the patient
  • 29. CCQ: COPD Clinical questionnaire
  • 31. Differences between COPD questionnaires SGRQ MRC Dyspnoea Questionnaire CCQ CAT • Measures impaired health and wellbeing • Measures dyspnoea only • Measures clinical disease control • Measures holistic impact of COPD on patients • Used largely in clinical trials – • Used in clinical practice • Used in clinical practice • Long (76-items) • Short (5-items) • Short (10-items) • Short (8 items) • Patient completed • Patient completed • Patient completed • Patient completed • Computer required • Paper based • Paper based • Paper based • Complex to administer • Simple to administer • Simple to administer • Simple to administer
  • 32. 2. Assess degree of airflow limitation • Use spirometry for grading severity • according to spirometry, • using four grades split at 80%, 50% and 30% of predicted value •
  • 33. Classification of Severity of Airflow Limitation in COPD* *Based on Post-Bronchodilator FEV1 © 2015 Global Initiative for Chronic Obstructive Lung Disease
  • 34. 3. Assess Risk of Exacerbations • To assess risk of exacerbations: • Use history of exacerbations and spirometry. • Two exacerbations or more within the last year or • an FEV1 < 50 % of predicted value are indicators of high risk. • Hospitalization for a COPD exacerbation associated with increased risk of death.
  • 35. Combined Assessment Of COPD • Assess symptoms • Assess degree of airflow limitation using spirometry • Assess risk of exacerbations • Combine these assessments for the purpose of improving management of COPD
  • 38. Assess risk of exacerbations next
  • 39. Patient Characteristics Spirometric 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 Combined Assessment of COPD • When assessing risk, choose the highest risk according to GOLD grade or exacerbation history. • One or more hospitalizations for COPD exacerbations should be considered high risk. © 2015 Global Initiative for Chronic Obstructive Lung Disease
  • 40. 4. Assess COPD Comorbidities • COPD patients are at increased risk for: • Cardiovascular diseases • Osteoporosis • Respiratory infections • Anxiety and Depression • Diabetes • Lung cancer • Bronchiectasis • These comorbid conditions may influence mortality and hospitalizations and should be looked for routinely, and treated appropriately
  • 42. Differential Diagnoses - Pulmonary • Asthma • Bronchogenic carcinoma • Bronchiectasis • Tuberculosis • Cystic fibrosis • Interstitial lung disease • Bronchiolitis obliterans • Pleural effusion • Pulmonary oedema • Recurrent aspiration • Recurrent pulmonary emboli • Foreign body • Alpha-1 antitrypsin deficiency • Tracheobronchomalacia
  • 43. Differential Diagnoses - Non-Pulmonary • Congestive Heart Failure • Hyperventilation syndrome/panic attacks • Vocal cord dysfunction • Obstructive sleep apnoea – undiagnosed • Aspergillosis • Chronic Fatigue Syndrome
  • 44. COPD and Asthma COPD • Onset in mid-life • Symptoms slowly progressive • Long smoking history Asthma • Onset early in life (often childhood) • Symptoms vary from day to day • Symptoms worse at night/early morning • Allergy, rhinitis, and/or eczema also present • Family history of asthma
  • 45.
  • 47. Physical Examination • Vitals:  RR,  HR,  O2 saturation • General: Barrel-chest, accessory muscle use • Cardiovascular: Quiet heart sounds • Respiratory: Decreased breath sounds, wheezing, rhonchi, crackles • Full Blood Count:  Haemoglobin/Haematocrit • ABG:  pH; /N pCO2 (>5kPa);  pO2 (<8kPa);  HCO3 (chronic respiratory acidosis)
  • 48. Additional Investigations Chest X-ray: • Seldom diagnostic but valuable to exclude alternative diagnoses and establish presence of significant comorbidities. Lung Volumes and Diffusing Capacity: • Help to characterize severity, but not essential to patient management. Oximetry and Arterial Blood Gases: • Pulse oximetry can be used to evaluate a patient’s oxygen saturation and need for supplemental oxygen therapy.
  • 49. Additional Investigations 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. Composite Scores: • Several variables (FEV1, exercise tolerance assessed by walking distance or peak oxygen consumption, weight loss and reduction in the arterial oxygen tension) identify patients at increased risk for mortality.
  • 51. Therapeutic Options • Smoking cessation has the greatest capacity to influence the natural history of COPD. Encourage all patients who smoke to quit. • Pharmacotherapy and nicotine replacement increase long-term smoking abstinence rates. • All COPD patients benefit from regular physical activity – 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. • None of the existing medications for COPD has been shown conclusively to modify the long-term decline in lung function. • Influenza and pneumococcal vaccination should be offered per local guidelines.
  • 52. Quit Smoking: Strategies • ASK Systematically identify all tobacco users at every visit • ADVISE Strongly urge all tobacco users to quit • ASSESS Determine willingness to make a quit attempt • ASSIST Aid the patient in quitting eg nicotine replacement • ARRANGE Schedule follow-up
  • 53. Therapeutic Options: Risk Reduction Tobacco-control: • clear, consistent, and repeated non-smoking messages. Primary prevention: • elimination or reduction of exposures in the workplace. Secondary prevention: • surveillance and early detection. Others • Reduce or avoid indoor air pollution from biomass fuel, burned for cooking and heating in poorly ventilated dwellings. • monitor public announcements of air quality and, depending on the severity of their disease, avoid vigorous exercise outdoors or stay indoors during pollution episodes.
  • 55. Therapeutic Options: COPD Medications 1. Beta2-agonists • Short-acting beta2-agonists: e.g. Salbutamol (Asthavent/Ventolin); Fenoterol (Berotec); Terbutaline (Bricanyl)} • Long-acting beta2-agonists: e.g. Salmeterol (Serevent); Formoterol (Foradil / Oxis) 2. Anticholinergics, e.g. Ipratropium bromide (Atrovent) • Short-acting anticholinergics • Long-acting anticholinergics 3. Combination short-acting beta2-agonists + anticholinergic in one inhaler • e.g. Atrovent beta (Ipratropium bromide 0.5mg + fenoterol hydrobromide 1.25mg/4ml 4. Combination long-acting beta2-agonist + anticholinergic in one inhaler
  • 56. Therapeutic Options: COPD Medications • 5. Methylxanthines Sustained release theophylline preparations e.g. Neulin • 6. Inhaled corticosteroids e.g. Beclomethasone; Beclate; Budesonide; Fluticasone propionate; Ciclesonide; Budeflam/ Inflammide; Flixotide • 7. Combination long-acting beta2-agonists + corticosteroids in one inhaler e.g. budesonide plus formoterol; fluticasone plus salmeterol (Seretide) • 8. Systemic corticosteroids • 9. Phosphodiesterase-4 inhibitors – roflumilast
  • 58. Therapeutic Options: Bronchodilators • Bronchodilator medications are central to the symptomatic management of COPD. • Bronchodilators are prescribed on an as-needed or on a regular basis to prevent or reduce symptoms. • The principal bronchodilator treatments are • beta2-agonists • anticholinergics • theophylline or • combination therapy.
  • 59. Therapeutic Options: Bronchodilators cont. • The choice of treatment depends on: availability of medications and each patient’s response in terms of symptom relief and side effects. Long-acting inhaled bronchodilators: • are convenient and more effective for symptom relief than short-acting bronchodilators. • reduce exacerbations and related hospitalizations and improve symptoms and health status. Combining bronchodilators of different pharmacological classes: • may improve efficacy and decrease the risk of side effects compared to increasing the dose of a single bronchodilator.
  • 60. Therapeutic Options: Inhaled Corticosteroids • 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. • Inhaled corticosteroid therapy is associated with an increased risk of pneumonia. • Withdrawal from treatment with inhaled corticosteroids may lead to exacerbations in some patients.
  • 61. Therapeutic Options: Combination Therapy • 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. • Combination therapy is associated with an increased risk of pneumonia.
  • 62. Therapeutic Options cont. Phosphodiesterase-4 Inhibitors • In patients with severe and very severe COPD (GOLD 3 and 4) and a history of exacerbations and chronic bronchitis, the phospodiesterase-4 inhibitor, roflumilast, reduces exacerbations treated with oral glucocorticosteroids. Systemic Corticosteroids • Chronic treatment with systemic corticosteroids should be AVOIDED because of an unfavourable benefit-to-risk ratio.
  • 63. Therapeutic Options: Theophylline • Low dose theophylline reduces exacerbations but does not improve post- bronchodilator lung function. • Theophylline is less effective and less well tolerated than inhaled long-acting bronchodilators (not recommended if those drugs are available and affordable). • Theophylline has a modest bronchodilator effect and some symptomatic benefit in stable COPD. • Addition of theophylline to salmeterol (laba) produces a greater increase in FEV1 and breathlessness than salmeterol alone.
  • 64. Therapeutic Options: Other Pharmacologic Treatments Influenza vaccines: • it 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. Antibiotics: • 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.
  • 65. Therapeutic Options: Other Pharmacologic Treatments cont. Mucolytics: • Patients with viscous sputum may benefit from mucolytics; overall benefits are very small. 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
  • 66. Therapeutic Options: Surgical Treatments Bullectomy • Resection of large bullae compressing normal lung Lung volume reduction surgery (LVRS) • 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. Double lung transplantation • For patients with very severe COPD, • It improves quality of life and functional capacity. • It is costly, can be lack of donor availability and requires lifelong immunosuppression.
  • 67. Therapeutic Options: Other Treatments Pulmonary Rehabilitation: • Aimed at keeping patient conditioned with exercise, perception of dyspnea, quality of life and self-efficacy. Oxygen Therapy: • The long-term administration of oxygen (> 15 hours per day) to patients with chronic respiratory failure increases survival in patients with severe, resting hypoxemia. Ventilatory Support: • Combination of non-invasive ventilation (NIV) with long-term oxygen therapy may be of some use in patients with pronounced daytime hypercapnia. Palliative Care, End-of-life Care, Hospice Care: • Communication with advanced COPD patients about end-of-life care and advance care planning gives patients and their families the opportunity to make informed decisions.
  • 69. COPD EXACERBATION • An exacerbation of COPD is: • “an acute event characterized by a worsening of the patient’s respiratory symptoms that is beyond normal day-to-day variations and leads to a change in medication.” • The goal of treatment is to minimize the impact of the current exacerbation and to prevent the development of subsequent exacerbations.
  • 70. COPD EXACERBATION cont. The most common causes of COPD exacerbations: • viral upper respiratory tract infections and • infection of the tracheobronchial tree. Diagnosis • relies exclusively on the clinical presentation of the patient complaining of an acute change of symptoms that is beyond normal day-to-day variation. • COPD exacerbations can often be prevented.
  • 71. Immediate management. • Assess severity of attack. • Start treatment prior to investigations. • Sit up and give oxygen e.g. 60%. • Salbutamol 5mg in saline nebulization. • Hydrocortisone 200mg IV or 30mg predisone per os. • If life threatening add ipratropium 0.5mg to beta 2 stimulant as nebulization • MgSO4 2g in 200ml N saline over 20 minutes • Intubate and Ventilate • If still not improving consider ICU.
  • 72. Manage Exacerbations: Assessments • Arterial blood gas measurements (in hospital): • PaO2 < 8.0 kPa with or without PaCO2 > 6.7 kPa when breathing room air indicates respiratory failure. • Chest radiographs: • useful to exclude alternative diagnoses. • ECG: • may aid in the diagnosis of coexisting cardiac problems. • Whole blood count: • identify polycythaemia, anaemia or bleeding.
  • 73. Manage Exacerbations: Assessments • Purulent sputum during an exacerbation: • indication to begin empirical antibiotic treatment. • Biochemical tests: • detect electrolyte disturbances, diabetes, and poor nutrition. • Spirometric tests: • not recommended during an exacerbation.
  • 74. Manage Exacerbations: Treatment options Oxygen: • titrate to improve the patient’s hypoxemia with a target saturation of 88-92%. Bronchodilators: • short-acting inhaled beta2-agonists with or without short-acting anticholinergics are usually the preferred bronchodilators for treatment of an exacerbation. Systemic Corticosteroids: • shortens recovery time, • improves lung function (FEV1) and arterial hypoxemia (PaO2), • reduce the risk of early relapse, treatment failure, and length of hospital stay. • dose of 40 mg prednisone per day for 5 days.
  • 75. Manage Exacerbations: Treatment Options cont. Antibiotics: • should be given to • patients with three cardinal symptoms: increased dyspnoea, increased sputum volume, and increased sputum purulence. • Patients who require mechanical ventilation. • It reduces the risk of early relapse, treatment failure, and length of hospital stay Non-invasive ventilation (NIV): • For patients hospitalized for acute exacerbations of COPD: • Improves respiratory acidosis, decreases respiratory rate, severity of dyspnoea, complications and length of hospital stay. • Decreases mortality and needs for intubation.
  • 76. Indications for hospital admission • Marked increase in intensity of symptoms • Severe underlying COPD • Onset of new physical signs • Failure of an exacerbation to respond to initial medical management • Presence of serious comorbidities • Frequent exacerbations • Older age • Insufficient home support
  • 77. Consequences Of COPD Exacerbations
  • 79. Manage Stable COPD: Overview • Identification and reduction of exposure to risk factors • Individualized assessment of symptoms, airflow limitation, and future risk of exacerbations • All COPD patients benefit from rehabilitation and maintenance of physical activity. • Pharmacologic therapy is used to • reduce symptoms, • reduce frequency and severity of exacerbations, and • improve health status and exercise tolerance. • Influenza vaccination
  • 81. Manage Stable COPD: Non- Pharmacologic
  • 82. Manage Stable COPD: Pharmacologic
  • 83. Manage Stable COPD: Pharmacologic Recommended First Choice
  • 84. Manage Stable COPD: Pharmacologic Alternative Choice
  • 85. Manage Stable COPD: Pharmacologic Other Possible Treatments
  • 87. Manage Comorbidities • COPD often coexists with other diseases (comorbidities) that may have a significant impact on prognosis. In general, presence of comorbidities should not alter COPD treatment and comorbidities should be treated as if the patient did not have COPD.
  • 88. Manage Comorbidities cont. • 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. • Cardiovascular disease (ischemic heart disease, heart failure, atrial fibrillation & hypertension) • most frequent and most important disease coexisting with COPD. • Benefits of cardioselective beta-blocker treatment in heart failure may outweigh potential risk.
  • 90. References • Global Initiative For Chronic Obstructive Lung Disease (GOLD): Teaching Slide Set; January 2015. • http://www.goldcopd.org