This document provides information about Chronic Obstructive Pulmonary Disease (COPD). It defines COPD as a progressive lung disease that makes breathing difficult. The two main conditions that make up COPD are chronic bronchitis and emphysema. Risk factors include cigarette smoking, air pollution, and genetic conditions. Symptoms vary between chronic bronchitis and emphysema. Management involves smoking cessation, medications like bronchodilators and steroids, oxygen therapy, and sometimes surgery. The severity of COPD is classified by lung function testing into four stages from mild to very severe.
2. SYNONYMS
Chronic obstructive pulmonary
disease(COPD) is also called as chronic
obstructive lung disease(COLD), chronic
obstructive airway disease(COAD),chronic
airflow obstruction(CAO).
3. DEFINITION
Chronic obstructive pulmonary disease is a
progressive disease that makes it hard to breath.
“progressive” means the disease get worse over
time.
In COPD, less air flows in and out of the airways
because of one or more of the following:
The airways and air sacs lose their elastic quality.
The walls between many of the air sacs are
destroyed.
The walls of the airways become thick and inflamed.
The airways make more mucus than usual, which
can clog them.
4.
5. RISK FACTORS
Exposures:
Cigarette smoking, pipe & cigar smoking is the
most important risk factor.
Breathing in second hand smoke, Air pollution,
or chemical fumes or dust from the environment
or workplace.
Previous Infectious diseases like HIV,
tuberculosis
Poverty & malnutrition
6. Host factors:
Genetic condition called alpha-1 antitrypsin
deficiency.(alpha-1 anti protease deficiency)
age:>40yrs
Airway hyperactivity as in asthma
7. Chronic bronchitis Emphysema
Incidence:
middle & late adult life
More in male than females
More in smokers than non smokers
More in urban than in rural dwellers
8. CHRONIC BRONCHITIS
Chronic bronchitis is defined as condition
associated with excessive tracheobronchial
mucus production to cause productive cough
for at least 3 months of the year for more
than 2 consecutive years.
Chronic bronchitis is characterized by
inflammation of airways extended from
trachea to small airways, alveoli.
9. EMPHYSEMA
Emphysema is defined as abnormal
permanent distension of air spaces distal to
the terminal bronchiole with destruction of
alveolar septa.
10. PATHOLOGY OF COPD
Chronic bronchitis & Emphysema occurs as a
result of inflammatory process involving the
airways and distal air spaces.
Smoking & other airway irritants cause
neutrophils, macrophages,T-
lymphocytes(CD8+) & other inflammatory cells
accumulate in airways.
Once they activated, they trigger inflammatory
response in which inflammatory mediators
navigate to site to destroy & remove foreign
debris
11. Repeated exposure to airway irritants cause
ongoing inflammatory response which causes
permanent inflammation of airways, chronic
bronchitis.
In emphysema, oxidants produced by smoking
& proteases produced by inflammatory
macrophages, epithelial cell cause protease &
anti protease imbalance which is responsible for
breakdown of lungs fragile elastic lamina,
destruction of alveolar septa.
Mediators: LTb4( attracts neutrophils,
lymphocytes),TNFα, IL1β, IL6(amplify
inflammatory response) &TGFβ(induce fibrosis
in small airways)
16. In Emphysema:
Severe destruction of small airways, alveoli.
Destruction of alveolar septa.
Formation of large pockets called bullae.
17.
18. CLASSIFICATION OF EMPHYSEMA
Centriacinar:
Destruction and distension are
limited to respiratory bronchiole and alveoli
closely related to them(with sparing of the
periphery).
Predominantly found in upper lobe
& superior segments of lower lobe, most
frequently associated with cigarette smoking.
19. Panacinar:
Generalized destruction of both central
& peripheral portion of acinus. Predominant
in lower half of the lungs, mostly associated
with alpha 1 antitrypsin deficiency.
Paraseptal:
Involves only distal acinus. It involves
distal airway structures, alveolar ducts & sacs.
Localized around septa of the lungs.
20.
21. SYMPTOMS
Chronic bronchitis Emphysema
•Ongoing cough with mucus
production(called smoker’s cough)
•Copious purulent sputum
•Breathlessness relatively late in onset
•Mucopurulent relapses more frequent
•Wheezing
•Chest tightness
•Minimal cough with expectoration
•Scanty mucoid sputum
•Breathlessness insidious in onset initially
on Exertional, gradually even at rest
•Mucopurelent relapses less frequent
• GeneralisedWeakness
•lethargy
22.
23. On examination:
Inspection:
Pt looks dyspnic
Use of accessory muscles
Barrel shaped chest (due to hyper inflation)
Prolonged expiration
Tripod positioning to facilitate action of accessory
muscles.
Patients with advanced disease have paradoxical inward
movement of the rib cage with inspiration (Hoover's sign).
Emphysema patients, termed "pink puffers" are thin and
non cyanotic at rest and have prominent use of accessory
muscles
Chronic bronchitis patients are more likely to be heavy and
cyanotic & termed as “blue bloaters”.
24.
25.
26. Palpation:
-decreased chest expansion
Percussion:
- hyper resonance on lung fields
Auscultation:
Decreased breath sounds
Normal vesicular breathing but
prolonged expiration
Expiratory ronchi
Coarse crepitatons on both phases
27. INVESTIGATIONS
Chest X-Ray:
Not sensitive for Dx
To exclude other diseases
Hyper-inflation signs
Low set flat diaphragm
ABG:
important for assessing patients with severe COPD.
Detect acute & chronic hypercapnia
Respiratory acidosis(pco2 raised, hypercarbia)
Pao2 is markedly reduced (hypoxemia)
Measurement of serum α1AT level, normal level 2-4 g/l.
28. ECG: May show features of right atrial
&ventricular hypertrophy.
Pulmonary function testing (spirometry):
Main method for diagnosing COPD.
low FEV1/FVC (< 70%)
Used for classification of COPD severity.
Obstructive pattern
FEV1-reduced (<80%)
FEV1/FVC-reduced (<70%)
PEF-reduced
TLC-increased
RV-increased
29. COMPLICATIONS OF COPD
Carbon dioxide narcosis: Persistant Co2
retention causes increase Paco2; hypercarbia,
causes drowsiness, altered sensorium,
headache.
Respiratory failure:
Type Ι respiratory failure(low Pao2, normal
Paco2) occurs in mild to moderate COPD.
Acute or Chronic Type ΙΙ respiratory failure
occurs in severe COPD.
Secondary polycythemia: Results from
hypoxemia stimulating erythropoiesis.
34. Specific management:
Mild COPD: Add short acting β2 agonists like
salbutamol 2-4mg or terbutaline 2.5-5mg 6 hourly.
Moderate COPD: Add long acting β-stimulants like
salmetrol,2puffs of 25 mcg each 2-3 times a day,
formetrol 2 puffs of 6 mcg each 1-3 times a day with
short acting anti cholinergic like ipratropium
bromide 40-80μg 6 hourly or long acting anti
cholinergic like tiotropium bromide 18μg once a day.
Severe COPD: Add inhaled glucocorticosteroids like
beclomethasone/budesonide/fluticasone. If response
is not satisfactory add systemic glucocorticosteroids
like prednisolone/methyl prednisolone.
35. Very severe COPD: Long term O2, ventilatory
support, management of cardiac failure, may
consider surgical management.
Methylxanthines like aminophylline or
theophylline can be administered when
necessary.
Long term domiciliary oxygen therapy should be
administered to patients with PaO2<55 mmhg,
>16 hrs/day, 2-3ltr/min to maintain SaO2>90%.
This reduses pulmonary hypertension,
polycythemia, dyspnoea, hypoxaemia.
Antibiotics like tetracycline or ampicillin is
needed when respiratory infection present, if no
response sputum culture sensitivity to be done &
antibiotic changed accordingly.
36. For out patients management doxycycline,
amoxicilline-clavulanate can be given. Patients
older than 65 years fluoroquinolones like
levofloxacin, gemifloxacin, moxifloxacin can be
given.
For hospitalised patients IV antibiotics like
azithromycin or fluoroquinolones or third
generation cephalosporins like ceftriaxone or
cefotaxime should be administered.
37. Severe acute exacerbation of COPD:
Oxygen: Initial therapy should be maintaining
SaO2 >90%, can be ).
Bronchodilators: Nebulisation of β2 agonists like
salbutamol 2.5mg every 20 min & anti
cholinergic agents like ipratropium bromide to
be administered.
Antibiotics: Indicated if sputum volume &
purulence is increased.
Most common organisms incluce S.pneumoniae,
H.influenzae, M,catarrhalis.
patients with severe exacerbation third
generation cephalosporins & fluoroquinolones or
an aminoglycoside to be given.
38. Corticosteroids: IV or oral corticosteroids to be
administered as they improve lung function &
hypoxemia.
Aminophylline: should be administered if
patient fails to respond to initial treatment
with Nebulization of β2 agonists. . Given as a
loading dose of 5mg/kg/hr as an infusion.
Diuretics: should be administered to patients
with gross cardiac failure.
Respiratory stimulants: Like Doxapram can be
if patient is not responding to conventional
agents. Dose 1.5-4mg/min as infusion.
39. Non-invasive positive pressure
Ventilation(NIPPV): Ventilation should be
tried with tight fitting face mask.
This is used in patient with normal mental
status, stable cardiovascular function.
Indications- severe dyspnoea, use of accessory
muscles, paradoxical abdominal motion,
PH<7.35 mmhg, PaCo2> 45 mmhg,
Respiratory rate>25/min.
40. Invasive mechanical ventilation: When NIV fails
patient should be intubated for mechanical
ventilation.
Indications- severe dyspnoea, use of accessory
muscles, paradoxical abdominal motion,
Respiratory rate>35/min
Severe acidosis-PH<7.25
Hypercapnia>60 mmhg
Hypoxia<40 mmhg
Altered sensorium
Respiratory arrest, unstable cardiovascular
function, sepsis, hypotension, shock.
41. Surgical management:
Bullectomy
Lung volume reduction surgery(LVRS)-
resection of damaged portion of lung,
improves exercise tolerance but doesn’t
improve life expectancy.
Lung transplantation- If FEV1<35% (PaO2<
60 mmhg), & PaCo2>50 mmhg.
42. GOLD
Stage
Severity Spirometry Management
0 At Risk Normal Avoid risk factors
I Mild FEV1/FVC <0.7 and FEV1 80%
predicted
Short acting β- 2
agonist
II Moderate FEV1/FVC <0.7 and 50% FEV1
<80% predicted
Long acting β- 2
agonist/short or long
acting anti cholinergics
III Severe FEV1/FVC <0.7 and 30% FEV1
<50% predicted
Add inhaled
steroids/methylxanthi
nes
IV Very Severe FEV1/FVC <0.7 and FEV1 <30%
predicted
or
FEV1 <50% predicted with
respiratory failure or signs of
right heart failure
Add oxygen,
ventilatory support,
management of RHF