Test 2 Respiratory Flashcards

(115 cards)

1
Q

Primary function of respiratory system

A

Provide O2 for metabolism in tissues
Remove CO2 that waste product of metabolism

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2
Q

Secondary function of respiratory function

A

Facilitate sense of smell
Produces speech
Maintains acid base balance
Maintains body water levels
Maintains heat balance

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3
Q

components of upper respiratory tract

A

Nasal cavity
Sinuses
Pharyngeal tonsils
Nasopharynx
Pharynx
Larynx
Epiglottis
Esophagus

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4
Q

Nose

A

Humidifies, warms and filters inspired air

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5
Q

Sinuses

A

Air filled cavities within hollow bone that surround nasal passages
Provide resonance during speech *

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6
Q

Pharynx

A

Located behind the oral and nasal cavities
Passage for both respiratory and digestive tracts

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7
Q

Divisions of pharynx

A

Nasopharynx
Oropharynx
Laryngopharynx

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8
Q

Larynx

A

Located above trachea and just below pharynx
“The voice box”
Two pairs of vocal cords

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9
Q

Glottis

A

Opening between the true vocal cords
Important role in coughing

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10
Q

Most fundamental defense mechanism of the lungs

A

Coughing

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11
Q

Epiglottis

A

Leaf shaped elastic structure attached to top of larynx
Prevents food from entering tracheobronchial tree by closing over glottis during swallowing

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12
Q

Components of the lower respiratory tract

A

Trachea
Bronchus
Bronchi
Bronchioles

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13
Q

Trachea

A

Located in front of esophagus
Branches into right and left main stem bronchi

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14
Q

Carina

A

Point where left and right main stem bronchi branch off

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15
Q

Main stem bronchi

A

Divide into 5 secondary or lobar bronchi that enter each of 5 lobes of lung
Bronchi are lined itch cilia, which propel mucus up and away from the lower airway to trachea where it can be expectorated or swallowed

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16
Q

Difference between right and left main stem bronchi

A

Right is slightly wider, shorter and more vertical than left

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17
Q

Bronchioles

A

Branch from the secondary bronchi and subdivide into the small terminal and respiratory bronchioles
Contain no cartilage and depend on elastic recoil of lung for patency

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18
Q

Terminal bronchioles

A

Contain no cilia and do not participate in gas exchange

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19
Q

Alveoli

A

*basic unit of gas exchange
On terminal bronchioles
Alveolus
Alveolar capillary network

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20
Q

Acinus (acini)

A

All structures distal to terminal bronchioles

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21
Q

Alveolar ducts

A

Branch from respiratory clusters

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22
Q

Surfactant

A

Secreted in the walls of alveoli
Phospholipid protein that reduces surface tension in alveoli
Without alveoli would collapse

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23
Q

lobes of lungs

A

3 in right 2 in left

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24
Q

Visceral pleura

A

Covers pulmonary surfaces (lungs)

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25
Parietal pleura
Lines the inside of thoracic cavity including upper surface of diaphragm
26
Pleural fluid
Produced by cells lining the pleura and lubricates visceral and parietal pleurae Allows them to guide smoothly and painlessly during respiration
27
Accessory muscles
Scalene muscles Sternocleidomastoid muscles Trapezius and pectoralis muscles
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Risk factors for respiratory disease
Smoking Chewing tobacco Allergies Frequent resp. Illness Chest injury Surgery Chemicals/pollutants Crowded living Fam history of infection disease Geographic residence and travel
29
Chest X-ray
Provides info regarding anatomic loco and appearance of lungs Cheap easy and quick
30
Sputum specimen
A specimen obtained by expectoration or tracheal suctioning to assist in identification of organisms or abnormal cells
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Sputum specimen pre procedure
Determine purpose Early morning is best 15 mL Rinse prior, several deep breaths, cough deeply
32
Bronchoscopy
Direct visual exam of larynx, trachea and bronchi with fiberoptic bronchoscope
33
Bronchoscopy pre procedure
Informed consent NPO midnight prior Vitals Monitor coagulation studied Remove dentures and glasses Meds for sedation Need crash cart available
34
Bronchoscopy post procedure
Vitals Semi- Fowler Assess gag reflux NPO until gag reflex returns Emesis basin Check for bloody sputum Monitor resp status, especially if had sedative Complications Notify if fever or difficulty breathing
35
Complications of Bronchoscopy
Bronchospasm, bacteremia, bronchial perforation indicated by facial or neck crepitus, dysrhythmias, fever, hemorrhage, hypoxemia, and pneumothorax
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Pulmonary angiography
Invasive fluoroscopic procedure following injection of iodine or radio plaque or contrast material through a catheter inserted through the antecubital or femoral vein into the pulmonary artery or one of its branches Lights up vasculator of lungs Helps see if they have blood clots
37
Pre procedure pulmonary angiography
Informed consent and allergies NPO 8 hours prior Monitor vitals Monitor coagulation studies Establish IV access Sedate Crash cart near Instruct that they must lie still and may feel urge to cough or experience flushing, nausea or salty taste
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Post procedure pulmonary angiography
Monitor vitals Don’t take blood pressure in extremity used for IV for 24 hrs Monitor peripheral neurovascular status Assess insertion site for bleeding Monitor for delayed reaction to dye
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Thoracentesis
Removal of fluid or air from pleural space via transthoracic aspiration
40
Pleural effusion
Gathering of fluid in the pleural space, can’t respirate well with it Is not pleural fluid, has unwanted matter
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Thoracentesis pre procedure
Informed consent Baseline vitals Ultrasound or CXR prior if perscribed Assess coagulation studies Sitting upright with arms and hear supported by table at bedside If can’t sit up lay on unaffected side Informed to NOT cough, breathe deeply or move
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Thoracentesis post procedure
Monitor vitals and resp status Pressure dressing and assess puncture site for bleeding and crepitus
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Complications of Thoracentesis
Pneumothorax, air embolism and pulmonary edema
44
Pulmonary function tests (PFTs)
Include a number of different tests used to evaluate lung mechanics, gas exchange and acid base disturbance through spirometric measurements, lung volumes and arterial blood gases
45
Pulmonary function tests pre procedure
Determine if any analgesics is being admin Consult physician regarding holding bronchodilators prior to testing Instruct: Void before Wear loose clothing Remove dentures No smoking or eating heavy meals for 4-6 hrs before
46
Pulmonary function tests post procedures
Resume to normal diet and bronchodilators that were held prior
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Inspiration reserve volume IRV
Breath in in in as much as possible and then hold How much extra can you take in?
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Tidal volume TV
Normal volume of air breathed in and out when not exerting self
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Expiratory reserve volume ERV
The maximum amount of air you can forcible breathe out after a breath
50
Residual volume RV
What’s left when a person breaths out as much as possible
51
Vital capacity VC
Everything you can take in minus the residual volume
52
Total lung capacity TLC
Everything you can take in including residual volume
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Percutaneous Lung biopsy
Performed to obtain tissue for analysis by culture or cytologic examinations
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Needle lung biopsy
Done to identify pulmonary lesions, changes in tissue and the cause of pleural effusion
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Lung biopsy pre procedure
Informed consent NPO prior Information of local anesthetic but may feel pressure during needle insertion and aspiration Admin analgesics and sedatives as prescribed
56
Lung biopsy post procedure
Monitor vitals Apply dressing to site and monitor for drainage and bleeding Monitor for resp distress Monitor for signs of pneumothorax and emboli
57
Ventilation perfusion lung scan
Perfusion scan: blood flow to lungs is evaluated Ventilation scan: determines patency of the pulmonary airways and detects abnormalities Radionuclide may be injected Sees if arteries match veins
58
Ventilation perfusion lung scan pre procedure
Informed consent Allergies for dye Remove jewelry Review breathing methods Establish IV access Admin sedation if perscribed Crash cart near
59
Skin tests
An intradermal injection used to assist and diagnosing various infectious diseases
60
Skin test procedure
Use test site free of excessive body hair dermatitis and blemishes Apply at upper 1/3 of inner surface of left arm Circle and mark injection test site Document date, time and test site
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skin test pre procedure
Determine hypersensitivity or previous reactions to skin tests
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Skin tests post procedure
Instruct not to scratch to prevent infection and abscess formation and to avoid scrubbing Interpret reaction at injection site 24-72 hours after Assess site for amount of induration (hard swelling) and presence of erythema and blister like elevations
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Arterial Blood Gases (ABGs)
Measures the dissolved O2 and CO2 in the arterial blood and reveals the acid base state and how well the O2 is being carried in the body Allen test
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Normal pH
7.35-7.45
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Normal PCO2 ABG
35-45 mmHg
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Normal HCO3 ABG
22-27 mmHg
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PO2 ABG
80-100 mmHg
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ABG pre procedure
Perform Allen test on both writsts Have rest for 30 minutes prior to Avoid suctioning prior to drawing blood Do not turn off O2 unless blood gases are ordered on room air
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ABG post procedure
Place specimen on ice Not temp on lab form Note O2 and type of ventilation Apply pressure to site for 5-10 minutes (longer if on anticoagulants or have bleeding disorder) Transport the specimens to lab w/in 15 minutes
70
Pulse Oximetry
Noninvasive test that registers O2 saturation of hemoglobin After a hypoxia client uses up the readily available O2 reserve O2 attached to the hemoglobin is drawn on the provided O2 to tissues Alerts hypoxemia before clinical signs occur
71
Pneumonias
Acute inflammation of parenchymal tissues functional parts = alveoli and bronchioles Affects 1% of pop each year 4 mil cases a year 6th leading cause of death Most common cause of death from infectious disease
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Nasopharyngeal defenses
Resistance factor of pneumonia Remove particles from air and destroy invading organisms Risks: hay fever, common cold, nasal trauma
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Glottic and cough reflexes
Host resistance for pneumonias Prevents aspiration into tracheobroncial tree Risk factors: stroke, abdominal or chest surgery, sedation, NG tube
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Mucociliary blanket
Host resistance for pnnemonias Remove secretions microorganisms and particles Risk factors: smoking, inhalation if irritating gases
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Pulmonary macrophages
Host resistance of pneumonias Removes microorganisms Risk factors: alcohol intoxication and smoking
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Complications of pneumonias
Bacteremia/septicemia Empyema Lung abscess
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Pneumonias etiology
Droplet inhalation Bacterial: streptococcus pneumonia, diplococcus pneumonia Viral: influenza, parainfluenza, RSV, CMV Other: mycoplasma pneumoniae Smoke inhalation Aspiration
78
Subjective pneumonia manifestations
Lassitude and severe malaise Chest pain that increases with inspiration, dyspnea
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Objective manifestations of pneumonias
^ temp ^ RR, HR, use of accessory muscles, orthopedia Cough and sputum Gray complexion Raleigh (fine crackles) Rhonchi Decreased breath sounds over consolidation Friction rub Dull to percussion E > A changes
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Sputum for diff types of pneumonias
Pneumococcal: purulent, rusty Staphylococcal: yellow, blood streaked Klebsiella: red gelatinous Mycoplasma: non productive that advances to muciod
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Diagnostics of pneumonias
^ WBC and ESR CXR is patchy or lobar pulmonary infiltrates Sputum/blood cultures
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ABGs for pneumonias
Hypoxemia Respiratory alkalosis
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Pathologic changes in pneumonia
Congestion 4-24 hrs Red hepatization 48 hrs Gray hepatization 1 week Resolution 7-12 days
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Congestion
Serous exudate from initial inflammatory response pours into alveoli
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Red hepatization
Extravasation of RBCs, fibrin, PMNs into alveoli Tissue is firm and red
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Gray hepatization
Fibrin accumulates and granulates, RBCS and PMNs start disintegrating
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Pneumonias treatment
Pneumococcal: penicillins and cephalosporins Gram negative: gentamycin or tobramycin
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Obstructive airway disorders
Asthma Chronic bronchitis Emphysema Chronic obstructive pulmonary disease Cystic fibrosis
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Restrictive airway disorders
Pleural effusion Hemothorax Pneumothorax Pneumoconioses Thoracic cage disorders Adult respiratory distress syndrome
90
Asthma
Hyper-responsive, reversible form of airway disease caused by restriction in airway size from bronchospasm, chronic inflammation and increased airway secretion - bronchial and bronchiolar narrowing from ^ smooth muscle tone - mucosal edema - hypersecretion of mucus
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Asthma epidemiology
9-12 mil in US ^ incidence prevalence and mortality Most common cause of chronic illness in <17
92
Extrinsic atopic asthma (type 1)
Immediate hypersensitivity response mediated by IgE Mast cells release histamine and prostaglandins on exposure to allergens Usually have fam history of allergies, urticaria or hay fever Usually affects children Good prognosis - complete remission in adolescence
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Intrinsic (non-atopic) idiopathic asthma (type 2)
Adult onset (> 30) Chronic mucopurulent bronchitis More serious, more difficult to control Poorer prognosis
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Exercise induced asthma
40-90% Triggers: hypocapnia, cool air with less water vapor
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Bronchospastic asthma triggers
Cold air - loss of heat and water Exercise Emotional upset - vagal pathways Exposure to bronchial irritants - receptors and vagal reflex
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Inflammatory asthma triggers
Exert effects through inflammatory response IgE mediated response to allergens - dust mite and cockroach excrement - molds and mildew - animal dander
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Asthma early response
Immediate bronchoconstriction on exposure to inhaled irritant or antigen Sx’s w/in 10-20 min Recovery 60-90 min Caused by re;ease of chem mediators from IgE coated mast cells on mucosa
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Asthma late response
Develops 3-5 hours after exposure to trigger may last for days or weeks Involves inflammation and increased airway responsiveness Caused by release of chemical mediators from mast cells, macrophages and epithelial cells (induce migration and activation of other inflammatory cell) Produces epithelial edema and injury changes in mucociliary function, reduced clearance or secretions ^ airway responsiveness
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Asthma manifestations 1
Bronchi widen and lengthen on inspiration BUT collapse on expiration Expiration becomes difficult d/t edema, narrowing and mucus obstruction Primary problem is getting air out of lungs Expiration requires use of accessory muscles
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Asthma manifestations 2
Decreased FEV and PEFR Dyspnea - orthopnea Wheezing esp. on expiration PaO2 60-72 mmHg PaCO2 low initially D/t ^ RR but ^ D/t decrease in alveolar ventilation V/Q mismatch Cyanosis Intercostal retraction Fatigue
101
Bronchial Asthma in children
Most frequent admitting dx in children’s hospitals Sex: 10-15% of boys 7-10% of girls Onset: 30% by age 1, 80-90% by age 4-5 Fam links: 1 parent = 25% risk, both = 50% Polygenic / multifactorial determinants
102
Asthma pharmacologic treatment
Beta 2 adrenergic bronchodilator - albuterol - epinephrine - xanthines Anticholinergic bronchodilator: Ipratropium (atovent) Corticosteroids - beclomethasone - hydrocortisone, methylprednisolone, IV if severe Heukotriene receptor antagonists Mast cell stabilizers FOR PREVENTION ONLY - cromolyn sodium
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Chronic Obstructive Pulmonary Disease (COPD)
Aka chronic obstructive lung disease (COLD) or chronic airway obstruction (CAO) Group of diseases that result in obstruction of airflow
104
COPD includes
Chronic bronchitis Emphysema
105
Chronic bronchitis
Inflammation on bronchial walls with hypertrophy of the mucous goblet cells Characterized by a chronic productive cough (copious mucus) Present for at least 3 months out of year OR 2 months/yr for 2 successive years Often have frequent and recurrent respiratory infections “blue bloater”
106
Bronchitis etiology
Cigarette smoking Inhalation of industrial gases and other toxic substances
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COPD etiologies
Air pollution, smoking, chronic respiratory infections, exposure to molds and fungi, allergic reactions
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Effects of bronchitis
Inhibits cilia and macrophages Inflammation of major and small airways Hypertrophy of mucosal glands Excessive secretion Narrowing and smooth muscle constriction
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Manifestations of bronchitis
DOE Decreased PaO2 ^ PaCO2 D/t decreased alveolar ventilation V/Q mismatch Hypoventilation of of alveoli d/t air trapping, hypoxemia, hypercapnia, cyanosis Scattered rhonchi and rales on forced expiration Abnormal ABGs Chronic cough Copious yellow green sputum Exercise intolerance Plycythemia Clubbing of fingers
110
Emphysema
Destruction of walls of alveoli Dilatation and less of elasticity of airspaces distal to terminal bronchioles and loss of normal elastic recoil Results in air trapping with ^ AP diameter “barrel chest” Larger airways become thinned and atrophied > become more collapsible Less prone to acute bronchitis or pneumonia but is very serious or fatal when they do get it “Pink Puffer”
111
Etiology emphysema
Cigarette smoking Often genetically determined - autosomal recessive - esp. early onset and severe progression - deficiency of alpha antitrysin which inhibits proteolytic enzymes of leukocytes - loss of inhibition -> digestion of lung tissue with bacteria
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Centrilobular emphysema
Assoc. with smoking Affects respiratory bronchioles and alveolar ducts Unevenly distributed BUT affects upper and posterior portions of lungs more severely
113
Panacinar emphysema
Destruction and enlargement of alveoli distal to terminal bronchioles Results of genetic abnormality or progression of chronic bronchitis * lower portions of lung more affected
114
Emphysema manifestations
Dyspnea even at rest Tachypnea V/Q mismatch NOT prominent d/t loss of capillaries with alveoli - cyanosis and heart failure less prominent - pink puffers Usually little cough or sputum ABGs usually normal or respiratory alkalosis d/t hyperventilation May be unable to eat Hyperinflation of lungs “barrel chest” Slowly debilitating
115
Treatment of bronchitis and emphysema
Control of environment irritants and infection Nutritional support Exercise training Breathing exercises and retraining Managing secretions Pharmacologic treatment Oxygen therapy Psycho-emotional support