Abnormal respiratory rate/ pattern:
– Tachypnea/ bradypnea
– Hyperpnea/hypopnea/apnea
– Kussmaul respiration – DKA (or any acidosis)
– Cheyne-Stokes respiration
Abnormal sputum
– Can be colored or clear, can increase or decrease in amount and frequency
Hemoptysis:
– Coughing up blood (cancer or TB)
Empyema:
– Pus in the pleural space, not a disease but a manifestation
▪ Hypoventilation
– Leads to Hypercapnia
▪ Hyperventilation
– Hypocapnia
▪ Cyanosis
▪ Clubbing
Disorders of the Respiratory System
Chest Wall Disorders
Disorders that compromise chest wall and restrict respiration
Causes:
Deformities
Musculoskeletal disorders
Immobilization
Obesity
Pathophysiology:
Mechanical restrictions of inspiration and expiration
Clinical manifestations:
Breathing difficulty
Of the underlying condition
Flail Chest
Multiple adjacent ribs are broken in multiple places, separating a segment
Etiology:
Severe trauma, falls
Pathophysiology:
Segment of chest wall moves independently in the opposite direction of the lung’s intention
Due to difference in pressure, flail segment goes in while the rest of the chest is moving out (vice versa) → paradoxical breathing
Clinical manifestations:
Chest pain
Dyspnea
Pneumothorax
Abnormal collection of air in pleural space
Etiology:
Physical trauma
Complication of medical/surgical intervention
Pathophysiology:
Uncoupling of the lung from the chest wall, air interferes with normal respiration
Increased pressure inside > atmospheric pressure,
– Compresses the lung
– Lung collapse (atelectasis)
Pressure displaces the mediastinum and cause cardiopulmonary impairment
Xray: black = air, tissue and fluid = white
Types:
Spontaneous pneumothorax:
– Rupture of a subpleural bleb
Secondary pneumothorax:
– Due to lung pathology, e.g. COPD
Open pneumothorax:
– Stab or bullet wounds
Tension pneumothorax:
– One-way valve allowing air and pressure to increase progressively inside pleural space
o Significant impairment of respiration and/or circulation
Clinical manifestations & diagnosis:
Chest pain, resp. distress
Diminished breath sounds
Hyper-resonant on percussion
X-ray
Pleural Effusion
Excess fluid accumulation in the pleural cavity
Causes/Types
Transudative effusion
– Congestive heart failure
– Liver cirrhosis
– Nephrotic syndrome
Exudative effusion
– Infection
– Malignancy
– Pulmonary embolism, infarction
– Pancreatitis
– Hemothorax
– Trauma
Pathophysiology:
Fluid limits expansion of lungs; impair breathing
Increased hydrostatic pressure
Injuries to the pleural lining
>300 ml = detectable clinical signs
Xray: tissue and fluid = white
Clinical manifestations & diagnosis:
Chest pain (sharp pain worsen by cough or deep breaths)
Impaired chest movement on the affected side
Dullness to percussion over the fluid
Diminished breath sounds on the affected side
Pleural friction rub
X ray confirms condition
Pulmonary Disorders
Restrictive lung diseases
Pulmonary, extra-pulmonary, diseases characterized by restriction of full expansion of lungs
Pathology: reduced lung volume, reduced ventilation/oxygenation, reduced effort in breathing
Main manifestation:
Dyspnea
Common diseases/conditions:
Aspiration
Atelectasis
Pulmonary fibrosis
Inhalation disorders
Pulmonary edema
ARDS
Obstructive lung diseases
Pulmonary diseases characterized by airway obstruction that is worse with expiration
Pathology:
o Inflamed and easily collapsible airways, frequent medical visits/ hospitalizations
Main manifestations:
Cough, dyspnea, and wheezing
Common diseases/conditions:
COPD
Chronic bronchitis/Emphysema
Bronchial Asthma
Bronchiectasis
Sleep breathing disorder (E.g. OSA)
Restrictive Lung disorders
Lung Aspiration
Entry of material from oropharynx or GI into resp. tract
Types of aspirate: pharyngeal secretions, food/drink, gastric content
Etiology:
Medical procedure; during positive pressure ventilation
Meconium aspiration syndrome
Risk factors:
Impaired consciousness (TBI), alcohol or drug overdose, general anesthesia
Tracheal intubation, presence of gastric tube
Pathophysiology:
Depends on particle size, volume, chemical composition of aspirated material, and underlying patient health status
Air way obstruction
Damage of lung tissue (acidity, microbes)
Clinical manifestations:
Range from no effect, to pneumonia, to death within minutes from asphyxiation
Inhalation Disorders
Entry of a substance with air inhalation into resp. tract
Types and Causes:
Toxic gases: e.g. CO, SO2
Pneumoconiosis (occupational lung disease)
– Silica
– Asbestos
– Coal
Pathophysiology & clinical manifestations:
Depend on dose inhaled, particle size, underlying patients’ health status
Atelectasis
Lung collapse resulting in reduced or absent gas exchange
May affect part or all of one lung
It can be a disease, or it can be caused by a disease
Etiology and Pathophysiology:
Post-surgical (most common cause)
Airway block (foreign body, mucus plug, tumor, lymph node, tubercle)
Poor surfactant
Clinical manifestations:
Breathing difficulty (rapid and shallow)
Low oxygen saturation
Cyanosis
Pleural effusion (transudate type)
Pulmonary Fibrosis
Scarring of lung tissue (alveoli)
Etiology:
Idiopathic
Inhalation, e.g. asbestos
Inflammation, e.g. pneumonitis
Autoimmune, e.g. SLE
Pathophysiology:
Replacement of normal lung parenchyma with fibrous tissue
Reduction of lung compliance
Defective perfusion
Clinical manifestations & evaluation:
Progressive dyspnea with exertion
X-ray to show fibrosis
Pulmonary Edema
Fluid inside the lungs
Etiology and diseases associated with lung edema:
Left side valvular dysfunction
Left ventricular failure
Injury to capillary endothelium
Blockage of lymphatic vessel
Pathophysiology:
Increase in atrial pressures
Increase in capillary permeability
Accumulation of fluid in interstitial space
Increased pulmonary capillary hydrostatic pressure
Clinical manifestations:
Dyspnea, orthopnea, PND
Cough (pink, frothy sputum)
Excessive sweating, anxiety, pale skin
Anxious
Acute Respiratory Distress Syndrome (ARDS)
Fulminant form of respiratory failure characterized by diffuse alveolo-capillary injury
Causes:
Sepsis (main reason)
Multiple trauma
Pneumonia
Near drowning
Drug overdose
Pathophysiology:
Injury to the pulmonary capillary endothelium
Pulmonary edema
Inflammation and platelet activation
Surfactant inactivation/loss
Clinical manifestations & diagnosis:
Dyspnea and hypoxemia
Hypoventilation, increased Pco2
Respiratory acidosis
Hypotension
Obstructive Lung disorders
Bronchial Asthma
The number 1 respiratory disease
Acute/chronic inflammatory/immune disorder of the airways
Etiology:
Complex environmental and genetic factors
Pathophysiology:
Children and adults
Hyper-responsive airways
Bronchospasm, inflammation, vascular congestion, increased mucous secretion
IgE mediated degranulation of mast cells
May lead to status asthmaticus
Precipitating factors:
Allergens, drugs, others
Clinical manifestations/ diagnosis:
*Expiratory wheezing, dyspnea, tachypnea, cough
Spirometry, family history, symptoms, etc.
*Seen everywhere in the world. The terminal airways are blocked from mucus and inflammation of the wall. This is an inflammatory disorder that is IgE mediated from mast cell degeneration. The smooth muscle wall responds quickly to antigen in exposed air. This disease can be acute or chronic and can run in a family. Status asthmaticus = severe acute asthmatic attack.
Chronic Bronchitis
Chronic inflammatory response within bronchi:
– Hyper-secretion of mucus, chronic productive cough at least 3 months/year & at least 2 consecutive years
Cause:
Smoking (main reason)
Air pollution
Long term exposure to irritants (occupation related)
Genetic factors
Pathophysiology:
Constant irritation will mucus production, size & number of mucous glands
Mucus is thicker than normal
Secondary bacterial infection adds to this inflammatory state
Clinical manifestations & evaluation:
Chronic, worsening productive cough
Diffuse, bilateral wheezes & rhonchi
Spirometry can measure the amount of airflow obstruction
Usually complicated by emphysema
Colored sputum = secondary bacterial infection
Bronchiectasis
Permanent enlargement of bronchioles most commonly secondary to infection.
– “ectasis” = dilation. You lose wall elasticity
Etiology:
Cystic fibrosis (50%), COPD
Infection; pneumonia, tuberculosis
Immune disorders
Pathophysiology:
Chronic inflammation