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1. Pulmonary Pathophysiology
2. Histology of the lung Respiratory epithelium
Connective tissue fibers, and cartilage: support and maintain open air way
Alveolar cells (type I and type II)
4. Normal Lung
5. Function of the lung Gas exchange
Protection against infection by alveolar macrophages
Surfactant secretion: allow expansion of alveoli with air
6. Lung function tests Tidal volume (TV): it is the amount of gas inhaled or exhaled with each resting breath.
Residual volume (RV): it is the amount of gas remaining in the lungs at the end of maximum exhalation.
7. Vital capacity (VC): it is the total amount of gas that can exhaled following maximum inhalation.
Total lung capacity (TLC): it is the amount of gas in the lung at the end of maximum inhalation.
TLC = RV+ VC
8. Reduction of Pulmonary Function Inadequate blood flow to the lungs: hypoperfusion
Inadequate air flow to the alveoli: hypoventilation
9. Noso-comial infections Factors that reduce airflow also compromise particle clearance and predispose to infection.
High rate of pneumonia in hospital patients due in large part to impaired ventilation and clearance.
10. Restricted lung movement and ventilation may arise due to:
Positioning
Constricting bandages
Central nervous system depression
Coma
11. Signs and Symptoms of Pulmonary Disease
12. 1- Dyspnea: subjective sensation of uncomfortable breathing, feeling “short of breath”
Ranges from mild discomfort after exertion to extreme difficulty breathing at rest.
Usually caused by diffuse and extensive rather than focal pulmonary disease.
13. Causes of Dyspnea :
Airway obstruction
Greater force needed to provide adequate ventilation
Wheezing sound due to air being forced through airways narrowed due to constriction or fluid accumulation
Decreased compliance of lung tissue
14. Signs of dyspnea:
Flaring nostrils
Use of accessory muscles in breathing
Retraction (pulling back) of intercostal spaces
15. 2- Cough
Attempt to clear the lower respiratory passages by forceful expulsion of air
Most common when fluid accumulates in lower airways
16. Causes of Cough:
Inflammation of lung tissue
Increased secretion in response to mucosal irritation
Inhalation of irritants
Intrinsic source of mucosal disruption – such as tumor invasion of bronchial wall
Excessive blood hydrostatic pressure in pulmonary capillaries
Pulmonary edema – excess fluid passes into airways
17. When cough can raise fluid into pharynx, the cough is described as a productive cough, and the fluid is sputum.
Production of bloody sputum is called hemoptysis
Not threatening, but can indicate a serious pulmonary disease
Tuberculosis, lung abscess, cancer, pulmonary infarction.
18. If sputum is purulent------- infection of lung or airway is indicated.
Cough that does not produce sputum is called a dry, or nonproductive cough.
Acute cough is one that resolves in 2-3 weeks from onset of illness or treatment of underlying condition.
Acute cough caused by upper respiratory tract (URT) infections, allergic rhinitis, acute bronchitis, pneumonia, congestive heart failure, pulmonary embolus, or aspiration.
19. A chronic cough is one that persists for more than 3 weeks.
In nonsmokers, almost always due to postnasal drainage syndrome, asthma, or gastroesophageal reflux disease
In smokers, chronic bronchitis is the most common cause, although lung cancer should be considered.
20. 3- Cyanosis
When blood contains a large amount of unoxygenated hemoglobin, it has a dark red-blue color which gives skin a characteristic bluish appearance.
Most cases arise as a result of peripheral vasoconstriction – result is reduced blood flow, which allows hemoglobin to give up more of its oxygen to tissues- peripheral cyanosis.
Best seen in nail beds
Due to cold environment, anxiety, etc.
21. Central cyanosis can be due to :
Abnormalities of the respiratory membrane
Mismatch between air flow and blood flow
Expressed as a ratio of change in ventilation (V) to perfusion (Q) : V/Q ratio
Pulmonary thromboembolus ---- reduced blood flow
Airway obstruction ---- reduced ventilation
In persons with dark skin can be seen in the whites of the eyes and mucous membranes.
22. Lack of cyanosis does not mean oxygenation is normal!!
In adults not evident until severe hypoxemia is present
Clinically observable when reduced hemoglobin levels reach 5 g/ dl.
Severe anemia and carbon monoxide poisoning give inadequate oxygenation of tissues without cyanosis
Individuals with polycythemia may have cyanosis when oxygenation is adequate.
23. 4- Pain
Originates in pleurae, airways or chest wall
Inflammation of the parietal pleura causes sharp or stabbing pain when pleura stretches during inspiration
Usually localized to an area of the chest wall, where a pleural friction rub can be heard
Laughing or coughing makes pain worse
Common with pulmonary infarction due to embolism
24. Inflammation of trachea or bronchi produce a central chest pain that is pronounced after coughing
Must be differentiated from cardiac pain
High blood pressure in the pulmonary circulation can cause pain during exercise that often mistaken for cardiac pain (angina pectoris).
25. 5- Clubbing
The selective bulbous enlargement of the end of a digit (finger or toe).
Usually painless
Commonly associated with diseases
that cause decreased oxygenation
Lung cancer
Cystic fibrosis
Lung abscess
Congenital heart disease
27. Introduction: Daily 10,000 liters of air - filtered..!
Pneumonia: Inflammation of lung.
Respiratory tract infections – commonest in medical practice.
Enormous morbidity & mortality.
28. Etiology: Decreased general resistance
Virulent infection - Lobar pneumonia
Clearing mechanism
Decreased Cough Reflex
Injury of the cilia and mucosa
Low alveolar defense
Pulmonary edema or congestion
Obstructions
Retention of secretions
29. Types: Viral
Bacterial
Mycoplasmal
Fungal
30. Patterns of infections: Airway - Bronchitis, Bronchiectasis
Parenchyma
Pneumonia
Bronchopneumonia
Lobar pneumonia
Lung abscess
Tuberculosis
31. Pneumonia Pathology:
Alveolar
Bronchopneumonia (Streptococcus pneumoniae, Haemophilus influenza, Staphylococcus aureus)
Lobar (Streptococcus pneumoniae)
Interstitial (Influenza virus, Mycoplasma pneumoniae)
Pathogenesis
Inhalation of air droplets
Aspiration of infected secretions or objects
Hematogenous spread
33. Bronchopneumonia Suppurative inflammation of lung tissue caused by Staph, Strep, Pneumo & H. influenza
Patchy consolidation – not limited to lobes.
Usually bilateral
Lower lobes common, but can occur anywhere
Complications:
Abscess
Empyema
Dissemination
34. Broncho-pneumonia
35. Broncho-pneumonia
36. Broncho-pneumonia
37. Bronchopneumonia:
39. Lobar Pneumonia: Fibrinosuppurative consolidation – whole lobe
Rare due to antibiotic treatment.
~95% - Strep pneumoniae
The course runs in four stages:
Congestion.
Red Hepatization.
Gray Hepatizaiton.
Resolution.
42. Lobar Pneumonia:
43. Lobar Pneumonia – Gray hep…
44. Lung Abscess: Focal suppuration with necrosis of lung tissue
Organisms commonly cultured:
Staphylococci
Streptococci
Gram-negative
Anaerobes
Frequent mixed infections
Mechanism:
Aspiration
Post pneumonic
Septic embolism
Neoplasms
Productive Cough, fever.
Clubbing
Complications: Systemic spread, septicemia.
45. Lung Abscess:
46. Abscess formation
47. Bronchopneumonia - Abscess formation
48. Lung Abscess:
49. Pulmonary tuberculosis Caused by Mycobacterium tuberculosis.
Transmitted through inhalation of infected droplets
Primary
Single granuloma within parenchyma and hilar lymph nodes (Ghon complex).
Infection does not progress (most common).
Progressive primary pneumonia
Miliary dissemination (blood stream).
51. Pulmonary tuberculosis Secondary
Infection (mostly through reactivation) in a previously sensitized individual.
Pathology
Cavitary fibrocaseous lesions
Bronchopneumonia
Miliary TB
54. Opportunistic pneumonias Infections that affect immunosuppressed patients
Associated disorders:
AIDS
Iatrogenic
Cancer patients
Transplant recipients
55. Usual interstitial pneumonia / idiopathic pulmonary fibrosis Progressive fibrosing disorder of unknown cause
Adults 30 to 50 years old
Respiratory and heart failure (cor pulmonale) ~ 5 y