Pathophysiology Exam 3 – Rapid Review Notes
Pulmonary System Anatomy
- Upper (conducting) portion: naso/oro/laryngopharynx
- Lower (respiratory) portion: larynx → trachea → bronchi → bronchopulmonary segments → alveoli
- Blood supply: bronchial & pulmonary arteries
- Alveolar cells: type I (gas exchange); type II (surfactant ↓ surface tension)
Neural Control & ANS Effects
- Respiratory centers: pons & medulla; efferent via phrenic nerve
- Parasympathetic (acetylcholine, vagus) → bronchoconstriction
- Sympathetic (β₂-adrenergic, epinephrine) → bronchodilation
Mechanics of Breathing
- Inspiration: diaphragm & external intercostals contract → ↑thoracic volume → negative intrapleural pressure
- Expiration: passive; active (forceful) uses internal intercostals & abdominals
- Functional residual capacity = air left after normal expiration
- Surfactant keeps alveoli open
Airway Resistance & Compliance
- Resistance ∝ \frac{1}{\text{radius}^4}; highest at nose, lowest in small bronchioles
- ↑Resistance factors: mucus, bronchospasm, stress, aging
- Compliance = \frac{\Delta V}{\Delta P}; ↑ in neonates, ↓ with age (rigid chest, ↓elastic fibers)
Ventilation & Diffusion
- Distribution: greatest at lung bases (upright)
- Diffusion barriers: surfactant → RBC (6 layers)
- Hypoventilation → ↑PaCO2 (resp. acidosis); Hyperventilation → ↓PaCO2 (resp. alkalosis)
Obstructive vs Restrictive Patterns
- Obstructive: air OUT problem (↑resistance, wheeze, hyperinflation)
- Restrictive: air IN problem (↓compliance, ↓volumes, crackles)
Obstructive Disorders
• Asthma (reversible)
- Intrinsic (non-allergic, adult); Extrinsic (IgE-mediated, pediatric)
- Immediate mediators: histamine, leukotrienes, prostaglandins
- S/S: wheeze, cough, tight chest, dyspnea
- Dx: ↓PEFR/FEV₁; Tx: trigger avoidance, β₂-agonists, steroids, O₂
• Chronic Bronchitis (Type B COPD, “blue bloater”) - Productive cough >3 mo/yr for 2 yrs
- Patho: mucous-gland hyperplasia, thick wall, pulmonary HTN
- S/S: cough, sputum, edema, cyanosis
- Tx: stop smoking, bronchodilators, hydration
• Emphysema (Type A COPD, “pink puffer”) - Alveolar wall destruction, loss of recoil; α₁-antitrypsin deficiency or smoking
- S/S: dyspnea, thin, barrel chest, pursed-lip breathing
- PFT: ↓FEV₁, ↑TLC; CXR: hyperinflation
- Tx: O₂, anticholinergics, steroids
• Bronchiectasis: irreversible bronchial dilation post‐infection; copious purulent sputum
• Cystic Fibrosis: AR CFTR mutation → thick secretions, recurrent infections
Restrictive Parenchymal Disorders
• Diffuse Interstitial Lung Disease (fibrotic)
- Immune injury → inflammation → fibrosis
- S/S: exertional dyspnea, dry cough, bibasilar crackles, clubbing
• Sarcoidosis: non-caseating granulomas; young women; S/S: fatigue, skin lesions; Tx: steroids
• ARDS: acute alveolar-capillary damage (sepsis, trauma, aspiration) - Patho: leaky capillaries → non-cardiogenic pulmonary edema, surfactant loss
- Hallmark: severe hypoxemia refractory to O₂; CXR “white-out”
Neuromuscular / Chest-Wall Causes
- Poliomyelitis, ALS, Guillain-Barré, Myasthenia gravis → ventilatory failure
- Deformities: kyphoscoliosis, flail chest, obesity restrict expansion
Pulmonary Infections
- Pneumonia: alveolar inflammation by bacteria/virus/aspiration
- S/S: fever, crackles, purulent sputum; CXR infiltrate; Tx: antibiotics
- SARS, TB also impact respiration (not detailed here)
Fluid & Electrolyte Basics
- Homeostasis: intake, absorption, distribution, excretion
- Regulators: hypothalamic thirst/ADH, RAAS, natriuretic peptides
- Edema mechanisms: ↑hydrostatic P, ↓oncotic P, lymph block, Na/H₂O retention
Key Electrolyte Ranges & Imbalance Signs
- Sodium 135–145 mEq/L
• Hyponatremia: cramps, confusion • Hypernatremia: thirst, dry mucosa - Potassium 3.5–5 mEq/L
• Hypo: weakness, arrhythmia • Hyper: flaccid paralysis, arrest - Calcium 8.5–10.5 mg/dL
• Hypo: tetany, spasms • Hyper: lethargy, constipation - Magnesium 1.5–2.5 mEq/L
• Hypo: cramps, arrhythmia • Hyper: ↓reflexes, respiratory depression - Chloride 98–108 mEq/L; Phosphate 2.5–4.5 mg/dL (see symptoms as needed)
Acid–Base Quick Table
Disorder | pH | PCO_2 | HCO_3^- | Primary Cause | Compensation |
---|---|---|---|---|---|
Metabolic Acidosis | ↓ | ↓ | ↓ | DKA, diarrhea | Hyperventilation |
Metabolic Alkalosis | ↑ | ↑ | ↑ | Vomiting | Hypoventilation |
Respiratory Acidosis | ↓ | ↑ | ↑ | COPD | Renal HCO_3^- retention |
Respiratory Alkalosis | ↑ | ↓ | ↓ | Hyperventilation (altitude) | Renal HCO_3^- excretion |
High-Yield Reminders
- Surfactant from type II cells critical for alveolar stability
- \text{Resistance} \uparrow as airway radius ↓; neonates have naturally higher resistance
- COPD hallmark: ↓FEV₁/FVC ratio; Restrictive: ↓TLC with normal ratio
- ARDS: treat underlying cause & provide supportive oxygenation
- RAAS ↑Na⁺/water reabsorption; Natriuretic peptides oppose RAAS
- Buffer systems (Hb, bicarbonate) & lungs/kidneys maintain pH 7.35–7.45