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Altered Ventilation and Diffusion (INFECTIOUS (Pneumonia (manifestations…
Altered Ventilation and Diffusion
INFECTIOUS
Pneumonia
cause
microorganisms: bacteria, viruses, fungi
manifestations
RBCS, WBCS, Fibrin accumulation in lungs
dehydration, metabolic acidosis
poor oxygen diffusion
hypoxia, fever, chills, cough, tachypnea, tachycardia, pleuritic pain, sputum production
mechanism
typical
pneumococcal bacteria attach to epithelium receptors- infect type 2 alveolar cells
atypical
immune-mediated mechanism
treatment
antibiotics
oxygen therapy
IV fluids, fever management
chest physiotherapy
OBSTRUCTIVE
COPD
Emphysema
cause
smoking
genetic inheritance of alpha antitrypsin
manifestations
air trapping: decrease in O2 uptake and CO2 release
chronic hypoxemia, hypercapnia, chronic cough, dyspnea, wheezing, barrel chest
mechanism
early
inflammation in small airways distal to respiratory bronchioles; proteolytic and antiproteolytic enzyme competition
late
loss of elastic recoil of alveoli, inner lining of arteries and arterioles of respiratory tract thickens, irreversible enlargement of air spaces
treament
smoking cessation
drug therapy: to increase AA, bronchodilators, steroid anti-inflammatory, mucolytic agents
supplemental O2, lung transplant
Chronic Bronchitis
mechanism
changes in bronchioles in response to chronic inflammation, hyperplasia, destruction of cilia, squamous cell metaplasia, or bronchial wall thickening
narrowing airway lumen, occluding lumen with mucous
cause
smoking
environmental pollutants
manifestations
similar to emphysema
chronic productive cough with excessive mucous for 3 months or more in 2 consecutive years
treatment
supplemental O2
drug therapy as emphysema
smoking cessation
Asthma
mechanism
chronic inflammatory disorder results in intermittent/persistent airway obstruction via bronchial hyper responsiveness, inflammation, bronchoconstriction, excess mucous production
cause
unknown; potential frequent exposures to environmental allergens
treatment
controlling environmental triggers
monitoring lung function
pharmacologic therapy to reverse inflammation, bronchoconstriction, and mucous secretion
manifestations
immune response triggers cascade of events including bronchospasm, mucous plugs, edema, exudate accumulation, and cell debris accumulation
over time: airway remodeling (smooth muscle hyperplasia, narrowing of airways, destruction of epithelium)
airway hyperactivity, wheezing, breathlessness, chest tightness, excessive sputum, cough
INFLAMMATORY
ARDS
manifestations
disrupted production of surfactant, damage to type 2 alveolar cells, atelactasis
O2 and CO2 diffusion issues, hyaline membrane formation, ventilation and diffusion impairment
poor lung expansion, hypoxemia, hypercapnia, acidosis, tachypnea, dyspnea, retractions, crackles
cause
injury: from inhalation of smoke, lung infections, aspiration of gastric fluids, lung trauma, anaphylaxis, lack of blood flow, etc
treatment
supportive, O2 supplementation, mechanical ventilation
mechanism
inflammatory response triggered from injury
chemical mediators promote collection of inflammatory cells, fluids, and proteins that leak into lung tissues and cause edema
GENETIC
Cystic Fibrosis
cause
autosomal recessive genetic transmission
treatment
clearing airways of mucous
controlling infections
bronchodialators, reducing inflamation
manifestations
air trapping, hyperinflation, access formation, lung tissue consolidation, persistent pneumonia, lung tissue fibrosis, cyst formation
tenacious secretions, chronic cough, mucoid sputum, tachypnea, wheezing/crackles, chest pain, hemopytosis, barrel chest, nasal polyps, finger clubbing
mechanism
impaired electrolyte transportation across epithelial cells on mucosal surfaces (water, chloride conduction)
mucous plugging, inflammation, infection in lungs as a result of abnormally thick respiratory tract secretions