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26 Cards in this Set

  • Front
  • Back

Pulmonary system function

gas exchange


ventilation

Pulmonary system orgnas

nose/mouth


trachea/bronchi


lungs/alveoli


respiratory muscles


thoracic cage

Ventilation

Contract (inspiratory muscles) then thoracic cage expands than create neg pressure




-this negative pressure draws air in


-opposite occurs for exhalation


-alveolar pressure increases creating positive pressure, which leads to exhalation

ventilation

nose/mouth draws air in


trachea/bronchi leads air to lungs


lungs alveoli, air sacs




other functions


warms, humidifies air


immune barrier (cilla and mucous traps particles


produces surfactant & other pro/hormones

Surfactant

phospholipid & PRO produced by epithelial cells of the alveoli




maintains surface tension




decrease surfactant and decrease surface tension can lead to collapse & alveolar instability

Gas Exchange

Right side heart pump O2 poor blood to lungs for oxygenation, CO2 removal


Impairment when


obstruction to air flow (airway resistance)


Decreased lung compliance (limited expansion of lungs)




So ventilation & perfusion mismatch

Bronchitis and Emphysema

alveoli are perfused but ventilation compromised




gas exchange doesn't take place


no oxygenation


results: hypoxemia

Opposite Situation

dead space ventilation


alveoli are ventilated but not perfused


CO2 builds




Results: Hypercarbia or hypercapnia

Common Pulmonary Dz

asthma


COPD


Emphysema


Bronchitis


Pneumonia


TB


Atelectasis


CF


ARDS

Asthma

spasm of the bronchioles


allergic rx caused by:


edema bronchioles, mucous secretion, spasm bronchioles, obstruction during expiration


increase airway resistance

Chronic Obstructive Pulmonary Dz


(COPD)

Emphysema


loss of elasticity and destruction of aveloli


reduces surface space for exchange of O2 and CO2 (increase airway resistance)


entrapment of air causing hypercapnia


Chronic Bronchitis


the airway filled w/ mucous causing caught


chronic inflammation leads to scarring & wall thickening of the bronchus (airway resistance)

COPD: nutriton concerns

progressive wt loss and muscle wasting


chronic depletion process which worsens w/ worsening respiratory function




impaired GI tract, Inadequate intake, meds, adaptive mechanism- lower O2 consumption, altered plum/CVD hemodynamics, hyper metabolism (inflammatory state, TNF)

COPD


Labs & Tests

Labs


Chem 7


Alb/ pre alb


ABG's




Tests


PFT


VQ Scan

COPD Meds

inhalers


bronchodilators


antibiotics


steriods

Pneumonia

inflammatory process


infectious


alveoli fill with fluid/blood cells

Tuberculosis

specific infectious organism


results


decrease macrophages to infected area


walling off of lesion by fibrous tissue


highly infectious

Nutrients needs

higher during repletion and lower during maintenance but still higher than normal

Atelectasis

collapsed alveoli


obstruction of airway


lack of surfactant




may require mech ventilation and nutrition support

Cystic Fibrosis

autosomal recessive disorder affects flow Na, Cl and water across cell membranes resulting in thick tenacious mucous production that obstructs glands & ducts




Sx


poor intake, decrease appetite


nutrient losses


irreversible neurological damage & poor growth

Cystic Fibrosis Complications

Pancreas


endocrine and exocrine function


Sweat/salivary glands


liver: steatosis


GI


Respiratory


bronchitis, pneumonia, atelectasis


tx with inhalants and chest physiotherapy

Pancreatic Insufficiency in CF

85-90% of CF


affects the digestive enzymes that breakdown macronutrients in the intestines leading to malabsorption


steatorrhea (fat in the feces)

CF related to DM

2 degree beta cell destruction


20% of adults w/ CF


Sx similar to both type 1 and 2 DM


Glucose intolerance


Dx w/ OGTT


leads to microvascular complications

Loss of Nutrients in CF

GERD


Chronic malabsorption


Steatorrhea (fat in feces)


Glucosuria (glucose in urine)


Increased work load of breathing


leading to FTT

CF Dx when

+ sweat test


+ lung dz


pancreatic function test


FTT


Genetic Test




manifest in infancy

CF nutrient needs

kcal 110-200% of std intake over 2yo


Fat 35-40% of total kcal


MCT oil to supplement




PRO 100-150% of est needs




high kcals, PRO diet w/ supplemental pancreatic enzymes & multi-vitamins

CF nutriton intervention

Pancreatic enzyme replacement


10-20 different enzymes


trial/error


based on stool output and wt gain


take w/ meals and snacks


FDA now requires approval


Creon is 1st FDA approved in US