Obstructive Lung Diseases (Gas#3) Flashcards

1
Q

Antitrypsin

A

patients with obstructive lung diseases lack this which leads to breakdown of protein

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2
Q

Chronic bronchitis

A

inflammation of the trachea and bronchi. Edema narrows airway& causes hyper-secretion of mucus. Basically, bronchi are narrowed due to increased mucus

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3
Q

How long do you have a cough if you have chronic bronchitis?

A

3 months or more for 2 years. Cough can go away & come back

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4
Q

When are people generally diagnosed with chronic bronchitis? when does it start?

A

generally diagnosed ages 40-55 years, starts after 20

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5
Q

Chronic bronchitis s/s

A

chronic inflammation, cilia damaged, mucous glands enlarged, thick mucus that obstructs bronchi, persistent cough with sputum, SOB, wheezing

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6
Q

Because patient with chronic bronchitis are cyanotic what problems do they have

A

Polycythemia (too many RBCs) occurs as compensation for hypoxemia, pulmonary infections are common (pneumonia), Pulmonary HTN which leads to cor pulmonale

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7
Q

cor pulmonale

A

enlargement of the right ventricle due to high pressure in the lungs

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8
Q

Right heart failure/cor pulmonale s/s

A

cough with or without sputum, dyspnea esp with exertion, S3& tricuspid regurgitation, atypical chest pain, rhonchi & wheezing, hepatomegaly & ascites, cyanosis

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9
Q

blue bloater

A

has low o2, doesnt struggle to breath, cyanotic, fat

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10
Q

pink puffer

A

has high co2, struggle to breath, thin

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11
Q

Emphysema

A

permanent enlargement of terminal bronchioles & enlargement and destruction of alveoli which reduces available area for gas exchange. Basically, alveoli lose their flexibility making it hard to expand & contract and alveoli are destroyed

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12
Q

Why do patients with emphysema have difficulty with breathing?

A

lungs lose elasticity in bronchioles and alveoli causing difficulty with exhalation

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13
Q

Centrilobular emphysema

A

bronchioles are destroyed usually in upper lungs. end alveolar remain the same but bronchioles are destroyed

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14
Q

Panlobular emphysema

A

destroys bronchioles & alveoli. usually effects lower lungs

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15
Q

Emphysema s/s

A

marked dyspnea 1st with exertion then dyspnea at rest, thin, tacypnea with prolonged expiration, barrel chest, diminished breath sounds

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16
Q

Bronchiectasis

A

abnormal dilation of a bronchi & bronchioles from long term obstruction r/t chronic infection d/t mucus accumulation & stasis (cystic fibrosis)

17
Q

Asthma

A

inflammation of respiratory track and spasm of bronchiolar smooth muscle, increase mucus, decreased airflow, decreased ventilation of alveoli

18
Q

Asthma s/s

A

cough, dyspnea, wheezing, expiratory& or inspiratory wheezes, stridor

19
Q

Peak flow monitor

A

used to asses the maximum expiratory flow

20
Q

during an asthma attack which do you give first, beta agonist or steroid?

A

beta agonist then steroid

21
Q

what do you do if your asthma symptoms do not improve after 15-20 minutes

A

call 911 or dr

22
Q

Status Asthmaticus & s/s

A

severe asthma unresponsive to therapy lasting longer than 24 hours, CO2 increases& pH falls, severe obstruction with less wheezing, fatigue

23
Q

Causes of status asthmaticus

A

aspirin, respiratory infection, massive exposer to allergens, abrupt discontinuation of drug therapy or overuse, waiting too long to take intervention

24
Q

Cystic Fibrosis

A

inherited autosomal recessive disease of exocrine glands, inability to transport chloride by epithelial cells making exocrine secretions very thick & tenacious

25
Q

effects of cystic fibrosis on the lungs

A

blocks alveolar ventilation, chronoic inflammation, edema of the capillary-alveolar interface, bronchial scarring & fibrosis destroys bronchial airways, reduced lung compliance, digital clubbing

26
Q

effects of cystic fibrosis on the pancreas

A

duct clogs, decreased insulin secretion & diabetes, destroys pancrease, digestive enzymes don’t reach small intestine

27
Q

Effects of cystic fibrosis on the liver

A

small bile duct obstruction, billiary cirrhosis, portal HTN, liver failure

28
Q

effects of cystic fibrosis on the intestine

A

blocks digestion & absorption, malabsorption of fats, CHO & proteins,

29
Q

effects of cystic fibrosis on heart

A

right sided heart failure

30
Q

effects of cystic fibrosis on reproductive organs

A

males: obstructed vas deferens, Females: thick musus secretion in cervix

31
Q

effects of cystic fibrosis on sweat glands

A

impaired reabsorption of sodium cloride in sweat ducts, salt loss in sweat (hyponatremia), heat exhaustion

32
Q

effects of cystic fibrosis on dental

A

gingivits, dental caries

33
Q

cystic fibrosis s/s

A

adventitious breath sounds, frequent respiratory infections, atelectasis r/t blockage of bronchioles, bronchiectasis with pockets of infection, cyanosis & hemoptysis (spitting of blood) at near terminal stage, cor pulmonale, barrel chest/nail clubbing at early stage

34
Q

management of cystic fibrosis

A

cool mist, hydration, chest PT, give pancreatic enzymes with meals & snacks, vitamins, antibiotics (prophylactic bactrium DS), mucolytics

35
Q

Cystic fibrosis diet

A

high in calories & protein, moderate in fat, extra fluids if warm outside,

36
Q

Why do we want to decrease carbs with a patient with COPD?

A

because carb metabolism produces CO2