Week 8 - Respiratory Flashcards

(53 cards)

1
Q

clinical manifestations of repiratory diseases

A
dyspnea
abnormal breathing patterns
hypo- & hyperventilation
cough
hemoptysis
cyanosis
pain
clubbing
abnormal sputum
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2
Q

dyspnea s&s

A

flaring nostrils
accessory muscle use
retraction of intercostal spaces

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3
Q

cheyne stokes

A

alternating periods of deep and shallow breathing

apnea for 15-60 seconds then rapid resps

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4
Q

cheyne stokes results from

A

injury to brainstem

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5
Q

during hypoventilation

A

co2 removal does not keep up with co2 production an paco2 increases causing hypercapnia, results in respiratory acidosis

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6
Q

causes of hypercapnia

A
  1. Depression of resp. centre by drugs
  2. Diseases/trauma of the medulla
  3. Spinal cord disruption
  4. Diseases of neuromuscular junction or respiratory muscles
  5. Thoracic cage abnormalities
  6. Large airway obstruction
  7. Increased work of breathing
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7
Q

hypoxemia causes

A
decreased oxygen content of inspired gas
hypoventilation
diffusion abnormalities
abnormal ventilation-perfusion ratios
pulmonary right-to-left shunt
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8
Q

acute cough

A

resolves within 2-3 weeks, URI

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9
Q

chronic cough

A

more than 3 weeks

postnasal drip, bronchitis

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10
Q

hemoptysis

A

coughing up blood caused from damage to lung parenchyma

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11
Q

asthma

A

chronic inflammatory disease of the airways, morbidity and mortality has risen over last 2 decades

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12
Q

asthma patho

A

Inflammation resulting in hyper-responsiveness of the airways to environmental triggers.
Produces bronchial smooth muscle spasm, edema formation, tenacious mucus production, ->obstruction

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13
Q

s&s asthma

A
Dyspnea, tachypnea
Wheezing on inspiration and expiration
Tachycardia
Circumoral cyanosis
Accessory muscle use
Diaphoresis
Pallor
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14
Q

asthma drugs

A
1st->bronchodilators
2nd->long acting bronchodilators
3rd->anticholinergic agents
4th->inhaled corticosteroids
5th->oral steroids
6th->IV steroids
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15
Q

s&s copd

A
Dyspnea
Cyanosis
Productive cough
Respiratory fatigue
Severe accessory muscle use
Orthopnea
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16
Q

chronic bronchitis

A

Chronic bronchitis is hypersecretion of mucous and productive cough (at least 3 months of the year for at least 2 years)
Patients have decreased exercise tolerance, infection is common

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17
Q

emphysema

A

Abnormal permanent enlargement of gas exchange airways
Obstruction results from changes in lung tissues
Loss of elastic recoil in alveolus and narrowed bronchiole

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18
Q

emphysema s&s

A
Dyspnea on exertion -> marked dyspnea
Little cough and little sputum production
Use of accessory muscles for ventilation
Often very thin
Braces for easier breathing
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19
Q

emphysema dx & tx

A

Pulmonary function tests indicate obstruction to expiratory phase of ventilation
TLC (total lung capacity) may be twice normal
ABG normal until late in disease

Smoking cessation most important tx
Inhaled anticholinergic agents
Relaxation exercises, reconditioning and breathing retraining helpful

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20
Q

tuberculosis

A

Infection of lower respiratory tract caused by mycobacterium tuberculosis, an acid-fast bacillus
Main reason for recent increases is AIDS - very susceptible to respiratory infections
Multidrug-resistant TB now present
Due to not taking medications and mutation of bacteria

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21
Q

tb patho

A

Transmitted in airborne droplets
Inspired bacilli cause pneumonitis (lung inflammation)
Neutrophils and macrophages seal colonies of bacilli into a tubercule
Infected tissues inside tubercule die and form a cheeselike substance (all within 10 days)
May lie dormant for years to whole lifetime
Poor nutritional status, IDDM, long term steroids

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22
Q

tb manifestations

A

Often asymptomatic
Fatigue, weight loss, lethargy, anorexia, low-grade fever in afternoon
Cough- purulent sputum, progresses to hemoptysis
Night sweats, general anxiety

23
Q

croup

A

Subglottic edema from the infection (in an already narrow airway)
Increased resistance to airflow -> increased work of breathing-> may cause dynamic collapse of upper airway
Watch for rhinorrhea, sore throat, low-grade fever-> seal-like barking cough
Most resolve spontaneously after a few days
If obstruction severe, needs immediate help

24
Q

croup s&s

A

Sore throat
Low-grade fever
Seal-like, barking cough

25
croup dx & tx
Some controversy over treatment If no stridor, then little treatment Now evidence of value of single dose of steroid with half-life of 36-72 hours Science neither supports or refutes use of mist
26
pneumonia
Infection of the lower respiratory tract | caused by bacteria, viruses, fungi, protozoa, or parasites
27
pneumonia risk factors
elderly, immunocompromised, lung disease, alcoholism, altered consciousness, smoking, intubation, malnutrition, immobilization
28
pneumococcal pneumonia
Best understood pneumoniae Inflammatory response and exudate cause alveolar edema This media causes multiplication of bacteria and spread of infection Phagocytosis takes place in consolidated alveoli Usually infection limited to 1-2 lobes
29
viral pneumonia
Mild and self-limiting Usually sets the stage for another infection (because it provides the perfect environment for bugs to grow) Primary infection = influenza pneumonia Caused by another infection such as chic pox, measles
30
pneumonia s&S
``` cough dyspnea fever chills malaise pleuritic chest pain ```
31
pneumonia dx
Confirmed by chest x-ray Elevated WBC Should do sputum Gram stain and possibly blood cultures
32
lun cancer general info
Arise from epithelium of respiratory tract Considered an epidemic in the U. S. Mortality rate still rising in women, higher even than breast cancer Most common cause is smoking Passive smoking = 30% higher risk Genetic predisposition to lung cancer Also environmental & occupational risk factors
33
lung cancer manifestations
Early symptoms are non-specific Coughing, sputum production, hemoptysis, airway obstruction, pleural effusions Disease usually well advanced before medical advice is sought Only proven reduction method is smoking cessation
34
cystic fibrosis
Autosomal recessive inherited disease In middle of chromosome 7 Gene mutation that results in abnormal expression of cystic fibrosis transmembrane regulator Results in abnormal secretions that obstruct tracts in respiratory, digestive, and reproductive systems Generally affects Caucasians Carriers are healthy
35
cystic fibrosis patho
Autosomal recessive inherited disease In middle of chromosome 7 Gene mutation that results in abnormal expression of cystic fibrosis transmembrane regulator Results in abnormal secretions that obstruct tracts in respiratory, digestive, and reproductive systems Generally affects Caucasians Carriers are healthy
36
cystic fibrosis clinical manifestations
Age of diagnosis 6 mos -> 1 year 10% not diagnosed until after age 10 Respiratory problems - persistent cough or wheeze and recurrent pneumonia GI problems - meconium ilius, failure to thrive, malabsorptive symptoms Males are typically infertile Severity not predictable by genotype, affected siblings may be very different
37
cystic fibrosis dx
Standard test is sweat test CF patients secrete high levels of electrolytes in their sweat sweat chloride concentration > 60 mEq/L
38
4 types of pneumonthorax
Spontaneous Tension Open Secondary
39
pleural effusion
``` Can be fluid - Exudative - Transudative Can be blood - Hemothorax Can be pus - Empyema ```
40
flail chest results from
rib or sternal fractures that disrupt mechanics of breathing
41
pneumothorax
accumulation of air in pleural space
42
tension pneumothorax
trapping of air in pleural space, life threatening
43
pleural effusion
accumulation of fluid in pleural space
44
empyema
presence of pus in pleural space
45
aspiration
passage of fluid and solid particles into lung
46
atelectasis
collapse of alveoli
47
bronchiectasis
inflammatory obstruction of small airways
48
bronchiolitis obliterans
an inflammatory, fibrotic | process that occurs as a complication of lung transplantation.
49
pulmonary fibrosis
excessive amount of connective tissue | in the lung
50
pneumoconiosis
inhalation of dust particles in workplace
51
pulmonary edema
presence of excess water in the lung caused by disturbances of capillary hydrostatic pressure, capillary oncotic pressure, or capillary permeability
52
ALI/ARDS
results from an acute, diffuse inflammatory injury to the alveolocapillary membrane and decreased surfactant production, which increases membrane permeability and causes pulmonary edema and atelectasis
53
acute bronchitis
acute infection or inflammation of the large airways or bronchi; it is usually self-limiting and caused by viruses.