Respiratory Apex Review Flashcards

1
Q

What does oxygen content (CaO2) tell you?

A

How much oxygen is present in 1 deciliter (100 mL) of blood

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2
Q

What is the formula for CaO2?

A

CaO2 = (1.34 x Hgb x SaO2) + (PaO2 x 0.003)

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3
Q

What does DO2 tell you?

A

How much O2 is delivered to the tissues per minute

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4
Q

What is the formula for DO2?

A

DO2 = CaO2 x CO x 10

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5
Q

___ is needed for oxygen delivery but not oxygen-carrying capacity.

A

CO

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6
Q

What is the reference value for CaO2?

A

20 mL O2 /dL

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7
Q

What is the reference value for DO2?

A

1,000 mL O2 per minute

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8
Q

What is the definition of oxygen consumption?

A

The difference between the amount of O2 that leaves the lungs and the amount of O2 that returns to the lungs

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9
Q

What is the formula for VO2?

A

VO2 = CO x (CaO2 -CvO2) x 10

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10
Q

What is the reference value for VO2?

A

250 mL/min or 3.5 mL/kg/min

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11
Q

What is 1 deciliter equal to?

A

100 mL

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12
Q

What two ways is oxygen transported by the blood?

A
  1. reversibly w/ Hgb (97%)
  2. Dissolves in the plasma (3%)
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13
Q

What percentage of oxygen reversibly binds with Hgb?

A

97%

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14
Q

What percentage of oxygen is dissolved in the plasma?

A

3%

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15
Q

Each gram of Hgb molecule can carry a theoretical max of ___ mL of molecular oxygen.

A

1.39

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16
Q

What is the normal Hgb for a male?

A

15 g/dL

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17
Q

What is the normal Hgb for a female?

A

13 g/dL

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18
Q

What is the normal Hct for a male?

A

45%

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19
Q

What is the normal Hct for a female?

A

39%

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20
Q

How is dissolved O2 measured?

A

By PaO2

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21
Q

What does PaO2 determine?

A

Gas exchange in the lungs (not a measure of oxygen content in the blood)

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22
Q

Oxygen dissolves in the plasma according to ____ law.

A

Henry’s

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23
Q

What is the solubility coefficient for oxygen?

A

0.003 mL/dL/mmHg

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24
Q

Oxygen is _____x less soluble than CO2.

A

20

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25
Q

What is the driving mechanism of DO2?

A

CO

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26
Q

VO2 stands for ______

A

oxygen consumption

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27
Q

What principle can be used to calculate oxygen consumption?

A

Fick’s principle

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28
Q

What does the oxyhemoglobin dissociation curve tell us?

A

the tendency of Hgb to bind to oxygen

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29
Q

A right-shifted curve of the oxyhemoglobin dissociation curve means Hgb has a ____ affinity for oxygen.

A

lower (right = release)

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30
Q

A left-shifted curve of the oxyhemoglobin dissociation curve means Hgb has a ____ affinity for oxygen.

A

higher (left = love or locked in)

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31
Q

What is the P50?

A

When Hgb is 50% saturated by oxygen

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32
Q

A low P50 indicates a ____ shifts of the oxyhemoglobin dissociation curve.

A

left

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33
Q

A high P50 indicates a ____ shifts of the oxyhemoglobin dissociation curve.

A

right

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34
Q

A left shift of the oxyhemoglobin dissociation curve is caused by _____, ______ temperature, and _______ 2,3-DPG.

A

alkalosis, decreased temperature, and decreased 2,3-DPG

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35
Q

A right shift of the oxyhemoglobin dissociation curve is caused by _____, ______ temperature, and _______ 2,3-DPG.

A

acidosis, increased temperature, increased 2,3-DPG

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36
Q

What three hemoglobin species can cause a left shift of the oxyhemoglobin dissociation curve?

A
  1. fetal hemoglobin
  2. methemoglobin
  3. carboxyhemoglobin
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37
Q

Above a PaO2 of _____ mmHg, hemoglobin is fully saturated with oxygen.

A

100

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38
Q

What does the Bohr effect say?

A

An increased partial pressure of CO2 and decreased pH cause Hemoglobin to release O2

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39
Q

Max O2 loading occurs at a PaO2 of what?

A

100 mmHg

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40
Q

Tissues with a high metabolic rate consume more ___ and produce more _____, ______, and ______.

A

O2; CO2, hydrogen ions, and heat

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41
Q

When is 2,3-DPG produced?

A

during RBC glycolysis (Rapoport-Luebering pathway)

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42
Q

What increases 2,3-DPG production?

A

Hypoxia

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43
Q

2,3 DPG is an important compensation mechanism during chronic ____.

A

anemia

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44
Q

In _____, the concentration of 2,3-DPG falls.

A

banked blood

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45
Q

What does not respond to 2,3-DPG?

A

Hgb F

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46
Q

What is the energy currency in the body?

A

Adenosine triphosphate (ATP)

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47
Q

What is the primary substrate used for ATP synthesis?

A

Glucose

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48
Q

What 3 key processes are involved in aerobic metabolism?

A
  1. glycolysis
  2. krebs cycle
  3. oxidative phosphorylation
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49
Q

How many ATP are gained with glycolysis?

A

net gain of 2 ATP

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50
Q

How many ATP are gained with Krebs cycle?

A

Net gain of 2 ATP

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51
Q

How may ATP are gained with oxidative phosphorylation?

A

net gain of 34 ATP

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52
Q

Anaerobic metabolism occurs when?

A

in the absence of oxygen

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53
Q

In the absence of oxygen, ______ is converted to lactic acid.

A

Pyruvate acid

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54
Q

Why does lactic acidosis occur during the absence of oxygen?

A

B/c pyruvate acid is converted to lactic acid during anaerobic metabolism

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55
Q

How is ATP produced?

A

by the oxidation of proteins, carbohydrates, and fats

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56
Q

The phosphate bond in ATP is a _____ energy bond.

A

high

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57
Q

Why must ATP be continuously replenished?

A

It cannot be stored

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58
Q

Which form of metabolism produces much more ATP?

A

aerobic

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59
Q

What is the primary goal of glycolysis?

A

to convert 1 glucose to 2 pyruvic acid molecules

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60
Q

The fate of pyruvic acid depends on whether or not _____ is available.

A

oxygen

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61
Q

In the absence of O2, pyruvic acid is converted to lactate where?

A

in the cytoplasm

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62
Q

If oxygen is present, where is pyruvic acid transported after glycolysis?

A

the mitochondria

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63
Q

During glycolysis of aerobic metabolism, the 2 molecules of pyruvic acid are converted into what?

A

2 molecules of acetyl coenzyme A

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64
Q

When is 2,3-DPG produced?

A

about halfway through glycolysis

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65
Q

During what pathway is 2,3-DPG produced?

A

the rapoport-luebering pathway

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66
Q

Where does the Krebs cycle take place?

A

in the matrix of the mitochondria

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67
Q

The krebs cycle is also known as what?

A

citric acid cycle

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68
Q

During the krebs cycle, the reaction begins when _____ and ______ react to produce citric acid.

A

acetyl coenzyme A
and
oxaloacetic acid

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69
Q

The Krebs Cycle reaction ends with the production of ____, ____, and _____.

A

oxaloacetic acid, NADH, and CO2

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70
Q

What is the primary goal of the krebs cycle reaction?

A

to produce a large quantity of H+ ions in the form of NADH

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71
Q

What is the primary goal of glycolysis and the Krebs cycle?

A

to liberate hydrogen from glucose

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72
Q

The NADH produced during the Krebs cycle is split into what?

A

NAD+, H+, and 2 electrons

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73
Q

During oxidative phosphorylation, the electrons produced from NADH are fed into the chemiosmotic mechanism. And a proton gradient is generated across a membrane which drives ________ with the help of ______.

A

ATP synthesis; ATP synthase

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74
Q

What serves at the final electron acceptor during oxidative phosphorylation?

A

oxygen

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75
Q

What are the 2 end products of oxidative phosphorylation?

A
  1. 34 ATP molecules
  2. water
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76
Q

What is the end product of anaerobic metabolism?

A

lactic acid

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77
Q

How much ATP molecules are created from pyruvic acid during the lactic acid pathway?

A

2 ATP

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78
Q

What type of acidosis is lactic acidosis?

A

anion gap metabolic acidosis

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79
Q

Why is there altered homeostasis in the setting of acidosis?

A

the body’s enzymes tend to not function properly in an acidic environment

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80
Q

How is serum lactate cleared?

A

the liver

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81
Q

What is the primary by-product of aerobic metabolism?

A

Carbon dioxide

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82
Q

What are the 3 primary ways that CO2 is transported/buffered in the blood?

A
  1. as bicarbonate
  2. bound to Hgb
  3. dissolved in the plasma
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83
Q

What % of CO2 is transported/buffered as bicarbonate?

A

70%

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84
Q

What % of CO2 is transported/buffered bound to Hgb?

A

23%

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85
Q

What % of CO2 is transported/buffered dissolved in the plasma?

A

7%

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86
Q

What is the enzyme that facilitates the formation of carbonic acid (H2CO3) from H2O and CO2?

A

Carbonic anhydrase

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87
Q

To maintain electroneutrality, for every molecule of HCO3- that leaves the erythrocyte, 1 _____ ion is transported in.

A

Cl-

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88
Q

What is the Hamburger shift?

A

To maintain electroneutraility, for every molecule of HCO3- that leaves the erythrocyte, 1Cl- ion is transported in.

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89
Q

Why is venous blood slightly more acidic?

A

The PvCO2 (venous blood) is about 5 mmHg higher than the PaCO2 (arterial blood).

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90
Q

What is the normal venous pH?

A

7.36 (as opposed to normal arterial pH = 7.4)

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91
Q

Metabolically active tissues create a more _____ environment.

A

acidic

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92
Q

A more acidic environment, enhances _____ from hemoglobin (Bohr effect) and _____ loading on hemoglobin (Haldene effect).

A

O2 offloading; CO2 loading

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93
Q

What is the Haldene effect?

A

CO2 loading onto Hgb in acidic environment

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94
Q

What is the Bohr effect?

A

O2 offloading in acidic environment

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95
Q

How is CO2 eliminated from the pulmonary blood?

A

alveolar ventilation

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96
Q

What is the Bicarbonate - Carbonic Acid Buffer Reaction?

A

H2O + CO2 <—> H2CO3 <—> H+ + HCO3-

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97
Q

What is required for the bicarbonate - carbonic acid buffer reaction to take place?

A

carbonic anhydrase

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98
Q

Where is carbonic anhydrase present? And where is it not?

A

Present in the erythrocyte
NOT present in the plasma

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99
Q

Why does the formation of carbonic acid reaction have to be fast?

A

RBCs only remain in capillary blood for a short period of time

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100
Q

What facilitates the formation of carbonic acid (H2CO3)?

A

Carbonic anhydrase

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101
Q

What is H2CO3?

A

Carbonic acid

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102
Q

Carbonic acid rapidly dissociates into ____ and _____.

A

H+ and HCO3-

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103
Q

What happens to the dissociates of carbonic acid?

A

the H+ is buffered by Hgb
the HCO3- is transported to plasm to act as a buffer

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104
Q

Where does the chloride shift (Hamburger shift) happen in reverse?

A

in the lungs as CO2 is excreted from the body

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105
Q

Venous Hct is _____ than arterial Hct.

A

@3% higher

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106
Q

Why is venous Hct higher than arterial Hct?

A

The chloride shift adds osmotically active ions (Cl-) to the erythrocyte in venous circulation. Water follows isosmotically, causing the erythrocyte to swell. The cell volume is increased relative to the plasm volume.

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107
Q

What is the carbamino compound buffer?

A

CO2 binds with amino groups on Hgb as well as other plasma proteins

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108
Q

What is the solubility coefficient of dissolved CO2?

A

0.067 mL/dL/mmHg

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109
Q

CO2 is 20x more soluble in the blood than what?

A

O2

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110
Q

The Haldene effect states that in the presence of deoxygenated Hgb, the CO2 dissociation curve shifts ____.

A

to the left

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111
Q

What does the Haldane effect describe?

A

CO2 carriage

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112
Q

The Haldane effect states that oxygen causes the erythrocyte to release ____.

A

CO2

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113
Q

The presence of oxygenated Hgb shifts the CO2 dissociation curve to the ____.

A

Right

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114
Q

The presence of deoxygenated Hgb shifts the CO2 dissociation curve to the ____.

A

left

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115
Q

What does the Bohr effect describe?

A

O2 carriage

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116
Q

The Bohr effect says what?

A

That CO2 and decreased pH cause the erythrocyte to release oxygen.

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117
Q

Why does oxygenated Hgb shift the CO2 dissociation curve to the right?

A

Blood can hold less CO2

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118
Q

Why does deoxygenated Hgb shift the CO2 dissociation curve to the left?

A

Blood can hold more CO2

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119
Q

Where in the body is the CO2 dissociation curve right shifted?

A

the lungs

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120
Q

Why is the CO2 dissociation curve right-shifted in the lungs?

A

This facilitates CO2 elimination

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121
Q

Where in the body is the CO2 dissociation curve left-shifted?

A

The systemic capillaries

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122
Q

Why is the CO2 dissociation curve left-shifted in the systemic capillaries?

A

This facilitates CO2 loading and transport by Hgb

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123
Q

Hypercapnia is defined as a PaCO2 > than ____mmHg.

A

45

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124
Q

What are the 3 etiologies of hypercapnia?

A
  1. increased CO2 production
  2. decreased CO2 elimination
  3. rebreathing
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125
Q

Sepsis, MH, thyroid storm, burns, and shivering are all causes of _____ CO2 production.

A

increased

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126
Q

Airway obstruction, ARDS, COPD, and opioid OD are all causes of ______ CO2 _____.

A

decreased CO2 elimination

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127
Q

What are some causes of rebreathing?

A

exhausted soda lime, faulty unidirectional valve in a circle system, or inadequate FGF in a Mapleson circuit

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128
Q

What are some consequences of hypercarbia?

A

hypoxemia, acidosis, cardiac depression, SNS stimulation, increased ICP

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129
Q

What is the formula for PaCO2?

A

PaCO2 = CO2 production / alveolar ventilation

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130
Q

With hypercapnia, the oxyhemoglobin curve shifts ____.

A

right

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131
Q

CO2 is a ______ depressant.

A

myocardial

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132
Q

CO2 directly ____ the peripheral vasculature

A

dilates

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133
Q

CO2 activates the ____ and increases ____ release from the adrenal medulla

A

SNS; catecholamine

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134
Q

With mild acidosis, the SNS stimulation r/t hypercapnia offsets what other s/e?

A

cardiac depression and direct peripheral vasodilation

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135
Q

CO2 is a smooth muscle dilator with the exception of what?

A

pulmonary vasculature

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136
Q

CO2 has what affect of PVR?

A

Hypercapnia increases PVR

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137
Q

An increased PVR increases the workload of the ____

A

right heart

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138
Q

Hypercapnia activates the ____ pump

A

H+/K+ …. Buffers CO2 acid in exchange for releasing K+ into plasma

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139
Q

What electrolyte effects does hypercapnia cause?

A

Increased K+ and increased Ca+

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140
Q

With acidosis, plasma proteins buffer H+ and release _____.

A

Ca+

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141
Q

Can CO2 freely diffuse across the BBB?

A

yes

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142
Q

Hypercapnia _____ ICP

A

increases

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143
Q

CO2 narcosis occurs when the PaCO2 is greater than what?

A

90 mmHg

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144
Q

During respiratory acidosis, the kidneys do what?

A

excrete H+ and conserve bicarbonate to return pH to normal

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145
Q

With acute respiratory acidosis, for every PaCO2 10 mmHg increase above 40 mmHg, pH decreases by ____.

A

0.08

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146
Q

With chronic respiratory acidosis, for every PaCO2 10 mmHg increase above 40 mmHg, pH decreases by ____.

A

0.03

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147
Q

Why is the decrease in pH less for chronic respiratory acidosis versus acute respiratory acidosis?

A

With chronic respiratory acidosis, there is HCO3- retention built up by the kidney

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148
Q

The carbon dioxide ventilatory response curve describes the relationship between ____ and ______.

A

PaCO2 and minute ventilation

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149
Q

What is the primary monitor of PaCO2?

A

the central chemoreceptor in the medulla

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150
Q

What are secondary monitors for PaCO2?

A

the peripheral chemoreceptors in the carotid bodies and transverse aortic arch

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151
Q

Where are the peripheral chemoreceptors that monitor PaCO2 located?

A

carotid bodies and transverse aortic arch

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152
Q

What conditions shift the CO2 response curve down and to the right?

A
  1. volatiles
  2. opioids
  3. NMBD
  4. metabolic alkalosis
  5. CEA
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153
Q

What conditions shift the CO2 response curve to the left?

A
  1. hypoxemia
  2. metabolic acidosis
  3. surgical stimulation
  4. intracranial HTN
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154
Q

What is the apneic threshold?

A

the highest PaCO2 at which a person will not breathe (once exceeded, the patient will begin to breathe)

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155
Q

Minute ventilation increases w/ PaCO2 in a linear fashion when PaCO2 is between ____ - ____ mmHg.

A

20-80

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156
Q

CO2 is a respiratory depressant when PaCO2 exceeds ____ - _____ mmHg.

A

80-100 mmHg

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157
Q

MAC of CO2 = _____ mmHg

A

200

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158
Q

What does the slope of the carbon dioxide ventilatory response curve represent?

A

The sensitivity of the entire respiratory apparatus to PaCO2

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159
Q

A left shift and increased slope of the carbon dioxide ventilatory response curve indicates what?

A

That Ve is higher than expected for a given PaCO2. This creates respiratory alkalosis

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160
Q

A right shift and decreased slope of the carbon dioxide ventilatory response curve indicates what?

A

That Ve is lower than expected for a give PaCO2. This creates respiratory acidosis.

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161
Q

What is the pacemaker for normal breathing?

A

Dorsal respiratory center

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162
Q

Where is the respiratory center located?

A

In the reticular activating system in the medulla and pons

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163
Q

The respiratory center receive afferent input from the central and peripheral chemoreceptors as well as _____.

A

Stretch receptors in the lungs

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164
Q

What two respiratory groups are a part of the medullary respiratory centers?

A

dorsal respiratory group and ventral respiratroy group

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165
Q

When is the dorsal respiratory group active?

A

During inspiration

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166
Q

When is the ventral respiratory group active?

A

During expiration

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167
Q

What two centers are part of the pontine respiratory centers?

A

pneumotaxic center and apneustic center

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168
Q

Where is the pneumotaxic center located?

A

upper pons

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169
Q

Where is the apneustic center located?

A

lower pons

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170
Q

What center inhibits the DRG?

A

pneumotaxic center (upper pons/of pontine)

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171
Q

What center stimulates DRG?

A

apneustic center (lower pons/pontine)

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172
Q

The respiratory rate & pattern are determined by what?

A

Medulla, Carotid bodies & Aortic arch & Lung baroreceptors

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173
Q

Where is the neural control of respiration located?

A

Respiratory center of medulla

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174
Q

The locations for chemical control of respiratory rate & pattern are determined by?

A

central chemoreceptors - medulla
peripheral chemoreceptors - carotid bodies and aortic arch

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175
Q

Where do the efferent pathways of the respiratory system terminate?

A

diaphragm, intercostals, and accessory muscles

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176
Q

What can modify the efferent response of the respiratory center?

A

The cerebral cortex

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177
Q

What is located in the medulla?

A

Dorsal respiratory group and ventral respiratory group

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178
Q

When is the DRG (dorsal respiratory group active)?

A

primarily active during inspiraiton

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179
Q

The respiratory pacemaker function is performed by the central pattern generator, which includes the ____, ______ (in the VRG), and other medullary strucutres.

A

DRG, pre-Botzinger complex (per Apex, if you see a question on this on the exam, first pick pre-botzinger complex if it is an option, if not pick DRG)

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180
Q

When is the ventral respiratory group active?

A

primarily active during expiration

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181
Q

When does the ventral respiratory group become more important?

A

during exercise or stress

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182
Q

What is located in the pons?

A

pneumotaxic center and apneustic center

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183
Q

What does the pneumotaxic center do?

A

inhibits the DRG (inhibits the pacemaker)

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184
Q

What does the apneustic center do?

A

stimulates the DRG (stimulates the pacemaker)

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185
Q

Is the pneumotaxic center located in the upper or lower pons?

A

Upper

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186
Q

What is the function of the pneumotaxic center?

A

To trigger the end of inspiration by inhibiting DRG

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187
Q

A strong stimulus of the pneumotaxic center promotes what kind of breathing?

A

rapid, shallow

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188
Q

A weak stimulus of the pneumotaxic center promotes what kind of breathing?

A

slow and deep

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189
Q

The apneustic center is located in the ____ pons.

A

lower

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190
Q

The apneustic center _____ the pneumotaxic center which causes inspiration.

A

antagonizes

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191
Q

What receptors are pulmonary stretch receptors?

A

J receptors

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192
Q

The action of the apneustic center is inhibited by what?

A

pulmonary stretch receptors/J receptors

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193
Q

What does the DRG do?

A

cause inspiration

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194
Q

Where is the DRG located?

A

Medulla

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195
Q

Where specifically in the medulla is the DRG located?

A

nucleus tractus solitarius

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196
Q

What does the VRG do?

A

causes expiration

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197
Q

Where is the VRG located?

A

medulla

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198
Q

Where specifically in the medulla is the VRG located?

A

nucleus ambiguous and nucleus retroambigus

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199
Q

The VRG has ___ and ___ function

A

inspiration and expiration

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200
Q

What does the VRG cause?

A

Expiration

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201
Q

When is the VRG primarily active?

A

expiration

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202
Q

What contains the pre-botzinger complex?

A

The Ventral Respiratory Group

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203
Q

Central chemoreceptors resond indirectly to what?

A

PaCO2

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204
Q

The BBB separates ___ from ____

A

blood from CSF

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205
Q

Which of the following can freely diffuse through the BBB: CO2, H+, and HCO3-?

A

Only CO2

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206
Q

After CO2 enter CSF, what does it do?

A

Dissociates into H+ and HCO3- (the rise in H+ is what stimulates respiration)

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207
Q

Respiratory changes to correct acidosis occur _____

A

within minutes

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208
Q

Can non-volatile (such as lactic acid) acids pass through BBB?

A

NO

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209
Q

How long is therapeutic hyperventilation (to reduce ICP) effective for?

A

A few hours to approximately 2 days

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210
Q

What respiratory technique is used to reduce ICP?

A

hyperventilation

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211
Q

What stimulates the central chemoreceptor?

A

hyeprcarbia and hypoxemia

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212
Q

What depresses the central chemoreceptors?

A

PROFOUND** hypercarbia and hypoxemia

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213
Q

Where are the central chemoreceptors located?

A

a few microns below the surface of the anterolateral aspect of the medulla

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214
Q

Ions, glucose, and amino acids can freely cross the BBB. T/F

A

False, are carried via active transport

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215
Q

What drives the respiratory pacemaker in the DRG?

A

H+

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216
Q

Do non-volatiles acids influence Ve on a short-term or long-term basis?

A

longer-term

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217
Q

HCO3= equilibrates between the blood & CSF - this process begins after a _____ and peaks at ____.

A

few hours; @2 days

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218
Q

What is the normal pH of CSF?

A

7.32

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219
Q

Where do peripheral chemoreceptors reside?

A

in the carotid bodies and aortic arch

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220
Q

What part of the carotid bodies do peripheral chemoreceptors reside?

A

bifurcation of the common carotid artery

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221
Q

What part of the aortic arch do peripheral chemoreceptors reside?

A

transverse aortic arch

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222
Q

What is the chief responsibility of the carotid body?

A

Monitor hypoxemia (PaO2 <60 mmHg)

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223
Q

Does the carotid body respond to SaO2 or CaO2?

A

No, neither - they respond to PaO2/hypoxemia

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224
Q

What is severed during CEA?

A

the afferent limb of the hypoxic ventilatory response

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225
Q

Why don’t we do bilateral CEA simultaneously or very close to each other?

A

B/c CEA severs the afferent limb of the hypoxic ventilatory response and it takes time for the body to recalibrate

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226
Q

What do sub-anesthetic doses of inhalation and IV anesthetics (0.1 MAC) do to the hypoxic ventilatory drive?

A

Depress the hypoxic ventiltory drive

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227
Q

What are secondary responsibilities of the carotid bodies?

A

monitoring of PaCO2, H+, and perfusion pressur

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228
Q

PaO2 <60 mmHg closes the ______ channels in ____ cells.

A

oxygen-sensitive K+; Type 1 Glomus

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229
Q

During the hypoxic ventilatory response, an action potential is propagated alon what nerve?

A

Hering’s nerve

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230
Q

Herings’s nerve –> _______ nerve

A

Glossopharyngeal nerve

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231
Q

CN 9 is what nerve?

A

Glossopharyngeal

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232
Q

The afferent pathway of the hypoxic ventilatory response terminates ______.

A

in the inspiratory center in the medulla

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233
Q

Volatile anesthetics impair ____,___,and ____ muscle function.

A

diaphragmatic, intercostal, and upper airway muscle function

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234
Q

CaO2 is reduced w/ these two processes but PaO2 usually remains normal: _____ and _____

A

anemia and carbon monoxide poisoning

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235
Q

Why does anemia and carbon monoxide poisoning not stimulate the hypoxic ventilatory response?

A

Even though CaO2 is reduced, PaO2 usually remains normal

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236
Q

Which reflex prevents alveolar overdistension?

A

Hering-Breuer inflation reflex

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237
Q

What receptors in smooth airway muscle in the lung influence respiratory pattern?

A

stretch receptors

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238
Q

What does the Hering-Breuer inflation reflex do?

A

Lung hyperinflation turns off the respiratory drive

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239
Q

What does the Hering-Breuer inflation reflex help to avoid?

A

overinflation

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240
Q

What is the Hering-Breuer deflation reflex?

A

Activates the respiratory drive when lung volume is too small

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241
Q

What does the Hering-Breuer deflation reflex help to prevent?

A

Atelectasis

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242
Q

J receptors are also known as _____ receptors

A

pulmonary C-fiber receptors

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243
Q

What increases the RR in the setting of pulmonary embolism or CHF?

A

J receptors (J receptors are activated by things that Jam traffic in the pulmonary vasculature).

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244
Q

What causes a newborn baby to take her first breath?

A

Paradoxical reflex of Head

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245
Q

What is the paradoxical reflex of head?

A

it causes a newborn to take its first breath

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246
Q

How do stretch receptors in the smooth airway muscle work?

A

they transduce pressure conditions inside the airway

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247
Q

Stretch receptors transmit pressure conditions along the _____ nerve to the _______.

A

vagus nerve; DRG

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248
Q

What is CN 10

A

Vagus

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249
Q

When does the Hering-Breuer Inflation reflex “turn off” the DRG/inspiration?

A

when lung inflation >1.5 L above FRC or 3x normal TV

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250
Q

J receptor stimulation causes _____

A

tachypnea

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251
Q

What is HPV?

A

A local reaction that occurs in response to a reduction in alveolar oxygen tension (not arterial PO2)

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252
Q

What is the goal of HPV?

A

To improve matching of ventilation and perfusion (aka minimize shunt)

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253
Q

What is the only region in the body that responds to hypoxia with vasoconstriction?

A

the pulmonary vasular bed

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254
Q

HPV is inhibited by volatile anesthetics > ____ MAC

A

1.5

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255
Q

What types of medications inhibit HPV?

A

phosphodiesterase inhibitors and dobutamine, vasodilators, and some CCB

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256
Q

Does hypervolemia or hypovolemia inhibit HPV?

A

Hypervolemia

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257
Q

_____ PEEP and _____ TV inhibits HPV.

A

Excessive; large

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258
Q

HPV is or is not inhibited by Ketamine, Propofol, and opioids?

A

HPV is NOT inhibited

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259
Q

HPV response begins within ____ and achieves full response in ____.

A

seconds; 15 minutes

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260
Q

HPV selectively increases the pulmonary vascular resistance in ______ areas to minimize shunt flow to these areas.

A

poorly ventilated

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261
Q

Neo, Epi, and Dopamine ____ shunt flow

A

Increase

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262
Q

What may distended constricted vessels in pulmonary vasculature and increase shunt flow?

A

Hypervolemia (LAP >25 mmHg) and elevated CO

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263
Q

Excessive PEEP or high TV increase what that would reduce optimal V/Q matching?

A

dead space

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264
Q

What 3 chemicals contribute to increased airway resistance?

A
  1. inositol triphosphate
  2. phospholipase C
  3. leukotrienes
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265
Q

The ___ of the airway has the most significant contribution to airflow resistance.

A

radius

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266
Q

What contributes to bronchoconstriction?

A

PNS (vagus nerve) and mast cells & non-cholinergic PNS

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267
Q

Non-cholinergic PNS (Nitric oxide) –> broncho____

A

dilation

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268
Q

SNS (circulating catecholamines) –> broncho____

A

dilation

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269
Q

Mast cells & non-cholingergic PNS –> broncho____

A

constriction

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270
Q

PNS (vagus nerve) –> broncho____

A

constriction

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271
Q

The vagus nerve supplies what kind of innervation to airway smooth muscle?

A

Parasympathetic

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272
Q

Stimulation of the ____ receptor produces bronchoconstriction

A

M3

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273
Q

What Mu receptor when stimulated produces bronchoconstriction?

A

M3

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274
Q

There are no sympathetic or para-sympathetic nerve endings in airway smooth muscle?

A

sympathetic

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275
Q

There is no ____ nerve endings in airway smooth muscle.

A

sympathetic

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276
Q

What receptors embedded in airway smooth muscle are activated by catecholamines in systemic circulation?

A

B2

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277
Q

Smooth muscle contraction –> _____ airway diameter

A

decreased

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278
Q

Decreased airway diameter –> increased ____

A

airway resistance

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279
Q

Smooth muscle relaxation –> ____ airway diameter

A

increased

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280
Q

The ____ nerve supplies parasympathetic innervation to airway smooth muscle.

A

Vagus nerve

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281
Q

Cholinergic nerve endings release Ach on to M3 receptors - parasympathetic or sympathetic?

A

Parasympathetic

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282
Q

What is a M3 receptor coupled to?

A

Gq protein

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283
Q

M3 receptor activation turns on the ___ protein, and this activates ____.

A

Gq; phospholipase C (PLC)

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284
Q

PLC activates what?

A

Inositol triphosphate (IP3) (ex of second messenger…. M3 –> PLC —> IP3)

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285
Q

What does IP3 stimulate and from where?

A

Release of Ca+2 from sarcoplasmic reticulum

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286
Q

Increased iCa2+ activates ____, and this enzyme enables the contractile mechanism –> bronchoconstriction.

A

myosin light chain kinase

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287
Q

Are mast cells in smooth airway epithelium?

A

Yes, highly concentrated

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288
Q

Coughing, allergy, or infection activate ____, ___, and ____, which in turn amplify the inflammatory response.

A

IgE, cytokines, and complement

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289
Q

__________-fibers release chemicals that promote bronchoconstriction.

A

Non-cholingergic c-fibers

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290
Q

Mast cell mediator?

A

histamine

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291
Q

B2 receptor is coupled to a ___ protein in airway smooth muscle

A

Gs

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292
Q

Activation of B2 receptor turns on Gs protein and this activates what?

A

Adenylate cyclase

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293
Q

Adenylate cyclase activates ____ (the second messenger)

A

cAMP

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294
Q

What does cAMP reduce?

A

release of Ca+2 from the sarcoplasmic reticulum

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295
Q

The bronchodilation pathway is turned off when _______ deactivates cAMP by converting it to AMP.

A

phosphodiesterase 3

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296
Q

NO is a potent smooth muscle ____

A

relaxant

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297
Q

Non-cholingergic PNS nerves release what onto airway smooth muscles?

A

vasoactive intestinal peptide

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298
Q

What increases NO production?

A

VIP

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299
Q

What does NO stimulate?

A

cGMP

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300
Q

What does cGMP do regarding the airway smooth muscle?

A

Smooth muscle relaxation and bronchodilation

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301
Q

What drug class is theophylline?

A

Methylxanthine

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302
Q

What drug class is zafirlukast?

A

Leukotriene modifier

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303
Q

What drug class is cromolyn?

A

mast cell stabilizer

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304
Q

What drug class is triamcinolone?

A

corticosteroid

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305
Q

What are the 3 types of pulmonary medications?

A
  1. bronchodilators
  2. anti-inflammatories
  3. methylxanthines
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306
Q

What are the 2 types of direct acting bronchodilators?

A
  1. beta 2 agonists
  2. anticholingergics
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307
Q

Beta __ agonists are bronchodilators

A

2

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308
Q

What are some beta 2 agonist examples?

A

albuterol, metaproterenol, salmeterol

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309
Q

What are some anticholinergics that are direct acting bronchodilators?

A

Atropine, glycopyrrolate, ipratropium

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310
Q

Anti-inflammatories that are pulmonary medications include: _____, ____, and ______.

A

inhaled corticosteroids, cromolyn, and leukotriene modifiers.

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311
Q

What are examples of leukotriene modifiers?

A

zileuton and montelukast

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312
Q

What are examples of inhaled corticosteroids?

A

beclomethasone, fluticasone, triamcinolone

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313
Q

Methylxanthines include what?

A

Theophylline

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314
Q

_____ and _____ are anesthetics with bronchodilating properties.

A

Volatile anesthetics and ketamine

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315
Q

What is the MOA of beta 2 agonists?

A

beta 2 stimulation –> increased cAMP –> decreased iCa2+

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316
Q

What are s/e of beta 2 agonists?

A

tachycardia, dysrhythmias, hypokalemia, hyperglycemia, tremors

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317
Q

Beta 2 agonists stabilize ______

A

mast cell membranes (which decrease mediator release)

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318
Q

What is the MOA of anticholingergics?

A

M3 antagonism –> decreased IP3 –> decreased iCa2+

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319
Q

What are s/e of anticholingergics?

A

inhibits secretions, urinary retention, blurry vision, cough

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320
Q

Anticholingergics increase ______ with narrow angle glaucoma.

A

intraocular pressure

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321
Q

Beclomethasone, Budesonide, Flunisolide, Fluticasone, and Triamcinolone are all what?

A

inhlated corticosteroids

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322
Q

What is the MOA of inhlaed corticosteroids?

A

stimulation of intracellular steroid receptors; regulates inflammatory protein synthesis (lowers airway inflammation and hyperresponsiveness)

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323
Q

S/e of inhaled corticosteroids?

A

dysphonia, myopathy of laryngeal muscles, oropharyngeal candidiasis, possible adrenal suppresion

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324
Q

What is the MOA of cromolyn?

A

Stabilizes mast cell membrane

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325
Q

What are the s/e of cromolyn?

A

neglibible s/e

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326
Q

Zileuton, Montelukast, Pranlukast, and Zarfirlukast are all what type of drug?

A

Leukotriene modifiers

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327
Q

What is the MOA of Leukotriene modifiers?

A

inhibits 5-lipoxygenase enzyme

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328
Q

Leukotriene modifiers decrease ____ synthesis

A

leukotriene

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329
Q

What are the s/e of leukotriene modifiers?

A

negligible

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330
Q

What is the MOA of methylxanthines?

A

inhibits phosphodiesterase –> increased cAMP

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331
Q

Theophylline is what type of drug?

A

methylxanthines

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332
Q

Methylxanthines inhibit what 2 things?

A

phosphodiesterase and adenosine receptors

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333
Q

Methylxanthines ____ endogenous catecholamine release

A

increase

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334
Q

What are the s/e of methylxanthines in plasma concentrations greater than 20?

A

N/V, diarrhea, HA, and disrupted sleep

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335
Q

When do seizures, tachydysrhythmias, and CHF occur with methylxanthine use?

A

plasma concentration >20

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336
Q

Steroids ____ arachidonic acid.

A

block

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337
Q

Which pulmonary function test is the MOST sensitive indicator of small airway disease?

A

Forced expiratory flow 25-75%

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338
Q

What measures how much air the lungs can hold at a single point in time?

A

Static lung volumes

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339
Q

What are examples of static lung volumes?

A

RV, ERV, TV, IRV, FRC, IC, VC, and TLC

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340
Q

What measures how quickly air can be moved in and out of the lungs over time?

A

Dynamic lung volumes

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341
Q

What are examples of dynamic lung volumes?

A

FEV1, FVC, FEV1/FVC, and MMEF

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342
Q

_________ measures how well the lungs can transfer gas across the alveolocapillary membrane.

A

Diffusing capacity

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343
Q

What is a normal FEV1

A

> 80% of predicted value

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344
Q

What is a normal FEV1/FVC ration?

A

> 75-80%

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345
Q

How are lung volumes and capcities measured?

A

spirometry

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346
Q

What is forced expiratory volume in 1 second (FEV1)?

A

volume of air that can be exhaled after a max inhalation in 1 second

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347
Q

FEV1 ____ with age

A

declines

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348
Q

What is forced vital capacity (FVC)?

A

Volume of air that can be exhaled after a max inhalation

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349
Q

What is the normal FVC for a male?

A

4.8 L

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350
Q

What is the normal FVC for a female?

A

3.7 L

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351
Q

What is FEV1/FVC ratio?

A

Compares volume of air expired in 1 second and total volume of air expired

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352
Q

The FEV1/FVC ratio is useful when diagnosis _____ vs _____

A

obstructive versus restrictive diseases

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353
Q

FEV1/FVC ratio <70% suggests what?

A

obstructive disease

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354
Q

A normal FEV1/FVC ratio occurs in what disease?

A

Restrictive

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355
Q

What is a normal FEV1/FVC?

A

> 75-80% of predicted value

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356
Q

What is forced expiratory flow at 25-75% vital capacity also called?

A

mid maximal expiratory flow rate (MMEF)

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357
Q

What does forced expiratory flow at 25-75% vital capacity show?

A

measures airflow in the middle of FEV (FEV 25-75%)

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358
Q

What is a normal forced expiratory flow at 25-75% vital capacity?

A

100 +/- 25% PREDICTED VALUE

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359
Q

What is maximum voluntary ventilation (MMV)?

A

max volume of air that can be inhaled and exhaled over the course of 1 minute

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360
Q

Maximum voluntary ventilation is the best test of ______-

A

endurance

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361
Q

What is the normal MMV for a male?

A

140-180 L

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362
Q

What is the normal MMV for a female?

A

80-120 L

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363
Q

What is diffusion capacity (DLCO)?

A

The volume of carbon monoxide that can traverse the alveolocapillary membrane per a given alveolar partial pressure of carbon monoxide

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364
Q

DLCO is based on _______ law

A

Fick’s law of diffusion

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365
Q

What is a normal DLCO?

A

17-25 mL/min/mmHg

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366
Q

Flow volume loops allow us to differentiate betwen what?

A

obstructive and restrictive respiratory diseases

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367
Q

On a flow-volume loop, _____ produces a waveform that moves from right to left with a negative deflection.

A

inhalation

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368
Q

On a flow-volume loop, _____ produces a waveform that moves from left to right with a positive deflection.

A

exhalation

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369
Q

What cannot be measured with spirometry.

A

RV

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370
Q

Independent risk factors that are patient-related for post-op pulmonary complication?

A

old age (>60)
COPD
CHF
smoking (>40 pack years)
ASA >2

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371
Q

Independent risk factors that are procedure-related for post-op pulmonary complication?

A

surgery >2 hours; GA; aortic or abdominal surgery

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372
Q

Independent risk factors that are diagnostic-related for post-op pulmonary complication?

A

Albumin <3.5 g/dL

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373
Q

What is a short-term benefit of smoking cessation?

A

reduction in carboxyhemoglobin

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374
Q

When should smoking cessation be done?

A

at least 6 weeks

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375
Q

What do you treat expiratory airflow obstruction with?

A

bronchodilators and corticosteroids

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376
Q

Moderate asthma, ABG analysis, and PFT have or have not been sown to increase the risk of post-op pulmonary complications for non-thoracic surgery.

A

HAVE NOT (key word = non-thoracic surgery)

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377
Q

What is smokings effects on the respiratory system?

A
  1. risk factor for pulmonary dx
  2. decreased mucociliary clearance
  3. airway hyperactivity
  4. reduced pulmonary immune function
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378
Q

What is smokings effects on the CV system?

A
  1. risk factor fo CV dx
  2. carbon monoxide –> decreased DO2
  3. catecholamine release
  4. coronary vasoconstriction
  5. decreased exercise tolerance
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379
Q

Short term effect of smoking cessation: carbon monoxide t1/2 = ___

A

4-6 hours

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380
Q

Short term effect of smoking cessation: P50 returns to near normal in ______

A

12 hours

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381
Q

Does short term cessation of smoking reduce pulmonary complciations?

A

no

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382
Q

Return of pulmonary function after smoking cessation takes at least ______.

A

6 weeks

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383
Q

A peak airway pressure of ____ is required to for initial reopening of the atelectatic regions.

A

30 cm H2O

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384
Q

Increasing the PIP to ____ for _____ appears to reverse anesthesia induced atelectasis almost completely.

A

40 cmH2O for 8 seconds (give a breath of 40 for 8 seconds)

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385
Q

A high FiO2 significantly contributes to what?

A

absorption atelectasis

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386
Q

Why should you use the lowest FiO2 the patient will tolerate?

A

B/c a high FiO2 significantly contributes to absorption atelectasis

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387
Q

List 3 types of surgery w/ the highest risk of PPC.

A
  1. aortic
  2. thoracic
  3. upper abdominal = neuro= peripheral vascular
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388
Q

A patient with severe kyphoscoliosis is expected to have a reduced ____ and ______. (pulmonary tests)

A

FRC; FEV1

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389
Q

_________ disease is characterized by small airway obstruction and increased resistance to expiratory flow.

A

obstructive

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390
Q

What type of respiratory disease has a proportionate reduction in all of the lung volumes along with poor compliance?

A

Restrictive

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391
Q

Restrictive respiratory disease has what type of lung volumes?

A

small

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392
Q

When is FEV1/FVC ratio decreased?

A

obstructive diseases

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393
Q

Patients with restrictive disease tend to have decreased ____ and ____, yet normal _____.

A

FEV1 and FRC; FEV1/FVE ratio

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394
Q

Getting air ____ is the problem in obstructive disease.

A

out

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395
Q

Restrictive or obstructive airway disease:
FEV1 ↓ to ↓↓↓↓

A

Obstructive

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396
Q

Restrictive or obstructive airway disease:
FEV1 ↓ to ↓↓↓

A

Restrictive

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397
Q

Restrictive or obstructive airway disease:
FVC ↑ to ↓↓↓

A

Obstructive

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398
Q

Restrictive or obstructive airway disease:
FVC ↓ to ↓↓↓

A

Restrictive

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399
Q

Restrictive or obstructive airway disease:
FEV1 to FVC Ratio ↓↓↓

A

Obstructive

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400
Q

Restrictive or obstructive airway disease:
FEV1 to FVC ratio normal

A

Restrictive

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401
Q

Restrictive or obstructive airway disease:
FEF 25-75% ↓↓↓

A

Obstructive

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402
Q

Restrictive or obstructive airway disease:
FEF 25-75% Normal

A

Restrictive

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403
Q

Restrictive or obstructive airway disease:
RV Normal to ↑

A

Obstructive

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404
Q

Restrictive or obstructive airway disease:
RV ↓↓↓

A

Restrictive

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405
Q

Restrictive or obstructive airway disease:
FRC Normal to ↑

A

Obstructive

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406
Q

Restrictive or obstructive airway disease:
FRC ↓↓↓

A

Restrictive

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407
Q

Restrictive or obstructive airway disease:
TLC Normal to ↑

A

Obstructive

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408
Q

Restrictive or obstructive airway disease:
TLC ↓↓↓

A

Restrictive

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409
Q

A normal spirometry waveform looks like what?

A

an up-side down ice cream cone

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410
Q

An example of a obstructive respiratory disease?

A

COPD

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411
Q

What does a spirometry waveform look like in obstructive disease?

A

The expiratory limb has a concave shape
LOOKS LIKE A CARRIAGE
“someone took a bite out of my ice cream cone”

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412
Q

What does a spirometry waveform look like in a restrictive lesion?

A

The shape of the loop is similar to the normal loop, but SMALLEr and RIGHT shifted
“on a restrictive diet you have to eat a smaller cone”

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413
Q

Pulmonary fibrosis is a ________ respiratory disease.

A

restrictive

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414
Q

In a fixed respiratory disease, the spirometry wvaeform is?

A

flat (both inspiratory and expiratory limbs)
“someone smashed my ice cream cone”
It needs to be fixed

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415
Q

What is an example of a fixed respiratory disease?

A

tracheal stenosis

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416
Q

In an extrathoracic obstruction, the patient ______ and the airway collapses.

A

inhales

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417
Q

In an extrathoracic obstruction, the patient exhales and____________.

A

pushes the obstruction open

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418
Q

What limb is flat for an extrathoracic obstruction spirometry waveform?

A

inspiratory limb is flat

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419
Q

The patient inhales and pulls open the obstruction in what type of thoracic obstruction?

A

intrathoracic

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420
Q

The patient exhales and the airway collapes in a _______obstruction.

A

intrathoracic

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421
Q

What limb is flat for an intrathoracic obstruction spirometry waveform?

A

expiratory limb

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422
Q

A bronchospasm immeditately following intubation in an asthma patient is MOST likely the result of?

A

Vagal stimulation

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423
Q

Airway smooth muscle is not innervated by the ______

A

SNS

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424
Q

What is the definition of asthma?

A

acute, reversible airway obstruction that is accompanied by chronic airway inflammation and bronchial hyperreactivity

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425
Q

With asthma, there is an acute, reversible ________, along with chronic airway and bronchial ________.

A

airway obstruction; inflammation; hyper-reactivity

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426
Q

What is atopy?

A

condition of being “hyper-allergic”

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427
Q

What is the greatest risk for developing asthma?

A

atopy

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428
Q

FEV1, FEV1/FVC ratio, and FEF 25-75% in asthma

A

all are reduced but improve w/ bronchodilator therapy

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429
Q

FEV1, FEV1/FVC ratio, and FEF 25-75% in asthma

A

all are reduced but improve w/ bronchodilator therapy

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430
Q

What is most common ABG for asthma?

A

respiratory alkalosis with hypocarbia

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431
Q

An elevated PaCO2 in asthma suggests what 3 possibilies?

A
  1. air trapping
  2. respiratory muscle fatigue
  3. impending respiratory failure
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432
Q

Key s/s of asthma:

A

wheezing, dyspnea, chest discomfort or tightness, productive or non-productive cough, prolonged expiratory phase, eosinophilia

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433
Q

During mechanism ventilation of an asthma patient, limit ____, prolong _____, and tolerate _____.

A

limit inspiratory time
prolong expiratory time
tolerate moderate permissive hypercapnia

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434
Q

What medications should be avoided in asthma patients?

A

Non-selective beta blockers and histamine releasing drugs

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435
Q

For asthma, use anesthetic agents that promote what?

A

bronchodilation

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436
Q

What anesthetic agents promote bronchodilation?

A

sevo, iso, ketamine, propofol, lidocaine

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437
Q

Name 4 drugs that release histamine.

A
  1. Sux
  2. Atracurium
  3. Morphine
  4. Meperidine
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438
Q

Smooth muscle hypertrophy, fibrosis, angiogenesis, and hypersecretion of mucus occur in what?

A

asthma

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439
Q

What type of external stressors provoke asthma S/S?

A

vagal stimulation and cold air

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440
Q

What drugs provoke asthma S/S? (4 total)

A

aspirin, nsaids, beta blockers, sulfites

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441
Q

What might the EKG show during a severe asthma attack?

A

RV strain with right axis deviation

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442
Q

Why might an EKG show RV strain with right axis deviation during a severe asthma attack?

A

PVR increases, and this increases workload of right heart

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443
Q

In asthma, PVR increases or decreases?

A

increases

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444
Q

The tachypnea and hyperventilation that occur during asthma attacks are the result of what?

A

Neural reflexes

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445
Q

Why might severe bronchospasm cause hypoxemia?

A

V/Q mismatch

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446
Q

PFTs are or are not predictive of post-op pulmonary complications.

A

ARE NOT

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447
Q

For what one surgery are PFT predictive of post-op pulmonary complications?

A

Lung reduction surgery

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448
Q

In asthma _____ may increase due to air trapping, but ______remains WNL.

A

FRC; TLC

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449
Q

CXR of asthma?

A

hyper-inflated lungs w/ diaphragmatic flattening

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450
Q

What is the preferred extubation technique for asthma patients?

A

Deep extubation (if not possible, use lidocaine or opioids)

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451
Q

What might benefit a patient with exercise-induced asthma during ventilation?

A

HME

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452
Q

What volatile agent reduces the risk of coughing and risk of bronchospasm?

A

Sevo

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453
Q

What is the only IV induction drug that causes bronchodilation?

A

Ketamine

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454
Q

What IV induction drug suppresses airway reflexes?

A

Propofol

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455
Q

_________1-3 minutes before extubation suppresses airway reflexes.

A

Lidocaine 1-1.5 mg/kg

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456
Q

How do you differentiate between light anesthesia and bronchospasm?

A

NMBD improve pulmonary compliance with light anesthesia but NOT bronchospasm

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457
Q

What is ketorolac’s effect on the airway?

A

it can increase airway resistance (caution in asthma)

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458
Q

What histamine receptor, when stimulated, reduces histamine release?

A

Presynaptic H2 receptor

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459
Q

What are some H2 antagonists?

A

Ranidtine and Famotidine

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460
Q

H2 antagonists allow for unopposed H1 stimulation, which can cause what in asthma patients?

A

bronchospasm (very low risk)

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461
Q

What BB is the best choice in asthma patients and why?

A

Esmolol b/c of its short t1/2 and B1 selectivity

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462
Q

What is F2 alpha prostaglandin?

A

a naturally occuring hormone

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463
Q

What does carboprost (hemabate) mimic?

A

the action of F2 alpha prostaglandin

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464
Q

What is the use of carboprost (hemabate)?

A

it is used to stop uterine bleeding

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465
Q

What is a s/e of carboprost (hemabate)?

A

bronchoconstriction in asthmatics

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466
Q

Which drug is LEAST likley to be effective in relieving s/s of acute bronchospasm?
1. Ketamine 1 mg/kg IV
2. Epi 1 mcg/kg IV
3. Hydrocortisone 2 mg /kg IV
4. Lidocaine 1.5 mg /kg IV

A

Hydrocortisone 2 mg /kg IV

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467
Q

What are causes of wheezing, besides asthma, when ventilated?

A

Kinked ETT, end-bronchial intubation, pulmonary aspiration

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468
Q

How does intraoperative bronchospasm present?

A
  1. wheezing
  2. decreased breath sounds
  3. increased PIP (/t decreased dynamic compliance)
  4. increased alpha angle on ETCO2 waveform
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469
Q

How do you treat acute bronchospasm?

A

100% FiO2, deepen anesthetic
short acting inhaled B2 agonist
inhaled ipratropium
epi 1 mcg/kg IV
hydrocortisone 2-4 mg /kg IV (doesn’t treat, prevents additional problems)
aminophylline
helium -oxygen gas mix

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470
Q

Name differential diagnosis for intra-op bronchospams/wheezing:

A
  1. mechanical obstruction of ETT
  2. light anesthesia
  3. acute asthma attack
  4. endobronchial intubation
  5. pneumo
  6. aspiration
  7. pulmonary edema
  8. PE
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471
Q

With light anesthesia, coughing and straining occur. This ____ FRC.

A

Decreases

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472
Q

Name 4 mechanical obstructions of ETT.

A

kinking, biting, secretions, overinflation of cuff

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473
Q

Why do increased PIP with normal plateau pressures occur during bronchospam?

A

d/t decreased dynamic pulmonary compliance

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474
Q

During bronchospasm, PIP is ____ and plateua pressure is _______

A

PIP is increased; plateau is normal

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475
Q

Is montelukast used in the treatment of acute bronchospasm?

A

NO

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476
Q

Alpha-1 antitrypsin deficiency: (select 2).
1. increases the risk of bronchospasm
2. causes pan-lobular emphysema
3. can be treated with IgG
4. is the most common metabolic disease affecting the liver

A

2 & 4
Pan-lobular emphysema and most common metabolic dx affectign the liver

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477
Q

COPD is characterized by a reduction in ___________ and a slower forced emptying of the lungs.

A

maximal expiratory flow

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478
Q

How is COPD different than asthma?

A

Air flow obstruction is not fully reversible

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479
Q

COPD is an umbrella term for what two diseases?

A

Chronic bronchitis and emphysema

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480
Q

What is the pathophysiology of chronic bronchitis?

A

hypertrophied bronchial mucus glands and chronic inflammation

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481
Q

What is the pathophysiology of emphysema?

A

enlargement and destruction of the airways distal to the terminal bronchioles

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482
Q

Etiologies of COPD include ____, ____, ____, and ____.

A

smoking, respiratory infection, exposure to environmental pollutants, and alpha-1 antitrypsin deficiency

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483
Q

Alpha-1 antitrypsin deficiency is r/t what disease?

A

COPD

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5
Perfectly
484
Q

Inability to fully exhale —> _____

A

gas trapping (↑RV)

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485
Q

ABG of chronically elevated PaCO2

A

respiratoyr acidosis

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486
Q

To combat respiratory acidosis, what do the kidneys do?

A

reabsorb bicarb

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487
Q

What happens if you administer supplemental O2 to patient with severe COPD?

A

it can cause oxygen-induced hypercapnia

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488
Q

Oxygen-induced hypercapnia in COPD is caused by what 2 things?

A
  1. inhibition of HPV
  2. Haldane effect
489
Q

To minimize the risk of oxygen-induced hypercapnia in patients with severe COPD, titrate FiO2 to maintain the SaO2 ___ to ___

A

88-92%

490
Q

With COPD there is progressive deterioration of what components in the lung?

A

elastic components

491
Q

What happens b/c of the deterioration of elastic components of the lungs of COPD patients?

A

there is a decreased recoil –> air trapping –> ↑RV

492
Q

In COPD there is a ____ airway rigidity.

A

reduced (causes collapse during exhalation)

493
Q

COPD Pathophysiology: ________ –> decreased pressure in airways –> airway collapse –> air trapping

A

increased gas velocity through narrowed airways

494
Q

What causes airflow obstruction and bronchospasm in COPD patients?

A

secretions

495
Q

Why does air trapping occur in COPD? (3 reasons)

A
  1. progressive deterioration of elastic components/decreased recoil
  2. reduced airway rigidity
  3. increased gas velocity
496
Q

In COPD, patients have a problem getting air ____

A

out

497
Q

COPD patients ahve _____ lungs

A

hyperinflated

498
Q

What are 3 changes to the lungs that occur with COPD?

A
  1. flattened diaphragm
  2. increased AP diameter
    pulmonary bullae
499
Q

COPD: _____ diaphragm

A

flattened

500
Q

COPD: ____ AP diameter

A

increased

501
Q

What happens if you try to restore a chronic COPDer to a normal PaCO2 on the vent?

A

The reabsorbed bicarb in the blood (d/t kidney compensation of acidosis) will then lead to risk of severe alkalosis –> reduced oxygen unloading and apnea

502
Q

Chronic bronchitis is defined by the presence of cough and sputum production for > ____ for ____.

A

3 months; 2 consecutive years

503
Q

What is the common cause of chronic bronchitis?

A

smoking

504
Q

Why does blood viscosity increase in chronic bronchitis?

A

RBCs are overproduced (erythrocytosis) to compensate for V/Q mismatch and hypoxemia

505
Q

Explain the pathophysiology of cor pulmonale in chronic bronchitis.

A

Chronic hypoxemia and hypercarbia –> increase PVR –> PHTN –> RV strain (right axis deviation) –> cor pulmonale

506
Q

____ heart function is normal in chronic bronchitis related cor pulmonale

A

left

507
Q

What is the most efficacious therapy for PHTN and prevention of erythrocytosis in chronic bronchitis?

A

oxygen therapy

508
Q

Blue bloaters are _____

A

chronic bronchitis

509
Q

_____ is associated with enlargement and destruction of the airways distal to the terminal bronchioles.

A

Emphysema

510
Q

Pink puffers are _____

A

emphysema

511
Q

____ is reduced in emphysema, which leads to increased dead space

A

surface area for gas exchange (r/t destruction of airways distal to terminal bronchioles)

512
Q

Why does PHTN occur in emphysema?

A

the pulmonary capillary beds are destroyed and the same amount of blood must travel to a smaller network of blood vessles

513
Q

Alpha-1 antitrypsin deficiency can cause what?

A

emphysema

514
Q

Emphysema PaO2 = ____

A

normal - slightly reduced

515
Q

Emphysema PaCO2 = ______

A

normal - decreased

516
Q

What is alpha-1 antitrypsin?

A

an enzyme

517
Q

Where is alpha-1 antitrypsin produced?

A

by the liver

518
Q

In alpha-1 antitrypsin deficiency, the ____ is unable to secrete this enzyme so it accumulates there. What does this cause?

A

Hepatocyte; cell death and cirrhosis

519
Q

What breaks down pulmonary connective tissue?

A

alveolar elastase

520
Q

What keeps the alveolar elastase enzyme in check?

A

alpha-1 antitrypsin

521
Q

Alpha-1 antitrypsin allows for an overactivity of what?

A

alveolar elastase enzyme

522
Q

COPD: RV is ↑ or ↓?

A

Increased

523
Q

COPD: FRC is ↑ or ↓?

A

Increased

524
Q

COPD: TLC is ↑ or ↓?

A

Increased

525
Q

COPD: FEV1 is ↑ or ↓?

A

Decreased

526
Q

COPD: FEV1/FVC is ↑ or ↓?

A

Decreased

527
Q

COPD: FEF 25-75% is ↑ or ↓?

A

Decreased

528
Q

An _______________ after bronchodilator therapy is diagnostic of COPD.

A

FEV1/FVC ratio <70%

529
Q

Supplemental O2 in COPD patients impairs the hypoxic drive. T/F

A

False - it can cause oxygen-induced hypercapnia

530
Q

What is the Haldane effect?

A

Describes how the oxygen tension in the blood determines the blood’s ability to buffer CO2

531
Q

According to the Haldane effect, well-oxygenated blood has a _____ capacity to buffer CO2 than deoxygenated blood.

A

Lower

532
Q

Identify the MOST appropriate strategy for mechanical ventilation in the patient with COPD.
a. I:E ratio 1:1
b. FiO2 <50%
c. RR 7
d. TV 10-12 mL/kg

A

RR 7

533
Q

For COPD patients, do not consider neuraxial anesthesia if the patient requires sensory block > ___.

A

T6

534
Q

What block is contraindicated in severe COPD? Why?

A

interscalene block; it causes paralysis of the ipsilateral hemidiaphragm

535
Q

In COPD patients, select a volatile with ______

A

low blood:gas solublity

536
Q

What are volatile agents affect upon HPV?

A

they impair HPV at >1.5 MAC and therefore increase shunt

537
Q

What volatile is associated with rupture of pulmonary blebs?

A

N2O

538
Q

COPD vent settings: TV _____

A

6-8 mL/kg IBW

539
Q

For vent settings of COPD, increase ____ time

A

expiratory

540
Q

Why should you avoid neuraxial anesthesia in COPD patients that would require sensory block > T6?

A

Block causes:
expiratory muscle function impairment, reduced ERV, and inability to cough and clear secretions

541
Q

What volatile is less likely to cause airway irritation in COPD?

A

Sevo

542
Q

What can be used to help gas redistribute from high compliance areas to those with longer time constants in COPD patients?

A

slow inspiratory flows

543
Q

When does dynamic hyperinflation occur?

A

When a new breath is given before the patient was able to exhale the previous breath fully

544
Q

Dynamic hyperinflation is also known as ____

A

breath staking

545
Q

What are 3 risk factors for dynamic hyperinflation?

A
  1. high minute ventilation
  2. increased airway resistance
  3. reduced expiratory flow (COPD)
546
Q

What are the consequences of dynamic hyperinflation?

A

barotrauma, pneumothorax, hypotension

547
Q

What is the treatment for dynamic hyperinflation/auto-PEEP?

A

remove the patient from the breathing circuit

548
Q

Removing the patient from the breathing circuit to treat auto-PEEP/dynamic hyperinflation allows what to happen?

A

allows the pressure in the lungs to equalize with atmospheric pressure

549
Q

What will show on the vent with dynamic hyperinflation?

A

The waveform’s baseline will increase with each breath

550
Q

What will the flow-volume loop look like with air trapping?

A

It will not return to zero at the end of expiration

551
Q

All of the following are examples of restrictive lung disease EXCEPT:
a. sarcoidosis
b. cystic fibrosis
c. negative pressure pulmonary edema
d. flail chest

A

Cystic fibrosis

552
Q

Restrictive lung disease describe disorders in which the lung is impaired when?

A

normal lung expansion during INSPIRATION is impaired

553
Q

Where are the areas of restriction in restrictive lung diseases?

A

pulmonary interstitium, pleura, rib cage, and/or abdomen

554
Q

Acute intrinsic restrictive ventilatory defects… name 2

A

aspiration
UA obstruction
reversal of opioid OD
cocaine OD
re-expansion of collapsed lung
neurogenic

555
Q

Chronic intrinsic restrictive ventilatory defects… name 2

A

Sarcoidosis
Amiodarone-induced pulmonary fibrosis

556
Q

Disease of the chest wall, mediastinum, and pleura restrictive ventilatory defects… name 3

A

Flail chest, pleural effusion, and ankylosing spondylitis

557
Q

Miscellanious restrictive ventilatory defects… name 3

A

Pregnancy, obesity, ascites

558
Q

FEV1 and FVC ______ is diagnostic for restrictive lung disease.

A

<70%

559
Q

Although FEV1 and FVC are decreased in restrictive lung disease, FEV1/FVC ration is ______

A

unchanged

560
Q

What is the most significant risk of restrictive lung disease?

A

barotrauma

561
Q

Vent settings for restrictive lung disease: TV - ____

A

6 mL/kg IBW (on smaller side)

562
Q

Vent settings for restrictive lung disease: RR - ____

A

14-18 breaths/min (on faster side)

563
Q

Vent settings for restrictive lung disease:PIP - ____

A

PIP <30 cm H2O

564
Q

Vent settings for restrictive lung disease: I:E ratio - ____

A

1:1 (prolonged inspiratory time)

565
Q

What are the characteristics of restrictive lung diseases? (name 3)

A
  1. decreased lung volumes and capacities
  2. decreased compliance
  3. intact pulmonary flow rates
566
Q

In _______ WOB is increased, manifesting as rapid and shallow breathing pattern.

A

restrictive respiratory disease

567
Q

What NM disorders cause restrictive ventilatory defects?

A

muscular dystrophies
Guillain-Barre
Spinal cord transection
Diseases of NM transmission

568
Q

Why are people with restrictive lung diseases more prone to rapid arterial desaturation during apnea?

A

B/c they have a reduced FRC

569
Q

All of the following reduce the incidence of ventilator-associated pneumonia EXCEPT:
a. oropharyngeal decontamination
b. minimizing the duration of mechanical ventilation
c. limiting sedation
d. PPI

A

PPI

570
Q

When does aspiration most commonly occur peri-op?

A

during anesthetic induction and intubation or within 5 minutes of extubation

571
Q

Aspiration can lead to what?

A

airway obstruction, bronchospasm, impaired gas exchange, bacterial respiratory infection

572
Q

What are risk factors for aspiration pneumonitis?

A

pregnancy, trauma, emergency surgery, GI obstruction

573
Q

What is Mendelson’s syndrome?

A

A chemical aspiration pneumonitis first described in OB patients receiving inhalation anesthesia

574
Q

What are risk factors for Mendelson’s syndrome?

A

gastric pH <2.5
Gastric volume >25 mL (0.4 mL/kg)

575
Q

What is the hallmark sign of aspiration?

A

hypoxemia

576
Q

What are S/S of aspiration?

A

hypoxemia, dyspnea, tachypnea, cyanosis

577
Q

What are the primary treatments for aspiration?

A

tilting head down or to side
suctioning upper airway
securing the airway
applying PEEP

578
Q

What are the rules regarding post-op care of aspirated patient?

A

A patient can be safely d/c home if they do NOT experience any of the following within 2-hours of the aspiration event:
- new cough or wheeze
- radiographic evidence of injury
- SpO2 decrease >10% or pre-op
- A-a gradient >300 mmHg

579
Q

What is the best method to prevent ventilator-associated pneumonia of the intubated patient?

A

minimize duration of mechanical ventilation

580
Q

Aspiration: gastric contents enter airway –> _____

A

risk of airway obstruction

581
Q

Aspiration: gastric contents cause a chemical burn to the airway and lung parenchyma –> ______

A

risk of bronchospasm and impaired gas exchange

582
Q

Aspiration: infectious material enters airway –» ______

A

bacterial infection

583
Q

T/F: All aspiration leads to infection.

A

False

584
Q

T/F: Routine use of prophylactic agents to prevent aspiration is recommended.

A

False

585
Q

Anticholinergics to reduce the risk of aspiration is or is not recommended.

A

Is NOT

586
Q

T/F: Many patients who experience aspiration remain asymptomatic.

A

True

587
Q

The most common findings of a CXR after aspiration are _____ and infiltrates in the _____ regions.

A

pulmonary edema; perihiar and dependent lung

588
Q

For aspiration, ABX are only indicated when?

A

The patient develops a fever or an increased WBC count > 48 hours

589
Q

What percent of people die after aspiration?

A

5%

590
Q

What percent of people require ventilation for longer than 6 hours after aspiration?

A

15%

591
Q

What percent of people require supportive care after aspiration?

A

20%

592
Q

What percent of people remain asymptomatic after aspiration?

A

60%

593
Q

Why does intubation have a risk for VAP?

A

the presence of an ETT bypasses the host’s defense mechanisms of cough and mucociliary clearance and allows organisms direct passage between the mouth and bronchopulmonary tree

594
Q

What does micoraspiration allow?

A

contaminants to slide between the ETT cuff and trachea

595
Q

What is leukocytosis?

A

high WBC

596
Q

What are early signs of VAP?

A

increased secretions in ETT and increasing O2 requirements (also high WBC and/or fever should raise suspicions)

597
Q

T/F: a CXR alone is non-specific for VAP.

A

True - could also be ARDS, atelectasis, or lung contusion

598
Q

What are the most common culprits of VAP?

A

Pseudomonas aeruginosa and S. aureus

599
Q

What is 1st line treatment for tensionpneumothorax?
a. chest tube insertion
b. 14g angiocath insertion at the 2nd ICS midclavicular line
c. pericardiocentesis
d. CPR

A

B (1st line in emergency; chest tube insertion is. the definitive treatment)

600
Q

What are the 3 types of pneumothorax?

A

close, communicating, and tension

601
Q

What are the hallmark characteristics of a tension pneumo?

A

hypoxemia
increased airway pressures
tachycardia
hypotension
elevated CVP

602
Q

What does point-of-care US show for a tension pneumo?

A

a lack of lung sliding and the absence of comet tails

603
Q

If you suspect a pneumo, you must d/c what immediately?

A

N2O

604
Q

Where can a 14g angiocath be inserted for a tension pneumo? (2 places)

A

2 ICS at mid-clavicular line OR 4th or 5th ICS at anterior axillary line

605
Q

What gauge angiogath is used in emergent treatment for tension pneumo?

A

14 g

606
Q

What causes flail chest?

A

blunt chest trauma w/ multiple fib fractures

607
Q

What is the key characteristic of flail chest?

A

paradoxical movement of the chest wall at the site of the fractures

608
Q

What are consequences of flail chest?

A

alveolar collpase, hypoventilation, hypercarbia, hypoxia

609
Q

What is. thetreatment for flail chest?

A

reducing pain with epidural or intercostal nerve block

610
Q

_______ pneumo: the defect is in the pulmonary tree or lung tissue, and air enters and exits the pleural space through the defect

A

closed

611
Q

T/F: In closed pneumos there is no communication between the pleural cavity and the atmosphere.

A

True

612
Q

Which pneumos present with mediastinal shift?

A

tension is the only one

613
Q

_____ pneumo: the defect is the chest wall, and air passes between the pleural space and the atmosphere

A

Open

614
Q

With an open pneumo, the lung collapses on _____ and partially re-expands on ____.

A

inspiration; expiration

615
Q

Treatment. ofa closed pneumo??

A

observation, catheter aspiration, chest tube

616
Q

Treatment of an open pneumo?

A

occlusive dsg that does not let air in (but lets air out), O2, chest tube, possible intubation

617
Q

Does a tension pneumo occur with a closed or open defect?

A

it can occur with either

618
Q

What is the pathophysiology of a tension pneumo?

A

Tension (aka increased intrathoracic pressure) is created when air enters the pleural space through a ball-valve defect in the chest wall - air is allowed to enter, but not exit, the pleural space

619
Q

In a tension pneumo, increased intrathoracic pressure causes a mediastinal shift towards _____ side.

A

the contralateral side.

620
Q

Why does hypotension occur with tension pneumos?

A

compression of the heart and vasculature reduces venous return and CO

621
Q

Why do you create an opening during emergent treatment of tension pneumo?

A

it will release the tension and relieve hemodynamic instability (does not cure however - that is CT)

622
Q

What line placement can cause a pneumothorax?

A

CVL insertion

623
Q

What block placement can cause a pneumothorax?

A

supraclavicular, interscalene, intercostal nerve blocks

624
Q

What surgeries can cause a pneumothorax?

A

Radical neck dissection
shoulder arthroscopy
mastectomy
axillary lymph node dissection
mediastinoscopy
laparoscopy
nephrectomy

625
Q

_____ after a chest trauma should raise suspicion about a pneumo.

A

Increasing peak inspiratory pressures

626
Q

What respiratory things can cause pneumo?

A

barotrauma, high PEEP, high PIP

627
Q

What is the blood:gas coefficient of N2O?

A

0.47

628
Q

What is a chylothorax?

A

lymph in chest

629
Q

What is a hemothorax?

A

blood in chest

630
Q

What is a fibrothorax?

A

organized blood clot in chest

631
Q

What is a pyothorax (empyema)?

A

pus in chest

632
Q

What is a pleural effusion?

A

serous fluid in chest

633
Q

What is the most common cause of hemothorax?

A

bleeding intercostal vessels

634
Q

WIth a hemothorax, what are the indications for thoracotomy?

A

Initial drainage >1,000 mL
continued bleeding >200 mL/hr
white lung on CXR
large air leak

635
Q

When can a patient with a hemothorax be managed with a VATS?

A

hemodynamically stable with bleeding <150 mL/hr

636
Q

The thoracic duct empties lymph into the _____.

A

left subclavian vein

637
Q

Injury to the thoracic duct during CVL insertion is more likely on the right tor left side?

A

left side

638
Q

Injury to the thoracic duct during CVL insertion can cause what?

A

chylothorax

639
Q

Negative intrathoracic pressure occurs during inspiration or expiration?

A

inspiration

640
Q

Positive intrathoracic pressure occurs during inspiration or expiration?

A

expiration

641
Q

During inspiration the chest wall moves ____ and lungs ____

A

out and lungs expand

642
Q

in flail chest, during inspiration the injured rib moves ____

A

in (and collapses affected region)

643
Q

in flail chest, during expiration the injured rib moves ____

A

out (and affected region doesn’t empty)

644
Q

Place the monitors for VEA in order according to their relative sensitivities (#1 is most sensitive).
a. TEE
b. precordial doppler
c. ETCO2
d. CVP

A
  1. TEE
  2. Doppler
  3. ETCO2
  4. CVP
645
Q

When a VAE of significant size travels to the R heart, what happens?

A

It lodges in the pulmonary outflow tract or pulmonary artery and produces an airlock that converts distal alveolar units to dead space

646
Q

Place in order (sitting, prone, lateral, supine)
In NS patient, the risk for VAE from highest to lowest: __>___>___>____

A

sitting > supine > prone > lateral

647
Q

What is the most sensitive diagnostic tool for VAE?

A

TEE

648
Q

What will a precordial doppler show with VAE?

A

“mill wheel” murmur

649
Q

VAE: ETCO2 ____

A

decreases

650
Q

VAE: EtN2 ____

A

increases

651
Q

VAE: BP ____

A

decreases

652
Q

What are consequences of VAE?

A

dysrhythmias, hypoxia, cyanosis, CV collapse

653
Q

Treatment for VAE?

A

FiO2 100%
Flood surgical field
d/c insufflation
left lateral decubitus position

654
Q

What is the durant maneuver?

A

left lateral decubitus position for VAE

655
Q

Consequences of air trapped in pulmonary circulation: _____ PAP

A

increased

656
Q

Consequences of air trapped in pulmonary circulation: _____ RV stroke work index

A

increased

657
Q

VAE can lead to what type of HF?

A

RV failure

658
Q

Consequences of air trapped in pulmonary circulation: _____ pulmonary venous return

A

decreased

659
Q

Consequences of air trapped in pulmonary circulation: _____ LV preload

A

decreased

660
Q

Consequences of air trapped in pulmonary circulation: _____ CO

A

decreased

661
Q

With durant maneuver, air will _____.

A

rise in the right heart (and minimizes entry into the pulmonary circulation)

662
Q

A patient with PHTN develops tricuspid regurgitation. Which treatments will MOST likely improve the patients conditions? (Select 3).
a. Hypothermia
b. NO
c. Nitroglycerin
d. N2O
e. PEEP
f. Hyperventilation

A

b, c, f

663
Q

PHTN is defined as a mean PAP >____

A

25 mmHg

664
Q

PVR increases as a function of _____, ____, and/or ____.

A

increased vascular smooth muscle tone, vascular cell proliferation, and/or pulmonary thrombi

665
Q

With PHTN you want to avoid conditions that increase what?

A

PVR

666
Q

What conditions increase PVR?

A

hypoxemia
hypercarbia
acidosis
hypothermia

667
Q

PHTN can progress to what?

A

RV failure aka cor pulmonale

668
Q

What are anesthesia considerations for PHTN?

A
  1. do not hold preop meds that lower PVR
  2. CO is fixed, pts are sensitive to inadequate preload
  3. Treat hypotension aggressively
  4. epidural anesthesia > spinal anesthesia
  5. inhaled NO
  6. high-frequency jet ventilation
669
Q

In PHTN, CO is dependent upon _____

A

preload

670
Q

Why does tricuspid regurg occur with PHTN?

A

There is a decreased RV stroke volume and increased RV volume at end of diastole. This stretches the tricuspid annulus leading. to regurg.

671
Q

List causes of PHTN.

A

COPD
Hypoxemia & Hypercarbia
LH dysfunction
Mitral valve dx
Congenital heart dx
Connective tissue disorders
Chronic thromboembolism
Portal HTN

672
Q

What is the formula for PVR?

A

PVR = (mean PAP - PAOP)/CO x 80

673
Q

What is normal PVR?

A

150-250 dynes

674
Q

What drugs increase PVR?

A

N2O
Ketamine
Des

675
Q

What drugs decreased PVR?

A

NO
Nitroglycerin
Phosphodiesterase Inhibitors (sildenafil)
Prostaglandins PGE1 and PGI2
CCB
ACEI

676
Q

Elevated RA pressures can open what? What happens if this occurs?

A

Foramen ovale, it causes right-to-left intracardiac shunt

677
Q

Hypoxemia increases or decreases PVR?

A

Increases PVR

678
Q

Hypercarbia increases or decreases PVR?

A

Increases PVR

679
Q

Acidosis increases or decreases PVR?

A

increases PVR

680
Q

SNS stimulation increases or decreases PVR?

A

Increases PVR

681
Q

Pain increases or decreases PVR?

A

Increases

682
Q

Hypothermia increases or decreases PVR?

A

Increases PVR

683
Q

Mechanical ventilation increases or decreases PVR?

A

Increases PVR

684
Q

PEEP increases or decreases PVR?

A

Increases

685
Q

Atelectasis increases or decreases PVR?

A

Increases

686
Q

Alkalosis increases or decreases PVR?

A

Decreases

687
Q

PHTN patients are____ dependent.

A

Preload

688
Q

Carbon monoxide:
a. shifts the oxyhemoglobin dissociation curve to the right
b. production is highest with Iso
c. binds to the O2 binding site on Hgb with an affinity 200x that of O2
d. poisoning is reversed with methylene blue

A

C

689
Q

Carbon monoxide shifts the oxyhemoglobin curve to the _____.

A

left

690
Q

Place in order the volatiles production of carbon monoxide.
Sevoflurane, Desflurane, Isoflurane

A

Des > Iso&raquo_space;> Sevo
Des produces the most

691
Q

Where is carbon monoxide produced in the anesthesia circuit?

A

soda lime, (particularly after desiccation)

692
Q

How is carbon monoxide poisoning treated?

A

Oxygen therapy

693
Q

What does Methylene blue treat?

A

Methemoglobinemia

694
Q

What patients are at risk for carboxyhemoglobinemia?

A

Burn victims, smokers, patients exposed to desiccated soda lime

695
Q

With Carboxyhemoglobin, CaO2 ____

A

is decreased

696
Q

What is required to dx carboxyhemoglobinemia?

A

Co-oximeter

697
Q

T/F: A pulse ox can be used to measure CoHgb.

A

False, pulse-ox does not measure carboxyhemoglobin and may give a falsely elevated result

698
Q

CO has an affinity for the binding site on Hgb ____x that of oxygen.

A

200x

699
Q

What two ways does carbon monoxide poisoning deprive tissues of O2?

A
  1. CO binds on Hgb, displacing O2 from Hgb and reducing CaO2
  2. Causes a left shift in oxyhemoglobin dissociation curve (less O2 released)
700
Q

Carbon monoxide poisoning results in an impairment of _____, reducing ATP production.

A

oxidative phosphorylation

701
Q

ABG in carbon monoxide poisoning: ______

A

metabolic acidosis

702
Q

T/F: Patients with carbon monoxide poisoning will appear cyanotic.

A

False - will have cherry red apperance

703
Q

The t1/2 of carboxyhemoglobin is ______ breathing RA.

A

4-6 hours

704
Q

Treating a patient with carbon monoxide poisoning with 100% supplemental O2 reduces the t1/2 of carboxyhemoglobin to _____.

A

60-90 minutes

705
Q

How long is O2 therapy continued. incarbon monoxide poisoning?

A

Until CoHgb is <5% or for 6 hours

706
Q

When is hyperbaric O2 indicated for carbon monoxide poisoning?

A

If CoHgb >25% or patient is symptomatic

707
Q

Soda lime is hydrated to _____.

A

13-15%

708
Q

What does desiccated mean regarding soda lime?

A

Becomes dehydrated

709
Q

In the presence of desiccated soda lime, what happens to Sevo?

A

Sevo forms compound A

710
Q

Compound A increases the risk of _____.

A

fire

711
Q

Identify the strongest indications for intubation and mechanical ventilation. (select 2)
a. PaCO2 > 60 mmHg
b. vital capacity 25 mL/kg
c. inspiratory force <25 cm H2O
d. RR 35

A

A and C

712
Q

Indications for mechanical ventilation -
Vital capacity _______

A

<15 mL/kg (normal = 65-75 mL/kg)

713
Q

Indications for mechanical ventilation -
Inspiratory force _______

A

<25 cm/H2O (normal = 75-100 cm/H2O)

714
Q

Indications for mechanical ventilation -
PaO2 _______

A

<200 mmHg (on 100% O2) (normal on 100% is >400)

715
Q

Indications for mechanical ventilation -
A-a gradient _______

A

> 450 mmHg (on 100% O2) (normal on 100% is <100)

716
Q

Indications for mechanical ventilation -
PaCO2 _______

A

> 60 mmHg

717
Q

Indications for mechanical ventilation -
RR_______

A

> 40 OR <6

718
Q

What drugs can be given via ETT in emergency situation?

A

NAVEL
Narcan
Atropine
Vasopressin
Epinephrine
Lidocaine

719
Q

Identify the absolute indications for one-lung ventilation. (Select 2).
a. esophageal resection
b. bronchopleural fistula
c. pulmonary infection
d. thoracic aortic aneurysm repair

A

B and C

720
Q

List 3 predictors of post-op pulmonary complications for patients undergoing pulmonary surgery.

A
  1. FEV1 <40% predicted
  2. DLCO <40% predicted
  3. VO2 max <15 mL/kg/min
721
Q

______ is indicated when pre-op assessment suggests an increased risk of post-op pulmonary complications in patients undergoing pulmonary surgery.

A

Split lung V/Q function testing

722
Q

Name 3 absolute indications for one-lung ventilation.

A

infection, massive hemorrhage, and bronchopleural fistula

723
Q

Name 3 relative indications for one-lung ventilation.

A

Improved surgical exposure, pulmonary edema, severe hypoxemia d/t lung disease

724
Q

A ____-sided double-lumen tube is typically preferred. Except when?

A

LEFT
The left main bronchus has distorted anatomy (tumor, TAA) OR surgical procedures - left pneumonectomy, left lung transplant, or left sleeve resection

725
Q

What is the ideal DLT size for females?

A

35-37

726
Q

What is the ideal DLT size for males?

A

39-41

727
Q

DLT should not be used for kids under ____

A

8 years of age

728
Q

What is the normal VO2 max for male?

A

35-40 mL/kg/min

729
Q

What is the normal VO2 max for female?

A

27-31 mL/kg/min

730
Q

What does VO2 measure?

A

cardiopulmonary reserve

731
Q

If you do not have a VO2 max reading, what can you ask teh pateint to gather similar info?

A

“can you climb 2 flights of stairs”

732
Q

What is the volume of the bronchial cuff of a DLT?

A

1-2 mL air

733
Q

The bronchial cuff of a DLT is a ___volume, ___ pressure cuff.

A

low; high

734
Q

How far should a DLT be inserted on a female?

A

@27 cm

735
Q

How far should a DLT be inserted on a male?

A

@29 cm

736
Q

What is the DLT size for kids 8-9?

A

26

737
Q

What is. theDLT size for kids 10 and up?

A

28 or 32

738
Q

During anesthesia in the lateral decubitus position, the ____ lung is better ventilated and the ____ lung is better perfused. What does this cause?

A

non-dependent lung; dependent
V/Q mismatch

739
Q

During OLV, blood from both lungs mix. What does this cause?

A

An increased shunt fraction and significant source of hypoxemia

740
Q

OLV: TV ____

A

6-8 mL/kg IBW

741
Q

OLV: RR _____

A

12-15

742
Q

What is the stepwise approach to hypoxemia during OLV?

A
  1. Verify delivery of 100% O2
  2. Check position of ETT via fiberoptic
  3. rule out physiologic cause (low CO, bronchospasm, mucus plug, etc)
  4. Apply CPAP to non-dependent lung or use a suction catheter to insufflate O2
  5. PEEP 5-10 to dependent lung
743
Q

If standard interventions work for hypoxemia during OLV, what should you do next?

A

a. intermittently reinflate non-dependent lung
b. ligate pulmonary artery
c. eliminate drugs that inhibit HPV

744
Q

If the DLT is in too far –> _______________

A

upper lobe is not ventilated

745
Q

If the DLT is not deep enough –> _______________

A

failure to achieve lung separation

746
Q

If the DLT is in the wrong bronchus –> _______________

A

wrong lung collapses

747
Q

What is the most common problem associated with one-lung ventilation?

A

intrapulmonary shunt

748
Q

How does the body attempt to compensate for V/Q mismatch during OLV?

A

HPV

749
Q

V/Q mismatch during OLV is made worse by ____, ____, and _____.

A

NMBD, Positive pressure ventilation, and surgical positioning devices

750
Q

What is the best method to verify the DLT is in the correct position?

A

Fiberoptic bronchoscope

751
Q

When confirming DLT placement, what structures should be visualized?

A

Tracheal lumen (incomplete c-rings that open posteriorly)
Blue of bronchial cuff barely visible in the correct bronchus w/ no herniation present

752
Q

When viewing the right bronchus, ___ takeoffs are rpesent.

A

3

753
Q

When viewing the left bronchus, ___ takeoffs are present.

A

2

754
Q

How do you auscultate to verify correct DLT positioning?

A
  1. inflate both cuff, clamp tracheal lumen, ventilate bronchial lumen (should hear BS on left for LDLT or right for RDLT)
  2. Clamp bronchial lumen and ventilate tracheal (should hear opposite of above)
  3. deflate bronchial cuff, keep bronchial lumen clamped, ventilate tracheal lumen (BS right and left)
755
Q

Right upper lobe take off of the lungs is only _____ beyond the carina.

A

a few centimeters

756
Q

When should you confirm DLT placement?

A

After insertion and after you change positions

757
Q

Why are left-sided DLT preferred?

A

Right upper lobe takeoff is only a few centimeters beyond the carina, and you must be careful to not occlude the RUL with right-sided DLT

758
Q

When you are ready. to begin OLV, you _____.

A

inflate teh bronchial cuff.

759
Q

Where do you apply the clamp for OLV?

A

Distal to. the y-piece and proximal to. the cap that you open to deflate. the lung

760
Q

What is the ideal inspiratory pressure during OLV?

A

<20 cmH2O above PEEP

761
Q

What serial assessment should you perform during OLV?

A

ABGs

762
Q

What is the normal I:E ratio?

A

1:2

763
Q

Why do some people recommended TIVA for OLV?

A

Volatiles impair HPV (if you do use, limit to 1-1.5 MAC)

764
Q

Apply ____ to the _____ lung starting at 2 cm H2O for hypoxia with OLV. What is the max?

A

CPAP, non-dependent, 10 cm H2O

765
Q

Is hypoxemia during OLV mroe common during surgery. onteh right or left lung?

A

Right lung, the left lung is smaller than the right, so there is less surface area for gas exchange when the left lung is ventilated (during right lung surgery)

766
Q

Unlike a DLT, the bronchial block CANNOT: (select 3):
a. insufflate O2 into the isolated lung
b. ventilate. the isolated lung
c. provide lung separation in nasotracheal intubation
d. prevent contamination from contralateral lung infection
e. provide lung separation in kids
f. suction secretions from isolated lung

A

B, D, F

767
Q

What are the two downsides to bronchial blockers?

A
  1. The operative lung is slow to collapse
  2. The high-pressure balloon can easily slip to enter the trachea (can cause contamination and block ventilation. of both lungs)
768
Q

Why is the lung on teh same side of the bronchial blocker slow to collapse?

A

The lumen of the bronchial blocker is narrow

769
Q

What can the lumen of the bronchial blocker do?

A

insufflate O2 into. the non-ventilated lung and suction air form the non-ventilated lung

770
Q

T/F: The lumen of the bronchial blocker can be used to suction blood, pus, or secretions from teh non-ventilated lung.

A

False

771
Q

Why is a bronchial blocker not the best choice for contamination?

A

The high-pressure ballon can easily slip out of place into the trachea

772
Q

ID the MOST common serious complications of mediastinoscopy (select 2)
a. chylothorax
b. pneumothorax
c. LRLN injury
d. Hemorrhage

A

B and D

773
Q

Why is a medistinoscopy performed?

A

To diagnose and stage lung CA

774
Q

What is an absolute CI to mediastinoscopy?

A

previous mediastinoscopy (d/t scarring)

775
Q

What can be compressed during mediastinoscopy?

A

Innominate artery

776
Q

Compression of the innominate artery can cause what?

A

Impairs cerebral perfusion

777
Q

Where should you place your pulse-ox during mediastinoscopy?

A

on RUE (compression of innominate artery –> dampened waveform)

778
Q

Where should you place your BP cuff during mediastinoscopy?

A

LUE (compression of innominate artery will not affect BP measurement)

779
Q

What. isa risk with mediastinoscopy?

A

Severe hemorrhage

780
Q

There is an association between oat cell carcinoma and _______.

A

Easton-Lambert syndrome

781
Q

Patients with ELS are sensitive. to what medications?

A

Sux and ND NMBD

782
Q

What are indications for tracheal resection?

A

Tracheal stenosis, tracheomalacia, tumor vascular lesions, and congenital malformations

783
Q

What is a post-op consideration for tracheal resection that would required fiberoptic intubation?

A

To reduce tension on the tracheal anastomosis, the patient’s neck must maintain a flexed position

784
Q

Where is. the incision made for medisastinoscopy?

A

midline of the lower neck at the suprasternal notch

785
Q

During mediastinoscopy, the scope is placed anterior to the ____ and posterior to the ____ and ___.

A

trachea; innominate artery and thoracic aorta

786
Q

A pneumothorax that occurs during mediastinoscopy most commonly occurs on the ____ side.

A

right

787
Q

What vital structures are at risk for injury during mediastinoscopy? (name 6)

A

thoracic aorta
innominate artery
vena cava
trachea
thoracic duct
phrenic and RLN

788
Q

Relative CI for mediastinoscopy?

A

tracheal deviation, thoracic aortic aneurysm, SVC obstruction

789
Q

Innominate (brachiocephalic) a. –> _____ artery —> _____ artery –> ______ artery

A

right common carotid –> right internal carotid –> right cerebral circulation at circle of willis

790
Q

What does innominate compression compromise?

A

circulation to the right side of the circle of willis

791
Q

Pre-op to tracheal resection, you must asses the patient for ____.

A

airflow limitations

792
Q

If a patient is at risk for airway obstruction during anesthetic induction, you should choose a technique that _____.

A

preserves spontaneous ventilation (ex: sevo)

793
Q

What are options to provide ventilation during tracheal resection?

A

ETT, jet ventilation, ECMO

794
Q

With. an upper tracheal lesion resection with a standard ETT, the ETT is ____or ____

A

advanced distally before the surgeon opens the trachea OR second ETT is placed into distal trachea after trachea is opened

795
Q

Where is the second ETT placed during lower tracheal lesion resection?

A

left main bronchus

796
Q

What. isat risk for compression during tracheal resection?

A

innominate artery

797
Q

What is a complication of neck hyperflexion?

A

Tetraplegia

798
Q

What are the MOST important strategies for managing mechanical ventilation. in patient w/ ARDS? (select 2)
a. low TV
b. reducing plateau pressure
c. high-frequency oscillatory ventilation
d. permissive hypocapnia

A

A and B

799
Q

____ is a form of non-cardiogenic pulmonary edema.

A

ARDS

800
Q

What. is the most common pulmonary etiology for ARDS?

A

Pneumonia

801
Q

What. is the most common extra-pulmonary etiology for ARDS?

A

Sepsis

802
Q

What causes ARDS?

A

inflammation injury (mediated by neutrophils and PLTs) –> diffuse alveolar destruction

803
Q

What are key features of ARDS:
1. _____
2. _____
3. _____
4. _____

A

Protein-rich pulmonary edema
loss of surfactant
hyaline membrane formation
possible long-term injury

804
Q

What does a CXR reveal in ARDs?

A

bilateral opacities

805
Q

For ARDs, diffuse patchy alveolar infiltrates appear peripherally about _____ after the inital insult, which then can progress. tocomplete alveolar consolidation.

A

12 hours

806
Q

The prone position may improve ____ during ARDS.

A

V/Q matching

807
Q

ARDs vent settings:
______ ventilation

A

PC

808
Q

ARDs vent settings:
______ TV

A

LOW TV (4-6 mL/kg IBW)

809
Q

ARDs vent settings:
TV ___ to ___ mL/kg IBW

A

4-6

810
Q

ARDs vent settings:
plateau pressure ____

A

<30 cm H2O

811
Q

ARDs vent settings:
RR ______

A

6-35

812
Q

ARDs vent settings:
I:E ratio of _____

A

1:1 - 1:3

813
Q

What is the target oxygenation goal for ARDs?

A

PaO2 55-80 mmHg or SpO2 88-95%

814
Q

What is used to make the diagnosis of ARDS?

A

Berlin definition

815
Q

What is mild form of ARDS?

A

PaO2/FiO2 ratio <201-300 mmHg with PEEP or CPAP >/= 5 cm H2O

816
Q

What is moderate form of ARDS?

A

PaO2/FiO2 ratio <101-200 mmHg with PEEP >/= 5 cm H2O

817
Q

What is severe form of ARDs?

A

PaO2/FiO2 ratio <100 mmHg with PEEP >/= 5 cm H2O

818
Q

Other than pneumonia or COVID, what are some pulmonary causes of ARDS? (name 3)

A
  1. aspiration
  2. smoke inhalatoin injury
  3. near-drowning
819
Q

What is the first satge of ARDs?

A

exudative

820
Q

What is. the onset of stage 1 ARDs?

A

6-72 hours after initial insult

821
Q

What. is the duration of stage 1 of ARDs?

A

7 days

822
Q

ARDS: injury to ______ disrupts the integrity of their tight junctions.

A

type 1 pneumocytes

823
Q

ARDS: damaged surfactant –> ___ alveolar surface tension –> increased alveolar ____ –> decreased _____

A

increased; collapse; gas exchange

824
Q

Why do alveoli collapse in ARDs?

A

There is not enough surfactant

825
Q

The damaged cells that accumulate in the airways during ARDs are called what?

A

Hyaline membranes

826
Q

What is the hallmark of ARDs?

A

hypoxemia despite increased supplemental oxygen

827
Q

ARDS: ____ A-aDO2 gradient

A

increased

828
Q

What is. the second stage of ARDs?

A

proliferative

829
Q

What is the duration of the second stage of ARDs?

A

7-21 days

830
Q

During the second stage of ARDs, the body does what?

A

creates new pulmonary surfactant, new type. 1 pneumocytes, tight junctions are restored, and alveolar fluid is drained by lymphatics

831
Q

What is stage 3 of ARDs?

A

fibrotic stage

832
Q

Extensive fibrotic changes from ARDS cause irreversible damage to the lung architecture and fibrosis. ofthe pulmonary vasculature lead sto _________

A

irreversible PHTN

833
Q

What are the 2 core strategies for mechanical ventilation in ARDs?

A
  1. low TV
  2. PEEP
834
Q

T/F: ARDs affects all alveoli in the same way.

A

False

835
Q

What is biotrauma?

A

excessive stretch of alveoli stimulates the release of inflammatory mediators

836
Q

Why should you use low TV with ARDs?

A

Positive pressure breaths, the TV follows the path of least resistance so stiff alveoli fill minimally and normal alveoli fill too much b/c the TV has to go somewhere

837
Q

When the lungs are ventilated at relatively low volumes, ____ can occur as repetitive opening and closing of recuritbal alveoli are exposed to high shear forces.

A

atelectrauma

838
Q

Why does PEEP reduce atelectrauma?

A

It maintains transpulmonary pressure above closing pressure, which prevents alveolar collapse during expiration

839
Q

For ARDs, weaning. by PS can begin when the FiO2/PEEP ration is ____

A

<0.4/8

840
Q

High inspired oxygen (>50%) causes ____ to the lung

A

oxidative stress

841
Q

With ARDs, permissive ____ may be required.

A

Hypercapnia

842
Q

What is the max FiO2 for a regualr nasal cannula?

A

40%

843
Q

What is teh fluid management strategy with ARDs?

A

Conservative fluid management supports oxygenation by reducing the hydrostatic pressure in the pulmonary capillaries

844
Q

The Mallampati exam assesses the _____.

A

oropharyngeal space

845
Q

The Inter-incisor gap exam assess _____.

A

How well the patient can open his mouth.

846
Q

What axis do you align for the sniffing position?

A

Oral, pharyngeal, and laryngeal

847
Q

A small inter-incisor gap creates a more acute angle between the ___ and ___ openings.

A

Oral and glottic

848
Q

What is a normal inter-incisor gap?

A

2-3 FB (4 cm)

849
Q

What can you see in Class 1 Mallampatti?

A

Pillars, Uvula, Soft Palate, Hard Palate (PUSH)

850
Q

What can you see in Class 2 Mallampatti?

A

Uvula, soft palate, hard palate

851
Q

What can you see in Class 3 Mallampatti?

A

Soft and hard palate (base. ofthe uvula may be seen)

852
Q

What can you see in Class 4 Mallampatti?

A

Hard palate

853
Q

To expose the glottic opening during DL, you must displace the tongue into the ____ space.

A

submandibular

854
Q

The _____ helps to estimate the size of the submandibular space.

A

thyromental distance

855
Q

What might happen if the submandibular space is small or poorly compliant?

A

You might not be able to move the tongue enough to expose the glottis

856
Q

A TMD less than ___ or greater than ___ correlates with an increased risk of difficult intubation.

A

6 cm; 9 cm

857
Q

The ____ assesses the function of the TMJ.

A

Mandibular protrusion test (MPT)

858
Q

How is a mandibular protrusion test performed?

A

The patient subluxes the jaw, and. the position of the lower incisors is compared to the position of the upper incisors

859
Q

What class MPT correlates with an increased difficulty of intubation?

A

3

860
Q

The ability to palce the patient into the sniffing position is highly dependent on the mobility of the ____ joint.

A

Atlanto-occpital joint

861
Q

What are some conditions that impair AO mobility? (name 3)

A

Arthritis, trauma, and down syndrome

862
Q

What. are the borders of the submandibular space:
superior border = __________
inferior border = ____________
lateral border = ___________

A

Superior = mentum
Inferior = hyoid bone
lateral = either side of neck

863
Q

How. do you assess for thyromental distance?

A

With the neck extended and mouth closed, you can measure the distance from the tip of the thyroid cartilage to the tip of the mentum

864
Q

DL may be more difficult if the TMD is <___ cm or >__ cm.

A

6 (3 FB); 9

865
Q

If. theTMD is >9 cm, the larynx assumes a more ___ position.

A

caudal

866
Q

If. theTMD is >9 cm, the larynx assumes a more ___ position.

A

caudal

867
Q

The upper lip bite test is also known as the _____ test.

A

mandibular protrustion

868
Q

Define a Class 1 MPT.

A

The patient can move LI past UI and bite the vermilion of the lip (where the lip meets the facial skin)

869
Q

Define a Class 2 MPT.

A

Patient can move LI in line with UI.

870
Q

Define a Class 3 MPT.

A

Patient cannot move LI past UI.

871
Q

What is normal AO flexion and extension?

A

90-165 degrees

872
Q

What is a normal AO extension?

A

35 degrees

873
Q

DL is difficult with an AO extension < ____ degrees.

A

23

874
Q

Explain the 3-3-2 Rule.

A

Inter-incisor gap > 3 FB
TMD > 3 FB
Thyrohyoid > 2 FB

875
Q

Tetanus does or does not impair AO mobility?

A

Does not

876
Q

Klippel-Feil does or does not impair AO mobility?

A

DOES

877
Q

Down Syndrome does or does not impair AO mobility?

A

Does

878
Q

Diabetes does or does not impair AO mobility?

A

does

879
Q

Pierre Robin Sequence does or does not impair AO mobility?

A

does not

880
Q

Beckwith syndrome does or does not impair AO mobility?

A

does not

881
Q

Ankylosing Spondylitis does or does not impair AO mobility?

A

does

882
Q

What. isthe Cormack and Lehane grading system?

A

Measures the laryngoscopic view we obtain during DL

883
Q

What can you see in a grade 1 cormack and lehane?

A

Complete or nearly complete view of glottic opening

884
Q

What can you see in a grade 2A cormack and lehane?

A

Posterior region of the glottic opening

885
Q

What can you see in a grade 2B cormack and lehane?

A

corniculate cartilages and posterior vocal cords (no glottic opening)

886
Q

What can you see in a grade 3 cormack and lehane?

A

epiglottis only

887
Q

What can you see in a grade 4 cormack and lehane?

A

soft palate only

888
Q

What can you not see with a grade 2 cormack and lehane score?

A

anterior commissure

889
Q

What can you not see with a grade 3 cormack and lehane score?

A

any part of the glottic opening

890
Q

What can you not see with a grade 4 cormack and lehane score?

A

any part of the larynx

891
Q

Identify the BEST predictors of difficult mask ventilation (SELECT 3)
a. mallampati class 3
b. old age
c. edentulousness
d. small mouth opening
e. high, arched palate
f. presence of a beard

A

B, C, F

892
Q

Always ask these 5 questions before you anesthetize anyone:

A
  1. will I be able. to mask ventilate? (BONES)
  2. Will I be able to intubate? (LEMON)
  3. Will I be able to place a supraglottic airway? (RODS)
  4. Will I be able to place an invasive airway? (SHORT)
  5. How fast must I secure the airway? (2,4,6,8)
893
Q

What. are complications r/t cricoid pressure?

A

Airway obstruction, difficult DL, impaired glottic visualization, difficult intubation, reduced LES tone

894
Q

What are the risk factors for difficult mask ventilation?

A

BONES
B - Beard
O - Obese (BMI > 26)
N - No teeth
E - elderly (>55)
S - Snoring

895
Q

What are risk factors for difficult supraglottic device placement?

A

Limited mouth opening
upper airway obstruction
altered pharyngeal anatomy (can prevent seal)
poor lung compliance (requires excessive PIP)
increased airway resistance (requires excessive PIP)
lower airway obstruction

896
Q

What are current NPO guidelines?

A

2 hours - clear liquids
4 hours - breast milk
6 hours - nonhuman milk, infant formula, solid food
8 hours - fired or fatty food

897
Q

Ingestion of clear liquids ___ before surgery reduces gastric volume. and increases gastric pH>

A

2 hours

898
Q

What does LEMON for difficult intubation stnad for?

A

L - Look externally (obesity, neck, head)
E - Evaluate 3-3-2
M - Mallampati
O - Obstruction?
N - Neck mobility

899
Q

What does RODS stand for for supraglottic airway placement?

A

R - Restricted mouth opening
O - Obstruction
D - Distorted airway
S - Stiff lungs or C-spine

900
Q

What does SHORT stand for for difficult surgical airway placement?

A

S - Surgery (neck surgery/previous scar)
H - Hematoma
O - Obesity
R - Radiation
T - Tumor

901
Q

Cricoid pressure is pressure applied to. thecricoid ring against ___ vertebra.

A

C5

902
Q

Cricoid Pressure: Pressure before LOC = ________

A

20 Newtons or @2 kg

903
Q

Cricoid Pressure: Pressure after LOC = ________

A

40 Newtons or @4 kg

904
Q

Pierre Robin sequence - difficutl maskin gor difficult DL?

A

DL

905
Q

Patient on CPAP - difficult masking or difficult DL?

A

Masking

906
Q

Geriatric Patient - difficult masking or difficult DL?

A

Masking

907
Q

Klippel-Feil - difficult masking or difficult DL?

A

DL

908
Q

Endentulous - difficult masking or difficult DL?

A

Masking

909
Q

What congenital conditions are associated with cervical spine anomalies? (select 2.)
a. treacher collins
b. klippel-feil
c. goldenhar
d. pierre robin

A

B and C

910
Q

____ is the chief concern in the patient with angioedema.

A

Upper airway obstruction

911
Q

Name 3 causes of angioedema.

A
  1. anaphylaxis
  2. ACEI
  3. C1 esterase deficiency
912
Q

How do you treat angioedema caused. byanaphylaxis?

A

Epinephrine, Antihistamines, and steroids

913
Q

How do you treat angioedema caused by ACEI or C1 esterase deficiency?

A

Icatibant, ecallantide, FFP, or C1 esterase concentrate

914
Q

What is Ludwig’s angina?

A

A bacterial infection characterized by rapidly progressing cellulitis in the floor of the mouth

915
Q

What is the most significant concern with Ludwig’s angina?

A

Posterior displacement of the tongue resulting in comple, supraglottic airway obstruction

916
Q

What is the best method to secure the airway in Ludwig’s angina?

A

Awake nasal intubation or awake trach

917
Q

Name 7 congenital conditions that impact airway management.

A
  1. Pierre Robin
  2. Treacher Colliins
  3. Trisomy 21
  4. Klippel-Feil
  5. Goldenhar
  6. Beckwidth
  7. Cri du Chat
918
Q

Angioedema is the result of ____ that can lead to swelling of the face, tongue, and airway.

A

increaed vascular permeability

919
Q

Why can ACEI cause angioedema?

A

They prevent bradykinin breakdown (genetics likley determine who is at risk)

920
Q

What is Icatibant?

A

Bradykinin receptor antagonist

921
Q

What is Ecallantide?

A

A plasma kallidrein inhibitor - stops the conversion of kinonogen to bradykinin

922
Q

Why can FFP be used at treatment for ACEI angioedema?

A

It contains enzymes that metabolize bradykinin

923
Q

What deficiency is the cause of hereditary angioedema?

A

C1 esterase deficiency

924
Q

What patients should receive prophylaxis of Danazol or C1 Esterase concentrate for procedures that require tracheal intubation or dental surgery?

A

Patients with hereditary angioedema

925
Q

For Ludwig’s Angina, _____ is contraindicated in patients with infection above the level of the trachea.

A

Retrograde intubation

926
Q

What congenital conditions impact airway management due to a large tongue? (2)

A

Beckwith syndrome
Trisomy 21 (down syndrome)
“Big Tongue”

927
Q

What congenital conditions impact airway management due to a small/underdeveloped mandible? (4)

A

Pierre Robin
Goldenhar
Treacher Collins
Cri du Chat
“Please Get That Chin”

928
Q

What congenital conditions impact airway management due to a cervical spin anomaly? (3)

A

Klippel-Feil
Trisomy 21
Goldenhar
“Kids Try GOLD”

929
Q

What physiologic characteristics occur with Pierre Robin?

A
  • small/underdeveloped mandible (micrognathia or mandibular hypoplasia)
  • tongue falls back & down (glossoptosis)
  • cleft palate
    NEONATES OFTEN REQUIRE INTUBATION
930
Q

What physiologic characteristics occur with Treacher Collins?

A
  • Small mouth
  • Small/underdeveloped mandible
  • nasal airway is blocked by tissue (choanal atresia)
  • ocular & auricular anomalies
931
Q

What physiologic characteristics occur with Trisomy 21?

A
  • Small mouth
  • Large tongue
  • Atlantoaxial instability
  • Small sublottic diameter (subglottic stenosis)
932
Q

What physiologic characteristics occur with Klippel-Feil?

A

There is congenital fusion of cervical vertebrae –> neck rigidity.

933
Q

What physiologic characteristics occur with Goldenhar?

A
  • Small/underdeveloped mandible
  • Cervcical spine abnormality
934
Q

What physiologic characteristics occur with Beckwith Syndrome?

A

Large otngue

935
Q

What physiologic characteristics occur with Cri du Chat?

A
  • Small/underdeveloped mandible
  • Laryngomalacia
  • Stridor
936
Q

What is the optimal position for tracheal intubation?
a. cervical flexion only
b. atlanto-occpital joint extension only
c. cervical flexion and atlanto-occipital joint extension
d. cervical extension and atlanto-occipital joint flexion

A

C

937
Q

What 3 axises are aligned in the sniffing position?

A

oral, pharyngeal, and laryngeal

938
Q

The “sniffing position” consists of ___ flexion and _____ extension.

A

cervical; atlanto-occpital

939
Q

Why are the three axes misaligned when a morbidly obese patient lies supine?

A

Excess adipose on the neck, shoulders, and back place the chest higher than the head

940
Q

What position should be used to align axes in. the morbidly obese during DL?

A

HELP position (Head Elevated Laryngoscopy Position)
Put the bed in reverse Trend. to unload the diaphragm and help prolong time between apnea and desaturation

941
Q

How does the head position affect the position of the ETT after intubation?
Nose to chest —> ______________

A

ETT tip moves towards the carina @2cm
(risk of endobronchial intubation)

942
Q

How does the head position affect the position of the ETT after intubation?
Nose away from chest —> ______________

A

ETT tip moves away from carina @ 2cm (risk of extubation)

943
Q

How does the head position affect the position of the ETT after intubation?
Lateral rotation of the head @0.7 cm —> ______________

A

ETT tip moves away from carina (risk of extubation)

944
Q

Cervical flexion moves _______ .

A

the chin towards the chest

945
Q

Atlanto-occipital extension _______.

A

extends the head on the neck

946
Q

When is optimal positioning achieved with the HELP position?

A

When the sternum and external auditory meatus are in the same horizontal plane

947
Q

How does steep trendelenburg position cause a risk for endobronchial intubation?

A

The abdominal contents are shifted towards the chest, reducing thoracic volume

948
Q

Explain the risk related to aggressive jaw thrust.

A

Aggressively thrusting the jaw anteriorly (excessive traction at the angle of. the mandible) can stretch the FACIAL nerve

949
Q

Explain how a patient with a nerve injury related to aggressive jaw thrust might present.

A
  • Affected side of face may sag
  • May drool
  • Chewing will be affected
950
Q

What is the risk related to a face mask strap that is too tight?

A

It can compress the BUCCAL branch. ofthe FACIAL nerve CN7

951
Q

Explain how a patient with a nerve injury related to a face mask strap that was too tight might present.

A

The patient will have difficulty opening and closing lips (ORBICULARES ORIS muscle is impaired)

952
Q

What is the nerve risk of the ETT connector resting on the face?

A

It can compress the supraorbital nerve

953
Q

How does a patient with supraorbital nerve injury present?

A

Eye pain, forehead numbness, photophobia

954
Q

Contraindications to the use of a nasopharyngeal airway include (SELECt 2)
a. dental trauma
b. coagulopathy
c. pierre robin syndrome
d. Le Fort 2 fracture

A

B and D

955
Q

How. do oral or nasal airways relieve upper airway obstruction?

A

It opens the airway by displacing hte tongue and epiglottis from the posterior wall of the pharynx

956
Q

How. doyou size an OPA?

A

Measure from the corner of the mouth to the earlobe or the angle. ofthe mandible

957
Q

How do you size a NPA?

A

Measure from the nare to the earlobe or the angle of the mandible

958
Q

Is a OPA or NPA better tolerated in a lightly anesthetized patient?

A

NPA (OPA can –> vomiting or laryngospasm)

959
Q

What are the 5 contraindications for NPA?

A
  1. Cribriform plate injury (LeFort 2 or 3 fracture)
  2. Coagulopathy
  3. Nasal fracture
  4. Previous transsphenoidal hypophysectomy
  5. Previous Caldwell-Luc procedure
960
Q

What are the uses of Wililams and Ovassapian OPAs?

A

Fiberoptic intubation (they have a hole in the center)

961
Q

What OPA do we use at Baptist?

A

Berman

962
Q

How should. an OPA sit in the mouth?

A

The flange should protrude outside the lips and the pharyngeal end should rest at the base of the tongue

963
Q

What can happen if an OPA is too short?

A

Airway can be obstructed. by causing the tongue to kink against the roof of the mouth

964
Q

What can happen if an OPA is too long?

A

The epiglottis can be displaced towards the glottis - causing trauma or obstruction

965
Q

To insert an NPA, gently retract the tip of the nose and introduce the airway in line with _____, _____ to. theface.

A

nasal passage; perpendicular

966
Q

What can happen with an NPA that is too short?

A

The obstruction is not relieved

967
Q

What can happen with an NPA that is too long?

A

The epiglottis can be displaced towards the glottis - causing trauma or obstruction

968
Q

Why is NPA inserted for cribriform plate injuries contraindicated?

A

Risk of brain injury

969
Q

What are S/S of cribriform plate injuries?

A

CSF rhinorrhea, Raccoon eyes, periorbital edema

970
Q

What is the cribriform plate?

A

A boney structure that separates the nasal cavity from the anterior cranial fossa

971
Q

Can you ID a Berman OPA?

A

look up on google lol

972
Q

Can you ID a Guedel OPA?

A

look up on google lol

973
Q

Can you ID a Ovassapian OPA?

A

look up on google lol

974
Q

Can you ID a Williams OPA?

A

look up on google lol

975
Q

Name 4 fractures that preclude the use of a NPA.

A
  1. LeFort 2
  2. LeFort 3
  3. Nasal
  4. Basiliar
976
Q

Name 3 fractures that lead to cribriform plate injury.

A
  1. LeFort 2
  2. LeFort 3
  3. Basilar
977
Q

Which intervention demonstrates the MOST accurate understanding of inflating the cuff on the endotracheal tube?
a. assess the pressure inside the pilot balloon with your fingers
b. add 10 mL air to the pilot balloon
c. attach. amanometer to the pilot balloon
d. attach a syringe to the balloon to create a minimal occlusive pressure

A

C

978
Q

What is the BURP maneuver?

A

With difficult glottic visualization during DL,
Backward
Upward,
Rightward
Pressure
may improve your view

979
Q

When does tracheal ischemia occur with an ETT?

A

If the cuff pressure exceeds tracheal mucosal perfusion pressure

980
Q

Cuff pressure should be less than ____.

A

25 cm H2O

981
Q

What is the murphy eye?

A

A small hole on the opposite side of the bevel

982
Q

What is the purpose of the Murphy eye?

A

To provide an alternate passage for air movement in case the tip of the ETT becomes occluded or abuts th tracheal wall

983
Q

PEDS ETT SIZE FORMULA???
Without cuff = ______

A

(age/4) + 4

984
Q

PEDS ETT SIZE FORMULA???
With cuff = ______

A

(age/4) + 3.5

985
Q

PEDS ETT
Depth Placement = ______

A

Internal diameter x 3

986
Q

The Macintosh blade ____ exposes. the glottis by applying tension to the ______ (in the ____) which lifts the epiglottis.

A

indirectly; hyoepiglottic ligament; vallecula

987
Q

The Miller blade ___ exposes the glottic opening by directly lifting the ____.

A

directly; epiglottis

988
Q

_____ diameter = ETT size

A

Internal

989
Q

What does inflation of the ETT cuff permit?

A

Positive pressure ventilation and protection from aspiration of gastric contents

990
Q

Which ETT have a low-volume, hihg-pressure cuff?

A
  1. red rubber tube
  2. silicon tube for LMA-Fastrach
  3. Bronchial balloon on a double lumen ETT
991
Q

Which ETT has high-volume, low-pressure cuffs?

A

Nearly all tubes in modern practice

992
Q

Cuff compliance - Low or high?

Low-Volume, High-Pressure Cuff

A

Low - it takes a small volume to increase the pressure inside the cuff

993
Q

Cuff compliance - Low or high?

High-Volume, Low-Pressure Cuff

A

High - it takes a larger volume to incrase the pressure inside the cuff

994
Q

Can you measure the internal pressure?

Low-volume, High-Pressure Cuffs

A

No

995
Q

Can you measure the internal pressure?

High-volume, Low-Pressure Cuffs

A

Yes - best to use a manometer

996
Q

What are the benefits of a low-volume, high-pressure cuff?

A

Better proctection against aspiration, lower incidence of sore thorat, easier visualization during intubation

997
Q

What are the benefits of a low-volume, high-pressure cuff?

A

Better protection against aspiration, lower incidence of sore throat, easier visualization during intubation

998
Q

What are the benefits of a high-volume, low-pressure cuff?

A

Cuff pressure closely resembles the pressure exerted on the trachea

999
Q

Risks with a low-volume, high-pressure cuff?

A

Prolonged intubation –> tracheal ischemia

1000
Q

Risks with a high-volume, low-pressure cuff?

A
  • Believing you can accurately estimate how much pressure is in the cuff
  • Adding too much air or using N2O –> increased cuff pressure –> tracheal ischemia
  • Easy to pass things around the cuff (esophageal stethoscopes, OGT, temp probe)
  • Protection against aspiration isn’t as good as a low-volume, high-pressure cuff
1001
Q

An ETT with a _____ valve is one method to protect patient against cuff pressure.

A

Lanz pressure-regulating

1002
Q

Which findings are MOST strongly associated with difficult video-assisted laryngoscopy? (select 2.)
a. history of neck radiation
b. mandibular protrusion score of 3
c. obesity
d. mallampati 4

A

A and B

1003
Q

Name 3 non-channeled video laryngoscopes.

A

Glidescope, C-MAC, and McGrath

1004
Q

Name 2 channeled video laryngoscopes.

A

Airtraq Avant and King Vision

1005
Q

What is the greatest risk with video laryngoscopy?

A

Pharyngeal injury

1006
Q

The GlideScope has a _____ anterior bend.

A

60-degree

1007
Q

What is anon-channeled video laryngoscope device?

A

It exposes the glottic structures, but the ETT is passed into. thetrachea separate from teh laryngoscope

1008
Q

What does an acute-angle blade facilitate?

A

Glottic exposure of a more anterior glottic opening

1009
Q

What is. achanneled video laryngoscope?

A

It integrates a channel or the ETT into the device (good for when you have trouble passing the tube)

1010
Q

What are predictors of a difficult VAL?

A

neck pathology (radiation, tumor, scar), short TMD, limited cervical motion, thick neck, Class 3 upper lip bite test

1011
Q

Match each LMA region with the anatomical border it touches.
Sides Pyriform sinuses
Distal end Upper esophageal sphincter
Proximal end Base of tongue

A

Sides - Pyriform sinuses
Distal end - upper esophageal sphincter (cricopharyngeus muscle)
Proximal end - base of tongue

1012
Q

what is the most commonly used supraglottic airway?

A

LMA

1013
Q

LMA:
Max PPV pressure = ______

A

20 cm H2O

1014
Q

LMA:
Max cuff pressure = ______

A

60 cm H2O

1015
Q

LMA:
Target cuff pressure = ______

A

40-60 cm H2O

1016
Q

What is the most common cause of nerve injury with an LMA?

A

cuff overinflation

1017
Q

What nerves are at risk for injury with LMA cuff overinflation?

A

lingual, hypoglossal, and RLN

1018
Q

If your LMA cuff pressure >60 cmH2O and you still cannot get a good seal, what could be the issue?

A

improper position, inadequate anesthesia, partial or complete laryngospasm

1019
Q

What prevents the epiglottis from obstructing the LMA airway tube?

A

two aperture bars across teh tube’s orifice

1020
Q

A ___ iscreasted after iar is added to the LMA’s inflatable cuff.

A

seal

1021
Q

While an LMA shields the larynx from pharyngeal secretions, it does not reliably protect against _____.

A

gastric regurgitation

1022
Q

The integrity of an LMA’s seal is primarily dependent on __ and ___ and less dependent on cuff volume and pressure.

A

size and position

1023
Q

What are other causes of nerve injuries due to LMA besides cuff overinflation?

A

Too small LMA, lidocaine lubrication, traumatic insertion

1024
Q

LMA Size 1
Patient Size - ____ kg

A

<5 kg

1025
Q

LMA Size 1.5
Patient Size - ____ kg

A

5-10 kg

1026
Q

LMA Size 2
Patient Size - ____ kg

A

10-20 kg

1027
Q

LMA Size 2.5
Patient Size - ____ kg

A

20-30 kg

1028
Q

LMA Size 3
Patient Size - ____ kg

A

30-50 kg

1029
Q

LMA Size 4
Patient Size - ____ kg

A

50-70 kg

1030
Q

LMA Size 5
Patient Size - ____ kg

A

70-100 kg

1031
Q

LMA Size 1
Cuff Inflation = ___ mL

A

4

1032
Q

LMA Size 1.5
Cuff Inflation = ___ mL

A

7

1033
Q

LMA Size 2
Cuff Inflation = ___ mL

A

10

1034
Q

LMA Size 2.5
Cuff Inflation = ___ mL

A

14

1035
Q

LMA Size 3
Cuff Inflation = ___ mL

A

20

1036
Q

LMA Size 4
Cuff Inflation = ___ mL

A

30

1037
Q

LMA Size 5
Cuff Inflation = ___ mL

A

40

1038
Q

LMA Size 1
Largest ETT that Fits = _____ mm

A

3.5

1039
Q

LMA Size 1.5
Largest ETT that Fits = _____ mm

A

4.0

1040
Q

LMA Size 2
Largest ETT that Fits = _____ mm

A

4.5

1041
Q

LMA Size 2.5
Largest ETT that Fits = _____ mm

A

5.0

1042
Q

LMA Size 3
Largest ETT that Fits = _____ mm

A

6.0

1043
Q

LMA Size 4
Largest ETT that Fits = _____ mm

A

6.0

1044
Q

LMA Size 5
Largest ETT that Fits = _____ mm

A

7.0

1045
Q

LMA Size 1
Largest Flexible Endoscope that Fits = _____ mm

A

2.7

1046
Q

LMA Size 1.5
Largest Flexible Endoscope that Fits = _____ mm

A

3.0

1047
Q

LMA Size 2
Largest Flexible Endoscope that Fits = _____ mm

A

3.5

1048
Q

LMA Size 2.5
Largest Flexible Endoscope that Fits = _____ mm

A

4.0

1049
Q

LMA Size 3
Largest Flexible Endoscope that Fits = _____ mm

A

5.0

1050
Q

LMA Size 4
Largest Flexible Endoscope that Fits = _____ mm

A

5.0

1051
Q

LMA Size 5
Largest Flexible Endoscope that Fits = _____ mm

A

5.5

1052
Q

Match each LMA with its unique feature:

LMAS - LMA ProseaL, LMA Flexible, LMA Fastrach

Features - Gastric drain, Designed for intubation, or wire-reinforced ariay tube

A

LMA ProSeal - Gastric drain
LMA Fastrach - designed for tracheal intubation
LMA Flexible - Wire-reinforced airway tube

1053
Q

What are features of hte LMA ProSeal?

A
  • gastric drain tube
  • larger mask
    -built-in bite block
1054
Q

What is the max PIP for PPV for the LMA ProSeal?

A

30 cm H2O (vs. 20 for LMA classic)

1055
Q

The LMA Fastrach is a _____ LMA.

A

intubating

1056
Q

What special feature does the LMA C-Trach contain?

A

A camera so you can visualize intubation

1057
Q

What are the chracteristics of the LMA Flexible?

A
  • has a flexible airway tube
  • is wire-reinforced
    -is useful for head and neck surgery
1058
Q

T/F: You can place suction directly to the gastric drain tube of LMA ProSeal for gastric decompression.

A

False. -Do NOT place suction directly to the drain tube. Instead, you must pass an OGT through the tube to decompress the stomach.

1059
Q

The LMA Supreme is a disposable version of the LMA _____.

A

ProSeal

1060
Q

T/F: You must leave the LMA Fastrach in place after using it for endotracheal intubation.

A

False - it can be removed after intubation or remain in place throughout the surgical procedure

1061
Q

When is an LMA Fastrach contraindicated and why?

A

During MRI; it has a metal handle

1062
Q

The specially designed endotracheal tube for LMA Fastrach uses a _____.

A

high-pressure cuff

1063
Q

The LMA Flexible is ___ and ___ than the LMA Classic.

A

longer and narrower

1064
Q

What type of surgery is the LMA Flesxible useful for?

A

Head and neck

1065
Q

What is the iGel?

A

A supraglottic airway that is an alternative to LMA. It can be used for spontaneous of or controlled ventilation.

1066
Q

How do you intubate though an iGel?

A

It requires guidance with a fiberoptic bronchoscope

1067
Q

What 2 LMA types are not safe for MRI?

A

LMA Flexible and LMA Fastrach

1068
Q

Does the iGel has a cuff?

A

No - can contribute to poor seal

1069
Q

Does the iGel has a gastric por?

A

Yes

1070
Q

What are complicatiosn of iGel airway?

A

tongue trauma, mucosal erosion of the cricoid cartilage, compression of the trachea, nerve injury, airway obstruction, regurgitation and aspiration

1071
Q

All of the following are CI to a LMA EXCEPT:
a. gastroparesis
b. asthma
c. tracheal tumor
d. hiatal hernia

A

B - asthma

1072
Q

What is the “go to” airway in the “can’t intubate and can’t ventilate” scenario?

A

LMA

1073
Q

When shoudl an LMA not be used?

A
  1. risk of gastric regurg/aspiration
  2. airway obstruction @ or below glottis
  3. poor lung compliance
  4. high airway resistance
  5. Risk. for tracheal collapse (tracheomalacia or external tracheal compression)
1074
Q

Which is preffered in a patient with reactive airway disease: LMA or ETT?

A

LMA

1075
Q

Compared to intubation, the ____ is less likely to activate the SNS.

A

LMA

1076
Q

Less anesthesia is needed to tolerate an LMA or an ETT?

A

LMA

1077
Q

Why do you need to maintain a deep enough plane of anesthesia during LMA?

A

To prevent swallowing which –> gastric insufflation –> increased risk of aspiration

1078
Q

When should you remove the LMA?

A

At the first sign of rejection during emergence; waiting until the patient is fully awake and following commands increases risk of aspiration

1079
Q

How can you assess for gastric insufflation?

A

Epigastric auscultation

1080
Q

What should you do if you see gastric contents inside the lMA?

A
  1. Leave LMA in place (may be gastric contents behind the LMA cuff, and removing it can worsen situation)
  2. Place. in trendelenburg (30 degrees) and deepen anesthesia if needed
  3. Give 100% FiO2 via a self-inflating resuscitation bag
  4. Use low FGF and TV
  5. Use flexible suction catheter to suction through the LMA
  6. Use FOB to evaluate (if gastric content is present in trachea consider intubation)
1081
Q

Why should you use a self-infalting resusctiation bag with possible aspiration with an LMA?

A

If gastric contents are present inside the breathing circuit you don’t want to push them into the lungs

1082
Q

The LMA shields the ____ opening.

A

Glottic

1083
Q

What do volatiles do to the pulmonary reflexes?

A

they obtund the reflexes
(As the patient emerges from GA, these reflexes wake up, ETT may trigger reflexes and –> cough or bronchospasm)

1084
Q

Why is there less risk of bronchospasm with an LMA?

A

The LMA sits over the glottis, there’s nothing inside the trachea to stimulate it during emergence

1085
Q

Place in order from most to least stimulating of the tendency of airway device placement to activate the SNS.

A
  1. combitube
  2. DL
  3. fiberoptic
  4. LMA
1086
Q

What is a Combitube?

A

A supraglottic, double lumen device that is blindly placed in the hypopharynx

1087
Q

What are CI the use of a Combitube?

A
  • intact gag reflex
  • prolonged use (>2-3 hours)
  • esophageal disease (zenker’s diverticulum)
  • ingestion of caustic substances
1088
Q

Do not use a Combitube size 37 Fr in someone <____.

A

4 feet

1089
Q

Do not use a Combitube size 41 Fr in someone <____.

A

6 feet

1090
Q

ID the CI to the Combitube airway: (select 3)
a. full stomach
b. zeker’s diverticulum
c. obesity
d. intact gag reflex
e. klippel-feil
f. prolonged use

A

B, D, F,

1091
Q

T/F: A Combituve airway does provide a secure airway.

A

true

1092
Q

What size Combitube is used for patients 4-6 feet tall?

A

Size 37 Fr

1093
Q

What size Combitube is used for patients >6 feet tall?

A

Size 41 Fr

1094
Q

What size Combitube is used for patients <4 feet tall?

A

There are no options for patients <4 feet tall.

1095
Q

What are benefits of Comtibue airways?

A
  • minimal training required
  • useful for obese population
  • can decompress the stomach
    -provides a secure airway
1096
Q

How does the King Laryngeal tube differ from the Combitube airway?

A

King only has a single lumen for ventilation and a single inflation port

1097
Q

What is the King LTS-D?

A

A disposable device that includes a second lumen that allows you to pass a gastric tube ot suction the stomach.

1098
Q

Inflation of the oropharyngeal balloon (proximal cuff) of the Combitube airway occludes the ____.

A

hypopharynx

1099
Q

Inflation of the distal balloon (distal cuff) of. theCombitube airway ocludes the ____.

A

esophagus

1100
Q

What balloon. is inflated first in a Combitube airway?

A

The oropharyngeal balloon

1101
Q

How much air do you place in a size 37 oropharyngeal balloon of a Combitube airway?

A

40-85 mL

1102
Q

How much air do you place in a size 41 oropharyngeal balloon of a Combitube airway?

A

40-100 mL + option for additional 50 mL

1103
Q

How much air do you place in the distal balloon of a Combitube airway?

A

5-12 mL air for both sizes

1104
Q

Cuff pressures of a Combitube airway should not exceed ____.

A

60 cm H2O

1105
Q

What is a risk of overzealous inflation of the cuffs of a Combitube airay?

A

Esophaugs rupture

1106
Q

What is Zenker’s Diverticulum?

A

A condition where diveticulum (pouches) form in the pharyngeal mucosa

1107
Q

The distal cuff of the King airway obstructs the ___, while the proximal cuff seals the __ and ___.

A

upper esophagus; oral and nasal pharynxes

1108
Q

How many inflation porst are there on a King’s airway?

A

1 - simultaneously inflates both the proximal and distal cuffs

1109
Q

What is the minimum weigh tfor a child-size Kings airway?

A

10 kg

1110
Q

For a king’s airway, the patient can only be ventilated through _____ betwene the two cuffs.

A

fenestrated apertures

1111
Q

When the tip of the Combitube airway is in the esophagus what lumen do you use to ventilate?

A

Blue -esophageal

1112
Q

When the tip of the Combitube airway is in the trachea what lumen do you use to ventilate?

A

The clear - tracheal tip

1113
Q

Regarding the operation of the flexible fiberoptic bronchoscope: (select 2)
a. the oral, pharyngeal, and laryngeal axes must align
b. pushing the level down points the tip up
c. the non-dominant hand controls the level
d. mask ventilation is impossible while the scope is in place

A

B and C

1114
Q

What is the gold standard for managina difficult airway in the awake, spontaneously ventilating patient?

A

FOB

1115
Q

What are the absolute CI for FOB?

A

there are none

1116
Q

What are the relative CI for FOB?

A

Hypoxia, bleeding, lack of cooperation

1117
Q

What should you use before nasal approach of FOB?

A

Defogger, antisialagogue, and vasoconstrictor

1118
Q

How does a flexible FOB work?

A

Light from an external source travels along the fiberoptic bundle and out from the distal tip. This light is reflected off the patient’s anatomy, allowing the operator to view the anatomy form the eyepiece or a camera attached to the eyepiece

1119
Q

FOB Scope movement:
non-dominant hand = _____

A

moves the level

1120
Q

FOB Scope movement:
dominant hand = _____

A

holds the cord

1121
Q

FOB Scope movement:
Pushing the lever down moves the tip ___.

A

up

1122
Q

FOB Scope movement:
Pushing the lever up moves the tip ___.

A

down

1123
Q

Horizontal movement of the FOB _____ the scope in either direction.

A

Rotates

1124
Q

What are indications for FOB besides difficult airway?

A

C-spine limitation - severe cervical stenosis, cervical fracture, Chiari malformation, vertebral artery insufficiency

Limited mouth opening - TMJ, facial burns, mandibular-maxillary fixation

1125
Q

What should be applied ot the tip of the FOB?

A

Anti-fog solution

1126
Q

hat type of drugs are best choices for awake FOB?

A

Short DOA and/or minimal respiratory depression
Ex: Precedex, REmifentanil, Ketamine, Midazolam

1127
Q

What should you do if the bevel of the ETT hangs up on the right arytenoid during fiberoptic intubation?

A

Pull back a little bit, rotate the ETT 90 degrees counterclockwise and advance the ETT again

1128
Q

What should you do in the FOB gets stuck in the Murphy eye during fiberoptic intubation?

A

You must remove the FOB and the ETT and repeat the procedure

1129
Q

The RLN is a brach of CN ___

A

10

1130
Q

The RLN provides sensory function to where?

A

below the vocal cords –> trachea

1131
Q

The RLN provides motor function to where?

A

All intrinsic muscles EXCEPT the cricothyroid

1132
Q

The Superior laryngeal nerve is. a branch of CN _

A

10

1133
Q

The external branch of the SLN provides sensory function ot where?

A

Nowhere

1134
Q

The internal branch of the SLN provides sensory function to where?

A

the posterior side of the epiglottis –> level of vocal cords

1135
Q

T/F: The true vocal cords are innervated by the RLN.

A

False - the true vocal cords are ligaments and are not innervated

1136
Q

The external branch of the SLN provides motor function to where?

A

Cricothyroid muscles

1137
Q

The internal branch of the SLN provides motor function to where?

A

Nowhere

1138
Q

What role does the cricothyroid muscle play?

A

Tenses vocal cords

1139
Q

What branch of the SLN provides motor function?

A

External branch

1140
Q

What branch of the SLN provides sensory function?

A

Internal branch

1141
Q

What CN is the glossopharyngeal nerve?

A

CN 9

1142
Q

What is the sensory function of the glossopharyngeal nerve?

A

Soft palate
oropharynx
tonsils
posterior 1/3 of tongue
vallecula
anterior side of epiglottis
afferent limb of gag reflex

1143
Q

What is the motor function of the glossopharyngeal nerve?

A

Swallowing and phonation

1144
Q

What CN is the trigeminal nerve?

A

CN 5

1145
Q

What is the V1 branch of the trigeminal nerve?

A

Ophthalmic (anterior ethmoidal)

1146
Q

What is the V2 branch of the trigeminal nerve?

A

Maxillary (sphenopalatine)

1147
Q

What is the V3 branch of the trigeminal nerve?

A

Mandibular (lingual)

1148
Q

What is the sensory function of Trigeminal V1?

A

nares & anterior 1/3 of nasal septum

1149
Q

What is the sensory function of Trigeminal V2?

A

Turbinates and septum

1150
Q

What is the sensory function of Trigeminal V3?

A

Anterior 2/3 of tongue

1151
Q

What is the motor function of Trigeminal V1?

A

None

1152
Q

What is the motor function of Trigeminal V2?

A

None

1153
Q

What is the motor function of Trigeminal V3?

A

None

1154
Q

What is the Bullard laryngoscope?

A

A rigid, fiberoptic device used for indirect laryngoscopy

1155
Q

When is the Bullard recommended?

A

For patients with small mouth openings, impaired cervical spine mobility, short thick necks, and congenital airway syndromes

1156
Q

Compared with DL, the Bullard casues less _____.

A

cervical spine displacement

1157
Q

What are the types of rigid, fiberoptic devices?

A

Bullard, WuScope, and UpsherScope

1158
Q

What is the minimum mouth opening for a Bullard laryngoscope?

A

7 mm

1159
Q

When using the Bullard, the patient’s head and neck must be in what position?

A

A neutral or slightly flexed position - any extension will make glottic visuialization more difficult

1160
Q

How do you expose the glottis with the Bullard?

A

The handle (blade) is pulled straight up (90 degree angle to the spine)

1161
Q

The Bullard has a disposable tip extender for tall patients. What is a consideration when using this?

A

Make sure to recover it - it is too large to be aspirated but can obstruct the upper airway

1162
Q

Compared to FOB, intubation with the BUllard is usually faster or slower?

A

faster

1163
Q

What are the names of the intubating styles?

A

Eschmann introducer and gum elastic bougie

1164
Q

The angled tip (coude) of an intubating stylet is used to facilitate intubation of a very _____ glottis. What Cormack & Lehane scores are it most useful for?

A

anterior; 2B or 3

1165
Q

Best time to use the EI = Class _____ view

A

3 (ei = eschmann introducer)

1166
Q

Second best time to use the EI = Class _____ view

A

2B

1167
Q

Worst time to use the EI = Class _____ view

A

3 - LOW change of success

1168
Q

What confirms placement when using the intubating stylet?

A

feeling the click of the tracheal rings

1169
Q

If you don’t feel the click of the tracheal rings to confirm placement of an intubating stylet, what is asecondary way to confirm placement?

A

“hold-up” sign - EI will encounter resistance at the carina (35-40 cm) … if you don’t feel this, you are in the esophagus!!

1170
Q

If using an intubating stylet when do you remove the laryngoscope?

A

After the entire intubation process

1171
Q

How far should the Eschmann introdducer be advanced into the trachea?

A

23-25 cm

1172
Q

Indications for the lighted stylet include: (select 3)
a. super morbid obesity
b. oropharyngeal bleeding
c. mandibular hypoplasia
d. epiglottitis
e. can’t ventilate and can’t intubate scenario
f. microstomia

A

B - severe oropharyngeal bleeding
C - mandibular hypoplasia
F - microstomia

1173
Q

What is a lighted stylet?

A

A blind intubation tehcnique that transilluminates the anterior neck to facilitate endotracheal intubation

1174
Q

What do you see when the lighted stylet is in the trachea?

A

A well-defined circumscribed glow below the thyroid prominence

1175
Q

What do you see when the lighted stylet is in the esophagus?

A

A more diffuse transillumination of the neck without the circumscribed glow

1176
Q

When the patient is supine, the trachea is located ____ to the esophagus.

A

anterior

1177
Q

What airways are lighted stylets useful for?

A

anterior airway, small mouth opening

1178
Q

T/F: The lighted stylet is a helpful tool to use in an emergency.

A

False - it should not be used in an emergency or a can’t ventilate can’t intubate scenario

1179
Q

When is a lighted stylet contraindicated?

A

Traumatic laryngeal injuries
(Also shouldn’t be used with tumors, foreign bodys, airway injury, or epiglottitis)

1180
Q

the trachlight in the adult, the tip should be bent to a ___ degree angle.

A

90

1181
Q

When using the Trachlight in a kid ,the angle should be ____ degrees to accomodate a more cephalad glottic opening.

A

60-80

1182
Q

Choose. theMOST appropriate indications for retorgrade intubation. (Select 2).
a. tracheal stenosis
b. unstable cervical spine
c. upper airway bleeding
d. can’t ventilate and can’t intubate scenario

A

B and C

1183
Q

What is retrograde intubation?

A

A blind procedure, where the tracheal intubation is accomplished by passing the ETT over a wire

1184
Q

What are contraindications for retrograde intubation?

A

Poor anatomy (neck deformity or mass)
Laryngotracheal disease (stenosis)
coagulopathy
infection

1185
Q

What are complications from retrograde intubation?

A

Bleeding, pneumothorax, trigeminal nerve trauma

1186
Q

What is the 1st step for retrograde intubation?

A

PUncture the cricothyroid membrane with a 14-18 g needle

1187
Q

How do you confirm proper placement of the needle in the tracheal lumen during retrograde intubation?

A

Aspirate for air

1188
Q

When is retrograde intubation best used and why?

A

When intubation has failed but ventilation is still possible; requires 5-7 minutes

1189
Q

Match each percutaneous airway technique with its absolute CI.

Transtracheal jet ventilation, cricothyroidotomy, tracheostomy

<6 y/o, UA obstruction, None

A

Jet ventilation - UA obstruction
Cricothyroidotomy - <6 y/o
Trach - none

1190
Q

What are the 3 ways to create a surgical airway?

A
  1. percutaneous cricothyroidotomy w/ transtracheal jet ventilation
  2. surgical cricothyroidotomy
  3. tracheostomy
1191
Q

Transtracheal jet ventilation requires a ____ oxygen source (___ psi) during inspiration. Exhalation is ____.

A

high-pressure; 50; passive

1192
Q

Why is transtracheal jet ventilation CI in UA obstruction?

A

Exhalation is passive, and UA obstruction can prevent exhalation –> barotrauma

1193
Q

Why does percutaneous cricothyroidotomy require a high-pressure oxygen source?

A

B.c the airway diameter is narrow

1194
Q

B/c ventilation can’t be controled durign percutaneous circothyroidotomy, the aptient is at risk for ___

A

hypercapnia

1195
Q

Why is surgical cricothyroidotomy CI in kids <6?

A

They have more pliable and mobile laryngeal and cricoid cartilages making it incredibly challenging; additionally, the thyroid isthmus commonly covers he cricothyroid membrane in kids

1196
Q

Besides kids <6, what are other CI for surgical cricothyroidotomy?

A

Laryngeal fracture or neoplasm

1197
Q

What is the mergency surgical airway technique of choice for kids <6?

A

percutaneous transtracheal ventilation (needle cric)

1198
Q

Incision for tracheostomies are usually made between the __ and __ tracheal rings.

A

2nd and 3rd

1199
Q

Following induction of GA, initial intubation attempts are unsuccessful and face mask ventilation is not adequate. According to the ASA Difficult Airway Algorithm, waht is the NEXT step?
a. supraglottic airway device
b. wake up patient
c. cricothyroidotomy
d. call for help

A

D - HELLLLPPPP

1200
Q

A reasonable approach is to limite attempts with any airway technique class to ___ attempts + ___ atempts by a clinicaln with higher skills.

A

3; 1

1201
Q

Anoxic injury can occur in as little as ___ minutes and can quickly progress to organ damage and death within the following ___ minutes.

A

4; 4-6

1202
Q

Deep extubation provides the MOST significant benefit in the patint with (select 2):
a. asthma
b. OSA
c. parkinson’s
d. CAD

A

A and D

1203
Q

___ and ___ are risks of deep extubation.

A

Airway obstruction and aspiration

1204
Q

What are the risks associated with awake extubations?

A

SNS stimulation increased
Increased ICP, IOP and IAP

1205
Q

Deep anesthetic plane = airway reflexes ____

A

attenuated

1206
Q

Light anesthetic plane = airway reflexes ____

A

hyperreactive (increased risk of laryngospasm)

1207
Q

Awake-disoriented anesthetic plane = airway reflexes ____

A

intact

1208
Q

What is Guedal stage 3?

A

Deep anesthetic plane

1209
Q

What is Guedal stage 2?

A

Light anesthetic plane

1210
Q

What is Guedal stage 1?

A

Awake-disoriented

1211
Q

What type of gaze occurs during light plane of anethesia?

A

disconjugate

1212
Q

What can you give to prevent CV and SNS stimluation during awake extubation?

A

BB, CCB, and vasodilators

1213
Q

What can you give to prevent coughing during awake extubation?

A

Lidocaine (IV or inside ETT cuff) and opioids

1214
Q

What is the BEST technique to manage the patient at high risk fo failed extubation?
a. eschmann introducer
b. airway exchange catheter
c. nasal airway
d. shikani stylet

A

B

1215
Q

What is an airway exchange catheter?

A

A long, thing, flexible hollow tube that maintains direct access to the airway following tracheal extubation

1216
Q

Besides being used for reintubation, the lumen of the airway exchange catheter can also be used to do what 3 things:

A
  1. measure ETCO2
    2.Jet ventilate
  2. Insufflate O2
1217
Q

The distal end of the AEC remains in the ____ (@____. cm at the lip).

A

trachea; 25-26 cm

1218
Q

The AEC can stay in place for how long?

A

Up to 72 hours