Week 9 One Lung Vent MH Flashcards

1
Q

The lower lung is known as __________

The upper lung is known as __________

A

Dependent lung = lower lung

Nondependent lung = upper lung

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2
Q

Axillary roll placed on upper chest wall, _____ in the axilla

A

NOT

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3
Q

In the _________ position, the dependent lung is better perfused (gravity) & ventilated

A

awake & lateral position

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4
Q

Upper lung is not ventilated but is still perfusing (although less than dependent lung), this causes a large ________________

A

right to left intrapulmonary shunt (20-30%)

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5
Q

Factors that inhibit hypoxic pulmonary vasoconstriction

A

Hypocapnia
Vasodilators: nitroglycerin (NTG), nitroprusside (SNP), b-adrenegic agonists (dobutamine), calcium channel blockers
Inhalation agents

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6
Q

During apnea: PCO2 increases _____for the first minute and then ______ for each additional minute of apnea

A

5mmHg

3mmHg

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7
Q

Hypoxia during one lung ventilation

A

FIO2 of 0.8 to 1.0
Check tidal volumes – want 10cc/Kg, suction ETT
Fiberoptic scope to ensure proper ETT placement
Adjust RR to keep PaCO2 at 40mmHg
Add 5cm H2O CPAP to nondependent lung – warn surgeon
Add 5cm H2O PEEP to dependent lung – tx’s atelectasis but may increase vascular resistance
Increase both CPAP and PEEP slowly
Ask surgeon to clamp or ligate nondependent PA
Return to two lung ventilation always an option

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8
Q

Double lumen tubes come in

A

left and right types (most common left)

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9
Q

Complications of double lumen tubes include

A

traumatic laryngitis, hypoxemia due to malpositioned tube, bronchial trauma from over inflation of cuff, inadvertent suturing of tube

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10
Q

Left/Right double lumen tube are the most commonly used by far, is easier to place due to anatomic differences in the bronchi

A

Left

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11
Q

MH is a rare inherited myopathy triggered by ___________, leading to an acute hypermetabolic state with a variable presentation

A

inhaled agents (not N2O) and/or succinylcholine

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12
Q

In MH, The __________ (Ca release channel) fails in the sarcoplasmic reticulum leading to decreased Ca reuptake from within the cell (myocyte) causing a 500-fold increase in intracellular Ca, leading to sustained muscle contraction, glycolysis, and heat production. Abnormal excitation-contraction coupling results in prolonged and irreversible muscle contracture.

A

ryanodine receptor

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13
Q

MH triggers are

A

Succinylcholine (Anectine)
Inhalational agents: halothane, isoflurane, sevoflurane, desflurane, enflurane
Other possible triggers: stress, muscle trauma, exercise, heat stroke

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14
Q

MH has an ___________ diagnosis

A

intraoperative

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15
Q

The first sign of MH is

A

First sign = most sensitive = unexplained tachycardia

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16
Q

The most specific sign of MH is

Other signs include

A

Most specific sign = increasing EtCO2 = hypercapnia, 2-3X

decrease in SaO2 & SpO2, rigidity despite muscle relaxant onboard, dysrhythmias, tachypnea, cyanosis, sweating, unstable BP, mottling of skin, trismus (masseter spasm) after succinylcholine, darkening of blood in surgical field, decreased mixed venous saturation, cola-colored urine, heating and exhaustion of CO2 absorber, hyperthermia (up to 2 degrees C per hour)

17
Q

Labs of MH indicate

A

Labs: initial metabolic acidosis then a combined metabolic & respiratory acidosis, hyperkalemia, hypercalcemia, hyperphosphatemia, creatinine kinase (CK) > 1000 IU, myoglobinuria, hypoxemia

18
Q

1st step for tx of MH includes

A

Call for help!

19
Q

Tx of MH is

A

Dantrolene 2.5 mg/Kg IV as soon as possible then Q5min. until symptoms controlled or up to 10 mg/Kg total, dantrolene must be mixed in sterile water, this is the mainstay of therapy

Continue dantrolene 1 mg/Kg IV Q6hrs for 72 hrs to prevent a recurrence
Calcium channel blockers should not be given while on dantrolene due to life-threatening hyperkalemia and myocardial depression that may occur

20
Q

Dantrolene works by

A

inhibiting Ca release from the sarcoplasmic reticulum
and
Intracellular dissociation of excitation-contraction coupling

21
Q

Safe drugs in MH patients include

A

propofol

22
Q

Gold standard pre-op test for MH diagnosis is the

A

Gold standard preop test = muscle biopsy with halothane-caffeine contracture test

23
Q

Some characteristics of patients with MH include

A

myopathy, short stature, cryptorchidism (undescended testicles), pectus carinatum (a chest wall deformity), lumbar lordosis and thoracic kyphosis (deformity of the spine), and unusual facial characteristics. Later reports have termed this combinations the King-Denborough syndrome, after the authors of the report.

24
Q

T/F Prior uneventful general anesthetic does not rule out the possibility of MH

A

True

25
Q

Boys < 9 yrs old who experience sudden cardiac arrest after succinylcholine in the absence of hypoxia should be treated for

A

acute hyperkalemia first: CaCl2 IV, Bicarbonate IV, they most likely have a subclinical muscular dystrophy

26
Q

The symptoms of MH usually develop within

A

one hour after exposure to trigger substances, but may even occur several hours later in rare instances.

27
Q

MH does not occur with every exposure to triggering agents, and susceptible patients may undergo

A

multiple uneventful episodes of anesthesia before developing an episode of MH