Week 9 One Lung Vent MH Flashcards
The lower lung is known as __________
The upper lung is known as __________
Dependent lung = lower lung
Nondependent lung = upper lung
Axillary roll placed on upper chest wall, _____ in the axilla
NOT
In the _________ position, the dependent lung is better perfused (gravity) & ventilated
awake & lateral position
Upper lung is not ventilated but is still perfusing (although less than dependent lung), this causes a large ________________
right to left intrapulmonary shunt (20-30%)
Factors that inhibit hypoxic pulmonary vasoconstriction
Hypocapnia
Vasodilators: nitroglycerin (NTG), nitroprusside (SNP), b-adrenegic agonists (dobutamine), calcium channel blockers
Inhalation agents
During apnea: PCO2 increases _____for the first minute and then ______ for each additional minute of apnea
5mmHg
3mmHg
Hypoxia during one lung ventilation
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
Double lumen tubes come in
left and right types (most common left)
Complications of double lumen tubes include
traumatic laryngitis, hypoxemia due to malpositioned tube, bronchial trauma from over inflation of cuff, inadvertent suturing of tube
Left/Right double lumen tube are the most commonly used by far, is easier to place due to anatomic differences in the bronchi
Left
MH is a rare inherited myopathy triggered by ___________, leading to an acute hypermetabolic state with a variable presentation
inhaled agents (not N2O) and/or succinylcholine
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.
ryanodine receptor
MH triggers are
Succinylcholine (Anectine)
Inhalational agents: halothane, isoflurane, sevoflurane, desflurane, enflurane
Other possible triggers: stress, muscle trauma, exercise, heat stroke
MH has an ___________ diagnosis
intraoperative
The first sign of MH is
First sign = most sensitive = unexplained tachycardia
The most specific sign of MH is
Other signs include
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)
Labs of MH indicate
Labs: initial metabolic acidosis then a combined metabolic & respiratory acidosis, hyperkalemia, hypercalcemia, hyperphosphatemia, creatinine kinase (CK) > 1000 IU, myoglobinuria, hypoxemia
1st step for tx of MH includes
Call for help!
Tx of MH is
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
Dantrolene works by
inhibiting Ca release from the sarcoplasmic reticulum
and
Intracellular dissociation of excitation-contraction coupling
Safe drugs in MH patients include
propofol
Gold standard pre-op test for MH diagnosis is the
Gold standard preop test = muscle biopsy with halothane-caffeine contracture test
Some characteristics of patients with MH include
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.
T/F Prior uneventful general anesthetic does not rule out the possibility of MH
True