Anesthesia
Keywords Defined - 2005
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DS083
INTRAOCULAR
PRESSURE: GAS SOLUBILITY: SF6, N2O
The
goal of using intravitreal gas during reattachment of retina
is to have a sustained bubble of stable size holding the retina
in place. Sulfur hexafluoride (SF6) is commonly used, and
is inert and poorly diffusible.
N2O
is 117 times more diffusible than SF6 and rapidly enters the
gas bubble, if administered after the injection of SF6 into
the vitreal cavity. The injected gas bubble will rapidly increase
to three times its original size and IOP increase from 14
to 30 mmHg. When N2O is discontinued, both bubble size and
IOP will decrease within 18 minutes. These rapid and wide
fluctuations in bubble size may adversely affect the outcome
of surgery. Therefore, administration of N2O should be discontinued
at least 20 minutes before the injection of gas (washout of
N2O 90% complete within 10 minutes).
SF6
gas bubble remains in place for at least 10 days (other intravitreal
gases remain 21-28 days). Therefore, N2O should be avoided
for general anesthesia within 3-4 weeks. Second exposure might
cause reexpansion of the bubble and elevated IOP with resultant
occlusion of retinal artery and loss of vision. This is more
likely if hypotension also occurs during anesthesia.
1.
Donlon JV, Doyle DJ, Feldman MA. Anesthesia for Eye, Ear,
Nose, and Throat Surgery. In Miller RD (ed.): Anesthesia.
6th edition. Churchill Livingstone, Philadelphia, PA. 2005:2533.
PR015
DOXORUBICIN:
ANESTHETIC IMPLICATIONS
The
side effects of doxorubicin include (myelosuppression) thrombocytopenia,
leukopenia, anemia, cardiac toxicity, hepatic toxicity, stomatitis
and red urine.
Cardiac
toxicity manifesting as life threatening cardiomyopathy occurs
in 1% to 5% of patients. The rapidly progressive congestive
heart failure (CHF) is often refractory to cardiac inotropic
drugs or mechanical cardiac assistance. Cardiomegaly and/or
pleural effusion may be evident on chest radiographs. QRS
voltages on the ECG may be decreased. Patients who have undergone
radiation therapy, particularly to the mediastinum, or patients
who are on concurrent cyclophosphamide therapy seem to be
more susceptible to the development of cardiomyopathy. Impairment
of left ventricular function for as long as 3 years after
discontinuing the doxorubicin has been observed.
In
contrast to life-threatening cardiomyopathy, about 10% of
treated patients show nonspecific, usually benign changes
on ECG (nonspecific ST-T changes, low QRS voltages, atrial
or ventricular premature beats) that do not necessarily reflect
an underlying cardiomyopathy.
Mild
degrees of cardiomyopathy can be detected preoperatively with
echocardiography, or exercise radionuclide angiography.
1.
Cancer. In Stoelting RK, Dierdorf SF. (ed.): Anesthesia and
Coexisting Disease. 4th edition. Churchill Livingstone, Philadelphia,
PA. 2000:588-92.
AS011
DRUGS
TO REDUCE THE DOSE OF SODIUM NITROPRUSSIDE
Sodium
nitroprusside (SNP) is an extremely potent vasodilator that
is available only for IV administration. It acts directly
on smooth muscle causing both arterial and venous dilation.
This results in decreased pre-load and afterload.
SNP
is used in spinal, intracranial (however, remember SNP causes
increased ICP by dilating cerebral capacitance and also directly
impairs cerebral autoregulation) and other surgeries for induced
hypotension to reduce blood loss and facilitate surgery.
The
benefits of deliberate hypotension must out weigh the risks
as it is associated with many complications. The dose should
be titrated to effect, but risk of toxicity is increased if
a dose of 10 mg/kg/min is exceeded. Toxicity is recognized
by the increasing tolerance to the drug.
Administration of SNP causes a reflex increase in sympathetic
tone and renin release. Drugs that blunt these responses markedly
enhance its effects (Beta blockers or ACE inhibitors), allowing
for lower doses and decreased potential for toxicity due to
buildup of cyanide.
Various
medications that can be use to reduce the dose of SNP are
as follows:
1. Calcium channel blockers (e.g. nicardipine, diltiazem)
2. Beta blockers (e.g. labetalol, esmolol and metoprolol)
3. Alpha 2 agonist such as clonidine
4. Isoflurane, opioids, and propofol
5. Captopril
6. Using nitroprusside in a 1:10 mixture with trimethaphan
1.
SJ Lustik. J clin. Anesthesia. 2004;16(1):25-33.
2.
Hackman T. Anesth Analg. 2003;96(4):976-81.
3.
Sum DC. Acta Anesth Sin. 1996;34(4):203-07.
4.
Bendo AA, Kass AS, Hartung J, Cottrell JE. Anesthesia for
Neurosurgery. In Barash PG, Cullen BF, Stoelting RK (eds):
Clinical Anesthesia. 4th edition. Lippincott Williams &
Wilkins, Philadelphia, PA. 2001:773-76.
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