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Interventional Neuroradiology
|Management in Diagnostic
Neuroradiology
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The introduction of the first
computed tomographic (CT) scanners in 1975
revolutionized the imaging of neurosurgical lesions.
Since that time, the diagnostic armamentarium of the
neuroradiologist in terms of neuroimaging has
expanded progressively. Diagnostic procedures
usually involve limited pain so that the
neuroradiologist frequently administers sedation.
The anesthesiologist is involved, however, in cases
for which difficulty with sedation is anticipated
for a myriad of reasons. These include extreme ages,
claustrophobia, serious neurologic or systemic
illness, and the inability of patients to remain
motionless to be able to achieve high-quality
images.
Many radiology departments have recently adopted the
guidelines for the sedation of children formulated
by the American Academy of Pediatrics Committee on
Drugs. These guidelines address patient selection,
dietary precautions, equipment, monitoring, and
discharge criteria. Furthermore, strict selection
criteria minimize sedation-related side effects. The
screening of patients before the procedure often
reveals those who have either anticipated airway
difficulties or serious medical conditions for whom
the presence of an anesthesiologist becomes
advisable. In one study, 13.1% of patients were
inadequately sedated for their procedure, resulting
in failure of 3.7% of procedures. Older children and
those undergoing magnetic resonance imaging (MRI)
and CT scans experienced higher failure rates. In
addition, Malviya found that 5.5% of children
sedated by nonanesthesiologists experienced an
untoward respiratory event. These events occurred
more commonly in American Society of
Anesthesiologists (ASA) status III and IV patients.
I. General
considerations
Once involved in the
neuroradiologic procedure, the anesthesiologist
faces the usual problems of providing anesthesia in
an environment foreign to and far from the operating
room. Nonferromagnetic equipment and monitoring
modalities are required in the MRI suite, and most
neuroradiographic procedures require that the
anesthesiologist be positioned at a distance from
the patient. Additionally, the issue of contrast
media with their attendant osmolar effects and
potential for toxic and allergic reactions must be
considered. Finally, the design of modern medical
facilities often requires that patients be either
recovered by qualified personnel in an area adjacent
to the radiology suite or transported over
relatively large distances through the medical
center to the regular postanesthesia care unit.
Evaluation. A
thorough preoperative evaluation should be performed
for each patient scheduled for a neurodiagnostic
procedure. In addition to elucidation of the
patient's medical and surgical history, experience
with sedatives and anesthetics, allergies, and
medications, particular attention must be directed
to the neurologic examination. Patients must be
carefully evaluated for signs of increased
intracranial pressure (ICP), preexisting neurologic
deficits, and, in the case of the emergency patient,
concomitant injury to the spine and other major
organ systems.
Equipment.
Equipment available in the radiology suite should
include compatible anesthesia delivery systems,
adequate supplies of medical gases, suction
apparatus, age-appropriate drugs and airway
equipment, and monitors for oxygen saturation,
end-tidal carbon dioxide (CO2),
electrocardiogram (ECG), and blood pressure
compatible with the imaging modality.
II. Computed
tomographic scan
Basic considerations.
Ionizing radiation is delivered to the patient
during CT scanning. Radiation detectors are
permanently fixed all of the way around the CT
gantry. For each image, an x-ray tube rotates in a
circle within the detector ring emitting a beam of
ionizing radiation that passes through the body. The
multiple detectors record the quantity of the x-ray
beam that is attenuated or absorbed as it passes
through the patient's tissues. This information from
various angles is electronically integrated and the
average attenuation value of each point in space is
expressed in Hounsfield units.
Attenuation by a substance is directly related to
its electronic density. Therefore, structures are
hypodense (of lower attenuation), isodense (of
similar attenuation), or hyperdense (of higher
attenuation) relative to the brain parenchyma. The
attenuation of vascular structures is increased by
the use of iodinated contrast drugs. While CT axial
images are displayed initially, high-resolution thin
images can be transformed into coronal or sagittal
sections through computer reformatting.
CT scanning is relatively insensitive for viewing
structures within the posterior fossa because of
image degradation by the artifact produced by the
interface of bone and brain parenchyma. This
modality remains the choice, however, for the
detection of skull fractures and acute subarachnoid
hemorrhage in the emergent setting. Spiral
acquisition CT scan is also popular because larger
anatomic regions can be imaged quickly, which is
particularly useful in the trauma situation. For
example, visualization from the aortic arch to the
circle of Willis can be accomplished in <1 minute of
scan time. With spiral acquisition scanning, unlike
conventional CT scan, the patient is moved at a
constant speed through the scanning field while the
x-ray tube rotates continuously. CT angiography
utilizes spiral acquisition scanning during the
administration of iodinated contrast as an
intravenous bolus. Complex intracranial aneurysms of
<2 mm in diameter can also be visualized with CT
angiography.
Management
Sedation. With the
current rapid CT scanners, very few adults or
school-aged children require sedation for CT
scanning. Occasionally, either intravenous midazolam
in titrated doses of 0.5 mg may be effective, or an
infusion of propofol at a dose of 25 to 100
mcg/kg/minute will sedate an anxious adult patient
for the brief procedure. If an adult or older child
manifests symptoms of increased ICP or serious
airway compromise, it could be better to proceed
with general anesthesia rather than attempt
sedation. Several suggested techniques for the
sedation of small children are listed in Table-1. In
addition to concerns about equipment, monitoring,
and airway management, it must be remembered that
the temperature of children within the cold
radiology suite environment must be carefully
maintained.
General anesthesia. In
the clinical situation where increased ICP is a
critical factor, the intravenous induction of
general anesthesia can be accomplished in children
through an indwelling catheter, the insertion of
which has been facilitated by the prior application
of EMLA (lidocaine 2.5% and prilocaine 2.5%) cream
to the dorsum of the patient's hands. In adults, an
intravenous induction utilizing thiopental, 3 to 4
mg/kg, or propofol, 1 to 2 mg/kg, followed by
succinylcholine, 1 mg/kg, with the addition of a
small dose of narcotic such as fentanyl, 50 to 100
mcg, and lidocaine, 1 mg/kg, to deepen the
anesthetic is appropriate for endotracheal
intubation. In small children, the issue of an
undiagnosed muscular dystrophy mitigates against the
use of succinylcholine. An induction utilizing
either rocuronium, 0.6 to 1 mg/kg, or mivacurium,
0.2 to 0.25 mg/kg, for relaxation is often
indicated. Anesthesia in children is maintained with
an intravenous infusion of propofol, 25 to 100
mcg/kg/minute, or low concentrations of inhaled
anesthetics. Rapid awakening at the end of the
procedure is desirable. An infusion of remifentanil,
0.1 to 0.2 mcg/kg/minute, is an alternative in
adults.
Table-1. Sedation
techniques for small children
|
Drug |
Dose |
Route |
Onset (min) |
Peak effect (min) |
Chloral
hydrate |
20-75
mg/kg (2 g maximum) |
p.o.,
p.r. |
20-30 |
30-90 |
Pentobarbital sodium |
2-4
mg/kg
5-7 mg/kg
(120 mg maximum) |
i.v.,
i.m. |
5-10 |
60-90 |
Midazolam |
0.02-0.15 mg/kg
0.3-0.75 mg/kg |
i.v.
p.o., p.r. |
1-5
(i.v.) |
20-30 |
Methohexitala |
1-2
mg/kg
20-30 mg/kg |
i.v.
p.r. |
5
10-15 |
45 |
a Might exacerbate temporal
lobe seizures.
p.o., by mouth; p.r., rectally; i.v.,
intravenously; i.m., intramuscularly. |
III. MRI
MRIs are acquired when protons on
water molecules within the patient's body are
excited through a combination of a strong magnetic
field and intermittent radiofrequency (RF) pulses.
Additional magnetic fields are applied to create
gradients and excite the protons to different
orientations within the basic magnetic field. In the
excited state, these protons gain energy and shift
from a low energy state to a high-energy state. This
process is termed resonance. When the RF pulse is
turned off, the protons lose energy in two ways: T1,
the longitudinal relaxation time, and T2, the
transverse relaxation time. Fortunately, no ionizing
radiation is employed with MRI, but a large,
powerful, external magnetic field is necessary.
Standard MRI sequences include T1-weighted images,
proton density, and T2-weighted images, as well as
T1 images with the intravenous administration of
gadolinium contrast material. Conventional
double-echo T2-weighted imaging has largely been
supplanted by fast-scan echo or hybrid rapid
acquisition relaxation enhancement (RARE)
sequencing. Additional imaging sequences include
gradient echo, blind-attenuated inversion recovery,
magnetic resonance angiography (MRA), perfusion
imaging, and diffusion weighting. Through constant
technologic improvement, MRI has achieved increased
accuracy with difficult clinical scenarios.
Currently, the areas optimally imaged by MRI include
the limbic system, pineal gland region, sella and
parasellar structures, cranial nerves, internal
auditory canal, cerebellopontine angle,
leptomeninges, and posterior fossa. Flair imaging
can detect processes in the area of the
periventricular and cortical surfaces.
While MRA provides images of arterial and dural
sinus blood flow, functional MRI is being utilized
with increasing frequency in patient evaluation.
Precise three-dimensional anatomic localization and
a contrast effect dependent on the level of blood
oxygenation facilitate functional studies of sight
and hearing. These permit the lateral identification
of the areas responsible for language before
epilepsy surgery. Diffusion-weighted imaging is
useful in the detection of acute cerebral
infarctions and is able to identify regions of
ischemia within minutes. Perfusion-weighted imaging
that utilizes intravenous gadolinium contrast can be
added to a diffusion-weighted study to demonstrate
the presence of cerebral tissue at risk for further
ischemia.
The frequency of adverse reactions to
gadolinium-based contrast of all types is much lower
than the frequency of adverse reactions to iodinated
contrast material. The reactions to gadolinium can,
however, range from mild erythema of the skin to
severe life-threatening reactions including
periorbital edema, respiratory distress, and
cardiovascular collapse. In patients who report a
previous reaction to gadolinium-based contrast,
pretreatment with corticosteroids, famotidine
(Pepcid), and diphenhydramine (Benadryl) and
substituting a different gadolinium-based contrast
agent can be helpful.
Monitoring. The
MRI suite presents a hostile environment to the
anesthesiologist. The following summarizes several
of the safety considerations:
Metallic objects within the patient can be affected,
depending on their metallic properties. Implants
(including vascular surgical clips, stents, cochlear
implants, and intrauterine devices) are subject to
magnetic flux, which can induce electrical currents
and cause local heating and movement. The function
of pacemakers, cardiac catheters, and insulin pumps
can be altered with exposure to the magnetic field.
The radiologist most commonly assesses the hazards
of metallic implants.
External metal wires, such as the ECG leads and
temperature probe, can burn the skin. It is
therefore necessary to use nonferromagnetic
monitoring modalities especially designed for and
compatible with the magnetic resonance (MR) scanner.
Pulse oximeters, even nonferrous and fiberoptically
cabled ones, should be placed on a distal extremity
as far from the scanner as possible. The occurrence
of scan artifacts and local skin irritation and
swelling has been reported in patients who have
either permanent eye makeup or tattoos that contain
ferromagnetic pigments.
Small loose metal objects can be pulled toward the
magnet and are obviously dangerous. Large objects
such as oxygen cylinders can also be pulled into the
magnet with considerable force and can be a serious
threat to both patients and health care personnel.
In general, no metallic objects are allowed in the
scanning room.
Noise is a problem in the MR scanner. The torque on
the loops of wire in which gradient currents are
induced during the RF pulses causes vibration and
audible noise that can average 95 decibels in a
1.5-Tesla scanner. Newer 3T machines generate twice
the noise, hampering communication and necessitating
ear protection for patients regardless of whether
they are awake, sedated, or asleep.
RF heating from induced currents is a potential
problem, particularly in small infants. Periodic
assessment of body temperature must be conducted.
Infants can also become cold within the magnet
because of the low ambient temperature in the
scanning room.
Newer, more powerful 3T MR scanners can induce
electric currents in patients that can stimulate the
peripheral nervous system. Paresthesias, cephalgia,
and muscle contractions have all been reported. The
RF impulse-induced electric currents can also cause
burns.
The anesthesiologist must find the point of least
distortion by orienting monitors in various
positions relative to the magnetic field. Most ECG
artifacts cannot be eliminated and monitors should
be MR-compatible and have good artifact suppression
characteristics. It is important to twist the ECG
cables, keeping the electrodes close together, and
position the electrodes near the center of the
imager with the cables padded to avoid direct
contact with the skin, to get the best images and to
reduce the possibility of burns.
Specialized equipment compatible with MRI is
currently available for monitoring blood pressure,
ETco2, Doppler, oxygen saturation, and
ECG. Compatible anesthesia machines and ventilators
are available as well. Plastic laryngoscopes are
also available although the batteries in the handle
could still be pulled into the magnetic field.
Problems remain in terms of patient accessibility,
hypothermia, and the physical limitations of
positioning obese patients within the magnet's bore.
Anesthetic management.
Many sedative techniques have proven quite
reasonable for MR scanning, including the scanning
of infants shortly after a meal to take advantage of
postprandial drowsiness. The anesthesiologist is
called to assist with MRI, however, when a patient
is complicated neurologically, manifests serious
illness, or has significant airway difficulties. In
general, securing the airway with an endotracheal
tube and then supplying ventilatory assistance
through hand ventilation, an MRI-compatible
ventilator, or a long circuit ensure an optimum
combination of monitoring, airway protection, and
anesthetic delivery. Certain centers have utilized
an intravenous infusion of propofol, either with or
without a laryngeal mask airway, to achieve the same
goals. Whatever the technique, the ability to
maintain adequate control of the airway in the face
of limited accessibility remains of paramount
importance.
IV. Positron emission
tomography (PET) and single-photon emission computed
tomography (SPECT)
These nuclear imaging modalities
are used to measure glucose consumption (PET) and
regional cerebral blood flow (SPECT), thereby
providing an indirect measurement of tissue
metabolism and oxygen utilization. PET scans use
positron-labeled molecules of which the most common
is 2-[18F] fluoro-2-deoxy-D-glucose
(FDG). The FDG is injected intravenously and taken
up into cerebral tissue. Because FDG cannot diffuse
out of the brain after phosphorylation, it is well
suited for imaging cerebral metabolism. PET scans
are used in the investigation of malignancy because
tumor cells have a much higher glucose metabolism. A
PET scan of the brain takes 15 to 30 minutes.
SPECT scans use radiotracers that emit single
photons. Three radiopharmaceutical agents have been
approved by the United States Food and Drug
Administration (FDA) for brain perfusion and SPECT
scanning. Of the three, Tc-99m
hexamethylpropyleneamine oxime ([99mTc]HMPAO)
is used most commonly. It reaches maximum uptake 10
minutes after injection but has a constant
distribution for hours afterward, which makes
scheduling a scan very flexible. SPECT scans are
used to investigate malignancy, cerebral ischemia,
neurodegenerative disorders, epilepsy, cortical
visual loss, and migraine headaches. A SPECT scan of
the brain takes 20 to 45 minutes. Almost all of the
radiopharmaceuticals are cleared through the urinary
tract. For both PET and SPECT scans, the radiation
exposure for the patient is usually equivalent to a
CT scan but may be as high as ten effective dose
equivalents.
Anesthetic considerations.
Many anesthetic drugs have been shown to alter
cerebral blood flow and metabolism, but, because of
the stability of the tracers after injection,
anesthetizing a patient for a scan should not
interfere with the results. Anesthetic
considerations include the necessity to provide all
appropriate monitoring modalities, medical gases,
drugs, suction, and airway equipment in a remote
location. Unlike MRI, PET scanners do not require
nonferromagnetic monitors, and the visualization of
and access to the patient are more easily
accomplished.
V. Cerebral
angiography
Cerebral angiography continues to
be important in the evaluation of subarachnoid
hemorrhage and carotid artery disease. The safest
and most widely used arterial access is the common
femoral artery so that the use of a transfemoral
catheter has replaced direct puncture of the carotid
artery. Digital subtraction angiography reduces the
volume of intra-arterial contrast required and the
overall duration of the procedure. Unfortunately,
neurologic problems related to the angiography
itself still occur. In a prospective study of 1,002
angiograms, the overall rate of ischemic events
within 0 to 24 hours of the procedure was 1.3% and
2.5% in patients studied for cerebrovascular
disease. Complications from the catheters include
transient global amnesia, cortical blindness,
multiple cholesterol emboli syndrome, and vascular
complications such as hematoma and pseudoaneurysm at
the puncture site.
Anesthetic management.
Although anesthesiologists are asked to participate
in diagnostic angiography on rare occasions, they
must bear in mind that contrast media cause
vasodilatation and a burning discomfort. Often the
degree of sedation needs to be increased in
anticipation of an intra-arterial injection of
contrast. As always, there is the possibility that a
reaction to the contrast material can occur.
VI. Myelography
Myelography is utilized to define
the contents of the thecal sac and any intrinsic or
extrinsic impressions. Contrast agents are
introduced directly into the subarachnoid space,
thereby bypassing the blood-brain barrier. The
newest myelographic contrast agents are nonionic, of
low osmolarity, and mix well with cerebrospinal
fluid. The main complications related to myelography
include headache, contrast-related complications,
either subdural or epidural contrast injection,
hematoma of the spinal canal, meningitis, seizures,
and various forms of neurologic injury. The
incidence of adverse events is higher in women and
increases with cervical versus lumbar puncture and
with the use of 22-gauge bevel-tipped versus
24-gauge Sprotte needles. Among the anesthetic
considerations is the need to carefully position
infants and children while the myelogram table is
rotated to achieve good flow of the contrast
material.
VII. Contrast
material
In addition to CT scan, iodinated
contrast is used for catheter angiography and
myelography. High-osmolar contrast agents are ionic
monomers at concentrations ranging from 60% to 76%
by weight. This material possesses five to eight
times the osmolality of human serum (280 mOsm/kg H2O).
Nonionic monomers and dimers as well as ionic dimers
are considered low-osmolar contrast agents (LOCAs)
when they have from two to three times the
osmolality of human serum. The LOCAs demonstrate
more hydrophilia and less tendency to bind to tissue
and are therefore more biologically inert. Despite
their higher cost, LOCAs are used for most
neurodiagnostic procedures.
Iodinated contrast agents are nephrotoxic. After an
initial mild vasodilatation, the renal vascular tree
undergoes prolonged vasoconstriction. Patients who
have preexisting renal insufficiency, diabetes
mellitus, and low cardiac output syndromes are at
risk for developing contrast agent-induced
nephrotoxicity. Renal insufficiency can be
ameliorated or prevented with adequate hydration and
the withholding of any other nephrotoxic medications
before the procedure. The use of fenoldopam,
N-acetylcysteine, and dopamine has consistently
failed to preserve renal function more effectively
than hydration alone. Patients at risk should
receive limited amounts of iodinated contrast media.
Diabetic patients who have nephropathy and who
receive metformin should be carefully monitored for
the development of metformin-induced lactic acidosis
after receiving iodinated contrast.
The hypertonicity of iodinated contrast media is
responsible for the side effects that occur after
injection. These include pain, flushing, nausea, and
vomiting. Patients' responses to iodinated contrast
material can range from a warm flushing and a
metallic taste during contrast injection to an
anaphylactoid reaction. Large multi-institutional
studies have demonstrated that patients given
nonionic contrast material have a 1 in 10,000 chance
of having a severe reaction. Patients likely to have
a problem with contrast include those who have had
previous idiosyncratic contrast reactions, patients
who have either asthma or multiple food and
medication allergies, and patients who have other
illnesses including preexisting azotemia and cardiac
disease. The use of corticosteroids such as oral
methylprednisolone, 32 mg, both 6 to 24 hours before
and 2 hours before the injection of the contrast
material, markedly reduces the chance of a severe
reaction to contrast. Additionally, some centers add
antihistamines and H2 blocking drugs to
the steroid regimen.
Not infrequently, a few hives about the face, neck,
and chest are the sole reaction that a patient
manifests to contrast. Often the only therapy
necessary in such cases is reassurance with perhaps
a dose of diphenhydramine, 25 mg to 50 mg
intravenously (i.v.). A severe reaction to contrast,
manifested by generalized skin irritation,
respiratory difficulties, and hypotension, requires
treatment with epinephrine, 100 mcg i.v., and
glucagon for refractory hypotension. Equipment must
be available in the radiology suite for immediate
airway control and the administration of additional
adjuncts such as beta2-agonists including albuterol
for treating bronchospasm. Occasionally, large
volumes of fluid as well as vasoactive drugs are
necessary to support the blood pressure. A prolonged
stay in the intensive care unit could be necessary
to stabilize the patient.
Delayed reactions can be seen in 1% to 3% of
patients receiving x-ray contrast material. These
are usually mild and consist of rashes and hives.
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