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BRAIN DEATH CRITERIA1*
Brain Death2* is a
clinical diagnosis which can be made when there is complete and
irreversible cessation of all brain function. Since it is now
technically possible to sustain cardiac, circulatory respiratory
and other organ function after the brain has ceased to be alive,
a diagnosis of brain death can be made before the heart beat
stops.
The diagnosis of brain death
is based primarily on clinical criteria. A confirmatory
laboratory test may be done to supplement the clinical
diagnosis.
An individual with
irreversible cessation of all brain function, including the
brain stem, is dead.
Historical Aspects
In 1564, Versalius a famous anatomist is said to have
conducted an autopsy in Madrid on a nobleman who had been his
patient. This autopsy was carried out in front of a large crowd
of citizens and when the thorax of the body was opened the heart
was beating. After that Versalius was compelled to leave Spain.
This and others episodes probably have made it necessary to
have physicians pronounce the death of patients.
PREREQUISITES
The presence of sedative
drugs, hypothermia, shock, or other potentially reversible
conditions that may depress brain function must be excluded for
these clinical criteria to be valid:
-
Body temperature must be
32.2 degree (90 degree F) or higher.
-
If barbiturates are
present in the blood, or were used therapeutically for
control of intracranial pressure or seizures, serum levels
should not exceed 1 mg % at the time of the clinical
examination.
-
Screen to exclude other
sedative drugs-where clinically indicated.
-
Absence of severe
hypotension (shock).
CLINICAL CRITERIA
The clinical examination
should be done by a neurologist, neurosurgeon, or critical care
attending who is familiar with the neurological examination and
with these criteria:
-
Coma with cerebral
unresponsitivity
-
Apnea
-
Absent brain stem reflexes
-
Persistence of condition
for 6 to 24 hours
-
Unresponsive Coma
The patient should be deeply
comatose with no movements, no withdrawal, seizures, or
posturing (decerebrate or decorticate), spontaneously or to
noxious stimulation. There may be spinal cord reflexes.
-
Apnea
Apnea may be demonstrated by
the absence of spontaneous respiration in the presence of an
adequate carbon dioxide (CO2) drive.
The apnea test is a clinical
bedside test to determine the response of the medullary brain
stem respiratory center to a CO2 stimulus. In the
absence of significant pulmonary disease or neuromuscular
paralysis, a lack of respiratory effort to hypercarbia implies
destruction of the most caudal part of the brain stem.
The test is begun by
pre-oxygenation with 100% oxygen via the ventilator for about 5
minutes. The ventilator is withdrawn and the trachea is
cannulated with an oxygen catheter. A passive flow of 100%
oxygen at 4 1/min allows the PCO2 to rise without
hypoxia. A baseline arterial blood gas (ABG) is drawn to ensure
that the PCO2 is normalized. Observe the patient's
undraped chest and abdomen for respiratory effort. After 5 and
l0 minutes an ABG is drawn and the patient returned to the
ventilator. A pulse oximeter should be used.
If in the presence of a
negative drug screen and in the absence of metabolic
intoxication, evidence of a paralyzing disease (e.g.
Guillan-Barre, Myesthenia Gravis), or of neuromuscular blockade,
there is no respiratory effort after an arterial PCO2
of more than 60 mm Hg has been achieved, the patient is apneic.
Usually an ABG is drawn at baseline, 5 and 10 minutes.
The apnea test is done near
the end of the period of observation. Patients whose PO2
cannot be maintained at normal levels may be excluded from a
formal, apnea test.
Recommended Procedure
-
Prerequisites:
-
Core temperature
should be at least 90°F (32.2o C).
-
The patient should
be hemodynamically stable.
-
A baseline ABG has
been obtained and the results show that the PaO2
is greater than 80, or O2 saturation is
at least 95% and the PCO2 in 35-45mmHg.
-
If the patient has
a history of COPD or other chronic pulmonary
disease, a pulmonary consult may be obtained.
-
If the patient has
received medications which may interfere with apnea
testing, consultation with a neurologist, a
neurosurgeon, an anesthesiologist, or a toxicologist
may be sought. If there is any question concerning
narcotic toxicity, a narcotic antagonist should be
given.
-
Equipment and
Personnel:
-
Suction catheter
of appropriate size with connecting tubing
-
Sterile gloves
-
Oxygen or suction
connecting tubing
-
Oxygen flow meter
with nipple
-
ABG kits, pulse
oximeter
-
Cardiac monitor
-
Nursing and
respiratory therapy personnel may be of assistance
in performing the procedure
-
Suction the patient
according to the standard procedure.
-
Pre-oxygenate the
patient with 100% oxygen on present means of respiratory
support for five minutes.
-
Remove patient from
the ventilator (if possible); observe the time the test
is started.
-
Insert catheter into
the endotracheal or tracheostomy tube. Care must be
taken not to intubate a mainstem bronchus; the tip of
the catheter should be at, or a few millimeters below,
the tip of the endotracheal or tracheostomy tube.
-
Attach the aspirator
manifold of the catheter to the oxygen flow meter via
the oxygen connecting tubing. Tape over the aspirator
manifold port or occlude it with your thumb throughout
the remainder of the procedure.
-
Set the flow meter for
4 lpm. Monitor SaO2 by pulse oximeter.
-
It is suggested that
starting PaCO2 be 35-45 Torr. The PaCO2
will be allowed to rise while the undraped thorax and
abdomen are observed and palpated carefully for signs of
spontaneous respirations.
-
An ABG should be drawn
at approx. 5 minutes and 10 minutes of elapsed time to
establish that the PaCO2 has reached 60mm Hg.
-
If there are any
respirations or if there is a loss of vital signs or
oxygen desaturation below 90%, draw ABG and discontinue
the test immediately. Reconnect the patient to
ventilatory support after 10 hyperinflating breaths with
the resuscitation bag using 100% oxygen.
-
The test is over after
approximately 10 minutes. If there is no respiratory
effort after an arterial PCO2 of more than
60mm Hg has been achieved, the patient is apneic. Repeat
testing for a period of time longer than 10 minutes may
be required if PaCO2 is below 60 at the end
of this test.
-
Discontinue the test
by hyperinflating with a resuscitation bag on 100%
oxygen for a brief period until the patient's vital
signs are stable and his/her color is normal. Resume
pre-test ventilation.

It is recognized that on some
occasions departure from the above procedures may be necessary.
The reasons for such departure, if taken, should be documented
in the patient's record.
-
Absent Brain Stem
Reflexes
-
Pupils - should be mid
position in size (4 mm) or dilated in the absence of
mydriatics and unreactive to bright light or noxious
stimulation.
-
Eye movements - there
should be no spontaneous eye movements, and the eyes
should remain in the neutral position on testing the
occulocephalic and occulovestibular reflexes. The
occulocephalic response is tested by rapid rotation of
the head to either side. In eliciting the
occulovestibular reflex, 20-30 ml of ice water are
instilled into each ear external auditory canal with an
intact tympanic membrane with the head elevated 30
degrees.

-
Corneal Reflex - No
blinking or eye movement when the cornea is touched
lightly with cotton.
-
Gag Reflex - No
gagging or coughing when the oropharynx or trachea is
stimulated.
-
Caloric testing

Head is
at 30°
from horizontal
Brings horizontal
semicircular canal into vertical and position of maximal
sensitivity
Each auditory canal
stimulated for 30 sec at temp of 30°
and 44°C
(7°
above & below body temp) with 5 minutes between each irrigation
Cold
stimulation: ipsilateral tonic deviation with nystagmus away
Warm
stimulation: nystagmus towards side of stimulation.
Bilateral
cold stimulation: tonic downward deviation with
nystagmus upward
Bilateral warm stimulation: tonic upward
deviation with nystagmus downward.
The presence of deep tendon or
other spinal reflexes does not preclude the diagnosis of brain
death.
-
Duration of Observation
The clinical examination may
be repeated after 12-24 hours. When there is a structural brain
damage and the diagnosis is known with certainty, a shorter
period of observation is adequate if central nervous system
depressant drugs, metabolic and anoxic causes have been
excluded.
5.
Confirmatory Tests for Determination of Brain Death
Although confirmatory tests are not
mandatory in most situations, additional testing (Table 5) may
be necessary for declaring brain death in patients in whom the
results of specific components of clinical testing cannot be
reliably evaluated.13
Clinical experience with confirmatory tests other than
conventional angiography, lectroencephalography, and
transcranial Doppler sonography is limited. Research involving
use of confirmatory tests for determination of brain death is
constrained by lack of blinded evaluation, absence of
interobserver reliability data, and sparse use of control
groups.

Conventional
Cerebral Angiography
Selective 4-vessel angiography may
be performed in the neuroradiology department. In patients with
brain death, intracerebral filling is absent at the level of the
carotid bifurcation or circle of Willis, whereas the external
carotid circulation is patent13
(Figure 3).

Electroencephalography
A 16- or 18-channel instrument and
guidelines developed by the American Electroencephalographic
Society are used to determine brain death.22,23
In patients with brain death, no electrical activity occurs
during a period of at least 30 minutes of
electroencephalographic recording.13
Transcranial
Doppler Sonography
In transcranial Doppler sonography,
intracranial arteries are insonated bilaterally (ie, middle
cerebral artery through the temporal bone above the zygomatic
arch). Ten percent of patients may not have temporal insonation
windows. Therefore, initial absence of Doppler signals cannot be
interpreted as consistent with brain death. Findings consistent
with brain death indicate high vascular resistance associated
with greatly increased intracranial pressure and include (1)
absent diastolic or reverberating flow, (2) systolic-only flow
or retrograde diastolic flow, and (3) small systolic peaks in
early systole. Blood flow velocities may be influenced by marked
changes in Pco2,
hematocrit, and cardiac output.12,13,24-27
Somatosensory and
Brain Stem Auditory Evoked Potentials
Testing for somatosensory evoked
potentials is done at the bedside with a portable instrument
that provides bilateral stimulation of median nerves. In studies13,28-31
of patients with brain death, most patients had no responses to
tests for somatosensory and brain stem auditory evoked
potentials. Both types of tests are less sensitive than
previously mentioned confirmatory tests.
Cerebral Blood
Flow and Magnetic Resonance Imaging Studies
In one investigation,32
patients who met clinical criteria for brain death had no
responses to tests for brain stem auditory evoked potentials and
no cerebral perfusion as measured by radionuclide cerebral
angiography and brain perfusion studies. Cerebral blood flow
studies with xenon 133 have also been used to confirm brain
death,33
and magnetic resonance imaging has been explored as a
noninvasive method for determining the nonfilling phenomenon
that occurs in brain death.34,35
In patients with brain
death, technetium Tc 99m brain scans show no uptake of the
radionuclide in brain parenchyma (“hollow skull phenomenon”).13
Neurophysiological technology and
neurodiagnostic testing have great promise for becoming the gold
standards for confirmatory tests of brain death. However,
current investigations of technology-driven confirmatory tests
still require further replication and clinical application.
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1* Note: These guidelines have
been developed to assist the physician in the determination of
brain death in adults and in children 5 years and older. For
children younger than 5 years of age, consultation with a
pediatric neurologist or neurosurgeon should be obtained.
2* Guidelines for
determination of death: Report of the medical consultants on the
diagnosis of death to the President's Commission for the study
of ethical problems in medicine and biomedical behavioral
research. JAMA. 246:2184-2186. 1981 |