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Alcor
personnel
prepare
patient
A-1068 for
cryopreservation
in
Fullerton,
California,
1985.
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The purpose of cryonics
is to preserve life.
Alcor therefore
intervenes in the dying
process at the earliest
moment that is legally
possible. If proper
procedures are followed
immediately after the
heart stops, then legal
death need not impact
the biology of cryonics
or its prospects for
success.
Ideal Cases
It is customary practice
in medicine to
discontinue care of
terminal patients, and
declare legal death,
when the heart stops
beating. The several
minutes of time between
when the heart stops and
the brain dies (by
conventional criteria)
provides a window of
opportunity for Alcor to
artificially restore
blood circulation and
preserve brain viability
even though a patient is
legally deceased.
Cryonics cases in which
life support techniques
are promptly used to
maintain brain viability
after the heart stops
are considered to be
ideal cases.
Standby
Alcor strongly
encourages members who
are terminally ill to
relocate to cooperative
hospice facilities in
Scottsdale, Arizona. If
relocation is not
possible, Alcor may
deploy equipment and a
transport team to a
remote location. As a
dying patient's
condition becomes
critical, Alcor
personnel wait nearby on
a 24-hour basis. This is
called "standby." When
the heart stops beating,
an independent nurse or
physician pronounces
legal death, and the
Alcor team begins life
support procedures as
described below.
Stabilization
The patient is placed in
an ice water bath, and
blood circulation and
breathing are
artificially restored by
a heart-lung
resuscitator (HLR). The
HLR, or "thumper," is a
mechanical device used
in emergency medicine to
perform CPR. In
cryonics, the term CPS
(cardiopulmonary
support) is used instead
of CPR because the
intent is to provide
life support, not
cardiac resuscitation.
Because cryonics
patients are legally
deceased, Alcor can use
methods that are not yet
approved for
conventional medical
use. This enables Alcor
to use new technologies
that can support the
brain longer and more
effectively than
traditional CPR. In
particular, the
combination of
simultaneous
compression-decompression
CPS and rapid cooling
are known to be
especially effective for
protecting the brain
during cardiac arrest.
Intravenous lines are
also established, and
protective medications
are administered. These
include:
-
Free radical
inhibitors
-
NOS (nitric oxide
synthase) inhibitors
-
PARP (Poly
ADP-ribose
polymerase)
inhibitors
-
Excitotoxicity
inhibitors
-
Anticoagulants
-
Pressors
-
pH buffers
-
Anesthetic
These drugs help
maintain blood pressure
during CPS, and protect
the brain from
"reperfusion" injury.
Anesthesia reduces brain
oxygen consumption,
which further protects
the brain.
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The
LUCAS
chest
compression
device,
shown in
the
photo at
right,
is used
by Alcor
to
re-establish
blood
circulation
and
oxygenation
in
cryonics
patients
following
cardiac
arrest.
Alcor
also
uses the
Michigan
Instruments
Thumper.
Both
devices
are
powered
by
pressurized
oxygen,
and
restore
blood
flow
much
better
than
manual
CPR. |
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Transport
If the patient is in a
hospital where the
administration is
unwilling to allow
cryonics procedures, the
patient is moved to an
alternate location while
CPS and cooling are
maintained without
interruption. Femoral
arteries and veins are
surgically accessed and
the patient is placed on
cardiopulmonary bypass.
This means that blood is
circulated through a
portable heart-lung
machine (pictured below)
that takes over the
function of the
patient's own heart and
lungs. External CPS is
no longer necessary, and
is discontinued.
Within minutes, a heat
exchanger in the
heart-lung machine
reduces the patient's
temperature to a few
degrees above the
freezing point of water.
Blood is also replaced
with an organ
preservation solution
that is specially
designed to support life
at low temperature. If
the patient is located
outside of Arizona, they
are packed in ice for
air shipment to Alcor's
facility in Scottsdale,
Arizona.
This treatment is
similar to procedures
used by transplant
surgeons to support the
life of organs moved
around the country for
transplant, except that
Alcor's procedures are
applied to whole
patients. Remarkably,
studies show that whole
animals can survive up
to three hours of cold
storage on ice using
existing medical
technology. Even longer
periods can be survived
if the preservation
solution is continuously
circulated. The MHP2
preservation solution
used by Alcor was
developed in 1984 during
pioneering experiments
in which animals were
successfully recovered
after 4 hours of
bloodless perfusion at
+4°C.
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After large
blood vessels
are surgically
accessed,
Alcor’s Air
Transportable
Perfusion kit
(ATP), shown in
the photo below,
is able to
quickly cool the
patient to
temperatures at
which oxygen is
no longer
necessary. The
ATP also
replaces blood
with an organ
preservation
solution that
supports life at
low temperature
(note the
solution
reservoir in the
case on the
left).
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Cryoprotective Perfusion
At Alcor a surgeon
connects major blood
vessels to a perfusion
circuit. The preferred
vascular access points
are the aortic arch and
right auricle of the
heart, which are
accessed by thoracic
surgery (median
sternotomy).
Traditionally,
neuropreservation
patients have been
treated by this same
procedure, except that
the descending aorta was
clamped. In 2000, Alcor
began treating
neuropreservation
patients by directly
accessing the carotid
and vertebral arteries.
This requires careful
surgical transection of
the spinal column
because vertebral
arteries are located
within the column.
A base perfusate similar
to the preservation
solution used during
transport is circulated
through the patient at a
temperature near 0°C
(the freezing point of
water) for several
minutes. This washes out
any remaining blood. The
cryoprotectant
concentration is then
linearly increased over
2 hours to one half the
final target
concentration. This slow
introduction minimizes
osmotic stress, and
allows time for the
cryoprotectant
concentration to
equilibrate (become the
same) inside and outside
cells. A rapid increase
to the final
concentration is then
made, and the final
concentration is held
until the venous outflow
concentration equals the
target concentration
(approximately one
hour). Temperature,
pressure, and
cryoprotectant
concentration data are
continuously monitored
and acquired by
computer.
The status of the brain
is visually monitored
through two small holes
in the skull made using
a standard neurosurgical
tool (14 mm Codman
perforator). This
permits verification of
brain perfusion by dye
injection, and
observation of the
osmotic response of the
brain. A healthy brain
slightly retracts from
the skull in response to
cryoprotectant
perfusion. An injured
brain swells, indicating
that the blood-brain
barrier has been
compromised. This injury
is often seen in
patients who suffered a
long period of untreated
cardiac arrest.
The cryoprotectant
solution Alcor uses to
prevent freezing is a
mixture of chemicals
developed by mainstream
cryobiologists for
long-term banking of
transplantable organs.
The solution has been
specifically validated
for structural
preservation of the
brain. At the end of
perfusion, these
chemicals are present at
a concentration of
approximately 60%. In
tissues adequately
penetrated by the
solution, the small
amount of remaining
water is not able to
freeze. Instead of
freezing, tissues
vitrify when they are
cooled to cryogenic
temperatures. Variable
penetration of the
solution appears to
result in a combination
of vitrification and
partial freezing in
various body tissues,
but total vitrification
(ice-free preservation)
of the brain, at least
under ideal conditions.
Cooling
After cryoprotective
perfusion, patients are
cooled under computer
control by fans
circulating nitrogen gas
at a temperature near
-125°C. The goal is to
cool all parts of the
patient below -124°C
(the glass transition
temperature) as quickly
as possible to avoid any
ice formation. This
requires approximately
three hours, at the end
of which the patient
will have "vitrified"
(reached a stable
ice-free state). The
patient is then further
cooled to -196°C over
approximately two weeks.
Patients are monitored
by sensitive "crackphone"
instruments during this
long cooling period to
detect fracturing events
that tend to occur when
large objects are cooled
below the glass
transition temperature.
Contrary to media
reports, fracturing is
not a result of
mishandling. It is a
universal problem for
large organs cooled to
liquid nitrogen
temperature. The federal
government recently
awarded $1.3 million
dollars to specifically
study the problem of
fracturing during
cryopreservation.
Long-Term Care
Currently Alcor patients
are stored under liquid
nitrogen at a
temperature of -196°C.
The liquid nitrogen is
held in vacuum-insulated
dewars that require
replenishment every few
weeks. Liquid nitrogen
is used because it is
inexpensive and
reliable.
Alcor is currently
experimenting with an
alternative "vapor
phase" storage system
that would retain the
safety and reliability
advantages of liquid
nitrogen, but allow
patients to be
maintained at controlled
temperatures warmer than
liquid nitrogen. This
will reduce or eliminate
fracturing injury.
Non-ideal Cases
Unfortunately not all
Alcor members can be
reached at the moment
their heart stops. In
cases of sudden illness
or serious injury, blood
circulation may stop for
hours before any
cryonics procedures are
possible. If a physician
determines that an Alcor
member in cardiac arrest
cannot be resuscitated
by current technology
(i.e. declares legal
death), the most
important actions are
administration of
heparin (a drug that
prevents blood clotting)
followed by chest
compressions to
circulate the heparin,
cooling with ice, and
prompt shipment on ice
to Alcor. Alcor will
cooperate with local
funeral directors in
making these
arrangements. Alcor will
also negotiate with
authorities to limit the
extent of any autopsy
that may be required.
The application of
cryonics to patients who
are clinically dead is
perhaps the single most
misunderstood aspect of
cryonics. How can
cryonics help someone
who is clinically dead?
The answer is that life
and death are not binary
"on-off" states. For
cells, organs, and
people, death is a
process, not an event.
For example, the brain
is commonly believed to
"die" after 5 minutes
without oxygen at normal
body temperature. This
is a myth. Brains have
been revived after one
hour of warm cardiac
arrest, and living human
brain cells have been
recovered after 4 hours
and even 8 hours of
clinical death at normal
temperature. What really
happens is that after 5
minutes without oxygen,
chemical changes occur
in the brain that cause
blood vessels to swell
when circulation is
restored. Without
special interventions,
this swelling eventually
stops the restored blood
flow, resulting in the
death of all brain cells
hours later. The
practical result is that
a brain that is deprived
of oxygen for more than
5 minutes is usually
doomed to die within
hours. But doomed is not
the same as dead.
The biological changes
known to occur in the
first hours following
cardiac arrest are
fundamentally minor and
reversible in principle.
Technology already
exists that could
recover people after
more than 5 minutes of
cardiac arrest, although
it is seldom used. The
conventional medical
research value of
donated brain tissue and
living brain cells
recovered from
post-mortem donors
further highlights the
minor nature of brain
changes in the early
hours of clinical death.
Ultimately the
difference between life
and death for a cell, an
organ, or an organism
reduces to a difference
in how atoms are
arranged inside it. It
therefore seems certain
that future medicine
capable of diagnosis and
repair at a molecular
level will be able to
resuscitate people after
longer periods of
clinical death than
medicine can today. How
much memory and
personality would
survive repair and
healing after hours of
cardiac arrest is not
currently known.
Ethics of Non-Ideal
Cases
Cryopreservation of
clinically dead patients
is double speculation.
First, as with all
cryonics cases, it is
assumed that the
cryopreservation process
will someday be
reversible. Second, it
is assumed that future
medicine will be able to
successfully recover
people after long
periods of cardiac
arrest. Alcor therefore
encourages members to
reduce their risk
profile for heart attack
and stroke, and relocate
close to Alcor during
serious illness if
possible. If despite
these precautions a
member experiences
unattended cardiac
arrest, Alcor will still
proceed with
cryopreservation unless
a member indicates
otherwise in their
paperwork.
Cryonics should never be
confused with funeral
arrangements. Alcor
rarely accepts cases
involving legal death of
a non-member. The
combination of strong
emotion, false hope,
unfamiliarity with
cryonics, low
probability of success,
and high cost of
cryonics without life
insurance make accepting
such cases ethically
difficult. People who
think they may someday
be interested in
cryonics should
therefore investigate
cryonics now. Waiting
until cryonics is needed
almost always means it
won't be available.
For Alcor members who
have chosen to be
cryopreserved under poor
conditions if necessary,
there is a final ethical
point. As long as
resuscitation medicine
remains an unfinished
science, it is unethical
to use the label "dead"
as a basis to dismiss
cryonics. Calling
someone "dead" is merely
medicine's way of
excusing itself from
resuscitation problems
it cannot fix today.
This makes people feel
better about abandoning
the patient and making
the unwarranted
assumption that nobody
could ever fix
the problem. Cryonics,
in contrast, is
conservative care
that acknowledges that
the real line between
life and death is
unclear and not
currently known. It is
humility in the face of
the unknown. It is the
right thing to do.
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