RULES
OF PROTOCOL
Since
the ACCII (formerly ACCT) originally published “Thermographic
Protocols” in 1988 there has been a significant reappraisal of
methodologies appropriate for the conduct of a legitimate infrared imaging
study. Infrared imaging has
been proven to provide an accurate depiction of the vascular changes that
reflect sympathetic nervous system function.
As such, control of ambient temperature and thermal stress on a
subject’s body temperature have become increasingly important, while, at
the same time, triplicate repetition of images has been shown to be
superfluous and unnecessarily costly.
CONTROL OF EXAMINATION ROOM CONDITIONS
Temperature:
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A cool examination room is imperative.
16-20°C
is the recommended temperature range, and it is important that the
ambient room temperature not exceed 20°C.
The core temperature of the patient’s body must be stressed
to provoke reactions in the sympathetic nervous system.
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Room temperature should be controlled so that ambient temperature does
not change more than 1°C
during the course of the examination.
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The examination room must have a thermometer to record the
room temperature before, during, and after the examination.
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Heat sources should be minimized in the examination room
and must be kept well away from the patient.
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In no case shall the temperature or humidity conditions in
the examination room be allowed to provoke sweating on the part of the
patient, as this would produce unacceptable artifact.
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Floor cover:
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The floor surface on which a patient stands must be
carpeted.
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Ventilation and Drafts:
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Typical doors and shaded windows should be sufficient to
maintain the examination room free of obvious drafts.
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Ventilation required to maintain the necessary cooling of
the examination room should be as draft-free as possible, with no
direct cold air blowing on the patient.
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Lighting:
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Standard fluorescent or diffused incandescent lights are
adequate.
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PATIENT PREPARATION
Pre-examination instructions:
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Shower or bathe the morning of the test to ensure that the
skin is as clean as possible; however, avoid hot water exposure to the
skin for at least two hours prior to the test.
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Avoid placing any material of any kind on the skin, such
as any skin lotions, deodorants, preparations, moisturizers,
liniments, topical analgesics, etc.
Avoid make-up if the face is to be examined.
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Wear loose clothing to the test; avoid anything binding
against the skin; avoid support undergarments or pantyhose. Do not wear jewelry, including rings if the hands are to be
examined.
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Eat lightly approximately two hours prior to the test, but
avoid any spicy or stimulating foods for 2 hours prior to the test.
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Avoid any source of nicotine for 4 hours prior to the
test.
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Avoid any source of caffeine (colas and coffee, including
decaffeinated coffee) for 4 hours prior to the test.
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Sunburn must be absolutely avoided for one week prior to
the test.
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Physical medicine procedures:
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Avoid skeletal manipulation, acupuncture, physical
therapy, the use of TNS units, or electrodiagnostic testing for 24
hours prior to the test.
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Exercise:
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Normal light exercise is acceptable.
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Bandages and braces:
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Remove all bandages and braces for at least 12 hours prior
to the test.
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Medications:
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The use or withdrawal of medications should be coordinated
with the prescribing physician; however, if possible, the test
should be performed in the morning, and all medications should be
withheld after midnight. Certain
medications have an effect on sympathetic function and could
complicate interpretation of the test.
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Unless there is compelling reason to the contrary:
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sympathetic blockers should be avoided for 12 hours prior
to the test.
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steroids should be avoided for 24 hours prior to the test.
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transdermal patches should be avoided for 24 hours prior
to the test.
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Examples of medications that may produce alterations in
surface temperature that could complicate the interpretation of an
infrared image include but are not limited to: beta blockers,
calcium channel blockers, alphaadrenergic blockers, vasodilators,
opioids, analgesics, antiinflammatories, high-dose niacin, and
topical or transdermal agents such as capsaicin cream or patch,
clonidine patch, or nicotine patch.
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Sympathetic blocks:
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For original diagnostic studies, all sympathetic and
neurolytic blocks must be avoided for at least 3 days prior to
the test, preferably one week prior.
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Post-block studies may be performed to:
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assess the effectiveness of the sympathetic block.
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evaluate for and/or localize the area of nociception in
cases of sympathetically-maintained pain and vasoconstriction
seen in patients showing normal somato-autonomic or viscero-autonomic
reflexes secondary to a pain generator(s).
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No equilibration is required for these post-block images,
as an intentionally-induced sympathetic artifact is already
present. Region-of-interest
spot views provide appropriate visualization, assuming that a
full-protocol original diagnostic study has already been
produced prior to the block.
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Equilibration and Disrobing
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Upon entrance to the thermal imaging lab, the patient
shall remove all clothing (including undergarments) and jewelry in the
area to be imaged and shall be issued a lightweight, loose examination
gown.
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The gowned patient shall remain in the
temperature-controlled examination room for at least 20 minutes,
provoking cooling of the body sufficient to stress the body’s core
temperature.
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The equilibration time may need to be extended, on a
case-by-case basis, in obese patients or in those with certain
endocrine disorders.
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In most cases (other than above), greater than 30 minutes
equilibration time is not generally advised.
Excessive equilibration times may cause patients to cool
excessively and begin to tremble, thus inducing artifacts in the
study.
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If a time/temperature stress test (qv)
is performed, no equilibration is required, as the purpose of the
procedure is to show sympathetic function in response to equilibration
over time.
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Equilibration is not required for post-sympathetic-block
follow-up evaluations (see above).
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The body part to be imaged must be selectively uncovered
for each view so that the infrared camera can detect surface infrared
emanations.
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NUMBER OF STUDIES AND VIEWS
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A “study” is a collection of infrared views necessary
to form a diagnostic impression.
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The views imaged should encompass the symptomatic region
of the body and all of its proximal and distal neurovascular
components. This is
usually interpreted as follows:
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Upper body study
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For evaluation of neck, upper back, or upper extremity
complaints
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Lower body study
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For evaluation of lower back, pelvic, and lower extremity
complaints
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Assuming that these protocols are followed, one study is
adequate for diagnostic purposes; triplicate imaging is no longer
required.
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The field of view chosen for imaging should be appropriate
to the image resolution inherent in the infrared camera equipment
being utilized; higher resolution cameras allow larger fields of view.
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It is recommended that all of the views imaged should also
be permanently archived, for purposes of comparison of changes over
time.
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STRESS STUDIES
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Autonomic stress testing may be required for some
conditions, particularly for the Complex Regional Pain Syndromes. This may be accomplished by immersing a body part
not being imaged in cold water to further stimulate the autonomic
nervous system; for example, if the hands and upper body are being
imaged, the feet are chosen for cold water immersion.
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Mechanical stress testing may be required to provoke
mechanically-induced symptoms.
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Sympathetic response to equilibration over time may be
conducted, known as a time/temperature stress test.
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Other stress tests may include water mist, warm water
immersion, directed air draft produced by fan, or alcohol spray.
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A description of the stress test must be entered in the
chart and described in the report, and it is also recommended that the
procedure be identified by legend affixed to the images.
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The stress views shall be imaged and recorded as the last
part of the study, after the standard views have been collected.
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Spot studies of a region-of-interest may be produced to
evaluate response to a sympathetic block.
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The ordering or examining physician may decide on the
appropriate stress test to be utilized for any given patient.
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EQUIPMENT
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Only high-resolution electronic infrared scanners are
appropriate.
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Temperature repeatability and accuracy of 0.1°C
temperature recording is necessary.
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When multiple views are used for bilaterally equivalent
areas, the equipment settings and technique should be identical.
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PATIENT IDENTIFICATION
The infrared image, captured on archival media, should
exhibit the following minimum information:
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Patient's name or identification code
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Facility/doctor identification
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Date the service was rendered
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