Scenar Therapy: A Comparison with Other Forms of Electrotherapy
Based on material from a
lecture by Y. Grinberg
SCENAR therapy is a form of electrotherapy. Other forms include electro-stimulation,
therapy with electro-sleep, dia-dynamic current, interference
therapy, therapy with sinusoidal modulated current, fluctuation and impulse
electro-therapy.
The
effects of electrical therapy may be divided into 3 groups, local (regional),
segmental and generalised.
Local reactions
include:
- activation of afferent sensory
nerves
Electrical
impulses stimulate receptors and nerve endings. Afferent impulses travel to the
central nervous system and give rise to the various segmental and general
reactions.
- influence on local blood flow
Impulses
can regulate the micro-circulation by stimulating contraction or relaxation of
the smooth muscle of the vascular wall, in particular the arterioles,
capillaries and venules with a resultant change in
local blood flow. This effect occurs through a combination of axon-reflexes,
bioactive substances (kinins, prostaglandins,
substance P, cytokines) and mediators (acetylcholine
and histamine). These chemical compounds are often filtered from the blood
through the endothelium/vessel wall into the interstitial space and may accumulate
in the superficial layers of the skin and various tissues.
- release of endogenous regulators of
inflammation and the immune response.
It
has been found that there is a reduction in secretion of mediators of
inflammation from the cell. Components of the complement system are suppressed
by synthesis of macrophages and there is a change in the metabolism of the
tissues. What this amounts to is a slowing down of the process of inflammation.
Segmental reactions:
These
appear at areas where the electrical impulses are applied and are essentially
spinal reflexes. Afferent impulses from sensory nervous fibres activate, via interneurones, motor neurones in the anterior horns of the
spinal cord. Efferent impulses then pass back to the area receiving the impulses
as well as to the organs corresponding to these segments of the spinal cord.
The interaction between visceral and somatic afferent impulses takes place at
the spinal level, and impulses are then sent to the bulbar and cortical
structures.
Generalised reactions:
These
occur as a result of transmission of ascending afferent impulses to the higher
centres of the brain. Visceral and somatic afferent impulses converge within
the central nervous system and are processed and the resultant efferent
impulses cause a general response from the whole system. General reactions also
occur as a result of direct stimulation of the glands of internal secretion and
of the cerebral cortex.
As an example of general
mechanisms of electro-therapy, let us look at DDC (Dia-Dynamic
Current or
P. Bernard current).
DDC
is made up of impulses half-sinusoidal in shape with a frequency of 50 – 100
Hz with delayed exponent background. DDC excites myelinated cutaneous nerves, which are sensitive to this
current. Ascending afferent impulses go towards the substantia gelatinosa in the posterior horns of the spinal cord
and then along paleo-spinal-thalamic,
neo-spinal-thalamic and spinal-reticular-thalamic tracts and activate opioid and serotonin-ergic systems of the brain stem.
This
gives pain relief in three ways. Firstly, a new dominant focus is formed in the
cortex, which causes de-localisation of the previously dominant focus of pain
and activates the parasympathetic nervous system. Secondly, a change in
sensitivity and a decrease in lability occur in the
thick A and thinner C nerve fibres. The faster A-fibres
depolarise the substantia gelatinosa and pain impulses arriving via the C-fibres are prevented from
continuing (Gate theory). Thirdly, activated cortical and sub-cortical
centres produce descending efferent impulses, which increase the blood flow and
stimulates local humoral mechanisms, viz., the
production and release of endorphins, increase in activity of enzymes, such as
acetyl cholinesterase, histaminase and kinases.
When
impulses are applied to the paravertebral zones, DDC
reduces activity of the Renshaw cells and so restores
the ability of the nervous system to damp down the transmission of pain
impulses.
Direct
action on the affected areas results in rhythmical contraction of a large
number of the myofibrils of the skeletal muscles and smooth muscles of the
blood vessel walls. This subsequently increases blood flow and opens anastomoses and collateral vessels. Metabolism in tissues
speeds up and the temperature in the area increases. The improved blood flow
allows redistribution of the ions and water in the interstitium,
promotes removal of the products of lysis in tissues,
permits rehydration of the tissues and helps to
reduce oedema. Reduction of the peri-neural oedema improves
conductivity and excitability of the nerves. These metabolic processes take
place at the areas stimulated by the impulses and also at the tissues and
organs that are innervated from the same segment of the spinal cord.
Based
on the above, DDC should be an effective therapy. However, practically, there
are many restrictions and contra-indications to this method. One of the
limitations of the effectiveness of this therapy is the adaptation of treated
tissues, mentioned by author P. Bernard himself. Another reason is the
essential energetic component in such current. To be non-damaging, the impulse
must be a bi-polar, rectangular impulse, where the duration of each phase is
not more than 100microseconds. In DDC, one half-period of a 50Hz impulse lasts 10milliseconds, i.e. 50 times longer then that
required to be non-damaging. Shortening the time would mean using an impulse of 5kHz, which is obviously unacceptable!
It
is generally accepted that the extent of the response of the organism depends
on the area which absorbs most of the electromagnetic energy. In modern
electro-therapy there is a tendency to attempt to achieve bigger therapeutic
effect using lower electro-magnetic energy by increasing the “informational
aspect” and reducing the “energy component” of the input. For this reason, the
shape (type) of the impulse signal is important.
There
are a number of ways of improving the effectiveness of electro-therapy:
- impulses should be
physiological;
- there needs to be less
habituation to these impulses;
- impulses are more effective if
variable;
- they need to be more
concentrated in order to reduce the general load and cause more specific
changes in the organism;
- if the impulses affect deeper
structures in the organism, their effect is more profound.
In
order to achieve greater therapeutic effect, the action should be applied by
means of electro-magnetic fields and current. To be non-damaging to nerves, the
impulses should last not more then 200microseconds. The time of the
relative and absolute refraction phase determines the frequency of repetition
of these impulses. In pathological states, these values can differ considerably
from values in normal states. For skeletal muscles, the absolute refractory
phase is 2.5 milliseconds and for motor neurones the time is <1millisecond.
Consequently the time between impulses needs to be longer than these times. As
mentioned, the times may vary with the pathology and the frequency of the
impulses may need to be varied from single units to hundreds of hertz to accommodate
this. In order to excite the nerves, the duration of the impulses and amplitude
must be varied considerably.
Practically,
these parameters are similar to Short-impulse Electro-Analgesia (SEA) where
mono- and bi-polar impulses are used, often formed in bundles and lasting 20-500 microsecs at frequencies 2-400Hz
As
in DDC, SEA causes rhythmical excitement of the myelinated nerves. These afferent impulses go towards the substantia gelatinosa of the spinal cord. Inhibitory interneurones in the lateral horns of the spinal cord
reduce the amount of substance P produced. This also reduces the possibility
for the transmission of impulses from afferent sensory conductors of the
lateral horns (A and C-fibres) to neurones of the reticular
formation and supra-spinal structures. Excitement of the interneurones of the posterior horns of the spinal cord
causes a release of opioid substances.
Serotonin is released from the lateral nucleus of the mes-encephalon
and from the peptide-ergic ventral nucleus of the
hypothalamus. As in DDC, fibrillation of the smooth muscles in the arterioles
and superficial skin muscles stimulates the utilisation of the allogenic substances and mediators, which are released in
response to pain. Increase in local blood flow stimulates local metabolic
processes and defensive reactions in the tissues. Reduction of the peri-neural oedema improves excitability and conductivity
of the skin conductors and promotes restoration of suppressed tactile
sensitivity.
Why
does SEA therapy, which seems to be optimal when we look at its mechanism, work
mainly for analgesia and not have wider applications?
1. This method
has a strict specific administration. Because of the type of current, it has
effects on the symptoms rather than a physiological action.
2. Habituation
of the organism to the impulses. Adaptation is an active response of the
organism to changes in the environment. When using electrotherapy, in order to
reduce adaptation to electrical impulses, various types of modulation,
frequency and wave forms are used. However, it is known that the nervous system
builds up a model of the external stimuli by modifying its own elements. As a
result, the nervous system blocks all signals, which are within fixed
parameters of intensity, time, and space. Only those signals that are outside
these parameters will cause a dynamic reaction.
3. In SEA
therapy, the choice of amplitude of the current is determined by the patient’s
sensations (as with other methods of electrotherapy). So excitement of some of
the fibres can be a coincidence. With some devices, because of the patient’s
subjective sensation, the impulses applied were only sufficient to stimulate
sensitive fibres and this determined the extent of the action on the organism.
4. Insufficient
theory exists to support this modality and the methods used were restricted to
studying pain relief.
SCENAR is close to SEA. What determines its significant effectiveness?
1. The “force-duration”
curve and strength of the acting stimuli differ from previous therapies.
The difference between SCENAR and DDC and SEA lies in the quality of action : SCENAR action causes obvious
physiological effects. In particular, it excites motor and sensory fibres,
increases the speed of blood flow, activates local humoral mechanisms, promotes the removal of the products of lysis from the cell, etc.
2. Almost
complete absence of adaptation of the organism to SCENAR action. Due to
bio-feedback, each subsequent impulse is different from the previous one. For
example, towards the end of the session, the power of action may be felt to be
increasing by the patient, but not usually decreasing.
3. Non-damaging
regime of action, technically (short excitatory impulses, bio-feedback, SCENAR-expertise)
and methodology (individually-dosing regime of action, therapy based on rules).
4. High level
of methodology. Various methods for treatment of certain diseases have been
developed as well as combination with general zones (including the three
pathways on the back, six points of the face etc.). Specific methods of action
are used for individually-dosed regimes and according to various rules.
5. SCENAR can
be used as a diagnostic and therapeutic tool at the same time, because there
are different reactions from healthy and pathological tissue. Using the
techniques now available we can assess the effectiveness of the procedures.
6. The successful
construction of the family of SCENAR devices makes it possible in one
session to combine the various effects of electro-analgesia, DDC, SEA and so
on. The size of the active electrode is about 1cm², which is quite small.
Therefore during the treatment we can achieve effects which are similar to the
effects of electro-acupuncture. Acupuncture points and reflective zones are at
areas of higher innervation (close proximity to
nervous trunks, above nervous plexus, lymphatic and blood vessels, at places
where a nerve exits/enters the bones). With the high conductivity of these
areas, the main energy of action can be applied to them, even though the size
of the electrode is bigger than the zones. We can suggest that SCENAR-therapy
smoothes away the differences between physiotherapy (electrotherapy) and
acupuncture, where general mechanisms and actions are similar to each other.
With
all this in mind, wherever other electrotherapies are effective, SCENAR therapy will also be useful and,
indeed, it has been found to be
very useful when other electrotherapies have failed. The peculiarities of SCENAR-therapy
mean that there are few contra-indications.
The
table below shows the indications and contra-indications for electrotherapy.
The recommendations for SCENAR-therapy are based on the experience of
the founders of SCENAR therapy in
Russia
: Dr Y.Gorfinkel and Dr. A. Revenko.
Abbreviation used in the table 1/2
DDC – Dia-Dynamic
Current;
TE – Trans-cranium Electro-Analgesia;
EST – Electro-Sleep Therapy;
SEA – Short impulse Electro-Analgesia;
ES – Electro Stimulation;
EP – Electro-Puncture;
AT – Ampli-pulse Therapy;
IT – Interference Therapy;
F – Fluctuorisation;
Sc – SCENAR therapy.
Table
1 Indication to
Electro-therapy
Disease |
DDC |
TE |
EST |
SEA |
ES |
EP |
AT |
IT |
F |
Sc |
Diseases of Peripheral Nervous System (neuritis, radiculitis, sympath-algia, trauma of the spinal cord) |
+ |
- |
- |
- |
- |
+ |
+ |
+ |
+ |
+ |
Acute traumas of the Musculo-skeletal System
(ligament injury, bruises, myalgia) |
+ |
- |
- |
- |
- |
- |
- |
+ |
- |
+ |
Peri-arthritis |
+ |
- |
- |
- |
- |
- |
+ |
+ |
- |
+ |
Muscular Atrophy |
+ |
- |
- |
- |
- |
- |
- |
- |
- |
+ |
Hypertonic Disease (I,II stages) |
+ |
- |
+ |
- |
+ |
- |
+ |
+ |
- |
+ |
Bronchial Asthma |
+ |
- |
+ |
- |
- |
+ |
+ |
- |
- |
+ |
Vascular Diseases (Raynaud’s, atheroscleriosis of the extremities, varicose veins,
endarteritis obliterans) |
+ |
- |
+ |
- |
- |
- |
+ |
+ |
- |
+ |
Cholecystitis |
+ |
- |
- |
- |
- |
- |
- |
- |
- |
+ |
Dyskinesia of the Bile Ducts |
+ |
- |
- |
- |
- |
- |
+ |
+ |
- |
+ |
Atonic and Spastic Colitis |
+ |
- |
- |
- |
- |
- |
+ |
+ |
- |
+ |
Pancreatitis |
+ |
- |
- |
- |
- |
- |
- |
- |
- |
+ |
Rheumatoid Arthritis |
+ |
- |
- |
- |
- |
- |
+ |
+ |
- |
+ |
Enuresis |
+ |
- |
+ |
- |
+ |
- |
+ |
+ |
- |
+ |
Deforming Osteoarthrosis |
+ |
- |
- |
- |
- |
- |
- |
- |
- |
+ |
Ankylosing spondylitis (Bechterev Disease) |
+ |
- |
- |
- |
- |
- |
- |
- |
- |
+ |
Chronic inflammation of the ovaries and tubes |
+ |
- |
- |
- |
- |
- |
- |
- |
- |
+ |
Adhesions |
+ |
+ |
- |
- |
- |
- |
- |
- |
- |
+ |
Neurasthenia |
+ |
- |
+ |
- |
- |
- |
- |
-- |
- |
+ |
Consequences of trauma to the brain, encephalopathy |
_ |
- |
+ |
- |
- |
- |
- |
- |
- |
+ |
Reactive and asthenia conditions |
- |
- |
+ |
- |
- |
- |
- |
- |
- |
+ |
Tiredness |
- |
+ |
+ |
- |
+ |
- |
- |
- |
- |
+ |
Disturbance of sleep |
- |
+ |
+ |
- |
- |
- |
- |
- |
- |
+ |
Atheroscleriosis of the brain vessels at the
initial stage |
- |
- |
+ |
- |
- |
- |
- |
- |
- |
+ |
Ischaemic Heart Disease |
- |
+ |
+ |
- |
- |
- |
- |
- |
- |
+ |
Neuro-circulatory Dystonia |
- |
- |
+ |
- |
+ |
- |
- |
- |
- |
+ |
Stomach and Duodenum Ulcer |
- |
+ |
+ |
- |
- |
- |
+ |
+ |
- |
+ |
Neuro-dermatitis |
- |
- |
+ |
- |
- |
- |
- |
- |
- |
+ |
Eczema |
- |
- |
+ |
- |
- |
- |
- |
- |
- |
+ |
Diseases of the mouth (stomatitis, para donthosis, peri-odontitis) |
- |
- |
+ |
- |
- |
- |
- |
- |
+ |
+ |
Juvenile bleeding from the uterus |
- |
- |
- |
+ |
- |
- |
- |
- |
- |
+ |
Hysterical Aphonia |
- |
- |
+ |
- |
- |
- |
- |
- |
- |
+ |
Alarming Conditions |
- |
- |
+ |
- |
- |
- |
- |
- |
- |
+ |
Pain syndrome in conjunction with cranial nerves (neuralgia, migraines, neuro-sensorial deafness) |
- |
+ |
- |
- |
+ |
- |
- |
- |
- |
+ |
Pain syndrome in conjunction with spinal nerves (spondylosis,
trapped nerve, autonomic pain) |
- |
+ |
- |
- |
+ |
- |
- |
- |
- |
+ |
Phantom limb pain |
- |
+ |
- |
+ |
+ |
- |
- |
- |
- |
+ |
Neuro-circulatory dystonia |
- |
+ |
- |
- |
- |
- |
- |
- |
- |
+ |
Itching Dermatoses |
- |
+ |
- |
- |
- |
- |
- |
- |
- |
+ |
Anaesthesiology for operative intervention |
- |
+ |
- |
- |
- |
- |
- |
- |
- |
+ |
Meteorological reaction |
- |
+ |
- |
- |
- |
- |
- |
- |
- |
+ |
Psycho-emotional stress |
- |
- |
- |
- |
- |
- |
- |
- |
- |
+ |
Pain syndrome (from the spinal column) |
- |
- |
- |
+ |
- |
- |
- |
- |
- |
+ |
Cephalgia |
- |
- |
- |
+ |
- |
- |
- |
- |
- |
+ |
Pain from Herpes Zoster |
- |
- |
- |
+ |
- |
- |
- |
- |
- |
+ |
Analgesia at general and combinative anaesthesia |
- |
- |
- |
+ |
+ |
| |