Low back painis the most frequent type of musculoskeletal pain
Conventional therapies can be ineffective, and some patients
may experience severe unexpected adverse effects
Neural prolotherapy treatment is a very effective treatment for
chronic painful conditions
Neural prolotherapy is probably one of the safest injection
therapies and easiest to administer with the least amount of
discomfort to the patient
INTRODUCTION
3.
Neural Prolotherapy isa new, exciting breakthrough in the treatment of pain
developed by a New Zealand physician, Dr. John Lyftogt, MD
Neural Prolotherapy involves multiple small injections along the path of
tender superficial nerves in the area of the patients pain with a small
amount of 5% Dextrose
The dextrose solution works by immediately blocking the nerve endings
(TRPV-1 or Capsacin receptors) that are responsible for the nerve pain and
inflammation with the associated superficial nerves
This leads to healing beneath the nerve to deeper structures like the
associated muscles, tendons, ligaments and cartilage of involved joints
INTRODUCTION
4.
Perineural
Subcutaneous
Injection (PSI)
Perineural Injection
Therapy(PIT)
Subcutaneous
Prolotherapy
Treatment
Neural
Prolotherapy
(NPT)
Injection close to subcutaneous nerves to restore their normal function
The American Academy of
Orthopaedic Medicine
To be favored in
Australia and
New Zealand
Introduced by
John Lyftogt
5.
Transient receptor
potential vanilloid
type1 (TRPV-1)
Located on the nervi-nervorum of the peripheral nervous
system
Na+
influx : formation and increased action potential causing the
neuropathic pain
Ca2+
influx : release of the neuropeptides Substance P “SP” and
Calcitonin Gene Related Peptide “CGRP” neurogenic
inflammation
Transient receptor potentialvanilloid type 1
(TRPV-1)
TRPV-1
Down-regulated
The nerve cell will be very “good”
Non-pain producing proteins, e.g. somatostatin
and galanin
Up-regulated
The nerve cell will be very “evil/bad”
Produce damaging and pain-producing proteins,
e.g P-substance and CGRP
8.
Injured or irritatednerve
Up-regulated TRPV-1 receptor/ TRPV-1 nerve
P Substance
CGRP or calcitonin-gene-related peptide
Neurogenic (nerve-caused) Inflammation
NEUROGENIC
INFLAMATION
Hilton’s law
“The nerve
supplyinga joint
also supplies the
ligaments,
tendon and
muscles that
move the joint
and the skin
covering the
joint”
TRPV1 nerves
connect to all
other
structures.
Treating the
nerves
supplying the
muscles moving
the joint
=
Treating the
nerves
supplying the
joint
=
Treating the
cutaneous
inflamed nerves
supplying the
skin over the
joint
Soliman, DMI. Journal of Sports Science 5 (2017) 113-118. doi: 10.17265/2332-7839/2017.02.006
Down regulateTRPV1 through an modulation effect reducing SP and
CGRP levels (Binds to presynaptic calcium channels inhibiting the
release of neurodegenerative peptides) decreasing neurogenic
inflammation pain reduction, regression of soft tissue swelling,
and relief of CCI constrictions, restoring normal nerve growth factor
flow, facilitating nerve repair, and providing almost instantaneous
analgesic effect lasting from hours to days.
Decreasing neurogenic infammation + analgesia effect
decreasing muscle spasm increases the function
HOW DOES NEURAL
PROLOTHERAPY
WORKS?
Dextrose 5 %
14.
CONCEPT: TIME FRAMEOF PAIN AND FUNCTIONAL BENEFIT
EFFECTS RESEARCH
DEXTROSE
Nerve Calming : 5-20 seconds – 2 days
Effect on Growth Factors : 20 min – 10 days
(Pain relief reason unclear)
Hyperosmolar/irritative or Needling Effect : 20
min -10 days (Pain relief reason unclear)
Tissue Maturation Over time (repair) : 10 days
– 3 months
Evaluates each patientthoroughly with a personal history and
physical examination, including observation of the gait
Careful examination with palpation of involved area is made as
it corresponds to the superficial nerves in that area when the
patient is experiencing their pain.
On an individual basis, further evaluation may include
ultrasound evaluation, X-rays and/or MRI before receiving
neural prolotherapy
In chronic pain cases, use expertise to provide a
comprehensive treatment approach that includes
rehabilitative exercises, nutrition, and specific supplements to
maximize your health and ability to heal.
EVALUATION
18.
Identify thearea of pain/anatomic fields
Using dermatomal anatomic distribution, identify the
nerves affected
Asses range of motion of the point affected to
determine peripheral nerves affected
Inject painful CCIs (Chronic constriction injuries)
Reassess same sites of pain after the procedure until
areas are pain free
EVALUATION
19.
Inject tenderpoints in the subcutaneous tissue along
the path of the affected nerve in each case.
3 mL syringes with a 0.5 inch needle were prepared with
a solution of 5% dextrose.
The tender points were each injected with 0.5 mL of
solution, at a 45 degree angle, 0.5- 1cm deep and
approximately 1-2 cm apart.
The solution was injected while withdrawing the needle
so as to create a skin bleb.
TECHNIQUE
20.
SOLUTIONS
5% to 20%dextrose water
5% dextrose water with 8,4% sodium
bicarbonate
10% mannitol with dextrose water
pH maintained between 7-8
21.
FREQUENCY OF TREATMENT
It is not possible to always
predict the exact number
of sessions required, since
each patient’s condition is
unique in terms of his or
her ability to repair and
heal an involved area.
Treatment is given weekly
on the average, for
maximum of 6 sessions
For short term treatment,
it’s given daily for 3 days,
then one week after the
third session
22.
WHAT TO EXPECT
Therelief from the initial treatment lasts
between 4 hours to a few days and will not
be permanent.
Typically, injections are done once weekly or
every other week.
Repetitive treatments will be required for
long term relief.
Generally patients return each week with
fewer regions to inject and 10-15% gradual
improvement weekly.