Neural Prolotherapy
Technique for Chronic
Pain Management
Prof. Dr. dr. Dessy Rakhmawati Emril, Sp. S (K)
Low back pain is 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
Neural Prolotherapy is a 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
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
Transient receptor
potential vanilloid
type 1 (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
Premkumar, LS. Current Neuropharmacology, 2008, 6, 151-163
Transient receptor potential vanilloid 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
Injured or irritated nerve
Up-regulated TRPV-1 receptor/ TRPV-1 nerve
P Substance
CGRP or calcitonin-gene-related peptide
Neurogenic (nerve-caused) Inflammation
NEUROGENIC
INFLAMATION
CHRONIC CONSTRICTION INJURY (CCI)
Alyan II. Med. J. Cairo Univ., Vol. 86, No. 5, September: 2727-2731, 2018
Neuronal
friction
Chronic
Constriction
Injury (CCI)
CHRONIC CONSTRICTION INJURY (CCI)
Hilton’s law
“The nerve
supplying a 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
Neurogenic
Inflammation
Healthy Nerve
Dextrose 5%
HOW DOES NEURAL
PROLOTHERAPY
WORKS?
 Down regulate TRPV1 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 %
CONCEPT: TIME FRAME OF 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
Others musculoskeletal pain
Neck pain
Low back pain
Fibromyalgia
Headaches
INDICATIONS
Local abscess
Cellulitis
Critical thrombocytopenia
Platelet dysfunction syndrome
Hemodynamic instability
Cellulitis
Critical thrombocytopenia
Platelet dysfunction syndrome
Hemodynamic instability
Local abscess
CONTRA
INDICATIONS
Evaluates each patient thoroughly 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
 Identify the area 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
 Inject tender points 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
SOLUTIONS
5% to 20% dextrose water
5% dextrose water with 8,4% sodium
bicarbonate
10% mannitol with dextrose water
pH maintained between 7-8
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
WHAT TO EXPECT
The relief 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.
THANK YOU

1. NRT for Chronic Pain slide share.pptx

  • 1.
    Neural Prolotherapy Technique forChronic Pain Management Prof. Dr. dr. Dessy Rakhmawati Emril, Sp. S (K)
  • 2.
    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
  • 6.
    Premkumar, LS. CurrentNeuropharmacology, 2008, 6, 151-163
  • 7.
    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
  • 9.
    CHRONIC CONSTRICTION INJURY(CCI) Alyan II. Med. J. Cairo Univ., Vol. 86, No. 5, September: 2727-2731, 2018 Neuronal friction Chronic Constriction Injury (CCI)
  • 10.
  • 11.
    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
  • 12.
  • 13.
     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
  • 15.
    Others musculoskeletal pain Neckpain Low back pain Fibromyalgia Headaches INDICATIONS
  • 16.
    Local abscess Cellulitis Critical thrombocytopenia Plateletdysfunction syndrome Hemodynamic instability Cellulitis Critical thrombocytopenia Platelet dysfunction syndrome Hemodynamic instability Local abscess CONTRA INDICATIONS
  • 17.
    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.
  • 23.