herniations by ozone DISCOLYSIS Alper Muradov MD StSofia Hospital SofiaBulgaria Epidemiology Low back pain is the commonest condition affecting the lumbar spine and is the most frequent cause of absence from work Around 80 of the population in western countries will experie ID: 927512
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Slide1
Percutaneous Treatment of LUMBAR disc herniations by ozone DISCOLYSIS
Alper
Muradov
M.D.
St.Sofia
Hospital
Sofia,Bulgaria
Slide2Epidemiology
Low back pain is the commonest condition affecting the lumbar spine, and is the most frequent cause of absence from work. Around 80% of the population in western countries will experience at least one episode of low back pain in their lifetime and 55% suffer from low back pain associated with
radicular
syndromes.
Slide3Epidemiology
In the United States alone around 200.000 patients with
lumbalgia
or sciatica are treated surgically every year. The short-term success rate after surgery for
lumbosacral
disc herniation is around 95-98% with a 2-6%, incidence of true recurrence of
herniation
. This percentage drops to around 80% in the long-term (more than 6 months) due to the onset of symptoms linked to Failed Back Surgery Syndrome (FBSS) characterised by recurrence and/or hypertrophic scarring with severe symptoms in 20% of patients and FBSS proper in 15%.
Slide4Mini Invasive Techniques
These techniques have minimized the invasive nature of open surgery and avoid or decrease the complications associated with surgery.
Reducing
intervertebral
disc size by mechanical aspiration of a part of the disc or partially dissolving the
herniation
by drying, reduces the conic pressure on the torn annulus and creates the space necessary for
retropulsion
whenever the circular fibres of the annulus regain a minimum capacity to contain the disc under tension. The strategy in these techniques is based on the fact, that a small change in volume produces large change in pressure.
Slide5Mini Invasive Techniques
LASER DISCECTOMY
COBLATION
THERMAL COACULATION
ASPIRATION
ENDOCOPY
CHEMONUCLEOLYSIS
Slide6Mini Invasive Techniques
According to the site
and the mechanism of action the MIS techniques can be divided in 3 groups:
DECOMPRESSIVE:
chemonucleolisys,percutaneous
decompression and
nucleodiscectomy
, LASER and thermal
discectomy
ANTIINFLAMATORY: Anti TNF therapy
COMBINED:Decompressive
and direct
antiinflamatory
like
coblation
nucleoplasty
and oxygen-ozone
dicolysis
Pathogenesis of Low Back Pain
Still
discutable
,but 2 Main group
s of factors are responsible:
MECHANIC FACTORS
DIRECT:
-Direct pressure of hernia on the spinal ganglion
-Deformation of the ligaments and
anullus
with stimulation of
noccireceptors
of
Luschka’s
nerve
INDIRECT:
-Ischemia due to compression on the arteries
-Venous stasis
INFLAMATORY FACTORS:
The
inflammatory factors are
- cell-mediated response to the disc
protrusion,possibly
related to segregation of the disc to the immune system)
-
biohumoral
factors like
Phospholipase
A2 (indirect inducer of pain mediators), Prostaglandin E2 (inflammatory inducer through
Phospholipase
A2), and Matrix
metaloproteinases
(MMPs)(inflammatory enhancers)
Pathogenesis
Herniation
of the nucleus
pulposus
is thought to trigger an autoimmune reaction, the
proteoglycan component of its nucleus being segregated from the immune system after birth.
Moreover the nucleus
pulposus
can also give rise to an inflammatory process through a non-immune-mediated mechanism supported by
histiocytes
, fibroblasts of the reactive
perihernial
tissue, and
chondrocytes
in the disc protrusions able to produce cytokines (Interleukin-1 alpha, Interleukin 6 and TNF-alpha). This lead to an increase in
phospholipase
A2 leading to the release of prostaglandin E2,
leucotrenes
and
thromboxanes
found in larger quantities in non-contained disc
herniations
and patients presenting more severe symptoms.
Prostaglandins cause pain. In small amounts, they enhance sensitivity of the nerve roots and other pain-producing substances like
bradykinin
.
Slide9DISCO-RADICULAR CONFLICT
COMPRESSION
Slide10DISCO-RADICULAR CONFLICT
MECHANICAL COMPRESSION
OF
THE NERVE ROOT
DOES
NOT
PROVOKE THE IRRADIATED
PAIN
DISCO-RADICULAR CONFLICT
PAIN
compression
edema
obstacle to circulation
ischemia+pH
Contracture of
paravertebral
muscles
NEUROLOGICAL
DISFUNCTION
Slide12DISCO-RADICULAR CONFLICT
INFLAMATION
AND
PAIN
Enzymes
Phospholypase
A2,prostaglandine E2
and
Interleukine
6 are elevated in herniated disc
and generate
Slide13DISCO-RADICULAR CONFLICT
COMPARTMENT SYNDROME
I
IN THE NERVE ROOT AND IN THE GANGLION
Slide14DISCO-RADICULAR CONFLICT
THIS LEADS TO EXTRINSIC COMPRESSION ON THE
ROOT
Slide15DISCO-RADICULAR CONFLICT
FIBROSIS
MECHANICAL INJURY
OEDEMA
VENOUS STASIS
FIBRINOLITIC DEFICIT
Slide16Mechanisms of Action of Ozone
Mechanical:
Stimulates disruption of intra/inter – molecular
valencies
and leads to collapse of the 3D structure of
proteoglycans
and collagen of the disc. with features of nucleus
pulposus
matrix
dehydratation
and signs of regression (so called “disk mummification”).
Slide17Mechanisms of Action of Ozone
Biochemical:
Strongly stimulating the local production of antioxidant enzymes
Intra- and trans-tissue oxygenation in the diseased site with reduced hypoxia and venous stasis.
Reduction of the cell-mediated process inhibiting proteinases release and an increase of the
immunosupressor
cytokines
Inhibition of inflammatory inducers (PPL) and pain-producing mediators ( ozone inhibits
sinthesys
of
prostaglandines
, liberation of
bradikinines
and other pain inducing products, secretion of proteinases from
macrofages
and polymorphous
neutrophyles
).
Slide18Mechanisms of Action of Ozone
Some studies on
histologic
disc
specimenns removed during open discectomy
confirmed the direct effect of Ozone on the mucopolysaccharides
making up the nucleus
pulposus
of the ruptured disc of water molecules and shrinkage of the
disc,exerting
compression on the nerve root.
Direct:
Slide19Ozone Injection
THROUH ALL THESE EFFECTS,OUR AIM IS TO OBTAIN
-DISC DEHIDRATATION
- NERVE METABOLISM CORRECTION
- PAIN RELEIF
Slide20O2-O3 Intradiscal Injection
Slide21O2-O3 Intradiscal Injection
Slide22Technique
Lateral position
Posterolateral
extraarticular
approach
Fluoroscopic C-arm system
Paralleling the vertebral plates
on AP and lateral
proections
Technique
-
Chiba needles 20G
-50 cc syringe
-Sterile drapes
Slide24Ozone Generators
Slide25Procedure
Paralleling The Needle
Slide26Procedure
Puncture of the disc
Slide27Procedure
Intradiscal
infiltration (Ozone discography)
Slide28Procedure
Epidural ozone diffusion
Slide29Procedure
Intraforaminal
injection of Local
Anesthetic(
Chirocaine
, Dexametasone and
Methylprednizolone
Procedure
Sterile draping
Slide31Indications
-Low back pain and/or nerve root pain resistant to previous medical treatment, physiotherapy and other therapies at least 3 month
-
Paresthesia
or hypoesthesia over the dermatome involved, mild muscle weakness and signs of root-ganglion irritation without motor loss.
-CT and/or MR signs of small and medium-sized herniated discs correlating with the patient’s symptoms with or without degenerative disease complicated by
intervertebral
disc changes –protrusion or
herniation
-FBSS-residue of surgical
discetomy
with
herniation
recurrence and/or hypertrophic fibrous scarring
Slide32Contraindications:
Favism
(G6PD deficiency)
Pregnancy
Disc
herniation
on CT/MRI corresponding to clinically severe motor deficit and/or sphincter disturbance
Free
discal
fragment
Severe spinal
stenosis
Spinal instability
-Severe
spondylosis
with development of big
osteophytes
Slide33Matherials and methods
For the period 2008 - 2014 , 3049 patients underwent
percutaneous
injection of O2-O3 mixture for treatment of symptomatic disc
herniations.All
patients had CT/MRI,and complained of back pain and leg
pain.The
patients were divided in four groups:
Group 1: L4-L5 or/and L5-S1
herniations
Group 2: Multiple level herniated discs
Group 3: Degenerative Disease complicated by
herniation
Group 4: Failed Back Surgery Syndrome(FBSS)
Slide34Results
The results after procedure were evaluated by
modified Mc Nab
method,VAS
and Oswestry Disability Index.
Group 1
excellent
80,2%
good
13,1%
poor
6,7%
( 93,3)
Group 2
excellent
75,6%
good
15,5%
poor
9,9%
( 91,1)
Group 3
excellent
49,1%
good 22,7 %
poor 28,2% (71,8)
Group 4 excellent 44,5% good
23,7% poor 31,8% (68,2)
Slide35Case 1
Before 4 months later
Slide36Case 2
Before 3 months later
Slide37Case 2
Before 3 months later
Slide38Case 3
Before 6 month later
Slide39Before 6 month later
Case 3
Slide40Case 4
Before 7 months later
Slide41Case 4
Before 7 months later
Slide42Case 5
Slide43Slide44Slide45Complications
NO Cases Of adverse reactions
NO Cases Of
spondylodiscitis
NO Cases Of root injury
Slide46Complications
Early-immediately after infiltration
Hypotension
Bradicardy
0,4%
Collaps
Late
Fibrotisation
over the site of infiltration
0,1%
Conclusion
Oxygen-ozone treatment of herniated disc is an effective and very safe procedure
Pain and functional results are similar to the outcomes for herniated discs treated with classic surgical
discectomy
Complication rate is extremely lower (<0,1 %)
Recovery time is significantly shorter
No need for general
anestesia
Do not modify normal spinal anatomy
Avoids bone demolition
Minimize
peridural
scarring
Conclusion
The O2-O3
intradiscal
injection is:
SAFE
No lesions of intrevertebral
disc and surrounding tissues
No
peridural
cicatrisation
No skin incision-lowered risk of infection
No muscle damage-no postoperative pain
No bone loss-no spinal instability
Do not except or impede open surgery if it is necessitated.
Slide49THANK YOU