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Updates in management of
Osteoarthritis
AHMED YOUSSEF
MUBARAK ALKABEER HOSPITAL
KUWAIT
Introduction
✦In the absence of a cure for
osteoarthritis, current therapeutic
modalities are primarily aimed at
reducing pain and improving joint
function by targeting symptom relief,
without facilitating any improvement in
the joint structure itself.
Introduction
✦Treatment plans should never be
defined rigidly based on X-ray
appearance of the joint, but instead
remain flexible so that they can be
altered in line with functional and
symptomatic responses obtained.
Non-pharmacological treatments
✦ SELF-MANAGEMENT AND EDUCATION
✓ Offer information on the natural history of
arthritis and provide resources for social support
and instructions on coping skills.
✓Recent data indicate that intensive dietary
restriction plus exercise safely achieved a mean
long-term (18 months) weight loss of 11.4% and
yielded a 50% improvement in osteoarthritis
Non-pharmacological treatments
✦EXERCISE:
✓ Is essential for all people with knee osteoarthritis,
irrespective of disease severity, age, comorbidity.􏰑􏰑􏰑􏰑
􏰑􏰑􏰑􏰑􏰑􏰑􏰑􏰑 􏰑􏰑 􏰑􏰑􏰑􏰑􏰑􏰑􏰑􏰑􏰑􏰑􏰑
✦ASSISTIVE DEVICES:
✓Alter the lower limb biomechanics in such a way as to
limit the exposure of one or more knee compartments
to potentially damaging and provocative mechanical
stresses.
Pharmacological treatments
✦Simple analgesics
✦NSAIDs
✦ Disease Modification Therapy
✦Symptomatic slow-acting drugs in osteoarthritis
(SYSADOAs).
✦Intra-articular therapies (corticosteroids,
hyaluronic acid)
✦Newer modalities (PRPs, MSCs, ASCs)
Disease Modification Therapy
Zoledronic acid
Risedronate sodium
Oral salmon calcitonin
Anakinra (IL1 - )
Eptoterminalfa (BMP)
PG-530742 (MMP -)
Icatibant (Bradykinin -)
Infliximab (TNF -)
Adapted from Hunter [64]. © 2010, rights managed by Nature Publishing
Group.
Disease Modification Therapy
Disease Modification Therapy
ymptomatic slow-acting drugs in
osteoarthritis (SYSADOAs).
✦Actions:
✓ Alleviate the symptoms of pain and functional
impairment.
✓ Evidence of a disease 􏰑􏰑􏰑􏰑􏰑􏰑􏰑􏰑􏰑modifying effect
on longterm.􏰑􏰑􏰑􏰑􏰑 􏰑􏰑 􏰑􏰑􏰑
✦Types:
✓ Glucosamin, Chondroitin sulpahte, Glucosamine plus
Glucosamine
✦Glucosamine is shown to induce reversal of pro
inflammatory and joint degeneration effects of IL1
on osteoarthritic cartilage and chondrocytes.
✦ A Cochrane review of 25 randomized controlled
trials (RCTs) of all glucosamine formulations in
4,963 OA patients overall failed to show any
benefits of glucosamine for pain.􏰑􏰑􏰑 􏰑􏰑􏰑􏰑􏰑􏰑 􏰑
􏰑 􏰑􏰑􏰑􏰑􏰑􏰑􏰑􏰑􏰑􏰑􏰑 􏰑􏰑􏰑 􏰑􏰑􏰑􏰑
Chondroitin sulphate
✦CS is reported to elicit anti-inflammatory effects, an
increase in type II collagen and proteoglycans, a
reduction in bone resorption and better
anabolic/catabolic balance in chondrocytes.
✦CS may also offer benefits on joint structure changes
in patients with mild to moderate disease. From
pooled results of three clinical trials of 2-year duration,
CS was shown to have a small 􏰑􏰑􏰑but significant
effect on the rate of decline in minimum 􏰑􏰑􏰑􏰑􏰑􏰑􏰑􏰑
Diacerein
✦Diacerein is an anti anthraquinone derivative with anti
inflammatory activity against IL1, anti catabolic and
pro anabolic effects on cartilage and synovial
membrane.􏰑
✦A Cochrane review of 6 RCTS of 1283 participants
that diacerin has a small but beneficial effect on
overall pain at 3–36 months, equivalent to a 9%
reduction in pain.
✦The safety of diacerein was called into question
Avocado Soyabean Unsaponfiable (ASU)
✦ASU is a complex mixture of many
natural vegetable extracts taken from
avocado and soybean oils, including fat-
soluble vitamins, sterols, triterpene
alcohols and furan fatty acids.􏰑􏰑
✦ In clinical studies over 3-6 months,
some improvement in pain, stiffness
and physical function has been
demonstrated with ASU (300 mg/day),
leading to a reduced need for
Intra-articular Ortho-biologic
Therapies
✦Actions:
✓Anabolic and anti-catabolic molecules that modify
arthritic or regenerative process.
✦Types:
✓Corticosteroids
✓HA
✓PRPs
✓MSCs
✓Adipose autologous tissues (ASCs)
Corticosteroids
✦Widely used.
✦However, a Cochrane review found that the
reduction in pain lasts for only 1–2 weeks.
✦Given this short duration of benefit, high cost and
potential adverse effects, corticosteroid may not be
merited in a chronic disease such as osteoarthritis.
✦Furthermore, repeat administration every three
months doesn’t appear to provide clinical benefit at
2 years with suggestion of MRI Increased cartilage
HA
✦The use of HA has been extensively
researched.
✦Recent meta-analysis found that the trials
are generally of low quality and that HA is
associated with a small and clinically
irrelevant reduction in pain but an
increased risk of serious adverse events.
PRPs
PRPs
✦Advantages of PRPs:
✓Reduction of pain
✓Anti-inflammatory
✓Anti-infective
✓Matrix Synthesis
✓Chondrogenesis
PRPs versus HA
Pluripotent MSCs
✦ Unspecialized
cells with self
renewal
potential and
able to
differentiate into
various adult
cells.
Pluripotent MSCs
✦Recruit other stem cells.
✦Secrete bioactive factors
✓Angiogenesis
✓Mitosis
✓Anti-scaring
✓Anti-apoptotic
✦Local modulation
✓Anti-inflammatory
✓Immunomodulatory (reduced T cell surveillance)
MSCs
✦Where? Bone marrow, adipose tissue,
synovium
✦ What? Concentrated or Expanded.
✦ How? Interarticular injection.
✦Where?
✓BMC(Iliac crest, Proxiaml tibia, proximal
humorous)
BMAC
Adipose stem cells (ASCs)
✦During the past decade, researchers have
explored the regenerative potential of
mesenchymal stem cells derived from
adipose tissue in the treatment of OA.
✦Lipogems is one such system where the
adipose tissue is mechanically
microfragmented and washed until free of
pro-inflammatory oil and blood residues.
Blue Party
Adipose stem cells (ASCs)
✦Adipose tissue consists of 100–
500 folds higher number of stem
cells compared to bone marrow
✦FDA approved on 2014 but level
one evidence is still lacking.
✦Donor site morbidity.
Take Home Message
✦Although guidelines showed that the newer
modalities of treatment of OA is lacking a good
based evidence, these modalities are being
extensively used depending on personal
preference and experience.
✦There is still a need for bigger randomized
controlled trials with little bias to consider these
modalities as one of the cornerstones in
Updates in managment of osteoarthritis.

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Updates in managment of osteoarthritis.

  • 1. Updates in management of Osteoarthritis AHMED YOUSSEF MUBARAK ALKABEER HOSPITAL KUWAIT
  • 2. Introduction ✦In the absence of a cure for osteoarthritis, current therapeutic modalities are primarily aimed at reducing pain and improving joint function by targeting symptom relief, without facilitating any improvement in the joint structure itself.
  • 3. Introduction ✦Treatment plans should never be defined rigidly based on X-ray appearance of the joint, but instead remain flexible so that they can be altered in line with functional and symptomatic responses obtained.
  • 4. Non-pharmacological treatments ✦ SELF-MANAGEMENT AND EDUCATION ✓ Offer information on the natural history of arthritis and provide resources for social support and instructions on coping skills. ✓Recent data indicate that intensive dietary restriction plus exercise safely achieved a mean long-term (18 months) weight loss of 11.4% and yielded a 50% improvement in osteoarthritis
  • 5. Non-pharmacological treatments ✦EXERCISE: ✓ Is essential for all people with knee osteoarthritis, irrespective of disease severity, age, comorbidity.􏰑􏰑􏰑􏰑 􏰑􏰑􏰑􏰑􏰑􏰑􏰑􏰑 􏰑􏰑 􏰑􏰑􏰑􏰑􏰑􏰑􏰑􏰑􏰑􏰑􏰑 ✦ASSISTIVE DEVICES: ✓Alter the lower limb biomechanics in such a way as to limit the exposure of one or more knee compartments to potentially damaging and provocative mechanical stresses.
  • 6. Pharmacological treatments ✦Simple analgesics ✦NSAIDs ✦ Disease Modification Therapy ✦Symptomatic slow-acting drugs in osteoarthritis (SYSADOAs). ✦Intra-articular therapies (corticosteroids, hyaluronic acid) ✦Newer modalities (PRPs, MSCs, ASCs)
  • 7. Disease Modification Therapy Zoledronic acid Risedronate sodium Oral salmon calcitonin Anakinra (IL1 - ) Eptoterminalfa (BMP) PG-530742 (MMP -) Icatibant (Bradykinin -) Infliximab (TNF -) Adapted from Hunter [64]. © 2010, rights managed by Nature Publishing Group.
  • 10. ymptomatic slow-acting drugs in osteoarthritis (SYSADOAs). ✦Actions: ✓ Alleviate the symptoms of pain and functional impairment. ✓ Evidence of a disease 􏰑􏰑􏰑􏰑􏰑􏰑􏰑􏰑􏰑modifying effect on longterm.􏰑􏰑􏰑􏰑􏰑 􏰑􏰑 􏰑􏰑􏰑 ✦Types: ✓ Glucosamin, Chondroitin sulpahte, Glucosamine plus
  • 11. Glucosamine ✦Glucosamine is shown to induce reversal of pro inflammatory and joint degeneration effects of IL1 on osteoarthritic cartilage and chondrocytes. ✦ A Cochrane review of 25 randomized controlled trials (RCTs) of all glucosamine formulations in 4,963 OA patients overall failed to show any benefits of glucosamine for pain.􏰑􏰑􏰑 􏰑􏰑􏰑􏰑􏰑􏰑 􏰑 􏰑 􏰑􏰑􏰑􏰑􏰑􏰑􏰑􏰑􏰑􏰑􏰑 􏰑􏰑􏰑 􏰑􏰑􏰑􏰑
  • 12. Chondroitin sulphate ✦CS is reported to elicit anti-inflammatory effects, an increase in type II collagen and proteoglycans, a reduction in bone resorption and better anabolic/catabolic balance in chondrocytes. ✦CS may also offer benefits on joint structure changes in patients with mild to moderate disease. From pooled results of three clinical trials of 2-year duration, CS was shown to have a small 􏰑􏰑􏰑but significant effect on the rate of decline in minimum 􏰑􏰑􏰑􏰑􏰑􏰑􏰑􏰑
  • 13. Diacerein ✦Diacerein is an anti anthraquinone derivative with anti inflammatory activity against IL1, anti catabolic and pro anabolic effects on cartilage and synovial membrane.􏰑 ✦A Cochrane review of 6 RCTS of 1283 participants that diacerin has a small but beneficial effect on overall pain at 3–36 months, equivalent to a 9% reduction in pain. ✦The safety of diacerein was called into question
  • 14. Avocado Soyabean Unsaponfiable (ASU) ✦ASU is a complex mixture of many natural vegetable extracts taken from avocado and soybean oils, including fat- soluble vitamins, sterols, triterpene alcohols and furan fatty acids.􏰑􏰑 ✦ In clinical studies over 3-6 months, some improvement in pain, stiffness and physical function has been demonstrated with ASU (300 mg/day), leading to a reduced need for
  • 15. Intra-articular Ortho-biologic Therapies ✦Actions: ✓Anabolic and anti-catabolic molecules that modify arthritic or regenerative process. ✦Types: ✓Corticosteroids ✓HA ✓PRPs ✓MSCs ✓Adipose autologous tissues (ASCs)
  • 16. Corticosteroids ✦Widely used. ✦However, a Cochrane review found that the reduction in pain lasts for only 1–2 weeks. ✦Given this short duration of benefit, high cost and potential adverse effects, corticosteroid may not be merited in a chronic disease such as osteoarthritis. ✦Furthermore, repeat administration every three months doesn’t appear to provide clinical benefit at 2 years with suggestion of MRI Increased cartilage
  • 17. HA ✦The use of HA has been extensively researched. ✦Recent meta-analysis found that the trials are generally of low quality and that HA is associated with a small and clinically irrelevant reduction in pain but an increased risk of serious adverse events.
  • 18. PRPs
  • 19. PRPs ✦Advantages of PRPs: ✓Reduction of pain ✓Anti-inflammatory ✓Anti-infective ✓Matrix Synthesis ✓Chondrogenesis
  • 21. Pluripotent MSCs ✦ Unspecialized cells with self renewal potential and able to differentiate into various adult cells.
  • 22. Pluripotent MSCs ✦Recruit other stem cells. ✦Secrete bioactive factors ✓Angiogenesis ✓Mitosis ✓Anti-scaring ✓Anti-apoptotic ✦Local modulation ✓Anti-inflammatory ✓Immunomodulatory (reduced T cell surveillance)
  • 23. MSCs ✦Where? Bone marrow, adipose tissue, synovium ✦ What? Concentrated or Expanded. ✦ How? Interarticular injection. ✦Where? ✓BMC(Iliac crest, Proxiaml tibia, proximal humorous)
  • 24. BMAC
  • 25. Adipose stem cells (ASCs) ✦During the past decade, researchers have explored the regenerative potential of mesenchymal stem cells derived from adipose tissue in the treatment of OA. ✦Lipogems is one such system where the adipose tissue is mechanically microfragmented and washed until free of pro-inflammatory oil and blood residues.
  • 27. Adipose stem cells (ASCs) ✦Adipose tissue consists of 100– 500 folds higher number of stem cells compared to bone marrow ✦FDA approved on 2014 but level one evidence is still lacking. ✦Donor site morbidity.
  • 28. Take Home Message ✦Although guidelines showed that the newer modalities of treatment of OA is lacking a good based evidence, these modalities are being extensively used depending on personal preference and experience. ✦There is still a need for bigger randomized controlled trials with little bias to consider these modalities as one of the cornerstones in