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RHEUMATOIDRHEUMATOID
ARTHRITISARTHRITIS
 Persistent, symmetrical, deforming peripheral arthropathyPersistent, symmetrical, deforming peripheral arthropathy..
 Autoimmune diseaseAutoimmune disease characterised bycharacterised by persistent inflammatorypersistent inflammatory
synovitis.synovitis.
 Causative Antigen :Causative Antigen : HLA DR4HLA DR4 (Human Leukocyte Antigen DR4).(Human Leukocyte Antigen DR4).
PathophysiologyPathophysiology
• Dendritic cellsDendritic cells ‘pick’ the Antigen to present it to T-lymphocytes.‘pick’ the Antigen to present it to T-lymphocytes.
• Cellular immune response….But,Cellular immune response….But, immune complexesimmune complexes areare
formed within the joint.formed within the joint.
• PolymorphsPolymorphs are attracted to the synovial joints.are attracted to the synovial joints.
• Phagocytosis andPhagocytosis and sustainedsustained inflammationinflammation..
• Synovial hypertrophySynovial hypertrophy;; destruction of cartilage and bonedestruction of cartilage and bone..
• Persistent synovitis causes anPersistent synovitis causes an effusion of synovial fluid rich ineffusion of synovial fluid rich in
protein and inflammatory cellsprotein and inflammatory cells..
Clinical ManifestationsClinical Manifestations
 Fatigue, malaise, stiffness,Fatigue, malaise, stiffness, diffusediffuse musculoskeletal pain.musculoskeletal pain.
 Joint pain, stiffness, loss of functionJoint pain, stiffness, loss of function (joints cant be fully(joints cant be fully
extended or flexed).extended or flexed).
 Morning stiffness of joints, which improves slightly during theMorning stiffness of joints, which improves slightly during the
day only to return slowly and worsen at night.day only to return slowly and worsen at night.
 Soft tissue swelling and erosions (starts in the PIP joints andSoft tissue swelling and erosions (starts in the PIP joints and
gradually spreads).gradually spreads).
 Ulnar deviationUlnar deviation andand volar subluxationvolar subluxation..
 ‘‘Sausage-shaped’ fingersSausage-shaped’ fingers
 Boutonniere deformity, Swan neck deformity, Piano keyBoutonniere deformity, Swan neck deformity, Piano key
fingers, Z-thumbfingers, Z-thumb..
 Gradual worsening of all symptoms.Gradual worsening of all symptoms.
Complications of RA
 Mayo Clinic researchers have concluded from a study (1955)
that not only do people with rheumatoid arthritis have a higher
risk of coronary heart disease than the general population, they
have:
 more silent, unrecognized heart attacks.
 more sudden cardiac deaths.
 Interestingly, however, rheumatoid arthritis patients are much
less likely to complain of chest pain.
Laboratory investigationsLaboratory investigations
 Rheumatoid factor +Rheumatoid factor +
 Elevated ESR, IgM, IgG, WBCs and platelet count.Elevated ESR, IgM, IgG, WBCs and platelet count.
 Hypochromic normocytic anaemia.Hypochromic normocytic anaemia.
 Synovial fluidSynovial fluid – yellowish, watery and turbid (due to high WBC– yellowish, watery and turbid (due to high WBC
and low glucose content).and low glucose content).
 X-ray of wrist, hands and feet – erosion of joint margin loss ofX-ray of wrist, hands and feet – erosion of joint margin loss of
joint space due to cartilage erosion.joint space due to cartilage erosion.
Drug TherapyDrug Therapy
1]1] NSAIDsNSAIDs
• Ibuprofen 1.2 – 3.2 gms in 3 – 4 doses;Ibuprofen 1.2 – 3.2 gms in 3 – 4 doses;
• Piroxicam 20 mg in 1 or 2 doses;Piroxicam 20 mg in 1 or 2 doses;
• Indomethacin 50 – 200 mg in 3 doses.Indomethacin 50 – 200 mg in 3 doses.
DMARDsDMARDs (Disease Modifying Anti Rheumatic Drugs)(Disease Modifying Anti Rheumatic Drugs)
 MethotrexateMethotrexate
• Drug of choiceDrug of choice for those who don’t respond to NSAIDs.for those who don’t respond to NSAIDs.
• 7.5 – 20 mg once weekly7.5 – 20 mg once weekly..
• Side effects –Side effects – stomatitis, hepatitis and gastric irritationstomatitis, hepatitis and gastric irritation..
 Antimalarials [Hydrochloroquine sulphate]Antimalarials [Hydrochloroquine sulphate]
• 200 – 400 mg per day200 – 400 mg per day..
• Low toxicity (pigmentary retinitis is rare but fatal, causing visualLow toxicity (pigmentary retinitis is rare but fatal, causing visual
loss).loss).
 Gold SaltsGold Salts
• For thoseFor those who can’t tolerate methotrexatewho can’t tolerate methotrexate..
• 10 mg (110 mg (1stst
week) to 25 mg (2week) to 25 mg (2ndnd
week), followed by maintenanceweek), followed by maintenance
dose of 50 mg weekly for upto 20 weeks.dose of 50 mg weekly for upto 20 weeks.
• Side effects – dermatitis, stomatitis, proteinuria and neutropeniaSide effects – dermatitis, stomatitis, proteinuria and neutropenia
((these can be controlled by corticosteroidsthese can be controlled by corticosteroids).).
 Corticosteroids 10 mg per day.Corticosteroids 10 mg per day.
 SulphasalazineSulphasalazine
• 22ndnd
line drug.line drug.
• Start with 0.5 mg, increase weekly by 0.5 mg till patient feelsStart with 0.5 mg, increase weekly by 0.5 mg till patient feels
better (to a maximum of 3 mg).better (to a maximum of 3 mg).
• Can causeCan cause hemolysis in G6PD deficiency caseshemolysis in G6PD deficiency cases..
 AzathioprineAzathioprine
• Antimetabolite; for those not responding to gold orAntimetabolite; for those not responding to gold or
antimalarials.antimalarials.
• Start withStart with 1 mg / kg, increased to a maximum of 3 mg1 mg / kg, increased to a maximum of 3 mg..
 PenicillaminePenicillamine
• ForFor severe RAsevere RA cases.cases.
• 250 mg daily initially to a maximum of 0.75 – 1 g per day250 mg daily initially to a maximum of 0.75 – 1 g per day..
• Given between meals to enhance absorption.Given between meals to enhance absorption.
• Side effects – fever, rash,Side effects – fever, rash, oral ulcersoral ulcers,, aplastic anaemiaaplastic anaemia..
 Minocycline 250 mg per dayMinocycline 250 mg per day for mild cases.for mild cases.
 TRIPLE THERAPYTRIPLE THERAPY
Methotrexate + Hydrochloroquine sulphate + SulfasalazineMethotrexate + Hydrochloroquine sulphate + Sulfasalazine
DMARDs
 Methotrexate (Rheumatrex, Trexall)
 Hydroxychloroquine (Plaquenil)
 Sulfasalazine (Azulfidine)
 Intramuscular Gold
 Tumor Necrosis Factor Inhibitors :
• Etanercept (Enbrel), Adalimumab (Humira), Infliximab (Remicade)
 T-cell Costimulatory Blocking Agents : Abatacept (Orencia)
 B cell Depleting Agents : Rituximab (Rituxan)
 Interleukin-1 (IL-1) Receptor Antagonist Therapy : Anakinra (Kineret)
 Leflunomide (Arava)
 Other Immunomodulatory and Cytotoxic agents :
• Azathioprine (Imuran), Cyclophosphamide, Cyclosporine A (Neoral,
Sandimmune)
Secondary TherapySecondary Therapy
 Physiotherapy, Occupational therapy.Physiotherapy, Occupational therapy.
 Weight loss, Orthoses.Weight loss, Orthoses.
 Regular exercises.Regular exercises.
THANK YOU!!!

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Rheumatoid Arthritis in a nutshell

  • 2.  Persistent, symmetrical, deforming peripheral arthropathyPersistent, symmetrical, deforming peripheral arthropathy..  Autoimmune diseaseAutoimmune disease characterised bycharacterised by persistent inflammatorypersistent inflammatory synovitis.synovitis.  Causative Antigen :Causative Antigen : HLA DR4HLA DR4 (Human Leukocyte Antigen DR4).(Human Leukocyte Antigen DR4). PathophysiologyPathophysiology • Dendritic cellsDendritic cells ‘pick’ the Antigen to present it to T-lymphocytes.‘pick’ the Antigen to present it to T-lymphocytes. • Cellular immune response….But,Cellular immune response….But, immune complexesimmune complexes areare formed within the joint.formed within the joint. • PolymorphsPolymorphs are attracted to the synovial joints.are attracted to the synovial joints. • Phagocytosis andPhagocytosis and sustainedsustained inflammationinflammation.. • Synovial hypertrophySynovial hypertrophy;; destruction of cartilage and bonedestruction of cartilage and bone.. • Persistent synovitis causes anPersistent synovitis causes an effusion of synovial fluid rich ineffusion of synovial fluid rich in protein and inflammatory cellsprotein and inflammatory cells..
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  • 5. Clinical ManifestationsClinical Manifestations  Fatigue, malaise, stiffness,Fatigue, malaise, stiffness, diffusediffuse musculoskeletal pain.musculoskeletal pain.  Joint pain, stiffness, loss of functionJoint pain, stiffness, loss of function (joints cant be fully(joints cant be fully extended or flexed).extended or flexed).  Morning stiffness of joints, which improves slightly during theMorning stiffness of joints, which improves slightly during the day only to return slowly and worsen at night.day only to return slowly and worsen at night.  Soft tissue swelling and erosions (starts in the PIP joints andSoft tissue swelling and erosions (starts in the PIP joints and gradually spreads).gradually spreads).  Ulnar deviationUlnar deviation andand volar subluxationvolar subluxation..  ‘‘Sausage-shaped’ fingersSausage-shaped’ fingers  Boutonniere deformity, Swan neck deformity, Piano keyBoutonniere deformity, Swan neck deformity, Piano key fingers, Z-thumbfingers, Z-thumb..  Gradual worsening of all symptoms.Gradual worsening of all symptoms.
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  • 12. Complications of RA  Mayo Clinic researchers have concluded from a study (1955) that not only do people with rheumatoid arthritis have a higher risk of coronary heart disease than the general population, they have:  more silent, unrecognized heart attacks.  more sudden cardiac deaths.  Interestingly, however, rheumatoid arthritis patients are much less likely to complain of chest pain.
  • 13. Laboratory investigationsLaboratory investigations  Rheumatoid factor +Rheumatoid factor +  Elevated ESR, IgM, IgG, WBCs and platelet count.Elevated ESR, IgM, IgG, WBCs and platelet count.  Hypochromic normocytic anaemia.Hypochromic normocytic anaemia.  Synovial fluidSynovial fluid – yellowish, watery and turbid (due to high WBC– yellowish, watery and turbid (due to high WBC and low glucose content).and low glucose content).  X-ray of wrist, hands and feet – erosion of joint margin loss ofX-ray of wrist, hands and feet – erosion of joint margin loss of joint space due to cartilage erosion.joint space due to cartilage erosion. Drug TherapyDrug Therapy 1]1] NSAIDsNSAIDs • Ibuprofen 1.2 – 3.2 gms in 3 – 4 doses;Ibuprofen 1.2 – 3.2 gms in 3 – 4 doses; • Piroxicam 20 mg in 1 or 2 doses;Piroxicam 20 mg in 1 or 2 doses; • Indomethacin 50 – 200 mg in 3 doses.Indomethacin 50 – 200 mg in 3 doses.
  • 14. DMARDsDMARDs (Disease Modifying Anti Rheumatic Drugs)(Disease Modifying Anti Rheumatic Drugs)  MethotrexateMethotrexate • Drug of choiceDrug of choice for those who don’t respond to NSAIDs.for those who don’t respond to NSAIDs. • 7.5 – 20 mg once weekly7.5 – 20 mg once weekly.. • Side effects –Side effects – stomatitis, hepatitis and gastric irritationstomatitis, hepatitis and gastric irritation..  Antimalarials [Hydrochloroquine sulphate]Antimalarials [Hydrochloroquine sulphate] • 200 – 400 mg per day200 – 400 mg per day.. • Low toxicity (pigmentary retinitis is rare but fatal, causing visualLow toxicity (pigmentary retinitis is rare but fatal, causing visual loss).loss).  Gold SaltsGold Salts • For thoseFor those who can’t tolerate methotrexatewho can’t tolerate methotrexate.. • 10 mg (110 mg (1stst week) to 25 mg (2week) to 25 mg (2ndnd week), followed by maintenanceweek), followed by maintenance dose of 50 mg weekly for upto 20 weeks.dose of 50 mg weekly for upto 20 weeks.
  • 15. • Side effects – dermatitis, stomatitis, proteinuria and neutropeniaSide effects – dermatitis, stomatitis, proteinuria and neutropenia ((these can be controlled by corticosteroidsthese can be controlled by corticosteroids).).  Corticosteroids 10 mg per day.Corticosteroids 10 mg per day.  SulphasalazineSulphasalazine • 22ndnd line drug.line drug. • Start with 0.5 mg, increase weekly by 0.5 mg till patient feelsStart with 0.5 mg, increase weekly by 0.5 mg till patient feels better (to a maximum of 3 mg).better (to a maximum of 3 mg). • Can causeCan cause hemolysis in G6PD deficiency caseshemolysis in G6PD deficiency cases..  AzathioprineAzathioprine • Antimetabolite; for those not responding to gold orAntimetabolite; for those not responding to gold or antimalarials.antimalarials. • Start withStart with 1 mg / kg, increased to a maximum of 3 mg1 mg / kg, increased to a maximum of 3 mg..
  • 16.  PenicillaminePenicillamine • ForFor severe RAsevere RA cases.cases. • 250 mg daily initially to a maximum of 0.75 – 1 g per day250 mg daily initially to a maximum of 0.75 – 1 g per day.. • Given between meals to enhance absorption.Given between meals to enhance absorption. • Side effects – fever, rash,Side effects – fever, rash, oral ulcersoral ulcers,, aplastic anaemiaaplastic anaemia..  Minocycline 250 mg per dayMinocycline 250 mg per day for mild cases.for mild cases.  TRIPLE THERAPYTRIPLE THERAPY Methotrexate + Hydrochloroquine sulphate + SulfasalazineMethotrexate + Hydrochloroquine sulphate + Sulfasalazine
  • 17. DMARDs  Methotrexate (Rheumatrex, Trexall)  Hydroxychloroquine (Plaquenil)  Sulfasalazine (Azulfidine)  Intramuscular Gold  Tumor Necrosis Factor Inhibitors : • Etanercept (Enbrel), Adalimumab (Humira), Infliximab (Remicade)  T-cell Costimulatory Blocking Agents : Abatacept (Orencia)  B cell Depleting Agents : Rituximab (Rituxan)  Interleukin-1 (IL-1) Receptor Antagonist Therapy : Anakinra (Kineret)  Leflunomide (Arava)  Other Immunomodulatory and Cytotoxic agents : • Azathioprine (Imuran), Cyclophosphamide, Cyclosporine A (Neoral, Sandimmune)
  • 18. Secondary TherapySecondary Therapy  Physiotherapy, Occupational therapy.Physiotherapy, Occupational therapy.  Weight loss, Orthoses.Weight loss, Orthoses.  Regular exercises.Regular exercises.