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Approach patient with
ARTHRITIS
DR. MOHAMMED O. AL-RUKBAN
Assistant Professor
Department of Family and Community Medicine
College of Medicine
King Saud University
Normal Joint..
Introduction..
 Causes include various self-limited
illness and disabling and life-
threatening.
 Is it Arthritis or Arthralgia?
 Musculoskeletal emergencies
(infection, sepsis, compartment
syndrome…).
Arthralgia..
 Fibromyalgia
 Bursitis
 Tendinitis
 Hypothyroidism
 Neuropathic pain
 Metabolic bone disease
 Depression
Monoarthritis..
 Trauma
 Infection:
 DGI ± Skin lesion.
 Nongonococcal bacterial infections: large joints.
 Mycobacterial and fungal infection.
 Crystal induced arthritis
 Monosodium Urate crystals (MPJ)
 Ca pyrophosphate dihydrate crystals (knee)
 Lyme disease
 Systemic Rheumatoid diseases:
 Seronegative spodyloarthropathy (Reactive arthritis, psoriatic
arthritis, Inflammatory BD..)
 Sarcoid periarthritis
 RA
 Osteoarthritis
Polyarthritis..
 Rheumatoid Arthritis
 Systemic lupus Erythrematosus
 Viral arthritis
 Reiter’s disease
 Psoriatic arthritis
 Reactive arthritis
Migratory Arthritis..
 Differential diagnosis:
 Rheumatic fever
 Gonococcemia
 Meningococcemia
 Viral Arthritis
 SLE
 Acute Leukemia
Rheumatic Fever..
 Majer Criteria:
1- Carditis 2- Polyarthritis 3- Chorea
4- Erythema Marginatum 5- Subcutaneous nodules
● Minor criteria:
1- Arthralgia 2- Ferver 3- Acute phase reactant
(ESR, CRP).
4- Prolong PR interval 5- Evidence of group A
streotococcal infection (AST, Throat culture…)
History.. Age
 <30= SLE, Ankylosis spodylitis,
Reactive Arthritis.
 30-50= RA, Systemic sclerosis, Gout.
 >50= OA, Pseudogout, PMR
 Any Age group= Psoriatic arthritis,
Enteropathic arthritis
History.. Sex
 >Female:
 SLE, RA, OA, Systemic sclerosis,
Ankylosis spodylitis, PMR.
 Male=Female:
 Psoriatic arthritis, Enteropathic
arthritis Pseudogout.
 >Male:
 Gout, Reactive Arthritis.
History.. Sx
 Site:
 Symmetrical= RA, SLE, Systemic sclerosis
 Asymmetrical=OA
 Large joints=OA
 DIP= OA, Psoriatic arthritis
 MCP, PIP= RA, SLE
 1st MTP= Gout, OA
 Spine= OA, Ankylosis spodylitis, Psoriatic arthritis,
Reactive arthritis
 Shoulder= PMR
History.. Sx
 Pain character:
 Aggravated by motion= Mechanical
 Relieved by motion= Inflammatory.
 Duration:
 <6 wks= viral arthritis, systemic rheumatic
diseases
 >6 wks=systemic rheumatic diseases
 Associated Sx:
 Morning stiffness: >1hr= RA, PMR, Inflammatory
>30 min= OA
History.. Sx
 Associated Sx:
 Multi-system involvement= Systemic
rheumatic diseases.
 Past Medical history:
 Trauma, fracture, surgical procedures…
 Medication list:
 Drug induced lupus.
 Diuretics.
Phy. Examination..
 Joint:
 Soft tissue swelling, warm, effusion…=
Inflammation.
 Inflammation signs extended= septic
arthritis, crystal induced arthritis, fracture.
 Passive motion (N), active(↓↓)= bursitis,
tendinitis, muscle injury.
 Passive motion (↓↓), active(↓↓)= Synovitis
Phy. Examination..
 General Examination:
 LAP, parotid enlargement, oral ulceration, heart
murmurs, pericardial or pleural friction rubs,
crackle…= systemic disease.
 Fever= infection, reactive arthritis, RA, SLE,
Crystal induced arthritis…
 Subcutaneous nodules= RA, RHD, Gout (tophi)
 Skin manifestations= psoriasis, RA, SLE…
 Eye disease (keratoconjunctivitis sicca, uveitis.
Conjunctivitis, episcleritis…)
Laboratory Studies..
 Can be misleading.
 Basic: CBC, Urinalysis, U&E, LFT.
 Acute phase reactant: ESR, CRP.
 Antibody tests:
 ANA= SLE
 Anti-dsDNA= SLE
 Anti-native DNA, anti-Sm= SLE
 RF= RA
 Anti-CCP antibody=RA
Rheumatoid Factor..
 Rheumatoid Arthritis
 Connective tissue diseases
 Viral infection
 Leishmaniasis
 Leprosy
 Tuberculosis
 Sarcoidosis
 Liver diseases
 Subacute bacterial endocarditis
Laboratory Studies..
 Uric acid concentration= Gout
 Synovial fluid analysis= infection,
crystal induced arthritis, inflammatory..
 Hepatitis B and C
 Parvovirus serology
Imaging Studies..
 X-ray:
 RA
 Chronic Gout
 OA
 Ankylosing spondylosis.
 MRI:
 Ankylosing spondylosis.
Rheumatoid Arthritis..
 Epidemiology :
 The world wide incidence of RA is
approximately 3 cases per 10,000
population and the prevalence rate is
approximately 1%
Rheumatoid Arthritis..
History..
 Malaise
 fever
 fatigue
 weight loss
 myalgias
 difficulty performing activities of daily
living
Examination..
 Joint affected
 swelling
 tenderness
 warmth
 decreased range of motion
 Atrophy of the interosseous
muscles
 deformities
Diagnosis..
 Morning stiffness
 Arthritis of 3 or more joint areas
 Arthritis of hand joints of at least one area
swollen in a wrist, MCP, or PIP joint
 Symmetric arthritis
 Rheumatoid nodules
 Serum RF
 Radiographic changes typical of RA
Deformities..
Extra-articular manifestations..
 Rheumatoid nodule
 Cardiovascular
 Pulmonary
 GI & Renal
 Hematological
 Skin
 Vasculitis
 Neurological
 Ocular
Progression of RA..
 Stage 1:
- no destructive changes.
- Osteoporosis.
 Stage 2:
- periarticular osteoporosis w/wo slight
subchondral bone destruction.
- joint mobility limit but no destruction.
- adjacent muscle atrophy.
- extra-articular soft tissue lesions.
Progression of RA..
 Stage 3
- cartilage and bone destruction in addition to
periarticular osteoporosis.
- joint deformity w/wo fibrous or bony ankylosis.
- extensive muscle atrophy.
- extra-articular soft tissue lesions.
 Stage 4
- criteria of stage 3.
- fibrous or bony ankylosis.
Laboratory ..
 Hematologic parameters
 Anaemia
 Thrombocytosis
 ↓ Serum iron & IBC
 ↑ Serum globuline
 ↑ ALP
 ↑ Acute phase reactant
 Immunological parameters
 Synovial fluid analysis
Prognosis..
 40 % of patient become disabled after
10 years.
 Persistent active cases more than 1
year likely to lead to joint deformities.
 Periods of activity cases have better
prognosis.
 Mortality rate 2.5 times than general
population
Systemic Lupus Erythrematosis
 Malar rash
 Discoid rash
 Photosensitivity
 Oral ulcers
 Arthritis
 Serositis
 Renal disease (proteinuria, cellular cast)
 Neurologic disease (seizure, psychosis)
 Hematologic disease
 Immunologic abnormalities
 ANA
Summary..
 Use of time.
 In one study: 60% of patients with early
synovitis diagnosed as:
 Rheumatoid Arthritis.
 Spondyloarthropathy.
 20% had a self limited arthritis.
 20% unclassifiable with good prognosis.
 In another study: 36% unclassifiable
 When to refer?
Approach_to_pateint_with_Arthritis.ppt

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Approach_to_pateint_with_Arthritis.ppt

  • 1. Approach patient with ARTHRITIS DR. MOHAMMED O. AL-RUKBAN Assistant Professor Department of Family and Community Medicine College of Medicine King Saud University
  • 3. Introduction..  Causes include various self-limited illness and disabling and life- threatening.  Is it Arthritis or Arthralgia?  Musculoskeletal emergencies (infection, sepsis, compartment syndrome…).
  • 4. Arthralgia..  Fibromyalgia  Bursitis  Tendinitis  Hypothyroidism  Neuropathic pain  Metabolic bone disease  Depression
  • 5. Monoarthritis..  Trauma  Infection:  DGI ± Skin lesion.  Nongonococcal bacterial infections: large joints.  Mycobacterial and fungal infection.  Crystal induced arthritis  Monosodium Urate crystals (MPJ)  Ca pyrophosphate dihydrate crystals (knee)  Lyme disease  Systemic Rheumatoid diseases:  Seronegative spodyloarthropathy (Reactive arthritis, psoriatic arthritis, Inflammatory BD..)  Sarcoid periarthritis  RA  Osteoarthritis
  • 6. Polyarthritis..  Rheumatoid Arthritis  Systemic lupus Erythrematosus  Viral arthritis  Reiter’s disease  Psoriatic arthritis  Reactive arthritis
  • 7. Migratory Arthritis..  Differential diagnosis:  Rheumatic fever  Gonococcemia  Meningococcemia  Viral Arthritis  SLE  Acute Leukemia
  • 8. Rheumatic Fever..  Majer Criteria: 1- Carditis 2- Polyarthritis 3- Chorea 4- Erythema Marginatum 5- Subcutaneous nodules ● Minor criteria: 1- Arthralgia 2- Ferver 3- Acute phase reactant (ESR, CRP). 4- Prolong PR interval 5- Evidence of group A streotococcal infection (AST, Throat culture…)
  • 9. History.. Age  <30= SLE, Ankylosis spodylitis, Reactive Arthritis.  30-50= RA, Systemic sclerosis, Gout.  >50= OA, Pseudogout, PMR  Any Age group= Psoriatic arthritis, Enteropathic arthritis
  • 10. History.. Sex  >Female:  SLE, RA, OA, Systemic sclerosis, Ankylosis spodylitis, PMR.  Male=Female:  Psoriatic arthritis, Enteropathic arthritis Pseudogout.  >Male:  Gout, Reactive Arthritis.
  • 11. History.. Sx  Site:  Symmetrical= RA, SLE, Systemic sclerosis  Asymmetrical=OA  Large joints=OA  DIP= OA, Psoriatic arthritis  MCP, PIP= RA, SLE  1st MTP= Gout, OA  Spine= OA, Ankylosis spodylitis, Psoriatic arthritis, Reactive arthritis  Shoulder= PMR
  • 12. History.. Sx  Pain character:  Aggravated by motion= Mechanical  Relieved by motion= Inflammatory.  Duration:  <6 wks= viral arthritis, systemic rheumatic diseases  >6 wks=systemic rheumatic diseases  Associated Sx:  Morning stiffness: >1hr= RA, PMR, Inflammatory >30 min= OA
  • 13. History.. Sx  Associated Sx:  Multi-system involvement= Systemic rheumatic diseases.  Past Medical history:  Trauma, fracture, surgical procedures…  Medication list:  Drug induced lupus.  Diuretics.
  • 14. Phy. Examination..  Joint:  Soft tissue swelling, warm, effusion…= Inflammation.  Inflammation signs extended= septic arthritis, crystal induced arthritis, fracture.  Passive motion (N), active(↓↓)= bursitis, tendinitis, muscle injury.  Passive motion (↓↓), active(↓↓)= Synovitis
  • 15. Phy. Examination..  General Examination:  LAP, parotid enlargement, oral ulceration, heart murmurs, pericardial or pleural friction rubs, crackle…= systemic disease.  Fever= infection, reactive arthritis, RA, SLE, Crystal induced arthritis…  Subcutaneous nodules= RA, RHD, Gout (tophi)  Skin manifestations= psoriasis, RA, SLE…  Eye disease (keratoconjunctivitis sicca, uveitis. Conjunctivitis, episcleritis…)
  • 16.
  • 17.
  • 18.
  • 19.
  • 20. Laboratory Studies..  Can be misleading.  Basic: CBC, Urinalysis, U&E, LFT.  Acute phase reactant: ESR, CRP.  Antibody tests:  ANA= SLE  Anti-dsDNA= SLE  Anti-native DNA, anti-Sm= SLE  RF= RA  Anti-CCP antibody=RA
  • 21. Rheumatoid Factor..  Rheumatoid Arthritis  Connective tissue diseases  Viral infection  Leishmaniasis  Leprosy  Tuberculosis  Sarcoidosis  Liver diseases  Subacute bacterial endocarditis
  • 22. Laboratory Studies..  Uric acid concentration= Gout  Synovial fluid analysis= infection, crystal induced arthritis, inflammatory..  Hepatitis B and C  Parvovirus serology
  • 23. Imaging Studies..  X-ray:  RA  Chronic Gout  OA  Ankylosing spondylosis.  MRI:  Ankylosing spondylosis.
  • 24.
  • 25. Rheumatoid Arthritis..  Epidemiology :  The world wide incidence of RA is approximately 3 cases per 10,000 population and the prevalence rate is approximately 1%
  • 27. History..  Malaise  fever  fatigue  weight loss  myalgias  difficulty performing activities of daily living
  • 28. Examination..  Joint affected  swelling  tenderness  warmth  decreased range of motion  Atrophy of the interosseous muscles  deformities
  • 29. Diagnosis..  Morning stiffness  Arthritis of 3 or more joint areas  Arthritis of hand joints of at least one area swollen in a wrist, MCP, or PIP joint  Symmetric arthritis  Rheumatoid nodules  Serum RF  Radiographic changes typical of RA
  • 30.
  • 31.
  • 32.
  • 33.
  • 34.
  • 36.
  • 37.
  • 38. Extra-articular manifestations..  Rheumatoid nodule  Cardiovascular  Pulmonary  GI & Renal  Hematological  Skin  Vasculitis  Neurological  Ocular
  • 39. Progression of RA..  Stage 1: - no destructive changes. - Osteoporosis.  Stage 2: - periarticular osteoporosis w/wo slight subchondral bone destruction. - joint mobility limit but no destruction. - adjacent muscle atrophy. - extra-articular soft tissue lesions.
  • 40. Progression of RA..  Stage 3 - cartilage and bone destruction in addition to periarticular osteoporosis. - joint deformity w/wo fibrous or bony ankylosis. - extensive muscle atrophy. - extra-articular soft tissue lesions.  Stage 4 - criteria of stage 3. - fibrous or bony ankylosis.
  • 41. Laboratory ..  Hematologic parameters  Anaemia  Thrombocytosis  ↓ Serum iron & IBC  ↑ Serum globuline  ↑ ALP  ↑ Acute phase reactant  Immunological parameters  Synovial fluid analysis
  • 42. Prognosis..  40 % of patient become disabled after 10 years.  Persistent active cases more than 1 year likely to lead to joint deformities.  Periods of activity cases have better prognosis.  Mortality rate 2.5 times than general population
  • 43. Systemic Lupus Erythrematosis  Malar rash  Discoid rash  Photosensitivity  Oral ulcers  Arthritis  Serositis  Renal disease (proteinuria, cellular cast)  Neurologic disease (seizure, psychosis)  Hematologic disease  Immunologic abnormalities  ANA
  • 44. Summary..  Use of time.  In one study: 60% of patients with early synovitis diagnosed as:  Rheumatoid Arthritis.  Spondyloarthropathy.  20% had a self limited arthritis.  20% unclassifiable with good prognosis.  In another study: 36% unclassifiable  When to refer?