27 April 2009

Rheumatoid Arthritis



Rheumatoid Arthritis
Presentation by: Anand Lal, M.D.


Rheumatoid Arthritis

* Chronic systemic inflammatory disease of unknown etiology
* Affects the Synovial Membranes of multiple joints
* Prevalence 1-2%
* Female : Male ratio 3:1
* Usual age of onset 20-40 years though individuals of any age group may be affected
* Pathologic finding: chronic synovitis with pannus formation. The pannus erodes cartilage, bone, ligament and tendons. In the acute phase effusion and other manifestations of inflammation are evident; in the later stages ankylosis of the joint may set in. In both the acute and chronic phase, there may be widespread inflammation of the tissues around the joint that can lead to significant joint destruction.

* Clinical presentation
o usually presents insidiously;
o prodromal syndrome of malaise, weight loss and vague periarticular pain and stiffness may be seen
o less commonly, the onset is acute, triggered by a stressful situation such as infection, trauma, emotional strain or in the postpartum period.
o the joint involvement is characteristically symmetric with associated stiffness, warmth tenderness and pain
* Clinical Features
o the stiffness is characteristically worse in the morning and improves during the day; its duration is a useful indicator of the activity of the disease. The stiffness may recur especially after strenuous activity.
o the usual joints affected by rheumatoid arthritis are the metacarpophalangeal jts, the PIP jts, the wrists, knees, ankles and toes.
o Entrapment syndromes may occur especially carpal tunnel syndrome

* Labs
o Rheumatoid factor, an IgM antibody is seen in the sera of 75% of patients with rheumatoid arthritis. High titers of rheumatoid factor are associated with severe disease.
o Rheumatoid factor is also found in other diseases like syphilis, sarcoidosis, infective endocarditis, TB, leprosy, parasitic infections; in advanced age and in asymptomatic relatives of patients with rheumatoid disease.
o Antinuclear antibody are seen in 20% of patients with rheumatoid arthritis, though their titer is lower than in SLE

* Labs
o The ESR is elevated both in the acute and chronic phases of the disease
o a moderate anemia is often present which is usually hypochromic normocytic
o the white count is normal or slightly increased but leukopenia may occur, often in presence of splenomegaly (e.g., Felty’s syndrome)
o the platelet count is often elevated in proportion to the degree of joint inflammation
o joint fluid examination is valuable. The fluid is translucent to opaque and has between 3000 and 50,000 WBCs /microL. There are 50% or more polymorphonuclear leukocytes. The culture is negative.

* X-ray
o of all the laboratory tests, x-ray changes are most specific for rheumatoid arthritis. However, they are not sensitive and usually are negative during the first 6 months of the disease

* X-rays
o the earliest changes occur in the wrist or feet and consist of soft tissue swelling and juxta-articular demineralization. Later, diagnostic changes consisting of joint space narrowing and erosions develop. The erosions are first seen at the ulnar styloid and at the juxta-articular margin, where the bony surface is not protected by cartilage. Diagnostic changes also occur in the cervical spine with C1-2 subluxation, but this can take several years to develop.

* Differential Diagnosis
o Rheumatic fever: migratory arthritis, elevated ASO and dramatic response to Aspirin
o Systemic Lupus Erythematosus: Butterfly rash, discoid lupus erythematous, photosensitivity, alopecia, high titers of Anti Ds-DNA, renal and CNS disease
o Osteoarthritis: no constitutional manifestations and no evidence of joint inflammation
o Gouty Arthritis: usually monoarticular initially but can become polyarticular in the later years
o Pyogenic arthritis: usually monoarticular, fever and chills, abnormal joint fluid
o Chronic Lyme disease: commonly monoarticular and associated with positive titers
o Human Parvovirus infection: arthralgia more common than arthritis, rash may be present, serologic evidence of parvovirus B19 infection
o Polymyalgia rheumatica is associated with proximal muscle weakness and stiffness
o several cancers produce paraneoplastic syndromes including polyarthritis; e.g., hypertrophic pulmonary osteoarthropathy produced by lung and gastrointestinal cancers. Diffuse swelling of the palmar fascia has been associated with several cancers including ovarian cancer.

* Treatment
* Treatment (Disease Modifying Agents (DMARDs)
* Prognosis
Rheumatoid Arthritis.ppt

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Reactive Arthritis



Reactive Arthritis
Presentation by: Walter Eisenhauer MMS, PA-C

Reactive Arthritis

* Also known as Reiter’s syndrome
o Named after Hans Reiter, a German Physician in 1916
o Symptoms of Arthritis, Conjunctivitis, Non Gonococcal Urethritis following bouts of bloody dysentery
o > 75% HLA B27 positive
* Secondary immune reaction, in susceptible individuals, to primary infection:
o Yersinia
o Campylobacter
o Shigella
o Salmonella
o Chlamydia
* Classified as a seronegative spondyloarthropathy
* Occurs 2-4 weeks after inciting infection
* Most responsible organisms have an affinity for mucous membranes
* Terms Reactive Arthritis & Reiter’s Syndrome Synonamous
* First manifestation usually non gonococcal Urethritis
o occurs in both venereal and non venereal forms of the disease
o Mucopurulent discharge
o Dysuria
o Prostatitis
o Epididymitis
* Females
o Dysuria
o Vaginal discharge
o Purulent cervicitis
* Conjunctivitis
o follows urethritis by several days
o Sx often mild and transient
o acute anterior Uveitis possible
* Articular symptoms typically appear last
* additive
* oligoarticular
* lower limbs most common
* Keratoderma blennorrhagicum
* Circinate Balanitis

Glossitis/ Mucocutaneous Lesions
* Aortic Valve involvement 1-2% of cases
* Amyloidosis
* Neurologic complications
o peripheral neuropathies
o encephalopathy
o transverse myelitis

* Clinical course
o Normally limited course running 3-12 months
o 15% with prolonged relapsing arthritis
+ ? Relapse
+ ?Reinfection
o Ankylosing Spondylitis in 10% of cases
o Relation to HIV- probably due to increased risk of concurrent infection not HIV as initiator
* Laboratory findings
o Normochromic, normocytic anemia
o Leukocytosis
o Acute phase reactants:
+ ESR
+ C-reactive Protein
* HLA-B27 positive 75%
* Synovial fluid- highly inflammatory
* Sterile cultures- negative gram stain
* X-Ray reveals periostitis with eventual new bone growth
* Treatment:
Idiopathic Inflammatory Bowel Disease
Whipple’s Disease
Ankylosing Spondylitis
Ankylosing Spondylitis
Clinical Picture
Syndosmophytes
Patient Instructions

* No cure but can be well managed
* Education of patients =increased compliance
* Early diagnosis important
* NSAIDS Vocational support
* Exercise Screen first degree relatives
* Surgical measures
Treatment

Reactive Arthritis.ppt

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Rheumatologic Examination



Rheumatologic Examination
Presentation by:Walter Eisenhauer MMS PA-C

Approach to Disorders of the Joints
* Etiologies of Joint Pain
+ Traumatic
+ Infectious
+ Degenerative
+ Metabolic
+ Immunologic
+ Neoplastic

Diagnosis

* Based on
+ History
+ Physical
+ Lab
+ X-ray
* Origination of Joint Symptoms
+ Synovium Cartilage Periarticular structures
+ Inflammatory Non-inflammatory

History

* Duration of Joint Symptoms
* Rapidity of Development
* Self Limited Symptoms Vs Persistent
* Number and Location of Affected Joints
* Pattern of Affected Joints
+ Symmetric
+ Asymmetric
* Sequence of Joint Involvement
+ Additive
+ Migratory
* Pain at Rest/Following Exercise
* Gelling
* Precipitating Events-Illness
* Morning Stiffness
* Symmetric Distribution of inflammatory changes-RA
* Weight Bearing Joints After Exercise-DJD
* Migratory-Rheumatic Fever
* Additive-RA
* Persistent Low Back Pain in Young Man-Ankylosing Spondylitis
* Acute Inflammation-Infection/Crystal Deposition Disease
* Chills/High Fever
* Constitutional Sx-RA/Neoplasm/infections
* Medications-Pronestyl Induced Lupus


Past Medical History

* Hepatitis
* Rubella, Mumps, Parvovirus
* Reynauds
* Iritis-Ankylosing Spondylitis
* Inflammatory Bowel Disease

Social History

* Sexual Practices
* Work
* S/S Depression-Anxiety
* Stress
* Diet-CA++/Purines

Physical Examination

* Skin
+ Nodules on extensor surfaces
+ Psoriatic Rashes
+ Nails
+ Signs of Vasculitis
+ Mucocutaneous lesions of Reiters Syndrome
+ Eye Dryness

Examination of the Joints

* Examine even Unaffected Joints
* Examine Peri-Articular Surfaces
+ Atrophy Effusions Erythema
+ Palpation
* Establish Range of Motion
* Palpate Exact Location of Tenderness
* Temperature
* Assess Muscle Strength/Tone
* History will help guide complementary exams:
+ Risk for CA and Assoc Wt Loss-Examine high risk systems
+ Abdomen/Bowel Sx- Examine abdomen
+ Fever-Cardiac
+ Pulmonary Sx-Lung

Classification of Joints

* Synarthrosis-No Movement
+ Suture-Cranial
+ Synchondrosis-Epiphysis/Diaphysis
* Amphiarthrosis-Slight movement
* Diarthrosis-Synovial
* Ball and Socket Saddle-Thumb Carpal/MC
* Hinge Gliding-intervertebral
* Pivot-Atlantoaxial
* Condyloid-Wrist

Examination

* Waiting Room Diagnosis
* Inspect Gait
* Ability to Disrobe etc- good eval of ROM
* Inspect Muscles
* Goniometer for ROM

Motor Examination

* S.I.T.S.
+ Size-measure all major muscle groups
* upper/lower arms
* upper/lower legs
* Inspect for Involuntary Movements
* Evaluate Tone
* Strength Testing
+ 0-4 grading

Motor Strength Testing

* 0- No Movement
* 1-Slight Contraction
* 2-Full Range of Motion/No Gravity
* 3-Full Range of Motion/Gravity
* 4- Some resistance
* 5- Full Resistance

Examination of the Upper Extremities

* Shoulder
+ Inspect
* Contour
* Girdle
* Clavicles
* Scapulae
* Muscles-SITT/Biceps/Deltoid/Traps
* AC Joint
* Bicipital Groove
* Shoulder Shrug-Inspect for symmetry
* Abduction-180
* Adduction-50
* Internal Rotation(behind small of back)-90
* External Rotation(behind neck)-90

Elbow
Fibromyalgia Syndrome
Rheumatologic Examination.ppt

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