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Ankylosing Spondylitis
DR NARESH SHETTY M.S.Ramaiah Medical College & Hospital. Bangalore
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Anklosing Spondylitis
Known also as Bechterew’s Disease Bechterew’s Syndrome Marie Strumpell Disease
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Etiology Chronic Inflammatory disease of unknown etiology.
Occurs in 6 per 10,000 population Male predominant ( 7:1) Autosomal inheritance, Incidence in relatives of affected subject is times that of general population
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Etiology 90% of patients have an association with HLA B27 antigen
Alternately presence of this antigen is associated with increased susceptibility to AS Lower frequency in Blacks
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The Cause of Ankylosing Spondylitis is unknown,
Causes of AS The Cause of Ankylosing Spondylitis is unknown, but a tendency to develop the condition may be Genetic
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Synovitis of Sacroiliac and vertebral facet joints
Pathology: Synovitis of Sacroiliac and vertebral facet joints Destruction of articular cartilage and periarticular bone Leads to bony ankylosis Costovertebral involvement can lead to diminished respiratory excursion
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Pathology Affects intervertebral discs, sacroiliac ligaments, symphysis pubis, manubrium sterni and bony insertion of large tendons Ant. Longitudinal ligament are especially affected Leads to bony bridging – bamboo spine
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Clinical Features: Starts insidiously
Teenager or young adult complains of low backache & stiffness or SI joint pain Symptoms are worse in the morning and after inactivity General fatigue, weight loss Involvement of hips, knees and shoulder There is symmetric involvement of large joints with changes in the hands which are similar but less severe than RA.
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Spine - Clinical Findings:
Loss of lumbar lordosis Later diminished spinal movement, increased thoracic kyphosis, loss of cervical extension Cervico-thoracic kyphosis is common Fused spine involvement of the appendicular skeleton (i.e. the limbs) is eventually seen in about 50% of the patients
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Other Clinical findings
May have diminished chest expansion due to involvement of costochondral & costovertebral joints B/L sacra-iliac joint involvement May involve Hip & Knee Joints Disease is slowly progressive over a few years with SI fusion, hip & Knee involvement and ankylosis of spine
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Associated features Extra-articular symptoms
Uveitis occurs in 25-40%. Need to be treated early or may cause visual impairment. Inflammatory bowel disease and/or psoriasis may be present Osteoporosis is a common feature Cardiac -aortic incompetence, cardiac conduction anomalies Chest Progressive, B/l apical cavitations/fibroses Asymptomatic GI inflammation present in 25-49% of Ankylosing Spondylitis
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Rome, 1961* Clinical Criteria
1. Low back pain and stiffness for more than 3 months, not relieved by rest 2. Pain and stiffness in the thoracic region 3. Limited motion in the lumbar spine 4. Limited chest expansion 5. History or of iritis or its sequelae 6.Radiologic Criterion - bilateral sacroiliac changes characteristic of Ankylosing Spondylitis
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Modified New York Classification -1984
Clinical Criteria Low back pain (3months) improved with exercise and not improved with rest. Limited movement of lumbar spine Chest expansion decreased < 2.5 cm Radiological criteria; Sacroiliitis grade> 2 bilateral or grade > 4 unilaterally Grade 0- Normal, Grade 1- suspicious, Grade 2- sclerosis with little erosion Grade 3- severe erosions Grade 4 – Complete Ankylosis Definite AS is present if radiological criteria is associated with at least one clinical criteria S
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To consider Ankylosing Spondyltis if:
Inflammatory spinal pain : Onset before age 40 Insidious onset Persistence for at least 3 months Morning stiffness that improves with exercise Chest pain Alternate buttock pain Acute anterior uveitis Other joints pain
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Progressive Disability
• Functional – Important predictors age, social support, lack of back exercise and smoking – Ward et al Arthritis Rheum 2002 Work AS patients 3X more likely than the normal population to leave the work force – Boonen et al Ann Rheum Dis 2001
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Diagnosis
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Laboratory tests Lab investigations
Raised ESR/CRP in 70% of AS, but no clear correlation with disease activity. Secondary anaemia Urinary 17-ketosteroids levels are increased HLA-B27 test: positive in most cases Synovial fluid : increase of mononuclear leukocytes ( in RA increase in polymorphonuclear leukocytes)
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HLA-B27: DISEASE ASSOCIATIONS
Ankylosing Spondylitis >90% Inflammatory Bowel Disease 50% Reiter's Syndrome 80 % Reactive Arthritis 85% Psoriatic Arthritis With Spondylitis 50% With Peripheral Arthritis 15% Whipple's Disease 30%
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Radiological findings-SI joint
• Initial changes are a bilateral sacroiliitis The stages of sacroiliitis are as follows; Initially affects lower and middle thirds of SI joint with the iliac side more severely affected Then sacral— periarticular osteoporosis, erosions and subchondral sclerosis Further erosion leads to widening of joints Progresses to bony ankylosis
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Radiological findings-Spine
Earliest vertebral change is flattening of the normal anterior concavity of the vertebral body (‘squaring’) Disease first affects lumbar spine and then ascends to thoracic spine affecting apophyseal joints,costotransverse joints, costovertebral joints and posterior ligaments.
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‘Bamboo Spine’ – bridging at several levels
Osteoporosis Hyperkyphosis of the thoracic spine
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X-RAY Cervical Spine Osteoporosis is a feature of longstanding disease. Because of the immobility and fragility of the spine. Cervical lordosis lost Ant. Bony bridging Cervical fractures following minor trauma are quite common. Unstable because they involve all three columns Atlantoaxial instability
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CT more sensitive than X-ray in detecting early changes
Radiology CT more sensitive than X-ray in detecting early changes MRI – useful to detect disease activity DEXA is useful for diagnosis of Osteoporosis Reliability of these Tests are still unclear
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MRI T1-Aweighted spin- echo image.
Erosions of vertebral-body endplates surrounded by low- signal-intensity bone-marrow oedema.
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Hip Joints Protrusio and hip flexion contractures are common.
Hip ankylosis Heterotropic ossification may follow THR; Heterotrophic ossification occurs in % of hip replacements and is more common with trochanteric osteotomy To avoid heterotropic ossification consider insertion of a cemented acetabular component followed by 750 rads around the component
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Treatment & Medications are available to reduce Symptoms & Pain
Management No Cure is known for AS Treatment & Medications are available to reduce Symptoms & Pain
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Management Combination of non-pharmocologic and pharmocological therapy depending on disease stage and symptoms Patient education essential- life long programme of exercise, use of individual, and group therapy as well as self-help groups Functional disability in AS progresses more rapidly in smokers and less so in those with better social support and regular exercises
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Three major Types 1.Anti-inflammatory 2.DMARDs 3. TNF Blockers
Medications Three major Types 1.Anti-inflammatory 2.DMARDs 3. TNF Blockers
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Anti-Inflammatory drugs
Control pain and counteract soft-tissue stiffness Reduces inflammation Includes NSAIDs such as Aspirin, ibuprofen, Indomethacin, naproxen, COX-2 inhibitors Cortisone effective in relieving pain & inflammation
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Has their own side effects
DMARD’S DMARD’s Such as Cyclosporines, methotrexate, Sulfasalazine, steriods Used to reduce immune system response through immunosupression Has their own side effects
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BIOLOGICS TNF-a blockers • Infliximab
TNF blockers have shown to be the most promising treatment , slowing the progress of AS in majority of cases They also have been effective in treating arthritis of joint but also the spinal arthritis associated with AS TNF-a blockers • Infliximab – IV 5mg/kg induction and 8 weekly intervals • Etanercept – SC 25mg/twice weekly • Humira
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Surgical Management Spinal correction for deformities
Spinal osteotomies; not easy Problems Positioning of patient Anaesthesia difficulty Injury to Cord Injury to major vessel like Aorta & Vena cava Cervical spine injury Paralytic Ileus
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Surgical Management Arthroplasty Surgery
THR ; Good pain relief, improves posture, improvement in range of movement Problems in surgery; Dislocation may be difficult, osteotomy of neck may be needed and head removed piecemeal. Edges of acetabulum need to be identified Heterotrophic ossification 20-40% TKR
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Rehabilitation Exercises Respiratory exercises Heat Therapy
Avoid excessive physical activity during acute phase
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Differential Diagnosis
Other Spondyloarthropathies Lumbar strain DISH(Forestier’s disease)- Degenerative joint disease Osteitis condensans illi(asymptomatic sclerosis of subchondral bone in parous women-only illiac area is involved)
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Complications Spinal fractures
Spine rigid + osteoporotic: Commonest site for fracture C5-7 Spinal Cord Compression , Atlanto-axial subluxation; Posterior Longitudinal Ligament Ossification Hyperkyphosis -may be difficult to lift head enough to walk and see Typical spinal ankylosis occurs after 10yrs Osteoporoses more likely in severe advanced, long- standing
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Prognosis Depends on stage at diagnoses & Initiation of effective therapy Worse in males Worse in patients poorly compliant with exercises Patients with peripheral arthritis take more sick leaves than those with axial involvement Worse for patients exposed to cold temperatures Worse in smokers, low socio-economic class
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Thank You
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