Samatha Madhavarapu. 21 m/o F with limping HPI Intermittent limp of R leg started 6 weeks ago....
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Transcript of Samatha Madhavarapu. 21 m/o F with limping HPI Intermittent limp of R leg started 6 weeks ago....
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Samatha Madhavarapu
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HPI• Intermittent limp of R leg started 6 weeks ago.• Constant limp since 3 days• Worse upon awakening• Stiffness in R knee.• Transient warmth and redness +• Not able to bear weight initially, improves over
2 hrs.• Was outdoors in Upstate at BBQ 8 weeks ago• No fever, rash, recent URI• No trauma, diarrhea,
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HPI Contd…PMH: NoneFH: grand father has seizure disorder. No
bone/joint problems Immunizations: UTDNKDAMeds: Tylenol PRN pain.Labs done 6 weeks ago: wbc7.6, 33.9/66.3,
ESR 18, xray R knee Normal.
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Physical ExamVital signs:HEENT : NormalHeart , Lungs ,Abdomen: NormalSkin: No rashR knee: decreased extension, no swelling, no
redness, no warmth.Other Jts: FROM.
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LABSBMP: 136/4.9/ 101/22/12/0.4/139/10.5Total Protein/ Albumin: 7.5/4.7LFT: 0.2/01, 38/19, 244CBC: 7.3/ 12/36.3/392ESR: 15
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Other LabsCRP: 0.2ANA negativeLyme Ab titre: 1.2Anti CCP antibody: 8.3HLA B 27: NegativeRF: 10.0Ultrasound of Knees: Small R knee jt effusion
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DD of Arthritis/extremity pain in Children
Rheumatic & Inflammatory Diseases
Seronegative Spondyloarthropathies
Infectious IllnessesReactive ArthritisImmunodeficiencies
Metabolic DisordersBone & Cartilage
DisordersNeoplastic DisordersHematologic
DisordersPain Syndromes
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Juvenile Rheumatoid ArthritisJRA most common rheumatic disease of
childhoodSynovitis of peripheral joints manifested as
swellingJRA is not a single disease, but a category of
diseases.It is a diagnosis of exclusion.
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Criteria for Classification of JRA Age of onset: < 16 yrs Arthritis in > or = 1 joint Duration of the Disease: > or = 6 weeks Onset type is defined by type of articular
involvement in the first 6 months after onset:
Poly arthritis: > or = 5 inflamed joints Oligo arthritis: < or = 4 inflamed joints Systemic Disease: arthritis with intermittent
fever
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Classification of Chronic Arthritis in Children
ACR, ELAR & ILAR classificationOnly ACR criteria have been
statistically validated.
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Characteristic ACR ELAR ILAR
Onset Types 3 6 6
Age of onset of arthritis < 16 yr <16 yr <16 yr
Duration of arthritis >= 6 wk
>= 3mn
>= 6wk
Juvenile Ankylosing Spondylitis
Doesn’t include
includes
Includes
Juvenile Psoriatic Arthritis
Doesn’t include
includes
includes
Inflammatory Bowel Disease
Doesn’t include
includes
includes
Exclusion of other diseases
YES YES YES
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Etiology• Unknown• Immunogenetic Susceptibility (Specific HLA
subtypes)• External Triggers - Viruses( EBV, Parvo virus B19, Rubella) - Host hyperreactivity to specific self
antigens(type 2 collagen) - Enhanced T-cell reactivity to bacterial
/mycobacterial heat shock proteins
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Epidemiology Incidence of JRA: 13.9/100,000 Sex: Pauci and poly articular disease more in girls Systemic onset –equal frequency in boys and girlsRace: Prevalence of JRA lower in Urban African –
American compared to Caucasians Oligo 40% newly diagnosed cases in Caucasians. Blacks with JRA were older and less likely to test
positive for ANA or to have uveitis, more likely to test positive for Ig M RF
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Pathogenesis• Synovitis: Villous hypertrophy & edema of
subsynovial tissues.• Vascular endothelial hyperplasia• Infiltration of mononuclear and plasma cells.• Pannus formation with erosion of cartilage and
bone.• Recriutment of T-cells specific to synovial non
specific antigens., facilitated by specific HLA types.
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Clinical FeaturesOnset insidious or abruptMorning stiffness and gellingEasy fatiguabilityJoint pain and swelling, limited joint movt,
mild /non erythematous.
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Oligoarthritis/Pauciarticular• Affects 4 or fewer joints• Typically larger joints (knees, ankles, wrists).• Starts with 1 joint• Monoarticular involvement of hip, upper
extremity large joints never presenting sign in JRA.
• If knee is affected-limping+, esp morning• Chronically- atrophy of extensor muscles of thigh,
tight hamstrings & knee flexion contractures.• Associated with HLA-DR8
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Polyarthritis/Polyarticular• Minimum 5 joints should be effected.• Both large & small jts of upper and lower
extremities• Resembles adult RA and HLA profile.• Associated with HLA –DR4• Rheumatoid nodules in severe form• Micrognathia- chronic TM joint disease• C-Spine involvement- atlantoaxial
subluxation
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Systemic Onset• Arthritis with visceral involvement• Characteristic intermittent spiking fevers to >/=
39c for >/= 2 weeks. • Febrile episode assoc with evenescent (< 1 hr)
macular rash, linear or circular, salmon colored ,2-5 mm, over trunk & proximal extremities.
• Koebner Phenomenon+• Arthralgia, myalgia• Hepatosplenomegaly,Lymaphadenopathy• Serositis/pericardial effusion• Photophobia (uveitis), irregular iris due to
synechiae
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LabsCBC with diff:
Lymphopenia,Thrombocytosis,microcytic anemia. Neutropenia is uncommon.
ESR: - Always elevated with systemic JRA. - Usually elevated with polyarticular but
within reference range in pauci articular. - When elevated, ESR helps to monitor
success of medical treatment
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Labs contdANA:Positive in 40-85% with oligo/poly articularUnusual with systemic onsetTiters do not correlate with disease
severity.Associated with increased risk of uveitisRF: Rare in systemic JRA. Marker of persistence of polyarticular JRA
into adulthood, devpt of rheumatoid nodules and poor functioning.
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Total protein and albumin: levels are often decreased during active disease
ALT test: to exclude hepatitis (viral or autoimmune) prior to starting NSAIDS
U/A: to r/o infection (trigger of JRA or transient postinfectious arthritis) and nephritis (seen in pts with SLE)
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ImagingX-ray: When 1 jt is affected , to r/o osteomyelitis or
septic arthritis. Soft tissue swelling, regional osteoporosis,
osteopenia, sub chondral bone erosions, narrowing of cartilage spaces, fusion of nueral arches.
MRI synovial inflammation, early minimal changes seen
Echo cardiography: Serositis
DEXA: osteopenia
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X rays
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ManagementMultidisciplinary Team for care of childrenCore Team:Parents and ChildPediatric RheumatologistPediatricianNurseSocial WorkerPhysical TherapistOccupational TherapistNutritionistOphthalmologist
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Main goal: maximize daily functioning , minimize drug toxicity
Key predictor of long term outcome is early diagnosis and referral to rheumatology team.
Diet: Include 3 servings of calcium rich foods
Activity: more active, better the prognosis
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NSAIDS• Used to treat all subtypes of JRA (40-60%
children show improvement).• Mean duration for anti-inflammatory effect in
JRA- 30 days• Most with pauci and few with poly respond to
NSAID alone . • Rofecoxib , celecoxib (selective Cox-2
inhibitors) ~ similar to naproxen effectiveness• Adverse : nausea, decreased appetite, abd
pain. Less gastritis.
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Methotrexate• Safest, most efficacious, least toxic of of 2nd
line agents for JRA.• Used in 60% patients with poly JRA• Inhibits DHFR, purine synthesis. • Pts unresponsive to PO MTX benefit from SC
or IM administration. • Well tolerated in children.• Pts who respond well have improved growth,
functionality, radiographic improvement.
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• For overwhelmingly inflammatory or systemic illness.• Bridge therapy for those who did not respond to conventional therapy• Ocular control of uveitis (drops or injections)• Intra articular use :initial therapy in pts with
only 1 or 2 joint involvement• Improvement in symptoms in 2-3 days,
which last for at least 6 mo in 60% and 1yr in 45%
Glucocorticoids
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Anti TNF alpha • Etanercept: Only one approved for children• Fusion protein with TNF receptor monomer fused to Fc portion of Ig G1.• Administered SC twice weekly used in active
polyarticular JRA who fail MXT therapy. • JRA assoc-chronic uveitis that is
inadequately responsive to steroid therapy.• Not to be used with h/o chronic infections• R/o TB before starting rx
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SulphasalazineImproved joint inflammation & labs
compared to placebo.GI irritation and rash.Steven johnson in pts with active systemic
JRA.CI in porphyria and G6PD deficiency
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Systemic JRA
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Prognostic features• Child with oligo: esp. girls, onset< 6yrs age
–chronic uveitis risk• Polyarticular: RF, rheumatoid nodules• Systemic onset: number of joints involved,
duration of inflammation, severity of arthritis.
• Limb length discrepancy, contractures,• Disability continues into adulthood in 20%• Chronic pain syndromes.• Psychological complications.
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LIVING WITH RHEUMATOID ARTHRITIShttp://www.youtube.com/watch?v=NqyB-
cTxvs8
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