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Arthritis in Children
Arthritis in Children
Asist.univ.Dr.Alexis Cochino
Definition. Causes.
inflammation of a joint/multiple joints due to:
Trauma Infection (septic/reactive arthritis) Autoimmunity Malignancy
Definition. Causes.
inflammation of a joint/multiple joints due to:
Trauma Infection (septic/reactive arthritis) Autoimmunity Malignancy
Causes
Developmental dysplasia (of the hip Other developmental conditions Trauma (abused child!) Infections
osteomyelitis, septic arthritis reactive arthritis, Lyme
JIA Other connective tissue disorders (SLE, Kawasakys) Clotting disorders Malignancy Referred pain Sickle cell crisis Overuse syndromes (in athletes)
JIA/JRA
chronic idiopathic arthritis>6 months synovial joints ~50% persistence at 10y Classification
1. Oligoarticular: <5 joints (~50%; F>M)
Persistent: <5 joints involved during the duration of followup. Extended: >4 joints involved during the duration of followup.
2.
3.
Systemic (fever, salmon-pink rash, lymphadenopathy, hepatosplenomegaly) (~10%; M>F) Psoriatic arthritis Entesitis related arthritis (inflammation at insertion of tendons, ligaments or fascia to bone; lower axial skeletal involvement; HLAB27 often present) Unclassified
4. 5.
6.
Diagnosis
Clinic+lab test (may be normal)+US/MRI/bone scans XR normal until late (50% focal bone mass); periosteal detachement earlier
Rheumatic fever
previously common (mid 1900s) post Strep A infection (pharyngeal/skin) Diagnosis criteria (modified Jones criteria, 1992)
Major
Polyarthritis Carditis Subcutaneous nodules Erythema marginatum Sydenham's chorea Fever Arthralgia ESR or CRP WBC PR interval culture / rapid Strep atg ASO previous RF
Minor
Strep.A inf.prove
D+: 2M/1M+2m + Strep.inf.prove Heart valve destruction (mitral>>aortic>tricuspid) Joint deformity (repeated attacks)
Sequellae
http://www.youtube.com/watch?v=HOalYWvVLU8&feature=related
Some numbers
Septic arthritis
1/5000 children
JIA
~5 prevalence of pediatric arthritis ~20 arthritis-related ambulatory care visits/1000 children/year ~1% of all hospitalizations ~ 1 death/million children/year
Presenting reason
Bone/joint signs:
Assymetry Limp Pain Joint effusion Function impairment (decreased ROM) Redness Fever Shivers Rashes Lymphadenopathy Hepatosplenomegaly
History
Age, sex Onset First time/recurrent Mono/poly articular Symptoms pattern Recent trauma/infection Systemic symptoms:
e.g. fever, weight loss, shivers, sweats
Clinical evaluation
Temperature Rash, throat, lips, tongue Subcut. nodes Lymph nodes Liver, spleen
Clinical evaluation
Limbs symetry Gait Look for foreign body
Clinical evaluation
Joint(s):
Tender, red, hot, swollen ROM No. of aff. joints Preferred position
Clinical evaluation
looking for joint effusion/tenderness
patellar tap test
metacarpophalangeal joints
bulge test
Lab tests
Blood
CBC+diff. ESR, CRP LDH Hb ELFO Uric acid Serology
Borrelia Strep
Synovial fluid
Aspect, viscosity Cells Chemistry Crystals Cultures
Stools:
Blood, cultures
Urine:
Urinalyses Culture Rapid atg tests
Pharyngeal swab
Culture Rapid Strep test
Clinical consultations
ophtalmology: q3-6 months ( in any JIA, but esp. oligoarticular JIA with ANA+)
Clinical consultations
orthopedics surgery hemato/oncology cardiology (ECG prolonged PR interval; heart US valves, coronary aa.) neurology (headache, chorea, ataxia) metabolic disorders
Imagistic studies
Ultrasound
Fast, mobile, pain-free, no X rays Use in:
Septic/reactive/AI/hemorrhagic
Early signs:
Effusion Hyperemia Soft tissue swelling
disadv.:
Operator-dependent Low resolution
Imagistic studies
MRI
Accurate, pain-free, no X rays Use: any arthritis Early signs:
Effusion Hyperemia Soft tissue swelling Bone/cartilage lesions
Time-consuming, expensive
Imagistic studies
XR:
Fast, largely available Use:
Chronic diss. Trauma Developmental
Imagistic studies
Bone scans
Use:
Prolonged evolution w/o localisation sympt/signs Paget, tumors, early osteomyelitis/avascular necrosis
Disadv.:
Low availability Expensive Radiation Very low resolution
Differentials
Developmental dysplasia (of the hip); risk factors:
first child, female, breech position, family history
Developmental
Slipped capital femoral epiphysis (M>F) Aseptic bone necrosis (Legg-Calve-Perthes disease; 3-10 yo; M>F)
Infections (osteomyelitis, septic arthritis) Infection-related arthritis (RF, Lyme) JIA Other connective tissue disorders (SLE, Kawasakys) Haemarthrosis Malignancy (leukemia, sarcoma, neuroblastoma) Referred pain (from inflam.process, e.g.appendicitis, psoas abscess) Sickle cell crisis Overuse syndromes (in athletes)
Not-to-be-overlooked !!!
(or delayed!)
Developmental dysplasia (of the hip) Developmental
Slipped capital femoral epiphysis Aseptic bone necrosis (Legg-Calve-Perthes disease) Sprain, contusion Fractures Osgood-Schlatter disease (patellar tendon insertion into the tibial tubercle) Patellofemoral syndrome
Trauma
Infections (osteomyelitis, septic arthritis) Infection-related arthritis (RF, Lyme) JIA Other connective tissue disorders (SLE) Malignancy (leukemia, sarcoma, neuroblastoma) Referred pain (from inflam.process) Sickle cell crisis Overuse syndromes (in athletes)
Treatment
Trauma ortho social services Haemarthrosis:
FFP, clotting factor antibiotics surgery
Septic arthritis
emergency start of i.v. antibiotics (staph, strep, pneumo, H.flu, E.coli, pseudomonas, kingella) total 4-6 weeks (7-10 days parenteral) surgery
Sicklemia:
emergency fluids and analgesics hematology
Treatment of JIA
Kynesitherapy Early arthritis concept Every drug used: the lowest efficient dose!! NSAIDs:
Ibuprofen, naproxen, diclofenac With meals!!! Attn: AEs (gastric, renal, cardiac, skin, lung)
CS:
p.o., i.v., puls therapy AEs (metabolic, CV, bone, eyes, gastric)
DMARDs:
Metothrexat, leflunomide, antimalarials, sulfasalazine AEs: liver, blood, eyes, skin
Biologics
Monoclonal antibodies (TNFa, Il-6, Il-1, CTLA-4) AEs: infections (TB especially; prior TB screening MANDATORY)