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Musculoskeletal problems in children

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Kathy Bailey Consultant Paediatric Rheumatologist Coventry and Warwickshire * Etiology and pathogenesis unknown, therefore classification is abritary on clinical ... – PowerPoint PPT presentation

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Title: Musculoskeletal problems in children


1
Musculoskeletal problems in children
  • Kathy Bailey
  • Consultant Paediatric Rheumatologist
  • Coventry and Warwickshire

2
Why is it important?
  • Common
  • History and examination essential
  • Missed diagnosis permanent disability
  • Simple problems require confident diagnosis
  • Will become part of curriculum!

3
How do children present?
4
How do children present?
  • Limp
  • stiffness
  • swelling
  • pain
  • restriction of movement
  • change in activities
  • not using limb
  • colour change in limb
  • fever
  • rash
  • unwell

5
Whats wrong with them?
  • HISTORY!!!
  • Inflammatory
  • mechanical
  • non-organic/psychosomatic

6
Whats wrong with them?
  • HISTORY!!!
  • Inflammatory
  • mechanical
  • non-organic/psychosomatic
  • Acute or chronic

7
Whats wrong with them?
  • HISTORY!!!
  • Inflammatory
  • mechanical
  • non-organic/psychosomatic
  • Acute or chronic
  • EXAMINATION
  • objective signs

8
Whats wrong with them?
  • HISTORY!!!
  • Inflammatory
  • mechanical
  • non-organic/psychosomatic
  • Acute or chronic
  • EXAMINATION
  • objective signs
  • TESTS
  • ???

9
History
  • Age of child
  • Duration
  • Symptoms
  • Impact on activities
  • Joints affected
  • Family History
  • Antecedents
  • infection/trauma/
  • illness

10
History
  • Associated features
  • Constitutional
  • Fever
  • Rash
  • Muscle weakness
  • Eyes
  • Weight loss
  • GI
  • bruising
  • LN/mucusitis
  • ....etc
  • Age of child
  • Duration
  • Symptoms
  • Impact on activities
  • Joints affected
  • Family History
  • Antecedents
  • infection/trauma/
  • illness

11
Examination
  • Height and weight
  • Temp/pulse/BP
  • General observations
  • Rash
  • Systems examination
  • Urinalysis

12
Musculoskeletal examination
  • PaediatricGaitArmsLegsSpine
  • www.arc.org.uk

www.arc.org.uk/arthinfo/emedia.asp
13
Examination - musculoskeletal
  • LOOK
  • gait
  • swelling
  • deformity
  • rash/colour changes

14
Examination
  • FEEL
  • heat
  • swelling
  • tenderness

15
Examination
  • MOVE restriction
  • /- pain
  • muscle strength

16
Differential Diagnosis
Inflammatory Mechanical Psychosomatic
Pain /-
Stiffness /-
Swelling /- /-
Sleep disturbance /- -
Instability /- /-
Physical signs /- (or )
17

Inflammatory Mechanical Idiopathic
Infection Reactive Post Strep JIA Connective tissue diseases - SLE - JDMS - Scleroderma - Vasculitis Hypermobility Osteochondroses - osgood-schlatter - Scheuermanns - Perthes Chondromalacia patella Osteochondritis dissecans Slipped upper femoral epiphysis Pain amplification syndromes - Localised - Generalised Growing pains
18
Inflammatory Conditions
  • Acute

19
Septic Arthritis
  • Fever
  • Localised tenderness
  • hot
  • Painful to move
  • Raised inflammatory markers

20
Septic Arthritis
  • Fever
  • Localised tenderness
  • hot
  • Painful to move
  • Raised inflammatory markers
  • JOINT ASPIRATION

21
Septic Arthritis Joint Distribution
  • Site
  • Knee 39
  • Hip 25
  • Ankle 14
  • Elbow 12
  • Organisms
  • Staph Aureus
  • Tuberculosis
  • Salmonella in sickle cell disease

22
Missed Septic Arthritis Knee
23
Osteomyelitis of distal tibia
24
Reactive Arthritis
  • May be history of recent infection
  • Single or multiple joints
  • No systemic features
  • Resolves by 6 weeks
  • Important to consider alternative diagnoses

25
Henoch Schonlein Purpura
  • Reactive Vasculitis (small vessel)
  • Palpable Purpura
  • Arthralgia/Arthritis
  • Abdominal pain
  • Nephritis
  • Headaches

26
Malignancy
  • 1 of patients referred to paediatric
    rheumatology have underlying malignancy

27
Malignancy
  • Acute Lymphoblastic Leukaemia
  • Bone pain and arthralgia in 20-40
  • Suspect from history, exam, or blood count
  • Bone Marrow aspirate

28
Malignancy
  • Acute Lymphoblastic Leukaemia
  • Neuroblastoma
  • Commonest solid tumour under infants
  • Bone pain from secondary spread
  • Urinary excretion of catecholamine metabolites
    (VMA)

29
Malignancy
  • Acute Lymphoblastic Leukaemia
  • Neuroblastoma
  • Primary Bone tumour
  • Osteoid osteoma benign
  • osteosarcoma

30
Malignancy
  • Features to raise concern
  • Bone pain (night time)
  • Weight loss
  • Night sweats or fevers
  • Abnormal bloods
  • Xray changes

31
Malignancy
32
Kawasaki Disease
  • 5 of following
  • Fever gt5 days unresponsive to Abx
  • Non purulent conjunctivitis
  • lymphadenopathy gt1.5cm
  • Rash - polymorphous
  • mucosal changes
  • extremities
  • early - swelling/palmar erythema
  • late peeling
  • OR 4 plus coronary artery aneurysms

33
Early features
34
Late features
35
Late features
36
KD - management
  • Prevent late sequel of coronary artery aneurysms
  • Intravenous IVIG
  • Aspirin
  • initially high, anti inflammatory
  • then low dose, anti platelet

37
Inflammatory Conditions
  • Chronic

38
Whats in a name?
  • JIA Juvenile Idiopathic Arthritis
  • JRA Juvenile Rheumatoid Arthritis
  • JCA Juvenile Chronic Arthritis

39
Whats in a name?
  • JIA Juvenile Idiopathic Arthritis
  • JRA Juvenile Rheumatoid Arthritis
  • JCA Juvenile Chronic Arthritis

40
Juvenile Idiopathic Arthritis
  • JIA commonest rheumatic condition in childhood
  • 30 150 per 100,000
  • 10 years follow up
  • 1/3 achieve remission
  • 30 have severe functional limitations
  • Fantini et al, ACR 1996

41
Definitions
  • Disease of childhood onset
  • under 16 years
  • Persistence of arthritis
  • 1 or more joints
  • 6 or more weeks
  • Exclusion of other diagnoses

42
Classification
  • Defined by clinical features in first 6 months

43
Classification
  • Defined by clinical features in first 6 months
  • Oligoarthritis 1-4 joints
  • Persistent
  • Extended

44
Oligoarthritis
  • Girls gtboys
  • Younger age
  • Best prognosis

45
Oligoarthritis
  • Girls gtboys
  • Younger age
  • Best prognosis
  • Associated with uveitis

46
Classification
  • Defined by clinical features in first 6 months
  • Oligoarthritis 1-4 joints
  • Polyarthritis 5 or more joints
  • RF positive
  • RF negative

47
Classification
  • Defined by clinical features in first 6 months
  • Oligoarthritis 1-4 joints
  • Polyarthritis 5 or more joints
  • Psoriatic Arthritis
  • Arthritis AND psoriasis
  • OR
  • Arthritis plus 2 of
  • Nail pitting
  • Dactylitis
  • First degree relative with confirmed psoriasis

48
Classification
  • Defined by clinical features in first 6 months
  • Oligoarthritis 1-4 joints
  • Polyarthritis 5 or more joints
  • Psoriatic Arthritis
  • Enthesitis Related Arthritis
  • Arthritis AND enthesitis
  • OR
  • Sacroiliac pain and HLA B27

49
Classification
  • Defined by clinical features in first 6 months
  • Oligoarthritis 1-4 joints
  • Persistent
  • Extended
  • Polyarthritis 5 or more joints
  • RF positive
  • RF negative
  • Psoriatic Arthritis
  • Enthesitis Related Arthritis
  • Systemic Arthritis

50
Systemic Arthritis
  • Daily fever for at least 2 weeks duration
    (quotidian for 3 days)
  • Plus one or more of
  • Evanescent rash
  • Generalized lymphadenopathy
  • Hepatosplenomegaly
  • Serositis
  • Arthritis
  • EXCLUSION OF OTHER DIAGNOSES

51
Quotidian Fever Systemic Arthritis
52
Evanescent salmon pink rash Systemic Arthritis
53
Prognosis
  • Poor indicators
  • Polyarticular onset and course
  • Rheumatoid factor positive girls
  • Systemic disease with persistent features
  • Delay in starting effective treatment
  • Good indicators
  • Oligoarticular disease

54
Treatment
  • Goals
  • Disease remission
  • Symptomatic improvement
  • Stiffness
  • Pain
  • Joint range of movement
  • Prevent joint damage
  • Normal growth and development
  • Education and normal adolesence
  • Prevent eye damage from Uveitis

55
Therapeutic approach
  • Multidisciplinary team
  • Paediatric rheumatologist
  • Nurse specialist
  • Occupational Therapist
  • Physiotherapist
  • Social worker
  • Ophthalmologist
  • Podiatrist

56
Drug treatments
  • Anti inflammatory drugs
  • NSAIDs
  • Glucocorticoids
  • Disease modifying drugs
  • Methotrexate
  • Etanercept
  • New biologic agents for recalcitrant disease

57
Mechanical conditions
58
Perthes(Legg-Calve Perthes)
  • Avascular necrosis of the femoral head
  • usually 2-10 (peak 4-6) yrs.
  • 3-5 boysgirls
  • Bilateral 30

59
PerthesLegg-Calve Perthes
  • Imaging
  • Asymmetry in femoral heads
  • Consider MRI or Nuclear medicine if clinical
    suspicion is high

60
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61
Slipped Upper Femoral Epiphysis
  • 10-13 years old
  • Overweight boys
  • 25 bilateral within 18/12
  • Slip of femoral head through growth plate
  • (posteriorly and inferiorly)

62
Slipped Upper Femoral Epiphysis
  • Imaging
  • AP and (frog) lateral films needed
  • CT/ MRI in cases of difficulty

63
Klein line should intersect femoral head
64
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65
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66
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67
Non - Accidental Injury
  • Inappropriate history
  • Physical signs dont match story
  • Other concerning features
  • Concerns raised by others

68
Anterior knee pain
  • Chondromalacia patella
  • Adolescent girls
  • Painful knees - kneeling
  • - going up stairs

69
Anterior knee pain
  • Osgood-Schlatter disease
  • Adolescent boys
  • Pain and swelling at tibial tuberosity
  • Increased by exercise

70
Anterior knee pain
  • Osgood-Schlatter disease
  • Adolescent boys
  • Pain and swelling at tibial tuberosity
  • Increased by exercise
  • Tenderness /- swelling of tibial tuberosity
  • Pain on resisted extension of knee

71
Osgood Schlatter - Radiology
  • Clinical diagnosis
  • DO NOT XRAY

72
Hypermobility
  • Very common
  • May be generalised or localised
  • Frequently responsible for musculoskeletal pain

73
Flat feet
  • Common cause of lower limb pain
  • If symptomatic correct with good footware and
    insoles

74
Idiopathic Musculoskeletal pain
75
Growing pains
  • 25-40 of children!
  • 3-5 years and 8-12 years
  • Typical history

76
Growing pains - history
  • Wake during night with pain
  • Eased with massage
  • May be worse after active day
  • No daytime symptoms
  • No abnormal physical signs

77
Idiopathic pain syndromes
  • No identifiable inflammatory or mechanical
    condition
  • Chronic pain
  • Impact on daily activities
  • Average age 9 12 years
  • Girls gt boys
  • Disease of the developed world

78
Spectrum of condition
Localised idiopathic pain eg RSD
CFS/ME Fibromyalgia
Diffuse idiopathic pain
79
Evaluation of musculoskeletal symptoms
80
Evaluation of musculoskeletal symptoms
  • History
  • History
  • History
  • Examination
  • Examination
  • Examination
  • Investigations targeted

81
Investigations
  • Blood Count
  • ? Appropriate to clinical features
  • Inflammatory markers
  • Usually mirror clinical features
  • Not always raised in inflammatory conditions
  • Blood and synovial fluid cultures
  • ANA/Rh Factor
  • Not helpful in making a diagnosis
  • Imaging
  • Need to use best modality and ask the right
    question

82
Summary
  • Musculoskeletal complaints are common in
    childhood
  • Serious pathology leads to long term disability
    if not appropriately managed
  • Diagnosis is dependant on good history and
    examination
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