Osteoarticular Infections Flashcards

(29 cards)

1
Q

What is the incidence of osteomyelitis

A

1-13 / 100 000

2.38/1000 admissions

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2
Q

What are the definitions of acute OM and chronic OM

A

OM: inflammation of bone and bone marrow due to infection

Acute - symptoms up to 4weeks
Chronic - symptoms >4wks with a vascular bone (sequestrum) or surrounded by new bone (involucrum) is present (Brodies’ abscess)

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3
Q

What are the common organisms for OM

A

S. Aureus
Kingella kingae - 12% in infants, 6 in older children
S. Pneumonia
S. Pyogenes

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4
Q

Where does OM typically occur?

A

Metaphysis of any long tubular bone because of presence of nutrient artery end emptying into venous sinusoids

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5
Q

Why is SA found more commonly with OM in younger children?

A

Because of trnasphyseal vessels prior to growth plate closure, and the joint capsule extends beyond epiphyseal plate allowing easier spread from metaphysis

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6
Q

What are clinical manifestations of OM or SA

A

Pseudoparalysis in affected area, limping
Pain
Swelling, erythema or fluctuance if abscess present = may look like overlying cellulitis

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7
Q

What are features of SA alone

A

Specific swelling of joint
Joint effusion
Pain on movement of isolated joint

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8
Q

What is included in the differential diagnosis of OM/SA and what are differentiating features?

A

AO/SA - pseudoparalysis/limp, history of fevers, tenders at site, decreased ROM, swelling/erythema

Transient synovitis of hip - age 4-10y, hip pain, limp, low-grade fever, preceding URTI, CRP<20

Fracture/trauma - acute onset with activity, hematoma, swelling, no fever

Lyme arthritis - endemic area, mono arthritis, no constitutional symptoms, less painful, CRP<40, may have Baker’s cyst

Cellulitis - rapid development of swelling, redness, pain, erythema before pain, more extensive than one focal area, +/- lymphangitis

CRMO - insidious onset, low-grade fever and malaise and wt loss in 1/3, worse at night, unusual sites, intense sclerosis with healing, may have dermatological conditions (psoriasis, palmoplantar pustulosis)

Heme malignancy: systemic complaints, arthralia, myalgia, metaphyseal licences or periosteal reactions, no localized pain, may have mild synovitis or joint swelling

Bone neoplastic lesion - diaphysis or flat bones, gradual onset, pain at night, refusal to weight bear, may have palpable mass

JIA - gradual onset, >6wk, may have extraarticular symptoms, less severe symptoms

SLE - constitutional symptoms, cutaneous symptoms, usually milder arthritis, heme or urine abN

Reactive arthritis - usually large joints, 2-3 weeks after an infection (GI or GU), may have ocular and urinary sx

PSRA - usually polyarticular non-migratory, persistent or recurrent, 3-14d after strep infection, may have other post-strep manifestations (GN, vasculitis, ARF)

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9
Q

What lab findings are suggestive of OM

A

WBC - may be elevated
CRP - elevated (t1/2 8h)
Blood culture
Imaging: X-ray, U/S for effusions, MRI with gadolinium and bone marrow edema, bone scans

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10
Q

Why is CRP better than ESR in OM

A

T1/2 - 8h - more sensitive (95%), decreases faster with therapy, normalizes by 10+/-0.5 days

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11
Q

When can you see x-ray changes with OM/SA? What are classic changes?

A

7-21d after onset of infection

  • lyric lesions
  • localized periosteal lifting
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12
Q

What is the earliest finding of OM on imaging

A

Bone marrow oedema

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13
Q

Is an MRI needed if there is supporting lab parameters and a positive clinical response to empiric therapy for OM

A

No

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14
Q

What is the sensitivity of bone scans?

What are FN and FP causes

A

80%

May be false negative if early in course, or if bone infarction

May be false positive with fractures, tumours f

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15
Q

How can SA be diagnosed ?

A

Optimal: joint aspiration
Other: U/S of joint, MRI

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16
Q

How common is it for blood, bone and joint fluid cultures to test negative

17
Q

What is the dominant pathogen in children <4yo presenting with SA +/- OM

18
Q

What other causes of OM/SA need to be considered in neonates, immunocompromised, or unique environmental exposures?

A

Entereobacteriaceae, fungi,

SCD - Salmonella

19
Q

If blood cultures are positive - when should they be repeated?

A

In 48h to ensure clearance

20
Q

When should surgery be considered in OM

A

If fails empiric antibiotics
If joint fluid collections
If soft tissue, periosteal abscess

21
Q

What is the empiric antibiotic choice for OM/SA

A

1st gen cephalosporin - cefazolin - covers MSSA and K kingae
- does: 100-150mg/kg/d q6-8h IV

22
Q

What is K Kingae resistant to?

A

Clindamycin
Vancomycin
Cloxacillin

23
Q

When should H influenza be considered as a pathogen? What antibiotic coverage should be used?

A

If unimmunised, or living in areas with invasive H. Flu is more common than usual

Cefuroxim 150mg/kg/d divide q8H IV

24
Q

If the isolate is MSSA what antibiotic can therapy be narrowed to?

A

Cloxacillin 150-200mg/kg/d IV divided q6h

25
How long does OM/SA need to be treated? When can step down to oral therapy occur?
SA - 3-4 weeks (if hip involved 4-6 weeks total) OM - 3-4 weeks total Step down when clinically improved - including able to weight bear , decreased CRP (50% by day 4, or down to at least 20-30) (usually 3-7d)
26
Why can we step down so early to PO in OM/SA if we require 6 weeks of therapy?
Because failure rates between IV and PO are the same (5-6% versus 4-5%) Fewer complications than with prolonged IV courses
27
What are contraindications to oral therapy?
Poor medication compliance or follow up Malabsorption Slow clinical resolution
28
What are oral options for OM/SA due to MRSA
Clindamycin Sentra Linezolid
29
What follow up is required for OM/SA
A normal CRP X-ray if growth plate was involved or if there was a large lyric lesion initially (look for sclerosis and healing) Usually ortho follow up needed