Acute and Chronic Osteomyelitis
Acute Osteomyelitis
Orthopaedic Diagnosis
History
2) Past History
3) Family History
4) Social background
5) Examination
Look / Feel / Move
Special tests
developmental milestones.
C ) Investigations
Plain Radiography
Patient - soft tissue , bones and joints
using contact media
2- CT
3) IMRI
5-30, 000, stronger than Earth’s magnetic field
4) Diagnostic ultrasound
5) Radionuclide imaging - 99 m Tc
B ) Blood tests
CBC, ESR CPP - Non specific
- Tissue typing
- Rheumatoid factor
- Synovial fluid analysis.
C) Bone-Biopsy
D) Diagnostic arthroscopy
Infection
Direct Introduction
(2) from contiguous infection
(3) indirect spread from blood stream
Factors predisposing to bone infection
- Malnutrition & general debility"
- DM
- Corticosteroid administration
- Immune deficiency
-immunosuppressive drugs.
- Venous stasis in limbs
- Peripheral l vascular diseases
- loss of sensibility
- intrinsic invasive measures
- Trauma
Principles of treatment
1 ) Analgesia
2) rest the affected part
3) indentify infecting organism, administer effective abx tr
4) release pus as soon as it’s detected
5) Stabilize bone if it's fractured
6) eradicate avascular & necrotic bone
7) maintain soft tissue and skin colour
Acute Haematogenous Osteomyelitis
Adults & Children - S. Aureus - 70%
-less often GABS (Str. Pyogenes) or
-alpha -haemolytic Diplococus , S. Pneumoniae
1-4. children - H. Influenzae.
- Kingalla kingne
Metophysis - involvement
1) Non-anastomosing losine terminal antony branches of nutrient artery
2) relative vascular stasis
3) lower oxygen tension
4) fire vessels in hypertrophic zone-bacteria pass through them and adhere to type I collagen
Pathology -
Inflammation, suppuration, bone necrosis reactive new bone formation, resolution & healing or chronicity
Metaphysis
-Intracapsular - SHE( SHOULDER , HIP and ELBOW JOINTS ) and spreads to it.
2) Periosteum looseliy attached in children spreads along shaft.
(3) physis is barrier to spread to joint
4) In infants ,bacteria spreads to joints
its through physis
Clinical features
(1) child over 4
(2) Pain, swelling , refused to move
(3) high grade fever
4) Infants - symptoms are mild
(5) Bony tenderness
(6) TL vertebrae are comon sites
Diagnostic Smaging
1)Plain xray
2) USG
3) 99m Tc - HDP : Increase activity in both perfusion and bone phase
4) MRI
B) Laboratory Tests
18 G needle.
Aspiration.
tissue aspiration 60% positive
CRP-12-24 hrs., ESP-24-48 hrs
D/P
4) Cellulitis
B) Acute suppurative Arthritis
2) Acute P
3) Rheumatism
4) Sickle cell crisis
D) Gaucher’s Disease
Treatment
Analgesia
Support affected part
Abx
Pus drainage
Fix facturas
Cover wound , remove dead bone
Choice of Abx.
Upto. 06 months - 3rd gen. cephalosp
Covers Aureus
6 months to 6 years - H. Influenza
Fluclox + 3rd gen ceohalosporin
Older chibaren & previously fit
flucloxacillin & Fusidic
acid
Elderly previously unfit patients
Like in
6 months children - G ‘-’ve organisms from GI Tract , respiratory system .
Pts. with Sickle Cell dis-
3rd gen ceohalosporins or fluoroquinolones
MArSA-
IV Vancomycin + 3rd Gen Cephalosporin
- Garre’s Sclerosing Osteomyelitis
Marked Sclerosis and Cortical thickening .
-Long history of bone pain and Swelling over bone
Treatment - Curettage
Acute suppurative Arthritis
S. Aureus
Involvement
I/A injections
Adjacent bone abscess
Blood spread from distant site
Clinical features
1 ) Pain / swelling ) refusal to move the part, fever
2)septiceamia in infants
3) rapid pulse, erythema over involved bone and swelling
4 ) restricted movement
Imaging
USG
X - Ray
MRI
G-stain
WBC-300/ ml is normal
- 1000/-non infective
> 50,000/ml - infective
D/D of Acute Osteomyelitis
Trauma
Irritable Joint
4) Haemophiliac Bleed
5) Rheumatic fever
6) Juvenile Rheumatoid Arthritis
7) Sickles cell Disease
10) Gaucher's Disease
11) Gout and Pseudogout
Complications
Subluxation
Damage to cartilage
Articular cartilage erosion
Gonococcal Arthritis
Neisseria Gonorrhoea.
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