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Acute
Osteomyelitis
Amalina Aminuddin
082012100067
• Infection of bone
• Mainly affect children
Introduction
Predisposing factors
• Malnutrition and
general debility
• Diabetes mellitus
• Corticosteroid
administration
• Immunosuppressive
drugs
• Venous stasis in the
limb
• Peripheral vascular
disease
• Loss of sensibility
• Iatrogenic invasive
measures
• Trauma
• Based on duration:
• Acute (< 2 weeks )
• Subacute (2-3 weeks )
• Chronic ( > 3 weeks )
• Based on route of
infection:
• Primary(hematogenou
s)
• Secondary
• Based on organism
• Pyogenic:
Staphylococci,
Streptococcus,
Pneumococci,
Gonococci, H.
influenza ,Kingella
kingae E. coli,
Salmonella sp,
• Non pyogenic:
tuberculosis, syphilis,
Classifications
Pathogenesis
Children
• Hairpin loops  stasis
• Low oxygen tension
• Structure in the
hypertrophic zone of the
physis
Infants
• anastomoses between
metaphyseal and
epiphyseal vessels
Adults
• Direct spread
from infection
foci
• Local trauma
• Hematogenous
Pathology
• Depend on:
• Patient’s age
• Site of infection
• Virulence of the
organism
• Host response.
Acute
inflammation
Subperiosteal
abscess
Sequestrum
Involcrum
Cloacae
In infants
• More common epiphysial
and adjacent joint spread
• Deformed joint, bizzare
new bone formation
In adults
• Medullary spread in long
bone
Clinical features
In child:
• Recent history of
infection
• Severe pain, malaise,
fever
• Acute tenderness near
one of the larger joints
• ‘Pseudoparalysis’.
Infants
• History of birth difficulties,
umbilical artery
catheterization or a site of
infection
• Fails to thrive
• Drowsy but irritable.
• Metaphyseal tenderness
and resistance to joint
movement
Adults
• History of some urological
procedure followed by a
mild fever and backache.
• Local tenderness
• Easily missed diagnosis
in elderly, and in those
with immune deficiency,
Diagnostic imaging
•Plain x-ray
•Ultrasonography
•Radionuclide
scanning
•Magnetic resonance
imaging
• Bone scan reveals increased tracer uptake in the right
tibia
• Sagittal T2 reveals
marrow edema in the
distal tibia which crosses
the physis to invade the
epiphysis
Investigations
• Aspiration analysis
• Blood culture
• CRP within 12–24 hours
• ESR within 24–48 hours
Differential diagnosis
Cellulitis
• Widespread
superficial redness
and lymphangitis.
• MRI
• Oral or intravenous
antibiotics
Acute suppurative arthritis
• Diffuse tenderness
• Joint movement abolished
Streptococcal necrotising myositis
• Intense pain ,board-like swelling
• MRI :muscle swelling, signs of tissue
breakdown.
•Intravenous antibiotics surgical
debridement , amputation
Acute rheumatism
•Less severe migratory pain
•signs of carditis, rheumatic nodules or
erythema marginatum
Sickle-cell crisis
• Salmonella
Gaucher’s disease
•“Pseudo-osteitis’
•enlargement of the spleen and liver.
Management
• Supportive treatment for pain and
dehydration.
• Splintage (Simple skin traction , plaster
slab )
• Appropriate antimicrobial therapy.
• Surgical drainage.
Age Group Types of antibiotics
Neonates up to 6months
• Flucloxacillin + 3rd gen cephalosporin
• Flucloxacillin + benzylpenicillin + gentamycin
Children 6months-
6years
• IV flucloxacillin + cefotaxime / cefuroxime
Older child & previously
fit adults
• IV flucloxacillin + fusidic acid
• For known strep infection : benzylpenicillin
• Allergic to penicillin : 2nd- or 3rd- gen of
cephalosporin like cefotaxime
Elderly & previously
unfit patient
• Combination of flucloxacillin + 2nd-/3rd- gen
cephalosporin
Condition Types of Antibiotics
Sickle-cell disease patient
• Chloramphenicol,
• Third-generation cephalosporin
/fluoroquinolone
Heroin Addicts &
immunocompromized patient
• Third-generation cephalosporins
• Flouroquinolone (ciprofloxacin)
Patient to be risk at MRSA with
acute hematogenous OM
• IV vancomycin + 3rd- gen of
cephalosporin
Drainage
• When ?
• Clinical features do not improve within 36 hours
• Signs of deep pus
• Pus is aspirated
• Drained by open operation under general anaesthesia.
• (no obvious abscess) drill into medullary cavity
• (extensive intramedullary abscess) cut a small window in the
cortex.
• Close wound without drain,
• Reapplied traction ,
• Encourage movements (crutches)
Complications
• Epiphyseal damage and altered bone
growth
• Suppurative arthritis
• Metastatic infection
• Pathological fracture
• Chronic osteomyelitis
Referance
• Louis Solomon, David Warwick,
Selvadurai, Apley's System of
Orthopaedics and Fractures 9th edition
• Maheshwari & Mhaskar ,Essential
Orthopedics, 5th edition
• http://www.nejm.org/doi/full/10.1056/NEJM
ra1213956

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Mellss yr4 ortho acute osteomyelitis

  • 2. • Infection of bone • Mainly affect children Introduction
  • 3. Predisposing factors • Malnutrition and general debility • Diabetes mellitus • Corticosteroid administration • Immunosuppressive drugs • Venous stasis in the limb • Peripheral vascular disease • Loss of sensibility • Iatrogenic invasive measures • Trauma
  • 4. • Based on duration: • Acute (< 2 weeks ) • Subacute (2-3 weeks ) • Chronic ( > 3 weeks ) • Based on route of infection: • Primary(hematogenou s) • Secondary • Based on organism • Pyogenic: Staphylococci, Streptococcus, Pneumococci, Gonococci, H. influenza ,Kingella kingae E. coli, Salmonella sp, • Non pyogenic: tuberculosis, syphilis, Classifications
  • 5. Pathogenesis Children • Hairpin loops  stasis • Low oxygen tension • Structure in the hypertrophic zone of the physis
  • 6.
  • 8. Adults • Direct spread from infection foci • Local trauma • Hematogenous
  • 9. Pathology • Depend on: • Patient’s age • Site of infection • Virulence of the organism • Host response.
  • 11. In infants • More common epiphysial and adjacent joint spread • Deformed joint, bizzare new bone formation In adults • Medullary spread in long bone
  • 12. Clinical features In child: • Recent history of infection • Severe pain, malaise, fever • Acute tenderness near one of the larger joints • ‘Pseudoparalysis’.
  • 13. Infants • History of birth difficulties, umbilical artery catheterization or a site of infection • Fails to thrive • Drowsy but irritable. • Metaphyseal tenderness and resistance to joint movement Adults • History of some urological procedure followed by a mild fever and backache. • Local tenderness • Easily missed diagnosis in elderly, and in those with immune deficiency,
  • 15.
  • 16.
  • 17.
  • 18. • Bone scan reveals increased tracer uptake in the right tibia
  • 19. • Sagittal T2 reveals marrow edema in the distal tibia which crosses the physis to invade the epiphysis
  • 20. Investigations • Aspiration analysis • Blood culture • CRP within 12–24 hours • ESR within 24–48 hours
  • 21. Differential diagnosis Cellulitis • Widespread superficial redness and lymphangitis. • MRI • Oral or intravenous antibiotics
  • 22. Acute suppurative arthritis • Diffuse tenderness • Joint movement abolished Streptococcal necrotising myositis • Intense pain ,board-like swelling • MRI :muscle swelling, signs of tissue breakdown. •Intravenous antibiotics surgical debridement , amputation
  • 23. Acute rheumatism •Less severe migratory pain •signs of carditis, rheumatic nodules or erythema marginatum Sickle-cell crisis • Salmonella Gaucher’s disease •“Pseudo-osteitis’ •enlargement of the spleen and liver.
  • 24. Management • Supportive treatment for pain and dehydration. • Splintage (Simple skin traction , plaster slab ) • Appropriate antimicrobial therapy. • Surgical drainage.
  • 25.
  • 26. Age Group Types of antibiotics Neonates up to 6months • Flucloxacillin + 3rd gen cephalosporin • Flucloxacillin + benzylpenicillin + gentamycin Children 6months- 6years • IV flucloxacillin + cefotaxime / cefuroxime Older child & previously fit adults • IV flucloxacillin + fusidic acid • For known strep infection : benzylpenicillin • Allergic to penicillin : 2nd- or 3rd- gen of cephalosporin like cefotaxime Elderly & previously unfit patient • Combination of flucloxacillin + 2nd-/3rd- gen cephalosporin
  • 27. Condition Types of Antibiotics Sickle-cell disease patient • Chloramphenicol, • Third-generation cephalosporin /fluoroquinolone Heroin Addicts & immunocompromized patient • Third-generation cephalosporins • Flouroquinolone (ciprofloxacin) Patient to be risk at MRSA with acute hematogenous OM • IV vancomycin + 3rd- gen of cephalosporin
  • 28. Drainage • When ? • Clinical features do not improve within 36 hours • Signs of deep pus • Pus is aspirated • Drained by open operation under general anaesthesia. • (no obvious abscess) drill into medullary cavity • (extensive intramedullary abscess) cut a small window in the cortex. • Close wound without drain, • Reapplied traction , • Encourage movements (crutches)
  • 29. Complications • Epiphyseal damage and altered bone growth • Suppurative arthritis • Metastatic infection • Pathological fracture • Chronic osteomyelitis
  • 30. Referance • Louis Solomon, David Warwick, Selvadurai, Apley's System of Orthopaedics and Fractures 9th edition • Maheshwari & Mhaskar ,Essential Orthopedics, 5th edition • http://www.nejm.org/doi/full/10.1056/NEJM ra1213956

Editor's Notes

  1. Hib 6, 10, 14 w, 18m
  2. Blood stream, infected tissue, open wound
  3. structure of the fine vessels in the hypertrophic zone of the physis allows bacteria moreeasily to pass through and adhere to type 1 collagen
  4. Neuropathic ulcer or an infected diabetic foot, operation or open injury
  5. inflammation, suppuration, bone necrosis, reactive new bone formation and,ultimately, resolution and healing or else intractable chronicity.
  6. physeal anlage may be damaged,further growth severely retarded ,joint permanently deformed. 6–9 months of life, small metaphyseal vessels penetrate physeal cartilage infection to the cartilaginous epiphysis. Exuberant periosteal reaction bizarre new bone formation along the diaphysis; longitudinal growth and remodelling the diaphyseal Eroding cortex  fracture, less periosteal new bone formation
  7. over 4 years, (a boil, a sore throat or a discharge from the ear) (e.g. above or below the knee, in the popliteal fossa or in the groin). the inability to move a part of the body owing to factors, as pain, other than those causing actual paralysis
  8. an inflamed intravenous infusion point or even a heel puncture.
  9. Osteomyelitis of the distal fibula with a subperiostal pus collection in an 11 year old gir
  10. involving the tibia of a 10-year-old male with foot pain, fever, and elevated ESR. A, AP radiograph of the right leg demonstrates focal demineralization with sclerosis of the distal tibia
  11.  large subperiosteal pus collection (red arrows) and a small focus of osteomyelitis in the distal left femoral metaphysis (white arrow).
  12. , . C, Bone scan reveals increased tracer uptake in the right tibia compared with normal uptake on the contralateral side
  13. Subperiostea abscess, the extraosseous soft tissues or an adjacent joint,16- or 18-gauge trocar needle, exmine for cell, orgnism, ab sensitivity white cell count, differential count, cultures, Gram stain
  14. source of skin infection may not be obvious
  15. coexis
  16. atty substances (sphingolipids) accumulate in cells and certain organs. The disorder is characterized by bruising, fatigue, anemia, low blood platelets, and enlargement of the liver and spleen
  17. Comfort but also to prevent joint contractures
  18. (Cefotaxime, cefuroxime)
  19. HIV, Pseudomonas aeruginosa, Proteus Microbilis, anaerobic Bacteroides sp.
  20. (swelling,oedema, fluctuation), When infc subside