Osteomyelitis medical therapy: Difference between revisions

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==Acute Osteomyelitis in Adults – Empiric Therapy==
==Acute Osteomyelitis in Adults – Empiric Therapy==
Although osteomyelitis in adults usually has a subacute or chronic course, acute hematogenous seeding may occur in elderly patients, intravenous drug users, or patients with indwelling catheters.  The most commonly isolated microorganisms are ''Staphylococcus aureus'' and ''Streptococcus pneumonia''.  Empiric antibiotics with anti-staphylococcal and anti-streptococcal coverage should be administered based on local resistance data.
Although osteomyelitis in adults usually has a subacute or chronic course, acute hematogenous seeding may occur in elderly patients, intravenous drug users, or patients with indwelling catheters.  The most commonly isolated microorganisms are ''[[Staphylococcus aureus]]'' and ''[[Streptococcus pneumonia]]''.  Empiric antibiotics with anti-staphylococcal and anti-streptococcal coverage should be administered based on local resistance data.


==Acute Osteomyelitis in Children – Empiric Therapy==
==Acute Osteomyelitis in Children – Empiric Therapy==

Revision as of 21:18, 28 April 2015

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]

Overview

Treatment of osteomyelitis typically requires a combination of complete surgical debridement and 4 to 6 weeks of antimicrobial therapy against the commonly recovered microorganisms based on the predisposing factors and local resistance pattern.

Acute Osteomyelitis in Adults – Empiric Therapy

Although osteomyelitis in adults usually has a subacute or chronic course, acute hematogenous seeding may occur in elderly patients, intravenous drug users, or patients with indwelling catheters. The most commonly isolated microorganisms are Staphylococcus aureus and Streptococcus pneumonia. Empiric antibiotics with anti-staphylococcal and anti-streptococcal coverage should be administered based on local resistance data.

Acute Osteomyelitis in Children – Empiric Therapy

Abbreviations: OSSA, oxacillin-sensitive Staphylococcus aureus; ORSA, Oxacillin-resistant Staphylococcus aureus; CRSA, Clindamycin-resistant Staphylococcus aureus. [1]

High prevalence of OSSA in community

  • High prevalence of ORSA with low prevalence of CRSA in community

    • Clindamycin ≥ 40 mg/kg/day administered in 4 equal doses
  • High prevalence of ORSA with high prevalence of CRSA in community

    • Vancomycin ≤ 40 mg/kg/day administered in 4 equal doses, adjust dosage to trough of 15–20 mcg/mL
    • Linezolid 30 mg/kg/day administered in 3 equal doses
  • Chronic Osteomyelitis in Adults – Pathogen-Based Therapy

    OSSA

  • ORSA

  • Penicillin-sensitive Streptococcus

  • Enterococcus or Streptococcus (MIC ≥ 0.5 μg/mL) or Abiotrophia or Granulicatella

    • Penicillin G 20 MU/day IV continuously or q4h for 4–6 wk ± Gentamicin 1 mg/kg IV or IM q8h for 1–2 wk
      OR
    • Ampicillin 12 g/day IV continuously or q4h for 4–6 wk ± Gentamicin 1 mg/kg IV or IM q8h for 1–2 wk
  • Enterobacteriaceae

  • Pseudomonas aeruginosa

  • Chronic Osteomyelitis in Children – Pathogen-Based Therapy

    Group A beta-hemolytic Streptococcus, Haemophilus influenzae type b, and Streptococcus pneumoniae

    • Ampicillin 150–200 mg/kg/day administered in 4 equal doses OR Amoxicillin 150–200 mg/kg/day administered in 4 equal doses
  • Vertebral Osteomyelitis

    Abbreviations: OSSA, oxacillin-sensitive Staphylococcus aureus; ORSA, Oxacillin-resistant Staphylococcus aureus; CRSA, Clindamycin-resistant Staphylococcus aureus. [2]

    OSSA or coagulase-negative staphylococci

  • ORSA

  • Streptococcus

  • Enterobacteriaceae, quinolone-susceptible

  • Enterobacteriaceae, quinolone-resistant

  • Pseudomonas aeruginosa

  • Anaerobes

  • References

    1. Peltola, Heikki; Pääkkönen, Markus (2014-01-23). "Acute osteomyelitis in children". The New England Journal of Medicine. 370 (4): 352–360. doi:10.1056/NEJMra1213956. ISSN 1533-4406. PMID 24450893.
    2. Zimmerli, Werner (2010-03-18). "Clinical practice. Vertebral osteomyelitis". The New England Journal of Medicine. 362 (11): 1022–1029. doi:10.1056/NEJMcp0910753. ISSN 1533-4406. PMID 20237348.