Necrotizing soft tissue infection: Difference between revisions
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**[[Clindamycin]] 600 to 900 mg IV q8h, for synergy and the Eagle phenomenon and decreased toxin production |
**[[Clindamycin]] 600 to 900 mg IV q8h, for synergy and the Eagle phenomenon and decreased toxin production |
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**If risk for MRSA, add [[vancomycin]] 15-20 mg/kg IV q8-12h |
**If risk for MRSA, add [[vancomycin]] 15-20 mg/kg IV q8-12h |
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**If water exposure, add two of: a fluoroquinolone, a carbapenem, a third-generation cephalosporin, and/or [[doxycycline]] (should have double-coverage pending susceptibilities) |
**If water exposure, add two of: a [[Fluoroquinolones|fluoroquinolone]], a [[Carbapenems|carbapenem]], a third-generation [[Cephalosporins|cephalosporin]], and/or [[doxycycline]] (should have double-coverage pending susceptibilities) |
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**Some recommend replacing [[clindamycin]] (and possibly [[vancomycin]]) with [[linezolid]]<ref>Nicolás Cortés-Penfield, Jonathan H Ryder, Should Linezolid Replace Clindamycin as the Adjunctive Antimicrobial of Choice in Group A Streptococcal Necrotizing Soft Tissue Infection and Toxic Shock Syndrome? A Focused Debate, ''Clinical Infectious Diseases'', 2022;, ciac720, https://doi.org/10.1093/cid/ciac720</ref> |
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*Then narrow based on the Gram stain an culture |
*Then narrow based on the Gram stain an culture |
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*Can consider IVIg, rarely, in [[streptococcal toxic shock syndrome|streptococcal]] or [[staphylococcal toxic shock syndrome]] |
*Can consider IVIg, rarely, in [[streptococcal toxic shock syndrome|streptococcal]] or [[staphylococcal toxic shock syndrome]] |
Revision as of 10:15, 4 September 2022
Background
Microbiology
- See Classification, below
- Most commonly caused by monomicrobial Streptococcus pyogenes, Staphylococcus aureus, Clostridium, or Vibrio, or polymicrobial infections that include Gram-positives, Gram-negatives, and anaerobes
Classification
- Although it is classically divided into Type 1 (polymicrobial) and Type 2 (monomicrobial), others have proposed an extension to include Type 3 (water-associated monomicrobial) and Type 4 (fungal).
- Type 1: polymicrobial, including Staphylococcus aureus, Gram-negative bacilli, and anaerobes
- Type 2: monomicrobial Gram-positive infections, primarily Streptococcus pyogenes (most common) but also Staphylococcus aureus or Clostridium (penetrating trauma, soil exposure)
- Type 3: monomicrobial Gram-negative infections, generally caused by water-associated Vibrio vulnificus or Aeromonas hydrophila
- Type 4: fungal, caused by Candida species, and exceedingly rare
Management
- Surgical debridement!
- Empiric antibiotics
- Piperacillin-tazobactam 4.5 g IV q8h (or, alternatively, meropenem)
- Clindamycin 600 to 900 mg IV q8h, for synergy and the Eagle phenomenon and decreased toxin production
- If risk for MRSA, add vancomycin 15-20 mg/kg IV q8-12h
- If water exposure, add two of: a fluoroquinolone, a carbapenem, a third-generation cephalosporin, and/or doxycycline (should have double-coverage pending susceptibilities)
- Some recommend replacing clindamycin (and possibly vancomycin) with linezolid[1]
- Then narrow based on the Gram stain an culture
- Can consider IVIg, rarely, in streptococcal or staphylococcal toxic shock syndrome
Eagle Effect
- Originally, referred to decreased effectiveness of penicillins at high concentrations
- Now, refers to decreased effectiveness of penicillins at high bacterial burden (when in stationary phase)
- Clindamycin kills enough of the bacteria that are in stationary phase that the bacteria return to logarithmic growth phase, where penicillins are more effective
Further Reading
- RCT of IVIG: Madsen MB et al. Immunoglobulin G for patients with necrotising soft tissue infection (INSTINCT): a randomised, blinded, placebo-controlled trial. Intensive Care Med. 2017;43:1585-93.
- ↑ Nicolás Cortés-Penfield, Jonathan H Ryder, Should Linezolid Replace Clindamycin as the Adjunctive Antimicrobial of Choice in Group A Streptococcal Necrotizing Soft Tissue Infection and Toxic Shock Syndrome? A Focused Debate, Clinical Infectious Diseases, 2022;, ciac720, https://doi.org/10.1093/cid/ciac720
References
- ^ 10.1093/cid/ciac720