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10 - Necrotizing Soft Tissue Infections

from Section 2 - Infectious Disease Emergencies

Published online by Cambridge University Press:  02 November 2023

Kaushal Shah
Affiliation:
Weill Cornell Medical Center, New York
Jarone Lee
Affiliation:
Massachusetts General Hospital, Boston
Clark G. Owyang
Affiliation:
Weill Cornell Medical Center, New York
Benjamin Christian Renne
Affiliation:
Massachusetts General Hospital, Boston
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Summary

For the clinical applications of this chapter, necrotizing soft tissue infections (NSTIs) will refer to infection of deep subcutaneous tissues and adjacent fascia.

Mortality is estimated to be around 20–50% in observational literature with variation by infection site and specific organism.

Paucity of early physical examination findings can lead to a delay in diagnosis, as classic superficial findings do not manifest until later in the disease course.

Infection leads to toxin production, cytokine activation and microthrombosis, which all contribute to ischemia, impaired antibiotic delivery and rapid progression.

Early surgical intervention decreases morbidity and mortality.

NSTIs can be classified based on microbial etiology, with polymicrobial etiology being the most common. Type I necrotizing fasciitis is polymicrobial in origin. Type II is monomicrobial, often caused by group A Streptococcus (typically, S. pyogenes). Staphylococcal NSTIs are increasing in prevalence due to community-associated methicillin-resistant S. aureus.

Exotoxin release by clostridia, staphylococci and streptococci can enhance cytokine release and promote an inflammatory cascade, which can lead to death if untreated.

NSTIs are more common in patients with comorbidities including diabetes mellitus, chronic alcoholism, chronic renal failure, HIV, liver failure (which is classically associated with Vibrio vulnificus) and other immunosuppressed states.

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Publisher: Cambridge University Press
Print publication year: 2023

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References

Stevens, DL, Bryant, AE, Goldstein, EJ. Necrotizing soft tissue infections. Infect Dis Clin North Am 2021;35(1):135155. https://doi.org/10.1016/j.idc.2020.10.004CrossRefGoogle Scholar

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