Necrotizing fasciitis
- Overview
- Theory
- Diagnosis
- Management
- Follow up
- Resources
Treatment algorithm
Please note that formulations/routes and doses may differ between drug names and brands, drug formularies, or locations. Treatment recommendations are specific to patient groups: see disclaimer
Look out for this icon: for treatment options that are affected, or added, as a result of your patient's comorbidities.
suspected necrotizing fasciitis, organism unknown
initial resuscitation
An urgent surgical consult should be sought as soon as the diagnosis is suspected.[3]Sartelli M, Coccolini F, Kluger Y, et al. WSES/GAIS/WSIS/SIS-E/AAST global clinical pathways for patients with skin and soft tissue infections. World J Emerg Surg. 2022 Jan 15;17(1):3. https://wjes.biomedcentral.com/articles/10.1186/s13017-022-00406-2 http://www.ncbi.nlm.nih.gov/pubmed/35033131?tool=bestpractice.com
Intensive hemodynamic support with intravenous fluids, and possibly vasoactive drugs, will be needed.[2]Sartelli M, Guirao X, Hardcastle TC, et al. 2018 WSES/SIS-E consensus conference: recommendations for the management of skin and soft-tissue infections. World J Emerg Surg. 2018 Dec 14;13:58. https://wjes.biomedcentral.com/articles/10.1186/s13017-018-0219-9 http://www.ncbi.nlm.nih.gov/pubmed/30564282?tool=bestpractice.com [3]Sartelli M, Coccolini F, Kluger Y, et al. WSES/GAIS/WSIS/SIS-E/AAST global clinical pathways for patients with skin and soft tissue infections. World J Emerg Surg. 2022 Jan 15;17(1):3. https://wjes.biomedcentral.com/articles/10.1186/s13017-022-00406-2 http://www.ncbi.nlm.nih.gov/pubmed/35033131?tool=bestpractice.com [5]Stevens DL, Bisno AL, Chambers HF, et al. Practice guidelines for the diagnosis and management of skin and soft tissue infections: 2014 update by the Infectious Diseases Society of America. Clin Infect Dis. 2014 Jul 15;59(2):e10-52. https://academic.oup.com/cid/article/59/2/e10/2895845 http://www.ncbi.nlm.nih.gov/pubmed/24973422?tool=bestpractice.com
Patients should receive adequate analgesia (e.g., an opioid).[2]Sartelli M, Guirao X, Hardcastle TC, et al. 2018 WSES/SIS-E consensus conference: recommendations for the management of skin and soft-tissue infections. World J Emerg Surg. 2018 Dec 14;13:58. https://wjes.biomedcentral.com/articles/10.1186/s13017-018-0219-9 http://www.ncbi.nlm.nih.gov/pubmed/30564282?tool=bestpractice.com
surgical debridement
Treatment recommended for ALL patients in selected patient group
Necrotizing fasciitis is a surgical emergency and the patient should be urgently taken to the operating room for debridement of all infected, devitalized tissues as soon as possible after initial resuscitation.[3]Sartelli M, Coccolini F, Kluger Y, et al. WSES/GAIS/WSIS/SIS-E/AAST global clinical pathways for patients with skin and soft tissue infections. World J Emerg Surg. 2022 Jan 15;17(1):3. https://wjes.biomedcentral.com/articles/10.1186/s13017-022-00406-2 http://www.ncbi.nlm.nih.gov/pubmed/35033131?tool=bestpractice.com
When debridement is performed, surgical incisions should extend beyond the areas of visible necrosis and the entire necrotic area excised.[3]Sartelli M, Coccolini F, Kluger Y, et al. WSES/GAIS/WSIS/SIS-E/AAST global clinical pathways for patients with skin and soft tissue infections. World J Emerg Surg. 2022 Jan 15;17(1):3. https://wjes.biomedcentral.com/articles/10.1186/s13017-022-00406-2 http://www.ncbi.nlm.nih.gov/pubmed/35033131?tool=bestpractice.com
Intraoperative tissue and fluid should be obtained for microbiological culture.
Intensive hemodynamic support is an important aspect of surgical management.[2]Sartelli M, Guirao X, Hardcastle TC, et al. 2018 WSES/SIS-E consensus conference: recommendations for the management of skin and soft-tissue infections. World J Emerg Surg. 2018 Dec 14;13:58. https://wjes.biomedcentral.com/articles/10.1186/s13017-018-0219-9 http://www.ncbi.nlm.nih.gov/pubmed/30564282?tool=bestpractice.com [3]Sartelli M, Coccolini F, Kluger Y, et al. WSES/GAIS/WSIS/SIS-E/AAST global clinical pathways for patients with skin and soft tissue infections. World J Emerg Surg. 2022 Jan 15;17(1):3. https://wjes.biomedcentral.com/articles/10.1186/s13017-022-00406-2 http://www.ncbi.nlm.nih.gov/pubmed/35033131?tool=bestpractice.com [5]Stevens DL, Bisno AL, Chambers HF, et al. Practice guidelines for the diagnosis and management of skin and soft tissue infections: 2014 update by the Infectious Diseases Society of America. Clin Infect Dis. 2014 Jul 15;59(2):e10-52. https://academic.oup.com/cid/article/59/2/e10/2895845 http://www.ncbi.nlm.nih.gov/pubmed/24973422?tool=bestpractice.com
Further surgical evaluation and debridement is necessary in most cases, and several procedures may be required to ensure that all necrotic tissue is removed.[5]Stevens DL, Bisno AL, Chambers HF, et al. Practice guidelines for the diagnosis and management of skin and soft tissue infections: 2014 update by the Infectious Diseases Society of America. Clin Infect Dis. 2014 Jul 15;59(2):e10-52. https://academic.oup.com/cid/article/59/2/e10/2895845 http://www.ncbi.nlm.nih.gov/pubmed/24973422?tool=bestpractice.com Data to guide optimal timing for surgical re-exploration are lacking; a reasonable approach may be serial debridement every 12-24 hours until minimal or no remaining necrotic tissue is encountered.[2]Sartelli M, Guirao X, Hardcastle TC, et al. 2018 WSES/SIS-E consensus conference: recommendations for the management of skin and soft-tissue infections. World J Emerg Surg. 2018 Dec 14;13:58. https://wjes.biomedcentral.com/articles/10.1186/s13017-018-0219-9 http://www.ncbi.nlm.nih.gov/pubmed/30564282?tool=bestpractice.com [3]Sartelli M, Coccolini F, Kluger Y, et al. WSES/GAIS/WSIS/SIS-E/AAST global clinical pathways for patients with skin and soft tissue infections. World J Emerg Surg. 2022 Jan 15;17(1):3. https://wjes.biomedcentral.com/articles/10.1186/s13017-022-00406-2 http://www.ncbi.nlm.nih.gov/pubmed/35033131?tool=bestpractice.com
After complete removal of necrotic tissue and final debridement, negative pressure wound therapy may be considered to help with granulation and healing of the wound.[15]Hua C, Urbina T, Bosc R, et al. Necrotising soft-tissue infections. Lancet Infect Dis. 2023 Mar;23(3):e81-94. http://www.ncbi.nlm.nih.gov/pubmed/36252579?tool=bestpractice.com
empiric broad-spectrum antibiotics
Treatment recommended for ALL patients in selected patient group
Until microbial etiology and antimicrobial susceptibilities are known, empiric broad-spectrum antibiotics should be administered targeting the most common etiologies for necrotizing fasciitis. These include type I infections (mixed infections with anaerobes such as Bacteroides or Peptostreptococcus with a facultative anaerobe such as certain Enterobacterales [ Escherichia coli, Enterobacter, Klebsiella, Proteus], MRSA, or non-group A streptococcus), and type II infections (group A streptococcus [i.e., Streptococcus pyogenes ]). Consider local resistance and epidemiologic patterns (including extended-spectrum beta-lactamase or carbapenemase-producing organisms).
Recommended empiric regimens include vancomycin, linezolid, tedizolid, or daptomycin combined with either: piperacillin/tazobactam or a carbapenem (e.g., meropenem, imipenem/cilastatin, ertapenem).
Until group A streptococcus involvement is excluded, empiric regimens should include an antimicrobial agent that inhibits toxin production. Evidence for clindamycin is strongest, although linezolid also has potential toxin-inhibiting properties.[5]Stevens DL, Bisno AL, Chambers HF, et al. Practice guidelines for the diagnosis and management of skin and soft tissue infections: 2014 update by the Infectious Diseases Society of America. Clin Infect Dis. 2014 Jul 15;59(2):e10-52. https://academic.oup.com/cid/article/59/2/e10/2895845 http://www.ncbi.nlm.nih.gov/pubmed/24973422?tool=bestpractice.com [35]Bonne SL, Kadri SS. Evaluation and management of necrotizing soft tissue infections. Infect Dis Clin North Am. 2017 Sep;31(3):497-511. http://www.ncbi.nlm.nih.gov/pubmed/28779832?tool=bestpractice.com
When further information is available and the etiologic agent has been determined, antibiotic therapy should be tailored to target the specific agent.
As there are currently no definitive clinical trials, the Infectious Diseases Society of America recommends continuing antibiotics until no further surgical debridement is needed, the patient has improved clinically, and fever has been absent for 48 to 72 hours.[5]Stevens DL, Bisno AL, Chambers HF, et al. Practice guidelines for the diagnosis and management of skin and soft tissue infections: 2014 update by the Infectious Diseases Society of America. Clin Infect Dis. 2014 Jul 15;59(2):e10-52. https://academic.oup.com/cid/article/59/2/e10/2895845 http://www.ncbi.nlm.nih.gov/pubmed/24973422?tool=bestpractice.com [55]Terzian WTH, Nunn AM, Call EB, et al. Duration of antibiotic therapy in necrotizing soft tissue infections: shorter is safe. Surg Infect (Larchmt). 2022 Jun;23(5):430-5. https://www.liebertpub.com/doi/10.1089/sur.2022.011 http://www.ncbi.nlm.nih.gov/pubmed/35451883?tool=bestpractice.com
Primary options
vancomycin: 15-20 mg/kg intravenously every 8-12 hours
More vancomycinAdjust dose according to serum vancomycin level.
or
linezolid: 600 mg intravenously every 12 hours
or
tedizolid phosphate: 200 mg intravenously every 24 hours
or
daptomycin: 4 mg/kg intravenously every 24 hours
-- AND --
piperacillin/tazobactam: 3.375 g intravenously every 6 hours
More piperacillin/tazobactamDose consists of 3 g piperacillin plus 0.375 g tazobactam.
or
imipenem/cilastatin: 1 g intravenously every 6-8 hours
More imipenem/cilastatinDose refers to imipenem component.
or
meropenem: 1 g intravenously every 8 hours
or
ertapenem: 1 g intravenously every 24 hours
-- AND --
clindamycin: 600-900 mg intravenously every 8 hours
More clindamycinOnly add clindamycin to the empiric regimen if linezolid is not already being used, until group A streptococcus involvement is excluded.
These drug options and doses relate to a patient with no comorbidities.
Primary options
vancomycin: 15-20 mg/kg intravenously every 8-12 hours
More vancomycinAdjust dose according to serum vancomycin level.
or
linezolid: 600 mg intravenously every 12 hours
or
tedizolid phosphate: 200 mg intravenously every 24 hours
or
daptomycin: 4 mg/kg intravenously every 24 hours
-- AND --
piperacillin/tazobactam: 3.375 g intravenously every 6 hours
More piperacillin/tazobactamDose consists of 3 g piperacillin plus 0.375 g tazobactam.
or
imipenem/cilastatin: 1 g intravenously every 6-8 hours
More imipenem/cilastatinDose refers to imipenem component.
or
meropenem: 1 g intravenously every 8 hours
or
ertapenem: 1 g intravenously every 24 hours
-- AND --
clindamycin: 600-900 mg intravenously every 8 hours
More clindamycinOnly add clindamycin to the empiric regimen if linezolid is not already being used, until group A streptococcus involvement is excluded.
Drug choice, dose and interactions may be affected by the patient's comorbidities. Check your local drug formulary.
Show drug information for a patient with no comorbidities
Primary options
vancomycin
or
linezolid
or
tedizolid phosphate
or
daptomycin
-- AND --
piperacillin/tazobactam
or
imipenem/cilastatin
or
meropenem
or
ertapenem
-- AND --
clindamycin
type I necrotizing fasciitis (polymicrobial)
surgical debridement
Necrotizing fasciitis is a surgical emergency and the patient should be urgently taken to the operating room for debridement of all infected, devitalized tissues as soon as possible after initial resuscitation.[3]Sartelli M, Coccolini F, Kluger Y, et al. WSES/GAIS/WSIS/SIS-E/AAST global clinical pathways for patients with skin and soft tissue infections. World J Emerg Surg. 2022 Jan 15;17(1):3. https://wjes.biomedcentral.com/articles/10.1186/s13017-022-00406-2 http://www.ncbi.nlm.nih.gov/pubmed/35033131?tool=bestpractice.com
When debridement is performed, surgical incisions should extend beyond the areas of visible necrosis and the entire necrotic area excised.[3]Sartelli M, Coccolini F, Kluger Y, et al. WSES/GAIS/WSIS/SIS-E/AAST global clinical pathways for patients with skin and soft tissue infections. World J Emerg Surg. 2022 Jan 15;17(1):3. https://wjes.biomedcentral.com/articles/10.1186/s13017-022-00406-2 http://www.ncbi.nlm.nih.gov/pubmed/35033131?tool=bestpractice.com
Further surgical evaluation and debridement is necessary in most cases, and several procedures may be required to ensure that all necrotic tissue is removed.[5]Stevens DL, Bisno AL, Chambers HF, et al. Practice guidelines for the diagnosis and management of skin and soft tissue infections: 2014 update by the Infectious Diseases Society of America. Clin Infect Dis. 2014 Jul 15;59(2):e10-52. https://academic.oup.com/cid/article/59/2/e10/2895845 http://www.ncbi.nlm.nih.gov/pubmed/24973422?tool=bestpractice.com Data to guide optimal timing for surgical re-exploration are lacking; a reasonable approach may be serial debridement every 12-24 hours until minimal or no remaining necrotic tissue is encountered.[2]Sartelli M, Guirao X, Hardcastle TC, et al. 2018 WSES/SIS-E consensus conference: recommendations for the management of skin and soft-tissue infections. World J Emerg Surg. 2018 Dec 14;13:58. https://wjes.biomedcentral.com/articles/10.1186/s13017-018-0219-9 http://www.ncbi.nlm.nih.gov/pubmed/30564282?tool=bestpractice.com [3]Sartelli M, Coccolini F, Kluger Y, et al. WSES/GAIS/WSIS/SIS-E/AAST global clinical pathways for patients with skin and soft tissue infections. World J Emerg Surg. 2022 Jan 15;17(1):3. https://wjes.biomedcentral.com/articles/10.1186/s13017-022-00406-2 http://www.ncbi.nlm.nih.gov/pubmed/35033131?tool=bestpractice.com
supportive care
Treatment recommended for ALL patients in selected patient group
Intensive hemodynamic support is an important aspect of surgical management.[2]Sartelli M, Guirao X, Hardcastle TC, et al. 2018 WSES/SIS-E consensus conference: recommendations for the management of skin and soft-tissue infections. World J Emerg Surg. 2018 Dec 14;13:58. https://wjes.biomedcentral.com/articles/10.1186/s13017-018-0219-9 http://www.ncbi.nlm.nih.gov/pubmed/30564282?tool=bestpractice.com [3]Sartelli M, Coccolini F, Kluger Y, et al. WSES/GAIS/WSIS/SIS-E/AAST global clinical pathways for patients with skin and soft tissue infections. World J Emerg Surg. 2022 Jan 15;17(1):3. https://wjes.biomedcentral.com/articles/10.1186/s13017-022-00406-2 http://www.ncbi.nlm.nih.gov/pubmed/35033131?tool=bestpractice.com [5]Stevens DL, Bisno AL, Chambers HF, et al. Practice guidelines for the diagnosis and management of skin and soft tissue infections: 2014 update by the Infectious Diseases Society of America. Clin Infect Dis. 2014 Jul 15;59(2):e10-52. https://academic.oup.com/cid/article/59/2/e10/2895845 http://www.ncbi.nlm.nih.gov/pubmed/24973422?tool=bestpractice.com
Patients should receive adequate analgesia (e.g., an opioid).[2]Sartelli M, Guirao X, Hardcastle TC, et al. 2018 WSES/SIS-E consensus conference: recommendations for the management of skin and soft-tissue infections. World J Emerg Surg. 2018 Dec 14;13:58. https://wjes.biomedcentral.com/articles/10.1186/s13017-018-0219-9 http://www.ncbi.nlm.nih.gov/pubmed/30564282?tool=bestpractice.com
intravenous antibiotics
Treatment recommended for ALL patients in selected patient group
In addition to urgent surgical debridement, antibiotics should be administered that cover the most common etiologies of type I necrotizing fasciitis (a mixed infection with anaerobes such as Bacteroides or Peptostreptococcus with a facultative anaerobe such as Escherichia coli, Enterobacter, Klebsiella, Proteus, MRSA, or non-group A streptococcus).
Recommendations for type I mixed infections include vancomycin, linezolid, tedizolid, or daptomycin combined with either: piperacillin/tazobactam or a carbapenem (e.g., meropenem, imipenem/cilastatin, ertapenem).[2]Sartelli M, Guirao X, Hardcastle TC, et al. 2018 WSES/SIS-E consensus conference: recommendations for the management of skin and soft-tissue infections. World J Emerg Surg. 2018 Dec 14;13:58. https://wjes.biomedcentral.com/articles/10.1186/s13017-018-0219-9 http://www.ncbi.nlm.nih.gov/pubmed/30564282?tool=bestpractice.com [5]Stevens DL, Bisno AL, Chambers HF, et al. Practice guidelines for the diagnosis and management of skin and soft tissue infections: 2014 update by the Infectious Diseases Society of America. Clin Infect Dis. 2014 Jul 15;59(2):e10-52. https://academic.oup.com/cid/article/59/2/e10/2895845 http://www.ncbi.nlm.nih.gov/pubmed/24973422?tool=bestpractice.com
When further information is available and the etiologic agent has been determined, antibiotic therapy should be tailored to target the specific agent.
As there are currently no definitive clinical trials, the Infectious Diseases Society of America recommends continuing antibiotics until no further surgical debridement is needed, the patient has improved clinically, and fever has been absent for 48 to 72 hours.[5]Stevens DL, Bisno AL, Chambers HF, et al. Practice guidelines for the diagnosis and management of skin and soft tissue infections: 2014 update by the Infectious Diseases Society of America. Clin Infect Dis. 2014 Jul 15;59(2):e10-52. https://academic.oup.com/cid/article/59/2/e10/2895845 http://www.ncbi.nlm.nih.gov/pubmed/24973422?tool=bestpractice.com [55]Terzian WTH, Nunn AM, Call EB, et al. Duration of antibiotic therapy in necrotizing soft tissue infections: shorter is safe. Surg Infect (Larchmt). 2022 Jun;23(5):430-5. https://www.liebertpub.com/doi/10.1089/sur.2022.011 http://www.ncbi.nlm.nih.gov/pubmed/35451883?tool=bestpractice.com
Primary options
vancomycin: 15-20 mg/kg intravenously every 8-12 hours
More vancomycinAdjust dose according to serum vancomycin level.
or
linezolid: 600 mg intravenously every 12 hours
or
tedizolid phosphate: 200 mg intravenously every 24 hours
or
daptomycin: 4 mg/kg intravenously every 24 hours
-- AND --
piperacillin/tazobactam: 3.375 g intravenously every 6 hours
More piperacillin/tazobactamDose consists of 3 g piperacillin plus 0.375 g tazobactam.
or
imipenem/cilastatin: 1 g intravenously every 6-8 hours
More imipenem/cilastatinDose refers to imipenem component.
or
meropenem: 1 g intravenously every 8 hours
or
ertapenem: 1 g intravenously every 24 hours
These drug options and doses relate to a patient with no comorbidities.
Primary options
vancomycin: 15-20 mg/kg intravenously every 8-12 hours
More vancomycinAdjust dose according to serum vancomycin level.
or
linezolid: 600 mg intravenously every 12 hours
or
tedizolid phosphate: 200 mg intravenously every 24 hours
or
daptomycin: 4 mg/kg intravenously every 24 hours
-- AND --
piperacillin/tazobactam: 3.375 g intravenously every 6 hours
More piperacillin/tazobactamDose consists of 3 g piperacillin plus 0.375 g tazobactam.
or
imipenem/cilastatin: 1 g intravenously every 6-8 hours
More imipenem/cilastatinDose refers to imipenem component.
or
meropenem: 1 g intravenously every 8 hours
or
ertapenem: 1 g intravenously every 24 hours
Drug choice, dose and interactions may be affected by the patient's comorbidities. Check your local drug formulary.
Show drug information for a patient with no comorbidities
Primary options
vancomycin
or
linezolid
or
tedizolid phosphate
or
daptomycin
-- AND --
piperacillin/tazobactam
or
imipenem/cilastatin
or
meropenem
or
ertapenem
type II necrotizing fasciitis due to group A streptococcus
surgical debridement
Necrotizing fasciitis is a surgical emergency and the patient should be urgently taken to the operating room for debridement of all infected, devitalized tissues as soon as possible after initial resuscitation.[3]Sartelli M, Coccolini F, Kluger Y, et al. WSES/GAIS/WSIS/SIS-E/AAST global clinical pathways for patients with skin and soft tissue infections. World J Emerg Surg. 2022 Jan 15;17(1):3. https://wjes.biomedcentral.com/articles/10.1186/s13017-022-00406-2 http://www.ncbi.nlm.nih.gov/pubmed/35033131?tool=bestpractice.com
When debridement is performed, surgical incisions should extend beyond the areas of visible necrosis and the entire necrotic area excised.[3]Sartelli M, Coccolini F, Kluger Y, et al. WSES/GAIS/WSIS/SIS-E/AAST global clinical pathways for patients with skin and soft tissue infections. World J Emerg Surg. 2022 Jan 15;17(1):3. https://wjes.biomedcentral.com/articles/10.1186/s13017-022-00406-2 http://www.ncbi.nlm.nih.gov/pubmed/35033131?tool=bestpractice.com
Further surgical evaluation and debridement is necessary in most cases, and several procedures may be required to ensure that all necrotic tissue is removed.[5]Stevens DL, Bisno AL, Chambers HF, et al. Practice guidelines for the diagnosis and management of skin and soft tissue infections: 2014 update by the Infectious Diseases Society of America. Clin Infect Dis. 2014 Jul 15;59(2):e10-52. https://academic.oup.com/cid/article/59/2/e10/2895845 http://www.ncbi.nlm.nih.gov/pubmed/24973422?tool=bestpractice.com Data to guide optimal timing for surgical re-exploration are lacking; a reasonable approach may be serial debridement every 12-24 hours until minimal or no remaining necrotic tissue is encountered.[2]Sartelli M, Guirao X, Hardcastle TC, et al. 2018 WSES/SIS-E consensus conference: recommendations for the management of skin and soft-tissue infections. World J Emerg Surg. 2018 Dec 14;13:58. https://wjes.biomedcentral.com/articles/10.1186/s13017-018-0219-9 http://www.ncbi.nlm.nih.gov/pubmed/30564282?tool=bestpractice.com [3]Sartelli M, Coccolini F, Kluger Y, et al. WSES/GAIS/WSIS/SIS-E/AAST global clinical pathways for patients with skin and soft tissue infections. World J Emerg Surg. 2022 Jan 15;17(1):3. https://wjes.biomedcentral.com/articles/10.1186/s13017-022-00406-2 http://www.ncbi.nlm.nih.gov/pubmed/35033131?tool=bestpractice.com
supportive care
Treatment recommended for ALL patients in selected patient group
Intensive hemodynamic support is an important aspect of surgical management.[2]Sartelli M, Guirao X, Hardcastle TC, et al. 2018 WSES/SIS-E consensus conference: recommendations for the management of skin and soft-tissue infections. World J Emerg Surg. 2018 Dec 14;13:58. https://wjes.biomedcentral.com/articles/10.1186/s13017-018-0219-9 http://www.ncbi.nlm.nih.gov/pubmed/30564282?tool=bestpractice.com [3]Sartelli M, Coccolini F, Kluger Y, et al. WSES/GAIS/WSIS/SIS-E/AAST global clinical pathways for patients with skin and soft tissue infections. World J Emerg Surg. 2022 Jan 15;17(1):3. https://wjes.biomedcentral.com/articles/10.1186/s13017-022-00406-2 http://www.ncbi.nlm.nih.gov/pubmed/35033131?tool=bestpractice.com [5]Stevens DL, Bisno AL, Chambers HF, et al. Practice guidelines for the diagnosis and management of skin and soft tissue infections: 2014 update by the Infectious Diseases Society of America. Clin Infect Dis. 2014 Jul 15;59(2):e10-52. https://academic.oup.com/cid/article/59/2/e10/2895845 http://www.ncbi.nlm.nih.gov/pubmed/24973422?tool=bestpractice.com
Patients should receive adequate analgesia (e.g., an opioid).[2]Sartelli M, Guirao X, Hardcastle TC, et al. 2018 WSES/SIS-E consensus conference: recommendations for the management of skin and soft-tissue infections. World J Emerg Surg. 2018 Dec 14;13:58. https://wjes.biomedcentral.com/articles/10.1186/s13017-018-0219-9 http://www.ncbi.nlm.nih.gov/pubmed/30564282?tool=bestpractice.com
intravenous antibiotics
Treatment recommended for ALL patients in selected patient group
Type II infection is most commonly due to group A streptococcus; clindamycin plus penicillin is recommended.
For patients with a penicillin allergy, vancomycin monotherapy may be used.
Primary options
penicillin G sodium: 2-4 million units intravenously every 4-6 hours
and
clindamycin: 600-900 mg intravenously every 8 hours
Secondary options
vancomycin: 15-20 mg/kg intravenously every 8-12 hours
More vancomycinAdjust dose according to serum vancomycin level.
These drug options and doses relate to a patient with no comorbidities.
Primary options
penicillin G sodium: 2-4 million units intravenously every 4-6 hours
and
clindamycin: 600-900 mg intravenously every 8 hours
Secondary options
vancomycin: 15-20 mg/kg intravenously every 8-12 hours
More vancomycinAdjust dose according to serum vancomycin level.
Drug choice, dose and interactions may be affected by the patient's comorbidities. Check your local drug formulary.
Show drug information for a patient with no comorbidities
Primary options
penicillin G sodium
and
clindamycin
Secondary options
vancomycin
intravenous immune globulin (IVIG)
Treatment recommended for SOME patients in selected patient group
The addition of IVIG may be considered for treatment of streptococcal toxic shock syndrome, although data on efficacy are conflicting.[2]Sartelli M, Guirao X, Hardcastle TC, et al. 2018 WSES/SIS-E consensus conference: recommendations for the management of skin and soft-tissue infections. World J Emerg Surg. 2018 Dec 14;13:58. https://wjes.biomedcentral.com/articles/10.1186/s13017-018-0219-9 http://www.ncbi.nlm.nih.gov/pubmed/30564282?tool=bestpractice.com [3]Sartelli M, Coccolini F, Kluger Y, et al. WSES/GAIS/WSIS/SIS-E/AAST global clinical pathways for patients with skin and soft tissue infections. World J Emerg Surg. 2022 Jan 15;17(1):3. https://wjes.biomedcentral.com/articles/10.1186/s13017-022-00406-2 http://www.ncbi.nlm.nih.gov/pubmed/35033131?tool=bestpractice.com [5]Stevens DL, Bisno AL, Chambers HF, et al. Practice guidelines for the diagnosis and management of skin and soft tissue infections: 2014 update by the Infectious Diseases Society of America. Clin Infect Dis. 2014 Jul 15;59(2):e10-52. https://academic.oup.com/cid/article/59/2/e10/2895845 http://www.ncbi.nlm.nih.gov/pubmed/24973422?tool=bestpractice.com
Primary options
immune globulin (human): 1 g/kg intravenously on day 1, followed by 0.5 g/kg on days 2 and 3; or 2 g/kg intravenously as a single dose
More immune globulin (human)Dose regimens vary; consult specialist for further guidance on dose.
These drug options and doses relate to a patient with no comorbidities.
Primary options
immune globulin (human): 1 g/kg intravenously on day 1, followed by 0.5 g/kg on days 2 and 3; or 2 g/kg intravenously as a single dose
More immune globulin (human)Dose regimens vary; consult specialist for further guidance on dose.
Drug choice, dose and interactions may be affected by the patient's comorbidities. Check your local drug formulary.
Show drug information for a patient with no comorbidities
Primary options
immune globulin (human)
type II necrotizing fasciitis due to Staphylococcus aureus
surgical debridement
Necrotizing fasciitis is a surgical emergency and the patient should be urgently taken to the operating room for debridement of all infected, devitalized tissues as soon as possible after initial resuscitation.[3]Sartelli M, Coccolini F, Kluger Y, et al. WSES/GAIS/WSIS/SIS-E/AAST global clinical pathways for patients with skin and soft tissue infections. World J Emerg Surg. 2022 Jan 15;17(1):3. https://wjes.biomedcentral.com/articles/10.1186/s13017-022-00406-2 http://www.ncbi.nlm.nih.gov/pubmed/35033131?tool=bestpractice.com
When debridement is performed, surgical incisions should extend beyond the areas of visible necrosis and the entire necrotic area excised.[3]Sartelli M, Coccolini F, Kluger Y, et al. WSES/GAIS/WSIS/SIS-E/AAST global clinical pathways for patients with skin and soft tissue infections. World J Emerg Surg. 2022 Jan 15;17(1):3. https://wjes.biomedcentral.com/articles/10.1186/s13017-022-00406-2 http://www.ncbi.nlm.nih.gov/pubmed/35033131?tool=bestpractice.com
Further surgical evaluation and debridement is necessary in most cases, and several procedures may be required to ensure that all necrotic tissue is removed.[5]Stevens DL, Bisno AL, Chambers HF, et al. Practice guidelines for the diagnosis and management of skin and soft tissue infections: 2014 update by the Infectious Diseases Society of America. Clin Infect Dis. 2014 Jul 15;59(2):e10-52. https://academic.oup.com/cid/article/59/2/e10/2895845 http://www.ncbi.nlm.nih.gov/pubmed/24973422?tool=bestpractice.com Data to guide optimal timing for surgical re-exploration are lacking; a reasonable approach may be serial debridement every 12-24 hours until minimal or no remaining necrotic tissue is encountered.[2]Sartelli M, Guirao X, Hardcastle TC, et al. 2018 WSES/SIS-E consensus conference: recommendations for the management of skin and soft-tissue infections. World J Emerg Surg. 2018 Dec 14;13:58. https://wjes.biomedcentral.com/articles/10.1186/s13017-018-0219-9 http://www.ncbi.nlm.nih.gov/pubmed/30564282?tool=bestpractice.com [3]Sartelli M, Coccolini F, Kluger Y, et al. WSES/GAIS/WSIS/SIS-E/AAST global clinical pathways for patients with skin and soft tissue infections. World J Emerg Surg. 2022 Jan 15;17(1):3. https://wjes.biomedcentral.com/articles/10.1186/s13017-022-00406-2 http://www.ncbi.nlm.nih.gov/pubmed/35033131?tool=bestpractice.com
After complete removal of necrotic tissue and final debridement, negative pressure wound therapy may be considered to help with granulation and healing of the wound.[15]Hua C, Urbina T, Bosc R, et al. Necrotising soft-tissue infections. Lancet Infect Dis. 2023 Mar;23(3):e81-94. http://www.ncbi.nlm.nih.gov/pubmed/36252579?tool=bestpractice.com
supportive care
Treatment recommended for ALL patients in selected patient group
Intensive hemodynamic support is an important aspect of surgical management.[2]Sartelli M, Guirao X, Hardcastle TC, et al. 2018 WSES/SIS-E consensus conference: recommendations for the management of skin and soft-tissue infections. World J Emerg Surg. 2018 Dec 14;13:58. https://wjes.biomedcentral.com/articles/10.1186/s13017-018-0219-9 http://www.ncbi.nlm.nih.gov/pubmed/30564282?tool=bestpractice.com [3]Sartelli M, Coccolini F, Kluger Y, et al. WSES/GAIS/WSIS/SIS-E/AAST global clinical pathways for patients with skin and soft tissue infections. World J Emerg Surg. 2022 Jan 15;17(1):3. https://wjes.biomedcentral.com/articles/10.1186/s13017-022-00406-2 http://www.ncbi.nlm.nih.gov/pubmed/35033131?tool=bestpractice.com [5]Stevens DL, Bisno AL, Chambers HF, et al. Practice guidelines for the diagnosis and management of skin and soft tissue infections: 2014 update by the Infectious Diseases Society of America. Clin Infect Dis. 2014 Jul 15;59(2):e10-52. https://academic.oup.com/cid/article/59/2/e10/2895845 http://www.ncbi.nlm.nih.gov/pubmed/24973422?tool=bestpractice.com
Patients should receive adequate analgesia (e.g., an opioid).[2]Sartelli M, Guirao X, Hardcastle TC, et al. 2018 WSES/SIS-E consensus conference: recommendations for the management of skin and soft-tissue infections. World J Emerg Surg. 2018 Dec 14;13:58. https://wjes.biomedcentral.com/articles/10.1186/s13017-018-0219-9 http://www.ncbi.nlm.nih.gov/pubmed/30564282?tool=bestpractice.com
intravenous antibiotics
Treatment recommended for ALL patients in selected patient group
In addition to urgent surgical debridement, antistaphylococcal antibiotics should be administered.
Antibiotics active against MRSA should be used until cultures confirm susceptibilities. Options include vancomycin, linezolid, tedizolid, or daptomycin; ceftaroline, telavancin, or dalbavancin are also reasonable choices, although clinical data are sparse.[2]Sartelli M, Guirao X, Hardcastle TC, et al. 2018 WSES/SIS-E consensus conference: recommendations for the management of skin and soft-tissue infections. World J Emerg Surg. 2018 Dec 14;13:58. https://wjes.biomedcentral.com/articles/10.1186/s13017-018-0219-9 http://www.ncbi.nlm.nih.gov/pubmed/30564282?tool=bestpractice.com [5]Stevens DL, Bisno AL, Chambers HF, et al. Practice guidelines for the diagnosis and management of skin and soft tissue infections: 2014 update by the Infectious Diseases Society of America. Clin Infect Dis. 2014 Jul 15;59(2):e10-52. https://academic.oup.com/cid/article/59/2/e10/2895845 http://www.ncbi.nlm.nih.gov/pubmed/24973422?tool=bestpractice.com
Nafcillin, oxacillin, or cefazolin may be used if methicillin susceptibility is confirmed.
Primary options
MRSA
vancomycin: 15-20 mg/kg intravenously every 8-12 hours
More vancomycinAdjust dose according to serum vancomycin level.
OR
MRSA
linezolid: 600 mg intravenously every 12 hours
OR
MRSA
tedizolid phosphate: 200 mg intravenously every 24 hours
OR
MRSA
daptomycin: 4 mg/kg intravenously every 24 hours
Secondary options
MRSA
ceftaroline fosamil: 600 mg intravenously every 12 hours
OR
MRSA
dalbavancin: 1500 mg intravenously as a single dose; or 1000 mg intravenously as a single dose followed by 500 mg one week later
OR
MRSA
telavancin: 10 mg/kg intravenously every 24 hours
Tertiary options
MSSA
nafcillin: 1-2 g intravenously every 4 hours
OR
MSSA
oxacillin: 1-2 g intravenously every 4 hours
OR
MSSA
cefazolin: 1 g intravenously every 6-8 hours
These drug options and doses relate to a patient with no comorbidities.
Primary options
MRSA
vancomycin: 15-20 mg/kg intravenously every 8-12 hours
More vancomycinAdjust dose according to serum vancomycin level.
OR
MRSA
linezolid: 600 mg intravenously every 12 hours
OR
MRSA
tedizolid phosphate: 200 mg intravenously every 24 hours
OR
MRSA
daptomycin: 4 mg/kg intravenously every 24 hours
Secondary options
MRSA
ceftaroline fosamil: 600 mg intravenously every 12 hours
OR
MRSA
dalbavancin: 1500 mg intravenously as a single dose; or 1000 mg intravenously as a single dose followed by 500 mg one week later
OR
MRSA
telavancin: 10 mg/kg intravenously every 24 hours
Tertiary options
MSSA
nafcillin: 1-2 g intravenously every 4 hours
OR
MSSA
oxacillin: 1-2 g intravenously every 4 hours
OR
MSSA
cefazolin: 1 g intravenously every 6-8 hours
Drug choice, dose and interactions may be affected by the patient's comorbidities. Check your local drug formulary.
Show drug information for a patient with no comorbidities
Primary options
MRSA
vancomycin
OR
MRSA
linezolid
OR
MRSA
tedizolid phosphate
OR
MRSA
daptomycin
Secondary options
MRSA
ceftaroline fosamil
OR
MRSA
dalbavancin
OR
MRSA
telavancin
Tertiary options
MSSA
nafcillin
OR
MSSA
oxacillin
OR
MSSA
cefazolin
type II necrotizing fasciitis due to Vibrio vulnificus
surgical debridement
Necrotizing fasciitis is a surgical emergency and the patient should be urgently taken to the operating room for debridement of all infected, devitalized tissues as soon as possible after initial resuscitation.[3]Sartelli M, Coccolini F, Kluger Y, et al. WSES/GAIS/WSIS/SIS-E/AAST global clinical pathways for patients with skin and soft tissue infections. World J Emerg Surg. 2022 Jan 15;17(1):3. https://wjes.biomedcentral.com/articles/10.1186/s13017-022-00406-2 http://www.ncbi.nlm.nih.gov/pubmed/35033131?tool=bestpractice.com
When debridement is performed, surgical incisions should extend beyond the areas of visible necrosis and the entire necrotic area excised.[3]Sartelli M, Coccolini F, Kluger Y, et al. WSES/GAIS/WSIS/SIS-E/AAST global clinical pathways for patients with skin and soft tissue infections. World J Emerg Surg. 2022 Jan 15;17(1):3. https://wjes.biomedcentral.com/articles/10.1186/s13017-022-00406-2 http://www.ncbi.nlm.nih.gov/pubmed/35033131?tool=bestpractice.com
Further surgical evaluation and debridement is necessary in most cases, and several procedures may be required to ensure that all necrotic tissue is removed.[5]Stevens DL, Bisno AL, Chambers HF, et al. Practice guidelines for the diagnosis and management of skin and soft tissue infections: 2014 update by the Infectious Diseases Society of America. Clin Infect Dis. 2014 Jul 15;59(2):e10-52. https://academic.oup.com/cid/article/59/2/e10/2895845 http://www.ncbi.nlm.nih.gov/pubmed/24973422?tool=bestpractice.com Data to guide optimal timing for surgical re-exploration are lacking; a reasonable approach may be serial debridement every 12-24 hours until minimal or no remaining necrotic tissue is encountered.[2]Sartelli M, Guirao X, Hardcastle TC, et al. 2018 WSES/SIS-E consensus conference: recommendations for the management of skin and soft-tissue infections. World J Emerg Surg. 2018 Dec 14;13:58. https://wjes.biomedcentral.com/articles/10.1186/s13017-018-0219-9 http://www.ncbi.nlm.nih.gov/pubmed/30564282?tool=bestpractice.com [3]Sartelli M, Coccolini F, Kluger Y, et al. WSES/GAIS/WSIS/SIS-E/AAST global clinical pathways for patients with skin and soft tissue infections. World J Emerg Surg. 2022 Jan 15;17(1):3. https://wjes.biomedcentral.com/articles/10.1186/s13017-022-00406-2 http://www.ncbi.nlm.nih.gov/pubmed/35033131?tool=bestpractice.com
supportive care
Treatment recommended for ALL patients in selected patient group
Intensive hemodynamic support is an important aspect of surgical management.[2]Sartelli M, Guirao X, Hardcastle TC, et al. 2018 WSES/SIS-E consensus conference: recommendations for the management of skin and soft-tissue infections. World J Emerg Surg. 2018 Dec 14;13:58. https://wjes.biomedcentral.com/articles/10.1186/s13017-018-0219-9 http://www.ncbi.nlm.nih.gov/pubmed/30564282?tool=bestpractice.com [3]Sartelli M, Coccolini F, Kluger Y, et al. WSES/GAIS/WSIS/SIS-E/AAST global clinical pathways for patients with skin and soft tissue infections. World J Emerg Surg. 2022 Jan 15;17(1):3. https://wjes.biomedcentral.com/articles/10.1186/s13017-022-00406-2 http://www.ncbi.nlm.nih.gov/pubmed/35033131?tool=bestpractice.com [5]Stevens DL, Bisno AL, Chambers HF, et al. Practice guidelines for the diagnosis and management of skin and soft tissue infections: 2014 update by the Infectious Diseases Society of America. Clin Infect Dis. 2014 Jul 15;59(2):e10-52. https://academic.oup.com/cid/article/59/2/e10/2895845 http://www.ncbi.nlm.nih.gov/pubmed/24973422?tool=bestpractice.com
Patients should receive adequate analgesia (e.g., an opioid).[2]Sartelli M, Guirao X, Hardcastle TC, et al. 2018 WSES/SIS-E consensus conference: recommendations for the management of skin and soft-tissue infections. World J Emerg Surg. 2018 Dec 14;13:58. https://wjes.biomedcentral.com/articles/10.1186/s13017-018-0219-9 http://www.ncbi.nlm.nih.gov/pubmed/30564282?tool=bestpractice.com
intravenous antibiotics
Treatment recommended for ALL patients in selected patient group
Predisposing risk factors for Vibrio vulnificus infection include hepatic disease, diabetes mellitus, chronic renal insufficiency, and adrenal insufficiency.[9]Kuo YL, Shieh SJ, Chiu HY, et al. Necrotizing fasciitis caused by Vibrio vulnificus: epidemiology, clinical findings, treatment and prevention. Eur J Clin Microbiol Infect Dis. 2007 Nov;26(11):785-92. http://www.ncbi.nlm.nih.gov/pubmed/17674061?tool=bestpractice.com
Doxycycline is used in the management of type II necrotizing fasciitis attributable to Vibrio vulnificus alongside a cephalosporin.[5]Stevens DL, Bisno AL, Chambers HF, et al. Practice guidelines for the diagnosis and management of skin and soft tissue infections: 2014 update by the Infectious Diseases Society of America. Clin Infect Dis. 2014 Jul 15;59(2):e10-52. https://academic.oup.com/cid/article/59/2/e10/2895845 http://www.ncbi.nlm.nih.gov/pubmed/24973422?tool=bestpractice.com
Primary options
doxycycline: 100 mg intravenously every 12 hours
-- AND --
ceftazidime sodium: 2 g intravenously every 8 hours
or
ceftriaxone: 2 g intravenously every 12-24 hours
These drug options and doses relate to a patient with no comorbidities.
Primary options
doxycycline: 100 mg intravenously every 12 hours
-- AND --
ceftazidime sodium: 2 g intravenously every 8 hours
or
ceftriaxone: 2 g intravenously every 12-24 hours
Drug choice, dose and interactions may be affected by the patient's comorbidities. Check your local drug formulary.
Show drug information for a patient with no comorbidities
Primary options
doxycycline
-- AND --
ceftazidime sodium
or
ceftriaxone
type II necrotizing fasciitis due to Aeromonas hydrophila
surgical debridement
Necrotizing fasciitis is a surgical emergency and the patient should be urgently taken to the operating room for debridement of all infected, devitalized tissues as soon as possible after initial resuscitation.[3]Sartelli M, Coccolini F, Kluger Y, et al. WSES/GAIS/WSIS/SIS-E/AAST global clinical pathways for patients with skin and soft tissue infections. World J Emerg Surg. 2022 Jan 15;17(1):3. https://wjes.biomedcentral.com/articles/10.1186/s13017-022-00406-2 http://www.ncbi.nlm.nih.gov/pubmed/35033131?tool=bestpractice.com
When debridement is performed, surgical incisions should extend beyond the areas of visible necrosis and the entire necrotic area excised.[3]Sartelli M, Coccolini F, Kluger Y, et al. WSES/GAIS/WSIS/SIS-E/AAST global clinical pathways for patients with skin and soft tissue infections. World J Emerg Surg. 2022 Jan 15;17(1):3. https://wjes.biomedcentral.com/articles/10.1186/s13017-022-00406-2 http://www.ncbi.nlm.nih.gov/pubmed/35033131?tool=bestpractice.com
Further surgical evaluation and debridement is necessary in most cases, and several procedures may be required to ensure that all necrotic tissue is removed.[5]Stevens DL, Bisno AL, Chambers HF, et al. Practice guidelines for the diagnosis and management of skin and soft tissue infections: 2014 update by the Infectious Diseases Society of America. Clin Infect Dis. 2014 Jul 15;59(2):e10-52. https://academic.oup.com/cid/article/59/2/e10/2895845 http://www.ncbi.nlm.nih.gov/pubmed/24973422?tool=bestpractice.com Data to guide optimal timing for surgical re-exploration are lacking; a reasonable approach may be serial debridement every 12-24 hours until minimal or no remaining necrotic tissue is encountered.[2]Sartelli M, Guirao X, Hardcastle TC, et al. 2018 WSES/SIS-E consensus conference: recommendations for the management of skin and soft-tissue infections. World J Emerg Surg. 2018 Dec 14;13:58. https://wjes.biomedcentral.com/articles/10.1186/s13017-018-0219-9 http://www.ncbi.nlm.nih.gov/pubmed/30564282?tool=bestpractice.com [3]Sartelli M, Coccolini F, Kluger Y, et al. WSES/GAIS/WSIS/SIS-E/AAST global clinical pathways for patients with skin and soft tissue infections. World J Emerg Surg. 2022 Jan 15;17(1):3. https://wjes.biomedcentral.com/articles/10.1186/s13017-022-00406-2 http://www.ncbi.nlm.nih.gov/pubmed/35033131?tool=bestpractice.com
supportive care
Treatment recommended for ALL patients in selected patient group
Intensive hemodynamic support is an important aspect of surgical management.[2]Sartelli M, Guirao X, Hardcastle TC, et al. 2018 WSES/SIS-E consensus conference: recommendations for the management of skin and soft-tissue infections. World J Emerg Surg. 2018 Dec 14;13:58. https://wjes.biomedcentral.com/articles/10.1186/s13017-018-0219-9 http://www.ncbi.nlm.nih.gov/pubmed/30564282?tool=bestpractice.com [3]Sartelli M, Coccolini F, Kluger Y, et al. WSES/GAIS/WSIS/SIS-E/AAST global clinical pathways for patients with skin and soft tissue infections. World J Emerg Surg. 2022 Jan 15;17(1):3. https://wjes.biomedcentral.com/articles/10.1186/s13017-022-00406-2 http://www.ncbi.nlm.nih.gov/pubmed/35033131?tool=bestpractice.com [5]Stevens DL, Bisno AL, Chambers HF, et al. Practice guidelines for the diagnosis and management of skin and soft tissue infections: 2014 update by the Infectious Diseases Society of America. Clin Infect Dis. 2014 Jul 15;59(2):e10-52. https://academic.oup.com/cid/article/59/2/e10/2895845 http://www.ncbi.nlm.nih.gov/pubmed/24973422?tool=bestpractice.com
Patients should receive adequate analgesia (e.g., an opioid).[2]Sartelli M, Guirao X, Hardcastle TC, et al. 2018 WSES/SIS-E consensus conference: recommendations for the management of skin and soft-tissue infections. World J Emerg Surg. 2018 Dec 14;13:58. https://wjes.biomedcentral.com/articles/10.1186/s13017-018-0219-9 http://www.ncbi.nlm.nih.gov/pubmed/30564282?tool=bestpractice.com
intravenous antibiotics
Treatment recommended for ALL patients in selected patient group
Aeromonas hydrophila infection may cause necrotizing fasciitis in patients with suppressed immune systems, burns, and trauma in an aquatic setting.[10]Markov G, Kirov G, Lyutskanov V, et al. Necrotizing fasciitis and myonecrosis due to Aeromonas hydrophila. Wounds. 2007 Aug;19(8):223-6. http://www.ncbi.nlm.nih.gov/pubmed/26110366?tool=bestpractice.com
Doxycycline is used in the management of type II necrotizing fasciitis attributable to Aeromonas hydrophila alongside a cephalosporin (e.g., ceftriaxone) or a fluoroquinolone (e.g., ciprofloxacin).[5]Stevens DL, Bisno AL, Chambers HF, et al. Practice guidelines for the diagnosis and management of skin and soft tissue infections: 2014 update by the Infectious Diseases Society of America. Clin Infect Dis. 2014 Jul 15;59(2):e10-52. https://academic.oup.com/cid/article/59/2/e10/2895845 http://www.ncbi.nlm.nih.gov/pubmed/24973422?tool=bestpractice.com
Systemic fluoroquinolone antibiotics may cause serious, disabling, and potentially long-lasting or irreversible adverse events. This includes, but is not limited to: tendinopathy/tendon rupture; peripheral neuropathy; arthropathy/arthralgia; aortic aneurysm and dissection; heart valve regurgitation; dysglycemia; and central nervous system effects including seizures, depression, psychosis, and suicidal thoughts and behavior.[56]Rusu A, Munteanu AC, Arbănași EM, et al. Overview of side-effects of antibacterial fluoroquinolones: new drugs versus old drugs, a step forward in the safety profile? Pharmaceutics. 2023 Mar 1;15(3):804. https://www.doi.org/10.3390/pharmaceutics15030804 http://www.ncbi.nlm.nih.gov/pubmed/36986665?tool=bestpractice.com Prescribing restrictions apply to the use of fluoroquinolones, and these restrictions may vary between countries. In general, fluoroquinolones should be restricted for use in serious, life-threatening bacterial infections only. Some regulatory agencies may also recommend that they must only be used in situations where other antibiotics that are commonly recommended for the infection are inappropriate (e.g., resistance, contraindications, treatment failure, unavailability). Consult your local guidelines and drug information source for more information on suitability, contraindications, and precautions.
Primary options
doxycycline: 100 mg intravenously every 12 hours
-- AND --
ceftriaxone: 2 g intravenously every 12-24 hours
or
ciprofloxacin: 400 mg intravenously every 8-12 hours
These drug options and doses relate to a patient with no comorbidities.
Primary options
doxycycline: 100 mg intravenously every 12 hours
-- AND --
ceftriaxone: 2 g intravenously every 12-24 hours
or
ciprofloxacin: 400 mg intravenously every 8-12 hours
Drug choice, dose and interactions may be affected by the patient's comorbidities. Check your local drug formulary.
Show drug information for a patient with no comorbidities
Primary options
doxycycline
-- AND --
ceftriaxone
or
ciprofloxacin
type II necrotizing fasciitis due to mucorales
surgical debridement
Necrotizing fasciitis is a surgical emergency and the patient should be urgently taken to the operating room for debridement of all infected, devitalized tissues as soon as possible after initial resuscitation.[3]Sartelli M, Coccolini F, Kluger Y, et al. WSES/GAIS/WSIS/SIS-E/AAST global clinical pathways for patients with skin and soft tissue infections. World J Emerg Surg. 2022 Jan 15;17(1):3. https://wjes.biomedcentral.com/articles/10.1186/s13017-022-00406-2 http://www.ncbi.nlm.nih.gov/pubmed/35033131?tool=bestpractice.com
When debridement is performed, surgical incisions should extend beyond the areas of visible necrosis and the entire necrotic area excised.[3]Sartelli M, Coccolini F, Kluger Y, et al. WSES/GAIS/WSIS/SIS-E/AAST global clinical pathways for patients with skin and soft tissue infections. World J Emerg Surg. 2022 Jan 15;17(1):3. https://wjes.biomedcentral.com/articles/10.1186/s13017-022-00406-2 http://www.ncbi.nlm.nih.gov/pubmed/35033131?tool=bestpractice.com
Further surgical evaluation and debridement is necessary in most cases, and several procedures may be required to ensure that all necrotic tissue is removed.[5]Stevens DL, Bisno AL, Chambers HF, et al. Practice guidelines for the diagnosis and management of skin and soft tissue infections: 2014 update by the Infectious Diseases Society of America. Clin Infect Dis. 2014 Jul 15;59(2):e10-52. https://academic.oup.com/cid/article/59/2/e10/2895845 http://www.ncbi.nlm.nih.gov/pubmed/24973422?tool=bestpractice.com Data to guide optimal timing for surgical re-exploration are lacking; a reasonable approach may be serial debridement every 12-24 hours until minimal or no remaining necrotic tissue is encountered.[2]Sartelli M, Guirao X, Hardcastle TC, et al. 2018 WSES/SIS-E consensus conference: recommendations for the management of skin and soft-tissue infections. World J Emerg Surg. 2018 Dec 14;13:58. https://wjes.biomedcentral.com/articles/10.1186/s13017-018-0219-9 http://www.ncbi.nlm.nih.gov/pubmed/30564282?tool=bestpractice.com [3]Sartelli M, Coccolini F, Kluger Y, et al. WSES/GAIS/WSIS/SIS-E/AAST global clinical pathways for patients with skin and soft tissue infections. World J Emerg Surg. 2022 Jan 15;17(1):3. https://wjes.biomedcentral.com/articles/10.1186/s13017-022-00406-2 http://www.ncbi.nlm.nih.gov/pubmed/35033131?tool=bestpractice.com
After complete removal of necrotic tissue and final debridement, negative pressure wound therapy may be considered to help with granulation and healing of the wound.[15]Hua C, Urbina T, Bosc R, et al. Necrotising soft-tissue infections. Lancet Infect Dis. 2023 Mar;23(3):e81-94. http://www.ncbi.nlm.nih.gov/pubmed/36252579?tool=bestpractice.com
supportive care
Treatment recommended for ALL patients in selected patient group
Intensive hemodynamic support is an important aspect of surgical management.[2]Sartelli M, Guirao X, Hardcastle TC, et al. 2018 WSES/SIS-E consensus conference: recommendations for the management of skin and soft-tissue infections. World J Emerg Surg. 2018 Dec 14;13:58. https://wjes.biomedcentral.com/articles/10.1186/s13017-018-0219-9 http://www.ncbi.nlm.nih.gov/pubmed/30564282?tool=bestpractice.com [3]Sartelli M, Coccolini F, Kluger Y, et al. WSES/GAIS/WSIS/SIS-E/AAST global clinical pathways for patients with skin and soft tissue infections. World J Emerg Surg. 2022 Jan 15;17(1):3. https://wjes.biomedcentral.com/articles/10.1186/s13017-022-00406-2 http://www.ncbi.nlm.nih.gov/pubmed/35033131?tool=bestpractice.com [5]Stevens DL, Bisno AL, Chambers HF, et al. Practice guidelines for the diagnosis and management of skin and soft tissue infections: 2014 update by the Infectious Diseases Society of America. Clin Infect Dis. 2014 Jul 15;59(2):e10-52. https://academic.oup.com/cid/article/59/2/e10/2895845 http://www.ncbi.nlm.nih.gov/pubmed/24973422?tool=bestpractice.com
Patients should receive adequate analgesia (e.g., an opioid).[2]Sartelli M, Guirao X, Hardcastle TC, et al. 2018 WSES/SIS-E consensus conference: recommendations for the management of skin and soft-tissue infections. World J Emerg Surg. 2018 Dec 14;13:58. https://wjes.biomedcentral.com/articles/10.1186/s13017-018-0219-9 http://www.ncbi.nlm.nih.gov/pubmed/30564282?tool=bestpractice.com
antifungal therapy
Treatment recommended for ALL patients in selected patient group
Although necrotizing mucormycosis predominantly affects immunocompromised people, it may also occur in immunocompetent individuals.[12]Jain D, Kumar Y, Vasishta RK, et al. Zygomycotic necrotizing fasciitis in immunocompetent patients: a series of 18 cases. Mod Pathol. 2006 Sep;19(9):1221-6. http://www.nature.com/articles/3800639 http://www.ncbi.nlm.nih.gov/pubmed/16741524?tool=bestpractice.com [13]Neblett Fanfair R, Benedict K, Bos J, et al. Necrotizing cutaneous mucormycosis after a tornado in Joplin, Missouri, in 2011. N Engl J Med. 2012 Dec 6;367(23):2214-25. http://www.nejm.org/doi/full/10.1056/NEJMoa1204781 http://www.ncbi.nlm.nih.gov/pubmed/23215557?tool=bestpractice.com [14]Ribes JA, Vanover-Sams CL, Baker DJ. Zygomycetes in human disease. Clin Microbiol Rev. 2000 Apr;13(2):236-301. http://cmr.asm.org/content/13/2/236.long http://www.ncbi.nlm.nih.gov/pubmed/10756000?tool=bestpractice.com
Primary options
amphotericin B lipid complex: 5 mg/kg intravenously every 24 hours
Secondary options
isavuconazonium sulfate: 372 mg intravenously/orally every 8 hours for 6 doses as a loading dose, followed by 372 mg every 24 hours (initiate maintenance dose 12-24 hours after last loading dose)
More isavuconazonium sulfate372 mg isavuconazonium is equivalent to 200 mg isavuconazole.
These drug options and doses relate to a patient with no comorbidities.
Primary options
amphotericin B lipid complex: 5 mg/kg intravenously every 24 hours
Secondary options
isavuconazonium sulfate: 372 mg intravenously/orally every 8 hours for 6 doses as a loading dose, followed by 372 mg every 24 hours (initiate maintenance dose 12-24 hours after last loading dose)
More isavuconazonium sulfate372 mg isavuconazonium is equivalent to 200 mg isavuconazole.
Drug choice, dose and interactions may be affected by the patient's comorbidities. Check your local drug formulary.
Show drug information for a patient with no comorbidities
Primary options
amphotericin B lipid complex
Secondary options
isavuconazonium sulfate
persistent cosmetic and functional defects after debridement
reconstructive surgery
Supportive surgical interventions, such as fecal diversion for colostomy in cases of Fournier gangrene with fecal contamination, or tracheostomy for patients with cervicofacial necrotizing fasciitis may be warranted.[3]Sartelli M, Coccolini F, Kluger Y, et al. WSES/GAIS/WSIS/SIS-E/AAST global clinical pathways for patients with skin and soft tissue infections. World J Emerg Surg. 2022 Jan 15;17(1):3. https://wjes.biomedcentral.com/articles/10.1186/s13017-022-00406-2 http://www.ncbi.nlm.nih.gov/pubmed/35033131?tool=bestpractice.com [18]Ord R, Coletti D. Cervico-facial necrotizing fasciitis. Oral Dis. 2009 Mar;15(2):133-41. http://www.ncbi.nlm.nih.gov/pubmed/19207484?tool=bestpractice.com
Where functional and cosmetic disability results from extensive surgical debridement for necrotizing fasciitis, reconstructive surgery may be required.[3]Sartelli M, Coccolini F, Kluger Y, et al. WSES/GAIS/WSIS/SIS-E/AAST global clinical pathways for patients with skin and soft tissue infections. World J Emerg Surg. 2022 Jan 15;17(1):3.
https://wjes.biomedcentral.com/articles/10.1186/s13017-022-00406-2
http://www.ncbi.nlm.nih.gov/pubmed/35033131?tool=bestpractice.com
[Figure caption and citation for the preceding image starts]: Late signs of necrotizing fasciitis with extensive cellulitis, induration, skin necrosis, and formation of hemorrhagic bullaeFrom: Hasham S, Matteucci P, Stanley PRW, et al. Necrotising fasciitis. BMJ. 2005 Apr 9;330(7495):830-3 [Citation ends].
After prolonged hospitalization and recurrent surgical interventions, physical therapy and rehabilitation may be needed for certain patients.
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