Suspected skin or soft tissue infection (adult)
Red, warm, swollen, painful skin. Adults only; children need a paediatric guideline.
Cellulitis & Skin/Soft Tissue Infection Management (IDSA 2014): Suspected skin or soft tissue infection (adult) → Assess severity, type and mimics → Red...
Pathway Overview
21 steps
21 total
Red, warm, swollen, painful skin. Adults only; children need a paediatric guideline.
Check vital signs first: look for sepsis and necrotising infection.
Pain out of proportion, rapid spread, hard wooden tissue, oedema beyond the redness, crepitus, bullae, skin necrosis or bruising, systemic toxicity.
Surgical exploration confirms the diagnosis. CT or MRI must not delay surgery.
Adult doses. Children: seek specialist advice.
Continue antibiotics until no more debridement is needed, the patient improves and fever has gone for 48–72 h.
Children, bites, water-exposed wounds, diabetic foot, periorbital or orbital cellulitis, neutropenia, severe immunocompromise, penicillin allergy.
Streptococci cause most cases. MRSA is an unusual cause of typical cellulitis.
Prior MRSA infection or colonisation, MRSA elsewhere, injection drug use, penetrating trauma, recent hospitalisation, Aboriginal and Torres Strait Islander or Pacific Islander people, or a high-MRSA area (for example NT, remote north Queensland, US community).
Check these before you choose an oral MRSA-active antibiotic.
Oral options for mild infection. Vancomycin IV for moderate or severe infection.
Systemic signs, hypotension, confusion, severe immunocompromise, failed oral therapy, poor adherence or cannot take oral medicines.
Purulent infection, suspected S. aureus or failed oral beta-lactam: add vancomycin IV. Switch to oral when improving.
Redness can worsen for a short time after antibiotics start. Compare with the marked border.
Treat predisposing factors (oedema, tinea, venous disease). 3–4 episodes a year: consider penicillin prophylaxis.
Look for an abscess, necrotising infection, resistant organism or another diagnosis.
Extend treatment beyond 5 days until improved.
Review in 48–72 hours. Return at once if the redness spreads fast, fever starts or pain becomes severe.
Drainage is the main treatment. Many drained abscesses need no antibiotic.
IDSA Practice Guidelines for the Diagnosis and Management of Skin and Soft Tissue Infections: 2014 Update (Stevens DL et al., Clin Infect Dis 2014;59:e10-e52)
Clinical Decision Support — Not a Substitute for Clinical Judgment
Individual patient factors may require deviation from these recommendations.
Known Limitations
Contraindicated Populations
Applicable Regions
AU: IV and oral beta-lactam doses follow the Safer Care Victoria Adult Sepsis Pathway (2025, skin source; adapted from Therapeutic Guidelines) and eTG-based durations (Aust Prescr 2019). Community MRSA is common in the NT and remote north Queensland. Doxycycline is TGA pregnancy category D; sulfamethoxazole C; clindamycin and cefalexin A.
US: IDSA 2014 alternatives: cefazolin 1 g IV 8-hourly, ceftriaxone, dicloxacillin 500 mg orally 6-hourly. Severe non-purulent infection: vancomycin plus piperacillin-tazobactam.
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The Cellulitis & Skin/Soft Tissue Infection Management (IDSA 2014) is a management clinical algorithm for Infectious Disease. It provides a structured decision tree to guide clinical decision-making, based on IDSA Practice Guidelines for the Diagnosis and Management of Skin and Soft Tissue Infections: 2014 Update (Stevens DL et al., Clin Infect Dis 2014;59:e10-e52).
This algorithm is based on IDSA Practice Guidelines for the Diagnosis and Management of Skin and Soft Tissue Infections: 2014 Update (Stevens DL et al., Clin Infect Dis 2014;59:e10-e52) (DOI: 10.1093/cid/ciu296).
Known limitations include: Adults only. Children need weight-based doses from a paediatric guideline.; MRSA rates differ by region. Use local susceptibility data (Australia: Therapeutic Guidelines: Antibiotic).; Bites, water-exposed wounds, diabetic foot, orbital cellulitis and neutropenia need specific pathways.; Doses assume normal renal function; adjust vancomycin and TMP-SMX in renal impairment.; Surgical site infections and pyomyositis are not covered; use a specific guideline.. Individual patient factors may require deviation from these recommendations.
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