Sandbox/cellulitis

Jump to navigation Jump to search

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Mugilan Poongkunran M.B.B.S [2]

Cellulitis Microchapters

Home

Patient Information

Overview

Historical perspective

Classification

Pathophysiology

Causes

Differentiating Cellulitis from other Diseases

Epidemiology and Demographics

Risk Factors

Natural History, Complications and Prognosis

Diagnosis

Diagnostic study of choice

History and Symptoms

Physical Examination

Laboratory Findings

Chest X Ray

CT

MRI

Ultrasound

Other Diagnostic Studies

Treatment

Medical Therapy

Surgery

Primary Prevention

Secondary Prevention

Cost-Effectiveness of Therapy

Future or Investigational Therapies

Case Studies

Case #1

Sandbox/cellulitis On the Web

Most recent articles

Most cited articles

Review articles

CME Programs

Powerpoint slides

Images

American Roentgen Ray Society Images of Sandbox/cellulitis

All Images
X-rays
Echo & Ultrasound
CT Images
MRI

Ongoing Trials at Clinical Trials.gov

US National Guidelines Clearinghouse

NICE Guidance

FDA on Sandbox/cellulitis

CDC on Sandbox/cellulitis

Sandbox/cellulitis in the news

Blogs on Sandbox/cellulitis

Directions to Hospitals Treating Cellulitis

Risk calculators and risk factors for Sandbox/cellulitis

Overview

Typically a combination of intravenous and oral antibiotics are administered for the treatment of cellulitis. Bed rest and elevation of the affected limbs are recommended to accompany the antibiotic treatment. In patients with edema of the extremities, compressive stockings may really aid in treating the fluid accumulation. Small abscesses surrounding the affected tissue can be treated with a simple incision and drainage of the fluid. It is advised to drink plenty of fluids during your treatment and recovery.

Non-Antibiotic Therapy

  • Elevation of the affected area facilitates gravity drainage of edema and inflammatory substances. The skin should be sufficiently hydrated to avoid dryness and cracking without interdigital maceration.
  • Treat underlying conditions such as tinea pedis, lymphedema, and chronic venous insufficiency, that predispose them to developing recurrent cellulitis.
  • Compressive stockings and diuretic therapy may help patients with edema.

Medical Therapy

  • The antibiotic selection for treatment of cellulitis depends on whether the clinical presentation is purulent or nonpurulent, as purulent cellulitis is potentially attributable to staphylococcus aureus, which should be empirically treated with Beta-lactam antibiotics.[1] Latest reports suggest that this bacterium has acquired resistance (MRSA) and newer drugs are to be used to kill off the pathogen. Reports from the laboratory regarding the sensitivity of the pathogen is a key factor in deciding the therapy.
  • Choice of the antibiotic therapy for cellulitis depends on the follwoing factors:
    • Age of the individual: Early hospitalization and parenteral therapy are required for treatment of cellulitis in neonates, except for the mildest of cases.
    • Co-morbid conditions
    • Site of lesion
    • Severity of lesion
    • Pathogen involved (gram positive or negative and aerobic or anaerobic)
    • Strain and resistance of the pathogen

Uncomplicated Cellulitis

Severe Cellulitis

  • In severe cases of the disease, parenteral therapy is advocated.
  • Higher generations of cephalosporins such as ceftriaxone, and cefuroxime are used.
  • Patients with a penicillin allergy can be given vancomycin and clindamycin.
  • In diabetic individuals, broad coverage antibiotics are used. Carbapenams, beta-lactam antibiotics with Beta-lactamase inhibitors are given in a combined regimen for antibiotic coverage.
  • The duration of therapy should be individualized depending on clinical response; 5 to 10 days is usually appropriate (7 to 10 days in neonates); longer duration of therapy may be warranted in patients with severe disease.

Empiric Therapy for Cellulitis in Neonates

▸ Click on the following categories to expand treatment regimens.

Age Groups

  ▸  Infants 0 to 4 weeks of age

  ▸  Infants <1 week of age

  ▸  Infants ≥1 week of age

Infants 0 to 4 weeks of age
Parental Regimen
Vancomycin 15 mg/kg IV q24h
PLUS
Cefotaxime 50 mg/kg IV q12h
OR
Gentamicin 2.5 mg/kg IV q18-24h
Infants 0 to 4 weeks of age
Oral Regimen
Clindamycin 5 mg/kg orally q12h
OR
Linezolid 10 mg/kg orally q8-12h
Infants <1 week of age (BW 1200 to 2000 g)
Parental Regimen
Vancomycin 10 to 15 mg/kg IV q12-18h
PLUS
Cefotaxime 50 mg/kg IV q12h
OR
Gentamicin 2.5 mg/kg IV q12h
Infants <1 week of age (BW 1200 to 2000 g)
Oral Regimen
Clindamycin 5 mg/kg orally q12h
OR
Linezolid 10 mg/kg orally q8-12h
Infants <1 week of age (BW >2000 g)
Parental Regimen
Vancomycin 10 to 15 mg/kg IV q8-12h
PLUS
Cefotaxime 50 mg/kg IV q8-12h
OR
Gentamicin 2.5 mg/kg IV q12h
Infants <1 week of age (BW >2000 g)
Oral Regimen
Clindamycin 5 mg/kg orally q8h
OR
Linezolid 10 mg/kg orally q8-12h
Infants ≥1 week of age (BW 1200 to 2000 g)
Parental Regimen
Vancomycin 10 to 15 mg/kg IV q8-12h
PLUS
Cefotaxime 50 mg/kg IV q8h
OR
Gentamicin 2.5 mg/kg IV q8-12h
Infants ≥1 week of age (BW 1200 to 2000 g)
Oral Regimen
Clindamycin 5 mg/kg orally q8h
OR
Linezolid 10 mg/kg orally q8h
Infants ≥1 week of age (BW > 2000 g)
Parental Regimen
Vancomycin 10 to 15 mg/kg IV q6-8h
PLUS
Cefotaxime 50 mg/kg IV q6-8h
OR
Gentamicin 2.5 mg/kg IV q8h
Infants ≥1 week of age (BW > 2000 g)
Oral Regimen
Clindamycin 5 mg/kg orally q6h
OR
Linezolid 10 mg/kg orally q8h

Note:

  • Treatment of cellulitis in neonates usually requires hospitalization and parenteral therapy. Oral therapy is given for completion of the treatment when the patogen is unknown.
  • Optimal dose should be based on determination of serum concentrations.

Empiric Therapy for Cellulitis in Adults and Children > 28 days

▸ Click on the following categories to expand treatment regimens.

MSSA

  ▸  Adults

  ▸  Children age >28 days

Adults
Parental Regimen
Cefazolin 1-2 g IV q8h
OR
Oxacillin 2g IV q4h
OR
Nafcillin 2g IV q4h
Alternative Regimen
Clindamycin 600-900 mg IV q8h
Adults
Oral Regimen
Dicloxacillin 500 mg orally q6h
OR
Cephalexin 500 mg orally q6h
Alternative Regimen
Clindamycin 300-450 mg orally q6-8h
Children age >28 days
Parental Regimen
Cefazolin 100 mg/kg per day IV in 3-4 doses
OR
Oxacillin 150-200 mg/kg per day IV in 4-6 doses
OR
Nafcillin 150-200 mg/kg per day IV in 4-6 doses
Alternative Regimen
Clindamycin 25-40 mg/kg per day IV in 3-4 doses
Children age >28 days
Oral Regimen
Dicloxacillin 25-50 mg/kg per day orally in 4 doses
OR
Cephalexin 25-50 mg/kg per day orally in 3-4 doses
Alternative Regimen
Clindamycin 20-30 mg/kg per day orally in 4 doses

▸ Click on the following categories to expand treatment regimens.

[2]

MRSA

  ▸  Adults

  ▸  Children age >28 days

Adults
Parental Regimen
Vancomycin 15-20 mg/kg/dose q8-12h, not to exceed 2 g per dose
Alternative Regimen
Linezolid 600 mg IV q12h
OR
Ceftaroline 600 mg IV q12h
OR
Tigecycline 100 mg IV once, thereafter 50 mg IV q12h
OR
Daptomycin 4 mg/kg IV q24h (for skin and soft tissue infections); 6 mg/kg IV once daily (for bacteremia)
Adults
Oral Regimen
Amoxicillin 500 mg orally q8h
PLUS
Trimethoprim-sulfamethoxazole 1 double strength tablet orally q12h
Alternative Regimen
Clindamycin 300 to 450 mg q8h
OR
Linezolid 600 mg orally q12h
OR
Tedizolid 200 mg orally q24h
OR
Amoxicillin 500 mg orally q8h PLUS Minocycline 200 mg once, then 100 mg orally q12h


OR
Amoxicillin 500 mg orally q8h PLUS Doxycycline 100 mg orally q12h

Children age >28 days
Oral Regimen
Amoxicillin 25-50 mg/kg per day orally divided in 3 doses
PLUS
Trimethoprim-sulfamethoxazole 8-12 mg trimethoprim component/kg per day orally divided in 2 doses
Alternative Regimen
Clindamycin 40 mg/kg per day orally divided in 3-4 doses
OR
Linezolid <12 years: 30 mg/kg per day orally divided in 3 doses, ≥12 years: 600 mg orally q12h
OR
Amoxicillin 25-50 mg/kg per day orally divided in 3 doses PLUS Minocycline 24 mg/kg orally once, then 4 mg/kg per day divided in 2 doses
OR
Amoxicillin 25-50 mg/kg per day orally divided in 3 doses PLUS Doxycycline ≤45 kg: 4 mg/kg per day orally divided in 2 doses, >45 kg: 100 mg orally q12h

Note:

  • The above antibiotic regimen is NOT for initial empirical treatment of infections involving the face.
  • Dose alteration for renal insufficiency may be needed in case of cephalosporins.
  • Clindamycin is an alternate therapy for patients at risk of severe hypersensitivity reaction to penicillins and cephalosporins.
  • Doxycycline is NOT recommended for children <8 years of age.

Special Cases

  • Bite Wounds (Mammalian).
    • Bite wounds suffered from a mammal often contain polymicrobial sources that are anaerobic in nature.[9]
    • Mild cases can be treated with amoxicillin and clavulanate, and in cases of penicillin allergy cotrimoxazole along with metronidazole is used.
    • In severe cases, piperacillin and tazobactum are used.
  • Acquatic punctures and lacerations.[10]
    • This is seen mainly in professional swimmers and divers both in freshwater and in brackish water.
    • Failure to recognize these wounds and delay treatment may cause a larger morbidity.
    • Wounds in fresh water are treated with doxycycline and ceftazidime (or fluroquinolones).
    • Wounds in brackish water are treated with ceftazidime and levofloxacin.

References

  1. Liu C, Bayer A, Cosgrove SE, Daum RS, Fridkin SK, Gorwitz RJ; et al. (2011). "Clinical practice guidelines by the infectious diseases society of america for the treatment of methicillin-resistant Staphylococcus aureus infections in adults and children". Clin Infect Dis. 52 (3): e18–55. doi:10.1093/cid/ciq146. PMID 21208910.
  2. 2.0 2.1 2.2 Liu C, Bayer A, Cosgrove SE, Daum RS, Fridkin SK, Gorwitz RJ; et al. (2011). "Clinical practice guidelines by the infectious diseases society of america for the treatment of methicillin-resistant Staphylococcus aureus infections in adults and children: executive summary". Clin Infect Dis. 52 (3): 285–92. doi:10.1093/cid/cir034. PMID 21217178.
  3. Moran GJ, Krishnadasan A, Gorwitz RJ; et al. (2006). "Methicillin-resistant S. aureus infections among patients in the emergency department". N. Engl. J. Med. 355 (7): 666–74. doi:10.1056/NEJMoa055356. PMID 16914702. Unknown parameter |month= ignored (help)
  4. Stryjewski ME, Chambers HF (2008). "Skin and soft-tissue infections caused by community-acquired methicillin-resistant Staphylococcus aureus". Clin. Infect. Dis. 46 Suppl 5: S368–77. doi:10.1086/533593. PMID 18462092. Unknown parameter |month= ignored (help)
  5. Stevens DL, Bisno AL, Chambers HF; et al. (2005). "Practice guidelines for the diagnosis and management of skin and soft-tissue infections". Clin. Infect. Dis. 41 (10): 1373–406. doi:10.1086/497143. PMID 16231249. Unknown parameter |month= ignored (help)
  6. Pallin DJ, Binder WD, Allen MB, Lederman M, Parmar S, Filbin MR; et al. (2013). "Clinical Trial: Comparative effectiveness of cephalexin plus trimethoprim-sulfamethoxazole vs. cephalexin alone for treatment of uncomplicated cellulitis: A randomized controlled trial". Clin Infect Dis. doi:10.1093/cid/cit122. PMID 23457080.
  7. Halilovic J, Heintz BH, Brown J (2012). "Risk factors for clinical failure in patients hospitalized with cellulitis and cutaneous abscess". J Infect. doi:10.1016/j.jinf.2012.03.013. PMID 22445732.
  8. Hepburn, Matthew J (2004-08-09). "Comparison of short-course (5 days) and standard (10 days) treatment for uncomplicated cellulitis". Archives of Internal Medicine. 164 (15): 1669–1674. doi:10.1001/archinte.164.15.1669. ISSN 0003-9926. PMID 15302637. Retrieved 2009-09-01. Unknown parameter |coauthors= ignored (help)
  9. Abrahamian FM, Goldstein EJ (2011). "Microbiology of animal bite wound infections". Clin. Microbiol. Rev. 24 (2): 231–46. doi:10.1128/CMR.00041-10. PMC 3122494. PMID 21482724. Unknown parameter |month= ignored (help)
  10. Noonburg GE (2005). "Management of extremity trauma and related infections occurring in the aquatic environment". J Am Acad Orthop Surg. 13 (4): 243–53. PMID 16112981.


Template:WikiDoc Sources