Impetigo medical therapy
Impetigo Microchapters |
Diagnosis |
---|
Treatment |
Case Studies |
Impetigo medical therapy On the Web |
American Roentgen Ray Society Images of Impetigo medical therapy |
Risk calculators and risk factors for Impetigo medical therapy |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Usama Talib, BSc, MD [2]
Overview
The mainstay of therapy for impetigo is antimicrobial therapy. Topical therapy is preferred unless there is an indication for systemic therapy.[1][2]Empiric therapy for mild disease includes either Mupirocin or Retapamulin applied topically. Empiric therapy for numerous lesions or poststreptococcoal glomerulonephritis includes either Dicloxacillin, Amoxicillin-Clavulanate, or Cephalexin. Penicillin is the drug of choice for impetigo caused by Streptococcus. Patients with impetigo caused by Methicillin-resistant Staphylococcus aureus are treated with either Doxycycline, Clindamycin, or Sulfamethoxazole-Trimethoprim. Non-bullous impetigo is self resolving and usually takes 1-2 weeks.[3][4]
Medical Therapy
- Topical therapy is preferred for patients with small amount of lesions and without any bullae[1][5]; but oral therapy is also accepted.[6]
- Oral regimens are used for patients with several lesions and patients with bullous impetigo.
- Non-medical therapy involves washing the lesions and the rest of the body with soap and water, and letting the impetigo dry in the air.
- Hand-washing and daily bathing is considered a method to prevent impetigo in children.[7]
- It is very important to remove the crusts before applying ointment, as the bacteria that cause the disease are located underneath them.
- The recommended duration of therapy is 7 days but will depend on the clinical response.
▸ Click on the following categories to expand treatment regimens.
Bullous Impetigo ▸ Adults ▸ Children Non-Bullous Impetigo ▸ Adults ▸ Children |
|
Antimicrobial regimen
- 1.1 Empiric antimicrobial therapy (covering methicillin-susceptible Staphylococcus aureus and β-hemolytic streptococci)
- 1.1.1 Limited number of lesions
- Preferred regimen (1): Mupirocin topically bid for 5 days
- Preferred regimen (2): Retapamulin topically bid for 5 days
- 1.1.2 Numerous lesions or outbreaks of post streptococcal glomerulonephritis
- Preferred regimen (1): Dicloxacillin 250 mg PO qid for 7 days
- Preferred regimen (2): Amoxicillin-Clavulanate 875/125 mg PO bid for 7 days
- Preferred regimen (3): Cephalexin 250 mg PO qid for 7 days
- Alternative regimen (1): (for penicillin-allergic patients) Doxycycline 100 mg PO bid for 7 days
- Alternative regimen (2): (for penicillin-allergic patients) Clindamycin 300–400 mg PO qid for 7 days
- Alternative regimen (3): (for penicillin-allergic patients) Sulfamethoxazole-Trimethoprim 1–2 double-strength tablets PO bid for 7 days
- 1.2 Culture-directed antimicrobial therapy
- 1.2.1 Streptococcus alone
- Preferred regimen: Penicillin V 250–500 mg PO qid for 7 days
- Alternative regimen (1): (for penicillin-allergic patients) Erythromycin 250 mg PO qid for 7 days
- Alternative regimen (2): (for penicillin-allergic patients) Clindamycin 300–400 mg PO qid for 7 days
- 1.2.2 Methicillin-resistant Staphylococcus aureus
- Preferred regimen (1): Doxycycline 100 mg PO bid for 7 days
- Preferred regimen (2): Clindamycin 300–450 mg PO qid for 7 days
- Preferred regimen (3): Sulfamethoxazole-Trimethoprim 1–2 double-strength tablets PO bid for 7 days
- 2. Impetigo, pediatric
- 2.1 Empiric antimicrobial therapy (covering methicillin-susceptible Staphylococcus aureus and β-hemolytic streptococci)
- 2.1.1 Limited number of lesions
- Preferred regimen (1): Mupirocin topically bid for 5 days
- Preferred regimen (2): Retapamulin topically bid for 5 days
- 2.1.2 Numerous lesions or outbreaks of poststreptococcal glomerulonephritis
- Preferred regimen (1): Amoxicillin-Clavulanate 25 mg/kg/day of amoxicillin component PO bid for 7 days
- Preferred regimen (2): Cephalexin 25–50 mg/kg/day PO tid–qid for 7 days
- Alternative regimen (1): (for penicillin-allergic patients) Clindamycin 25–30 mg/kg/day PO tid for 7 days
- Alternative regimen (2): (for penicillin-allergic patients) Sulfamethoxazole-Trimethoprim 8–12 mg/kg/day PO bid for 7 days
- 2.2 Culture-directed antimicrobial therapy
- 2.2.1 Streptococcus alone
- Preferred regimen: Penicillin V 60,000–100,000 U/kg PO qid for 7 days
- Alternative regimen (1): (for penicillin-allergic patients) Erythromycin 40 mg/kg/day PO tid–qid for 7 days
- Alternative regimen (2): (for penicillin-allergic patients) Clindamycin 20 mg/kg/day PO tid for 7 days
- 2.2.2 Methicillin-resistant Staphylococcus aureus
- Preferred regimen (1): Clindamycin 25–30 mg/kg/day PO tid for 7 days
- Preferred regimen (2): Sulfamethoxazole-Trimethoprim 8–12 mg/kg/day PO bid for 7 days
References
- ↑ 1.0 1.1 Rhody C (2000). "Bacterial infections of the skin". Prim Care. 27 (2): 459–73. PMID 10815055.
- ↑ Brown J, Shriner DL, Schwartz RA, Janniger CK (2003). "Impetigo: an update". Int J Dermatol. 42 (4): 251–5. PMID 12694487.
- ↑ Cole C, Gazewood J (2007). "Diagnosis and treatment of impetigo". Am Fam Physician. 75 (6): 859–64. PMID 17390597.
- ↑ Koning S, van der Sande R, Verhagen AP, van Suijlekom-Smit LW, Morris AD, Butler CC; et al. (2012). "Interventions for impetigo". Cochrane Database Syst Rev. 1: CD003261. doi:10.1002/14651858.CD003261.pub3. PMID 22258953.
- ↑ Sander Koning, Renske van der Sande, Arianne P. Verhagen, Lisette W. A. van Suijlekom-Smit, Andrew D. Morris, Christopher C. Butler, Marjolein Berger & Johannes C. van der Wouden (2012). "Interventions for impetigo". The Cochrane database of systematic reviews. 1: CD003261. doi:10.1002/14651858.CD003261.pub3. PMID 22258953.
- ↑ Ranti S. Bolaji, Tushar S. Dabade, Cheryl J. Gustafson, Scott A. Davis, Daniel P. Krowchuk & Steven R. Feldman (2012). "Treatment of impetigo: oral antibiotics most commonly prescribed". Journal of drugs in dermatology : JDD. 11 (4): 489–494. PMID 22453587. Unknown parameter
|month=
ignored (help) - ↑ Stephen P. Luby, Mubina Agboatwalla, Daniel R. Feikin, John Painter, Ward Billhimer, Arshad Altaf & Robert M. Hoekstra (2005). "Effect of handwashing on child health: a randomised controlled trial". Lancet. 366 (9481): 225–233. doi:10.1016/S0140-6736(05)66912-7. PMID 16023513. Unknown parameter
|month=
ignored (help) - ↑ 8.0 8.1 8.2 8.3 8.4 8.5 Stevens DL, Bisno AL, Chambers HF, Everett ED, Dellinger P, Goldstein EJ; 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.
- ↑ 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.
- ↑ Stevens DL, Bisno AL, Chambers HF, Dellinger EP, Goldstein EJ, Gorbach SL; et al. (2014). "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. 59 (2): 147–59. doi:10.1093/cid/ciu296. PMID 24947530.