eMedicine Specialties > Emergency Medicine > Infectious Diseases

Impetigo: Treatment & Medication

Author: Rashid M Rashid, MD, PhD, Resident Physician, Department of Dermatology, MD Anderson Cancer Center, University of Texas and The Morzak Center
Coauthor(s): Andrew C Miller, MD, Chief Resident and Clinical Assistant Instructor, Departments of Emergency Medicine and Internal Medicine, State University of New York Downstate Medical Center, Kings County Hospital Center; Mark A Silverberg, MD, FACEP, MMB, Assistant Professor, Assistant Residency Director, Department of Emergency Medicine, State University of New York Downstate College of Medicine; Consulting Staff, Department of Emergency Medicine, Staten Island University Hospital, Kings County Hospital, University Hospital, State University of New York Downstate at Brooklyn
Contributor Information and Disclosures

Updated: Sep 15, 2009

Treatment

Emergency Department Care

The emerging resistance of S aureus to beta-lactams, macrolides, and even mupirocin requires consideration of the prevalence of community-acquired methicillin-resistant Staphylococcus aureus (CA-MRSA) in the locale of the patient. Treatment of bullous impetigo should now always consider this possibility. Trimethoprim-sulfamethoxazole, clindamycin, and rifampin all retain sensitivity in the vast majority of CA-MRSA strains.

  • Wound cleaning with gentle abrasion is indicated. Deep abrasive scrubbing is not required.
  • Topical mupirocin is adequate treatment for single lesions of nonbullous impetigo or small areas of involvement. A 7-day course is usually standard, although a few large studies have been performed to verify this as the most effective approach.
  • Systemic antibiotics are indicated for extensive involvement or for bullous impetigo.
  • If there are large areas of involvement resulting in denuded skin from ruptured bullae, then adequate fluid resuscitation is indicated with intravenous rehydration fluid at a volume and rate similar to standard volume replacement for burns.
  • Early and appropriate treatment usually prevents scarring and localized spread.
  • Good hygiene and hand washing should be encouraged. Household spread is common otherwise. If skin care is not reviewed with the patient, the chance of re-infection or persistent infection is high. Skin care details should include adjuvants to topical antibiotics. The easiest adjuvants to use for patients are the bleach bath (1 cup of bleach in a bathtub of water at a safe level and with supervision), mixing vinegar and water at a 1:4 ratio for rinsing the area, and chlorhexidine scrubs.

Consultations

The need for consultation is determined by the extent of involvement and the age of the patient. Neonates with bullous impetigo require a consultation with neonatology. Recurrent disease should trigger a specialist consult.

Medication

Antibiotics are the mainstay of therapy, but they should be done in isolation without the adjuvants discussed above.

The drug chosen must provide coverage against coagulase-positive S aureus and GABHS. In areas with high percentage of CA-MRSA, the empiric antibiotic choice should provide coverage for this possibility.

Topical antibiotics

These agents pose fewer potential problems than systemic antibiotics, but their use is reserved only for cases involving lesions that are small or few in number.


Mupirocin ointment (Bactroban)

DOC for few small lesions in absence of lymphadenopathy.

Adult

Apply to lesions tid for 5 d; clean lesions prior to application

Pediatric

Apply as in adults

Pregnancy

B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals

Precautions

Prolonged use may result in growth of nonsusceptible organisms


Retapamulin (Altabax)

Topical antibiotic available as a 1% ointment. First of new antibiotic class called pleuromutilins. Inhibits protein synthesis by binding to 50S subunit on ribosome. Indicated for impetigo caused by Staphylococcus aureus or Streptococcus pyogenes.

Adult

Apply topically to affected site bid for 5 d

Pediatric

<9 months: Not established
>9 months: Apply as in adults

Pregnancy

C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus

Precautions

May cause irritation at application site (1.4%); avoid application to eye area; keep out of reach of children

Systemic antibiotics

Therapy must cover all likely pathogens in the context of the clinical setting.


Cephalexin (Keflex)

First-generation cephalosporin that inhibits bacterial growth by inhibiting bacterial cell wall synthesis; bactericidal and effective against rapidly growing organisms forming cell walls. Primarily active against skin flora; typically used for skin-structure coverage and as prophylaxis in minor procedures. Does not cover MRSA.
DOC for cases involving large number of lesions, large areas of involvement, or regional lymphadenopathy.

Adult

250-500 mg PO qid for 7 d

Pediatric

25-50 mg/kg/d PO divided qid

Aminoglycosides increase nephrotoxic potential

Pregnancy

B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals

Precautions

Adjust dose in renal impairment


Erythromycin (EES, Erythrocin, Ery-Tab)

DOC in penicillin- or cephalosporin-allergic patient. Inhibits RNA-dependent protein synthesis, possibly by stimulating dissociation of peptidyl tRNA from ribosomes, which inhibits bacterial growth. Does not cover MRSA.

Adult

250-500 mg PO qid for 7 d

Pediatric

30-50 mg/kg/d PO divided qid for 7 d

May increase toxicity of theophylline, digoxin, carbamazepine, and cyclosporine; may potentiate anticoagulant effects of warfarin; lovastatin or simvastatin increases risk of rhabdomyolysis

Documented hypersensitivity; hepatic impairment

Pregnancy

B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals

Precautions

Resistance may exist in some areas (as many as 30% of cases); caution in liver disease; estolate preparations may cause cholestatic jaundice; GI adverse effects, including nausea and vomiting, are common (administer doses after meals); discontinue use if nausea, vomiting, malaise, abdominal colic, or fever occur


Dicloxacillin (Dycill, Dynapen)

Bactericidal antibiotic that inhibits cell wall synthesis. Used in treatment of infections caused by penicillinase-producing staphylococci; may be used to initiate therapy when staphylococcal infection suspected. Very effective but less well tolerated than cephalexin. Does not cover MRSA.

Adult

250 mg PO qid for 7 d

Pediatric

20-50 mg/kg/d PO divided qid for 7 d

Decreases efficacy of oral contraceptives; increases effects of anticoagulants; probenecid and disulfiram may increase levels

Pregnancy

B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals

Precautions

Monitor PT in patients taking anticoagulant medications; toxicity may increase in renal impairment


Clindamycin (Cleocin)

Semisynthetic antibiotic produced by 7(S)-chloro-substitution of 7(R)-hydroxyl group of parent compound lincomycin. Inhibits bacterial growth, possibly by blocking dissociation of peptidyl tRNA from ribosomes, causing RNA-dependent protein synthesis to arrest. Widely distributes in the body without penetration of CNS. Protein bound and excreted by the liver and kidneys.
Alternative therapy for S aureus resistant to erythromycin and MRSA. Used for treatment of serious skin and soft tissue staphylococcal infections. Also effective against aerobic and anaerobic streptococci (except enterococci).

Adult

300 PO q8h for 10 d

Pediatric

10-30 mg/kg/d PO divided q6-8h for 10 d

Increases duration of neuromuscular blockade induced by tubocurarine and pancuronium; erythromycin may antagonize effects of clindamycin; antidiarrheals may delay absorption of clindamycin

Documented hypersensitivity; regional enteritis; ulcerative colitis; hepatic impairment; antibiotic-associated colitis

Pregnancy

B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals

Precautions

Adjust dose in severe hepatic dysfunction; no adjustment necessary in renal insufficiency; associated with severe and possibly fatal colitis by allowing overgrowth of Clostridium difficile

More on Impetigo

Overview: Impetigo
Differential Diagnoses & Workup: Impetigo
Treatment & Medication: Impetigo
Follow-up: Impetigo
Multimedia: Impetigo
References

References

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  3. Allen CH, Patel B, Endom EE. Primary bacterial infections of the skin and soft tissues, changes in epidemiology and management. Clin Ped Emerg Med. 2004;5:246-255.

  4. Dagan R. Impetigo in childhood: changing epidemiology and new treatments. Pediatr Ann. Apr 1993;22(4):235-40. [Medline].

  5. Elsayed S, Laupland KB. Emerging gram-positive bacterial infections. Clin Lab Med. Sep 2004;24(3):587-603, v. [Medline].

  6. Epps RE. Impetigo in pediatrics. Cutis. May 2004;73(5 Suppl):25-6. [Medline].

  7. Leyden JJ. Review of mupirocin ointment in the treatment of impetigo. Clin Pediatr (Phila). Sep 1992;31(9):549-53. [Medline].

  8. Loffeld A, Davies P, Lewis A, Moss C. Seasonal occurrence of impetigo: a retrospective 8-year review (1996-2003). Clin Exp Dermatol. Sep 2005;30(5):512-4. [Medline].

  9. Luby S, Agboatwalla M, Schnell BM, Hoekstra RM, Rahbar MH, Keswick BH. The effect of antibacterial soap on impetigo incidence, Karachi, Pakistan. Am J Trop Med Hyg. Oct 2002;67(4):430-5. [Medline].

  10. Nishijim S, Ohshima S, Higashida T, Nakaya H, Kurokawa I. Antimicrobial resistance of Staphylococcus aureus isolated from impetigo patients between 1994 and 2000. Int J Dermatol. Jan 2003;42(1):23-5. [Medline].

  11. Oranje AP, Chosidow O, Sacchidanand S, et al. Topical retapamulin ointment, 1%, versus sodium fusidate ointment, 2%, for impetigo: a randomized, observer-blinded, noninferiority study. Dermatology. 2007;215(4):331-40. [Medline].

  12. Zetola N, Francis JS, Nuermberger EL, Bishai WR. Community-acquired meticillin-resistant Staphylococcus aureus: an emerging threat. Lancet Infect Dis. May 2005;5(5):275-86. [Medline].

Further Reading

Contributor Information and Disclosures

Author

Rashid M Rashid, MD, PhD, Resident Physician, Department of Dermatology, MD Anderson Cancer Center, University of Texas and The Morzak Center
Rashid M Rashid, MD, PhD is a member of the following medical societies: American Academy of Dermatology, Council for Nail Disorders, Houston Dermatological Society, and Texas Medical Association
Disclosure: Nothing to disclose.

Coauthor(s)

Andrew C Miller, MD, Chief Resident and Clinical Assistant Instructor, Departments of Emergency Medicine and Internal Medicine, State University of New York Downstate Medical Center, Kings County Hospital Center
Andrew C Miller, MD is a member of the following medical societies: American College of Emergency Physicians, American College of Physicians, American Medical Association, Emergency Medicine Residents Association, Islamic Medical Association of North America, Medical Society of the State of New York, and Society for Academic Emergency Medicine
Disclosure: Nothing to disclose.

Mark A Silverberg, MD, FACEP, MMB, Assistant Professor, Assistant Residency Director, Department of Emergency Medicine, State University of New York Downstate College of Medicine; Consulting Staff, Department of Emergency Medicine, Staten Island University Hospital, Kings County Hospital, University Hospital, State University of New York Downstate at Brooklyn
Mark A Silverberg, MD, FACEP, MMB is a member of the following medical societies: American College of Emergency Physicians, American Medical Association, Council of Emergency Medicine Residency Directors, and Society for Academic Emergency Medicine
Disclosure: Nothing to disclose.

Medical Editor

Eric M Kardon, MD, FACEP, Attending Emergency Physician, Georgia Emergency Medicine Specialists; Physician, Division of Emergency Medicine, Athens Regional Medical Center
Eric M Kardon, MD, FACEP is a member of the following medical societies: American College of Emergency Physicians
Disclosure: Nothing to disclose.

Pharmacy Editor

Francisco Talavera, PharmD, PhD, Senior Pharmacy Editor, eMedicine
Disclosure: eMedicine Salary Employment

Managing Editor

Eric L Weiss, MD, DTM&H, Director of Stanford Travel Medicine, Medical Director of Stanford Lifeflight, Assistant Professor, Departments of Emergency Medicine and Infectious Diseases, Stanford University School of Medicine
Eric L Weiss, MD, DTM&H is a member of the following medical societies: American College of Emergency Physicians, American College of Occupational and Environmental Medicine, American Medical Association, American Society of Tropical Medicine and Hygiene, Physicians for Social Responsibility, Southeastern Surgical Congress, Southern Association for Oncology, Southern Clinical Neurological Society, and Wilderness Medical Society
Disclosure: Nothing to disclose.

CME Editor

John D Halamka, MD, MS, Associate Professor of Medicine, Harvard Medical School, Beth Israel Deaconess Medical Center; Chief Information Officer, CareGroup Healthcare System and Harvard Medical School; Attending Physician, Division of Emergency Medicine, Beth Israel Deaconess Medical Center
John D Halamka, MD, MS is a member of the following medical societies: American College of Emergency Physicians, American Medical Informatics Association, Phi Beta Kappa, and Society for Academic Emergency Medicine
Disclosure: Nothing to disclose.

Chief Editor

Pamela L Dyne, MD, Professor of Clinical Medicine/Emergency Medicine, David Geffen School of Medicine at UCLA; Attending Physician, Department of Emergency Medicine, Olive View-UCLA Medical Center
Pamela L Dyne, MD is a member of the following medical societies: American Academy of Emergency Medicine, American College of Emergency Physicians, and Society for Academic Emergency Medicine
Disclosure: Nothing to disclose.

 
 
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