Updated: Apr 23, 2009
Human bite wounds have a notorious reputation, which is mostly based on one injury, the closed-fist injury. Human bites in other areas pose no greater risk than animal bites. Three general types of injuries can lead to complications: (1) closed-fist injury, (2) chomping injury to the finger, and (3) puncture-type wounds about the head caused by clashing with a tooth. Otherwise, the general principles of contaminated wound management apply to human bite wounds.
For more information, see Medscape's Wound Management Resource Center.
In a closed-fist injury, forces sufficient to break the skin from striking an opponent's tooth often inoculate the extensor tendon and its sheath. As the hand is flexed at the time of impact, the bacterial load is transferred caudally when the hand is opened and the tendon slides back to its relaxed state. Resulting contamination cannot be removed readily through normal cleansing and irrigation.
When a finger is bitten, such as in a chomping-type injury, tendons and their overlying sheaths are in close proximity to the skin. The wound may appear to be a minor abrasion-type injury, but careful inspection is required to rule out deep injury.
When a tooth strikes the head, even a deep puncture wound may appear innocuous. Deep, subgaleal, bacterial contamination is possible. This is especially true in young children who have relatively thin soft scalp and forehead tissue.
Exact incidence of human bite wounds is unknown, and many cases do not come to medical attention. Institutionalized patients with poor impulse control create a high-risk environment for human bite wounds. Lesch-Nyhan syndrome is an uncommon disorder that includes self-mutilation through biting.
In a 4-year retrospective review in the United Kingdom, 421 (13%) human bites were identified out of 3136 case notes. The majority of those bitten were young males, with 44% of the males aged 16-25 years. The male-to-female ratio was 3:1.1
Bites, Animal
Bites, Insects
Hand Infections
The acute, non-infected human bite
The infected human bite wound
Other considerations
The only drug therapy of significance in human bites is antibiotic treatment. Bacterial flora include that of the mouth and skin. Theoretically, penicillin treats oral pathogens and may suffice for prophylactic treatment as Staphylococcus species probably only infect bite wounds secondarily.
Once a human bite is infected, beta-lactamase–producing staphylococci must be addressed. Eikenella corrodens may not be covered by first-generation cephalosporins. Additionally, Eikenella species are resistant to clindamycin, penicillinase-resistant semisynthetic penicillins, and metronidazole. A broad-spectrum antibiotic, rather than combination therapy, is the usual choice for infected bite wounds. An in vitro study of 50 infected human bites by Talan et al indicated that amoxicillin-clavulanic acid and moxifloxacin demonstrated excellent activity against common isolates.7
Therapy must cover all likely pathogens in the context of the clinical setting.
Drug combination that extends antibiotic spectrum of this penicillin to include bacteria normally resistant to beta-lactam antibiotics. DOC for noninfected human bite wounds. Dosing is based on amoxicillin component. Indicated for skin and skin structure infections caused by beta-lactamase-producing strains of Staphylococcus aureus.
875 mg PO bid for 5 d
45 mg/kg/d PO divided q12h
Risk of bleeding increases when coadministered with warfarin or heparin, possibly because of additive effects
Documented hypersensitivity
B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals
Use may precipitate pseudomembranous colitis;
give for minimum of 10 d to eliminate organism and prevent sequelae (endocarditis, rheumatic fever); following treatment, perform cultures to confirm eradication of streptococci
Drug combination that uses beta-lactamase inhibitor with ampicillin; covers skin, enteric flora, and anaerobes. DOC for infected bites.
1.5 (1 g ampicillin + 0.5 g sulbactam) to 3 g (2 g ampicillin + 1 g sulbactam) IV q6h; not to exceed 4 g/d sulbactam or 8 g/d ampicillin
<12 years: Not established
Probenecid and disulfiram elevate ampicillin levels; allopurinol decreases ampicillin effects and has additive effects on ampicillin rash; may decrease effects of oral contraceptives
Documented hypersensitivity
B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals
Adjust dose in renal failure; evaluate rash and differentiate from hypersensitivity reaction
Alternative drug for infected bites; second-generation cephalosporin indicated for management of infections caused by susceptible gram-positive cocci and gram-negative rods. Many infections that are caused by gram-negative bacteria and are resistant to some cephalosporins and penicillins respond to cefoxitin.
2 g IV q8h
>3 months: 80-160 mg/kg/d IV divided q4-6h
Probenecid may increase effects; coadministration with aminoglycosides or furosemide may increase nephrotoxicity (closely monitor renal function)
Documented hypersensitivity
B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals
Bacterial or fungal overgrowth of nonsusceptible organisms may occur with prolonged use or repeated treatment; caution in patients with previously diagnosed colitis
Inhibits the A subunits of DNA gyrase, resulting in inhibition of bacterial DNA replication and transcription.
400 mg PO/IV qd
<18 years: Not recommended
>18 years: Administer as in adults
Antacids and electrolyte supplements reduce absorption; loop diuretics, probenecid, and cimetidine increase serum levels; NSAIDs enhance CNS stimulating effect; may increase toxicity of theophylline, caffeine, cyclosporine, and digoxin (monitor digoxin levels); may increase effects of anticoagulants (monitor PT); ferrous sulfate decreases bioavailability (administer moxifloxacin 4 h prior or 8 h following ferrous sulfate); coadministration with drugs that prolong QTc interval (quinidine, procainamide, amiodarone, sotalol, erythromycin, tricyclic antidepressants) increase risk of life-threatening arrhythmia
Documented hypersensitivity; known Q-T prolongation; concurrent administration of drugs that cause Q-T prolongation
C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus
In prolonged therapy, perform periodic evaluations of organ system functions (eg, renal, hepatic, hematopoietic); superinfections may occur with prolonged or repeated antibiotic therapy; fluoroquinolones have induced seizures in CNS disorders and caused tendinitis or tendon rupture
These agents are used to immunize patients against tetanus.
Used for passive immunization of any person with a wound that may be contaminated with tetanus spores.
Prophylaxis: 250-500 U IM in opposite extremity to tetanus toxoid lesion
Clinical tetanus: 3000-10,000 U IM
Prophylaxis: 250 U IM in opposite extremity to tetanus toxoid
Clinical tetanus: 3000-10,000 U IM
None reported
Since antibodies in globulin preparation may interfere with immune response to vaccination, do not administer within 3 mo of live-virus immune globulin administration; may be necessary to revaccinate persons who received immune globulin shortly after live-virus vaccination
C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus
Persons with isolated IgA deficiency have potential for developing antibodies to IgA and may have anaphylactic reactions to subsequent administration of blood products that contain IgA; do not perform skin testing since intradermal injection of concentrated gamma globulin may cause localized area of inflammation and can be misinterpreted, causing medication to be withheld from a patient not allergic to this material; true allergic responses to human gamma globulin given in prescribed IM manner are extremely rare; do not admix with other medications since usually incompatible
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Smith DK, Grohskopf LA, Black RJ, et al. Antiretroviral postexposure prophylaxis after sexual, injection-drug use, or other nonoccupational exposure to HIV in the United States: recommendations from the U.S. Department of Health and Human Services. MMWR Recomm Rep. Jan 21 2005;54(RR-2):1-20. [Medline].
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Lindsey D, Christopher M, Hollenbach J, et al. Natural course of the human bite wound: incidence of infection and complications in 434 bites and 803 lacerations in the same group of patients. J Trauma. Jan 1987;27(1):45-8. [Medline].
Miura I, Ohshima A, Takahashi N, et al. A new non-random chromosomal translocation t(3;6)(q27;p21.3) associated with BCL6 rearrangement in two patients with non-Hodgkin's lymphoma. Int J Hematol. Oct 1996;64(3-4):249-56. [Medline].
Pretty IA, Anderson GS, Sweet DJ. Human bites and the risk of human immunodeficiency virus transmission. Am J Forensic Med Pathol. Sep 1999;20(3):232-9. [Medline].
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Smith PF, Meadowcroft AM, May DB. Treating mammalian bite wounds. J Clin Pharm Ther. Apr 2000;25(2):85-99. [Medline].
Turner TW. Evidence-based emergency medicine/systematic review abstract. Do mammalian bites require antibiotic prophylaxis?. Ann Emerg Med. Sep 2004;44(3):274-6. [Medline].
human bites, human bite wound, closed-fist injury, chomping injury, puncture-type wound, infected human bite wounds, bite wounds, bite injury
Jeffrey Barrett, MD, Assistant Professor, Department of Emergency Medicine, Temple University School of Medicine
Jeffrey Barrett, MD is a member of the following medical societies: American Academy of Emergency Medicine and Society for Academic Emergency Medicine
Disclosure: Nothing to disclose.
Robert M McNamara, MD, FAAEM, Chair and Professor, Department of Emergency Medicine, Temple University School of Medicine
Robert M McNamara, MD, FAAEM is a member of the following medical societies: American Academy of Emergency Medicine, American Medical Association, Pennsylvania Medical Society, and Society for Academic Emergency Medicine
Disclosure: Nothing to disclose.
Samuel M Keim, MD, Associate Professor, Department of Emergency Medicine, University of Arizona College of Medicine
Samuel M Keim, MD is a member of the following medical societies: American Academy of Emergency Medicine, American College of Emergency Physicians, American Medical Association, American Public Health Association, and Society for Academic Emergency Medicine
Disclosure: Nothing to disclose.
Francisco Talavera, PharmD, PhD, Senior Pharmacy Editor, eMedicine
Disclosure: eMedicine Salary Employment
James Steven Walker, DO, MS, Clinical Professor of Surgery, Department of Surgery, University of Oklahoma Health Sciences Center
James Steven Walker, DO, MS is a member of the following medical societies: American Academy of Emergency Medicine, American College of Emergency Physicians, American College of Osteopathic Emergency Physicians, and American Osteopathic Association
Disclosure: Nothing to disclose.
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.
Jonathan Adler, MD, Attending Physician, Department of Emergency Medicine, Massachusetts General Hospital; Division of Emergency Medicine, Harvard Medical School
Jonathan Adler, MD is a member of the following medical societies: American Academy of Emergency Medicine and Society for Academic Emergency Medicine
Disclosure: Nothing to disclose.
Clinical guidelines
Management of human bite wounds. University of Texas, School of Nursing, Family Nurse Practitioner Program. Management of human bite wounds. Austin (TX): University of Texas, School of Nursing; 2007 May. 22 p.
Antiretroviral postexposure prophylaxis after sexual, injection-drug use, or other nonoccupational exposure to HIV in the United States: recommendations from the U.S. Department of Health and Human Services. Smith DK, Grohskopf LA, Black RJ, Auerbach JD, Veronese F, Struble KA, Cheever L, Johnson M, Paxton LA, Onorato IM, Greenberg AE. Antiretroviral postexposure prophylaxis after sexual, injection-drug use, or other nonoccupational exposure to HIV in the United States: recommendations from the U.S. Department of Health and Human Services. MMWR Recomm Rep 2005 Jan 21;54(RR-2):1-26. [126 references] PubMed
Practice guidelines for the diagnosis and management of skin and soft-tissue infections. Stevens DL, Bisno AL, Chambers HF, Everett ED, Dellinger P, Goldstein EJ, Gorbach SL, Hirschmann JV, Kaplan EL, Montoya JG, Wade JC. Practice guidelines for the diagnosis and management of skin and soft-tissue infections. Clin Infect Dis 2005 Nov 15;41(10):1373-406. [236 references] PubMed
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