Updated: Aug 5, 2009
Human bite wounds are notoriously deceptive and are often underestimated and undertreated. While controversies regarding optimal management continue, the basic tenets of meticulous wound care are no different than those for contaminated wounds.
The goals of therapy are to prevent or appropriately treat infection and to minimize the soft tissue deformity. Recognition and early, aggressive treatment are mandatory to prevent infection and associated complications.
Approximately 10-15% of human bite wounds become infected, and this considerable infection rate is multifactorial. Patients often wait until infection is established before presenting late in the course of their injury, thus necessitating medical attention. Wounds evaluated earlier are frequently more extensive than estimated on initial examination by the inexperienced observer and are frequently managed inadequately.
The bacterial inoculum of human bite wounds is rich in oral flora, as saliva contains as many as 100,000,000 organisms per mL, representing as many as 190 different species. Moreover, most of these injuries occur on the hands, and hand wounds of any cause have a higher infection rate than similar wounds in other anatomic locations.
The possibility of transmission of disease through human bites must be considered. Human bites have been shown to transmit hepatitis B, hepatitis C, herpes simplex virus (HSV), syphilis, tuberculosis, actinomycosis, and tetanus. Evidence suggests that it is biologically possible to transmit HIV through human bites, although this is quite unlikely.
For additional information on hepatitis B and hepatitis C, see Medscape’s Hepatitis B Resource Center and Hepatitis C Resource Center.
Human bite wounds occur as 2 separate entities: clenched-fist injuries and occlusive bites.
Clenched-fist injury
Clenched-fist injuries are the most common and possess the greater clinical significance. They occur as the closed fist strikes the teeth of another individual with sufficient force to create a small wound, usually 3-8 mm in length. The injury usually occurs over the dorsal surface of the middle finger metacarpophalangeal joint of the dominant hand. Potential injuries include joint penetration, metacarpal fracture, and extensor tendon laceration. Digital nerve or digital artery injury is rare.
As the fingers extend following injury, the bacterial inoculum may be carried proximally with the extensor tendons. This makes adequate irrigation of the wound more difficult. These are the most serious human bite wounds, and they require the most aggressive treatment.
Occlusive bites
Occlusive bites occur when the teeth bite a part of the body with sufficient force to violate the integrity of the skin. Although less serious than clenched-fist injuries, those occurring on the hand must be treated with greater attention, as they have a higher infection rate than occlusive bites to other parts of the body.
Regardless of mechanism and anatomic location, the bacterial inoculum deserves special consideration because it is composed of the rich oral flora of aerobes and anaerobes. Cultures of human bite wounds are commonly polymicrobial in nature, and aerobes and anaerobes are represented almost equally. Several bacterial species produce beta-lactamase, rendering them resistant to penicillin.
Commonly isolated aerobes include Eikenella corrodens and Staphylococcus, Streptococcus, and Corynebacterium species. Staphylococcus aureus is associated with some of the most severe infections, resulting in the highest complication rates. E corrodens is a slow-growing, gram-negative bacillus frequently associated with chronic infection and abscess formation. Commonly isolated anaerobes include Bacteroides and Peptostreptococcus species.
In addition to the infection risk, the potential for transmission of life-threatening disease is also present in human bites. Hepatitis B has been transmitted through human bites, as 75% of patients with hepatitis B infection have detectable antigen in their saliva. Less likely is the transmission of HIV, although several cases in the literature suggest this mode of transmission.1,2 HIV is found in the saliva of affected patients, although at lower levels than in the blood. In addition, salivary inhibitors render the virus noninfective in most cases.
Human bites are believed to be the third-most-common bite wounds, following dog and cat bites. The true frequency is difficult to estimate because the vast majority probably go unreported and because many patients do not seek medical attention.
Of those reported, approximately 60% occur in the upper extremities, while another 15% occur in the head and neck region. The remainder occur on the breasts, genitals, thighs, and other areas.
Upper extremity bites most frequently occur on the dominant extremity. Head and neck injuries most commonly occur on the ears, nose, or lips.
A thorough, detailed history is necessary to facilitate communication between various health care professionals involved in the treatment of the patient and to document why the plan of care was appropriate.
When questioned as to the nature of the injury, patients often mislead the examiner out of embarrassment or fear of legal repercussion. These cases are often assault cases and are more likely to involve the judicial system. With that in mind, documentation should be clear, concise, and complete.
Cellulitis
Tetanus
Although rare, human bites have been shown to transmit Clostridium tetani. Assess all patients for tetanus immune status and update as appropriate. Erring on the side of caution when deciding to administer tetanus toxoid or tetanus immune globulin is best. These wounds are often several days old and are heavily contaminated or even infected upon first presentation. Bites with no significant skin penetration (abrasions or contusions) require no further care.
A multidisciplinary approach can lead to maximum patient benefit in certain circumstances.
After initial immobilization of hand injuries in a position of function and elevation, provide instruction regarding resumption of activity.
The question of which patients require antibiotic therapy is a matter of considerable debate. Antibiotics cannot avert or cure infections in the face of poor wound care, reflecting the importance of meticulous treatment of the wound as the cornerstone of therapy. In regard to antibiotic therapy, it is best to err on the side of caution because the risks of antibiotic therapy are minimal, while the potential complications of bite wound infections are considerable.
In general, superficial noninfected wounds involving sites other than the hand that are evaluated early in the compliant patient without significant comorbidities may be treated without antibiotics if the wound is left open to heal by secondary intention.
Wounds of the hand, infected wounds, and wounds of the head and neck closed primarily mandate antibiotic therapy.
Wounds treated on an outpatient basis may be treated with oral antibiotics, whereas wounds requiring admission to the hospital should be treated with intravenous antibiotics.
Prophylaxis in the noninfected wound should be continued for 5-7 days, whereas therapeutic antibiotics should be administered for 10-14 days.
Selection of the appropriate antibiotic involves multiple factors, including culture results if obtained and available, drug sensitivities, patient age, drug interactions, expected compliance, and renal and hepatic function.
Empiric antimicrobial therapy must be comprehensive and should cover all likely pathogens in the context of the clinical setting.
Drug combination treats bacteria resistant to beta-lactam antibiotics. The most effective and economical choice for outpatient therapy unless contraindicated.
In children >3 mo, base dosing protocol on amoxicillin content. Because of different amoxicillin/clavulanic acid ratios in 250-mg tab (250/125) vs 250-mg chewable tab (250/62.5), do not use 250-mg tab until child weighs >40 kg.
500/125 mg PO tid or 875/125 mg PO bid
40 mg/kg/d PO, divided q8h (based on amoxicillin component)
Probenecid decreases renal excretion, increasing blood levels of amoxicillin; coadministration with warfarin or heparin, increases risk of bleeding; may decrease effectiveness of oral contraceptive agents
Documented hypersensitivity
B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals
Administer for a minimum of 10 d to eliminate organism and to prevent sequelae (eg, endocarditis, rheumatic fever); following treatment, perform cultures to confirm eradication of streptococci; renal insufficiency may require dose reduction
Alternative for oral therapy in the penicillin-allergic patient. Inhibits protein synthesis and thus bacterial growth by binding to 30S and possibly 50S ribosomal subunits of susceptible bacteria.
100 mg PO bid
<8 years: Not established
>8 years: 2-4 mg/kg/d PO divided q12h
Bioavailability decreases with antacids containing aluminum, calcium, magnesium, iron, or bismuth subsalicylate; tetracyclines can increase hypoprothrombinemic effects of anticoagulants; tetracyclines can decrease effects of oral contraceptives, causing breakthrough bleeding and increased risk of pregnancy
Documented hypersensitivity; severe hepatic dysfunction; lactation
D - Fetal risk shown in humans; use only if benefits outweigh risk to fetus
Caution in patients who are cachectic or debilitated and in hepatic or renal disease; photosensitivity may occur with prolonged exposure to sunlight or tanning equipment; reduce dose in renal impairment; consider drug serum level determinations in prolonged therapy; tetracycline use during tooth development (last half of pregnancy through age 8 y) can cause permanent discoloration of teeth; Fanconilike syndrome may occur with outdated tetracyclines
Third-generation cephalosporin with broad-spectrum, gram-negative activity; lower efficacy against gram-positive organisms; higher efficacy against resistant organisms. Arrests bacterial growth by binding to one or more penicillin-binding proteins. Once-daily IM dosing may benefit the noncompliant patient. Also may be used as an IV antibiotic for patients admitted to the hospital.
1 g IV/IM qd
50 mg/kg/d IV/IM qd
Probenecid may increase ceftriaxone levels; coadministration with ethacrynic acid, furosemide, and aminoglycosides may increase nephrotoxicity
Documented hypersensitivity
B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals
Adjust dose in renal impairment; caution in breastfeeding women and allergy to penicillin
Second-generation cephalosporin indicated for gram-positive cocci and gram-negative rod infections. Infections caused by cephalosporin- or penicillin-resistant gram-negative bacteria may respond to cefoxitin.
1-2 g IV q4-8h
25-50 mg/kg/d IV divided q6h
Probenecid may increase effects of cefoxitin; 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
Drug combination of beta-lactamase inhibitor with ampicillin. Covers skin, enteric flora, and anaerobes. Not ideal for nosocomial pathogens.
1.5 (1 g ampicillin + 0.5 g sulbactam) to 3.0 g (2 g ampicillin + 1 g sulbactam) IV/IM q6-8h; not to exceed 4 g/d sulbactam or 8 g/d ampicillin
<12 years: Not established
>12 years: Administer as in adults
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
Inhibits biosynthesis of cell wall mucopeptide and is effective during stage of active growth.
3.1 g IV q6h
<12 years: Not established
>12 years: Administer as in adults
Tetracyclines may decrease effects of ticarcillin; high concentrations of ticarcillin may physically inactivate aminoglycosides if administered in same IV line; effects when administered concurrently with aminoglycosides are synergistic; probenecid may increase penicillin levels
Documented hypersensitivity; severe pneumonia, bacteremia, pericarditis, emphysema, meningitis, and purulent or septic arthritis should not be treated with oral penicillin during acute stage
B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals
Perform CBCs prior to initiation of therapy and at least weekly during therapy; monitor for liver function abnormalities by measuring AST and ALT during therapy; exercise caution in patients diagnosed with hepatic insufficiencies; perform urinalysis, BUN, and creatinine determinations during therapy, and adjust dose if values become elevated; monitor blood levels to avoid possible neurotoxic reactions
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Goldstein EJ, Citron DM, Hudspeth M, Hunt Gerardo S, Merriam CV. In vitro activity of Bay 12-8039, a new 8-methoxyquinolone, compared to the activities of 11 other oral antimicrobial agents against 390 aerobic and anaerobic bacteria isolated from human and animal bite wound skin and soft tissue infections in humans. Antimicrob Agents Chemother. Jul 1997;41(7):1552-7. [Medline].
Goldstein EJ, Citron DM, Hudspeth M, Hunt Gerardo S, Merriam CV. Trovafloxacin compared with levofloxacin, ofloxacin, ciprofloxacin, azithromycin and clarithromycin against unusual aerobic and anaerobic human and animal bite-wound pathogens. J Antimicrob Chemother. Mar 1998;41(3):391-6. [Medline].
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[Guideline] 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. [41 references].
human bite infections, human bites, infection, oral flora, saliva, hand wounds, clenched-fist injury, occlusive bites, hepatitis B, hepatitis C, herpes simplex virus, HSV, syphilis, tuberculosis, actinomycosis, tetanus, HIV, AIDS, Eikenella corrodens, E corrodens, Staphylococcus aureus, S aureus, Clostridium tetani, C tetani, Streptococcus, Corynebacterium, Bacteroides, Peptostreptococcus, bacteremia, sepsis
Don R Revis Jr, MD, Consulting Staff, Department of Surgery, Division of Plastic and Reconstructive Surgery, University of Florida College of Medicine
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