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Tetanus Overview

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Author: Brenda Cosens, RN, Operations Manager, Mental Retardation Provider Services Division, Metrocare Services, Incorporated

Brenda Cosens is a member of the following medical societies: Emergency Nurses Association

Coauthor(s): Robert Suter, DO, MHA, Medical Director, Department of Emergency Services, Springbranch Medical Center, Greater Houston Emergency Physicians, Associate Professor, Department of Emergency Medicine, University of Texas Southwestern and Medical College of Georgia

Editors: William G Gossman, MD, Associate Clinical Professor of Emergency Medicine, Creighton University School of Medicine; Consulting Staff, Department of Emergency Medicine, Creighton University Medical Center; Francisco Talavera, PharmD, PhD, Senior Pharmacy Editor, eMedicine; 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; John Halamka, MD, Chief Information Officer, CareGroup Healthcare System, Assistant Professor of Medicine, Department of Emergency Medicine, Beth Israel Deaconess Medical Center; Assistant Professor of Medicine, Harvard Medical School; Jonathan Adler, MD, Attending Physician, Department of Emergency Medicine, Massachusetts General Hospital; Division of Emergency Medicine, Harvard Medical School

Author and Editor Disclosure

Synonyms and related keywords: blood, body fluids, other potentially infectious materials, OPIM, needle stick, sharps injury, hepatitis, HBV, HCV, HDV, human immunodeficiency virus, HIV, acquired immunodeficiency syndrome, AIDS, tetanus, hepatitis A, hepatitis B, hepatitis C, hepatitis D, occupational transmission of disease, occupational exposure to body fluids 



Background

Concern regarding the management of occupational exposure to human immunodeficiency virus (HIV) was heightened when it was realized that HIV is transmitted by body fluids. In spite of this concern, the risk of hepatitis continues to be the greater occupational threat.

Pathophysiology

The major pathogens of concern in occupational body fluid exposure are HIV and hepatitis A, B, C, and D. These pathogens are viruses that require percutaneous or mucosal introduction for infectivity. The major target organs are the immune system (HIV) and the liver (hepatitis). A lesser theoretical concern is tetanus, which attacks the CNS.

Frequency

United States

The rate of occupational transmission from an HIV-positive source is believed to be 0.3% for a percutaneous exposure and 0.09% for a mucous membrane exposure. The rate of transmission from a hepatitis B-positive source to a nonimmunized host is 6-24% and 1-10% for exposure to hepatitis C.



History

  • No symptoms of disease should be expected from the needle-stick exposure, upon a timely presentation.
  • The history should focus on the patient's medical history, including immunizations and risk factors for both HIV and hepatitis.
  • Specific questions include the following:
    • Complete immunization record, including tetanus and hepatitis B
    • Previous occupational exposure to body fluids
    • Intravenous drug abuse
    • Sexual history
    • Body piercing or tattooing
    • Receiving blood and/or blood products
    • Any history of dialysis
    • Travel outside the United States in the last year

Physical

  • No abnormal physical findings, other than evidence of the reported trauma, should be expected upon a timely presentation.
  • At a minimum, a baseline screening examination of the lungs, liver, and lymph nodes should be documented for future reference.

Causes

  • Risk factors for occupational exposure to body fluids include the following:
    • Failure to adhere to universal precautions
    • Using equipment designed without appropriate safety features
    • Performance of exposure-prone procedures



Lab Studies

  • Source patient (if available)
    • HIV
    • Hepatitis B antigen
    • Hepatitis C antibody
    • Aspartate aminotransferase/alanine aminotransferase (AST/ALT) and alkaline phosphatase levels
  • Victim/health care worker
    • Hepatitis B surface antibody
    • HIV
    • Hepatitis C antibody testing at 2 weeks, 4 weeks, and 8 weeks
  • Prior to initiating retrovirals
    • Pregnancy test (stat)
    • CBC count with differential and platelets
    • Serum creatinine/BUN levels
    • Urinalysis with microscopic analysis
    • AST/ALT levels
    • Alkaline phosphatase level
    • Total bilirubin level



Prehospital Care

  • If the exposure is mucosal or the wound is large enough to irrigate, irrigate with copious amounts of saline or other clean fluid.

Emergency Department Care

  • Irrigate and clean wound.
  • The need for tetanus and/or hepatitis B prophylaxis is based on medical history. Health care providers should have been immunized against hepatitis B. Hepatitis A prophylaxis may (rarely) need to be considered depending on the source-patient situation.
  • The need for HIV or chemoprophylaxis (antiretrovirals) is based on an assessment of the risk by using the 3-step process developed by the Centers for Disease Control and Prevention (CDC).
  • Step 1: Determine exposure code.
    • Is the source material blood, bloody fluid, other potentially infectious material, or an instrument contaminated with one of these substances?
      • If not, there is no risk of HIV transmission.
      • If yes, what type of exposure occurred?
    • If the exposure was to intact skin only, there is no risk of HIV transmission.
    • If the exposure was to mucous membrane or integrity-compromised skin, was the volume of fluid small (ie, few drops, short duration) or large (ie, several drops or major splash, long duration)?
      • If small, the category is exposure code 1.
      • If large, the category is exposure code 2.
    • If the exposure was percutaneous, was it a solid needle or a superficial scratch (ie, less severe)?
      • If yes, the category is exposure code 2.
    • Was it from a large-bore hollow needle, a device with visible blood, or a needle used in a source patient's artery or vein (ie, more severe)?
      • If yes, the category is exposure code 3.
  • Step 2: Determine HIV status code.
    • What is the HIV status of the exposure source?
      • If HIV negative, no postexposure prophylaxis is needed.
      • If HIV positive, was the exposure low titer or high titer?
      • Low-titer exposures are asymptomatic patients with high CD4 counts. These are HIV status code 1.
      • High-titer exposures are patients with primary HIV infection, high or increasing viral load or low CD4 counts, or advanced acquired immunodeficiency syndrome (AIDS). These are HIV status code 2.
      • If HIV status is unknown or the source is unknown, the HIV status code is unknown.
  • Step 3: Match exposure code with HIV status code to determine if any postexposure prophylaxis is indicated.
    • Postexposure prophylaxis recommendation
      • Exposure code 1 and HIV status code 1: Postexposure prophylaxis may not be warranted. Exposure type does not pose a known risk. The exposed health care worker and the treating clinician should decide whether the risk for drug toxicity outweighs the benefit of postexposure prophylaxis.
      • Exposure code 1 and HIV status code 2: Consider the basic regimen. Exposure type poses a negligible risk for HIV transmission. A high HIV titer in the source may justify consideration of postexposure prophylaxis. The exposed health care worker and the treating clinician should decide whether the risk for drug toxicity outweighs the benefit of postexposure prophylaxis.
      • Exposure code 2 and HIV status code 1: Recommend the basic regimen. Most HIV exposures are in this category. No increased risk for HIV transmission has been observed, but use of postexposure prophylaxis is appropriate.
      • Exposure code 2 and HIV status code 2: Recommend expanded regimen. Exposure type represents an increased HIV transmission risk.
      • Exposure code 3 and HIV status code 1 or 2: Recommend expanded regimen. Exposure type represents an increased HIV transmission risk.
      • HIV status code unknown: If the source or, in the case of an unknown source, the setting where the exposure occurred suggests possible risk for HIV exposure and the exposure code is 2 or 3, consider the postexposure prophylaxis basic regimen.
  • Basic regimen: 4 weeks of zidovudine (600 mg/d in 2-3 divided doses) and lamivudine (150 mg twice daily)
  • Expanded regimen: Basic regimen plus either indinavir (800 mg q8h) or nelfinavir (750 mg 3 times/d).
  • Interferon ribavirin prophylaxis decreases risk by 40%. Exposed workers should be counseled on the risks of disease transmission based upon their specific exposure.

Consultations

Consult an infectious disease specialist if risks and/or benefits of drug treatment cannot be easily defined.



When indicated, medications are used to prevent disease transmission.

Drug Category: Immunizations

Vaccines containing epitopes that can elicit an immune response are very effective in inducing a protective response.

Drug NameDiphtheria and tetanus vaccine (Diftavax)
DescriptionUsed to induce active immunity against tetanus in selected patients. The immunizing agent of choice for most adults and children <7 y are tetanus and diphtheria toxoids. Necessary to administer booster doses to maintain tetanus immunity throughout life.
Pregnant women should receive only tetanus toxoid, not a diphtheria antigen-containing product.
May administer into deltoid or midlateral thigh muscles in children and adults. Preferred site of administration in infants is the mid-thigh laterally.
Adult DosePrimary immunization: 0.5 mL IM, give 2 injections 4-8 wk apart and a third dose 6-12 mo after second injection
Booster dose: 0.5 mL q10y
Pediatric DoseAdminister as in adults
ContraindicationsDocumented hypersensitivity; history of neurologic symptoms following administration of this product; FDA recommends that elective tetanus immunization be deferred during any outbreak of poliomyelitis because tetanus toxoid injections are an important cause of provocative poliomyelitis
InteractionsPatients receiving immunosuppressants, including corticosteroids or radiation therapy, may remain susceptible despite immunization due to poor immune response; cimetidine may enhance or augment delayed-hypersensitivity responses to skin-test antigens; avoid concurrent use of medication with systemic chloramphenicol since it may impair amnestic response to tetanus toxoid; concurrent use of tetanus-immune globulin may delay development of active immunity by several days (interaction is nevertheless clinically insignificant and does not preclude its concurrent use)
PregnancyC - Fetal risk revealed in studies in animals but not established or not studies in humans; may use if benefits outweigh risk to fetus
PrecautionsNot for use to treat actual tetanus infections or for immediate prophylaxis of unimmunized individuals (use tetanus antitoxin instead, preferably human tetanus immune globulin); diminished antibody response to active immunization may be seen in patients receiving immunosuppressive therapy; better to defer primary diphtheria immunization until immunosuppressive therapy discontinued; routine immunization of symptomatic and asymptomatic HIV-infected persons is recommended

Drug NameTetanuimmune globulin (Hyper-Tet)
DescriptionUsed for passive immunization of any person with a wound that might be contaminated with tetanus spores. Administer if immunization status is unclear or patient is allergic to diphtheria/tetanus vaccine.
Adult DoseProphylaxis: 250-500 U IM in opposite extremity to tetanus toxoid lesion
Clinical tetanus: 3000-10,000 U IM
Pediatric DoseProphylaxis: 250 U IM in opposite extremity to tetanus toxoid
Clinical tetanus: 3000-10,000 U IM
ContraindicationsBecause 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
InteractionsNone reported
PregnancyC - Fetal risk revealed in studies in animals but not established or not studies in humans; may use if benefits outweigh risk to fetus
PrecautionsPersons with isolated immunoglobulin A (IgA) deficiency have potential for developing antibodies to IgA and could have anaphylactic reactions to subsequent administration of blood products that contain IgA; do not perform skin testing because intradermal injection of concentrated gamma globulin may cause localized area of inflammation and can be misinterpreted, causing the 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 administer with other medications since usually incompatible

Drug NameHepatitis B vaccine (Recombivax HB, Engerix-B)
DescriptionRecombinant vaccine used to provide immunization against all known subtypes of hepatitis B virus.
Adult Dose1 mL IM as early as possible (24 h) following a needlestick
1-month booster: 1 mL
6-month booster: 1 mL
Pediatric Dose0.5 mL IM as early as possible (12 h) after birth
<10 years:
Initial dose:
Recombivax HB: 0.25 mL
Engerix-B: 0.5 mL
1-month booster:
Recombivax HB: 0.25 mL
Engerix-B: 0.5 mL
6-month booster:
Recombivax HB: 0.25 mL
Engerix-B: 0.5 mL
>10 years:
Initial dose:
Recombivax HB: 0.5 mL
Engerix-B: 1 mL
1-month booster:
Recombivax HB: 0.5 mL
Engerix-B: 1 mL
6-month booster:
Recombivax HB: 0.5 mL
Engerix-B: 1 mL
ContraindicationsDocumented hypersensitivity; patients with IgA deficiency
InteractionsMay decrease effects of immunosuppressive agents
PregnancyC - Fetal risk revealed in studies in animals but not established or not studies in humans; may use if benefits outweigh risk to fetus
PrecautionsImmunosuppressed patients may require larger doses to respond as well as healthy individuals; vaccine does not protect against the hepatitis A virus; instances of multiple sclerosis exacerbations following administration of hepatitis B vaccine have occurred; caution with thrombocytopenia or coagulation disorders

Drug Category: Antiretrovirals

These agents are inhibitors of reverse transcriptase and thus, cause chain termination when incorporated into a growing viral strand.

Drug NameZidovudine (AZT, ZDV, Retrovir)
DescriptionThymidine analog that inhibits viral replication.
Educate patient on risk versus benefits, including, but not limited to, the lack of substantiated evidence that postexposure chemoprophylaxis will prevent infection. Patient should also learn about side effects, lack of data regarding mutagenesis, and teratogenesis. Obtain a signed consent form.
Perform pretreatment laboratory tests including CBC counts with differential and platelets, serum creatinine level, UA with microscopic analysis, AST level, alkaline phosphatase level, total bilirubin level, and pregnancy test.
Adult Dose200 mg PO tid for 4 wk
Pediatric Dose90-180 mg/m2/dose PO q6h
ContraindicationsDocumented hypersensitivity
InteractionsAcetaminophen may decrease bioavailability; toxicity increases when administered concurrently with amphotericin B, flucytosine, vincristine, vinblastine, doxorubicin, cimetidine, indomethacin, probenecid, lorazepam, aspirin, acyclovir, ganciclovir, dapsone, and pentamidine
PregnancyC - Fetal risk revealed in studies in animals but not established or not studies in humans; may use if benefits outweigh risk to fetus
PrecautionsCaution in impaired hepatic or renal function; reduce or stop therapy in patients who develop hematologic disorders, such as thrombocytopenia, granulocytopenia, and severe anemia

Drug NameLamivudine (3TC, Epivir)
DescriptionThymidine analog that inhibits viral replication.
Adult Dose150 mg PO bid for 4 wk
Pediatric Dose4 mg/kg PO bid
ContraindicationsDocumented hypersensitivity
InteractionsTrimethoprim/sulfamethoxazole increases bioavailability of lamivudine; lamivudine increases concentration of zidovudine when administered concurrently
PregnancyC - Fetal risk revealed in studies in animals but not established or not studies in humans; may use if benefits outweigh risk to fetus
PrecautionsAdjust dose in renal impairment; caution in history of pancreatitis



Further Outpatient Care

  • Follow up with occupational health or infectious disease in 24-72 hours.
  • Discuss need for safe sex practices until follow-up laboratory testing is negative for HIV. Most now recommend a follow-up screen at 3 or 6 months.

In/Out Patient Meds

  • Antiretrovirals, as indicated, by the 3-step assessment process (see Treatment section)

Deterrence/Prevention

  • Universal precautions

Complications

  • Infection

Prognosis

  • Most health care workers with occupational exposure to body fluids do not develop disease. For those who do, prognosis is the same as for other routes of transmission.

Patient Education

  • Refer to occupational health for extensive patient education. Having a brochure available to be given out in the ED is helpful to alleviate fear.
  • For excellent patient education resources, visit eMedicine's Infections Center. Also, see eMedicine's patient education article Tetanus.



Medical/Legal Pitfalls

  • With the advent of CDC recommendations for HIV postexposure prophylaxis, failure to counsel patients on the existence of retroviral treatment (eg, explain its risk/benefits) could be the source of a significant judgment if the patient subsequently develops HIV.
  • Involvement of an informed patient in the decision-making process is essential.



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Needle-stick Guideline excerpt

Article Last Updated: Oct 11, 2007