You are in: eMedicine Specialties > Emergency Medicine > INFECTIOUS DISEASES Body Fluid ExposuresArticle Last Updated: Jul 2, 2007AUTHOR AND EDITOR INFORMATIONAuthor: Darrell Looney, MD, Attending Physician, Associate Professor of Emergency Medicine, Department of Emergency Medicine, Long Island College Hospital Darrell Looney is a member of the following medical societies: American Academy of Emergency Medicine, American College of Emergency Physicians, and National Medical Association Coauthor(s): Peter B Richman, MD, Consulting Staff, Department of Emergency Medicine, Morristown Memorial Hospital; Richard Shih, MD, Program Director, Department of Emergency Medicine, Morristown Memorial Hospital; Director of Toxicology Fellowship, New Jersey Poison Center, Newark Beth Israel Medical Center Editors: Samuel M Keim, MD, Associate Professor, Department of Emergency Medicine, University of Arizona College of Medicine; Francisco Talavera, PharmD, PhD, Senior Pharmacy Editor, eMedicine; Barry J Sheridan, DO, Chief, Department of Emergency Medical Services, Brooke Army Medical Center; 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: needle sticks, needlestick, needlestick injury, body fluid exposures, splash exposures, mucous membrane exposures, sharps injury, hepatitis B virus, HBV, hepatitis C virus, HCV, human immunodeficiency virus, HIV INTRODUCTIONBackgroundOccupational transmission of blood-borne infections may occur through parenteral, mucous membrane, and nonintact skin exposure. The greatest risk for transdermal transmission is via a skin penetration injury sustained with a sharp hollow-bore needle that was recently removed from a blood-contaminated source. Although many infections may be transmitted by such contact, the most consequential are hepatitis B virus (HBV), hepatitis C virus (HCV), and human immunodeficiency virus (HIV). In addition, skin and soft tissue infection at the site of inoculation through introduction of staphylococcal species is an issue of concern and must not be neglected. Tetanus prophylaxis is also an important issue of concern. Another important concept is the fact that many clinical pathways adopt plans for management primarily of health care personnel but are woefully lacking when faced with the outside individual at risk for significant exposure. PathophysiologyWhen intact, the integumentary system serves as an effective physical barrier to the entry of infectious elements into the body. However, a special situation exists in terms of mucous membranes. Across these membranes, lies a layer of mucus secreted by specialized columnar cells that are closely associated with each other through gap junctions, which are little more than specialized cell surface projections that allow intercellular communication. The presence of a moist mucous layer tends to prolong the viability of fragile viruses, such as HIV and HBV, which cannot survive long in drier environments. However, HBV has been demonstrated to survive in dried blood for extended periods. Higher vascularity coupled with a relatively permeable cellular layer gives rise to a presumed heightened risk of transmission of HBV, HCV, and HIV across this organ system and into the bloodstream. Still, at least for occupational HIV exposures, transmission rarely occurs. Intact, keratinized skin does not possess these characteristics and is virtually impermeable unless disrupted. Viral transmission here is not readily possible, hence the association with transmission caused by needlestick injury or (less frequently) through open wounds. In terms of blood and body fluids, semen and vaginal secretions with visible blood should be considered potentially infectious vehicles. Similarly, cerebrospinal fluid, amniotic fluid, pleural fluid, synovial fluid, and peritoneal and pericardial fluids carry a high suspicion of risk for transmission. In addition, unless blood is present, saliva, sputum, sweat, tears, feces, nasal secretions, urine, and vomitus carry a low risk of transmission of HBV, HCV, and HIV. FrequencyUnited StatesSharps injuries occur at a rate of 1.8 per year per physician and 0.98 per year per nurse, while working on the same medical ward. Statistically, twice as many nurses as doctors have been reported with occupationally acquired HIV infection. Whether this is a functionality of the significance of the exposure (ie, severity of the stick) or the route of exposure remains to be studied. If the inoculum were blood and positive for both hepatitis B surface antigen (HBsAg) and hepatitis B e antigen (HBeAg), the risk for developing clinical hepatitis due to HBV infection may lie somewhere between 22% and 31%. The risk for developing HIV remains around 0.3%. Mortality/Morbidity
CLINICALHistoryPatients present with a history of exposure. Typically, this is a splash-type exposure to mucosal or nonintact skin or a needle-stick injury to intact skin. Patients may often report exposures to intact keratinized skin out of uninformed concern or they are aware of some preexisting injury and may be predisposed to infection. Reassurance through awareness of the risks for viral transmission in various scenarios is of significant importance to both the health care provider and the patient.
PhysicalDuring the physical examination, be sure to assess body area of exposure and depth of any wounds. The neurovascular status in the setting of extremity wounds is an important and often omitted element. The clinician should remain suspicious of occult injury, such as paper cuts or abrasions, which may threaten the integrity of the skin. For mucosal exposures, especially on the face, keep in mind that the exposure may not be limited to only one area, and it may occur simultaneously in nasal, mucosal, and conjunctival mucosae. CausesMost exposures are the result of a departure from universal precautions on some level—whether it is the result of recapping, failure to use personal protective equipment, or the unintentional sharp left in an inappropriate container for disposal. When dealing with blood and body fluid exposures, document whether the exposure represents a departure from universal precautions, Occupational Safety and Health Administration (OSHA) standards, or a true accident (eg, projectile vomiting, precipitous labor with spontaneous rupture of membranes). This information is vital to the institutional safety committee whose function is to monitor the safety of the environment for the entire facility and make recommendations for upgrades and changes in policy. DIFFERENTIALSHepatitis HIV Infection and AIDS Sexual Assault Workers' Compensation
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| Drug Name | Zidovudine (AZT, ZDV, Retrovir) |
|---|---|
| Description | Thymidine analog that inhibits viral replication. |
| Adult Dose | 200 mg PO tid 1-2 mg/kg/dose IV q4h |
| Pediatric Dose | 90-180 mg/m2/dose PO q6h 1-2 mg/kg/dose IV q4h Usually, now the AZT 180 mg/m2/dose, given bid (max 600 mg/d) Body surface area calculation Usually confusing to most physicians; 5 equations are used currently, although the Mostellar equation is most often recommended. The Mosteller formula For example, BSA = SQRT[(cm*kg)/3600] In inches and pounds: BSA (m²) = ([Height(in) X Weight(lb)]/3131)½ The DuBois and DuBois formula BSA (m²) = 0.20247 X Height(m)0.725 X Weight(kg)0.425 A variation of DuBois and DuBois that gives virtually identical results: BSA (m²) = 0.007184 X Height(cm)0.725 X Weight(kg)0.425 The Haycock formula The Gehan and George formula BSA (m²) = 0.0235 X Height(cm)0.42246 X Weight(kg)0.51456 The Boyd formula For more information on BSA calculation, see Standardization of Body Surface Area Calculations. |
| Contraindications | Documented hypersensitivity |
| Interactions | Acetaminophen may decrease bioavailability of zidovudine; zidovudine toxicity increases when administered concurrently with amphotericin B, flucytosine, doxorubicin (Adriamycin), vincristine, vinblastine, cimetidine, indomethacin, probenecid, lorazepam, aspirin, acyclovir, ganciclovir, dapsone, and pentamidine |
| Pregnancy | C - Safety for use during pregnancy has not been established. |
| Precautions | Caution in impaired hepatic or renal function; reduce or stop therapy in hematologic disorders such as thrombocytopenia, granulocytopenia, and severe anemia |
| Drug Name | Lamivudine (3TC, Epivir) |
|---|---|
| Description | Thymidine analog that inhibits viral replication. |
| Adult Dose | 150 mg PO bid |
| Pediatric Dose | 4 mg/kg PO bid |
| Contraindications | Documented hypersensitivity |
| Interactions | Trimethoprim/sulfamethoxazole increases bioavailability of lamivudine; lamivudine increases concentration of zidovudine when administered concurrently |
| Pregnancy | C - Safety for use during pregnancy has not been established. |
| Precautions | Primary toxicities and/or adverse effects include headache, abdominal pain, diarrhea, and pancreatitis (rare); toxicity of zidovudine and 3TC when used in combination is approximately equal to that of zidovudine alone; adjust dose in renal impairment; caution in children with history of pancreatitis |
These agents block modification of precursor poly proteins responsible for the synthesis of reverse transcriptase and HIV-1 protease.
| Drug Name | Indinavir (IDV, Crixivan) |
|---|---|
| Description | Prevents formation of protein precursors necessary for HIV infection of uninfected cells and viral replication. |
| Adult Dose | 800 mg PO q8h on empty stomach |
| Pediatric Dose | Not established |
| Contraindications | Documented hypersensitivity |
| Interactions | Indinavir increases blood concentrations of astemizole (recalled from US market), cisapride, midazolam, isoniazid, stavudine, trimethoprim, terfenadine (recalled from US market), triazolam, and PO contraceptives; fluconazole and rifampin decrease blood concentration of indinavir; quinidine and ketoconazole increase blood concentrations of indinavir; indinavir decreases blood concentration of lamivudine |
| Pregnancy | C - Safety for use during pregnancy has not been established. |
| Precautions | Caution in hepatic impairment; primary toxicities and/or adverse effects include nephrolithiasis, crystalluria, hematuria, nausea, headache, indirect hyperbilirubinemia, elevated LFT results, and hyperglycemia/diabetes mellitus; caution in hepatic impairment |
| Drug Name | Nelfinavir (Viracept) |
|---|---|
| Description | Inhibits HIV-1 protease, resulting in production of an immature and noninfectious virus. |
| Adult Dose | 750 mg PO tid ac |
| Pediatric Dose | <2 years: Not established 2-12 years: 20-30 mg/kg PO tid ac >12 years: Administer as in adults |
| Contraindications | Documented hypersensitivity |
| Interactions | Nelfinavir increases blood concentrations of astemizole (recalled from US market), cisapride, midazolam, isoniazid, stavudine, trimethoprim, terfenadine (recalled from US market), triazolam, and PO contraceptives; fluconazole and rifampin decrease blood concentrations of nelfinavir; quinidine and ketoconazole increase nelfinavir blood concentrations; nelfinavir decreases lamivudine blood concentrations |
| Pregnancy | B - Usually safe but benefits must outweigh the risks. |
| Precautions | If PO contraception desired, should use alternative or additional contraceptive measures while taking nelfinavir as opposed to standard oral contraceptive therapy Primary toxicities and/or adverse effects include diarrhea and hyperglycemia/diabetes mellitus due to effects on pancreas; caution in hepatic impairment |
Patients who may not have been immunized against Clostridium tetani products should receive tetanus immune globulin (Hyper-Tet).
| Drug Name | Tetanus immune globulins (Hyper-Tet) |
|---|---|
| Description | Used for passive immunization of any person with a wound that might be contaminated with tetanus spores. See Tetanus Immunoglobulin Drug Data Sheet. |
| Adult Dose | Currently, only tetanus immunoglobulin for IM use is available from BPL (020 8258 2200 - 24 hours); no product suitable for IV use will be available in foreseeable future Prophylaxis IM for tetanus prone wounds (licensed): 250 U for most uses (500 U if more than 24 h have elapsed or there is risk of heavy contamination or following burns) Available in 1-mL ampules containing 250 U |
| Pediatric Dose | Prophylaxis: 250 U IM in opposite extremity as tetanus toxoid Clinical tetanus: 3,000-10,000 U IM |
| Contraindications | Administration within 3 mo of live-virus immune globulin because antibodies in globulin preparation may interfere with immune response to vaccination (may be necessary to revaccinate persons who received immune globulin shortly after live-virus vaccination) |
| Interactions | None reported |
| Pregnancy | C - Safety for use during pregnancy has not been established. |
| Precautions | Persons 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 ID 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 administered in prescribed IM manner are extremely rare; do not admix with other medications because usually incompatible |
These agents are used for tetanus immunization. A booster injection in previously immunized individuals is recommended to prevent this potentially lethal syndrome.
| Drug Name | Tetanus toxoid |
|---|---|
| Description | Induce active immunity against tetanus in selected patients. Tetanus and diphtheria toxoids are immunizing agents of choice for most adults and children (>7 y). Necessary to administer booster doses to maintain tetanus immunity throughout life. Pregnant patients should receive only tetanus toxoid, not a diphtheria antigen–containing product. May be administered into deltoid or midlateral thigh muscles of children and adults. In infants, preferred site of administration is mid thigh laterally. |
| Adult Dose | Primary immunization: 0.5 mL IM; administer 2 injections 4-8 wk apart and a third dose 6-12 mo after second injection Booster dose: 0.5 mL q10y |
| Pediatric Dose | Administer as in adults |
| Contraindications | Documented hypersensitivity; history of any type of neurologic symptoms or signs following administration of this product; immunization during poliomyelitis outbreak (FDA recommends that elective tetanus immunization be deferred during any outbreak of poliomyelitis because tetanus toxoid injections are an important cause of provocative poliomyelitis) |
| Interactions | Patients receiving immunosuppressants, including corticosteroids or radiation therapy, may remain susceptible despite immunization because of poor immune response; cimetidine may enhance or augment delayed-type hypersensitivity responses to skin test antigens; avoid concurrent use of medication with systemic chloramphenicol because 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) |
| Pregnancy | C - Safety for use during pregnancy has not been established. |
| Precautions | Do not use to treat actual tetanus infections or for immediate prophylaxis of unimmunized individuals (instead use tetanus antitoxin, preferably human tetanus immune globulin); diminished antibody response to active immunization may be observed 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 |
| Media file 1: Flowsheet for management of blood/body fluid exposures. | |
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Article Last Updated: Jul 2, 2007