Difference between revisions of "Healthcare occupational exposure to blood or other body fluids"

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==HIV==
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==Background==
*[[HIV Prophylaxis (Non-Occupational)]]
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*The majority of persons (e.g. source patients) chronically infected with hepatitis B and C (65% to 75%) are not aware of their infection <ref>[https://www.ncbi.nlm.nih.gov/pubmed/23740193 Fretz R, Negro F, Bruggmann P et al. Hepatitis B and C in Switzerland - healthcare provider initiated testing for chronic hepatitis B and C infection. Swiss Med Wkly. 2013 May 17;143:w13793.]</ref>
*[[HIV Prophylaxis (Occupational)]]
 
  
==Hep B==
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==Clinical Features==
# risk of infc 2- 30% after needle stick
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*Frequently from needlestick injuries or other occupational exposures to bodily fluids
# can survive on dried blood for 1 wk
 
# found in all fluids but highest conc in blood and therefore highest risk with blood
 
# hep b surface antibodies confers life long immunity
 
# don't need to test pt or source if pt certain fully/ successfully immunized- antibodies > 10 IU at some time
 
# if pt not successfully immunized, give hep b immune globulin
 
# failed 3 shots/ 1 series- give hep booster and immune globulin x 2 doses over 1 mo
 
# failed 6 shots/ 2 series- give sequential immune globulin
 
  
Patient Unvaccinated, Source Pos
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==Differential Diagnosis==
--> HBIG + vaccine
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*[[Laceration]]
 +
*Retained [[foreign body]]
  
==Hep C==
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==Evaluation==
# no prophylaxsis
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''Most commonly, the only actionable lab on the day of exposure is a rapid [[HIV]] test from the source-patient (for consideration of [[PEP]])''
# no interferon, no antivirals, no globulin
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*Less severe percutaneous exposures are associated with solid and blunt tip needles
# not xmitted efficiently through needle stick- 2% rate
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*More severe percutaneous exposures are associated with deep punctures, large bore hollow needles, visible blood on the device, and needles used in patients arteries and veins.
# get basline hcv test and ALT
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*Smaller volume (few drops) exposures are considered to be lower risk than higher volume (major blood splash) for mucous membranes and non-intact skin exposures.
 +
*Most occupational exposures to HIV are not associated with transmission.
 +
===Source-patient labs===
 +
*Rapid HIV
 +
*Consider [[hepatitis]] panel and possibly RPR
 +
**Hepatitis B and C infectivity of source patient:
 +
***HBs-Ag (active infection)
 +
***HBc-Ab IgM (window period)
 +
***HepC-Ab, plus or minus viral load
  
Post Exp Viral Hep Counseling
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===Exposed-patient labs===
# can still breast feed
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*In some systems, NO immediate laboratory testing is performed
# no organ/ blood donation
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*In many systems, a standardized baseline lab panel is sent in the ED and then followed up at employee health the next day
# no worry about modifiying sex pattern or becoming preg
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*If giving HIV [[PEP]]:
 +
**Rapid [[HIV]] (to confirm they do not ''already'' have HIV)
 +
**CBC, C7, LFTs, pregnancy test
  
www.needlestick.mednet.ucla.edu
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==Management==
 +
===[[HIV]]===
 +
*Consider [[HIV post-exposure prophylaxis]]
  
==Source==
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{{HIV post-exposure prophylaxis regimens}}
6/06 MISTRY
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 +
===[[Hepatitis B]]===
 +
*Not normally indicated, assuming patient has had full course of Hepatitis B vaccination (as all healthcare workers should have)
 +
**If exposed-patient NOT already vaccinated, see [[Hepatitis_B#Hepatitis_B_Post-Exposure_Prophylaxis|Hepatitis B Post-Exposure Prophylaxis]]
 +
 
 +
===[[Hepatitis C]]===
 +
*No prophylaxis regimen has any benefit
 +
 
 +
==Disposition==
 +
*Outpatient management with employee health follow-up
 +
 
 +
==See Also==
 +
*[[HIV post-exposure prophylaxis]]
 +
 
 +
==References==
 +
<references/>
  
 
[[Category:ID]]
 
[[Category:ID]]

Latest revision as of 15:31, 17 June 2019

Background

  • The majority of persons (e.g. source patients) chronically infected with hepatitis B and C (65% to 75%) are not aware of their infection [1]

Clinical Features

  • Frequently from needlestick injuries or other occupational exposures to bodily fluids

Differential Diagnosis

Evaluation

Most commonly, the only actionable lab on the day of exposure is a rapid HIV test from the source-patient (for consideration of PEP)

  • Less severe percutaneous exposures are associated with solid and blunt tip needles
  • More severe percutaneous exposures are associated with deep punctures, large bore hollow needles, visible blood on the device, and needles used in patients arteries and veins.
  • Smaller volume (few drops) exposures are considered to be lower risk than higher volume (major blood splash) for mucous membranes and non-intact skin exposures.
  • Most occupational exposures to HIV are not associated with transmission.

Source-patient labs

  • Rapid HIV
  • Consider hepatitis panel and possibly RPR
    • Hepatitis B and C infectivity of source patient:
      • HBs-Ag (active infection)
      • HBc-Ab IgM (window period)
      • HepC-Ab, plus or minus viral load

Exposed-patient labs

  • In some systems, NO immediate laboratory testing is performed
  • In many systems, a standardized baseline lab panel is sent in the ED and then followed up at employee health the next day
  • If giving HIV PEP:
    • Rapid HIV (to confirm they do not already have HIV)
    • CBC, C7, LFTs, pregnancy test

Management

HIV

Preferred HIV PEP Regimen[2][3]

PEP should be started as soon as possible after significant exposure and continued for 28 days[4]

  • Raltegravir (Isentress; RAL) 400 mg PO twice daily, plus
  • Truvada, 1 PO once daily (Tenofovir DF [Viread; TDF] 300 mg emtricitabine [Emtriva; FTC] 200 mg)

Other Considerations

  • If known source patient with resistant HIV strain, consult HIV service for source-patient-specific PEP
  • Consider interactions with current medication interactions and contraindications, such as renal impairment with Truvada

Hepatitis B

  • Not normally indicated, assuming patient has had full course of Hepatitis B vaccination (as all healthcare workers should have)

Hepatitis C

  • No prophylaxis regimen has any benefit

Disposition

  • Outpatient management with employee health follow-up

See Also

References

  1. Fretz R, Negro F, Bruggmann P et al. Hepatitis B and C in Switzerland - healthcare provider initiated testing for chronic hepatitis B and C infection. Swiss Med Wkly. 2013 May 17;143:w13793.
  2. Kuhar D, et al. Updated US Public Health Service Guidelines for the Management of Occupational Exposures to Human Immunodeficiency Virus and Recommendations for Postexposure Prophylaxis. September 2013. 34(9):875-892. DOI: 10.1086/672271. http://www.jstor.org/stable/10.1086/672271
  3. Updated Guidelines for Antiretroviral Postexposure Prophylaxis After Sexual, Injection Drug Use, or Other Nonoccupational Exposure to HIV—United States, 2016. Centers for Disease Control and Prevention, U.S. Department of Health and Human Services
  4. Kuhar DT et al. Updated US Public Health Service guidelines for the management of occupational exposures to human immunodeficiency virus and recommendations for postexposure prophylaxis. Infect Control Hosp Epidemiol. 2013 Sep;34(9):875-92. doi: 10.1086/672271.