Table 1.
Categories of Exposure to Suspected or Confirmed Rabid Animal and Actions Required | |
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Category I |
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Action required: not regarded as exposures, no post-exposure prophylaxis is required | |
Category II |
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Action required: thorough local wound care and vaccine injection as soon as possible | |
Category III |
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Action required: thorough local wound care and administration of vaccine and RIG as soon as possible | |
Passive Immunization: Rabies Immunoglobulin (RIG) | |
Target population |
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Type, dose |
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Time and site |
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Active Immunization: Vaccines | |
Types | Cell culture vaccine (CCV) and embryonated egg-based vaccines (CCEEVs): |
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and | |
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Potency | ≥2.5 IU per single IM |
Route of administration, dose, vaccine type, and injection sites |
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Sites: | |
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Sites: | |
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Pre-Exposure Prophylaxis | |
Indication |
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IM vaccination regimen | 3 doses, one IM dose on each of days 0, 7, and 21 or 28 |
ID vaccination regimen | 3 doses, one ID injection of 0.1 mL on each of days 0, 7, and 21 or 28 * |
Booster injections | Only for those working under continuous or frequent risk of exposure †, if rabies-virus neutralizing antibody titers is <0.5 IU/mL |
Post-Exposure Prophylaxis | |
Indication |
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Wound care |
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IM vaccination regimen § | 5-dose, Essen regimen (1-1-1-1-1): |
one dose on each of days 0, 3, 7, 14, and 28 | |
4-dose, Zagreb regimen (2-0-1-0-1 or 2-1-1): | |
2 doses on day 0 (one in each of the two deltoid or thigh sites) followed by one dose on each of days 7 and 21 | |
4-dose shortened Essen regimen (1-1-1-1-0) for fully immunocompetent, exposed people who received wound care + high quality RIG + WHO prequalified rabies vaccine: | |
One dose on each of days 0, 3, 7, and 14 | |
For immunocompromised individuals including patients with HIV/AIDS: | |
5-dose CCEEV regimen + wound care + local infiltration with human RIG. Evaluation of the rabies-virus neutralizing antibody 2–4 weeks after vaccination and administration of an additional vaccine dose if needed. | |
ID vaccination regimen § | The updated Thai Red Cross regimen (2-2-2-0-2): |
Injections of 0.1 mL at two sites (deltoid and thigh) on each of days 0, 3, 7, and 28 | |
Short Post-Exposure Prophylaxis for Previously Vaccinated Individuals | |
Exposed or re-exposed individuals, or individuals with rabies-virus neutralizing antibody titers of ≥0.5 IU/mL: | |
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Individuals exposed or re-exposed three months after complete vaccination: | |
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Individuals with category III re- exposure who were vaccinated with a vaccine of unproven potency, or have received an incomplete course of vaccination: | |
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Sources: Rabies vaccines: WHO position paper (2010) [13] and WHO Expert Consultation on Rabies (2013) [1]; Abbreviations: CCEEV, cell culture vaccine and embryonated egg-based vaccines; CCV, cell culture vaccine; HDCV, human diploid cells vaccine; ID, intradermal; IM, intramuscular; PCECV, purified chick embryo cell vaccine; PDEV, purified duck embryo vaccine; PVRV, purified Vero rabies vaccine; RIG, rabies immunoglobulin; WHO, World Health Organization; * within 6–8 h, several individuals should be vaccinated in order to utilize all the volume of the opened vials, reducing thus the overall cost; † antibody monitoring, is preferred to booster injections. Every six months for those at risk of exposure to high concentrations of live rabies virus (e.g., laboratory workers dealing with rabies virus and other lyssaviruses), and every two years for those not at continuous risk of exposure (e.g., veterinarians and animal health officers); § at exceptional circumstances and when it is not possible to complete post-exposure prophylaxis with the same CCEEV, a rabies CCV fulfilling the WHO requirements should be used.