When to Administer HTIG and HRIG
Human Tetanus Immunoglobulin (HTIG) should be given for contaminated wounds in patients with incomplete tetanus vaccination (<3 doses or unknown status), while Human Rabies Immunoglobulin (HRIG) must be administered immediately at 20 IU/kg for all previously unvaccinated persons with rabies exposure, regardless of wound type. 1, 2
Human Tetanus Immunoglobulin (HTIG) Administration
Indications Based on Wound Type and Vaccination History
Clean, minor wounds:
- HTIG is not indicated regardless of vaccination history 2
- Give tetanus toxoid booster only if >10 years since last dose 2
All other wounds (contaminated with dirt, puncture wounds, traumatic wounds):
- Give HTIG if: 2
- Unknown vaccination history, OR
- <3 documented tetanus toxoid doses
- Do not give HTIG if: 2
- ≥3 documented tetanus toxoid doses (give toxoid booster only if >5 years since last dose)
HTIG Dosing and Administration
- Administer at a separate site from tetanus toxoid using a separate needle and syringe 2
- Follow manufacturer's package insert for specific dosing 2
- Must be given within 6 months of potential exposure for immunocompromised patients (e.g., rituximab-treated) 3
Human Rabies Immunoglobulin (HRIG) Administration
Indications for HRIG
HRIG is required for all previously unvaccinated persons with rabies exposure, including: 1, 4
- Bite exposures (any penetration of skin by teeth)
- Non-bite exposures (scratches breaking skin, mucous membrane contamination)
- Exposures from any high-risk animal (bats, raccoons, skunks, foxes, monkeys, cats, dogs)
HRIG is NOT indicated for: 1, 3
- Previously vaccinated persons (those who completed pre-exposure or post-exposure vaccination with cell culture vaccine)
- Persons with documented rabies virus neutralizing antibody titer
Critical Timing for HRIG Administration
Administer HRIG as soon as possible, ideally within 24 hours of exposure 4
- If not given on day 0, HRIG can be administered up to and including day 7 of the vaccine series 1, 4
- Beyond day 7, HRIG is contraindicated because vaccine-induced antibody response is presumed to have occurred 1, 5
- Begin treatment regardless of time interval since exposure, as rabies incubation periods exceeding 1 year have been documented 4, 3
HRIG Dosing and Administration
Dose: 20 IU/kg (0.133 mL/kg) body weight for all ages 1, 4
Administration technique: 1, 6
- Infiltrate the full calculated dose thoroughly around and into all wounds if anatomically feasible
- Inject any remaining volume intramuscularly at a site distant from vaccine administration
- Never administer in the same syringe or anatomical site as the vaccine
Common Pitfalls to Avoid
- Never exceed the recommended 20 IU/kg dose - excess HRIG can partially suppress active antibody production 1, 5
- Never give HRIG to previously vaccinated persons - it interferes with anamnestic response and is contraindicated 3, 6
- Never delay HRIG while attempting to locate or test the animal - this is a medical urgency 4
- Failure to infiltrate adequate HRIG at wound sites has been associated with rare postexposure prophylaxis failures 1
Special Populations
Immunocompromised patients (e.g., rituximab-treated): 3
- Still require HRIG at standard 20 IU/kg dose
- Use extended 5-dose vaccine schedule (days 0,3,7,14,28) instead of standard 4-dose regimen
- Consider serologic testing to confirm adequate antibody response
Previously vaccinated persons re-exposed to rabies: 3, 6
- Give only 2 vaccine doses (days 0 and 3)
- Do not give HRIG - it is contraindicated in this population
Concurrent Wound Management
For both tetanus and rabies exposures: 1
- Immediately wash wounds thoroughly with soap and water for 15 minutes
- Apply povidone-iodine solution or other virucidal agent
- Assess need for tetanus prophylaxis in all rabies exposures
- Consider antibiotic prophylaxis based on wound characteristics
- Avoid suturing when possible