Rabies
Description
Rabies, an acute, fatal encephalomyelitis caused
by neurotropic viruses in the family Rhabdoviridae, genus Lyssavirus,
is almost always transmitted by an animal bite that inoculates the
virus into wounds. Very rarely, rabies has been transmitted by nonbite
exposures that introduce the virus into open wounds or mucous membranes.
All mammals are believed to be susceptible, but reservoirs are carnivores
and bats. Although dogs are the main reservoir in resource-poor countries,
the epidemiology of the disease differs sufficiently from one region
or country to another to warrant the medical evaluation of all mammal
bites.
Occurrence
Rabies is found on all continents except Antarctica.
In certain areas of the world, canine rabies remains highly endemic,
including (but not limited to) parts of Brazil, Bolivia, Colombia,
Ecuador, El Salvador, Guatemala, India, Mexico, Nepal, Peru, the
Philippines, Sri Lanka, Thailand, and Vietnam. The disease is also
found in dogs in most of the other countries of Africa, Asia, and
Central and South America, except as noted in Table
3–13, which lists countries that have reported no cases
of rabies during the most recent 2-year period for which information
is available (formerly referred to as “rabies-free countries”).
Additional information can be obtained from the
World Health Organization, local health authorities of the country,
the embassy, or the local consulate's office in the United States.
Table 3–13.
Countries and political units reporting no cases of rabies
during 1999*
Africa |
Cape Verde, Libya, Mauritius,
Réunion, São Tome and Principe, and
Seychelles |
Americas |
North: Bermuda, St. Pierre
and Miquelon
Caribbean: Antigua and Barbuda, Aruba, Bahamas, Barbados,
Cayman Islands, Guadeloupe, Jamaica, Martinique, Montserrat,
Netherlands Antilles (Bonaire, Curaçao, Saba, Saint
Eustatius, and Sint Maarten), Saint Kitts (Saint Christopher)
and Nevis, Saint Lucia, Saint Martin, Saint Vincent and Grenadines,
and Virgin Islands (UK and US)
South: Uruguay |
Asia |
Armenia, Cyprus, Hong Kong,
Japan, Kuwait, Lebanon, Qatar, and Singapore |
Europe |
Albania, Finland, Gibraltar,
Greece, Iceland, Ireland, Isle of Man, Italy, Malta,
Norway (mainland), Portugal, Spain* (except Ceuta/Melilla),
Sweden, Switzerland, and United Kingdom |
Oceania† |
Australia,* Cook Islands,
Fiji, French Polynesia, Guam, Hawaii, Kiribati, Micronesia,
New Caledonia, New Zealand, Palau, Papua New Guinea,
Samoa, and Vanuatu |
|
|
Risk for Travelers
Travelers to rabies-endemic countries should be
warned about the risk of acquiring rabies, although rabies vaccination
is not a requirement for entry into any country. Travelers with extensive
unprotected outdoor, evening, and nighttime exposure in rural areas,
such as might be experienced while bicycling, camping, or engaging
in certain occupational activities, might be at high risk even if
their trip is brief.
Clinical Description
The disease progresses from a nonspecific prodromal
phase to paresis or paralysis; spasms of swallowing muscles can be
stimulated by the sight, sound, or perception of water (hydrophobia);
delirium and convulsions can develop, followed by coma and death.
Prevention
Preexposure vaccination with human diploid cell
rabies vaccine (HDCV), purified chick embryo cell (PCEC) vaccine,
or rabies vaccine adsorbed (RVA) may be recommended for international
travelers based on the local incidence of rabies in the country to
be visited, the availability of appropriate antirabies biologicals,
and the intended activity and duration of stay of the traveler. Preexposure
vaccination may be recommended for veterinarians, animal handlers,
field biologists, spelunkers, missionaries, and certain laboratory
workers. Table 3–14 provides
criteria for preexposure vaccination. Preexposure vaccination does
not eliminate the need for additional medical attention after a rabies
exposure, but simplifies postexposure prophylaxis in populations
at risk by eliminating the need for rabies immune globulin (RIG)
and by decreasing the number of doses of vaccine required. Preexposure
vaccination is of particular importance for travelers at risk of
exposure to rabies in countries where locally available rabies vaccines
might carry a high risk of adverse reactions. Preexposure vaccination
can also provide protection when there is an unapparent or unrecognized
exposure to rabies and when postexposure prophylaxis might be delayed.
Purified equine rabies immune globulin (ERIG) has
been used effectively in developing countries where human rabies
immune globulin (RIG) might not have been available. If necessary,
such heterologous product is preferable to no RIG administration
in human rabies postexposure prophylaxis. The incidence of adverse
reactions after the use of these products has been low (0.8%–6.0%),
and most of those that occurred were minor. However, such products
are neither evaluated by U.S. standards nor regulated by the U.S.
Food and Drug Administration, and their use cannot be unequivocally
recommended at this time. In addition, unpurified antirabies serum
of equine origin might still be used in some countries where neither
human RIG nor ERIG are available. The use of this antirabies serum
is associated with higher rates of serious adverse reactions, including
anaphylaxis.
Travelers should be advised that any animal bite
or scratch should receive prompt local treatment by thorough cleansing
of the wound with copious amounts of soap and water and a povidone-iodine
solution if available; this local treatment will significantly reduce
the risk of rabies. Travelers who might have been exposed to rabies
should be advised to always contact local health authorities immediately
for advice about postexposure prophylaxis and should also contact
their personal physician or state health department as soon as possible
thereafter.
Tables 3–15 and 3–16 provide
information on preexposure and postexposure prophylaxis. Routine
serologic testing is not necessary for travelers who receive the
recommended preeexposure or postexposure regimen with HDCV, PCEC,
or RVA vaccines. Exposed travelers previously vaccinated with noncell
culture vaccines should receive the complete postexposure regimen
unless they have developed a laboratory-confirmed antibody response
to the primary vaccination. Serologic testing is still recommended
for travelers whose immune response might be diminished by drug therapy
or by diseases. Rabies preexposure prophylaxis might not be indicated
for travelers to the countries in Table 3–13,
and postexposure prophylaxis is rarely necessary after exposures
to terrestrial animals in these countries.
Table 3–14. Criteria
for preexposure immunization for rabies
Continuous |
Virus present continuously, often in high concentrations
Specific exposures likely to go unrecognized
Bite, nonbite, or aerosol exposure |
Rabies research laboratory workers,* rabies biologics production
workers |
Primary course: Serologic testing every 6 months; booster
vaccination if antibody titer is below acceptable level† |
Frequent |
Exposure usually episodic with source recognized, but exposure
might also be unrecognized
Bite, nonbite, or aerosol exposure possible |
Rabies diagnostic laboratory workers*, spelunkers, veterinarians
and staff, and animal control and wildlife workers in rabies-epizootic
areas |
Primary course: Serologic testing every 2 years; booster
vaccination if antibody titer is below acceptable level† |
Infrequent (greater than general population) |
Exposure nearly always episodic with source recognized
Bite or nonbite exposure |
Veterinarians, animal control and wildlife workers in areas
with low rabies rates; veterinary students; and travelers visiting
areas where rabies is enzootic and immediate access to appropriate
medical care, including biologics, is limited. |
Primary course: No serologic testing or booster vaccination |
Rare (general population) |
Exposure always episodic, with source recognized
Bite or nonbite exposure |
U.S. population at large, including individuals in rabies-epizootic
areas |
No preexposure immunization necessary. |
Table 3–15.
Preexposure immunization for rabies*
HDCV† |
1.0 |
3 |
0, 7, 21 or 28 |
Intramuscular |
PCEC |
1.0 |
3 |
0, 7, 21 or 28 |
Intramuscular |
RVA |
1.0 |
3 |
0, 7, 21 or 28 |
Intramuscular |
|
|
Table 3–16.
Postexposure immunization for rabies*
Not previously immunized |
RIG† |
20 IU/kg body weight |
1 |
0 |
Infiltrated at bite site (if possible); remainder
intramuscular. |
HDCV
PCEC
RVA |
1.0 mL |
5 |
0, 3, 7, 14, 28 |
Intramuscular |
Previously immunized‡ |
HDCV
PCEC
RVA§ |
1.0 mL |
2 |
0, 3 |
Intramuscular |
|
|
Adverse Reactions
Travelers should be advised that they can experience
local reactions such as pain, erythema, and swelling or itching at
the injection site, or mild systemic reactions, such as headache,
nausea, abdominal pain, muscle aches, and dizziness. Approximately
6% of persons receiving booster vaccinations with HDCV can experience
an immune complex-like reaction characterized by urticaria, pruritus,
and malaise. Once initiated, rabies postexposure prophylaxis should
not be interrupted or discontinued because of local or mild systemic
reactions to rabies vaccine.
Precautions and Contraindications
Pregnancy. Pregnancy is not a contraindication
to postexposure prophylaxis.
Age. In infants and children, the dose of HDCV,
PCEC, or RVA for preexposure or postexposure prophylaxis is the
same as that recommended for adults. The dose of RIG for postexposure
prophylaxis is based on body weight (Table
3–16).
For more information about rabies, see the CDC rabies site at http://www.cdc.gov/ncidod/dvrd/rabies
—
Charles Rupprecht
|