Poliomyelitis is an acute infection that involves the gastrointestinal tract and, occasionally, the central nervous system. It is acquired by fecal-oral transmission. Clinical manifestations of poliovirus infection range from asymptomatic (the majority of infections) to symptomatic, including acute flaccid paralysis of a single limb to quadriplegia; respiratory failure; and, rarely, death.
In the prevaccine era, infection with poliovirus was common, with epidemics occurring in the summer and fall in temperate areas. The incidence of poliomyelitis fell rapidly after the licensure of inactivated polio vaccine in 1955 and oral polio vaccine in the 1960s. The last cases of indigenously acquired polio in the United States occurred in 1979. Although a polio eradication program led to elimination of polio in the Western Hemisphere, where the last case associated with wild poliovirus was detected in 1991, an outbreak of vaccine-derived poliovirus type 1 occurred in the Dominican Republic and Haiti in July 2000. In spite of this recent outbreak in the Western Hemisphere, the global polio eradication initiative has reduced the number of reported polio cases worldwide by >90% since the mid-1980s, and worldwide eradication of the disease appears feasible in the near future. Risk for Travelers
Travelers to countries where polio is epidemic or still endemic should be fully immunized. Because of polio eradication efforts, the number of countries where travelers are at risk for polio has decreased dramatically. Concurrent with the decline in polio incidence, the number of polio-endemic countries decreased from more than 120 in 1988 to approximately 50 in 1998. Approximately 75% of the world's population resides in areas now considered free of wild poliovirus circulation, including the Western Hemisphere, the Western Pacific Region (which encompasses China), and the European
Most of the world's remaining poliovirus transmission is in two large endemic areas in south Asia and sub-Saharan Africa. Accelerated polio eradication strategies are being used in seven reservoir countries--Bangladesh, Democratic Republic of the Congo, Ethiopia
, India, Nepal, Nigeria, and Pakistan--as well as in Afghanistan, Angola, Liberia, Sierra Leone
, Somalia, Sudan, and Tajikistan. Preventive Measures Vaccine
A person is considered to be fully immunized if he or she has received a primary series of at least three doses of inactivated poliovirus vaccine (IPV), live oral poliovirus (OPV), or any combination of IPV and OPV. To eliminate the risk for vaccine-associated paralytic poliomyelitis, OPV was no longer recommended for routine immunization in the United States as of January 1, 2000. Manufacture of the only OPV licensed for use in the United States has ceased, and OPV is no longer available in this country. OPV remains the vaccine of choice, however, for global polio eradication activities. Infants and Children
Because OPV is no longer recommended for routine immunization in the United States, all infants and children should receive four doses of IPV at 2, 4, and 6 through 18 months of age, and 4 through 6 years of age. If accelerated protection is needed, the minium interval between doses is 4 weeks, although the preferred interval between the second and third doses is 2 months. Infants and children who have initiated the poliovirus vaccination series with one or more doses of OPV should receive IPV to complete the series. Adults
Adults who are traveling to polio-endemic areas and are unimmunized or whose vaccination status is unknown should receive IPV. Two doses of IPV should be administered at intervals of 4 to 8 weeks; a third dose should be administered 6 to 12 months after the second. If three doses of IPV cannot be administered within the recommended intervals before protection is needed, the following alternatives are recommended:
If more than 8 weeks is available before protection is needed, three doses of IPV should be administered at least 4 weeks apart.
If less than 8 weeks, but more than 4 weeks, is available before protection is needed, two doses of IPV should be administered at least 4 weeks apart.
If less than 4 weeks is available before protection is needed, a single dose of IPV is recommended.
The remaining doses of vaccine should be administered later, at the recommended intervals, if the person remains at increased risk for poliovirus exposure. Adults who are traveling to polio-endemic areas and have received a primary series with either IPV or OPV can receive another dose of IPV. Available data do not indicate the need for more than a single lifetime booster dose with IPV for adults. Adverse Reactions Allergy.
--Minor local reactions (pain and redness) can occur following IPV. No serious adverse reactions to IPV have been documented.
IPV should not be administered to people who have experienced a severe allergic (anaphylactic) reaction after a previous dose of IPV or to streptomycin, polymixin B, or neomycin. Because IPV contains trace amounts of streptomycin, polymixin B, and neomycin, hypersensitivity reactions can occur among people sensitive to these antibiotics. Pregnancy.
--Although no adverse events of IPV have been documented among pregnant women or their fetuses, vaccination of pregnant women should be avoided on theoretical grounds. However, if a pregnant woman
is unimmunized and requires immediate protection against polio, IPV can be administered as recommended in the adult schedule. Breast-feeding
does not interfere with successful immunization against polio. Precautions and Contraindications
A dose of IPV may be administered to an infant or a child with diarrhea. Minor upper respiratory illnesses with or without fever; mild to moderate local reactions to a previous dose of IPV; current antimicrobial therapy; and the convalescent phase of acute illness are not contraindications for vaccination. Immunosuppression.
--IPV is the only polio vaccine recommended for use in immunodeficient travelers and their household contacts. Many immunodeficient people are immune to polioviruses as a result of previous vaccination or exposure to the wild virus when they were immunocompetent. Administration of IPV to immunodeficient travelers is safe. Although a protective immune response cannot be ensured, IPV might confer some protection.
© Center for Disease Control