Copyright 2000 American Medical Association. All Rights Reserved. Applicable FARS/DFARS Restrictions Apply to Government Use.2000American Medical AssociationThis is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
A temporary shortage of adult tetanus and diphtheria toxoids (Td) in the United States has resulted from two coincident situations: (1) a decrease in the number of lots released by Wyeth Lederle (Pearl River, New York), and (2) a temporary decrease in inventory of vaccine following routine maintenance activities at the production facilities by Aventis Pasteur (Swiftware, Pennsylvania) that lasted longer than anticipated. Approximately one half of the usual number of Td doses has been distributed this year. Although there have been no decreases in production of tetanus toxoid (TT), availability is low because of increased use during the Td shortage. On the basis of information provided by Aventis Pasteur, the Public Health Service expects vaccine supplies to be restored early in 2001. Until then, Aventis Pasteur will be limiting orders to assure the widest possible distribution of available doses.
The shortage will only impact persons aged ≥7 years who (1) require tetanus prophylaxis in wound management, (2) have not completed a primary series (three doses) of vaccine containing Td, or (3) have not been vaccinated during the preceding 10 years with Td, diphtheria and tetanus toxoids and acellular pertussis vaccine (DTaP) or diptheria and tetanus toxoids (DT).1 This shortage will not affect vaccination of children aged <7 years who require additional doses of a vaccine-containing TT; they should receive DTaP or pediatric DT,2 which are not in short supply. Td is preferred to TT because Td provides protection against both tetanus and diphtheria.1 However, during this shortage, if Td is not available, TT can be used as an alternative for persons aged ≥7 years who require immediate boosting with TT (e.g., wound management), or who are unlikely to return to a clinic if vaccination is delayed. If TT is administered, patients and health-care providers must weigh risks and benefits of subsequent vaccination with Td. Arthus-type reactions may occur among persons who receive multiple doses of TT, especially within short intervals (<10 years). However, if vaccination with Td is delayed for >10 years following their last Td administration, persons may be protected inadequately against diphtheria.
Clinics experiencing shortages of Td may need to prioritize their use of available supplies. If administration of Td is delayed, clinics should implement a call-back system when vaccine is available. Recommendations for use (highest to lowest priority) of Td are:
Persons traveling to a country where the risk for diphtheria is high.*
Persons requiring tetanus vaccination for prophylaxis in wound management.
Persons who have received <3 doses of vaccine containing Td.
Pregnant women and persons at occupational risk for tetanus-prone injuries who have not been vaccinated with Td within the preceding 10 years.
Adolescents who have not been vaccinated with a vaccine containing Td within the preceding 10 years.
Adults who have not been vaccinated with Td within the preceding 10 years.
Shortage of Tetanus and Diphtheria Toxoids. JAMA. 2000;284(21):2712. doi:10.1001/jama.284.21.2712