2006 AAHA Canine Vaccine Guidelines
In 2005, AAHA’s Canine Vaccine Task Force met to reexamine and revise guidelines on the use of vaccines in dogs. The results of the Task Force’s work are summarized and tabulated in this article and are published in their entirety on the AAHA website (www.aahanet.org). The 2006 AAHA Canine Vaccine Guidelines contain information on new technological developments in vaccines, an introduction to conditionally licensed vaccines, and detailed recommendations on the use of available vaccines. Perhaps the most noteworthy addition to the guidelines is a separate set of recommendations created for shelter facilities. Vaccines are classified as core (universally recommended), noncore (optional), or not recommended. The Task Force recognizes that vaccination decisions must always be made on an individual basis, based on risk and lifestyle factors.
Executive Summary
Since the publication of the AAHA Canine Vaccine Guidelines in 2003, the profession and the biologics industry have moved in the direction advocated in that document by the Canine Vaccine Task Force. The profession has witnessed no negative medical ramifications to the recommendations issued by the Task Force, several well-documented studies have demonstrated the extended duration of immunity (DOI) and supported the extended vaccine intervals advocated by the guidelines, and the industry has responded in the main by supporting the use of products with extended DOI protocols. While a number of rabies vaccines have long been available as licensed for 3 years by the US Department of Agriculture (USDA), vaccines against other infectious diseases of dogs have generally been licensed as 1-year vaccines. At least one manufacturer has been successful in obtaining a 3-year license from the USDA Center for Veterinary Biologics (USDA/CVB).
In early 2005, the Canine Vaccine Guidelines Task Force was reconvened with the charge of updating the guidelines and developing a plan to simplify the revision process and make it more responsive to the emergence of new vaccines and developments. To that end, the guidelines will be published in their entirety electronically on the AAHA web site (www.aahanet.org), where they can be readily accessed by the profession.
The Task Force recognizes that individual readers will find some sections of immediate interest and others of background interest. However, practitioners are urged to read the entire document for reference, with special attention to certain key sections that have been revised and new sections that have been added.
Revised sections include those addressing the vaccine licensing process and the medical and legal implications of vaccine medicine. Because serologic interpretation in conjunction with or in lieu of vaccination is of major interest to the profession, the section addressing serologic testing has been expanded. The question is not the validity of serology but the application and indication for serologic testing.
A key section of the 2003 guidelines focused on vaccine adverse events and emphasized the importance of reporting adverse events to the appropriate agency. A vaccine adverse event is any undesirable or unintended outcome (including failure to achieve the desired result) that occurs in conjunction with vaccine administration. The section on vaccine adverse events has been updated to reflect recent developments in reporting procedures. The Task Force reiterates its recommendation that practitioners take the time to document and report all adverse events. As changes in protocols are adopted and innovative vaccines and vaccine technologies gain ground, such vigilance is even more essential.
Included in the 2006 guidelines is a section highlighting the science of vaccine development, specifically such technologies as live vectored, subunit, gene-deleted, and deoxyribonucleic acid vaccines. In adding this material, the Task Force’s intent is to introduce its audience to new concepts and future technologies and to stimulate awareness of where the science of vaccine development is headed.
The Task Force has also introduced the subject of conditionally licensed vaccines in one of the several tables included in this update. These vaccines have demonstrated safety and purity and in preliminary studies have demonstrated a reasonable expectation of efficacy. Though only granted conditional licenses by the USDA/CVB, these products may have definite indications in individual animals and bear consideration in selected animals.
Another notable addition to these updated guidelines is a section devoted to shelter medicine. The impetus for separate shelter vaccination guidelines was the Task Force’s recognition that this rapidly developing area of veterinary practice faces unique challenges. What best serves a clinical companion animal practice may not be ideal in an environment housing an ever-changing population. This section discusses some of the special considerations and issues confronting shelter medicine and provides tables listing vaccines that are recommended, optional, and not recommended for the shelter environment.
For many readers, a highlight of the 2006 guidelines will be the recommendations for selecting appropriate vaccines to be administered to the individual patient. The vaccine type, optimal time of administration for puppies and adult dogs, and general comments are compiled in an easy-to-use table within the main guidelines. Vaccines are now categorized as core, noncore (or optional), and not recommended. Core vaccines are those that all dogs should receive in one form or other. Optional vaccines should be administered selectively, based on the animal’s geographic and lifestyle exposure and an assessment of risk/benefit ratios. The table does not mention specific products or manufacturers; it is the position of the Task Force that all major manufacturers produce quality canine vaccines and that these decisions are best left to the clinician.
Even in their revised and updated form, the 2006 guidelines reflect the same underlying principles that imbued the 2003 edition:
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Vaccination is a medical decision and a medical procedure that should be individualized based on the risk and lifestyle of the individual animal.
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An extended vaccine interval is reasonable, safe, and effective in preventing most infectious diseases.
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Veterinary medicine must remain vigilant of emerging diseases, changes in incidence of known diseases, and adverse events associated with vaccine administration. It is incumbent on veterinarians to proactively report adverse events.
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Decisions surrounding vaccination of client-owned pets should include a discussion with clients and always be fully documented in the medical record.


