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Appendices

The first 20% of the full text of this section appears below.

Section 1. Active and Passive Immunization

INFORMING PATIENTS AND PARENTS

Parents and patients should be informed about the benefits and risks of disease preventive and therapeutic procedures, including immunization. The patient, parents, and/or legal guardian should be informed about benefits to be derived from vaccines in preventing diseases in immunized people and in the community where they live and about the risks of those vaccines. Questions should be encouraged and adequate time should be allowed so that information is understood.

The National Childhood Vaccine Injury Act (NCVIA) of 1986 included requirements for notifying all patients and parents about vaccine benefits and risks. Whether vaccines are purchased with private or public funds, this legislation mandates that a vaccine information statement (VIS) be provided each time a vaccine covered under the National Vaccine Injury Compensation Program (VICP) is administered (see Table 1.2). This applies in all settings, such as clinics, offices, and hospitals (eg, for the birth dose of hepatitis B vaccine). Providing this information before the day of immunization is desirable. For vaccines not yet included in the VICP, VISs are available but are not mandated unless the vaccine is purchased through a contract with the Centers for Disease Control and Prevention (CDC [ie, the Vaccines for Children Program, state immunization grants, or state purchases through the CDC]). Copies of current VISs are available on the NIP Web site (www.cdc.gov/nip/publications/VIS/default.htm) and the Immunization Action Coalition Web . . . [Go to Full Text]

 

Related text in Red Book:

Record Keeping and Immunization Information Systems

Red Book 2006: 37-39. [Extract] [Full Version]  

Parental Misconceptions About Immunizations

Red Book 2006: 51-54. [Extract] [Full Version]  

Standards for Child and Adolescent Immunization Practices

Red Book 2006: 844-846. [Extract] [Full Version]  








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