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Sudden Infant Death Syndrome (SIDS) and Vaccination
The age at which infants begin their primary course of vaccinations (2 to 4 months old) is also the peak age for the incidence of sudden infant death syndrome (SIDS). The similar timing of these two events has led some people to believe that the events might be related. However, recent studies have concluded that vaccinations are not a risk factor for SIDS or sudden unexpected death in infants. The incidence of SIDS is declining in the United States due to public education campaigns regarding infant sleeping position, reduced exposure of infants to cigarette smoke and fewer potentially hazardous sleeping environments. Recent reports and studies, combined with the decrease in SIDS rate despite the increase in vaccinations, support the conclusion that routine childhood vaccinations do not contribute to SIDS. | |||||
What is SIDS? Sudden Infant Death Syndrome (SIDS) is the diagnosis given for the sudden death of an infant under one year of age that remains unexplained after a thorough case investigation (i.e., autopsy, death scene exam, review of health status prior to dying and other family medical history). SIDS is the leading cause of death in infants between one month and one year of age. Most SIDS deaths occur when a baby is between one and four months of age. Who is at risk for SIDS?
It is also important to note...
What causes SIDS? The cause(s) of SIDS are not known. However, the "triple-risk" model appears to be the most accepted description of the chain of events that may lead to SIDS. This model suggests that three factors or events lead to SIDS: First, an infant that appears normal and healthy has an underlying defect. This defect may be located in the brainstem, which is responsible for heart rate, respiratory controls and overall body regulatory mechanisms. Second, the infant, like all infants under or around the age of 6 months, passes through a critical development period in which rapid changes in sleep and wake patterns, breathing, heart rate, blood pressure and temperature occur. Finally, other factors (like tummy sleeping, cigarette smoke exposure, and mild respiratory infections) tip the delicate balance causing SIDS. According to the triple-risk model, an infant will die of SIDS only if he or she possesses all three factors described above. For example, if an infant with an underlying defect is passing through the normal critical development period and is subjected to outside stressors (like tummy sleeping or cigarette smoke exposure), the infant is at high risk of dying from SIDS. Current programs to reduce the risk of SIDS have focused on these modifiable risk factors in an attempt to remove any additional stressors from a vulnerable infant. Because it is impossible to identify which infants are vulnerable, the risk reduction programs are targeted at every child. According to the "Targeting SIDS: A Strategic Plan" located on the National Institute of Child Health and Human Development (NICHD website): Between 1992 and 1998, the proportion of infants placed to sleep on their stomachs declined from about 70 percent to about 17 percent. Between 1992 and 1998, the SIDS rate declined by about 40 percent, from 1.2 per 1,000 live births to 0.72 per 1,000 live births. How do we know that some SIDS deaths are not due to vaccines? This issue has been studied for many years and several lines of evidence reassure us about the safety of vaccines. A study utilizing the Vaccine Safety Datalink (VSD) data, which included children who were under a health maintenance organization (HMO) health plan, found that there was no association between immunization and deaths in young children. The study investigated deaths in children one month to 7 years of age between 1991 and 1995. Data were analyzed by comparing vaccination histories for each vaccine during the week and month prior to the date of death for each child. Five hundred and seventeen deaths occurred between 1991-1995, most (59%) during the first year of life. Of these deaths, the results did not show an association between immunizations and childhood deaths. The Vaccine Adverse Event Reporting System (VAERS), established by the Food and Drug Administration (FDA) and the Centers for Disease Control and Prevention (CDC), also monitors the safety of vaccines. VAERS provides a mechanism for the collection and analysis of adverse events associated with vaccines currently licensed in the United States. Adverse events are defined as health effects that occur after immunization that may or may not be related to the vaccine. VAERS data are continually monitored in order to detect previously unknown adverse events or increases in known adverse events. Studies that looked at the age distribution and seasonality of deaths reported to VAERS5, SIDS and VAERS reports following DTP vaccination6, and SIDS and VAERS reports following Hepatitis B vaccination7 found no association between SIDS and vaccination. The FDA carefully investigates all deaths following vaccination that are reported to VAERS. Between 1990 and 1992 the FDA and the Institute of Medicine (IOM) reviewed 208 deaths reported to VAERS. Only one death was believed to have resulted from a vaccine: a 28-year-old woman who died from Guillain-Barre Syndrome (GBS) after tetanus vaccination. The IOM concluded that the vast majority of deaths reported to VAERS are coincidental and not causally related to vaccination. About the Author www.cdc.gov |
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