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Family to
Receive Compensation in Unique Case
Court rules that child’s
Underlying Disorder was exacerbated Following
Vaccination
March • 2008
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A previously healthy
19-month-old child received five vaccines (MMR,
varicella, IPV, DTaP, and Haemophilus influenzae) in
2000 because she was behind in the recommended childhood
immunization schedule. She subsequently developed
neurodegeneration including some signs of mild autism
spectrum disorder. A muscle biopsy and genetic testing
revealed that she had a preexisting mitochondrial
dysfunction disorder. The US Court of Federal Claims has
agreed to pay the family from a federal fund that
compensates people injured by vaccines.
The decision to compensate the family is summarized in
the following quote from the
Division of Vaccine Injury Compensation (DVIC), "[We
have] concluded that the facts of this case meet the
statutory criteria for demonstrating that the
vaccinations child received on July 19, 2000,
significantly aggravated an underlying mitochondrial
disorder, which predisposed her to deficits in cellular
energy metabolism, and manifested as a regressive
encephalopathy with features of autism spectrum
disorder."
The full text of the
decision by the US Court of Federal Claims has been
posted (link)
although the formal decision has not yet been announced
by the Vaccine Injury Compensation Program. More
information will be made available in May when this
report is scheduled to be made public. In the meantime,
federal officials are prohibited from making public
statements about a specific case in order to protect the
confidentiality of medical records.
Encephalopathy has been shown to occur at an increased
rate following whole cell DTP vaccine. That vaccine has
been replaced by the acellular pertussis vaccine (DTaP),
but rare cases of encephalopathy still occur. The
detailed investigation of this child that identifyed the
underlying mitochondrial dysfunction disorder may
provide an important clue to understanding why these
rare complications occur. Moreover, future
investigations might help identify a means to screen for
such disorders, although because there are many
different mitochondrial dysfunction disorders and
testing is invasive and expensive, screening is
difficult.
Other children with encephalopathy following vaccines
have been compensated through the Vaccine Injury
Compensation Program. What attracted public attention to
this case was that it had been submitted as a test case
by petitioners seeking compensation for children with
autism following exposure to thimerosal containing
vaccines. The decision to award compensation in this
case has nothing to do with the thimerosal that may have
been present in one or two of the vaccines that the
child received (in 2000, only two of the five vaccines
this child received would have contained thimerosal; the
others were already thimerosal free). The underlying
mitochondrial dysfunction disorder in this case
predisposes to neurodegeneration following significant
stresses associated with infections, and possibly the
multiple vaccines that this girl received. After the
decision was made to award compensation, the case was
withdrawn as a test case.
Additional research is needed to determine if other
children with autism, especially those with “the
regressive form” of autism have the same or similar
underlying mitochondrial dysfunction disorders.
The advisory groups who make recommendations regarding
vaccines will undoubtedly examine this case carefully
and make decisions regarding the potential need for
changes in recommendations for administering multiple
vaccines to children who have fallen behind in the
recommended childhood immunization schedule.
For more information:
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This page
was last updated on
March 10, 2008 |
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