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Fetal Alcohol Spectrum Disorders (FASD) are conditions that impact the lives of
thousands of children each year. These disorders are completely preventable, but once obtained
have lifelong implications for the children who suffer from them.
There are multiple disorders within FASD, the most severe being Fetal Alcohol
Syndrome (FAS). FAS includes abnormal facial features, growth problems, central nervous
problems, and can be confirmed by having the knowledge of alcohol consumption by the mother,
although this is not always necessary. FASD includes a group of conditions that can range from
mild to severe. These conditions can have a devastating impact on individuals physical,
behavior, and/or educational outcomes.
The Center for disease Control and Prevention, reports that approximately two out of
every 1,000 births is effected by Fetal Alcohol Syndrome (FAS) (Data, 2014). FASD has been
reported as high as 50 in every 1,000 births, making it more common than Autism. FASD is a
leading cause of preventable intellectual diseases affecting our children today (about FASD,
2014).
Taking care of children with a FASD requires a lifetime of medical intervention. These
medical costs add up to nine times that of a child without a FASD. The American government is
estimated to spend more than $6 billion annually on caring for those with a FASD (about FASD,
2014). A major deficit area, that requires costly treatment in children with FASD, is that of
Executive function.
frequently met to discuss methods being used during therapy times to ensure reliability of the
results.
This study was based on an isolated population group within the FAS community. Due
to none of the participants living with their biological parents the external validity of this
intervention is impacted. From this study it would not be fair to say that this intervention would
be effective for all FAS affected clients.
Sampling
The participants in this study ranged in age from six years to 11 year, 11 months. These
participants were all placed in out of home placements due to prenatal substance abuse or
continual substance abuse in the home. The children were tested to confirm FAS or Alcohol
Related Neurodevelopmental Disorder (ARND). From those confirmed 90 were invited to
participate and 78 families consented to participate in the study. Before placing the children in
groups each child was given a base-line research evaluation. After this, participants were
randomly placed in treatment and non-treatment control groups using simple random assignment.
Forty children were placed in the treatment group and 38 were placed in the control group. The
benefits to this form of selection is that the study has a high internal validity rate. One
disadvantage is that one group does not receive treatment, which may pose some ethical concern.
The research question posed is If children with reduced executive functioning (EF) due
to Fetal Alcohol Syndrome are treated with cognitive behavioral therapy will they have improved
EF and other outcomes? While this study addresses EF through cognitive behavior therapy it
leaves out a large portion of the FAS population. This omission lessens the external validity of
this research.
Measurement
Wells, Chasnoff, Schmidt, Telford & Schwartz focused on children diagnosed with FAS
or ARND living in foster or adoptive homes. Each childs health history was reviewed. Any
children with serious head injuries, lead poisoning or dysmorphic syndrome unrelated to FAS
were excluded from the study. All other participants were tested and given a diagnosis of FAS or
ARND. This diagnosis was based on three criteria: growth retardation, facial dysmorphology,
and central nervous system abnormalities. The testing began with a digital facial photographs to
assist in gaining accurate facial measurements. Following this all children were given a
neuropsychological evaluation to determine central nervous system function. Those with delays
in all three categories were diagnosed with FAS while the participants with confirmed alcohol
exposure without facial dysmorphology were diagnosed with ARND.
This study included parental involvement, therefore if the variables included children still
living with their biological family the outcomes may have changed. Parents who give birth to
FAS/ARND children may not be willing, or may not be capable of following through with the
new skills learned, and may have caused a marked decrease in the success of this treatment. In
addition to this, if the clients that had other closed head injuries, lead poisoning or facial
dysmorphology unrelated to FAS were included in the study the validity of the study may have
been compromised. Researchers may not have been able to determine what was causing
improvements or delays within this group.
Data Collection
Multiple baseline tests including, Behavior Rating Inventory of Executive Function
(BREIF), Roberts Apperception Test for Children (RATC), and the Wechsler Intelligence Scale
for Children-Third Edition (WISC-III) were given at the beginning and then repeated after 7
months. The BRIEF is an assessment that the primary care giver fills out regarding the executive
function behaviors at home and at school. The RATC is a test given to children measuring their
perception of common interpersonal situations. Finally the WISC-III was used to determine the
IQ of each child. The baseline data was then compared to the post data to determine the
effectiveness of neurocognitive habilitation therapy.
Overall the data collection methods were effective. Some areas of improvment existed.
Input from caregivers, as well as the children were taken. The BREIF was being used to
determine function at home and at school yet there was no mention of gaining any input from
school personnel. Also, there is the possibility of parental input not being accurate making it
important to have other sources complete this type of questionnaire to obtain accurate results.
Parents are also receiving training on how to parent FAS children, yet there is no measure of
their parenting skills. Without looking at their skills, while at the same time relying on their
answers regarding their children, it is hard to determine if the parents perspective is changing or
the child is changing. These areas may need to be addressed to improve the accuracy of future
studies.
If these adjustments were made in data collection it may give a more accurate picture of
the children receiving treatment. It is possible that the education provided to the parents
allowed them to view their children in a new way. This perspective change may have impacted
how they answered the questions on the follow-up assessment, thus improving their scores
without behavior change.
traumatic brain injury. Wells, Chasnoff, Schmidt, Telford & Schwartz reported that children
in the intervention group demonstrated significant improvements in executive and emotional
functioning when compared with the control group (2012). Neurocognitive habilitation therapy
looks like a promising treatment for FAS/ARND sufferers in the future.
In order to implement this type of intervention it would be necessary to have several
professionals that function at a masters and doctorate level. To perform all of the interventions
therapists, physical therapists, and psychologists would be needed. It would be important to
have these professionals in order to effectively implement the intervention as well as measure the
success for each client.
Neurocognitive habilitation therapy is a new type of intervention for the FAS/ARND
population, therefore obtaining proper training at this time would be difficult. Without proper
training achieving competence may create ethical issues.
Conclusion
FAS/ARND children face a life long struggle of functioning at what society deems a
normal level. Their social, academic, and cognitive skills are lacking. This is a social issue that
needs to be give more focus. Neurocognitive habilitation therapy is showing signs of being a
viable treatment option in the future, but more research is needed. This populations disabilities
were not created by their own choices or by genetic disorders, but are instead completely
preventable. Our society needs to create a plan to surround these children and adults with the
support they need to live a meaningful life.
References
About FASD. (2014, May 30). FASD Center for Excellence. Retrieved June 4, 2014, from
http://fasdcenter.samhsa.gov/aboutUs/aboutFASD
Data & Statistics. (2014, May 23). Centers for Disease Control and Prevention. Retrieved June
5, 2014, from http://www.cdc.gov/ncbddd/fasd/data.html
Rasmussen, C. (2005). Executive Functioning and Working Memory in Fetal Alcohol Spectrum
Disorder. Alcoholism: Clinical And Experimental Research, 29(8), 1359-1367.
doi:10.1097/01.alc.0000175040.91007.d0
Richardson, R. (2009). Psychological & Educational Insight: A Closer Look At Fetal
Alcohol Spectrum Disorders And Executive Functioning. Exceptional Mental Health Provider
training manual. richardsonsconsulting.com/resource_center_art.html
Wells, A. M., Chasnoff, I. J., Schmidt, C. A., Telford, E., & Schwartz, L. D. (2012).
Neurocognitive habilitation therapy for children with fetal alcohol spectrum disorders: An
adaptation of the Alert Program. American Journal Of Occupational Therapy, 66(1),
24-34. doi:10.5014/ajot.2012.002691