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A Word from DBSA's Scientific Advisory
Board (SAB) Chair
All 65 of our SAB
members and their colleagues are constantly in search of new ways to
recognize, treat and prevent mood disorders. Not all of our work will
produce groundbreaking new treatments. Sometimes it will give us new
knowledge about brain chemistry or allow us to rule out a treatment that
doesn’t work. As we move toward new and meaningful discoveries, we
must also make sure that people are educated about mood disorders. We
must do everything in our power to reduce stigma. Greater acceptance of
mood disorders can lead to increased research funding, and appropriate
insurance coverage. It can also motivate more patients and families to
seek help sooner.
The effect of
antidepressant medications on young people has been in the news often in
recent weeks. We know that mood disorders can lead to suicide. This is
especially tragic when it happens to a child, but this tragedy can no
more be traced to one cause than it can be solved with one answer.
One thing is certain:
children with mood disorders need treatments that will help them to lead
stable, healthy lives. Their parents and health care providers need as
many options as possible. They need the information necessary to make
informed, educated choices.
Many people became
concerned late in 2003, when the British Regulatory Agency recommended
against the use of selective serotonin reuptake inhibitor (SSRI)
antidepressants in patients under the age of 18. In response to this
ruling, the American College of Neuropsychopharmacology (ACNP) formed a
task force to examine this issue. In a review of all available data from
published clinical trials conducted in young people, the ACNP task force
failed to find any statistically significant increase in suicide
attempts, self-harm or suicidal thinking related to SSRI treatment. They
also pointed out that in the relatively few years since prescribing of
these medications has become widespread, there has been an unprecedented
decline – averaging 33% – in rates of youth suicide in 15 countries.
However, in a public
meeting held on February 2, the Food and Drug Administration (FDA) noted
that only a few of the trials of SSRI’s in youth showed clear
superiority to placebo. Many trials showed no difference. The FDA also
examined a large database of unpublished trials, which suggested that
there may be an increased rate of suicidality in young people taking
these SSRIs. This led the FDA’s Psychopharmacologic Drugs Advisory
Panel to recommend stronger warnings about the use of SSRI’s in youth.
In the meantime, they are analyzing the unpublished data more closely.
The decision to take
SSRIs, or any other type of treatment, is one that must be made
individually by each patient and his or her family and health care
providers. It is important that every individual have as many safe,
effective choices as possible. It is also essential that patients,
family members and health care providers have sufficient information to
be able to weigh the potential benefits against any possible risks.
Even today’s reduced
incidence of suicide and self-harm in young people is clear evidence of
critical unmet needs. Our children need more specialized health care
providers. Primary care providers, as well as educational, juvenile
justice and foster care systems should have knowledge of mood disorders
and treatments. Everyone concerned with the welfare of our children must
make special efforts to meet these needs.
Children deserve
wellness as much, if not more than adults do. The fact that this
wellness is often even more difficult to reach than it is for adults
means that it is even more important that we remain steadfast and
dedicated to maximizing every child’s chance to achieve it.
Ellen Frank,
DBSA's Scientific Advisory Board Chair
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