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A marked fall in antidepressant
use occurs when women first learn that they are pregnant,
according to a report.
"It is alarming to see that there is still a fear regarding
antidepressant use during pregnancy. We knew that some women
were going to discontinue using their antidepressants during
pregnancy but we didn't think it would be so prevalent and
inappropriately used (amongst those who remain on it)," senior
author Dr. Anick Berard told Reuters Health.
"The risks of untreated depression during pregnancy are
significant," Berard, from the CHU Sainte-Justine Hospital in
Montreal, said. "Given the safety of most antidepressants
during pregnancy, a careful evaluation of the risk/benefit
ratio should be done before deciding to discontinue their use.
Although physicians and women think they are protecting their
unborn child, they might be doing just the contrary."
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People who feel chronically
stressed on the job may face an increased risk of depression, a
large study suggests.
Researchers found that among more than 24,000 working
Canadian adults, nearly 5 percent had suffered from major
depression in the past year. Those under heavy stress at work
appeared to be at particular risk, according to findings in the
American Journal of Public Health.
A number of studies have found health risks associated with
chronic job stress, including high blood pressure and heart
disease, as well as depression. However, the depression studies
have been limited to either certain occupations or single
companies, noted Dr. Emma Robertson Blackmore, the lead author
of the new study and an assistant professor of psychiatry at
the University of Rochester Medical School in New York.
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Among patients who have had a
heart attack and subsequently develop depression, a lack of
response to antidepressant treatment signals a high risk of
another cardiac episode, according to a secondary analysis of
data from Myocardial Infarction and Depression-Intervention
Trial (MIND-IT).
MIND-IT involved 2,177 patients who were hospitalized with
an acute heart attack. During follow-up, 375 patients developed
post-heart attack depression. Two hundred nine of these
patients were randomly assigned to receive mirtazapine, sold
under the trade name Remeron, or to "care as usual."
If there was an inadequate response to mirtazapine after 8
weeks, the patients were switched to citalopram, sold under the
trade name Celexa, according to the report in the American
Journal of Psychiatry.
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Eli Lilly yesterday added strong warnings to the label of Zyprexa, its best-selling medicine for schizophrenia, citing the drug’s tendency to cause weight gain, high blood sugar, high cholesterol and other metabolic problems.
For
the first time, Zyprexa’s label now acknowledges that the drug causes
high blood sugar more than some other medicines for schizophrenia and bipolar disorder, called atypical antipsychotics.
Lilly previously argued that Zyprexa had not been proved to cause high blood sugar at a more frequent rate than its competitors.
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A perplexing finding about suicide rates:
As many know, the
CDC has reported that the suicide rates have jumped since 2004,
especially in young people, and especially in girls aged 10-14. While
this is noteworthy in itself, it is also near the time when the first
black box warnings concerning the link between antidepressants and
suicide came out.
The controversy about antidepressants and suicide has a long history, but it can be summarized with a few key points:
First, even in the early psychoanalytic days, experts observed that
people often attempted suicide as they began to improve from
depression. Consider that suicide attempts are often highest
immediately following discharge from a hospital. The explanation was
that their motivation, or cognition, improved before their sadness; so
while at first they were too depressed to do anything-- including
suicide, as they began to improve they got well enough to plan and
execute a suicide.
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