NEW YORK – Now that all antidepressants carry a black box warning regarding pediatric suicidality, physicians who treat children and adolescents with depression need to institute closer monitoring and pay careful attention to informed consent, Bruce Waslick, M.D., said at a psychopharmacology update sponsored by the American Academy of Child and Adolescent Psychiatry.
In response to analyses identifying an increased risk of suicide during the early weeks of antidepressant treatment, the Food and Drug Administration recommends that children and adolescents be actively monitored for worsening of depression, response to treatment, and emergence of suicidality.
“I am not trying to dissuade you from using antidepressants,” said Dr. Waslick of the division of child psychiatry at Columbia University, New York.
The importance of pharmacotherapy was highlighted by findings from the Treatment for Adolescents With Depression Study (TADS), which showed that cognitive-behavioral therapy plus fluoxetine was superior to either modality alone. (See box.) “You will need to make a risk-benefit calculation and try to give patients and parents some understanding about the safety concerns. Try to give them a rational view of the available evidence and take their preferences into account,” Dr. Waslick said. “Based on my experience with TADS and from an objective reading of the literature, I do think antidepressants have a role in the treatment of kids with depression.”
The FDA's black box decision followed a year of controversy and media attention that left fluoxetine the sole antidepressant with a pediatric indication for major depressive disorders. That decision, in turn, has left clinicians without clear guidance on several issues, such as what to do if an adequate trial of fluoxetine proved to be unsuccessful.
There also are no clear guidelines on medicolegal issues and physician liability, but closer monitoring during the initial phase of treatment is key. According to the FDA, patients should be seen weekly for the first 4 weeks, biweekly for the next 4 weeks, and then monthly or as clinical need dictates. Informed consent is very important. “I don't know if it will protect you regarding liability issues, but I think it's the right thing to do,” he said.
Besides the black box warning, the FDA plans to send letters to parents. “I've seen a draft of the letter, and it emphasizes the risks and doesn't talk too much about the benefits,” Dr. Waslick said. “This is black box plus.”
After the initial reports of potential suicidality associated with paroxetine (Paxil), the FDA requested that all manufacturers of selective serotonin reuptake inhibitors and atypical antidepressants go through their data in an effort to find suicide-related events in both active treatment and placebo patients.
Companies were asked to prepare vignettes about these events, detailing the circumstances and outcome, so that FDA officials might determine whether they were indeed drug related and see whether there was some way of assessing risk.
The initial analysis of these data, done by chief FDA scientist Andrew Mosholder, M.D., found 109 “possibly suicide-related” events in 4,100 subjects. Twice as many events were reported in patients taking the active drug than in those taking placebo.
In February 2004, a public hearing was held on antidepressant safety but Dr. Mosholder was not permitted to present his data. When word of the FDA's action was leaked to the media, a firestorm resulted, with charges that dangers were being suppressed, leading to congressional investigations. The FDA's position was that the initial analysis was unreliable and that investigations were ongoing. In an attempt to have the data analyzed in a blinded fashion, FDA officials contracted with a group of independent suicide experts from Columbia University to undertake a more definitive analysis.
The Columbia University panel analyzed the suicide events in two ways: when reported as an adverse event/serious adverse event, and according to scores on suicide items on depression questionnaires. The panel concluded that there was what Dr. Waslick called a “low-magnitude, low-frequency suicide [ideation or behavior] signal” in the adverse events/serious adverse events data set.
However, evaluation of the systematically collected rating scale scores found no evidence of a suicide signal, Dr. Waslick said. Despite that discrepancy, the FDA concluded that no antidepressant is completely risk free and determined that all the drugs–even the older tricyclics and MAO inhibitors–would carry the black box warning.
Dr. Waslick said he has been prescribing these drugs for 15 years and always assumed any suicidality was a result of the underlying disease. “But the FDA has concluded that this adverse event signal is evidence that a relationship exists between antidepressant treatment and emergent suicidality.”