NOTE BY Ann Blake-Tracy (www.drugawareness.org):
Paragraphs seven and eight read: “The researchers treated 72 people suffering from major
depressive disorder (MDD) with one of two SSRIs, fluoxetine or venlafaxine, or with a placebo. All were evaluated by a clinician using the Hamilton Depression Rating Scale, a standard instrument that assesses the severity of a wide range of depression symptoms. Of the 37 participants on medication,five (13.5 percent) had worsening thoughts of suicide.” “All of the participants were also examined using QEEG, which evaluates brain function based on thebrain‘s electrical activity. Among the 13.5 percent of participants who got worse, the researchersfound a sharp drop in brain activity within 48 hours of the start of medication. The dropoccurred in the midline and right-frontal sections of the brain, areas known to control emotions.”SSRI Stories note: In regard to placebo & suicidality, it should be remembered that the majority of placebo patients are ‘wash-out’ patients from other antidepressants and thus are actually inantidepressant withdrawal which can be extremely dangerous.
http://www.physorg.com/news189972383.htmlSimple test can detect signs of suicidal thoughts in people taking antidepressants
(PhysOrg.com) — UCLA researchers have developed a non-invasive biomarker that may serve as a type of early warning system for doctors and patients.
While antidepressant medications have proven to be beneficial in helping people overcome majordepression, it has long been known that a small subset of individuals taking these drugs can actually experience a worsening of mood, and even thoughts of suicide. No clinical test currently exists to make this determination, and only time usually weeks can tell before a psychiatrist knows whether a patient is getting better or worse.
Now, UCLA researchers have developed a non-invasive biomarker, or indicator, that may serve as a type of early warning system.
Reporting in the April edition of the peer-reviewed journal Acta Psychiatrica Scandinavica, Aimee Hunter, an assistant research psychologist in the UCLA Department of Psychiatry, and colleagues report that by using quantitative electroencephalographic (QEEG), a non-invasive measurement of electrical activity in the brain, they were able to observe a sharp reduction of activity in a specific brainregion in individuals who proved susceptible to thoughts of suicide within 48 hours of the start of treatment.
Prior research, Hunter said, has shown that between 8 and 14 percent of depressed patients develop thoughts of suicide while taking the most common forms of depression drugs, known as selective serotonin reuptake inhibitors (SSRI). Although reports have suggested that SSRIs are to blame, no firm link between these drugs and thoughts of suicide has been established.
This study suggests, for the first time, a link between worsening suicidality and specific changes inbrain function while on these medications.
The researchers treated 72 people suffering from major depressive disorder (MDD) with one of twoSSRIs, fluoxetine or venlafaxine, or with a placebo. All were evaluated by a clinician using the Hamilton Depression Rating Scale, a standard instrument that assesses the severity of a wide range of depression symptoms. Of the 37 participants on medication, five (13.5 percent) had worseningthoughts of suicide.
All of the participants were also examined using QEEG, which evaluates brain function based on thebrain‘s electrical activity. Among the 13.5 percent of participants who got worse, the researchers found a sharp drop in brain activity within 48 hours of the start of medication. The drop occurred in the midline and right-frontal sections of the brain, areas known to control emotions.
Of note, eight of the 35 participants taking a placebo (22.9 percent) also had increased thoughts of suicide. However, the placebo participants did not show the precipitous drop in brain activity within the first 48 hours.
“This is the first study to show a change in brain function after the start of medication that appears to be linked to the subsequent development of worsening thoughts of suicide during antidepressant treatment,” Hunter said. “Importantly, changes in this biomarker did not predict worsening suicidal thoughts in the placebo-treated subjects, so the results suggest that the biomarker specifically detected medication-related worsening only.”
QEEG is a relatively inexpensive instrument that is non-invasive; measurements are obtained by placing electrodes on the scalp. As a result, Hunter said, further development of this biomarker could potentially lead to a tool that could be used by clinicians to predict, in the early stages of treatment, whether an individual suffering from depression will develop thoughts of suicide.
Provided by University of California Los Angeles
atracyphd,
My daughter ClaireD’Angelo now 39 years of age has been a patient of a leading Psychiatrist Dr Dennis Tannenbaum and prescribed many drugs over the past 12 years.
She is now experiencing Thyroid and pituatary problems and whilst her medications have been constantly changed her depression and anxiety remains aand her general health is suffering.
What alternative to a psychiatrist , neuorologist, is open to us in Australia in order to prevent her continuing with these problems for the rest of her life.
Is their any branch of your organization in Australia or persons you can recommend with whom we can approach.
Yours sincerely,
Peter G Reynolds
Health science research
peterh@radecinternational.com
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