NeuroStar® TMS Therapy
FDA-cleared, non-medication depression treatment
(855) 940-4867
Do you often lose track of where you left your keys or your phone? Do you find it difficult to recall what you've just read? Do you occasionally forget to take your medications?
If you have depression and memory loss symptoms, these issues might sound familiar to you. So, how can depression cause memory loss and what can we do about it? The answers lie within the connections and chemistry of our brains.
Persistent stress increases the brain's levels of the hormone cortisol, which, in turn, decreases the level of a chemical messenger called
BDNF . This impairs the growth of nerve cells within the hippocampus of the brain.
We rely on the hippocampus for almost everything related to memory, including memory encoding (getting the information into our memory systems), storage, and retrieval. That is why shrinkage in the hippocampus can result in forgetfulness.
If you have depression and memory loss symptoms, you may have noticed problems with both your short-term memory and long-term memory. Occasionally forgetting where you put your phone or whether you turned off a light may not be a big deal, but losing track of where you are in a major work project or finding that you have only vague memories of a vacation you took a few years ago can have a real impact on your ability to accomplish and enjoy important life activities.
Depression also affects the frontal lobe—the part of the brain behind the forehead.
Studies of thousands of people with depression have found significantly reduced volume in this region.
The frontal lobe of the brain helps us to pay attention, so if you have depression, you may find that you're easily distracted. Perhaps you cannot concentrate fully during conversations with colleagues. You lose focus while reading a book, or you find it difficult to follow the plot of a TV show. Your friends, family, or co-workers might have even pointed these changes out to you.
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The attention issues associated with frontal lobe shrinkage in depression can exacerbate the memory difficulties caused by a smaller hippocampus.
So depression can, in fact, cause memory loss. But fortunately, depression treatments can help reverse these brain changes.
Professor Ian Hickie, lead researcher of the world's biggest depression study on brain volume, has
explained that "the hippocampus is unique in its ability to rapidly generate new connections between cells, and what are lost here [in depression] are connections between cells rather than the cells themselves." That means depression treatments can potentially stimulate the growth of
new nerve cells and strengthen novel connections between them. Given that repeated episodes of depression increase the risk to the brain, Hickie and other researchers recommend seeking treatment early.
Transcranial Magnetic Stimulation (TMS) is a non-drug, non-invasive treatment option that helps to form new connections between nerve cells in the
hippocampus and other brain regions affected by depression. It specifically
increases levels of BDNF throughout the brain, thereby stimulating nerve cell growth. Patients whose depression improves with TMS treatment show
improved performance on cognitive tests of verbal and visual memory, attention, and processing speed.
TMS is FDA-cleared and covered by most insurance when at least two antidepressant medications haven't been effective.
When undergoing treatment for depression, it can be reassuring to know you'll also be proactively addressing other brain changes that accompany the condition. Treatment that boosts your mood can also boost your memory, empowering you to live your best life and cherish the memories you make along the way.
Take our short quiz to see if TMS therapy or nasal esketamine could be right for you
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NeuroStar Adult Indications for Use
The NeuroStar Advanced Therapy System is indicated for the treatment of depressive episodes and for decreasing anxiety symptoms for those who may exhibit comorbid anxiety symptoms in adult patients suffering from Major Depressive Disorder (MDD) and who failed to achieve satisfactory improvement from previous antidepressant medication treatment in the current episode.
The NeuroStar Advanced Therapy System is intended to be used as an adjunct for the treatment of adult patients suffering from Obsessive-Compulsive Disorder (OCD).
NeuroStar Adolescent Indications for Use
NeuroStar Advanced Therapy is indicated as an adjunct for the treatment of Major Depressive Disorder (MDD) in adolescent patients (15-21).
Important Safety Information
NeuroStar Advanced Therapy is only available by prescription. A doctor can help decide if NeuroStar Advanced Therapy is right for you. Patients’ results may vary.
The most common side effect is pain or discomfort at or near the treatment site. These events are transient; they occur during the TMS treatment course and do not occur for most patients after the first week of treatment. There is a rare risk of seizure associated with the use of TMS therapy (<0.1% per patient).
Visit neurostar.com for full safety and prescribing information.
Important Safety Information
What is the most important information I should know about SPRAVATO®?
SPRAVATO® can cause serious side effects, including:
Do not take SPRAVATO® if you:
If you are not sure if you have any of the above conditions, talk to your healthcare provider before taking SPRAVATO®.
Before you take SPRAVATO®, tell your healthcare provider about all of your medical conditions, including if you:
Tell your healthcare provider about all the medicines that you take, including prescription and over-the-counter medicines, vitamins and herbal supplements. Taking SPRAVATO® with certain medicine may cause side effects.
Especially tell your healthcare provider if you take central nervous system (CNS) depressants, psychostimulants, or monoamine oxidase inhibitors (MAOIs) medicine. Keep a list of them to show to your healthcare provider and pharmacist when you get a new medicine.
How will I take SPRAVATO®?
What should I avoid while taking SPRAVATO®?
Do not drive, operate machinery, or do anything where you need to be completely alert after taking SPRAVATO®. Do not take part in these activities until the next day following a restful sleep. See “What is the most important information I should know about SPRAVATO®?”
What are the possible side effects of SPRAVATO®?
SPRAVATO® may cause serious side effects including:
See “What is the most important information I should know about SPRAVATO®?”
Increased blood pressure. SPRAVATO® can cause a temporary increase in your blood pressure that may last for about 4 hours after taking a dose. Your healthcare provider will check your blood pressure before taking SPRAVATO® and for at least 2 hours after you take SPRAVATO®. Tell your healthcare provider right away if you get chest pain, shortness of breath, sudden severe headache, change in vision, or seizures after taking SPRAVATO®.
Problems with thinking clearly. Tell your healthcare provider if you have problems thinking or remembering.
Bladder problems. Tell your healthcare provider if you develop trouble urinating, such as a frequent or urgent need to urinate, pain when urinating, or urinating frequently at night.
The most common side effects of SPRAVATO® include:
If these common side effects occur, they usually happen right after taking SPRAVATO® and go away the same day.
These are not all the possible side effects of SPRAVATO®.
Call your doctor for medical advice about side effects. You may report side effects to Johnson & Johnson at 1-800-526-7736, or to the FDA at 1-800-FDA-1088.
What is SPRAVATO® (esketamine) CIII nasal spray?
SPRAVATO® is a prescription medicine used:
SPRAVATO® is not for use as a medicine to prevent or relieve pain (anesthetic). It is not known if SPRAVATO® is safe or effective as an anesthetic medicine.
It is not known if SPRAVATO® is safe and effective for use in preventing suicide or in reducing suicidal thoughts or actions. SPRAVATO® is not for use in place of hospitalization if your healthcare provider determines that hospitalization is needed, even if improvement is experienced after the first dose of SPRAVATO®.
It is not known if SPRAVATO® is safe and effective in children.
Please see full Prescribing Information, including Boxed WARNINGS, and Medication Guide for SPRAVATO® and discuss any questions you may have with your healthcare provider.
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