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Technical Details of the TMS Treatment Process for MDD

Transcranial Magnetic Stimulation (TMS) is a non-invasive brain stimulation technique that directly targets the neural circuits responsible for mood regulation in patients with Major Depressive Disorder (MDD). The science behind TMS involves applying rapidly changing magnetic fields to induce electrical currents in the brain. Below is a breakdown of the technical aspects of TMS, focusing on how devices like the Blossom TMS system operate and their role in clinical treatment.

1. The TMS Device and Components

TMS devices, like the Blossom TMS machine, are composed of several critical components that ensure safe, effective, and patient-friendly treatment.

  • Magnetic Coil: The primary component is the coil, which generates the magnetic fields that penetrate the scalp and skull. The Blossom TMS system uses a Figure-8 coil design, which is standard for precise targeting of specific brain regions, such as the left dorsolateral prefrontal cortex.
  • Cooling System: One of the key innovations in the Blossom TMS device is its liquid-cooled coil, designed to operate quietly and comfortably during long treatment sessions. Traditional TMS systems may overheat or become noisy during extended use, but the Blossom TMS coil remains cool, ensuring uninterrupted sessions and enhancing patient comfort.
  • Stimulation Control and Software: The TMS device includes sophisticated software that allows clinicians to program specific stimulation protocols, adjust the frequency of pulses, and track patient data. For example, the Blossom TMS machine offers pre-set FDA-cleared protocols for treating MDD and can be tailored to deliver different stimulation frequencies, such as 10 Hz, 20 Hz, or Theta Burst Stimulation (TBS) depending on patient needs.

2. Electromagnetic Pulse Generation and Delivery

  • Pulse Characteristics: TMS devices use electromagnetic induction to generate electrical activity in the brain. In technical terms, the coil creates a rapidly changing magnetic field, which, according to Faraday’s Law, induces an electric current in the neurons beneath the coil. These pulses can reach depths of 1.5-2.5 cm into the brain, targeting specific areas associated with depression.
  • Frequency and Duration: The frequency of the pulses is critical to the treatment outcome. For instance, high-frequency TMS (10 Hz or more) is generally used to stimulate underactive regions in MDD, while Theta Burst Stimulation (TBS), a more recent and rapid protocol, involves delivering short bursts of high-frequency stimulation over a shorter time span (e.g., 3-5 minutes compared to the typical 30-40 minutes for traditional protocols).
  • Magnetic Field Strength: The magnetic field generated by the coil in TMS is typically around 1.5 to 2 Tesla, which is roughly the same strength as an MRI machine. This field strength is sufficient to modulate brain activity without causing any permanent changes to the neurons.

3. Targeting Specific Brain Regions

  • Neuro-navigation: Advanced TMS systems can integrate neuronavigation tools to enhance precision. This allows the clinician to visualize the exact location in the brain where the magnetic pulses are being directed, ensuring that stimulation targets the dorsolateral prefrontal cortex, the region implicated in MDD.
  • Coil Placement: Correct placement of the coil is crucial for achieving therapeutic effects. The motor threshold (MT) mapping process ensures that the stimulation intensity is personalized for each patient based on their individual cortical excitability, reducing the risk of discomfort or ineffective treatment.

4. Safety Mechanisms

  • Risk Mitigation: The device also includes safeguards against risks like seizures, which, while rare, are a known potential side effect of repetitive TMS at high frequencies. Blossom TMS includes advanced algorithms to prevent excessive stimulation and ensure that treatment is delivered within the safe parameters defined by clinical guidelines.

5. Data and Treatment Tracking

  • Patient Data Management: Some TMS devices store critical patient data, including motor thresholds, treatment progress, and session logs, which are essential for monitoring long-term outcomes. More affordable devices are streamlined for simplicity and allow the clinic’s EHR to handle the patients data.
  • Customizable Protocols: Advanced systems like Blossom also allow for custom protocol designs, making it possible to experiment with new, research-backed approaches (within FDA guidelines) for treatment-resistant MDD. This flexibility is a significant advantage for clinicians looking to optimize therapy for individual patients.

6. Innovations and Future Directions

  • Quiet Coil Technology: The quiet coil design of the Blossom TMS system reduces the noise typically associated with TMS devices, making treatments more comfortable for patients. This innovation also improves the overall clinical experience, especially in environments where patients undergo frequent sessions.
  • Upcoming Technologies: Future innovations in TMS are likely to include further personalization of treatments, integration with neuroimaging for real-time feedback, and enhanced coil designs that allow for deeper brain stimulation without compromising patient safety or comfort.

Summary

TMS therapy for MDD is a highly technical process that relies on sophisticated devices like the Blossom TMS system to deliver safe and effective treatments. With features like liquid-cooled coils, advanced software for treatment customization, and quiet operation, the Blossom TMS system represents the cutting edge of brain stimulation technology. The precision and adaptability of TMS make it a powerful tool in treating MDD, offering hope to those who have not found relief through medication or other therapies.

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Email: Sales@sebersmedical.com

Address: 230 S Broad Street, 17th Floor Philadelphia, PA 19102

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Disclaimer:

Regulations in the United States

*United States Federal Law regulates the sale of Medical Devices. The Blossom TMS Therapy System is indicated for the treatment of Major Depressive Disorder in adult patients, who have failed to achieve satisfactory improvement from prior antidepressant medication in the current episode. (K220625) All other devices on this website are not approved and/or cleared for use in treatment and/or diagnosis in the United States. All investigational devices must be labeled in accordance with the labeling requirements of the IDE regulation (§ 812.5) and bear a label that states:
“CAUTION.
Investigational Device. Restricted by federal (or United States) law to research use.”