SEEG is a pre-eclampsia micro-assessment tool, which uses stereodirectional technology to incorporate intracircle electrodes, to record intracircle electro-electric activity and direct electrical stimulation to determine the epilepsy zone for patients with epilepsy, and has become more widespread in recent years at home and abroad.
SEEG is used mainly for pre-operative assessments of impregnable epilepsy that cannot be identified after an unsolved assessment but which is highly suspicious of the beginning of the facility ‘ s stove or of the potential stress and functioning of the area. The electrodes are more accurately placed within the skull through the penetration of the electrodes inside the auxiliary skull of the neurosurgery robot, which, while using SEEG to locate the eclampsia area, can be connected to the radio-frequency current thermal condensator, and the radio-frequency condensation damage (SEEG RF-TC) led by SEEG is cured or reduced.
The advantages are that it is not necessary to open a skull, to reduce the fear of a skull-opening operation, to reduce pain, to reduce the length of treatment, to improve the efficacy of treatment, to reduce the number of complications, to recover quickly after the surgery, to achieve a truly micro-creative treatment for difficult epilepsy, and to improve the quality of life of patients by better control of epilepsy.
SEEG into the adaptive certificate
Episcopal epilepsy, which is clearly identified as difficult to treat, has led to a working hypothesis of a reasonable network of origin and transmission of epilepsy through an ingenuity assessment.
2. The location of epilepsy symptoms, electrophysiological patterns and anatomical structures contradict the precise location of the area.
3. Eclample areas involve critical functional areas, requiring accurate positioning of the brain function area and precision determination of the extent of the surgical removal to avoid or minimize the potential for functional impairment.
The eclampsia area is limited or located in the depths and is placed in the SEEG electrodes for the purpose of radio-frequency digestion treatment.
These conditions must be 1 and 2 or 3 or 4 conditions must be met so as to avoid the introduction of “spreadnet” electrodes without a reasonable working assumption.
SEEG’s on a taboo.
1. Patients subject to the taboos of whole vasectomy.
2. Patients infected with skin, subcutaneous soft tissue or otherwise blocked by the implant.
3. Failure to complete the visual inspection required for registration (e.g. MR).
4. Patients with severe mental disorders, severe cognitive disorders and failure to comply with the test, which makes it difficult to ensure the safety of electrodes.
5. Local skull thickness & lt; 2.0 mm, patients who cannot securely steer screws.
6. The target areas are suspected blood-rich pathologies such as arrerovenous malformation, AVM etc.
