IONM in Cranial Surgery: Difference between revisions
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The following are stimulation parameters for the Penfield and Taniguchi techniques: | The following are stimulation parameters for the Penfield and Taniguchi techniques: | ||
Penfield | Penfield | ||
Stimulator type: Bipolar | Stimulator type: Bipolar | ||
Pulse type: Bi or Monophasic | Pulse type: Bi or Monophasic | ||
Frequency: 50 Hz | Frequency: 50 Hz | ||
Pulse width: 300-1000 microsec | Pulse width: 300-1000 microsec | ||
Intensity: 2-20 mA | Intensity: 2-20 mA | ||
Duration: 2-5 sec 20 microsec | Duration: 2-5 sec | ||
Taniguchi | |||
Stimulator type: Monopolar | |||
Pulse type: Monophasic Anodal | |||
Frequency: 250-500 Hz | |||
Pulse width: 500 microsec | |||
Intensity: 2-20 mA | |||
Duration: 20 microsec | |||
==Skull base or CP angle tumors== | ==Skull base or CP angle tumors== |
Revision as of 19:18, 18 August 2021
Introduction
Cortical mapping
The resection of tumors located within or near the eloquent cortex can result in postoperative sensory, motor and language deficits. Cortical brain mapping techniques have been used for many years to help the neurosurgeon identify and avoid these important brain structures. For tumors that impact the primary motor cortex, the main concern includes loss of motor functions in the contralateral face and upper and lower extremities. Two techniques have been developed for intraoperative cortical and subcortical mapping of the corticospinal tracts - the Penfield and Taniguchi techniques. Direct stimulation of the motor cortex along the homunculus can elicit compound muscle action potentials that are recorded by electrodes placed on corresponding muscle groups.
The following are stimulation parameters for the Penfield and Taniguchi techniques:
Penfield
Stimulator type: Bipolar Pulse type: Bi or Monophasic Frequency: 50 Hz Pulse width: 300-1000 microsec Intensity: 2-20 mA Duration: 2-5 sec
Taniguchi
Stimulator type: Monopolar Pulse type: Monophasic Anodal Frequency: 250-500 Hz Pulse width: 500 microsec Intensity: 2-20 mA Duration: 20 microsec
Skull base or CP angle tumors
Deep brain stimulation
Intracranial vascular procedures
Neurovascular information
The brain is very sensitive to changes in blood flow. Cerebral blood flow is maintained and regulated by a homeostatic process called autoregulation. Cerebral blood flow is maintained at approximately 40-70 ml per minute for every 100 g of brain tissue, which occurs over a wide range of arterial blood pressures (~60 - 160 mm Hg) in a healthy brain. To maintain constant cerebral blood flow, several homeostatic mechanisms converge to maintain a balance between vasoconstriction and vasodilation, which includes myogenic, neurogenic, metabolic, and endothelial components (Armstead, Anesthesiol Clin. 2016; 34(3): 465–477).
Cranial nerve monitoring
The cranial nerves are monitored with for a variety of surgical procedures. The modalities that are monitored typically include spontaneous and triggered EMG recordings and motor evoked potentials.
1. The recurrent laryngeal nerve, a branch of the vagus nerve (CN X), is monitored for thyroidectomies. The recurrent laryngeal nerve, one of approximately 11 branches of CN X, innervates the intrinsic muscles of the larynx. This nerve is monitored using an endotracheal tube that is lined with recording electrodes.
2. The facial nerve (CN VII) is monitored for parotidectomies, tympanoplasties, mastoidectomies, microvascular decompressions, etc. Major branches of CN VII include the temporal, zygomatic, buccal, marginal mandibular, and cervical. The temporal branch innervates the frontalis, orbicularis oculi and corrugator supercilii muscles. The zygomatic branch innervates the orbicularis oculi muscle. The buccal branch innervates the orbicularis oris, buccinator and zygomaticus muscles. The marginal mandibular branch innervates the mentalis muscle. The cervical branch innervates the platysma, a sheet of muscle fibers extending from the collarbone to the jaw. Pairs of recording electrodes are typically placed at the muscles of each branch.
3. The glossopharyngeal (CN IX) can be monitored for microvascular decompressions and acoustic neuroma resections. For acoustic neuroma resections, multiple cranial nerves could be at risk of injury depending on the size of the tumor, including the vestibulocochlear (CN VIII), facial (CN VII) nerve, vagus nerve (CN X), hypoglossal nerve (CN XII), and accessory nerve (CN XI).