Electrophysiology

Retinitis PigmentosaElectrophysiology is used to diagnose and follow progression of disorders affecting vision similar to the manner electrocardiograms (ECGs) are used to monitor heart disease. The retina of the eye, optic pathways in the brain and visual cortex, create electrical signals that can be recorded directly from the eye or extracted by computer from brain electrical signals recorded from the scalp, similar to recording electroencephalograms (EEG).

Moran Eye Center electrophysiologists are leaders in the field. We are actively involved in research to improve electrophysiological testing. Dr. Donnell Creel was the first expert to teach electrophysiology in much of China and Nepal. In the video below, Dr. Creel demonstrates how to perform multifocal ERGs, with Mandarin Chinese subtitles.

Watch our video about Multifocal ERGs

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Services

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  • Electroretinograms
  • Multifocal Electroretinograms
  • Visually Evoked Potentials
  • Multifocal Visually Evoked Potentials
  • Electro-Oculograms
  • Auditory Brainstem Responses
  • Goldmann-Weekers Dark Adaptometry
  • Saccadic Velocities

Watch our video about Multifocal ERGs

Electroretinograms

The electroretinogram (ERG) is an electrical response of the retina to photic stimulation. The ERG is similar to an electrocardiogram in that it reflects the electrical health of the retina, similar to the ECG reflecting the health of the heart muscles. The eye does not “beat” so the retina must be stimulated to initiate its electrical response.

A flash of light or bright appearance of a pattern elicits a biphasic negative/positive waveform. Chemical changes in the retina start in 18 nanoseconds. The a-wave is the initial electrochemical discharge of the rods (night receptors) and cones (day and color receptors) and is fully formed in 10-15 milliseconds. The b-wave is generated by the mid-retina where editing begins before electrochemical signals are sent into the brain via the optic nerves. There are several methods used to record ERGs depending on whether one is most interested in the global health of the retina or whether one wishes to map the retina using multifocal patterns to determine areas producing blind spots.

Multifocal electroretinograms are used to map the retina detecting blind spots and are usually best to detect drug toxicity. Abbreviated recording methods are used with infants and in the operating room as part of exams under anesthesia. None of these procedures are painful. The eye is numbed with drops, so contact lenses are not uncomfortable.


Visually Evoked Potentials

The terms visually evoked response (VER) and visually evoked potential (VEP) are synonymous. They refer to electrical potentials recorded from scalp overlying visual cortex at the back of the head, which are extracted from the electroencephalogram (EEG) by signal averaging performed by computer. The most common stimuli are checkerboard patterns displayed on a television monitor or flashes of light. Usually, the recording electrode is placed on the midline overlying the central pole of the occipital cortex at the back of the head.

Visually evoked potentials are used primarily to measure the functional integrity of the optic nerves and pathways to the visual cortex of the brain. Any abnormality that affects the visual pathways or cortex in the brain can affect the VEP. A few examples are cortical blindness, due to meningitis; demyelination, associated with multiple sclerosis; optic neuritis; optic atrophy; stroke; compression of the optic pathways, such as by tumors; oxygen deprivation; visual-field defects; neurofibromatosis; and several dozen others.

In general, slowing neuronal transmission such as produced by myelin plaques, common in multiple sclerosis or gliomas on optic nerves in neurofibromatosis, slow the speed of the VEP wave peaks.  Compression of the optic pathways, such as from hydrocephalus or from a tumor, reduces the amplitude of wave peaks.

There are several methods of recording VEPs. In patients over about three years of age, VEPs are usually recorded using a television monitor to present patterned stimuli. In sedated patients and infants, flashes of light from a strobe flash or an array of LEDs are used to stimulate the eye.

Multifocal VEPs can be recorded to map the projection over the occipital cortex. Visually evoked potentials are also recorded in the operating room as part of an exam under anesthesia or during a surgical procedure. The various methods of recording VEPs, along with a number of examples of VEPs from patients, can be viewed at the following:

webvision.med.utah.edu/book/electrophysiology/visually-evoked-potentials/


webvision.med.utah.edu/book/electrophysiology/the-electroretinogram-clinical-applications/

Electro-Oculogram/the

The electro-oculogram (EOG) measures the potential between the cornea and the back of the eye. The potential produces a dipole field with the cornea electrically positive compared to the back of the eye.  With the cornea constantly positive, movement of the eye produces a shift of this electrical potential. By attaching skin electrodes near the inner and outer corners of the eye, the potential can be measured by having the patient move their eyes horizontally.

The procedure is simply that the patient keeps their head still while moving the eyes back and forth, alternating between the two red lights.  The movement of the eyes produces a voltage swing of approximately 5 millivolts between the electrodes on each side of the eye, which is charted on graph paper or stored in the memory of a computer.  Typically the voltage becomes smaller in the dark, reaching its lowest potential after about 8-12 minutes: the so-called "dark trough.” When the lights are turned on, the potential rises reaching its peak in about 10 minutes. When the size of the "light peak" is compared to the "dark trough," the relative size should be at least near 2:1. That is, twice as big in light compared to low voltage in dark. A ratio of less than about 1.7 is considered abnormal.

The origin of electro-oculographic potentials is the pigment epithelium of the retina. Although, the light rise of the potential requires both a normal pigment epithelium and normal mid-retinal function. A number of retinal diseases produce an abnormal electro-oculogram (EOG), which can also be demonstrated with the electroretinogram (ERG). The most common use of the electro-oculogram is to confirm Best's disease.  Best's dystrophy is usually identified by the appearance of the fundus and can be confirmed by recording both the electroretinogram (ERG) and electro-oculogram (EOG): the ERG will be normal, and the EOG will be abnormal.


Auditory Brainstem Responses

"Brainstem auditory evoked potential" (BAEP), "brainstem auditory evoked response" (BAER), and "auditory brainstem response" (ABR) are synonymous terms. They all refer to a test that is little used in ophthalmology. For decades, this test has been commonly used as a clinical tool in neurology and audiology to detect pathology in the brainstem.

Auditory brainstem responses are recorded by placing an electrode at the top of the head in reference to an electrode on the ear lobe or mastoid behind ear. Click stimuli of several intensities, including about 70 dB above minimum hearing threshold, are presented to one ear through earphones at a rate of 10 or more per second. A computer averages brain potentials evoked by about 2000 clicks. These small-amplitude potentials are very reliable, and usually five peaks can be identified in the first 10 milliseconds. The best feature of this test is that each peak has been associated with the level of the brainstem generating each component. Alterations in the brainstem, which are adjacent to the auditory pathways, will also alter the brainstem auditory evoked potential (BAEP). The auditory relay center in the mid-pontine region of brainstem lies adjacent to the cranial nerve nuclei IV, V, VI, and VII, so there is a high probability that anomalies associated with these nerves will produce abnormal ABRs.

It has been shown that brainstem auditory evoked potentials reflect abnormal brainstem pathways in visual centers controlling eye movement such as in Duane's retraction syndrome. We have found that half of patients with Marcus-Gunn ptosis demonstrate abnormal brainstem auditory evoked potentials as do about one-third of patients with blepharospasm. Although this test does not have the broad-base application to ophthalmology, it is of diagnostic use in patients with eye movement disorders that may be of central origin. The brainstem auditory pathways are also the second most common sites of demyelination seen in patients with multiple sclerosis. Neuro-ophthalmologists and neurologists often request the ABR.

 

Goldmann-Weekers Dark Adaptometry

This test measures how quickly and how well people adapt to the dark.  When passing from the light into dark, the light sensitivity of the eye improves up to one-thousand-fold or more. This is due to increase in the sensitivity of night receptor cells in the retina (rods) and is called dark adaptation. A person views a black and white three-stripe circle the size of a tennis ball that blinks on about once per second. Over a period of about 30 minutes, a dark-adaptation curve, which reflects level of dark adaptation is created.

 

Saccadic Velocities

To quantitate eye movement disorders, some doctors measure the relative strength and speed of eye muscles. The patient has small discs placed near the inner and outer corners of the eye, which measures electrical potentials when the patient moves their eyes horizontally a set distance.

The procedure is similar to an electro-oculogram without the dark adaptation. The patient keeps their head still while moving the eyes back and forth, alternating between the two small red lights. The movement of the eyes produces a voltage swing between the electrodes on each side of the eye, which is charted on graph paper or stored in the memory of a computer, and reflects relative speed and strength of eye muscles. 

To learn more about any of these topics, one may search Internet.

Donnell J. Creel, Ph.D.

Dr. Donnell Creel is Director of the Electrophysiology Service and a Research Professor at the Moran Eye Center. He joined the University of Utah Ophthalmology Department in 1979. Dr. Creel’s main clinical interest is diagnostic use of electrophysiological tests in patients, mainly the application of evoked potentials and electroretinography. His research includes ocular problems associated with genetic inheritance and the role of melanin pigmentation in the development and function of the visual and auditory systems. Research efforts include visual and auditory anatomical studies, evoked potentials, and psychophysical studies.

In a 1971 article in Nature, Dr. Creel first made the connection that visual anomalies in Siamese cats are associated with albinism. He hypothesized that all albino mammals, including humans, likely have optic misrouting. He created the visually evoked potential test that is used to confirm forms of albinism, and he published the first visual evoked potential studies in human albinos in 1974. Dr. Creel published the first paper showing visual tract anomalies in human ocular albinos in Science in 1978. His publications include multiple first-author publications in Science, including two cover articles, and a feature article in New England Journal of Medicine. He is an author of a chapter on Albinism in Internet text, The Metabolic and Molecular Bases of Inherited Disease (2012).

Dr. Creel donates his time overseas on teaching missions several times each year, primarily in China, where he is on the faculty of two medical schools. He is the English Editor for the Chinese Journal of Ocular Fundus Diseases. He also teaches at the Tilganga Eye Center in Kathmandu, Nepal. He was the first expert to teach electrophysiology in parts of China and Nepal, and he carries out ongoing lectures, training, and internet education to these countries. Dr. Creel has published over 100 peer-reviewed papers and chapters, and he has authored the two most-viewed chapters on Internet concerning visual electrophysiology.





Dr. Creel

Krista Kinard, M.D.

Krista Kinard spends time recording electrophysiology from patients as part of her last year of ophthalmology residency training. Beginning July, 2013, she will focus on specializing in neuro-ophthalmology as the Neuro-ophthalmology Fellow at the Moran Eye Center. Additional areas of training and specialization include ultrasound of the orbit.  Electrophysiology techniques include ffERG, mfERG, VEPs, ABRs, and EOG. After completing training, Dr. Kinard will be working at the Spokane Eye Clinic specializing in neuro-ophthalmology, ultrasound, electrophysiology, and general ophthalmology, providing medical and surgical care.  

Krista Kinard

 

Abraham Granados, Jr.

Abraham Granados, Jr. was a physician and surgeon in his native country of Guatemala. Abraham immigrated to the United States and is an outstanding ophthalmic tech at the Moran Eye Center. Abraham was awarded the prestigious University Staff Excellence Award for 2010 at the University of Utah School of Medicine, which recognizes the top medical-support employee within the entire School of Medicine. Abraham’s skills include recording visual and auditory electrophysiology. We enjoy the luxury of having a medical doctor fluent in Spanish in the Division.

Abraham Granados



 

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