Special Diagnostic Studies
OVERVIEW OF SPECIAL DIAGNOSTIC STUDIES
These special studies have been selected for discussion because of their great diagnostic value in identifying diseases and disorders of certain organs and systems. Tests after death serve to identify previously undiagnosed disease; evaluate accuracy of predeath diagnosis; provide information about sudden, suspicious, or unexplained deaths; assist in organ donation and postmortem legal investigations; and promote quality control in healthcare settings.
THE EYE
• Visual Field Testing
This procedure is used in conjunction with a basic eye examination in order to quantify the sensitivity of the peripheral vision. The test can be used to evaluate and rule out glaucoma and to evaluate the integrity of the visual pathway. Small blind spots in the visual field begin to appear early in glaucoma. The visual field exam may detect diseases that affect the eye, optic nerve, or brain and screen for visual sequelae of cerebrovascular accident or head or eye trauma.
Reference Values
Normal
Negative for depressions of sensitivity other than the physiologic blind spot
Procedure
The patient is seated in front of the visual field analyzer with the forehead resting against the machine.
The patient is instructed to stare at the fixation light.
The patient is asked to click a button when he or she sees lights of varying intensity that are displayed at intervals.
Check one eye at a time.
Inform the patient that the procedure time is about 5 to 10 minutes for each eye.
Clinical Implications
Abnormal findings show the depressions of sensitivity that appear in glaucoma or pathology affecting the optic nerve (i.e., ischemic neuropathy).
Positive results should be confirmed with a repeat examination.
Repeat testing for positive findings will show larger spots and progression of disease (Fig. 16.1).
Interventions
Pretest Patient Care
Explain the purpose and procedure of the test.
Although there may be some slight discomfort during the procedure, assure the patient that there is no pain involved. The only discomfort is related to feeling sleepy, similar to being hypnotized.
If evaluating for glaucoma, explain that risk factors include age, race, family history, and elevated intraocular pressure.
Follow guidelines in Chapter 1 for safe, effective, informed pretest care.
Posttest Patient Care
Review test results (Fig. 16.2) and counsel the patient regarding abnormal findings; explain the need for possible follow-up testing and treatment. Modify the nursing care plan as needed.
Follow guidelines in Chapter 1 for safe, effective, informed posttest care.
NOTE
For the previous section, information was produced by the Eye Clinic of Wisconsin. Laser Diagnostic Technologies of San Diego, California, supplied the technical information.
• Retinal Nerve Fiber Analysis
This procedure evaluates glaucoma by use of microscopic laser technology to precisely measure the thickness of the retinal nerve fiber of the eye and is recorded in computerized data for analysis. It is this nerve layer that receives and transmits images and gives us vision.
Reference Values
Normal
No abnormalities of retinal nerve fiber
Normal thickness of retinal nerve layer
Procedure
Dilation of the eye is not necessary.
Have the patient sit upright in the examining chair.
Place the patient’s forehead and chin in cuplike holders and check one eye at a time. Twenty sectional images are obtained in <1 second and then analyzed to determine thickness of the nerve layer.
Clinical Implications
Abnormal appearance of the optic nerve is associated with changes in the eye that occur in glaucoma. Changes may be associated with vision loss.
Interventions
Pretest Patient Care
Explain test purpose and procedure. No pain or discomfort is associated with this test. There are no bright flashes of light.
Contact lenses may be left in place.
Follow guidelines in Chapter 1 for safe, effective, informed pretest care.
Posttest Patient Care
Evaluate outcomes, counsel appropriately, and explain if there is need for further testing and possible treatment of abnormal outcomes. Modify the nursing care plan as needed.
Follow guidelines in Chapter 1 for safe, effective, informed posttest care.
• Fluorescein Angiography (FA)
The purpose of this test is to detect vascular disorders of the retina that may be the cause of poor vision. Fluorescein, a yellow-red contrast substance, is injected intravenously over a 10- to 15-second period. Under ideal conditions, retinal capillaries 5 to 10 µm in diameter can be visualized using fluorescein angiography (FA). Images of the eye, taken by a special camera, are studied to detect the presence of retinal disorders. Choroidal circulation is not seen with color photographs.
Reference Values
Normal
Normal retinal vessels, retina, and circulation
Procedure
Give a series of three drops to dilate the pupil of the eye. Complete dilation occurs within 30 minutes of giving the last drop.
When dilation is complete, take a series of color photographs of both eyes.
Have the patient sit with the head immobilized in a special headrest in front of a fundus camera.
Inject fluorescein dye intravenously.
Take a series of photographs as the dye flows through the retinal blood vessels over a period of 3 to 4 minutes.
Take a final series of photographs 8 to 10 minutes after the injection.
PROCEDURAL ALERT
Some patients may experience nausea for a short period of time following the injection.
The eyedrops may sting or cause a burning sensation.
Clinical Implications
Abnormal results reveal:
Diabetic retinopathy
Aneurysm
Macular degeneration
Diabetic neovascularization
Blocked blood vessels
Leakage of fluid from vessels
Interventions
Pretest Patient Care
Determine whether the patient has any known allergies to medications or contrast agent.
Instruct the patient about the purpose, procedure, and side effects of the test.
Follow guidelines in Chapter 1 for safe, effective, informed pretest care.
Posttest Patient Care
Inform the patient that he or she may experience color changes in the skin (yellowish) and urine (bright yellow or green) for 36 to 48 hours after the test.
Advise the patient to wear dark glasses and not to drive while the pupils remain dilated (4 to 8 hours). During this time, patients are unable to focus on nearby objects and react abnormally to changes in light intensity.
Review test results; report and record findings. Modify the nursing care plan as needed.
Follow guidelines in Chapter 1 for safe, effective, informed posttest care.
• Electroretinography (ERG)
Electroretinography (ERG) is used to study hereditary and acquired disorders of the retina, including partial and total color blindness (achromatopia), night blindness, retinal degeneration, and detachment of the retina in cases in which the ophthalmoscopic view of the retina is prohibited by some opacity, such
as vitreous hemorrhage, cataracts, or corneal opacity. When these disorders exclusively involve either the rod system or the cone system to a significant degree, the ERG shows corresponding abnormalities.
as vitreous hemorrhage, cataracts, or corneal opacity. When these disorders exclusively involve either the rod system or the cone system to a significant degree, the ERG shows corresponding abnormalities.
In this test, an electrode is placed on the eye to obtain the electrical response to light. When the eye is stimulated with a flash of light, the electrode will record potential (electric) change that can be displayed and recorded on an oscilloscope. The ERG is indicated when surgery is considered in cases of questionable retinal viability.
Reference Values
Normal
Normal A and B waves
NOTE
“A” waves are produced by photoreceptor cells and “B” waves by Müller radial cells.
Procedure
Have the patient hold eyes open during the procedure.
The patient may be sitting up or lying down.
Instill topical anesthetic eyedrops.
Place bipolar cotton wick electrodes, saturated with normal saline, on the cornea.
Use two states of light adaptation to detect rod and cone disorders along with different wavelengths of light to separate rod and cone function. Normally, the more intense the light, the greater the electrical response.
Room (ambient) light
Room darkened for 20 minutes and then a white light is flashed
Bright flash (In cases of trauma, when there is vitreous hemorrhage, a much more intense flash of light must be used.)
Use chloral hydrate or a general anesthesia for infants and small children who are being tested for a congenital abnormality.
Total examining time is about 1 hour.
Clinical Implications
Changes in the ERG are associated with:
Diminished response in ischemic vascular diseases, such as arteriosclerosis and giant cell arteritis
Siderosis (poisoning of the retina when copper is embedded intraocularly [this is not associated with stainless steel foreign bodies])
Drugs that produce retinal damage, such as chloroquine and quinine
Retinal detachment
Opacities of ocular media
Decreased response, such as in vitamin A deficiency or mucopolysaccharidosis
Diseases of the macula do not affect the standard ERG. Macular disorder can be detected using a focal ERG.
Interventions
Pretest Patient Care
Explain the purpose and procedure of the test. For the most part, the patient will experience little or no discomfort. The electrode may feel like an eyelash in the eye.
Follow guidelines in Chapter 1 for safe, effective, informed pretest care.
Posttest Patient Care
Review test results; report and record findings. Modify the nursing care plan as needed.
Follow guidelines in Chapter 1 for safe, effective, informed posttest care.
CLINICAL ALERT
Caution the patient not to rub the eyes for at least 1 hr after testing to prevent accidental corneal abrasion.
• Eye and Orbit (Ophthalmic) Ultrasound
Ultrasound can be used to describe both normal and abnormal tissues of the eyes when no alternative visualization is possible because of opacities caused by corneal edema, vitreal hemorrhage, or cataracts. This information is valuable in the management of eyes with large corneal leukomas or conjunctival flaps and in the evaluation of the eyes for keratoprosthesis. Orbital lesions can be detected and distinguished from inflammatory and congestive causes of exophthalmus with a high degree of reliability. An extensive preoperative evaluation before vitrectomy or surgery for vitreous hemorrhages is also done. In this case, the vitreous cavity is examined to rule out retinal and choroidal detachments and to detect and localize vitreoretinal adhesions, choroidal lesions, and intraocular foreign bodies. It can also be used to detect optic nerve drusen. Persons who are to have intraocular lens implants after removal of cataracts must be measured for the length of the eye (within 0.1 mm). The ophthalmic ultrasound can produce biometric readings for lens calculation prior to cataract surgery.
Reference Values
Normal
Normal image pattern indicating normal soft tissue of eye, retrobulbar orbital areas, retina, choroid, and orbital fat
Procedure
Anesthetize the eye area by instilling eyedrops.
Ask the patient to fix the gaze and hold very still. If imaging a lesion, movement is required for a retinal detachment evaluation.
Place a small, very-high-frequency transducer directly on the eye or position over a water standoff pad placed onto the eye surface.
Take multiple images.
If a lesion in the eye is detected, as much as 30 minutes may be required to differentiate the pathologic process accurately.
Orbital examination can be done in 8 to 10 minutes.
Follow guidelines in Chapter 1 for safe, effective, informed intratest care.
PROCEDURAL ALERT
When a ruptured globe is suspected or surgery has been performed, ophthalmic ultrasound can be performed over a closed eyelid.
Caution must be used to avoid excessive pressure applied to the globe causing expulsion of the contents and increased risk for introduction of bacteria.
Clinical Implications
Abnormal patterns are seen in:
Alkali burns with corneal flattening and loss of anterior chamber
Detached retina
Keratoprosthesis
Extraocular thickening in thyroid eye disease
Pupillary membranes
Cyclotic membranes
Vitreous opacities
Orbital mass lesions
Inflammatory conditions
Vascular malformations
Foreign bodies
Hypotony
Optic nerve drusen
Congenital cataract
Posterior vitreous detachment
Retinoschisis
Choroidal hemorrhage or detachment
Trauma
Abnormal patterns are also seen in tumors of various types based on specific ultrasonic patterns:
Solid tumors (e.g., meningioma, glioma, neurofibroma)
Cystic tumors (e.g., mucocele, dermoid, cavernous hemangioma)
Angiomatous tumors (e.g., diffuse hemangioma)
Lymphangioma
Infiltrative tumors (e.g., metastatic lymphoma, pseudotumor)
Interfering Factors
If, at some time, the vitreous humor in a particular patient was replaced by gas or silicone oil, no result may be obtained.
Interventions
Pretest Patient Care
Explain the purpose and procedure of the test. For the most part, the patient will experience little to no discomfort.
Follow guidelines in Chapter 1 for safe, effective, informed pretest care.
Posttest Patient Care
Review test results; report and record findings. Modify the nursing care plan as needed.
Caution the patient not to rub the eyes until the effects of the anesthesia have disappeared to prevent accidental corneal abrasion. Minor blurred vision may be experienced for a short time.
Follow guidelines in Chapter 1 for safe, effective, informed posttest care.
BRAIN AND NERVOUS SYSTEM
• Electroencephalogram (EEG) and Epilepsy/Seizure Monitoring
The electroencephalogram (EEG) measures and records electrical impulses from the brain cortex. It is used to investigate causes of seizures, to diagnose epilepsy, and to evaluate brain tumors, brain abscesses, subdural hematomas, cerebral infarcts, and intracranial hemorrhages, among other conditions. It can be a tool for diagnosing narcolepsy, Parkinson’s disease, Alzheimer’s disease, and certain psychoses. It is common practice to consider the EEG pattern, along with other clinical procedures, drug levels, body temperature, and thorough neurologic examinations, to establish electrocerebral
silence, otherwise known as “brain death.” The American Clinical Neurophysiology Society sets guidelines for obtaining these recordings. When an electrocerebral silence pattern is recorded in the absence of any hope for neurologic recovery, the patient may be declared brain dead despite cardiovascular and respiratory support.
silence, otherwise known as “brain death.” The American Clinical Neurophysiology Society sets guidelines for obtaining these recordings. When an electrocerebral silence pattern is recorded in the absence of any hope for neurologic recovery, the patient may be declared brain dead despite cardiovascular and respiratory support.
Epilepsy/seizure monitoring using simultaneous video and EEG recordings (online computer) is done to verify a diagnosis of epilepsy, when seizures begin, and how they appear. The results differentiate and define seizure type, localize region of seizure onset, quantify seizure frequency, and identify candidates for medical implantation of vagus nerve stimulator or surgical treatment of seizures. Hospital admission is required.
Reference Values
Normal
Normal, symmetric patterns of electrical brain activity
Range of alpha: 8 to 11 Hz (cycles per second)
Seizure monitoring: expected outcome of at least three typical recorded seizures that may be different from what the patient usually experiences because medications have been reduced; also, onset area and type of seizures
No cross-circulation of internal carotid arteries
Evidence of hemispheres to support language and memory
Procedure for Electroencephalogram
Scalp hair should be recently washed.
Fasten electrodes containing conduction gel to the scalp with a special skin glue or paste. Seventeen to 21 electrodes are used according to an internationally accepted measurement known as the 10-20 System. This system correlates electrode placement with anatomic brain structure.
Place the patient in a recumbent position, instruct to keep the eyes closed, and encourage the patient to sleep during the test (resting EEG). (seizure activating procedure [see numbers 4 to 6])
Before beginning the test, some patients may be instructed to breathe deeply through the mouth 20 times per minute for 3 minutes. This hyperventilation may cause dizziness or numbness in the hands or feet but is nothing to be alarmed about. This activating breathing procedure induces alkalosis, which causes vasoconstriction, which in turn may activate a seizure pattern.
Place a light flashing at frequencies of 1 to 30 times per second close to the face. This technique, called photic stimulation, may cause an abnormal EEG pattern not normally recorded.
Be aware that certain persons may be intentionally sleep deprived before the test to promote sleep during the test. Administer an oral medication to promote sleep (e.g., diazepam [Valium] or chloral hydrate). The sleep state is valuable for revealing abnormalities, especially different forms of epilepsy. Make recordings while the patient is falling asleep, during sleep, and while the patient is waking.
Remove electrodes, glue, and paste after the test. The patient may then wash the hair.
Follow guidelines in Chapter 1 for safe, effective, informed intratest care.
Procedure for Seizure Monitoring
Apply electrodes, take the EEG, and explain video and EEG monitoring (for up to 6 days). An electrode panel is applied and must be covered when the patient eats. The patient remains in bed except to use the bathroom; a helmet is worn when out of bed.
Perform neuropsychological testing to evaluate memory (remember objects), language (circles, squares), and problem solving (4 to 6 hours of testing).
A cerebral angiogram to assess cross-circulation in carotids is followed by a Wada test to determine the dominant hemisphere for language and whether the opposite hemisphere can support memory. An intravenous line is started and a catheter is threaded through the femoral artery to the internal carotid to inject sodium amobarbital to “put the brain to sleep” for 5 minutes in each half of the
brain. The Wada test is also known as the amobarbital study or intracarotid Amytal test, or the Brevital test when sodium methohexital is used.
Perform a functional brain magnetic resonance imaging (MRI) study. Procedure time is about 90 minutes. The patient wears earphones and is asked to respond to questions, sounds, and pictures by pressing a special button.
A combined positron emission tomography/computed tomography (PET/CT) scan is often done to provide further information about brain hemispheres.
Clinical Implications
Abnormal EEG pattern readings reveal seizure activity (e.g., grand mal epilepsy, petit mal epilepsy) if recorded during a seizure. If a patient suspected of having epilepsy shows a normal EEG, the test may have to be repeated using sleep deprivation or special electrodes. The EEG may also be abnormal during other types of seizure activity (e.g., focal [psychomotor], infantile myoclonic, or jacksonian seizures); between seizures, 20% of patients with petit mal epilepsy and 40% with grand mal epilepsy show a normal EEG pattern, and the diagnosis of epilepsy can be made only by correlating the clinical history with the EEG abnormality, if one exists.
An EEG may often be normal in the presence of cerebral pathology. However, most brain abscesses and glioblastomas produce EEG abnormalities.
Electroencephalographic changes due to cerebrovascular accidents depend on the size and location of the infarcts or hemorrhages.
Following a head injury, a series of EEGs may be helpful in predicting the likelihood of posttraumatic epilepsy, especially if a previous EEG is available for comparison.
In cases of dementia, the EEG may be normal or abnormal.
In early stages of metabolic disease, the EEG is normal; in the later stages, it is abnormal.
The EEG is abnormal in most diseases or injuries that alter the level of consciousness. The more profound the change in consciousness, the more abnormal the EEG pattern.
Abnormal procedure results (e.g., identification of major connections between the anterior and posterior circulation, or abnormal connection between the internal carotid arteries, or isolation of seizure onset and number and types of seizures)
Interfering Factors
Sedative drugs, mild hypoglycemia, or stimulants can alter normal EEG tracings.
Oily hair, hair spray, and other hair care products interfere with the placement of EEG patches and the procurement of accurate EEG tracings.
Artifacts can appear in technically well-performed EEGs. Eye and body movements cause changes in brain wave patterns and must be noted so that they are not interpreted as abnormal brain waves.
Interventions
Pretest Patient Care
Explain test purpose and procedure to allay patient fears and concerns. Emphasize that electroencephalography is not painful, that it is not a test of thinking or intelligence, that no electrical impulses pass through the body, and that it is not a form of shock therapy. The transmitted impulses are magnified at least 1 million times and transcribed to permanent hard copy for further study.
Explain seizure monitoring procedures, purposes, and risks. Risks of angiogram and Wada test include allergy to sodium amobarbital, cross-circulation leading to respiratory arrest, and stroke related to allergy to contrast agent used in angiography.
Allow food if the patient is to be sleep deprived. However, no coffee, tea, or cola is permitted within 12 hours of the test. Emphasize that food should be eaten to prevent hypoglycemia.
Allow, but do not encourage, smoking before the test.
Have the patient wash and thoroughly rinse hair with clear water the evening before the test so that the EEG patches remain firmly in place during the test. Tell the patient to not apply conditioners or oils after shampooing.
If a sleep study is ordered, the adult patient should sleep as little as possible the night before (i.e., stay up past midnight) so that sleep can occur during the test.
Call the electroencephalography department for special instructions if a sleep deprivation study is ordered for a child.
Medications are generally reduced before the Wada test. A liquid breakfast is permitted.
EEG and video monitoring of seizures occur for up to 6 days, with medications gradually reduced by one third for 3 days.
Follow guidelines in Chapter 1 regarding safe, effective, informed pretest care.
Posttest Patient Care
Wash the hair after the test. Application of oil to the adhesive before shampooing can ease its removal.
Allow the patient to rest after the test if a sedative was given during the test. Put bedside rails in the raised position for safety. Resume medications (if reduced preprocedure).
Skin irritation from the electrodes usually disappears within a few hours.
Review test results; report and record findings. Modify the nursing care plan as needed. If a repeat testing is necessary, provide explanations and support to the patient. Explain possible treatment of uncontrolled seizures (e.g., newer antiseizure medications, surgical implantation of vagus nerve stimulator). Explain role of female hormones in epilepsy: Seizures may be worsened by hormones; adult epilepsy involves areas of the brain sensitive to reproductive hormones; and, at menopause, seizures tend to increase, worsen, or lessen.
Follow guidelines in Chapter 1 for safe, effective, informed posttest care.
• Evoked Responses/Potentials: Brainstem Auditory Evoked Response (BAER); Visual Evoked Response (VER); Somatosensory Evoked Response (SSER)
These tests use conventional EEG recording techniques with specific electrode site placement for each procedure and include computer data processing to evaluate electrophysiologic integrity of the auditory, visual, and sensory pathways. These are brain responses “time locked” to some event. See Chart 16.1 for wave and standard deviation (SD) measurements.
Brainstem auditory evoked response (BAER). This study allows evaluation of suspected peripheral hearing loss, cerebellopontine angle lesions, brainstem tumors, infarcts, multiple sclerosis, and comatose states. Special stimulating techniques permit recording of signals generated by subcortical structures in the auditory pathway. Stimulation of either ear evokes potentials that can reveal lesions in the brainstem involving the auditory pathway without affecting hearing. Evoked potentials of this type are also used to evaluate hearing in newborns, infants, children, and adults through electrical response audiometry.
Visual evoked response (VER). This test of visual pathway function is valuable for diagnosing lesions involving the optic nerves and optic tracts, multiple sclerosis, and other disorders. Visual stimulation excites retinal pathways and initiates impulses that are conducted through the central visual path to the primary visual cortex. Fibers from this area project to the secondary visual cortical areas on the brain’s occipital convexity. Through this path, a visual stimulus to the eyes causes an electrical response in the occipital regions, which can be recorded with electrodes placed along the vertex and the occipital lobes. It is also used to assess development of blue-yellow pathway in infants.
Somatosensory evoked response (SSER). This test assesses spinal cord lesions, stroke, and numbness and weakness of the extremities. It studies impulse conduction through the somatosensory pathway. Electrical stimuli are applied to the median nerve in the wrist or peroneal nerve near the knee at a level near that which produces thumb or foot twitches. The milliseconds it takes
for the current to travel along the nerve to the cortex of the brain is then measured. SSERs can also be used to monitor sensory pathway conduction during surgery for scoliosis or spinal cord decompression and/or ischemia. Loss of the sensory potential can signal impending cord damage.
for the current to travel along the nerve to the cortex of the brain is then measured. SSERs can also be used to monitor sensory pathway conduction during surgery for scoliosis or spinal cord decompression and/or ischemia. Loss of the sensory potential can signal impending cord damage.
CHART 16.1 Wave and Standard Deviation Measurements for Evoked Response/Potential | ||||||||||||||||||||||||||||||||||||||||||||||
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Procedures
Obtain BAERs through electrodes placed on the vertex of the scalp and on each earlobe. Stimuli in the form of clicking noises or tone bursts are delivered to one ear through earphones. Because sound waves delivered to one ear can be heard by the opposite ear, a continuous masking noise is simultaneously delivered to the opposite ear.
Place electrodes used in VER on the scalp along the vertex and occipital lobes. Ask the patient to watch a checkerboard pattern flash for several minutes, first with one eye and then with the other, while brain waves are recorded.
Record SSERs through several pairs of electrodes. Apply electrical stimuli to the median nerve at the wrist or to the peroneal nerve at the knee. Scalp electrodes placed over the sensory cortex of the opposite hemisphere of the brain pick up the signals and measure, in milliseconds, the time it takes for the current to travel along the nerve to the cortex of the brain.
Follow guidelines in Chapter 1 for safe, effective, informed intratest care.
Clinical Implications
Abnormal BAERs are associated with the following conditions:
Acoustic neuroma
Cerebrovascular accidents
Multiple sclerosis
Lesions affecting any part of the auditory nerve or brainstem area
Abnormal VERs are associated with the following conditions:
Demyelinating disorders such as multiple sclerosis
Lesions of the optic nerves and eye (prechiasmal defects)
Lesions of the optic tract and visual cortex (postchiasmal defects)
Abnormal visual evoked potentials may also be found in persons without a history of retrobulbar neuritis, optic atrophy, or visual field defects. However, many patients with proven damage to the postchiasmal visual path and known visual field defects may have normal visual evoked potentials.
Abnormal SSERs are associated with the following conditions:
Spinal cord lesions
Cerebrovascular accidents
Multiple sclerosis
Cervical myelopathy accident
Interfering Factors
Some difficulty in interpreting brainstem evoked potentials may arise in persons with peripheral hearing defects that alter evoked potential results (i.e., subthreshold stimulation of peripheral nerves and inadequate skin preparation).
Maximum depolarization stimulation is divided into two protocols:
Brachial plexus (BP) protocol involves stimulation of the median, ulnar, and superficial sensory radial nerves just proximal to the wrist.
Lumbosacral (LS) protocol involves stimulating the posterior tibial and common peroneal nerves, which are the primary divisions of the LS plexus forming the sciatic nerve.
Interventions
Pretest Patient Care
Explain test purpose and procedure.
Have the patient wash and rinse hair before testing. Instruct the patient not to apply any other hair preparations.
Follow guidelines in Chapter 1 for safe, effective, informed pretest care.
Posttest Patient Care
Allow the patient to wash his or her hair (assist if necessary). Remove gel from other skin areas.
Review test results; report and record findings. Modify the nursing care plan as needed.
Monitor the patient for neurologic changes.
Follow guidelines in Chapter 1 for safe, effective, informed posttest care.
• Cognitive Tests: Event-Related Potentials (ERPs)
Event-related potentials (ERPs) are used as objective measures of mental function in neurologic diseases that produce cognitive defects. These measurements use the method of auditory evoked response testing in which sound stimuli are transmitted through earphones. A rare tone is associated with a prominent endogenous P3 component that reflects the differential cognitive processing of that tone. Although a systematic neurologic increase in P3 component latency occurs as a
function of increasing age in normal persons, in many instances of neurologic diseases associated with dementia, the latency of the P3 component has been reported to exceed substantially the normal age-matched value.
function of increasing age in normal persons, in many instances of neurologic diseases associated with dementia, the latency of the P3 component has been reported to exceed substantially the normal age-matched value.
This test is useful in evaluating persons with dementia or decreased mental functioning. It is also helpful in differentiating persons with real organic brain defects affecting cognitive function from those who are unable to interact with the examiner because of motor or language defects or those unwilling to cooperate because of problems such as depression or schizophrenia.
Reference Values
Normal
No shift of P3 components to longer latencies
ERP: absolute latency of P3 waveform
P3 wave mean and SD 294 ± 21 msec
Procedure
This procedure is the same as that for auditory brainstem response.
Ask patients to count the occurrences of audible rare tones they hear through the earphones.
Follow guidelines in Chapter 1 for safe, effective, informed intratest care.
Clinical Implications
An increased or abnormal P3 latency is associated with neurologic diseases producing dementia, such as the following:
Alzheimer’s disease
Metabolic encephalopathy such as that associated with hypothyroidism or alcoholism with severe electrolyte disturbances
Brain tumor
Hydrocephalus
Interfering Factors
Latency of P3 component normally increases with age.
Interventions
Pretest Patient Care
Explain the purpose and procedure of the test.
Follow guidelines in Chapter 1 regarding safe, effective, informed pretest care.
Posttest Patient Care
Review test results; report and record findings. Modify the nursing care plan as needed.
Monitor for neurologic disease.
Follow guidelines in Chapter 1 for safe, effective, informed posttest care.
• Brain Mapping: Computed Tomography (CT)
Brain mapping uses transitional EEG data and specialized computer digitization to display the diagnostic information as a topographic map of the brain and spinal cord. The computer analyzes EEG signals for amplitude and distribution of alpha, beta, theta, and delta frequencies and displays the analysis as a color map. Specific or minute abnormalities are enhanced and allow comparison with normal data. This methodology is used for assessing cognitive function and for evaluating patients with migraine headaches, trauma, or episodes of vertigo or dizziness. Persons who lose periods of time and select patients with generalized seizures, dementia of organic origin, ischemic abnormalities,
or certain psychiatric disorders are also candidates for this testing. With this procedure, it is possible to localize a specific area of the brain that may otherwise show up as a generalized area of deficit in the conventional EEG. Children or adults who demonstrate hyperactivity, dyslexia, dementia, or Alzheimer’s disease may benefit from evaluation through brain mapping.
or certain psychiatric disorders are also candidates for this testing. With this procedure, it is possible to localize a specific area of the brain that may otherwise show up as a generalized area of deficit in the conventional EEG. Children or adults who demonstrate hyperactivity, dyslexia, dementia, or Alzheimer’s disease may benefit from evaluation through brain mapping.
Reference Values
Normal
Normal frequency signals and evoked responses presented as a color-coded map of electrical brain activity
Procedure
Ensure that the patient is rested and awake for the test so that no sleep signals appear as indicators of beta wave activity.
After the skin of the scalp is cleansed with an abrasive solution, place 42 electrodes at designated areas on the scalp and hold in place with adhesive or paste formulated for this purpose.
Place the patient in a recumbent position and instruct him or her to keep the eyes closed and to refrain from any movement.
Follow guidelines in Chapter 1 for safe, effective, informed intratest care.
Clinical Implications
Abnormal brain maps can pinpoint the following conditions:
Areas of focal seizure discharge in persons who experience generalized seizures
Areas of focal irritation in persons with migraine
Areas of ischemia
Areas of dysfunction in states of dementia
Areas of possible brain abnormalities associated with schizophrenia or other psychotic states
Interfering Factors
Tranquilizers may alter results.
Unwashed hair or the use of hair preparations can interfere with electrode placement.
Eye and body movements cause changes in signals and wave patterns.
Interventions
Pretest Patient Care
Explain test purpose and procedure. There are no known risks. Emphasize the fact that electrical impulses pass from the patient to the machine and not the opposite.
Tell the patient that food and fluids can be taken before testing. However, no coffee, tea, or caffeinated drinks should be ingested for at least 8 hours before test.
Ensure that hair has been recently washed.
Ensure that tranquilizers are not taken before testing (check with healthcare provider). Other prescribed medications such as antihypertensives and insulin may be taken. If in doubt, contact the testing laboratory for guidelines.
Follow guidelines in Chapter 1 for safe, effective, informed pretest care.
Posttest Patient Care
Remove the conduction gel and encourage the patient to wash his or her hair. Provide supplies if possible.
Review test results; report and record findings. Modify the nursing care plan as needed.
Monitor the patient for seizure activity and other neurologic changes.
Follow guidelines in Chapter 1 for safe, effective, informed posttest care.
• Electromyography (EMG); Electroneurography; Electromyoneurogram (EMNG)
Electromyoneurography combines electromyography (EMG) and electroneurography. These studies, done to detect neuromuscular abnormalities, measure nerve conduction and electrical properties of skeletal muscles. Together with evaluation of range of motion, motor power, sensory defects, and reflexes, these tests can differentiate between neuropathy and myopathy. The electromyogram can define the site and cause of muscle disorders such as myasthenia gravis, muscular dystrophy, and myotonia; inflammatory muscle disorders such as polymyositis; and lesions that involve the motor neurons in the anterior horn of the spinal cord. EMG can also localize the site of peripheral nerve disorders such as radiculopathy and axonopathy. Skin and needle electrodes measure and record electrical activity. Electrical sound equivalents are amplified and recorded for later studies.
Reference Values
Normal
Normal EMG and electromyoneurogram (EMNG)
Procedure
The test is done in a copper-lined room to screen out outside interference.
The patient may lie down or sit during the test.
Apply a surface disk or lead strap to the skin around the wrist or ankle to ground the patient. Choose the muscles and nerves examined according to the patient’s signs and symptoms, history, and physical condition (select nerves innervate specific muscles).
Encourage the patient to relax (massage certain muscles to get the patient to relax) or to contract certain muscles (e.g., to point to toes) at specific times during the test.
Testing is divided into two parts.
The first test determines nerve conduction.
Coat metal surface electrodes with electrode paste and firmly place over a specific nerve area. Pass electrical current (maximum, 100 mA for 1 msec) through the area to cause sensations, similar to shock from carpeting or static electricity or the equivalent of an AA battery, that are directly proportional to the time the current is applied. Patients with mild forms of neuromuscular disorders may feel mild discomfort, whereas those with polyneuropathies may experience moderate discomfort.
Read the amplitude wave on an oscilloscope and record on magnetic tape for later studies.
Electrical current leaves no mark but can cause unusual sensations that are not usually considered unpleasant. How fast and how well a nerve transmits messages can be measured. Nerves in the face, arms, or legs are appropriate for testing in this way.
The second test determines muscle potential.
Insert a monopolar electrode (a 1.25- to 7.5-cm-long small-gauge needle) and incrementally advance into the muscle. Manipulate the needle without actually removing it to see if readings change, or place the needle in another muscle area.
The electrode usually causes no pain unless the tip is near a terminal nerve. Ten or more needle insertions may be necessary. The needle electrode detects electricity normally present in muscle.
Observe the oscilloscope for normal wave forms and listen for normal quiet sounds at rest. A “machine-gun popping” sound or a rattling sound like hail on a tin roof is normally heard when the patient contracts the muscle.
If the patient reports pain, remove the needle because the pain stimulus yields false results.
Total examining time is 45 to 60 minutes if testing is confined to a single extremity; testing may take up to 3 hours for more than one extremity. There is no completely “routine” EMG. The length of the test depends on the clinical problem.
Follow guidelines in Chapter 1 regarding safe, effective, informed intratest care.
PROCEDURAL ALERT
Enzyme levels that reflect muscle activity (e.g., aspartate aminotransferase, lactate dehydrogenase, creatine phosphokinase) must be determined before actual testing because the EMG causes elevation of these enzymes for up to 10 d postprocedure.
Although rare, hematomas may form at needle insertion sites. Take measures, such as application of pressure to the site, to control bleeding. Notify the healthcare provider. Ascertain whether the patient is taking anticoagulants or aspirin-like drugs.
Clinical Implications
Abnormal neuromuscular activity occurs in diseases or disturbances of striated muscle fibers or membranes in the following conditions:
Muscle fiber disorders (e.g., muscular dystrophy)
Cell membrane hyperirritability; myotonia and myotonic disorders (e.g., polymyositis, hypocalcemia, thyrotoxicosis, tetanus, rabies)
Myasthenia (muscle weakness states) caused by the following conditions:
Myasthenia gravis
Cancer due to nonpituitary adrenocorticotropic hormone (ACTH) secretion by the tumor
Bronchial cancer
Sarcoid
Deficiencies
Familial hypokalemia
McArdle’s phosphorylase
Hyperadrenocorticism
Acetylcholine-blocking agents
Curare
Botulin
Kanamycin
Snake venom
Disorders or diseases of lower motor neurons
Lesions involving motor neuron on anterior horn of spinal cord (myelopathy)
Tumor
Trauma
Syringomyelia
Juvenile muscular dystrophy
Congenital amyotonia
Anterior poliomyelitis
Amyotrophic lateral sclerosis
Peroneal muscular atrophy
Lesions involving the nerve root (radiculopathy)
Guillain-Barré syndrome
Entrapment of the nerve root
Tumor
Trauma
Herniated disk
Hypertrophic spurs
Spinal stenosis
Damage to or disease of peripheral or axial nerves
Entrapment of the nerve
Carpal or tarsal tunnel syndrome
Facial, ulnar, radial, or peroneal palsy
Neuralgia paresthetica
Endocrine
Hypothyroidism
Diabetes
Toxic
Heavy metals
Solvents
Antiamebicides
Chemotherapy
Antibiotics
Early peripheral nerve degeneration and regeneration
Interfering Factors
Conduction can vary with age and normally decreases with increasing age.
Pain can yield false results.
Electrical activity from extraneous persons and objects can produce false results as a result of movement.
The test is ineffective in the presence of edema, hemorrhage, or thick subcutaneous fat.
Interventions
Pretest Patient Care
Explain test purpose and procedure. There is a risk for hematoma if the patient is on anticoagulant therapy.
Sedation or analgesia may be ordered.
Follow guidelines in Chapter 1 for safe, effective, informed pretest care.
Posttest Patient Care
If the patient experiences pain, provide pain relief through appropriate interventions. Obtain an order for an analgesic if necessary.
Promote rest and relaxation.
Review test results; report and record findings. Modify the nursing care plan as needed.
Monitor the patient for nerve and muscle disease. Provide assistance as necessary.
Follow guidelines in Chapter 1 for safe, effective, informed posttest care.
• Electronystagmogram (ENG)
This study aids in the differential diagnosis of lesions in the brainstem and cerebellum. It can confirm the causes of unilateral hearing loss of unknown origin, vertigo, or ringing in the ears. Evaluation of the vestibular system and the muscles controlling eye movement is based on measurements of the nystagmus cycle. In health, the vestibular system maintains visual fixation during head movements by means of nystagmus, the involuntary back-and-forth eye movement caused by initiation of the vestibular-ocular reflex.
Reference Values
Normal
Vestibular-ocular reflex: Normal nystagmus accompanying head turning is expected.
Procedure
The test is usually done in a darkened room with the patient sitting or lying down.
Remove any earwax before testing.
Tape five electrodes at designated positions around the eye.
During the study, ask the patient to look at different objects, to open and close his or her eyes, and to change head position.
Toward the end of the test, gently blow air into each external ear canal, starting on the affected side. Instill cold water and then warm water into the ears during the test to record eye movement in response to various stimuli.
Follow guidelines in Chapter 1 for safe, effective, informed intratest care.
PROCEDURAL ALERT
Water irrigation of the ear canal should not be done when there is a perforated eardrum. Instead, a finger cot may be inserted into the ear canal to protect the middle ear.
Clinical Implications
Prolonged nystagmus and postural instability following a head turn is abnormal and can be caused by lesions of the vestibular or ocular system, as in the following conditions:
Cerebellar disease
Brainstem lesion
Peripheral lesion occurring in elderly persons; head trauma; middle ear disorders
Congenital disorders
Ménière’s disease
Interfering Factors
Test results are altered by the inability of the patient to cooperate, poor eyesight, blinking of the eyes, or poorly applied electrodes.
The patient’s anxiety or medications such as central nervous system depressants, stimulants, or antivertigo agents can cause false-positive test results.
Interventions
Pretest Patient Care
Explain test purpose and procedure. No pain or known risks are associated with the test. The procedures to stimulate involuntary rapid eye movements are uncomfortable.
Have the patient remove makeup.
Have the patient abstain from all caffeinated and alcoholic beverages for at least 48 hours. Heavy meals should be avoided before testing.
In most cases, medications such as tranquilizers, stimulants, or antivertigo agents should be withheld for 5 days before the test. If in doubt, consult the healthcare provider who ordered the test.
Follow guidelines in Chapter 1 for safe, effective, informed pretest care.
CLINICAL ALERT
The test is contraindicated in persons who have pacemakers.
Posttest Patient Care
Allow the patient to rest as necessary.
If present, nausea, vertigo, and weakness may require treatment and medication. Check with the healthcare provider who ordered the test.
Review test results; report and record findings. Modify the nursing care plan as needed.Stay updated, free articles. Join our Telegram channel
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