7.5 Antiemetics

Nausea and vomiting are common conditions. Nausea is the unpleasant sensation of having the urge to vomit, and vomiting(emesis) is the forceful expulsion of gastric contents.^[1] There are many potential causes of nausea and vomiting, such as:

• Morning sickness during pregnancy
• Gastroenteritis and other infections
• Migraines
• Motion sickness
• Food poisoning
• Side effects of medicines, including those for cancer chemotherapy
• GERD and ulcers
• Intestinal obstruction
• Poisoning or exposure to a toxic substance
• Diseases of other organs (cardiac, renal, or liver)

Nausea and vomiting are common and are usually not serious. However, the health care provider should be contacted immediately if the following conditions occur:

• Vomiting for longer than 24 hours
• Blood in the vomit (also called hematemesis)
• Severe abdominal pain
• Severe headache and stiff neck
• Signs of dehydration, such as dry mouth, infrequent urination, or dark urine

Treatment of nausea and vomiting should be tailored to the cause. There are several medications that work on different neuroreceptors that when used can treat nausea and vomiting. For severe cases of vomiting, intravenous fluids may also be needed to treat the accompanying dehydration. ^[2],[3]

Pathophysiology

The vomiting center can be activated directly by irritants or indirectly following input from four principal areas: gastrointestinal tract, cerebral cortex and thalamus, vestibular region, and chemoreceptor trigger zone (CRTZ). See Figure 7.14 for an illustration of the pathophysiology of nausea and vomiting.^[4]

An important part of the emesis circuit is the chemoreceptor trigger zone (CTZ), located in the area postrema in the brain. The CTZ is not restricted by the blood–brain barrier, which allows it to respond directly to toxins in the bloodstream such as anesthesia and opioids. The CTZ also receives stimuli from several other locations in the body including the vestibular center; visceral organs such as the GI tract, kidneys, and liver; the thalamus; and the cerebral cortex.

The vestibular center and cerebral cortex can stimulate the vomiting center directly or indirectly through the CTZ. The vestibular system is located within the inner ear and gives a sense of balance and spatial orientation for the purpose of coordinating movement with balance. The feeling of nausea associated with motion sickness often arises from stimuli from the vestibular center. The gastrointestinal tract sends stimuli to the CTZ via cranial nerves IX and X related to obstruction, distension, inflammation, and infection. The cerebral cortex and other parts of the brain can also stimulate a sense of nausea related to odors, tastes, and images and send these stimuli to the CTZ. The CTZ forwards these signals to the vomiting center in the brain. Pain can also directly stimulate the vomiting center.

The vomiting center (VC) is located in the medulla in the brain. In response to these stimuli, the vomiting center initiates vomiting by inhibiting peristalsis and producing retro-peristaltic contractions beginning in the small bowel and ascending into the stomach. It also produces simultaneous contractions in the abdominal muscles and diaphragm that generate high pressures to propel the stomach contents upwards. Additionally, autonomic stimulation of the heart, airways, salivary glands, and skin cause other symptoms associated with vomiting such as salivation, palor, sweating, and tachycardia. Several neurotransmitters are involved in the nausea and vomiting process, and antiemetic medications are targeted to specific neuroreceptors.^[5]

Table 7.5a compares the neurotransmitters involved in the nausea and vomiting process, classes of antiemetic medication targeting these neurotrasmitters, prototype antiemetic medications, and associated mechanisms of action.^[6] Each medication class is also discussed in more detail later in this section.

Table 7.5a Neurotransmitters and Associated Medications Used to Treat Nausea and Vomiting

Neurotransmitter	Medication Class	Antiemetic Drug	Mechanism of Action
Acetylcholine (M1)	Anticholinergics	scopolamine	Blocks ACh receptors in vestibular system
Histamine (H1)	Antihistamines	meclizine	Blocks H1 receptors and thus blocks ACh in vestibular system
Dopamine (DA2)	Dopamine antagonists	prochlorperazine	Blocks dopamine in CTZ and may block ACh
Dopamine and ACh (DA2 and M1)	Prokinetics	metoclopramide	Blocks dopamine in CTZ and stimulates ACh in GI tract
Serotonin (5HT)	Serotonin antagonists	ondansetron	Blocks serotonin in GI tract, CTZ, and VC
Substance P (NK1)	Neurokinin antagonists	aprepitant	Inhibits substance P neurokinin receptors
Cannabinoid (CB1)	Tetrahydrocannabinols (THC)	dronabinol or medical marijuana	Activated CB1 receptor leading to inhibitory effects on cerebral cortex

Nursing Considerations

Assessment

When administering antiemetics, identify factors contributing to the symptoms of nausea and vomiting so that treatment can correctly target the cause. Document the frequency and amount of emesis and effects on the patient’s appetite and fluid intake. Assess for symptoms of dehydration, such as decreased blood pressure associated with tachycardia, decreased skin turgor, and decreased urine output or dark concentrated urine. If lab tests are ordered, monitor hemoglobin, hematocrit, and serum sodium levels for additional signs of dehydration.

Implementation

Advocate for the most effective route of administration if the patient is vomiting. Consider timing of administration of antiemetics in advance of meals when appetite is affected. Follow drug label administration information and monitor the patient closely for potential side effects associated with that category of medication. For example, when administering anticholinergics and antihistamines, monitor for anticholinergic side effects, especially in elderly patients.

Evaluation

Monitor for improvement of nausea and vomiting and notify the provider if expected improvement does not occur so that other treatment can be initiated. Continue to monitor for dehydration. Teach the patient nonpharmacological interventions for nausea such as:

• Drink enough fluids to avoid dehydration. If you are having trouble keeping liquids down, drink sips of clear liquids every few minutes.
• Eat bland foods; stay away from spicy, fatty, or salty foods.
• Eat smaller meals more often.
• Avoid strong smells because they can sometimes trigger nausea and vomiting.
• If you are pregnant and have morning sickness, eat crackers before you get out of bed in the morning.^[7]

Antiemetic Medication Classes

Anticholinergics

Scopolamine is an example of an anticholinergic medication that is often used to treat motion sickness or nausea and vomiting associated with surgical recovery from anesthesia and/or opiate analgesia.

Mechanism of Action

Anticholinergics block ACh receptors in the vestibular center and within the brain to prevent nausea-inducing stimuli to the Chemoreceptor Trigger Zone (CTZ) and the Vomiting Center (VC). They also dry GI secretions and reduce smooth muscle spasms.

Specific Administration Considerations

The scopolamine transdermal patch (see Figure 7.15)^[8] is designed for continuous release of scopolamine following application to an area of intact skin on the head, behind the ear. The system is formulated to deliver approximately 1 mg of scopolamine to the systemic circulation over 3 days. It is contraindicated in patients with glaucoma. It has been reported to exacerbate psychosis, induce seizures, and cause drowsiness, confusion, and sedation. Due to its anticholinergic properties, scopolamine can decrease gastrointestinal motility and cause urinary retention. Nurses should perform more frequent monitoring during treatment with Transderm Scōp and discontinue Transderm Scōp in patients who develop difficulty in urination. Transderm Scōp contains an aluminized membrane; skin burns have been reported at the application site in patients wearing an aluminized transdermal system during an MRI scan. Remove Transderm Scōp before undergoing an MRI.

Application instructions:

• Only wear one transdermal system at any time.
• Do not cut the transdermal system.
• Apply the transdermal system to the skin in the postauricular area (hairless area behind one ear).
• After the transdermal system is applied on the dry skin behind the ear, wash hands thoroughly with soap and water and dry hands.
• If the transdermal system becomes displaced, discard the transdermal system, and apply a new transdermal system on the hairless area behind the other ear.
• For surgeries other than cesarean section, apply one Transderm Scōp transdermal system the evening before scheduled surgery. Remove the transdermal system 24 hours following surgery.

Patient Teaching & Education

Transderm Scōp may impair the mental and/or physical abilities required for the performance of hazardous tasks such as driving a motor vehicle, operating machinery, or participating in underwater sports. Concomitant use of other drugs (e.g., alcohol, sedatives, hypnotics, opiates, and anxiolytics) that cause central nervous system (CNS) adverse reactions, or that have anticholinergic properties, may increase this impairment. Inform patients not to operate motor vehicles or other dangerous machinery or participate in underwater sports until they are reasonably certain that Transderm Scōp does not affect them adversely. Scopolamine can cause temporary dilation of the pupils resulting in blurred vision if it comes in contact with the eyes. Advise patients to wash their hands thoroughly with soap and water and dry their hands immediately after handling the transdermal system. Upon removal, fold the used transdermal system in half with the sticky side together, and discard in household trash in a manner that prevents accidental contact or ingestion by children, pets, or others.^[9]

Antihistamines

Meclizine is an example of an antihistamine that is often used to treat motion sickness.

Mechanism of Action

Antihistamines block H1 receptors in the vestibular center and may also block acetylcholine (ACh).

Specific Administration Considerations

Antihistamines are contraindicated in patients with glaucoma or an enlarged prostate gland. Dosage should be started one hour before travel begins.

Patient Teaching & Education

• Do not exceed recommended dosage.
• Be advised that drowsiness may occur.
• Avoid alcohol, sedatives, and tranquilizers, which may increase drowsiness.
• Avoid alcoholic drinks.
• Be careful when driving a motor vehicle or operating machinery.^[10]

Dopamine Antagonists

Prochlorperazine is an example of a dopamine antagonist used to treat nausea and vomiting. It can also be used as an antipsychotic medication.

Mechanism of Action

Prochlorperazine blocks dopamine in the Chemoreceptor Trigger Zone (CTZ). It also calms the central nervous system and may also block acetylcholine.

Specific Administration Considerations

Prochlorperazine can be administered orally, intramuscularly, rectally or intravenously. It is contraindicated in children under age 2 or under 20 pounds. Severe side effects have occurred when used to treat psychosis.

Patient Teaching & Education

Patients should be instructed to take medications as prescribed.  They should avoid alcohol and other CNS depressants.  Patients may experience increased photosensitivity and extreme temperatures should be avoided.  Patients should be advised that urine may turn pinkish to reddish-brown.^[11]

Prokinetics

Metoclopramide is an example of a prokinetic medication (see Figure 7.16).^[12]

Mechanism of Action

Metoclopramide blocks dopamine and may also sensitize tissues to acetylcholine. It is used to promote peristalsis to empty the gastrointestinal tract and thus reduce nausea.

Specific Administration Considerations

Metoclopramide can be administered orally, intramuscularly, and intravenously. The onset of pharmacological action of metoclopramide is 1 to 3 minutes following an intravenous dose, 10 to 15 minutes following intramuscular administration, and 30 to 60 minutes following an oral dose. Pharmacological effects persist for 1 to 2 hours.

Metoclopramide should not be used whenever stimulation of gastrointestinal motility might be dangerous (e.g., in the presence of gastrointestinal hemorrhage, mechanical obstruction, or perforation). Metoclopramide is contraindicated in patients with pheochromocytoma because the drug may cause a hypertensive crisis. Metoclopramide should not be used in epileptics or patients receiving other drugs that are likely to cause extrapyramidal reactions because the frequency and severity of seizures or extrapyramidal reactions may be increased. Rare reports of neuromalignant syndrome have occured.

Patient Teaching & Education

Teach patients to immediately inform the healthcare provider if they experience new feelings of depression or abnormal muscle movements they cannot control such as:

• lip smacking, chewing, or puckering of the mouth
• frowning or scowling
• sticking out the tongue
• blinking and moving the eyes
• shaking of the arms and legs^[13]

Serotonin Antagonists

Ondansetron is an example of a serotonin (5HT) antagonist often used to treat severe nausea and vomiting associated with chemotherapy, postoperative nausea and vomiting, and hyperemesis during pregnancy. (See Figure 7.17 for an image of odansetron blocking the 5-HT₃ receptor.^[14])

Mechanism of Action

Ondansetron blocks serotonin receptors in the GI tract, the chemoreceptor trigger zone (CTZ), and the vomiting center (VC). See Figures 7.18 and 7.19 for images of the injectable and oral formulations of ondansetron.^[15],[16]

Specific Administration Considerations

Ondansetron is available as an orally disintegrating tablet and as an injectable for those patients too nauseated to tolerate oral medication. It is contraindicated with apomorphine. Serotonin syndrome can occur if administered concurrently with other serotonin antagonists or selective serotonin reuptake inhibitors. Ondansetron can cause headaches, drowsiness, constipation, fever, and diarrhea. A rare but serious adverse effect of ondansetron is QT prolongation that can cause an abnormal cardiac rhythm.

Patient Teaching & Education

Teach patients to immediately inform their healthcare provider if they experience a change in heart rate, lightheadedness, or feel faint or have any signs and symptoms of hypersensitivity reactions such as fever, chills, rash, or breathing problems.^[17]

Neurokinin Receptor Antagonists

Aprepitant is an example of a neurokinin antagonist used to prevent nausea and vomiting associated with chemotherapy and surgery.

Mechanism of Action

Aprepitant inhibits substance-P neurokinin receptors in the brainstem.

Nursing Considerations

Aprepitant is usually administered concurrently with dexamethasone (a corticosteroid) and ondansetron. It can be administered orally or intravenously. It has clinically significant CYP3A4 drug interactions with medications such as pimozide, diltiazem, and rifampin, and can decrease INR levels when taken concurrently with warfarin. It can also reduce the effectiveness of oral contraceptives.

Patient Teaching & Education

Teach patients taking warfarin that they will need to monitor their INR levels more closely, which may require adjustment of the warfarin dosage, while taking aprepitant. Teach patients using an oral contraceptive to use backup birth control.^[18]

Tetrahydrocannabinoids (THC)

Dronabinol or medical marijuana is an example of a THC medication used to treat nausea in patients with cancer or AIDS (see Figures 7.20 and 7.21).^[19]

 

Mechanism of Action

THC has inhibitory effects in the cerebral cortex causing an alteration in mood and the body’s perception of its surroundings, which may relieve nausea and vomiting, as well as stimulate the appetite.

Specific Administration Considerations

THC will cause a dose-related “high” (easy laughing, elation, and heightened awareness). It is abusable and, thus, is a controlled substance and scheduled medication. THC should be used cautiously in elderly patients because they may be more sensitive to the neurological, psychoactive, and postural hypotensive effects of the drug. In general, dose selection for an elderly patient should be cautious, usually starting at the low end of the dosing range.

Patient Teaching & Education

Teach patients to not drive, operate machinery, or engage in any hazardous activity when using THC. Keep out of reach of children and pets.^[20]

Herbal and Vitamin Supplements

Ginger has been used in traditional Indian and Chinese medicine as an antiemetic. Although its mechanism of action is not completely understood, ginger is thought to antagonize the 5HT and cholinergic receptors and may have direct activity on the gastrointestinal tract. Although ginger can cause reflux and heartburn and may potentially cause bleeding because of its anticoagulant effects, dosages of up to 2 g per day in divided doses of 250 mg are considered safe even in pregnant women. Pyridoxine (vitamin B6) has also been recommended for treating nausea and vomiting in pregnancy. Typical dosages of pyridoxine 10 to 25 mg every eight hours cause minimal adverse effects. ^[21]

Antiemetics Medication Grid

Now let’s take a closer look at the medication grid comparing medications used to treat nausea. See Table 7.5b.^[22]

Medication grids are intended to assist students to learn key points about each medication.  Because information about medication is constantly changing, nurses should always consult evidence-based resources to review current recommendations before administering specific medication. Basic information related to each class of medication is outlined below.  Detailed information on a specific medication can be found for free at Daily Med. On the home page, enter the drug name in the search bar to read more about the medication.  Prototype/generic medications listed in the grids below are also hyperlinked directly to a Daily Med page.

Table 7.5b Medication Grid Comparing Antiemetics

Class	Prototype/ Generic	Administration Considerations	Therapeutic Effects	Adverse/Side Effects
Anticholinergic	scopolamine	Apply patch to hairless skin behind ear for 3 days or apply the night before surgery and remove 24 hours later Do not cut patch After application, thoroughly wash and dry hands Remove before an MRI Contraindicated in patients with glaucoma	Prevent or reduce nausea and vomiting associated with motion sickness or surgery	Monitor for anticholinergic effects such as decreased GI motility and urinary retention Discontinue if it exacerbates psychosis or causes seizures or cognitive impairment
Antihistamine	meclizine	Contraindicated in patients with glaucoma or an enlarged prostate gland Dosage should be started one hour before travel begins	Prevent or reduce nausea and vomiting associated with motion sickness	May cause drowsiness
Dopamine antagonist	prochlorperazine	Can be administered PO, IM, PR, or IV	To control nausea and vomiting associated with surgery	Drowsiness, dizziness, amenorrhea, blurred vision, skin reactions, and hypotension may occur
Prokinetic	metoclopramide	Can be administered PO, IM, and IV Onset of action is 1 to 3 minutes following an IV dose, 10 to 15 minutes following IM administration, and 30 to 60 minutes following an oral dose Pharmacological effects persist for 1 to 2 hours	To prevent or treat nausea and vomiting associated with surgery or chemotherapy	Restlessness, drowsiness, fatigue, depression, and suicide ideation Should be immediately discontinued if symptoms of tardive dyskinesia (abnormal muscle movements) or neuromalignant syndrome occur (hyperthermia, muscle rigidity, altered consciousness, irregular pulse or blood pressure, tachycardia, diaphoresis, and cardiac arrhythmias)
Serotonin antagonist	ondansetron	Can be administered as oral disintegrating tablet, PO, or IV	Prevention or treatment of severe nausea and vomiting associated with surgery, chemotherapy, or hyperemesis in pregnancy	Hypersensitivity reactions, including fever, chills, rash, or breathing problems Headache, drowsiness, constipation, fever, and diarrhea May cause QT prolongation Can cause serotonin syndrome if given concurrently with other serotonin antagonists or SSRIs
Neurokinin receptor antagonist	aprepitant	Can be administered PO or IV	Prevention of nausea and vomiting associated with chemotherapy and surgery	Hypersensitivity reaction, such as hives, rash. and itching; skin peeling or sores; or difficulty in breathing or swallowing If taking warfarin, increase monitoring of INR levels If taking oral contraceptives, use a backup method of birth control
THC	dronabinol or medical marijuana	Administered PO Most patients respond to 5 mg three or four times daily Dosage may be escalated during a chemotherapy cycle or at subsequent cycles, based on initial results	For treatment of nausea and vomiting associated with cancer chemotherapy when other treatment fails	Use cautiously in elderly patients because they may be more sensitive to the neurological, psychoactive, and postural hypotensive effects of the drug. In general, dose selection for an elderly patient should be cautious, usually starting at the low end of the dosing range