MOBILE VIEW  | 

CAPSAICIN

Classification   |    Detailed evidence-based information

Therapeutic Toxic Class

    A) Capsaicin is a chemical irritant found in many plant species, especially in the genus Capsicum. Many of the peppers of the capsicum species are prepared and used in a variety dishes. The oleoresin of capsicum is a major ingredient of "pepper spray". This management includes a discussion about the various uses of capsaicin and its potential sources and routes of exposure.

Specific Substances

    A) CAPSICUM SPECIES - BOTANICAL NAMES
    1) Capsicum annuum L. var. annuum
    2) Capsicum annuum var. glabriusculum (Dunal) Heiser & Pickersgill
    3) Capsicum chinense Jacq.
    4) Capsicum frutescens L.
    COMMON NAMES
    1) Cayenne pepper
    2) Chili pepper
    3) Habanero pepper
    4) Tabasco pepper
    PERSONAL PROTECTION
    1) Capsaicin spray
    2) Capsicum spray
    3) Pepper mace
    4) Pepper spray projectile
    5) Oleoresin capsicum (OC)
    6) OC spray
    7) OC gas
    8) Riot control agent
    OTHER
    1) Trans-8-methyl-N-vanillyl-6-nonenamide
    2) Pelargonic acid vanillylamide (synthetic analogue of capsaicin)
    3) Pelargonic acid morpholide (synthetic form of capsaicin)
    4) Desmethyldihydrocapsaicin

Available Forms Sources

    A) SOURCES
    1) PLANT: Found in various plant species, especially of the genus Capsicum and is part of the Solanaceae family. Such plants include Capsicum frutescens, and Capsicum annuum. There are approximately 20 species of Capsicum, which are perennial herbs native to tropical America. The fruits and seed of most peppers can be injurious except for sweet pepper varieties or bell peppers (Nelson et al, 2007).
    2) PERSONAL PROTECTION: Pepper mace may come in sprays of 1% to 10% concentrations.
    B) USES
    1) CULINARY
    a) Many of the peppers of the capsicum species are prepared and used in a variety of dishes. Although these peppers are used in many foods, they can act as a mucous membrane irritant and may cause release of substance P from sensory nerve fibers. This substance can stimulate pain fibers and release inflammatory mediators (Nelson et al, 2007).
    1) Dermal exposure can cause erythema, but not vesiculation. Eye exposure to the pepper juice can produce moderate chemical conjunctivitis and pain. Oral exposure can cause burning and stinging of the oral mucosa.
    2) LAW ENFORCEMENT
    a) Pepper spray is commonly used in law enforcement for training of personnel as well as to directly incapacitate individual suspects or for crowd control. A retrospective case review of pepper spray exposures reported to the California Poison Control System between 2002 and 2011 revealed that more severe outcomes, requiring medical evaluation, occurred when pepper spray was used during law enforcement training (odds ratio (OR) 7.39; 95% CI, 2.98 to 18.28), with direct intentional exposure for purposeful use to incapacitate (OR 3.02; 95% CI, 1.80 to 5.06), and with law enforcement use on individual target suspects or crowd control (OR 2.45; 95% CI, 1.42 to 4.23) (Kearney et al, 2014).
    1) The more severe outcomes, requiring medical evaluation, included ocular symptoms (ie, persistent pain, blurred vision, foreign body sensation, discharge or exudate, periorbital swelling), dermal symptoms (ie, rash, blisters), and respiratory symptoms (ie, shortness of breath, chest tightness, wheezing) (Kearney et al, 2014).
    3) MEDICINAL
    a) Capsicum contains about 0.02% to 0.5% capsaicin as well as a volatile oil (1.5%), a fixed oil, carotenoids and 0.2% Vitamin C. It is used medicinally as an irritant and carminative (Tyler et al, 1981).
    b) Capsaicin has been investigated for the topical treatment of various dermatological diseases (Bernstein, 1988). Paradoxically, capsaicin is available as a topical nonprescription cream used to treat painful lesions by depleting the sensory nerve endings of substance P to provide analgesia (Nelson et al, 2007).
    4) PERSONAL PROTECTION
    a) PEPPER SPRAY: The oleoresin of capsicum is a major ingredient of "pepper gas". Personal protection weapons carried by many civilians and law enforcement personnel. These weapons can provide temporary immobilization of an assailant when sprayed into the face, especially the eyes. Pepper gases may contain other substances including CS. (tear gas).
    1) "Pepperball Tactical Powder" pellets have been used to control riots. Each pellet weighs just over 3 grams and has a thin rigid plastic casing (diameter 17.2 mm). It has 2.45 grams of a white powder containing capsaicin, present as a 0.5% (w/w) mixture with barium sulfate and non-crystalline amorphous precipitated silica. When pellets are fired, the plastic casing will rupture on impact and the contents will be discharged (Hay et al, 2006).

Life Support

    A) This overview assumes that basic life support measures have been instituted.

Clinical Effects

    0.2.1) SUMMARY OF EXPOSURE
    A) USES: HOME: Many of the peppers of the capsicum species are prepared and used in a variety foods and dishes. MEDICAL: Topical formulations are used to treat painful skin conditions. LAW ENFORCEMENT: The oleoresin of capsicum is used in some pepper "gas" sprays by law enforcement or for personal protection. PLANTS: Found in plants of the genus Capsicum (primarily chili peppers).
    B) PHARMACOLOGY: Topical application stimulates pain fibers and causes release of immunoreactive somatostatin. Most likely causes the depletion of substance P in pain and heat neurons resulting in the inability of those neurons to report pain for a period.
    C) TOXICOLOGY: Activates pain and heat neurons resulting in those sensations. Adverse effects are due to capsaicin's irritation of the skin, eyes, and respiratory tract.
    D) EPIDEMIOLOGY: Exposure is common; severe toxicity is rare. In the home setting, exposure to capsaicin is most commonly from capsaicin in peppers and occurs during food preparation. In the emergency department, exposure is most often from aerosolized capsaicin used for personal protection or riot control.
    E) WITH POISONING/EXPOSURE
    1) MILD TO MODERATE TOXICITY: Irritation, erythema, and burning pain without vesiculation following dermal or mucous membrane exposure are common. Lacrimation, blepharospasm, respiratory irritation, cough, vomiting, and diarrhea may also develop. Painful contact dermatitis may persist for several hours following exposure to pepper spray (capsaicin). Large oral ingestions can cause nausea, vomiting, abdominal pain, and rectal mucosal pain.
    2) SEVERE TOXICITY: Rare, but may include corneal abrasions, bronchospasm, severe respiratory distress, and acute lung injury. Hypokalemia, seizures and hypotension were reported in an infant following ingestion of capsaicin. Fatalities are extremely rare.
    3) PREDISPOSING CONDITIONS: Patients with underlying pulmonary disease, particularly asthma, emphysema, chronic bronchitis, or reactive airways, are at greater risk for more severe toxicity after exposure to aerosolized capsaicin.
    0.2.3) VITAL SIGNS
    A) WITH POISONING/EXPOSURE
    1) Hypothermia may develop acutely because of concurrent stimulation of the hypothalamic cooling center and warmth receptors. Conversely, hyperthermia can develop and is thought to be due to the desensitization or inactivation of heat dissipation mechanisms.
    0.2.20) REPRODUCTIVE
    A) Capsaicin topical patches have been classified as FDA pregnancy category B. There are no adequate and well-controlled studies of capsaicin topical patch use during pregnancy. It is not known if capsaicin is excreted into human breast milk. Infant capsaicin exposure can be minimized by the mother avoiding nursing after capsaicin treatment on the day of treatment since the drug is administered as a single 60-minute application and rapidly clears from the mother's bloodstream.

Laboratory Monitoring

    A) Most patients do not require laboratory evaluation.
    B) Monitor arterial blood gases, pulse oximetry, and pulmonary function tests, and obtain a chest radiograph in any patient with severe respiratory symptoms.

Treatment Overview

    0.4.2) ORAL/PARENTERAL EXPOSURE
    A) MANAGEMENT OF MILD TO MODERATE TOXICITY
    1) Adequate decontamination of dermal and ocular exposures and supportive care are the mainstays of treatment for mild to moderate exposures. DERMAL: Copious water irrigation may provide temporary pain relief. Magnesium-aluminum hydroxide-simethicone suspension (eg, Maalox (R)) applied as a dressing to the skin can provide immediate pain relief. EYE: Copious water irrigation may provide temporary pain relief. Ophthalmic topical anesthetics can be used in cases of severe ocular pain. Pain generally decreases an hour after exposure.
    B) MANAGEMENT OF SEVERE TOXICITY
    1) Supplemental oxygen should be administered to patients with signs of respiratory distress. Administer inhaled beta agonists for significant respiratory distress. Chest radiography can be obtained to examine for signs of pulmonary edema or acute lung injury. In extreme cases, mechanical ventilation may be necessary. Severe respiratory effects would only be expected in cases of exposure in enclosed spaces, repeated exposures, exposures in young children, or in cases of underlying respiratory disease.
    C) DECONTAMINATION
    1) PREHOSPITAL: DERMAL: Remove the patient's clothes and wash and irrigate the skin thoroughly. Apply a magnesium-aluminum hydroxide-simethicone suspension (eg, Maalox (R)) as a dressing to the skin to provide immediate pain relief. EYES: Copious water irrigation. INHALATION: Move patient to fresh air.
    2) HOSPITAL: DERMAL: Remove the patient's clothes and wash and irrigate the skin thoroughly. Apply a magnesium-aluminum hydroxide-simethicone suspension (eg, Maalox (R)) as a dressing to the skin to provide immediate pain relief. EYES: Copious water irrigation. INGESTION: Immediately dilute with 4-8 ounces of milk/water. Activated charcoal and gastric lavage are not indicated. INHALATION: Move to fresh air. If symptomatic, evaluate for irritation, bronchitis, or pneumonitis. 100% humidified oxygen as needed.
    D) AIRWAY MANAGEMENT
    1) Patients with severe respiratory distress may need ventilatory support in very rare cases.
    E) ANTIDOTE
    1) None
    F) ENHANCED ELIMINATION PROCEDURES
    1) There is no means of enhanced elimination.
    G) PATIENT DISPOSITION
    1) HOME CRITERIA: Patients with minor signs or dermal or ocular irritation can be observed at home.
    2) OBSERVATION CRITERIA: Patients with respiratory irritation or persistent dermal or persistent dermal or ocular irritation should be evaluated in a healthcare facility.
    3) ADMISSION CRITERIA: Patients with persistent respiratory symptoms should be admitted.
    4) CONSULT CRITERIA: Consult a poison center or medical toxicologist for assistance in managing severe poisonings.
    H) PITFALLS
    1) There can be minor aerosolization of capsaicin if patches are removed rapidly. Caregivers should avoid direct dermal contact with contaminated skin or clothing, and may develop mild respiratory irritation caring for a patient with heavy dermal exposure to capsaicin spray.
    I) PHARMACOKINETICS
    1) Dermal absorption is rapid although relief from pain after topical application may take weeks.
    J) TOXICOKINETICS
    1) Irritation to ocular and upper respiratory mucous membranes following an aerosolized exposure can be expected to be immediate.
    K) DIFFERENTIAL DIAGNOSIS
    1) Exposure to other respiratory and skin irritants, such as ammonia, chlorine, acids, alkaline substances, other lacrimators, may produce similar symptoms.
    0.4.3) INHALATION EXPOSURE
    A) Refer to "ORAL OVERVIEW" for more specific information.
    B) INHALATION: Move patient to fresh air. Monitor for respiratory distress. If cough or difficulty breathing develops, evaluate for respiratory tract irritation, bronchitis, or pneumonitis. Administer oxygen and assist ventilation as required. Treat bronchospasm with an inhaled beta2-adrenergic agonist. Consider systemic corticosteroids in patients with significant bronchospasm.
    0.4.4) EYE EXPOSURE
    A) DECONTAMINATION: Remove contact lenses and irrigate exposed eyes with copious amounts of room temperature 0.9% saline or water for at least 15 minutes. If irritation, pain, swelling, lacrimation, or photophobia persist after 15 minutes of irrigation, the patient should be seen in a healthcare facility.
    B) Ophthalmic topical anesthetics provide relief in most patients. Pain generally decreases an hour after exposure.
    0.4.5) DERMAL EXPOSURE
    A) OVERVIEW
    1) SUMMARY: Remove the patient's clothes and wash and irrigate the skin thoroughly. Apply a magnesium-aluminum hydroxide-simethicone suspension (eg, Maalox (R)) as a dressing to the skin to provide immediate pain relief.
    2) PEPPER SPRAY - An antacid suspension containing magnesium-aluminum hydroxide-simethicone, applied topically, has been shown to provide more rapid pain relief than saline treatments following dermal exposure to pepper-mace sprays containing capsaicin. Pain scores were significantly lower in the magnesium-aluminum hydroxide treatment group as compared to saline at 10, 20 and 30 minutes.
    3) DECONTAMINATION: Remove contaminated clothing and jewelry and place them in plastic bags. Wash exposed areas with soap and water for 10 to 15 minutes with gentle sponging to avoid skin breakdown. A physician may need to examine the area if irritation or pain persists (Burgess et al, 1999).
    4) Cold water has been recommended, but seldom provides long lasting relief.
    5) Vinegar water irrigation has been touted as producing relief, but has only been moderately successful.
    6) EMLA, an emulsion of lidocaine and prilocaine, may be used to treat skin that has been severely irritated by capsaicin. Relief from pain occurs approximately one hour after application of this mixture.
    7) Vegetable oil has been tested, and does provide better long term relief from the pain of "chile burns."

Range Of Toxicity

    A) TOXICITY: Respiratory of ocular exposure to very small amounts will produce toxic effects. Severe respiratory effects would only be expected in cases of exposure in enclosed spaces, repeated exposures, exposures in young children, or in cases of underlying respiratory disease. Concentrations of less than 10(-4) molar will cause a burning sensation when applied to the tongue.
    B) THERAPEUTIC DOSE: A thin layer of cream is typically applied to the affected area 3 to 4 times a day. A patch is typically applied for 60 minutes every 3 months.

Gastrointestinal

    3.8.2) CLINICAL EFFECTS
    A) ORAL SUBMUCOSAL FIBROSIS
    1) WITH POISONING/EXPOSURE
    a) Submucous fibrosis is a condition in which changes in the connective tissue of the palate occurs, was seen in India where there is a high intake of chili peppers. Recurrent oral vesicle formation was seen in 13% of one series of 104 cases (Smith et al, 1970).
    B) NAUSEA AND VOMITING
    1) WITH POISONING/EXPOSURE
    a) Nausea and vomiting may occur after ingestion of the plant containing capsaicin (Morton, 1971; Tominack & Spyker, 1987; Snyman et al, 2001) or following contact with pepper spray (Forrester & Stanley, 2003).
    b) Nausea has been reported in individuals exposed to "Pepperball Tactical Powder" pellets containing capsaicin. These pellets have been used to control riots (Hay et al, 2006).
    C) DIARRHEA
    1) WITH POISONING/EXPOSURE
    a) Diarrhea was seen in children who had jalapeno peppers and Tabasco(R) sauce placed in their mouth as punishment. An anal burning sensation also occurred (Tominack & Spyker, 1987).
    D) GASTRIC HEMORRHAGE
    1) WITH POISONING/EXPOSURE
    a) Epithelial cell damage and destruction may occur in the gastrointestinal tract with chronic administration of capsaicin (Desai et al, 1976).
    b) The effects on mucosal surfaces may range from mild erythema to edema and minute hemorrhagic spots (Viranuvatti et al, 1972; Desai et al, 1977; Kumar et al, 1984).
    c) Studies done in rats (Lippe et al, 1989; Holzer, 1989) and in humans (Graham et al, 1988), have failed to demonstrate gastric mucosal injury from capsicum.
    d) The administration of meals containing red pepper (0.1 to 1.5 g) or black pepper (1.5 g) to healthy human volunteers caused gastric cell exfoliation. Mucosal micro-bleeding was seen after spice administration and one subject had grossly visible gastric bleeding (Myers et al, 1987).
    E) TASTE SENSE ALTERED
    1) WITH POISONING/EXPOSURE
    a) Capsaicin is a lipid soluble phenol that may produce a pungent taste to water at a concentration of 1 to 11 parts per million of water (Tyler et al, 1981).
    1) Biting plants which contain capsaicin may cause acute stinging of lips, tongue, and oral mucosa.
    F) PERFORATION OF ESOPHAGUS
    1) WITH POISONING/EXPOSURE
    a) CASE REPORT: A 47-year-old man presented to the emergency department with severe abdominal and chest pain associated with severe retching and vomiting after eating ghost peppers a pepper grown in India and considered one of the hottest chili peppers with a measured "heat" of 1,000,000 Scoville Heat Units that is more than twice that of a habanero pepper. The patient was unresponsive to supportive therapy, including administration of an antacid, lidocaine and NG tube placement and lavage, and a chest x-ray was performed, revealing left-sided pleural effusion and patchy infiltrates. Pneumomediastinum with air around the distal esophagus, indicating a possible esophageal perforation (a 2.5 cm tear was present in the distal esophagus) and left-sided pneumothorax, was observed with an abdominal and pelvis CT scan and was confirmed with surgical intervention. Following surgery, the patient's hospital course was complicated with transient hypotension and a right sided pleural effusion requiring chest tube placement. The patient was extubated on day 14. With continued supportive care, the patient slowly improved with the ability to tolerate liquids on hospital day 17 (Arens et al, 2015).

Hematologic

    3.13.2) CLINICAL EFFECTS
    A) INCREASED FIBRINOLYSIS
    1) WITH POISONING/EXPOSURE
    a) One study done on Thai people who eat capsicum-containing peppers daily showed higher antithrombin III, lower plasma fibrinogen, increase fibrinolytic activity, and hypocoagulability (Visudhiphan et al, 1982).
    3.13.3) ANIMAL EFFECTS
    A) ANIMAL STUDIES
    1) PLATELET AGGREGATION
    a) ANIMALS: Capsicum inhibited platelet aggregation more potently than aspirin or indomethacin, but did not alter blood coagulation as measured by PT or PTT (Wang et al, 1985).

Dermatologic

    3.14.2) CLINICAL EFFECTS
    A) ERUPTION
    1) WITH POISONING/EXPOSURE
    a) Erythema and burning without vesiculation often occurs when applied topically to human skin (Smith et al, 1970; Burnett, 1989; Watson et al, 1996; Herman et al, 1998a), but blistering and rash may occur, especially after chronic or prolonged exposures (Morton, 1971).
    b) Exposure to pepper-mace spray containing 5% capsaicin has been reported to cause immediate and severe discomfort to the skin (Herman et al, 1998). Treatment with a topical solution of magnesium hydroxide/aluminum hydroxide/simethicone suspension improved symptoms immediately and then resolved completely within 2 minutes of topical application.
    c) "Pepperball Tactical Powder" pellets containing capsaicin have been used to control riots. When pellets are fired, the plastic casing ruptures on impact and the contents are discharged. Exposed individuals have experienced severe pain, erythema, stinging, and swelling. The injury sites may become infected, may cause scarring, and may heal with subsequent hyperpigmentation (Hay et al, 2006).
    d) According to a retrospective review of cases reported to the California Poison Control System between 2002 and 2011, 249 of 3671 (6.8%) cases reported pepper spray exposure in individuals 6 years of age or older who had severe outcomes warranting medical evaluation. Of the 249 patients, 44 patients (17.7%) reported rash and blisters (Kearney et al, 2014).
    B) PAIN
    1) WITH POISONING/EXPOSURE
    a) A condition in which an intense burning sensation and pain in the hands, possibly radiating up the arms, may occur after the hands are exposed to capsaicin-containing peppers during cooking or meal preparation. . Actual burns do not usually appear (Weinberg, 1981).
    b) "Pepperball Tactical Powder" pellets containing capsaicin have been used to control riots. When pellets are fired, the plastic casing will rupture on impact and the contents will be discharged. Exposed individuals have experienced severe pain, erythema, stinging, and swelling (Hay et al, 2006).
    C) DERMATITIS
    1) WITH POISONING/EXPOSURE
    a) Workers handling wet chilies developed dermatitis of the hands; the irritant even appears to penetrate rubber gloves. The dried fruit of plants containing capsaicin may have a vesicant effect, but in most cases, simply produces a burning sensation and mild erythema.

Endocrine

    3.16.3) ANIMAL EFFECTS
    A) ANIMAL STUDIES
    1) HYPOGLYCEMIA
    a) RATS: The aqueous extract of the fruits of Capsicum annum L of tropical regions caused a dose-dependent decrease in fasting blood glucose levels in rats either by oral or intraperitoneal route of administration.
    1) Pretreatment with 500 mg/kg of the extract administered orally or intraperitoneally improved the oral glucose curves, and the oral administration of extract reduced the intracardiac glucose tolerance curve.
    2) The hypoglycemic effect of capsicum may involve both the inhibition of intestinal glucose transport and its action upon systemic glucose metabolism (Ivorra et al, 1989).

Immunologic

    3.19.2) CLINICAL EFFECTS
    A) INCREASED TOLERANCE
    1) WITH POISONING/EXPOSURE
    a) Repeated dosing may not produce actual desensitization but rather a mental attitude change that permits tolerance (Rozin et al, 1982).
    b) Desensitization to the burning sensations and the rhinorrhea induced by topical capsaicin (75 mcg) developed and these effects were completely abolished after 4 to 5 applications of the drug (Geppetti et al, 1988).
    c) Desensitization of chemosensitive unmyelinated sensory nerve fibers with eventual loss of local tissue reaction may occur with topical application (Tominack & Spyker, 1987).

Reproductive

    3.20.1) SUMMARY
    A) Capsaicin topical patches have been classified as FDA pregnancy category B. There are no adequate and well-controlled studies of capsaicin topical patch use during pregnancy. It is not known if capsaicin is excreted into human breast milk. Infant capsaicin exposure can be minimized by the mother avoiding nursing after capsaicin treatment on the day of treatment since the drug is administered as a single 60-minute application and rapidly clears from the mother's bloodstream.
    3.20.2) TERATOGENICITY
    A) ANIMAL STUDIES
    1) Fetal teratogenicity was not evident when animals were treated during fetal organogenesis with capsaicin patches (at 11-fold margin over the maximum human recommended dose (MHRD) based on Cmax exposure) or with liquid (at 37-fold margin over the MHRD) (Prod Info QUTENZA(R) topical patch, 2013).
    3.20.3) EFFECTS IN PREGNANCY
    A) PREGNANCY CATEGORY
    1) Capsaicin topical patches have been classified as FDA pregnancy category B (Prod Info QUTENZA(R) topical patch, 2013).
    2) There are no adequate and well-controlled studies of capsaicin topical patch use during pregnancy (Prod Info QUTENZA(R) topical patch, 2013)
    B) ANIMAL STUDIES
    1) Exposure to capsaicin during gestation and lactation did not affect offspring survival, growth, learning and memory tests, sexual maturation, mating, pregnancy, and fetal development in an animal peri- and postnatal reproduction toxicology study (Prod Info QUTENZA(R) topical patch, 2013).
    2) Growth retardation and fewer matings and pregnancies occurred with prenatal capsaicin use in comparison with untreated rodents (Traurig et al, 1984).
    3.20.4) EFFECTS DURING BREAST-FEEDING
    A) BREAST MILK
    1) No adequate or well-controlled studies describing the use of capsaicin during human lactation are available. It is not known if capsaicin is excreted into human breast milk. Infant capsaicin exposure can be minimized by the mother avoiding nursing after capsaicin treatment on the day of treatment since the drug is administered as a single 60-minute application and rapidly clears from the mother's bloodstream (Prod Info QUTENZA(R) topical patch, 2013).
    B) ANIMAL STUDIES
    1) In an animal peri- and postnatal reproduction toxicology study, milk samples showed measurable levels of capsaicin after exposure (at 11-fold margin over the maximum human recommended dose) during gestation and lactation (Prod Info QUTENZA(R) topical patch, 2013).
    3.20.5) FERTILITY
    A) ANIMAL STUDIES
    1) Exposure to capsaicin patches significantly reduced the number and percent of motile sperm at doses of 13- to 28-fold over the maximum human recommended dose based on Cmax exposure. Sperm counts were reduced 79% compared with 69% with placebo. These reductions in sperm count did not demonstrate any adverse effects on fertility (Prod Info QUTENZA(R) topical patch, 2013).

Summary Of Exposure

    A) USES: HOME: Many of the peppers of the capsicum species are prepared and used in a variety foods and dishes. MEDICAL: Topical formulations are used to treat painful skin conditions. LAW ENFORCEMENT: The oleoresin of capsicum is used in some pepper "gas" sprays by law enforcement or for personal protection. PLANTS: Found in plants of the genus Capsicum (primarily chili peppers).
    B) PHARMACOLOGY: Topical application stimulates pain fibers and causes release of immunoreactive somatostatin. Most likely causes the depletion of substance P in pain and heat neurons resulting in the inability of those neurons to report pain for a period.
    C) TOXICOLOGY: Activates pain and heat neurons resulting in those sensations. Adverse effects are due to capsaicin's irritation of the skin, eyes, and respiratory tract.
    D) EPIDEMIOLOGY: Exposure is common; severe toxicity is rare. In the home setting, exposure to capsaicin is most commonly from capsaicin in peppers and occurs during food preparation. In the emergency department, exposure is most often from aerosolized capsaicin used for personal protection or riot control.
    E) WITH POISONING/EXPOSURE
    1) MILD TO MODERATE TOXICITY: Irritation, erythema, and burning pain without vesiculation following dermal or mucous membrane exposure are common. Lacrimation, blepharospasm, respiratory irritation, cough, vomiting, and diarrhea may also develop. Painful contact dermatitis may persist for several hours following exposure to pepper spray (capsaicin). Large oral ingestions can cause nausea, vomiting, abdominal pain, and rectal mucosal pain.
    2) SEVERE TOXICITY: Rare, but may include corneal abrasions, bronchospasm, severe respiratory distress, and acute lung injury. Hypokalemia, seizures and hypotension were reported in an infant following ingestion of capsaicin. Fatalities are extremely rare.
    3) PREDISPOSING CONDITIONS: Patients with underlying pulmonary disease, particularly asthma, emphysema, chronic bronchitis, or reactive airways, are at greater risk for more severe toxicity after exposure to aerosolized capsaicin.

Vital Signs

    3.3.1) SUMMARY
    A) WITH POISONING/EXPOSURE
    1) Hypothermia may develop acutely because of concurrent stimulation of the hypothalamic cooling center and warmth receptors. Conversely, hyperthermia can develop and is thought to be due to the desensitization or inactivation of heat dissipation mechanisms.
    3.3.3) TEMPERATURE
    A) WITH POISONING/EXPOSURE
    1) HYPOTHERMIA may develop acutely because of concurrent stimulation of the hypothalamic cooling center and warmth receptors (Tominack & Spyker, 1987).
    2) HYPERTHERMIA developed to various stimuli in rats after chronic administration of high doses. The possible mechanism is thought to be the desensitization or inactivation of heat dissipation mechanisms because of desensitized hypothalamic warmth receptor (Virus & Gebhart, 1979).

Heent

    3.4.3) EYES
    A) WITH POISONING/EXPOSURE
    1) SUMMARY: Tearing, stinging, and erythema result from accidental spraying of capsaicin into the eyes. Animal experimentation has shown more severe eye damage.
    2) CORNEAL damage may occur following exposures.
    a) SENSORY NEURON CHANGES: Topical application of capsaicin to the cornea produced changes in the fine structures of the sensory neurons (Carpenter & Lynn, 1981).
    b) ABRASIONS: Corneal abrasions were identified in 7 patients out of 30 (23%), by fluorescein staining following aerosol exposure to oleoresin capsicum (Watson et al, 1996). In a descriptive, retrospective review of 100 individuals exposed to aerosol pepper spray, 7 developed corneal abrasions. Based on this review, it could not be determined if the pepper spray compound, the carrier or propellant, or the patient rubbing their eyes produced the ocular effects observed (Brown et al, 2000).
    1) Conjunctival inflammation/hyperemia and corneal epithelium injuries were noted in 2 patients who were exposed to pepper spray. Several days after exposure, one patient was still noted to have a corneal erosion which improved with steroid therapy. Despite corneal healing, the patient had punctate epitheliopathy. In both cases, clinical improvement was noted over weeks to months, but the patients were lost to follow-up (Holopainen et al, 2003).
    c) EPITHELIAL DEFECT with STROMAL OPACITY: A woman was sprayed in the eyes with pepper spray during the course of her arrest and received no ocular irrigation for more than 9 hours. The right eye was asymptomatic. However, worsening ocular irritation in the left eye was noted at 24 hours and an initial ophthalmology exam revealed a visual acuity of 20/80, keratopathy, and an epithelial defect with moderate inflammation of the eye. Inflammation resolved over 2 weeks with supportive care, but the patient had a persistent stromal opacity with a corrected visual acuity of 20/40 (Epstein & Majmudar, 2001).
    d) ANIMALS: A single subcutaneous injection of 12.5, 25, or 50 mg/kg of capsaicin led to changes in the cornea of the mouse and rat, with histologic findings characterized by a loss of nerve axons in the corneal epithelium (Shimizer et al, 1984).
    1) These capsaicin-induced corneal lesions were latter shown to be suppressed by pretreatment with a subcutaneous injection of 6-hydroxydopamine and/or DSP4 (N-(2 chloroethyl)-N-ethyl-2-bromobenzylamine) (Shimizu et al, 1987).
    e) According to a retrospective review of cases reported to the California Poison Control System between 2002 and 2011, 249 of 3671 (6.8%) cases reported pepper spray exposure in individuals 6 years of age or older who had severe outcomes warranting medical evaluation. Of the 249 patients, 134 patients (53.8%) reported persistent pain, blurred vision, foreign body sensation, discharge or exudate, and periorbital swelling. Twelve cases documented corneal abrasions (Kearney et al, 2014).
    3) LACRIMATION: In a prospective, randomized study of 47 volunteers exposed to pepper spray (oleoresin capsicum), mean corneal sensitivity was 0.6 cm 10 minutes after exposure compared with 5.7 cm before exposure. Punctate epithelial erosions were observed in 21% of the eyes. On a short questionnaire, pain, blurring of vision, and tearing were rated by all subjects as significant at 10 minutes; however, all symptoms were markedly improved by 1 hour (Zollman et al, 2000).
    4) In a prospective, randomized study of 47 volunteers exposed to pepper spray (oleoresin capsicum), corneal sensitivity was decreased markedly at 10 minutes after exposure, improving by 1 hour (Zollman et al, 2000)
    5) BLEPHAROSPASM and obvious pain were seen in rats who had 50 mcg/mL dropped in their eyes (Grant & Schuman, 1993).
    6) IRRITATION may occur following eye exposures.
    a) CASE REPORT: A boy who accidentally sprayed capsaicin into his eyes from a dog repellent experienced stinging, tearing, and erythema, which cleared by the following day (Grant & Schuman, 1993).
    b) CASE SERIES: In a series of 81 patients who presented to the emergency department following aerosol exposure of oleoresin capsicum from law enforcement action, 45 (56%) developed ocular burning, 36 (44%) developed conjunctival injection, 32 (40%) developed erythema, 13 (16%) lacrimation and 7 (9%) developed corneal abrasion (Watson et al, 1996).
    7) KERATOUVEITIS was seen in rats who had retrobulbar injection of capsaicin. Inflammation onset was 6 to 12 hours (Waldrep & Crosson, 1988).
    3.4.5) NOSE
    A) WITH POISONING/EXPOSURE
    1) RHINORRHEA has occurred from inhalation or direct contact to the nasal mucosa.
    a) Touching the nasal mucosa after handling plants containing capsaicin may cause considerable irritation or pain.
    b) Fumes from burned plants or capsaicin sprays are highly irritating (Morton, 1971; Collier & Fuller, 1984).
    c) Topical application of capsaicin (75 mcg) to the human nasal mucosa was more potent than methacholine (50 mg) in inducing rhinorrhea (Geppetti et al, 1988).

Cardiovascular

    3.5.2) CLINICAL EFFECTS
    A) HYPOTENSIVE EPISODE
    1) WITH POISONING/EXPOSURE
    a) CASE REPORT: An 8-month-old infant was hypotensive and acidotic with hypokalemia and seizures when he was presented for medical care. He had a 7-day history of cough and 3 days of diarrhea and vomiting. He had been treated with an infusion made from capsaicin powder (dose and duration not specified). The child died on the day of hospital admission. It is not clear to what extent his underlying illness as opposed to the capsaicin exposure contributed to the clinical presentation (Snyman et al, 2001).
    B) MYOCARDIAL INFARCTION
    1) WITH POISONING/EXPOSURE
    a) CASE REPORT: A 25-year-old man, who had been taking oral cayenne pepper pills, for weight loss, once daily for 5 days prior to onset of symptoms, presented to the emergency department with a 2-hour history of severe chest pain, with the pain radiating to his left arm, neck, and jaw. An ECG showed ST segment elevation in leads II, III, and aVF, indicating an inferior wall acute myocardial infarction (AMI). The patient's troponin T concentration peaked at 4.6 ng/mL (normal less than 0.01 ng/mL). A coronary angiogram, performed 3 hours post-onset of chest pain, revealed patent coronary arteries. With supportive treatment, including administration of sublingual nitroglycerin, the patient's pain and ECG abnormalities resolved. The patient had no risk factors for coronary artery disease and denied the use of illicit substances, suggesting that the AMI was a result of coronary vasospasm secondary to capsaicin use (Sogut et al, 2012).
    3.5.3) ANIMAL EFFECTS
    A) ANIMAL STUDIES
    1) HYPOTENSION
    a) When injected into rats, an initial fall, transient rise, then a secondary fall in blood pressure was noted. Treatment with adrenoceptors or cholineceptors was ineffective (Donnerer & Lembeck, 1982; Toda et al, 1972).

Carcinogenicity

    3.21.3) HUMAN STUDIES
    A) MUCOUS MEMBRANE DISORDER
    1) The carcinogenic potential of capsaicin is currently the subject of discussion. Although a precancerous condition, oral submucosal fibrosis, associated with connective tissue hyperplasia of the palate and faucial pillars, has a strong association with the ingestion of chili peppers (Burnett, 1989).

Respiratory

    3.6.2) CLINICAL EFFECTS
    A) BRONCHOSPASM
    1) WITH POISONING/EXPOSURE
    a) Capsaicin vapors, especially from burning, may cause significant pulmonary irritation and prolonged cough (Snyman et al, 2001; Morton, 1971; Collier & Fuller, 1984).
    1) CASE REPORT (CHILD): Capsaicin spray produced severe bronchospasm and pulmonary edema in a child (Winograd, 1977).
    2) Increased airway resistance may be seen after inhalation of capsaicin (Fuller, 1991).
    b) Bronchospasm, independent of histamine or acetylcholine mechanism, can be created by placing capsaicin on human bronchial preparations in vitro. The effect is similar to what is seen with substance P (Lundberg et al, 1983).
    c) CASE SERIES: Five patients presented to the emergency department with shortness of breath or wheezing after exposure to oleoresin capsicum spray (Watson et al, 1996).
    d) According to a retrospective review of cases reported to the California Poison Control System between 2002 and 2011, 249 of 3671 (6.8%) cases reported pepper spray exposure in individuals 6 years of age or older who had severe outcomes warranting medical evaluation. Of the 249 patients, 79 patients (31.7%) reported shortness of breath, chest tightness, and wheezing. Ten cases documented wheezing and bronchospasm (Kearney et al, 2014).
    B) RESPIRATORY FINDING
    1) WITH POISONING/EXPOSURE
    a) CASE REPORT: A 32-year-old healthy male, corrections officer, was exposed to pepper spray (approximately 3 to 4 feet from the source) during training and developed persistent shortness of breath and an inability to exercise. Forty-eight hours after exposure, a posterior and lateral chest x-ray and a CT scan of the chest were consistent with a pneumomediastinum and pneumopericardium likely due to severe coughing which gradually resolved. Upon further examination 3 months later, pulmonary function studies and lung volumes were within normal limits, but the patient was noted to have high resistance which was consistent with mild airway dysfunction. The patient denied any history of reactive airway disease. The authors concluded that, in general, individuals with a history of reactive airway disease or COPD may be at risk to develop hypersensitivity following exposure, but further study was suggested (Miller & Skolnick, 2006).
    b) CASE REPORT: A 47-year-old woman presented to an outpatient pulmonary clinic with a 9-month history of chronic respiratory symptoms, including episodic dyspnea and wheezing that occurred every 1 to 2 days and would last for 4 to 5 hours. Interview of the patient revealed that she had been exposed to high concentrations of oleoresin capsicum gas (capsaicin) for greater than 20 minutes, and subsequently developed right-sided pleuritic chest pain, dyspnea, and cough, progressing to episodic dyspnea and cough over the next several months. At the outpatient clinic, her pulmonary function tests and chest x-ray were normal, with no evidence of infiltrates or bronchial disease, although she did have a positive methacholine challenge test, with a greater than 20% reduction in her FEV1. She was prescribed a budesonide/formoterol combination inhaler and, two months later, reported improvement but continued to have episodic dyspnea. She also reported greater sensitivity to environmental irritants (eg, scents, perfumes, cigarette smoke). Her score was 43 on the chemical sensitivity scale for sensory hyperreactivity (score range 1 to 55; 43 or higher is considered a high score). It is suspected that the patient developed airway sensory hyperreactivity syndrome following intense exposure to capsaicin (Copeland & Nugent, 2013).
    C) HYPERVENTILATION
    1) WITH POISONING/EXPOSURE
    a) Capsaicin, when inhaled using a nebulizer which produced a 10(-7) concentration, increased the mean inspiratory flow by inducing more rapid, but not shallower breathing (Maxwell et al, 1987).
    D) IRRITATION SYMPTOM
    1) WITH POISONING/EXPOSURE
    a) SMOKE EXPOSURE: The smoke of burning chilies is also an irritant.

Neurologic

    3.7.2) CLINICAL EFFECTS
    A) PAIN
    1) WITH POISONING/EXPOSURE
    a) Capsaicin renders the skin of humans and animals insensitive to various types of chemical pain stimuli (Bernstein et al, 1981).
    B) SEIZURE
    1) WITH POISONING/EXPOSURE
    a) CASE REPORT: An 8-month-old infant was hypotensive and acidotic with hypokalemia and seizures when he was presented for medical care. He had a 7-day history of cough and 3 days of diarrhea and vomiting. He had been treated with an infusion made from capsaicin powder (dose and duration not specified). The child died on the day of hospital admission. It is not clear to what extent his underlying illness as opposed to the capsaicin exposure contributed to the clinical presentation (Snyman et al, 2001).
    C) VASODILATATION
    1) WITH POISONING/EXPOSURE
    a) Skin treated with capsaicin will have reduced flare (vasodilatation) and reduced heat sensitivity. There is some evidence that the damage may be long lasting, especially with chronic exposure (Carpenter & Lynn, 1981).

Monitoring Parameters Levels

    4.1.1) SUMMARY
    A) Most patients do not require laboratory evaluation.
    B) Monitor arterial blood gases, pulse oximetry, and pulmonary function tests, and obtain a chest radiograph in any patient with severe respiratory symptoms.
    4.1.2) SERUM/BLOOD
    A) TOXICITY
    1) Most patients do not require laboratory evaluation.
    4.1.4) OTHER
    A) OTHER
    1) Monitor arterial blood gases, pulse oximetry, and pulmonary function tests, and obtain a chest radiograph in any patient with severe respiratory symptoms.

Life Support

    A) Support respiratory and cardiovascular function.

Patient Disposition

    6.3.1) DISPOSITION/ORAL EXPOSURE
    6.3.1.1) ADMISSION CRITERIA/ORAL
    A) Patients with persistent respiratory symptoms should be admitted.
    6.3.1.2) HOME CRITERIA/ORAL
    A) Patients with minor signs or dermal or ocular irritation can be observed at home.
    6.3.1.3) CONSULT CRITERIA/ORAL
    A) Consult a poison center or medical toxicologist for assistance in managing severe poisonings.
    6.3.1.5) OBSERVATION CRITERIA/ORAL
    A) Patients with respiratory irritation or persistent dermal or persistent dermal or ocular irritation should be evaluated in a healthcare facility.

Monitoring

    A) Most patients do not require laboratory evaluation.
    B) Monitor arterial blood gases, pulse oximetry, and pulmonary function tests, and obtain a chest radiograph in any patient with severe respiratory symptoms.

Oral Exposure

    6.5.1) PREVENTION OF ABSORPTION/PREHOSPITAL
    A) PREHOSPITAL: DERMAL: Remove the patient's clothes and wash and irrigate the skin thoroughly. Apply a magnesium-aluminum hydroxide-simethicone suspension (eg, Maalox (R)) as a dressing to the skin to provide immediate pain relief. EYES: Copious water irrigation. INHALATION: Move patient to fresh air.
    6.5.2) PREVENTION OF ABSORPTION
    A) SUMMARY: Immediately dilute with 4-8 ounces of milk/water. Activated charcoal and gastric lavage are not indicated.
    B) DILUTION
    1) DILUTION: If no respiratory compromise is present, administer milk or water as soon as possible after ingestion. Dilution may only be helpful if performed in the first seconds to minutes after ingestion. The ideal amount is unknown; no more than 8 ounces (240 mL) in adults and 4 ounces (120 mL) in children is recommended to minimize the risk of vomiting (Caravati, 2004).
    6.5.3) TREATMENT
    A) MONITORING OF PATIENT
    1) Most patients do not require laboratory evaluation.
    2) Monitor arterial blood gases, pulse oximetry, and pulmonary function tests, and obtain a chest radiograph in any patient with severe respiratory symptoms.

Inhalation Exposure

    6.7.1) DECONTAMINATION
    A) Move patient from the toxic environment to fresh air. Monitor for respiratory distress. If cough or difficulty in breathing develops, evaluate for hypoxia, respiratory tract irritation, bronchitis, or pneumonitis.
    B) OBSERVATION: Carefully observe patients with inhalation exposure for the development of any systemic signs or symptoms and administer symptomatic treatment as necessary.
    C) INITIAL TREATMENT: Administer 100% humidified supplemental oxygen, perform endotracheal intubation and provide assisted ventilation as required. Administer inhaled beta-2 adrenergic agonists, if bronchospasm develops. Consider systemic corticosteroids in patients with significant bronchospasm (National Heart,Lung,and Blood Institute, 2007). Exposed skin and eyes should be flushed with copious amounts of water.
    6.7.2) TREATMENT
    A) BRONCHOSPASM
    1) BRONCHOSPASM SUMMARY
    a) Administer beta2 adrenergic agonists. Consider use of inhaled ipratropium and systemic corticosteroids. Monitor peak expiratory flow rate, monitor for hypoxia and respiratory failure, and administer oxygen as necessary.
    2) ALBUTEROL/ADULT DOSE
    a) 2.5 to 5 milligrams diluted with 4 milliliters of 0.9% saline by nebulizer every 20 minutes for three doses. If incomplete response, administer 2.5 to 10 milligrams every 1 to 4 hours as needed OR administer 10 to 15 milligrams every hour by continuous nebulizer as needed. Consider adding ipratropium to the nebulized albuterol; DOSE: 0.5 milligram by nebulizer every 30 minutes for three doses then every 2 to 4 hours as needed, NOT administered as a single agent (National Heart,Lung,and Blood Institute, 2007).
    3) ALBUTEROL/PEDIATRIC DOSE
    a) 0.15 milligram/kilogram (minimum 2.5 milligrams) diluted with 4 milliliters of 0.9% saline by nebulizer every 20 minutes for three doses. If incomplete response administer 0.15 to 0.3 milligram/kilogram (maximum 10 milligrams) every 1 to 4 hours as needed OR administer 0.5 mg/kg/hr by continuous nebulizer as needed. Consider adding ipratropium to the nebulized albuterol; DOSE: 0.25 to 0.5 milligram by nebulizer every 20 minutes for three doses then every 2 to 4 hours as needed, NOT administered as a single agent (National Heart,Lung,and Blood Institute, 2007).
    4) ALBUTEROL/CAUTIONS
    a) The incidence of adverse effects of beta2-agonists may be increased in older patients, particularly those with pre-existing ischemic heart disease (National Asthma Education and Prevention Program, 2007). Monitor for tachycardia, tremors.
    5) CORTICOSTEROIDS
    a) Consider systemic corticosteroids in patients with significant bronchospasm. PREDNISONE: ADULT: 40 to 80 milligrams/day in 1 or 2 divided doses. CHILD: 1 to 2 milligrams/kilogram/day (maximum 60 mg) in 1 or 2 divided doses (National Heart,Lung,and Blood Institute, 2007).
    B) Treatment should include recommendations listed in the ORAL EXPOSURE section when appropriate.

Eye Exposure

    6.8.1) DECONTAMINATION
    A) EYE IRRIGATION, ROUTINE: Remove contact lenses and irrigate exposed eyes with copious amounts of room temperature 0.9% saline or water for at least 15 minutes. If irritation, pain, swelling, lacrimation, or photophobia persist after 15 minutes of irrigation, an ophthalmologic examination should be performed (Peate, 2007; Naradzay & Barish, 2006).
    6.8.2) TREATMENT
    A) LOCAL ANESTHESIA
    1) TOPICAL PROPARACAINE vs. FLURBIPROFEN: In a prospective randomized study of 47 subjects with ocular exposure to pepper spray (oleoresin capsicum), topical proparacaine 0.5% improved ocular symptoms (ie, pain, blurred vision, tearing) in 16 of 29 eyes, while topical flurbiprofen, a nonsteroidal antiinflammatory, was effective in 2 eyes. A decrease in pain was noted in most subjects an hour after exposure (Zollman et al, 2000).
    B) IRRITATION SYMPTOM
    1) Animals whose eyes were exposed to 50 micrograms/milliliter capsaicin were treated with local anesthetic which did relieve pain, but did not alter the erythema (Grant, 1986).
    C) Treatment should include recommendations listed in the ORAL EXPOSURE section when appropriate.

Dermal Exposure

    6.9.1) DECONTAMINATION
    A) ANTACID SUSPENSION
    1) MAGNESIUM-ALUMINUM HYDROXIDE: A double-blind, randomized, controlled, prospective study (n=10) compared the effectiveness of magnesium-aluminum hydroxide-simethicone suspension (eg, Maalox (R)) with saline treatment following dermal capsicin exposure. Dressings were embedded with the antacid solution or saline and then applied to the exposed skin. Statistically significant pain relief was reported at 10, 20 and 30 minutes in the magnesium-aluminum hydroxide group, as compared to the saline group; no differences were found at 60, 90 and 120 minutes (Lee & Ryan, 2003).
    2) A magnesium hydroxide-aluminum hydroxide-simethicone suspension was topically applied to several individuals following dermal exposure to pepper-mace sprays containing capsaicin. All patients experienced immediate and sustained relief following application of the antacid suspension to the different cutaneous areas (Herman et al, 1998a). A mechanism of action has not been established.
    B) WARM WATER
    1) Wash exposed areas several times with warm water and soap. The capsaicin is more soluble in warm water than in cold water and is more soluble in alcohol as well.
    2) Small amounts of alcohol might solubilize the remaining capsaicin if it is felt that previous washings have not decontaminated the area, and the exposed area is not abraded or a mucous membrane.
    C) COLD WATER
    1) Cold water has been recommended but seldom provides long term relief (Weinberg, 1981). In a study done by Jones et al (1987) cool tap water immersion provided initial relief, but not as enduring a pain relief as immersion in vegetable oil.
    6.9.2) TREATMENT
    A) LOCAL ANESTHETIC
    1) Lidocaine gel was useful in treating a case of capsaicin-induced Hunan hand (Weinberg, 1981).
    2) EMLA, an emulsion of lidocaine and prilocaine, may be used to treat skin that has been severely irritated by capsaicin. Relief from pain occurs approximately one hour after application of this mixture (Robieux et al, 1990; Robieux et al, 1992).
    B) GENERAL TREATMENT
    1) RANDOMIZED STUDY: A randomized controlled trial was conducted comparing the efficacy of an antacid suspension (aluminum hydroxide-magnesium hydroxide), 2% lidocaine gel, baby shampoo, milk, or water for treatment of acute pain following dermal exposure to oleoresin capsaicin (pepper spray). Forty-nine adult volunteers were sprayed in the face with pepper spray, began initial self-decontamination with water 2 minutes later, and then were randomized to treatment with one of the five treatment groups (antacid, lidocaine, baby shampoo, milk, or water). The volunteers then rated their pain on a 10-cm visual analog scale (VAS) every 10 minutes over a 60-minute period. The results showed that, although there was a significant difference in pain over time, there appeared to be no significant difference in pain between the treatment groups (Barry et al, 2008).
    2) VEGETABLE OIL - May provide some relief.
    3) In a study by Jones et al (1987), 20 volunteers immersed their hands in a standardized green chile slurry for 40 minutes:
    a) One hand was placed in cool water; the other in vegetable oil for 75 minutes.
    b) Pain was evaluated on a visual analog scale. Cool tap water gave relief more quickly, while vegetable oil provided longer lasting relief.
    c) A mechanism of action has not been established.
    C) Treatment should include recommendations listed in the ORAL EXPOSURE section when appropriate.

Case Reports

    A) PEDIATRIC
    1) A 4-week-old infant was unintentionally sprayed in the face with his mother's self-defense (5% pepper gas) spray. There was an immediate onset of gasping and epistaxis followed by hypotonia, apnea, and cyanosis. Chest radiograph showed bilateral parenchymal infiltrates (Wiley et al, 1995).
    a) The infant had progressive worsening of pulmonary gas exchange and copious tracheal secretions, profound anemia, hematuria, and transient hyperkalemia. He was treated with 138 hours of venoarterial extracorporeal membrane oxygenation (ECMO) and 48 hours after ending ECMO the patient was stable and breathing spontaneously (Wiley et al, 1995).

Summary

    A) TOXICITY: Respiratory of ocular exposure to very small amounts will produce toxic effects. Severe respiratory effects would only be expected in cases of exposure in enclosed spaces, repeated exposures, exposures in young children, or in cases of underlying respiratory disease. Concentrations of less than 10(-4) molar will cause a burning sensation when applied to the tongue.
    B) THERAPEUTIC DOSE: A thin layer of cream is typically applied to the affected area 3 to 4 times a day. A patch is typically applied for 60 minutes every 3 months.

Therapeutic Dose

    7.2.1) ADULT
    A) GENERAL
    1) The dose of capsicum (not capsaicin) used for induction of peristalsis is approximately 60 mg (Tyler et al, 1981).
    2) Adults in many tropical countries ingest up to 3 g/day of capsicum in food products (Desai et al, 1976).
    B) TOPICAL PATCH
    1) The recommended dose is a single, 60-minute application of up to 4 patches (8% capsaicin; 179 mg/patch), which may be repeated no more often than every 3 months (Prod Info QUTENZA(R) topical patch, 2013).
    C) TOPICAL CREAM, GEL, OR LOTION
    1) Apply to the affected area not more than 3 or 4 times/day (OTC Product Information, as posted to the DailyMed site 05/2014; OTC Product Information, as posted to the DailyMed site 03/2013; OTC Product Information, as posted to the DailyMed site 09/2011).
    7.2.2) PEDIATRIC
    A) TOPICAL CREAM OR PATCH
    1) Safety and efficacy have not been established in pediatric patients younger than 18 years (OTC Product Information, as posted to the DailyMed site 05/2014; Prod Info QUTENZA(R) topical patch, 2013).
    B) TOPICAL GEL
    1) 12 YEARS OR OLDER: Apply to the affected area not more than 3 or 4 times/day (OTC Product Information, as posted to the DailyMed site 03/2013).
    C) TOPICAL LOTION
    1) 6 YEARS OR OLDER: Apply to the affected area not more than 3 or 4 times/day (OTC Product Information, as posted to the DailyMed site 09/2011).

Maximum Tolerated Exposure

    A) DERMAL EXPOSURE
    1) Erythema and burning without vesiculation often occurs when applied topically to human skin (Smith et al, 1970), but blistering and rash may occur especially after chronic or prolonged exposures (Morton, 1971).
    2) Exposure to pepper-mace spray containing 5% capsaicin has been reported to cause immediate and severe discomfort to the skin (Herman et al, 1998).
    B) INHALATION EXPOSURE
    1) Capsaicin vapors, especially from burning, may cause significant pulmonary irritation and prolonged cough (Snyman et al, 2001; Morton, 1971; Collier & Fuller, 1984).
    a) CASE REPORT (SPRAY): One case has been reported where a capsaicin spray produced severe bronchospasm and pulmonary edema (Winograd, 1977).
    b) Increased airway resistance may be seen after inhalation of capsaicin (Fuller, 1991).
    c) CASE SERIES (SPRAY): Five patients presented to the emergency department with shortness of breath or wheezing after exposure to oleoresin capsicum spray (Watson et al, 1996).
    C) CONCENTRATION LEVEL
    1) HUMAN: Concentrations of less than 10(-4) molar will cause a burning sensation when applied to the tongue.
    2) EXPERIMENTAL: When capsaicin doses of 0.01, 0.1, 1, 10, and 100 mcg were injected intradermally, the magnitude and duration of pain, as well as the area and duration of mechanical hyperalgesia increased as a negative accelerating function of dose (Simone et al, 1989).

Pharmacologic Mechanism

    A) When given as a pretreatment or by rapid IV infusion in experimental animals, capsaicin has shown antitussive and antibronchoconstrictor activity (O'Neill, 1991 (Suppl A)).

Toxicologic Mechanism

    A) SUBSTANCE P
    1) Capsaicin appears to first induce the release of substance P (SP) from a neuron, then block the synthesis and transport of SP to the effector side of the axon reflex (Tominack & Spyker, 1987; Bernstein, 1988); De & Ghosh, 1990.
    2) Substance P depolarizes neurons to produce dilation of blood vessels, stimulation of smooth muscle, and activation of sensory nerve endings (Tominack & Spyker, 1987; Helme et al, 1987).
    B) Capsaicin effects were characterized as an initial intense excitation of certain sensory neurons. This is followed by a lengthy period of insensitivity to physicochemical stimuli, including the natural environmental stimuli for the sensory nerve endings (Buck & Burks, 1986).
    C) Capsaicin is without effects in the motor system (Tominack & Spyker, 1987).
    D) Capsaicin's site of action may be at the axon rather than on the receptor terminals (Carpenter & Lynn, 1981). Capsaicin has been shown to stimulate pain fibers and release immunoreactive somatostatin (Gamse et al, 1981).

Physical Characteristics

    A) This compound exists as a white solid.

Molecular Weight

    A) 305.4

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