Caffeine Toxicity

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Caffeine Toxicity

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Caffeine (1,3,7-trimethylxanthine; see the image below) is the most widely consumed stimulant drug in the world. [1] It is present in a variety of forms: medications, coffee, tea, soft drinks, and chocolate. Because caffeine overdoses, intentional or unintentional, are relatively common in the United States, physicians and other medical personnel must be aware of caffeine toxicity to recognize and treat it appropriately.

When acute caffeine ingestion is suspected, the history should address the following:

Use of prescription medications or over-the-counter (OTC) drugs

Use of illicit drugs

Recent caffeine ingestion or recent behavior compatible with such ingestion

When ingested in excessive amounts for extended periods, caffeine produces a specific toxidrome (caffeinism), which consists primarily of the following features:

Central nervous system (CNS) – Headache, lightheadedness, anxiety, agitation, tremulousness, perioral and extremity tingling, confusion, psychosis, seizures

Cardiovascular – Palpitations or racing heart rate, chest pain

Gastrointestinal (GI) – Nausea and vomiting, abdominal pain, diarrhea, bowel incontinence, anorexia

CNS findings on physical examination include the following:

Anxiety, agitation

Tremors

Seizures

Altered mental status

Head, eyes, ears, nose, and throat findings

Pupils that are dilated but reactive to light

The thyroid should be examined because thyrotoxicosis may mimic caffeine toxicity.

Cardiovascular findings on physical examination include the following:

Widened pulse pressure

Sinus tachycardia, dysrhythmias

Hypotension

Tachypnea

GI findings on physical examination include the following:

Vomiting

Abdominal cramping

Hyperactive bowel sounds

See Presentation for more detail.

In hemodynamically stable patients with mild symptoms and a clear history of caffeine ingestion, no laboratory studies are indicated. Laboratory studies are indicated in patients with moderate-to-severe symptoms of caffeine toxicity. The following studies may be helpful:

Complete blood count (CBC)

Serum electrolyte, glucose, blood urea nitrogen (BUN), and creatinine concentrations

Routine screening for other potentially treatable toxins

Total creatine kinase (CK) concentrations

Dipstick urinalysis

Rapid urine drug screen

Serum ethanol concentrations and osmolality (in cases of unknown ingestion or suspected coingestion)

Serum pregnancy test

Thyroid studies

Arterial blood gas analysis

Serum caffeine concentration determinations do not influence management.

In hemodynamically stable patients with only mild symptoms, no diagnostic imaging is required. The following studies may be considered in particular circumstances:

Chest radiograph – In patients with chest pain, fever, altered mental status, or respiratory complaints

Unenhanced computed tomography (CT) of the head – In patients with seizures or altered mental status despite initial resuscitation

Patients with chest pain, palpitations, tachycardia, or an irregular heart rhythm should be evaluated with electrocardiography (ECG) and telemetry monitoring.

See Workup for more detail.

Prehospital care is primarily supportive, and most cases resolve. Emergency management of more severe cases includes the following:

ABCs (Airway, Breathing, Circulation)

Management of hypotension

Correction of dysrhythmias

Management of seizures (with benzodiazepines or barbiturates)

Correction of metabolic disturbances (hypokalemia, rhabdomyolysis, hyperglycemia, metabolic acidosis)

Treatment of prolonged vomiting

Decontamination with activated charcoal, sorbitol, or both

In rare severe cases, hemoperfusion or hemodialysis

Consultations may include a regional poison control center, a medical toxicologist, or a psychiatrist (once the patient is medically stable). Medically unstable patients are admitted for the appropriate level of care, depending on the clinical presentation.

See Treatment and Medication for more detail.

About 85% of adults in the United States drink at least one caffeinated beverage a day, [2] as do 73% of children. [3] Caffeine intake intake in US children and adolescents remained stable from 1999 to 2010, but sources of caffeine changed: the contribution of soda decreased from 62% to 38% while that of coffee increased from 10% to nearly 24% and energy drinks (which did not exist in 1999) increased to nearly 6%. [3]  In a 2014 nationally representative cross-sectional survey, nearly nearly two thirds of US adolescents aged 13-17 years reported ever using energy drinks, and 41% had done so in the past 3 months. [4]

A study published by the US Food and Drug Administration (FDA) reported that in 2003-2008, the average adult consumed about 300 mg caffeine/day, with teenagers consuming roughly 100 mg/d. [5] In quantities found in food and beverages, caffeine is unlikely to cause acute medical problems; however, a changing market in which energy drinks are not subject to FDA regulatory standards has raised concerns over caffeine-related health problems.

In 1989, the US Food and Drug Administration (FDA) limited the amount of caffeine in OTC products to a maximum of 200 mg/dose. Caffeine is present in concentrated forms in OTC products such as alertness-promoting medications (eg, NoDoz, Vivarin), menstrual aids (eg, Midol), analgesics (eg, Excedrin, Anacin, BC Powder), and diet aids (eg, Dexatrim). Caffeine is also a component of prescription medications (eg, Fioricet, Cafergot) and herbal preparations.The ingestion of such concentrated sources of caffeine is the general cause of acute caffeine toxicity. See the image below for caffeine equivalents of common products.

Caffeine has differing CNS, cardiovascular, and metabolic effects based on the quantity ingested. Average doses of caffeine (85-250 mg, the equivalent of 1-3 cups of coffee) may result in feelings of alertness, decreased fatigue, and eased flow of thought. High doses (250-500 mg) can result in restlessness, nervousness, insomnia, and tremors. In high doses, caffeine can cause a hyperadrenergic syndrome resulting in seizures and cardiovascular instability.

Because caffeine overdoses, intentional or unintentional, are relatively common in the United States, physicians and other medical personnel must be aware of caffeine toxicity to recognize and treat it appropriately.

In cola beverages, caffeine is permitted by the FDA for flavor use at a 0.02% (0.2 mg/mL) concentration, equivalent to 20 mg in a 100-mL beverage or 71 mg in a 12-ounce beverage (Code of Federal Regulations, title 21, sec. 182.1180). [6] Because caffeine is not considered a nutrient, the FDA does not require manufacturers to label the amount of caffeine present in food and beverages, although caffeine must be listed as an ingredient if the manufacturer adds it to their product. [7]

Although caffeine is found in food and over-the-counter products, more than 97% of caffeine consumed by adults and teenagers comes from beverages, including coffee, tea, cola-products, and energy drinks. [5] Unlike cola-beverages, energy drinks and shots are typically classified as dietary supplements; thus, individuals who consume these products are likely unaware of how much caffeine they are actually consuming. [7]  See Table 1, below.

Table 1. Reported Caffeine Content of Common  Beveragesref4} (Open Table in a new window)

Item

Amount

Caffeine Content, mg

Coca-Cola Classic

12 oz

35

Brewed black tea, generic

8 oz

45-74

Red Bull Regular

8.4 oz

80

Brewed coffee, generic

8 oz

57

Regular 5-Hour Energy

2 oz

138

Rockstar

16 oz

160

Monster Energy

16 oz

160

Espresso, generic

1 oz

170

NOS

16

280

Starbucks Tall Americano

16

330

The caffeine content of dietary supplements is virtually unregulated by the FDA. Prior to the Dietary Supplement Health and Education Act (DSHEA) of 1994, dietary supplements were subject to the same regulatory requirements as other foods; however, after DSHEA, the safety of dietary supplements became the sole responsibility of manufacturers. Consequentially, there are no limitations on the amount of caffeine in dietary supplements and manufacturers are not required to list the caffeine content of their products.

In 2018, the FDA issued a new guidance regulating the sale of “bulk quantities” (packages containing enough powder or liquid for thousands of recommended servings) of pure or highly concentrated caffeine in powder or liquid forms sold directly to consumers. However the FDA did not address preexisting beverages. [8]  

The rising popularity of caffeinated energy drinks over the past decade has raised new concerns about their impact on public health. As illustrated above, energy drinks contain substantially more caffeine than conventional cola beverages, with caffeine content ranging from 75-300 mg per serving. Many also contain caffeine-containing ingredients such as guarana, kola nut, or yerba mate. Consequentially, they may contain more caffeine than reported in Table 1 above. [9] These energy drinks are also sold in larger sizes (16-23.5 fl oz). It is not uncommon for individuals to consume multiple caffeinated beverages over the course of a day.

Caffeine has differing CNS, cardiovascular, and metabolic effects based on the quantity ingested. Average doses of caffeine (85-250 mg, the equivalent of 1-3 cups of coffee) may result in feelings of alertness, decreased fatigue, and eased flow of thought. High doses (250-500 mg) can result in restlessness, nervousness, insomnia, and tremors. In high doses, caffeine can cause a hyperadrenergic syndrome resulting in seizures and cardiovascular instability.

Because caffeine overdoses, intentional or unintentional, are relatively common in the United States, physicians and other medical personnel must be aware of caffeine toxicity to recognize and treat it appropriately.

Caffeine, a methylxanthine, is closely related to theophylline. Caffeine is rapidly and completely absorbed from the GI tract; it is detectable in the plasma 5 minutes after ingestion, with peak plasma levels occurring in 30-60 minutes. The volume of distribution in adults is approximately 0.5 L/kg.

Caffeine is primarily metabolized by the cytochrome P450 (CYP) oxidase system in the liver. The plasma half-life of caffeine varies considerably from person to person, with an average half-life of 5-8 hours in healthy, nonsmoking adults. Caffeine clearance is accelerated in smokers; clearance is slowed in pregnancy, in liver disease, and in the presence of some CYP inhibitors (eg, cimetidine, quinolones, erythromycin). In addition, the hepatic enzyme system responsible for caffeine metabolism can become saturated at high levels, resulting in a marked increase in serum concentration with small additional doses.

Various mechanisms mediate the effects of caffeine in the human body. Caffeine directly stimulates respiratory and vasomotor centers of the brain and acts as an adenosine antagonist, resulting in peripheral vasodilatation and CNS stimulation. Caffeine is a potent releaser of catecholamines (norepinephrine and, to a lesser extent, epinephrine) that increases cardiac chronotropic and inotropic activity, bronchodilation, and peripheral vasodilatation. Caffeine is also a phosphodiesterase inhibitor. However, because extremely high concentrations of caffeine are required to inhibit this enzyme, whether this effect contributes to the clinical effects of caffeine in vivo is unknown.

In addition to its cardiovascular effects, caffeine induces a number of metabolic changes, including hyperglycemia (by stimulating gluconeogenesis and glycogenolysis), increased renal filtration, ketosis, and hypokalemia. Caffeine is a potent stimulator of gastric acid secretion and GI motility.

Death from caffeine toxicity is rare, but it has been reported due to dysrhythmias, seizures, and aspiration of emesis. Oral doses of caffeine greater than 10 g can be fatal in adults. [10] A daily intake of 400 mg—about four or five cups of coffee—is considered safe for adults, while 200 mg is considered safe for pregnant women. [7, 11]

Caffeine poisoning is a relatively common toxicologic emergency in the United States, and the number of cases has steadily increased in the past decade. The Substance Abuse and Mental Health Services Administration (SAMHSA) reported a jump in the number of emergency department visits involving energy drinks, increasing roughly 10-fold from 2005 (1128 visits) to 2008 and 2009 (16,053 and 13,114 visits, respectively). More than half of the visits made by patients age 18-25 years involved the combination of energy drinks with alcohol or other drugs. [12]  Between 2007 and 2011 the number of energy drink related visits to the emergency room doubled.  [13]

The American Association of Poison Control Centers (AAPCC) reported 1122 single exposures to caffeine-containing energy drinks in 2016, with five major outcomes but no deaths. The AAPCC also reported 3702 single exposures to caffeine as a street drug, with 16 major outcomes but no deaths. [14]

Caffeinated alcoholic beverages were a public health concern because caffeine can mask some sensory cues that people might normally rely on to determine their level of intoxication. The US Food and Drug Administration (FDA) banned their sales in 2010. [7] In spite of the ban, mixing alcohol with energy drinks is still common practice and popular. In 2015, 13.0% of students in grades 8, 10, and 12 and 33.5% of young adults aged 19 to 28 reported consuming alcohol mixed with energy drinks at least once in the past year. Furthermore, the CDC reports that drinkers aged 15 to 23 who mix alcohol with energy drinks are 4 times more likely to binge drink at high intensity. [15] It is very important for the physician to inquire about co-ingestion of caffeine-containing drinks when obtaining a history for possible drug overdose or alcohol poisoning.

Death is an uncommon result of caffeine poisoning, but may be due to caffeine-related dysrhythmias, seizures, and aspiration of emesis. Oral doses of caffeine greater than 10 g can be fatal in adults. [10]

The AAPC reported no deaths related to caffeine in 2016. [14] The FDA’s Center for Food Safety and Applied Nutrition (CFSAN) Adverse Event Reporting System (CAERS) reported 29 deaths related solely to Monster, 5-Hour Energy, and Rockstar energy drinks from 2004-2013. [16]

Caffeine is the most commonly used drug in the world, and its use is prevalent in essentially all races and ethnic groups. [1] No scientific data have demonstrated that the outcomes of caffeine exposure differ on the basis of race or sex. [17]

Whether or not the effects of caffeine on adults can be generalized to children is unclear; however, studies suggest that children are differently affected by caffeine. One study comparing the effects of caffeine in men and boys found that the same dose of caffeine raised blood pressure in both groups but only decreased heart rate in boys. They also found that boys exhibited increased motor activity and speech rates and decreased reaction time compared with men. [18]

Another study found that an intake of 5 mg/kg body weight leads to elevated blood pressure and lower heart rate, without concomitant changes in energy metabolism in children aged 9-11 years. This amounts to 160 mg caffeine/day in a 10-year-old child weighing 30 kg, which is equivalent to the caffeine content of a single 16-oz Monster or Rockstar energy drink. [19]

In 2016, the AAPCC reported that the most exposures to caffeinated energy drinks were in children younger than 6 years. The second highest number of exposures were in adults aged 20 years and older. [14]

Additional age-related concerns arise from the fact that many energy drinks are marketed toward youth and youth-related activities, such as extreme sports. Students and athletes often drink them to enhance performance. A survey of 496 college students found that 51% of those surveyed drank more than 1 energy drink per month, with the majority of students drinking several  energy drinks per week. The main impetus was the desire for increased energy and concentration, with the most common complaint being insufficient sleep or a disruption in their regular sleep cycles. [20]

Reid TR. Caffeine. Natl Geogr Mag. 2005. 3-32. [Full Text].

Mitchell DC, Knight CA, Hockenberry J, Teplansky R, Hartman TJ. Beverage caffeine intakes in the U.S. Food Chem Toxicol. 2014 Jan. 63:136-42. [Medline]. [Full Text].

Branum AM, Rossen LM, Schoendorf KC. Trends in caffeine intake among U.S. children and adolescents. Pediatrics. 2014 Mar. 133 (3):386-93. [Medline]. [Full Text].

Miller KE, Dermen KH, Lucke JF. Caffeinated energy drink use by U.S. adolescents aged 13-17: A national profile. Psychol Addict Behav. 2018 Aug 20. [Medline].

Laszlo SP. Caffeine Intake By the U.S. Population. US Food and Drug Administration. Available at http://www.fda.gov/downloads/AboutFDA/CentersOffices/OfficeofFoods/CFSAN/CFSANFOIAElectronicReadingRoom/UCM333191.pdf. Accessed: December 28, 2016.

US National Archives and Records Administration. Code of Federal Regulations. Title 21. Caffeine. 2011. Available at http://www.gpo.gov/fdsys/granule/CFR-2011-title21-vol3/CFR-2011-title21-vol3-sec182-1180/content-detail.html. Accessed: December 28, 2016.

US Food and Drug Administration. FDA to Investigate Added Caffeine. About FDA. Available at http://www.fda.gov/ForConsumers/ConsumerUpdates/ucm350570.htm. June 21, 2016; Accessed: December 28, 2016.

Guidance for Industry: Highly Concentrated Caffeine in Dietary Supplements. US Food and Drug Administration. 2018 April 16. Available at https://www.fda.gov/Food/GuidanceRegulation/GuidanceDocumentsRegulatoryInformation/ucm604318.htm.

Clauson KA, Shields KM, McQueen CE, Persad N. Safety issues associated with commercially available energy drinks. J Am Pharm Assoc (2003). 2008 May-Jun. 48(3):e55-63; quiz e64-7. [Medline].

Heckman MA, Weil J, Gonzalez de Mejia E. Caffeine (1, 3, 7-trimethylxanthine) in foods: a comprehensive review on consumption, functionality, safety, and regulatory matters. J Food Sci. 2010 Apr. 75 (3):R77-87. [Medline].

EFSA Panel on Dietetic Products, Nutrition, and Allergies (NDA). Scientific Opinion on the safety of caffeine. European Food Safety Authority. Available at http://ec.europa.eu/food/fs/sc/scf/out22_en.html. Accessed: December 28, 2016.

The DAWN Report: Emergency Department Visits Involving Energy Drinks. Rockville, MD. Substance Abuse and Mental Health Services Administration, Center for Behavioral Health Statistics and Quality. (November 22, 2011).

Energy Drinks. National Center for Complementary and Integrative Health. Available at https://nccih.nih.gov/health/energy-drinks. 2018 July 26; Accessed: 2018 August 19.

Gummin DD, Mowry JB, Spyker DA, Brooks DE, Fraser MO, Banner W. 2016 Annual Report of the American Association of Poison Control Centers’ National Poison Data System (NPDS): 34th Annual Report. Clin Toxicol (Phila). 2017 Nov 29. 55 (10):1556-9519. [Medline]. [Full Text].

Fact Sheets – Alcohol and Caffeine. Centers for Disease Control and Prevention. Available at https://www.cdc.gov/alcohol/fact-sheets/caffeine-and-alcohol.htm. 2017 June 9; Accessed: 2018 August 19.

US Food and Drug Administration. CAERS Reports Allegedly Related to Multiple Energy Drinks. Center for Food Safety and Applied Nutrition. Available at https://cspinet.org/sites/default/files/attachment/foia-energy-drinks.pdf. Accessed: August 19, 2018.

Hartley TR, Lovallo WR, Whitsett TL. Cardiovascular effects of caffeine in men and women. Am J Cardiol. 2004 Apr 15. 93(8):1022-6. [Medline].

Turley KR, Desisso T, Gerst JW. Effects of caffeine on physiological responses to exercise: boys versus men. Pediatr Exerc Sci. 2007 Nov. 19(4):481-92. [Medline].

Turley KR, Gerst JW. Effects of caffeine on physiological responses to exercise in young boys and girls. Med Sci Sports Exerc. 2006 Mar. 38(3):520-6. [Medline].

Malinauskas BM, Aeby VG, Overton RF, Carpenter-Aeby T, Barber-Heidal K. A survey of energy drink consumption patterns among college students. Nutr J. 2007 Oct 31. 6:35. [Medline]. [Full Text].

Mortelmans LJ, Van Loo M, De Cauwer HG, Merlevede K. Seizures and hyponatremia after excessive intake of diet coke. Eur J Emerg Med. 2008 Feb. 15(1):51. [Medline].

Kromhout HE, Landstra AM, van Luin M, van Setten PA. [Acute caffeine intoxication after intake of ‘herbal energy capsules’]. Ned Tijdschr Geneeskd. 2008 Jul 12. 152(28):1583-6. [Medline].

Carrillo JA, Benitez J. Clinically significant pharmacokinetic interactions between dietary caffeine and medications. Clin Pharmacokinet. 2000 Aug. 39(2):127-53. [Medline].

Torraca L, Wang RY. Emergency toxicology. Methylxanthines: Theophylline and Caffeine. 2nd ed. 1998. 775-83.

Blake KV, Massey KL, Hendeles L, Nickerson D, Neims A. Relative efficacy of phenytoin and phenobarbital for the prevention of theophylline-induced seizures in mice. Ann Emerg Med. 1988 Oct. 17(10):1024-8. [Medline].

Kapur R, Smith MD. Treatment of cardiovascular collapse from caffeine overdose with lidocaine, phenylephrine, and hemodialysis. Am J Emerg Med. 2009 Feb. 27(2):253.e3-6. [Medline].

Laskowski LK, Henesch JA, Nelson LS, Hoffman RS, Smith SW. Start me up! Recurrent ventricular tachydysrhythmias following intentional concentrated caffeine ingestion. Clin Toxicol (Phila). 2015. 53 (8):830-3. [Medline].

Meier B. In a New Aisle, Energy Drinks Sidestep Some Rules. New York Times. March 19, 2013. Available at http://www.nytimes.com/2013/03/20/b usiness/in-a-new-aisle-energy-drinks-sidestep-rules.html?ref=business.

McCusker RR, Goldberger BA, Cone EJ. Caffeine content of energy drinks, carbonated sodas, and other beverages. J Anal Toxicol. 2006 Mar. 30(2):112-4. [Medline].

Item

Amount

Caffeine Content, mg

Coca-Cola Classic

12 oz

35

Brewed black tea, generic

8 oz

45-74

Red Bull Regular

8.4 oz

80

Brewed coffee, generic

8 oz

57

Regular 5-Hour Energy

2 oz

138

Rockstar

16 oz

160

Monster Energy

16 oz

160

Espresso, generic

1 oz

170

NOS

16

280

Starbucks Tall Americano

16

330

David Yew, MD Assistant Clinical Professor, Department of Surgery, University of Hawaii, John A Burns School of Medicine; Medical Director and Flight Physician, Hawaii Life Flight, AirMed International

David Yew, MD is a member of the following medical societies: American College of Emergency Physicians, Air Medical Physician Association

Disclosure: Nothing to disclose.

Sophie Kim Boston College

Disclosure: Nothing to disclose.

Francisco Talavera, PharmD, PhD Adjunct Assistant Professor, University of Nebraska Medical Center College of Pharmacy; Editor-in-Chief, Medscape Drug Reference

Disclosure: Received salary from Medscape for employment. for: Medscape.

John G Benitez, MD, MPH Associate Professor, Department of Medicine, Medical Toxicology, Vanderbilt University Medical Center; Managing Director, Tennessee Poison Center

John G Benitez, MD, MPH is a member of the following medical societies: American Academy of Clinical Toxicology, American Academy of Emergency Medicine, American College of Medical Toxicology, American College of Preventive Medicine, Undersea and Hyperbaric Medical Society, Wilderness Medical Society, American College of Occupational and Environmental Medicine

Disclosure: Nothing to disclose.

Michael A Miller, MD Clinical Professor of Emergency Medicine, Medical Toxicologist, Department of Emergency Medicine, Texas A&M Health Sciences Center; CHRISTUS Spohn Emergency Medicine Residency Program

Michael A Miller, MD is a member of the following medical societies: American College of Medical Toxicology

Disclosure: Nothing to disclose.

James E Keany, MD, FACEP Associate Medical Director, Emergency Services, Mission Hospital Regional Medical Center, Children’s Hospital of Orange County at Mission

James E Keany, MD, FACEP is a member of the following medical societies: American College of Emergency Physicians, American College of Sports Medicine, California Medical Association

Disclosure: Nothing to disclose.

China N Byrns Department of Cell and Molecular Biology, University of Hawaii at Manoa

China N Byrns is a member of the following medical societies: Phi Beta Kappa

Disclosure: Nothing to disclose.

Jeffrey T Laczek, MD Gastroentology Fellow, Walter Reed Army Medical Center

Disclosure: Nothing to disclose.

Caffeine Toxicity

Research & References of Caffeine Toxicity|A&C Accounting And Tax Services
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