Updated: Jun 12, 2009
According to the World Health Organization (WHO), tobacco use is widespread, affecting one third of the global adult population. Reportedly, tobacco is the single largest preventable cause of morbidity and premature death in the United States. Most people who smoke report initiation of tobacco use during childhood or adolescence, with 75% of adult tobacco users reporting initial use when aged 11-17 years.
Although overall smoking rates are declining, smoking rates in American adolescents have shown a gradual increase since 1987, with an increase of almost one third from 1991-1997. In addition, the rate of smokeless tobacco use has increased over the last 15 years. In addition to the immediate health impact of smoking and tobacco use, adolescent smokers are more likely to become adult smokers and to use alcohol and illicit substances. Studies also suggest that the earlier adolescents start to smoke, the more cigarettes they will smoke as an adult, which is associated with more severe tobacco-related health complications.
Additionally, molecular research now suggests that early smoking may lead to changes in lung cells, especially during a critical period of lung development in adolescence, increasing the lung cancer risk independent of smoking duration or intensity. This risk is accentuated in females because of earlier maximum lung growth compared with that in males (age 18 y in females vs 24 y in males).1
Absorption of nicotine from inhaled cigarette smoke is rapid, and a bolus of nicotine reaches the brain within 10-16 seconds. Once in the brain, nicotine activates nicotinic acetylcholine receptors, leading to the release of dopamine.
The daily use of tobacco in US schools has reached epidemic proportions. More than 3 million adolescents in the United States smoke; 6,000 adolescents start smoking every day, and one half of these adolescents become daily smokers.
Studies show that 5 million people who smoke in the United States are aged 12-17 years; more than 500,000 people who smoke in the United States are aged 8-11 years.
Other studies suggest that, by the year 2000, 15% of eighth graders, 24% of tenth graders, and 31% of high school seniors used tobacco daily. Tobacco use among individuals aged 18 years who are not in school has been estimated to be as high as 75%. Rates of tobacco use in adolescents are higher in rural areas than in urban areas.
Most adolescents who smoke daily are addicted to nicotine, and 50% report withdrawal symptoms when trying to stop smoking. More than one half of these smokers report wanting to stop smoking, and more than one half of them have tried to stop smoking in the last year.2
According to the WHO, by the early 1990s, 1.1 billion people used tobacco, representing one third of the global adult population. The use of tobacco in developing countries is increasing, with 48% of men and 7% of women using tobacco regularly. In developed countries, where the use of tobacco by women has markedly increased, 42% of men and 24% of women use tobacco regularly.
The WHO has estimated that, by the year 2030, tobacco will be the world's leading cause of morbidity and mortality, accounting for 10 million deaths per year. Worldwide, tobacco will cause more deaths than the deaths caused by HIV infection, tuberculosis, maternal mortality, motor vehicle collisions, suicide, and homicide combined. A long-term tobacco user has a 50% chance of dying prematurely of a tobacco-related disease. Other studies suggest that one third of adolescents who become regular smokers will die of a smoking-related disease.
In the United States, the prevalence of cigarette smoking among Hispanic, African American, and white adolescents is increasing, with the most dramatic increases in African American teens, although smoking rates continue to be much higher in whites. These differences in tobacco use among whites remain when studies control for lifestyle and demographic factors.
While definitive studies have not been completed, factors suspected to play a role in these race-based differences include marketing strategies and attitudes toward smoking. As examples, African American adolescents are less likely to perceive smoking as fun, African American parents tend to have a more punitive approach to tobacco use, and African American females are less likely to use smoking for weight control.3
While the incidence of adolescent tobacco use is increasing overall, males are still more likely to smoke and use tobacco than are females, except in white adolescents, in whom rates are the same in males and females.
The following are stages in the development of adolescent smoking:4
The following are signs and symptoms that constitute nicotine dependence:
According to the US Preventive Services Task Force (USPSTF) guidelines, clinicians should ask adolescents about use of tobacco products and provide cessation interventions to current users. The guideline engages a “5-A” approach to counseling that includes the following:7
Brief (<10 min) behavioral counseling and pharmacotherapy are each effective alone, although they are most effective when used together. The task force also advises clinicians to ask all pregnant women, regardless of age, about tobacco use. Those who currently smoke should receive pregnancy-tailored counseling supplemented with self-help materials.
In adults with nicotine addiction, combination therapy with NRT and non-NRTs, particularly bupropion or other antidepressants, have been shown to double abstinence rates.
Nicotine replacement in adolescents has been shown to be safe, but studies have not demonstrated that these medications are effective in promoting long-term cessation in adolescents. As a result, the use of these medications is not recommended by the US Public Health Service in their most recently updated clinical practice guideline on treating tobacco use and dependence.9
These agents help prevent nicotine withdrawal. They deliver nicotine systemically via oral or nasal mucosa or transdermal delivery systems. They are most effective for smoking cessation when used in conjunction with a support program, such as counseling, group therapy, or behavioral therapy.
Nicotine is quickly absorbed through the oral mucosa. Closely approximates time course of plasma nicotine levels observed after cigarette smoking. Available as gum or lozenge.
Gum: Chew 1 piece of gum PO q1-2h while awake for 6 wk, then reduce dose to 1 piece of gum q2-4h during weeks 7-9, then reduce dose to 1 piece of gum q4-8h during weeks 10-12
Note: Initiate with 4-mg gum if 25 or more cigarettes smoked/d, initiate with 2-mg gum if <25 cigarettes smoked/d
Lozenge: Dissolve 1 lozenge PO q1-2h while awake for 6 wk, then reduce dose to 1 lozenge q2-4h during weeks 7-9, then reduce dose to 1 lozenge q4-8h during weeks 10-12
Note: Initiate with 4-mg lozenge if first cigarette smoked within 30 min of waking; if first smoked is >30 min after waking, initiate with 2-mg lozenge
<18 years: Not established; use only with physician supervision
May decrease diuretic effects of furosemide and decrease cardiac output; may decrease absorption of glutethimide; may increase circulating cortisol and catecholamines; do not use if patient continues to smoke, use snuff, chew tobacco, or use other nicotine products, as it may increase toxicity of nicotine
Documented hypersensitivity; nonsmokers; children; pregnancy; life-threatening arrhythmias; severe or worsening angina pectoris
D - Fetal risk shown in humans; use only if benefits outweigh risk to fetus
Do not smoke cigarettes in addition to nicotine replacement; caution in peptic ulcer, coronary artery disease, angina, hypertension, peripheral arterial disease, diabetes, severe renal dysfunction, and hepatic dysfunction; chew gum 4-6 times or until tingling sensation or peppery taste appears, then place between cheek and teeth until tingling dissipates, repeat this chewing process for about 30 min
Quickly absorbed and closely approximates time course of plasma nicotine levels observed after cigarette smoking. Each inhaler cartridge delivers 4 mg of nicotine. Once activated, may be used over several min to simulate smoking, although the drug is generally absorbed from oral mucosa.
Individualize dose by self-titration to the level of nicotine required; most successful use demonstrated 6-16 cartridges/d
Most effective with continuous puffing over 20 min
Recommended duration of treatment is 3 mo, then gradually reduce daily dose over 6-12 wk
Not established
May decrease diuretic effects of furosemide and decrease cardiac output; may decrease absorption of glutethimide; may increase circulating cortisol and catecholamines; do not use if patient continues to smoke, uses snuff, chews tobacco, or uses other nicotine products, as it may increase toxicity of nicotine
Documented hypersensitivity; nonsmokers; children; pregnancy; life-threatening arrhythmias; severe or worsening angina pectoris
D - Fetal risk shown in humans; use only if benefits outweigh risk to fetus
Do not smoke cigarettes in addition to nicotine replacement; caution in peptic ulcer, coronary artery disease, angina, hypertension, peripheral arterial disease, diabetes, severe renal dysfunction, and hepatic dysfunction; may cause rhinitis, and throat and mouth irritation
Intranasal nicotine may closely approximate the time course of plasma nicotine levels observed after cigarette smoking.
1-2 sprays/h intranasally, each spray contains 0.5 mg of nicotine, not to exceed more than 10 sprays (5 mg) per h or 40 sprays/24 h
Not established
May decrease diuretic effects of furosemide and decrease cardiac output; may decrease absorption of glutethimide; may increase circulating cortisol and catecholamines; do not use if patient continues to smoke, use snuff, chew tobacco, or use other nicotine products as it may increase toxicity of nicotine
Documented hypersensitivity; nonsmokers; children; pregnancy; life-threatening arrhythmias; severe or worsening angina pectoris
D - Fetal risk shown in humans; use only if benefits outweigh risk to fetus
Do not smoke cigarettes in addition to nicotine replacement; caution in peptic ulcer, coronary artery disease, angina, hypertension, peripheral arterial disease, diabetes, severe renal dysfunction, and hepatic dysfunction; may cause coughing or exacerbation of asthma; may also cause burning or irritation upon administration
Transdermal patches are most appropriate for individuals who smoke more than 10 cigarettes each day.
Nicotrol: Apply one 15-mg transdermal patch qd for 6 wk; remove at bedtime; decrease to 10 mg/d for weeks 7-8, then 5 mg/d for weeks 9-10, then discontinue
Habitrol or Nicoderm CQ: Apply one 21-mg patch qd for 6wk, then one 14-mg patch qd for 2 wk, followed by one 7-mg patch qd for 2 wk for a total of 10 wk
Not established
May decrease diuretic effects of furosemide and decrease cardiac output; may decrease absorption of glutethimide; may increase circulating cortisol and catecholamines; do not use if patient continues to smoke, use snuff, chew tobacco, or use other nicotine products as it may increase toxicity of nicotine
Documented hypersensitivity; nonsmokers; children; pregnancy; life-threatening arrhythmias; severe or worsening angina pectoris
D - Fetal risk shown in humans; use only if benefits outweigh risk to fetus
Do not smoke cigarettes in addition to nicotine replacement; caution in peptic ulcer, coronary artery disease, angina, hypertension, peripheral arterial disease, diabetes, severe renal dysfunction, and hepatic dysfunction; may cause skin irritation; if persistent insomnia occurs, remove patch at bedtime
These agents modulate noradrenergic neurotransmission and increase smoking cessation rates.
Used in conjunction with a support group and/or behavioral counseling. Inhibits neuronal dopamine reuptake in addition to being a weak blocker of serotonin and norepinephrine reuptake.
150-mg tab PO qd for 3 d, then increase to 150 mg bid with at least 8 h between each dose for 7-12 wk
Not established
Carbamazepine, cimetidine, phenytoin, and phenobarbital may decrease effects; toxicity increases with concurrent administration of levodopa and MAOIs
Documented hypersensitivity; seizure disorder, anorexia nervosa, concurrent use with MAOIs; concurrent use with other bupropion products (eg, Wellbutrin)
B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals
Caution in renal or hepatic insufficiency; doses >450 mg/d significantly decrease seizure threshold; may cause hypertension; may increase risk of suicidal ideation or worsening depression
For excellent patient education resources, visit eMedicine's Public Health Center, Lung and Airway Center, and Substance Abuse Center. Also, see eMedicine's patient education articles Cigarette Smoking and Substance Abuse.
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nicotine abuse, nicotine dependence, tobacco use, cigarette use, smoking, tobacco-related disease, smoking-related disease
Donna G Grigsby, MD, Associate Professor, Department of Pediatrics, University of Kentucky College of Medicine
Donna G Grigsby, MD is a member of the following medical societies: American Academy of Pediatrics and Kentucky Pediatric Society
Disclosure: Nothing to disclose.
Kristin M Rager, MD, MPH, Assistant Professor of Pediatrics, Department of Pediatrics, Division of Adolescent Medicine, University of Kentucky College of Medicine
Kristin M Rager, MD, MPH is a member of the following medical societies: American Academy of Pediatrics, Kentucky Pediatric Society, North American Society for Pediatric and Adolescent Gynecology, and Society for Adolescent Medicine
Disclosure: Nothing to disclose.
Todd R Cheever, MD, Consulting Staff, Department of Psychiatry, University of Kentucky College of Medicine
Todd R Cheever, MD is a member of the following medical societies: American Medical Association, American Psychiatric Association, and Kentucky Medical Association
Disclosure: Nothing to disclose.
Chet Johnson, MD, Medical Director, Child Development Unit, Department of Pediatrics, Professor, University of Kansas Medical Center
Chet Johnson, MD is a member of the following medical societies: American Academy of Pediatrics
Disclosure: Nothing to disclose.
Mary L Windle, PharmD, Adjunct Assistant Professor, University of Nebraska Medical Center College of Pharmacy, Pharmacy Editor, eMedicine
Disclosure: Pfizer Inc Stock Investment from financial planner; Avanir Pharma Stock Investment from financial planner ; WebMD Salary and stock Employment and investment from financial planner
Carrie Sylvester, MD, MPH, Director of Education in Child and Adolescent Psychiatry, Professor, Departments of Psychiatry and Pediatrics, Northwestern University Medical School
Carrie Sylvester, MD, MPH is a member of the following medical societies: American Academy of Child and Adolescent Psychiatry, American Academy of Pediatrics, American Medical Women's Association, American Psychiatric Association, and American Society for Adolescent Psychiatry
Disclosure: Nothing to disclose.
Caroly Pataki, MD, Professor of Clinical Psychiatry and Behavioral Sciences, Department of Psychiatry, Division Chair, Child and Adolescent Psychiatry, Director of Training, Child and Adolescent Psychiatry Residency Program, University of Southern California Keck School of Medicine
Caroly Pataki, MD is a member of the following medical societies: American Academy of Child and Adolescent Psychiatry, New York Academy of Sciences, and Physicians for Social Responsibility
Disclosure: Nothing to disclose.
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