Skip to main content
NIHPA Author Manuscripts logoLink to NIHPA Author Manuscripts
. Author manuscript; available in PMC: 2009 Jul 1.
Published in final edited form as: AIDS Educ Prev. 2009 Jun;21(3 Suppl):14–27. doi: 10.1521/aeap.2009.21.3_supp.14

Review: The need for smoking cessation among HIV-positive smokers

Shadi Nahvi 1, Nina A Cooperman 1
PMCID: PMC2704483  NIHMSID: NIHMS113791  PMID: 19537951

Abstract

Most HIV-positive persons in the U.S. smoke cigarettes. Despite substantial clinical advances in HIV care in the era of highly active antiretroviral therapy (HAART), HIV-positive persons are at high risk of tobacco-related disease and death. HIV-positive persons have complex social, economic, psychiatric, and medical needs which may impact smoking behavior and response to smoking cessation interventions, but there is a dearth of research on smoking cessation interventions tailored to HIV-positive persons. HIV care providers should treat tobacco use with the array of evidence-based smoking cessation treatments available, updating their clinical practice as new data emerge. This paper reviews the literature on the health consequences of tobacco use in HIV-positive persons, the treatment of tobacco dependence, and the research to date on smoking cessation interventions in HIV-positive persons, and presents recommendations for future research and intervention.

Keywords: HIV, Tobacco, Smoking cessation


Tobacco use is the leading preventable cause of morbidity and mortality in the United States (McGinnis & Foege, 1993), but the health consequences of cigarette smoking are not borne equally among all populations. The prevalence of current tobacco use in HIV-positive smokers is estimated at between 50 and 70% (Burkhalter, Springer, Chhabra, Ostroff, & Rapkin, 2005; Cooperman, Schoenbaum, Klein, & Arnsten, 2007; Gritz, Vidrine, Lazev, Amick, & Arduino, 2004; Niaura et al., 2000), markedly higher than the 20% prevalence in the U.S. general population (Centers for Disease Control and Prevention, 2007). The significant clinical gains made in the control of HIV in the HAART era may be threatened by the cardiovascular, pulmonary, neoplastic and infectious complications of tobacco use in HIV-positive persons. Despite a call for research in the NIH State-of-the-Science statement on tobacco use to evaluate tobacco control interventions in people with co-occurring conditions (NIH State-of-the-Science Panel, 2006), few studies have investigated smoking cessation interventions in HIV-positive persons, and smoking cessation treatment has not been a priority in HIV treatment programs. The objectives of this review are to 1) examine the burden of tobacco use and tobacco-related disease in HIV-positive persons; 2) discuss evidence-based tobacco dependence treatment; 3) describe issues unique to HIV-positive smokers; 4) review the research to date on smoking cessation interventions for HIV-positive smokers; and 5) identify priorities for future research and intervention.

The burden of tobacco use in HIV-positive persons

Over 85% of HIV-infected individuals in the U.S. have a lifetime history of smoking (Burkhalter et al., 2005), and current cigarette smoking is highly prevalent among HIV-positive persons. Among those with a lifetime history of cigarette smoking, HIV-positive persons are approximately half as likely to be currently abstinent from tobacco use as compared to HIV-negative individuals (Gritz et al., 2004). On average, HIV-positive smokers have been smoking for 22.8 years (Burkhalter et al., 2005) and smoke 16 to 23 cigarettes per day (Benard et al., 2007; Lloyd-Richardson et al., 2008). Among HIV-positive current smokers, most are moderately to highly nicotine dependent (Benard et al., 2007; Lloyd-Richardson et al., 2008).

The marked prevalence of tobacco use in HIV-positive persons has a corresponding health cost. With the decline in AIDS-related death in the HAART era (Palella et al., 1998; Walensky et al., 2006), the proportion of deaths due to tobacco-associated disease, including cardiovascular disease, pulmonary disease and non-HIV related malignancy has increased in HIV-positive persons (Palella et al., 2006). Tobacco use has been found to be independently associated with mortality in HIV-positive smokers (Crothers et al., 2005; Feldman et al., 2006). Despite the marked reductions in HIV-associated illness and mortality, HIV-positive persons have increased mortality rates compared to the general population (Lohse et al., 2007); addressing the disproportionate burden of tobacco use in HIV-positive persons may help to close that gap.

Cigarette smoking is of particular concern among HIV-positive persons given the prevalence of insulin resistance, dyslipidemia, hypertension, abdominal obesity and cardiovascular disease among HIV-positive persons in the HAART era (Carr et al., 1998; Thiebaut et al., 2000; Triant, Lee, Hadigan, & Grinspoon, 2007). Antiretroviral therapy may confer cardiovascular risk; the incidence of myocardial infarction has been shown to increase with increased exposure to antiretroviral therapy in a large prospective cohort (The DAD Study Group, 2007; The Data Collection on Adverse Events of Anti-HIV Drugs (DAD) Study Group, 2003). Of note, data from this cohort suggest that current smoking confers greater risk of myocardial infarction (RR= 2.83, 95% CI 2.04, 3.93) than protease inhibitor therapy (RR= 1.16, 95% CI 1.10, 1.23) (The DAD Study Group, 2007). HIV-positive persons also have higher rates of acute myocardial infarction and cardiovascular risk factors including hypertension, diabetes and dyslipidemia than HIV-negative patients (Triant et al., 2007). In addition, the estimated risk of cardiovascular mortality is higher in HIV-positive patients compared to the general population (De Socio et al., 2007); the main contributor to the increased risk is the high proportion of HIV-positive smokers.

HIV infection may increase susceptibility to chronic obstructive pulmonary disease (COPD) (Crothers, 2007; Crothers et al., 2006). In an observational study of HIV-positive and HIV-negative men, HIV infection was found to be an independent risk factor for COPD, adjusting for age and pack-years of smoking (Crothers et al., 2006). HIV-positive persons were 50-60% more likely to have COPD than HIV-negative persons. The increased risk of COPD in HIV-positive persons is exacerbated by tobacco use. Among a cohort of HIV-positive veterans, cigarette smoking was found to be strongly associated with respiratory symptoms and non-infectious pulmonary disease; COPD was five times more likely in current and former smokers than in never smokers (Crothers et al., 2005).

The association of cigarette smoking and cancer risk is well-established. Among HIV-positive persons, large cohort (Clifford et al., 2005; Engels et al., 2006; Kirk et al., 2007) and population-based studies (Chaturvedi et al., 2007) have demonstrated a three to four-fold increased incidence of lung cancer compared to HIV-negative persons. Though the association between HIV disease and lung cancer persists after adjustment for tobacco use in a number of studies (Chaturvedi et al., 2007; Engels et al., 2006; Kirk et al., 2007), this increased risk partially reflects the high prevalence of tobacco use among HIV-positive persons. This is of particular concern because lung cancer is the leading cause of non-AIDS-defining malignancy in HIV-positive persons (Frisch, Biggar, Engels, & Goedert, 2001), and the prognosis is poor (Biggar et al., 2005).

Tobacco use also increases the risk of opportunistic and non-opportunistic infections in persons with HIV. Cigarette smoking is independently associated with increased risk of oral candidiasis, oral hairy leukoplakia and oral warts, after adjustment for CD4 count (Chattopadhyay et al., 2005a, 2005b; Palacio, Hilton, Canchola, & Greenspan, 1997). Adjusting for antiretroviral therapy, cigarette smoking increases the risk of pneumocystis carinii pneumonia (Miguez-Burbano et al., 2005; Miguez-Burbano et al., 2003). Multiple studies have described the association between cigarette smoking and risk of bacterial pneumonia; cigarette smoking is associated with a 1.5 to 3-fold increased risk of bacterial pneumonia in HIV-positive persons (Crothers et al., 2005; Kohli et al., 2006; Le Moing et al., 2006; Miguez-Burbano et al., 2005).

Several studies have investigated the relationship between cigarette smoking and quality of life in HIV-positive persons (Crothers et al., 2005; Reynolds, Neidig, & Wewers, 2004; J. Turner et al., 2001; Vidrine, Arduino, & Gritz, 2007). Among HIV-positive individuals, current cigarette smoking was independently related to a decrease in general health perception, physical functioning, energy, role functioning, and cognitive functioning and an increase in physical pain, adjusting for age, immunologic function and other covariates (J. Turner et al., 2001). Another study found that HIV-positive current smokers experience greater physical symptoms and decreased quality of life compared to former and never smokers (Crothers et al., 2005). Alternatively, among HIV-positive smokers who engaged in a smoking cessation intervention, smoking abstinence was significantly related to a decrease in HIV-related symptom burden but not improved health related quality of life (Vidrine et al., 2007). In sum, HIV-positive smokers have a poorer quality of life than HIV-positive non-smokers. While quitting smoking may improve HIV symptoms, it may not be enough to improve overall health-related quality of life.

Smoking cessation interventions

Evidence-based smoking cessation treatment

Ample clinical evidence exists to support the use of a range of smoking cessation interventions in the general population. However there are no clinical practice guidelines to guide the provision of smoking cessation treatment in HIV-positive persons. Evidence-based treatments with demonstrated efficacy in the general population should thus be incorporated into the care of HIV-positive smokers. Such interventions are outlined below.

Smokers have misperceptions about the risks of smoking and the value, safety and efficacy of using evidence-based cessation methods (Bonnie, Stratton, Wallace, & Committee on Reducing Tobacco Use: Strategies Barriers and Consequences, 2007). Fewer than 20% of quitters use proven treatments, leading to lower cessation and higher relapse rates (S. Zhu, Melcer, Sun, Rosbrook, & Pierce, 2000). It is common for smokers to make multiple quit attempts prior to successful smoking cessation, and multiple courses of treatment or extended treatment may be necessary (Fiore et al., 2008).

Behavioral interventions

U.S. Public Health Service guidelines recommend brief individual smoking cessation counseling with five components (known as the “5 A’s”) at each clinical encounter. Providers are advised to systematically ask about tobacco use, advise smokers to quit, assess willingness to quit, assist with quitting, and arrange follow up (Fiore et al., 2008). Brief advice has been shown to increase the likelihood that a smoker will successfully quit and remain a nonsmoker 12 months later (Lancaster & Stead, 2004) and is easily generalizable to complex clinical settings.

Smokers’ telephone quitlines are a cost-effective intervention with broad reach and demonstrated efficacy for long-term smoking cessation (Abrams et al., 2003; Fiore et al., 2008; Stead, Perera, & Lancaster, 2006). They offer telephone counseling, smoking cessation educational materials, and some offer nicotine replacement therapy (NRT). Quitlines have been shown to be effective in reaching racial and ethnic minorities (S. H. Zhu et al., 2002), however in low income HIV-positive persons, lack of access to continuous telephone service may be a barrier to their utilization. Despite this potential barrier, HIV-positive persons report interest in telephone-based smoking cessation counseling (Lazev, Vidrine, Arduino, & Gritz, 2004).

Various individual and group smoking cessation counseling approaches have been used in the general population. Motivational interviewing (MI) is a patient-centered approach utilized to amplify an individual’s ambivalence about a health-related behavior and enhance readiness to change (Miller & Rollnick, 2002). MI is based on four general principles: 1) express empathy, 2) develop discrepancy, 3) roll with resistance and 4) support self-efficacy. Motivational interviewing is effective in increasing quit attempts, however its efficacy in promoting cessation in motivated smokers is unclear (Fiore et al., 2008).

Cognitive behavioral interventions are another form of counseling known to help smokers quit or reduce cigarette smoking (Niaura, 2008; Simon, Carmody, Hudes, Snyder, & Murray, 2003). Interventions are designed to modify critical cognitions and actions that maintain behaviors such as smoking by promoting the thoughts and skills necessary to create behavioral change. Cognitive-behavioral interventions help a person identify thoughts, feelings and events that are associated with a behavior and subsequently teach skills to cope with those thoughts and events.

Pharmacotherapy

Smoking cessation medications have been demonstrated to increase quit rates 1.5 to 2 fold (Gonzales et al., 2006; Hurt et al., 1997; Jorenby et al., 2006; Silagy, Lancaster, Stead, Mant, & Fowler, 2004). Medications approved by the FDA for smoking cessation include nicotine replacement therapy (patch, lozenges, inhalers, gum and nasal spray), bupropion and varenicline. Selection of individual agents may be guided by patient preference, patients’ prior experience with medications, patient characteristics, medical contraindications and cost considerations (Fiore et al., 2008).

All formulations of nicotine replacement therapy have similar efficacy for smoking cessation (Stead, Perera, Bullen, Mant, & Lancaster, 2008). The combination of nicotine replacement therapies is more efficacious than a single agent alone (Stead et al., 2008). Initial dosing is determined by the number of cigarettes smoked per day, and the dose is tapered over the course of treatment. The optimal duration of treatment is not known, but a standard course of treatment is generally 10-12 weeks. Nicotine replacement therapy is safe in stable cardiovascular disease, and should be used with caution in patients with myocardial infarction in the last two weeks, serious arrhythmia, unstable angina, and uncontrolled hypertension (Fiore et al., 2008). There are no known interactions between nicotine replacement therapy and HAART.

Bupropion SR (sustained release) approximately doubles quit rates (Hurt et al., 1997). Bupropion SR alone, or in combination with nicotine replacement therapy, has been shown to be more efficacious than nicotine replacement therapy or placebo (Jorenby et al., 1999). Side effects include insomnia and dry mouth. Because bupropion may lower the seizure threshold, it is contraindicated in people with a history of seizures and should be used with caution in people with a risk of seizures. Bupropion is metabolized by the hepatic cytochrome P450 CYP2B6 system, and its metabolism has been shown to be inhibited by the antiretroviral medications nelfinavir, ritonavir and efavirenz in vitro (Hesse, von Moltke, Shader, & Greenblatt, 2001). Short-term ritonavir administration does not significantly alter bupropion pharmacokinetics in healthy volunteers (Hesse, Greenblatt, von Moltke, & Court, 2006) and no medication-associated adverse events were observed in a case series of ten HIV-positive persons using either ritonavir, nelfinavir or efaverinz with bupropion (Park-Wyllie & Antoniou, 2003).

Varenicline is a partial agonist of the α4β2 nicotinic acetylcholine receptor, which mediates nicotine dependence. Varenicline, which relieves nicotine withdrawal symptoms and reduces the rewarding properties of nicotine, has been shown to be more efficacious than bupropion or placebo for smoking cessation (Gonzales et al., 2006; Jorenby et al., 2006). Side effects include nausea, insomnia, headache and abnormal dreams. Given adverse neuropsychiatric events observed in post marketing surveillance, including drowsiness, agitation, depressed mood, suicidal ideation and attempted and completed suicide, providers should monitor patients for the development or exacerbation of neuropsychiatric symptoms (U.S. Food and Drug Administration). No drug-drug interactions have been described to date with antiretroviral therapy and varenicline.

The unique needs of HIV-positive smokers

HIV-positive persons have a complex range of social, economic, psychiatric, and medical needs which may impact smoking behavior and response to smoking cessation interventions. Psychiatric comorbidity, substance use, motivational level, health risk perception and medication adherence issues are important considerations in the development and dissemination of smoking cessation interventions for HIV-positive smokers.

Social and economic issues

The consequences of tobacco use are not borne equally among all populations--African Americans, Latinos, and Native Americans face well-documented disparities in chronic disease risk, access to appropriate treatment, and cardiovascular mortality (Smedley, Stith, & Nelson, 2002). Socioeconomic status is a major determinant of both smoking prevalence (Centers for Disease Control and Prevention, 2007) and AIDS incidence (Zierler et al., 2000). There is also a higher prevalence of tobacco use among gay and bisexual men than among the general population (Stall, Greenwood, Acree, Paul, & Coates, 1999). Racial and ethnic minorities and socioeconomically disadvantaged persons may also be less likely to receive smoking cessation advice and treatment (Browning, Ferketich, Salsberry, & Wewers, 2008; Houston, Scarinci, Person, & Greene, 2005; Lopez-Quintero, Crum, & Neumark, 2006). Community-specific interventions may be necessary to effectively reduce tobacco use among HIV-positive smokers, but there is a dearth of clinical research to guide the provision of effective tailored interventions. Barriers to access to smoking cessation and HIV treatment will also need to be addressed to optimize provision of smoking cessation services to HIV-positive persons.

Co-morbid psychiatric illness and drug abuse

The high prevalence of cigarette smoking among HIV-infected individuals may be a reflection of the high prevalence of psychiatric illness and substance abuse among HIV-positive persons. Between 50 and 90% of those with psychiatric illness or substance use disorders smoke cigarettes (Nahvi, Richter, Li, Modali, & Arnsten, 2006; Richter & Arnsten, 2006; Richter, Gibson, Ahluwalia, & Schmelzle, 2001; Williams & Ziedonis, 2004) and those with mental illness (including substance use disorders) consume over 40% of the cigarettes smoked in the U.S. (Lasser et al., 2000). Although prevalence estimates for psychiatric and substance use disorders among those with HIV vary by study and disorder, studies have reported that, among those with HIV, 21-28% report current illicit drug use (Cofrancesco et al., 2008; Pence, Miller, Whetten, Eron, & Gaynes, 2006) and the prevalence of mental illness may be as high as 63% (Tegger et al., 2008).

Among those with HIV, individuals who use drugs or alcohol are more likely to be current cigarette smokers (Burkhalter et al., 2005; Gritz et al., 2004; Webb, Vanable, Carey, & Blair, 2007). In qualitative analyses, shared psychological and physical cues and withdrawal symptoms have been reported to be associated with opiate and nicotine dependence (McCool & Richter, 2003), which may make smoking cessation more difficult for drug users. Some may smoke cigarettes to help improve psychiatric symptoms; research has shown that cigarette smoking may improve symptoms of conditions such as attention deficit disorder and schizophrenia, and quitting smoking is associated with symptoms of depression (Williams & Ziedonis, 2004). Furthermore, depressive symptoms are associated with increased nicotine dependence (Benard et al., 2007) and decreased readiness to quit smoking (Burkhalter et al., 2005) in HIV-positive smokers. Co-morbid psychiatric illness and substance abuse are thus important considerations when helping HIV-positive smokers to quit.

Risk perception and coping

HIV-positive smokers may not be aware of or concerned about the health risks of smoking, and may use cigarette smoking as a coping mechanism. In focus groups with 13 HIV-positive men who were current and former cigarette smokers, although the men acknowledged that smoking can be expensive, addictive, and cause health problems, they minimized the health risks and believed that there were benefits to smoking (Reynolds et al., 2004). The men found smoking to be soothing and helpful with social interaction. Some stated that smoking was a useful coping tool and were reluctant to quit. The study participants also felt that they would probably not live long enough to suffer the serious health problems associated with smoking.

Motivation to quit and quit attempts

Despite the high prevalence of smoking and significant barriers to quitting among those with HIV, many are interested in quitting and have made quit attempts. Studies have reported that 40% to 63% HIV-positive smokers are contemplating quitting or preparing to quit smoking (Benard et al., 2007; Burkhalter et al., 2005; Mamary, Bahrs, & Martinez, 2002), similar to smokers in the general population (Velicer et al., 1995). Approximately 70% of HIV-positive smokers have made a previous quit attempt (Benard et al., 2007; Mamary et al., 2002), with an average of 2.8 quit attempts since their HIV diagnosis (Burkhalter et al., 2005). Studies have reported that between 69% and 84% of HIV-positive smokers are interested in smoking cessation programs or nicotine replacement therapy (Burkhalter et al., 2005; Mamary et al., 2002).

Adherence to pharmacotherapy

Poor adherence to smoking cessation pharmacotherapy could prevent HIV-positive smokers from successfully quitting. The effect of smoking cessation treatment is significantly reduced among individuals who are not adherent to their pharmacotherapy regimen (Stein, Anderson, & Niaura, 2006), and medication adherence is an important clinical issue among those with HIV. Many HIV-positive individuals need to take multiple medications and manage different medication schedules. Issues such as drug abuse, psychiatric illness, and other life stressors are known to impact medication adherence among those with HIV (Arnsten et al., 2002; Arnsten et al., 2007; Leserman, Ironson, O’Cleirigh, Fordiani, & Balbin, 2008) and are likely to impact their ability to adhere to smoking cessation pharmacotherapy as well. Research has shown that cigarette smoking is associated with deceased adherence to HAART (Peretti-Watel, Spire, Lert, & Obadia, 2006; Shuter & Bernstein, 2008; Yuan, L’Italien, Mukherjee, & Iloeje, 2006), suggesting that adherence to smoking cessation pharmacotherapy could be difficult for some HIV-positive smokers.

Provider-level barriers

For smoking cessation interventions to reach smokers, health care providers must recognize and address tobacco use. In a survey of Veterans Affairs HIV and non-HIV providers and HIV-positive and HIV-negative patients (Crothers et al., 2007), HIV providers failed to recognize current smoking status more often than non-HIV providers. Patients’ HIV status was an independent predictor of a provider’s failure to recognize current smoking. Recognition of smoking status was not impacted by comorbid illness, cough, dyspnea, degree of immune competence or HIV viral suppression. Furthermore, only a minority (39%) of HIV providers reported confidence in their ability to influence smoking cessation. To increase access to evidence-based smoking cessation treatment, HIV provider-level barriers must be addressed. Provider training, particularly when coupled with systems changes such as reminder systems, has been shown to increase the provision of tobacco cessation interventions (Fiore et al., 2008), however such research has not been conducted in HIV care settings to date.

HIV clinics and providers are uniquely positioned to provide smoking cessation interventions. Smoking cessation interventions delivered by different clinicians increase abstinence rates in the general population (Fiore et al., 2008). The interdisciplinary treatment model of HIV care programs, in which case management, counseling, nursing and medical treatment are co-located, is thus an ideal setting for the delivery of smoking cessation interventions. Routine HIV follow up may enhance the provision of smoking cessation advice; repeated counseling has been shown to increase smoking abstinence rates (Fiore et al., 2008). HIV providers are skilled at addressing and supporting medication adherence and troubleshooting medication adverse effects. HIV providers have also developed skills in addressing addictive disorders and integrating addiction treatment with HIV care (Basu, Smith-Rohrberg, Bruce, & Altice, 2006; B. Turner, Laine, Lin, & Lynch, 2005) that could be utilized to provide smoking cessation services. These strengths must be leveraged to systematically integrate smoking cessation treatment into HIV care.

Smoking cessation interventions for HIV-positive smokers

A review published in 2000 outlined a research agenda to facilitate expansion of smoking cessation services to HIV-positive persons. The authors called for research that 1) tests the efficacy and generalizability of proven smoking cessation interventions; and 2) understands the special concerns that may surround cessation among HIV-positive smokers (Niaura et al., 2000). Despite these recommendations, there continues to be a dearth of clinical research to help elucidate and disseminate effective interventions for HIV-positive smokers.

Persons with HIV were likely to be excluded from participation in the clinical trials that demonstrated the efficacy of nicotine replacement therapy, bupropion, or varenicline for smoking cessation (Ahluwalia, Harris, Catley, Okuyemi, & Mayo, 2002; Gonzales et al., 2006; Hurt et al., 1997; Jorenby et al., 2006; Jorenby et al., 1999). A number of studies (reviewed below) have evaluated the feasibility and effectiveness of smoking cessation treatment in HIV-positive smokers using nicotine replacement therapy; no trials to our knowledge have evaluated the efficacy of bupropion or varenicline for smoking cessation in HIV-positive smokers. Differences in smoking patterns, nicotine dependence and psychosocial factors decrease the generalizability of results of clinical trials conducted in the general population.

Pilot research suggests that smoking cessation interventions are feasible in HIV care settings. Three small studies evaluating standard smoking cessation interventions in HIV-positive smokers are summarized in Table 1. Results suggest that nicotine replacement therapy, in combination with counseling, may increase smoking cessation and decrease tobacco use in HIV-positive smokers (Cummins, Trotter, Moussa, & Turham, 2005; Elzi et al., 2006; Wewers, Neidig, & Kihm, 2000). Further research is necessary to confirm these findings in controlled trials.

Table 1.

Studies of standard smoking-cessation interventions among HIV-positive smokers

Source Setting Participants Interventions Outcomes
Cummins et al., 2005 Outpatient clinic
and primary care
community
service in New
South Wales
HIV+ outpatients
I: Current smokers interested
in quitting (sex, age NR)
C: no comparison group
I (N=27): 8-12 weeks NRT
 Single counseling session
 Smoking diary
 Educational materials
C: no comparison group
Completion of treatment:
N= 16 (59%)
Self-reported abstinence:
44% at end of NRT course
15% at 5 month follow up
Elzi et al., 2006 Swiss HIV
Cohort Study
(SHCS) clinics in
Basel,
Switzerland
HIV+ SHCS participants
I: Current smokers interested
in quitting
82% male, age M = 43
C: Current smokers
67% male, age M = 40
I (N=34): NRT (course NR)
Fifteen 30 minute counseling
sessions
C (N=383): usual care
Completion of treatment NR
Self-reported abstinence:
I: 50% at 3 months
 38% at 12 months*
C:15% at 3 months
 7% at 12 months*
*OR=6.2 (95% CI 2.8, 14.3)
Wewers et al., 2000 AIDS Clinical
Trials Unit in
Ohio providing
primary and
research care
Male, HIV+ smokers
interested in quitting
I: age M = 42
27 cigarettes/day
C: age M = 37
28 cigarettes/day
I (N=8): Nicotine patch × 8 wks
 Weekly peer-led telephone
 counseling and smoking
 cessation skills training
C (N=7): Written self-help
 materials
Completion of treatment:
I: N= 7 (87.5%)
C: NR
Biochemically-confirmed
continuous abstinence:
I: 62.5% at 8 weeks
 50% at 8 months
C: 0% at 8 weeks
 0% at 8 months

I = intervention arm C = comparison arm NR = not reported

Tailored interventions

HIV-positive persons have a complex range of psychiatric, social, economic and medical needs, but research on smoking cessation interventions specifically tailored to HIV-positive persons is in its infancy. To address motivational issues of HIV-positive smokers, including low interest, confidence or readiness to quit smoking, Ingersoll et al. evaluated a motivational smoking cessation intervention among 40 HIV-positive smokers reporting interest in smoking cessation (Ingersoll, Cropsey, & Heckman, 2007). All participants received nicotine patches and were randomly assigned to receive a single session of motivational counseling or written self-help material. There was no difference in smoking cessation outcomes by treatment arm, however both groups significantly reduced cigarettes smoked per day and mean Carbon Monoxide level.

The largest trial to date randomized 95 HIV-positive smokers to receive usual care (brief physician counseling, self-help written materials and nicotine replacement therapy) or a cellular telephone intervention (including eight telephone counseling contacts and usual care components) (Vidrine, Arduino, Lazev, & Gritz, 2006). The cellular phone counseling was tailored to HIV-positive smokers, addressing benefits of smoking cessation such as preventing HIV-related diseases and reducing HIV treatment-associated side effects. Biochemically verified point prevalence abstinence was 36.8% in the cellular telephone group, 3.6× higher than the usual care group, at three month follow up. These data suggest that tailored, intensive interventions are feasible and may be effective for short-term smoking cessation in HIV-positive persons.

Future directions

Much remains to be learned about effective tobacco control measures in HIV-positive persons. Further research is necessary to elucidate and expand the provision of effective smoking cessation interventions in 1) clinical, 2) behavioral, and 3) systems-based domains:

  1. Clinical research. The efficacy, safety and tolerability of smoking cessation medications in HIV-positive persons warrants further evaluation in controlled clinical trials with long-term follow up. Medication interactions with antiretroviral therapy and effects of medication adherence must be further explored.

  2. Behavioral research. Smoking cessation interventions with demonstrated efficacy in the general population may be less effective among HIV-positive smokers. Tailoring interventions to address the complex social, economic, psychiatric and medical needs of HIV-positive smokers may be necessary, and must be rigorously evaluated.

  3. Systems-based research. Multiple barriers to the provision of smoking cessation treatment exist. Systems-based interventions effective in expanding routine screening for tobacco use and provision of cessation services must be developed and disseminated.

As HIV-positive persons live longer in the HAART era, the burden of tobacco-related disease and mortality must be addressed through the development and dissemination of effective smoking cessation treatment. The disproportionate prevalence of tobacco use in HIV-positive persons contributes to the increasing incidence of cardiovascular, pulmonary and non-HIV associated neoplastic disease in HIV-positive persons. Despite the marked prevalence of tobacco use and tobacco-related disease, data suggest that HIV-positive smokers are interested in smoking cessation treatment and can successfully quit. The strengths of HIV care systems and providers should be leveraged to systematically integrate tobacco cessation treatment into HIV care. In the absence of clear guidelines, HIV providers should treat tobacco use with the array of evidence-based smoking cessation treatments available, updating their clinical practice as new data emerge. Without smoking cessation treatment, thousands will benefit from antiretroviral therapy only to suffer the consequences of tobacco-related disease and death.

ACKNOWLEDGMENTS

We acknowledge Dr. Julia Arnsten and colleagues at the Albert Einstein College of Medicine Division of General Internal Medicine for their thoughtful comments on this manuscript. We also thank Racheline G. Habousha, MSLS, AHIP, for assistance with the literature search, and further thank the National Institutes of Health for organizing the “Current Issues in Cigarette Smoking and HIV/AIDS” workshop.

Dr. Nahvi is supported by the Bronx Center to Reduce and Eliminate Ethnic and Racial Health Disparities (NIH 5P60 MD000514), the New York State Department of Health Empire Clinical Research Investigator Program, and the Clinical Addiction Research and Education Program (NIH R25 DA023021).

Dr. Cooperman is supported by the National Institute of Drug Abuse Grant # R01DA015302, and a Center for AIDS Research Grant # P30AI51519 from the National Institute of Allergy and Infectious Diseases.

References

  1. Abrams DB, Niaura R, Brown RA, Emmons KM, Goldstein MG, Monti PM. The Tobacco Dependence Treatment Handbook: A Guide to Best Practices. Guilford Press; New York: 2003. [Google Scholar]
  2. Ahluwalia JS, Harris KJ, Catley D, Okuyemi KS, Mayo MS. Sustained-Release Bupropion for Smoking Cessation in African Americans: A Randomized Controlled Trial. JAMA. 2002;288(4):468–474. doi: 10.1001/jama.288.4.468. [DOI] [PubMed] [Google Scholar]
  3. Arnsten JH, Demas PA, Grant RW, Gourevitch MN, Farzadegan H, Howard AA, et al. Impact of active drug use on antiretroviral therapy adherence and viral suppression in HIV-infected drug users. Journal of General Internal Medicine. 2002;17(5):377–381. doi: 10.1046/j.1525-1497.2002.10644.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Arnsten JH, Li X, Mizuno Y, Knowlton AR, Gourevitch MN, Handley K, et al. Factors associated with antiretroviral therapy adherence and medication errors among HIV-infected injection drug users. Journal of Acquired Immune Deficiency Syndromes: JAIDS. 2007;46(Suppl 2):S64–71. doi: 10.1097/QAI.0b013e31815767d6. [DOI] [PubMed] [Google Scholar]
  5. Basu S, Smith-Rohrberg D, Bruce RD, Altice F. Models for Integrating Buprenorphine Therapy into the Primary HIV Care Setting. Clinical Infectious Diseases. 2006;42(5):716–721. doi: 10.1086/500200. [DOI] [PubMed] [Google Scholar]
  6. Benard A, Bonnet F, Tessier J-F, Fossoux H, Dupon M, Mercie P, et al. Tobacco addiction and HIV infection: Toward the implementation of cessation programs. ANRS CO3 Aquitaine Cohort. AIDS Patient Care and STDs. 2007;21(7):458–468. doi: 10.1089/apc.2006.0142. [DOI] [PubMed] [Google Scholar]
  7. Biggar RJMD, Engels EAMD, Ly SMS, Kahn AMS, Schymura MJP, Sackoff JP, et al. Survival After Cancer Diagnosis in Persons With AIDS. JAIDS Journal of Acquired Immune Deficiency Syndromes. 2005;39(3):293–299. doi: 10.1097/01.qai.0000164033.02947.e3. [DOI] [PubMed] [Google Scholar]
  8. Bonnie RJ, Stratton K, Wallace RB, Committee on Reducing Tobacco Use: Strategies Barriers and Consequences . Ending the Tobacco Problem: A Blueprint for the Nation. The National Academies Press; Washington, D.C.: 2007. [Google Scholar]
  9. Browning KK, Ferketich AK, Salsberry PJ, Wewers ME. Socioeconomic disparity in provider-delivered assistance to quit smoking. Nicotine & Tobacco Research. 2008;10(1):55–61. doi: 10.1080/14622200701704905. [DOI] [PubMed] [Google Scholar]
  10. Burkhalter JE, Springer CM, Chhabra R, Ostroff JS, Rapkin BD. Tobacco use and readiness to quit smoking in low-income HIV-infected persons. Nicotine & Tobacco Research. 2005;7(4):511–522. doi: 10.1080/14622200500186064. [DOI] [PubMed] [Google Scholar]
  11. Carr A, Samaras K, Burton S, Law M, Freund J, Chisholm DJ, et al. A syndrome of peripheral lipodystrophy, hyperlipidaemia and insulin resistance in patients receiving HIV protease inhibitors. AIDS. 1998;12(7):F51–F58. doi: 10.1097/00002030-199807000-00003. [DOI] [PubMed] [Google Scholar]
  12. Centers for Disease Control and Prevention State-specific prevalence of cigarette smoking among adults and quitting among persons aged 18-35 years--United States, 2006. Morbidity and mortality weekly report. 2007;56(38):993–996. [PubMed] [Google Scholar]
  13. Chattopadhyay A, Caplan DJ, Slade GD, Shugars DC, Tien H-C, Patton LL. Incidence of oral candidiasis and oral hairy leukoplakia in HIV-infected adults in North Carolina. Oral Surgery Oral Medicine Oral Pathology Oral Radiology & Endodontics. 2005a;99(1):39–47. doi: 10.1016/j.tripleo.2004.06.081. [DOI] [PubMed] [Google Scholar]
  14. Chattopadhyay A, Caplan DJ, Slade GD, Shugars DC, Tien H-C, Patton LL. Risk indicators for oral candidiasis and oral hairy leukoplakia in HIV-infected adults. Community Dentistry and Oral Epidemiology. 2005b;33(1):35–44. doi: 10.1111/j.1600-0528.2004.00194.x. [DOI] [PubMed] [Google Scholar]
  15. Chaturvedi AK, Pfeiffer RM, Chang L, Goedert JJ, Biggar RJ, Engels EA. Elevated risk of lung cancer among people with AIDS. AIDS. 2007;21(2):207–213. doi: 10.1097/QAD.0b013e3280118fca. [DOI] [PubMed] [Google Scholar]
  16. Clifford GM, Polesel J, Rickenbach M, Dal Maso L, Keiser O, Kofler A, et al. Cancer risk in the Swiss HIV Cohort Study: associations with immunodeficiency, smoking, and highly active antiretroviral therapy. Journal of the National Cancer Institute. 2005;97(6):425–432. doi: 10.1093/jnci/dji072. [DOI] [PubMed] [Google Scholar]
  17. Cofrancesco J, Jr., Scherzer R, Tien PC, Gibert CL, Southwell H, Sidney S, et al. Illicit drug use and HIV treatment outcomes in a US cohort. AIDS. 2008;22(3):357–365. doi: 10.1097/QAD.0b013e3282f3cc21. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Cooperman NA, Schoenbaum E, Klein R, Arnsten JH. Cigarette smoking among older men and women with or at-risk for HIV infection. Poster presented at the Society for Research on Nicotine and Tobacco 13th Annual Meeting; Austin, TX. 2007. [Google Scholar]
  19. Crothers K. Chronic obstructive pulmonary disease in patients who have HIV infection. Clinics in Chest Medicine. 2007;28(3):575–587. doi: 10.1016/j.ccm.2007.06.004. [DOI] [PubMed] [Google Scholar]
  20. Crothers K, Butt AA, Gibert CL, Rodriguez-Barradas MC, Crystal S, Justice AC, et al. Increased COPD among HIV-positive compared to HIV-negative veterans. Chest. 2006;130(5):1326–1333. doi: 10.1378/chest.130.5.1326. [DOI] [PubMed] [Google Scholar]
  21. Crothers K, Goulet JL, Rodriguez-Barradas MC, Gibert CL, Butt AA, Braithwaite RS, et al. Decreased awareness of current smoking among health care providers of HIV-positive compared to HIV-negative veterans. Journal of General Internal Medicine. 2007;22(6):749–754. doi: 10.1007/s11606-007-0158-8. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Crothers K, Griffith TA, McGinnis KA, Rodriguez-Barradas MC, Leaf DA, Weissman S, et al. The impact of cigarette smoking on mortality, quality of life, and comorbid illness among HIV-positive veterans. Journal of General Internal Medicine. 2005;20(12):1142–1145. doi: 10.1111/j.1525-1497.2005.0255.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Cummins D, Trotter G, Moussa M, Turham G. Smoking cessation for clients who are HIV-positive. Nursing Standard. 2005;20(12):41–47. doi: 10.7748/ns2005.11.20.12.41.c4016. [DOI] [PubMed] [Google Scholar]
  24. De Socio GVL, Martinelli L, Morosi S, Fiorio M, Roscini AR, Stagni G, et al. Is estimated cardiovascular risk higher in HIV-infected patients than in the general population? Scandinavian Journal of Infectious Diseases. 2007;39(9):805–812. doi: 10.1080/00365540701230884. [DOI] [PubMed] [Google Scholar]
  25. Elzi L, Spoerl D, Voggensperger J, Nicca D, Simcock M, Bucher HC, et al. A smoking cessation programme in HIV-infected individuals: a pilot study. Antiviral Therapy. 2006;11(6):787–795. [PubMed] [Google Scholar]
  26. Engels EA, Brock MV, Chen J, Hooker CM, Gillison M, Moore RD. Elevated incidence of lung cancer among HIV-infected individuals. Journal of Clinical Oncology. 2006;24(9):1383–1388. doi: 10.1200/JCO.2005.03.4413. [DOI] [PubMed] [Google Scholar]
  27. Feldman JG, Minkoff H, Schneider MF, Gange SJ, Cohen M, Watts DH, et al. Association of cigarette smoking with HIV prognosis among women in the HAART era: a report from the women’s interagency HIV study. American Journal of Public Health. 2006;96(6):1060–1065. doi: 10.2105/AJPH.2005.062745. [DOI] [PMC free article] [PubMed] [Google Scholar]
  28. Fiore MC, Jaén CR, Baker TB, Bailey WC, Benowitz NL, Curry SJ, et al. Clinical Practice Guideline. U.S. Department of Health and Human Services. Public Health Service; Rockville, MD: 2008. Treating Tobacco Use and Dependence. [Google Scholar]
  29. Frisch M, Biggar RJ, Engels EA, Goedert JJ. Association of Cancer With AIDS-Related Immunosuppression in Adults. JAMA. 2001;285(13):1736–1745. doi: 10.1001/jama.285.13.1736. [DOI] [PubMed] [Google Scholar]
  30. Gonzales D, Rennard SI, Nides M, Oncken C, Azoulay S, Billing CB, et al. Varenicline, an alpha4beta2 Nicotinic Acetylcholine Receptor Partial Agonist, vs Sustained-Release Bupropion and Placebo for Smoking Cessation: A Randomized Controlled Trial. JAMA. 2006;296(1):47–55. doi: 10.1001/jama.296.1.47. [DOI] [PubMed] [Google Scholar]
  31. Gritz ER, Vidrine DJ, Lazev AB, Amick BC, 3rd, Arduino RC. Smoking behavior in a low-income multiethnic HIV/AIDS population. Nicotine & Tobacco Research. 2004;6(1):71–77. doi: 10.1080/14622200310001656885. [DOI] [PubMed] [Google Scholar]
  32. Hesse L, Greenblatt DJ, von Moltke LL, Court MH. Ritonavir has minimal impact on the pharmacokinetic disposition of a single dose of bupropion administered to human volunteers. Journal of Clinical Pharmacology. 2006;46(5):567–576. doi: 10.1177/0091270006286981. [DOI] [PubMed] [Google Scholar]
  33. Hesse L, von Moltke LL, Shader RI, Greenblatt DJ. Ritonavir, efavirenz, and nelfinavir inhibit CYP2B6 activity in vitro: potential drug interactions with bupropion. Drug Metabolism & Disposition. 2001;29(2):100–102. [PubMed] [Google Scholar]
  34. Houston TK, Scarinci IC, Person SD, Greene PG. Patient smoking cessation advice by health care providers: The role of ethnicity, socioeconomic status, and health. American Journal of Public Health. 2005;95(6):1056–1061. doi: 10.2105/AJPH.2004.039909. [DOI] [PMC free article] [PubMed] [Google Scholar]
  35. Hurt R, Sachs DP, Glover ED, Offord KP, Johnston JA, Dale LC, et al. A comparison of sustained-release bupropion and placebo for smoking cessation. New England Journal of Medicine. 1997;337(17):1195–1202. doi: 10.1056/NEJM199710233371703. [DOI] [PubMed] [Google Scholar]
  36. Ingersoll KS, Cropsey KL, Heckman CJ. A Test of Motivational Plus Nicotine Replacement Interventions for HIV Positive Smokers [epub ahead of print] AIDS and Behavior. 2007 doi: 10.1007/s10461-007-9334-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
  37. Jorenby D, Hays JT, Rigotti NA, Azoulay S, Watsky EJ, Williams KE, et al. Efficacy of Varenicline, an alpha4beta2 Nicotinic Acetylcholine Receptor Partial Agonist, vs Placebo or Sustained-Release Bupropion for Smoking Cessation: A Randomized Controlled Trial. JAMA. 2006;296(1):56–63. doi: 10.1001/jama.296.1.56. [DOI] [PubMed] [Google Scholar]
  38. Jorenby D, Leischow SJ, Nides MA, Rennard SI, Johnston JA, Hughes AR, et al. A controlled trial of sustained-release bupropion, a nicotine patch, or both for smoking cessation. New England Journal of Medicine. 1999;340(9):685–691. doi: 10.1056/NEJM199903043400903. [DOI] [PubMed] [Google Scholar]
  39. Kirk GD, Merlo C, O’ Driscoll P, Mehta SH, Galai N, Vlahov D, et al. HIV infection is associated with an increased risk for lung cancer, independent of smoking. Clinical Infectious Diseases. 2007;45(1):103–110. doi: 10.1086/518606. [DOI] [PMC free article] [PubMed] [Google Scholar]
  40. Kohli R, Lo Y, Homel P, Flanigan TP, Gardner LI, Howard AA, et al. Bacterial pneumonia, HIV therapy, and disease progression among HIV-infected women in the HIV epidemiologic research (HER) study. Clinical Infectious Diseases. 2006;43(1):90–98. doi: 10.1086/504871. [DOI] [PubMed] [Google Scholar]
  41. Lancaster T, Stead LF. Physician advice for smoking cessation. Cochrane Database of Systematic Reviews. 2004;(Issue 4) doi: 10.1002/14651858.CD000165.pub3. Art. No.: CD000165. DOI: 10.1002/14651858.CD000165.pub2. [DOI] [PubMed] [Google Scholar]
  42. Lasser K, Boyd JW, Woolhandler S, Himmelstein DU, McCormick D, Bor DH. Smoking and Mental Illness: A Population-Based Prevalence Study. JAMA. 2000;284(20):2606–2610. doi: 10.1001/jama.284.20.2606. [DOI] [PubMed] [Google Scholar]
  43. Lazev A, Vidrine D, Arduino R, Gritz E. Increasing access to smoking cessation treatment in a low-income, HIV-positive population: the feasibility of using cellular telephones. Nicotine & Tobacco Research. 2004;6(2):281–286. doi: 10.1080/14622200410001676314. [DOI] [PubMed] [Google Scholar]
  44. Le Moing V, Rabaud C, Journot V, Duval X, Cuzin L, Cassuto JP, et al. Incidence and risk factors of bacterial pneumonia requiring hospitalization in HIV-infected patients started on a protease inhibitor-containing regimen. HIV Medicine. 2006;7(4):261–267. doi: 10.1111/j.1468-1293.2006.00370.x. [DOI] [PubMed] [Google Scholar]
  45. Leserman J, Ironson G, O’Cleirigh C, Fordiani JM, Balbin E. Stressful Life Events and Adherence in HIV [Epub ahead of print] AIDS Patient Care and STDs. 2008 doi: 10.1089/apc.2007.0175. [DOI] [PMC free article] [PubMed] [Google Scholar]
  46. Lloyd-Richardson EE, Stanton CA, Papandonatos GD, Betancourt RM, Stein M, Tashima K, et al. HIV-positive smokers considering quitting: Differences by race/ethnicity. American Journal of Health Behavior. 2008;32(1):3–15. doi: 10.5555/ajhb.2008.32.1.3. [DOI] [PMC free article] [PubMed] [Google Scholar]
  47. Lohse N, Hansen A-BE, Pedersen G, Kronborg G, Gerstoft J, Sorensen HT, et al. Survival of persons with and without HIV infection in Denmark, 1995-2005. Annals of Internal Medicine. 2007;146(2):87–95. doi: 10.7326/0003-4819-146-2-200701160-00003. [DOI] [PubMed] [Google Scholar]
  48. Lopez-Quintero C, Crum RM, Neumark YD. Racial/Ethnic Disparities in Report of Physician-Provided Smoking Cessation Advice: Analysis of the 2000 National Health Interview Survey. Am J Public Health. 2006;96(12):2235–2239. doi: 10.2105/AJPH.2005.071035. [DOI] [PMC free article] [PubMed] [Google Scholar]
  49. Mamary EM, Bahrs D, Martinez S. Cigarette smoking and the desire to quit among individuals living with HIV. Aids Patient Care and STDS. 2002;16(1):39–42. doi: 10.1089/108729102753429389. [DOI] [PubMed] [Google Scholar]
  50. McCool RM, Richter KP. Why do so many drug users smoke? Journal of Substance Abuse Treatment. 2003;25(1):43–49. doi: 10.1016/s0740-5472(03)00065-5. [DOI] [PubMed] [Google Scholar]
  51. McGinnis JM, Foege WH. Actual causes of death in the United States. JAMA. 1993;270(18):2207–2212. [PubMed] [Google Scholar]
  52. Miguez-Burbano MJ, Ashkin D, Rodriguez A, Duncan R, Pitchenik A, Quintero N, et al. Increased risk of Pneumocystis carinii and community-acquired pneumonia with tobacco use in HIV disease. International Journal of Infectious Diseases. 2005;9(4):208–217. doi: 10.1016/j.ijid.2004.07.010. [DOI] [PubMed] [Google Scholar]
  53. Miguez-Burbano MJ, Burbano X, Ashkin D, Pitchenik A, Allan R, Pineda L, et al. Impact of tobacco use on the development of opportunistic respiratory infections in HIV seropositive patients on antiretroviral therapy. Addiction Biology. 2003;8(1):39–43. doi: 10.1080/1355621031000069864. [DOI] [PubMed] [Google Scholar]
  54. Miller WR, Rollnick S. Motivational Interviewing: Preparing People for Change. 2d ed Guilford Press; New York: 2002. [Google Scholar]
  55. Nahvi S, Richter K, Li X, Modali L, Arnsten J. Cigarette smoking and interest in quitting in methadone maintenance patients. Addictive Behaviors. 2006;31:2127–2134. doi: 10.1016/j.addbeh.2006.01.006. [DOI] [PubMed] [Google Scholar]
  56. Niaura R. Nonpharmacologic therapy for smoking cessation: characteristics and efficacy of current approaches. American Journal of Medicine. 2008;121(4 Suppl 1):S11–19. doi: 10.1016/j.amjmed.2008.01.021. [DOI] [PubMed] [Google Scholar]
  57. Niaura R, Shadel WG, Morrow K, Tashima K, Flanigan T, Abrams DB. Human immunodeficiency virus infection, AIDS, and smoking cessation: the time is now. Clinical Infectious Diseases. 2000;31(3):808–812. doi: 10.1086/314048. [DOI] [PubMed] [Google Scholar]
  58. NIH State-of-the-Science Panel National Institutes of Health State-of-the-Science Conference Statement: Tobacco Use: Prevention, Cessation, and Control. Annals of Internal Medicine. 2006;145(11):839–844. doi: 10.7326/0003-4819-145-11-200612050-00141. [DOI] [PubMed] [Google Scholar]
  59. Palacio H, Hilton JF, Canchola AJ, Greenspan D. Effect of cigarette smoking on HIV-related oral lesions. Journal of Acquired Immune Deficiency Syndromes & Human Retrovirology. 1997;14(4):338–342. doi: 10.1097/00042560-199704010-00005. [DOI] [PubMed] [Google Scholar]
  60. Palella FJ, Baker RK, Moorman AC, Chmiel JS, Wood KC, Brooks JT, et al. Mortality in the highly active antiretroviral therapy era: changing causes of death and disease in the HIV outpatient study. Journal of Acquired Immune Deficiency Syndromes: JAIDS. 2006;43(1):27–34. doi: 10.1097/01.qai.0000233310.90484.16. [DOI] [PubMed] [Google Scholar]
  61. Palella FJ, Delaney KM, Moorman AC, Loveless MO, Fuhrer J, Satten GA, et al. Declining Morbidity and Mortality among Patients with Advanced Human Immunodeficiency Virus Infection. New England Journal of Medicine. 1998;338(13):853–860. doi: 10.1056/NEJM199803263381301. [DOI] [PubMed] [Google Scholar]
  62. Park-Wyllie LY, Antoniou T. Concurrent use of bupropion with CYP2B6 inhibitors, nelfinavir, ritonavir and efavirenz: a case series. AIDS. 2003;17(4):638–640. doi: 10.1097/00002030-200303070-00025. [DOI] [PubMed] [Google Scholar]
  63. Pence BW, Miller WC, Whetten K, Eron JJ, Gaynes BN. Prevalence of DSM-IV-defined mood, anxiety, and substance use disorders in an HIV clinic in the Southeastern United States. Journal of Acquired Immune Deficiency Syndromes: JAIDS. 2006;42(3):298–306. doi: 10.1097/01.qai.0000219773.82055.aa. [DOI] [PubMed] [Google Scholar]
  64. Peretti-Watel P, Spire B, Lert F, Obadia Y. Drug use patterns and adherence to treatment among HIV-positive patients: evidence from a large sample of French outpatients (ANRS-EN12-VESPA 2003) Drug & Alcohol Dependence. 2006;82(Suppl 1):S71–79. doi: 10.1016/s0376-8716(06)80012-8. [DOI] [PubMed] [Google Scholar]
  65. Reynolds NR, Neidig JL, Wewers ME. Illness representation and smoking behavior: a focus group study of HIV-positive men. Journal of the Association of Nurses in AIDS Care. 2004;15(4):37–47. doi: 10.1177/1055329003261969. [DOI] [PubMed] [Google Scholar]
  66. Richter K, Arnsten JH. A rationale and model for addressing tobacco dependence in substance abuse treatment. Substance Abuse Treatment, Prevention, and Policy. 2006;1:1–23. doi: 10.1186/1747-597X-1-23. [DOI] [PMC free article] [PubMed] [Google Scholar]
  67. Richter K, Gibson CA, Ahluwalia JS, Schmelzle KH. Tobacco use and quit attempts among methadone maintenance clients. American Journal of Public Health. 2001;91(2):296–299. doi: 10.2105/ajph.91.2.296. [DOI] [PMC free article] [PubMed] [Google Scholar]
  68. Shuter J, Bernstein SL. Cigarette smoking is an independent predictor of nonadherence in HIV-infected individuals receiving highly active antiretroviral therapy. Nicotine & Tobacco Research. 2008;10(4):731–736. doi: 10.1080/14622200801908190. [DOI] [PubMed] [Google Scholar]
  69. Silagy C, Lancaster T, Stead L, Mant D, Fowler G. Nicotine replacement therapy for smoking cessation (Cochrane review) Cochrane Database of Systematic Reviews 2004. 2004;(Issue 3) doi: 10.1002/14651858.CD000146.pub2. Art. No.: CD 000146. DOI: 10.1002/14651858.CD 000146.pub2. [DOI] [PubMed] [Google Scholar]
  70. Simon JA, Carmody TP, Hudes ES, Snyder E, Murray J. Intensive smoking cessation counseling versus minimal counseling among hospitalized smokers treated with transdermal nicotine replacement: a randomized trial. American Journal of Medicine. 2003;114(7):555–562. doi: 10.1016/s0002-9343(03)00081-0. [DOI] [PubMed] [Google Scholar]
  71. Smedley BD, Stith AY, Nelson AR. Unequal Treatment: Confronting Racial and Ethnic Disparities in Health Care. National Academies Press; Washington, DC: 2002. [PubMed] [Google Scholar]
  72. Stall RD, Greenwood GL, Acree M, Paul J, Coates TJ. Cigarette smoking among gay and bisexual men. Am J Public Health. 1999;89(12):1875–1878. doi: 10.2105/ajph.89.12.1875. [DOI] [PMC free article] [PubMed] [Google Scholar]
  73. Stead L, Perera R, Bullen C, Mant D, Lancaster T. Nicotine replacement therapy for smoking cessation. Cochrane Database of Systematic Reviews: Reviews 2008. 2008;(Issue 1) doi: 10.1002/14651858.CD000146.pub3. DOI: 10.1002/14651858.CD000146.pub3. [DOI] [PubMed] [Google Scholar]
  74. Stead L, Perera R, Lancaster T. Telephone counselling for smoking cessation. Cochrane Database of Systematic Reviews. 2006;3 doi: 10.1002/14651858.CD002850.pub2. CD002850. [DOI] [PubMed] [Google Scholar]
  75. Stein MD, Anderson BJ, Niaura R. Nicotine replacement therapy: patterns of use after a quit attempt among methadone-maintained smokers. Journal of General Internal Medicine. 2006;21(7):753–757. doi: 10.1111/j.1525-1497.2006.00504.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  76. Tegger MK, Crane HM, Tapia KA, Uldall KK, Holte SE, Kitahata MM. The effect of mental illness, substance use, and treatment for depression on the initiation of highly active antiretroviral therapy among HIV-infected individuals. AIDS Patient Care & Stds. 2008;22(3):233–243. doi: 10.1089/apc.2007.0092. [DOI] [PubMed] [Google Scholar]
  77. The DAD Study Group Class of Antiretroviral Drugs and the Risk of Myocardial Infarction. New England Journal of Medicine. 2007;356(17):1723–1735. doi: 10.1056/NEJMoa062744. [DOI] [PubMed] [Google Scholar]
  78. The Data Collection on Adverse Events of Anti-HIV Drugs (DAD) Study Group Combination Antiretroviral Therapy and the Risk of Myocardial Infarction. New England Journal of Medicine. 2003;349(21):1993–2003. doi: 10.1056/NEJMoa030218. [DOI] [PubMed] [Google Scholar]
  79. Thiebaut R, Daucourt V, Mercie P, Ekouevi DK, Malvy D, Morlat P, et al. Lipodystrophy, Metabolic Disorders, and Human Immunodeficiency Virus Infection: Aquitaine Cohort, France, 1999. Clinical Infectious Diseases. 2000;31(6):1482–1487. doi: 10.1086/317477. [DOI] [PubMed] [Google Scholar]
  80. Triant VA, Lee H, Hadigan C, Grinspoon SK. Increased acute myocardial infarction rates and cardiovascular risk factors among patients with human immunodeficiency virus disease. Journal of Clinical Endocrinology and Metabolism. 2007;92(7):2506–2512. doi: 10.1210/jc.2006-2190. [DOI] [PMC free article] [PubMed] [Google Scholar]
  81. Turner B, Laine C, Lin Y.-t., Lynch K. Barriers and Facilitators to Primary Care or Human Immunodeficiency Virus Clinics Providing Methadone or Buprenorphine for the Management of Opioid Dependence. Arch Intern Med. 2005;165(15):1769–1776. doi: 10.1001/archinte.165.15.1769. [DOI] [PubMed] [Google Scholar]
  82. Turner J, Page-Shafer K, Chin DP, Osmond D, Mossar M, Markstein L, et al. Adverse impact of cigarette smoking on dimensions of health-related quality of life in persons with HIV infection. AIDS Patient Care & STDs. 2001;15(12):615–624. doi: 10.1089/108729101753354617. [DOI] [PubMed] [Google Scholar]
  83. U.S. Food and Drug Administration [Retrieved October 24, 2008];Information for Healthcare Professionals: Varenicline (marketed as Chantix) 2008 May 16; from http://www.fda.gov/cder/drug/InfoSheets/HCP/vareniclineHCP.htm.
  84. Velicer WF, Fava JL, Prochaska JO, Abrams DB, Emmons KM, Pierce JP. Distribution of smokers by stage in three representative samples. Preventive Medicine. 1995;24:401–411. doi: 10.1006/pmed.1995.1065. [DOI] [PubMed] [Google Scholar]
  85. Vidrine DJ, Arduino RC, Gritz ER. The effects of smoking abstinence on symptom burden and quality of life among persons living with HIV/AIDS. AIDS Patient Care & STDs. 2007;21(9):659–666. doi: 10.1089/apc.2007.0022. [DOI] [PubMed] [Google Scholar]
  86. Vidrine DJ, Arduino RC, Lazev AB, Gritz ER. A randomized trial of a proactive cellular telephone intervention for smokers living with HIV/AIDS. AIDS. 2006;20(2):253–260. doi: 10.1097/01.aids.0000198094.23691.58. [DOI] [PubMed] [Google Scholar]
  87. Walensky RP, Paltiel AD, Losina E, Mercincavage LM, Schackman BR, Sax PE, et al. The survival benefits of AIDS treatment in the United States. Journal of Infectious Diseases. 2006;194(1):11–19. doi: 10.1086/505147. [DOI] [PubMed] [Google Scholar]
  88. Webb MS, Vanable PA, Carey MP, Blair DC. Cigarette smoking among HIV+ men and women: examining health, substance use, and psychosocial correlates across the smoking spectrum. Journal of Behavioral Medicine. 2007;30(5):371–383. doi: 10.1007/s10865-007-9112-9. [DOI] [PMC free article] [PubMed] [Google Scholar]
  89. Wewers ME, Neidig JL, Kihm KE. The feasibility of a nurse-managed, peer-led tobacco cessation intervention among HIV-positive smokers. Journal of the Association of Nurses in AIDS Care. 2000;11(6):37–44. doi: 10.1016/S1055-3290(06)60353-1. [DOI] [PubMed] [Google Scholar]
  90. Williams JM, Ziedonis D. Addressing tobacco among individuals with a mental illness or an addiction. Addictive Behaviors. 2004;29(6):1067–1083. doi: 10.1016/j.addbeh.2004.03.009. [DOI] [PubMed] [Google Scholar]
  91. Yuan Y, L’Italien G, Mukherjee J, Iloeje UH. Determinants of discontinuation of initial highly active antiretroviral therapy regimens in a US HIV-infected patient cohort. HIV Medicine. 2006;7(3):156–162. doi: 10.1111/j.1468-1293.2006.00355.x. [DOI] [PubMed] [Google Scholar]
  92. Zhu S, Melcer T, Sun J, Rosbrook B, Pierce JP. Smoking cessation with and without assistance: A population-based analysis. American Journal of Preventive Medicine. 2000;18(4):305–311. doi: 10.1016/s0749-3797(00)00124-0. [DOI] [PubMed] [Google Scholar]
  93. Zhu SH, Anderson CM, Tedeschi GJ, Rosbrook B, Johnson CE, Byrd M, et al. Evidence of real-world effectiveness of a telephone quitline for smokers. New England Journal of Medicine. 2002;347(14):1087–1093. doi: 10.1056/NEJMsa020660. [DOI] [PubMed] [Google Scholar]
  94. Zierler S, Krieger N, Tang Y, Coady W, Siegfried E, DeMaria A, et al. Economic deprivation and AIDS incidence in Massachusetts. Am J Public Health. 2000;90(7):1064–1073. doi: 10.2105/ajph.90.7.1064. [DOI] [PMC free article] [PubMed] [Google Scholar]

RESOURCES