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Lucy McCarty, Averi McCarthy, Michael Rusu, Alleya Wagner, and Emma Wukelich
5 April 2021
SMOKING CESSATION PROGRAMS 2
Abstract
therapy is more successful than non-pharmacological smoking cessation therapy. The smoking
cessation programs researched were nicotine patches and gum, Chantix, combination therapy,
and non-pharmacological interventions. It was found through our research that there was
significant evidence supporting the use of smoking cessation programs. All forms of smoking
cessation programs that were researched showed some success in either reducing cigarette
effective in helping smokers to reduce cravings and quit smoking. Even in smokers with no
desire to stop smoking, cessation programs effectively decreased their tobacco consumption.
This research included ten sources with qualitative studies, longitudinal studies, and a
literature review. There was no definite evidence regarding proof one individual smoking
cessation program was more successful than another. However, there was evidence that the use
of any combination of smoking cessation therapies lead to greater results than all types of
individual therapy. Overall, the research showed that smoking cessation programs effectively
helped people quit smoking regardless of therapy and the use of multiple therapies led to higher
Literature Review
Introduction
In order to discover the most effective smoking cessation methods in the medical
profession, information was acquired using the Maag Library’s nursing databases. Specifically,
MedLINE, Proquest, and CINAHL were used to find the ten sources used to examine and collect
data regarding the effectiveness of various smoking cessation programs, both pharmacological
and nonpharmacological.
Nicotine Patch
Smoking cessation has been a hot topic in research due to the number of people that want
to quit smoking, considering the lasting effects of smoking tobacco. Many, old and new, nicotine
replacement therapies (NRT) are available on the market today, including nicotine patches that
have long been used in smoking cessation treatments to ease the transition to becoming smoke-
free. Extensive research has been performed to evaluate the effectiveness of patches compared to
other therapies. The goal of NRT is to replace the nicotine that would otherwise come from
smoking to reduce symptoms of withdrawal. Nicotine patches have advantages over other forms
of NRT stated as, “Nicotine patches differ from the other products in that they deliver the
nicotine dose slowly and passively” (Hartmann, 2018, p. 5). Nicotine patches have been proven
to help an individual quit smoking longer than six months. However, there is no conclusive
evidence that solely using patches is more effective than solely using other forms of NRT. As
Lindson (2018, p.2) said, “High‐certainty evidence from eight studies suggests that using either a
form of fast‐acting NRT or a nicotine patch results in similar long‐term quit rates (RR 0.90, 95%
CI 0.77 to 1.05, 8 studies, 3319 participants; I2 = 0%)”. It has been shown that the choice to use
one therapy over another is affected by factors such as expense, availability, and personal
SMOKING CESSATION PROGRAMS 4
response to each therapy. Hartman (2018, p.2) stated, “Side effects from using NRT are related
to the type of product, and include skin irritation from patches and irritation to the inside of the
Research has proven that combinations of NRT have led to greater results than individual
therapy. Again, no conclusive evidence has been provided over which therapies to use together
will bring the best results. It plays into the same factors as choosing an individual therapy.
Patches have not only been studied against other forms of NRT but also have been compared to
different patches based on dosing and duration. Nicotine patches were examined at higher doses
and longer durations to determine if there was more success in smoking cessation. The studies
concluded that participants did have a higher rate of smoking cessation with higher dosages and
durations. The concern with higher dosages and durations was the adverse effects on the
participant. “Results suggest that many smokers can tolerate much higher doses than those
offered by current NRT products and that the evaluation of such dosing is warranted” (Przulj,
2019, p.520).
Overall, nicotine patches do aid in the process of quitting smoking and lead to much
higher success rates long term. Further study will need to be conducted to determine the most
effective monotherapy form of NRT. “Overall evidence favored the combination of NRT over
single-type NRT for smoking cessation” (Lindson, 2019, p.26). Lindson went on to say, “Using
nicotine patch and another type of NRT (such as gum or lozenge) together made it 15% to 36%
more likely that a person would successfully stop smoking than if they used one type of NRT
alone”. However, it is unlikely that new results will change due to the number of individual
Secondly, higher dosages and durations of nicotine patches did prove to have higher
success rates of smoking cessation due to individuals controlling their nicotine intake while
smoking. Lindson (2019, p.2) continued to state, “People were also more likely to quit
successfully if they used higher dose nicotine patches (containing 25 mg (worn over 16 hours) or
compared to 2 mg of nicotine)”. Research has shown that NRT is highly individualized, but there
is not enough evidence to accurately state that the sole use of nicotine patches offers a higher rate
Nicotine Gum
According to Hansson et al. (2019, p. 5), nicotine replacement therapy increases the
chances of stopping smoking by 50% regardless of the type of nicotine replacement therapy.
“Relief of cravings and withdrawal symptoms represents the primary intended use of nicotine
replacement therapy (NRT) and relief of these symptoms is also the principal mechanism of
action of NRT in the support of smoking cessation” (Hansson et al., 2019, p.1). In a randomized,
two-way crossover study conducted on 240 healthy adult smokers given either one dose of 6 mg
or 4 mg nicotine gum, it was discovered that the dose of nicotine gum is an essential factor for
the efficacy of NRT in the treatment of tobacco dependence. Healthy adult volunteers were
recruited for this study and then were randomly allocated in equal proportion to one of two
treatments using a random number generator. Each participant was given a piece of gum; they
were to place the gum in their mouth without looking at it and chew slowly for 30 minutes.
Subjects were then sent home with electronic diaries to record how strong their urge to smoke
was on a 100 mm visual analog scale (VAS) at various time intervals. On the VAS, 100
SMOKING CESSATION PROGRAMS 6
represented an extreme urge to smoke, and zero represented no urge to smoke. In the first 60
minutes, the average urge to smoke was 44 mm with 6 mg gum and 39 mm with 4 mg gum. The
study discovered that the mean reduction in urges to smoke was statistically greater with 6 mg
than 4 mg gum for all examined time intervals (Hannson et al., 2019, p. 1-6).
“For those smokers who, despite numerous quit attempts, are unable to stop or smokers
with low motivation to quit, the concept of smoking reduction, i.e. decreased number of daily
cigarettes smoked, maybe an alternative approach to controlling their smoking” (Wennike et al.,
2003, p. 1). A study was completed on volunteer participants who were 18 years or older, were
either unwilling or unable to stop smoking but interested in reducing their smoking. A total of
411 smokers were randomized to receive active gum or the placebo for up to 1 year. “Subjects
who scored 5 or less in the Fagerström Test for Nicotine Dependence (FTND) were allocated to
the low‐dose group and randomized to either nicotine 2 mg gum or placebo whereas those who
scored 6–10 were allocated to the high‐dose group and randomized to nicotine 4 mg gum or
The study found that a linear relationship was present between a decrease in smoking and
a decrease in plasma thiocyanate and exhaled carbon that was greater in the nicotine gum group
than the placebo group after 4 and 12 months (Wennike et al., 2003, p. 1). “In the active group
at month 12, while still using nicotine gum, mean cigarette consumption was 46% of baseline
value, while mean CO was reduced to 62%; plasma cotinine to 93% and plasma thiocyanate to
75% of baseline” (Wennike et al., 2003, p. 4). This study implies that smokers who are not
interested in smoking cessation can be given nicotine gum to help reduce the number of
cigarettes that they smoke daily, helping to reduce the levels of carbon monoxide and other
Chantix
Along with the use of over-the-counter nicotine replacement therapies, physicians can
also prescribe medications that block the pleasant effects of nicotine on the brain. The United
States Food and Drug Administration (FDA) has provided approval for practitioners to prescribe
varenicline for individuals to use for nicotine addiction. It is one of the seven pharmaceutical
interventions that the FDA has permitted approval for smoking cessation (Burke, 2016, p. 435).
Varenicline is not used as frequently due to the concerns of prescribing practitioners regarding
varenicline for smoking cessation (Burke, 2016, p. 436). The review was completed for PubMed
abstracts with the dates between January 1966 and December 2015. Varenicline was the key
primary word used for the literature search and evaluation. The authors of the literature review
provide disclosure of providing training for medical education credits for Phizer and research
The reviews were broken down into three samples: dosing studies, Phase II studies, and
Phase III studies. The sample for the dosing study was 320 random smokers. There were two
studies of 638 random smokers and 647 random smokers in the Phase II studies. Two trials were
The measurement of the trials was based on two factors. The first was the check-in
points of the participants at 7, 12, 24, and 52 weeks. The confirmations of the trial ending were
the verification of nicotine abstinence by biochemical testing and validation. The trial
participants were provided written education and counseling for smoking cessation (Burke, 2016,
p. 437).
SMOKING CESSATION PROGRAMS 8
Burke (2016, p. 438) reported that varenicline is a successful intervention for persons
who are seeking to stop smoking. The patients who can utilize this technique safely include
those with such diagnoses, including mental health and diseases of the heart and lungs.
Practitioners need to assess the hazards and advantages of using varenicline before determining
if the patient will be started on the medication. The dosage needs to be adjusted to manage
potential side effects of the medication. Self-titrated dosing by the participants had the highest
smoking cessation highest efficacy. Adjusting doses demonstrated improved side effect
Ebbert (2010) completed a literature review to identify the efficacy of varenicline for
smoking cessation. The authors report no conflicts of interest in the article's completion. The
review identifies how to avoid negative side effects of the treatment. Two double-blind Phase III
trials were reviewed. Of the 377 adult smokers in the studies, half were provided a placebo, and
half were provided varenicline. The meta-analysis Ebbert (2010, p. 357) included in the
placebo (Ebbert, 2010, p. 357). The study participants checked in throughout the study. The
dosage of varenicline was 1 milligram twice a day versus the placebo dosage. The results of this
study were participants who received varenicline had higher smoking cessation success
compared to those receiving a placebo. The results were 44% for medication versus 37% for
placebo. A study to verify the safety and effectiveness of long-term varenicline treatment was
reviewed by Ebbert (2010, p. 358). There were 377 smokers in the study divided into
varenicline or placebo administration. After one year, the cohort receiving varenicline was 37%,
while the cohort receiving placebo was 8% for smoking cessation. Ebbert concluded that when
SMOKING CESSATION PROGRAMS 9
smoking adults take varenicline, they have the highest level of smoking cessation attainment
(2010, p. 361). The comparison group is individuals who take other first-line pharmaceutical
treatments for eliminating tobacco dependence. Obstacles to a client's success include such items
as previous smoking cessation failures and unfavorable side effects. Recommendations for
success by Ebbert (2010, p. 361) incorporate fluctuating the medication dosage to minimize the
Nonpharmacological
influences can also aid smokers in reduction and quitting. Smoking cessation is a “social event,”
and those smokers with more social support have a better chance of quitting, as noted by
O’Keefe et al. (2018). In a study, 46 participants between the ages of 33-56 were selected based
on the criteria that they had attended any phase of CEASE (Clinical Effort Against Secondhand
Smoke Exposure) cessation classes. The participants were then split into two groups, based on
their self-reported smoking status; 11 “doers” (quitters) and 35 “non-doers” (smokers). These 46
individuals were given in-depth interviews (IDI) and placed into exploratory focus group
discussions (FGD), which were led by Peer Motivators. “Medical personnel are not as effective
in leading cessation classes as are Peer Motivators (PMs)” (O’Keefe et al., 2018, p. 3).
The 46 individuals completed 8 FGDs, which were recorded and transcribed. “The codes,
themes and subthemes from the FGDs were compared and contrasted to identify similarities and
differences between doers and non-doers” (O’Keefe et al., 2018, p. 3). Most of the non-doers
(smokers) had more reasons for why they smoked cigarettes and were also more apt to place
blame on external triggers for their smoking, such as stress, family, etc. Most of the doers
(quitters) credited their ability to quit on support from their PMs. Doers were also motivated by
SMOKING CESSATION PROGRAMS 10
the well-being of others and their family support systems. The study found that the feedback
most commonly reported by all participants was the appreciation they had to be a participant in a
community-cessation effort and the desire for the program to reach more smokers (O’Keefe et
al., 2018, p. 7). “For many of these smokers, CEASE became the social capital they needed to
conquer the most addictive drug we know” (O’Keefe et al., 2018, p. 7).
Harm reduction aimed at promoting e-cigarettes and vaping among tobacco users is a
topic that has come under much speculation. “Public Health England recommends the use of e-
cigarette for smokers who do not succeed in quitting smoking with other methods or who do not
want to stop smoking” (Pasquereau et al., 2017, p.1). A study was conducted on 2,057 cigarette
users. Of those, 1,805 were conventional smokers, and 252 were dual users (e-cigarettes and
conventional cigarettes). Participants were given a baseline survey. “Intention to quit smoking
during the next 6 months, attempt to stop at least 24 hours during the last 30 days and use of
nicotine replacement therapy (NRT) during the last 30 days were asked at baseline” (Pasquereau
These outcomes were again measured at a six-month follow-up. “The three outcomes
assessed at 6 months were: a minimum 50% reduction in the number of cigarettes smoked per
day, quit attempts of at least 7 days and smoking cessation of at least 7 days at the time of
follow-up” (Pasquereau et al., 2017, p. 1). The study found that dual users were more likely than
exclusive cigarette users to have halved their cigarette consumption. Dual users were also more
likely to have made a quit attempt of at least a week. “Among people who smoke, those also
using an e-cigarette regularly are more likely to try to quit smoking and reduce their cigarette
Combination Therapy
SMOKING CESSATION PROGRAMS 11
In many instances, pharmacological therapy has a much higher success rate when used in
combination with other forms of therapy. This can be seen in a study Vogeler, McClain, and
Evoy conducted in 2016 on whether varenicline, also known as Chantix, worked better as a
single drug therapy for smoking cessation, or if combining varenicline with bupropion, also
known as Wellbutrin, had a higher success rate with smoking cessation. The study had 1,320
cessation service at the study site, and the sample size for this
group was 427. The results for this group showed, “A significantly
McClain, Evoy, 2016, p.4). The next two groups that were studied
included those older than eighteen years old who were smoking at
least ten cigarettes a day for more than six months and had expired-
air CO level ≥ 10 ppm (recent exposure to high levels of CO2). The sample size for
these groups combined was 387. This study concluded, “Results showed a significant difference
in the primary endpoint of 4-week smoking abstinence for weeks 8–11 with combination
treatment (39.8%) versus varenicline plus placebo (25.9%)” (Volger, McClain, Evoy, 2016, p.3).
The last group observed in the study were those greater than the age of 18, who were smoking
more than ten cigarettes a day, for more than six months, who also were in good health. This
group showed, “Results displayed significantly higher prolonged abstinence rate at 12 weeks
SMOKING CESSATION PROGRAMS 12
(OR = 1.49; 95% CI = 1.05–2.12; p value 0.03) and 26 weeks (OR = 1.52; 95% CI = 1.04–2.22;
p value 0.03)” (Volger, McClain, Evoy, 2016, p.4). Overall, the results from each group of the
study concluded that taking varenicline alone yielded less success than if the patient took
varenicline with bupropion or varenicline with bupropion with an SSRI. The success rates from
taking polytherapy were much higher than taking a monotherapy drug by at least ten percent
The next study researched, examined data on medication use and abstinence or cessation
from smoking cigarettes using a randomized comparative effectiveness trial of nicotine patch
monotherapy, varenicline, and combination nicotine patch and lozenge therapy. 241 patients
were given a nicotine patch, 424 patients were given varenicline, 421 patients were given a
nicotine patch and lozenge, and all 1,086 patients received cessation counseling along with their
pharmacologic therapy. Adherence to the cessation therapy was evaluated at the twenty-seventh
day, and data was then compared between all three groups.
shows that adherence is highest for the nicotine patch, and next highest for varenicline,
and lowest for combination nicotine patch and lozenge therapy, due to low lozenge use.”
These results show that physically taking medication and having to remember to take medication
shows to be less effective than placing a transdermal patch on your skin once every few days
because it requires less energy and effort in remembering to place the patch.
While the patch had an overall success in cessation, the study concludes, “Varenicline
and combination NRT did not promote abstinence among adherent latent classes but did promote
SMOKING CESSATION PROGRAMS 13
abstinence among those partially adherent, relative to patch alone.” (McCarthy, Varsella, 2019,
p.1). Meaning for those who only took the varenicline medication part of the time, had better
success in smoking abstinence, than those who only partly adhered to using the nicotine patch.
Conclusion
Overall, the research showed that smoking cessation programs did effectively help people
quit smoking regardless of the type of therapy used. However, it was discovered that the
combination of any of these therapies proved to be more effective than the use of only one of the
therapies. While some smokers were able to achieve full abstinence from tobacco with these
programs, other smokers benefited from harm reduction by simply reducing their cigarette
consumption. According to the CDC, 480,000 Americans die every year due to smoking-related
illnesses. Smoking cessation programs, therefore, could be responsible for saving countless lives
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