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Abstract

Aim:

In the face of increasing tobacco consumption in Sub-Saharan Africa, it is crucial to not only curb the uptake of tobacco, but to ensure that tobacco users quit. Considering the minimal attention that tobacco cessation interventions receive in Sub-Saharan Africa, this review aims to describe studies that evaluated tobacco cessation interventions in the region.

Methods:

A search of studies published till December 2019 that evaluated tobacco cessation interventions in Sub-Saharan Africa and examined tobacco quit rates was conducted in PubMed-Medline, Web of Science and Scopus. Study designs were not limited to randomised control trials but needed to include a control group.

Results:

Of the 454 titles and abstracts reviewed, eight studies, all conducted in South Africa, were included. The earliest publication was from 1988 and the most recent from 2019. Five studies were randomised control trials, two were quasi-experimental and one was a case–control study. Populations studied included community-based smokers (four studies) and university students, while the relevant clinic-based studies were conducted in pregnant women, tuberculosis patients and HIV-infected patients. Sample sizes were 23 in the case–control study, 87–561 in randomised control trials, and 979 (pregnant women) and 4090 (three rural communities) in the quasi-experimental studies. Four studies included nicotine replacement therapy in the interventions while four utilised only psychotherapy without adjunct pharmacotherapy. Quit rates were evaluated by exhaled carbon monoxide levels (five studies), blood carbon monoxide, urinary cotinine levels and self-reported quit rates. Four studies (two each with and without pharmacotherapy) reported significantly better outcomes in the intervention versus the control groups while one study findings (without pharmacotherapy) were significant in women but not men.

Conclusion:

This review highlights that scant attention has been paid to tobacco cessation intervention in Sub-Saharan Africa. The heterogeneity of these studies precluded comparisons across interventions or populations. There is a need for evidence-based low-cost tobacco cessation intervention that target high-risk population in Sub-Saharan Africa.

Keywords

Tobacco cessation interventions Sub-Saharan Africa South Africa smoking tobacco use quit rates

Introduction

Tobacco is the leading preventable cause of mortality globally contributing to cancer, cardiac disease, stroke, chronic lung diseases and other non-communicable diseases.¹ It accounts for more than eight million deaths annually. In addition, tobacco smoking exacerbates tuberculosis and HIV infection leading to poorer outcomes.² Consequently, stopping tobacco use is among the single most effective lifestyle measure to improve health. Substantial evidence shows that smoking cessation reduces mortality from tobacco-related diseases and improves health.³ Unfortunately, smoking is a powerful addiction and despite numerous quit attempts, many individuals who smoke frequently fail to stop smoking, during which time they are unfortunately losing life-years.^1,4 Smoking cessation programmes are therefore necessary to provide the support required for smokers to quit.⁵

The World Health Organisation (WHO) has emphasised the importance of providing support for tobacco cessation in its MPOWER measures, which is a practical tool proposed to reduce tobacco use; the ‘O’ is to ‘offer help to quit tobacco use’.² Effective tobacco cessation interventions (TCI) have shown to greatly increase the likelihood of successfully quitting tobacco. The probability of successful quitting can be doubled with the use of proven cessation medications and professional support. Therefore, providing access to and encouraging the use of tobacco cessation services should be a critical component of any tobacco control strategy.²

In 2011, The Lancet Non-Communicable Disease (NCD) Action Group and the NCD Alliance identified tobacco control as the ‘most urgent and immediate priority’ intervention to reduce NCDs,⁶ with this tenet echoed at the United Nations High-level meeting on NCDs in the same year.⁷ To reduce the global smoking prevalence by 30% by 2025 from a 2010 baseline, countries were urged to fully implement the WHO Framework Convention on Tobacco Control (WHO FCTC). As described in the WHO FCTC Article 14,¹ tobacco cessation is a cost-effective healthcare intervention, and governments and healthcare providers need to provide resources and improve access to programmes to help tobacco users quit.

Furthermore, tobacco control is increasingly considered a vital element for human development because tobacco use contributes to poverty on multiple fronts. These include the cost of purchasing tobacco, healthcare costs for treatment of tobacco-related diseases, and the loss of human capital from tobacco-attributable morbidity and mortality.² Consequently, curbing tobacco use has been recognised as important in promoting sustainable development and incorporated within the Sustainable Development Goals (SDGs) 2030 agenda. Comprehensive tobacco cessation measures are among the key initiatives required to achieve the SDG targets on tobacco control.²

Nevertheless, tobacco use is rising in some countries, especially among vulnerable groups such as women and the youth. This is true in Sub-Saharan Africa (SSA), where the tobacco industry concertedly targets these vulnerable groups.⁸ Therefore, in the face of increasing tobacco consumption on the continent, including in women and the youth, it is crucial to not only curb the uptake of tobacco, but it is also essential to ensure that tobacco users quit. There are highly effective and inexpensive TCI that are recommended even in resource-constrained settings such as SSA.² A small window of opportunity currently exists, particularly in developing regions, to reverse these trends and decrease the epidemic of tobacco-related morbidity and mortality, given the long delay between smoking uptake and the development of disease.^3,9 Therefore, the aim of this systematic review was to examine studies that evaluated TCI in SSA countries.

Methodology

Sources of information and selection of eligible studies

The Preferred Reporting Items for Systematic Reviews and Meta-Analysis (PRISMA) framework was used for reporting this review,¹⁰ while the Cochrane Handbook for Systematic Reviews of Interventions, version 6.0, was applied when conducting the review.¹¹ A search of PubMed-Medline, Scopus and Web of Science was conducted of literature published till 5 December 2019. Relevant studies that evaluated TCI in SSA and examined tobacco/smoking quit rates or reductions in tobacco use/smoking were evaluated for inclusion. Study designs were not limited to randomised control trials (RCTs) but needed to include a control group. Key search terms included ‘tobacco cessation’ OR ‘smoking cessation’ OR ‘quit smoking’ OR ‘quit tobacco’ OR ‘stop smoking’ AND ‘Africa’ OR ‘sub-Saharan Africa’. For example, the search string used in PubMed-Medline was as follows: (‘tobacco cessation’ OR ‘smoking cessation’ OR ‘quit smoking’ OR ‘quit tobacco’ OR ‘stop smoking’) AND ( ‘Africa’ OR ‘sub-Saharan Africa’).

Data collection, extraction, assessment and synthesis

Two authors (N.P., A.N. or N.P., M.K.) sequentially screened titles, abstracts and then full texts for inclusion (Figure 1). The literature was screened for any paper that evaluated a tobacco cessation programme in SSA. The outcome examined was tobacco/smoking cessation/reduction in the intervention and control groups following the evaluation of the intervention (differences in prevalence). The outcomes used were those defined in the included studies and comprised self-reported tobacco use/abstinence or biochemically verified changes (urinary cotinine, or blood or exhaled carbon monoxide (CO) levels). In multi-country studies, data pertaining to SSA needed to be specifically reported. Any disagreements regarding the included papers were resolved through discussion or reviewed by a third author (A.P.K.). The reasons for excluding studies were also recorded.

Figure 1.

Preferred reporting items for systematic reviews and meta-analysis (PRISMA) diagram.

The data extracted from the selected studies included variables relating to the study design and setting, sample size, participant characteristics, the intervention, training of counsellors, assessments done, and outcomes evaluated. Data extraction was done by one author (N.P.), and another author (A.N.) verified the accuracy and validity of the extracted data. A risk of bias assessment was also conducted using the Cochrane risk of bias assessment tool for RCTs¹¹ and the Risk Of Bias In Non-Randomised Studies – of interventions (ROBINS-I) tool for the other included studies.¹²

Statistical analyses

The heterogeneity of the included studies precluded comparisons across interventions or populations. Therefore, a meta-analysis could not be conducted. A qualitative description of the studies, interventions and outcomes are instead presented.

Results

There were 645 titles retrieved and after removal of duplicates, 452 titles remained (Figure 1). An additional two titles were retrieved after personal communication with the authors, resulting in a total of 454 titles being reviewed. Twenty-seven full texts were evaluated for eligibility and eight, including a conference abstract, were selected for this review. The methodological details of the latter study were obtained from a qualitative paper on the same study.¹³

Study settings, designs, populations and sample sizes of included studies

All eight included studies were from South Africa with five studies conducted solely in the Western Cape Province of the country^14–18 (Tables 1 and 2). A study each was conducted in Tshwane¹⁹ and Klerksdorp²⁰ while a single study was multicentred with sites in Cape Town, Johannesburg and Durban.²¹ Seven studies included both men and women, and a single study was conducted in pregnant women.¹⁸

Table 1.

Overview of included studies that utilised nicotine replacement therapy (with or without psychotherapy).

First author, year	Baddeley, 1988¹⁴	Schuurmans, 2004¹⁷	Koegelenberg, 2014²¹	Golub, 2017²⁰
Study location	Cape Town, South Africa	Cape Town, South Africa	7 centres in Cape Town, Johannesburg, and Durban, South Africa	Klerksdorp, South Africa
Year/s conducted	Not provided	Not provided	2011–2012	2016
Aim	To compare the effectiveness of 2 mg nicotine gum together with group psychological support vs. psychological treatment only, in matched groups of heavy smokers who were motivated to stop	To determine whether 2 weeks of pre-treatment with nicotine patches affected withdrawal symptoms or smoking cessation success rate of subsequent nicotine patch use	To assess the efficacy and safety of using varenicline with a nicotine patch compared with varenicline alone for smoking cessation	To compare smoking cessation in HIV-infected patients randomised to intensive anti-smoking counselling alone vs. counselling and NRT patches and gum
Setting and population	Smokers from the general population	Healthy smokers from the general population	Community-based relatively healthy smokers	HIV-infected patients attending three HIV clinics
Study design	Case–control cohort; participants matched for sex, number of cigarettes smoked/day, number of years of smoking, and number of attempts to stop	Double-blind randomised controlled trial with parallel groups	Randomised, blinded, placebo-controlled clinical trial	Randomised control trial
Inclusion criteria	Heavy smokers who were motivated to stop smoking	⩾18-year-old healthy smokers, daily cigarette consumption ⩾15 for >3 years, exhaled CO >10 parts per million (ppm) and ⩾1 quit attempt(s) in the last 12 months	18- to 75-year-old smokers who sought assistance for smoking cessation, had smoked ⩾10 cigarettes/day during the previous year and month, and had not stopped smoking for >3 months in the past year	Self-reported HIV-infected smokers interested in quitting; smoking status confirmed on urinary cotinine
Recruitment strategy	Volunteers responded to English and Afrikaans adverts in the local press	Volunteers responded to adverts in local English and Afrikaans newspapers	Not described	Not described
Intervention	Nicotine gum as desired (self-provided) and group psychological support	Pre-treatment for 2 weeks: 15 mg active nicotine-patch. From quit date onwards: active patch of 15 mg/16 h for 8 weeks followed by 10 and 5 mg for 2 weeks each	Nicotine-patch treatment commenced 2 weeks before target quit date and continued for a further 12 weeks. Varenicline for 12 weeks	10 weeks of nicotine patches and gum together with counselling
Control	Group psychological support only	Pre-treatment for 2 weeks: placebo patch. From quit date onwards: active patch of 15 mg/16 hours for 8 weeks followed by 10 mg and 5 mg for 2 weeks each	Placebo patch treatment commenced 2 weeks before target quit date and continued for a further 12 weeks; varenicline for 12 weeks	Counselling only at Day 0, 2 weeks, 4 weeks, 2 months, 3 months and 6 months
Counselling received	Six session multicomponent programme on behaviour modification	20 minutes of counselling at each of six visits and 10–15 min counselling by study doctor at screening visit	10 minutes of smoking cessation counselling based on the 2008 US Public Health Service guidelines update was provided to all participants at each visit. Weekly visits for 4 weeks, then 4-weekly × three visits	Six counselling sessions lasting about 20 minutes using the 5As model of the National Cancer Institute; topics covered included health effects of smoking and coping mechanisms to deal with triggers
Duration of intervention and follow-up	3-week programme; assessed thereafter at 6 weeks and 6 months	2 weeks pre-treatment, then quit date to 6 months	26 weeks: 2 weeks prior to quit date, 12 week treatment period and further 12 week follow-up; 6 month assessment	10 week NRT and regular counselling up to 6 months
Selection and training of counsellors	Details of counsellors or the training they received was not provided	Counsellors were experienced nurses from the smoking cessation clinic; details of training were not provided	Details of counsellors or the training they received was not provided	Details of counsellors or the training they received was not provided
Primary outcome	Smoking abstinence verified biochemically	Severity of withdrawal symptoms	Complete abstinence from smoking for the last 4 weeks of treatment	Stopped smoking at 6 month follow-up visit
Secondary outcomes	Not described	Sustained abstinence at 26 weeks	Point-prevalence abstinence at 6 months; continuous abstinence rate for weeks 9–24; incidence of adverse events	Not described
Assessment of outcomes	Blood carbon monoxide (CO) levels	Primary outcome: Wisconsin scale; Secondary outcome: exhaled CO	Biochemically validated exhaled CO	Biochemically verified CO breath test, and urine cotinine for TB patients on isoniazid
Frequency of assessments	Baseline, 6 weeks and 6 months	Quit date, 2, 6, 10 and 26 weeks	Week 9 to 12 of commencing intervention	6 month follow-up visit
Sample size	23 in total; intervention: 12control: 11	200 in total; 100 participants per arm	435 in total; intervention: 216; control: 219	561 in total; intervention: 280; control: 281
Gender distribution	Number of men to women: intervention: 6:6, control: 7:4	n = 200, 45% female	intervention: men: n = 87 (39.2%); control: men: n = 84 (37.5%)	Women: 22%
Age (years) of participants	Intervention: 45.8 ; control: 46.5	Intervention: 43.2 ± 10.3;Control: 43.7 ± 10.8	Mean (SD): intervention: 46.6 (11.9); control: 46.1 (11.9)	Median age: 37 (IQR: 31–46)
Results	Abstinence rates at 6 months: intervention: 6/12 (50%); control: 3/11 (27%); p = 0.246	Primary outcome: no significant difference in withdrawal symptoms; secondary outcome: sustained abstinence at 6 months: overall: 17% (n = 34); intervention: 22% (n = 22); control: 12% (n = 12); p = 0.03	Continuous abstinence rate higher with combination treatment at 12 weeks (55.4%vs 40.9%; OR, 1.85; 95% CI, 1.19–2.89; p = 0.007) and 24 weeks (49.0% vs 32.6%; OR, 1.98; 95% CI, 1.25–3.14; p = 0.004); 6 month point-prevalence abstinence rate (65.1% vs 46.7%; OR, 2.13; 95% CI, 1.32–3.43; p = 0.002)	Quit smoking at 6 months: Counselling + NRT vs. counselling alone: 16.4% vs. 14.6%, p = 0.640).
Conclusions	No significant difference in smoking quit rates in the intervention (psychological treatment and nicotine gum) and control (psychological treatment only) groups	Nicotine-patch pre-treatment, that is, 2 weeks before quit date increased sustained abstinence rates significantly at 6 months in intervention vs. control group but did not reduce early withdrawal symptoms	NRT added to varenicline was more effective than varenicline alone at attaining tobacco abstinence at 12 weeks (end of treatment) and at 6 months	No increase in smoking cessation in HIV-infected participants who received NRT compared to those who did not

NRT: nicotine replacement therapy; CO: carbon monoxide; IQR: interquartile range; OR: odds ratio; CI: confidence interval.

Table 2.

Overview of included studies that utilised only psychotherapy without adjunct pharmacotherapy.

First author, year	Steenkamp, 1991¹⁶	Everett-Murphy, 2010¹⁸	Louwagie, 2014¹⁹	Hofmeyr, 2019¹⁵
Study location	Swellendam, Robertson and Riversdale in south-western Cape, South Africa	Cape Town, South Africa	Tshwane, South Africa	UCT, Cape Town, South Africa
Years conducted	1979–1983	2006–2007	2011–2013	2017–2018
Aim	To reduce smoking rates in two communities through HII and LII compared with no intervention	To evaluate the impact of brief smoking cessation counselling on quit rates in pregnant smokers attending public sector antenatal clinics	To determine the efficacy of brief MI, administered by LHWs, to assist with tobacco cessation in TB patients who smoked	To evaluate a CM smoking cessation programme vs. only information and monitoring in treatment-seeking student smokers
Setting and population	General population of three rural communities	Pregnant women who smoked and attended one of four public sector antenatal clinics managed by midwives	Newly diagnosed TB patients who attended one of six primary care TB clinics	UCT students who currently smoked
Study design	Quasi-experimental prospective clinical trial with cross-sectional surveys conducted before and after a 4 year intervention programme (1979 and 1983); anti-smoking trial was part of the CORIS study	Quasi-experimental with a natural history cohort and an intervention cohort	Multi-centre two-group parallel individual randomised controlled trial	Randomised control trial
Inclusion criteria	15- to 64-year-old residents of the selected areas; for HII, a smoker defined as smoking at least 1 cigarette or 1 g of tobacco per day	Mixed ethnic descent pregnant women (<24 weeks gestation) of low socioeconomic status who smoked	⩾18-year-old current smokers newly diagnosed with TB or on TB treatment for <1 month	⩾18-year-old students who were current smokers; lifetime smoking of at least 100 cigarettes; had smoked in the last 10 h; smoked at least five cigarettes a day; reported an interest in quitting smoking and taking part in a smoking cessation programme; and had a CO in expired air reading of ⩾8 parts per million (ppm)
Recruitment strategy	Recruited using an intensive postal campaign	Control group: all self-reporting smokers who were registered at the clinics between February and November 2006 Intervention group: registered at the same clinics, but a year later, between February and November 2007	Newly diagnosed adult TB patients were screened for smoking status using a baseline questionnaire, with current smokers identified by LHWs	Potential participants contacted via email sent to all students through UCT’s central mailing list. Interested students completed an online questionnaire; eligible students invited for in-person interviews and CO measurement. Eligible students who signed up randomised to treatment or control group using computer-generated stratified random assignment
Intervention	HII and LII: multiple risk factor interventions to prevent CHD, that is, CHD risk factor education and mass media programme using posters, billboards, mailing and local newspapers targeting the whole community; HII only: interpersonal intervention for high-risk individuals, such as smokers	Smoking cessation intervention, incorporating the ACOG 5As best practice guidelines included brief counselling by midwives and peer counsellors; self-help Quit Guide booklet provided; posters summarising the 5As hung in examination rooms	Same as control below and participants received brief MI session of 15–20 min from the LHWs	Participants received information and monitoring, plus CM. CM involved the timeline follow back method where smoking behaviour in the 7 days prior to the session was examined. It is a calendar-based method that asks individuals to retrospectively estimate, and complete on a calendar, their tobacco use in the period prior to the interview date
Control	Nil	Usual care	Participants received a short, standardised smoking cessation message of four sentences from the TB nurse and ‘Smoking cessation in tuberculosis services smoking cessation’ booklet supplied by the National Council Against Smoking of South Africa	Participants received an aid-to-quit information document to help them quit smoking; their quit attempts were monitored
Counselling received	Only for HII group; not described	Only intervention group: ACOG 5As brief smoking cessation counselling with MI principles linked to each step	Control group: four sentences; intervention group: MI	Only intervention group: CM
Duration and frequency of intervention	4 years; duration and frequency of HII not described	Duration and frequency of intervention not described	A single brief MI session of 15–20 min	One baseline session for ±2 h and four intervention sessions for 10 min, in person, individual meetings
Follow-up	4 years	Till end of pregnancy, that is, delivery	6-month follow-up visit	3 and 6 months after quit date
Selection and training of counsellors	Details of counsellors or the training they received was not provided	In-service training for midwives, two afternoon sessions of 2 h each. Training included time for reflection on their current approach, their personal experiences of smoking cessation counselling, and opportunities for role play. ‘Health Care Providers Guide to Counselling Pregnant Women about Smoking’ booklet, adapted from the ACOG guide, was provided	8 LHWs with ⩾11 years schooling and ⩾1 year experience as LHWs selected and trained as data collectors and tobacco cessation counsellors; LHWs received a 3-day MI training from an experienced brief MI counsellor and trainer. The TB nurse in charge of each clinic had one day’s training on the project and in delivering the brief tobacco cessation message	Details of counsellors or the training they received was not provided
Primary outcome	Net change in smoking habits, that is, residual change in the intervention areas after allowing for change in the control area, that is, intervention effect	Quitting smoking defined as urinary cotinine level < 100 ng/ml	Sustained 6 month smoking abstinence	7-day point-prevalence abstinence measured at 6 months and at the end of the intervention period; smoking intensity of non-abstinent participants measured
Secondary outcomes	Not described	Reduction in smoking, that is, at least half the level of urinary cotinine as at study entry, and self-reported quitting, reduction and quit attempts	Sustained 3-month smoking abstinence; 7-day point-prevalence abstinence at 1, 3 and 6 months; quit attempts	Decrease in smoking intensity of non-abstainers
Assessment of outcomes	Self-reported smoking/tobacco use	Urinary cotinine using a Cotinine Direct ELISA kit	Self-reported smoking abstinence; biochemically verified exhaled CO (piCO + Smokerlyzer CO monitor), ⩾10 parts per million (ppm) signifies smoking, sub-sample (n = 165) tested at 6 months	CO ⩽ 6 ppm (breath reading); CO levels measured in expired air using a Micro + Smokerlyzer^® monitor
Frequency of assessments	Baseline and 4 years later	Baseline <24 weeks gestation, mid-pregnancy (28–35 weeks), late pregnancy (36–39 weeks)	At participants’ routine 1-, 3- and 6-month TB treatment visits	At all sessions
Sample size	4090 participants participated in both surveys; HII: 1251; LII: 1531; control: 1308	979 self-reporting pregnant smokers; 443 in the control; 536 in the intervention group	409 in total; intervention group, n = 205; control group, n = 204	87 in total; intervention: n = 40; control: n = 47
Gender distribution	Men: 1852 (45.3%); women: 2238 (54.7%)	Women: 100%	Intervention: 188/205 (91.7% men); control: 180/204 (88.2% men)	Overall: 78% male; Intervention: 80% men; Control: 76% men
Age (years) of participants	15–64 years at baseline; men: 43.2–44.8 (±12.3–12.8); women: 43.0–44.3 (±12.3–12.4)	intervention: 24.1 (6.0); control: 24.0 (6.0)	Intervention: 40.3 (SD ± 10.3); control: 42.3 (SD ± 10.1)	±22
Results	Net reduction in smoking rates compared with control group: men: HII: 8.4%, LII: 2.0%; women: HII: 30.6%, LII: 19.2%; net reduction in amount smoked/day compared with control group: men: HII: 13.0%, LII: 4.6%; women: HII: 20.5%, LII: 8.1%; quit rate: men (p > 0.05): HII: 22.8%, LII: 16.9%, control: 20.1%; women: HII: 31.4% vs. 15.5% (control), p < 0.01; LII: 28.3% vs 15.5%, p < 0.05	Differences between intervention and control arms: quit rates 5.3% (95% CI: 3.2–7.4%, p < 0.0001) in an intention to treat analysis; smoking reduction: 11.8% (95% CI: 5.0–18.4%, p = 0.0006)	Self-reported 6-month sustained abstinence: 21.5% (intervention) vs. 9.3% (control); RR = 2.29, 95% CI = 1.34, 3.92, absolute difference of 12%. Biochemically verified (n = 166) 6-month sustained abstinence: intervention group: RR 2.21, 95% CI = 1.08, 4.51.Self-reported 3-month sustained abstinence: 25.4% (intervention); 12.8% (control); RR = 1.98, 95% CI = 1.24, 3.18	Abstinence at the end of the intervention period: intervention: 45%, control: 6% (p < 0.001); Abstinence at the end of 6 months: intervention: 10%, control: 6% (p = 0.536)No statistically significant effect on smoking intensity of non-abstainers in intervention arm
Conclusions	Community-based intervention programme is effective in reducing smoking. However, quit rates were significant in women but not men	A smoking cessation intervention based on best practice guidelines, among high risk, pregnant smokers, was effective	Significantly improved sustained smoking abstinence for at least 6 months in TB patients who received MI from LHWs compared with brief advice alone	CM promoted abstinence in the intervention period but not at the 6-month follow-up period

UCT: University of Cape Town; HII: high-intensity intervention; LII: low-intensity intervention; MI: motivational interviewing; LHWs: lay healthcare workers; TB: tuberculosis; CM: contingency management; CORIS: Coronary Risk Factor Study; CO: carbon monoxide; CHD: coronary heart disease; ACOG: American College of Obstetricians and Gynaecologists; CI: confidence interval; RR: relative risk.

Five studies were RCTs,^{15,17,19–21} two were quasi-experimental^16,18 and one was a case–control study.¹⁴ Participants or sites were randomly selected for seven of the eight studies; in the case–control study; however, participants self-selected for the intervention, that is, the use of nicotine gum.¹⁴

Four studies targeted community-based smokers,^14,16,17,21 three studies were conducted in patients attending public sector health clinics (one each in antenatal,¹⁸ tuberculosis (TB)¹⁹ and antiretroviral²⁰ clinics), and one study was conducted in students at the University of Cape Town (UCT).¹⁵ Sample sizes were 23 in the case–control study,¹⁴ 87–561 in RCTs,^{15,17,19–21} and 979 (pregnant women) and 4090 (three rural communities in the CORIS Study) in the quasi-experimental studies.^16,18

The sources of heterogeneity in the included studies comprise the wide range of interventions (discussed below), the different study designs and the specific population groups targeted for the interventions. These differences precluded comparability across studies.

Interventions of included studies

Studies that utilised nicotine replacement therapy

Four studies included pharmacotherapy (nicotine replacement therapy (NRT)) in the interventions^14,17,20,21 (Table 1). The NRT offered varied across the four studies with two studies comparing NRT and counselling versus counselling alone while the other two studies compared different NRT regimens. These were as follows: (1) group psychological treatment only versus self-provided 2-mg nicotine gum together with group psychological support,¹⁴ (2) intensive anti-smoking counselling alone versus counselling and nicotine patches and gum,²⁰ (3) 2-week pre-treatment with placebo versus 15-mg active nicotine patch followed by active patch for both groups,¹⁷ and (4) using varenicline alone versus varenicline with a nicotine patch.²¹

The intervention periods for the use of NRT were 3 weeks of self-provided nicotine gum used as desired,¹⁴ 10 weeks of nicotine patches and gum,²⁰ two additional weeks of nicotine patches,¹⁷ and 14 weeks of nicotine patches.²¹

All four NRT studies included psychological support using different counselling schedules. These included a multicomponent programme on behaviour modification,¹⁴ 10-min sessions based on the 2008 US Public Health Service guidelines²¹ or 20 min using the 5As model of the National Cancer Institute.²⁰

All four NRT studies assessed smoking cessation biochemically; blood CO was tested in a single study¹⁴ while the other three examined exhaled CO.^17,20,21 Outcomes were assessed at baseline, during the intervention, immediately after the intervention period and after 6 months.^14,17,20,21 Sustained abstinence at 6 months was significantly higher in the intervention versus the control groups in two studies^17,21 and non-significantly different in the other two NRT studies.^14,20

Studies that utilised psychotherapy only

The interventions in studies that utilised only psychotherapy without adjunct pharmacotherapy comprised (1) ‘interpersonal intervention’ (high-intensity intervention (HII)) and/or ‘mass media programmes’ (low-intensity intervention (LII)) versus no intervention,¹⁶ (2) brief counselling and self-help quit materials versus usual care,¹⁸ (3) brief motivational interviewing (MI) versus short, standardised smoking cessation message of four sentences¹⁹ and (4) ‘contingency management’ (CM) versus an aid-to-quit information document¹⁵ (Table 2). In the CORIS Study, the duration of the mass media programmes, that is, the LII was 4 years; however, the duration, frequency or details of the interpersonal intervention, that is, the HII was not described.¹⁶ The smoking cessation intervention incorporating the American College of Obstetricians and Gynaecologists (ACOG) 5As best practice guidelines with brief counselling provided by midwives and peer counsellors was used in the study on pregnant women; the duration and frequency of the intervention was also not described.¹⁸ Lay healthcare workers (LHWs) administered a single brief MI session of 15–20 min in the study in newly diagnosed TB patients.¹⁹ In the UCT study, there was one baseline session for ±2 h and four sessions for 10 min.¹⁵ The latter study used CM which involved the timeline follow back (TLFB) method, where smoking behaviour in the 7 days prior to the session was examined.

Smoking cessation was assessed by self-report in both the CORIS Study,¹⁶ and in the study with TB patients.¹⁹ However, a sub-sample of patients in the latter study had biochemically verified exhaled CO assessments at 6 months. Participants in the UCT study had their CO levels measured in expired air at all sessions.¹⁵ Urinary cotinine levels were assessed in the pregnant women study at three time-points: baseline, mid-pregnancy and late pregnancy.¹⁸

In the CORIS Study, the quit rates after 4 years were significantly higher in women exposed to both the HII and the LII compared with the control group; however, these findings were not significant in men.¹⁶ Quit rates and reductions in smoking were significantly higher in the intervention versus the control group in pregnant women.¹⁸ Sustained smoking abstinence for at least 6 months was significantly higher in TB patients who received MI from LHWs compared with brief advice alone.¹⁹ In the UCT students exposed to CM, abstinence was not significantly higher than the control group at 6 months.¹⁵

In summary, there was no significant difference in smoking cessation in the intervention and control groups in two NRT studies^14,20 while two NRT studies reported significantly higher tobacco abstinence at 6 months in the intervention groups.^17,21 In studies that utilised only psychotherapy without adjunct pharmacotherapy, smoking cessation was significantly higher in the intervention versus the control groups in pregnant women¹⁸ and TB patients¹⁹ but not in students.¹⁵ The community-based intervention programme was effective in reduce smoking overall but quit rates in women only.¹⁶

Risk of bias

Tables 3 and 4 describe the risk of bias for the RCTs and the non-RCTs, respectively, among the included studies. Among the RCTs, two studies each were at high risk of bias for blinding of participants and personnel (performance bias)^15,19 and incomplete outcome data (attrition bias)^17,21 while a single study was at high risk of bias for blinding of outcome assessments (detection bias)¹⁹ (Table 3). The overall risk of bias was moderate for the non-RCTs (Table 4).^14,16,18

Table 3.

Risk of bias assessment for the included randomised control trials with the supporting evidence.

Author, reference	Random sequence generation (selection bias)	Allocation concealment (selection bias)	Blinding of participants and personnel (performance bias)	Blinding of outcome assessment (detection bias)	Incomplete outcome data (attrition bias)	Selective reporting (reporting bias)	Other bias
Schuurmans et al.¹⁷	Low risk: “Randomization done through a computer-generated list”.	Low risk: “Numbering of identical boxes containing patches was carried out prior to the study by a person not involved in the study. The treatment code was only broken after the last follow-up visit had been completed and data recorded”	Low risk: “Double blind with parallel groups”.	Low risk	High risk	Low risk	Unclear
Koegelenberg et al.²¹	Low risk: centrally generated block randomisation	Low risk: “Randomized at second visit into one of the two groups of the study in a 1:1 ratio using centrally generated block randomization within each site (blocks of 4 with 2 active and 2 placebo patches)”	Low risk: “Double blinded. Both investigators and participants were blinded”	Low risk	High risk: “Only 62.3% of randomized participants completed the study”	Low risk	Low risk
Golub et al.²⁰,	Unclear	Unclear	Unclear	Unclear	Unclear	Unclear	Unclear
Louwagie et al.¹⁹	Low Risk: “Randomization sequence with a 1:1 allocation and random block sizes of 2, 4, 6, 8”	Low Risk: “Current smokers were allocated to either intervention or control arm by means of sequentially numbered sealed opaque envelopes”	High Risk: “Not possible to blind respondents and LHCWs to the intervention received because there was only one LHCW per site at 4 of the 6 sites”	High risk	Low risk: “Loss to follow up rate similar to intervention and control groups. All patients lost to follow up were considered smokers in the ITT analysis”	Low risk: “Results were analyzed as per protocol whereby non- eligible participants and patients lost to follow up were excluded from the analysis”	Unclear
Hofmeyr et al.¹⁵	Low risk: “Computer-generated stratified random assignment”	Low risk: “Importantly it was the first-time treatment allocation was revealed to participants” (after taking CO reading)	High Risk: “Neither treatment subjects nor RAs were blind to treatment allocation”	Low risk: “CO (breath reading). RAs followed a carefully structured script during sessions”	Low risk: “Dropouts not statistically significant”	Low risk	Unclear: “Given that the weekly CO readings could not biochemically verify the 7 day PPA measures hence there is a potential of misreporting the abstinence and the gaming of the intervention”

CO: carbon monoxide; LHCW: lay health-care worker; ITT: intention-to-treat; RAs: research assistants; PPA: point prevalence abstinence.

Table 4.

Risk of bias assessment for the non-randomised included studies.

Author, reference	Pre-intervention		At intervention	Post-intervention				Overall risk of bias
	Bias due to confounding	Bias in selection of participants into the study	Bias in classification of interventions	Bias due to deviations from intended interventions	Bias due to missing data	Bias in measurement of outcomes	Bias in selection of the reported result	Overall risk of bias
Steenkamp et al.¹⁶	Moderate	Moderate	Low	Moderate	Serious	Moderate	Low	Moderate
Everett-Murphy et al.¹⁸	Moderate	Low	Low	Moderate	Moderate	Moderate	Low	Moderate
Baddeley et al.¹⁴	Moderate	Low	Moderate	Moderate	Low	Moderate	Low	Moderate

Low risk of bias (the study is comparable to a well-performed randomised trial); moderate risk of bias (the study provides sound evidence for a non-randomised study but cannot be considered comparable to a well-performed randomised trial); serious risk of bias (the study has some important problems).

Discussion

To our knowledge, this is among the first studies to examine TCIs in SSA. As illustrated by the included studies, there is a wide range of behavioural and pharmacological TCIs. Numerous approaches were utilised in the TCIs and these differed in terms of intensity, cost (although not examined in this review) and effectiveness. The NRT studies ranged from the self-selection of nicotine gum in a case–control study¹⁴ to the use of patches and gum in an RCT²⁰ and pre-treatment with nicotine patches in two RCTs.^17,21 Similarly, the studies with psychotherapy as their focus incorporated different techniques and principles. These included the ACOG 5As best practices, brief MI and CM. The different aims, interventions and designs of the included studies precluded comparisons across the studies and a meta-analysis from being conducted.

Of the TCI studies in SSA included in this review, all were conducted in a single country, that is, South Africa. The dearth of TCI studies in SSA is of concern considering that tobacco cessation support services complement other tobacco control initiatives and contribute to decreasing the prevalence of tobacco use.² The prevalence of adult tobacco smoking in SSA is significant with the prevalence ⩾15% in seven countries in 2017. These were Lesotho (21%), Sierra Leone (19%), South Africa (17%), Madagascar (16%), Mauritius (16%), Seychelles (16%) and Botswana (15%).² Therefore, there is an urgent need in the region for evidence-based TCI for tobacco users who wish to quit.

This is particularly relevant when considering that assisting tobacco users to quit is one of the most cost-effective preventive primary healthcare services. Indeed, of the four studies in this review that utilised only psychotherapy without adjunct pharmacotherapy, three were found to be effective and may be adapted to low-resource settings. These interventions consisted of brief counselling using the ACOG 5As best practice guidelines in pregnant women, brief MI in TB patients, and ‘interpersonal intervention’ (not described) and/or ‘mass media programmes’. Notably, in the study in UCT students, which was not found to be effective, students also received monetary incentives at each assessment if their exhaled CO was ⩽6 ppm. Such an intervention is unlikely to be cost-effective nor sustainable in low-resource settings.

Notably, psychological support using different counselling schedules was a component of all included studies that used NRT, emphasising the importance of psychotherapy in tobacco cessation programmes. Two of these studies tested the utility of psychotherapy with or without NRT and reported no significant differences in quit rates between groups. This possibly further highlights the role of psychotherapy in tobacco cessation. The other two NRT studies tested different NRT regimes and reported significant findings. One study tested the use of an additional 2 weeks of active nicotine patch (14 weeks vs 12 weeks) and the other study the use of varenicline with or without nicotine patches. However, the findings of the latter two studies are unlikely to influence tobacco cessation public health policies in most SSA countries because of the high cost and unsustainable financial implications of pharmacological treatment. Furthermore, out-of-pocket expenditure on pharmacological treatments for tobacco cessation is not feasible for the poor majority residing in SSA because they are not cheap nor affordable.²² Therefore, tobacco cessation medications are likely to be reserved for upscaling of TCIs when resources are available. SSA countries should follow a stepwise approach when developing their TCIs taking cost and effectiveness of different cessation interventions into consideration.²

The counselling offered in most studies included in this review comprised intensive face-to-face therapy, which is usually affordable for middle- and high-income countries only.² However, in resource-constrained setting, a more pragmatic approach is necessary. This may include the integration of brief advice into primary healthcare setting as an initial step in encouraging tobacco cessation. Importantly, tobacco cessation should urgently be integrated into healthcare programmes such as TB and HIV/AIDS because of worse outcomes reported in smokers as well as family planning and maternal health because of poorer outcomes in pregnant women.^23,24 A study each in this review was conducted in patients with TB, HIV and pregnant women; a rollout of low-cost TCIs in these vulnerable groups will likely yield high returns.

Nevertheless, numerous barriers exist to implementing such support. Although tobacco users frequently encounter healthcare providers, they do not receive cessation advice despite the opportunities provided.²⁴ Barriers to delivering cessation advice among healthcare providers may include their smoking behaviour, lack of knowledge, awareness or motivation, inadequate counselling skills, other urgent priorities and insufficient time due to overburdened clinics. To overcome these barriers, governments need to prioritise the integration of brief cessation advice in primary healthcare settings by incorporating it into healthcare policies and programmes. Equally crucial is to ensure that the training and skills required to impart such advice is provided. In addition, a practical solution to address the multiple demands placed on senior healthcare professionals, who are frequently overburdened and in short supply in SSA, is to shift tobacco cessation counselling to lower-level healthcare workers.²⁵

It is essential to monitor and evaluate all tobacco cessation strategies and programmes to ensure the adoption of best practices. Therefore, the implementation, efficacy and cost-effectiveness of such programmes will need to be carefully reviewed, that is, both the use of lower-level healthcare workers and the integration of brief tobacco cessation advice into TB, HIV and antenatal services.

This underscores the need for existing healthcare systems to be strengthened to implement tobacco cessation promotion and tobacco dependence treatment initiatives. Unfortunately, SSA countries have a poor record in implementing TCI as illustrated by the following:² (1) tobacco use status was routinely recorded on medical records in only three SSA countries (Kenya, Nigeria and Seychelles). (2) Smoking cessation support was offered in some primary healthcare facilities in 10 SSA countries, but the cost was only partially covered in four countries and not covered at all in three countries. (3) NRT was available in 19 SSA countries; in six of these countries, a prescription was required. However, the cost was covered fully or partially in only eight of these countries. (4) Seven SSA countries have a national tobacco cessation strategy and 10 countries have national tobacco cessation clinical guidelines. (5) Only four SSA countries have national toll-free quit lines.²

This highlights that governments need to invest in promoting cessation, by developing evidence-based cost-effective national strategies and guidelines and allocating adequate resources for programme implementation. In keeping with the findings of this review, they need to promote and provide counselling for those that stop smoking, and implement mass communication programmes that encourage quitting.¹ The latter is important because a lack of knowledge about quit strategies and peer-pressure, among other factors, also contribute to continued smoking or a failure to quit.⁴ Moreover, while not reflected in the current review, a plethora of evidence from high-income countries demonstrates the benefits of pharmacotherapy in aiding successful tobacco cessation. Given that the use of pharmacotherapy increases the likelihood of successfully quitting tobacco,² SSA governments should strive to improve the availability, accessibility and affordability of cessation medicines.

For optimal effect, governments need to implement such programmes in conjunction with other demand-reduction tobacco control policies.² These include higher tobacco taxes, smoke-free spaces, prohibitions on tobacco advertising, promotion and sponsorship, large pictorial health warnings on tobacco packages, and anti-tobacco mass media campaigns. Such messages encourage quitting and create supportive environments.

The limitations of this study are that heterogeneity across studies precluded a meta-analysis from being conducted. The strengths are that three databases were used to search for relevant studies.

Conclusion

This review highlights that scant attention has been paid to TCI in SSA. All included studies were conducted in South Africa only. Furthermore, some of the interventions in the included studies cannot easily be introduced in resource-constrained settings and overburdened healthcare systems. For example, the long duration of the counselling sessions is not feasible for implementation. In others, the lack of accessibility and affordability of NRT in most SSA countries makes such interventions currently impractical and unattainable for most SSA tobacco users. However, NRT and other pharmacological aids to quit smoking can approximately double the chance that an individual will successfully quit.

It is essential to monitor and evaluate all tobacco cessation strategies and programmes to ensure the adoption of best practices. Currently, the limited availability of quality data prevents the implementation of tailored services in SSA. Additional studies are required that examine the effectiveness of best-practice cessation interventions in settings of graded resource availability, that is, from brief advice in primary healthcare to combination pharmacotherapies. Furthermore, there needs to be close collaborations between governments, academic institutions, non-governmental organisations and other stakeholders for the implementation and monitoring of optimal TCI services.

Supplemental Material

PRISMA-2009-checklist--2 – Supplemental material for A narrative systematic review of tobacco cessation interventions in Sub-Saharan Africa

Supplemental material, PRISMA-2009-checklist--2 for A narrative systematic review of tobacco cessation interventions in Sub-Saharan Africa by Nasheeta Peer, Ashika Naicker, Munira Khan and Andre-Pascal Kengne in SAGE Open Medicine

Footnotes

Declaration of conflicting interests

The author(s) declared no potential conflicts of interest with respect to the research, authorship, and/or publication of this article.

Funding

The author(s) received no financial support for the research, authorship, and/or publication of this article.

ORCID iD

Nasheeta Peer

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