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Smokeless tobacco cessation interventions: A systematic review
For correspondence: Dr Ravi Mehrotra, ICMR-National Institute of Cancer Prevention & Research, Plot I-7, Sector 39, Noida 201 301, Uttar Pradesh, India e-mail: ravi.mehrotra@gov.in
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Abstract
Background & objectives:
Smokeless tobacco (SLT) consumption is a global health issue with about 350 million users and numerous adverse health consequences like oral cancer and myocardial disorders. Hence, cessation of SLT use is as essential as smoking cessation. An update on the available literature on SLT cessation intervention studies is provided here.
Methods:
Through an extensive literature search on SLT cessation intervention studies, using keywords such as smokeless tobacco, cessation, interventions, quitlines, brief advice, nicotine replacement therapy, nicotine gum, nicotine lozenge, nicotine patch, bupropion, varenicline, mHealth, etc., 59 eligible studies were selected. Furthermore, efficacy of the interventions was assessed from the reported risk ratios (RRs) [confidence intervals (CIs)] and quit rates.
Results:
Studies were conducted in Scandinavia, India, United Kingdom, Pakistan and the United States of America, with variable follow up periods of one month to 10 years. Behavioural interventions alone showed high efficacy in SLT cessation; most studies were conducted among adults and showed positive effects, i.e. RR [CI] 0.87 [0.7, 1.09] to 3.84 [2.33, 6.33], quit rate between 9-51.5 per cent, at six months. Regular telephone support/quitlines also proved beneficial. Among pharmacological modalities, nicotine lozenges and varenicline proved efficacious in SLT cessation.
Interpretation & conclusions:
Globally, there is limited information available on SLT cessation intervention trials, research on which must be encouraged, especially in the low-resource, high SLT burden countries; behavioural interventions are most suitable for such settings. Appropriate training/sensitization of healthcare professionals, and school-based SLT use prevention and cessation programmes need to be encouraged.
Keywords
Behavioural
intervention
nicotine replacement therapy
smokeless tobacco
tobacco dependence
tobacco use cessation
Smokeless tobacco (SLT) use, a form of tobacco consumed without combustion/burning, has become a global health issue with about 350 million users, maximally seen in the South-East Asian Region. Its use is associated with a myriad of adverse effects, with the major ones being oral cancer, myocardial infarction and other cardiovascular diseases1.
Article 14 of the World Health Organization Framework Convention on Tobacco Control (WHO-FCTC) deals with tobacco addiction and dependence treatment measures. It states that ‘each Party shall develop and disseminate appropriate, comprehensive and integrated guidelines based on scientific evidence and best practices, taking into account national circumstances and priorities, and shall take effective measures to promote cessation of tobacco use and adequate treatment for tobacco dependence2.’ The formulation of this Article demonstrates the fact that the FCTC realizes the addictive potential of tobacco. Hence, the same came into existence at the Conference of the Parties 4 with the objective of development of effective treatment guidelines and measures to promote adequate treatment for tobacco dependence, by the member Parties3. However, the average implementation of Article 14, as reported in the Global Progress Report on Implementation of the WHO-FCTC in 20164, has not been significant, i.e. 50 per cent, between 2012 and 2016, as compared to the other substantive articles of the Convention5. According to the guidelines of Article 14, tobacco cessation has multiple dimensions to it, comprising behavioural interventions [brief advice, telephone counselling via national toll-free quitlines (NQLs)], pharmacotherapy, nicotine replacement therapy (NRT) and non-nicotine therapy - bupropion and varenicline, involvement of the healthcare system/healthcare workers, noting individual's tobacco use2.
In spite of widespread use and adverse health consequences of SLT, there is a dearth of evidence-based published literature on SLT cessation as compared to that on smoking cessation. A systematic review and meta-analysis available for SLT cessation intervention trials was the Cochrane review reporting data till 2015, majorly for studies performed in the United States of America (USA), with a few in the Scandinavian countries6. Here we provide a global update on the existing literature regarding studies on the demand reduction measures concerning SLT dependence and cessation, along with evidence-based discussion of the efficacy of each.
Material & Methods
To search the literature and systematically review the various demand reduction measures for SLT dependence and cessation, an online search strategy was performed since inception (1966) for PubMed to 2017, and the resultant data evaluated, as shown in Figure.

- Flow chart showing search strategy. *These were the number of articles which were chosen for screening of their abstracts after excluding other articles deemed irrelevant based on their titles.
Extensive PubMed and Google literature search was performed using a combination of keywords such as smokeless tobacco, cessation, interventions, dependence, treatment, quitlines, behavioural, brief advice, nicotine replacement therapy, nicotine gum, nicotine lozenge, nicotine patch, bupropion, varenicline, dentist, mHealth and mobile. This search produced 28,756 results, the titles of which were assessed and those not relevant were excluded. Abstracts of the remaining publications and full papers were reviewed to identify those that fulfilled the inclusion criteria. Among these, 59 articles were found to be of potential interest and were included.
The criteria for data selection, obtained from the search above, were as follows:
Inclusion criteria
Studies performed for SLT cessation interventions; studies performed for cessation of both smoking and SLT but also reporting data specific to SLT cessation; those with the most recent results for consecutively reported studies; SLT cessation intervention studies performed either on adults or adolescents were included. Only English language literature was included.
Exclusion criteria
Studies only for smoking cessation; studies for cessation of both smoking and SLT but not providing separate information for SLT cessation; literature reviews; repetitive data (example: extracts from already included Cochrane articles); articles on tobacco use screening and counselling; study protocols; studies with differing objectives; old published data for the same study; unavailability of the complete report for reference in case of lack of clarity of information in the abstract; documents in languages other than English, were excluded.
The current status of availability of the SLT dependence and cessation measures globally and the efficacy of each of the SLT cessation intervention was assessed based on the risk ratio (RR) [confidence intervals (CIs)] and quit rates reported for each of them in the various resultant studies.
Results
Behavioural interventions for smokeless tobacco (SLT) cessation
Twenty randomized controlled trials (RCTs) (case-control studies) on behavioural interventions for SLT cessation were reported; sixteen were conducted in the USA78910111213141516171819202122, three in India232425 while only one study was reported from Sweden26. Most studies had majority of adult participants while three were conducted among the youth132024. Among the 19 studies having a follow up of six months or more, 10 studies reported statistically and clinically significant benefits with RR (CI) ranging between 1.33 (1.09, 1.63) and 3.84 (2.33, 6.33)9101113141718192223, in five studies the CIs did not specify a clinical benefit but did not exclude one either, with an RR (CI) between 1.08 (0.84, 1.39) and 3.72 (0.79, 7.47)712162026 and four studies had RRs just below or above one and relatively narrow CI suggesting no important benefit or harm i.e. RR (CI) from 0.87 (0.7, 1.09) upto 1.07 (0.87, 1.31)8152124. Overall, the RR (CI) ranged from 0.87 (0.7, 1.09) to 3.84 (2.33, 6.33). The one case-control pilot study conducted by Jhanjee et al25 showed an RR (CI) of 1.80 (0.77, 4.25) at the end of three months of treatment (Table I). Therefore, the trials suggested a benefit of behavioural interventions in SLT cessation.
| Authors | Year | Country | Study type | Subject characteristics | Intervention period/method | Follow up period | Risk ratio and CI | |||
|---|---|---|---|---|---|---|---|---|---|---|
| Total | Case (n) | Control (n) | Age (yr) | |||||||
| NRT with behavioural interventions | ||||||||||
| Boyle et al40 | 1992 | USA | RCT | 100 | 50 | 50 | Average age 32 | 6 wk | 1, 6 and 12 months | 1.00 (0.52-1.94) |
| Hatsukami et al41 | 1996 | USA | RCT | 210 males | 106 | 104 | Average age 31 | Pharmacotherapy - 8 wk, | 12 months | 0.98 (0.63-1.54) |
| Behaviour therapy - 10 wk | ||||||||||
| Howard-Pitney et al42 | 1999 | USA | RCT | 410 males | 206 | 204 | Average age 36 | 6 months | 1.12 (0.86-1.45) | |
| Hatsukami et al43 | 2000 | USA | RCT | 402 | 201 | 201 | Average age 31 | 10 wk | Up to 62 wk | 1.27 (0.92-1.74) |
| Stotts et al44 | 2003 | USA | RCT | 303 males | 198 | 105 | 14-19 | 6 wk | 12 months | 1.26 (0.57-2.78) |
| Croucher et al54 | 2003 | UK | Pilot study | 130 UK-resident Bangladeshi women | 65 | 65 | Average age 42.5 | 4 wk | 1.25 (0.58-2.68) | |
| Ebbert et al45 | 2007 | USA | RCT | 42 males | 10 | 11 | Average age 34-38 (20-56) | 8 wks | 6 months | 1.10 (0.19-6.41) |
| Ebbert et al46 | 2009 | USA | RCT | 270 (264 males and 6 females) | 136 | 134 | 18 and above (average age 37) | 12 wk | 6 months | 1.40 (0.88-2.22) |
| Ebbert et al47 | 2010 | USA | RCT | 60 males | 30 | 30 | 18 yr and above (average age: randomized group 43.6±16.0, control group 42.4±11.7) | 12 wk | 6 months | 0.73 (0.34-1.55) |
| Croucher et al53 | 2012 | UK | Cohort | 239 South Asians | 219 | 20 | Average age 45 | 4 wk | 1 yr | 1.62 (0.94-2.80) |
| Croucher et alb52 | 2012 | UK | Cohort | 419 UK resident Bangladeshi women | 330 | 89 | Average age 48.9 | 4 wk | 4.93 (2.02-12.00) | |
| Ebbert et al49 | 2013 | USA | RCT | 52 | 25 | 27 | Average age 41 (18-55) | 8 wk | 6 months | 1.73 (0.65-4.59) |
| Ebbert et al48 | 2013 | USA | Pilot study | 130 (125 males and 5 females) | 40 | 41 | 18 yr and above (average age 38) | 12 wk | 6 months | 1.03 (0.32-3.27) |
| Danaher et al50 | 2015 | USA | RCT | 407 (397 males and 10 females) | 205 | 202 | Average age 35 | 12 wk | 3 and 6 months | 1.53 (1.12-2.09) |
| Severson et al51 | 2015 | USA | RCT | 1067 males | 357 | 354 | Average age 36 | 12 wk | 3 and 6 months | 1.36 (1.12-1.66), 1.43 (1.20-1.71) |
| Behavioural interventions only | ||||||||||
| Gupta et al23 | 1992 | India | Cohort study | 7033 males and females SLT users | 4619 | 2414 | 15 yr and above | Intervention group: Concentrated programme of education against tobacco use. Control group: minimal advice against tobacco use | 10 yr | 2.79 (2.36, 3.29) |
| Cummings et al8 | 1995 | USA | RCT | 733 males | 316 | 417 | Average age 36 | 2 yr | 2 yr | 0.98 (0.76-1.27) |
| Stevens et al7 | 1995 | USA | RCT | 518 males | 245 | 273 | 15 yr and above | 18 months | 3 and 12 months | 1.47 (0.83-2.60) |
| Severson et al9 | 1998 | USA | RCT | 633 | 394 | 239 | 15 yr and above | 3 and 12 months | 3 and 12 months | 3.03 (1.44-6.37) |
| Walsh et al10 | 1999 | USA | RCT | 360 | 171 | 189 | Intervention group: Oral exam (3-5 min) with feedback, photos of ST effects, advice to quit, self-help manual, optional brief counselling (15-20 min) about quit date, triggers, tobacco withdrawal); optional nicotine gum (to mitigate withdrawal symptoms), optional phone counselling. Controls: Oral examination only | Up to 1 yr | 2.21 (1.5-3.25) | |
| Andrews et al11 | 1999 | USA | RCT | 633 (632 males and 1 female) | 394 | 239 | 15 yr and above (Average age 36.2) | Intervention: Determine tobacco use, identify oral disease, strong advice to quit, set quit date within two wk, motivation video, written material, call patient within two wk; Usual care | 3 and 12 months | 3.26 (1.49-7.17) |
| Cigrang et al12 | 2002 | USA | Pilot study | 60 males | 31 | 29 | Average age 31 (19-47) | Programme using motivational interviewing consisted of a treatment manual, video, and two supportive phone calls (about 10 min each) from a cessation counsellor | 3 and 6 months | 2.18 (0.62-7.65) |
| Walsh et al13 | 2003 | USA | RCT | 307 males | 141 | 166 | 14-18 | Peer-led component (50-60 min): Interactive, peer-led team directing education with videotape and brief discussion (10-15 min), slide show (20-30 min), and small-group discussion on tobacco industry advertising (10 min). Dental component with oral cancer screening examination by a dentist or hygienist. Included advice to quit, a self-help guide, tobacco cessation counselling in small groups (15 min), and a phone call on the quit date (5-10 min). Control group: No intervention | 1 and 12 months | 1.95 (1.22-3.10) |
| Boyle et al14 | 2004 | USA | RCT | 221 males | 109 | 112 | Average age 36 | Behavioural therapy 1. S-H materials (control) 2. S-H material + 4 proactive telephone counselling calls. Initial call four days after S-H material mailing. Subsequent calls were negotiated and placed emphasis on support, problem-solving, and use of cognitive-behavioural strategies including monitoring tobacco behaviour patterns, goal setting, finding alternative coping options and planning for high-risk situations or cues associated with tobacco use | 6 months | 1.61 (1.09-2.39) |
| Gansky et al15 | 2005 | USA | RCT | 637 | 285 | 352 | 17-20 | Intervention: 1. Three-hour video conference training for athletic trainers/dentists/hygienists; follow up newsletter for athletic trainers 2. Oral cancer screening by dentists/hygienists 3. Athletic trainer follow up and referral with follow up by trainer on quit date, plus 3 booster sessions one week apart 4. Peer-led component with education meeting (50-60 min). Control: anti-tobacco education | 1 yr | 0.98 (0.80-1.20) |
| Severson et al16 | 2007 | USA | RCT | 1069 males | 535 | 534 | Average age 39 (17-82) | Assisted self-help including: 1. Phone support (two calls, 10-15 min, with quit date setting and tobacco withdrawal management) 2. Self-help manual (60 pages) 3. Self-help videos (20 min). Controls received a self-help manual | 12 months | 1.32 (0.94-1.86) |
| Stigler et al24 | 2007 | India | Cohort study | 209 girls and boys | 100 | 109 | 10-16 | Four months | 2 yr (here, outcome of 1 yr) | 0.87 (0.7-1.09) |
| Severson et al18 | 2008 | USA | RCT | 2523 males | 1260 | 1263 | Average age 36.8 | Intervention (enhanced website): a guided interactive programme for quitting tobacco, useful resources and other weblinks, web forums namely ‘Talk with Others’ and ‘Ask an Expert’, planning to quit and staying quit modules Controls (basic website): a static website having a pocket guide titled “Enough Snuff ”and a section with useful materials and links | 3 & 6 months | 1.59 [1.26, 2.02] |
| Boyle et al (the Chew Free Minnesota study)17 | 2008 | USA | RCT | 406 (399 males and 7 females) | 201 | 205 | Average age 40 | A self-help manual plus proactive phone-based cessation counselling. Phone-based treatment included up to 4 calls in support of quitting and personalized cognitive and behavioural tobacco treatment strategies (e.g., setting a quit date, examining use patterns, developing stress-reduction skills, avoiding known triggers to use). Controls received usual care (i.e., self-help manual only) | 3 and 6 months | 3.16 (1.99-5.03) |
| Severson et al19 | 2009 | USA | RCT | 785 males | 392 | 393 | Average age 30 | Telephone counselling by a trained cessation counsellor who offered assistance in quitting ST use (3 calls: First call one week after dental examination, second call three weeks after quitting materials were mailed, third call a few days after participant’s quit date or two weeks after the second call); a mailed videotape and self-help guide tailored for the military. Controls received usual care | 6 months | 3.84 (2.33-6.33) |
| Walsh et al20 | 2010 | USA | RCT | 4731 males | 123 | 123 | 14-18 | Peer-led educational session (45 min), oral exam with feedback, and three nurse-led group cessation counselling sessions (one hour each, optional). Peer-led sessions included video/slide presentation and discussion about the presentations and how the tobacco industry targets young males. Oral examination included feedback about any tobacco-related lesions, advice to quit using ST, assessing of readiness to quit. The first nurse-led session focused on assessment, education, preparation to get ready to quit, and the importance of social support; the second session focused on setting a quit date and skills to cope with cravings and temptation to use; the third session reviewed progress and focused on relapse prevention. Controls received no intervention | 1 yr | 1.08 (0.84-1.39) |
| Danaher et al21 | 2013 | USA | RCT | 1716 (1656 males and 60 females) | 857 | 859 | Average age 21 (14-25) | Behavioural therapy 1. Basic condition (control): Static website content including an ‘Enough Snuff’ pocket guide, a resource section with informational materials and links to websites offering content for ST cessation and relaxation strategies 2. Enhanced condition: Interactive and multimedia features with functionality to create online lists, watch videos, and a Web blog moderated by research staff. Automated email reminders encouraged website use and provided supportive measures | 3 and 6 months | 1.07 (0.87-1.31) |
| Danaher et al22 | 2015 | USA | RCT | 1683 (1641 males and 42 females) | 1259 | 424 | Average age 38 | Behavioural therapy: 1. Web only: Automated, tailored and interactive intervention delivered as text, activities, and videos 2. Quitline only: Proactive telephone counselling through the California Tobacco Chewers’ Helpline 3. Web + Quitline: Received the Web and Quitline Interventions 4. Control: Self-help printed guide | 3 and 6 months | 1.33 (1.09-1.63) |
| Virtanen et al (the FRITT study)26 | 2015 | Scandinavia (Sweden) | RCT | 241 males and females | 94 | 100 | 18-75 | Behavioural therapy: 1. Structured tobacco use intervention based upon the 5 A’s specifically referring to oral health with reference to pharmacotherapy, more intensive counselling in the primary care clinic and the telephone quitline. Hand-outs supplied 2. Usual care | 6 months | 3.72 (0.79-17.47) |
| Jhanjee et al25 | 2017 | India | Pilot study | 100 women | 50 | 50 | Average age 43 | 3 months | 1.80 [0.77, 4.25] | |
| Non-nicotine therapy (with behavioural interventions): Bupropion | ||||||||||
| Glover et al59 | 2002 | USA | Double-blind RCT | 70 males | 35 | 35 | 18 & above | 7 wk | 5 wk | 2.73 [1.07, 7.72] (at 7 wk), 1.93 [0.71, 5.47] (at follow up) |
| Dale et al60 | 2002 | USA | RCT | 68 (67 males, 1 female) | 34 | 34 | Average age 37 | 12 wk | 24 wk | 1 [0.27, 3.68] |
| Dale et al61 | 2007 | USA | RCT | 225 males | 113 | 112 | Average age 38 (19-72) | 12 wk | 24 & 52 wk | 0.87 [0.51, 1.46] |
| Non-nicotine therapy (with behavioural interventions): Varenicline | ||||||||||
| Fagerstrom et al62 | 2010 | Scandinavia (Sweden & Norway) | RCT | 431 (385 males & 46 females) | 213 | 218 | Average age 43.9 | 12 wk | 6 months | 1.33 [1.05, 1.69] |
| Ebbert et al63 | 2011 | USA | RCT | 76 males | 38 | 38 | Average age 41 | 12 wk | 3 & 6 months | 1.42 [0.79, 2.55] |
| Jain et al64 | 2014 | India | Double-blind RCT | 237 (mostly males) | 119 | 118 | Average age 34.2 | 12 wk | 2.60 [1.20, 4.20] | |
SLT, smokeless tobacco; RCT, randomized controlled trials
Twelve non-case-control studies employing behavioural interventions for SLT cessation interventions were found, among which eight had a follow up of six months or more2728293031323334 and four had a follow up of less than six months35363738. Of these, two studies were performed in India3032, one in Pakistan and United Kingdom (UK)33 and the rest were done in the USA272829313438. Among the group having intervention/follow up of less than six months, the quit rate ranged from eight per cent (at the end of one month, Gala et al) to 58 per cent (after 1.5 months, Fisher et al)3738. The quit rate of SLT users in the trials having a longer follow up of six months or more was between 9 per cent (at six months, Walsh et al) and 51.5 per cent (after 12 months, Mishra et al)2730 (Table II).
| Authors | Country | Year | Study type | Subject characteristics | Intervention period | Follow up period | Quit rate (%) | |
|---|---|---|---|---|---|---|---|---|
| n | Age (yr) | |||||||
| Behavioural interventions only | ||||||||
| Eakin et al35 | USA | 1989 | Pilot study | 25 males | 3 months | 16 | ||
| Masouredis et al36 | USA | 1997 | RCT | 1208 males | 3 months | 24 | ||
| Walsh et al27 | USA | 1998 | Pilot study | 304 males | Minor and major league players | 6 months | 9 | |
| Boyle et al28 | USA | 1999 | Media campaign | 205 males | 21-79 Average age=37.5 | 1 yr | 11.5 | |
| Fisher et al37 | USA | 2001 | Cohort study | 50 (49 males, 1 female) | 18 and above | 6 wk | 58 | |
| Lichtenstein et al29 | USA | 2002 | 363 female romantic partners of male smokeless tobacco users | Average age=40 | 6 months | 32 | ||
| Gala et al38 | USA | 2008 | Cohort study | 18 males | 18 and above | 1 month | 8 | |
| Mishra et al30 | India | 2009 | Cohort study | 104 males | 1 yr | 51.5 | ||
| Meier et al31 | USA | 2013 | Institutional intervention | 2293 males | 18-56 (average age =20.6) | 4 yr | 16.4 | |
| Mishra et al32 | India | 2014 | Community-based intervention | 304 women | 1 yr | 33.5 | ||
| Siddiqi et al33 | UK, Pakistan | 2016 | Pilot study | 32 (16 males and 16 females) | 18 and above | 6 months | 12.5 | |
| Gupta et al34 | India | 2016 | Quitline | 1105 | Majority between 16-25 | 1 call session | 1 wk, 1 month, 3 months, 6 months, 1 yr | 20.0 (at 18 months) |
| NRT with behavioural interventions | ||||||||
| Sinusas et al56 | USA | 1993 | Preliminary trial | 14 males | 2-4 months | Up to 12 months | 21 (at the end of treatment), 7 (at follow up) | |
| Hatsukami et al57 | USA | 2003 | Pilot study | 40 males | Average age=31.9 | 12 wk | At 26 wk | 25 (at end of treatment) 15 (at follow up) |
| Ebbert et al58 | USA | 2007 | Open-label, one-arm, phase II clinical trial | 30 (29 males, 1 female) | Average age=35.4 | 12 wk | 6 months | 53 (at end of treatment), 47 (at follow up) |
| Wallstrom et al55 | Sweden | 2010 | Prospective, open, non-randomized intervention trial | 50 males | Average age=42.2 | Six wk | 3, 6, 12 months | 30 (at 12 months) |
| Mushtaq et al39 | USA | 2015 | Cohort study | 374 males | Average age=41.3 | 7 months | 43 | |
| Non-Nicotine therapy with behavioural interventions: Varenicline | ||||||||
| Ebbert et al47 | USA | 2010 | Pilot study | 20 males | Average age=42.8 | 12 wk | 6 months | 15 (at 12 wk) 10 (at 6 months) |
NRT, Nicotine replacement therapy
National toll-free quitlines (NQLs): Telephone support has been shown to be efficacious in SLT cessation. Among the aforementioned studies, 10 RCTs conducted in the USA, in which telephone support formed part of the intervention showed their benefit, with RR (CI) ranging between 1.32 (0.94, 1.86) and 3.84 (2.33, 6.33) (Table I)791012131416171922. Four non case-control studies28343539 reported a beneficial effect of telephone support for SLT cessation. A quit rate of 20 per cent among SLT users at the end of 18 months of the quitline activity in Rajasthan (India), a voluntary activity of Rajasthan Cancer Foundation, was reported34. A media campaign (comprising of quitline component) in Nebraska (USA)28 reported a quit rate of 11.5 per cent at the end of 12 months and Eakin et al (USA)35 reported a quit rate of 16 per cent at the end of three months in their multi-component behavioural intervention programmes including frequent telephone contact/counselling with the SLT users. Mushtaq et al39 reported a quit rate of 43 per cent at the end of seven months; however, the intervention also involved delivery of NRT in addition (Table II).
Pharmacotherapy for SLT cessation
Nicotine replacement therapy (NRT): Fifteen RCTs on NRT for SLT cessation were found. Twelve trials were performed in the USA404142434445464748495051 while three were conducted in the UK among Bangladeshi-resident women525354. Except one44, the rest of the studies had adult participants. Among the 12 studies from the USA with a follow up of six or more months, neither nicotine patch4243444549 nor nicotine gum4041 increased abstinence; however, the five studies of nicotine lozenges showed increased SLT abstinence, with RR (CI) between 0.73 (0.34, 1.55) and 1.53 (1.12, 2.09)4647485051 (Table I). In the Bangladeshi Stop Tobacco Project, NRT proved effective among 419 Bangladeshi female resident SLT users of UK with RR (CI) of 4.93 (2.02, 2.00) at four weeks, whereas the opposite was noted for nicotine gum or patch among 239 and 130 Bangladeshi origin participants living in the UK525354 (Table I).
Five non-case-control studies on NRT usage for SLT cessation were found. All were conducted among adults and had a follow up period of six months or more. Only one study was performed in Sweden55 and the rest in the USA39565758. Three studies tested the efficacy of nicotine gum alone in SLT cessation555657, while one study58 employed nicotine lozenge; Mushtaq et al39, utilised nicotine gums, patches and lozenges in their participants. A higher benefit of nicotine lozenge in SLT cessation was also observed by Ebbert et al58, i.e. 47 per cent quit rate at six months. The quit rate for NRT in general in SLT cessation ranged from 7 to 47 per cent (Table II).
Non-nicotine therapy: A total of six RCTs, three each for bupropion and varenicline for SLT cessation, were found, and all were conducted among adults. All the three bupropion-related studies596061 were performed in the USA, with one having a follow up of less than six months59 and the other two having a follow up period of more than six months6061; however, none of these studies showed a positive effect on tobacco abstinence. The three trials of varenicline, were conducted in Scandinavia62, USA63 and India64 with one having a follow up of less than six months64 and the other two having a follow up period of more than six months. These studies showed increased tobacco abstinence rates at six months compared to placebo (Table I). A single non-case-control pilot study in USA reported a quit rate of 15 per cent among adult participants at the end of 12 wk of treatment with varenicline and 10 per cent at the end of six months of follow up65.
Discussion
Globally, a dearth in the published literature regarding SLT cessation intervention trials has been observed (only for 3% WHO-FCTC ratified Parties, i.e. 5/179 Parties - Sweden, Norway, India, United Kingdom and Pakistan, apart from the USA). Further, a deficiency in the tobacco cessation support availability in most low-resource and high SLT burden Parties has been reported in the MPOWER 2017, which is required to be strengthened66.
Studies assessing the efficacy of SLT cessation interventions, especially behavioural interventions, must be carried out by all countries, especially those having a high burden of SLT consumption, as behavioural interventions have been found to have maximum benefit in SLT cessation as compared to pharmacotherapy7891011121314151617181920212223242526272829303132333435363738. The Cochrane review (2015) on the SLT cessation intervention trials also showed results along similar lines, with behavioural interventions proving most efficacious for SLT cessation6. Another Cochrane review (2012) also suggested almost similar efficacy of behavioural interventions in both smoking and SLT cessation67. The importance of behavioural intervention in the form of brief advice by healthcare professionals for successful SLT cessation has also been undermined and not much research has been performed. The Global Adult Tobacco Survey (GATS) performed in India, Bangladesh, Kenya, Pakistan, Thailand and Uganda reported a considerable variation while tobacco cessation counselling by health professionals (greater consideration for smokers than SLT users)68. Two trials in India have been performed successfully utilizing brief advice for tobacco cessation among both smokers and SLT users i.e. an overall quit rate of 67.3 per cent was reported by Kaur et al69, and 2.6 per cent by Sarkar et al70, however, the quit rate for SLT users has not been mentioned separately. There is also a lack of formal training for tobacco cessation among health profession students and school personnel, as seen in the Global Health Professions Student Survey and Global School Personnel Survey, respectively68. Hence, the same must be encouraged and expanded up to the grass root level, i.e. among health workers working in the villages. However, the likelihood of healthcare professionals giving brief advice will be more if tobacco use is recorded in the medical history; but only 20 per cent of countries follow this71.
Quitlines and telephone support for SLT cessation have proven efficacious as noted in literature79101213141617192228343539. In a Cochrane review6, the pooled risk ratio of 10 studies conducted in the USA, in which telephone support formed part of the intervention, indicated benefit in SLT cessation. It was also noted that a combination of oral examination and telephone support was more beneficial (RR- 2.07, CI-1.61, 2.66), than oral examination alone6. However, according to the MPOWER 2017 data66, only one-third, i.e. 31 per cent, Parties have NQLs, the establishment of which needs to be encouraged. In addition, the phone number of the quitlines could be mentioned on the SLT product packet health warnings. To ensure broader coverage, the primary healthcare system, services for treating tuberculosis and human immunodeficiency virus/acquired immunodeficiency syndrome, dental set-ups and non-communicable diseases programmes could also be involved72.
mHealth services for SLT cessation can be employed as an easy and cost-effective option, especially in the low-income group countries, for smoking cessation. Very few WHO-FCTC ratified countries have provided this facility (24 Parties)72. A national, bilingual mCessation programme (tobacco cessation through mobile text messages) was started in 2016 in India. Evaluation at the end of the first year, of more than 12,000 registered users, demonstrated an average quit rate of about seven per cent among both smokers and SLT users six months after enrolment66. Based on the information from 12 studies reported in the Cochrane review, 201673 (performed mostly in high-income countries such as USA, Australia, UK, Switzerland, New Zealand), smokers who received the mobile phone-based support were around 1.7 times more likely to quit than those who did not, proving this intervention efficacious, which could also be utilized for SLT cessation.
Most studies had adult participants. SLT prevention and cessation programmes must be facilitated in schools such as Project MYTRI24, especially among students of the lower strata of the society and with a higher early tobacco usage initiation tendency (smoking and/or SLT or both).
In conclusion, SLT cessation intervention-based research needs encouragement globally, especially in the low-income group countries which are deficient in tobacco cessation support. Behavioural interventions have been proven to be an efficacious and feasible modality for tobacco cessation in all settings (low and high resource). Sensitization and imparting of training regarding the same to health professionals and SLT use prevention and cessation-related school programmes need to be encouraged.
Financial support & sponsorship: None.
Conflicts of Interest: None.
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