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What's new in smoking cessation? - Australian Prescriber

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<strong>What's</strong> <strong>new</strong> <strong>in</strong> smok<strong>in</strong>g <strong>cessation</strong>?<br />

John Litt, Senior Lecturer <strong>in</strong> General Practice, School of Medic<strong>in</strong>e, Fl<strong>in</strong>ders University,<br />

Adelaide<br />

Summary<br />

Tobacco smok<strong>in</strong>g is the ma<strong>in</strong> preventable cause<br />

of morbidity and mortality <strong>in</strong> Australia. Recently<br />

published evidence-based guidel<strong>in</strong>es for general<br />

practitioners recommend the 5As framework<br />

which is consistent with other <strong>in</strong>ternational<br />

guidel<strong>in</strong>es. Active follow-up of smokers by<br />

Quitl<strong>in</strong>e and the use of nurses to provide smok<strong>in</strong>g<br />

<strong>cessation</strong> activities are two <strong>in</strong>terventions that are<br />

likely to expand the reach of smok<strong>in</strong>g <strong>cessation</strong><br />

services and <strong>in</strong>crease their effectiveness.<br />

Comb<strong>in</strong>ation pharmacotherapies for nicot<strong>in</strong>e<br />

dependence should be considered <strong>in</strong> smokers<br />

who have had difficulty quitt<strong>in</strong>g despite the<br />

concurrent use of brief behavioural counsell<strong>in</strong>g<br />

and pharmacotherapy.<br />

Key words: nicot<strong>in</strong>e, patient support.<br />

Introduction<br />

(Aust Prescr 2005;28:73–5)<br />

Every year <strong>in</strong> Australia, tobacco smok<strong>in</strong>g causes an estimated<br />

19 000 deaths and up to 10% of hospital separations <strong>in</strong> people<br />

aged 35 years and over. 1 The 50-year follow-up of the British<br />

doctors study shows that up to 66% of lifelong smokers are<br />

likely to die from a tobacco-related disease with half these<br />

deaths occurr<strong>in</strong>g prematurely. 2 No other s<strong>in</strong>gle avoidable factor<br />

accounts for such a high proportion of deaths. 1<br />

Health professionals have several strategies they can use<br />

to encourage patients to quit smok<strong>in</strong>g. In addition to the<br />

publication of the first <strong>Australian</strong> smok<strong>in</strong>g <strong>cessation</strong> guidel<strong>in</strong>es<br />

for general practice <strong>in</strong> 2004 1 , there have been a number of other<br />

developments. These <strong>in</strong>clude:<br />

■ <strong>in</strong>creas<strong>in</strong>g evidence for the effectiveness of:<br />

– active callback programs by the Quitl<strong>in</strong>e 3,4<br />

– nurses provid<strong>in</strong>g smok<strong>in</strong>g <strong>cessation</strong> <strong>in</strong> the primary care<br />

sett<strong>in</strong>g 5<br />

■ the need to consider the use of comb<strong>in</strong>ation<br />

pharmacotherapies <strong>in</strong> assist<strong>in</strong>g smokers to quit. 6<br />

Smok<strong>in</strong>g <strong>cessation</strong> guidel<strong>in</strong>es for <strong>Australian</strong><br />

general practice<br />

The <strong>Australian</strong> general practice guidel<strong>in</strong>es for smok<strong>in</strong>g <strong>cessation</strong><br />

follow the 5As framework (Table 1). To assist busy practitioners<br />

<strong>in</strong> summaris<strong>in</strong>g the effective smok<strong>in</strong>g <strong>cessation</strong> activities a<br />

time-tiered synopsis of the 5As approach has also been<br />

published.* This <strong>in</strong>tervention can be delivered <strong>in</strong> one m<strong>in</strong>ute<br />

or less. 7<br />

Active callback programs by telephone quit<br />

l<strong>in</strong>es<br />

Several recent randomised controlled trials <strong>in</strong> Australia and the<br />

USA have found an advantage <strong>in</strong> offer<strong>in</strong>g telephone follow-up<br />

to smokers referred to a quit l<strong>in</strong>e. Active follow-up (4–5 calls on<br />

average) <strong>in</strong> the first three months of quitt<strong>in</strong>g is associated with<br />

higher 12-month quit rates (between 22% 3 and 25.8% 4 ) than<br />

more passive referrals to the Quitl<strong>in</strong>e. This represents four more<br />

people quitt<strong>in</strong>g for every 100 counselled.<br />

Nurse-delivered smok<strong>in</strong>g <strong>cessation</strong> strategies<br />

A systematic review has found that nurses have a similar impact<br />

to doctors when provid<strong>in</strong>g smok<strong>in</strong>g <strong>cessation</strong> <strong>in</strong> primary care. 5<br />

The ma<strong>in</strong> f<strong>in</strong>d<strong>in</strong>gs of the systematic review were:<br />

■ smokers offered advice by a nurse had an <strong>in</strong>creased<br />

likelihood of quitt<strong>in</strong>g compared to smokers without nurs<strong>in</strong>g<br />

<strong>in</strong>tervention (3–4 extra quitters for each 100 counselled)<br />

■ smok<strong>in</strong>g <strong>in</strong>tervention <strong>in</strong> the 13 trials <strong>in</strong>volv<strong>in</strong>g<br />

non-hospitalised adults gave an approximately 80% <strong>in</strong>crease<br />

<strong>in</strong> the odds of success<br />

■ there was no evidence from <strong>in</strong>direct comparisons that higher<br />

<strong>in</strong>tensity <strong>in</strong>terventions were more effective <strong>in</strong> achiev<strong>in</strong>g<br />

successful quitt<strong>in</strong>g.<br />

Overall, the results revealed that brief smok<strong>in</strong>g <strong>cessation</strong><br />

<strong>in</strong>terventions provided by nurses significantly <strong>in</strong>crease the odds<br />

of quitt<strong>in</strong>g compared to usual care.<br />

Comb<strong>in</strong>ation pharmacotherapies <strong>in</strong> assist<strong>in</strong>g<br />

smokers to quit<br />

With the slow fall <strong>in</strong> the prevalence of smok<strong>in</strong>g, the current<br />

population of smokers represent a mix of 'hardened' smokers<br />

who have attempted to quit on a number of occasions and<br />

others, for example younger smokers. 8 Both groups are<br />

exposed to <strong>in</strong>creas<strong>in</strong>g community awareness of the harmful<br />

effects of smok<strong>in</strong>g and expand<strong>in</strong>g legislative changes to quit.<br />

* A summary copy of the time-tiered 5As approach to smok<strong>in</strong>g<br />

<strong>cessation</strong> can be found on the Cancer Council SA website<br />

http://www.cancersa.org.au/i-cms_file?page=544/GPdeskprompt.<br />

pdf [cited 2005 May 10]<br />

| VOLUME 28 | NUMBER 3 | JUNE 2005 73


Table 1<br />

5As smok<strong>in</strong>g <strong>cessation</strong> framework *<br />

5As Strategy Suggested approach<br />

Ask Identify and document smok<strong>in</strong>g status at least Hand out brief patient survey <strong>in</strong> the wait<strong>in</strong>g room to identify<br />

every 12 months<br />

smok<strong>in</strong>g status<br />

Assess Interest <strong>in</strong> quitt<strong>in</strong>g How do you feel about your smok<strong>in</strong>g at the moment?<br />

How would you rate your <strong>in</strong>terest <strong>in</strong> quitt<strong>in</strong>g right now on a scale<br />

of 1–10 where 10 equals very <strong>in</strong>terested <strong>in</strong> quitt<strong>in</strong>g?<br />

What do you like and dislike about smok<strong>in</strong>g?<br />

Barriers to quitt<strong>in</strong>g<br />

Level of nicot<strong>in</strong>e dependence<br />

Quitt<strong>in</strong>g history<br />

High risk situations<br />

What would be the hardest th<strong>in</strong>g about quitt<strong>in</strong>g?<br />

Time to first cigarette from wak<strong>in</strong>g (less than 30 m<strong>in</strong>utes)<br />

Smokes 15 or more cigarettes a day<br />

Evidence of withdrawal symptoms with previous quit attempts<br />

What has worked before?<br />

What hasn't worked?<br />

What would be the hardest cigarette to give up?<br />

Advise<br />

Provide clear, brief and non-judgemental advice<br />

to quit<br />

As your doctor, I strongly suggest that you stop smok<strong>in</strong>g<br />

Quitt<strong>in</strong>g is the most important th<strong>in</strong>g you can do to stay healthy<br />

Address the three doma<strong>in</strong>s<br />

Nicot<strong>in</strong>e dependence<br />

Habit<br />

Psychological aspects of smok<strong>in</strong>g<br />

Assist Quit services Refer to Quitl<strong>in</strong>e 131 848 †<br />

Pharmacotherapy<br />

Address barriers to quitt<strong>in</strong>g<br />

Offer Quit book<br />

Enrol <strong>in</strong> Quitl<strong>in</strong>e callback program<br />

Discuss pharmacotherapy e.g. nicot<strong>in</strong>e replacement therapies<br />

and bupropion<br />

Commonly:<br />

– stress<br />

– weight ga<strong>in</strong><br />

– negative emotions<br />

– lack of support<br />

– fear of failure<br />

– low self-confidence<br />

Arrange Follow-up Review pharmacotherapy<br />

Advise about relapse prevention<br />

Review progress<br />

Support<br />

Offer your support<br />

Enlist support of significant others<br />

*<br />

adapted from 'Smok<strong>in</strong>g <strong>cessation</strong> guidel<strong>in</strong>es for <strong>Australian</strong> general practice' 1 , GPs Assist<strong>in</strong>g Smokers Program (GASP) 7 and<br />

'Treatment of tobacco use and dependence' 9<br />

†<br />

<strong>in</strong> all states except Queensland<br />

Identification of read<strong>in</strong>ess to change, level of nicot<strong>in</strong>e<br />

dependence and number of previous quit attempts will assist<br />

the practitioner <strong>in</strong> the approach to <strong>cessation</strong>, especially the use<br />

of pharmacotherapy.<br />

Like other pharmacological treatments, comb<strong>in</strong>ation therapy<br />

us<strong>in</strong>g drugs with different modes of action has been tried with<br />

differ<strong>in</strong>g degrees of success. 6 Comb<strong>in</strong>ation therapy can <strong>in</strong>clude<br />

two alternative forms of nicot<strong>in</strong>e replacement therapy (NRT) or<br />

nicot<strong>in</strong>e replacement and buproprion when 'the smoker has not<br />

been successful on an adequate trial of one of these therapies'. 1<br />

Most formulations of NRT provide doses of nicot<strong>in</strong>e that are<br />

below that achieved by smok<strong>in</strong>g. 1 Comb<strong>in</strong>ation NRT <strong>in</strong>cludes a<br />

formulation that provides basal levels of nicot<strong>in</strong>e (for example<br />

nicot<strong>in</strong>e patch) with 'top up' doses when withdrawal and crav<strong>in</strong>g<br />

74 | VOLUME 28 | NUMBER 3 | JUNE 2005


are more likely to be a problem, for example first th<strong>in</strong>g <strong>in</strong> the<br />

morn<strong>in</strong>g. Top up doses can be provided by a nicot<strong>in</strong>e <strong>in</strong>haler,<br />

lozenge or gum. Comb<strong>in</strong>ation therapies should be considered <strong>in</strong><br />

smokers who have failed despite behavioural <strong>in</strong>tervention and a<br />

reasonable trial of a s<strong>in</strong>gle formulation.<br />

References<br />

1. Zwar N, Richmond R, Borland R, Stillman S, Cunn<strong>in</strong>gham M,<br />

Litt J. Smok<strong>in</strong>g <strong>cessation</strong> guidel<strong>in</strong>es for <strong>Australian</strong> general<br />

practice. Canberra: Commonwealth Department of Health<br />

and Age<strong>in</strong>g; 2004.<br />

http://www.health.gov.au/<strong>in</strong>ternet/wcms/publish<strong>in</strong>g.<br />

nsf/Content/health-pubhlth-publicat-document-smok<strong>in</strong>g_<br />

<strong>cessation</strong>-cnt.htm [cited 2005 May 10]<br />

2. Doll R, Peto R, Boreham J, Sutherland I. Mortality <strong>in</strong> relation<br />

to smok<strong>in</strong>g: 50 years' observations on male British doctors.<br />

Br Med J 2004;328:1519.<br />

3. Borland R, Segan CJ, Liv<strong>in</strong>gston PM, Owen N. The<br />

effectiveness of callback counsell<strong>in</strong>g for smok<strong>in</strong>g <strong>cessation</strong>:<br />

a randomized trial. Addiction 2001;96:881-9.<br />

4. Zhu SH, Anderson CM, Tedeschi GJ, Rosbrook B,<br />

Johnson CE, Byrd M, et al. Evidence of real-world<br />

effectiveness of a telephone quitl<strong>in</strong>e for smokers.<br />

N Engl J Med 2002;347:1087-93.<br />

5. Rice VH, Stead LF. Nurs<strong>in</strong>g <strong>in</strong>terventions for smok<strong>in</strong>g<br />

<strong>cessation</strong>. The Cochrane Database of Systematic Reviews<br />

2004, Issue 1. Art. No.: CD001188.pub2. DOI:10.1002/<br />

14651858.CD001188.pub2.<br />

6. George TP, O'Malley SS. Current pharmacological treatments<br />

for nicot<strong>in</strong>e dependence. Trends Pharmacol Sci 2004;25:42-8.<br />

7. Litt J, L<strong>in</strong>g M-Y, McAvoy B. How to help your patients quit:<br />

practice-based strategies for smok<strong>in</strong>g <strong>cessation</strong>. Asia Pac<br />

Fam Med 2003;2:175-9.<br />

8. White V, Hill D, Siahpush M, Bobevski I. How has the<br />

prevalence of cigarette smok<strong>in</strong>g changed among <strong>Australian</strong><br />

adults? Trends <strong>in</strong> smok<strong>in</strong>g prevalence between 1980 and<br />

2001. Tob Control 2003;12(Suppl 2):ii67-74.<br />

9. Rigotti NA. Cl<strong>in</strong>ical practice. Treatment of tobacco use and<br />

dependence. N Engl J Med 2002;346:506-12.<br />

Conflict of <strong>in</strong>terest: none declared<br />

Self-test questions<br />

The follow<strong>in</strong>g statements are either true or false<br />

(answers on page 79)<br />

7. Telephone follow-up by a quit l<strong>in</strong>e service <strong>in</strong>creases the<br />

chance of a smoker successfully quitt<strong>in</strong>g smok<strong>in</strong>g.<br />

8. Patients should not use two forms of nicot<strong>in</strong>e<br />

replacement therapy at the same time.<br />

New drugs<br />

Some of the views expressed <strong>in</strong> the follow<strong>in</strong>g notes on <strong>new</strong>ly approved products should be regarded as tentative, as there may have been little<br />

experience <strong>in</strong> Australia of their safety or efficacy. However, the Editorial Executive Committee believes that comments made <strong>in</strong> good faith at an early<br />

stage may still be of value. As a result of fuller experience, <strong>in</strong>itial comments may need to be modified. The Committee is prepared to do this. Before<br />

<strong>new</strong> drugs are prescribed, the Committee believes it is important that full <strong>in</strong>formation is obta<strong>in</strong>ed either from the manufacturer's approved product<br />

<strong>in</strong>formation, a drug <strong>in</strong>formation centre or some other appropriate source.<br />

Bivalirud<strong>in</strong><br />

Angiomax (CSL)<br />

vials conta<strong>in</strong><strong>in</strong>g 250 mg lyophilised powder for reconstitution<br />

Approved <strong>in</strong>dication: percutaneous coronary <strong>in</strong>tervention<br />

<strong>Australian</strong> Medic<strong>in</strong>es Handbook section 7.1<br />

Patients hav<strong>in</strong>g procedures such as percutaneous translum<strong>in</strong>al<br />

coronary angioplasty need to be anticoagulated. While hepar<strong>in</strong><br />

can be used, some patients still develop ischaemia and there is<br />

a risk of major bleed<strong>in</strong>g.<br />

Bivalirud<strong>in</strong> is a direct <strong>in</strong>hibitor of thromb<strong>in</strong> related to the<br />

anticoagulant prote<strong>in</strong> produced by leeches. By reversibly<br />

b<strong>in</strong>d<strong>in</strong>g to thromb<strong>in</strong>, bivalirud<strong>in</strong> stops the conversion of<br />

fibr<strong>in</strong>ogen to fibr<strong>in</strong> and <strong>in</strong>hibits platelet aggregation.<br />

The anticoagulant effect beg<strong>in</strong>s with<strong>in</strong> a few m<strong>in</strong>utes of<br />

<strong>in</strong>travenous adm<strong>in</strong>istration. The clott<strong>in</strong>g time, activated partial<br />

thromboplast<strong>in</strong> time (APTT), prothromb<strong>in</strong> time and thromb<strong>in</strong><br />

time are all <strong>in</strong>creased. Bivalirud<strong>in</strong> is given as a bolus dose<br />

followed by an <strong>in</strong>fusion. It has a half-life of approximately<br />

25 m<strong>in</strong>utes, with most of the dose be<strong>in</strong>g metabolised <strong>in</strong>to<br />

am<strong>in</strong>o acids. As 20% of the dose is excreted unchanged <strong>in</strong> the<br />

ur<strong>in</strong>e impaired renal function prolongs the half-life.<br />

An early study of bivalirud<strong>in</strong> found that it caused less<br />

bleed<strong>in</strong>g but had no greater efficacy than high-dose hepar<strong>in</strong><br />

<strong>in</strong> prevent<strong>in</strong>g ischaemic complications <strong>in</strong> patients hav<strong>in</strong>g<br />

coronary angioplasty. 1 Development of the drug did not<br />

proceed, however when the results were reanalysed several<br />

years later they showed a statistical advantage for bivalirud<strong>in</strong>. 2<br />

As the drugs used dur<strong>in</strong>g the procedure had changed <strong>in</strong> the<br />

<strong>in</strong>terven<strong>in</strong>g years, there was a need to evaluate bivalirud<strong>in</strong> with<br />

the <strong>new</strong> approaches.<br />

The REPLACE-2 trial randomised 6010 patients to receive<br />

bivalirud<strong>in</strong> or hepar<strong>in</strong> plus a glycoprote<strong>in</strong> IIb/IIIa <strong>in</strong>hibitor. All<br />

patients also received aspir<strong>in</strong> and the use of clopidogrel was<br />

| VOLUME 28 | NUMBER 3 | JUNE 2005 75

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