Statistical analysis of pharmacotreatment effect and associated interactions in smoking cessation Dr Neil Walker, Oxford Biomedical Research Centre.

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Presentation transcript:

Statistical analysis of pharmacotreatment effect and associated interactions in smoking cessation Dr Neil Walker, Oxford Biomedical Research Centre

Objectives Use observational data (Stop Smoking Service) to: Make inference on effectiveness of pharmacotreatment in smoking cessation Identify subgroups (demographic or treatment regime) who perform strongly with particular treatments

Stop Smoking Service 12 – week programme offered to smokers wanting to quit throughout UK. Programme of meetings, max=12 (face-to-face, group session, telephone conversations) Initial assessment (smoking patterns, motivation) to tailor programme to individual needs Medication: Nicotine Replacement Therapy (NRT), Champix and Zyban Follow-up sessions: progress, medication, encouragement

Quit Manager database Electronic system for tracking patients using Stop Smoking Service: Standard personal & demographic information (name, DOB, address…) Session information (date, duration etc) Outcome recorded at 4,12,26 & 52 weeks (increasing number lost to follow-up at later times) Anonymised data extracted from Quit Manager for current analysis

Pharmacotreatment Champix (Varenicline) – prescribed course of tablets, proven efficacy in RCTs. Mode of action: Nicotine receptor partial agonist. Zyban (Bupropion) – prescribed tablets. Mode of action: Norepinephrine-dopamine Reuptake Inhibitor (NDRI). Nicotine Replacement Therapy (NRT) – available over the counter/on prescription. Patches, typically in combination with oral product (chewing gum, nasal spray etc).

Observational data Data provided by Quit-51: operate a number of Stop Smoking Services in England Data recorded on patients attempting to quit through Stop Smoking Service Opportunity to analyse a large observational dataset: Can assess smoking quit rates and association with wide range of potential explanatory variables in “real world” setting

Stop Smoking Service treatment programme NCSCT accredited 12-week programme. Includes: Sessions with NCSCT-accredited adviser(s) Initial assessment to establish suitable programme Quit date agreed (“Not a puff” criteria) Weekly/fortnightly follow-up sessions (medication, monitor progress, encouragement)

Quit Manager Patient’s progress recorded electronically; Patient details (name, DOB, medical history etc) Details on individual sessions Outcomes (quit success/failure) recorded at 4, 12, 26 & 52 weeks Patient data (anonymised) extracted to create database for analysis

DATA Data from 10 PCTs: London (Havering [ ], Redbridge [ ], Waltham Forest [ ], Barking & Dagenham [ ]). Sussex (East Sussex Downs and Weald [ ], Hastings and Rother [ ]) West Midlands (Sandwell [ ], Walsall Teaching [ ], Telford and Wrekin [ ], Worcestershire [ ]) N=89740 in total

Quantitative + qualitative information Has patient managed to quit? Self-report at 4 weeks then at 12, 26 & 52 weeks. CO validation at 4 weeks (i.e. CO < 10 ppm) Standard demographic information: Age, Sex, Occupation… Service used: Group, one-to-one with adviser, treatment prescribed…

Statistical models

1.Main effects: Assess overall effects of explanatory variables. Logit(y) = Treatment + Age + Sex + Service Treatment*Age + Treatment*Sex + Treatment*Service 2.Treatment interactions: Do treatments benefit particular subgroups? Logit(y) = Treatment + Age + Sex + Service + Treatment*Age + Treatment*Sex + Treatment*Service

RESULTS Raw data – quit rate by pharmacotreatment

RESULTS Raw data – quit rate by age

RESULTS Raw data – quit rate by service used

RESULTS Main effects GLMM Raw dataModel statistics VariableLevels n quit / n total (% quit rate) β (logit scale)Wald-stat (df)p-value Sex 10.6 (1, )0.001 male20012/26491 (75.5%)0 female21713/29684 (73.1%) (1, )0.001 Age Category (2, )< /2258 (51.7%) /8518 (71.8%) (1, )< /45402 (75.9%) (1, )<0.001 Service Used 69.5 (7, )<0.001 Treatment (3, )<0.001 No treatment specified 5093/6492 (78.5%)0 Champix10969/13593 (80.7%) (1, )<0.001 NRT25329/35650 (71.0%) (1, )0.006 Zyban336/443 (75.8%) (1, )0.2

RESULTS Interactions GLMM (interactions only) InteractionLevel β (logit scale) Wald-stat (df)p-value NRT*Age Category (2, ) 0.4 Champix* Age Category (2, ) 0.2 Zyban* Age Category (2, )0.997 NRT* Sex (1, )0.02 NRT*female-0.17 Champix* Sex (1, ) 0.5 Zyban* Sex (1, ) 0.5 NRT* Service Used 33.8 (7, )<0.001 NRT*drop-in0 NRT*GP-0.30 NRT*group0 NRT*one-to-one-0.40 NRT*pharmacy+0.14 NRT*telephone service NRT*workplace+0.10 NRT*unknown-0.26 Champix* Service Used Zyban* Service Used (5, )0.4

RESULTS NRT * Sex interaction, raw data

RESULTS NRT * service, raw data

Inference – main effects Statistical evidence of effects associated with: Pharmacotreatment – highest quit rates seen in patients using Champix Sex – Men using stop smoking service are more likely to quit Age – low quit rates among young smokers, flattens off with increasing age Service used – statistical evidence that the type of service used can influence chance of successful quit (Group sessions most effective)

Inference - interactions Patients using NRT have lower chance of quitting than on other regimes – this particularly pronounced in females Some evidence that effectiveness of NRT varies according to programme regime (positive interaction with “pharmacy” & “workplace”, negative in conjunction with “telephone service”).

Conclusions Statistical evidence in real world setting to support the use of Champix as an aid to smoking cessation. Quit rate associated with NRT low in relation to other treatments. This particularly so for women. Evidence that effectiveness of NRT can be enhanced in combination with particular treatment programmes. Quit rate low in young age group, rises sharply up to approximately 30 years, then flattens. No statistical evidence for interaction between age and treatment(s) though. Data from 10 PCTs – can we generalise results to rest of UK? Haven’t taken into account the different costs of treatments

Further Work Interactions between treatment & other factors Geographical differences? Using later time points (12,26, 52 weeks) for analysis (but data more scarce) How results compare to RCTs Non-linear modelling of age

Thank you, merci, grazie, obrigado… Thanks to Emma Croghan and Hayley Bates (North-51) for providing the data.