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Cochrane Database of Systematic Reviews

Intervenciones para aumentar la adherencia a los fármacos para la dependencia del tabaco

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Información

DOI:
https://doi.org/10.1002/14651858.CD009164.pub2Copiar DOI
Base de datos:
  1. Cochrane Database of Systematic Reviews
Versión publicada:
  1. 23 febrero 2015see what's new
Tipo:
  1. Intervention
Etapa:
  1. Review
Grupo Editorial Cochrane:
  1. Grupo Cochrane de Tabaquismo

Copyright:
  1. Copyright © 2015 The Cochrane Collaboration. Published by John Wiley & Sons, Ltd.

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Autores

  • Gareth J Hollands

    Correspondencia a: Behaviour and Health Research Unit, University of Cambridge, Cambridge, UK

    [email protected]

  • Máirtín S McDermott

    School of Information Systems and Technology, University of Wollongong, Wollongong, Australia

  • Nicola Lindson‐Hawley

    Nuffield Department of Primary Care Health Sciences, University of Oxford, Oxford, UK

  • Florian Vogt

    Institute of Pharmaceutical Science, King's College London, London, UK

  • Amanda Farley

    Public Health, Epidemiology and Biostatistics, University of Birmingham, Birmingham, UK

  • Paul Aveyard

    Nuffield Department of Primary Care Health Sciences, Oxford University, Oxford, UK

Contributions of authors

Draft the protocol: All authors

Develop the search strategy: GJH, MM

Search for trials: GJH, MM, FV, AF

Obtain copies of trials: GJH

Select which studies to include: GJH, MM

Extract data from studies: GJH, MM, FV, AF, NL

Enter data into RevMan: GJH, MM

Carry out the analysis: GJH

Interpret the analysis: All authors

Draft the final review: All authors

Update the review: GJH

Sources of support

Internal sources

  • King's College London, UK.

    Database access

  • University of Cambridge, UK.

    Computer use, database access

External sources

  • No sources of support supplied

Declarations of interest

Gareth Hollands and Paul Aveyard are authors of one study included in this review. All other authors declare that they have no competing interests.

Acknowledgements

The authors would like to thank Monaz Mehta (Managing Editor), Lindsay Stead (Managing Editor, who ran searches of the Tobacco Addiction Group Specialized Register), and all at the Cochrane Tobacco Addiction Group. We also greatly appreciate the input of the peer reviewers who have commented on this review throughout its development.

Version history

Published

Title

Stage

Authors

Version

2019 Aug 16

Interventions to increase adherence to medications for tobacco dependence

Review

Gareth J Hollands, Felix Naughton, Amanda Farley, Nicola Lindson, Paul Aveyard

https://doi.org/10.1002/14651858.CD009164.pub3

2015 Feb 23

Interventions to increase adherence to medications for tobacco dependence

Review

Gareth J Hollands, Máirtín S McDermott, Nicola Lindson‐Hawley, Florian Vogt, Amanda Farley, Paul Aveyard

https://doi.org/10.1002/14651858.CD009164.pub2

2011 Jun 15

Interventions to increase adherence to medications for tobacco dependence

Protocol

Gareth J Hollands, Florian Vogt, Máirtín McDermott, Amanda C Parsons, Paul Aveyard

https://doi.org/10.1002/14651858.CD009164

Differences between protocol and review

The criteria for eligible interventions was refined between the protocol and the review. The original primary intention of the review was to examine the effect of interventions to increase adherence where this was the clearly intended focus of those intervening. However, this primary intention was not adequately reflected in the original criteria. As such, a large number of studies of interventions that could in theory alter adherence but where this was not the researchers' intention would have been relevant for inclusion. Furthermore, this lack of clarity meant that most extant studies that featured any intervention in smokers would have to be examined at the full‐text screening stage because a clear focus on increasing adherence (which can typically be derived from the title and abstract screening process) was not necessary for consideration for inclusion.

Keywords

MeSH

PICO

Population
Intervention
Comparison
Outcome

El uso y la enseñanza del modelo PICO están muy extendidos en el ámbito de la atención sanitaria basada en la evidencia para formular preguntas y estrategias de búsqueda y para caracterizar estudios o metanálisis clínicos. PICO son las siglas en inglés de cuatro posibles componentes de una pregunta de investigación: paciente, población o problema; intervención; comparación; desenlace (outcome).

Para saber más sobre el uso del modelo PICO, puede consultar el Manual Cochrane.

Study flow diagram
Figuras y tablas -
Figure 1

Study flow diagram

Risk of bias summary: review authors' judgements about each risk of bias item for each included study.
Figuras y tablas -
Figure 2

Risk of bias summary: review authors' judgements about each risk of bias item for each included study.

Comparison 1 Primary outcome (adherence), Outcome 1 Adherence ‐ Dichotomous outcomes.
Figuras y tablas -
Analysis 1.1

Comparison 1 Primary outcome (adherence), Outcome 1 Adherence ‐ Dichotomous outcomes.

Comparison 1 Primary outcome (adherence), Outcome 2 Adherence ‐ Continuous outcomes.
Figuras y tablas -
Analysis 1.2

Comparison 1 Primary outcome (adherence), Outcome 2 Adherence ‐ Continuous outcomes.

Comparison 2 Secondary outcomes, Outcome 1 Short‐term abstinence < 6 months.
Figuras y tablas -
Analysis 2.1

Comparison 2 Secondary outcomes, Outcome 1 Short‐term abstinence < 6 months.

Comparison 2 Secondary outcomes, Outcome 2 Long‐term abstinence ≥ 6 months.
Figuras y tablas -
Analysis 2.2

Comparison 2 Secondary outcomes, Outcome 2 Long‐term abstinence ≥ 6 months.

Summary of findings for the main comparison. Interventions to increase adherence compared to standard care for improving adherence to medications for tobacco dependence and abstinence from smoking

Interventions to increase adherence compared to standard care for improving adherence to medications for tobacco dependence and abstinence from smoking

Patient or population: Adult smokers
Settings: Typically in‐person clinical settings
Intervention: Interventions to increase adherence through providing information and facilitating problem‐solving
Comparison: Standard care

Outcomes

Relative effect (95% CI)

Illustrative comparative risks (95% CI)

No of Participants
(studies)

Quality of the evidence
(GRADE)

Assumed risk

Corresponding risk

Standard care

Interventions to increase adherence

Adherence to medications for tobacco dependence (dichotomous outcomes)

RR 1.14
(1.02 to 1.28)

Study population

1630
(5 RCTs)

⊕⊕⊕⊝
MODERATE 1

368 per 1000 achieve a specified satisfactory level of adherence

419 per 1000 (375 to 471) achieve a specified satisfactory level of adherence

Adherence to medications for tobacco dependence (continuous outcomes)

SMD 0.07

(‐0.03 to 0.17)

The mean level of adherence is 0

The mean level of adherence is 0.07 standard deviations higher (0.03 lower to 0.17 higher)

1529
(4 RCTs)

⊕⊕⊝⊝
LOW 1,2

Short‐term abstinence from smoking (<6 months)

RR 1.07
(0.95 to 1.21)

Study population

1755
(4 RCTs)

⊕⊕⊝⊝
LOW 1,3

363 per 1000 achieve abstinence

389 per 1000 (345 to 439) achieve abstinence

Long‐term abstinence from smoking (≥6 months)

RR 1.16
(1.01 to 1.34)

Study population

3049
(4 RCTs)

⊕⊕⊝⊝
LOW 1,4

171 per 1000 achieve abstinence

198 per 1000 (173 to 229) achieve abstinence

The corresponding risk (and its 95% confidence interval) is based on the assumed risk in the comparison group and the relative effect of the intervention (and its 95% CI). CI: Confidence interval;

GRADE Working Group grades of evidence
High quality: Further research is very unlikely to change our confidence in the estimate of effect.
Moderate quality: Further research is likely to have an important impact on our confidence in the estimate of effect and may change the estimate.
Low quality: Further research is very likely to have an important impact on our confidence in the estimate of effect and is likely to change the estimate.
Very low quality: We are very uncertain about the estimate.

1All studies are judged to be at high or unclear risk of bias which lowers confidence in estimate of effect

2Includes sufficient sample size for single adequately powered trial but 95% CI overlaps no effect and ranges from very small harm to small benefit

3Includes sufficient sample size for single adequately powered trial but 95% CI overlaps no effect and ranges from small harm to substantial benefit

4Substantial heterogeneity with inconsistency in point estimates and limited overlap of confidence intervals

Figuras y tablas -
Summary of findings for the main comparison. Interventions to increase adherence compared to standard care for improving adherence to medications for tobacco dependence and abstinence from smoking
Table 1. Brief descriptions of adherence interventions

Study

Brief description of specific intervention components intended to increase adherence*

Additional contact time relative to standard care?

Medication for which adherence was targeted

Chan

2010

Added counselling contact time to standard behavioural support, focusing specifically on medication adherence

Yes

NRT

Chan

2011

Added counselling contact time to standard behavioural support, focusing specifically on medication adherence

Yes

NRT

Marteau

2012

Tailored and communicated about NRT dosage using a more potent rationale (genotype versus phenotype)

No

NRT

Mooney

2005

Personalised feedback of questionnaire responses regarding medication

No

NRT

Mooney

2007

Personalised feedback of externally validated medication adherence

Yes

Bupropion

Nollen

2011

Added counselling contact time to standard behavioural support, focusing specifically on medication adherence

Yes

Varenicline

Schmitz

2005

Personalised feedback of externally validated medication adherence

Yes

Bupropion

Smith

2013

Added counselling contact time to standard behavioural support, focusing specifically on medication adherence

Yes

NRT

* For further details see Characteristics of Included Studies

Figuras y tablas -
Table 1. Brief descriptions of adherence interventions
Comparison 1. Primary outcome (adherence)

Outcome or subgroup title

No. of studies

No. of participants

Statistical method

Effect size

1 Adherence ‐ Dichotomous outcomes Show forest plot

5

1630

Risk Ratio (M‐H, Fixed, 95% CI)

1.14 [1.02, 1.28]

2 Adherence ‐ Continuous outcomes Show forest plot

4

1529

Std. Mean Difference (IV, Fixed, 95% CI)

0.07 [‐0.03, 0.17]

Figuras y tablas -
Comparison 1. Primary outcome (adherence)
Comparison 2. Secondary outcomes

Outcome or subgroup title

No. of studies

No. of participants

Statistical method

Effect size

1 Short‐term abstinence < 6 months Show forest plot

4

1755

Risk Ratio (M‐H, Fixed, 95% CI)

1.07 [0.95, 1.21]

2 Long‐term abstinence ≥ 6 months Show forest plot

4

3049

Risk Ratio (M‐H, Fixed, 95% CI)

1.16 [1.01, 1.34]

Figuras y tablas -
Comparison 2. Secondary outcomes