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Cochrane Database of Systematic Reviews

Cafeína como adyuvante analgésico para el dolor agudo en adultos

Información

DOI:
https://doi.org/10.1002/14651858.CD009281.pub3Copiar DOI
Base de datos:
  1. Cochrane Database of Systematic Reviews
Versión publicada:
  1. 11 diciembre 2014see what's new
Tipo:
  1. Intervention
Etapa:
  1. Review
Grupo Editorial Cochrane:
  1. Grupo Cochrane de Dolor y cuidados paliativos

Copyright:
  1. Copyright © 2019 The Cochrane Collaboration. Published by John Wiley & Sons, Ltd.

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Contraer

Autores

  • Christopher J Derry

    Pain Research and Nuffield Department of Clinical Neurosciences (Nuffield Division of Anaesthetics), University of Oxford, Oxford, UK

  • Sheena Derry

    Correspondencia a: Oxford, UK

    [email protected]

  • R Andrew Moore

    Plymouth, UK

Contributions of authors

All authors contributed to writing the protocol.

For the original review CD and SD carried out searches and data extraction. RAM contacted pharmaceutical companies and conduct Internet searches for otherwise unpublished data. All authors were involved with data analysis and preparation of the manuscript. RAM will be responsible for any update, though the paucity of recent studies with caffeine make any update unlikely in the near future.

For this update SD and RAM carried out the searches. All authors contributed to updating the text.

Sources of support

Internal sources

  • Oxford Pain Relief Trust, UK.

    General institutional support

External sources

  • No sources of support supplied

Declarations of interest

CD has no conflicts relating to this review or any similar product.

SD has no conflicts relating to this review or any similar product.

RAM has no conflicts relating to this review or any similar product.

For transparency we have received research support from charities, government, and industry sources at various times, but none relate to this review. We are funded by the NIHR for work on a series of reviews informing the unmet need of chronic pain and providing the evidence for treatments of pain.

Acknowledgements

We wish to thank Prof Henry McQuay for his insight and useful discussions, and the peer reviewers and Cochrane PaPaS Group editorial team for their helpful comments on the original review.

CRG Funding Acknowledgement: The National Institute for Health Research (NIHR) is currently the largest single funder of the Cochrane Pain, Palliative and Supportive Care Review Group. Disclaimer: The views and opinions expressed therein are those of the authors and do not necessarily reflect those of the NIHR, NHS or the Department of Health.

Version history

Published

Title

Stage

Authors

Version

2014 Dec 11

Caffeine as an analgesic adjuvant for acute pain in adults

Review

Christopher J Derry, Sheena Derry, R Andrew Moore

https://doi.org/10.1002/14651858.CD009281.pub3

2012 Mar 14

Caffeine as an analgesic adjuvant for acute pain in adults

Review

Christopher J Derry, Sheena Derry, R Andrew Moore

https://doi.org/10.1002/14651858.CD009281.pub2

2011 Aug 10

Caffeine as an analgesic adjuvant for acute pain in adults

Protocol

Christopher J Derry, Sheena Derry, R Andrew Moore

https://doi.org/10.1002/14651858.CD009281

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' graph: review authors' judgements about each risk of bias item presented as percentages across all included studies.
Figuras y tablas -
Figure 2

'Risk of bias' graph: review authors' judgements about each risk of bias item presented as percentages across all included studies.

'Risk of bias' summary: review authors' judgements about each risk of bias item for each included study.
Figuras y tablas -
Figure 3

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

Individual studies comparing the primary outcome for analgesic + caffeine versus analgesic alone ‐ any pain condition
Figuras y tablas -
Figure 4

Individual studies comparing the primary outcome for analgesic + caffeine versus analgesic alone ‐ any pain condition

Forest plot of comparison: 3 Analgesic plus caffeine versus analgesic alone by dose of caffeine, outcome: 3.1 Primary outcome.
Figuras y tablas -
Figure 5

Forest plot of comparison: 3 Analgesic plus caffeine versus analgesic alone by dose of caffeine, outcome: 3.1 Primary outcome.

Comparison 1 Analgesic plus caffeine versus analgesic alone by pain condition, Outcome 1 Primary outcome.
Figuras y tablas -
Analysis 1.1

Comparison 1 Analgesic plus caffeine versus analgesic alone by pain condition, Outcome 1 Primary outcome.

Comparison 2 Analgesic plus caffeine versus analgesic alone by drug, Outcome 1 Primary outcome.
Figuras y tablas -
Analysis 2.1

Comparison 2 Analgesic plus caffeine versus analgesic alone by drug, Outcome 1 Primary outcome.

Comparison 3 Analgesic plus caffeine versus analgesic alone by dose of caffeine, Outcome 1 Primary outcome.
Figuras y tablas -
Analysis 3.1

Comparison 3 Analgesic plus caffeine versus analgesic alone by dose of caffeine, Outcome 1 Primary outcome.

Analgesic plus caffeine compared with analgesic alone for acute pain

Patient or population: adults with acute pain

Settings: community

Intervention: analgesic plus caffeine

Comparison: same dose of analgesic alone

Outcomes

Outcome with analgesic alone

Outcome with analgesic plus caffeine

RR and NNT
(95% CI)

No of participants
(studies)

Quality of the evidence
(GRADE)

Comments

Effective pain relief

41%

48%

RR 1.2 (1.1 to 1.3)

NNT 14 (9.9 to 24)

4262

(27 separate comparisons)

High

Small effect size but large numbers of participants contributing. There is a large amount of data that cannot be incorporated into this review, but this result is robust to analysis assuming all missing data show no effect. In fact, the results of this review are consistent with an almost completely different analysis in 10,000 participants demonstrating the effect of caffeine to have a similar effect size

Serious adverse events

1 event

1 event

Not calculated

Not calculated

Very low

Neither event judged related to study medication. Single dose studies are not powered to assess serious adverse events

CI: confidence interval; NNT: number needed to treat to benefit; RR: risk ratio

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.

Figuras y tablas -
Comparison 1. Analgesic plus caffeine versus analgesic alone by pain condition

Outcome or subgroup title

No. of studies

No. of participants

Statistical method

Effect size

1 Primary outcome Show forest plot

16

4262

Risk Ratio (M‐H, Fixed, 95% CI)

1.18 [1.11, 1.26]

1.1 Postoperative/postpartum

10

2139

Risk Ratio (M‐H, Fixed, 95% CI)

1.16 [1.08, 1.25]

1.2 Headache

5

1503

Risk Ratio (M‐H, Fixed, 95% CI)

1.30 [1.11, 1.52]

1.3 Dysmenorrhoea

1

620

Risk Ratio (M‐H, Fixed, 95% CI)

1.11 [0.92, 1.34]

Figuras y tablas -
Comparison 1. Analgesic plus caffeine versus analgesic alone by pain condition
Comparison 2. Analgesic plus caffeine versus analgesic alone by drug

Outcome or subgroup title

No. of studies

No. of participants

Statistical method

Effect size

1 Primary outcome Show forest plot

12

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

1.1 Paracetamol

8

2186

Risk Ratio (M‐H, Fixed, 95% CI)

1.14 [1.06, 1.22]

1.2 Ibuprofen

4

707

Risk Ratio (M‐H, Fixed, 95% CI)

1.52 [1.25, 1.84]

Figuras y tablas -
Comparison 2. Analgesic plus caffeine versus analgesic alone by drug
Comparison 3. Analgesic plus caffeine versus analgesic alone by dose of caffeine

Outcome or subgroup title

No. of studies

No. of participants

Statistical method

Effect size

1 Primary outcome Show forest plot

16

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

1.1 Caffeine < 70 mg

5

596

Risk Ratio (M‐H, Fixed, 95% CI)

1.14 [0.97, 1.34]

1.2 Caffeine 70 mg to 150 mg

14

2983

Risk Ratio (M‐H, Fixed, 95% CI)

1.21 [1.12, 1.32]

1.3 Caffeine > 150 mg

6

745

Risk Ratio (M‐H, Fixed, 95% CI)

1.21 [1.07, 1.35]

Figuras y tablas -
Comparison 3. Analgesic plus caffeine versus analgesic alone by dose of caffeine