Scolaris Content Display Scolaris Content Display

Cochrane Database of Systematic Reviews

Antibióticos para las sibilancias o la tos persistente después de la bronquiolitis aguda en niños

Información

DOI:
https://doi.org/10.1002/14651858.CD009834.pub3Copiar DOI
Base de datos:
  1. Cochrane Database of Systematic Reviews
Versión publicada:
  1. 22 agosto 2017see what's new
Tipo:
  1. Intervention
Etapa:
  1. Review
Grupo Editorial Cochrane:
  1. Grupo Cochrane de Vías respiratorias

Copyright:
  1. Copyright © 2017 The Cochrane Collaboration. Published by John Wiley & Sons, Ltd.

Cifras del artículo

Altmetric:

Citado por:

Citado 0 veces por enlace Crossref Cited-by

Contraer

Autores

  • Gabrielle B McCallum

    Correspondencia a: Child Health Division, Menzies School of Health Research, Charles Darwin University, Darwin, Australia

    [email protected]

  • Erin J Plumb

    Child Health Division, Menzies School of Health Research, Charles Darwin University, Darwin, Australia

  • Peter S Morris

    Child Health Division, Menzies School of Health Research, Charles Darwin University, Darwin, Australia

  • Anne B Chang

    Child Health Division, Menzies School of Health Research, Charles Darwin University, Darwin, Australia

Contributions of authors

GBM and ABC wrote the protocol. PSM reviewed the protocol. For the 2012 review, GBM and ABC, and for the 2016 search, GBM and EJP, independently reviewed the search, double‐entered data, and wrote the manuscript. ABC amended the manuscript, and PSM reviewed the manuscript.

Sources of support

Internal sources

  • The authors declare that no such funding was received for this systematic review, Other.

External sources

  • National Health Medical Research Council, Australia.

    Salary support for GBM, early career fellowship, grant number 1111705

  • National Health Medical Research Council, Australia.

    Salary support for ABC, practitioner fellowship, grant number 1058213

  • NHMRC Centre of Research Excellence Grant, Australia.

    CRE in respiratory health in Aboriginal and Torres Strait Islander children, grant number 1040830

Declarations of interest

Three review authors (GBM, PSM, and ABC) were authors of the McCallum 2015 paper. Review author EJP, who was not involved in the McCallum 2015 trial, extracted data for this review.

Acknowledgements

We thank Dr. Chris Cates, Dr. Emma Dennett, Jessica Thomas, and Emma Jackson for support for the protocol and the review. We also thank Elizabeth Stovold from the Cochrane Airways Group for performing the searches.

Dr. Chris Cates served as the Editor for this review and commented critically on the review.

The Background and Methods sections of this review are based on a standard template used by Cochrane Airways.

This project was supported by the National Institute for Health Research (NIHR) via Cochrane Infrastructure funding to the Cochrane Airways Group. The views and opinions expressed therein are those of the review authors and do not necessarily reflect those of the Systematic Reviews Programme, NIHR, NHS, or the Department of Health.

Version history

Published

Title

Stage

Authors

Version

2017 Aug 22

Antibiotics for persistent cough or wheeze following acute bronchiolitis in children

Review

Gabrielle B McCallum, Erin J Plumb, Peter S Morris, Anne B Chang

https://doi.org/10.1002/14651858.CD009834.pub3

2012 Dec 12

Antibiotics for persistent cough or wheeze following acute bronchiolitis in children

Review

Gabrielle B McCallum, Peter S Morris, Anne B Chang

https://doi.org/10.1002/14651858.CD009834.pub2

2012 Jun 13

Antibiotics for persistent cough or wheeze following acute bronchiolitis in children

Protocol

Gabrielle B McCallum, Peter S Morris, Anne B Chang

https://doi.org/10.1002/14651858.CD009834

Differences between protocol and review

The previous review used a hierarchy of assessment and was difficult to read. For this review update, instead of using a hierarchy of assessment, we modified primary and secondary outcomes for the purpose of providing clarity. We included an additional primary outcome for exacerbation rate and moved adverse events and bacterial resistance to secondary outcomes. We updated the methods to reflect current reporting, which included adding a risk of bias tool and an SOF table. For this review update, we planned but did not perform three sensitivity analyses, which we will likely perform in the future; we updated the inclusion criteria to make them more applicable to the primary question. Using a random‐effects model (when we detected heterogeneity), we performed our analysis by treatment received.

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 trial.
Figuras y tablas -
Figure 3

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

Forest plot of comparison: 1 Prevention of post‐bronchiolitis syndrome (antibiotics vs placebo), outcome: 1.1 Number of participants who were not cured at follow‐up (up to 6 months).
Figuras y tablas -
Figure 4

Forest plot of comparison: 1 Prevention of post‐bronchiolitis syndrome (antibiotics vs placebo), outcome: 1.1 Number of participants who were not cured at follow‐up (up to 6 months).

Forest plot of comparison: 1 Prevention of post‐bronchiolitis syndrome (antibiotics vs placebo), outcome: 1.2 Number of participants who were rehospitalised within 6 months.
Figuras y tablas -
Figure 5

Forest plot of comparison: 1 Prevention of post‐bronchiolitis syndrome (antibiotics vs placebo), outcome: 1.2 Number of participants who were rehospitalised within 6 months.

Forest plot of comparison: 1 Prevention of post‐bronchiolitis syndrome (antibiotics vs placebo), outcome: 1.3 Proportion of participants with wheeze (within 6 months of intervention).
Figuras y tablas -
Figure 6

Forest plot of comparison: 1 Prevention of post‐bronchiolitis syndrome (antibiotics vs placebo), outcome: 1.3 Proportion of participants with wheeze (within 6 months of intervention).

Comparison 1 Prevention of post‐bronchiolitis syndrome (antibiotics vs placebo), Outcome 1 Number of participants who were not cured at follow‐up (up to 6 months).
Figuras y tablas -
Analysis 1.1

Comparison 1 Prevention of post‐bronchiolitis syndrome (antibiotics vs placebo), Outcome 1 Number of participants who were not cured at follow‐up (up to 6 months).

Comparison 1 Prevention of post‐bronchiolitis syndrome (antibiotics vs placebo), Outcome 2 Number of participants who were rehospitalised within 6 months.
Figuras y tablas -
Analysis 1.2

Comparison 1 Prevention of post‐bronchiolitis syndrome (antibiotics vs placebo), Outcome 2 Number of participants who were rehospitalised within 6 months.

Comparison 1 Prevention of post‐bronchiolitis syndrome (antibiotics vs placebo), Outcome 3 Proportion of participants with wheeze (within 6 months of intervention).
Figuras y tablas -
Analysis 1.3

Comparison 1 Prevention of post‐bronchiolitis syndrome (antibiotics vs placebo), Outcome 3 Proportion of participants with wheeze (within 6 months of intervention).

Summary of findings for the main comparison. Antibiotics compared with placebo or no treatment for persistent respiratory symptoms following acute bronchiolitis

Antibiotics compared with placebo or no treatment for persistent respiratory symptoms following acute bronchiolitis

Patient or population: children < 24 months with persistent respiratory symptoms following acute bronchiolitis
Setting: post‐acute bronchiolitis phase > 14 days
Intervention: antibiotics^
Comparison: placebo or no treatment^

Outcomes

Anticipated absolute effects* (95% CI)

Relative effect
(95% CI)

No. of participants
(studies)

Quality of the evidence
(GRADE)

Comments

Risk with placebo

Risk with antibiotics

Number of participants who were not cured at follow‐up
Follow‐up: 6 months

234 per 1000

174 per 1000
(102 to 282)

OR 0.69
(0.37 to 1.28)

249
(2 RCTs)

⊕⊕⊝⊝
LOWa

Number of participants rehospitalised for a respiratory illness
Follow‐up: 6 months

238 per 1000

271 per 1000
(173 to 398)

OR 1.19
(0.67 to 2.12)

240
(2 RCTs)

⊕⊕⊝⊝
LOWa

Proportion of participants with recurrent wheeze
Follow‐up: 6 months

123 per 1000

99 per 1000
(47 to 195)

OR 0.47

(0.06 to 3.95)

240
(2 RCTs)

⊕⊕⊝⊝
LOWa

^Intervention/Comparison group: treatment initiated during child's hospitalisation for acute bronchiolitis

*The risk in the intervention group (and its 95% confidence interval) is based on assumed risk in the comparison group and the relative effect of the intervention (and its 95% CI)
CI: confidence interval; OR: odds ratio

We used GRADEPro software to create this table (GRADEpro GDT 2015)

GRADE Working Group grades of evidence
High quality: We are very confident that the true effect lies close to that of the estimate of the effect
Moderate quality: We are moderately confident in the effect estimate: The true effect is likely to be close to the estimate of the effect, but there is a possibility that it is substantially different
Low quality: Our confidence in the effect estimate is limited: The true effect may be substantially different from the estimate of the effect
Very low quality: We have very little confidence in the effect estimate: The true effect is likely to be substantially different from the estimate of effect

aQuality downgraded because of small numbers of studies and participants and high attrition in the Tahan study. Hence, we cannot be confident of the effect estimate

Figuras y tablas -
Summary of findings for the main comparison. Antibiotics compared with placebo or no treatment for persistent respiratory symptoms following acute bronchiolitis
Comparison 1. Prevention of post‐bronchiolitis syndrome (antibiotics vs placebo)

Outcome or subgroup title

No. of studies

No. of participants

Statistical method

Effect size

1 Number of participants who were not cured at follow‐up (up to 6 months) Show forest plot

2

249

Odds Ratio (M‐H, Fixed, 95% CI)

0.69 [0.37, 1.28]

2 Number of participants who were rehospitalised within 6 months Show forest plot

2

240

Odds Ratio (M‐H, Random, 95% CI)

0.54 [0.05, 6.21]

3 Proportion of participants with wheeze (within 6 months of intervention) Show forest plot

2

240

Odds Ratio (M‐H, Random, 95% CI)

0.47 [0.06, 3.95]

Figuras y tablas -
Comparison 1. Prevention of post‐bronchiolitis syndrome (antibiotics vs placebo)