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Cochrane Database of Systematic Reviews

Inmunonutrición como tratamiento adyuvante para las quemaduras

Información

DOI:
https://doi.org/10.1002/14651858.CD007174.pub2Copiar DOI
Base de datos:
  1. Cochrane Database of Systematic Reviews
Versión publicada:
  1. 23 diciembre 2014see what's new
Tipo:
  1. Intervention
Etapa:
  1. Review
Grupo Editorial Cochrane:
  1. Grupo Cochrane de Lesiones

Copyright:
  1. Copyright © 2014 The Cochrane Collaboration. Published by John Wiley & Sons, Ltd.

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Autores

  • Hannah B Tan

    Victorian Adult Burns Service, The Alfred Hospital, Prahran, Australia

    Monash University, Melbourne, Australia

  • Stefan Danilla

    Departamento de Cirugia, Hospital Clínico Universidad de Chile, Santiago, Chile

  • Alexandra Murray

    Victorian Adult Burns Service, The Alfred Hospital, Melbourne, Australia

  • Ramón Serra

    Health Research and Development, Hospital de Las Fuerzas Armadas Punta Arenas, Santiago, Chile

  • Regina El Dib

    Department of Anaesthesiology, Botucatu Medical School, UNESP–Universidade Estadual Paulista, Botucatu, São Paulo, Brazil

  • Tom OW Henderson

    Victorian Adult Burns Service, The Alfred Hospital, Melbourne, Australia

    University of Oxford Clinical School, Oxford University, Oxford, UK

  • Jason Wasiak

    Correspondencia a: Department of Radiation Oncology, The Epworth Hospital, Richmond, Australia

    [email protected]

    [email protected]

Contributions of authors

Hannah Beatrix Tan: trial screening, manuscript drafting and editing, assessing quality.

Stefan Danilla: manuscript drafting, trial screening, extracting data, assessing quality, performing statistical analysis.

Alexandra Murray: trial screening, manuscript drafting and editing.

Ramon Serra: searching grey literature, manuscript drafting, extracting data, assessing quality.

Regina El Dib: manuscript drafting, trial screening.

Tom Henderson: trial screening, manuscript drafting.

Jason Wasiak: trial screening, manuscript drafting and editing, assessing quality.

Declarations of interest

All authors: none known.

Acknowledgements

Sincere thanks to Dr Zhaowei Zhou (Department of Cardiothoracic Surgery, Hammersmith Hospital, London, UK) for translating Chinese articles, to Dr María Teresa Valenzuela for sending letters to the authors of selected articles and to Frances Phillips (Head of Dietetics and Nutrition, Royal Perth Hospital, Perth, AUS) for providing insights into clinical content.

Version history

Published

Title

Stage

Authors

Version

2014 Dec 23

Immunonutrition as an adjuvant therapy for burns

Review

Hannah B Tan, Stefan Danilla, Alexandra Murray, Ramón Serra, Regina El Dib, Tom OW Henderson, Jason Wasiak

https://doi.org/10.1002/14651858.CD007174.pub2

2008 Apr 23

Immunonutrition as an adjuvant therapy for burns

Protocol

Stefan Danilla, Regina P El Dib, Ramón Serra, Gabriel Cavada, Maria Valenzuela

https://doi.org/10.1002/14651858.CD007174

Differences between protocol and review

  1. Performed trial sequential analysis for mortality on glutamine intervention post hoc according to the peer review process.

  2. Changed population of interest from “patients with severe burn injuries” to "patients of any age with a burn of any severity" because of the heterogeneity of the definition of "severe" burn injury.

  3. Removed the following secondary outcomes: mortality due to sepsis, rates of multiple organ failure (MOF).

  4. Combined the following secondary outcomes into "Rate of non‐wound infection": pneumonia, urinary tract infection, burn wound sepsis, central venous catheter–associated bloodstream infection.

  5. Did not perform the following subgroup analyses.

    1. Minor versus major burns (major burns are defined as burns to at least 20% of the total body surface).

    2. Early versus delayed nutrition.

    3. Children (birth to 18 years of age) versus adults (19 years of age or older).

    4. Different types of immunonutrients in the experimental group.

    5. Different types of nutrition in the control group.

    6. Different doses of immunonutrients.

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.

Risk of bias graph: review authors' judgements about each risk of bias item presented as percentages across all included studies.
Figuras y tablas -
Figure 3

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

Comparison 1 All‐cause mortality, Outcome 1 Glutamine vs control.
Figuras y tablas -
Analysis 1.1

Comparison 1 All‐cause mortality, Outcome 1 Glutamine vs control.

Comparison 1 All‐cause mortality, Outcome 2 Ornithine α‐ketoglutarate vs control.
Figuras y tablas -
Analysis 1.2

Comparison 1 All‐cause mortality, Outcome 2 Ornithine α‐ketoglutarate vs control.

Comparison 1 All‐cause mortality, Outcome 3 Branched‐chain amino acids vs control.
Figuras y tablas -
Analysis 1.3

Comparison 1 All‐cause mortality, Outcome 3 Branched‐chain amino acids vs control.

Comparison 1 All‐cause mortality, Outcome 4 Fish oil vs control.
Figuras y tablas -
Analysis 1.4

Comparison 1 All‐cause mortality, Outcome 4 Fish oil vs control.

Comparison 1 All‐cause mortality, Outcome 5 Combined immunonutrients vs control.
Figuras y tablas -
Analysis 1.5

Comparison 1 All‐cause mortality, Outcome 5 Combined immunonutrients vs control.

Comparison 2 Length of hospital stay, Outcome 1 Glutamine vs control.
Figuras y tablas -
Analysis 2.1

Comparison 2 Length of hospital stay, Outcome 1 Glutamine vs control.

Comparison 2 Length of hospital stay, Outcome 2 Ornithine α‐ketoglutarate vs control.
Figuras y tablas -
Analysis 2.2

Comparison 2 Length of hospital stay, Outcome 2 Ornithine α‐ketoglutarate vs control.

Comparison 2 Length of hospital stay, Outcome 3 Branched‐chain amino acids.
Figuras y tablas -
Analysis 2.3

Comparison 2 Length of hospital stay, Outcome 3 Branched‐chain amino acids.

Comparison 2 Length of hospital stay, Outcome 4 Fish oil vs control.
Figuras y tablas -
Analysis 2.4

Comparison 2 Length of hospital stay, Outcome 4 Fish oil vs control.

Comparison 2 Length of hospital stay, Outcome 5 Combined immunonutrients vs control.
Figuras y tablas -
Analysis 2.5

Comparison 2 Length of hospital stay, Outcome 5 Combined immunonutrients vs control.

Comparison 3 Rate of burn wound infection, Outcome 1 Glutamine vs control.
Figuras y tablas -
Analysis 3.1

Comparison 3 Rate of burn wound infection, Outcome 1 Glutamine vs control.

Comparison 3 Rate of burn wound infection, Outcome 2 Ornithine α‐ketoglutarate vs control.
Figuras y tablas -
Analysis 3.2

Comparison 3 Rate of burn wound infection, Outcome 2 Ornithine α‐ketoglutarate vs control.

Comparison 3 Rate of burn wound infection, Outcome 3 Combined immunonutrients vs control.
Figuras y tablas -
Analysis 3.3

Comparison 3 Rate of burn wound infection, Outcome 3 Combined immunonutrients vs control.

Comparison 4 Rate of non‐wound infection, Outcome 1 Glutamine vs control.
Figuras y tablas -
Analysis 4.1

Comparison 4 Rate of non‐wound infection, Outcome 1 Glutamine vs control.

Comparison 4 Rate of non‐wound infection, Outcome 2 Fish oil vs control.
Figuras y tablas -
Analysis 4.2

Comparison 4 Rate of non‐wound infection, Outcome 2 Fish oil vs control.

Comparison 4 Rate of non‐wound infection, Outcome 3 Combined immunonutrients vs control.
Figuras y tablas -
Analysis 4.3

Comparison 4 Rate of non‐wound infection, Outcome 3 Combined immunonutrients vs control.

Comparison 1. All‐cause mortality

Outcome or subgroup title

No. of studies

No. of participants

Statistical method

Effect size

1 Glutamine vs control Show forest plot

3

111

Risk Ratio (M‐H, Fixed, 95% CI)

0.25 [0.08, 0.78]

1.1 Enteral

2

85

Risk Ratio (M‐H, Fixed, 95% CI)

0.23 [0.06, 0.93]

1.2 Parenteral

1

26

Risk Ratio (M‐H, Fixed, 95% CI)

0.29 [0.04, 2.27]

2 Ornithine α‐ketoglutarate vs control Show forest plot

3

155

Risk Ratio (M‐H, Fixed, 95% CI)

0.93 [0.37, 2.36]

2.1 Enteral

3

155

Risk Ratio (M‐H, Fixed, 95% CI)

0.93 [0.37, 2.36]

3 Branched‐chain amino acids vs control Show forest plot

1

Risk Ratio (M‐H, Fixed, 95% CI)

Totals not selected

3.1 Parenteral

1

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

4 Fish oil vs control Show forest plot

1

Risk Ratio (M‐H, Fixed, 95% CI)

Totals not selected

4.1 Enteral

1

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

5 Combined immunonutrients vs control Show forest plot

4

163

Risk Ratio (M‐H, Fixed, 95% CI)

1.10 [0.47, 2.60]

5.1 Enteral

4

163

Risk Ratio (M‐H, Fixed, 95% CI)

1.10 [0.47, 2.60]

Figuras y tablas -
Comparison 1. All‐cause mortality
Comparison 2. Length of hospital stay

Outcome or subgroup title

No. of studies

No. of participants

Statistical method

Effect size

1 Glutamine vs control Show forest plot

7

255

Mean Difference (IV, Fixed, 95% CI)

‐5.65 [‐8.09, ‐3.22]

1.1 Enteral

5

199

Mean Difference (IV, Fixed, 95% CI)

‐6.29 [‐9.12, ‐3.46]

1.2 Parenteral

2

56

Mean Difference (IV, Fixed, 95% CI)

‐3.84 [‐8.63, 0.95]

2 Ornithine α‐ketoglutarate vs control Show forest plot

1

Mean Difference (IV, Fixed, 95% CI)

Totals not selected

2.1 Enteral

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

3 Branched‐chain amino acids Show forest plot

1

Mean Difference (IV, Fixed, 95% CI)

Totals not selected

3.1 Parenteral

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

4 Fish oil vs control Show forest plot

1

Mean Difference (IV, Fixed, 95% CI)

Totals not selected

4.1 Enteral

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

5 Combined immunonutrients vs control Show forest plot

3

113

Mean Difference (IV, Fixed, 95% CI)

1.93 [‐4.41, 8.28]

5.1 Enteral

3

113

Mean Difference (IV, Fixed, 95% CI)

1.93 [‐4.41, 8.28]

Figuras y tablas -
Comparison 2. Length of hospital stay
Comparison 3. Rate of burn wound infection

Outcome or subgroup title

No. of studies

No. of participants

Statistical method

Effect size

1 Glutamine vs control Show forest plot

2

81

Risk Ratio (M‐H, Fixed, 95% CI)

0.42 [0.16, 1.06]

1.1 Enteral

2

81

Risk Ratio (M‐H, Fixed, 95% CI)

0.42 [0.16, 1.06]

2 Ornithine α‐ketoglutarate vs control Show forest plot

1

Risk Ratio (M‐H, Fixed, 95% CI)

Totals not selected

2.1 Enteral

1

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

3 Combined immunonutrients vs control Show forest plot

3

122

Risk Ratio (M‐H, Fixed, 95% CI)

0.79 [0.51, 1.20]

3.1 Enteral

3

122

Risk Ratio (M‐H, Fixed, 95% CI)

0.79 [0.51, 1.20]

Figuras y tablas -
Comparison 3. Rate of burn wound infection
Comparison 4. Rate of non‐wound infection

Outcome or subgroup title

No. of studies

No. of participants

Statistical method

Effect size

1 Glutamine vs control Show forest plot

2

67

Odds Ratio (M‐H, Fixed, 95% CI)

0.73 [0.27, 1.95]

1.1 Bacteraemia

2

67

Odds Ratio (M‐H, Fixed, 95% CI)

0.73 [0.27, 1.95]

2 Fish oil vs control Show forest plot

1

Risk Ratio (M‐H, Fixed, 95% CI)

Totals not selected

2.1 Pneumonia

1

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

3 Combined immunonutrients vs control Show forest plot

3

266

Risk Ratio (M‐H, Fixed, 95% CI)

1.16 [0.86, 1.57]

3.1 Pneumonia

3

122

Risk Ratio (M‐H, Fixed, 95% CI)

0.83 [0.59, 1.15]

3.2 Urinary tract infection

2

72

Risk Ratio (M‐H, Fixed, 95% CI)

2.46 [0.98, 6.20]

3.3 Bacteraemia

2

72

Risk Ratio (M‐H, Fixed, 95% CI)

1.77 [0.81, 3.88]

Figuras y tablas -
Comparison 4. Rate of non‐wound infection