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Cochrane Database of Systematic Reviews

Cuidado cardiaco rápido para pacientes adultos sometidos a cirugía cardíaca

Información

DOI:
https://doi.org/10.1002/14651858.CD003587.pub3Copiar DOI
Base de datos:
  1. Cochrane Database of Systematic Reviews
Versión publicada:
  1. 12 septiembre 2016see what's new
Tipo:
  1. Intervention
Etapa:
  1. Review
Grupo Editorial Cochrane:
  1. Grupo Cochrane de Anestesia

Copyright:
  1. Copyright © 2016 The Cochrane Collaboration. Published by John Wiley & Sons, Ltd.

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Autores

  • Wai‐Tat Wong

    Department of Anaesthesia and Intensive Care, The Chinese University of Hong Kong, Shatin, Hong Kong

  • Veronica KW Lai

    Department of Anaesthesia and Intensive Care, The Chinese University of Hong Kong, Shatin, Hong Kong

  • Yee Eot Chee

    Department of Anaesthesiology, Queen Mary Hospital, Pokfulam, Hong Kong

  • Anna Lee

    Correspondencia a: Department of Anaesthesia and Intensive Care, The Chinese University of Hong Kong, Shatin, Hong Kong

    [email protected]

    Hong Kong Branch of The Chinese Cochrane Centre, The Jockey Club School of Public Health and Primary Care, Faculty of Medicine, The Chinese University of Hong Kong, Shatin, Hong Kong

Contributions of authors

Designing the update for the review: Wai‐Tat Wong (WTW), Veronica Ka Wai Lai (VKWL), Yee Eot Chee (YEC), Anna Lee (AL).

Co‐ordinating the review: AL.

Screening search results: WTW, AL.

Organizing retrieval of papers: VKWL, AL.

Screening retrieved papers against inclusion criteria: WTW, AL.

Appraising quality of papers: VKWL, AL.

Abstracting data from papers: VKWL, AL.

Writing to authors of papers for additional information: AL.

Managing data for the review: VKWL, AL.

Entering data into Review Manager (RevMan 5.3): VKWL.

Checking data entry in Review Manager (RevMan 5.3): WTW, AL.

Analysing RevMan statistical data: VKWL, AL.

Performing there statistical analyses not using RevMan: VKWL, AL.

Interpreting data: all review authors.

Making statistical inferences: all review authors.

Writing the review: all review authors.

Providing guidance on the review: AL.

Securing funding for the review: not applicable.

Sources of support

Internal sources

  • Department of Anaesthesia and Intensive Care, The Chinese University of Hong Kong, Hong Kong.

External sources

  • No sources of support supplied

Declarations of interest

WTW, VKWL and YEC declare no potential conflict of interests in this review. AL co‐authored a previous related systematic review (Myles 2003), along with Professor Paul Myles; two of his trials are included in this updated review (Myles 1997; Myles 2002). As AL was also co‐author of a trial included in this updated review (Zhu 2015), WTW and VKWL independently performed data extraction.

Acknowledgements

We would like to thank Rodrigo Cavallazzi (Content Editor), Nathan Pace (Statistical Editor) Janet Wale (Consumer Editor) and Jane Cracknell (Managing Editor) for help and editorial advice provided during preparation of this updated systematic review.

Thanks to Dr John Carlisle, Prof Nathan Pace, Dr Karen Hovhannisyan, Dr R Peter Alston, Prof Paul Myles, Dr Vesna Svircevic and Ms Jane Cracknell for help and editorial advice provided during the previous update (Zhu 2012). Thanks to Dr Zhirajr Mokini for translating a study (Nougarede 2004) from French to English.

We would like to acknowledge the work done in the original Cochrane review by Claire Hawkes, Srinivasan Dhileepan and David Foxcroft (Hawkes 2003), and in the previous update by Fang Zhu (Zhu 2012).

Version history

Published

Title

Stage

Authors

Version

2016 Sep 12

Fast‐track cardiac care for adult cardiac surgical patients

Review

Wai‐Tat Wong, Veronica KW Lai, Yee Eot Chee, Anna Lee

https://doi.org/10.1002/14651858.CD003587.pub3

2012 Oct 17

Fast‐track cardiac care for adult cardiac surgical patients

Review

Fang Zhu, Anna Lee, Yee Eot Chee

https://doi.org/10.1002/14651858.CD003587.pub2

2003 Oct 20

Early extubation for adult cardiac surgical patients

Review

Claire A Hawkes, Srinivasan Dhileepan, David R Foxcroft

https://doi.org/10.1002/14651858.CD003587

Differences between protocol and review

Inclusion criteria and mortality time points in this updated systematic review are different from those in the original review by Hawkes et al (Hawkes 2003). This update and our previous updated review (Zhu 2012) includes more types of postoperative adverse outcomes, health‐related quality of life and healthcare costs. These patient‐centred outcomes are important for clinical decision making.

Notes

None.

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.

Forest plot of comparison: 2 Time‐directed extubation protocols, outcome: 2.4 Subgroup analysis.
Figuras y tablas -
Figure 4

Forest plot of comparison: 2 Time‐directed extubation protocols, outcome: 2.4 Subgroup analysis.

Comparison 1 Dose of opioid‐based cardiac anaesthesia, Outcome 1 Mortality.
Figuras y tablas -
Analysis 1.1

Comparison 1 Dose of opioid‐based cardiac anaesthesia, Outcome 1 Mortality.

Comparison 1 Dose of opioid‐based cardiac anaesthesia, Outcome 2 Postoperative complications.
Figuras y tablas -
Analysis 1.2

Comparison 1 Dose of opioid‐based cardiac anaesthesia, Outcome 2 Postoperative complications.

Comparison 1 Dose of opioid‐based cardiac anaesthesia, Outcome 3 Service outcomes.
Figuras y tablas -
Analysis 1.3

Comparison 1 Dose of opioid‐based cardiac anaesthesia, Outcome 3 Service outcomes.

Comparison 2 Time‐directed extubation protocol, Outcome 1 Mortality.
Figuras y tablas -
Analysis 2.1

Comparison 2 Time‐directed extubation protocol, Outcome 1 Mortality.

Comparison 2 Time‐directed extubation protocol, Outcome 2 Postoperative complications.
Figuras y tablas -
Analysis 2.2

Comparison 2 Time‐directed extubation protocol, Outcome 2 Postoperative complications.

Comparison 2 Time‐directed extubation protocol, Outcome 3 Service outcomes.
Figuras y tablas -
Analysis 2.3

Comparison 2 Time‐directed extubation protocol, Outcome 3 Service outcomes.

Comparison 2 Time‐directed extubation protocol, Outcome 4 Subgroup analysis.
Figuras y tablas -
Analysis 2.4

Comparison 2 Time‐directed extubation protocol, Outcome 4 Subgroup analysis.

Summary of findings for the main comparison. Low‐dose opioid‐based GA vs high‐dose opioid‐based GA

Low‐dose opioid‐based general anaesthesia compared with high‐dose opioid‐based general anaesthesia for adults undergoing cardiac surgery

Patient or population: adult cardiac surgical patients
Setting: people undergoing various cardiac surgical procedures in hospitals in Europe, North America, Asia, Australasia and Middle East

Intervention: low‐dose opioid‐based general anaesthesia
Comparison: high‐dose opioid‐based general anaesthesia

Outcomes

Anticipated absolute effects* (95% CI)

Relative effect
(95% CI)

Number of participants
(studies)

Quality of the evidence
(GRADE)

Comments

Risk with high‐dose opioid‐based general anaesthesia

Risk with low‐dose opioid‐based general anaesthesia

Mortality ‐ Death at any time after surgery

Low

OR 0.53
(0.25 to 1.12)

1994
(8 RCTs)

⊕⊕⊝⊝
LOWa,b

No death recorded in 3 trials

10 per 1000

5 per 1000
(3 to 11)

Moderate

30 per 1000

16 per 1000
(8 to 33)

High

110 per 1000

61 per 1000
(30 to 122)

Postoperative myocardial infarction

Study population

RR 0.98
(0.48 to 1.99)

1683
(8 RCTs)

⊕⊕⊝⊝
LOWa,b

No postoperative myocardial infarction recorded in 2 trials

30 per 1000

30 per 1000
(15 to 60)

Postoperative stroke

Study population

RR 1.17
(0.36 to 3.78)

562
(5 RCTs)

⊕⊕⊝⊝
LOWb,c

No stroke recorded in 1 trial

18 per 1000

21 per 1000
(6 to 67)

Postoperative tracheal reintubation

Study population

RR 1.77
(0.38 to 8.27)

594
(5 RCTs)

⊕⊕⊝⊝
LOWb,d

No reintubation recorded in 3 trials

7 per 1000

12 per 1000
(3 to 55)

Time to extubation (hours)

Mean time to extubation (hours) was 5.2 to 35.1

Mean time to extubation (hours) in the intervention group was 7.4 lower (10.51 lower to 4.29 lower).

2486
(14 RCTs)

⊕⊕⊝⊝
LOWe,f

Length of intensive care unit stay (hours)

Mean length of intensive care unit stay (hours) was 2.6 to 112.8.

Mean length of intensive care unit stay (hours) in the intervention group was 3.7 lower (6.98 lower to 0.41 lower).

1394
(12 RCTs)

⊕⊕⊝⊝
LOWf,g

Length of hospital stay (days)

Mean length of hospital stay (days) was 5.1 to 27.0.

Mean length of hospital stay (days) in the intervention group was 0.3 lower (1.04 lower to 0.43 higher).

913
(8 RCTs)

⊕⊕⊝⊝
LOWf,h

*The risk in the intervention group (and its 95% confidence interval) is based on the assumed risk in the comparison group using the EuroSCORE risk classification (Michel 2003) and the relative effect of the intervention (and its 95% CI).

CI: confidence interval; RR: risk ratio; OR: odds ratio.

GRADE Working Group grades of evidence
High quality: We are very confident that the true effect lies close to that of the estimate of effect.
Moderate quality: We are moderately confident in the effect estimate: The true effect is likely to be close to the estimate of effect but may be substantially different.
Low quality: Our confidence in the effect estimate is limited: The true effect may be substantially different from the estimate of 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.

aOf the 8 trials, 2 had ≥ 1 high risk of bias domain (downgrade 1 point owing to study limitations).

bOptimal information size not met (downgrade 1 point owing to imprecision).

cOf the 5 trials, 1 had ≥ 1 high risk of bias domain (downgrade 1 point owing to study limitations).

dOf the 5 trials, 2 had ≥ 1 high risk of bias domain (downgrade 1 point owing to study limitations).

eOf the 14 trials, 4 had ≥ 1 high risk of bias domain (downgrade 1 point owing to study limitations).

fUnexplained reasons for high heterogeneity.

gOf the 12 trials, 3 had ≥ 1 high risk of bias domain (downgrade 1 point owing to study limitations).

hOf the 8 trials, 3 had ≥ 1 high risk of bias domain (downgrade 1 point owing to study limitations).

Figuras y tablas -
Summary of findings for the main comparison. Low‐dose opioid‐based GA vs high‐dose opioid‐based GA
Summary of findings 2. Time‐directed extubation protocol vs usual care

Time‐directed extubation protocol compared with usual care for adults undergoing cardiac surgery

Patient or population: adult cardiac surgical patients
Setting: people undergoing various cardiac surgical procedures in hospitals in Europe, North America, Asia and Middle East
Intervention: time‐directed extubation protocol
Comparison: usual care

Outcomes

Anticipated absolute effects* (95% CI)

Relative effect
(95% CI)

Number of participants
(studies)

Quality of the evidence
(GRADE)

Comments

Risk with usual care

Risk with time‐directed extubation protocol

Mortality ‐ Death at any time after surgery

Low

OR 0.80
(0.45 to 1.45)

1802
(10 RCTs)

⊕⊕⊝⊝
LOWa,b

No deaths recorded in 4 trials. Low to moderate heterogeneity (I2 = 37%) may be explained by the inclusion of a trial (Reyes 1997) that had the highest rate of mortality of all trials considered. When excluded, the OR changed to 0.31 (95% CI 0.11 to 0.90, P = 0.03, I2 = 0%).

10 per 1000

8 per 1000
(5 to 14)

Moderate

30 per 1000

24 per 1000
(14 to 43)

High

110 per 1000

90 per 1000
(53 to 152)

Postoperative myocardial infarction

Study population

RR 0.59
(0.27 to 1.31)

1378
(8 RCTs)

⊕⊕⊝⊝
LOWb,c

No postoperative myocardial infarction was recorded in 1 trial.

61 per 1000

36 per 1000
(16 to 80)

Postoperative stroke

Study population

RR 0.85
(0.33 to 2.16)

1646
(11 RCTs)

⊕⊕⊝⊝
LOWb,d

No stroke was recorded in 2 trials.

12 per 1000

10 per 1000
(4 to 26)

Postoperative reintubation

Study population

RR 1.34
(0.74 to 2.41)

1261
(12 RCTs)

⊕⊕⊝⊝
LOWb,e

No reintubation was recorded in 3 trials.

28 per 1000

38 per 1000
(21 to 68)

Time to extubation (hours)

Mean time to extubation (hours) was 3.4 to 18.9.

Mean time to extubation (hours) in the intervention group was 6.25 lower (8.84 lower to 3.67 lower).

2024
(16 RCTs)

⊕⊕⊝⊝
LOWf,g

No variation in time to extubation in the early extubation group in 1 trial

Length of intensive care unit stay (hours)

Mean length of intensive care unit stay (hours) was 17.9 to 95.0.

Mean length of intensive care unit stay (hours) in the intervention group was 7.16 lower (10.45 lower to 3.88 lower).

1888
(13 RCTs)

⊕⊕⊝⊝
LOWf,h

No variation in length of ICU stay in early extubation group in 1 trial

Length of hospital stay (days)

Mean length of hospital stay (days) was 5.1 to 13.0.

Mean length of hospital stay (days) in the intervention group was 0.44 lower (1.04 lower to 0.16 higher).

1334
(8 RCTs)

⊕⊕⊝⊝
LOWf,i

*The risk in the intervention group (and its 95% confidence interval) is based on the assumed risk in the comparison group using the EuroSCORE risk classification (Michel 2003) and the relative effect of the intervention (and its 95% CI).

CI: confidence interval; RR: risk ratio; OR: odds ratio.

GRADE Working Group grades of evidence
High quality: We are very confident that the true effect lies close to that of the estimate of 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 may be substantially different.
Low quality: Our confidence in the effect estimate is limited: The true effect may be substantially different from the estimate of 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.

aOf the 10 trials, 3 had 1 high risk of bias domain (downgrade 1 point owing to study limitations).

bOptimal information size not met (downgrade 1 point owing to imprecision).

cOf the 8 trials, 3 had 1 high risk of bias domain (downgrade 1 point owing to study limitations).

dOf the 11 trials, 5 had 1 high risk of bias domain (downgrade 1 point owing to study limitations).

dOf the 12 trials, 5 had 1 high risk of bias domain (downgrade 1 point owing to study limitations).

fUnexplained reasons for high heterogeneity.

gOf the 16 trials, 6 had 1 high risk of bias domain (downgrade 1 point owing to study limitations).

hOf the 13 trials, 5 had 1 high risk of bias domain (downgrade 1 point owing to study limitations).

iOf the 8 trials, 2 had 1 high risk of bias domain (downgrade 1 point owing to study limitations).

Figuras y tablas -
Summary of findings 2. Time‐directed extubation protocol vs usual care
Comparison 1. Dose of opioid‐based cardiac anaesthesia

Outcome or subgroup title

No. of studies

No. of participants

Statistical method

Effect size

1 Mortality Show forest plot

8

Peto Odds Ratio (Peto, Fixed, 95% CI)

Subtotals only

1.1 Death in hospital after surgery

7

1896

Peto Odds Ratio (Peto, Fixed, 95% CI)

0.58 [0.24, 1.39]

1.2 Death at 1 year after surgery

2

446

Peto Odds Ratio (Peto, Fixed, 95% CI)

0.55 [0.17, 1.82]

1.3 Death at any time after surgery

8

1994

Peto Odds Ratio (Peto, Fixed, 95% CI)

0.53 [0.25, 1.12]

2 Postoperative complications Show forest plot

10

Risk Ratio (IV, Random, 95% CI)

Subtotals only

2.1 Postoperative myocardial infarction

8

1683

Risk Ratio (IV, Random, 95% CI)

0.98 [0.48, 1.99]

2.2 Stroke

5

562

Risk Ratio (IV, Random, 95% CI)

1.17 [0.36, 3.78]

2.3 Acute renal failure

4

492

Risk Ratio (IV, Random, 95% CI)

1.19 [0.33, 4.33]

2.4 Major bleeding

4

469

Risk Ratio (IV, Random, 95% CI)

0.48 [0.16, 1.44]

2.5 Reintubation

5

594

Risk Ratio (IV, Random, 95% CI)

1.77 [0.38, 8.27]

3 Service outcomes Show forest plot

14

Mean Difference (IV, Random, 95% CI)

Subtotals only

3.1 Time to extubation (hours)

14

2486

Mean Difference (IV, Random, 95% CI)

‐7.40 [‐10.51, ‐4.29]

3.2 Length of intensive care unit stay (hours)

12

1394

Mean Difference (IV, Random, 95% CI)

‐3.70 [‐6.98, ‐0.41]

3.3 Length of hospital stay (days)

8

913

Mean Difference (IV, Random, 95% CI)

‐0.30 [‐1.04, 0.43]

Figuras y tablas -
Comparison 1. Dose of opioid‐based cardiac anaesthesia
Comparison 2. Time‐directed extubation protocol

Outcome or subgroup title

No. of studies

No. of participants

Statistical method

Effect size

1 Mortality Show forest plot

10

Peto Odds Ratio (Peto, Fixed, 95% CI)

Subtotals only

1.1 Death in the intensive care unit

2

370

Peto Odds Ratio (Peto, Fixed, 95% CI)

0.87 [0.19, 3.88]

1.2 Death in hospital after surgery

5

582

Peto Odds Ratio (Peto, Fixed, 95% CI)

0.23 [0.05, 1.04]

1.3 Death at 1 month after surgery

4

1122

Peto Odds Ratio (Peto, Fixed, 95% CI)

1.13 [0.59, 2.19]

1.4 Death at any time after surgery

10

1802

Peto Odds Ratio (Peto, Fixed, 95% CI)

0.80 [0.45, 1.45]

2 Postoperative complications Show forest plot

15

Risk Ratio (IV, Random, 95% CI)

Subtotals only

2.1 Postoperative myocardial infarction

8

1378

Risk Ratio (IV, Random, 95% CI)

0.59 [0.27, 1.31]

2.2 Stroke

11

1646

Risk Ratio (IV, Random, 95% CI)

0.85 [0.33, 2.16]

2.3 Acute renal failure

9

1541

Risk Ratio (IV, Random, 95% CI)

1.11 [0.42, 2.91]

2.4 Major bleeding

10

1244

Risk Ratio (IV, Random, 95% CI)

0.92 [0.53, 1.61]

2.5 Major sepsis

3

477

Risk Ratio (IV, Random, 95% CI)

2.40 [0.31, 18.25]

2.6 Wound infection

2

868

Risk Ratio (IV, Random, 95% CI)

0.67 [0.25, 1.83]

2.7 Reintubation

12

1261

Risk Ratio (IV, Random, 95% CI)

1.34 [0.74, 2.41]

3 Service outcomes Show forest plot

16

Mean Difference (IV, Random, 95% CI)

Subtotals only

3.1 Time to extubation (hours)

16

2024

Mean Difference (IV, Random, 95% CI)

‐6.25 [‐8.84, ‐3.67]

3.2 Length of intensive care unit stay (hours)

13

1888

Mean Difference (IV, Random, 95% CI)

‐7.16 [‐10.45, ‐3.88]

3.3 Length of hospital stay (days)

8

1334

Mean Difference (IV, Random, 95% CI)

‐0.44 [‐1.04, 0.16]

4 Subgroup analysis Show forest plot

11

Risk Ratio (IV, Random, 95% CI)

Subtotals only

4.1 Reintubation after extubation in ICU

8

934

Risk Ratio (IV, Random, 95% CI)

1.99 [0.93, 4.23]

4.2 Reintubation after extubation outside ICU

3

127

Risk Ratio (IV, Random, 95% CI)

3.82 [0.44, 33.24]

Figuras y tablas -
Comparison 2. Time‐directed extubation protocol