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Table 2 Summary of findings in the eight studies focused on patient–ventilator asynchrony in ventilated patients in Part A

From: Patient–ventilator asynchrony, impact on clinical outcomes and effectiveness of interventions: a systematic review and meta-analysis

Overview of study design

Patients or study population: adult patients requiring mechanical ventilation in the ICU

Exposure: high patient–ventilator asynchrony

Comparison: low patient–ventilator asynchrony

Outcome

Illustrative comparative risksd (95% CI)

Relative effect (95% CI)

No. of participants (studies)

Certainty of the evidence (GRADE)

Comments

Assumed risk

Corresponding risk

Control

Intervention

Duration of mechanical ventilation (days)

Study population

673 (8 studies)

Lowa,b

 
 

MD: 5.16 (2.38 to 7.94)

ICU mortality

Study population

OR2.73 (1.76 to 4.24)

576 (6 studies)

Lowa,b

 

267 per 1000

498 per 1000 (390 to 607)

Hospital mortality

Study population

OR1.94 (1.14 to 3.30)

420 (6 studies)

Lowa,b

 

348 per 1000

509 per 1000 (378 to 638)

Incidence of reintubation

Study population

OR2.21 (0.72 to 8.83)

363 (4 studies)

Lowa,c

 

110 per 1000

214 per 1000 (82 to 457)

Incidence of tracheostomy

Study population

OR2.13 (0.96 to 4.71)

425 (5 studies)

Lowa,c

 

133 per 1000

246 per 1000 (128 to 420)

  1. GRADE Working Group grades of evidence
  2. High certainty: we are very confident that the true effect lies close to the estimate of the effect
  3. Moderate certainty: 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
  4. Low certainty: our confidence in the effect estimate is limited; the true effect may be substantially different from the estimate of the effect
  5. Very low certainty: we have very little confidence in the effect estimate; the true effect is likely to be substantially different from the estimate of effect
  6. CI, confidence interval; ICU, intensive care unit; MD, mean difference; OR, odds ratio
  7. aDowngraded one point because of a high risk of bias associated with statistical analysis and reporting
  8. bDowngraded one point because of imprecise (optimal information size)
  9. cDowngraded one point because of imprecise (confidence interval)
  10. dThe corresponding risk (and its 95% CI) is based on the assumed risk in the comparison group and the relative effect (and its 95% CI) estimated for the intervention group. Assumed risk was estimated from the meta-analysis of control risks