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Table 2 Summary of finding table in included RCT studies

From: Efficacy of therapeutic drug monitoring-based antibiotic regimen in critically ill patients: a systematic review and meta-analysis of randomized controlled trials

Outcomes

Certainty assessment

No. of patients

Effect

 

No. of studies

Risk of bias

Inconsistency

Indirectness

Imprecision

TDM

Placebo

Relative (95%CI)

Absolute (95%CI)

Certainty

28-Day mortality

5

Not serious

Not serious

Not serious

Seriousa

137/510 (26.9%)

142/501 (28.3%)

RR 0.94 (0.77–1.14)

17 fewer per 1000

(from 65 fewer to 42 more

Moderate

Hospital mortality

3

Very seriousb

Not serious

Not serious

Seriousa

101/342 (29.5%)

103/339 (30.4%)

RR 0.96 (0.76 to 1.20)

12 fewer per 1000

(from 73 fewer to 61 more)

Very low

ICU length of stay

3

Not serious

Seriousc

Not serious

Seriousd

446

443

 

MD 0

(2.18 lower to 2.19 higher)

Low

Clinical cure

3

Very seriousb

Seriousc

Seriouse

Very seriousf

72/123 (58.5%)

54/127 (42.5%)

RR 1.23 (0.91 to 1.67)

98 more per 1000

(from 38 fewer to 285 more)

Very low

Target attainment in day 1

4

Very seriousb

Seriousc

Seriouse

Seriousg

250/446 (56.1%)

214/429 (49.9%)

RR 1.14 (0.88 to 1.48)

70 more per 1000

(from 60 fewer to 239 more)

Very low

Target attainment at day 3

3

Very seriousb

Seriousc

Seriouse

Very seriousf

118/221 (53.4%)

92/215 (42.8%)

RR 1.35 (0.90 to 2.03)

150 more per 1000

(from 43 fewer to 441 more)

Very low

  1. CI confidence interval, MD mean difference, RR risk ratio
  2. a95% confidence interval for risk ratio includes 1.0
  3. bHigh risk of the selection of the reported result
  4. cThe value of I2 is over 50% which should be considered as serious
  5. d95% confidence interval for MD includes 0
  6. eThe definition of the outcome varies between studies
  7. f95% confidence interval for risk ratio includes 1.0 which means no effect for outcome and 1.25 which means serious benefit, and the number of events is under the optimal information size assuming the relative risk reduction of 25%
  8. g95% confidence interval for risk ratio includes 1.0 which means no effect for outcome and 1.25 which means serious benefit