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Table 2 Quality assessment of included randomized controlled trials

From: Optimal dosing of antibiotics in critically ill patients by using continuous/extended infusions: a systematic review and meta-analysis

Author (year) Country

Number of centres

Number of patients

Blinding

concealed allocation

Intention-to-treat analysis

Stopped early for benefit

Post randomization Withdrawal

Georges (1999) France [12]

1

18

N

NR

NR

N

NR

Hanes (2000) USA [13]

1

32

N

NR

NR

N

Y (1 from each group)

Nicolau (2001) USA [14]

1

41

N

NR

NR

N

Y (5 from CI group and 1 from control group)

Wysocki (2001) France [15]

10

160

N

Y (consecutive sealed opaque envelopes)

Y

N

Y (15 from CI and 26 from control group)

Bujik (2002) Netherlands [16]a

1

18

N

NR

NR

N

NR

Georges (2005) France [17]

1

50

N

NR

NR

N

NR

Rafati (2006) Iran [18]

1

40

N

NR

NR

N

NR

Roberts (2007) Australia [19]

1

57

N

Y (sequential opaque sealed envelopes)

Y

N

N

Sakka (2007) Germany [20]

1

20

N

Y (sealed envelopes)

NR

N

NR

Adembri (2008) Italy [21]

1

16

N

Y (closed envelopes)

NR

N

Y (1 died, 1 developed ARF; group(s) not specified)

Wang (2009) China [32]

1

30

N

NR

NR

N

NR

Chyta (2012) Czech [22]

1

240

N

Y (sealed opaque envelopes)

Y

N

N for mortality and LoS, but Y (14 in CI and, 12 in control group) for cure data

Dulhunty (2012) Australia [29]

5

60

Y

Y (sequentially numbered sealed envelopes)

Y

N

N

  1. Y, Yes; N, No; NR, not reported; CI, continuous infusion; LoS, length of stay; ARF, acute renal failure.
  2. aPartial randomization: first six patients allocated to continuous-infusion group; next 12 patients randomized to continuous infusion or intermittent administration groups.