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Table 3 Rating of quality of evidence with GRADE system

From: Comparison of vaginal hysterectomy and laparoscopic hysterectomy: a systematic review and meta-analysis

Certainty assessment

Number of patients

Effect

Certainty

Importance

Number of studies

Study design

Risk of bias

Inconsistency

Indirectness

Imprecision

Other considerations

LH

VH

Relative (95% CI)

Absolute (95% CI)

Overall complications

17

randomised trials

serious†

not serious

not serious

not serious

none

169/887 (19.1%)

212/1055 (20.1%)

RR 1.11 (0.85 to 1.45)

22 more per 1000 (from 30 fewer to 90 more)

MODERATE

none

Grade I complications

17

randomised trials

serious†

not serious

not serious

not serious

none

128/887 (14.4%)

144/1055 (13.6%)

RR 1.20 (0.90 to 1.61)

27 more per 1000 (from 14 fewer to 83 more)

MODERATE

none

Grade II complications

17

randomised trials

serious†

not serious

not serious

not serious

none

29/887 (3.3%)

55/1055 (5.2%)

RR 0.78 (0.49 to 1.24)

11 fewer per 1000 (from 13 more to 27 fewer)

MODERATE

none

Grade III complications

17

randomised trials

serious†

not serious

not serious

not serious

none

12/887 (1.4%)

14/1055 (1.3%)

RR 1.03 (0.49 to 2.16)

0 fewer per 1000 (from 7 fewer to 15 more)

MODERATE

none

Urinary tract injuries

17

randomised trials

serious†

not serious

not serious

not serious

none

9/781 (1.2%)

10/1020 (1.0%)

RR 1.20 (0.50 to 2.85)

2 more per 1000 (from 5 fewer to 18 more)

MODERATE

none

Operating time

18

randomised trials

serious†

not serious

not serious

not serious

none

922

1089

MD 34.01 h lower (45.54 lower to 24.48 lower)

MODERATE

none

Length of hospital stay

14

randomised trials

serious‡

serious§c

not serious

not serious

none

636

809

MD 6.57 h lower (18.65 lower to 5.5 higher)

LOW

none

Blood loss

16

randomised trials

serious†

serious§

not serious

not serious

none

595

598

MD 35.91 mL lower (102.26 lower to 30.43 higher)

LOW

none

Intraoperative conversion

7

randomised trials

serious†

not serious

not serious

not serious

none

15/771 (1.9%)

24/939 (2.6%)

RR 0.94 (0.49 to 1.81)

2 fewer per 1000 (from 13 fewer to 21 more)

MODERATE

none

Recuperation

4

randomised trials

serious‡

serious§

not serious

not serious

none

130

130

MD 0.66 days higher (0.77 lower to 0.9 higher)

LOW

none

Pain on day of surgery (assessed with: Visual analogue scale)

5

randomised trials

serious†

not serious

not serious

not serious

none

325

491

MD 0.8 higher (0.08 lower to 1.68 higher)

MODERATE

none

Pain at 24 h after surgery (assessed with: Visual analogue scale)

4

randomised trials

serious†

not serious

not serious

not serious

none

155

157

MD 0.53 lower (0.7 lower to 0.35 lower)

MODERATE

none

Pain at 48 h after surgery (assessed with: Visual analogue scale)

4

randomised trials

serious†

not serious

not serious

not serious

none

295

461

MD 0.2 lower (0.61 lower to 0.22 higher)

MODERATE

none

  1. CI Confidence interval, RR risk ratio, and MD mean difference
  2. † High risk of allocation and blinding
  3. ‡ High risk of blinding and incomplete outcome data
  4. § High heterogeneity