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. 2014 Aug 15;2014(8):CD005355. doi: 10.1002/14651858.CD005355.pub5

Summary of findings 5. Peri‐cervical tourniquet compared to no treatment to reduce blood loss during myomectomy for fibroids.

Peri‐cervical tourniquet compared to no treatment to reduce blood loss during myomectomy for fibroids
Patient or population: Women with fibroids
 Settings: Low and high income countries
 Intervention: Tourniquet around the cervix only, or around both the cervix and the infundibulopelvic ligament 
 Comparison: No treatment
Outcomes Illustrative comparative risks (95% CI) Relative effect
 (95% CI) No of participants
 (studies) Quality of the evidence
 (GRADE) Comments
No treatment Peri‐cervical tourniquet
Blood loss (ml) 
 Estimated blood loss during myomectomy The mean blood loss in the control groups was
 756.4 ml (for cervical tourniquet) &2359.0 ml (for cervical plus infundibulopelvic ligament tourniquet) The mean blood loss in the intervention groups was
 240.70 ml lower 
 (359.61 ml lower to 121.79 ml lower) for the cervical tourniquet study & 1870 ml lower (2547.16 ml lower to 1192.84 ml lower) for the cervical plus infundibulopelvic ligament tourniquet study MD ‐240.70 (‐359.61 to ‐121.79) for cervical touniquet study & ‐1870 (‐2547.16 to ‐1192.84) for the cervical plus infundibulopelvic ligament tourniquet study 121
 (2 studies) ⊕⊕⊝⊝
 low1 We rated down the quality of evidence (by 2) because the data were derived from two small studies that were not pooled together due to significant clinical and statistical heterogeneity.
One study used polyglactin suture round both the cervix and infundibulopelvic ligament, while the other used a Foley catheter round the cervix.
Need for blood transfusion 
 Participants who received blood transfusion 539 per 1000 for cervical tourniquet study &786 per 1000 for cervical plus infundibulopelvic ligament study 204 per 1000 
 for cervical tourniquet study &71 per 1000 for cervical plus infundibulopelvic ligament study OR 0.22 
 (0.09 to 0.55) or cervical tourniquet study &
OR 0.02
(0.00 to 0.23) for cervical plus infundibulopelvic ligament study
121
 (2 studies) ⊕⊕⊝⊝
 low1 We rated down the quality of evidence (by 2) because the data were derived from two small studies which were not pooled together because of significant heterogeneity.
One study used polyglactin suture round both the cervix and infundibulopelvic ligament, while the other used a Foley catheter round the cervix.
Duration of surgery (min) 
 Operative time The mean duration of surgery in the control groups was
 118 min The mean duration of surgery in the intervention groups was
 4 min lower 
 (29.28 lower to 21.28 higher) MD ‐4.00
(‐29.28 to 21.28)
28
 (1 study) ⊕⊝⊝⊝
 very low We rated down the quality of evidence (by 3) because the data were derived from one small study and the effect estimate was imprecise
CI: Confidence interval; MD: mean difference; OR: Odds ratio
GRADE Working Group grades of evidence
 High quality: Further research is very unlikely to change our confidence in the estimate of effect.
 Moderate quality: Further research is likely to have an important impact on our confidence in the estimate of effect and may change the estimate.
 Low quality: Further research is very likely to have an important impact on our confidence in the estimate of effect and is likely to change the estimate.
 Very low quality: We are very uncertain about the estimate.

1In one trial the allocation concealment was unclear and in the other trial allocation concealment was achieved by sealed sequentially‐numbered opaque envelopes containing computer‐generated random numbers.