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Cochrane Database of Systematic Reviews

Tratamiento quirúrgico para la enfermedad tubárica en mujeres a las que se les realizará fecundación in vitro

Information

DOI:
https://doi.org/10.1002/14651858.CD002125.pub4Copy DOI
Database:
  1. Cochrane Database of Systematic Reviews
Version published:
  1. 22 October 2020see what's new
Type:
  1. Intervention
Stage:
  1. Review
Cochrane Editorial Group:
  1. Cochrane Gynaecology and Fertility Group

Copyright:
  1. Copyright © 2020 The Cochrane Collaboration. Published by John Wiley & Sons, Ltd.

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Authors

  • Pedro Melo

    Correspondence to: Buckinghamshire Hospitals NHS Trust, Aylesbury, UK

    [email protected]

    [email protected]

  • Ektoras X Georgiou

    Buckinghamshire Hospitals NHS Trust, Aylesbury, UK

  • Neil Johnson

    Discipline of Obstetrics and Gynaecology, School of Medicine, Robinson Research Institute, The University of Adelaide, Adelaide, Australia

  • Sabine F. van Voorst

    Faculty of Medicine, University of Maastricht, Maastricht, Netherlands

  • Annika Strandell

    Obstetrics and Gynecology, University of Gothenburg, Gothenburg, Sweden

  • Ben Willem J Mol

    Department of Obstetrics and Gynaecology, Monash University, Clayton, Australia

  • Christian Becker

    Nuffield Department of Women's & Reproductive Health, University of Oxford, Oxford, UK

  • Ingrid E Granne

    Nuffield Department of Women's & Reproductive Health, University of Oxford, Oxford, UK

Contributions of authors

PM was the lead author in writing the full review update and was involved in preparing all sections of the review. EXG was involved in data extraction for the review. CB and IEG made substantial editorial amendments to the review.

NJ conceptualised the protocol and the review primarily, and carried out the search, selection of trials and risk of bias assessment as a first reviewer and first author in the first version of the review and as a second reviewer in the previous update.

SVV updated the review in 2010 as a first reviewer performing the search, selection of trials and risk of bias assessment. She proofread the current review.

Ben Willem Mol and Annika Strandell proofread the updated review.

Sources of support

Internal sources

  • University of Auckland, School of Medicine, Auckland, New Zealand

External sources

  • None, Other

Declarations of interest

PM has no interests to declare.

EXG has no interests to declare.

NJ works as a gynaecologist at Auckland Gynaecology Group and Fertility Specialist at Repromed Auckland. Within the last 3 years NJ has had consultancy with Guerbet, Myovant Sciences, Vifor Pharma and Roche Diagnostics and has received research funding from Guerbet, AbbVie and Myovant Sciences.

SVV ‐ at the time of the update in 2010 ‐ was a medical student of the faculty of Health, Medicine and Life Sciences of the University of Maastricht. She is now a resident in Obstetrics and Gynaecology at the Erasmus Medical Center, Rotterdam, the Netherlands. She has no financial conflicts of interest.

AS led one of the trials included in this review (Strandell 1999). She is a gynaecologist at Sahlgrenska Hospital, associate professor at the University of Gothenburg and employed at the regional centre for Health Technology Assessment in Göteborg, Sweden. She has received fees from Guerbet for an expert consultancy.

BWJM is an author on one of the trials included in this review (Dreyer 2016) and confirms he took no part in selecting this study, extracting data or assessing risk of bias. In addition, BWJM is supported by a NHMRC Investigator grant (GNT1176437) and reports consultancy for ObsEva, Merk KGaA, iGenomix and Guerbet.

CMB has received research support by Bayer, Volition Rx, Roche Diagnostics and MDNA Life Sciences. He has also received consultancy fees from ObsEva, AbbVie and Myovant.

IEG's institution has received research support from Finox and Bayer.

Acknowledgements

We would like to thank Helen Nagels, CGF Managing Editor, for her support and guidance in the preparation of this review; Marian Showell, Cochrane Information Specialist, for her help in preparing and conducting the search strategies; and Ms Xiaojing Wu for assessing two Chinese manuscripts and extracting relevant data. We also thank Martin Sowter for his significant contributions to previous versions of this systematic review, and the peer reviewers (Dr Vivienne Moore, Dr Vanessa Jordan and Dr Mohan Kamath) whose helpful comments made this a better piece of work.

Finally, we wish to thank the trial authors who contributed to this review by supplying additional details of their research in all the versions of this review, particularly Evangelos Makrakis, Herve Déchaud, Nahed Hammadieh, Vaeceslav Moshin, Kareem Labib and Kim Dreyer.

Version history

Published

Title

Stage

Authors

Version

2020 Oct 22

Surgical treatment for tubal disease in women due to undergo in vitro fertilisation

Review

Pedro Melo, Ektoras X Georgiou, Neil Johnson, Sabine F. Voorst, Annika Strandell, Ben Willem J Mol, Christian Becker, Ingrid E Granne

https://doi.org/10.1002/14651858.CD002125.pub4

2010 Jan 20

Surgical treatment for tubal disease in women due to undergo in vitro fertilisation

Review

Neil Johnson, Sabine van Voorst, Martin C Sowter, Annika Strandell, Ben Willem J Mol

https://doi.org/10.1002/14651858.CD002125.pub3

2004 Jul 19

Surgical treatment for tubal disease in women due to undergo in vitro fertilisation

Review

Neil Johnson, Sabine van Voorst, Martin C Sowter, Annika Strandell, Ben Willem J Mol

https://doi.org/10.1002/14651858.CD002125.pub2

2001 Jul 23

Surgical treatment for tubal disease in women due to undergo in vitro fertilisation

Review

Neil NP Johnson, W Mak, M C Sowter

https://doi.org/10.1002/14651858.CD002125

Differences between protocol and review

In the current version of the review, ongoing pregnancy rate and viable pregnancy rate were combined with clinical pregnancy rate, as ongoing pregnancy is currently not a recognised outcome by The International Glossary on Infertility and Fertility Care 2017 (Zegers‐Hochschild 2017). We no longer report on biochemical pregnancy rates, contrary to the previous version of this review, because clinical pregnancy and live birth rates are more clinically relevant outcomes.

We added the following outcomes to the meta‐analysis:

  • Mean number of oocytes, to investigate concerns of tubal surgery affecting the ovarian blood supply;

  • Mean number of embryos, to investigate whether tubal surgery had an impact upon fertilisation.

We added a subgroup analysis for women younger or older than 40 years to account for the effect of age on expected ovarian response, although this was not possible due to a lack of data.

We carried out analyses of dichotomous outcomes using RR, instead of OR, in this review, in line with Cochrane guidance recommending RR as it is a more easily interpretable measure of relative effect (Higgins 2011).

We have also updated the list of outcomes according to the most recent edition of the Cochrane Handbook of Systematic Reviews of Interventions. Additionally, we have used GradePRO to grade the evidence and produce a Summary of Findings Table for the main comparison of tubal surgery versus no tubal surgery.

Keywords

MeSH

PICOs

Population
Intervention
Comparison
Outcome

The PICO model is widely used and taught in evidence-based health care as a strategy for formulating questions and search strategies and for characterizing clinical studies or meta-analyses. PICO stands for four different potential components of a clinical question: Patient, Population or Problem; Intervention; Comparison; Outcome.

See more on using PICO in the Cochrane Handbook.

Study flow diagram.

Figures and Tables -
Figure 1

Study flow diagram.

Methodological quality graph: review authors' judgements about each methodological quality item presented as percentages across all included studies.

Figures and Tables -
Figure 2

Methodological quality graph: review authors' judgements about each methodological quality item presented as percentages across all included studies.

Methodological quality summary: review authors' judgements about each methodological quality item for each included study.

Figures and Tables -
Figure 3

Methodological quality summary: review authors' judgements about each methodological quality item for each included study.

Forest plot of comparison: Tubal surgery (all methods) versus no tubal surgery, outcome: 8.1 Clinical pregnancy rate.

Figures and Tables -
Figure 4

Forest plot of comparison: Tubal surgery (all methods) versus no tubal surgery, outcome: 8.1 Clinical pregnancy rate.

Forest plot of comparison: 2 Proximal tubal occlusion (all methods) vs laparoscopic salpingectomy, outcome: 2.1 Live birth rate.

Figures and Tables -
Figure 5

Forest plot of comparison: 2 Proximal tubal occlusion (all methods) vs laparoscopic salpingectomy, outcome: 2.1 Live birth rate.

Forest plot of comparison: 2 Proximal tubal occlusion (all methods) vs laparoscopic salpingectomy, outcome: 2.4 Clinical pregnancy rate.

Figures and Tables -
Figure 6

Forest plot of comparison: 2 Proximal tubal occlusion (all methods) vs laparoscopic salpingectomy, outcome: 2.4 Clinical pregnancy rate.

Comparison 1: Tubal surgery (all methods) vs no tubal surgery, Outcome 1: Surgical complication rate ‐ conversion to laparotomy

Figures and Tables -
Analysis 1.1

Comparison 1: Tubal surgery (all methods) vs no tubal surgery, Outcome 1: Surgical complication rate ‐ conversion to laparotomy

Comparison 1: Tubal surgery (all methods) vs no tubal surgery, Outcome 2: Surgical complication rate ‐ pelvic infection

Figures and Tables -
Analysis 1.2

Comparison 1: Tubal surgery (all methods) vs no tubal surgery, Outcome 2: Surgical complication rate ‐ pelvic infection

Comparison 1: Tubal surgery (all methods) vs no tubal surgery, Outcome 3: Clinical pregnancy rate

Figures and Tables -
Analysis 1.3

Comparison 1: Tubal surgery (all methods) vs no tubal surgery, Outcome 3: Clinical pregnancy rate

Comparison 1: Tubal surgery (all methods) vs no tubal surgery, Outcome 4: Multiple pregnancy rate

Figures and Tables -
Analysis 1.4

Comparison 1: Tubal surgery (all methods) vs no tubal surgery, Outcome 4: Multiple pregnancy rate

Comparison 1: Tubal surgery (all methods) vs no tubal surgery, Outcome 5: Miscarriage rate

Figures and Tables -
Analysis 1.5

Comparison 1: Tubal surgery (all methods) vs no tubal surgery, Outcome 5: Miscarriage rate

Comparison 1: Tubal surgery (all methods) vs no tubal surgery, Outcome 6: Ectopic pregnancy rate

Figures and Tables -
Analysis 1.6

Comparison 1: Tubal surgery (all methods) vs no tubal surgery, Outcome 6: Ectopic pregnancy rate

Comparison 1: Tubal surgery (all methods) vs no tubal surgery, Outcome 7: Mean number of oocytes

Figures and Tables -
Analysis 1.7

Comparison 1: Tubal surgery (all methods) vs no tubal surgery, Outcome 7: Mean number of oocytes

Comparison 1: Tubal surgery (all methods) vs no tubal surgery, Outcome 8: Mean number of embryos

Figures and Tables -
Analysis 1.8

Comparison 1: Tubal surgery (all methods) vs no tubal surgery, Outcome 8: Mean number of embryos

Comparison 1: Tubal surgery (all methods) vs no tubal surgery, Outcome 9: Multiple pregnancy rate (per clinical pregnancy)

Figures and Tables -
Analysis 1.9

Comparison 1: Tubal surgery (all methods) vs no tubal surgery, Outcome 9: Multiple pregnancy rate (per clinical pregnancy)

Comparison 1: Tubal surgery (all methods) vs no tubal surgery, Outcome 10: Miscarriage rate (per clinical pregnancy)

Figures and Tables -
Analysis 1.10

Comparison 1: Tubal surgery (all methods) vs no tubal surgery, Outcome 10: Miscarriage rate (per clinical pregnancy)

Comparison 2: Proximal tubal occlusion (all methods) vs laparoscopic salpingectomy, Outcome 1: Live birth rate

Figures and Tables -
Analysis 2.1

Comparison 2: Proximal tubal occlusion (all methods) vs laparoscopic salpingectomy, Outcome 1: Live birth rate

Comparison 2: Proximal tubal occlusion (all methods) vs laparoscopic salpingectomy, Outcome 2: Surgical complication rate ‐ wound infection

Figures and Tables -
Analysis 2.2

Comparison 2: Proximal tubal occlusion (all methods) vs laparoscopic salpingectomy, Outcome 2: Surgical complication rate ‐ wound infection

Comparison 2: Proximal tubal occlusion (all methods) vs laparoscopic salpingectomy, Outcome 3: Surgical complication rate ‐ pelvic infection

Figures and Tables -
Analysis 2.3

Comparison 2: Proximal tubal occlusion (all methods) vs laparoscopic salpingectomy, Outcome 3: Surgical complication rate ‐ pelvic infection

Comparison 2: Proximal tubal occlusion (all methods) vs laparoscopic salpingectomy, Outcome 4: Clinical pregnancy rate

Figures and Tables -
Analysis 2.4

Comparison 2: Proximal tubal occlusion (all methods) vs laparoscopic salpingectomy, Outcome 4: Clinical pregnancy rate

Comparison 2: Proximal tubal occlusion (all methods) vs laparoscopic salpingectomy, Outcome 5: Multiple pregnancy rate

Figures and Tables -
Analysis 2.5

Comparison 2: Proximal tubal occlusion (all methods) vs laparoscopic salpingectomy, Outcome 5: Multiple pregnancy rate

Comparison 2: Proximal tubal occlusion (all methods) vs laparoscopic salpingectomy, Outcome 6: Miscarriage rate

Figures and Tables -
Analysis 2.6

Comparison 2: Proximal tubal occlusion (all methods) vs laparoscopic salpingectomy, Outcome 6: Miscarriage rate

Comparison 2: Proximal tubal occlusion (all methods) vs laparoscopic salpingectomy, Outcome 7: Ectopic pregnancy rate

Figures and Tables -
Analysis 2.7

Comparison 2: Proximal tubal occlusion (all methods) vs laparoscopic salpingectomy, Outcome 7: Ectopic pregnancy rate

Comparison 2: Proximal tubal occlusion (all methods) vs laparoscopic salpingectomy, Outcome 8: Mean number of oocytes

Figures and Tables -
Analysis 2.8

Comparison 2: Proximal tubal occlusion (all methods) vs laparoscopic salpingectomy, Outcome 8: Mean number of oocytes

Comparison 2: Proximal tubal occlusion (all methods) vs laparoscopic salpingectomy, Outcome 9: Mean number of embryos

Figures and Tables -
Analysis 2.9

Comparison 2: Proximal tubal occlusion (all methods) vs laparoscopic salpingectomy, Outcome 9: Mean number of embryos

Comparison 2: Proximal tubal occlusion (all methods) vs laparoscopic salpingectomy, Outcome 10: Multiple pregnancy rate (per clinical pregnancy)

Figures and Tables -
Analysis 2.10

Comparison 2: Proximal tubal occlusion (all methods) vs laparoscopic salpingectomy, Outcome 10: Multiple pregnancy rate (per clinical pregnancy)

Comparison 2: Proximal tubal occlusion (all methods) vs laparoscopic salpingectomy, Outcome 11: Miscarriage rate (per clinical pregnancy)

Figures and Tables -
Analysis 2.11

Comparison 2: Proximal tubal occlusion (all methods) vs laparoscopic salpingectomy, Outcome 11: Miscarriage rate (per clinical pregnancy)

Comparison 3: Transvaginal aspiration of hydrosalpingeal fluid vs laparoscopic salpingectomy, Outcome 1: Surgical complication rate

Figures and Tables -
Analysis 3.1

Comparison 3: Transvaginal aspiration of hydrosalpingeal fluid vs laparoscopic salpingectomy, Outcome 1: Surgical complication rate

Comparison 3: Transvaginal aspiration of hydrosalpingeal fluid vs laparoscopic salpingectomy, Outcome 2: Clinical pregnancy rate

Figures and Tables -
Analysis 3.2

Comparison 3: Transvaginal aspiration of hydrosalpingeal fluid vs laparoscopic salpingectomy, Outcome 2: Clinical pregnancy rate

Comparison 3: Transvaginal aspiration of hydrosalpingeal fluid vs laparoscopic salpingectomy, Outcome 3: Miscarriage rate

Figures and Tables -
Analysis 3.3

Comparison 3: Transvaginal aspiration of hydrosalpingeal fluid vs laparoscopic salpingectomy, Outcome 3: Miscarriage rate

Comparison 3: Transvaginal aspiration of hydrosalpingeal fluid vs laparoscopic salpingectomy, Outcome 4: Ectopic pregnancy rate

Figures and Tables -
Analysis 3.4

Comparison 3: Transvaginal aspiration of hydrosalpingeal fluid vs laparoscopic salpingectomy, Outcome 4: Ectopic pregnancy rate

Comparison 3: Transvaginal aspiration of hydrosalpingeal fluid vs laparoscopic salpingectomy, Outcome 5: Mean number of oocytes

Figures and Tables -
Analysis 3.5

Comparison 3: Transvaginal aspiration of hydrosalpingeal fluid vs laparoscopic salpingectomy, Outcome 5: Mean number of oocytes

Comparison 3: Transvaginal aspiration of hydrosalpingeal fluid vs laparoscopic salpingectomy, Outcome 6: Mean number of embryos

Figures and Tables -
Analysis 3.6

Comparison 3: Transvaginal aspiration of hydrosalpingeal fluid vs laparoscopic salpingectomy, Outcome 6: Mean number of embryos

Comparison 3: Transvaginal aspiration of hydrosalpingeal fluid vs laparoscopic salpingectomy, Outcome 7: Miscarriage rate (per clinical pregnancy)

Figures and Tables -
Analysis 3.7

Comparison 3: Transvaginal aspiration of hydrosalpingeal fluid vs laparoscopic salpingectomy, Outcome 7: Miscarriage rate (per clinical pregnancy)

Summary of findings 1. Tubal surgery versus no surgery for tubal disease in women due to undergo in vitro fertilisation

Tubal surgery compared to no surgery for tubal disease in women due to undergo in vitro fertilisation

Patient or population: tubal disease in women due to undergo in vitro fertilisation
Setting: assisted reproduction clinic
Intervention: tubal surgery
Comparison: no tubal surgery

Outcomes

Anticipated absolute effects* (95% CI)

Relative effect
(95% CI)

Number of participants
(studies)

Quality of the evidence
(GRADE)

Comments

Risk with no tubal surgery

Risk with tubal surgery

Live birth rate

No studies reported on this outcome for the main comparison.

Surgical complication rate
‐ conversion to laparotomy

Salpingectomy (all methods)

0 per 1,000

0 per 1,000
(0 to 0)

Peto OR 5.80
(0.11 to 303.69)

204
(1 RCT)

⊕⊝⊝⊝
Very lowa,b,d

We are uncertain of the effect of salpingectomy on the rate of conversion to laparotomy.

Surgical complication rate
‐ pelvic infection

Salpingectomy (all methods)

0 per 1,000

0 per 1,000 (0 to 0)

Peto OR 5.80 (0.11 to 303.69)

204 (1 RCT)

⊕⊝⊝⊝
Very lowa,b,d

We are uncertain of the effect of salpingectomy on the rate of pelvic infection.

Transvaginal aspiration of hydrosalpingeal fluid

0 per 1,000

0 per 1,000 (0 to 0)

Not estimable

176 (1 RCT)

There were insufficient data to estimate differences between groups.

Clinical pregnancy rate

Salpingectomy (all methods)

186 per 1,000

376 per 1,000
(268 to 524)

RR 2.02
(1.44 to 2.82)

455
(4 RCTs)

⊕⊕⊕⊝
Moderatea

Salpingectomy probably increases clinical pregnancy rate.

Tubal occlusion (all methods)

123 per 1,000

396 per 1,000
(212 to 740)

RR 3.21
(1.72 to 5.99)

209
(2 RCTs)

⊕⊕⊝⊝
Lowa,b

Tubal occlusion may increase clinical pregnancy rate.

Transvaginal aspiration of hydrosalpingeal fluid

178 per 1,000

297 per 1,000
(196 to 453)

RR 1.67
(1.10 to 2.55)

311
(3 RCTs)

⊕⊝⊝⊝
Very lowa,b,c

We are uncertain whether transvaginal aspiration of hydrosalpingeal fluid increases clinical pregnancy rate.

Miscarriage rate

Salpingectomy (all methods)

53 per 1,000

48 per 1,000
(18 to 126)

Peto OR 0.91
(0.33 to 2.52)

329
(3 RCTs)

⊕⊕⊝⊝
Lowa,b

Salpingectomy may have little or no difference in miscarriage rate.

Tubal occlusion (all methods)

67 per 1,000

40 per 1,000
(4 to 411)

Peto OR 0.55
(0.04 to 8.43)

65
(1 RCT)

⊕⊝⊝⊝
Very lowa,b,d

We are uncertain of the effect of tubal occlusion on miscarriage rate.

Transvaginal aspiration of hydrosalpingeal fluid

44 per 1,000

56 per 1,000
(21 to 148)

Peto OR 1.27
(0.44 to 3.66)

311
(3 RCTs)

⊕⊝⊝⊝
Very lowa,b,c

We are uncertain of the effect of transvaginal aspiration of hydrosalpingeal fluid on miscarriage rate.

Ectopic pregnancy rate

Salpingectomy (all methods)

23 per 1,000

8 per 1,000
(1 to 55)

Peto OR 0.29
(0.04 to 2.11)

329
(3 RCTs)

⊕⊕⊝⊝
Lowa,b

Salpingectomy may reduce ectopic pregnancy rate.

Tubal occlusion (all methods)

0 per 1,000

0 per 1,000
(0 to 0)

Peto OR 3.67
(0.04 to 384.48)

65
(1 RCT)

⊕⊝⊝⊝
Very lowa,b,d

We are uncertain of the effect of tubal occlusion on miscarriage rate.

Transvaginal aspiration of hydrosalpingeal fluid

15 per 1,000

10 per 1,000
(2 to 61)

Peto OR 0.59
(0.08 to 4.61)

311
(3 RCTs)

⊕⊝⊝⊝
Very lowa,b,c

We are uncertain of the effect of transvaginal aspiration of hydrosalpingeal fluid on ectopic pregnancy rate.

*The risk in the intervention group (and its 95% confidence interval) is based on the assumed risk in the comparison group and the relative effect of the intervention (and its 95% CI).

CI: confidence interval; IVF/ICSI: in vitro fertilisation/intracytoplasmic sperm injection; OR: odds ratio; RCT: randomised controlled trial; RR: risk ratio.

GRADE Working Group grades of evidence
High quality: further research is very unlikely to change our confidence in the estimate 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.

aDowngraded one level for imprecision: wide confidence intervals.

bDowngraded one level for imprecision: low number of participants.

cDowngraded one level for risk of bias: at least one study with two domains at high risk of bias.

dDowngraded one level for imprecision: single small study.

Figures and Tables -
Summary of findings 1. Tubal surgery versus no surgery for tubal disease in women due to undergo in vitro fertilisation
Summary of findings 2. Laparoscopic proximal tubal occlusion versus laparoscopic salpingectomy for tubal disease in women due to undergo in vitro fertilisation

Laparoscopic proximal tubal occlusion versus laparoscopic salpingectomy for tubal disease in women due to undergo in vitro fertilisation

Patient or population: tubal disease in women due to undergo in vitro fertilisation
Setting: assisted reproduction clinic
Intervention: proximal tubal occlusion
Comparison: laparoscopic salpingectomy

Outcomes

Anticipated absolute effects* (95% CI)

Relative effect
(95% CI)

№ of participants
(studies)

Certainty of the evidence
(GRADE)

Comments

Risk with laparoscopic salpingectomy

Risk with proximal tubal occlusion

Live birth rate

Laparoscopic proximal tubal occlusion vs laparoscopic salpingectomy

268 per 1,000

325 per 1,000
(204 to 523)

RR 1.21
(0.76 to 1.95)

165
(1 RCT)

⊕⊝⊝⊝
Very lowa,b,c

We are uncertain of the effect of laparoscopic proximal tubal occlusion on live birth rate compared to laparoscopic salpingectomy.

Surgical complication rate
‐ wound infection

No study reported on this outcome for laparoscopic proximal tubal occlusion.

Surgical complication rate
‐ pelvic infection

No study reported on this outcome for laparoscopic proximal tubal occlusion.

Clinical pregnancy rate

Laparoscopic proximal tubal occlusion vs laparoscopic salpingectomy

410 per 1,000

332 per 1,000
(254 to 439)

RR 0.81
(0.62 to 1.07)

347
(3 RCTs)

⊕⊝⊝⊝
Very lowa,c,d

We are uncertain of the effect of laparoscopic proximal tubal occlusion on clinical pregnancy rate compared to laparoscopic salpingectomy.

Miscarriage rate

Laparoscopic proximal tubal occlusion vs laparoscopic salpingectomy

30 per 1,000

23 per 1,000
(5 to 98)

Peto OR 0.74
(0.16 to 3.34)

265
(2 RCTs)

⊕⊕⊝⊝
Lowa,c

Laparoscopic proximal tubal occlusion may reduce miscarriage rate slightly compared to laparoscopic salpingectomy.

Ectopic pregnancy rate

Laparoscopic proximal tubal occlusion vs laparoscopic salpingectomy

0 per 1,000

0 per 1,000
(0 to 0)

Peto OR 7.39
(0.15 to 372.38)

100
(1 RCT)

⊕⊝⊝⊝
Very lowa,b,c

We are uncertain of the effect of laparoscopic proximal tubal occlusion on ectopic pregnancy rate compared to laparoscopic salpingectomy.

*The risk in the intervention group (and its 95% confidence interval) is based on the assumed risk in the comparison group and the relative effect of the intervention (and its 95% CI).

CI: confidence interval; IVF/ICSI: in vitro fertilisation/intracytoplasmic sperm injection; OR: odds ratio; RCT: randomised controlled trial; RR: risk ratio.

GRADE Working Group grades of evidence
High certainty: We are very confident that the true effect lies close to that of the estimate of the effect
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
Low certainty: Our confidence in the effect estimate is limited: The true effect may be substantially different from the estimate of the effect
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

aDowngraded one level for imprecision: low number of participants.

bDowngraded one level for imprecision: single small study.

cDowngraded one level for imprecision: wide confidence intervals.

dDowngraded one level for inconsistency: high degree of heterogeneity.

Figures and Tables -
Summary of findings 2. Laparoscopic proximal tubal occlusion versus laparoscopic salpingectomy for tubal disease in women due to undergo in vitro fertilisation
Summary of findings 3. Transvaginal aspiration of hydrosalpingeal fluid versus laparoscopic salpingectomy for tubal disease in women due to undergo in vitro fertilisation

Transvaginal aspiration of hydrosalpinx versus laparoscopic salpingectomy for tubal disease in women due to undergo in vitro fertilisation

Patient or population: tubal disease in women due to undergo in vitro fertilisation
Setting: assisted reproduction clinic
Intervention: transvaginal aspiration of hydrosalpinx
Comparison: laparoscopic salpingectomy

Outcomes

Anticipated absolute effects* (95% CI)

Relative effect
(95% CI)

№ of participants
(studies)

Certainty of the evidence
(GRADE)

Comments

Risk with laparoscopic salpingectomy

Risk with transvaginal aspiration of hydrosalpingeal fluid

Live birth rate

No studies reported on this outcome.

Surgical complication rate

0 per 1,000

0 per 1,000
(0 to 0)

not estimable

160
(1 RCT)

There were insufficient data to estimate differences between groups.

Clinical pregnancy rate

400 per 1,000

276 per 1,000
(176 to 428)

RR 0.69 (0.44 to 1.07)

160
(1 RCT)

⊕⊝⊝⊝
Very lowa,b,c

We are uncertain of the effect of transvaginal aspiration of hydrosalpingeal fluid on clinical pregnancy rate compared to laparoscopic salpingectomy.

Miscarriage rate

38 per 1,000

38 per 1,000
(8 to 180)

Peto OR 1.00 (0.20 to 5.08)

160
(1 RCT)

⊕⊝⊝⊝
Very lowa,b,c

We are uncertain of the effect of transvaginal aspiration of hydrosalpingeal fluid on miscarriage rate compared to laparoscopic salpingectomy.

Ectopic pregnancy rate

0 per 1,000

0 per 1,000
(0 to 0)

Peto OR 7.39 (0.15 to 372.38)

160
(1 RCT)

⊕⊝⊝⊝
Very lowa,b,c

We are uncertain of the effect of transvaginal aspiration of hydrosalpingeal fluid on ectopic pregnancy rate compared to laparoscopic salpingectomy.

*The risk in the intervention group (and its 95% confidence interval) is based on the assumed risk in the comparison group and the relative effect of the intervention (and its 95% CI).

CI: confidence interval; IVF/ICSI: in vitro fertilisation/intracytoplasmic sperm injection; OR: odds ratio; RCT: randomised controlled trial; RR: risk ratio.

GRADE Working Group grades of evidence
High certainty: We are very confident that the true effect lies close to that of the estimate of the effect
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
Low certainty: Our confidence in the effect estimate is limited: The true effect may be substantially different from the estimate of the effect
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

aDowngraded one level for imprecision: low number of participants.

bDowngraded one level for imprecision: single small study.

cDowngraded one level for imprecision: wide confidence intervals.

Figures and Tables -
Summary of findings 3. Transvaginal aspiration of hydrosalpingeal fluid versus laparoscopic salpingectomy for tubal disease in women due to undergo in vitro fertilisation
Comparison 1. Tubal surgery (all methods) vs no tubal surgery

Outcome or subgroup title

No. of studies

No. of participants

Statistical method

Effect size

1.1 Surgical complication rate ‐ conversion to laparotomy Show forest plot

1

204

Peto Odds Ratio (Peto, Fixed, 95% CI)

5.80 [0.11, 303.69]

1.1.1 Salpingectomy (all methods) vs no tubal surgery

1

204

Peto Odds Ratio (Peto, Fixed, 95% CI)

5.80 [0.11, 303.69]

1.2 Surgical complication rate ‐ pelvic infection Show forest plot

3

Peto Odds Ratio (Peto, Fixed, 95% CI)

Subtotals only

1.2.1 Salpingectomy (all methods) vs no tubal surgery

1

204

Peto Odds Ratio (Peto, Fixed, 95% CI)

5.80 [0.11, 303.69]

1.2.2 Transvaginal aspiration of hydrosalpingeal fluid vs no tubal surgery

2

176

Peto Odds Ratio (Peto, Fixed, 95% CI)

Not estimable

1.3 Clinical pregnancy rate Show forest plot

7

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

1.3.1 Salpingectomy (all methods) vs no tubal surgery

4

455

Risk Ratio (M‐H, Fixed, 95% CI)

2.02 [1.44, 2.82]

1.3.2 Tubal occlusion (all methods) vs no tubal surgery

2

209

Risk Ratio (M‐H, Fixed, 95% CI)

3.21 [1.72, 5.99]

1.3.3 Transvaginal aspiration of hydrosalpingeal fluid vs no tubal surgery

3

311

Risk Ratio (M‐H, Fixed, 95% CI)

1.67 [1.10, 2.55]

1.4 Multiple pregnancy rate Show forest plot

1

Peto Odds Ratio (Peto, Fixed, 95% CI)

Subtotals only

1.4.1 Transvaginal aspiration of hydrosalpingeal fluid vs no tubal surgery

1

135

Peto Odds Ratio (Peto, Fixed, 95% CI)

2.15 [0.59, 7.85]

1.5 Miscarriage rate Show forest plot

6

Peto Odds Ratio (Peto, Fixed, 95% CI)

Subtotals only

1.5.1 Salpingectomy (all methods) vs no tubal surgery

3

329

Peto Odds Ratio (Peto, Fixed, 95% CI)

0.91 [0.33, 2.52]

1.5.2 Tubal occlusion (all methods) vs no tubal surgery

1

65

Peto Odds Ratio (Peto, Fixed, 95% CI)

0.55 [0.04, 8.43]

1.5.3 Transvaginal aspiration of hydrosalpingeal fluid vs no tubal surgery

3

311

Peto Odds Ratio (Peto, Fixed, 95% CI)

1.27 [0.44, 3.66]

1.6 Ectopic pregnancy rate Show forest plot

6

Peto Odds Ratio (Peto, Fixed, 95% CI)

Subtotals only

1.6.1 Salpingectomy (all methods) vs no tubal surgery

3

329

Peto Odds Ratio (Peto, Fixed, 95% CI)

0.29 [0.04, 2.11]

1.6.2 Tubal occlusion (all methods) vs no tubal surgery

1

65

Peto Odds Ratio (Peto, Fixed, 95% CI)

3.67 [0.04, 384.48]

1.6.3 Transvaginal aspiration of hydrosalpingeal fluid vs no tubal surgery

3

311

Peto Odds Ratio (Peto, Fixed, 95% CI)

0.59 [0.08, 4.61]

1.7 Mean number of oocytes Show forest plot

4

Mean Difference (IV, Fixed, 95% CI)

Subtotals only

1.7.1 Salpingectomy (all methods) vs no tubal surgery

2

191

Mean Difference (IV, Fixed, 95% CI)

0.79 [‐0.87, 2.45]

1.7.2 Tubal occlusion (all methods) vs no tubal surgery

2

244

Mean Difference (IV, Fixed, 95% CI)

0.54 [‐0.80, 1.88]

1.7.3 Transvaginal aspiration of hydrosalpingeal fluid vs no tubal surgery

2

176

Mean Difference (IV, Fixed, 95% CI)

0.96 [‐0.67, 2.59]

1.8 Mean number of embryos Show forest plot

4

Mean Difference (IV, Fixed, 95% CI)

Subtotals only

1.8.1 Salpingectomy (all methods) vs no tubal surgery

2

191

Mean Difference (IV, Fixed, 95% CI)

0.31 [‐1.10, 1.72]

1.8.2 Tubal occlusion (all methods) vs no tubal surgery

2

209

Mean Difference (IV, Fixed, 95% CI)

0.26 [‐1.07, 1.58]

1.8.3 Transvaginal aspiration of hydrosalpingeal fluid vs no tubal surgery

2

176

Mean Difference (IV, Fixed, 95% CI)

0.98 [‐0.24, 2.19]

1.9 Multiple pregnancy rate (per clinical pregnancy) Show forest plot

1

Peto Odds Ratio (Peto, Fixed, 95% CI)

Subtotals only

1.9.1 Transvaginal aspiration of hydrosalpingeal fluid vs no tubal surgery

1

38

Peto Odds Ratio (Peto, Fixed, 95% CI)

2.05 [0.45, 9.42]

1.10 Miscarriage rate (per clinical pregnancy) Show forest plot

6

Peto Odds Ratio (Peto, Fixed, 95% CI)

Subtotals only

1.10.1 Salpingectomy (all methods) vs no tubal surgery

3

106

Peto Odds Ratio (Peto, Fixed, 95% CI)

0.45 [0.14, 1.48]

1.10.2 Tubal occlusion (all methods) vs no tubal surgery

1

22

Peto Odds Ratio (Peto, Fixed, 95% CI)

0.04 [0.00, 2.45]

1.10.3 Transvaginal aspiration of hydrosalpingeal fluid vs no tubal surgery

3

78

Peto Odds Ratio (Peto, Fixed, 95% CI)

0.65 [0.19, 2.27]

Figures and Tables -
Comparison 1. Tubal surgery (all methods) vs no tubal surgery
Comparison 2. Proximal tubal occlusion (all methods) vs laparoscopic salpingectomy

Outcome or subgroup title

No. of studies

No. of participants

Statistical method

Effect size

2.1 Live birth rate Show forest plot

2

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

2.1.1 Proximal tubal occlusion (laparoscopy) vs laparoscopic salpingectomy

1

165

Risk Ratio (M‐H, Fixed, 95% CI)

1.21 [0.76, 1.95]

2.1.2 Proximal tubal occlusion (hysteroscopy) vs laparoscopic salpingectomy

1

85

Risk Ratio (M‐H, Fixed, 95% CI)

0.46 [0.24, 0.89]

2.2 Surgical complication rate ‐ wound infection Show forest plot

1

85

Peto Odds Ratio (Peto, Fixed, 95% CI)

0.14 [0.00, 6.98]

2.2.1 Proximal tubal occlusion (hysteroscopy) vs laparoscopic salpingectomy

1

85

Peto Odds Ratio (Peto, Fixed, 95% CI)

0.14 [0.00, 6.98]

2.3 Surgical complication rate ‐ pelvic infection Show forest plot

1

Peto Odds Ratio (Peto, Fixed, 95% CI)

Subtotals only

2.3.1 Proximal tubal occlusion (hysteroscopy) vs laparoscopic salpingectomy

1

85

Peto Odds Ratio (Peto, Fixed, 95% CI)

7.57 [0.15, 381.46]

2.4 Clinical pregnancy rate Show forest plot

4

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

2.4.1 Proximal tubal occlusion (laparoscopy) vs laparoscopic salpingectomy

3

347

Risk Ratio (M‐H, Fixed, 95% CI)

0.81 [0.62, 1.07]

2.4.2 Proximal tubal occlusion (hysteroscopy) vs laparoscopic salpingectomy

1

85

Risk Ratio (M‐H, Fixed, 95% CI)

0.53 [0.32, 0.89]

2.5 Multiple pregnancy rate Show forest plot

1

Peto Odds Ratio (Peto, Fixed, 95% CI)

Subtotals only

2.5.1 Proximal tubal occlusion (hysteroscopy) vs laparoscopic salpingectomy

1

85

Peto Odds Ratio (Peto, Fixed, 95% CI)

0.14 [0.00, 6.98]

2.6 Miscarriage rate Show forest plot

3

Peto Odds Ratio (Peto, Fixed, 95% CI)

Subtotals only

2.6.1 Proximal tubal occlusion (laparoscopy) vs laparoscopic salpingectomy

2

265

Peto Odds Ratio (Peto, Fixed, 95% CI)

0.74 [0.16, 3.34]

2.6.2 Proximal tubal occlusion (hysteroscopy) vs laparoscopic salpingectomy

1

85

Peto Odds Ratio (Peto, Fixed, 95% CI)

2.03 [0.21, 20.04]

2.7 Ectopic pregnancy rate Show forest plot

2

Peto Odds Ratio (Peto, Fixed, 95% CI)

Subtotals only

2.7.1 Proximal tubal occlusion (laparoscopy) vs laparoscopic salpingectomy

1

100

Peto Odds Ratio (Peto, Fixed, 95% CI)

7.39 [0.15, 372.38]

2.7.2 Proximal tubal occlusion (hysteroscopy) vs laparoscopic salpingectomy

1

85

Peto Odds Ratio (Peto, Fixed, 95% CI)

Not estimable

2.8 Mean number of oocytes Show forest plot

2

265

Mean Difference (IV, Fixed, 95% CI)

0.40 [‐0.67, 1.48]

2.8.1 Proximal tubal occlusion (laparoscopy) vs laparoscopic salpingectomy

2

265

Mean Difference (IV, Fixed, 95% CI)

0.40 [‐0.67, 1.48]

2.9 Mean number of embryos Show forest plot

2

Mean Difference (IV, Fixed, 95% CI)

Subtotals only

2.9.1 Proximal tubal occlusion (laparoscopy) vs laparoscopic salpingectomy

1

100

Mean Difference (IV, Fixed, 95% CI)

0.17 [‐1.38, 1.72]

2.9.2 Proximal tubal occlusion (hysteroscopy) vs laparoscopic salpingectomy

1

85

Mean Difference (IV, Fixed, 95% CI)

0.10 [‐1.77, 1.97]

2.10 Multiple pregnancy rate (per clinical pregnancy) Show forest plot

1

Peto Odds Ratio (Peto, Fixed, 95% CI)

Subtotals only

2.10.1 Proximal tubal occlusion (hysteroscopy) vs laparoscopic salpingectomy

1

38

Peto Odds Ratio (Peto, Fixed, 95% CI)

0.22 [0.00, 13.62]

2.11 Miscarriage rate (per clinical pregnancy) Show forest plot

3

Peto Odds Ratio (Peto, Fixed, 95% CI)

Subtotals only

2.11.1 Proximal tubal occlusion (laparoscopy) vs laparoscopic salpingectomy

2

95

Peto Odds Ratio (Peto, Fixed, 95% CI)

0.82 [0.17, 3.86]

2.11.2 Proximal tubal occlusion (hysteroscopy) vs laparoscopic salpingectomy

1

38

Peto Odds Ratio (Peto, Fixed, 95% CI)

4.59 [0.40, 53.35]

Figures and Tables -
Comparison 2. Proximal tubal occlusion (all methods) vs laparoscopic salpingectomy
Comparison 3. Transvaginal aspiration of hydrosalpingeal fluid vs laparoscopic salpingectomy

Outcome or subgroup title

No. of studies

No. of participants

Statistical method

Effect size

3.1 Surgical complication rate Show forest plot

1

160

Peto Odds Ratio (Peto, Fixed, 95% CI)

Not estimable

3.2 Clinical pregnancy rate Show forest plot

1

160

Risk Ratio (M‐H, Fixed, 95% CI)

0.69 [0.44, 1.07]

3.3 Miscarriage rate Show forest plot

1

160

Peto Odds Ratio (Peto, Fixed, 95% CI)

1.00 [0.20, 5.08]

3.4 Ectopic pregnancy rate Show forest plot

1

160

Peto Odds Ratio (Peto, Fixed, 95% CI)

7.39 [0.15, 372.38]

3.5 Mean number of oocytes Show forest plot

1

160

Mean Difference (IV, Fixed, 95% CI)

0.34 [‐0.85, 1.53]

3.6 Mean number of embryos Show forest plot

1

160

Mean Difference (IV, Fixed, 95% CI)

0.35 [‐0.70, 1.40]

3.7 Miscarriage rate (per clinical pregnancy) Show forest plot

1

54

Peto Odds Ratio (Peto, Fixed, 95% CI)

1.53 [0.28, 8.45]

Figures and Tables -
Comparison 3. Transvaginal aspiration of hydrosalpingeal fluid vs laparoscopic salpingectomy