Hysterectomy with opportunistic salpingectomy versus hysterectomy alone

Laura A M van Lieshout, Miranda P Steenbeek, Joanne A De Hullu, M Caroline Vos, Saskia Houterman, Jack Wilkinson, Jurgen Mj Piek, Laura A M van Lieshout, Miranda P Steenbeek, Joanne A De Hullu, M Caroline Vos, Saskia Houterman, Jack Wilkinson, Jurgen Mj Piek

Abstract

Background: Ovarian cancer has the highest mortality rate of all gynaecological malignancies with an overall five-year survival rate of 30% to 40%. In the past two decades it has become apparent and more commonly accepted that a majority of ovarian cancers originate in the fallopian tube epithelium and not from the ovary itself. This paradigm shift introduced new possibilities for ovarian cancer prevention. Salpingectomy during a hysterectomy for benign gynaecological indications (also known as opportunistic salpingectomy) might reduce the overall incidence of ovarian cancer. Aside from efficacy, safety is of utmost importance, especially due to the preventive nature of opportunistic salpingectomy. Most important are safety in the form of surgical adverse events and postoperative hormonal status. Therefore, we compared the benefits and risks of hysterectomy with opportunistic salpingectomy to hysterectomy without opportunistic salpingectomy.

Objectives: To assess the effect and safety of hysterectomy with opportunistic salpingectomy versus hysterectomy without salpingectomy for ovarian cancer prevention in women undergoing hysterectomy for benign gynaecological indications; outcomes of interest include the incidence of epithelial ovarian cancer, surgery-related adverse events and postoperative ovarian reserve.

Search methods: The Cochrane Gynaecology and Fertility (CGF) Group trials register, CENTRAL, MEDLINE, Embase, PsycINFO, CINAHL and two clinical trial registers were searched in January 2019 together with reference checking and contact with study authors.

Selection criteria: We intended to include both randomised controlled trials (RCTs) and non-RCTs that compared ovarian cancer incidence after hysterectomy with opportunistic salpingectomy to hysterectomy without opportunistic salpingectomy in women undergoing hysterectomy for benign gynaecological indications. For assessment of surgical and hormonal safety, we included RCTs that compared hysterectomy with opportunistic salpingectomy to hysterectomy without opportunistic salpingectomy in women undergoing hysterectomy for benign gynaecological indications.

Data collection and analysis: We used standard methodological procedures recommended by Cochrane. The primary review outcomes were ovarian cancer incidence, intraoperative and short-term postoperative complication rate and postoperative hormonal status. Secondary outcomes were total surgical time, estimated blood loss, conversion rate to open surgery (applicable only to laparoscopic and vaginal approaches), duration of hospital admission, menopause-related symptoms and quality of life.

Main results: We included seven RCTs (350 women analysed). The evidence was of very low to low quality: the main limitations being a low number of included women and surgery-related adverse events, substantial loss to follow-up and a large variety in outcome measures and timing of measurements.No studies reported ovarian cancer incidence after hysterectomy with opportunistic salpingectomy compared to hysterectomy without opportunistic salpingectomy in women undergoing hysterectomy for benign gynaecological indications. For surgery-related adverse events, there were insufficient data to assess whether there was any difference in both intraoperative (odds ratio (OR) 0.66, 95% confidence interval (CI) 0.11 to 3.94; 5 studies, 286 participants; very low-quality evidence) and short-term postoperative (OR 0.13, 95% CI 0.01 to 2.14; 3 studies, 152 participants; very low-quality evidence) complication rates between hysterectomy with opportunistic salpingectomy and hysterectomy without opportunistic salpingectomy because the number of surgery-related adverse events was very low. For postoperative hormonal status, the results were compatible with no difference, or with a reduction in anti-Müllerian hormone (AMH) that would not be clinically relevant (mean difference (MD) -0.94, 95% CI -1.89 to 0.01; I2 = 0%; 5 studies, 283 participants; low-quality evidence). A reduction in AMH would be unfavourable, but due to wide CIs, the postoperative change in AMH can still vary from a substantial decrease to even a slight increase.

Authors' conclusions: There were no eligible studies reporting on one of our primary outcomes - the incidence of ovarian cancer specifically after hysterectomy with or without opportunistic salpingectomy. However, outside the scope of this review there is a growing body of evidence for the effectiveness of opportunistic salpingectomy itself during other interventions or as a sterilisation technique, strongly suggesting a protective effect. In our meta-analyses, we found insufficient data to assess whether there was any difference in surgical adverse events, with a very low number of events in women undergoing hysterectomy with and without opportunistic salpingectomy. For postoperative hormonal status we found no evidence of a difference between the groups. The maximum difference in time to menopause, calculated from the lower limit of the 95% CI and the natural average AMH decline, would be approximately 20 months, which we consider to be not clinically relevant. However, the results should be interpreted with caution and even more so in very young women for whom a difference in postoperative hormonal status is potentially more clinically relevant. Therefore, there is a need for research on the long-term effects of opportunistic salpingectomy during hysterectomy, particularly in younger women, as results are currently limited to six months postoperatively. This limit is especially important as AMH, the most frequently used marker for ovarian reserve, recovers over the course of several months following an initial sharp decline after surgery. In light of the available evidence, addition of opportunistic salpingectomy should be discussed with each woman undergoing a hysterectomy for benign indication, with provision of a clear overview of benefits and risks.

Conflict of interest statement

JP, JdH, MCV, JW, SH and MS have no interests to declare.

LvL is first author of the included study, van Lieshout 2018. She took no part in selecting the study for inclusion, or in extracting and entering data from it.

Figures

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1
Study flow diagram.
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2
'Risk of bias' summary: review authors' judgements about each risk of bias item for each included study.
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'Risk of bias' graph: review authors' judgements about each risk of bias item presented as percentages across all included studies.
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Forest plot of comparison: 1 Hysterectomy with opportunistic salpingectomy versus hysterectomy without opportunistic salpingectomy, outcome: 1.1 Surgery‐related adverse events.
 With OS: hysterectomy with opportunistic salpingectomy; without OS: hysterectomy without opportunistic salpingectomy
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Forest plot of comparison: 1 Hysterectomy with opportunistic salpingectomy versus hysterectomy without opportunistic salpingectomy, outcome: 1.2 Postoperative hormonal status (AMH).
 With OS: hysterectomy with opportunistic salpingectomy; without OS: hysterectomy without opportunistic salpingectomy
1.1. Analysis
1.1. Analysis
Comparison 1 Hysterectomy with opportunistic salpingectomy versus hysterectomy without bilateral salpingectomy, Outcome 1 Surgery‐related adverse events.
1.2. Analysis
1.2. Analysis
Comparison 1 Hysterectomy with opportunistic salpingectomy versus hysterectomy without bilateral salpingectomy, Outcome 2 Postoperative hormonal status (AMH).
1.3. Analysis
1.3. Analysis
Comparison 1 Hysterectomy with opportunistic salpingectomy versus hysterectomy without bilateral salpingectomy, Outcome 3 Postoperative hormonal status (AMH per time point).
1.4. Analysis
1.4. Analysis
Comparison 1 Hysterectomy with opportunistic salpingectomy versus hysterectomy without bilateral salpingectomy, Outcome 4 Postoperative hormonal status (FSH).
1.5. Analysis
1.5. Analysis
Comparison 1 Hysterectomy with opportunistic salpingectomy versus hysterectomy without bilateral salpingectomy, Outcome 5 Postoperative hormonal status (FSH per time point).
1.6. Analysis
1.6. Analysis
Comparison 1 Hysterectomy with opportunistic salpingectomy versus hysterectomy without bilateral salpingectomy, Outcome 6 Postoperative hormonal status (LH).
1.7. Analysis
1.7. Analysis
Comparison 1 Hysterectomy with opportunistic salpingectomy versus hysterectomy without bilateral salpingectomy, Outcome 7 Postoperative hormonal status (LH per time point.
1.8. Analysis
1.8. Analysis
Comparison 1 Hysterectomy with opportunistic salpingectomy versus hysterectomy without bilateral salpingectomy, Outcome 8 Postoperative hormonal status (estradiol).
1.9. Analysis
1.9. Analysis
Comparison 1 Hysterectomy with opportunistic salpingectomy versus hysterectomy without bilateral salpingectomy, Outcome 9 Postoperative hormonal status (estradiol per time point).
1.10. Analysis
1.10. Analysis
Comparison 1 Hysterectomy with opportunistic salpingectomy versus hysterectomy without bilateral salpingectomy, Outcome 10 Total surgical time.
1.11. Analysis
1.11. Analysis
Comparison 1 Hysterectomy with opportunistic salpingectomy versus hysterectomy without bilateral salpingectomy, Outcome 11 Estimated blood loss.
1.12. Analysis
1.12. Analysis
Comparison 1 Hysterectomy with opportunistic salpingectomy versus hysterectomy without bilateral salpingectomy, Outcome 12 Conversion rate to open surgery.
1.13. Analysis
1.13. Analysis
Comparison 1 Hysterectomy with opportunistic salpingectomy versus hysterectomy without bilateral salpingectomy, Outcome 13 Duration of hospital admission.
1.14. Analysis
1.14. Analysis
Comparison 1 Hysterectomy with opportunistic salpingectomy versus hysterectomy without bilateral salpingectomy, Outcome 14 Quality of life.
2.1. Analysis
2.1. Analysis
Comparison 2 Subgroup analyses, Outcome 1 Incidence of intraoperative adverse events depending on surgical approach.
3.1. Analysis
3.1. Analysis
Comparison 3 Sensitivity analysis (random‐effects model), Outcome 1 Postoperative hormonal status (AMH).
4.1. Analysis
4.1. Analysis
Comparison 4 Sensitivity analysis (skewed data), Outcome 1 Postoperative hormonal status (AMH).

Source: PubMed

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