Percutaneous-assisted vs mini-laparoscopic hysterectomy: comparison of ultra-minimally invasive approaches

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This study found that both percutaneous-assisted hysterectomy and mini-laparoscopic hysterectomy are viable ultra-minimally invasive approaches for gynecological conditions, with mini-laparoscopic procedures showing less post-operative pain at four hours.

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This study compared feasibility and safety of percutaneous-assisted hysterectomy (PSS-H) versus 3 mm mini-laparoscopy hysterectomy (m-LPS-H) in 126 patients undergoing minimally invasive hysterectomy for benign conditions and low/intermediate risk endometrial cancer, using intra/perioperative outcomes, post-operative pain, and cosmetic satisfaction. Baseline characteristics and clinical indications were similar, with no significant differences in operative time, estimated blood loss, uterine manipulator usage, conversion to standard laparoscopy, or overall intra-operative complication rates. Early post-operative complications occurred in five PSS-H cases and none in the m-LPS-H group, while pain favored m-LPS-H at 4 hours; cosmetic satisfaction at 30 days did not differ. The paper explicitly limits conclusions by comparing two non-identical groups from a single-center experience (80 vs 46), with statistically non-significant trends for several safety outcomes. This paper is centrally about endometriosis and/or adenomyosis — it includes women whose primary hysterectomy indication was “fibroids/adenomyosis,” directly incorporating adenomyosis in the enrolled population.

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Abstract

To assess the feasibility and the safety of the ultra-minimally invasive (U-MIS) approaches in gynecology, we compared our experience in percutaneous assisted hysterectomy (PSS-H) with a series of 3 mm mini-laparoscopy hysterectomy (m-LPS-H). 126 patients affected by benign and malignant gynecological conditions were considered eligible for minimally invasive hysterectomy: 80 patients received PSS approach and 46 m-LPS approach. For both groups, we evaluated intra and perioperative outcomes, post-operative pain and cosmetic outcomes. The baseline characteristics were comparable between the two study groups. As well, no differences were reported in the clinical indications for hysterectomy, principally fibroids/adenomyosis, endometrial hyperplasia and early stage endometrial cancer. The median operative time was 88.5 (40-190) minutes for PSS-H group and 95.0 (42-231) minutes in m-LPS-H group (p = 0.131). No differences were detected in median estimated blood loss (p = 0.104) as well, in the uterine manipulator usage (p = 0.127) between the two different surgical approaches. Only 1 (2.2%) conversion to standard laparoscopy occurred in m-LPS-H group (p = 0.691). One intra-operative complication was recorded 1 (1.3%) in the PSS-H group (p = 0.367). The post-operative early complication was recorded in five cases of PSS-H group (p = 0.158), none for m-LPS-H procedures. The results in post-operative pain detection was statistically significant after 4 h in favor of m-LPS-H group (p = 0.001). After 30 days no differences in cosmetic satisfaction were detected between the two groups (p = 0.206). PSS-H and m-LPS-H are two valid U-MIS alternatives for benign gynecological conditions and low/intermediate risk endometrial cancer.
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Abstract

To assess the feasibility and the safety of the ultra-minimally invasive (U-MIS) approaches in gynecology, we compared our experience in percutaneous assisted hysterectomy (PSS-H) with a series of 3 mm mini-laparoscopy hysterectomy (m-LPS-H). 126 patients affected by benign and malignant gynecological conditions were considered eligible for minimally invasive hysterectomy: 80 patients received PSS approach and 46 m-LPS approach. For both groups, we evaluated intra and perioperative outcomes, post-operative pain and cosmetic outcomes. The baseline characteristics were comparable between the two study groups. As well, no differences were reported in the clinical indications for hysterectomy, principally fibroids/adenomyosis, endometrial hyperplasia and early stage endometrial cancer. The median operative time was 88.5 (40–190) minutes for PSS-H group and 95.0 (42–231) minutes in m-LPS-H group (p = 0.131). No differences were detected in median estimated blood loss (p = 0.104) as well, in the uterine manipulator usage (p = 0.127) between the two different surgical approaches. Only 1 (2.2%) conversion to standard laparoscopy occurred in m-LPS-H group (p = 0.691). One intra-operative complication was recorded 1 (1.3%) in the PSS-H group (p = 0.367). The post-operative early complication was recorded in five cases of PSS-H group (p = 0.158), none for m-LPS-H procedures. The results in post-operative pain detection was statistically significant after 4 h in favor of m-LPS-H group (p = 0.001). After 30 days no differences in cosmetic satisfaction were detected between the two groups (p = 0.206). PSS-H and m-LPS-H are two valid U-MIS alternatives for benign gynecological conditions and low/intermediate risk endometrial cancer. Similar content being viewed by others

References

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Additional information Publisher's Note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations. Rights and permissions About this article Cite this article Cianci, S., Perrone, E., Rossitto, C. et al. Percutaneous-assisted vs mini-laparoscopic hysterectomy: comparison of ultra-minimally invasive approaches. Updates Surg 73, 2347–2354 (2021). https://doi.org/10.1007/s13304-020-00893-5 Received: Accepted: Published: Version of record: Issue date: DOI: https://doi.org/10.1007/s13304-020-00893-5

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adenomyosis

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Endometrial Neoplasms Endometrial Neoplasms Laparoscopy Female Humans Hysterectomy Minimally Invasive Surgical Procedures Operative Time Postoperative Pain Retrospective Studies

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