Many gynecologic surgeons regard uteri of ≥17-week size as a relative contraindication to total laparoscopic hysterectomy (TLH) due to the markedly distended, tortuous uterine vasculature, which complicates secure vascular control and elevates conversion rates9. The core technical challenge in these cases is achieving safe, reliable occlusion of the uterine arteries. Currently, bipolar electrocoagulation and titanium vascular clamps are the primary modalities for vessel control; however, both demand extensive dissection to skeletonize the uterine vessels and ureters, thereby prolonging operative time and increasing procedural complexity, especially when the vessel caliber is large10. Additionally, bipolar energy risks collateral thermal injury to the ureter, while mechanical clamping may result in vessel wall slippage and secondary bleeding upon clamp release. These drawbacks have limited the applicability of TLH in patients with substantially enlarged uteri.
We introduce Laparoscopic Extracorporeal Knot-Tying for Uterine Vessel Occlusion during Hysterectomy with Cervical Cerclage (LEKTUVOHCC), a novel minimally invasive technique designed for markedly enlarged uteri. Our findings confirmed that this technique is both feasible and effective even in uteri approximating a 28-week gestational size. The procedure began with the placement of an extracorporeal laparoscopic knot-pusher to fashion a Roeder's knot around the cervical isthmus, thereby achieving en bloc occlusion of the uterine arteries. Once vascular control is secured, the uterine corpus is transected supracervically to rapidly debulk the specimen. This staged approach restores deep pelvic exposure, optimizes visualization of critical structures, and enables precise dissection throughout the operation.
Since the novel surgery we designed involves placing the cervical ligature around the cervical isthmus, if there were cervical fibroids or uterine broad ligament fibroids, they may prevent the cervical ligature from being positioned accurately and tightened properly, increasing the risk of cervical ligature slipping off. To ensure the effectiveness of the ligature and guarantee the patient's safety, as well as avoid the risk of massive bleeding due to improper tightening or ligature slippage, we decided to exclude patients with these two types of special location fibroids.
Our data indicated that this technique achieved a median intraoperative blood loss (IBL) of just 80 mL) markedly lower than the averages reported by Purohit et al. and Tchartchian et al.11,12. The blood transfusion rate was 3.23% in our study, which was much lower than reported by Mamik et al. with a median IBL of 275 mL and a transfusion rate of 8.4%13. By substantially reducing IBL, this technique minimizes reliance on allogeneic transfusion, which carries well-documented risks of infectious and immunologic complications14 and helps to conserve scarce erythrocyte supplies, addressing broader public health concerns related to blood product shortage15.
The analysis of our institutional learning curve further demonstrated that both IBL and operative time (OT) declined significantly after approximately 15 cases. In the latter half of our cohort (cases 16-31), the median IBL and OT were significantly reduced compared to the first 15 cases (116 min vs 214 min, 60 mL vs 150 mL), indicating that proficiency in this technique for large uteri can be attained after a relatively short series of procedures. This contrasts with the 50-60 cases typically required to master conventional laparoscopic hysterectomy16 and the roughly 20 cases needed to achieve proficiency with robotic hysterectomy in large uteri17. Such a shortened learning curve not only expedites the safe dissemination of the technique but also enhances surgical efficiency, further mitigating the risks associated with prolonged OT and IBL.
The key features of this technique include the following:
The best site for trocar insertion
The procedure began by establishing a 10 mm optical trocar midway between the umbilicus and xiphoid process, which optimized cranial visualization and instrument triangulation. Three additional 5 mm ports provided direct access to the utero-ovarian and broad ligaments while preserving ergonomic hand positioning.
Division of the utero-ovarian, round, and broad ligaments
With the pneumoperitoneum in place, the utero-ovarian, round, and broad ligaments were sequentially coagulated and transected. This ligamentous division fully mobilized the adnexa, cleared the anterior and lateral uterine surfaces, and created a working space for subsequent cervical cerclage.
Intracervical Roeder's knot cerclage for en bloc uterine artery occlusion
An extracorporeal knot-pusher was used to position a size-1 braided polyglactin suture around the cervical isthmus, where a Roeder's knot is tied and tensioned at the 10 o'clock position. Once advanced fully, uniform blanching of the uterus body confirmed complete arterial occlusion. To ensure sustained hemostasis, two additional Roeder's knots were sequentially applied to the residual cervical stump. In our series, only one patient case 7, whose uterus measured approximately 28 weeks' gestational equivalent, had an IBL of 750 mL and required a blood transfusion. Investigation revealed that the initial knot had been under-tensioned, resulting in incomplete vessel closure. This experience led us to standardize knot-tension monitoring and refine our tying technique, after which no further transfusions were necessary.
Injection of diluted vasopressin into the uterine myometrium before loop ligation
Prior to cervical cerclage, diluted vasopressin was injected into the myometrium to induce vigorous myometrial contraction. This vasopressin-mediated constriction "milks" intramural blood into the systemic circulation, rendering the uterine wall pale and turgid. At the point of maximal blanching, a Roeder's knot was advanced around the cervical isthmus to effect en bloc occlusion of the uterine arteries, thereby preventing retrograde bleeding into the impending specimen. Conceptually analogous to an in situ autologous blood transfusion, this maneuver facilitated the return of retained uterine blood to the systemic circulation of the patient prior to the transection of the uterine corpus. Although a minor perioperative hemoglobin drop is anticipated, two patients in our series exhibited postoperative HGB gains, most likely reflecting the reinfused intramural volume. Compared with conventional TLH, this vasopressin-augmented protocol substantially reduced net IBL.
Supracervical debulking and bladder mobilization prior to uterine vessel division
To develop the surgical spaces, the uterine corpus was first removed, and bladder reflection was then performed by incising the vesico-uterine peritoneum, which fully exposes the uterine vessels for en bloc coagulation and division.
Conclusion
Laparoscopic Extracorporeal Knot-Tying for Uterine Vessel Occlusion during Hysterectomy with Cervical Cerclage (LEKTUVOHCC) offers a robust, minimally invasive solution for uteri equivalent to ≥17 weeks' gestation. By integrating extracorporeal Roeder's knot ligation at the cervical isthmus, achieving en bloc uterine artery occlusion, with staged supracervical debulking, this technique substantially minimizes IBL, obviates allogeneic blood transfusion, and streamlines operative workflow. This two-stage protocol preserves standard laparoscopic ergonomics, shortens postoperative recovery, and reduces healthcare resource utilization. Our series demonstrated that procedural proficiency and concomitant reductions in operative time (OT) and intraoperative blood loss (IBL) occurred after approximately 15 cases, reflecting a comparatively brief learning curve versus conventional laparoscopic or robotic hysterectomy for large uteri.
The novel procedure does not require any special equipment. All that is needed is a simple knot-tying device, which is very cheap and readily available, so it is worth promoting in remote areas or in grassroots hospitals.
Limitations of this single-center study include its relatively small cohort and nonrandomized design. To corroborate these promising results, we plan a multicenter, randomized controlled trial with an expanded sample size to rigorously evaluate the technique's safety profile, efficacy, and cost-effectiveness in the management of large benign uterine pathology.