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. 2025 Mar 7;19(1):103. doi: 10.1007/s11701-025-02255-y

Comparative study between Hugo™ RAS and intuitive da Vinci Xi systems in different gynecologic surgeries: a single-institution perspective study

Kim-Seng Law 1,2,
PMCID: PMC11889050  PMID: 40053244

Abstract

The objective is to compare the feasibility, safety, and complications of the novel robot-assisted system Hugo™ RAS to the established Intuitive da Vinci Xi system in different gynecologic surgeries. This is a retrospective and propensity score-matching study conducted at a tertiary teaching hospital. The participants were women with various indications for gynecologic surgery who underwent robotic procedures. The results of our first 40 cases of gynecologic procedures performed with Hugo™ RAS were compared to those of a 1:3 propensity-matched cohort using the da Vinci Xi system. Length of hospital stay, blood loss, surgical time, console time, and perioperative complications were the main outcome measures. There were no differences in the length of hospital stay, blood loss, and complication rates between the novel Hugo™ RAS and da Vinci Xi system in different gynecologic procedures. However, the surgical time was longer with Hugo™ RAS in the staging of endometrial cancer. The Hugo™ RAS is a feasible and safe robotic platform for different indications in gynecologic surgery.

Supplementary Information

The online version contains supplementary material available at 10.1007/s11701-025-02255-y.

Keywords: da Vinci Xi, Gynecologic surgery, Hugo™ RAS, Robotic surgery

Introduction

Minimally invasive surgery (MIS) has been the mainstay of surgical procedures for most gynecologic diseases, with increasing application of robotic surgery globally, since the introduction of the Intuitive™ da Vinci system in 2003. The surgical platform provides precise manipulation, tremor filtering effects, magnified surgical fields with less blood loss, shorter hospital stays, and rapid recovery [1, 2]. There is a higher incidence of adhesive disease and morbid obesity, and larger uteri with fewer intraoperative complications in the robotic cohort than in the conventional open abdominal hysterectomy and vaginal hysterectomy cohorts, while shorter hospital stays and fewer postoperative complications than in the laparoscopic-assisted vaginal hysterectomy, vaginal hysterectomy, and abdominal hysterectomy cohorts [3].

By 2024, the da Vinci robotic series has dominated the robotic surgical market for almost 20 years, with nearly 9210 platforms installed in 72 countries worldwide. Innovative surgical platforms were introduced into the market in 2019. The Medtronic Hugo™ RAS first gained EU approval in 2021, and 100 platforms have been installed with more than 10,000 procedures having been performed by July 2024 [46]. This novel surgical platform is currently used in only seven centers in East Asia for gynecologic procedures by September 2024, including one in Taiwan and all others in Japan. The procedure has been performed in 51 cases in our institute (TTMHH), 23, 14, 26, 68, 6, and 17 cases in Kitasato Institute, Sapporo Medical University, Tottori University Hospital, Yamanashi Pref. Central Hospital, Fujita Medical University, and Kyoto University Hospital, respectively, by August 2024. Clinical studies were announced in the USA by Medtronic in May 2024.

The innovative open console (Fig. 1) enables surgeons to communicate with operating room personnel effortlessly and effectively during the entire procedure. Furthermore, the ergonomic design is more comfortable and fatigue-free for surgeons compared to an immersive console design, especially during a complicated and long surgery. Another key feature is the four independent arm carts, which enable the adjustment of various configurations adaptable to different clinical scenarios and easy movement between different operating rooms, thereby enhancing the versatility of the platform.

Fig. 1.

Fig. 1

The open console facilitates direct communication between the surgeon and the operating room personnel, as well as provides a more comfortable posture for the surgeon per se during a long procedure

Few reports on gynecology [7, 8], except the prolapse of the pelvic organ (POP) procedure, using the new surgical platform have been published in the past 2 years [9]. Herein, we described our first 40 cases of Hugo™ RAS procedure in different gynecologic surgeries and compared it to the established Intuitive da Vinci Xi system to evaluate its feasibility, safety, and perioperative results.

Methods

Study design and participants

Electronic records of patients who underwent Hugo™ RAS for various gynecologic indications between March 2023 and July 2024 were retrospectively analyzed, and the results were compared to those using the da Vinci Xi system with matched demographics and disease characteristics. The study was approved by the Institutional Review Board of Tung’s Taichung Metroharbor Hospital, and the informed consent was waived.

Main outcome measures

To investigate the feasibility of the Hugo™ RAS in different gynecologic diseases, the length of stay, blood loss, surgical time, and perioperative complication rates were compared to those of the established Intuitive da Vinci Xi systems.

Statistical analysis

To reduce treatment discrepancies between the Hugo robotic surgery and da Vinci robotic surgery, propensity score matching was used to pair the two surgical methods based on age, height, weight, and the weight of the excised surgical components. Descriptive statistics were used to describe demographic variables. Continuous variables are presented as mean and range and were compared using Student’s t test. Categorical variables are expressed numerically as percentages and were compared using the Chi-square test or Fisher’s exact test, as appropriate.

Results

Between May 2023 and July 2024, 40 women, including 4, 4, 6, 20, 2, 3, and 1 cases of adenomyosis, cervical cancer, endometrial cancer, uterine leiomyomas, adenomyosis combined with uterine myomas, cesarean scar defect, and ovarian cancer, respectively, underwent hysterectomy (both benign and malignant, n = 25), myomectomy (n = 12), and scar defect repair (n = 3) (Table 1) with mean uterine weight of 338.6 g (62–1975 g). The mean blood loss was 317.68 ml, which was slightly higher in patients undergoing myomectomy (520.83 ml) and hysterectomy with myomas (502.5 ml), but comparable in others. The mean surgical time, docking time, and console time were 279.92 min (137–628), 7 min (2–20), and 131.7 min (25–455), respectively (Table 2).

Table 1.

Surgical characteristics and demographics of the Hugo™ RAS cohort

No. Length of hospital stay (days) Diagnoses Surgical procedure Docking time (min) Console time (min) Blood loss (ml) Complications
1 4 Endometrial cancer Hugo RAS staging 10 215 50
2 3 Cesarean scar defect with prolonged menses Hugo RAS scar repair 5 75 10
3 3

1. Large subserosal myoma

2. Right paratubal cyst

Hugo RAS myomectomy/enucleation of paratubal cyst 5 25 200 Ileus
4 2 Uterine myomas Hugo RAS myomectomy 14 115 150
5 4 Cervical cancer stage IIIC 1 (p) Hugo RAS radical hysterectomy + BSO + BPLD 8 272 10 Fever
6 2 Uterine mass with post-menopausal bleeding Hugo RAS hysterectomy + BSO 7 46 50
7 3

1. Left ovarian mucinous cystadenomas

2. Uterine myomas

3. Adenomyosis

Hugo RAS hysterectomy + LSO + RS 3 178 200
8 3 Persistent endometrial hyperplasia with atypia (failed medications) Hugo RAS hysterectomy + BS 3 50 10
9 2 Cesarean scar defect with prolonged menses Hugo scar defect repair 3 68 2
10 9

1. Post-menopausal bleeding with rule out endometrial cancer

2. Rectal cancer s/p under chemotherapy

Hugo RAS hysterectomy + BSO 7 38 300 Vomiting, ileus
11 3 Large uterine myomas with compression Hugo RAS hysterectomy + BSO 3 56 350
12 4 Multiple huge uterine myomas Hugo RAS myomectomy 3 129 200
13 4 Huge uterine myomas with compression Hugo RAS hysterectomy + BSO 3 167 1800
14 3

1. Recurrent multiple myomas

2. Submucosal myomas

Hugo RAS myomectomy + Tru clear myomectomy 3 370 1000 Spotting
15 3 Adenomyosis with elevated serum Ca-125 Hugo RAS hysterectomy + BS + adhesiolysis 8 98 300
16 4 Endometrial cancer Hugo RAS staging 5 255 100 Hematuria
17 2 Cesarean scar defect with persisted spotting Hugo scar defect repair 10 70 20
18 3 Multiple uterine myomas Hugo RAS hysterectomy + BSO 5 59 500 Dizziness
19 2

Uterine myomas with degeneration

2 ovarian endometriomas

Hugo RAS myomectomy + enucleation of ovarian endometriomas 7 32 100
20 4 Multiple uterine myomas/ovarian endometriomas Hugo RAS myomectomy + enucleation of ovarian endometriomas 5 202 1000
21 2

1. LEGH with post-menopausal bleeding

2. Breast cancer under Tamoxifen

Hugo RAS hysterectomy + BSO 5 202 100
22 2 Multiple uterine myomas Hugo RAS myomectomy 15 101 100
23 3 Huge uterine myomas Hugo RAS hysterectomy + BS 9 190 1400
24 2 Uterine myomas with dysmenorrhea Hugo RAS myomectomy 2 60 100
25 4 Large uterine myomas Hugo RAS myomectomy 10 130 600
26 2 Adenomyosis with severe dysmenorrhea Hugo RAS hysterectomy + BS 12 120 50
27 3 Endometrial cancer Hugo RAS staging 3 155 20
28 6 Post-menopausal bleeding with r/o uterine sarcoma Hugo RAS hysterectomy + BSO 4 182 15 Fever, infection, leg weakness
29 2 large broad ligament’s myomas Hugo RAS myomectomy 20 80 300
30 52 Endometrial cancer Hugo RAS staging 10 190 100 Fever, small intestinal perforation
31 5 Ovarian cancer s/p neoadjuvant chemotherapy Hugo RAS maximal debulking + hyperthermic intraperitoneal chemotherapy (HIPEC) 2 163 100
32 4 Multiple large uterine myomas Hugo RAS myomectomy 3 125 1500
33 3 Adenomyosis with severe anemia failed Mirena twice Hugo RAS hysterectomy + BS (single port) 5 65 300
34 3 Uterine myomas with compression Hugo RAS myomectomy 20 150 1000
35 3 Cervical cancer Ib3 s/p neoadjuvant chemotherapy Hugo RAS radical hysterectomy + BSO 11 455 150
36 2 Adenomyosis with failed Mirena and persisted dysmenorrhea Hugo RAS hysterectomy + BS (single port) 5 88 200
37 4 Cervical cancer s/p CCRT with partial response of tumor Hugo RAS hysterectomy + BSO 8 77 150 Spotting
38 2 Submucosal myomas Hugo RAS hysterectomy + BSO 4 90 100
39 3 CIN3 with margin involved Hugo RAS hysterectomy + BS 5 85 50
40 3 Residual endometrial polys/breast cancer under Tamoxifen Hugo RAS hysterectomy + BS 10 40 20

BSO, bilateral salpingooophorectomy; BPLD, bilateral pelvic lymph node dissection; LSO, left salpingooophorectomy; RS, right salpingectomy; LEGH, lobular endocervical glandular hyperplasia; CCRT, concurrent chemoradiotherapy; BS, bilateral salpingectomy

Table 2.

Demographics of the Hugo™ RAS cohort

Parameters Hugo (n = 40)
Age, year 47.65 (34–84)
BMI, kg/m2 26.17 (19.52–35.86
Obesity 8 (20)
Uterine weight, gm 338.6 (62–1975)
Myoma, gm 374.3 (5–1040)
Length of hospital stay, day 4.42 (2–52)
Blood loss, ml 317.68 (2–1800)
 Hysterectomy + adenomyosis 212.5 (50–300)
 Hysterectomy + Cervical cancer 202.5 (10–500)
 Hysterectomy + endometrial cancer 64.17 (15–100)
 Hysterectomy + leiomyomas and adenomyosis 175 (50–300)
 Hysterectomy + myoma 502.5 (20–1800)
 Hysterectomy + others 10 (10–10)
 Myomectomy + myoma 520.83 (100–1500)
 Scar repair 10.67 (2–20)
Surgery time, min 279.92 (137–628)
 Hysterectomy + adenomyosis 209.8 (190–240)
 Hysterectomy + cervical cancer 338 (170–628)
 Hysterectomy + endometrial cancer 371.3 (290–460)
 Hysterectomy + leiomyomas and adenomyosis 203 (154–252)
 Hysterectomy + myoma 280.2 (164–607)
 Hysterectomy + others 172 (172–172)
 Myomectomy + myoma 291.1 (137–627)
 Scar repair 155 (141–164)
Docking time, min 7 (2–20)
Console time, min 131.7 (25–455)
Surgery type
 Hysterectomy 25 (62.5)
 Myomectomy 12 (30)
 Scar repair 3 (7.5)
Disease
 Adenomyosis 4 (10)
 Cervical cancer 4 (10)
 Endometrial cancer 6 (15)
 Leiomyomas and adenomyosis 2 (5)
 Myoma 20 (50)
 Others 1 (2.5)
 Scar repair 3 (7.5)
Complication (7 days) 9 (22.5)
Complication (30 days) 5 (12.5)
Transfusion 10 (25)

BMI, body mass index

After propensity score matching, compared to the 111 patients who underwent da Vinci surgery in our series, there were no differences in blood loss [235.42 ml (0–3100) vs. 342.57 ml (10–1800), p = 0.198], incidence of perioperative complications [25 (22.52%) vs. 9 (24.32%), p > 0.99, within 7 days (Table S1); 15 (13.51%) vs. 5 (13.51%), p > 0.99, within 30 days (Table S2)], and length of hospital stay [3.51 days (2–9) vs. 4.59 days (2–52), p = 0.426). However, the surgical time was longer with Hugo™ RAS (228.23 min [84–483] vs. 290.05 min [137–628], p < 0.011), especially in the procedure in the staging of endometrial cancer (381 vs. 324.86 min, p < 0.025) (Table 3).

Table 3.

Comparison between the cohorts using the Hugo™ RAS and da Vinci Xi system

Parameter Da Vinci (n = 111) Hugo (n = 37) p
Age, year 48.86 (26–83) 48.46 (34–84) 0.836
BMI, kg/m2 26.01 (17.8–37.74) 26.38 (19.52–35.86) 0.665
Obesity 42 (37.84) 15 (40.54) 0.922
Uterine weight, gm 335 (5–1990) 338.6 (62–1975) 0.972
Myoma, gm 361.5 (3–1088) 374.3 (5–1040) 0.9
Length of hospital stay, day 3.51 (2–9) 4.59 (2–52) 0.426
Blood loss, ml 235.42 (0–3100) 342.57 (10–1800) 0.198
 Hysterectomy + adenomyosis 280 (100–750) 212.5 (50–300) 0.664
 Hysterectomy + cervical cancer 118 (20–400) 202.5 (10–500) 0.514
 Hysterectomy + endometrial cancer 68.53 (10–300) 64.17 (15–100) 0.904
 Hysterectomy + leiomyomas and adenomyosis 164.1 (2–500) 175 (50–300) 0.93
 Hysterectomy + myoma 206.43 (0–1700) 502.5 (20–1800) 0.14
 Myomectomy + myoma 486.25 (15–3100) 520.83 (100–1500) 0.871
Surgery time, min 228.23 (84–483) 290.05 (137–628) 0.011
 Hysterectomy + adenomyosis 190.4 (127–255) 209.75 (190–240) 0.523
 Hysterectomy + cervical cancer 271.8 (110–456) 338 (170–628) 0.578
 Hysterectomy + endometrial cancer 227.76 (149–483) 371.33 (290–460) 0.002
 Hysterectomy + leiomyomas and adenomyosis 199.95 (113–364) 203 (154–252) 0.948
 Hysterectomy + myoma 224.36 (84–480) 280.25 (164–607) 0.337
 Myomectomy + myoma 261.89 (89–460) 291.08 (137–627) 0.47
Surgery type
 Hysterectomy 83 (74.77) 25 (67.57) 0.521
 Myomectomy 28 (25.23) 12 (32.43) 0.521
Disease
 Adenomyosis 5 (4.5) 4 (10.81) 0.228
 Cervical cancer 5 (4.5) 4 (10.81)  > 0.99
 Endometrial cancer 17 (15.32) 6 (16.22) 0.067
 Leiomyomas and adenomyosis 20 (18.02) 2 (5.41) 0.849
 Myoma 56 (50.45) 20 (54.05)  > 0.99
 Others 5 (4.5) 1 (2.7) 0.573
 Ovarian cancer 3 (2.7) 0 (0) 0.234
Complication (7 days) 25 (22.52) 9 (24.32)  > 0.99
Complication (30 days) 15 (13.51) 5 (13.51)  > 0.99
Transfusion 27 (24.32) 10 (27.03) 0.913

BMI, body mass index

Discussion

Main findings

There were no differences in the length of hospital stay, blood loss, and perioperative complication rates between the Hugo™ RAS and the established da Vinci Xi system in our study cohorts. A variety of procedures, including single-port hysterectomy, three-arm setting, and ovarian interval debulking surgery (IDS) combined with HIPEC, were added to conventional simple hysterectomy, radical hysterectomy, endometrial staging procedure, and myomectomy, all resulting in favorable perioperative outcomes. The feasibility of the platform has been clearly demonstrated for almost all common surgical indications in the gynecology field. The main obstacle to be tackled is the limited option of instruments available for procedures performed with only monopolar scissors, bipolar coagulation, and Cadiere forceps to choose from. Although there is a built-in pedal for the ligasure™ (Medtronic), it was not available during the period when this study was carried out. A slight lag time between instrumental shifts sometimes can be a problem for a seamless procedure.

Interpretation of findings

The novel Hugo™ RAS can perform most gynecologic procedures well, and with experience gained in the journey, little modification is required in the configuration of presetting arms to fit different situations. We found that with the compact setting as originally suggested by Gueli Alletti et al. [10] (Fig. 2), a longer instrument and limited space of the assistant through the Palmer point might hinder the smoothness of the procedure, whereas a slight modification of the down placement of the fourth trocar (the straight port placement) coupled with a modified butterfly configuration (Fig. 3) may greatly decrease the incidence of arms collisions during complex procedure. Although its original design is not specifically for single-port applications, we demonstrated the feasibility of single-arm hysterectomy in two cases (Fig. 4). Further evaluation of the modifications of the presetting angles and arm placement is necessary to carry out the procedure smoothly in the future. The procedure of interval debulking with complete resection of the ovarian tumor (R0) in a case of stage IIIB ovarian cancer coupled with intraoperative hyperthermic intraperitoneal chemotherapy (HIPEC) was successfully performed, which is believed to be the first case report using the new surgical platform in this scenario. A slightly longer surgical time is expected when adapting to a new robotic platform, with totally different docking procedure as well as adaptability of limited instrument option, especially for more complicated procedures. However, for more commonly performed surgeries, such as simple hysterectomy and myomectomy, there was no difference in surgical time between our study cohort and the da Vinci cohort.

Fig. 2.

Fig. 2

The compact configuration requires the assistants to enter through Palmer’s point, which limits their ability to help due to the longer distance to the target tissue

Fig. 3.

Fig. 3

The modified butterfly configuration provides assistants with a more spacious working area

Fig. 4.

Fig. 4

Single-port hysterectomy using the Glove Port (Nelis Medical, Korea) and three-arm setting in a single umbilical incisional wound. BS: bilateral salpingectomy

With the introduction of a different setting of surgical console and separate docking arms, a more surgeon-friendly platform will reduce the muscle strains of upper musculoskeletal as well as wrist portion and easy adjustment of angle during operative time will enable the reaching to a wider surgical field.

There is an easy shifting from da Vinci platform to Hugo™ RAS with short learning curve as demonstrated in our study with most of the surgical time, blood loss and hospital stay are comparable to da Vinci platform. With the innovation of different surgical design, it is anticipated there will be more surgeon-friendly and ease to use with comparable results and cost effective in term of unit price.

Strengths and limitations

This is a small retrospective study in a single institution, and the experience in this novel surgical platform of one surgeon inevitably introduced recall bias when retrieving data from previous cases using the da Vinci Xi procedure due to its long-lapsing and retrospective nature. However, every procedure and all demographic details were documented precisely in the first 40 cases using the Hugo™ RAS. The configuration was modified according to different clinical situations and new settings were adapted to various situations, which might provide a more practical and valuable experience compared with the recommendations of in vivo studies, as suggested by Gueli Alletti et al. [10]. The author has been practicing da Vinci surgery since 2013 with a total of 351 different procedures being carried out as of June, 2024 and has been a proctor for TR300 in da Vinci accredited advance course as well as an instructor for IRCAD Taiwan (MIS training center). He is also a sole proctor in Hugo™ RAS in gynecologic surgery in the Greater China since August 2024. There are no single case of conversion to laparotomy both in the da Vinci cohort and Hugo™ RAS during the study period.

Conclusions

The Hugo™ RAS is feasible and safe in most gynecologic procedures with more options of instruments anticipated in the future.

Supplementary Information

Below is the link to the electronic supplementary material.

Author contributions

Kim-Seng Law was responsible for the conception, planning, carrying out, and analysis of the study, as well as writing the manuscript.

Funding

The author received no funding for this study.

Data availability

All data supporting the findings of this study are available within the paper and its Supplementary Information.

Declarations

Conflict of interest

The author reports no conflict of interest.

IRB approval

This study received IRB approval from our institutions (Approval Number 113040 dated 17 July 17, 2024). The requirement for informed consent was waived by the Institutional Review Board.

Prior presentation

Nil.

Footnotes

Publisher's Note

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Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Supplementary Materials

Data Availability Statement

All data supporting the findings of this study are available within the paper and its Supplementary Information.


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