Robotic-assisted surgery (RAS) is increasingly adopted in the pediatric population. This retrospective multicenter study aimed to report application of RAS for gynecological indications in pediatric patients. The medical records of all girls with gynecological pathology, operated in 4 different institutions over a 3-year period, were retrospectively collected. Robot docking time, total operative time, length of stay (LOS), requirement time of pain medication, complication rate, conversion rate, and pathology were analyzed. Twenty-three girls, with median age of 12.3 years (range 0.6–17.8) and median weight of 47.2 kg (range 9–73), received the following RAS procedures: ovarian cystectomy for ovarian cyst/mass (n = 10), salpingo-oophorectomy for ovarian complex mass (n = 6), bilateral gonadectomy for Turner syndrome SRY + (n = 1), salpingectomy for fallopian tube lesion (n = 1), paratubal cyst excision (n = 1), Gartner cyst excision (n = 1), paravaginal ganglioneuroma resection (n = 1), fistula closure in urogenital sinus (n = 1), and vaginoplasty using ileal flap in cloaca malformation (n = 1). Median operative time was 144.9 min (range 64–360), and median docking time was 17.3 min (range 7–50). Conversion to open or laparoscopy was not necessary in any case. Median LOS was 2.1 days (range 1–7), and median analgesic requirement was 2.2 days (range 1–6). One patient (4.3%) needed redo-surgery for recurrent Gartner cyst (Clavien 3b). This preliminary experience showed that RAS is safe and feasible for surgical treatment of gynecological pathology in pediatric patients, although no conclusive data are available to confirm its superiority over traditional laparoscopy. Randomized, prospective, comparative studies are needed to identify the gold standard approach for such indication.
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Introduction
Robotic-assisted surgery (RAS) has gained widespread diffusion over the last years, demonstrating the ability to overcome the technical limitations of conventional laparoscopy. Enhancements provided by robotic assistance include three-dimensional view and magnification, increased dexterity with 7-degrees of freedom of robotic instruments, tremor filtering, and improved surgeons’ ergonomics [1, 2]. Some major drawbacks must be considered before using RAS in children: anesthesia, placement of trocars, and technical difficulties related to small space [3]. Nevertheless, RAS has been described as safe and feasible option for a wide range of surgical indications in children, including urological, oncological, and gastrointestinal pathologies [4‐8]. Several reports have investigated safety and feasibility of RAS in pediatric population, compared with different approaches (open or laparoscopic) [9‐12].
To the current state, the field of pediatric gynecology remains the least explored, with only few pediatric reports of application of RAS for gynecological indications [13‐16].
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This descriptive, retrospective study aimed to report a multicenter experience regarding the application of RAS for gynecological indications in pediatric patients.
Materials and methods
All children and adolescents up to 18 years of age, operated using RAS for gynecological indications in 4 different institutions over a 3-year period, were included. The exclusion criteria were patients over 18 years old as well as all gynecological surgical conditions not treated with RAS.
The surgical centers were contacted via mail and those accepting to participate to the study, were required to fill a study form, with requested information, for each enrolled patient.
Patient baseline, including age at time of surgery, weight, possible comorbidities, clinical presentation, pre-operative diagnosis, and side of pathology, were reported in the first section.
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Details of operative technique, such as type of procedure, number of robotic and/or accessory ports, use of sealing device, method for specimen extraction, were reported in the second section.
Operative results, including robot docking time, total operative time, length of stay (LOS), requirement time of pain medication, complication rate, conversion rate, pathology, and follow-up results, were analyzed in the third section.
All data were elaborated using the statistical software Microsoft Excel, Windows vers.11. Descriptive statistics were used to present findings, and quantitative variables were expressed as median (range) to report the data.
The study received appropriate Institute Review Board (IRB) approval.
Results
Patient baseline
Twenty-three girls, with median age at surgery of 12.3 years (range 0.6–17.8) and median weight of 47.2 kg (range 9–73), received RAS for gynecological indication in the study period and were included. Associated comorbidities were reported in 5/23 (21.7%). Most patients (16/23, 69.5%) were symptomatic at time of diagnosis, with non-specific abdominal/pelvic pain being the most frequent presentation. Pre-operative work-up included abdominal ultrasonography (US), pelvic computed tomography (CT) and/or magnetic resonance imaging (MRI), and voiding cystourethrogram (VCUG) in selected cases. Serum tumor markers, such as beta human chorionic gonadotropin (β-HCG), alfa-fetoprotein (α-FP), Cancer Antigen 125 (Ca125), lactic dehydrogenase (LDH), and human epididymis secretory protein 4 (HE-4), were performed in all patients with adnexal mass. Pre-operative diagnosis was ovarian cyst (n = 4), ovarian “complex” mass (n = 12), fallopian tube lesion (n = 3), uterine cyst (n = 1), gonadal dysgenesis (n = 1), pelvic paravaginal mass (n = 1), cloaca malformation (n = 1), and high-confluence urogenital sinus (UGS) (n = 1). One patient (4.3%) presented concomitant ovarian “complex” mass and paratubal cyst.
Installation and operative technique
All RAS procedures were carried out using the da Vinci Xi Surgical System (Intuitive Surgical, Sunnyvale, CA, USA). The patient was placed supine on the operative table and appropriate age-sized Foley catheter was inserted using sterile precautions pre-operatively.
Three robotic arms, one 12-mm with 12–8 mm reducer, for the 3D, 0-degree, robotic optic, and two 8-mm ports to accommodate the robotic instruments, were placed on the umbilical line in all procedures. A fourth 5-mm accessory port was also placed. The robot was finally docked over the patient’s feet. Robotic vessel sealer was adopted in all procedures. Indocyanine green (ICG) near-infrared fluorescence (NIRF) was adopted in ovarian mass to check the resection margins and guide intra-operative decision making and in paratubal lesion to check the vascular permeability of the fallopian tube following the removal of the lesion (Fig. 1). A 10-mm bag-retrieval, introduced through the umbilical port, was adopted for specimen extraction.
Fig. 1
After removal of giant paratubal cyst (a, b), ICG-guided fluorescence was helpful to check the vascular permeability of fallopian tube (c)
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Video 1 reproduces the technique of robotic-assisted resection of ovarian mass using ICG-NIRF.
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Supplementary file1 (MP4 46006KB)
Operative results
The RAS procedures included: ovarian cystectomy (n = 10), salpingo-oophorectomy (n = 6), bilateral gonadectomy (n = 1), salpingectomy (n = 1), paratubal cyst excision (n = 1), Gartner cyst excision (n = 1), paravaginal ganglioneuroma resection (n = 1), fistula closure in UGS (n = 1), and vaginoplasty using ileal flap in cloaca malformation (n = 1). Median operative time was 144.9 min (range 64–360), and median docking time was 17.3 min (range 7–50). Conversion to open or laparoscopy was not necessary in any case. Median LOS was 2.1 days (range 1–7), and median analgesic requirement was 2.2 days (range 1–6). One patient (4.3%) needed redo-surgery for recurrent Gartner cyst (Clavien 3b).
Pre-operative MRI and specimen of right ovarian immature teratoma
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The median length of follow-up was 2.2 years (range 0.5–4.5). No patients required adjuvant chemotherapy following surgery and none reported recurrence of tumoral pathology.
Outcomes of RAS in pediatric gynecological indications
Patient
Age (years)
Side
Comorbidity
Pre-operative diagnosis
Surgical procedure
OT (min)
LOS (days)
Post-operative complications
Pathology results
1
10
Right
No
Ovarian mass
Salpingo-oophorectomy
85
1
0
Mature cystic teratoma
2
16
Left
No
Giant ovarian cyst (12 cm)
Ovarian cystectomy
72
1
0
Serous cystadenoma
3
17
Right
No
Giant ovarian cyst (10 cm)
Ovarian cystectomy
75
1
0
Serous cystadenoma
4
12
Right
Type I neurofibromatosis
Ovarian mass
Salpingo-oophorectomy
124
3
0
Immature teratoma
5
12
Right
Rheumatoid arthritis
Ovarian mass
Salpingo-oophorectomy
95
2
0
Immature teratoma
6
13
Left
No
Ovarian mass + paratubal cyst
Salpingo-oophorectomy
78
2
0
Immature teratoma + paratubal cyst
7
3
Bilateral
Turner syndrome SRY +
Gonadal dysgenesis
Bilateral gonadectomy
64
2
0
Streak gonads
8
13
Right
No
Fallopian tube lesion
Salpingectomy
96
2
0
Tubal cystadenoma
9
17
N/A
No
Uterine cyst
Excision
200
3
Cyst recurrence (Clavien 3b)
Gartner cyst
10
7
Right
No
Ovarian
Mass
Ovarian cystectomy
155
2
0
Mature cystic teratoma
11
14
Left
No
Pelvic paravaginal mass
Excision
198
2
0
Ganglioneuroblastoma
12
10
N/A
No
Cloaca
Vaginoplasty using ileal flap
360
7
0
N/A
13
0.6
N/A
No
Urogenital sinus
Fistula closure
155
3
0
N/A
14
17
Right
DSD
Ovarian mass
Ovarian cystectomy
145
1
0
Ovotestis
15
13
Left
DSD
Ovarian mass
Salpingo-oophorectomy
120
1
0
Ovotestis
16
13
Right
Epilepsy, mild cystic fibrosis
Ovarian mass
Salpingo-oophorectomy
80
1
0
Immature teratoma
17
17.8
Right
Epilepsy, Hashimoto thyroiditis
Paratubal cyst
Paratubal cystectomy
115
2
0
Serous papillary cystadenoma
18
13.2
Left
No
Ovarian mass
Ovarian cystectomy
228
3
0
Mature cystic teratoma
19
12.9
Right
No
Ovarian mass
Ovarian cystectomy
218
2.1
0
Mature cystic teratoma
20
8
Right
No
Ovarian mass
Ovarian cystectomy
185
2.7
0
Mature cystic teratoma
21
14.8
Right
No
Ovarian mass
Ovarian cystectomy
198
2.3
0
Mature cystic teratoma
22
14.7
Bilateral
No
Ovarian cyst (6 cm)
Ovarian cystectomy
155
1.5
0
Functional follicular cyst
23
15
Left
No
Ovarian cyst
(7 cm)
Ovarian cystectomy
132
1
0
Functional follicular cyst
RAS robotic-assisted surgery, OT operative time, LOS length of stay, DSD disorder of sex development
Discussion
Despite the growing number of indications in pediatric urology, the application of RAS remains still limited in other fields of pediatric surgery. Analyzing the pediatric literature, very few reports on RAS application in gynecology are available, with limited case series or single-case observations [13‐15].
Our study collected the number of 4 pediatric surgery units with high volume robotic activity and 24 patients, operated over a 3-year period, were enrolled. Despite the small number of patients included, our preliminary results were promising and showed that RAS may be fully applicable even to gynecological indications in pediatric patients. Improved dexterity, coordination, and visualization were provided by robot assistance. The absence of intra- and post-operative complications also confirmed the safety and feasibility of this approach in children.
Moreover, our study added new elements to the current knowledge. First, the previous reports have described benign ovarian pathology as main indication to RAS [13‐15]. Our study introduced further undescribed indications, such as tubal, uterine, and vaginal malformations, and demonstrated the feasibility of complex reconstructive procedures of internal genitalia such as vaginoplasty using ileal flap using robotic approach.
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Based on our experience, we believe that the key-points for an optimal management of such pathology using RAS are correct trocar placement, use of sealing device and ICG-NIRF technology, use of endobag for specimen extraction, and teamwork. The most critical step is the placement of trocars, especially in children [17]. Improper placement of the trocars would limit robotic manipulation in the abdominal cavity and increase the chances of instrument conflicts due to the small surface area of the abdominal wall of children and the relatively small space in the abdominal cavity. As described by Xie et al. [14], we always adopted three robotic arms and a fourth accessory laparoscopic port for the bedside surgeon. We placed the robotic ports on the umbilical line to keep proper distance from the pelvic area and have enough working space for manipulation of giant masses or insertion of retrieval bag. Our standard operation order was to insert the trocar for the scope first and then insert the trocars for the robotic arms. Furthermore, if use of specimen retrieval bag is planned, our suggestion is to place 12-mm umbilical robotic port with 12–8 mm reducer to use the 8-mm robotic scope. At time of specimen extraction, the optic is moved to one working arm and the 10-mm retrieval bag is inserted into the abdominal cavity through the umbilical robotic port and the specimen extraction is finally done under direct vision.
Use of robotic vessel sealer is very helpful to perform a bloodless dissection of anatomic structures or resection of giant tumors. In some indications, such as ovarian tumors, use of ICG-NIRF was very helpful to visualize the resection margins of the mass and help guide intra-operative decision between salpingo-oophorectomy and ovarian-sparing surgery. This technology required an intra-operative administration of ICG (0.5 mg/kg) via intravenous route and in a matter of 60 s, fluorescence appeared in the target organs, allowing to identify the resection margins and the vascularization of the mass [18‐20]. Recently, ICG-NIRF was also adopted during removal of paratubal lesion, to check the vascular permeability of the fallopian tube following the resection of the lesion.
Use of endobag is needed for extraction of resected tumors with high suspicion of malignancy. We suggest adopting large endobags (volume up to 1000 mL) and extract the specimen by enlarging the umbilical incision and, whenever possible, aspirating the liquid content of cystic masses before extraction, to avoid additional large Pfannestiel incision.
Finally, the teamwork is essential to perform a smooth operation, shorten the learning curve for docking, and ultimately reduce total operative time and anesthetic times.
Limitations of the presented study are the small number series, the limited follow-up period, and the multi-institutional participation, that made the data hardly comparable. The number of accumulated procedures in children is difficult to compare with that in adults. Thus, it was necessary collect the data of different pediatric surgery units to collect more conspicuous evidence.
Conclusion
This preliminary experience showed that RAS is safe and feasible for surgical treatment of pediatric gynecological pathology, although no conclusive data are available to confirm its superiority over traditional laparoscopy. Case–control and comparative prospective studies will help to delineate better the advantages of this new technology as well as its optimal use in pediatrics. The primary focus for future studies should therefore be on quality management, optimization of patient outcomes for the largest number of patients, and surgical and team training.
Declarations
Conflict of interest
The authors have no relevant financial or non-financial interests to disclose.
Ethics approval
This is a retrospective study. No ethical approval is required.
Consent to participate
Written informed consent was obtained from all individual participants included in the study and their parents.
Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
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