Introduction
Ovarian endometriosis (endometrioma, OMA) is a disease
in which endometrial-like tissues grow inside or on the sur-
face of the ovaries, undergoing hemorrhagic changes with
Chuan Lin and Guihua Chen contributed equally to this work.
Extended author information available on the last page of the article
Abstract
This study aims to introduce and evaluate a novel suturing technique for treating ovarian endometriomas (OMA) using
robot-assisted laparoscopy (RAL), termed the Reapproximation of Ovarian Stroma (ROS) method. The primary focus is to
assess the efficacy of ROS-RAL in treating OMA and preserving ovarian reserve, as measured by anti-Müllerian hormone
(AMH) levels, compared to conventional laparoscopy (CL). In this retrospective study, we evaluated 154 patients who
underwent OMA resection via either CL or RAL at Jeonbuk National University Hospital in Korea between February 1,
2017, to December 31, 2023. Among the participants, 85 patients received CL using conventional ovarian surgery, while
69 patients received ROS-RAL surgery. AMH levels were measured preoperatively and at postoperative intervals of 1, 6,
12, 24, and 36 months to determine the rate of AMH decline. The incidence of diminished ovarian reserve (DOR) was
assessed to evaluate the impact on ovarian function over time. Univariate and multivariate logistic regression analyses
were conducted to identify factors associated with decreased ovarian reserve following OMA surgery. The ROS-RAL
group exhibited higher AMH levels at postoperative months 1, 12, and 36 compared to the CL group ( p < 0.05). Further-
more, the rate of AMH decline at all postoperative time points was significantly lower in the ROS-RAL group ( p < 0.05).
At 36 months postoperatively, the incidence of DOR was also notably lower in the ROS-RAL group than in the CL
group (27.54% vs. 44.71%, p = 0.028). Multivariate logistic regression analysis showed that ROS-RAL (OR: 0.207, 95%
CI: 0.068–0.561, p = 0.003), higher preoperative AMH levels (OR: 0.43, 95% CI: 0.29–0.59, p < 0.001), unilateral cysts
(OR: 3.36, 95% CI: 1.24–9.74, p = 0.020), and younger age (OR: −0.12, 95% CI: −0.16 to −0.08, p < 0.001) were found
as protective factors for postoperative ovarian reserve function. Additionally, the postoperative recurrence rate in the CL
group was 5.88%, while no recurrence cases were observed in the RAL group. This study demonstrates that the novel
ROS-RAL surgery offers significant advantages in treating OMA and preserving ovarian function postoperatively in
patients with OMA. Future research should incorporate larger sample sizes and evaluate the influence of surgical expertise
and refinement in technique to substantiate and expand upon these results, ultimately contributing to optimized treatment
strategies for OMA.
Keywords
Ovarian endometriomas · Conventional laparoscopy · Robot-assisted laparoscopy · Reapproximation of
ovarian stroma
Received: 13 November 2025 / Accepted: 17 December 2025
© The Author(s) 2025
Robotic assisted versus conventional laparoscopic ovarian suture
reapproximation in ovarian cystectomy of ovarian endometriomas in
preserving ovarian reserve
Chuan Lin1,2,3,4,5 · Guihua Chen5 · Mingda Wang5,6 · Chongkai Zhai7 · Seong-Tshool Hong5,10 · Hee-Suk Chae1,8,9
1 3
Journal of Robotic Surgery (2026) 20:138
surrounding pelvic tissues and damaging the ovarian cortex,
thereby impairing its function. Patients with OMA experi -
ence symptoms such as pelvic pain, dyspareunia, abnormal
menstruation, infertility, and decreased ovarian function,
severely affecting their quality of life and reproductive
health [3]. Lifestyle factors and dietary patterns have also
been shown to influence the development and progression
of endometriosis [ 4]. OMA negatively impact fertility and
can reduce ovarian reserve [ 5]. With the growing demand
for fertility preservation, protection of ovarian function has
become particularly critical [6, 7].
Despite its seriousness, there is currently no medication
specifically for OMA, and only management drugs, such as
hormonal treatments, are used for the purpose of relieving
the symptoms. Surgical excision is generally recommended
to treat OMA, particularly for patients with cysts larger than
4 cm in diameter, significant pain, poor response to medica-
tion, or infertility issues with a desire for childbearing [ 8].
Application of laparoscopy in OMA treatment improves
clinical outcomes compared to conventional laparotomy.
Laparoscopic surgery offers several advantages, includ -
ing less postoperative pain, shorter hospital stays, lower
rates of adhesion formation, and a smaller impact on ovar -
ian function [9, 10]. Additionally, laparoscopic cystectomy
effectively reduces the recurrence of endometriotic cysts
[11], and when combined with progestins or short-term
contraceptives, can significantly lower postoperative pain
rates. Consequently, laparoscopic excision is widely used
in clinical [ 12]. However, conventional laparoscopy (CL)
has certain limitations. For example, the restricted range
and flexibility of the instruments can make the surgery more
challenging [13]. The two-dimensional surgical view makes
it difficult to identify and completely excise hidden patho -
logical lesions. Furthermore, prolonged surgeries can lead
to surgeon fatigue, potentially affecting surgical precision.
In particularly, CL has not shown satisfactory results for
OMA, especially in advanced-stage endometriosis of stage
3 or higher [ 14]. Although advanced magnetic resonance
imaging techniques have improved preoperative assessment
of deep infiltrating lesions and complex pelvic anatomy,
they do not fundamentally address the ovarian damage
caused by the surgical procedure itself [ 15]. The advent
of da Vinci robot-assisted laparoscopy (RAL) has demon -
strated the potential to overcome the limitations of CL. In
patients with stage III-IV OMA, classified according to the
ASRM endometriosis scoring system, which often involves
extensive and dense pelvic adhesions1 [ 16], RAL—featur -
ing 360° rotating mechanical arms and multiple degrees of
freedom—improves surgical ergonomics and enables more
precise adhesion dissection in most surgical cases [ 17].
Compared to CL, RAL allows surgeons to perform com -
plex and delicate procedures in confined spaces, facilitating
the full dissection of “frozen pelvis” conditions in stage
IV endometriosis patients without requiring colon resec -
tion [18]. Despite the advancements in surgical flexibility
offered by RAL, the current surgical outcomes of OMA sur-
gery performed with RAL does not demonstrate a clear ben-
efit in preserving postoperative ovarian re serve [ 19]. This
is because the surgical procedures employed in both meth -
ods are fundamentally the same. In typical CL and RAL
OMA surgeries, bleeding sites encountered after a strip -
ping cystectomy are cauterized before suturing. However,
cauterization inevitably causes significant thermal dam -
age to the ovary, as the process involves burning tissue to
achieve hemostasis. Suture techniques have been proposed
due to concerns about ischemic irreversible thermal damage
caused by cauterization. In the case of a method of achiev -
ing hemostasis through pure suturing without cauterization,
the ovary is penetrated, and the entire ovary is ligated mul -
tiple times during suturing. While this approach avoids the
thermal damage caused by cauterization, the tight physical
force exerted on the entire ovary results in ischemic damage
by reducing blood flow to the ovarian cortex and stroma.
Consequently, the surgical outcomes of the suturing method
are not significantly better than those of the cauterization
Method
[20].
Since current surgical techniques for OMA are basically
similar regardless of whether CL or RAL is used, the out -
comes of RAL OMA surgery are not markedly different
from those of CL [ 19]. Considering the surgical flexibility
of RAL compared to CL, RAL has the potential to facilitate
the development of new surgical methods that could over -
come the limitations of current OMA surgeries. By leverag-
ing its advanced capabilities, RAL may pave the way for
improved approaches to enhance surgical outcomes and bet-
ter preserve ovarian function in patients with OMA.
Preservation of ovarian function is one of the primary
clinical concerns in patients with OMA. With the widespread
use of assisted reproductive technologies, accumulating evi-
dence suggests that assisted reproductive technologies may
be associated with an increased risk of certain birth defects,
such as congenital heart disease, and may impose a substan-
tial psychological burden on patients [ 21–24]. Therefore,
promoting natural conception while reducing reliance on
assisted reproductive technologies has become an impor -
tant goal in the clinical management of OMA. Accordingly,
numerous studies have explored the beneficial effects of
optimizing ovarian physiology and improving metabolic
homeostasis on reproductive outcomes [ 25–27]. Given
the critical importance of ovarian reserve for fertility and
pregnancy, there is an urgent need to develop a new surgi -
cal method that effectively removes OMA while preserving
ovarian reserve. In this work, we developed a novel RAL
surgical method called Reapproximation of Ovarian Stroma
1 3
138 Page 2 of 10
Journal of Robotic Surgery (2026) 20:138
(ROS), leveraging the surgical flexibility offered by RAL.
This ROS-RAL OMA surgical method is to suture only
the vascular-rich ovarian stroma while avoiding the cortex
after cystectomy, with the aim of avoiding thermal damage
caused by cauterization and reducing physical damage to
the ovarian cortex caused by tightly sewn sutures. At this
time, the ovarian incision site is either tied with a suture just
around the edges of the incision to maintain the shape of the
ovary, or left unsutured. This approach proved effective in
treating advanced-stage endometriosis and demonstrated a
significant advantage in preserving ovarian function post -
operatively, even in patients with OMA of advanced-stage
endometriosis.
Methods
Study population
Patient data were extracted from electronic medical records
within the timeframe of February 1, 2017, to December
31, 2023, using the keyword “ovarian endometriosis.” A
total of 259 patient records were retrieved. Inclusion crite -
ria: (1). Age > 18 years; (2). Underwent surgical treatment,
specifically laparoscopy or the Da Vinci robotic system;
(3). Postoperative histopathological confirmation of ovar -
ian endometriosis; (4). Presence of an OMA larger than
4 cm in diameter. Exclusion criteria: Exclusion criteria:
(1) Incomplete general patient information; (2) History of
ovarian surgery or hormone treatment within six months
prior to surgery; (3) Other surgeries performed during the
operation besides excision of ovarian endometriotic cysts,
such as myomectomy, salpingectomy, etc.; (4) Incomplete
postoperative follow-up data; (5) Presence of severe sys -
temic diseases, such as malignant tumors, serious disorders
of the heart, liver, kidney, hematologic, endocrine systems,
or autoimmune diseases. Ultimately, 154 patients were
included in the study, with 85 in the laparoscopy group and
69 in the Da Vinci robotic group (Supplemental Fig. 1). All
procedures were conducted in accordance with the Declara-
tion of Helsinki and approved by the Ethics Committee of
Jeonbuk National University, Korea (Approval No. 2024-
08-037-004). Written informed consent was obtained from
all participants prior to inclusion.
Surgical procedure
All CL and ROS-RAL OMA surgeries were performed
under general anesthesia by the same gynecologic surgeon,
H.S. Chae, with assistance from C. Lin.
The CL OMA surgery procedure
Using a Veress needle, a pneumoperitoneum was estab -
lished through a 10 mm vertical incision below the umbi -
licus, followed by the insertion of a 10 mm laparoscope.
Two additional 5 mm trocars were placed to insert auxiliary
instruments. After performing ovarian adhesion dissection,
the endometriotic cyst was opened, and its contents were
aspirated. Once the cleavage plane between the normal
ovarian tissue and the cyst wall was identified, the cyst wall
was separated from the ovarian parenchyma using atrau -
matic forceps and counter-traction. If the cleavage plane
was unclear, scissors were used to trim the cyst wall. After
cyst excision, the subsequent surgical steps can be divided
into two types based on whether bipolar electrocoagula -
tion is applied to the bleeding site. One approach involves
achieving hemostasis with electrocoagulation before sutur -
ing, while the other completely avoids electrocoagulation
and achieves hemostasis solely through ovarian suturing.
The sutures were applied from the ovarian surface to the
vicinity of the mesovarium to ensure effective hemostasis
(Fig. 1).
The ROS- RAL OMA surgery procedure
After making a 12 mm transverse subumbilical incision,
a camera port was inserted through the incision to create
pneumoperitoneum. Then two 8 mm da Vinci ports were
placed in the left and right lower quadrants of abdomen,
respectively. A 12 mm trocar as an assistant port was placed
between camera port and left da Vinci port. An incision is
made on the cyst and the contents of OMA were suctioned.
Adhesions between OMA and surrounding structures were
lysed to expose the ovary. The cleavage plane between the
normal ovarian tissue and the capsule of OMA was identi -
fied. Then, OMA were removed by stripping the capsule of
the cyst from the normal ovarian tissue using traction and
countertraction forces. Then, only the stroma was closed,
without penetrating the cortex, thereby minimizing mechan-
ical injury to functional ovarian tissue. The reconstruction
was completed using interrupted figure-of-eight sutures. In
most cases, the edge of the ovarian incision was left unsu -
tured. However, sometimes, only the edges of the ovarian
incision were sutured to close the ovary in order to maintain
its shape (Fig. 2). All sutures used were 3 − 0 polyglactin
910 (Vicryl®, Ethicon Ltd., Edinburgh, UK).
Data collection
Preoperative data recorded included patient age, body mass
index (BMI), cyst size, cyst number, laterality, serum can -
cer antigen (CA) 125 levels. Endometriosis was classified
1 3
Page 3 of 10 138
Journal of Robotic Surgery (2026) 20:138
Fig. 2 Schematic diagram of ROS-RAL suturing the OMA: The cyst
removal process is performed similarly to CL techniques. During sutur-
ing, absorbable sutures are inserted into the ovarian stroma, passed
through the bleeding deep tissues, and exited through the stroma on
the opposite side. This process is repeated, and the sutures are tight -
ened to form an “X” shape. A knot is tied at the crossing point. The
sutures do not pass through the ovarian surface cortex, and hemostasis
is achieved by intermittently suturing only the ovarian stroma. Postop-
eratively, the edge of the ovarian incision was left unsutured. In most
cases, the ovarian incision was left unsutured; however, to preserve the
ovarian shape, sutures may occasionally be applied starting from the
edges of the incision, with hemostasis performed as described above
Fig. 1 Schematic diagram of the procedure for CL OMA surgery:
expose the cyst and make a longitudinal incision along the free side
of the ovary, cutting through the ovarian cortex to the cyst wall. Aspi-
rate the cyst fluid, and use dissecting forceps to bluntly separate the
boundary between the cyst wall and the ovarian cortex. Completely
peel off the cyst wall and hemostasis can be divided into two types:
One approach involves achieving hemostasis with electrocoagulation
before suturing, while the other completely avoids electrocoagulation
and achieves hemostasis solely through ovarian suturing. The sutur -
ing involved the full thickness of the ovarian cortex and the medulla,
including both the inner and outer cortical layers, and was performed
using interrupted figure-of-eight stitches
1 3
138 Page 4 of 10
Journal of Robotic Surgery (2026) 20:138
SPSS version 22.0. All hypothesis tests were two-sided,
with a significance level set at p < 0.05.
Results
Baseline characteristics of participants
A total of 154 patients were included in this study, with 85
undergoing CL surgery and 69 undergoing RAL surgery
(Table 1). There were no significant differences between
the two groups in terms of age (CL: 30.13 ± 6.15 vs. RAL:
29.38 ± 6.26, p = 0.457) and BMI (CL: 21.45 ± 2.80 vs.
RAL: 21.50 ± 2.73, p = 0.689). However, the RAL group had
significantly larger cyst sizes (7.25 ± 3.47 vs. 6.19 ± 2.28,
p = 0.024) and a higher number of cysts (3.90 ± 2.60 vs.
2.40 ± 1.42, p < 0.001) compared to the CL group. Addition-
ally, the proportion of bilateral cases was higher in the RAL
group (50.72% vs. 31.76%, p = 0.017), and most patients in
this group were at stage IV of endometriosis (84.06% vs.
62.35%, p = 0.003). The rASRM score was also significantly
higher in the RAL group (75.29 ± 35.37 vs. 57.09 ± 35.54,
p = 0.002). There were no significant differences between
the two groups in CA 125 levels, duration of surgery, and
hemoglobin decline.
The surgical results
The intraoperative images demonstrate notable differences
in the ovarian presentation between the CL and RAL groups.
Supplemental Fig. 2A depicts the typical intraoperative
findings of CL OMA surgery. Following cyst excisioncon -
ventional suturing techniques are employed to perform full-
thickness suturing of both the ovarian cortex and stroma.
according to the revised American Society for Reproductive
Medicine (rASRM) classification [16]. The size of the cyst
was determined as the average of the sum of the long and
transverse axes of the cyst, and in the case of bilateral cysts,
it was determined as the sum of the sizes of the cysts on both
sides. The number of cysts is referenced from the operative
records, but in the case of laparoscopy, there are cases where
it is not recorded, and in these cases, the number of cysts was
determined based on magnetic resonance imaging. The total
operation time was defined as the time from skin incision to
closure. Serum hemoglobin (Hb) levels were measured pre-
operatively and on the 1st days postoperatively. Anti-Mülle-
rian hormone (AMH) levels were measured preoperatively
and at 1, 6, 12, 24, and 36 months postoperatively. The
serum AMH level was determined using a commercial kit
(AMH Gen II assay; Beckman Coulter Inc., USA) and the
Result
was recorded in ng/ml. The changes and decline rates
in AMH levels (ΔAMH%) at each postoperative time point
were documented, as well as the incidence of diminished
ovarian reserve (DOR). ΔAMH% was calculated using the
formula: 100 x (preoperative AMH - postoperative AMH) /
preoperative AMH. According to the Bologna criteria, DOR
was defined as AMH < 1.1 ng/ml [28].
Statistical analysis
Continuous variables following a normal distribution were
expressed as mean ± standard deviation (χ ± s) and compared
using an independent samples t-test. Categorical variables
were expressed as percentages or frequencies and compared
using Pearson’s chi-squared test. Univariate and multivari-
ate analyses were conducted using binary logistic regression
models, with odds ratios (OR) and 95% confidence intervals
(CI) calculated. Statistical analyses were performed using
Table 1 Baseline characteristics of CL group versus the RAL group
Total CL RAL p
N = 154 N = 85 N = 69
Age, years 29.79 ± 6.19 30.13 ± 6.15 29.38 ± 6.26 0.457
BMI, kg/m2 21.56 ± 3.09 21.45 ± 2.80 21.50 ± 2.73 0.689
Cyst size, cm 6.67 ± 2.92 6.19 ± 2.28 7.25 ± 3.47 0.024
Cyst number 3.07 ± 2.16 2.40 ± 1.42 3.90 ± 2.60 < 0.001
Laterality, n (%) 0.017
Unilateral 92 (59.74) 58 (68.24) 34 (49.28)
Bilateral 62 (40.26) 27 (31.76) 35 (50.72)
CA 125, U/ml 65.22 ± 136.8 52.07 ± 62.84 81.43 ± 191.71 0.186
Endometriosis stage, N (%) 0.003
III 43 (27.92) 32 (37.65) 11 (15.94)
IV 111 (72.08) 53 (62.35) 58 (84.06)
r ASRM score 65.25 ± 36.50 57.09 ± 35.54 75.29 ± 35.37 0.002
Duration of operation, min 91.71 ± 36.21 89.19 ± 32.67 94.81 ± 40.17 0.339
Hb loss, g/dl 1.63 ± 0.80 1.57 ± 0.84 1.70 ± 0.76 0.315
BMI: body mass index, CA125: cancer antigen 125, CL: conventional laparoscopy, Hb: Hemoglobin, RAL: robot-assisted laparoscopy, r-ASRM
score: revised American Society for Reproductive Medicine score
1 3
Page 5 of 10 138
Journal of Robotic Surgery (2026) 20:138
postoperatively, the AMH levels in the RAL were higher
than those in the CL group (2.78 ± 1.91 vs. 2.20 ± 1.70 ng/
ml, p = 0.047). This significant difference persisted at 12
months (2.62 ± 1.82 vs. 2.06 ± 1.59 ng/ml, p = 0.043) and 36
months (2.27 ± 1.64 vs. 1.66 ± 1.50 ng/ml, p = 0.018) post-
operatively (Table 2, Supplemental Fig. 3A). Regarding the
decline rates in AMH levels, the RAL group had lower rates
at all measured time points: 1 month (17.40 ± 36.00% vs.
40.76 ± 26.95%, p < 0.001), 6 months (19.74 ± 40.09% vs.
43.08 ± 34.85%, p < 0.001), 12 months (21.68 ± 38.79% vs.
43.35 ± 28.58%, p < 0.001), 24 months (24.08 ± 37.89% vs.
44.00 ± 28.88%, p < 0.001), and 36 months (30.43 ± 37.30%
vs. 48.27 ± 35.76%, p < 0.001) (Table 2, Supplemental
Fig. 3B).
Incidence of diminished ovarian reserve (DOR) post-
surgery
There was no significant difference in the preoperative inci-
dence of DOR between the CL group and the RAL group
(CL: 12.94%, RAL: 14.49%, p = 0.780). At 1 month postop-
eratively, the incidence of DOR was similar between the two
groups (CL: 18.82%, RAL: 18.84%, p = 0.998). Over time,
the incidence of DOR gradually increased in the CL group.
By 36 months postoperatively, the incidence of DOR in the
CL group was significantly higher than in the RAL group,
with this difference being statistically significant (27.54%
vs. 44.71%, p = 0.028) (Table 3, Supplemental Fig. 3C).
Univariate and multivariate logistic regression
analysis of DOR incidence at 3-year follow-up
In the univariate and multivariate logistic regression analy -
sis of DOR incidence at 3 years post-surgery between the
CL group and the RAL group, several variables were found
to be significantly associated with DOR. Univariate analysis
revealed that age (OR: 1.20, p < 0.001), laterality (bilateral,
OR: 2.26, p = 0.017), surgical duration (OR: 1.01, p = 0.041),
RAL surgery (OR: 0.47, p = 0.029), and preoperative AMH
levels (OR: 0.41, p < 0.001) were associated with DOR. In
contrast, variables such as the number and size of ovarian
cysts, BMI, CA 125 levels, and endometriosis stage (III and
IV) did not show significant associations in the univariate
analysis. In the multivariate analysis, younger age (OR:
0.12, 95% CI: 0.08–0.16, p < 0.001), bilateral cysts (OR:
Bluish discoloration observed in portions of the surgical-
side ovary suggests potential ischemic injury. In contrast,
Supplemental Fig. 2B illustrates the intraoperative findings
during RAL surgery. The innovative ROS suturing technique
eliminates the need for suturing the ovarian cortex, selec -
tively targets the vascular-rich ovarian stroma, effectively
reducing the mechanical stress exerted on ovarian tissue by
sutures. This approach not only improves ovarian perfusion,
but also allows tissue suturing to be performed more eas -
ily and with greater precision and control compared with
conventional laparoscopic suturing, owing to the enhanced
dexterity provided by the robotic system, thereby improv -
ing operative efficiency. Notably, Supplemental Fig. 2-B3
reveals that the surgical-side ovary in the ROS-RAL group
exhibits coloration consistent with the non-operated contra-
lateral ovary, indicating that ovarian perfusion has been well
preserved. At this time, the edges of the ovarian incision
were sutured to close the ovary. Supplemental Fig. 2-B3
shows that the surgical-side ovary in the ROS-RAL group
demonstrates no discoloration compared with the non-oper-
ated contralateral ovary, indicating that ovarian perfusion
has been well preserved.
AMH levels and decline rates
Preoperative AMH levels showed no significant differ -
ence between the two groups (CL: 3.68 ± 2.69 ng/ml,
RAL: 3.78 ± 2.43 ng/ml, p = 0.817). However, at 1 month
Table 2 AMH levels and AMH decline rate between CL group and
RAL group
CL RAL p
AMH, ng/ml
Pre-operation 3.68 ± 2.69 3.78 ± 2.43 0.817
1 month 2.20 ± 1.70 2.78 ± 1.91 0.047
6 months 2.07 ± 1.43 2.53 ± 1.58 0.062
12months 2.06 ± 1.59 2.62 ± 1.82 0.043
24 months 2.00 ± 1.51 2.48 ± 1.69 0.065
36 months 1.66 ± 1.50 2.27 ± 1.64 0.018
ΔAMH, %
1 month 40.76 ± 26.95 17.40 ± 36.00 < 0.001
6 months 43.08 ± 34.85 19.74 ± 40.09 < 0.001
12 months 43.35 ± 28.58 21.68 ± 38.79 < 0.001
24 months 44.00 ± 28.88 24.08 ± 37.89 < 0.001
36 months 48.27 ± 35.76 30.43 ± 37.30 < 0.001
AMH: anti-Müllerian hormone, CL: conventional laparoscopy, RAL:
robot-assisted laparoscopy
Table 3 DOR between CL group and RAL group
The incidence of DOR
Pre-operation 1 month 6 months 12 months 24 months 36 months
CL, n (%) (n = 85) 11 (12.94) 16(18.82) 20 (23.53) 23 (27.06) 29 (34.12) 38(44.71)
RAL, n (%) (n = 69) 10 (14.49) 13 (18.84) 14 (20.29) 16 (23.19) 18 (26.09) 19 (27.54)
P 0.780 0.998 0.630 0.583 0.282 0.028
AMH: anti-Müllerian hormone, CL: conventional laparoscopy, DOR: diminished ovarian reserve, RAL: robot-assisted laparoscopy
1 3
138 Page 6 of 10
Journal of Robotic Surgery (2026) 20:138
[29, 30]. In both surgical methods, hemostasis of the vascu-
lar-rich ovarian stroma, from which the OMA is removed,
is typically achieved through cauterization prior to suturing
or by tightly ligating the incised ovary using the suturing
method. While these approaches are effective for achieving
hemostasis, they result in ischemic damage to the operated
ovary. The cauterization method achieves hemostasis by
burning the bleeding vessels, and the burned site inevitably
causes ischemic damage, leading to a reduction in ovarian
reserve. Studies on OMA surgery repeatedly reported that
cauterization method significantly reduces ovarian reserve
and function, and can even cause ovarian dysfunction or
failure [31, 32]. Due to the limitations of ovarian reserve
preservation with cauterization method, suturing method,
which achieve hemostasis by tightly ligating the bleed -
ing ovary, have been explored. Comparative studies have
shown that suture-based hemostatic methods, compared to
cauterization method, slightly reduce the impact on ovarian
reserve, but the improvement is not significant [33–36]. The
Limitation
of suturing methods lies in ischemic damage to
the distal area of the blood vessel due to restricted blood
flow, highlighting the need for the development of new sur-
gical methods.
The unsatisfactory outcomes of current OMA surgeries
Result
from ischemic damage caused by both cauterization
and suturing methods, regardless of whether they are per -
formed using CL or RAL. However, the surgical flexibility
of RAL offers significant potential for the development of
innovative surgical techniques. Leveraging this flexibility,
3.36, 95% CI: 1.24–9.74, p = 0.020), RAL surgery (OR:
0.207, 95% CI: 0.068–0.561, p = 0.003), and higher preoper-
ative AMH levels (OR: 0.43, 95% CI: 0.29–0.59, p < 0.001)
remained significantly associated with DOR (Table 4).
Postoperative recurrence
During a 36-month postoperative follow-up, five patients in
the CL group experienced a recurrence of OMA, resulting in
a recurrence rate of 5.88%, whereas no cases of recurrence
were observed in the RAL group (Supplemental Fig. 3D).
The average age of the five patients who experienced
recurrence was 29.8 years, and their cysts had an average
diameter of 5.5 cm. All five patients received postoperative
pharmacological therapy to prevent recurrence; specifically,
two patients were prescribed oral dienogest (Visanne ®),
while the remaining three were administered combined oral
contraceptives.
Discussion
Preserving ovarian reserve during OMA surgery remains a
significant challenge, whether performed using RAL or CL.
Despite the greater precision and flexibility offered by RAL,
the preservation of ovarian reserve following RAL-OMA
surgery does not differ significantly from that of CL. Grow-
ing evidence indicates that both CL and RAL OMA surger-
ies have significantly negative impacts on ovarian reserve
Table 4 The regression analysis of DOR at 36 months after surgery
Variable Univariate analysis Multivariate analysis
OR (95% CI) p OR (95% CI) p
Age 1.20 (1.12, 1.28) < 0.001 -0.12 (-0.16, -0.08), < 0.001
BMI 1.02 (0.92, 1.14) 0.655 NA
Cyst size 0.95 (0.85, 1.07) 0.429 NA
Cyst number 1.01 (0.86, 1.17) 0.943 NA
Laterality
Unilateral Ref Ref
Bilateral 2.26 (1.15, 4.41) 0.017 3.36 (1.24, 9.74) 0.020
CA 125 0.99 (0.99, 1.00) 0.055 NA
Endometriosis stage
Ⅲ Ref NA
Ⅳ 1.76 (0.82, 3.79) 0.148 NA
r ASRM score 1.01 (1.00, 1.02) 0.062 NA
Duration of operation 1.01 (1.00, 1.02) 0.041 1.01 (0.997, 1.02) 0.170
Hb loss 0.99 (0.66, 1.48) 0.949 NA
Surgical approach
CL Ref Ref
RAL 0.47 (0.24, 0.93) 0.029 0.207 (0.068, 0.561) 0.003
Pre-operation AMH 0.41 (0.31, 0.56) < 0.001 0.43 (0.29, 0.59) < 0.001
AMH: anti-Müllerian hormone, BMI: body mass index, CA125: cancer antigen 125, CL: conventional laparoscopy, DOR: diminished ovarian
reserve, Hb: Hemoglobin, NA: not available, RAL: robot-assisted laparoscopy, r-ASRM score: revised American Society for Reproductive
Medicine score, Ref: reference
1 3
Page 7 of 10 138
Journal of Robotic Surgery (2026) 20:138
of recurrence were observed in the RAL group (Supplemen-
tal Fig. 3D).
In summary, this study demonstrated the clinical advan -
tages of RAL using the ROS surgical technique for the
excision of OMA, offering superior postoperative ovarian
function preservation compared to traditional RAL or CL.
With a follow-up period of up to three years, this study
provides long-term data illustrating the impact of ROS-
RAL OMA surgery on ovarian reserve. However, despite
the statistical significance of these findings, our study had
some limitations. First, the relatively small sample size may
limit its generalizability. Second, as a single-center study,
the results may be influenced by the specific surgical team’s
expertise, potentially limiting the broader applicability of
the conclusions. Additionally, surgical skills and experience
may impact outcomes, and future studies should consider
this factor.
Conclusion
ROS-RAL OMA surgery offers significantly favorable
long-term outcomes in preserving ovarian function in OMA
patients and positively impacts reducing postoperative cyst
recurrence. Larger, multicenter studies are recommended to
further validate these findings.
Supplementary Information The online version contains
supplementary material available at h t t p s : / / d o i . o r g / 1 0 . 1 0 0 7 / s 1 1 7 0 1 - 0
2 5 - 0 3 0 8 9 - 4.
Acknowledgements
The authors sincerely thank the clinical and
research staff of Jeonbuk National University Hospital for their assis -
tance and contributions to this study.
Author contributions Conceptualization and Methodology: CL, GHC,
MDW. Investigation and Formal analysis: MDW, CKZ. Visualization
and Writing - Original Draft: CL, GHC, MDW. Supervision and Proj-
ect administration: STH, HSC. Funding acquisition: HSC. Writing -
Review & Editing: all authors.
Funding This paper was supported by Fund of Biomedical Research
Institute, Jeonbuk National University Hospital.
Data availability Data can be made available upon reasonable request
to the corresponding author.
Declarations
Competing interests The authors declare no competing interests.
Ethics approval and consent to participate This study adheres to the
principles of the Declaration of Helsinki and has received approval
from the Ethics Committee of Jeonbuk National University in Korea
(Ethics Approval Number: 2024-08-037-004).
Consent for publication Not applicable.
we developed a novel OMA surgical method, termed ROS-
RAL, which has demonstrated a dramatic improvement in
the preservation of ovarian reserve and function. In ROS-
RAL OMA surgery, hemostasis in the vascular-rich ovarian
stroma, where the OMA is removed, is achieved through
meticulous interrupted suturing to reapproximate the incised
ovary. Unlike previous cauterization or suturing methods,
where hemostasis is harshly achieved through forcible tech-
niques causing ischemic damage, hemostasis in ROS-RAL
surgery is passively achieved by interrupted suturing of the
incised ovarian stroma. The reapproximation of the incised
ovarian stroma by interrupted suturing in ROS-RAL surgery
provides sufficient hemostasis and allows the natural clo -
sure of the incised ovarian cortex. Overzealous hemostasis
using energy devices can lead to thermal spread, resulting
in ischemic damage to the inner ovarian stromal connec -
tive tissue that contains ovarian follicles. The ROS-RAL
technique allows for targeted and precise suture ligation
of bleeding sites, preventing unnecessary devasculariza -
tion and destruction of normal ovarian tissue, optimizing
the restoration of ovarian blood supply, and thereby better
preserving ovarian reserve. Considering that targeted sutur-
ing on connective tissues such as stroma, widely adopted in
general surgery, has been shown to be effective for hemo -
stasis, it is not surprising that the reapproximation of the
incised ovarian stroma achieves sufficient hemostasis in the
ROS-RAL surgical method.
The most unique aspect of ROS-RAL OMA surgery is
its use of targeted interrupted sutures on the incised ovar -
ian stroma to achieve hemostasis through reapproximation
of the incised ovarian stroma. This method reapproximates
the incised ovarian stroma, allowing the ovarian cortex to
close naturally and the incised ovary to heal gradually. This
approach minimizes trauma to ovarian tissue and optimizes
postoperative restoration of ovarian blood supply, thereby
more effectively preserving ovarian reserve. Our study dem-
onstrated that ROS-RAL OMA surgery was significantly
more effective in preserving ovarian reserve in patients with
OMA compared to current OMA surgical methods. The
ROS-RAL OMA group exhibited significantly higher AMH
levels at all postoperative time points (1, 12, and 36 months)
(Table 2) compared to the CL group, with a notably lower
rate of AMH decline. Furthermore, the incidence of DOR at
the 36-month follow-up was significantly lower in the RAL
group than in the CL group (27.54% vs. 44.71%, P = 0.028)
(Table 3). In addition, the study explored factors influenc -
ing postoperative DOR and identified that age, bilateral
endometriomas, the CL surgical platform, and preoperative
AMH levels were associated with DOR incidence (Table 4).
Notably, during the 36-month postoperative follow-up, five
patients in the CL group experienced a recurrence of OMA,
resulting in a recurrence rate of 5.88%. In contrast, no cases
1 3
138 Page 8 of 10
Journal of Robotic Surgery (2026) 20:138
17. Bankar GR, Keoliya A (2022) Robot-Assisted surgery in gynecol-
ogy. Cureus 14(9):e29190
18. Brudie LA et al (2012) Peri-operative outcomes of patients with
stage IV endometriosis undergoing robotic-assisted laparoscopic
surgery. J Robot Surg 6(4):317–322
19. Lee J, Hong DG (2022) Serum anti-Müllerian hormone recovery
after ovarian cystectomy for endometriosis: A retrospective study
among Korean women. Med (Baltim) 101(40):e30977
20. Falcone T, Flyckt R (2018) Clinical management of endometrio-
sis. Obstet Gynecol 131(3):557–571
21. Goudakou M et al (2012) Cryptic sperm defects May be the
cause for total fertilization failure in oocyte donor cycles. Reprod
Biomed Online 24(2):148–152
22. Prapas Y et al (2017) GnRH antagonist administered twice the
day before hCG trigger combined with a step-down protocol May
prevent OHSS in IVF/ICSI antagonist cycles at risk for OHSS
without affecting the reproductive outcomes: a prospective ran -
domized control trial. J Assist Reprod Genet 34(11):1537–1545
23. Gullo G et al (2023) Assisted reproductive techniques and risk
of congenital heart diseases in children: a systematic review and
Meta-analysis. Reprod Sci 30(10):2896–2906
24. Burgio S et al (2022) Psychological variables in medically
assisted reproduction: a systematic review. Prz Menopauzalny
21(1):47–63
25. Gullo G et al (2015) Myo-inositol: from induction of ovula -
tion to menopausal disorder management. Minerva Ginecol
67(5):485–486
26. Laganà AS et al (2022) Does Alpha-lipoic acid improve effects
on polycystic ovary syndrome? Eur Rev Med Pharmacol Sci
26(4):1241–1247
27. Coldebella D et al (2023) Inositols administration: further insights
on their biological role, vol 35. ITALIAN JOURNAL OF GYN -
AECOLOGY & OBSTETRICS, pp 30–36. 01
28. Younis JS, Ben-Ami M, Ben-Shlomo I (2015) The Bologna crite-
ria for poor ovarian response: a contemporary critical appraisal. J
Ovarian Res 8:76
29. Busacca M et al (2006) Postsurgical ovarian failure after laparo -
scopic excision of bilateral endometriomas. Am J Obstet Gynecol
195(2):421–425
30. Benaglia L et al (2010) Rate of severe ovarian damage following
surgery for endometriomas. Hum Reprod 25(3):678–682
31. Li CZ et al (2009) The impact of electrocoagulation on ovarian
reserve after laparoscopic excision of ovarian cysts: a prospective
clinical study of 191 patients. Fertil Steril 92(4):1428–1435
32. Hwu YM et al (2011) The impact of endometrioma and lapa -
roscopic cystectomy on serum anti-Müllerian hormone levels.
Reprod Biol Endocrinol 9:80
33. Zhang CH, Wu L, Li PQ (2016) Clinical study of the impact on
ovarian reserve by different hemostasis methods in laparoscopic
cystectomy for ovarian endometrioma. Taiwan J Obstet Gynecol
55(4):507–511
34. Wang Y et al (2019) Effect of laparoscopic endometrioma cystec-
tomy on anti-Müllerian hormone (AMH) levels. Gynecol Endo -
crinol 35(6):494–497
35. Moreno-Sepulveda J et al (2022) The effect of laparoscopic
endometrioma surgery on Anti-Müllerian hormone: A systematic
review of the literature and Meta-Analysis. JBRA Assist Reprod
26(1):88–104
36. Haghgoo A et al (2021) Increasing trend of serum antimullerian
hormone level after long term follow up of endometrioma resec -
tion. J Endometr Pelvic Pain Disorders 13(2):98–103
Publisher’s note Springer Nature remains neutral with regard to juris-
dictional claims in published maps and institutional affiliations.
Open Access This article is licensed under a Creative Commons
Attribution-NonCommercial-NoDerivatives 4.0 International License,
which permits any non-commercial use, sharing, distribution and
reproduction in any medium or format, as long as you give appropri -
ate credit to the original author(s) and the source, provide a link to the
Creative Commons licence, and indicate if you modified the licensed
material. You do not have permission under this licence to share
adapted material derived from this article or parts of it. The images or
other third party material in this article are included in the article’s Cre-
ative Commons licence, unless indicated otherwise in a credit line to
the material. If material is not included in the article’s Creative Com -
mons licence and your intended use is not permitted by statutory regu-
lation or exceeds the permitted use, you will need to obtain permission
directly from the copyright holder. To view a copy of this licence, visit
h t t p : / / c r e a t i v e c o m m o n s . o r g / l i c e n s e s / b y - n c - n d / 4 . 0 /.
References
1. Koninckx PR et al (2021) Pathogenesis based diagnosis and treat-
ment of endometriosis. Front Endocrinol (Lausanne) 12:745548
2. Yılmaz Hanege B, Güler Çekıç S, Ata B (2019) Endometrioma
and ovarian reserve: effects of endometriomata per se and its sur-
gical treatment on the ovarian reserve. Facts Views Vis Obgyn
11(2):151–157
3. Fiorentino G et al (2023) Biomechanical forces and signals oper-
ating in the ovary during folliculogenesis and their dysregulation:
implications for fertility. Hum Reprod Update 29(1):1–23
4. Habib N et al (2022) Impact of lifestyle and diet on endometriosis:
a fresh look to a busy corner. Prz Menopauzalny 21(2):124–132
5. Muzii L et al (2018) Antimüllerian hormone is reduced in the
presence of ovarian endometriomas: a systematic review and
meta-analysis. Fertil Steril 110(5):932–940e1
6. Gullo G et al (2020) Closed vs. Open oocyte vitrification methods
are equally effective for blastocyst embryo transfers: prospective
study from a sibling oocyte donation program. Gynecol Obstet
Invest 85(2):206–212
7. De Paola L et al (2025) The era of increasing cancer survivor -
ship: trends in fertility preservation, medico-legal implications,
and ethical challenges. Open Med (Wars) 20(1):20251144
8. Singh SS, Suen MW (2017) Surgery for endometriosis: beyond
medical therapies. Fertil Steril 107(3):549–554
9. Busacca M, Vignali M (2009) Endometrioma excision and ovar -
ian reserve: a dangerous relation. J Minim Invasive Gynecol
16(2):142–148
10. Hart R et al (2005) Excisional surgery versus ablative surgery
for ovarian endometriomata: a Cochrane review. Hum Reprod
20(11):3000–3007
11. Busacca M et al (1999) Recurrence of ovarian endometrioma after
laparoscopic excision. Am J Obstet Gynecol 180(3 Pt 1):519–523
12. Dioun S et al (2021) Trends in the use of minimally inva -
sive adnexal surgery in the united States. Obstet Gynecol
138(5):738–746
13. V olodarsky-Perel A et al (2023) Robotic-assisted versus conven-
tional laparoscopic approach in patients with large rectal endo -
metriotic nodule: the evaluation of safety and complications.
Colorectal Dis 25(11):2233–2242
14. Nezhat CR et al (2015) Robotic-assisted laparoscopy vs conven -
tional laparoscopy for the treatment of advanced stage endome -
triosis. J Minim Invasive Gynecol 22(1):40–44
15. Alonzo L et al (2024) Magnetic Resonance Imaging of Endome -
triosis: The Role of Advanced Techniques. J Clin Med, 13(19)
16. Revised American fertility society classification of endometrio -
sis: 1985. Fertil Steril, (1985) 43(3): p. 351–352
1 3
Page 9 of 10 138
Journal of Robotic Surgery (2026) 20:138
Authors and Affiliations
Chuan Lin1,2,3,4,5 · Guihua Chen5 · Mingda Wang5,6 · Chongkai Zhai7 · Seong-Tshool Hong5,10 · Hee-Suk Chae1,8,9
Seong-Tshool Hong
[email protected]
Hee-Suk Chae
[email protected]
1 Department of Obstetrics and Gynecology, Jeonbuk National
University, Jeonju, Republic of Korea
2 Department of Obstetrics and Gynecology, Women and
Children’s Hospital of Chongqing Medical University,
Chongqing, China
3 Department of Obstetrics and Gynecology, Chongqing
Health Center for Women and Children, Chongqing, China
4 Chongqing Research Center for Prevention & Control of
Maternal and Child Diseases and Public Health, Chongqing,
China
5 Department of Biomedical Sciences, Institute for Medical
Science, Jeonbuk National University Medical School,
Jeonju, Republic of Korea
6 Department of Critical Care Medicine, Shandong Provincial
Hospital, Shandong First Medical University, Jinan, China
7 The Geographical Indication Medicines and Life Health
Engineering Research Center of Henan Province, Luoyang
Polytechnic, Luoyang, China
8 Research Institute of Clinical Medicine of Jeonbuk National
University- Biomedical Research Institute of Jeonbuk
National University Hospital, Jeonju, Republic of Korea
9 Department of Obstetrics and Gynecology, Biomedical
Research Institute, Research Institute of Clinical Medicine of
Jeonbuk National University, Jeonbuk National University
Hospital, Jeonbuk National University Medical School, 20,
Geonji-ro, Deokjin-gu, Jeonju 561-712, Jeonbuk, Republic of
Korea
10 Research Institute of Clinical Medicine, Jeonbuk National
University Medical School, 20, Geonji-ro, Deokjin-gu,
Jeonju 561-712, Jeonbuk, Republic of Korea
1 3
138 Page 10 of 10
Text is read by the "Ask this paper" AI Q&A widget below.
Extraction quality varies by source — PMC NXML preserves structure
cleanly, OA-HTML may include some navigation residue, and OA-PDF can
have broken hyphenation. The publisher copy
(via DOI)
is the canonical version.