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. 2025 Aug 19;17(16):2699. doi: 10.3390/cancers17162699

Safety and Efficacy of Transvaginal Natural Orifice Transluminal Endoscopic (vNOTES) Right Colectomy: A Systematic Review

Georgia Dimopoulou 1, Konstantinos Perivoliotis 2,*, Evangelos Lolis 3, Dimitrios Symeonidis 4, Konstantinos Tepetes 4, Ioannis Baloyiannis 4
Editor: Alain P Gobert
PMCID: PMC12385156  PMID: 40867328

Simple Summary

Currently, there is absence of pooled evidence regarding the overall morbidity, the postoperative recovery profile, and the oncological efficiency of vNOTES right colectomy. Our study highlighted an acceptable rate of overall and intraoperative complications of this technique. The efficacy of the approach has been highlighted on several efficiency markers, including the operation duration and the length of hospital stay.

Keywords: transvaginal, right, colectomy, notes, vaginal

Abstract

Background/Objectives: We aim to provide pooled data on the safety and efficacy of Transvaginal Natural Orifice Transluminal Endoscopic (vNOTES) right colectomy. Methods: This systematic review was conducted according to the Cochrane Handbook and the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines. The primary endpoint was the overall complication rate. Quality assessment was based on the NHLBI quality assessment tools. Results: Overall, six studies were included in this review. Overall morbidity rate was 21.9% (95% CI: 10.7–33.2%, p < 0.001), while intraoperative adverse events were noted in 19.9% (p < 0.001) of cases. Mean operation duration was 176.42 (p < 0.001) minutes. Overall hospital stay was 8.68 days (p = 0.002). Conclusions: Our analyses confirm the safety and efficacy of the approach. Given several study limitations, further large-scale and high-quality trials are required.

1. Introduction

1.1. Rationale

The advent of minimally invasive techniques marked a paradigm shift in surgical practice that resulted in improved cosmesis, reduced postoperative pain, and enhanced aspects of postoperative recovery [1,2,3]. In addition to laparoscopic and robotic surgeries, single-incision approaches were also described as a means of further minimizing total transabdominal entrance points to one [4,5].

Natural Orifice Translumenal Endoscopic Surgery (NOTES) is another alternative that is considered by many as the natural sequalae of single-incision techniques [6]. However, the combination of technical challenges and a steep learning curve have prohibited a wider adoption of NOTES [7,8].

Similarly, in the domain of colorectal surgery, natural orifice approaches have been utilized for specific procedural steps, such as dissection and specimen retrieval, or the completion of the operation in total [6,8,9]. Typical examples are the trans-anal total mesorectal excision (TaTME) and the transvaginal extraction of colectomy specimens (natural orifice specimen extraction (NOSE)) [6,7,10].

For female patients with right colonic pathology, transvaginal NOSE was shown in multiple reports to be a valid option for opting out of an abdominal incision, thus augmenting patient satisfaction and attenuating wound-related morbidity [11,12]. On the other hand, due to anatomical restrictions, alteration of the operative field of view, and single-port related loss of triangulation and instrument clashing, Transvaginal NOTES (vNOTES) right colectomy represents a major leap in terms of operative difficulty [9,13]. This is clearly depicted by the fact that the existing literature on vNOTES right colectomy largely comprises a relatively small number of case series and early feasibility studies, with varying methodologies and outcome measures [9,14,15]. Additionally, to the best of our knowledge, there is currently no pooled evidence regarding the overall morbidity, the postoperative recovery profile, or the oncological efficiency of this technique.

1.2. Aim

The present study aims to critically synthesize the current data regarding the safety and efficacy of vNOTES right colectomy, thereby elucidating the potential role of this approach in the surgical management of right-sided colonic pathology.

2. Materials and Methods

2.1. Study Protocol

This systematic review was conducted in accordance with the Cochrane Handbook and the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines [16,17].

The study protocol has been registered (https://doi.org/10.17605/OSF.IO/JEZX8).

2.2. Search Strategy

A comprehensive search strategy was applied across major databases to identify eligible studies. Screening was performed in PubMed, Scopus, and Cochrane databases from inception until March 2025. The following keywords were used, combined with Boolean logic nexuses:

“vaginal”, “transvaginal”, “natural orifice”, “notes”, “right colectomy”, “right colon”

Reference screening was also performed in the eligible articles.

2.3. Endpoints

The primary endpoint of our study was the overall complication rate. Secondary outcomes included specific intraoperative (i.e., hemorrhage, blood loss, bladder injury, conversion) and postoperative adverse events (hematoma, ileus, vaginal infection, bacteremia, anastomotic bleeding). Further analyses were performed in efficacy (operation duration, length of hospital stay, mobilization, and time to first flatus) and oncological (recurrence rates and lymph node yield) points of interest.

2.4. Eligibility and Exclusion Criteria

All human studies reporting on adult patients submitted to vNOTES right colectomy and providing data on outcomes of interest were considered as eligible.

The following exclusion criteria were considered: (1) non-human studies, (2) studies not reporting data on outcomes of interest, (3) pediatric population, (4) articles in the form of editorials, letters, or conference abstracts, and (5) studies in which transvaginal access was used for specimen extraction only (NOSE).

2.5. Quality Assessment

The methodology used to assess quality was structured around standardized checklists tailored to different study designs: case reports, prospective cohorts, and case series. For each type, a set of specific criteria was defined based on the National Heart, Lung, and Blood Institute (NHLBI) quality assessment tools. Each study was systematically evaluated against these criteria. This approach ensures a transparent and consistent evaluation of study quality, highlighting strengths and weaknesses in reporting and design.

2.6. Study Selection and Data Collection

After the completion of database screening, duplicate entries were removed. Following title and abstract screening, the remaining records were submitted to a full text review to evaluate consistency with the predefined eligibility criteria. Data extraction and quality assessment were performed independently and blindly by two reviewers (G.D. and I.B.). In the case of a discrepancy that was not resolved through mutual discussion, the opinion of a third reviewer (K.P.) was considered.

From the eligible studies, data regarding study characteristics (first author, date of publication, type of study, country, number of involved centers, study period, number of patients, body mass index (BMI), age, and follow up period), patient and tumor characteristics (previous operations, American Society of Anesthesiologists (ASA) score, Tumor Node Metastasis (TNM) status, and tumor location), and technical operative details (preoperative bowel preparation, patient position, pneumoperitoneum, access, number of trocars, anastomosis technique, approach, number of surgeons, and access closure) were extracted. Additionally, data regarding the prespecified outcomes were recorded.

2.7. Statistical Analysis

All statistical analyses were performed in IBM SPSS version 29 and Open Meta Analyst. Continuous and categorical data were provided as mean (standard deviation (SD)) and N, respectively. In the case that these were not provided, they were estimated from the respective data (median, range, interquartile range (IQR)), using the algorithm proposed by Hozo et al. [18]. Moreover, combined group means and SDs were calculated [16].

Pooled continuous outcomes were reported as mean, with the corresponding 95% confidence interval (95% CI). The effect size of binary outcomes was the raw proportion (RP), with the 95% CI. For the identification of publication bias, the respective funnel plot of the primary endpoint was provided.

Statistical analysis was based on the DerSimonian–Laird method. Heterogeneity was estimated through the calculation of I2, while Cochran Q test results confirmed the significance. The random-effect (RE) and fixed-effect (FE) models were applied based on the estimated significance. Statistical significance was considered at the level of p < 0.05.

3. Results

3.1. Search Results

An initial literature search (Figure 1) identified 869 records. After the removal of 310 duplicates, 559 titles and abstracts were screened. During the first screening step, 550 records (25 reviews and 525 irrelevant studies) were excluded. Subsequently, nine manuscripts were retrieved and underwent a full-text assessment. One study was excluded due to reporting on NOSE procedure, and two [13,14] for providing data on hybrid NOTES. Two studies were identified to be conducted in the same research center with similar methodology, as well as inclusion and exclusion criteria [15,19]. However, due to not totally overlapping study periods and the differences in patient characteristics, both were included. Overall, six studies [9,15,19,20,21,22] were included in this review.

Figure 1.

Figure 1

PRISMA flow diagram.

3.2. Study Characteristics

Overall, 49 patients that underwent vNOTES right colectomy were included in this review (Table 1). In total, five studies [15,19,20,21,22] were performed in a single institution, and one [9] in multiple centers. Most eligible studies reported on performed vNOTES right colectomies in the form of individual case reports or case series [20,21,22]. Study periods ranged from 2006 to 2024. BMI and age allocation of included patients is also provided in Table 1. Mean postoperative follow-up ranged from 1 to 60 months.

Table 1.

Main characteristics of the included studies.

First Author Publication Date Type of Study Country Single-/Multi-Center Study Period Number of Patients BMI Age Follow Up (Months)
Seow-en et al. 2024 case report Singapore single 2024 1 32 (0) 59 (0) 60 (0)
Xiao et al. 2023 retrospective China single 2019–2022 30 22 (3.1) n/a n/a
Song et al. 2021 case report China single 2021 1 18.4 (0) 65 (0) 1 (0)
Xiao et al. 2021 prospective China single 2018–2020 12 n/a 70 (7.5) 30 (0)
Bullian et al. 2014 prospective Germany multi 2008–2013 4 26 (2.75) 63.5 (5.5) n/a
Burghardt et al. 2008 case report Germany single 2008 1 22 (0) 66 (0) n/a

Data regarding further patient and tumor characteristics are also provided in Appendix A Table A1 and Table A2. In terms of technical characteristics, all procedures were performed in the lithotomy position, with a pneumoperitoneum pressure ranging from 12 to 14 mmHg. All cases were performed laparoscopically, and multiple transvaginal single-access ports were used. Significant heterogeneity was noted in terms of the number of transvaginal trocars. The use of abdominal accessory trocars was reported in two studies. Dissection was performed in a medial to lateral or an inferior to superior approach. Both intracorporeal and extracorporeal anastomoses were described. Information regarding the number of operating surgeons and experience was scarce. In all reported cases, the access closure was performed with direct suturing.

3.3. Quality Assessment

A structured quality assessment (Appendix A Table A3, Table A4 and Table A5) was conducted using standardized checklists tailored to the respective study design—case report or prospective cohort. Among the case reports, one study [22] achieved a perfect score of 100%, while the rest demonstrated acceptable-quality grades (87.5%). For cohort studies, quality scores ranged from 78.6% to 85.7%.

3.4. Primary Outcomes

The pooled complication rate of vNOTES right colectomy (Table 2, Figure 2) was 21.9% (95% CI: 10.7–33.2.0%, p < 0.001). No significant heterogeneity was noted (I2 = 0%). The effect of each study was evaluated through a leave-one-out analysis (Appendix A Figure A1). The pooled estimate ranged from 21.1% (Xiao et al. 2021 [15]) to 25% (Xiao et al. 2023 [19]). Statistical significance of the pooled results and the heterogeneity levels were retained in all cases, respectively.

Table 2.

Statistical analysis results of primary and secondary outcomes. Model results and heterogeneity.

Model Metric Estimate Lower Bound Upper Bound Std. Error p-Value Tau2 Q Het. p-Value I2
Primary outcome
Overall Complications BF-E Proportion 0.219 0.107 0.332 0.05 <0.001 0 0.18 0.99 0
Secondary outcome
Intraoperative Complications BF-E Proportion 0.199 0.094 0.303 0.053 <0.001 0 3.19 0.67 0
Intraoperative Hemorrhage BF-E Proportion 0.097 0.02 0.175 0.04 0.014 0 2.691 0.747 0
Intraoperative Blood Loss (mL) CF-E Mean 29.9 26.42 33.57 1.826 <0.001 0 0.001 0.972 0
Intraoperative Bladder Injury BF-E Proportion 0.104 0.022 0.185 0.042 0.013 0 0.755 0.98 0
Conversion BF-E Proportion 0.053 −0.006 0.112 0.03 0.076 0 2.841 0.725 0
Hematoma BF-E Proportion 0.049 −0.008 0.106 0.029 0.093 0 1.851 0.869 0
Ileus BF-E Proportion 0.062 −0.032 0.155 0.048 0.196 0 1.406 0.843 0
Vaginal Infection BF-E Proportion 0.109 −0.016 0.234 0.064 0.088 0 0.744 0.946 0
Bacteremia BF-E Proportion 0.109 −0.016 0.234 0.064 0.088 0 0.744 0.946 0
Anastomotic Bleeding BF-E Proportion 0.062 −0.032 0.155 0.048 0.196 0 1.406 0.843 0
Recurrence BF-E Proportion 0.062 −0.032 0.155 0.048 0.196 0 1.406 0.843 0
Operation Duration (minutes) CF-E Mean 176.42 170.76 182.08 2.88 <0.001 0 1.348 0.510 0
Length of Hospital Stay (days) CR-E Mean 8.68 3.29 14.07 2.74 0.002 14.7 37.2 <0.001 97.3
Lymph Node Yield CR-E Mean 20.6 15.2 25.9 2.74 <0.001 14 13.8 <0.001 92.8

Figure 2.

Figure 2

Overall complication forest plot.

3.5. Secondary Outcomes

Similarly, the intraoperative complication rate (Appendix A Figure A2) was 19.9% (95% CI: 0.9–30.3%, p < 0.001). Of these, the most common was intraoperative bladder injury (Appendix A Figure A3), with an overall risk of 10.4% (95% CI: 2.2–18.5%, p = 0.013). Although significant hemorrhage (Appendix A Figure A4) was reported in 9.7% (95% CI: 2–17.5%, p = 0.014) of cases, the mean intraoperative blood loss (Appendix A Figure A5) was 29.9 mL (95% CI: 26.42–33.57 mL, p < 0.001). Conversion (Appendix A Figure A6) due to technical difficulties was required in 5.3% (95% CI: −0.6–11.2%, p = 0.076) of the procedures; however, this was not significant.

The pooled rates of specific postoperative complications, including hematoma (Appendix A Figure A7, 4.9% 95%CI: −0.8–10.6%, p = 0.093), ileus (Appendix A Figure A8, 6.2% 95%CI: −3.2–15.5%, p = 0.196), vaginal infection (Appendix A Figure A9, 10.9% 95%CI: −1.6–23.4%, p = 0.088), bacteremia (Appendix A Figure A10, 10.9% 95%CI: −1.6–23.4%, p = 0.088) and anastomotic bleeding (Appendix A Figure A11, 6.2% 95%CI: −3.2–15.5%, p = 0.196) did not reach statistical significance. Furthermore, an insignificant 6.2% (Appendix A Figure A12, 95%CI: −3.2–15.5%, p = 0.196) rate of tumor recurrence was estimated. Mean lymph node yield (Appendix A Figure A13) was 20.6 (95% CI: 15.2–25.9, p < 0.001).

Mean operation duration (Appendix A Figure A14) was 176.42 min (95% CI: 170.76–182.08, p < 0.001). The reported overall mean hospital stay (Appendix A Figure A15) was 8.68 days (95% CI: 3.29–14.07, p < 0.001). Data regarding patient mobilization and the time to first flatus were scarce and, thus, no further analysis was performed. More specifically, patients mobilized at 18 to 24 h; while regarding the latter, first flatus was achieved at 24 to 40 h postoperatively.

3.6. Publication Bias

To evaluate potential publication bias, we generated the primary outcome funnel plot (Figure 3). Visual inspection of the plot revealed a symmetrical distribution of the eligible studies, thus minimizing the risk of publication bias.

Figure 3.

Figure 3

Overall complication funnel plot.

4. Discussion

The description of NOTES further pushed the boundaries of minimally invasive colorectal surgery [13,14,15]. Due to its elasticity, expedited healing, and optimal cosmesis, the transvaginal route was initially used for specimen retrieval, thus abolishing the need for transabdominal incisions [11,12]. Further evolvement of this conception was vNOTES, in which mobilization, vessel ligation, and colonic transection are performed through the vagina [11,12].

To introduce the camera and the working instruments during vNOTES, a transvaginal single-port device is utilized [15]. However, due to the proximity and the interference between ports, dissection is impeded [15]. Another important technical difficulty is the differentiation of the surgical visualization compared to in other minimally invasive modalities [15]. In laparoscopic, single-incision, and robotic approaches, a top-down view of the surgical field is achieved; however, in vNOTES, the camera is inserted from a lower pivotal point, thus resulting in a horizontal view. Subsequently, for a complete mesocolic excision to be performed, alteration of the dissection strategy may be required [21,22].

It becomes apparent that the safety of vNOTES right colectomy should be carefully examined prior to its widespread adoption. We estimated a pooled overall complication rate of vNOTES right colectomy of 21.9%, with bladder injury being the most common. In an 8257-patient meta-analysis, Solaini et al. [23] compared the two most prominent minimally invasive techniques for right colonic surgery and estimated the mean morbidity rates of the laparoscopic and robotic approaches to be 23.4% and 21.4%, respectively.

To tackle the previously mentioned technical difficulties, and to facilitate proper exposure of the embryological planes, assistant ports or hybrid vNOTES approaches may be utilized [15]. However, in some cases, this may not be achieved, and a standard laparoscopic or open conversion may be required. Our pooled analysis estimated an insignificant 5.3% overall conversion rate of vNOTES. Comparably, according to previous publications, the conversion rate of single-incision right colectomy may reach the level of 7.4% [23].

Early publications raised significant concerns regarding the morbidity related to intra-abdominal bacterial seeding from the opening of a natural orifice during NOTES [13]. However, in a recent systematic review by Li et al. [24], these risks were shown to be minimal. Similarly, in a feasibility cohort by Xiao et al. [15], one patient out of twelve developed vaginal discharge, and one developed bacteremia. We calculated the pooled vaginal complications of vNOTES right colectomy to be non-significant, at 10.9%.

Even though operative time can be affected by multiple parameters, including case complexity, technical competency, and theater personnel coordination, it still is one of the most important efficacy metrics, with a direct impact on clinical and logistic outcomes [25]. In a network meta-analysis by Rausa et al. [26], the mean operative times between the different minimally invasive approaches were not significantly different. Interestingly, Liu et al. [27] reported that single-incision techniques required a mean 129 to 217 min, 23.49 min shorter compared to standard laparoscopic right colectomies. We estimated that the mean operation duration of vNOTES right colectomy was 176.42 min. Although we did not perform pairwise comparisons with other modalities, the estimated effect size is within the reported range from other publications.

The adoption of the ERAS protocols promoted the enhancement of postoperative recovery, thus increasing patient satisfaction and minimizing of hospitalization costs [28]. Minimization of incisions is among the various technical interventions described in these protocols [28]. In other minimally invasive techniques for right colectomy, the first flatus landmark is achieved at 2.3–3.3 days postoperatively, and patients are discharged after 5.8–6.1 days [29]. Regarding vNOTES, due to lack of data, pooled evidence could not be provided.

In terms of oncological efficacy, we estimated that the average lymph node yield of vNOTES colectomy was 20.06. In addition to this, the estimated recurrence rate during the analyzed follow-up was 6.2%; however, this was not statistically significant. These results are consistent with the current literature regarding the oncological endpoints of minimally invasive right colectomies. More specifically, in a systematic review by Apostolou et al. [30], the number of harvested lymph nodes in single-incision right colectomy was 19.2. Similarly, Stipa et al. [11] estimated that, following laparoscopic NOSE colorectal resections, the mean lymph node yield was 12, with no evidence of disease recurrence. The oncological efficacy of transvaginal approaches was further confirmed in the meta-analysis by Chang et al. [31]. In this study, transvaginal and transabdominal specimen extraction displayed similar 2- and 3-year disease free survival, with no reports of pelvic or vaginal seeding.

The main advantage of the vNOTES approach is minimization of the need for a transabdominal incision. Through a posterior colpectomy and a single-port device, functional access to the abdominal cavity is installed [15]. In pure vNOTES, the entire operation is performed through the single-port device, whereas, in hybrid techniques, only certain procedural steps are completed transvaginally [13,14]. The importance of these lies to the extent of the required abdominal incision. In the former, no transabdominal access is utilized, whereas, in the latter, standard laparoscopic ports may be inserted. The reduction in the cumulative length of a surgical wound is important due to multiple reasons. First, due to the association between surgical injury and the inflammatory cascade, a decrease in incision length directly improves multiple clinical parameters [32]. Second, reducing the length of the incision promotes cosmesis, increases patient satisfaction, and enhances patient well-being [33]. Finally, transabdominal incisions are associated with significant complications, such as the development of infection, seroma, wound dehiscence, and incisional hernias that may eventually require reoperation [34]. Therefore, by utilizing a natural orifice access, the risk for such adverse events is avoided.

Another sequalae of abdominal wounds is postoperative pain [33]. Through laparoscopic and robotic resections, incision wounds were minimized to port placement and specimen extraction, thus decreasing postoperative pain compared to open resections [26]. Less pain translates to earlier mobilization, better functional recovery, reduced risk for respiratory compromise, and overall patient acceptance [33]. The use of the vaginal natural orifice to either extract the specimen or complete the operation would theoretically abate postoperative pain scores. In a prospective randomized controlled trial by Leung et al. [35], hybrid NOTES colectomy for left-side tumors had significantly lowered maximum pain scores during the first week, compared to conventional laparoscopic colectomy. Moreover, in a meta-analysis by He et al. [36], NOSE application in colorectal resections led to reductions in postoperative pain and prescribed analgesics. In our review, pooled postoperative pain estimates were not provided, due to the scarcity of data. Visual analog scale scores during the first postoperative days were reported in some cases and never exceeded the 4-point threshold.

Furthermore, concerns regarding sexual function and long-term pelvic floor outcomes remain insufficiently addressed. Most eligible records were case series and prospective or retrospective cohorts, with no distinct methodology for the assessment of these respective endpoints with objective or patient-reported validated tools. Therefore, until more evidence is available, careful patient selection and informed consent remain critical for incorporating this novel technique into clinical practice.

Optimal patient selection is of paramount importance when attempting to introduce vNOTES for the management of colorectal tumors. In addition to general and colorectal-specific medical history, the attending physician should also evaluate, in detail, the patient’s gynecological history [14]. According to a 2021 consensus [37] on the safe implementation of vNOTES, several exclusion criteria were proposed, including history of rectovaginal endometriosis and severe pelvic inflammatory disease. Additionally, history of pelvic radiotherapy was also suggested as an important factor for not implementing vNOTES [37]. On the other hand, the consensus statement did not identify nulliparity, previous caesarian section, or high BMI as contraindications for vNOTES [38]. In a cohort study by Park et al. [14], in which a hybrid vNOTES right colectomy was performed, bulky tumors > 5 cm, severe pelvic adhesions, history of endometriosis, and patients at child-bearing age were excluded. The rationale was that vaginal narrowing might prohibit the establishment of peritoneal access and specimen removal, while extensive pelvic adhesions increase the risk for adjacent organ injury [14]. Similar criteria were also used by Xiao et al. [15], who suggested a 6 cm tumor size cut-off.

Finally, another important consideration is the learning curve and technical prerequisites of vNOTES right colectomy. Surgeons require advanced laparoscopic skills and experience with Natural Orifice Transluminal Endoscopic Surgery (NOTES) techniques, which may limit the procedure’s widespread adoption [38,39]. As shown in various settings, reaching proficiency in NOTES requires the performance of a significant number of cases [40,41]. In terms of colorectal surgery, data is notably inconsistent [42]. For instance, in a review by Lau et al. [42], the number of procedures required to reach stabilization of the TaTME learning curve ranged from 5 to 140 cases. Additionally, evidence for the vNOTES right colectomy learning curve is currently scarce. More specifically, in our study, the number of experienced operating surgeons was not systematically reported.

Strengths

This systematic review is the first to provide overall estimates for vNOTES right colectomy performance. Our analyses assessed multiple clinical parameters that represent aspects of safety, perioperative efficiency, and oncological efficacy. The utilization of a standardized methodology allowed us to combine the data from the current literature reports and provide an accurate overall estimate on these endpoints. These indicators could act as guidance for clinicians evaluating the potential role of vNOTES techniques in right colon cancer. Finally, our review highlighted the lack of evidence in several clinical parameters, thus promoting further research in this field.

Limitations

Prior to the appraisal of our results, several study limitations should be considered. First, most trials reporting on vNOTES right colectomy were either individual case reports or cohort studies, with minimal sample sizes. Subsequently, the lack of blinding in assessing outcomes alongside specific methodology deficits significantly impacts the overall quality of evidence. Additionally, it was noted that there was no standardization of the approach, with multiple variances in the applied technique, thus reducing the reproducibility of our results. Moreover, the discrepancies in terms of patient and underlying pathology characteristics further reduce the ability to extrapolate our findings to a wider surgical population. In addition, despite a thorough assessment of the included studies, two of them were conducted in the same research center during partially overlapping periods, thus posing the risk of duplicate data. Furthermore, the lack of systematic long-term follow-up could possibly impact the results of oncological endpoints. Similarly, the absence of comparative data does not allow us to safely reach conclusions regarding the performance of vNOTES over other traditional minimally invasive techniques. Finally, surgical outcomes are significantly affected by the experience of the surgeons, and, thus, insufficient relevant data may lead to unsafe conclusions.

5. Conclusions

To the best of our knowledge, this study is the first attempt to provide pooled evidence regarding the safety and efficacy of vNOTES right colectomy. Our study highlighted an acceptable rate of overall and intraoperative complications. Additionally, the results of our analyses on several efficiency markers, including the operation duration, the length of hospital stay, and postoperative recovery endpoints, validated the efficacy of the approach. However, due to several study limitations, further high-quality trials are required to standardize the surgical technique and provide comparative data with other minimally invasive approaches.

Abbreviations

The following abbreviations are used in this manuscript:

NOTES Natural Orifice Translumenal Endoscopic Surgery
TaTME Trans-Anal Total Mesorectal Excision
NOSE Natural Orifice Specimen Extraction
vNOTES Transvaginal NOTES
PRISMA Preferred Reporting Items for Systematic Reviews and Meta-Analyses
NHLBI National Heart, Lung, And Blood Institute
SD Standard Deviation
IQR Interquartile Range
95% CI 95% Confidence Interval
RP Raw Proportion
RE Random Effects
FE Fixed-Effect
CF-E Continuous Fixed-Effect
CR-E Continuous Random-Effect
BF-E Binary Fixed-Effect
n/a Not Applicable
BMI Body Mass Index
ASA American Society of Anesthesiologists
TNM Tumor Node Metastasis

Appendix A

Table A1.

Patient and Tumor Characteristics.

First Author Previous Abdominal Operations ASA T N M Tumour Location
I II III Tis 1 2 3 4 0 1 2 0 Cecum/Ascending Hepatic Flexure/ Transverse Tumor Size (cm)
Seow-en et al. 0 0 1 0 1 0 1 0 1 1 0 3
Xiao et al. n/a n/a n/a n/a n/a n/a
Song et al. 0 0 1 0 0 1 0 1 0 0 1 0 2.5 (0)
Xiao et al. n/a 10 2 0 1 2 1 2 3 8 4 0 5 n/a n/a 6.75 (1.5)
Bullian et al. n/a 1 1 2 n/a n/a n/a n/a n/a n/a n/a n/a n/a n/a n/a n/a
Burghardt et al. 1 0 1 0 0 1 0 1 1 0 n/a

Table A2.

Operative Technique Characteristics.

First Author Bowel Preparation Position Pneumoperitoneum (mmHg) Access Laparoscopic/Robotic Trocar Anastomosis Approach Number of Surgeons Access Closure
Abdominal Vaginal
Seow-en et al. no lithotomy & trendelenburg 12 wound protector & glove lap 1 4 intracorporeal antiperistaltic stapled side-to-side inferior to superior direct suture
Xiao et al. n/a lithotomy 14 Single Port Access System HTKD Medical™ lap 0 5 intracorporeal stapled antiperistaltic side-to-side caudal n/a n/a
Song et al. mechanical & oral antibiotics lithotomy & trendelenburg n/a StarPort™ lap 0 3 extracorporeal stapled end-to-side caudal n/a direct suture
Xiao et al. n/a lithotomy 14 Single Port Access System HTKD Medical™ lap 0 5 intracorporeal stapled antiperistaltic side-to-side caudal n/a n/a
Bullian et al. n/a n/a n/a n/a lap n/a n/a n/a n/a n/a direct suture
Burghardt et al. n/a lithotomy n/a 12mm trocar lap 2 1 intracorporeal stapled side-to-side n/a n/a n/a

Table A3.

Quality Assessment Checklist for Case Reports.

Seow-en et al.
(2024)
Song et al.
(2021)
Burghardt et al.
(2008)
Q1. Were the patient’s demographic
characteristics clearly described?
YES NO NO
Q2. Was the patient’s history clearly described
and presented as a timeline?
YES YES YES
Q3. Was the current clinical condition of the
patient clearly described?
YES YES YES
Q4. Were diagnostic tests or assessment methods and the results clearly described? YES YES YES
Q5. Was the intervention(s) or treatment procedure(s) clearly described? YES YES YES
Q6. Was the post-intervention clinical condition clearly described? YES YES YES
Q7. Were adverse events (harms) or unanticipated events identified and described? YES YES YES
Q8. Does the case report provide takeaway lessons? YES YES YES

Table A4.

Quality Assessment Checklist for Cohorts.

Xiao et al.
(2023)
Xiao et al.
(2020)
Bullian et al.
(2014)
1. Was the research question or objective in this paper clearly stated? YES YES YES
2. Was the study population clearly specified and defined? YES YES YES
3. Was the participation rate of eligible people at least 50%? YES YES YES
4. Were all the subjects selected or recruited from the same or similar populations (including the same period)? Were inclusion and exclusion criteria for being in the study prespecified and applied uniformly to all participants? YES YES NO
5. Was sample size justification, power description, or variance and effect estimates provided? YES YES NO
6. For the analyses in this paper, were the exposure(s) of interest measured prior to the outcome(s) being measured? YES YES YES
7. Was the timeframe sufficient so that one could reasonably expect to see an association between exposure and outcome if it existed? YES YES YES
8. For exposures that can vary in amount or level, did the study examine different levels of exposure as related to the outcome (e.g., categories of exposure, or exposure measured as continuous variable)? YES YES YES
9. Were the exposure measures (independent variables) clearly defined, valid, reliable, and implemented consistently across all study participants? YES YES YES
10. Was the exposure(s) assessed more than once over time? NO NO NO
11. Were the outcome measures (dependent variables) clearly defined, valid, reliable, and implemented consistently across all study participants? YES YES YES
12. Were the outcome assessors blinded to the exposure status of participants? YES YES NO
13. Was loss to follow-up after baseline 20% or less? NO NO NO
14. Were key potential confounding variables measured and adjusted statistically for their impact on the relationship between exposure(s) and outcome(s)? YES YES YES

Table A5.

Quality Assessment Scores.

Study Study Type Total Items Assessed Items Answered “Yes” Quality Score (%)
Seow-en et al. (2024) Case Report 8 8 100
Song et al. (2021) Case Report 8 7 87.5
Burghardt et al. (2008) Case Report 8 7 87.5
Xiao et al. (2020) Cohort 14 12 85.7
Xiao et al. (2023) Cohort 14 12 85.7
Bullian et al. (2014) Cohort 14 11 78.6

Figure A1.

Figure A1

Leave one out analysis of the primary outcome.

Figure A2.

Figure A2

Intraoperative Complications Forest Plot.

Figure A3.

Figure A3

Intraoperative Bladder Injury Forest Plot.

Figure A4.

Figure A4

Intraoperative Hemorrhage Forest Plot.

Figure A5.

Figure A5

Intraoperative Blood Loss (mL) Forest Plot.

Figure A6.

Figure A6

Conversion Forest Plot.

Figure A7.

Figure A7

Postoperative Hematoma Forest Plot.

Figure A8.

Figure A8

Postoperative Ileus Forest Plot.

Figure A9.

Figure A9

Postoperative Vaginal Infection Forest Plot.

Figure A10.

Figure A10

Postoperative Bacteremia Forest Plot.

Figure A11.

Figure A11

Postoperative Anastomotic Bleeding Forest Plot.

Figure A12.

Figure A12

Recurrence Forest Plot.

Figure A13.

Figure A13

Lymph Node Yield Forest Plot.

Figure A14.

Figure A14

Operation Duration (minutes) Forest Plot.

Figure A15.

Figure A15

Length of Hospital Stay (days) Forest Plot.

Author Contributions

Conceptualization, G.D. and K.P.; data curation, G.D., K.P. and E.L.; writing—original draft preparation, G.D., K.P. and E.L.; writing—review and editing, D.S. and K.T.; supervision, D.S., I.B. and K.T.; project administration, I.B. All authors have read and agreed to the published version of the manuscript.

Conflicts of Interest

The authors declare no conflicts of interest.

Funding Statement

This research received no external funding.

Footnotes

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