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. 2025 Apr 8;29(1):98. doi: 10.1007/s10151-025-03141-3

Robotic-assisted versus laparoscopic surgery for colorectal cancer in high-risk patients: a systematic review and meta-analysis

S Gahunia 1,✉,#, J Wyatt 1,2,#, S G Powell 1,2, S Mahdi 1, S Ahmed 1, K Altaf 1
PMCID: PMC11978707  PMID: 40198499

Abstract

Background

Evidence of superiority of robotic-assisted surgery for colorectal resections remains limited. This systematic review and meta-analysis aims to compare robotic-assisted and laparoscopic surgical techniques in high-risk patients undergoing resections for colorectal cancer.

Methods

Systematic searches were performed using Pubmed, Embase and Cochrane library databases from inception until December 2024. Randomised and non-randomised studies reporting outcomes of robotic-assisted or laparoscopic resections in the following high-risk categories were included: obesity, male gender, the elderly, low rectal cancer, neoadjuvant chemoradiotherapy and previous abdominal surgery. Comparative meta-analyses for all sufficiently reported outcomes were completed. Risk of bias was assessed using the ROBINS-I and RoB 2 tools for non-randomised and randomised studies, respectively.

Results

48 studies, including a total of 34,846 patients were eligible for inclusion and 32 studies were utilised in the comparative meta-analyses. Conversion to open rates were significantly lower for robotic-assisted surgery in patients with obesity, male patients and patients with low rectal tumours (obese OR 0.41 [CI 0.32–0.51], p < 0.00001); male gender (OR 0.28 [CI 0.22–0.34], p < 0.00001); low tumours OR 0.10 [CI 0.02–0.58], p = 0.01). Length of stay was significantly reduced for robotic-assisted surgery in patients with obesity (SMD 0.25 [CI − 0.41 to − 0.09], p = 0.002). Operative time was significantly longer in all subgroups (obesity SMD 0.57 [CI 0.31–0.83], p < 0.0001; male gender SMD 0.77 [CI 0.17–1.37], p = 0.01; elderly SMD 0.50 [CI 0.18–0.83], p = 0.002; low rectal tumours SMD 0.48 [CI 0.12–0.84], p = 0.008; neoadjuvant chemoradiotherapy SMD 0.72 [CI 0.34–1.09], p = 0.0002; previous surgery SMD 1.55 [CI 0.05–3.06], p = 0.04). When calculable, blood loss, length of stay, complication rate and lymph node yield were comparable in all subgroups.

Conclusions

This review provides further evidence of non-inferiority of robotic-assisted surgery for colorectal cancer and demonstrates conversion rates are superior in specific, technically challenging operations.

Supplementary Information

The online version contains supplementary material available at 10.1007/s10151-025-03141-3.

Keywords: Robotic-assisted surgery, Obesity, Male gender, Conversion to open, Operative time

Introduction

Robotic-assisted surgery (RAS) has significantly impacted colorectal surgical management over the past two decades and has become established as a safe and viable alternative to laparoscopic surgery. RAS provides technical advantages including articulation of instruments, three-dimensional vision, remote operating and improved ergonomics [1, 2]. Its benefits over laparoscopic surgery have been widely documented in urological and gynaecological surgery [35]. In colorectal surgery, however, there is more limited evidence. The largest and most robust randomised control trial to date, the ROLARR trial, compared RAS with conventional laparoscopic surgery in patients undergoing rectal cancer resections [6]. This trial utilised conversion to open rates as the primary outcome and demonstrated the non-inferiority of RAS but no benefit. Subgroup analyses hinted at possible lower conversion rates for patients with obesity or male patients but the trial was not powered to detect significant differences in these patient groups. Considering the significant cost burdens [7] and barriers to training [8] associated with RAS, further evidence is required to clarify the benefits of this approach.

RAS may provide the most benefit in more technically challenging or high-risk operations. The following patient groups are independently associated with technical challenges or inferior outcomes in colorectal cancer resections and, as such, make up the subgroups of interest for this study: male gender [912], obesity [13], low rectal tumours [9, 11], neoadjuvant chemoradiotherapy [9, 11, 12], the elderly [10, 14] and patients with previous abdominal surgery [15, 16]. In male patients, the narrower anatomical pelvis provides more limited space for dissection during total mesorectal excision (TME). Similarly, limited space and poor visualisation are problems encountered in both low rectal tumours and patients with obesity. Neoadjuvant radiotherapy is associated with tissue oedema, fibrosis and scarring, and adhesion formation from previous abdominal surgery can alter dissection planes and is associated with a higher risk of iatrogenic injury. Elderly patients do not provide specific anatomical challenges but are at higher risk of significant comorbidities which impact perioperative physiology, tissue healing and recovery.

Whilst there are an increasing number of observational studies comparing robotic surgery to laparoscopic surgery in high-risk patients, randomised control trials are lacking. Therefore, the highest quality evidence will be provided by systematic review and meta-analysis of observational studies. Suwa et al. conducted a meta-analysis comparing outcomes in patients with and without obesity undergoing robotic colorectal surgery [17]. They concluded obesity is associated with a significantly longer operating time and an increased risk of conversion to open, in keeping with findings from laparoscopic surgery. No previous meta-analyses compare RAS to laparoscopic approaches in high-risk groups.

This review aims to perform a direct comparison of robotic-assisted versus laparoscopic surgery in high-risk patients to ascertain any benefit of RAS in addition to proving non-inferiority.

Methods

This systematic review has been reported according to the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines [18]. A prospective review protocol was registered with the International Prospective Register of Systematic Reviews (PROSPERO) database (registration no. CRD42022326555).

Search strategy

A systematic search was performed using Pubmed, the Cochrane Library and EMBASE databases. The following search algorithm was used for each database: (Robotic) AND (colorectal surgery OR rectal surgery) AND (high risk OR obese OR obesity OR male OR gender OR age OR elderly OR location OR tumour location OR low tumour OR chemoradiation OR radiation OR previous surgery OR abdominal surgery) AND (outcomes). Results were filtered to human studies published in the English language. The final searches took place no later than December 2024.

Eligibility criteria

Inclusion

All randomised and non-randomised studies which report original data on any outcome of robotic colorectal surgery in high-risk patients are included. The high-risk categories we identified are obesity, male gender, age > 65 years, low tumour location, previous chemoradiation and previous abdominal surgery. These categories were chosen after careful inspection of current data concerning the risk factors for complications in colorectal surgery [10, 19].

Exclusion

All studies published in languages other than English were excluded from this review. Case reports were excluded and studies with no comparison to either laparoscopic surgery or a corresponding lower-risk category were excluded.

Study selection and data extraction

Each article identified by the initial search was manually and independently screened, using the study title and abstract in reference to the eligibility criteria. Screened articles were then included in a full-text review to confirm final eligibility.

The primary outcome was conversion to open rate. Secondary outcomes included overall complication rate (all Clavien Dindo grades), estimated blood loss, length of stay, operative time, readmission rate and the lymph node yield.

Data was manually and independently extracted onto a prospectively designed database. Corresponding authors were contacted if necessary to provide clarity or further detail during data extraction. All non-randomised studies underwent bias analysis using the ROBINS-I tool [20] and the RoB 2 tool was used for randomised trials [21].

Statistical analysis

Meta-analyses are presented as Forest plots. For the pooling of dichotomous data, the Mantel–Haenszel method was used and results are presented as an odds ratio (OR) with a corresponding 95% confidence interval (CI). For continuous data, the inverse variance (IV) method was used and results are presented as a standardised mean difference (SMD) with 95% CI. Analysis was completed using a random-effects model. When original studies reported outcomes using a median and a range or interquartile range (IQR), mean and standard deviation (SD) was estimated using previously published methods [22, 23]. Review Manager v5.4 (RevMan) software (Cochrane Collaboration, Oxford, UK) was used for comparative meta-analyses. Pooled weighted meta-analyses (PWM) were calculated using a random-effects model and either the metaprop or metan commands in Stata v14 (Stata Corp) software for dichotomous and continuous data, respectively. Pooled weighted meta-analyses are presented with corresponding 95% confidence intervals.

Results

Study selection

A total of 1841 records were identified from database searches, Fig. 1. Title and abstract screening excluded 1329 irrelevant records. Full-text screening of 211 papers was completed and 162 studies were excluded for not meeting the eligibility criteria. 48 papers were eligible for inclusion in this review. In order to have comparable homogenous data, the 32 studies [2455] which performed a direct case-matched comparison of laparoscopic and robotic-assisted surgery in high-risk patients were included in comparative meta-analyses. The remaining 16 studies [6, 5670] comparing high-risk to lower-risk patients undergoing robotic-assisted surgery were included in pooled summary meta-analyses but not in the comparative meta-analyses.

Fig. 1.

Fig. 1

PRISMA diagram

Study characteristics

The included studies comprise 42 retrospective observational studies, four prospective cohort studies and two randomised control trials. The eligible studies include a total of 34,846 patients. A summary of study characteristics and their inclusion criteria is listed in Table 1.

Table 1.

Study characteristics

Author and year Type of study Site(s) of resection Inclusion criteria Total number Laparoscopic Robotic
Obesity
 Hellan 2014 Retrospective Rectal BMI > 30 126 0 126
 Keller 2015 Retrospective Rectal + colonic BMI > 30 68 0 68
 Lagares-Garcia 2015 Prospective Rectal + colonic BMI > 30 34 0 34
 Cardinali 2016 Retrospective Colonic BMI > 30 15 8 7
 Gorgun 2016 Retrospective Rectal BMI > 30 56 27 29
 Shiomi 2016 Retrospective Rectal VFA > 130 cm2 82 30 52
 Ackerman 2017 Retrospective PSM Rectal BMI > 30 130 66 64
 Baukloh 2017 Prospective Rectal BMI > 30 57 0 57
 Bayraktar 2017 Retrospective Rectal BMI > 30 30 0 30
 Jayne 2017 RCT Rectal BMI > 30 107 0 107
 Schootman 2017 Retrospective PSM Colonic BMI > 30 4404 3589 815
 Harr 2017 Retrospective Rectal + colonic BMI > 30 108 0 108
 Pai 2017 Prospective Rectal BMI > 30 33 0 33
 Duchalais 2018 Retrospective Rectal BMI > 30 58 0 58
 Panteleimonitis 2018 Retrospective PSM Rectal BMI > 30 124 61 63
 Peacock 2020 Retrospective Rectal BMI > 30 161 0 161
 Ozben 2021 Retrospective Colonic BMI > 30 42 0 42
 Hannan 2022 Retrospective Rectal + colonic BMI > 30 34 0 34
 Juang 2023 Retrospective PSM Rectal + colonic BMI > 40 1296 648 648
 Albayati 2022 Retrospective Rectal BMI > 30 2385 1824 561
 Glencer 2022 Retrospective Rectal BMI > 30 6722 4711 2011
 Zhao 2024 Retrospective PSM Rectal VFA > 100 cm2 242 121 121
Male
 Ackerman 2017 Retrospective PSM Rectal Male 614 311 303
 Baukloh 2017 Prospective Rectal Male 229 0 229
 Jayne 2017 RCT Rectal Male 317 0 317
 Serin 2015 Retrospective Rectal Male 79 65 14
 Schootman 2017 Retrospective PSM Colonic Male 6489 5259 1230
 Esen 2018 Retrospective Rectal Male 83 42 41
Elderly
 Fernandez 2013 Retrospective Rectal ≥ 65 years  72 59 13
 Ceccarelli 2017 Retrospective Rectal + colonic ≥ 65 years  38 0 38
 Oldani 2017 Retrospective Rectal + colonic ≥ 70 years  9 0 9
 De’Angelis 2018 Retrospective PSM Rectal + colonic ≥ 70 years  160 102 58
 Palomba 2021 Retrospective Rectal + colonic ≥ 65 years  83 51 32
 Srinath 2022 Retrospective Colonic ≥ 80 years  171 86 85
 Ali 2023 Retrospective Rectal ≥ 70 years  108 63 45
 Lu 2024 Retrospective Colonic ≥ 80 years  7550 7061 489
Low tumour location
 Park 2010 Retrospective Rectal 1–8 cm from AV 123 82 41
 Baek 2013 Retrospective Rectal Mean 5.5 cm from AV 84 37 47
 Park 2013 Retrospective Rectal Mean 3.5 cm from AV 80 40 40
 Kuo 2014 Retrospective Rectal 2–6 cm from AV 64 28 36
 Yoo 2015 Retrospective Rectal < 5 cm from AV 70 26 44
 Feng 2022 RCT Rectal < 5 cm from AV 347 173 174
Chemoradiotherapy
 Saklani 2013 Retrospective Rectal Chemoradiotherapy 138 64 74
 Serin 2015 Retrospective Rectal Chemoradiotherapy 79 65 14
 Kim 2016 Retrospective Rectal Chemoradiotherapy 99 66 33
 Huang 2017 Retrospective Rectal Chemoradiotherapy 78 38 40
 Chen 2021 Retrospective PSM Rectal Chemoradiotherapy 171 95 76
 Fiorenzo 2021 Prospective Rectal Chemoradiotherapy 102 64 38
 Morohashi 2022 Retrospective Rectal Chemoradiotherapy 55 0 55
 Yamanashi 2022 Retrospective PSM Rectal Chemoradiotherapy 60 30 30
Previous abdominal surgery
 Park 2017 Retrospective Rectal + colonic Previous open or laparoscopic procedure that invaded peritoneal space 850 612 238
 Huang 2020 Retrospective PSM Rectal Previous abdominal siurgery 32 0 32
 Milone 2021 Retrospective PSM All GI resections Previous open abdominal surgery 98 62 36
 Total 34,846 25,666 9180

PSM propensity score matching, RCT randomised control trial, BMI body mass index, VFA visceral fat area, AV anal verge, GI gastrointestinal

The included studies report on both rectal and colonic resections. 23 studies utilised in the comparative meta-analyses reported on surgery undertaken for rectal cancer only, and nine studies reported on segmental colectomies alone or both colonic and rectal resections. Given this confounding variable, a sensitivity analysis utilising only rectal resections has been completed for each meta-analysis. The results of sensitivity analyses are reported in each section and accompanying forest plots are presented in Fig. S1.

Only one randomised control trial (RCT) was used in the comparative meta-analyses for low rectal tumours. A further sensitivity analysis was undertaken without the RCT to ensure outcomes remained the same, which they did. The forest plots for these analyses are presented in Fig. S2.

Bias and quality analysis

All non-randomised studies selected for inclusion were screened for risk of bias with the ROBINS-I tool, Fig. 2. The two randomised control trials were assessed using the RoB 2 tool and found to be at low risk of bias. Overall, the included studies showed a moderate to high risk of bias, largely to due to the presence of confounding bias. Visual assessment of the funnel plots for each meta-analysis demonstrated no evidence of significant reporting bias.

Fig. 2.

Fig. 2

Risk of bias analysis. Diagrammatic representation of the risk of bias assessed using the ROBINS-I 2 tool from the Cochrane group, presented using the robvis tool

Obesity

Obesity was defined as a BMI greater than 30 or visceral fat area (VFA) > 100 cm2 in all studies in the meta-analyses. Ten case-matched studies reported on robotic-assisted versus laparoscopic surgery in patients with obesity and were included in the meta-analyses [24, 27, 31, 37, 42, 44, 4850, 55]. These studies included a total of 4371 robotic-assisted cases and 11,085 laparoscopic. Forest plots of select meta-analyses are presented in Fig. 3. All meta-analyses not presented in Fig. 3 can be found in Fig. S3.

Fig. 3.

Fig. 3

Forest plots. Forest plots representing the comparative meta-analyses of select outcomes. M-H Mantel–Haenszel, CI confidence interval, SD standard deviation

A meta-analysis including the seven studies which reported operative time found significantly longer operations using robotic-assisted surgery (SMD 0.57 [CI 0.31–0.83], p < 0.0001). Nine studies reported conversion-to-open rates, and meta-analysis demonstrated a significantly lower conversion rate in robotic-assisted surgery (OR 0.41 [CI 0.32–0.51], p < 0.00001). Six studies reported on length of stay, and meta-analysis suggested a reduced length of stay in patients undergoing robotic-assisted surgery (SMD 0.25 [CI − 0.41 to − 0.09], p = 0.002). Blood loss (SMD 0.23 [CI − 0.51 to 0.05], p = 0.11), overall complication rate (OR 0.96 [CI 0.81–1.14], p = 0.68), and lymph node yield (SMD 0.11 [CI − 0.07 to 0.28], p = 0.24) were comparable between groups.

A pooled weighted mean (PWM) of conversion to open rate was 7.6% [CI 5.2–10.1%] and was calculated utilising 21 studies reporting outcomes of robotic-assisted surgery in patients with obesity [6, 24, 27, 31, 37, 42, 44, 4850, 5666]. Table 2 presents all calculable PWMs for each outcome in each subgroup.

Table 2.

Pooled weighted means

Mean (%) 95% CI (%) Mean (mins) 95% CI (mins)
Conversion to open rate Operative time
 Obesity 7.6 5.2–10.1 Obesity 289 251–327
 Male gender 9.1 5.4–12.7 Male gender 271 117–425
 Elderly 5.7 1.3–10.2 Elderly 264 56–462
 Low rectal tumours NC NC Low rectal tumours 318 223–414
 Neoadjuvant chemoradiotherapy 5.6 0.7–11.8 Neoadjuvant chemoradiotherapy 348 256–441
 Previous abdominal surgery 0.5 0–1.3 Previous abdominal surgery 270 224–317
Mean (%) 95% CI (%) Mean (days) 95% CI (days)
Perioperative complication rate Length of stay
 Obesity 28 21.7–34.3 Obesity 6.5 4.2–8.8
 Male gender 19 5.4–32.7 Male gender 5.2 2.6–7.8
 Elderly 38.3 24.2–52.5 Elderly 9.8 5.4–14.2
 Low rectal tumours 22.0 14.3–29.7 Low rectal tumours 11.2 7.7–14.8
 Neoadjuvant chemoradiotherapy 26.8 17.1–36.4 Neoadjuvant chemoradiotherapy 10.3 6.7–13.9
 Previous abdominal surgery 15.1 0–32.7 Previous abdominal surgery 8.2 3.6–12.9

CI confidence interval, NC not calculable

On sensitivity analysis, looking at rectal resections alone, all outcomes remain the same.

Male gender

Four studies examined male gender as a high-risk factor and included a total of 934 robotic-assisted cases and 3762 laparoscopic cases [24, 29, 42, 43]. All but one of the studies looked at resections for rectal cancer alone, with the fourth study including all types of colectomies. There were no significant differences between the two groups with regards to complication rate (OR 1.09 [CI 0.91–1.30], p = 0.36) or length of stay (SMD 0.19 [CI − 0.51–0.13], p = 0.25). Operative time was again significantly longer in the robotic-assisted group (SMD 0.77 [CI 0.17–1.37], p = 0.01). However, conversion to open was significantly lower in the robotic-assisted group (OR 0.28 [CI 0.22–0.34], p < 0.00001), Fig. 3.

PWM conversion to open rate from five studies of robotic-assisted surgery in male patients [6, 24, 42, 43, 60] was 9.1% [CI 5.4–12.7%].

Sensitivity analysis of rectal resections alone did not alter the primary outcome but did alter operative time to be equivalent between the two groups (SMD 0.75 [CI − 0.70 to 2.19] p = 0.31) and length of stay then favoured RAS (SMD − 0.40 [CI − 0.75 to 0.06] p = 0.02).

Elderly

Six studies were eligible for inclusion in the comparative meta-analyses. The authors reported outcomes of robotic-assisted versus laparoscopic surgery in elderly patients, including a total of 722 robotic-assisted cases and 7422 laparoscopic [28, 30, 36, 45, 51, 54]. Definitions of elderly varied between studies, but all patients had a pooled mean age of 84.3 ± 2.3 years.

Operative time was significantly longer in the robotic-assisted group (SMD 0.50 [CI 0.18–0.83], p = 0.002). There was no difference between the two groups with regards to conversion to open (OR 0.28 [CI 0.07–1.11], p = 0.07), complication rate (OR 1.02 [CI 0.59–1.78], p = 0.94), length of stay (SMD 3.20 [CI − 10.45 to 4.06], p = 0.39), estimated blood loss (SMD 0.04 [CI − 0.29 to 0.22], p = 0.77) or lymph node yield (SMD 0.34 [CI − 0.78 to 0.10], p = 0.13).

PWM conversion to open rate from six studies of elderly patients undergoing robotic-assisted colorectal resections [28, 30, 36, 51, 67, 68] was 5.7% [CI 1.3–10.2%].

On sensitivity analysis of rectal resections alone, all outcomes remain the same with the exception of lymph node yield which was greater in laparoscopic surgery (OR 0.55 [CI − 0.94 to − 0.16], p = 0.006).

Low rectal tumour

Six studies looked at low rectal tumours, including 382 robotic-assisted cases and 386 laparoscopic [25, 34, 38, 40, 46, 52]. The pooled mean distance of the tumour from the anal verge was 4 ± 1.5 cm. Of the two studies that reported on conversion to open rates, these were found to be significantly lower in the robotic-assisted group (OR 0.10 [CI 0.02–0.58], p = 0.01).

Operative time was significantly longer in the robotic-assisted group (SMD 0.48 [CI 0.12–0.84], p = 0.008), Fig. 3. There was no difference between the two groups with regards to complication rate (OR 0.94 [CI 0.58–1.52], p = 0.81), estimated blood loss (SMD − 0.37 [CI − 0.89 to 0.15], p = 0.16), length of stay (SMD − 0.34 [CI − 0.87 to 0.18], p = 0.20) or lymph node yield SMD − 0.07 [CI − 0.34 to 0.19], p = 0.59).

When a robotic-assisted technique was used, only one patient from a pooled total of 338 from five studies required conversion to open for a low rectal cancer [25, 34, 38, 40, 52].

Neoadjuvant radiotherapy

Seven studies examined patients who had received long-course neoadjuvant chemoradiotherapy for low rectal cancer, with a total number of 305 robotic-assisted cases and 422 laparoscopic [26, 32, 33, 41, 43, 47, 53], Fig. 3. Operative time was significantly longer in the robotic-assisted group (SMD 0.72 [CI 0.34–1.09], p = 0.0002). There was no difference between the two groups with regards to conversion to open (OR 0.47 [CI 0.09–2.43], p = 0.37), complication rate (OR 1.10 [CI 0.66–1.81], p = 0.72), estimated blood loss (SMD 0.17 [CI − 0.74 to 0.40], p = 0.56), length of stay (SMD 0.07 [CI − 0.22 to 0.08], p = 0.36) or lymph node yield (SMD 0.18 [CI − 0.28 to 0.64], p = 0.44).

After neoadjuvant radiotherapy, PWM conversion to open rate from six studies [6, 33, 41, 43, 47, 53] was 5.6% [CI 0.7–11.8%].

All studies reported on rectal cancers only and, therefore, sensitivity analyses were not completed.

Previous abdominal surgery

Two studies looked at patients who had previous abdominal surgery, with a total number of 274 robotic-assisted cases and 674 laparoscopic [35, 39]. There was no significant difference between the two groups with regards to conversion to open (OR 0.42 [CI 0.08–2.21], p = 0.30), complication rate (OR 0.89 [CI 0.35–2.27], p = 0.80) or length of stay (SMD 0.06 [CI − 0.14 to 0.27], p = 0.54). Again, operative time was significantly longer for RAS (SMD 1.55 [CI 0.05–3.06], p = 0.04), Fig. 3.

The same two studies were the only ones to report conversion to open rates after previous surgery and PWM was 0.5% [CI 0–1.3%].

Both studies included colonic and rectal resections and so sensitivity analysis was not possible. Furthermore, both studies included a wide range of previous surgeries, including some minimally invasive operations, and only one utilised an adhesion severity scoring system, limiting the robustness of primary data and meta-analysis.

Discussion

This review has demonstrated significantly lower conversion to open rates in male patients, patients with obesity and patients with low rectal tumours undergoing robotic-assisted surgery for colorectal cancer when compared to laparoscopic surgery. It has also demonstrated shorter length of stay in patients with obesity undergoing robotic-assisted surgery, and male patients when looking at rectal resections alone.

As the prevalence of RAS has increased, so has the evidence demonstrating equivalent outcomes for robotic-assisted and laparoscopic colorectal surgery. The exception to this has been conversion rates. Observational studies and meta-analyses of RAS have consistently shown superiority in conversion to open rates [7173]. However, before this review, obesity was the only high-risk subgroup explored with level 1 or 2 evidence, suggesting lower conversion to open rates as well as decreased length of stay [61, 74]. This review confirms these findings. There is strong evidence depicting the relationship between obesity and colorectal cancer [7577] and, as the prevalence of obesity continues to increase worldwide [78], so will the proportion of these patients in a colorectal surgeon’s workload.

Furthermore, the results demonstrate the advantage of robotic-assisted surgery in male patients and patients with low rectal tumours. Conversion rates are significantly lower with RAS, confirming in practice the benefits of improved instrument articulation in narrow spaces. When just rectal resections were examined, length of stay was shorter for RAS in male patients.

The pooled weighted means show that male patients and patients with obesity have the highest conversion to open rates among all the subgroups analysed. Conversion to open surgery in any population is associated with increased morbidity and mortality in addition to adverse long-term oncological outcomes [79, 80]. Suwa et al. [17] found higher conversion rates and significantly longer operative times in patients with obesity undergoing robotic colorectal cancer resections compared to patients without obesity. Similarly, Baukloh et al. [60] conducted a multicentre prospective study in 348 patients undergoing robotic surgery due to rectal cancer and found male patients had significantly higher rates of major complications and anastomotic leakage. Therefore, RAS should be considered the modality of choice for male patients and/or patients with obesity, especially those with low rectal tumours, to decrease conversion rates and improve outcomes in these high-risk subgroups.

In elderly patients, this review finds no evidence of superior outcomes for RAS when compared to laparoscopic surgery but does find significantly longer operating times. Therefore, it is questionable whether elderly patients not belonging to any other high-risk subgroup will benefit from RAS. This is even more important considering this subgroup is at greater risk from lengthier surgery [81, 82].

Longer surgery for any patient is an independent risk factor for postoperative complications and increased length of stay [83, 84]. This finding is likely due to the setup and docking required for robotic-assisted surgery and the established learning curve for surgeons and theatre staff. However, once RAS becomes more established in individual centres, operative time decreases and is on par with a laparoscopic approach. Furthermore, evidence is emerging to suggest the learning curve for RAS may be faster than the learning curve for laparoscopy, and implementation of robotic training programmes can be associated with reduced operating times and fewer complications [85, 86].

The limitations of this meta-analysis lie largely in the primary evidence. Out of the 32 studies included in the comparative meta-analyses, all but one are non-randomised observational studies with significant bias due to confounding. The majority of sample sizes were small. Furthermore, the ‘previous abdominal surgery’ subgroup analyses are at higher risk of error given the inherent biases in the primary studies’ methodologies. The studies included span over a decade, from 2010 to 2024. Within that time, robotic-assisted surgery has progressed significantly, drawing into question the comparability of older and newer studies. Finally, the source studies are at an overall moderate to high risk of bias which can have an effect on the reliability of data syntheses.

Conclusions

This systematic review and meta-analysis demonstrates equivalent or superior outcomes of RAS when compared to laparoscopic surgery in high-risk colorectal patients. Conversion to open rates are significantly lower for robotic-assisted surgery in male patients, patients with obesity and patients with low rectal tumours, when compared to laparoscopy. Length of stay is also significantly reduced in patients with obesity undergoing all resection types, and in male patients undergoing rectal resections alone. These findings suggest robotic-assisted surgery should be considered as the preferred modality in these cohorts. However, operative times remain significantly longer in robotic-assisted surgery, which must be weighed against the cost implications and learning curve.

Supplementary Information

Below is the link to the electronic supplementary material.

Abbreviations

OR

Odds ratio

PWM

Pooled weighted means

RAS

Robotic-assisted surgery

SD

Standard deviation

SMD

Standardised mean difference

TME

Total mesenteric excision

Author contributions

SG was responsible for initial searches, study screening, data extraction and quality analysis. SGP and SM were responsible for data extraction. JW and KA were responsible for data analysis. SA and KA conceived the review. JW and SG completed the first draft of the manuscript and all co-authors critically reviewed, revised the manuscript and provided final approval.

Funding

No funding was sought or required for the preparation of this manuscript.

Data availability

No datasets were generated or analysed during the current study.

Declarations

Conflict on interest

Drs. Sukhpreet Gahunia, James Wyatt, Simon G. Powell, Shareef Mahdi, Shakil Ahmed and Kiran Altaf have no competing interests or financial ties to disclose.

Footnotes

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

S. Gahunia and J. Wyatt share joint first authorship.

References

  • 1.Lg T, Cc O (2016) 30 years of robotic surgery. World J Surg 40(10):2550–2557 [DOI] [PubMed] [Google Scholar]
  • 2.Peters BS, Armijo PR, Krause C, Choudhury SA, Oleynikov D (2018) Review of emerging surgical robotic technology. Surg Endosc 32(4):1636–1655 [DOI] [PubMed] [Google Scholar]
  • 3.Eoh KJ, Nam EJ, Kim SW, Shin M, Kim SJH, Kim JA (2021) Nationwide comparison of surgical and oncologic outcomes in endometrial cancer patients undergoing robotic, laparoscopic, and open surgery: a population-based cohort study. Cancer Res Treat 53(2):549–557 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 4.O’Malley DM, Smith B, Fowler JM (2015) The role of robotic surgery in endometrial cancer: robotic surgery in endometrial cancer. J Surg Oncol 112(7):761–768 [DOI] [PubMed] [Google Scholar]
  • 5.Zahid A, Ayyan M, Farooq M, Cheema HA, Shahid A, Naeem F (2022) Robotic surgery in comparison to the open and laparoscopic approaches in the field of urology: a systematic review. J Robot Surg. 10.1007/s11701-022-01416-7 [DOI] [PubMed] [Google Scholar]
  • 6.Jayne D, Pigazzi A, Marshall H, Croft J, Corrigan N, Copeland J (2017) Effect of robotic-assisted vs conventional laparoscopic surgery on risk of conversion to open laparotomy among patients undergoing resection for rectal cancer: the ROLARR randomized clinical trial. JAMA. 318(16):1569 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 7.Jeon Y, Park EJ, Baik SH (2019) Robotic surgery for rectal cancer and cost-effectiveness. J Min Invasive Surg 22(4):139–149 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 8.Shaw RD, Eid MA, Bleicher J, Broecker J, Caesar B, Chin R (2022) Current barriers in robotic surgery training for general surgery residents. J Surg Educ 79(3):606–613 [DOI] [PubMed] [Google Scholar]
  • 9.Eriksen MT, Wibe A, Norstein J, Haffner J, Wiig JN, Norwegian Rectal Cancer Group (2005) Anastomotic leakage following routine mesorectal excision for rectal cancer in a national cohort of patients. Colorectal Disease. 7(1):51–7 [DOI] [PubMed] [Google Scholar]
  • 10.Kirchhoff P, Dincler S, Buchmann P (2008) A multivariate analysis of potential risk factors for intra- and postoperative complications in 1316 elective laparoscopic colorectal procedures. Ann Surg 248(2):259–265 [DOI] [PubMed] [Google Scholar]
  • 11.Park JS, Choi GS, Kim SH, Kim HR, Kim NK, Lee KY (2013) Multicenter analysis of risk factors for anastomotic leakage after laparoscopic rectal cancer excision: the Korean Laparoscopic Colorectal Surgery Study Group. Ann Surg 257(4):665–671 [DOI] [PubMed] [Google Scholar]
  • 12.Qu H, Liu Y, D-s B (2015) Clinical risk factors for anastomotic leakage after laparoscopic anterior resection for rectal cancer: a systematic review and meta-analysis. Surg Endosc 29(12):3608–3617 [DOI] [PubMed] [Google Scholar]
  • 13.Yamashita M, Tominaga T, Nonaka T, Fukda A, Moriyama M, Oyama S (2021) Impact of obesity on short-term outcomes of laparoscopic colorectal surgery for Japanese patients with colorectal cancer: a multicenter study. Asian J Endosc Surg 14(3):432–442 [DOI] [PubMed] [Google Scholar]
  • 14.de Moreira Azevedo JG, Silveira Mendes CR, Lima MA et al (2021) Laparoscopic colorectal surgery and discharge within 24 h—who is at risk for readmission? Colorectal Dis 23(10):2714–22 [DOI] [PubMed] [Google Scholar]
  • 15.Lee SY, Kim CH, Kim YJ, Kim HR (2016) Laparoscopic surgery for colorectal cancer patients who underwent previous abdominal surgery. Surg Endosc 30(12):5472–5480 [DOI] [PubMed] [Google Scholar]
  • 16.Yamamoto M, Okuda J, Tanaka K, Kondo K, Asai K, Kayano H (2013) Effect of previous abdominal surgery on outcomes following laparoscopic colorectal surgery. Dis Colon Rectum 56(3):336–342 [DOI] [PubMed] [Google Scholar]
  • 17.Suwa Y, Joshi M, Poynter L, Endo I, Ashrafian H, Darzi A (2020) Obese patients and robotic colorectal surgery: systematic review and meta-analysis. BJS Open 4(6):1042–1053 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 18.Page MJ, McKenzie JE, Bossuyt PM, Boutron I, Hoffmann TC, Mulrow CD (2021) The PRISMA 2020 statement: an updated guideline for reporting systematic reviews. BMJ. 10.1136/bmj.n71 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 19.Sciuto A, Merola G, Palma GDD, Sodo M, Pirozzi F, Bracale UM (2018) Predictive factors for anastomotic leakage after laparoscopic colorectal surgery. World J Gastroenterol 24(21):2247–2260 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 20.Sterne JA, Hernán MA, Reeves BC, Savović J, Berkman ND, Viswanathan M (2016) ROBINS-I: a tool for assessing risk of bias in non-randomised studies of interventions. BMJ. 10.1136/bmj.i4919 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 21.Sterne JAC, Savović J, Page MJ, Elbers RG, Blencowe NS, Boutron I (2019) RoB 2: a revised tool for assessing risk of bias in randomised trials. BMJ 366:l4898 [DOI] [PubMed] [Google Scholar]
  • 22.Luo D, Wan X, Liu J, Tong T (2018) Optimally estimating the sample mean from the sample size, median, mid-range, and/or mid-quartile range. Stat Methods Med Res 27(6):1785–1805 [DOI] [PubMed] [Google Scholar]
  • 23.Wan X, Wang W, Liu J, Tong T (2014) Estimating the sample mean and standard deviation from the sample size, median, range and/or interquartile range. BMC Med Res Methodol. 10.1186/1471-2288-14-135 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 24.Ackerman SJ, Daniel S, Baik R, Liu E, Mehendale S, Tackett S (2018) Comparison of complication and conversion rates between robotic-assisted and laparoscopic rectal resection for rectal cancer: which patients and providers could benefit most from robotic-assisted surgery? J Med Econ 21(3):254–261 [DOI] [PubMed] [Google Scholar]
  • 25.Baek SJ, Al-Asari S, Jeong DH, Hur H, Min BS, Baik SH (2013) Robotic versus laparoscopic coloanal anastomosis with or without intersphincteric resection for rectal cancer. Surg Endosc. 27(11):4157–63 [DOI] [PubMed] [Google Scholar]
  • 26.Chen TC, Liang JT (2022) Robotic versus laparoscopic surgery for rectal cancer after neoadjuvant chemoradiotherapy: a propensity-score matching analysis. J Formos Med Assoc 121(8):1532–1540 [DOI] [PubMed] [Google Scholar]
  • 27.Cardinali L, Belfiori G, Ghiselli R, Ortenzi M, Guerrieri M (2016) Robotic versus laparoscopic right colectomy for cancer: short-term outcomes and influence of body mass index on conversion rate. Minerva Chir 71(4):217–222 [PubMed] [Google Scholar]
  • 28.de’Angelis N, Abdalla S, Bianchi G et al (2018) Robotic versus laparoscopic colorectal cancer surgery in elderly patients: a propensity score match analysis. J Laparoendosc Adv Surg Tech. 28(11):1334–45 [DOI] [PubMed] [Google Scholar]
  • 29.Esen E, Aytac E, Ağcaoğlu O, Zenger S, Balik E, Baca B (2018) Totally robotic versus totally laparoscopic surgery for rectal cancer. Surg Laparosc Endosc Percutan Tech 28(4):245–249 [DOI] [PubMed] [Google Scholar]
  • 30.Fernandez R, Anaya DA, Li LT, Orcutt ST, Balentine CJ, Awad SA (2013) Laparoscopic versus robotic rectal resection for rectal cancer in a veteran population. Am J Surg 206(4):509–517 [DOI] [PubMed] [Google Scholar]
  • 31.Gorgun E, Ozben V, Costedio M, Stocchi L, Kalady M, Remzi F (2016) Robotic versus conventional laparoscopic rectal cancer surgery in obese patients. Colorectal Dis 18(11):1063–1071 [DOI] [PubMed] [Google Scholar]
  • 32.Huang YM, Huang YJ, Wei PL (2017) Outcomes of robotic versus laparoscopic surgery for mid and low rectal cancer after neoadjuvant chemoradiation therapy and the effect of learning curve. Medicine 96(40):e8171 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 33.Kim YS, Kim MJ, Park SC, Sohn DK, Kim DY, Chang HJ (2016) Robotic versus laparoscopic surgery for rectal cancer after preoperative chemoradiotherapy: case-matched study of short-term outcomes. Cancer Res Treat 48(1):225–231 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 34.Kuo LJ, Lin YK, Chang CC, Tai CJ, Chiou JF, Chang YJ (2014) Clinical outcomes of robot-assisted intersphincteric resection for low rectal cancer: comparison with conventional laparoscopy and multifactorial analysis of the learning curve for robotic surgery. Int J Colorectal Dis 29(5):555–562 [DOI] [PubMed] [Google Scholar]
  • 35.Milone M, de Angelis N, Beghdadi N, Brunetti F, Manigrasso M, Simone G (2021) Conversions related to adhesions in abdominal surgery. Robotic versus laparoscopic approach: a multicentre experience. Int J Med Robot Comput Assist Surg. 10.1002/rcs.2186 [DOI] [PubMed] [Google Scholar]
  • 36.Palomba G, Dinuzzi VP, Capuano M, Anoldo P, Milone M, Palma GD (2022) Robotic versus laparoscopic colorectal surgery in elderly patients in terms of recovery time: a monocentric experience. J Robot Surg 16(4):981–987 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 37.Panteleimonitis S, Pickering O, Abbas H, Harper M, Kandala N, Figueiredo N (2018) Robotic rectal cancer surgery in obese patients may lead to better short-term outcomes when compared to laparoscopy: a comparative propensity scored match study. Int J Colorectal Dis 33(8):1079–1086 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 38.Park JS, Choi GS, Lim KH, Jang YS, Jun SH (2010) Robotic-assisted versus laparoscopic surgery for low rectal cancer: case-matched analysis of short-term outcomes. Ann Surg Oncol 17(12):3195–3202 [DOI] [PubMed] [Google Scholar]
  • 39.Park S, Kang J, Park EJ, Baik SH, Lee KY (2017) Laparoscopic and robotic surgeries for patients with colorectal cancer who have had a previous abdominal surgery. Ann Coloproctol 33(5):184–191 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 40.Park SY, Choi GS, Park JS, Kim HJ, Ryuk JP (2013) Short-term clinical outcome of robot-assisted intersphincteric resection for low rectal cancer: a retrospective comparison with conventional laparoscopy. Surg Endosc 27(1):48–55 [DOI] [PubMed] [Google Scholar]
  • 41.Saklani AP, Lim DR, Hur H, Min BS, Baik SH, Lee KY (2013) Robotic versus laparoscopic surgery for mid–low rectal cancer after neoadjuvant chemoradiation therapy: comparison of oncologic outcomes. Int J Colorectal Dis 28(12):1689–1698 [DOI] [PubMed] [Google Scholar]
  • 42.Schootman M, Hendren S, Loux T, Ratnapradipa K, Eberth JM, Davidson NO (2017) Differences in effectiveness and use of robotic surgery in patients undergoing minimally invasive colectomy. J Gastrointest Surg 21(8):1296–1303 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 43.Serin KR, Gultekin FA, Batman B, Ay S, Kapran Y, Saglam S (2015) Robotic versus laparoscopic surgery for mid or low rectal cancer in male patients after neoadjuvant chemoradiation therapy: comparison of short-term outcomes. J Robot Surg 9(3):187–194 [DOI] [PubMed] [Google Scholar]
  • 44.Shiomi A, Kinugasa Y, Yamaguchi T, Kagawa H, Yamakawa Y (2016) Robot-assisted versus laparoscopic surgery for lower rectal cancer: the impact of visceral obesity on surgical outcomes. Int J Colorectal Dis 31(10):1701–1710 [DOI] [PubMed] [Google Scholar]
  • 45.Srinath H, Kim TJ, Mor IJ, Warner RE (2022) Robot-assisted vs laparoscopic right hemicolectomy in octogenarians. J Am Med Dir Assoc 23(4):690–694 [DOI] [PubMed] [Google Scholar]
  • 46.Yoo BE, Cho JS, Shin JW, Lee DW, Kwak JM, Kim J (2015) Robotic versus laparoscopic intersphincteric resection for low rectal cancer: comparison of the operative, oncological, and functional outcomes. Ann Surg Oncol 22(4):1219–1225 [DOI] [PubMed] [Google Scholar]
  • 47.Angehrn FV, Schneider R, Wilhelm A, Daume D, Koechlin L, Fourie L (2022) Robotic versus laparoscopic low anterior resection following neoadjuvant chemoradiation therapy for stage II–III locally advanced rectal cancer: a single-centre cohort study. J Robot Surg 16(5):1133–1141 [DOI] [PubMed] [Google Scholar]
  • 48.Juang S, Chung K, Cheng K et al (2023) Outcomes of robot-assisted versus laparoscopic surgery for colorectal cancer in morbidly obese patients: a propensity score-matched analysis of the US Nationwide Inpatient Sample. J Gastroenterol Hepatol 38(9):1510–1519 [DOI] [PubMed] [Google Scholar]
  • 49.Glencer AC, Lin JA, Trang K et al (2022) Assessing the role of robotic proctectomy in obese patients: a contemporary NSQIP analysis. J Robot Surg 16(6):1391–1399 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 50.Albayati S, Hitos K, Berney CR et al (2022) Robotic-assisted versus laparoscopic rectal surgery in obese and morbidly obese patients: ACS-NSQIP analysis. J Robot Surg 17(2):637–643 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 51.Ali M, Wang Y, Yu W, Baral S, Jun R, Wang D (2023) Benefits of minimally invasive surgery for rectal cancer in older adults compared with younger adults: a retrospective study. J Robot Surg 17(4):1825–1833 [DOI] [PubMed] [Google Scholar]
  • 52.Feng Q, Tang W, Zhang Z et al (2022) Robotic versus laparoscopic abdominoperineal resections for low rectal cancer: a single-center randomized controlled trial. J Surg Oncol 126(8):1481–1493 [DOI] [PubMed] [Google Scholar]
  • 53.Yamanashi T, Miura H, Tanaka T et al (2022) Short-term outcomes of robot-assisted versus conventional laparoscopic surgery for mid and low rectal cancer after neoadjuvant chemoradiotherapy: a propensity score-matched analysis. J Robot Surg 17(3):959–969 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 54.Lu CC, Lu CT, Chang KY, Chun-Li W, Wu CY (2024) Robot-assisted vs. laparoscopic right hemicolectomy in octogenarians and nonagenarians: an analysis of the US nationwide inpatient sample 2005–2018. Aging Clin Exp Res 36(1):193 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 55.Zhao S, Li R, Zhou J et al (2024) Comparison of robotic versus laparoscopic surgery for visceral obesity in mid–low rectal cancer: a propensity-matched analysis. J Robot Surg. 10.1007/s11701-024-01945-3 [DOI] [PubMed] [Google Scholar]
  • 56.Bayraktar O, Aytaç E, Özben V, Atasoy D, Bilgin İA, Erenler Bİ (2018) Does robot overcome obesity-related limitations of minimally invasive rectal surgery for cancer? Surg Laparosc Endosc Percutan Tech 28(1):8–11 [DOI] [PubMed] [Google Scholar]
  • 57.Hellan M, Ouellette J, Lagares-Garcia JA, Rauh SM, Kennedy HL, Nicholson JD (2015) Robotic rectal cancer resection: a retrospective multicenter analysis. Ann Surg Oncol 22(7):2151–2158 [DOI] [PubMed] [Google Scholar]
  • 58.Keller DS, Madhoun N, Flores-Gonzalez JRI et al (2016) Effect of BMI on short-term outcomes with robotic-assisted laparoscopic surgery: a case-matched study. J Gastrointest Surg 20(3):488–93 [DOI] [PubMed] [Google Scholar]
  • 59.Lagares-Garcia J, O’Connell A, Firilas A, Robinson CC, Dumas BP, Hagen ME (2016) The influence of body mass index on clinical short-term outcomes in robotic colorectal surgery: robotic colorectal surgery and obesity. Int J Med Robot Comput Assist Surg 12(4):680–685 [DOI] [PubMed] [Google Scholar]
  • 60.Baukloh JK, Reeh M, Spinoglio G, Corratti A, Bartolini I, Mirasolo VM (2017) Evaluation of the robotic approach concerning pitfalls in rectal surgery. Eur J Surg Oncol 43(7):1304–11 [DOI] [PubMed] [Google Scholar]
  • 61.Harr JN, Haskins IN, Amdur RL, Agarwal S, Obias V (2018) The effect of obesity on laparoscopic and robotic-assisted colorectal surgery outcomes: an ACS-NSQIP database analysis. J Robot Surg 12(2):317–323 [DOI] [PubMed] [Google Scholar]
  • 62.Pai A, Alsabhan F, Park JJ, Melich G, Sulo S, Marecik SJ (2017) The impact of obesity on the perioperative, clinicopathologic, and oncologic outcomes of robot assisted total mesorectal excision for rectal cancer. Polish J Surg 89(4):23–28 [DOI] [PubMed] [Google Scholar]
  • 63.Duchalais E, Machairas N, Kelley SRL et al (2018) Does obesity impact postoperative outcomes following robotic-assisted surgery for rectal cancer? Surg Endosc 32(12):4886–92 [DOI] [PubMed] [Google Scholar]
  • 64.Peacock O, Limvorapitak T, Hu CY, Bednarski B, Tillman M, Kaur H (2020) Robotic rectal cancer surgery: comparative study of the impact of obesity on early outcomes. Br J Surg 107(12):1552–1557 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 65.Ozben V, Aliyeva Z, Bilgin IA, Aytac E, Baca B, Hamzaoglu I (2021) Does obesity impact surgical and pathological outcomes in robotic complete mesocolic excision for colon cancer? J Laparoendosc Adv Surg Tech 31(11):1247–1253 [DOI] [PubMed] [Google Scholar]
  • 66.Hannan E, Troy A, Feeney G, Ullah MF, Ryan C, McNamara E (2022) The impact of body mass index on outcomes in robotic colorectal surgery: a single-centre experience. J Robot Surg 16(2):279–285 [DOI] [PubMed] [Google Scholar]
  • 67.Ceccarelli G, Andolfi E, Biancafarina A, Rocca A, Amato M, Milone M (2017) Robot-assisted surgery in elderly and very elderly population: our experience in oncologic and general surgery with literature review. Aging Clin Exp Res 29(S1):55–63 [DOI] [PubMed] [Google Scholar]
  • 68.Oldani A, Bellora P, Monni M, Amato B, Gentilli S (2017) Colorectal surgery in elderly patients: our experience with DaVinci Xi® System. Aging Clin Exp Res 29(S1):91–99 [DOI] [PubMed] [Google Scholar]
  • 69.Morohashi H, Sakamoto Y, Miura T, Ichinohe D, Kubota S, Yamazaki K (2022) Short-term outcomes of robotic-assisted surgery following neoadjuvant chemotherapy for lower rectal cancer. Asian J Endosc Surg 15(3):577–584 [DOI] [PubMed] [Google Scholar]
  • 70.Huang CW, Su WC, Chang TK, Ma CJ, Yin TC, Tsai HL (2020) Impact of previous abdominal surgery on robotic-assisted rectal surgery in patients with locally advanced rectal adenocarcinoma: a propensity score matching study. World J Surg Oncol 18(1):308 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 71.Dolejs SC, Waters JA, Ceppa EP, Zarzaur BL (2017) Laparoscopic versus robotic colectomy: a national surgical quality improvement project analysis. Surg Endosc 31(6):2387–2396 [DOI] [PubMed] [Google Scholar]
  • 72.Ng KT, Tsia AKV, Chong VYL (2019) Robotic versus conventional laparoscopic surgery for colorectal cancer: a systematic review and meta-analysis with trial sequential analysis. World J Surg 43(4):1146–1161 [DOI] [PubMed] [Google Scholar]
  • 73.Wang X, Cao G, Mao W, Lao W, He C (2020) Robot-assisted versus laparoscopic surgery for rectal cancer: a systematic review and meta-analysis. J Cancer Res Ther 16(5):979 [DOI] [PubMed] [Google Scholar]
  • 74.Wee IJY, Kuo LJ, Ngu JCY (2019) The impact of robotic colorectal surgery in obese patients: a systematic review, meta-analysis, and meta-regression. Surg Endosc 33(11):3558–3566 [DOI] [PubMed] [Google Scholar]
  • 75.Dai Z (2007) Obesity and colorectal cancer risk: a meta-analysis of cohort studies. World J Gastroenterol 13(31):4199 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 76.Elangovan A, Skeans J, Landsman M, Ali SMJ, Elangovan AG, Kaelber DC (2021) Colorectal cancer, age, and obesity-related comorbidities: a large database study. Dig Dis Sci 66(9):3156–3163 [DOI] [PubMed] [Google Scholar]
  • 77.Moghaddam AA, Woodward M, Huxley R (2007) Obesity and risk of colorectal cancer: a meta-analysis of 31 studies with 70,000 events. Cancer Epidemiol Biomark Prev 16(12):2533–2547 [DOI] [PubMed] [Google Scholar]
  • 78.De Lorenzo A, Romano L, Di Renzo L, Di Lorenzo N, Cenname G, Gualtieri P (2020) Obesity: a preventable, treatable, but relapsing disease. Nutrition 71:110615 [DOI] [PubMed] [Google Scholar]
  • 79.Clancy C, O’Leary DP, Burke JP, Redmond HP, Coffey JC, Kerin MJ (2015) A meta-analysis to determine the oncological implications of conversion in laparoscopic colorectal cancer surgery. Colorectal Dis 17(6):482–490 [DOI] [PubMed] [Google Scholar]
  • 80.Masoomi H, Moghadamyeghaneh Z, Mills S, Carmichael JC, Pigazzi A, Stamos MJ (2015) Risk factors for conversion of laparoscopic colorectal surgery to open surgery: does conversion worsen outcome? World J Surg 39(5):1240–1247 [DOI] [PubMed] [Google Scholar]
  • 81.Cheng H, Clymer JW, Po-Han Chen B, Sadeghirad B, Ferko NC, Cameron CG (2018) Prolonged operative duration is associated with complications: a systematic review and meta-analysis. J Surg Res. 229:134–44. 10.1016/j.jss.2018.03.022 [DOI] [PubMed] [Google Scholar]
  • 82.Hersey AE, Durand WM, Eltorai AEM, DePasse JM, Daniels AH (2019) Longer operative time in elderly patients undergoing posterior lumbar fusion is independently associated with increased complication rate. Global Spine J 9(2):179–184 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 83.Harrison OJ, Smart NJ, White P, Brigic A, Carlisle ER, Allison AS (2014) Operative time and outcome of enhanced recovery after surgery after laparoscopic colorectal surgery. JSLS 18(2):265–272 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 84.Poles G, Stafford C, Francone T, Roberts PL, Ricciardi R (2018) What is the relationship between operative time and adverse events after colon and rectal surgery? Am Surg 84(5):712–716 [PubMed] [Google Scholar]
  • 85.Flynn J, Larach JT, Kong JCH, Waters PS, Warrier SK, Heriot A (2021) The learning curve in robotic colorectal surgery compared with laparoscopic colorectal surgery: a systematic review. Colorectal Dis 23(11):2806–2820 [DOI] [PubMed] [Google Scholar]
  • 86.Olthof PB, Giesen LJX, Vijfvinkel TS, Roos D, Dekker JWT (2021) Transition from laparoscopic to robotic rectal resection: outcomes and learning curve of the initial 100 cases. Surg Endosc 35(6):2921–2927 [DOI] [PMC free article] [PubMed] [Google Scholar]

Associated Data

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Supplementary Materials

Data Availability Statement

No datasets were generated or analysed during the current study.


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