Platinum Priority – Review – Kidney Cancer
Editorials by Alexandre Mottrie, Marco Borghesi and Vincenzo Ficarra on pp. 1034–1036 and by Anthony T. Corcoran, Alexander Kutikov and Robert G. Uzzo on pp. 1037–1038 of this issue

Robotic Versus Laparoscopic Partial Nephrectomy: A Systematic Review and Meta-Analysis eulogo1

By: Omar M. Aboumarzouka b lowast , Robert J. Steinc, Remi Eyraudc, Georges-Pascal Haberc, Piotr L. Chlostad, Bhaskar K. Somanie and Jihad H. Kaoukc

European Urology, Volume 62 Issue 1, December 2012, Pages 1023-1033

Published online: 01 December 2012

Keywords: Robotic, Laparoscopic, Partial Nephrectomy, Renal cancer, Systematic review, Nephron Sparing

Abstract Full Text Full Text PDF (1,9 MB)



Centres worldwide have been performing partial nephrectomies laparoscopically for greater than a decade. With the increasing use of robotics, many centres have reported their early experiences using it for nephron-sparing surgery.


To review published literature comparing robotic partial nephrectomy (RPN) with laparoscopic partial nephrectomy (LPN).

Evidence acquisition

An online systematic review of the literature according to Cochrane guidelines was conducted from 2000 to 2012 including studies comparing RPN and LPN. All studies comparing RPN with LPN were included. The outcome measures were the patient demographics, tumour size, operating time, warm ischaemic time, blood loss, transfusion rates, length of hospital stay, conversion rates, and complications. A meta-analysis of the results was conducted. For continuous data, a Mantel-Haenszel chi-square test was used; for dichotomous data, an inverse variance was used. Each was expressed as a risk ratio with a 95% confidence interval p<0.05 considered significant.

Evidence synthesis

A total of 717 patients were included, 313 patients in the robotic group and 404 patients in the laparoscopic group (seven studies). There was no significant difference between the two groups in any of the demographic parameters except for age (age: p=0.006; sex: p=0.54; laterality: p=0.05; tumour size: p=0.62, tumour location: p=57; or confirmed malignant final pathology: p=0.79). There was no difference between the two groups regarding operative times (p=0.58), estimated blood loss (p=0.76), or conversion rates (p=0.84). The RPN group had significantly less warm ischaemic time than the LPN group (p=0.0008). There was no difference regarding postoperative length of hospital stay (p=0.37), complications (p=0.86), or positive margins (p=0.93).


In early experience, RPN appears to be a feasible and safe alternative to its laparoscopic counterpart with decreased warm ischaemia times noted.

Take Home Message

Robotic partial nephrectomy is feasible and is a safe alternative to laparoscopic partial nephrectomy. The robotic procedure has the added benefit of shorter ischaemic times, resulting in more nephron preservation and lending true meaning to the term nephron-sparing surgery.

Keywords: Robotic, Laparoscopic, Partial Nephrectomy, Renal cancer, Systematic review, Nephron Sparing.

1. Introduction

Partial nephrectomy (PN) is the gold standard for treatment of small renal masses, with laparoscopy becoming a more commonly used approach [1]. With advancements in laparoscopic techniques, equipment, and operator skills, laparoscopic PN (LPN) has emerged as a viable alternative to open PN with comparable oncologic outcomes, less morbidity, and faster postoperative recovery [1], [2], [3], and [4]. However, LPN is technically challenging and has a steeper learning curve because it requires not only precise tumour margin resection but complex and time-dependent renal reconstruction [5], [6], [7], [8], and [9]. This led the European Association of Urology to propose that these techniques be performed only in experienced centres [1].

Current robotic surgical systems provide not only optically magnified three-dimensional imaging but also a greater range of fully articulated wristed-instrument motion. This provides precision control with scaling of the surgeons’ movements [1] and [2].

Numerous centres have published their experiences with robotic PN (RPN) [1], [2], [3], [6], [7], [9], [10], and [11]. RPN outcomes have been reported to be similar to laparoscopic or open procedures in terms of oncologic and functional outcomes [6], [7], [8], and [9]. Enhanced precision robotic handling has reduced the technical challenges posed by LPN, helped reduce the surgical learning curve needed, and shortened operative and ischaemic times with less blood loss compared with LPN [1], [2], and [4]. Several studies have emerged recently comparing experience with outcomes of RPN and LPN [2], [8], [11], and [12].

We conducted a systematic review of the literature with a meta-analysis of the results to compare RPN and LPN in terms of operative and ischaemic times, blood loss, hospital stay, conversion rates, positive surgical margin rates, and perioperative complications.

2. Evidence acquisition

2.1. Search strategy and study selection

The systematic review was performed according to the Cochrane review guidelines. The search strategy was conducted to find relevant studies from Medline (2000–2012), Embase (2000–2011), Cochrane Central Register of Controlled Trials—CENTRAL (in the Cochrane Library, Issue 1, 2011), CINAHL (2000–2012),, Google Scholar, and individual urologic journals. The search was conducted on February 6, 2012.

Search terms used included robot, robotic, robotics, laparoscopic, laparoscopy, partial, nephron sparing, and nephrectomy. Medical Subject Heading (MeSH) phrases included (“Robotics”[MeSH]) AND “Nephrectomy”[MeSH]); ((“Robotics”[MeSH]) AND “Nephrectomy”[MeSH]) AND “Laparoscopy”[MeSH]); (((“Robotics”[MeSH]) AND “Laparoscopy”[MeSH]) AND “Nephrectomy”[MeSH]) AND Partial).

Papers in languages other than English were included if data were extractable. References of searched papers were also evaluated for potential inclusion. Authors of the included studies were contacted wherever the data were not available or not clear. If data were not provided or clarified, the study was excluded.

Two reviewers (O.A. and R.S.) identified all studies that appeared to fit the inclusion criteria for full review. Four reviewers (O.A., R.S., R.E., and B.S.) independently selected studies for inclusion in the review. Disagreement between the extracting authors was resolved by consensus by all authors.

2.2. Data extraction and analysis

Studies comparing RPN with LPN were included. The main outcome was to assess the pre-, peri-, and postoperative results between the two procedures. The secondary outcome will be to assess the learning curve required and a cost analysis. The following variables were extracted from each study: patient demographics, tumour size, operating time, warm ischaemic time, blood loss, transfusion rates, length of hospital stay, conversion rates, and complications. The data of each study were grouped into a meta-analysis, in an intention-to-treat basis, to allow a numerical representation of the results. Only similar results that were pooled from the included studies were meta-analysed. A subgroup analysis was conducted to evaluate whether or not the tumour location or the complication classification varied between the two procedures. For continuous data, a Mantel-Haenszel chi-square test was used and expressed as the mean difference with 95% confidence interval (CI). For dichotomous data, an inverse variance was used and expressed as risk ratio with 95% CI. In both cases p<0.05 was considered significant.

Taking into consideration that the first 25 procedures can be attributed to the learning curve for the procedures, we conducted a subgroup analysis to compare the two procedures regarding operative times, estimated ischaemic times, blood loss, length of hospital stay, and complication rates.

Heterogeneity will be analysed using a chi-square test on n-of-1 degree of freedom, with an α of 0.05 used for statistical significance and with the I2 test [13]. I2 values of 25%, 50%, and 90% correspond to low, medium, and high levels of heterogeneity. A fixed-effect model was used unless statistically significant high heterogeneity (ie, I2>90%) existed between studies. A random-effects model was used if heterogeneity existed. Although not included in the meta-analysis, studies of relevance were included in the systematic review for a general overview.

An assessment of the methodological quality of the included studies in the meta-analysis was conducted in line with the Cochrane handbook [13] and [14]. For quality assessment, the selection bias, performance bias, detection bias, attrition bias, and reporting bias were assessed in each of the included studies. We used Review Manager (RevMan v.5.0.23) to plot the quality assessment.

3. Evidence synthesis

The literature search yielded 521 studies, of which 447 were excluded due to nonrelevance based on the titles and 51 excluded due to nonrelevance based on the abstracts (Fig. 1). Full manuscripts were evaluated in 25 studies, of which 12 were included in the systematic review [4], [8], [12], [15], [16], [17], [18], [19], [20], [21], [22], and [23]. Of the 12 initially included studies, 7 were included in a pooled meta-analysis [4], [12], [19], [20], [21], [22], and [23]. Most of the studies were published within the last 5 yr, reflecting the increased use of this procedure.


Fig. 1 Flowchart for article selection process of the review.

After reading the full manuscripts, we excluded 13 studies for various reasons [1], [2], [3], [7], [10], [11], [24], [25], [26], [27], [28], [29], and [30]. Laydner and Kaouk was a systematic review of RPN [24]. Lee et al. compared RPN with the open procedure rather than LPN [25]. Yu et al. assessed the use, costs, and outcomes of laparoscopic surgery in urology with no specific comparison of RPN versus LPN [26]. Aron et al. was excluded because the authors provided data of their larger cohort of patients over a longer period of time published more recently [11] and [12]. The study by Spana et al. only looked at complications of RPN [7]. Gupta et al. reported on RPN for large tumours with no comparison with LPN (27). Long et al. compared the outcomes of LPN and RPN of just complex renal tumours and therefore was excluded; however, a previously published study comparing LPN and RPN for the same group was included [12] and [30]. Although the remaining excluded studies were on RPN, no comparison with LPN was made [1], [2], [3], [6], [10], [28], and [29].

All the included studies were cohort observational studies with no randomisation, and all reported on their centres’ experience with RPN compared with LPN. All the studies reported on the patient demographics, tumour size, operating time, warm ischaemic time, blood loss, transfusion rates, length of hospital stay, conversion rates, and complications (plotted into Table 1, Fig. 2, and Fig. 3). Table 2 depicts the data of the five studies that were excluded from the meta-analysis due to lack of data [8], [15], [16], [17], and [18]. All corresponding authors of the studies were contacted for data or clarification either by e-mail or by postal address. The corresponding authors of the seven studies in the meta-analysis replied with the missing or unclear data where appropriate [4], [12], [19], [20], [21], [22], and [23]. After numerous attempts at contacting the authors of the five remaining studies, no reply was received. Hence they were excluded because their data could not be pooled for analysis [8], [15], [16], [17], and [18]. The authors failed to report the standard deviation of their results that are needed for meta-analysis of the data. The emphasis of this review is on the seven studies included in the meta-analysis.

Table 1 Study results of robotic versus laparoscopic partial nephrectomy

Study Patients, RPN vs LPN, no. Age, RPN vs LPN, yr Male:female, RPN vs LPN Right:left, RPN vs LPN Pathology, malignant:benign, RPN vs LPN
Ellison et al. [23] 108 vs 108 59.4±12.1 vs 55.9±10.6 66:42 vs 62:42 52:56 vs 57:51 92:16 vs 84:24
Haber et al. [12] 75 vs 75 62.6±11.3 vs 60±12.05 44:31 vs 40:35 36:39 vs 43:32 59:16 vs 59:16
Jeong et al. [19] 31 vs 26 53.4±14 vs 58.7±8.4 0.94:1 vs 1:1 NA 22:9 vs 18:8
Kural et al. [20] 11 vs 20 50.81±13.15 vs 58.9±15.4 8:3 vs 14:6 3:8 vs 8:12 11:0 vs 16:4
Pierorazio et al. [4] 48 vs 102 60.15±9.13 vs 54.8±11.59 27:21 vs 63:39 22:26 vs 55:47 36:12 vs 84:18
Seo et al. [21] 13 vs 14 54.2±12.4 (33–72) vs 53.9±11.6 (34–72) 10:3 vs 8:6 4:9 vs 10:4 11:2 vs 9:5
Williams et al. [22] 27 vs 59 55.74±11.23 vs 54.6±11.69 17:10 vs 41:18 13:14 vs 28:31 22:4 vs 58:2

LPN=laparoscopic partial nephrectomy; RPN=robotic partial nephrectomy; NA=not available.


Fig. 2 Forest plots of outcomes: (a) tumour size in millimetres; (b) tumour location; (c) operative time; (d) warm ischaemic time; (e) estimated blood loss; (f) length of hospital stay; (g) positive margin; (h) conversion. The following studies are cited: Ellison [23], Haber [12], Jeong [19], Kural [20], Pierazio [4], Seo [21], and Williams [22]. CI=confidence interval; IV=inverse variance; LPN=laparoscopic partial nephrectomy; M-H=Mantel-Haenszel; RPN=robotic partial nephrectomy; SD=standard deviation.


Fig. 3 Forest plots of complications and Clavien classifications: (a) complications; (b) Clavien classifications 1–2 and 3–4. The following studies are cited: Ellison [23], Haber [12], Kural [20], Pierazio [4], Seo [21], and Williams [22].

Table 2 Study results of robotic versus laparoscopic partial nephrectomy of studies excluded

Study Tumour size, RPN vs LPN. mm (mean) Patients, RPN vs LPN, no. Age, RPN vs LPN, yr Male:female, RPN vs LPN Right:left, RPN vs LPN Operating time, RPN vs LPN, min (mean) Warm ischaemia time, RPN vs LPN, min (mean) Blood loss, RPN vs LPN, ml (mean) Length of stay, RPN vs LPN, d (mean) Location U/M/L pole, RPN vs LPN Positive surgical margins, RPN vs LPN Pathology, malignant:benign, RPN vs LPN
Benway and Bhayani [6] 28 vs 25 129 vs 118 59.2 vs 59.2 NA NA 189 vs 174 19.7 vs 28.4 155 vs 196 2.4 vs 2.7 NA 5 vs 1 87:42 vs 89:29
Deane et al. [17] 31 (25–40) vs 23 (17–62) 11 vs 11 53.2 vs 54 10:1 vs 7:4 4:7 vs 4:7 228.7 (98–375) vs 289.5 (145–369) 32.1 (30–45) vs 35.3 (15–49) 115 (75–500) vs 198 (25–300) 2 vs 3.1 8/0/3 vs 3/3/5 0 vs 0 11:0 vs 8:3
Caruso et al. [15] 19.5 vs 21.8 10 vs 10 58 vs 61 NA NA 279 vs 253 26.4 vs 29.3 240 vs 200 2.6 vs 2.65 3/3/4 vs 4/1/5 0 vs 1 8:2 vs 5:5
DeLong et al. [18] 26 vs 28 13 vs 15 59.7 vs 53.6 8:5 vs 8:7 7:6 vs 8:7 344 vs 254 29.7 (21–45) vs 39.9 (24–51) Median: 100 vs 150 Not clear NA NA 13:0 vs 9:6
Cho et al. [16] 27 (9–35) vs 28 (15–35) 10 vs 10 63 (36–78) vs 56 (31–79) 8:2 vs 5:5 3:7 vs 5:5 376 (179–470) vs 361 (197–477) 31 (26–36) vs 40 (27–50) 329 (50–700) vs 328 (200–550) 7 (5–12) vs 14 (6–51) 3/4/3 vs 5/5/0 0 vs 0 9:1 vs 8:2

LPN=laparoscopic partial nephrectomy; RPN=robotic partial nephrectomy; U=upper; M=middle; L=lower; NA=not available.

3.2. Characteristics of the included studies

Although a literature search was conducted between 2000 and 2012, comparison studies were published between 2009 and 2012, four conducted in the United States, two in Korea, and one in Turkey. Among the 717 patients, the ages of 313 patients (the robotic group) ranged from 37 to 73 yr; the ages of 404 patients (the laparoscopic group) ranged from 42 to 73 yr. In the RPN group there were 188 men; 130 procedures were right sided. In the LPN group there were 241 men; 201 procedures were right sided. Jeong et al. did not report on the laterality of their procedure [19].

All seven studies reported on the tumour size, operative times, warm ischaemic times, estimated blood loss, transfusion requirement, length of hospital stay, conversion rates, and malignant and benign rates [4], [12], [19], and [23]. Three studies reported on tumour location [12], [20], and [21]. Six studies reported surgical margins and complications [4], [12], [20], [21], [22], and [23]; however, only three studies classified their complications using the Clavien scheme [4], [22], and [23]. The data of all the studies were given as means plus or minus the standard deviation, which allowed for a meta-analysis of the pooled data.

3.3. Meta-analysis results

Table 1 depicts the demographics of the studies including number of patients, age, sex, laterality, and pathology. There was no significant difference between the two groups for any of the demographic parameters except for age (age: p=0.006, MD: 2.38, 95% CI, 0.69–4.06; sex: p=0.54, odds ratio [OR]: 1.00, 95% CI, 0.81–1.24; laterality: p=0.05, OR: 1.00; 95% CI, 0.80–1.25; malignant pathology: p=0.79, OR: 1.05, 95% CI, 0.72–1.54).

There was no statistical difference found between RPN and LPN regarding tumour size (p=0.62; MD: 0.52; 95% CI, −1.56 to 2.60), tumour location (p=1; OR: 1.0; 95% CI, 0.71–1.4), or positive margins (p=0.93; OR: 0.97; 95% CI, 0.43–2.17) (Fig. 2).

There was no perioperative difference between the two groups regarding operative times (p=0.58; MD: 8.64; 95% CI, −21.72 to 39.00), estimated blood loss (p=0.15; MD: −24.04; 95% CI, −56.86 to 8.77), or conversion rates (p=0.84; OR: 1.12; 95% CI, 0.38–3.32). However, the RPN group had significantly less warm ischaemic time than the LPN group (p=0.0008; MD: −2.74; 95% CI, −4.35 to −1.14) (Fig. 2). There was no difference regarding postoperative length of hospital stay (p=0.37; MD: 0.11; 95% CI, −0.13 to 0.35) (Fig. 2).

There was no statistical difference between the two groups regarding complications (p=0.86; OR: 0.96; 95% CI, 0.65–1.43). There was no difference between the two groups regarding the Clavien classification (CC) of complications CC 1 and 2 (p=0.89; OR: 1.24; 95% CI, 0.77–2.01) and CC 3 and 4 (p=0.6; OR: 0.81; 95% CI, 0.37–1.80) (Fig. 3).

3.3.1. Subgroup analysis

Removing the studies with <25 procedures, there was no difference found between the two groups regarding operative times (p=0.55; MD: 11.32; 95% CI, −25.90 to 48.55), estimated blood loss (p=0.13; MD: −27.53; 95% CI, −63.13 to 8.07), or postoperative length of hospital stay (p=0.31; MD: 0.14; 95% CI, −0.13 to 0.41), Fig. 4. Furthermore, there was no difference regarding the complication rates (p=0.81; OR: 0.95; 95% CI, 0.64–1.42). However, similar to the general analysis, the RPN group had significantly less warm ischaemic time than the LPN group (p=0.001; MD: −2.83; 95% CI, −4.53 to −1.13) (Fig 2 and Fig 4).


Fig. 4 Forest plots of subgroup analysis: (a) subgroup analysis of operative times; (b) subgroup analysis of estimated ischaemic times; (c) subgroup analysis of blood loss; (d) subgroup analysis of length of hospital stay; (e) subgroup analysis of complications. The following studies are cited: Ellison [23], Haber [12], Jeong [19], Pierazio [4], Seo [21], and Williams [22].

3.4. Methodological quality assessment

All the studies were observational controlled studies. Figure 5 depicts the summary of the quality assessment based on the reviewing author's judgement of risks of bias for each included study. Only Pierorazio et al. had a high risk of selection bias due to the difference noted between the demographics of the LPN and RPN groups (the RPN group tended to be older) [4]. Otherwise the studies had a low risk of bias in all the categories. None of the studies were randomised or blinded, and the LPN groups were considered the control group.


Fig. 5 Quality assessment (risk of bias summary: review authors’ judgements about each risk of bias item for each included study). The following studies are cited: Ellison [23], Haber [12], Jeong [19], Kural [20], Pierazio [4], Seo [21], and Williams [22].

3.5. Discussion

3.5.1. Summary of the main results

This review found no significant difference between RPN and LPN, except that the RPN group had significantly less warm ischaemic time (Fig. 2). With the exception of Pierorazio et al. and Ellison et al, there was no difference between the two groups regarding age, sex, tumour size, laterality, or location. However, a pooled analysis did show that the RPN group had older patients, implying the procedure can safely accommodate a wider age range than its laparoscopic counterpart.

Regarding the operative parameters, no significant difference was found pertaining to the operative time, blood loss, or conversion rate (Fig. 2). No statistical significance was found regarding the postoperative and oncologic parameters such as hospital stay, surgical margins, or complications (Fig 2 and Fig 3).

Four studies reported less warm ischaemia time in the RPN group [4], [20], [22], and [23]. One study had less blood loss in the LPN group [12]; another had less blood loss in the RPN group [4]. Seo et al. reported that the overall operative time in the LPN group was shorter; however, they further subdivided the operative time into laparoscopic time, defined as the insertion of the ports to their removal, which did not show any difference between the two groups [21]. Ellison et al. also found that the LPN group had shorter operative times, overall ischaemic time, and shorter length of hospital stay [23]. Pierorazio et al. reported that the RPN group had less operative time [4]. Despite the subtle variations between the groups, the pooled meta-analysis found no statistical difference between the two groups regarding most of the outcome parameters, except for warm ischaemic time favouring the RPN group with less time needed [4], [12], [19], [20], [21], [22], and [23].

Although the only significant parameter favouring RPN, it is of vital importance because return of renal function depends on the duration of ischaemic time [31]. In fact, it is recommended that the pedicle clamping necessary during PN should be limited to 20min of warm ischaemia [31] and [32]. Although the kidney can tolerate longer cold ischaemic times, up to 2h, an international collaborative review suggested it should not go beyond 35min [32]. Nevertheless, controversy exists regarding the importance of warm ischaemia time compared with other modifiable risk factors such as the amount of benign renal parenchyma preserved. Warm ischaemia was used in all studies in this review when hilar clamping was performed (Fig. 2 and Table 2). Because PN is essentially nephron-sparing surgery, every minute is vital for preservation of renal function. Therefore, it can be deduced that RPN is superior to LPN in preserving nephrons and ultimately renal function.

The meta-analysis for one of the outcome parameters had significant heterogeneity, two other parameters had medium-level heterogeneity, and the remaining comparisons were considered as having low heterogeneity (Fig. 2). No cause for the heterogeneity was found because no difference regarding the risk of bias, timing and length of the studies, inclusion criteria, or country was isolated. Subgroup analysis conducted based on isolating small and large numbered cohort studies had no effect on the heterogeneity; however, no statistical significance between the two groups remained. Heterogeneity also applied to the warm ischaemia time. However, when small and large numbered cohorts were isolated, the heterogeneity did not change, and no change was found regarding the statistical difference, which favoured the RPN with less time. The discrepancy between the patient cohorts in the studies could explain the significant heterogeneity; however, no difference was found with the end result.

Regarding the five studies not included in the meta-analysis due to lack of data, three studies found no significant difference in any of the outcome parameters measured [15], [16], and [17]. DeLong et al. reported that the LPN had significantly less operative time but significantly longer warm ischaemic time [18]. Benway et al. reported significantly less blood loss, shorter warm ischaemic time, and shorter hospital stay in the RPN group; otherwise no difference was noted regarding the other outcome parameters [8].

3.5.2. Learning curve

Pierorazio et al. conducted a further analysis to determine whether or not a learning curve has an effect on the end result. Comparing their first 25 patients to their most recent patients, they found a significant improvement in the operative time, warm ischaemic time, and estimated blood loss in the LPN group [4]. However, similar differences were not found in the RPN group when comparing the earlier and later patient data. Ellison et al. also found that the ischaemic time, blood loss, and operative times improved after the first 33 cases, suggesting the learning curve does improve with time and more familiarity with the procedure by both the surgeon and the operating team [23]. Mottrie et al. also found that the impact of surgeons’ learning curve improved with time [1]. They showed that with more experience, the operative time, warm ischaemia time, and the need for pelvicaliceal repairs due to injury were reduced; however, no impact was found regarding blood loss or complications. In the largest reported series comparing early and later experiences of RPN, they showed that once the learning curve was past, there was a significantly decreased blood loss, transfusion rate, conversion rate, rate of postoperative complications, mean operative time, and length of hospital stay [33]. With further experience with RPN, lower complication rates and better results, especially with more complex tumours, compared with LPN may be noted. Nevertheless, further study is needed for verification, especially at a multi-institutional level.

3.5.3. Cost analysis

None of the studies conducted a cost analysis comparison between the laparoscopic and robotic groups. Nonetheless, Yu et al. compared the costs of various urologic procedures carried out open, laparoscopically, or using robots [26]. They found that robotic surgery was significantly more expensive than both laparoscopic and open procedures. But it was associated with a significantly shorter hospital stay with fewer complications and transfusion rates compared with laparoscopic and open procedures. Despite this, no social cost analysis was found in the literature that factors in the implications of a quicker recovery and shorter convalescence. It is estimated that RPN costs about $1600 more per person or an additional 6% per case [26].

Despite the increase in costs, numerous reports have suggested that RPN is feasible for tumours >4cm, complex tumours, in patients with prior abdominal surgery, in children, and even as single-port surgery [27], [34], [35], [36], [37], and [38]. A systematic review that included >700 patients who underwent RPN showed that RPN was feasible and had similar results to laparoscopic and open techniques [24].

3.5.4. Strengths and limitations of the review

The main limitation of this review is the inclusion of studies with small patient cohorts in the meta-analysis. Three of the seven studies included had ≥150 patients; the remaining studies had fewer numbers [4], [12], and [23]. This can skew the results because these studies might be reporting on their initial experiences. However, with more experience reported beyond the initial learning curve, results of such comparative analysis may differ. Removing studies with <25 procedures in either group, we found no difference in the end results in any of the parameters.

This review was impartial and conducted systematically and methodically in keeping with Cochrane standards. This represents the evidence available in the literature comparing early experiences of RPN with LPN.

It is evident that a large multicentre trial comparing the two procedures in addition to open PN is required once the learning curve for RPN has been overcome. This study needs to include a cost analysis between the procedures, including postdischarge convalescence and return to work analysis, in addition to patient and surgeon perspectives regarding pain and overall satisfaction with the procedure.

4. Conclusions

Meta-analysis of the literature reveals that RPN is a feasible and safe alternative to LPN with similar outcomes and low complication rates. RPN was found to have significantly less ischaemic time. Further studies are needed to evaluate the benefits of RPN and its cost effectiveness compared with LPN.

Author contributions: Omar M. Aboumarzouk had full access to all the data in the study and takes responsibility for the integrity of the data and the accuracy of the data analysis.

Study concept and design: Aboumarzouk

Acquisition of data: Aboumarzouk, Stein, Eyraud, Haber.

Analysis and interpretation of data: Aboumarzouk.

Drafting of the manuscript: Aboumarzouk, Stein, Somani.

Critical revision of the manuscript for important intellectual content: Aboumarzouk, Stein, Haber, Chlosta, Somani, Kaouk.

Statistical analysis: Aboumarzouk.

Obtaining funding: None.

Administrative, technical, or material support: Aboumarzouk, Stein, Eyraud, Somani.

Supervision: Aboumarzouk, Kaouk.

Other (specify): Bhaskar Somani and Jihad Kaouk have equal senior authorship.

Financial disclosures: Omar M. Aboumarzouk certifies that all conflicts of interest, including specific financial interests and relationships and affiliations relevant to the subject matter or materials discussed in the manuscript (eg, employment/ affiliation, grants or funding, consultancies, honoraria, stock ownership or options, expert testimony, royalties, or patents filed, received, or pending), are the following: None.

Funding/Support and role of the sponsor: None.

Acknowledgement statement: Omar M. Aboumarzouk acknowledges Dr. Isra Ashi for her support and advice.


  • [1] A. Mottrie, G. De Naeyer, P. Schatteman, P. Carpentier, M. Sangalli, V. Ficarra. Impact of the learning curve on perioperative outcomes in patients who underwent robotic partial nephrectomy for parenchymal renal tumours. Eur Urol. 2010;58:127-133 Abstract, Full-text, PDF, Crossref.
  • [2] E.K. Cha, D.J. Lee, J.J. Del Pizzo. Current status of robotic partial nephrectomy (RPN). BJU Int. 2011;108:935-941 Crossref.
  • [3] G. Gautam, B.M. Benway, S.B. Bhayani, K.C. Zorn. Robot-assisted partial nephrectomy: current perspectives and future prospects. Urology. 2009;74:735-740 Crossref.
  • [4] P.M. Pierorazio, H.D. Patel, T. Feng, J. Yohannan, E.S. Hyams, M.E. Allaf. Robotic-assisted versus traditional laparoscopic partial nephrectomy: comparison of outcomes and evaluation of learning curve. Urology. 2011;78:813-819 Crossref.
  • [5] B.K. Hollenbeck, D.A. Taub, D.C. Miller, R.L. Dunn, J.T. Wei. National utilization trends of partial nephrectomy for renal cell carcinoma: a case of underutilization?. Urology. 2006;67:254-259 Crossref.
  • [6] B.M. Benway, S.B. Bhayani. Surgical outcomes of robot-assisted partial nephrectomy. BJU Int. 2011;108:955-961 Crossref.
  • [7] G. Spana, G.P. Haber, L.M. Dulabon, et al. Complications after robotic partial nephrectomy at centers of excellence: multi-institutional analysis of 450 cases. J Urol. 2011;186:417-421
  • [8] B.M. Benway, S.B. Bhayani, C.G. Rogers, et al. Robot assisted partial nephrectomy versus laparoscopic partial nephrectomy for renal tumors: a multi-institutional analysis of perioperative outcomes. J Urol. 2009;182:866-872
  • [9] C.G. Rogers, A. Metwalli, A.M. Blatt, et al. Robotic partial nephrectomy for renal hilar tumors: a multi-institutional analysis. J Urol. 2008;180:2353-2356 discussion 2356 Crossref.
  • [10] B.M. Benway, S.B. Bhayani, C.G. Rogers, et al. Robot-assisted partial nephrectomy: an international experience. Eur Urol. 2010;57:815-820 Abstract, Full-text, PDF, Crossref.
  • [11] M. Aron, P. Koenig, J.H. Kaouk, M.M. Nguyen, M.M. Desai, I.S. Gill. Robotic and laparoscopic partial nephrectomy: a matched-pair comparison from a high-volume centre. BJU Int. 2008;102:86-92 Crossref.
  • [12] G.P. Haber, W.M. White, S. Crouzet, et al. Robotic versus laparoscopic partial nephrectomy: single-surgeon matched cohort study of 150 patients. Urology. 2010;76:754-758 Crossref.
  • [13] J.P. Higgins, S.G. Thompson, J.J. Deeks, D.G. Altman. Measuring inconsistency in meta-analyses. BMJ. 2003;327:557-560 Crossref.
  • [14] Higgins JPT, Green S, editors. Cochrane handbook for systematic reviews of interventions, v.5.1 [updated March 2011]. Cochrane Collaboration Web site.
  • [15] R.P. Caruso, C.K. Phillips, E. Kau, S.S. Taneja, M.D. Stifelman. Robot assisted laparoscopic partial nephrectomy: initial experience. J Urol. 2006;176:36-39 Crossref.
  • [16] C.L. Cho, K.L. Ho, S.S. Chu, P.C. Tam. Robot-assisted versus standard laparoscopic partial nephrectomy: comparison of perioperative outcomes from a single institution. Hong Kong Med J. 2011;17:33-38
  • [17] L.A. Deane, H.J. Lee, G.N. Box, et al. Robotic versus standard laparoscopic partial/wedge nephrectomy: a comparison of intraoperative and perioperative results from a single institution. J Endourol. 2008;22:947-952 Crossref.
  • [18] J.M. DeLong, O. Shapiro, A. Moinzadeh. Comparison of laparoscopic versus robotic assisted partial nephrectomy: one surgeon's initial experience. Can J Urol. 2010;17:5207-5212
  • [19] W. Jeong, S.Y. Park, E.I. Lorenzo, C.K. Oh, W.K. Han, K.H. Rha. Laparoscopic partial nephrectomy versus robot-assisted laparoscopic partial nephrectomy. J Endourol. 2009;23:1457-1460 Crossref.
  • [20] A.R. Kural, F. Atug, I. Tufek, H. Akpinar. Robot-assisted partial nephrectomy versus laparoscopic partial nephrectomy: comparison of outcomes. J Endourol. 2009;23:1491-1497 Crossref.
  • [21] I.Y. Seo, H. Choi, Y. Boldbaatr, J.W. Lee, J.S. Rim. Operative outcomes of robotic partial nephrectomy: a comparison with conventional laparoscopic partial nephrectomy. Korean J Urol. 2011;52:279-283 Crossref.
  • [22] Williams SB, Kacker R, Alemozaffar M, Francisco IS, Mechaber J, Wagner AA. Robotic partial nephrectomy versus laparoscopic partial nephrectomy: a single laparoscopic trained surgeon's experience in the development of a robotic partial nephrectomy program. World J Urol. In press.
  • [23] J.S. Ellison, J.S. Montgomery, J.S. Wolf Jr., K.S. Hafez, D.C. Miller, A.Z. Weizer. A matched comparison of perioperative outcomes of a single laparoscopic surgeon versus a multisurgeon robot-assisted cohort for partial nephrectomy. J Urol. 2012;188:45-50 Crossref.
  • [24] H. Laydner, J.H. Kaouk. Robotic partial nephrectomy: the new horizon. Arab J Urol. 2012;10:2-9 Crossref.
  • [25] S. Lee, J. Oh, S.K. Hong, S.E. Lee, S.S. Byun. Open versus robot-assisted partial nephrectomy: effect on clinical outcome. J Endourol. 2011;25:1181-1185 Crossref.
  • [26] H.Y. Yu, N.D. Hevelone, S.R. Lipsitz, K.J. Kowalczyk, J.C. Hu. Use, costs and comparative effectiveness of robotic assisted, laparoscopic and open urological surgery. J Urol. 2012;187:1392-1399 Crossref.
  • [27] Gupta GN, Boris R, Chung P, Marston Linehan W, Pinto PA, Bratslavsky G. Robot-assisted laparoscopic partial nephrectomy for tumors greater than 4cm and high nephrometry score: feasibility, renal functional, and oncological outcomes with minimum 1 year follow-up. Urol Oncol. In press.
  • [28] B.J. Scoll, R.G. Uzzo, D.Y. Chen, et al. Robot-assisted partial nephrectomy: a large single-institutional experience. Urology. 2010;75:1328-1334 Crossref.
  • [29] Mottrie A, Schatteman P, De Wil P, De Troyer B, Novara G, Ficarra V. Validation of the preoperative aspects and dimensions used for an anatomical (PADUA) score in a robot-assisted partial nephrectomy series. World J Urol. In press.
  • [30] J.A. Long, R. Yakoubi, B. Lee, et al. Robotic versus laparoscopic partial nephrectomy for complex tumors: comparison of perioperative outcomes. Eur Urol. 2012;61:1257-1262
  • [31] R.H. Thompson, B.R. Lane, C.M. Lohse, et al. Every minute counts when the renal hilum is clamped during partial nephrectomy. Eur Urol. 2010;58:340-345 Abstract, Full-text, PDF, Crossref.
  • [32] F. Becker, H. Van Poppel, O.W. Hakenberg, et al. Assessing the impact of ischaemia time during partial nephrectomy. Eur Urol. 2009;56:625-635 Abstract, Full-text, PDF, Crossref.
  • [33] J.H. Kaouk, S.P. Hillyer, R. Autorino, et al. 252 robotic partial nephrectomies: evolving renorrhaphy technique and surgical outcomes at a single institution. Urology. 2011;78:1338-1344
  • [34] Y. Gong, C. Du, D.Y. Josephson, T.G. Wilson, R. Nelson. Four-arm robotic partial nephrectomy for complex renal cell carcinoma. World J Urol. 2010;28:111-115 Crossref.
  • [35] J.H. Kaouk, R.K. Goel. Single-port laparoscopic and robotic partial nephrectomy. Eur Urol. 2009;55:1163-1170 Abstract, Full-text, PDF, Crossref.
  • [36] R.S. Lee, A.S. Sethi, C.C. Passerotti, et al. Robot assisted laparoscopic partial nephrectomy: a viable and safe option in children. J Urol. 2009;181:823-828 discussion 828–9
  • [37] M.N. Patel, L.S. Krane, A. Bhandari, et al. Robotic partial nephrectomy for renal tumors larger than 4cm. Eur Urol. 2010;57:310-316 Abstract, Full-text, PDF, Crossref.
  • [38] F.G. Petros, M.N. Patel, E. Kheterpal, et al. Robotic partial nephrectomy in the setting of prior abdominal surgery. BJU Int. 2011;108:413-419


a Wales Deanery, Urology Department, Cardiff, Wales, UK

b Islamic University of Gaza, College of Medicine, Gaza, Palestine

c Cleveland Clinic, Glickman Urologic and Kidney Institute, Cleveland, OH, USA

d Department of Urology, Institute of Oncology, UJK University, Kielce, Poland and Department of Urology, the Medical Centre of Postgraduate Education, Warsaw, Poland

e University Hospitals Southampton NHS Trust, Southampton, UK

lowast Corresponding author. Wales Deanery, Urology Department, Cardiff, Wales, UK and Islamic University of Gaza, College of Medicine, Gaza, Palestine. Tel. +44 7886 885677. Please visit to read and answer questions on-line. The EU-ACME credits will then be attributed automatically.

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