For men diagnosed with localized prostate cancer, radical surgical resection of the prostate versus watchful waiting improves disease-specific survival . However, due to the morbidity of the procedure in terms of a high likelihood of blood transfusion, incontinence and erectile dysfunction, radiotherapy was the preferred treatment prior to Walsh's anatomic discoveries and technical refinement toward anatomic radical prostatectomy . The use of robotic assistance has transformed the surgical treatment of prostate cancer. In effect, surgeons have a wider margin for error in terms of pelvic venous blood loss, as both the median and range of blood loss have decreased in the transition from open to robotic-assisted radical prostatectomy [3▪]. Moreover, patient perception of new technology coupled with smaller incisions and less blood loss may increase the appeal of radical prostatectomy as compared to radiation therapy options and the potential anxiety of active surveillance.
Although cancer control is the primary goal of this operation, unintended side-effects associated with surgical resection, such as urinary incontinence and erectile dysfunction, present a technical challenge for urologic surgeons. Likewise for patients, postoperative health-related quality of life (HRQOL) is of important consideration when selecting a course of treatment for prostate cancer [4▪,5]. Among postoperative HRQOL outcomes, decreased potency following radical prostatectomy is commonly reported and is associated with poor postoperative quality of life [5,6]. Surgical technique has evolved in recent decades to improve postoperative potency without sacrificing oncologic control. Recent data suggest that the prevalence of postprostatectomy erectile dysfunction ranges from 64 to 80%, when the operation is performed using a nerve-sparing technique . However, the ability to accurately quantify postprostatectomy erectile function remains challenging despite the use of validated HRQOL instruments, such as the University of California, Los Angeles Prostate Cancer Index, Expanded Prostate Cancer Index, and the Sexual Health Inventory for Men [8–11] Difficulties in administering such instruments to ensure patient versus physician reporting and the use of continuous scores in the instruments to measure what many perceive to be a dichotomous outcome of potent versus impotent remain barriers to the widespread adoption of standardized measurement of sexual function. Therefore, variation in methodology and outcomes from published series confound cross-study interpretation . Despite difficulty in accurately assessing postprostatectomy erectile function, there have been continued efforts to refine surgical approaches and develop operative techniques in an effort to improve functional outcomes after radical prostatectomy. The evolution in the understanding of prostate anatomy with advances in surgical technique in the context of robotic surgery is evaluated in this review.
WALSH ANATOMIC RETROPUBIC RADICAL PROSTATECTOMY
In 1982, Walsh published his technique for an anatomic approach to radical prostatectomy, taking into careful consideration the blood supply and periprostatic anatomy in an effort to reduce blood loss and overall morbidity. Through his study of cadaveric models he identified the pelvic plexus as the autonomic innervation of the corpora cavernosum and the basis for neurophysiologic control of erectile function. He noted that the neurovascular bundle (NVB) coursed in a dorsolateral fashion to the prostate between the rectum and the urethra, proposing that injury to this structure is correlated with decreased postprostatectomy potency. His technique to avoid injury to these nerves involved incising the lateral pelvic fascia anterior to the NVB and dividing the lateral pedicle close to the prostate, avoiding injury to the branches of the pelvic plexus and the surrounding capsular vessels . This served as the basis for the ‘nerve-sparing’ radical prostatectomy in which the neurovascular bundles are preserved, resulting in improved postprostatectomy potency . Further review revealed that potency may be preserved when sparing either bilateral or unilateral NVBs [14–16]. Importantly, no significant difference in positive surgical margins was noted for nerve-sparing procedures in men with organ-confined disease or with extracapsular extension, suggesting that the nerve-sparing operation provides oncologic control while preserving functional outcomes [17▪,18,19].
EXPANSION OF ANATOMIC PRINCIPLES
The introduction of the nerve-sparing prostatectomy paved the way for further detailed study of the periprostatic neuroanatomy. In 2004, Costello et al. expanded upon Walsh's initial efforts, again using cadaveric models to further detail the precise anatomy of the neurovascular bundles as they relate to the prostate and seminal vesicles. They identified three functional components of the neurovascular bundle. The posterior and posterolateral component runs within Denonvillier's and pararectal fascia and innervates the rectum. A second component in the lateral NVB supplies the levator ani, and finally the cavernosal nerves and prostatic neurovascular supply originally described by Walsh and Donker  lie along the posterolateral surface. At the base of the prostate and at the seminal vesicles, the organization of these nerve bundles is rather chaotic, further detailing the complexity of the NVBs and the challenges of performing a technically sound nerve-sparing procedure . In 2006, Eichelberg et al. further illustrated the great variability in the distribution of nerves, using postoperative specimens to demonstrate that while the majority of the periprostatic nerves were found in the posterolateral location as initially described, approximately one-third were located on the anterior surface. They suggest using a higher incision along the ventral surface of the prostate during nerve-sparing to account for this variability . Takenaka, et al. confirmed this finding and described the nerves to be on the lateral and anterolateral surface of the prostate distributed as multiple fine fibers. Other authors have proposed performing a more anterior incision of the lateral pelvic fascia . Taking into account these recent findings regarding the anterior distribution of the nerves, Walsh recently refined his technique, describing a ‘high-anterior release’ of the apical NVB to avoid injury via excessive traction or electrocautery .
EVOLUTION OF NERVE-SPARING WITH ROBOTIC SURGERY
Efforts to detail precise periprostatic anatomy were spurred with the introduction of the robotic-assisted laparoscopic radical prostatectomy (RALP) in 2001 . Robotic surgery offered a new perspective on prostatic anatomy, allowing for a 12-fold magnified three-dimensional view and articulating robotic arms providing wristed, seven-degree motion. Furthermore, the pneumoperitoneum assists in providing a bloodless field for improved visualization of precise anatomic structures . In 2003, Tewari et al. detailed the prostatic anatomy from the perspective of this laparoscopic approach and identified webs of several smaller nerves with a more variable course than previously thought. This was further described as a ‘hammock-like’ distribution, suggesting that the nerves are dispersed along the lateral surface and do not form a single distinct structure.
INTRAFASCIAL AND INTERFASCIAL NERVE-SPARING
By taking into account the previously described anatomic principles and implications of delicate and athermal nerve dissection, several techniques have been proposed to optimize recovery of sexual function using a robot-assisted laparoscopic approach. The intraoperative magnification offered by the robot and wristed surgical instruments enables identification and preservation of periprostatic fascial planes housing the nerve fibers . A thorough understanding of these planes is crucial for performing an anatomic dissection while avoiding mechanical and thermal injury to the NVBs . The endopelvic fascia comprises multilayered connective tissue that encases the prostate and bladder and supports these structures by inserting onto the pubic bone as the puboprostatic ligaments. The layer of fascia that directly covers the prostate is the prostatic fascia, forming an intrafascial plane between this and the capsule. Just exterior to this laterally is the levator fascia, part of the parietal fascial layer, which serves as the boundary for an interfascial plane. Posteriorly, this same interfascial plane is bound by Denonvilliers fascia. Dissection along these avascular planes allows preservation of the neurovascular bundles, as the majority of the NVB is thought to run between the anterior extension of Denonvilliers fascia and the levator fascia. Dissection external to this – in the extrafascial plane – risks direct injury to the NVB and is shown to have significantly poorer sexual function outcomes [29–31]. Many authors advocate an interfascial dissection as a method of performing a nerve-sparing procedure without compromising oncologic control in appropriately selected patients . Some caution against performing an intrafascial nerve-sparing operation at the risk of positive surgical margins, particularly in those patients with T3 disease. Other studies have supported its use in that it offers improved potency with similar oncologic outcomes [33–35].
The ‘Veil of Aphrodite’ was first described by Menon and Hemal in 2004 [36,37] and refers to a plane of cavernosal nerves extending from the posterolateral to anterolateral surface of the prostate in a curtain-like distribution. Just as open surgeons utilize a high anterior release of the lateral pelvic fascia to preserve the anterior nerves, robotic prostatectomists propose this similar technique. An avascular interfascial plane is entered between the prostatic fascia and the lateral pelvic fascia. The ideal site of entry into this plane is debatable, as some authors propose incising the fascia laterally at the base and developing a plane towards the apex, whereas others suggest improved visibility using a posterior approach through Denonvilliers fascia [37,38]. Regardless of the initial entry point, the goal is to dissect within the interfascial plane to dissect the prostate medially while preserving the NVB laterally, creating a ‘veil’ of spared neurovascular tissue that is suspended from the pubourethral ligaments. Subsequent data have confirmed that this technique does not increase positive surgical margins and offer improved potency outcomes as compared to a conventional nerve-sparing procedure [37,39,40]. Menon et al. report that in 85 patients in whom the ‘Veil of Aphrodite’ technique was used, 94% had erections sufficient for penetration at a median follow-up of 18 months when using phosphodiesterase-5 inhibitors. However, Ganzer et al.[42▪] used immunohistochemical staining to map the distribution of the parasympathetic proerectile nerve fibers to largely course posterior to the horizontal axis of the prostate, calling into question whether high-release ‘Veil of Aphrodite’ dissections result in greater periprostatic tissue bulk scaffolding along the neurovascular bundle to attenuate nerurapraxia and improve erectile function rather than leaving more nerve fibers behind.
As the understanding of the anatomic distribution of the nerves continued to evolve, methods for tissue dissection were also examined. Ong et al. used canine models to demonstrate that the use of electrocautery for hemostasis during dissection of the NVB results in significant decreased erectile response and recommend avoiding its use during nerve-sparing procedures. Further support of athermal dissection for preservation of erectile function is illustrated by Ahlering et al. in a case series demonstrating better erectile function for nerve-sparing without the use of cautery . A recent systematic review showed significant improvement in 12-month potency rates using a cautery-free technique [45▪]. Additionally, while some advocate using the harmonic scalpel during prostate pedicle ligation and nerve-sparing due to less nerve injury relative to electrocautery, the heated tip of the harmonic scalpel may easily damage unmyelinated nerve fibers that comprise the neurovascular bundle .
MINIMIZING NEUROVASCULAR BUNDLE DISPLACEMENT DURING NERVE-SPARING AND NEURAPRAXIA
Although many studies have focused on achieving the optimal fascial plane of dissection, other authors have investigated the effect of intraoperative traction to the NVB on surgical outcomes. The mechanical stretch neuropathy has been demonstrated in vivo animal models . Mulhall et al. suggested that in addition to nerve dissection, neurogenic erectile dysfunction may also develop transiently due to mechanical traction. Rassweiler et al.[49,50] minimize traction to the NVB during seminal vesicle dissection, asserting the cavernous nerves are at especially high risk of traction injury during this step because the NVB runs in such close proximity. Kaul et al. believe delayed dorsal vein complex ligation and endopelvic fascia sparing reduces traction on the NVB and cavernous nerves during dissection of the prostatic fascia. Tewari et al. exclusively employ sharp dissection and avoid excessive traction during NVB release.
Mattei et al. hypothesized that excessive traction on the NVB and the resultant neuropraxia have negative effects both on continence and erectile function, detailing their technique for a tensionless, energy-free approach. They also describe vascular control in an athermal manner, using only microclips, and additionally advocate preservation of the bladder neck, early release of the NVB, dissection of the seminal vesicles only after complete lateral dissection of the NVB, and the use of the fourth robotic arm for constant tension-free exposure. However, media from some of these studies demonstrate assistant surgeon suction counter-traction of the neurovascular bundle to facilitate nerve-sparing. In contrast, Kowalczyk et al.[53▪] demonstrated an earlier return of sexual function and potency after a technical modification specifically avoiding assistant countertraction on the NVB during dissection (Fig. 1). They found clinically significant higher sexual function scores at 5-months postoperatively in a retrospective series of patients undergoing RALP, after adjusting for preoperative variables and nerve-sparing status, whereas no difference was found at 12-months, which the authors attribute to temporary neuropraxia. Additionally, after eliminating continuous assistant counter-traction of the neurovascular bundle, Alemozaffar et al.[54▪] minimized lateral displacement of the neurovascular bundle inherent in the use of blunt dissection to peel the neurovascular bundle away from the prostate (Fig. 2), demonstrating improved 5 and 12-month recovery of sexual function (Fig. 3).
SURGICAL LEARNING CURVE
Several high-volume surgeons with large series have reported on sequential surgical, oncologic, and functional outcomes, lending insight into the effect of a learning curve on RALP. Secin et al. have also reported a large international, multicenter study on the effect of the learning curve on positive surgical margin outcomes. However, less is known regarding a learning curve effect on sexual function. Zorn et al. reported improvement in operative time, blood loss, positive margins, and urinary continence, but no significant differences were demonstrated in sexual function at 12 months in a 700 patient series, despite increased surgeon experience. Conversely, Alemozaffar et al., through video review, demonstrated a learning curve for preservation of erectile function during robotic-assisted radical prostatectomy that comprised 413 cases to consistently achieve the nerve-sparing dissection plane, 268 cases to become independent of continuous countertraction to facilitate nerve-sparing dissection, and 400 cases to attenuate transient lateral displacement of the neurovascular bundle. Additionally, trainee involvement at the surgeon console during the nerve-sparing step was associated with worse erectile function recovery, emphasizing the existence of a significant learning curve for maximizing erectile function outcomes [54▪]. Moreover, this finding highlights the need for procedure-specific robotic simulators to overcome the nerve-sparing learning curve for neophyte robotic surgeons.
Gumus et al. also defined a learning curve in reporting improved potency rates in a smaller series of 120 men. Although cross-comparisons are made difficult by varying definitions of potency in the literature, the authors suggest that a surgeon without previous experience may be able to achieve similar functional results as some high-volume centers after 80 cases. However, there was no mention of specific technical modifications that improved potency outcomes.
From Walsh's initial description of an anatomic approach to radical prostatectomy to the advent of robotic prostate surgery, advances in the understanding of the neurovascular supply of the prostate have been met with continued evolution in surgical technique. Further understanding of prostatic fascial planes, the adoption of athermal, cautery-free technique and efforts to minimize traction during nerve dissection has enabled continued advances in optimizing recovery of sexual function.
Conflicts of interest
There are no conflicts of interest.
REFERENCES AND RECOMMENDED READING
Papers of particular interest, published within the annual period of review, have been highlighted as:
- ▪ of special interest
- ▪▪ of outstanding interest
Additional references related to this topic can also be found in the Current World Literature section in this issue (pp. 102–103).
1. Bill-Axelson AA, Holmberg LL, Ruutu MM, et al. Radical prostatectomy versus watchful waiting in early prostate cancer. N Engl J Med 2011; 364:1708–1717.
2. Walsh PC. Anatomic radical prostatectomy: evolution of the surgical technique
. J Urol 1998; 160 (6 Pt 2):2418–2424.
3▪. Novara G, Ficarra V, Rosen RC, et al. Systematic review and meta-analysis of perioperative outcomes and complications after robot-assisted radical prostatectomy. Eur Urol 2012; 62:431–452.
This article is a systematic review and meta-analysis comparing robot-assisted radical prostatectomy to retropubic radical prostatectomy and laparoscopic radical prostatectomy. The authors identified complication rates and risk factors for complication rates for robot-assisted radical prostatectomy along with surgical techniques for the robot-assisted surgery to improve these complications.
4▪. Alemozaffar M, Regan MM, Cooperberg MR, et al. Prediction of erectile function following treatment for prostate cancer. JAMA 2011; 306:1205–1214.
This purpose of this article is to predict long-term erectile function following prostate cancer treatment. The authors conclude that by stratifying individual pretreatment patient characteristics, posttreatment erectile function can be predicted, thus improving the patients’ decision-making process regarding their treatment options.
5. Sanda MG, Dunn RL, Michalski J, et al. Quality of life and satisfaction with outcome among prostate-cancer survivors. N Engl J Med 2008; 358:1250–1261.
6. Penson DF, Feng Z, Kuniyuki A, et al. General quality of life 2 years following treatment for prostate cancer: what influences outcomes? Results from the prostate cancer outcomes study. J Clin Oncol 2003; 21:1147–1154.
7. Murphy DG, Challacombe BJ, Costello AJ. Outcomes after robot-assisted laparoscopic radical prostatectomy. Asian J Androl 2009; 11:94–99.
8. Wheat JC, Hedgepeth RC, He C, et al. Clinical interpretation of the expanded prostate cancer index composite-short form sexual summary score. J Urol 2009; 182:2844–2849.
9. Rosen RC, Riley A, Wagner G, et al. The international index of erectile function (IIEF): a multidimensional scale for assessment of erectile dysfunction. Urology 1997; 49:822–830.
10. Wei JT, Dunn RL, Litwin MS, et al. Development and validation of the expanded prostate cancer index composite (EPIC) for comprehensive assessment of health-related quality of life in men with prostate cancer. Urology 2000; 56:899–905.
11. Litwin MS, Hays RD, Fink AA, et al. Quality-of-life outcomes in men treated for localized prostate cancer. JAMA 1995; 273:129–135.
12. Hu JC, Yu H-y, Kowalczyk KJ. Challenges of interpreting and improving radical prostatectomy outcomes: technique, technology, training, and tactical reporting. Eur Urol 2011; 59:1073–1074.
13. Walsh PC, Donker PJ. Impotence following radical prostatectomy: insight into etiology and prevention. J Urol 1982; 128:492–497.
14. Walsh PC, Mostwin JL. Radical prostatectomy and cystoprostatectomy with preservation of potency. Results using a new nerve-sparing technique. Br J Urol 1984; 56:694–697.
15. Walsh PC, Epstein JI, Lowe FC. Potency following radical prostatectomy with wide unilateral excision of the neurovascular bundle. J Urol 1987; 138:823–827.
16. Finley DS, Rodriguez EE, Skarecky DW, Ahlering TE. Quantitative and qualitative analysis of the recovery of potency after radical prostatectomy: effect of unilateral vs. bilateral nerve sparing. BJU Int 2009; 104:1484–1489.
17▪. Moore BM, Savdie R, PeBenito RA, et al. The impact of nerve sparing on incidence and location of positive surgical margins in radical prostatectomy. BJU Int 2012; 109:533–538.
This article examined whether the risk for positive surgical margins was increased during nerve-sparing surgery for either organ confined disesase or extracapsular extenstion. The authors concluded that the nerve sparing approach does not increse the rate of positive surgical margins when the patients are selected appropriately.
18. Palisaar R-J, Noldus J, Graefen M, et al. Influence of nerve-sparing (NS) procedure during radical prostatectomy (RP) on margin status and biochemical failure. Eur Urol 2005; 47:176–184.
19. Lepor H, Tareen B. Neurovascular bundle resection: does it improve the margins? Urol Oncol 2010; 28:215–218.
20. Costello AJ, Brooks MM, Cole OJ. Anatomical studies of the neurovascular bundle and cavernosal nerves. BJU Int 2004; 94:1071–1076.
21. Eichelberg CC, Erbersdobler AA, Michl UU, et al. Nerve distribution along the prostatic capsule. Eur Urol 2007; 51:105–110.
22. Takenaka A, Murakami G, Soga H, et al. Anatomical analysis of the neurovascular bundle supplying penile cavernous tissue to ensure a reliable nerve graft after radical prostatectomy. J Urol 2004; 172:1032–1035.
23. Amend B, Hennenlotter J, Kuehs U, et al.
Prostatic peripheral nerve distribution may impact the functional outcome of nerve-sparing prostatectomy. World J Urol 2011. [Epub ahead of print]
24. Nielsen ME, Schaeffer EM, Marschke P, Walsh PC. High anterior release of the levator fascia improves sexual function
following open radical retropubic prostatectomy. J Urol 2008; 180:2557–2564.
25. Binder J, Kramer W. Robotically-assisted laparoscopic radical prostatectomy. BJU Int 2001; 87:408–410.
26. Ficarra VV, Cavalleri SS, Novara GG, et al. Evidence from robot-assisted laparoscopic radical prostatectomy: a systematic review. Eur Urol 2007; 51:45–56.
27. Tewari A, Peabody JO, Fischer M, et al. An operative and anatomic study to help in nerve sparing during laparoscopic and robotic radical prostatectomy. Eur Urol 2003; 43:444–454.
28. Walz JJ, Graefen MM, Huland HH. Surgical anatomy of the prostate in the era of radical robotic prostatectomy. Curr Opin Urol 2011; 21:173–178.
29. Walz J, Burnett AL, Costello AJ, et al. A critical analysis of the current knowledge of surgical anatomy related to optimization of cancer control and preservation of continence and erection in candidates for radical prostatectomy. Eur Urol 2010; 57:179–192.
30. Chauhan S, Coelho RF, Rocco B, et al. Techniques of nerve-sparing and potency outcomes following robot-assisted laparoscopic prostatectomy. Int Braz J Urol 2010; 36:259–272.
31. Shikanov S, Woo J, Al-Ahmadie H, et al. Extrafascial versus interfascial nerve-sparing technique for robotic-assisted laparoscopic prostatectomy: comparison of functional outcomes and positive surgical margins characteristics. Urology 2009; 74:611–616.
32. Zorn KC, Gofrit ON, Orvieto MA, et al. Robotic-assisted laparoscopic prostatectomy: functional and pathologic outcomes with interfascial nerve preservation. Eur Urol 2007; 51:755–762.
33. Potdevin L, Ercolani M, Jeong J, Kim IY. Functional and oncologic outcomes comparing interfascial and intrafascial nerve sparing in robot-assisted laparoscopic radical prostatectomies. J Endourol 2009; 23:1479–1484.
34. Secin FP, Savage C, Abbou C, et al. The learning curve for laparoscopic radical prostatectomy: an international multicenter study. J Urol 2010; 184:2291–2296.
35. Galfano A, Ascione A, Grimaldi S, et al. A new anatomic approach for robot-assisted laparoscopic prostatectomy: a feasibility study for completely intrafascial surgery. Eur Urol 2010; 58:457–461.
36. Menon M, Hemal A. Vattikuti Institute prostatectomy: a technique of robotic radical prostatectomy: experience in more than 1000 cases. J Endourol 2004; 18:611–619.
37. Menon M, Shrivastava A, Kaul S, et al. Vattikuti Institute prostatectomy: contemporary technique and analysis of results. Eur Urol 2007; 51:648–657.
38. Ischia JJ, Sengupta SS, Webb DD. Early release of pedicles and posterior development of the ‘Veil of Aphrodite’ in robotic-assisted laparoscopic prostatectomy (RALP). BJU Int 2010; 106:1856–1861.
39. Savera AT, Kaul S, Badani K, et al. Robotic radical prostatectomy with the ‘Veil of Aphrodite’ technique: histologic evidence of enhanced nerve sparing. Eur Urol 2006; 49:1065–1073.
40. Kaul SS, Bhandari AA, Hemal AA, et al. Robotic radical prostatectomy with preservation of the prostatic fascia: a feasibility study. Urology 2005; 66:1261–1265.
41. Menon MM, Shrivastava AA, Bhandari MM, et al. Vattikuti Institute prostatectomy: technical modifications in 2009. Eur Urol 2009; 56:89–96.
42▪. Ganzer R, Stolzenburg JU, Wieland WF, Brundl J. Anatomic study of periprostatic nerve distribution: immunohistochemical differentiation of parasympathetic and sympathetic nerve fibres. Eur Urol 2012; 62:1150–1156.
This is a peer-reviewed journal article in which the authors characterize the distribution of periprostatic nerves using immunohistochemical analysis to identify proerectile parasympathetic nerves from sypathetic nerves on whole-mount sections of prostates following nonnerve-sparing laparoscpic radical prostatectomy The purpose was to identify the quality of nerves in the ventrolateral position of the prostate to enhance surgical planning for improved potency results. They found that only a minority of the ventrolateral periprostatic nerves were of parasympathetic proerectile quality, and thus a high incision of the prostate during nerve-sparing operations may help to preserve more parasympathetic nerves at the base and middle, but is of little help at the apex.
43. Ong AM, Su L-M, Varkarakis I, et al. Nerve sparing radical prostatectomy: effects of hemostatic energy sources on the recovery of cavernous nerve function in a canine model. J Urol 2004; 172 (4 Pt 1):1318–1322.
44. Ahlering TE, Rodriguez EE, Skarecky DW. Overcoming obstacles: nerve-sparing issues in radical prostatectomy. J Endourol 2008; 22:745–750.
45▪. Ficarra V, Novara G, Ahlering TE, et al.
Systematic review and meta-analysis of studies reporting potency rates after robot-assisted radical prostatectomy. Eur Urol 2012.
This is a systematic review and meta-analysis designed to evaluate the prevalence and risk factors of erectile dysfunction after robotic-assisted radical prostatectomy and to identify surgical techniques that may improve the rate of potency recovery. The purpose was to compare Robot-assissted radical prostatectomy to open radical prostatectomy had laparoscopic radical prostatectomy in terms of postoperative potency rates. The authors are the first to conclude that there is a significant advantage of RALP compared with the open radical retropubic prostatectomy approach in terms of 12-month potency rates and that the use of a cautery-free technique improves the incidence of potency recovery.
46. Chen C, Kallakuri S, Vedpathak A, et al.
The effects of ultrasonic and electrosurgery devices on nerve physiology. Br J Neurosurg 2012. [Epub ahead of print]
47. Wall EJ, Massie JB, Kwan MK, et al. Experimental stretch neuropathy. Changes in nerve conduction under tension. J Bone Joint Surg Br Vol 1992; 74:126–129.
48. Mulhall JP, Slovick RR, Hotaling JJ, et al. Erectile dysfunction after radical prostatectomy: hemodynamic profiles and their correlation with the recovery of erectile function. J Urol 2002; 167:1371–1375.
49. Rassweiler J, Wagner AA, Moazin M, et al. Anatomic nerve-sparing laparoscopic radical prostatectomy: comparison of retrograde and antegrade techniques. Urology 2006; 68:587–591.
50. Kaul S, Savera A, Badani K, et al. Functional outcomes and oncological efficacy of Vattikuti Institute prostatectomy with Veil of Aphrodite nerve-sparing: an analysis of 154 consecutive patients. BJU Int 2006; 97:467–472.
51. Tewari AA, Takenaka AA, Mtui EE, et al. The proximal neurovascular plate and the tri-zonal neural architecture around the prostate gland: importance in the athermal robotic technique of nerve-sparing prostatectomy. BJU Int 2006; 98:314–323.
52. Mattei A, Naspro R, Annino F, et al. Tension and energy-free robotic-assisted laparoscopic radical prostatectomy with interfascial dissection of the neurovascular bundles. Eur Urol 2007; 52:687–695.
53▪. Kowalczyk KJ, Huang AC, Hevelone ND, et al. Stepwise Approach for Nerve Sparing Without Countertraction During Robot-Assisted Radical Prostatectomy: Technique and Outcomes. Eur Urol 2011; 60:536–547.
This is a retrospective study in which the authors compare potency outcomes following nerve-sparing robot-assisted radical prostatectomy when performed with and without countertraction on the neurovascular bundle. They demonstrate that use of countertraction results in neuropraxia and delayed recovery of sexual function and potency. The authors describe a stepwise surgical technique to perform nerve-sparing without countertraction.
54▪. Alemozaffar M, Duclos A, Hevelone ND, et al. Technical refinement and learning curve for attenuating neurapraxia during robotic-assisted radical prostatectomy
to improve sexual function
. Eur Urol 2012; 61:1222–1228.
This is a retrospective study of 400 consecutive nerve-sparing robot-assisted radical prostatectomy in which the authors demonstrate and quantify the learning curve for improving sexual function outcomes. The specific technical modifications that were made over the course of the 400 surgeries that contributed to the improvement in outcomes are included in the article.. The authors conclude that improved postoperative sexual function was associated with greater surgeon experience, younger patient age, and better preoperative sexual function. The authors find that attentuating lateral displacement of the neurvascular bundle decreases neuropraxia, thus improving postoperative sexual function.
55. Zorn KC, Wille MA, Thong AE, et al. Continued improvement of perioperative, pathological and continence outcomes during 700 robot-assisted radical prostatectomies. Can J Urol 2009; 16:4742–4749.
56. Gumus E, Boylu U, Turan T, Onol FF. The learning curve of robot-assisted radical prostatectomy. J Endourol 2011; 25:1633–1637.