
The da Vinci Single Port (SP) robotic surgical system was introduced by Intuitive Surgical, Inc. (ISRG) in 2018 after being approved by the US Food and Drug Administration (FDA) in May of that year.1 Since its introduction, ISRG has continued to develop improved access instrumentation, and the company has received clearance for the SP platform to be used for a variety of genitourinary disease states. In 2020, the FDA approved the SP Access Port Kit to enhance SP access for several surgical procedures, including radical prostatectomy, pyeloplasty, nephrectomy, and partial nephrectomy.2 The SP platform is intended to enable surgeons to perform robot-assisted surgical procedures with the same precision as the traditional multiport techniques that have been developed over the last 20 years.
Since the introduction of the SP platform, many urologists from around the world have attempted different techniques and approaches to traditional multiport robotic surgical procedures, but those techniques present several challenges that need to be addressed before their widespread adoption. One notable challenge is the lack of availability of SP platforms in all hospital systems. According to the latest ISRG investor reports, there are currently 150 total SP deployments compared with more than 7900 multiport robotic systems.3 Furthermore, the SP platform has not yet been approved by the FDA for general surgical procedures, which comprise the largest percentage of robot-assisted procedures performed using da Vinci platforms worldwide.4
Since the introduction of the SP platform, 3 general methods have been described for prostatic access and surgery: perineal, transvesical, and extraperitoneal. The transperitoneal approach is not included because a primary benefit of SP surgery is the potential to avoid peritoneal access and facilitate surgical procedures in “hostile” abdomens with significant scarring related to prior surgeries.