
The deployment signals a shift toward more versatile, minimally invasive platforms that can improve outcomes and expand robotic surgery beyond current specialties, influencing hospital investment strategies.
Robotic‑assisted surgery has moved from niche procedures to a mainstream pillar of modern operating rooms, driven by advances in imaging, instrumentation, and regulatory approvals. The FDA's clearance of the Hugo RAS system adds a new competitor to a market long dominated by a single manufacturer, offering hospitals an alternative that promises comparable clinical benefits with distinct ergonomic features. Early adopters like Cleveland Clinic are positioning themselves at the forefront of this evolution, leveraging the technology to attract patients seeking cutting‑edge, minimally invasive care.
The Hugo RAS distinguishes itself through modular robotic arms that can be re‑oriented to suit patient anatomy, granting surgeons greater flexibility in accessing the prostate. Its open‑console design departs from traditional enclosed stations, allowing surgeons to operate while maintaining a more natural line of sight and using foot pedals alongside hand controls. These innovations aim to reduce surgeon fatigue and improve precision, potentially translating into lower intra‑operative blood loss, shorter hospital stays, and faster recovery—key metrics that hospitals track for both clinical quality and reimbursement.
Beyond urology, the system’s adaptable architecture suggests broader applicability across thoracic, colorectal, and gynecologic procedures. As more institutions evaluate the Hugo RAS, competitive pricing and diversified technology stacks could lower barriers to entry for midsize hospitals, expanding patient access to robotic surgery. The ripple effect may accelerate research into procedure‑specific outcomes, drive further FDA clearances, and reshape the strategic roadmap for health systems investing in next‑generation surgical platforms.
Cleveland Clinic recently became the first health system in the U.S. to use a new robotic-assisted surgery system for prostatectomy.
The FDA approved the Hugo RAS system in December. The system includes modular arms that let surgeons select operating angles and an open-console setup in which the surgeon uses foot pedals and hand controls to operate the robot, according to a Feb . 17 news release.
Jihad Kaouk, MD, professor and chair of Cleveland Clinic’s Glickman Urologic Institute and Zegarac-Pollock Endowed Chair in Robotic Surgery, was the principal investigator for the study that supported FDA approval of the robotic system.
“This case exemplifies Cleveland Clinic’s mission to lead surgical innovation and expand access to minimally invasive surgery for patients,” Dr. Kaouk said in the news release. “The potential for this new technology extends beyond urology to other specialties, and we look forward to building our experience with this new system and exploring the added benefit for patients.”
Minimally-invasive surgery is tied to reduced blood loss in patients, reduced length of stay, shorter recovery times and less postoperative pain, Cleveland Clinic said.
The post Cleveland Clinic 1st to use new robot for prostate surgery appeared first on Becker's Hospital Review | Healthcare News & Analysis.
Comments
Want to join the conversation?
Loading comments...