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Study reveals safety and feasibility of robotically-assisted PCI

May 10, 2016 By Abigail Esposito

Cath Lab at JCMC Mountain States Health Alliance_submitted for staff written casestudy

The technology of performing robotically-assisted PCI is relatively new and was recently approved by the FDA. Image source: www.dicardiology.com

A first-of-its kind study using robotic technology to remotely control coronary guidewires and stents illuminates the feasibility of performing percutaneous coronary intervention (PCI) on patients with complex coronary lesions. Similar clinical outcomes compared to the PCI procedure performed manually were reported. Results of the 18-month complex robotically-assisted percutaneous coronary intervention (CORA-PCI) trial were presented as a late-breaking clinical trial at the Society for Cardiovascular Angiography and Interventions 2016 Scientific Sessions in Orlando.

The technology of performing robotically-assisted PCI is relatively new and was recently approved by the FDA. Previous studies were performed largely on patients with simple coronary lesions.

“For the first time, we’ve shown nearly identical outcomes with a group of complex patients,” said Ehtisham Mahmud, MD, the study’s lead author and division chief, cardiovascular medicine and director, interventional cardiology and cardiac cath lab at the University of California, San Diego School of Medicine. He noted that approximately 80% of lesions treated in the CORA-PCI trial were complex, which is more reflective of contemporary interventional cardiology practice.

Consecutive robotic and manual procedures were performed by a single operator and a total of 334 PCI procedures were analyzed (108 R, 157 lesions; 226 M, 336 lesions) in 315 patients (age 67.7 ± 11.8). The majority of patients (78%) were male. Clinical success was similar between the groups (99.1% for robotic PCI versus 99.6% for manual PCI, p=0.64).

In the robotically-assisted PCI group, over 90% of the procedures were performed entirely robotically or with minimal manual assistance. Procedure time was longer (robotic PCI 44:30 ± 26:04 min versus manual PCI 36:34 ± 23:03 min, p=0.005) and remained significant after accounting for Syntax score, primary lesion length and complexity (p=0.026); however, the longer procedure time was limited to the low complexity lesions. Propensity matched analysis (n=94 each group) confirmed the longer procedure time in the R-PCI group with comparable clinical success (98.9% versus 100%, p=1.0). No increase in resource utilization or patient radiation exposure was reported with robotic PCI.

According to Mahmud, the data presented show that using robotic technology to perform PCI is a viable alternative to manual PCI with the potential benefits of reducing radiation exposure and orthopedic injuries to the interventional cardiologist.

Society for Cardiovascular Angiography and Interventions
www.scai.org

 

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