Lung cancer is the leading cause of cancer deaths worldwide.1
Explore additional research and evidence about Ion robotic bronchoscopy—Outcomes, experiences, and techniques from some of the early adopters of the Ion technology.
A single-center study included 407 patients with 503 lung nodules (median size: 21 mm). 24.4% of the nodules had a bronchus sign. This study assessed the diagnostic success and clinical outcomes in a large multisurgeon cohort using radial probe endobronchial ultrasound (R-EBUS) and 2D fluoroscopy.
A multicenter review of 225 patients compared robotic-assisted bronchoscopy (RAB) with Ion and CT-guided transthoracic biopsy (CTTB) to evaluate lung nodules. Both methods had similar diagnostic yield, but CTTB had a significantly higher complication rate.
A single-center study of 241 patients who underwent Ion robotic-assisted bronchoscopy with fixed cone beam CT (CBCT). The study looked at technical factors and clinical outcomes of combining CBCT with the Ion system.
A comparison study of three software platforms. Each create virtual airway maps to reach a target lesion. It examined differences in segmentation capabilities between planning software for electromagnetic navigation platforms and Ion PlanPoint.
A multicenter, prospective study including 365 patients who had Ion robotic-assisted bronchoscopy with 2D fluoroscopy. This abstract covers the group in the performance stage, focusing on procedural outcomes like diagnostic yield, sensitivity for malignancy, and safety.
A review of the first 200 biopsy procedures at UT Southwestern Medical Center. This study details the diagnostic accuracy, sensitivity for malignancy, specificity, safety, and other procedural outcomes
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Ion Endoluminal System
The Ion Endoluminal System assists the user in navigating a catheter and endoscopic tools in the pulmonary tract using endoscopic visualization of the tracheobronchial tree for diagnostic and therapeutic procedures. The Ion Endoluminal System enables fiducial marker placement. It does not make a diagnosis and is not for pediatric use.
The Flexision Biopsy Needle is used with the Ion Endoluminal System to biopsy tissue from a target area in the lung.
The PlanPoint Software uses patient CT scans to create a 3D plan of the lung and navigation pathways for use with the Ion Endoluminal System.
The Ion Endoluminal System, the Flexision Biopsy Needle and the PlanPoint Software are class IIa medical devices CE marked (CE 2460) under the European Medical Devices Regulation (EU 2017/745), manufactured by Intuitive Surgical, Inc. Refer to Instructions For Use before use.
Some products, features or technologies may not be available in all countries. Please contact your local Intuitive representative for product availability in your region. Refer to the product specific User Manual for indications, contraindications, warnings and other product information.
Individuals’ outcomes may depend on a number of factors—including but not limited to—patient characteristics, disease characteristics, and/or physician experience.