The ability to magnify the field of view while increasing inherent spatial resolution with Hi-Def technology enhances visualization during critical aspects of endovascular interventions and has the potential to translate into additional accuracy and precision in X-ray imaging guided procedures with enhanced real time visualization during complex endovascular procedures.
Canon Medical provides an innovative technology with the world’s first Hi-Def detector—offering more than twice the spatial resolution of conventional flat panel detectors (FPD)—for resolving fine details. This unique hybrid 12" x 12" or 12" x 16" FPD combines high definition imaging technology based on CMOS that boosts spatial resolution up to 6.6 line pairs per millimeter (lp/mm) with 76 micron pixels (Figure 1). This unique Alphenix system offers the standard magnification modes 16", 12", 10", 8", 6" or 4.3" fields of view (FOV) and three additional Hi-Def modes with 3", 2.3" and 1.5" FOV, allowing increased spatial resolution without interruption of procedure workflow. At any given point in time, both modes are available, and when needed, the selection between the two modes can be quickly changed using an FOV switch, without adding additional delay to the procedure.

A patient with no remarkable medical history presented to the emergency room with the worst headache of her life. Magnetic resonance angiography demonstrated a right carotid cavernous aneurysm measuring 11 × 7 mm. Lumbar puncture and head CT scan were negative for subarachnoid hemorrhage. The aneurysm size and location were confirmed with diagnostic cerebral angiography.
Under 2.3" x 2.3" FOV Hi-Def mode roadmap guidance, a 2.5Fr microcatheter over a 0.014" microwire was introduced and placed in the right distal M1 segment (Figure 3). An 2.4Fr microcatheter with a 45° angle was introduced concomitantly over the 0.014" microwire to cannulate the aneurysm neck. Under Hi-Def magnification, a single 9 × 33 mm coil was partially deployed into the aneurysm dome. Subsequently, a 4.5 × 23 mm LVIS Blue stent was introduced into the 2.5Fr microcatheter and deployment was started just distal to the aneurysm neck. Under 2.3" x 2.3" FOV Hi-Def mode, deployment showed good wall apposition throughout the curve of the cavernous carotid artery. The partially deployed coil was then fully deployed, followed by a second 5 × 20 mm coil. After the second coil deployment, DSA contrast runs were obtained and showed stasis in the aneurysm dome. The imaging mode was switched to large FOV, and a DSA contrast run was obtained to make sure the distal circulation was patent post-treatment. The patient was extubated and remained neurologically intact.

Advancements in medical device and imaging technology as well as accruing clinical evidence have accelerated the growth of endovascular treatment of cerebrovascular diseases. However, these procedures often necessitate the acquisition of many high-quality image sets and the use of long total fluoroscopy times, resulting in patients being potentially exposed to considerable radiation dose levels. And, with an increasing number of neurointerventional procedures being spurred by rapid advances in minimally invasive techniques and technologies for image guidance, this trend is likely to continue in the future. To mitigate this risk of unnecessary radiation exposure, and to provide data for decision support in justification and optimization, patient radiation dose tracking is considered to be of crucial importance. The ALARA principle, to limit radiation dose to “as low as reasonably achievable” should always be used; however, radiation doses should not be reduced at the expense of necessary image quality. Efforts focused solely on minimizing instantaneous radiation dose rates may paradoxically result in higher cumulative radiation dose delivered to the patient if there is an increase in overall irradiation time and/or increased utilization of higher dose acquisition modes to overcome inadequate visualization.
To quantify the clinical impacts and radiation dose of this novel dual-resolution detector, DICOM Radiation Dose Structured Report (RDSR) data was collected for all neurointerventional procedures performed before and after installation of the Hi-Def detector at a single center over a 45-month period. There were 1,702 pre- and 4,598 post-Hi-Def cases encompassing over 400,000 irradiation events in total. Normal and high-resolution magnification modes could be freely selected via the push of a button within the user interface. No other modifications were made to either the equipment or clinical protocols. Data from all cases were included and represented an equal mix of approximately 50% diagnostic and 50% interventions which remained consistent in both pre/post populations. A real-time patient skin dose tracking system (DTS) was used to monitor peak skin dose during the Hi-Def cases (Figure 5). A two-sample Student’s t-test analysis was performed to compare various technical parameters included in the RDSR. And, to further investigate any potential impacts on radiation dose, the cumulative air kerma, dose area product, and peak skin dose were plot as a function of Hi-Def utilization as a percentage of the total number of irradiation events (Figure 6).