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Artis zeego

Manufactured by Siemens
Sourced in Germany

The Artis Zeego is a multi-axis robotic system designed for angiography and interventional radiology procedures. It provides versatile imaging capabilities to support a wide range of clinical applications. The system features a ceiling-mounted, robotic C-arm that can be positioned around the patient to capture high-quality images from various angles.

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34 protocols using artis zeego

1

Digital Subtraction Angiography with C-arm

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Digital subtraction angiography was performed on a C-arm angiography system with flat panel detectors (Artis zeego; Siemens Healthcare GmbH, Erlangen, Germany). The fluoroscope was operated in the automatic mode for control of tube peak kilovoltage kVp, Cu filtration thickness, and milliamperes. Digital subtraction angiography was performed by 3 experienced interventional neuroradiologists.
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2

Carotid Artery Angiography in Rabbits

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Similar to the CTPI subgroup, rabbits in the DSA subgroup were fixed onto the operation table in supine position. After supplemental anesthesia and skin preparation, the right main carotid artery was exposed and punctured. Depending on the group (IR-0, IR-6, IR-12, or IR-24), angiography of the lower abdominal aorta was performed to assess changes in the blood flow changes of the right hindlimb using a 2.7 F microcatheter (Terumo, Japan) through the carotid artery at 0, 6, 12, or 24 h. The DSA equipment used in this study was Artis Zeego (Siemens, Erlangen, Germany). Iodixanol (320 mg/mL) was injected with a velocity of 3 mL/s through the microcatheter using a power injector. The injection pressure was 200 psi and the total dose of the contrast agent was 9 mL. The DSA acquisition frame rate was six frames per sec and each acquisition process lasted until the inferior vena cava was visualized.
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3

Rapid UF-CBCT Imaging for TACE Therapy

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We used a multiaxis robotic CBCT system (Artis zeego, Siemens Healthcare, Forchheim Germany) to conduct patient examinations during TACE therapy. This UF-CBCT system offers the possibility to rotate the tube-detector system around the patient with a maximum speed of up to 100°/sec. The system is equipped with a latest generation 30 × 40 cm flat panel detector made of amorphous silicon with cesium iodide scintillator (aSi:CsI). During UF-CBCT acquisition the system acquires projection images on a 200° circular trajectory with a constant angular frame increment (AI); that is, each AI degree the system acquired an image. This means that the image acquisition frame rate differs between the acceleration phase, the phase with constant speed, and the deceleration phase of the CBCT.
The correlation between UF-CBCT rotation speed (vcbct), readout speed (vro), and angular frame increment (AI) is as follows:
AI(/°image)=vcbct(/°s)  vro(image/s).
With a given angular increment for a UF-CBCT acquisition the maximum readout speed of the detector may limit the maximum CBCT rotation speed.
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4

Intraoperative CBCT Imaging and Navigation

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Surgical procedures were conducted in the Guided Therapeutics (GTx) operating room, which integrates an Artis Zeego (Siemens Healthcare) system for intraoperative CBCT imaging13 (link),22 (link) (Fig. 1). This system is based on a flat-panel detector (1,920 × 2,480) and x-ray source (up to 125 kV) mounted on a robotic C-arm gantry. CT acquisition consisted of 248 x-ray projections obtained during a 10-second orbit, yielding images encompassing 25 × 25 × 18 cm using 0.5-mm3 voxels.
The custom navigation software (GTx-Eyes) provides different 3D visualizations, including triplanar views, bone-surface renderings, and clipping planes23 . It also provides real-time feedback on the location and trajectory of planar cutting instruments in 2D and 3D views (Fig. 2). This has been validated in preclinical orthopaedic oncology studies in pelvic and extremity models24 (link),25 (link) and in head and neck surgery26 ,27 (link). Various cutting instruments can be navigated using an intraoperative calibration jig (see Appendix Supplemental Figure 1).
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5

Brachytherapy Seed Implantation Protocol

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Regarding the production of BNT (Figure 1), three-column 125I seeds were regularly placed on a sticky medical device with a 5 mm interval distance, which was adhered to NFNT. The position was consistent with the occlusion according to pre-operative CT and esophagography results; 125I seeds exceeded the tumor length by 2 cm above and below the tumor. Finally, No. 7 non-absorbable nylon wire was used to fix 125I seeds to prevent displacement. Every 125I radioactive seed (Tianjin Saide Biopharmaceutical Co., Ltd., China) was 4.5 mm × 0.8 mm, with an average energy of 27-35 keV, half-life of 59.6 days, tissue penetration capacity of 1.7 cm, and single seed radioactivity of 0.8 mCi. Fluoroscopy was performed with a flat-panel detector and digital subtraction angiography (Artis Zeego, Siemens, Germany).
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6

Hybrid Operating Room FEVAR Procedure

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All procedures were performed under general anaesthesia in a hybrid operating room with a fixed imaging system and computed tomography fusion (Artis Zeego, Siemens Healthineers AG, Erlangen, Germany). Surgical access was performed with a bilateral femoral cutdown and double purse string sutures of Prolene (Ethicon, Somerville, NJ, USA) fitted with a snugger were used in all access vessels to potentially allow removal of the sheaths in order to restore blood flow to the artery. The detailed explanation of the FEVAR procedure execution in our centre has been previously described [15 (link),16 (link)].
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7

CBCT-Guided Robotic Lung Biopsy

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Each patient underwent initial CBCT imaging for procedural planning and guidance using a robotic c-arm system and iPilot software (Artis zeego, Siemens Healthineers). No additional electromagnetic navigation or shape-sensing system was used. All CBCT imaging was performed using an 8-second protocol (396 projection images acquired at 0.5 deg/projection) during an inspiratory breath hold at Vt, using a ventilation protocol as described further.
In each patient, the target lesion was highlighted using a process called segmentation, on the initial CBCT scan, for overlay on live fluoroscopic images. Subsequently, CBCT augmented fluoroscopy (AF) was used to navigate a steerable catheter (Edge Firm Tip, Medtronic, varying degrees) to the target lesion. Once the navigation catheter was optimally aligned, a biopsy tool was inserted and advanced to the lesion. r-EBUS was used in all cases; these images were classified as concentric, eccentric, or none. Then, CBCT was performed again, for tool-in-lesion confirmation to assess if the biopsy tool was visible within the lesion in 3 orthogonal planes (axial, sagittal, and coronal). If the tool touched the lesion but was not inside the lesion, this was considered tool-touch-lesion (TTL). It was considered a center strike if the tool was in the middle third of the lesion in all views. Rapid onsite pathologic evaluation was utilized in all cases.
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8

Detailed Lower Extremity DSA Imaging

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DSA images were obtained using an angiographic system (Artis Zeego; Siemens, Germany). Medical restraint bands were used to limit the movement of the affected limb during the angiography, so as not to affect the quality of image acquisition. A 5-F catheter was placed through the 6F contralateral sheath in the affected limb through the common femoral artery for all arteriographic procedures. Four successive DSA scans were performed over the entire lower extremity. The first segment contained the catheter tip and the femoral head, and the C-arm was tilted 30° medially to fully view the superficial and deep femoral arteries. The second segment observed from the anteroposterior view included the knee joint as the lower boundary of the field of view (FOV). The upper boundary of the third segment observed from the anteroposterior view was 5 cm above the upper edge of the patella. The fourth segment of the lower boundary observed from lateral view contained the entire affected foot. A power-injector was set to deliver the contrast material (320 mg iodine/ml) at a flow rate of 3 cc/s. The dose of contrast material was 9 cc for the first three segments and 15 cc for the last segment. A high-pressure syringe was set to a pressure of 300 PSI and the number of angiographic frames was 15 per second.
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9

Ultrasonic-Guided Ferrofluid Droplet Manipulation

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There are two sets of magnetic actuation systems in the experiment. A Helmholtz electromagnetic coil setup consists of three sets of orthogonally placed coils, signals are generated by four motor drivers (ESCON70/10, Maxon) and controlled by a PC. By adjusting mathematical expressions into the control program, we can use this setup to generate 1D, 2D and 3D magnetic fields with specific requirements. When the system is matched with an ultrasonic device (Terason t3200, Teratech Corporation, USA), it can carry out real-time ultrasonic-guided ferrofluid droplet motion. In addition, a 6-DOF robotic arm and three coils are assembled together, and paired with a fluoroscopy imaging device (Artis zeego, SIEMENS) to guide the movement of ferrofluid droplets in real time. Magnetic field gradient force and magnetic torque can be generated in this system.
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10

Hybrid Neurosurgical Robotic C-Arm System

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A floor-mounted multi-axis robotic C-arm monoplane DSA system (Artis zeego, Siemens Healthcare, Forchheim, Germany) equipped with “syngo X workplace” software (Siemens Healthcare, Forchheim, Germany) was employed in all cases. The system and software consist of a 3-dimensional rotational angiograph (3DRA), syngo DynaCT, syngo 3D stenosis measurement, syngo Aneurysm Guidance Neuro and syngo Needle Guidance software (syngo X workplace, Siemens Healthcare, Forchheim, Germany). The hybrid OR was also installed with a radiation-transmitting surgical table (MAGNUS OR Table System, Maquet GmbH, Rastatt, Germany), which allows for head flexion/extension, tilting to the right and left and Trendelenburg positions. We also have a radiolucent skull clamp and horseshoe headrest (Doro Radiolucent Headrest System, Pro Med Instruments, GmbH, Germany). This table and the instrument enable 3DRA and 3D CT in various patient positions. This system allows simultaneous endovascular and surgical treatment without moving the patient to another location or table. During cranial surgery, the multi-axis robotic C-arm is folded and placed so that it does not interfere with the microscope or other movement lines (Fig. 1).
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