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Artis zee system

Manufactured by Siemens
Sourced in Germany

The Artis Zee System is a high-performance imaging platform designed for interventional procedures. It provides real-time, high-quality imaging to support diagnostic and therapeutic applications. The Artis Zee System is equipped with advanced imaging technologies to deliver reliable and accurate visual information during complex medical procedures.

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8 protocols using artis zee system

1

Ruptured and Unruptured Cerebral Aneurysm Analysis

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The patients were enrolled from January 2015 to September 2018. The inclusion criteria were as follows: patients who had 3D digital subtraction angiography by Siemens Artis Zee System (Siemens Healthcare, Erlangen, Germany); a confirmed ruptured or unruptured diagnosis of aneurysm; sufficient image quality for 3D vessel construction with no artifacts to accurately represent aneurysm and parent vasculature; saccular aneurysm; and available clinical charts. Aneurysms combined with other vascular abnormalities such as arteriovenous malformation, arteriovenous fistula, and Moyamoya disease were excluded. A total of 719 aneurysms in 579 patients were enrolled in this study.
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2

Quantitative Coronary Angiography Procedure

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Coronary angiography analyses were performed using an Artis zee system (Siemens Healthineers). Prior to image acquisition, 200 μg of intracoronary nitroglycerin was administered to ensure maximal arterial dilation. The procedure involved percutaneous access, typically through the radial or femoral artery, introduction of a guide catheter into the ostium of the coronary artery, and injection of a contrast agent. Quantitative measurements were taken from digital recordings of the angiograms, analyzed offline by blinded operators at the cardiovascular core laboratory using CAAS software (Version 5.10, Pie Medical Imaging).
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3

Retrospective Analysis of aSAH and MIA Patients

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We retrospectively collected images and medical records from a consecutive series of patients with both aSAH and MIA treated at 3 hospitals in China (Beijing Tiantan Hospital, Beijing Hospital, and Peking University International Hospital) from January 2016 to December 2018. The inclusion criteria were as follows: patients with the diagnosis of aSAH and having at least two saccular IAs; patients with 3D-DSA diagnosed by Siemens Artis Zee System (Siemens Healthcare, Erlangen, Germany); sufficient image quality for segmentation; and patients with available clinical information. The ruptured IA was confirmed through microscopic visual assessment for patients with craniotomy treatment or through a definitive hemorrhage pattern on CT for patients who underwent endovascular or no treatment [21 (link)] (Figure 1). Patients in whom the ruptured IA could not be confirmed and those with other cerebrovascular diseases were excluded. Patients with aneurysm that has un-clear neck from the parent vessel were also excluded. All aneurysms included were randomly divided into 2 cohorts: the derivation cohort (70% of the IAs) and the validation cohort (30% of the IAs).
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4

Cerebral Artery Reconstruction from DSA Images

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As shown in Figure 3, the reconstructed four models based on digital subtraction angiography (DSA) images, i.e., twin A-RB, twin A-LB, twin B-LB, and twin B-LB with ACA branches virtually removed (only for the purpose of configuration comparisons), were reconstructed using Mimics Research 23.0 (Materialise NV, Leuven, Belgium), based on 390 non-invasive scanned DSA images for each brain by the Artis Zee system (Siemens Medical Solutions USA, Inc., Malvern, PA, USA). To cover the volume of cerebral arteries, the scanning was conducted with a collimated section width of 1 mm, a pitch of 1.5, and a gantry rotation time of 0.5 s in a total of 9 s. To balance arterial curvature and smoothness, reducing tolerance 0.03 with 5 iterations and smooth factor 0.4 with 10 iterations were adopted in the reconstruction. Reconstructed models were used for comparisons of morphologies and hemodynamics between the twins.
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5

Videofluoroscopic Swallow Studies in Mice

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Videofluoroscopic swallow studies assays were performed as previously described (Glass and Connor, 2016 (link)). Mice were identified by alphanumeric codes to mask genotype identities to workers during VFSS assays. The food used for imaging was a 2:1 mixture of Fritos Mild Cheddar CheeseTM dip and 40% weight/volume barium suspension. Mice were acclimated to cheese mixtures daily for a few days immediately prior to VFSS, and all food was withheld overnight prior to the VFSS study. On the day of data acquisition, each mouse was placed alone in a cage and was imaged during continuous volitional eating at 30 fps with an Artis Zee system (Siemens Healthcare, Forchheim, Germany). The duration of VFSS acquisition for each mouse was limited to the amount of time required to record several visible swallows, typically at least 10 s. For all experiments, each mouse generated VFSS data for only one time point. Following VFSS, mice were weighed.
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6

Saccular Cerebral Aneurysm Characterization

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The data supporting the findings of this study are available from the corresponding author upon reasonable request. All patients were from the Beijing TianTan Hospital of Capital Medical University. This study was conducted by the Declaration of Helsinki and approved by the Ethics Committee of Tiantan Hospital affiliated to Capital Medical University (2018-0117/2018-09-06), and written informed consent was obtained from each patient before the operation. The cohort of patients enrolled was from January 2015 to September 2018. The inclusion criteria were: patients who had 3D digital subtraction angiography by Siemens Artis Zee System (Siemens Healthcare, Erlangen, Germany); a confirmed ruptured or unruptured diagnosis of the aneurysm; sufficient image quality for 3D vessel construction with no artifacts to accurately represent aneurysm and parent vasculature; saccular aneurysm; and available clinical charts. Aneurysms accompanied with other vascular abnormalities such as moyamoya disease, arteriovenous malformation, and arteriovenous fistula were excluded. A total of 719 aneurysms in 579 patients met the criteria were enrolled for analysis.
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7

Cerebral Aneurysm Diagnosis and Imaging

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The diagnosis of rIAs was established by admission computed tomography (CT), which also was utilized to evaluate the SAH severity as reflected by the modified Fisher grade. The aneurysm size was defined as the maximum diameter of the IAs measured on two-dimensional imaging and three-dimensional digital subtraction angiography using the Siemens Artis Zee System (Siemens, Erlangen, Germany). Anterior circulation aneurysms were those located in the anterior cerebral artery, anterior communicating artery, middle cerebral artery, internal carotid artery, and posterior communicating artery, whereas posterior circulation aneurysms were located in the basilar artery, posterior cerebral artery, and intracranial segment of the vertebral artery. All images were read by two neurointerventionists (B.Z. and X.H.) who were blinded to each other’s interpretations and the patients’ clinical information. Disagreements were resolved by a third reader (A.L.).
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8

Quantitative Coronary Angiography Protocol

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Angiograms were acquired with a cine-angiographic equipment (Siemens Artis Zee system, Forchheim, Germany) in different orthogonal views. The percent diameter stenosis (%) of the coronary lesions was obtained by quantitative coronary angiography (QCA) software with digital calibration. Significant stenosis was defined as ≥ 70% diameter narrowing in a coronary artery or coronary artery stenosis with fractional flow reserve (FFR) ≤ 0.80.
Lesion classification was defined according to the Society for Cardiac Angiography and Interventions (SCAI) lesion classification system [12 (link)], which uses type C lesion characteristics [13 (link)] as the key determinant of lesion complexity. Accordingly, we defined four different lesion types (SCAI type 1–4) based on the SCAI classification system.
Multivessel PCI was defined as stenting in two or more major coronary arteries or bypass grafts which supply different myocardial territories.
Overlapping stenting was defined as the presence of ≥ 2 stents within a single treated lesion and an overlapping stent zone of at least 1 mm.
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