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Allura

Manufactured by Philips
Sourced in Netherlands

The Allura is a diagnostic imaging system designed for interventional procedures. It provides high-quality imaging capabilities to assist healthcare professionals in performing various medical interventions.

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12 protocols using allura

1

Endovascular Aneurysm Treatment Techniques

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All procedures were carried out under general anesthesia using a biplane angiography system (Philips Allura Xper FD20/15, Koninklijke Philips N.V., Amsterdam, The Netherlands). Cerebral vessel access was established using a 6F 088 Neuron MAX Long Sheath 90/4 Straight (Penumbra, Inc., Alameda, CA, USA). Subsequently, a three-dimensional rotational angiography was performed to plan the procedure. In all cases that involved placement of a LEO+(Baby) or Enterprise stent, jailing technique was used: First, a microcatheter system was navigated in the aneurysm; second, another microcatheter system was navigated distal to the aneurysm, and the stent was then partially unsheathed and the aneurysm was coiled. After the aneurysms were fully packed with coils, the stent was completely unsheathed. In the cases in which the Atlas stent was used, the flow diverter was first deployed, and then a microwire/microcatheter system was navigated through the stent into the aneurysm for subsequent coiling.
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2

Transcatheter Embolization Procedures

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All procedures of transcatheter embolization were performed in an angiographic room by interventional radiologists with at least 10 year of experience in the field, using digital subtraction angiography (DSA) (Philips Allura Xper FD20, Angio system, Netherlands). Procedures technically varied according to different type of transcatheter embolization. Squid was always administered after a super-selective catheterization with a DMSO-compatible microcatheter.
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3

Multimodal Imaging of Duodenum

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We used an X-ray imaging system (Philips Allura Xper FD20), the Image Processing Center (Evis Lucera, Olympus Cv-260)the Evis Lucera Xenon Light Source (Olympus Cv-260), and Electronic Endoscopy of the Duodenum (Evis Lucera Olympus Tjf Type 260v).
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4

Prostate Artery Embolization Protocol

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The technique has been described in details elsewhere [20 (link)]. In short, embolic particles were injected proximally in the prostate artery and after achieving stasis of the flow, the microcatheter was advanced into the intraprostatic branches. The purpose of initial flow-directed embolization followed by complete occlusion of the microcirculation was to induce a significant infarction. Perioperatively, 5000 units of heparin in bolus were administered followed by 1000–2000 units per hour on the discretion of the operator. Under local anesthesia, a 5F sheath (Fortress, Biotronik) was employed to access the right common femoral artery. The prostate arteries were localized on each hemipelvis and super-selectively catheterized with a 2.0-F microcatheter (Progreat, Terumo Interventional Systems). Before manually injecting 300–500-μm tris-acryl gelatine microspheres (Embosphere, Merit Medical) particles under fluoroscopic guidance, a cone-beam CT (Allura, Phillips) was performed to confirm catheter placement and visualize any aberrant collaterals. Branches not supplying the prostate were protected by coil embolization or by advancing the microcatheter distally to their origin before injection of embolic particle suspension. Every milliliter of particle suspension injected was followed by three milliliters of saline.
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5

Coronary Artery Patency Assessment

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Patency was determined at the end of follow-up, per coronary angiography (Philips Allura Xper FD20, Eindhoven, The Netherlands). Access was via the femoral artery, with the internal mammary catheter (6 Fr) introduced in the proximal LIMA. Images were recorded in at least 2 directions and were graded by 2 independent investigators to the FitzGibbon criteria (classes A and B are defined as patent, class O is defined as nonpatent).11 (link)
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6

Biplane Fluoroscopy for Electrophysiology

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The biplane fluoroscopy system (Philips Allura®), x‐ray filtration by 0.4 mm copper and 1 mm aluminum was set to 3.75 frames/s in the fluoroscopy mode and 7.5 frames/s in the cine mode as our standard setup for electrophysiology procedures. For storage and documentation of the ablation procedure primarily the last image hold or the last run hold option from fluoroscopy were used, whereas recordings of short cine sequences only were performed in case of poor image quality. All operators were urged to use maximum collimation and avoid excessive zooming. For radiation protection of the operator and the staff a standard shielding with 1 mm led equivalent value was mounted at the fluoroscopy table added by a 0.5 mm lead equivalent value transparent shield.
Initially, a posterior–anterior projection was used for catheter placement and turned to RAO 35° and LAO 50° without cranio‐caudal angulations for transseptal puncture and ablation.
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7

Cardiac Angiography Using Philips Allura X-ray

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We used the X-ray system (Philips Allura Xper FD10/10 biplane), which is a cardiac angiography system.
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8

Quantitative Coronary Angiography Analysis

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A digital subtraction angiography machine (Allura, Philips, Amsterdam, Netherlands) performed coronary angiography, and angiography images were recorded at 15 frames/s. The field of view (FOV) was 20 cm × 20 cm − 22 cm × 22 cm, the matrix was 512 × 512, the tube current was 500−800 mA, and the tube voltage was 60−120 kV. The non-ionic contrast agent with an iodine content of 350−370 mgI/ml was injected. Before coronary angiography, nitroglycerin was injected into the target vessel to exclude coronary spasms caused by medical devices. An experienced technician using QCA software (Beijing Crealife Technology Co., Ltd., Beijing, China) selected the angiogram in the diastolic period. Meanwhile, the technician analyzed the quantitative coronary angiography values of the target vessels. QCA software automatically delineated the lumen contour of the target vessels, and a manual correction was allowed when the error of measurement existed. An intermediate QCA technician was selected to analyze the QCA; after that, a senior technician verified all data.
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9

Time-of-Flight MRA and Rotational DSA

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We included only high-field (1.5T or 3T) time-of-flight MRA. A small number of patients had both time-of-flight MRA and gadolinium-enhanced MRA. We excluded gadolinium-enhanced MRA images from this study. Since patients had MRA performed at different facilities, the MR scanners and MRA protocols used were often different from patient to patient. Twenty-one models of MR equipment from 5 companies (Canon Medical Systems, GE Healthcare, Hitachi Medical Systems, Philips Healthcare, and Siemens Healthineers) were included in this study. However, the imaging procedures used standard algorithms and were of satisfactory image quality. We excluded a small minority of MRA images that had a low-to midfield (below 1.5T) MRA or poor visualization due to artifacts.
DSA was performed with a biplane angiography system (Allura, Philips Healthcare). We acquired anteroposterior and lateral images from 2D DSA for the bilateral internal carotid artery (ICA) and vertebral artery and then performed rotational angiography on affected or suspected arteries. We added 2D DSA of the profile angle, which was obtained through 3D reconstruction with rotational angiography, to identify the shape of the aneurysm. We excluded patients who did not undergo rotational angiography.
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10

Coronary Angiography for Transplant Vasculopathy

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Routine XRCA was performed on standard equipment (Allura, Philips, Amsterdam, The Netherlands) using a 6F guiding catheter via right radial or right femoral artery access. The coronary arteries were imaged after administration of intracoronary nitro-glycerine (50 μg) into the right coronary artery (RCA) or left main coronary artery. At least two orthogonal projections of each coronary artery were acquired. Two interventional cardiologists (J.F.I. and S.D.) independently graded the severity of CAV (hereafter called XRCA-CAV) with a scale ranging from 0 (=not significant) to 3 (=severe) on the basis of luminographic pathology [4] (link), which remains the clinical reference standard even though it can only be used to detect latestage CAV. In cases of differences in CAV grading, a consensus was sought after joint reinvestigation.
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