Integris allura

Manufactured by Philips

Sourced in Netherlands

The Integris Allura is a medical imaging device manufactured by Philips. It is used for various diagnostic and interventional procedures. The core function of the Integris Allura is to provide high-quality medical imaging capabilities to healthcare professionals.

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Lab products found in correlation

Solitaire fr, by Medtronic (1 mentions) Trevo xp, by Stryker (1 mentions) Allura xper, by Philips (1 mentions) Axiom artis, by Siemens (1 mentions) Eub 7500, by Hitachi (1 mentions) Ultravist 370, by Bayer (1 mentions)

7 protocols using integris allura

3D TOF MRA Imaging Protocol

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1.5 tesla (T) (n = 28) or 3T (n = 16) MR scanners were used for the acquisition of the 3D TOF MRA images. Intracranial 3D TOF MRA was performed in conjunction with the conventional MRI, using a multiple overlapped and acquisition technique. In the imaging with the 3D TOF MRA, the following ranges of parameters were used: 3D fast imaging with steady procession; TR, 21-38 ms; TE, 2.4-7.2 ms; flip angle, 18-25 degrees; effective section thickness, 0.5-1.2 mm; FOV, 130-190 × 130-220 (maximum intensity projection [MIP] images) and 175-240 × 190-270 (source images [SI]); and 256-640 × 192-512 matrix covering an area from the clivus to the genu of the corpus callosum. Both rotational MIP images and SI (axial acquired partitions) were used in the evaluation of the follow-up results.
The DSA was performed using a biplane system (Integris Allura; Philips Medical Systems, Best, the Netherlands) via transfemoral catheterization and selective injection of contrast media into the carotid or vertebral arteries. Imaging was performed to a standard and with adequate working projections as required.

Cho Y.D., Kim K.M., Lee W.J., Sohn C.H., Kang H.S., Kim J.E, & Han M.H. (2014). Time-of-Flight Magnetic Resonance Angiography for Follow-Up of Coil Embolization with Enterprise Stent for Intracranial Aneurysm: Usefulness of Source Images. Korean Journal of Radiology, 15(1), 161-168.

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Intraarterial Treatment for Ischemic Stroke

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A neurointerventionalist (C.J.) performed intraarterial treatment (IAT) of all the cases on a biplane angiography machine (Integris Allura, Philips, the Netherlands). We used a 9 French balloon guiding catheter. In case of a tortuous cervical ICA, a second guiding catheter was used for the coaxial system. The primary device for IAT was a stent retriever (Solitaire FR; Covidien, Irvine, California; Trevo-XP; Stryker, Kalamazoo, MI, USA). Mechanical aspiration device, thrombolytics, or permanent stenting were also used at the discretion of operator. The reperfusion grading was measured by using modified treatment in cerebral infarction before and after IAT [13 (link)].

Woo H.G., Jung C., Sunwoo L., Bae Y.J., Choi B.S., Kim J.H., Kim B.J., Han M.K., Bae H.J., Jung S, & Cha S.H. (2019). Dichotomizing Level of Pial Collaterals on Multiphase CT Angiography for Endovascular Treatment in Acute Ischemic Stroke: Should It Be Refined for 6-Hour Time Window?. Neurointervention, 14(2), 99-106.

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Coronary Angiography Protocol

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Coronary angiography was performed by a standard percutaneous femoral or radial approach with 6F or 7F diagnostic or guiding catheters. Angiographic images were recorded at 15 frames per second by monoplane or biplane x‐ray systems (AXIOM‐Artis, Siemens; Innova, GE; AlluraXper, Philips; INTEGRIS Allura, Philips). The contrast medium was injected manually with a forceful and stable injection or by the pump at a rate of ≈4 mL/s. The degree of stenosis (DS) of the LAD artery was visually estimated by experienced operators who were not involved in data analysis.

Wang C., Hu Z., Hou Z., Wang Y., Song L., Xu B., Guan C., Ning Y., Feng W, & Zhang Y. (2023). Impact of Preoperative Quantitative Flow Ratio of the Left Anterior Descending Artery on Internal Mammary Artery Graft Patency and Midterm Patient Outcomes After Coronary Artery Bypass Grafting. Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, 12(11), e029134.

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Diagnosing Diabetic Foot Syndrome

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The diagnosis of diabetic foot syndrome was established using a standard algorithm, which involved a detailed patient history and clinical and laboratory examination. The duration of the disease, intermittent lameness, pain at rest, presence and nature of soft tissue damage, pulse on main arteries, analysis of laboratory research methods, and history of concomitant diseases were considered. Non-invasive examinations were conducted to further assess the condition. This included determining the regional systolic pressure index on the foot arteries using a portable Super Dopplex ultrasound machine (China), Doppler ultrasound using the Hitachi EUB 7500 device (Japan) equipped with a linear sensor (L 5-10 MHz), and measurement of transcutaneous oxygen tension (TpO2) in the foot tissues using the TSM 400 device manufactured by Radiometer Copenhagen (Denmark). Invasive studies included angiography according to Seldinger, using the Philips Integris Allura (Holland) device. In addition, X-rays of the bones of the foot and lower leg were performed when necessary. The degree of ischemia was assessed according to the GLASS (2014) system.

Ivanova Y., Gramatiuk S., Kryvoruchko I., Tymchenko M., Goltsev K, & Sargsyan K. (2023). Investigating the joint application of negative pressure wound treatment and tissue therapy for chronic wounds in patients with diabetes. Journal of Medicine and Life, 16(7), 1098-1104.

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Primary PCI via Radial or Femoral Access

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All enrolled patients were treated by primary PCI using the digital x-ray system "Integris Allura" (Philips Healthcare, Best, The Netherlands) and managed by radial (n = 187) or femoral (n = 59) vascular access. We infused "Ultravist-370" (Bayer Pharma GmbH, Leverkusen, Germany) contrast. Bare-metal stent Rebel TM (Platinum Chromium Coronary Stent System, Boston Scientific, Natick, MA, USA) for primary PCI with implantation in infarct-related artery was performed. All enrolled patients received standard adjuvant treatment. 18 (link)

Petyunina O., Kopytsya M., Kobets A, & Berezin A. (2023). Myocardial Mechanical Dispersion Predicts Adverse Cardiac Remodeling in Patients with ST Segment Elevation Myocardial Infarction Who Underwent Primary Percutaneous Coronary Intervention. Turk Kardiyoloji Dernegi arsivi : Turk Kardiyoloji Derneginin yayin organidir, 51(2).

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Conventional Coronary Angiography Procedure

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Conventional coronary angiography was performed immediately after admission of the patients to the hospital using Digital X-Ray system "Integris Allura" (Philips Healthcare, Best, The Netherlands), and managed by radial or femoral vascular access. Coronary arteries were visualized with two-to-three orthogonal projections per conventional protocol. The number of views obtained was decided by the operator depending on coronary anatomy. The main coronary arteries were left main coronary artery, left anterior descending branch, left circumflex branch, right main coronary artery, and right coronary descending branch. In this study, the contrast "Ultravist-370" (Baier Pharma GmbH, Germany) and automatic contrast injector were used. The contrast amount used in coronary angiography in each injection was 8 -10 mL at 4 mL/s for the left coronary artery and 6 mL at 3 mL/s for the right coronary artery (radiation exposure 20 to 35 mGycm). After coronary angiography, two experienced interventional cardiologists discussed the captures and filled in the final report of the results of the procedure after reaching consensus.

Kutia I., Kopytsya M., Hilova Y., Petyunina O.V., & Berezin A.Е. (2020). The predictive value of vascular endothelial growth factor-A gene polymorphism for clinical outcomes among acute ST-segment elevation myocardial infarction patients: A single center prospective study. Biomedical Research and Therapy, 7(5), 3744-3759.

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Quantitative Angiographic Analysis of PCI

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Thrombolysis in myocardial infarction (TIMI) grade 3 coronary flow in the treated vessel and a residual stenosis less than 30% were the criteria used to define a successful PCI. Quantitative angiographic analyses (Integris Allura; Philips, The Netherlands) were performed online and offline by two experienced technician who were unaware of treatment assignment with the averaging scores if they were none in agreement.

De Luca G., Sauro R., Capasso M., Lanzillo T., Manganelli F., Carbone G., Lanni F., Pagliuca M.R., Palmieri V., Serino V., Rosato G., Suryapranata H, & Di Lorenzo E. (2015). Impact of diabetes on the benefits from everolimus-eluting stent as compared to first-generation drug-eluting stent in patients with ST elevation myocardial infarction. Diabetes & vascular disease research, 12(5).

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