Integris h5000f

Manufactured by Philips

Sourced in United States

The Integris H5000F is a medical imaging system designed for fluoroscopic procedures. It provides high-quality digital imaging capabilities to support various medical applications. The system is equipped with advanced features, but a detailed description cannot be provided while maintaining an unbiased and factual approach.

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Lab products found in correlation

Artis zee, by Siemens (1 mentions) 0.035 guidewire, by Terumo (1 mentions)

5 protocols using integris h5000f

Numerical Simulation of Skin Dose Maps

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A numerical simulation engine based on ray tracing for radiation transport theory20 was used to compute skin dose maps for each simulated case. The validity of this simulation has been verified independently elsewhere.18 (link)
Two C-arm fluoroscopes were simulated: one was a flat-panel system (Artis zee, Siemens Medical Systems, Malvern, Pennsylvania, USA) with a 48 cm A-plane detector and a 25 cm B-plane detector, and the other was an X-ray image-intensified (XRII) system (Integris H5000F, Phillips Medical Systems, Andover, Massachusetts, USA) with a 9-inch XRII. Because large image receptors are unusual in cardiology, only data acquired using the B-plane detector on the Artis zee system were used in this study. The X-ray field sizes (formats) that were available on the two simulated systems are listed in table 1. To facilitate interpretation of data, similar formats were grouped as indicated in the ‘Format group’ column in table 1.

Pasciak A.S., Bourgeois A.C, & Jones A.K. (2014). C-arm rotation as a method for reducing peak skin dose in interventional cardiology. Open Heart, 1(1), e000141.

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Minimally Invasive Lung Intervention

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A total of 22 female pigs (46.95 ± 4.67 kg) were used in this study. All the animals were euthanized at the end of the experiment. An Olympus peripheral bronchoscope (TJF-260V, 4 mm in diameter) was inserted into the endotracheal tube and directed to the target sites. All procedures were performed on an X-ray fluoroscopy table (Integris H5000F, Philips Medical Systems) to take advantage of real-time fluoroscopic imaging guidance and cone-beam CT (CBCT) imaging if needed.

Shah I.A., Seol H.Y., Cho Y., Ji W., Seo J., Lee C., Chon M.K., Shin D., Kim J.H., Choo K.S., Park J., Kim J., Yoo H, & Kim J.H. (2023). Conversion of the bronchial tree into a conforming electrode to ablate the lung nodule in a porcine model. Communications Medicine, 3, 129.

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In Vivo Evaluation of 3D Balloon Spacer

Cited 1 time

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For the in vivo functional efficacy evaluation, we assessed the following parameters: 3D balloon spacer adjustment and 3D balloon spacer patency in surviving pigs. Procedures were performed under fluoroscopy guidance [6 (link)]. The pivot system was delivered using the 0.035” guidewire (Terumo Corporation, Tokyo 151-0072, Japan) until the collapsed 3D leaflet crossed the tricuspid valve, and the distal end of the device was directed towards the right lower pulmonary artery. To assess the spacer, we injected a fluid (saline and dye mixture) through the injection tube while monitoring the size and position of the spacer using fluoroscopy and echocardiography. Once the inflation was confirmed, the injection tube was simply removed by pulling it out. At the end of the procedure, a spiral anchor was deployed in the inferior vena cava (IVC). Sixteen pigs were used to evaluate the expansion ability, size control ability, and patency via X-ray fluoroscopy (Integris H5000F; Philips Medical Systems, Amsterdam, The Netherlands).

Chon M.K., Jung S.J., Seo J.Y., Shin D.H., Park J.H., Kim H.S., Hahn J.Y., Kim E.K., Lee S.W., Park Y.H., Lee S.H, & Kim J.H. (2023). The Development of a Permanent Implantable Spacer with the Function of Size Adjustability for Customized Treatment of Regurgitant Heart Valve Disease. Bioengineering, 10(9), 1016.

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Fluoroscopic Transcatheter Tricuspid Valve Repair

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TR was created by the destruction of the valve structure under fluoroscopic guidance (Integris H5000F, Philips Medical Systems). Both snare catheter (Ensnare or Gooseneck Snare) and 0.014-in guidewire from the superior vena cava or IVC were intentionally delivered into the RV cavity and then snared the 0.014-inch guidewire in the RV cavity to form a loop. If the loop was found to entangle the subvalvular structure of the TV, it was forcefully pulled out to destroy the valve. This maneuver was repeated until chordal rupture or flail motion of the leaflet was confirmed by means of echocardiography.

Chon M.K., Lee S.W., Hahn J.Y., Park Y.H., Kim H.S., Lee S.H., Shin D.H., Lee P.H., Kim E.K., Lee J.H., Park J.H., Choi Y.J., Reinthaler M., Barbieri F., Park J.W., Park J, & Kim J.H. (2022). A Novel Device for Tricuspid Regurgitation Reduction Featuring 3-Dimensional Leaflet and Atraumatic Anchor: Pivot-TR System. JACC: Basic to Translational Science, 7(12), 1249-1261.

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Verifying TR Pivot Device Success

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We technically verified the procedural success for the TR pivot device by means of X-ray fluoroscopy (Integris H5000F, Philips Medical Systems)

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