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Progreat microcatheter

Manufactured by Terumo
Sourced in Japan

The Progreat microcatheter is a medical device used for selective and superselective catheterization of the peripheral, visceral, and neurovascular systems. It is designed to provide access and support for the delivery of diagnostic and therapeutic agents.

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10 protocols using progreat microcatheter

1

Transarterial Embolization of Hepatic Tumors

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Using a transfemoral approach, a 5-F RH catheter (Cook) was used to catheterize the celiac trunk or anatomic variant to gain access to the hepatic arteries, which was achieved with a 2.7-F Progreat microcatheter (Terumo). Diagnostic angiographic runs were obtained on the celiac trunk and proper hepatic and right and left hepatic arteries to define tumor arterial supply. Through the microcatheter, a vial of 100–300 or 300–500μm in size CalliSpheres microspheres (Jiangsu Hengrui Callisyn Biomedical Co., Ltd., Suzhou, China) loaded with 60 mg of pirarubicin or epirubicin were injected to occlude each tumor artery. If tumor staining was still present on repeated imaging after all DEB, 560–710 μm gelatin sponge particles or polyvinyl alcohol (ALICON Pharm SCI & TECH) were added until near-stasis was achieved, defined as the disappearance of tumor stain on angiography. The procedures were conducted by two interventional radiologists with more than 15 years of experience.
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2

Feline Carotid Artery Embolization

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All animal experiments were conducted in accordance with the guidelines issued by our Institutional Animal Care and Use Committee (Approval No: 2012-038). Sixty healthy adult domestic male cats weighing 2.8-3.3 kg were anesthetized with an intramuscular injection of ketamine HCl (2.5 mg/kg; Huons, Jechun, Korea) and xylazine (0.125 mg/kg; Bayer Korea, Seoul, Korea). Cats were allowed to breathe ambient air spontaneously during the procedure. Briefly, the right femoral artery was isolated and its distal portion was ligated with 4.0 silk. An 18-guage intravenous catheter was then inserted into the artery proximal to the ligated portion. A 2.2F microcatheter (Progreat microcatheter, Terumo, Tokyo, Japan) equipped with a microguidewire (GT guidewire, Terumo, Tokyo, Japan) was then passed through the intravenous catheter into the lumen of the artery. The tip of the microcatheter was positioned in the right or left common carotid artery at the level of the fourth cervical vertebra under fluoroscopic guidance. Triolein (triglyceride, 1, 2, 3-tri [cis-9-octadecenoyl] glycerol) was supplied by Sigma-Aldrich (St. Louis, MO, USA).
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3

Radioembolization with Y-90 Resin Microspheres

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All 90Y procedures were performed under local anaesthesia by or under direct supervision of an expert interventional radiologist (GM) and nuclear medicine physician (CD). Previously published work describes the details of the 90Y treatment.13 (link) Briefly, patients first underwent a detailed baseline angiogram and embolization of enterohepatic arteries with micro-coils according to the expertise of the interventional radiologist. Technetium-99m-macroaggregated albumin (99mTC-MAA) was injected in the target vessels and a planar scintigraphy was performed to determine the lung shunt fraction. Two weeks later patients underwent bi-lobar or uni-lobar injection of 90Y resin microspheres (SIR spheres, Sirtex Inc, Cosgrove, Australia) under local anaesthesia. The activity of 90Y injected in the patient was calculated based on the body surface area method. In patients where it was possible to use the partition model, the partition model was used instead of the body surface area method. Dependent on the site of lesions, the 90Y resin microspheres were injected intra-arterially via a micro catheter to the right and left liver lobe (superselective). A Progreat® micro catheter (Terumo, Europe) or an anti-reflux catheter (Surefire Inc., Westminster, CO, USA) was used for injection of the microspheres. Patients received antiemetics and morphine derivates before 90Y injection when required.
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4

Interventional Radiologists' Venous Embolization

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Two experienced interventional radiologists, both with >30 years of experience, performed all embolization procedures in both hospitals.
The technique has been described by the authors in previous publications and has not changed substantially for plug embolization (Group VP). In all cases, the four venous axes were closed [8 (link),10 (link)].
In the VPPF group, the existence of direct venous connections to the systemic venous circulation was ruled out. When these were found, the connection and flow were reduced by releasing a VP of the appropriate caliber. On a few occasions, it was required to close the connection with an occlusion balloon. Coaxially to the MPA 5F catheter, a 2.7 F 130 cm Progreat microcatheter (Terumo, Tokyo, Japan) was introduced, and a foam of 2 mL of 2% polidocanol was mixed with 8 mL of air and 1 mL of iodinated contrast. This mixture was injected slowly until the vessel was obstructed, verifying that there was no migration of the foam towards the systemic venous circulation. Occlusion (lOV, ROV, LHV, and RHV) was confirmed through venography performed after embolization (Figure 3). During the intervention, all the data were collected.
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5

Renal Artery Embolization Protocol

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All interventions were completed by three interventional physicians, who had more than 10 years of medical experience. The patients were placed in the supine position. The right or left femoral artery was punctured by the modified Seldinger technique after the induction of local anesthesia. Abdominal aortic angiography was conducted first to confirm the number and position of the renal arteries. Selected renal artery angiography was then performed to confirm the involved artery; subsequently, a progreat microcatheter (Terumo, Tokyo, Japan) was superselectively inserted into the involved artery. Embolization was performed with different embolic agents, including gelatin sponge (GS) particles, microcoils, and n-butyl cyanoacrylate glue. Finally, renal artery angiography was repeated to confirm that embolization was complete.
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6

Selective TACE for Hepatocellular Carcinoma

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All eligible HCC patients were invited to receive selective conventional TACE (TACE), defined as catheterization at the subsegmental hepatic artery performed by two interventional radiologists through the transfemoral route. Superior mesenteric artery and celiac axis arteriogram were selective at the beginning of procedure using a 5Fr selective catheter (Cobra or MIK catheter) and a 0.035-inch J-tip Terumo guidewire. We performed selective catheterization to the tumor feeding hepatic arteries or in extrahepatic collaterals as distal as possible in each tumor lesion using a microcatheter (A 1.98-Fr tip Asahi Masters Parkway Soft microcatheter from Asahi, a 2.0-Fr tip Progreat microcatheter from Terumo or a 2.4-Fr tip Renegrade STC microcatheter from Boston Scientific) with coaxial technique. We slowly administered the mixture of iodized oil; range 4-16 ml (Lipiodol, Guerbet), the doxorubicin hydrochloride; range 10-40 mg (Adriamycin, Pfizer) under real time monitoring on Digital Subtraction Angiography (Phillips AlluraClarity FD20). The amount of anticancer-in-oil-emulsion was determined by total tumor size and number of nodules. Subsequently, this feeding artery was embolized using gelatin sponge particles. We completed the procedure when the tumor feeding branch was completely obstructed and tumor staining from digital subtraction angiography completely disappeared.
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7

Stem Cell Transplantation Protocol

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The procedure of stem cell transplantation has been described previously [5 (link), 6 (link), 10 (link)]. Briefly, a 5 F catheter (Sim1, Beacon®, USA) was selectively navigated through transfemoral route into the celiac trunk. Within the Sim1 catheter, another caliber catheter (Progreat microcatheter, Terumo, Japan) was selectively advanced into superior pancreatico-duodenal (SPD) artery and cells were injected accordingly, unless vascular anomalies were detected. Post-procedure, the patients were monitored for any immediate complications for the next 24 h.
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8

Microsphere Delivery and Contrast Agents

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LUMI40‐90, LUMI70‐150, and DC70‐150 were provided in 2 mL vials. Doxorubicin hydrochloride powder (>99% purity, Dox) was obtained from Hisun (China) and irinotecan hydrochloride (>99% purity, Iri) was obtained from ScinoPharm (Taiwan). Contrast agents used were Isovue™ 300, 370, and Iomeron™ 400 (Bracco Imaging, USA), Ultravist™ 370 (Bayer HealthCare Pharmaceuticals Inc., USA), Omnipaque™ 350 and Visipaque™ 320 and 370 (GE Heathcare, USA), Optiray™ 350 and Oxilan™ 350 (Guerbet LLC, USA). Microcatheters used for microsphere delivery were 2.0 and 2.4 Fr PROGREAT® Microcatheters (Terumo Corp., Japan).
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9

In vitro Microsphere Delivery Force

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Both LUMI40‐90 and LUMI70‐150 were delivered using different dilutions and contrast agent mixtures and the ease of delivery or cases of catheter blockage noted using a 3 mL syringe and Terumo Progreat microcatheters (2.4 and 2.0 Fr) set in a defined tortuous path in a water bath at 37°C. Force to deliver certain suspensions was obtained by attaching a force meter (Omega Engineering Inc.) to a custom mounted syringe adaptor to record the force required to expel the microsphere suspension. Furthermore, the Colorview camera system was set to focus on the transparent catheter hub and microsphere delivery was subsequently recorded as a record of the effect of dilution and bead size on catheter blocking.
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10

Splenic Artery Embolization Techniques

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All procedures were performed by one of eight consultant interventional radiologists along with one of five interventional radiology fellows. The access was from the femoral artery, using either a 6-Fr 11 cm Radifocus™ introducer sheath (Terumo, Tokyo, Japan) or 6-Fr 35 cm Pinnacle® destination sheath (Terumo, Tokyo, Japan), a guiding 4-Fr or 5-Fr catheter (Cook Medical, Bloomington, USA) to selectively catheterize the celiac trunk and/or splenic artery, and when needed 2-Fr, 2.4-Fr, 2.7-Fr Progreat® microcatheters (Terumo, Tokyo, Japan). Embolic materials according to operator preference included 5-10 mm Amplatzer vascular plugs 4 (AVP 4) (St Jude Medical, Plymouth, USA), 5-14 mm pushable coils and detachable microcoils Concerto Helix (0.018″ Medtronic, Minnesota, USA), Ruby (0.018″ Penumbra, California, USA), POD (0.025″ Penumbra, California, USA), VortX (0.018″ or 0.035″ Boston scientific, Massachusetts, USA), and Gelfoam (Pfizer, Michigan, USA).
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