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5 f catheter

Manufactured by Cook Medical
Sourced in United States, Japan

The 5-F catheter is a medical device designed for use in various diagnostic and therapeutic procedures. It is a flexible tube with a diameter of 5 French (F), which is approximately 1.67 millimeters. The catheter is intended to be inserted into blood vessels or other body cavities to facilitate the passage of tools or fluids.

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10 protocols using 5 f catheter

1

Transarterial Chemoembolization for Liver Cancer

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TACE was performed by one of four physicians. TACE was performed by placing a 5-F catheter (Cook, Bloomington, Indiana) or a 2.8-F microcatheter (Renegade Hi-Flo Straight, Boston Scientific, Natick, Mass; Progreat, Terumo, Tokyo, Japan) as superselectively as possible into tumor-feeding arteries. Initially, a lobaplatin solution with a concentration of 0.5 mg/mL was infused into the tumor-feeding vessels. The total lobaplatin level was 20-50 mg and depended on the patient’s body weight. Then, an emulsion of 3–10 mL lipiodol (Lipiodol Ultrafluide; Guerbet, Aulnay-Sous-Bois, France) and 20–60 mg doxorubicin hydrochloride was administered into the feeder vessels. Finally, polyvinyl alcohol particles 300 μm in diameter (Polyvinyl Alcohol Foam Embolization Particles; Cook) mixed with contrast material were administered into the tumor-feeding vessels until arterial flow stasis was achieved. After embolization, angiography of the feeding artery was performed to determine the extent of vascular occlusion. If the feeding artery was not completely occluded, polyvinyl alcohol particle embolism was performed again.
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2

TACE Procedure for Hepatic APS Embolization

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The TACE procedure was performed by operators with a minimum of 5 years of experience. First, angiography of the hepatic common artery was used to identify the location, severity and direction of the vessels of APS. Then, a 5-F catheter (Cook, Bloomington, Indian, USA) or a 3-F microcatheter (Progreat, Terumo, Tokyo, Japan) was advanced into the feeding artery of APS. Polyvinyl alcohol particles (500–1,000 um, Cook, USA) that were mixed with contrast media (Hengrui Pharmaceutical Co. Ltd, Jiangsu, China) were then injected to block the APS. An arteriography was then performed to confirm the occlusion of APS. Depending on tumor size and liver function, 2–20 mL of lipiodol (Lipiodol Ultrafluido, Guerbet, France) was mixed with 20–40 mg doxorubicin hydrochloride (Hisun Pharmaceutical Co. LTD, Zhejiang, China) to create an emulsion that was subsequently injected into the tumor feeding arteries. Gelatin sponge particles (300–700 um, Cook, USA) were used to supplement embolization until the stagnation of artery flow appeared.
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3

Transarterial Chemoembolization Protocol

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TACE was performed based on our institutional standard protocol and has been described previously (13 (link), 14 (link)). Briefly, angiography was performed to determine tumor staining and tumor-supplying vessels, and a 5-F catheter (Cook, Bloomington, Indiana, USA) or 3-F microcatheter (Progreat, Terumo, Tokyo, Japan) was inserted as far as possible into the tumor supplying vessels. Then, an emulsion of 2–20 mL iodized oil (Lipiodol Ultra-Fluid; Laboratoire Andre Guerbet, Aulnay-sous-Bois, France) and 20–60 mg doxorubicin hydrochloride was injected into the target vessels. Finally, gelatin sponge particles (300–700μm, Alicon, Hangzhou, China) were injected for additional embolization until the stasis of arteries flow was achieved. After embolization, reexamination angiography of the feeding artery was performed to confirm the devascularization.
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4

Transcatheter Arterial Chemoembolization for Hepatic Tumors

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TACE was performed by placing a 5-F catheter (Cook, Bloomington, Indiana, USA) or a 2.7-F microcatheter (Progreat, Terumo, Tokyo, Japan) into hepatic tumor feeding arteries. Initially, an emulsion of 2–20 mL lipiodol and 20–60 mg epirubicin was administered into the target vessels under fluoroscopic guidance. Next, gelatin sponge particles (350–710 μm, Alicon, Hangzhou, China) were administered into the tumor donor arteries. Embolization was operated under fluoroscopic guidance until the stasis of arteries flow was occurred. Finally, reexamination angiography of the hepatic artery was performed to validate the devascularization.
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5

Transarterial Chemoembolization for Liver Cancer

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TACE was performed by two radiologists with >10 years of interventional therapy experience.8 (link),13 (link) Following the introduction of 5 F catheter (Cook Medical, Bloomington, IN, USA) through the femoral artery, superior mesenteric artery angiography and hepatic arteriography were performed to determine portal patency and intrahepatic tumor blood supply. Then, the 2.7 F microcatheter was placed in the tumor-feeding arteries and confirmed by angiography. Chemoembolization was performed using 50 mg pirarubicin with 5–20 mL of lipiodol (Guerbet Laboratories, Roissy, France). Gelatin sponge particles (350–560 µm) or embolism microspheres (300–500 µm) were added to supplement embolism. When the contrast column cleared within two to five heartbeats, it was considered the endpoint of the embolization.
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6

Percutaneous Vascular Obstruction Biopsy

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Sedation was achieved by continuous infusion of propofol (4–6 mg/kg, Jiangsu Enhua Pharmaceutical Co., Ltd., Xuzhou, China). Local anesthesia with 2% lidocaine (5–10 mL) was applied to the puncture site. The steps for the procedure were as follows: (I) the FV access was successfully established by a 9F sheath (90 cm in length for the SVC and PA; 45 cm for the IVC; Cook Medical, Indiana, USA) under the guidance of digital subtraction angiography (DSA; Artis-zeego, Siemens Healthineers, Munich, Germany). (II) A 0.035-inch soft guide wire (Terumo Medical, Tokyo, Japan) and a 5F catheter (100 cm in length; Cook Medical) were introduced through the sheath and reopened the obstructive blood vessels. (III) The initial soft guide wire was replaced with strengthened guide wire to adjust the sheath direction. (IV) The 9F sheath was advanced to the proximal end of the vascular obstructive site, and the location was confirmed by vascular angiography. (V) Forceps biopsy (clamp diameter =6 mm, length =120 mm; Nanjing Micro-tech) was introduced through the 9F sheath to the obstructed area, pushed forward 5–10 mm, and then tightened and pulled out of the sheath. The specimens were evaluated by expert pathologists. The IVFB was performed 3–6 times to obtain satisfactory specimens.
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7

Transarterial Chemoembolization for Tumors

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The Seldinger puncture technique was used to puncture the femoral artery, and the 5F catheter (Cook Medical, Bloomington, IN) was delivered to common hepatic or superior mesenteric artery under digital subtraction angiography. Angiography was performed to determine the variations of blood vessels, the presence of arteries in tumor blood supply, and the dyeing conditions. When the superselected catheterization reached the blood supply vessel of tumors, 30 mg epirubicin (Pfizer, New York, NY) was added to 5 to 20 mL of super liquid iodized oil for chemoembolization. If the remaining tumor feeding arteries were still abundant, embospheres with different diameters (Merit Medical Inc, South Jordan, UT) were selected for supplementary embolism. Routine hepatic treatment was performed after surgery.
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8

Transarterial Chemo-Embolization for Liver Tumors

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TACE procedures were performed by three experienced radiologists with a minimum of 10 years of experience in interventional therapy. A 5 F catheter (Cook, Bloomington, IN, USA) was inserted into the hepatic artery. Then, a 3F micro-catheter (Progreat, Terumo, Tokyo, Japan) was used to insert the tumor-feeding arteries. Subsequently, lipiodol (Lipiodol Ultrafluido, Guerbet, Villepinte, France) was mixed with doxorubicin hydrochloride to create an emulsion at the ratio of 1 mL/2 mg. Depending on the size of the tumor and liver function, 5–20 mL emulsion was injected slowly into the tumor-feeding arteries until stasis of the feeding arteries of the tumor. If it was necessary, supplement embolization was performed using gelatin sponge particles (300–700 um, Cook, USA).
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9

Standardized TACE Procedure for HCC

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All patients in both groups received TACE once at least. TACE was conducted by specialists with 10 years` experiences. Under the guidance of digital subtraction angiography (DSA), a 5-F catheter (Cook, Bloomington, Indiana, USA) was placed into the hepatic artery and a 2.7-F microcatheter (Progreat, Terumo, Tokyo, Japan) was inserted selectively into tumor feeding arteries. About 2–20 mL lipiodol and 20–60 mg epirubicin were prepared to make emulsion. Then, the emulsion was administrated into the tumor feeding arteries through the microcatheter. Gelatin sponge particles (350–710 μm, Alicon, Hangzhou, China) were used to embolize completely the tumor feeding arteries. Finally, hepatic artery angiography was performed to validate the complete embolism of the feeding arteries. If the residual lesions were confirmed by enhanced CT, the repeated TACE would be recommended.
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10

TACE for Hepatic Tumor Treatment

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TACE was initiated before apatinib and camrelizumab administration. Under local anesthetic, TACE treatment was conducted through the femoral artery. To determine the number, size, location, and feeding arteries of the tumors, a 5-F catheter (COOK) was inserted and angiography was performed. Then, an emulsion of chemotherapeutic drugs (lobaplatin, 30–50 mg; epirubicin, 10–30 mg) mixed with lipiodol was administered through the hepatic artery. Thereafter, embolization via a microcatheter (2.7 F; Terumo Medical Corp., Tokyo, Japan; or 2.4 F; Merit Maestro, South Jordan, Utah, USA) was performed either selectively or superselectively. Selective embolization with 300 μm polyvinyl alcohol particles (Biosphere Medical, Paris, France; or Jiangsu Hengrui Medicine Co., Ltd., Jiangsu, China) or gelatin sponge particles was performed to achieve blood flow stasis in the tumor-feeding artery. Post-TACE syndrome was recorded, and liver function indices were assessed within 1 week of each TACE session.
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