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0.035 inch stiff guide wire

Manufactured by Cook Medical
Sourced in United States

The 0.035-inch stiff guide wire is a medical device designed to facilitate the insertion and positioning of catheters or other interventional devices within the human body. It is a thin, flexible wire with a stiff core, intended to provide support and guidance during medical procedures.

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4 protocols using 0.035 inch stiff guide wire

1

Transhepatic Biliary Stent Placement

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Patients were placed in a supine position. The right intrahepatic biliary tract was punctured under combined ultrasonic and fluoroscopic guidance. A 0.035-inch normal guidewire (Terumo, Tokyo, Japan) and a 4 to 5F VER catheter (Cordis, Hialeah, FL) were used to detect the obstructed site. When the guidewire and catheter had entered the duodenum, the normal guidewire was exchanged with a 0.035-inch stiff guidewire (Cook, Bloomington, IN). The uncovered SEMS (Micro-Tech, Nanjing, China) was placed at the obstructed site via this stiff guidewire. The stents were 8 mm in diameter and 50 to 70 mm in length.
All patients received antibiotic therapy and hemostasis for 3 to 5 days after SEMS insertion
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2

Bare and Covered Stents for Malignant Biliary Obstruction

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Both bare and covered stents were inserted under the fluoroscopic guidance. The methods of bare and covered stents insertion were same. A 21G Chiba needle (Cook, Bloomington, IN) was punctured into the intrahepatic biliary tract via the right approach. The contrast-medium was injected into the biliary tract to confirm the DMBO site and the length of obstruction. A 4F angiographic catheter (Cordis, Warren, FL) with a 0.035-inch normal guide wire (Terumo, Tokyo, Japan) was then employed to pass through the obstruction. When the catheter and guide wire entered the duodenum, a 0.035-inch stiff guide wire (Cook) was used to replace the normal guide wire. The stent introducer sheaths were sent to the DMBO site via the stiff guide-wire and the stents were released to recanalize the obstruction.
All patients were placed an 8.5F temporary biliary drainage catheter (Cook) and administered preventive anti-inflammatory medications and hemostasis for 5 days.
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3

Percutaneous Biliary Obstruction Stenting

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All procedures were performed with fluoroscopic guidance. A 21G Chiba needle (Cook, IN, USA) was used to puncture the right intrahepatic biliary tract using combined ultrasonic and fluoroscopic guidance, with cholangiography being conducted to image the obstruction. A 4F VER catheter (Cordis, Warren, FL, USA) with a 0.035-inch normal guide wire (Terumo, Tokyo, Japan) was then employed to pass through the obstruction. When the catheter and guide wire entered the duodenum, a 0.035-inch stiff guide wire (Cook) was used to replace the normal guide wire. The stent (Micro-Tech, Nanjing, China) was released at the site of the obstruction via the stiff guide wire.
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4

Celiac Artery Aneurysm Stenting Procedure

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Fluoroscopic guidance and local anesthesia were used during all stent insertion procedures in this study. All procedures were performed in the digital substraction angiography room.
The treatment was performed via a right femoral approach. A 5F vascular sheath was inserted into the right femoral artery, a 0.035-inch soft guide wire (Terumo, Tokyo, Japan) and a 4F angiographic catheter (Cordis, NJ, USA) were inserted to the vascular sheath, and the angiographic catheter was placed at the ostium of the celiac artery.
CAA was confirmed via celiac angiography, after which the guide wire was exchanged for 0.035-inch stiff guide wire (Cook, IN, USA). This guide wire was then used to insert a metal stent which was used to seal the CAA (Fig. 1b). Stent selection criteria were: (a) stents had to fully cover the CAA neck (a minimum of 5 mm on both sides), and (b) the stent had a diameter that was 1.1–1.2 times the celiac artery diameter. After stent insertion was complete, patency was confirmed and CAA was reevaluated via celiac angiography.
For 6 months following intervention, all patients underwent dual anti-platelet treatment (aspirin 100 mg/day + clopidogrel 75 mg/day), after which daily aspirin intake was maintained for life.
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