Journal List > J Korean Radiol Soc > v.38(3) > 1068139

Kim and Lee: Placement of an Implantable Central Venous Access Device1

Abstract

Purpose

To evaluate the efficacy and safety of placement of a central venous catheter with infusion port into the superior vena cava

Materials and Methods:

Central venous catheters with a infusion port were implanted in 21 patients (M:F = 4:17, age range: 15 — 63, mean age: 41) diagnosed as suffering from breast cancer (n=9), lymphoma(n=7), thymoma(n=2) rhabdomyosarcoma(n=2) and rectal cancer(n=l). The peripheral portion of the subclavean vein was punctured under fluoroscopic guidance during injection of contrast media at the site of the ipsilateral peripheral vein (20 cases) and under ultrasonographic guidance! 1 case). 9.6F central venous catheters placed in the superior vena cava via the subclavian vein and the connected infusion ports were implanted in the subcutaneous pocket near the puncture site of the right anterosuperior chest wall.

Results:

Catheter insertion in the superior vena cava and port implantation in the subcutaneous pocket were successful in all patients. Mean procedure time was 23 minutes and there were no early complications. Because the incision site had not healed, one patient underwent resuturing 3 weeks after the procedure. In one case, thrombotic occlusion of the catheter occurred, but successful recanalization, involving urokinase infusion, was performed. At the end of the chemotherapy schedule, at 180, 157 and 139 days after the procedure, three central venous catheters with a infusion port were removed in the radiologic suite. Catheter days are 5 days-180 days (mean, 119) from now(1997. 7. 1).

Conclusion:

Radiologic placement under fluoroscopic guidance of a central venous catheter with a infusion port is easy, safe and useful for patients requring long-term venous access.

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Fig. 1.
Placement of an implantable central venous access device on right anterosuperior chest
jkrs-38-437f1.tif
Fig. 2.
CEMO-PORT㧸, Implantable Vascular Access Kit (titanium portal connected with 9.6fr silicone catheter, Percutaneous entry needle, “J” tipped guide wire, dilator/peel sheath assembly, HDC Corporation, San Jose, CA, USA)
jkrs-38-437f2.tif
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