RFA is a procedure in which an electrical generator
originates alternating current delivered at high
frequency (460,000 Hz) by a needle electrode. Ions
in the tissue follow the alternating current delivered
by the needle. The ionic agitation causes frictional
heating resulting in protein denaturation and desiccation.
Target tissue necrosis is achieved as the tissue
gradually desiccates and eventually loses its ability
to conduct current. A rise in impedance occurs as
the lesion becomes more resistant to current flow.
Tissue necrosis is completed once the tissue impedance
reaches a clinically relevant level. When system
achieves Roll-Off™ there is a reduction in
power concurrent with an increase in impedance, signaling
the clinical endpoint. The term Roll-Off refers to
a precipitous decrease in current/rise in impedance,
which has been shown to be a significant predictor
of local control after RFA.
Roll-Off might not occur if the electrode is bathed
in blood which would continue to conduct electricity
even after local tumor ablation and tissue dessication
had occurred.
An advanced RFA system includes a 200 watt generator
and a 4.0cm electrode designed to improve efficiency.
Theoretically, the 4.0cm needle will enable the ablation
of 49% more volume with a single deployment than
a 3.5cm needle. In addition, the new CoAccess™ electrode
is designed to allow pre-treatment biopsy to be performed
through the same percutaneous channel used for RFA.
• LeVeen® Needle
Electrode or LeVeen CoAccess™ Electrode
System
• RF 3000 Radio
Frequency Generator