A system and associated method for altering or destroying tissues and anatomical or other structures in medical applications for the purpose of treating diseases or disorders. In one aspect, the system includes a device configured to deploy devices for altering the lobes of a prostate.

The present disclosure relates to the field of microwave ablation treatment devices, and in particular, to a microwave ablation needle head and a microwave ablation needle. A microwave ablation needle head, comprising an outer tube, a cooling tube, a coaxial cable, and an electrode. The outer tube comprises a first branch tube and a second branch tube which are sequentially provided in a direction from the distal end to the proximal end of the outer tube, and the end of the first branch tube away from the second branch tube forms the distal end of the outer tube, and the material of the first branch tube is a ceramic material or a polymer material. The cooling tube is provided within the outer tube, the cooling tube and the outer tube are spaced apart from each other, and a first cooling flow channel is formed between the cooling tube and the outer tube, the material of the cooling tube is a polymer material, and the distal end of the cooling tube is located inside the distal end of the first branch tube, so as to form a mounting space in a distal end region of the cooling tube. The microwave ablation needle head can effectively suppress induced currents, and eliminate the effect of induced currents on ablation shapes.

An ablation probe tip 100 having a shaft 102 with an insertion end 104 and an annular aperture 120 near the insertion end 104. A center of ablation 124 is located within the shaft 102 and surrounded by the annular aperture shaft 102. The ablation probe tip 100 may be part of an ablation probe system 50 that includes an ablation source 60 that provides ablation means 62 to the ablation probe tip 100. The center of ablation 124 is a focal region from which the ablation means 62 radiates through the annular aperture 120 to form an ablation zone 150, 160, 170. The system 50 has at least one intra-operative control selected from the group of: ablation zone positioning control, ablation zone shaping control, ablation center control, ablation zone temperature control, guided ablation volume/diameter control, and power loading control.

Ferritin or iron-based image enhancement agents identify target tissue for treatment or ablation and are heated by microwave absorption. Microwave heat substrates enhance microwave hyperthermal ablation treatment, and may be percutaneously delivered and imaged by x-ray CT during placement of the microwave treatment antenna, allowing more precise positioning and more complete ablation of a tumor site. One method of treating a target tissue uses image-guided delivery of a heat substrate with a reverse-phase change polymer, and may apply energy to fix a mass of the material in the tissue. The fixed polymer may increase hyperthermia, form a thermal boundary, or blockade a vessel or passage so as to reduce or prevent undesired conductive cooling by contiguous tissue, or may deliver a localized treatment drug at the site, upon heating or as it degrades over time.

A flexible microwave ablation antenna and a microwave ablation needle including the same are disclosed. The flexible microwave ablation antenna including: a radiator for transmitting microwave for ablation; a coaxial cable for propagating the microwave for ablation generated by a microwave generator to the radiator; wherein the flexible microwave ablation antenna is bendable. Preferably, an annular composite structure is disposed around a periphery of the coaxial cable to suppress the electromagnetic wave from propagating along the coaxial cable in a reverse direction. The annular composite structure includes an annular non-metallic layer and an annular metallic layer surrounding the annular non-metallic layer. The annular metallic layer is electrically insulated from the coaxial cable.

The invention relates to a holder device for holding a medical instrument, the device comprising:

a base that is to be carried by an apparatus comprising a medical imaging probe associated with the medical instrument; and

a carrier structure for carrying the medical instrument and movably mounted on the base so as to be capable of moving on the base between a first position and a second position.

The invention also relates to an installation including both such a device and a needle-guide.

A system for neuromodulation includes a split-ring resonator (SRR) comprising a resonance circuit, the SRR being implantable in a cranial target site and a source of microwave signals, wherein the microwave signals are deliverable wirelessly to couple with the SRR to produce a localized electrical field, wherein the localized electrical field inhibits one or more neurons at the cranial target site with submillimeter spatial precision.

A surgical probe includes a connection hub, an antenna assembly, and an outer jacket. The antenna assembly is coupled to the connection hub, extends distally from the connection hub, and includes a radiating portion coupled thereto at the distal end thereof. The radiating portion is configured to deliver energy to tissue to treat tissue. The outer jacket is coupled to the connection hub, extends distally therefrom, and is disposed about the radiating portion. The outer jacket includes a distal end member configured to be spaced-apart from the radiating portion a target axial distance. One or more of the couplings between the antenna assembly and the connection hub, the radiating portion and the antenna assembly, and the outer jacket and the connection hub defines a flexible configuration permitting axial movement therebetween to maintain the target axial distance between the radiating portion and the distal end member.

An electrosurgical apparatus for treating fluid-filled biological growths by replacing the fluid within the growth with a substance that assists in delivering treatment energy.

The treatment energy may be microwave energy or may be thermal energy derived from microwave energy. The apparatus comprises an instrument having a radiating tip portion, and a fluid delivery mechanism for transporting fluid to and from a treatment zone located around the radiating tip portion. The fluid delivery mechanism comprises a rigid insertion element arranged to extend into the treatment zone, whereby fluid can be aspirated from the treatment zone, and a substance injected into the treatment zone to replace the aspirated fluid. The injected substance has dielectric properties selected to facilitate uniform delivery of treatment energy to biological tissue in the treatment zone.

An integrated ablation needle (100), comprising a cannula (10) and an electrode needle (20) that is movably and penetratingly installed within the cannula (10); the electrode needle (20) comprises a needle tip (21) located at the far end and a needle rod (23) connected to the near end of the needle tip (21); at least a portion that is near to the needle tip (21) of the needle rod (23) is provided with a sampling groove (231); and the far end of the cannula (10) is provided with a cutting edge (11). The cannula (10) moves along the axial direction relative to the needle rod (23) so as to expose or cover the sampling groove; when the sampling groove (231) is exposed, a tissue portion around the needle rod (23) enters the sampling groove (231); and when the sampling groove (231) is covered, the cutting edge (11) cuts off tissue inside and outside of the sampling groove (231), such that the tissue within the sampling groove (231) is acquired as a biopsy sample. Further provided is an ablation system (1000) comprising an integrated ablation needle (100). The integrated ablation needle (100) and the ablation system (1000) integrate ablation and biopsy functions on the same ablation needle (100), without needing to independently execute a biopsy step, thus avoiding repeated puncturing, reducing damage to the human body, and reducing operation time.