Abstract: A medical probe includes an elongate member having a proximal end and a distal end, an ablative element mounted to the distal end of the elongate member, and a cage assembly mounted to the distal end of the elongate member, the cage assembly at least partially covers the ablative element. A method of treating tissue in a body includes inserting an ablative element in the body, placing the ablative element adjacent the tissue, and maintaining a distance between the ablative element and the tissue using a protective catheter element that circumscribes at least a portion of the ablative element.

Abstract: Catheter devices and methods for intravascular heating and/or cooling of human or veterinary patients. The catheter devices generally comprise catheters having inflow and outflow lumens and at least one curvilinear balloon connected to the inflow and outflow lumens such that heat exchange fluid may be circulated through the balloon(s). The catheter is inserted into the vasculature and heated or cooled fluid is circulated through the balloon(s) to heat or cool blood flowing in heat-exchange proximity to the balloon(s), thereby affecting heating or cooling of all or a portion of the patient's body.

Abstract: System method and apparatus for accurately carrying out the in situ heating of a targeted tissue. Small implants are employed with the targeted tissue which exhibit an abrupt change of magnetic permeability at an elected Curie temperature. The permeability state of the implant is monitored utilizing a magnetometer. The implants may be formed as a setpoint temperature determining component combined with a non-magnetic heater component to enhance the tissue heating control of the system. With the system, a very accurate quantum of heat energy can be supplied to a neoplastic lesion or tissue carrying infectious disease so as to maximize the induction of heat shock proteins. The system also may be utilized in conjunction with non-magnetic arterially implanted stents for the hyperthermia therapy treatment of restenosis and in conjunction with the mending of boney tissue.

Abstract: The present invention relates to a tissue warming device for use with an ultrasound probe having top and bottom sides located diametrically opposite to each other viewed from a frontal cross-section of the probe. The device includes a sheath configured and dimensioned to receive at least a portion of the probe. A first sack, which is associated with the sheath, covers at least a portion of the top side of the probe. The sack includes first and second passages. The first passage allows warm fluid to be directed into the first sack for expansion thereof. The second passage allows fluid to be removed from the first sack. When expanded with warm fluid, the first sack warms body tissue disposed adjacent thereto. The warm fluid may be a warm liquid, such as an aqueous liquid.

Abstract: A method of marking an orientation of a cut specimen of tissue prior to excision thereof from a body includes steps of disposing a tissue-marking probe in the body adjacent the cut specimen, the tissue-marking probe including a tissue-marking tool configured to selectively mark the cut specimen. A surface of the cut specimen is then marked with the tissue-marking tool such that the orientation of the cut specimen within the body is discernable after the cut specimen is excised from the body. The tissue-marking tool may be configured to selectively bow out of and back into a window defined near a distal tip of the probe and the marking step may include a step of selectively bowing the tissue-marking tool out of the window and following the surface of the cut specimen while rotating the probe. The tissue-marking tool may include an RF cutting tool and the marking step may include a step of coagulating or cauterizing a selected portion of the surface of the cut specimen with the RF cutting tool.

Abstract: To reduce the amount of air input to a patient warming blanket, when the blanket is of a size that does not require the full amount of air output from a convective warmer for optimal pressurization, a regulator is provided to the inlet of the blanket to restrict the amount of air input to the blanket, thereby reducing the airflow rate to one that is appropriate for the optimal inflation or pressurization of the warming blanket. Respective regulators that allow different amounts of air under pressure to pass therethrough may be correspondingly fitted to blankets of different sizes and/or dimensions. Each regulator fitted to the inlet of the blanket may be configured in the form of an adapter with multiple orifices for passage of air, or a filter made of an air permeable material having a preselected porosity.

Abstract: An air mattress includes a mattress envelope having a compartment and comprising a thermal functional layer and an outer layer overlapped thereon and an air cushion including a plurality of individual air chambers evenly disposed in the compartment of the mattress envelope and an air supplying tube communicatively interconnecting the air chamber with each other. A thermal control arrangement includes a liquid supplying tube spirally extending at the thermal functional layer of the mattress envelope for guiding a flow of thermal liquid and a thermal energy generator arranged to regulate a temperature of the thermal liquid such that when the thermal liquid passes through the liquid supplying tube, the thermal liquid thermo-communicating with the thermal functional layer of the mattress envelope towards the outer layer so as to regulate a temperature of the mattress envelope.

Abstract: A method of performing CPR on the patient while altering the body temperature of a patient comprises covering at least a thoracic region of the patient with a cover. A heat transfer liquid is directed to flow through liquid passages in the cover for contact with the thoracic region of the patient. Oxygen is supplied to the lungs of the patient, and the thoracic region of the patient is compressed directly through the cover while heat transfer liquid is being directed through the liquid passages in the cover. Apparatus for adjusting the body temperature of a patient generally comprising an enclosure sized and shaped for receiving at least a torso of the patient's body. A heat transfer liquid has a temperature between about 0° C. and about 5° C. A pump drives the heat transfer liquid into the enclosure for connect with the patient's body at a rate greater than about 6 liters per minute.

Abstract: A thermotherapy device has a plurality of heat generation portions disposed on a flexible band-like body, the heat generation portions each comprising a base sheet and an oxygen permeable sheet forming the flexible band-like body, a bag-like accommodation portion formed between the base sheet and the oxygen permeable sheet, and a composition that generates heat filled in the accommodation portion, wherein the filling ratio R satisfies expression (1) below and is less than 0.7, and the heating value of the exothermic composition is not less than 0.26 kcal/cm2 per planar area of the accommodation portion: R??0.016S+0.94??(1) wherein S is the planar area of the accommodation portion of the exothermic composition (unit: cm2), and R is defined by the following expression: R=(mass of the exothermic composition in the accommodation portion)/(maximum mass of the exothermic composition that can be filled in the accommodation portion).

Abstract: A surgical device having a body portion that is gripped by a user, the body portion having a distal end equipped with a soft tip and the proximal end optionally connected to an external vacuum or gas/air source. The surgical device is particularly suitable for use in ophthalmic surgical procedures to remove fluid from the eye or introduce gas/air into the eye. The soft tip is fabricated to protect the delicate tissues if the eye and is further modified so as to enhance a user's visibility of the device in the surgical field.

Abstract: Retrograde methods of accessing and treating collagenous pelvic tissue from a fixed point behind the endo-pelvic fascia, particularly from a space of retzius, are disclosed. Performing treatment from the space of retzius provides for simple and reliable placement and application of the system which in turn enhances both safety and efficacy of such retrograde methodologies. Generally, the systems of the present invention comprise at least a two-part assembly including a penetrating cannula or trocar and an expansible energy applying applicator that is preferably dismounted from behind the endo-pelvic fascia, particularly the space of retzius. The systems and methods are particularly well suited for the treatment of incontinence and other conditions related to insufficient collagenous pelvic tissue support.

Abstract: A radiation delivery module (8) includes a body (48) supportable on a patient's skin and defines a skin surface plane generally aligned with the patient's skin surface (40). A radiation source (22) is mounted to the body and produces a beam (34) of tissue-damaging radiation directed transverse to and at the skin surface plane. The radiation beam creates a radiation spot (42) having a length (36) and a width (44) at the skin surface plane, the length being at least about 5 to 10 times the width. A number of scanned diode laser radiation sub-sources (64) each directing a radiation beam component (66) at the radiation spot may be used. The radiation source may include a rod lens as a focusing optical element. The radiation delivery module may also include a radiation source translator (18) so that the radiation spot moves in a direction generally perpendicular to the length of the radiation spot.

Abstract: The present invention relates to a medical device for treating prostate diseases by using near-infrared LEDs (light emitting diodes), and more particularly, to a medical device for treating prostate diseases in which a probe having installed therein near-infrared LEDs and a vibrator is constructed to be inserted into the rectum, to radiate near-infrared rays to the prostate from a position closest to the prostate and render a direct physical massage function to the prostate, thereby effectively treating prostate-related diseases. Also, the present invention relates to a pad mechanism supplementing the probe mechanism, being brought into close contact with the perineal region to radiate red visible rays and transmit vibration to the organs around the prostate, thereby curing the natures of diseases in the organs around the prostate, and a disposable probe condom used in a state in which it is worn over the probe mechanism.

Abstract: A thermal blanket for warming the limbs includes a surface, an inactive region of the surface adapted to lie against the thoracic and/or abdominal area of a person extending at least from the thighs to the abdomen of the person, active regions of the surface adapted to circulate pressurized air to limbs of the person, and an inflatable pneumatic structure adapted to distribute pressurized air to the active regions. When warmed, pressurized air is introduced into the pneumatic structure, prewarming and/or comfort warming is provided.

Abstract: A guide element is used to guide a cutting device when removing breast tissue. The cutting device may have a tissue collection element for collecting tissue. The tissue collection element may be detachable so that the collection element may be removed independent from the cutting device.

Abstract: A convective warmer to which blankets of different dimensions may be connected is capable of providing air to the various blankets at flow rates that optimally inflate those blankets to achieve the optimal clinical result for the patients covered by those blankets. The blanket connected to the warmer may range from a full size adult warming blanket to a pediatric or neonate warming blanket. There is provided on each blanket a code, marking or marker, to be read by a sensor(s) provided at the outlet of the warmer, that identifies the type of blanket when the blanket is coupled to the warmer. Consequently, heated air may be automatically output by the warmer to the blanket at the appropriate flow rate of that blanket to optimally inflate the blanket without any need for intervention by a user. In addition to being used to control the flow rate of the heated air, the code from the blanket may also be used to control the temperature of the heated air to be input to the blanket.

Abstract: Methods and apparatus for preventing myocardial infarction, or lessening the size/severity of an evolving myocardial infarction, by cooling at least the affected area of the myocardium using an intravascular heat exchange catheter. The heat exchange catheter may be inserted into the vasculature (e.g., a vein) and advanced to a position wherein a heat exchanger on the catheter is located in or near the heart (e.g., within the vena cava near the patient's heart). Thereafter, the heat exchange catheter is used to cool the myocardium (or the entire body of the patient) to a temperature that effectively lessens the metabolic rate and/or oxygen consumption of the ischemic myocardial cells or otherwise protects the ischemic myocardium from undergoing irreversible damage or infarction.

Abstract: A connector assembly for catheters having closed loop flow circuits, such as some balloon catheters and heat exchange catheters. The connector assembly comprises first and second connector bodies that may be connected and disconnected from one another. When the connector bodies are disconnected, a syringe or negative pressure source may be attached to withdraw residual fluid from the catheter's closed loop circuit and to deflate any expandable portion of the closed loop circuit (e.g., balloon or expandable heat exchanger). A one way flow valve prevents make up air or other fluid from entering the catheter while the negative pressure is being applied. Also disclosed are sterility barrier assemblies for all types of catheters.

Abstract: A cryotherapy system is provided with multiple cryoprobes, each of which has a shaft with a closed distal end adapted for insertion into a body and conduits for flowing a cryogenic fluid through the shaft to reduce a temperature of the distal end. A source is provided for the cryogenic fluid, and flow-control metering valves are provided in fluid communication with the conduits and source of the cryogenic fluid. A compressor is provided in fluid communication with the conduits of the cryoprobes to define a self-contained fluid system. The flow-control metering valves and the compressor are controlled by a computer processor to provide the desired flows of the cryogenic fluid through the conduits of the self-contained fluid system.

Abstract: A patient cooling system comprises an inflatable patient mattress having an airflow system and integral manifold incorporated therein and a patient enclosure or tent coupled to the inflatable patient mattress and supported by a framework of inflatable tubes drawing air off of the same air supply used to supply the mattress and to thermally control the area in the tent. The framework of inflatable tubes is divided into left and right sections, which are further subdivided into lower body and upper body sections. An inflatable connector with a stem and protuberance is provided to secure the framework in a closed position. The patient-supporting mattress comprises a plurality of inflatable compartments extending transversely across the width of the mattress that can be alternately pressurized for pressure relief therapy. Air is recirculated from the area in the tent and the integral manifold through the airflow system and into a thermal control unit.