Abstract: Systems and methods for delivering medicament to a subject use one or more sensors to generate signals that represent characteristics of the ultrasonic energy emitted into or by a respiratory medicament delivery device. Parameters based on these signals indicate energy amplitude in one or more frequency ranges. Such parameters can be used to determine respiratory parameters, patient adherence, and/or other parameters.

Abstract: A nasal delivery device for delivering substance to a nasal cavity of a subject, the delivery device comprising: a substance supply unit for supplying a dose of substance to be delivered to the nasal cavity of the subject, the substance supply unit including an inlet and an outlet; a nosepiece unit including a nosepiece for fitting to a nasal cavity of the subject and being in fluid communication with the outlet of the substance supply unit; and a mouthpiece unit including a mouthpiece in fluid communication with the inlet of the substance supply unit and through which the subject in use exhales such as to entrain substance from the container chamber and deliver the same through the nosepiece, and at least one temperature modifier for reducing a temperature of the exhaled air flow such as to reduce the absolute humidity thereof.

Abstract: Gas flow reversing element (1) for the use of a gas supply (14) under excess pressure, in particular inspiratory gases, for selectively generating a gas flow (8) from or to a line connector (6) which can in particular be connected to an airway of a patient, said gas flow reversing element (1) being designed as a main piece (2), the main piece (2) at least comprising an inflow region (9), a nozzle region (15) and a mixing region (16), and further a branching piece (3), the inflow region (9) connecting a pressure connector (4), for connection to the gas supply (14), to at least one closable outlet opening (5) arranged in the mixing region (16), and the branching piece (3) connecting the nozzle region (15) of the main piece (2) to the line connector (6), wherein a nozzle (7), particularly an injector nozzle, is configured and arranged in the nozzle region (15) in such a way that, a gas flow (8) flowing along a first flow path (20) through the main piece (2) from the pressure connector (4) subsequently through th

Abstract: Systems and methods for delivering therapy and/or medicament to a subject use one or more sensors to generate signals that represent characteristics of ultrasonic energy emitted during the use of respiratory medicament delivery devices. Parameters based on these signals indicate energy amplitude in one or more frequency ranges. Such parameters can be used to characterize the emitted ultrasonic energy and control and/or monitor device operation and/or patient adherence.

Abstract: A flexible tube holding device includes a handle having a groove along a length of a back side thereof, the groove being sized to at least partially accept a desired flexible tube, such as an endotracheal tube. The device is generally J-shaped from the side, and further includes a blade connected to the handle, the blade having a proximal blade section connected to the handle and having an opening along a back side thereof, and a tube retention section connected to the proximal blade section at an end thereof opposite the handle and along the opening. The tube retention section is sized to accept and hold at least most of a cross-section of a tip portion of the flexible tube and shaped to retain the tip portion. The flexible tube is held in place manually or using a quick-release closure mechanism. The flexible tube holding device may be part of an intubation system.

Abstract: A patient interface has a single loop headstrap and a mask for covering at least the nostrils of the user. The single loop headstrap extends from the mask at either end. A short length of supple conduit is coupled to the mask by a swivel or ball joint to allow rotation of the conduit relative to the mask through different angles and orientations.

Abstract: An interface includes a mask. The mask includes a frame and a seal supported by the frame. Headgear is connected to the mask. The interface includes at least one of (i) an adjustment mechanism that can be set to a use length for a loop defined by the mask and the headgear; and (2) a break-fit assembly that can selectively lengthen the loop defined by the mask and the headgear and return to the use length.

Abstract: A swivel connector includes a patient member that has a first end for connecting to a patient facemask. The first end of the patient member is in fluid communication with a second end of the patient member. A first end of a gas supply member is for connecting to a supply of gases. A second end of the gas supply member is rotatably and fluidly coupled to the second end of the patient member, thereby gases flow between the patient member and the gas supply member. An axis of the first end of the patient member is at a non-zero angle with respect to an axis of the second end of both members. Likewise, an axis of the first end of the gas supply member is at a non-zero angle with respect to an axis of the second end of both members.

Abstract: The resuscitation method and device incorporates a T-piece and/or bag and mask resuscitation device that transforms into short term (and then long term) CPAP device. This results in continuum of respiratory care in the Delivery Room, and potentially in the nursery. The respiratory support is uninterrupted. The device can include a modular design, which adds heat and humidity in a modular way, when the long term CPAP requires it. The resuscitation device and method includes a PIP phase and a PEEP phase. This is driven either manually or by a finger and gas power. The exhalation phase is PEEP, where the PEEP is a small positive pressure to ensure the lungs remain open. When the baby is spontaneously breathing, meaning no longer in need of PIP, the PEEP can be adjusted to be continuous positive pressure, or CPAP. If the CPAP is short term, there is minimal need for heating or humidifying the air. When the CPAP is used longer term, a heater and humidifier can be applied to the air source of the CPAP.

Abstract: A method and apparatus to identify the source of oxygen delivery failure to a patient. The apparatus comprises a pressure sensor to detect a patient's breathing pressure and ambient pressure, an oxygen flow analyzer to measure oxygen flow to the patient, and a processor to analyze the breathing pressure values, ambient pressure value, and oxygen flow rate values. When the oxygen flow rate value is greater than a predetermined threshold value, the processor is programmed to compare the breathing pressure values to the ambient pressure value and output an apnea alarm or an oxygen delivery device displacement alarm.

Abstract: A method and apparatus to deliver a variable flow of oxygen to a patient is described. The apparatus may include a flow control valve, a pressure sensor to detect a patient's breathing pressure and ambient pressure, an oxygen flow analyzer to measure oxygen flow to the patient, and a processor to analyze the breathing pressure values, ambient pressure value, and oxygen flow rate values and to determine when a patient is inhaling. When the processor determines the patient is inhaling, the processor calculates an optimal oxygen flow rate to deliver to a patient, which may depend on a pre-selected flow rate and an oxygen backlog, and the processor sends a signal to the flow control valve to deliver the optimal oxygen flow rate to the patient.

Abstract: The present invention relates to a mouthpiece for controlled delivery of a breathing gas including oxygen, preferably an increased ratio of oxygen with respect to ambient air, to the respiratory tracts of a user comprising a valve having two modes; a closed default mode, which substantially impedes any flow of the breathing gas through the valve; and an active open mode, which allows for a substantial flow of the breathing gas through the valve, wherein the open mode can be activated by the user manipulating the valve with his/her mouth. The invention also relates to the use of such a valve in a device for delivery of breathing gas and further to an apparatus for controlled delivery of the breathing gas to the respiratory tracts of a user. Finally, the invention also relates to a method for controlled delivery of the breathing gas to the respiratory tracts of a user.

Abstract: A method is provided for treating a neuromuscular defect in a subject. One step of the method includes locating a target nerve. After locating the target nerve, a treatment probe is provided. The treatment probe includes an elongated body member having a proximal end portion and a distal end portion. The distal end portion includes an energy delivery mechanism for stimulating or ablating the target nerve, a monitoring mechanism, and a fluid aspiration/delivery mechanism. Next, the target nerve is verified as an appropriate target for ablation by stimulating and then monitoring the target nerve via the energy delivery mechanism and the monitoring mechanism, respectively. After verifying the target nerve, a tumescent fluid is injected into the tissue surrounding the target nerve. An electric current is then delivered to the energy delivery mechanism to substantially ablate the target nerve.

Abstract: A tray (100) for accommodating a coiled medical device, such as a catheter assembly (700), includes a first compartment (101), a second compartment (102), and a third compartment (103). The catheter assembly (700) and devices associated with a catheterization procedure, such as syringes (701,702) containing sterile water and lubricating jelly and a specimen container (703) can be disposed within the tray. Printed instructions (1001) can be included with the tray (100). When a CSR wrap (1000) is disposed about the tray (100), the printed instructions can be placed atop the CSR wrap (1000) but beneath an outer sterile wrap (1002). The printed instructions (1001) can include a patient portion (1202) that is detachably coupled to a health care services portion (1201) such that it can be taken home with the patient after the procedure.

Abstract: A method of a forming a hollow, drug-eluting medical device includes providing composite member having an outer member and a core member disposed within a lumen of the outer member. The composite member is shaped into a pattern. Openings are formed through the outer member of the composite member. The composite member is processed to remove the core member from the lumen of the outer member without harming the outer member, leaving a hollow tubular member already formed into the desired pattern. The lumen of the outer member is filled with a therapeutic substance.

Abstract: An antibacterial catheter includes a body having a urine passage, and an antibacterial carbon material disposed in the urine passage. The antibacterial carbon material has a BET specific surface area in a range between 500 m2/g and 1800 m2/g, and contains a plurality of pores including micropores that have a diameter less than 2 nm. The antibacterial carbon material has a micropore-to-pore volume ratio ranging from 30% to 50%. Because the antibacterial carbon material is disposed in the urine passage of the catheter, the bacteria outside the human body may not easily enter into the urinary bladder and the bacteria inside the urinary bladder can be destroyed, such that the urinary system can be effectively prevented from the bacterial infection.

Abstract: Systems, devices, and methods are provided for delivering chemical and electrical stimulation across one or more neural circuits. The systems, devices, and methods can also be used for sensing and recording specific neural activity. In certain embodiments, a system includes first and second fluid reservoirs, a manifold, and a delivery tube. The manifold may include first and second chambers therein. The first chamber may be in fluid communication with the first reservoir, and the second chamber may be in fluid communication with the second reservoir. The delivery tube may include a first conduit in fluid communication with the first chamber, a second conduit in fluid communication with the second chamber, and a third conduit configured to house an electrode therein. In this manner, a distal tip of the delivery tube is configured to be positionable adjacent to the one or more neural circuits for providing chemical and electrical stimulation thereto.

Abstract: An interventional catheter for treating an artery includes an elongated body sized and shaped to be transcervically introduced into a common carotid artery at an access location in the neck. The elongated body has an overall length such that the distal most section can be positioned in an intracranial artery and at least a portion of the proximal most section is positioned in the common carotid artery during use.

Abstract: Described are peritoneal catheter devices and methods for positioning these devices in a medical patient. The peritoneal catheter includes a catheter tube having a proximal end portion opposite a distal end portion, a stationary flange attached to the catheter tube near the distal end portion, and a mobile flange positioned on the catheter tube between the stationary flange and the proximal end portion. In use, the stationary flange is positioned to cover a hole in the rectus muscle and the mobile flange is selectively moved along the catheter tube to sandwich the rectus muscle of the patient between the stationary flange and the mobile flange. Optionally an interior cuff is mounted on the catheter tube adjacent to the stationary flange but between the stationary flange and the mobile flange and wherein the selectively positioning the mobile flange includes sandwiching the interior cuff between the stationary flange and the mobile flange.

Abstract: A system for strain relieving intravenous (IV) assembly includes a dressing and an anchor portion for use with the dressing. In various embodiments, the dressing may cover an injection site into a portion of a patient's body for an intravenous (IV) assembly that provides fluid communication between the injection site and a fluid reservoir remote from the injection site through a flexible tube. In an illustrative example, the anchor portion may include a first member and a second member. The first member may be secured, for example, to the dressing and may, in some examples, wrap around the tubing so as to resist axial movement of the tubing relative to the dressing. The second member may be secured to the dressing and may wrap around the tubing and a portion of the patient's body so as to resist radial movement of the tubing relative to the body.

Abstract: Certain exemplary embodiments provide systems, methods, and/or devices configured to utilize a cannula-needle having a tubular body adapted to house thereinside a needle of a catheter. The cannula-needle has a peripheral wall extending along a longitudinal direction with a predetermined length from an open proximal end to a distal end, the distal end provided with a hole.

Abstract: A device for restraining a guide wire includes a base having a recessed formation configured to receive a portion of the guide wire, and a flexible lid configured to fit on the base. The lid has a main sheet portion covering the portion of the guide wire and a plurality of fingers separated by gaps and extending downwardly from a peripheral edge of the main sheet portion to surround the base. Sandwiched between the lid and base, the guide wire extends through gaps between the finger members. Constructed of sheet material, the lid is flexibly movable between a closed configuration wherein the fingers are flexed inwardly engaging the base, and an open configuration wherein the fingers are flexed outwardly releasing the base.

Abstract: A tube system for medical application has a tube with at least one tube lumen. A guide wire is inserted in at least a tube section in at least one tube lumen. An adhesive coating is present between an outer wall of the inserted guide wire and an inner wall of the guide wire-tube lumen. This results in a tube system with better handling characteristics.

Abstract: An intravascular balloon catheter device is disclosed having an inner member, an outer member disposed about the inner member and further comprising a balloon. A sheath is disposed about the outer member that moves relative to the balloon so as to selectively expose some or all of the balloon for inflation. A clamp may be used to selectively secure the sheath at a desired position relative to the balloon.

Abstract: A thrombectomy and balloon angioplasty catheter for the removal of blood clots and debris from a blood vessel and/or for the dilation of a narrowed or completely closed segment in the blood vessel is disclosed. The catheter includes a shaft having a proximal end and a distal end, an angioplasty balloon mounted to the shaft adjacent the distal end of the shaft, and an occlusion balloon mounted to the shaft at a location proximally spaced from the angioplasty balloon. A guide wire lumen is arranged on the shaft. The guide wire lumen extends from a first position adjacent the distal end of the shaft to a second position proximal the angioplasty balloon and distal the proximal end of the shaft.

Abstract: A subdural drainage system includes: (a) a subdural drainage device having an opening formed therethrough, said subdural drainage device having an upper portion, a body portion, and a lower portion; (b) a housing having an upper portion and lower portion, with said housing connected to said subdural drainage device; said housing movable between (i) a first configuration and (ii) a second configuration; and (c) an elongated element positioned inside said housing, said elongated element having an upper portion, a lower portion and a deformable member connected to the lower portion; said elongated element being configured such that said elongated element is moved between (i) a retracted position with said elongated element inside a portion of said subdural drainage device and said deformable member inside said housing, and (ii) an extended position with said elongated element extending through said subdural drainage device such that said deformable member automatically extends to an extended, deformed position i

Abstract: Implantable physiological shunt systems and related fluid flow control devices and accessories for use therewith. Devices, systems and methods relating to implantable medical fluid flow control devices, rotors and magnets with increased resistance to inadvertent setting changes. Devices, systems and methods relating implantable medical fluid flow control devices, rotors and magnets which provide improved magnetic coupling to fluid flow control device accessories such as adjustment tools.

Abstract: The invention describes a sinus balloon catheter and methods of use. Specifically a sinus balloon catheter for dilating a sinus cavity lumen is provided with a tip that can be extended. The catheter comprises a guide tube with a proximal and distal end, a sleeve member, a balloon disposed upon the sleeve member and a rounded tip arranged at the distal end and extendable along with the extension of the sleeve member.

Abstract: A method for use with a balloon catheter device that includes a selectively bendable portion with a balloon disposed thereon, a control device for controlling bending of the selectively bendable portion, and a camera located at an end of a distal portion, includes inserting the distal portion into the nostril while the distal portion is straight; viewing an image provided by the camera; stopping insertion of the distal portion after the ethmoidal bulla is viewed in the image; articulating the distal portion in an upward direction to view the opening to the frontal sinus ostium or a downward direction to view the opening to the maxillary sinus ostium using the control device; inserting the distal portion into the frontal sinus ostium or the maxillary sinus ostium while the distal portion remains in the bent position; and inflating the balloon in the frontal sinus ostium or the maxillary sinus ostium.

Abstract: An applicator assembly includes a plurality of ampoules formed of a frangible material and containing liquid to be applied, a container having a proximal end, a distal end, and an interior portion defining a chamber adapted to receive the plurality of ampoules, an application member attached to the distal end of the container; and at least one actuator projecting from the container, wherein the at least one actuator is actuatable to independently fracture the plurality of ampoules, thereby independently releasing the liquid into the application member. The at least one actuator may be moveable from a first position to a second position, the applicator having a smaller profile when the actuator is in the second position than when the actuator is in the first position.

Abstract: An in-situ material delivery device for handheld, stereotactic table or MRI stage use may comprise a work element configured to selectively open and close at least one articulable beak configured to penetrate tissue to a target delivery site, or follow a central lumen of another device or other guiding modality, and then to deliver selected materials. Such a device may deliver a variety of materials such as markers, radio-active pellets, medications, other devices, and other materials of solid, liquid or gaseous form to a target site, and materials of similar nature may also be captured and removed from a target site. A single tube with or without coatings or an inner sheath and an outer sheath which may be co-axially disposed relative to a work element may be configured to actuate a beak or beaks and internal delivery mechanisms simultaneously. One embodiment of this device may be applicable to field use or one time use.

Abstract: Exemplary methods of improving the delivery of a substance encapsulated in a delivery vehicle to cells of interest in skin, tissue or tumor are disclosed herein.

Abstract: An article having at least one microneedle (160, 260) is provided. The microneedle includes a base (162), an elongated body (161) having a central axis (130) and a body diameter (168), a tip portion (166), a first channel (170), and a second channel (176). The tip portion includes a tip (164), a beveled surface (140), and a bevel opening (172) in the beveled surface. The first channel extends axially from the bevel opening through at least a portion of the elongated body and has a first wall that is substantially aligned with the central axis. The second channel extends radially from the first channel to the bevel opening and has a second wall that is oriented substantially orthogonal to the central axis. The first channel and second channel merge to form the bevel opening.

Abstract: A device with a positioning frame which can be adhered onto the skin and with a transdermal therapeutic system which can be inserted into a cut-out that passes through the positioning frame. The active substance dispensing outlet side of the inserted transdermal therapeutic system facing the skin. The device includes a tool unit which can be inserted into the cut-out of the positioning frame and centered in said cut-out in order to produce openings at least in the uppermost layer of the skin.

Abstract: Devices are disclosed that can be used with a medical instrument that comprises an elongated sheath and a hub that comprises a sideport. The hub and the sheath of the medical instrument are configured to permit at least a portion of an elongated medical implement to pass through them. The devices can include a plurality of engagement members that cooperate to define an opening through which the elongated medical implement can pass and a biasing surface. The devices can further include an adapter that includes an attachment mechanism to directly engage the sideport to secure the adapter to the medical instrument and a locking member for coupling with the adapter. The adapter and the locking member can interact to advance the plurality of engagement members along the biasing surface to transition the engagement members from an open state to a locked state.

Abstract: A locking device for medical tube coupling includes an elongated body positionable during use adjacent an exterior surface of the medical tube coupling, a first flange carried on one end of the body, a slot formed through a thickness of the first flange in an open communication with an edge surface thereof, and a second flange carried on a longitudinally opposite end of the body and extending in a direction of the first flange. The second flange may include the same slot and/or a cavity in an inner surface thereof. The locking device may be made adjustable to lock a connection between a tube and the medical tube coupling and/or securely cap the inlet port of the medical tube coupling when tube is removed. The device may also include a third flange being disposed on the elongated body between the first and second flanges.

Abstract: A soft grip medical connector comprises a housing with an upstream end, a downstream end and a lumen extending through a central portion thereof. A flexible member comprises a valve portion integrally formed with a sleeve portion. The valve portion is positioned within a section of the housing and is configured to control a flow of fluid through the housing lumen. The sleeve is inverted to envelope at least a portion of the outer surface of the housing. In some embodiments the gripping portion is integrally formed with the valve portion. In some embodiments, the connector is also generally configured to create a positive pressure in a catheter lumen upon removal of a syringe or other medical device from the upstream end of the connector. Methods of making a medical fluid connector generally comprise forming a valve member with a sleeve extending there from, and assembling the valve, sleeve and housing.

Abstract: Liquid transfer devices based on commonly owned WIPO International Publication No. WO 2007/052252 entitled Needleless Additive Control Valve. The liquid transfer devices include either an integral vial adapter and/or an integral infusion set for reducing cost and facilitating use by reducing user steps.

Abstract: A medical device includes a printed circuit board, a connector mounted on the printed circuit board, and a polymeric body molded over the connector and the printed circuit board. The connector is configured to receive a medical lead and electrically and mechanically couple the lead to the printed circuit board. The connector comprises a housing and feedthrough assembly that includes a polymeric housing and a conductor. The housing defines a bore configured to receive the lead and defines a feedthrough opening through which the conductor extends. The housing and feedthrough assembly is sealed except for an aperture in communication with the bore. The connector further includes a contact disposed in the bore. The conductor electrically couples the contact with the printed circuit board. When a lead is properly received by the bore, the contact couples the lead to the printed circuit board via the conductor.

Abstract: An electrode for use with an implantable medical device includes a titanium surface, and a titanium nitride layer formed on at least a portion of the titanium surface. At least some titanium of the portion of the titanium surface is removed from the titanium surface prior to forming the titanium nitride layer. The textured titanium nitride layer is formed by reacting nitrogen proximate to the portion of the titanium surface with titanium at the portion of the titanium surface.

Abstract: A method of manufacturing a detection/stimulation lead for implantation into a venous, arterial, or lymphatic network is shown and described. The method includes providing a microcable comprising a sheath of insulating material covering an electrically conductive core. The method further includes surrounding a portion of the microcable with an electrically conductive metal ring. The method also includes crimping the ring such that the thickness of the sheath is penetrated by a portion of the metal ring and such that an electrical connection is formed between the metal ring and the electrically conductive core.

Abstract: Electrical neurostimulation leads for use in craniofacial peripheral nerve neurostimulation (e.g. occipital neurostimulation). Paddle leads, lead wires, lead wire anchors, tools, or other hardware can be designed for implantation in the craniofacial region. This can address problems of electrical neurostimulation in the craniofacial region such as lead migration, hardware breakage, patient discomfort, or other problems.

Abstract: A percutaneously implantable paddle lead includes an elongated lead body having a proximal portion and a distal portion; a plurality of terminals disposed on the proximal portion of the lead; a flexible paddle body coupled to the distal portion of the lead; and a plurality of electrodes disposed in the paddle body and electrically coupled to the terminals on the proximal portion of the lead. The percutaneously implantable paddle lead also includes a bonding material in contact with the paddle body and holding the paddle body in a compacted form prior to, and during, insertion into a percutaneous implantation tool. The bonding material is configured and arranged to release the paddle body during or soon after implantation into a patient so that the paddle body can deploy into its paddle-like form. Alternatively, at least one current-degradable fastener can be used instead of the binding material.

Abstract: A therapeutic electron transfer device including a half-cell and an ionically conductive path for ion transfer between an organism and the half-cell. The half-cell includes an electrically conductive electrode, an active material in contact with the electrode, and an electrically conductive path for electron transfer between the organism and the electrode. The active material includes an oxidizing agent or a reducing agent, such that electron transfer occurs spontaneously from or to the organism, respectively. A kit includes therapeutic electron transfer device and instructions for use. Two therapeutic electron transfer devices may be used simultaneously or alternately to provide electrons to an organism, withdraw electrons from an organism, or both.

Abstract: Medical devices and methods for providing breathing therapy (e.g., for treating heart failure, hypertension, etc.) may determine at least the inspiration phase of one or more breathing cycles based on the monitored physiological parameters and control delivery of a plurality of breathing therapy sessions (e.g., each of the breathing therapy sessions may be provided during a defined time period). Further, each of the plurality of breathing therapy sessions may include delivering stimulation after the start of the inspiration phase of each of a plurality of breathing cycles to prolong diaphragm contraction during the breathing cycle.

Abstract: An efferent contraction training device may include a fixing unit, an electrical stimulation pad and a driving unit. The fixing unit may be configured to fix an articulation of a patient. The fixing unit may include a first member and a second member connected to the first member. The second member of the fixing unit may have an angle with respect to the first member changed in accordance with movements of the articulation of the patient. The electrical stimulation pad may apply an electrical stimulation to a muscle of the articulation to provide the articulation with an efferent contraction exercise. The driving unit may drive the electrical stimulation pad. Thus, the efferent contraction training device may be effectively used for rehabilitating the patient with the paralytic musculature.

Abstract: The present invention relates to a seating apparatus for the diagnosis and treatment, and more particularly, to a seating apparatus for diagnosis and treatment of diagnosing and curing urinary incontinence, erectile dysfunction and defecation disorders which enables to diagnose symptoms of urinary incontinence, erectile dysfunction and defecation disorders by measuring contraction pressure and contraction duration of pelvic floor muscles, muscles of perineum and anal sphincters of a user, who puts on cloth while seated, simultaneously with curing symptoms of urinary incontinence, erectile dysfunction and defecation disorders throughout biofeedback exercise and training.

Abstract: Generally, the disclosure is directed one or more methods or systems of cardiac pacing employing a right ventricular electrode and a plurality of left ventricular electrodes. Pacing using the right ventricular electrode and a first one of the left ventricular electrodes and measuring activation times at other ones of the left ventricular electrodes. Pacing using the right ventricular electrode and a second one of the ventricular electrodes and measuring activation times at other ones of the left ventricular electrodes. Computing a first degree of resynchronization based on a sum of differences of activation times and corresponding activation times. Pacing using the right ventricular electrode and a second one of the ventricular electrodes and measuring activation times at other ones of the left ventricular electrodes. Computing a second degree of resynchronization based on the sum of differences of activation times and corresponding activation times.

Abstract: A system and method for treating pain without paresthesia by spinal cord stimulation.

Abstract: An operating room cable assembly for electrically coupling at least one implantable electrical stimulation lead to a trial stimulator includes an elongated body; a trial stimulator connector disposed at one end of the elongated body; and a lead connector disposed at another end of the elongated body. The lead connector includes a connector body, a connector cover, a cover fastener disposed on the connector body, at least one lead channel to each receive a lead or lead extension, conductors coupled to the elongated body to make electrical contact with terminals disposed on the lead or lead extension, and a layer of medical adhesive disposed along a bottom surface of the lead connector. The layer of medical adhesive and the lead connector are configured and arranged for disposition over an exit wound from which the at least one lead or lead extension extends out of a skin of a patient.