US20180000420A1 - Proximal connector for guidewire assembly - Google Patents
Proximal connector for guidewire assembly Download PDFInfo
- Publication number
- US20180000420A1 US20180000420A1 US15/637,293 US201715637293A US2018000420A1 US 20180000420 A1 US20180000420 A1 US 20180000420A1 US 201715637293 A US201715637293 A US 201715637293A US 2018000420 A1 US2018000420 A1 US 2018000420A1
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- Prior art keywords
- proximal
- insulative element
- contact
- guidewire
- connector
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-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B5/00—Measuring for diagnostic purposes; Identification of persons
- A61B5/68—Arrangements of detecting, measuring or recording means, e.g. sensors, in relation to patient
- A61B5/6846—Arrangements of detecting, measuring or recording means, e.g. sensors, in relation to patient specially adapted to be brought in contact with an internal body part, i.e. invasive
- A61B5/6847—Arrangements of detecting, measuring or recording means, e.g. sensors, in relation to patient specially adapted to be brought in contact with an internal body part, i.e. invasive mounted on an invasive device
- A61B5/6851—Guide wires
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B5/00—Measuring for diagnostic purposes; Identification of persons
- A61B5/01—Measuring temperature of body parts ; Diagnostic temperature sensing, e.g. for malignant or inflamed tissue
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B5/00—Measuring for diagnostic purposes; Identification of persons
- A61B5/02—Detecting, measuring or recording pulse, heart rate, blood pressure or blood flow; Combined pulse/heart-rate/blood pressure determination; Evaluating a cardiovascular condition not otherwise provided for, e.g. using combinations of techniques provided for in this group with electrocardiography or electroauscultation; Heart catheters for measuring blood pressure
- A61B5/026—Measuring blood flow
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B5/00—Measuring for diagnostic purposes; Identification of persons
- A61B5/03—Detecting, measuring or recording fluid pressure within the body other than blood pressure, e.g. cerebral pressure; Measuring pressure in body tissues or organs
- A61B5/036—Detecting, measuring or recording fluid pressure within the body other than blood pressure, e.g. cerebral pressure; Measuring pressure in body tissues or organs by means introduced into body tracts
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B5/00—Measuring for diagnostic purposes; Identification of persons
- A61B5/06—Devices, other than using radiation, for detecting or locating foreign bodies ; determining position of probes within or on the body of the patient
- A61B5/061—Determining position of a probe within the body employing means separate from the probe, e.g. sensing internal probe position employing impedance electrodes on the surface of the body
- A61B5/062—Determining position of a probe within the body employing means separate from the probe, e.g. sensing internal probe position employing impedance electrodes on the surface of the body using magnetic field
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M25/00—Catheters; Hollow probes
- A61M25/01—Introducing, guiding, advancing, emplacing or holding catheters
- A61M25/09—Guide wires
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B2562/00—Details of sensors; Constructional details of sensor housings or probes; Accessories for sensors
- A61B2562/12—Manufacturing methods specially adapted for producing sensors for in-vivo measurements
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B2562/00—Details of sensors; Constructional details of sensor housings or probes; Accessories for sensors
- A61B2562/22—Arrangements of medical sensors with cables or leads; Connectors or couplings specifically adapted for medical sensors
- A61B2562/225—Connectors or couplings
- A61B2562/227—Sensors with electrical connectors
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B5/00—Measuring for diagnostic purposes; Identification of persons
- A61B5/02—Detecting, measuring or recording pulse, heart rate, blood pressure or blood flow; Combined pulse/heart-rate/blood pressure determination; Evaluating a cardiovascular condition not otherwise provided for, e.g. using combinations of techniques provided for in this group with electrocardiography or electroauscultation; Heart catheters for measuring blood pressure
- A61B5/021—Measuring pressure in heart or blood vessels
- A61B5/0215—Measuring pressure in heart or blood vessels by means inserted into the body
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M25/00—Catheters; Hollow probes
- A61M25/01—Introducing, guiding, advancing, emplacing or holding catheters
- A61M25/09—Guide wires
- A61M2025/09058—Basic structures of guide wires
- A61M2025/09083—Basic structures of guide wires having a coil around a core
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M25/00—Catheters; Hollow probes
- A61M25/01—Introducing, guiding, advancing, emplacing or holding catheters
- A61M25/09—Guide wires
- A61M2025/09058—Basic structures of guide wires
- A61M2025/09083—Basic structures of guide wires having a coil around a core
- A61M2025/09091—Basic structures of guide wires having a coil around a core where a sheath surrounds the coil at the distal part
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M25/00—Catheters; Hollow probes
- A61M25/01—Introducing, guiding, advancing, emplacing or holding catheters
- A61M25/09—Guide wires
- A61M2025/09108—Methods for making a guide wire
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M25/00—Catheters; Hollow probes
- A61M25/01—Introducing, guiding, advancing, emplacing or holding catheters
- A61M25/09—Guide wires
- A61M2025/09133—Guide wires having specific material compositions or coatings; Materials with specific mechanical behaviours, e.g. stiffness, strength to transmit torque
Definitions
- the present disclosure relates generally to a guidewire assembly including a proximal portion configured for electrical connection to an external device.
- the present disclosure relates to a guidewire assembly having a proximal connector disposed on a proximal portion thereof, the proximal connector including at least one electrical contact and at least one reflowed insulative segment bonded or sealed to an adjacent electrical contact.
- Various diagnostic and therapeutic procedures in or on the body of a patient may be performed or facilitated by inserting a catheter into a body lumen and thereafter navigating the diagnostic or therapeutic catheter to the target site prior to, for example, delivering a medical device to the target site.
- a guidewire is often used.
- the guidewire typically has a reduced diameter relative to the catheter or device; the reduced diameter aids a physician in inserting and navigating the guidewire to the target site.
- the catheter or device is then passed over the guidewire and guided to the target site.
- One method of maneuvering a guidewire to a target site within a patient is to place one or more position sensors on the guidewire, track the position sensors with a navigation system, and display a real-time or rendered image of the guidewire for the clinician manipulating the guidewire to view.
- the raw signal generated by the position sensor and/or physiological data sensor located within the body may be transmitted to an external device, in which the raw signal is re-translated into locational or physiological data.
- the re-translated longitudinal or physiological data is then processed and the results continuously displayed on a monitor and/or saved.
- some known guidewires utilize one or more cables or leads extending along an internal portion of the guidewire between the sensor and a proximal connector.
- Some known guidewires utilize a physical electrical connection between the proximal connector and an external device to transfer power or communicate generated signals thereto, while other known guidewires utilize a wireless connection between the proximal connector and the external device.
- the proximal connector includes at least one electrically isolated area for the connection to be made. The isolated area(s) are generally bonded or sealed to an insulative element so as to prevent liquid or moisture from entering the internal portion of the guidewire, contacting internal electrical components, and causing an electrical short.
- the present disclosure is directed to a guidewire assembly comprising: a guidewire having a distal portion and a proximal portion; a sensor disposed at the distal portion of the guidewire; and a proximal connector disposed at the proximal portion of the guidewire.
- the proximal connector comprises at least one proximal contact and at least one reflowed insulative element disposed adjacent the at least one proximal contact.
- the present disclosure is further directed to a guidewire comprising: a distal portion comprising a sensor; a shaft portion coupled to the distal portion; and a proximal connector coupled to the shaft portion.
- the proximal connector comprises at least one proximal contact and at least one reflowed insulative element disposed adjacent the at least one proximal contact.
- the present disclosure is further directed to a guidewire assembly obtained by a process comprising: forming a proximal connector, the proximal connector comprising a first proximal contact and a first insulative element disposed adjacent a distal end of the first proximal contact; distally advancing a heat shrink tube over the proximal connector; heating the heat shrink tube and the proximal connector to reflow the first insulative element so as to couple the first insulative element to the distal end of the first proximal contact; and removing the heat shrink tube from the proximal connector.
- FIG. 1 is a diagrammatic view of a conventional system for performing one or more diagnostic or therapeutic procedures utilizing a guidewire assembly.
- FIG. 2 is a cross-sectional view of one embodiment of a guidewire assembly of the present disclosure.
- FIG. 3 is a perspective view of the guidewire assembly of FIG. 2 .
- FIGS. 4, 4A, and 4B are a flowchart of one embodiment of a method of making a proximal connector for use in the guidewire assembly of FIGS. 2 and 3 .
- FIGS. 5A-5E are perspective views of the proximal connector at various stages of the method illustrated in FIGS. 4, 4A, and 4B
- a guidewire assembly that includes a sensor at a distal end thereof for determining the relative position of the guidewire assembly within the patient or for relaying data relative to certain physiological parameters of the patient, such as temperature, pressure, or rate of fluid (e.g. blood) flow.
- the guidewire assembly may include a proximal connector at the proximal end thereof that includes at least one electrical contact and at least one insulative segment electrically isolating the electrical contact from the remainder of the guidewire assembly and from any other electrical contacts included in the proximal connector.
- the isolated electrical contact(s) and the insulative segment(s) adjacent thereto are sealed or bonded to one another in order to prevent such fluid or moisture contact with the internal electrical components from occurring. Further, it is also generally desirable to provide a guidewire assembly having sufficient rigidity to aid in delivery of the catheter or other medical device and having a substantially uniform longitudinal or concentric alignment between the electrical contact(s) and the insulative segment(s).
- a guidewire assembly including a sensor at a distal end thereof and a proximal connector at a proximal end thereof, wherein the proximal connector is rigid, is substantially longitudinally or concentrically aligned along a length thereof, and is sealed to prevent fluid or moisture from contacting the internal electrical components of the guidewire assembly. It is also desirable to provide methods or processes of making and using such guidewire assemblies.
- the present disclosure is directed to a guidewire assembly, and the process of making and using the guidewire assembly, that provides a proximal connector that is rigid, longitudinally and concentrically aligned, and sealed so as to prevent fluid or moisture from contacting internal electrical components of the guidewire assembly.
- the guidewire assembly includes a sensor at a distal end thereof and a proximal connector at a proximal end thereof for electrically connecting the sensor to an external device, such as a display or monitoring device.
- the proximal connector includes at least one electrical contact (or proximal contact) and an insulative element positioned adjacent to the electrical contact. The material forming the insulative element is capable of being reflowed during production of the guidewire assembly so as to create a bond or seal (preferably a hermetic seal) with the adjacent electrical contact.
- a reflowable material such as nylon
- an electrical contact and adjacent insulative element are securely bonded together while also creating a seal or barrier between external fluid or moisture and internal electrical components.
- use of a reflowable material as the insulative elements in forming the proximal connector provides an improved longitudinal or concentric alignment along a length of the proximal connector as well as the desired rigidity of the proximal portion of the guidewire assembly.
- the method of making a proximal connector for use in a guidewire assembly also provides a streamlined and more efficient method of manufacturing the proximal connector as compared to other conventional methods of manufacturing a proximal connector known in the art.
- FIG. 1 illustrates one exemplary embodiment of a conventional system 100 for performing one or more diagnostic or therapeutic procedures utilizing a guidewire assembly 102 .
- system 100 includes a guidewire assembly 102 , an interface cable 104 capable of being coupled to and electrically communicating with guidewire assembly 102 , and an external device 106 , such as a signal processor, computer, or other control unit, capable of being coupled to and electrically communicating with interface cable 104 .
- Guidewire assembly 102 includes a sensor 108 , such as a positional sensor or a physiological data sensor, positioned on a distal portion 110 of guidewire assembly 102 .
- Sensor 108 is configured to electrically communicate with interface cable 104 and thus external device 106 .
- external device 106 , interface cable 104 , and guidewire assembly 102 are configured such that signals generated by sensor 108 are transmitted through guidewire assembly 102 , to interface cable 104 , and to external device 106 so as to communicate information obtained by sensor 108 , such as location, position, or physiological data, to a user.
- External device 106 may include, for example and without limitation, an electronic control unit (ECU), a display device, a user input device, memory, and the like.
- system 100 may further include other conventional components such as, for example and without limitation, additional sensors, catheters, medical devices, coupling or connecting means, and the like.
- system 100 may utilize wireless transmission of a signal generated by sensor 108 to external device 106 , such as via a transmitter or transceiver unit (not shown) adapted to wirelessly communicate via a radio frequency signal with a communication unit (not shown) arranged in connection with external device 106 .
- FIG. 2 is a cross-sectional view of a guidewire assembly of the present disclosure
- FIG. 3 is a perspective view of the guidewire assembly of FIG. 2
- Guidewire assembly 202 includes a distal portion 210 , a proximal portion 212 , and a flexible sheath 214 extending therebetween.
- distal portion 210 includes a distal tip 216 coupled to a distal end of a distal spring coil 218 , and an outer jacket 220 which is coupled at a distal end thereof to a proximal end of distal spring coil 218 .
- Outer jacket 220 serves as a housing for a sensor 208 and includes a window or opening 222 through which sensor 208 is exposed to the outer portion of guidewire assembly 202 and thus the medium, e.g. blood, surrounding guidewire assembly 202 when introduced into a patient.
- Sensor 208 may include any sensor known in the art and suitable for use within a guidewire assembly during a therapeutic or diagnostic procedure, such as and without limitation, a pressure sensor, a temperature sensor, a rate of fluid (e.g. blood) flow sensor, and or a positioning or location sensor.
- Flexible sheath 214 is coupled at a distal end thereof to a proximal end of outer jacket 220 and may comprise a single tubular member as shown in FIGS.
- flexible sheath 214 may be in the form of a tubular member as shown in FIGS. 2 and 3 or may be in the form of a coil spring (not shown).
- a core wire 224 (not shown in FIG. 3 ) extends from proximal portion 212 through distal portion 210 and into distal tip 216 .
- Core wire 224 includes a recess 226 in which sensor 208 is disposed.
- Flexible sheath 214 and core wire 224 may be comprised of any material known in the art suitable for use in a guidewire assembly.
- Proximal portion 212 of guidewire assembly 202 includes proximal connector 228 configured to communicate with an external device, such as external device 106 shown in FIG. 1 .
- Proximal connector 228 as illustrated in FIGS. 2 and 3 , includes a first proximal contact 230 , a second proximal contact 232 , and a third proximal contact 234 , each of which are annular or tubular components, such as a ring electrode, longitudinally aligned with one another along core wire 224 .
- First, second, and third proximal contacts 230 , 232 , and 234 are electrically insulated from one another and from the remainder of guidewire assembly 202 by first insulative element 236 , second insulative element 238 , and third insulative element 240 , each of which are annular or tubular elements longitudinally aligned with one another as well as with first, second, and third proximal contacts 230 , 232 , and 234 .
- first insulative element 236 is positioned distal to and adjacent first proximal contact 230
- second insulative element 238 is positioned distal to and adjacent second proximal contact 232
- third insulative element 240 is positioned distal to and adjacent third proximal contact 234 . That is, first, second, and third proximal contacts 230 , 232 , and 234 are positioned in an alternating relationship with first, second, and third insulative elements 236 , 238 , and 240 .
- proximal connector 228 may include one, two, four, five or more proximal contacts and/or insulative elements without departing from the scope of the present disclosure so long as the proximal contacts and insulative elements are arranged in an alternating configuration such that each proximal contact is insulated from one another and from the remainder of guidewire assemble 202 by at least one insulative element.
- a first transmitting cable 242 , a second transmitting cable 244 , and a third transmitting cable 246 extend from first, second, and third proximal contacts 230 , 232 , and 234 , respectively, to sensor 208 so as to electrically couple first, second, and third proximal contacts 230 , 232 , and 234 for transmission of a signal generated by sensor 208 or for transmission of power to sensor 208 .
- Proximal connector 228 further includes an atraumatic proximal tip 248 coupled to a proximal end of third proximal contact 234 that closes or otherwise seals a proximal end of guidewire assembly 202 .
- proximal tip 248 for example and without limitation, comprises an adhesive.
- proximal tip 248 may comprise an epoxy, metal, or other material known in the art suitable for use in a guidewire assembly.
- first, second, and third proximal contacts 230 , 232 , and 234 may be comprised of, for example and without limitation, a gold plated stainless steel tubing. In other embodiments, for example and without limitation, first, second and third proximal contacts 230 , 232 , and 234 may be comprised of platinum, gold, copper, or other electrically conductive materials as would be known to one of skill in the art.
- First, second, and third insulative elements 236 , 238 , and 240 may be comprised of any material that may be reflowed so as to create a bond or seal (preferably a hermetic seal) with an adjacent proximal contact to prevent or minimize fluid or moisture from contacting internal electrical components of guidewire assembly 202 .
- first, second, and third insulative elements 236 , 238 , and 240 may comprise a reflowable thermoplastic material, such as nylon or polyester block amides.
- first, second, and third insulative elements 236 , 238 , and 240 may be coated with a hydrophobic material, such as polytetrafluoroethylene (PTFE) or fluorinated ethylene propylene (FEP).
- PTFE polytetrafluoroethylene
- FEP fluorinated ethylene propylene
- guidewire assembly 202 may be manufactured utilizing any number of suitable manufacturing techniques that can produce the desired structure.
- proximal connector 228 of guidewire assembly 202 is manufactured by first providing 400 proximal connector 228 comprising first proximal contact 230 , second proximal contact 232 , and third proximal contact 234 positioned around core wire 224 as shown in FIG. 5A and as described above in detail.
- First, second, and third proximal contacts 230 , 232 , and 234 may be positioned on and coupled to core wire 224 (also referred to as a chamfered wire) by any suitable method known to those skilled in the art.
- First insulative element 236 is then advanced distally 402 onto proximal connector 228 and positioned such that a distal end of first insulative element 236 is adjacent a proximal end of flexible sheath 214 (not shown in FIGS. 5A-5E ) and a proximal end of first insulative element 236 is adjacent a distal end of first proximal contact 230 , as shown in FIG. 5B .
- second insulative element 238 is advanced distally 404 onto proximal connector 228 and positioned such that a distal end of second insulative element 238 is adjacent a proximal end of first proximal contact 230 and a proximal end of second insulative element 238 is adjacent a distal end of second proximal contact 232 , as shown in FIG. 5B .
- Third insulative element 240 is then advanced distally onto proximal connector 228 and positioned such that a distal end of third insulative element 240 is adjacent a proximal end of second proximal contact 232 and a proximal end of third insulative element 240 is adjacent a distal end of third proximal contact 234 , as shown in FIG. 5B .
- a fourth insulative element 250 is then advanced distally onto proximal connector 228 and positioned such that a distal end of fourth insulative element 250 is adjacent a proximal end of third proximal contact 234 , as shown in FIG. 5B . As shown in FIG.
- each of the first, second, and third proximal contacts 230 , 232 , and 234 as well as each of the first, second, third, and fourth insulative elements 236 , 238 , 240 , and 250 are generally longitudinally or concentrically aligned with one another.
- first, second, third, and fourth insulative elements 236 , 238 , 240 , and 250 are comprised of any material that may be reflowed, such as nylon.
- proximal connector 228 may comprise, in other embodiments of the present disclosure, one, two, four, five, or more proximal contacts. It will be further appreciated by one skilled in the art that in embodiments comprising other than three proximal contacts as described above with respect to FIG. 4 , insulative elements should be positioned on proximal connector 228 in an alternating arrangement with respect to the proximal contacts such that an insulative element is present at least at the distal end of proximal connector 228 , and in some embodiments also at the proximal end of proximal connector 228 .
- a heat shrink material 252 is advanced distally 410 over proximal connector 228 such that heat shrink material 252 is positioned over an entirety of proximal connector 228 (i.e., a proximal end 254 of heat shrink material 252 extends past a proximal end 256 of proximal connector 228 and a distal end 258 of heat shrink 252 extends past a distal end 260 of proximal connector 228 ), as shown in FIG. 5C .
- Heat shrink material 252 is in the form of a hollow cylindrical tube and may be comprised of any suitable material known in the art suitable for use in a reflow process, such as polyethylene and fluorinated ethylene propylene (FEP).
- FEP fluorinated ethylene propylene
- proximal end 254 of heat shrink material 252 extends beyond proximal end 256 of proximal connector 228 by a minimum of 4 mm.
- proximal end 254 of heat shrink material 252 extends beyond proximal end 256 of proximal connector 228 by about 4-10 mm.
- proximal end 254 of heat shrink material 252 extends beyond proximal end 256 of proximal connector 228 by a minimum of 10 mm or more.
- distal end 258 of heat shrink material 252 extends beyond distal end 260 of proximal connector 228 by a minimum of 4 mm.
- a proximal portion 262 of heat shrink material 252 overlying fourth insulative element 250 is heated 414 so as to tack or couple proximal portion 262 of heat shrink material 252 to fourth insulative element 250 .
- heat shrink material 252 may be held in place over proximal connector 228 so as to reduce movement of heat shrink material 252 with respect to proximal connector 228 during subsequent manufacturing of proximal connector 228 .
- a distal portion 264 of heat shrink material 252 overlying first insulative element 236 may be heated so as to tack or couple distal portion 264 of heat shrink material 252 to first insulative element 236 .
- heat shrink material 252 may be heated with a hot air pencil or hot air gun for a minimum of about 30 seconds at a temperature of from about 350 degrees Fahrenheit to about 400 degrees Fahrenheit.
- the step of positioning fourth insulative element 250 on proximal connector 228 may be omitted in an alternative embodiment.
- the step of heating 414 a proximal portion 262 of heat shrink material 252 overlying fourth insulative element 250 is also omitted.
- heat shrink material 252 and proximal connector 228 is then heated 416 so as to reflow first, second, third, and fourth insulative elements 236 , 238 , 240 , and 250 thus coupling adjacent insulative elements and proximal contacts and creating a seal from external fluid and moisture therebetween.
- heat shrink material 252 and proximal connector 228 are placed entirely within (and centered within) a hot air nozzle and heated for about 40 seconds to about 60 seconds at a temperature of from about 305 degrees Fahrenheit to about 325 degrees Fahrenheit.
- Heat shrink material 252 is then removed 418 from proximal connector 228 , as shown in FIG. 5D .
- heat shrink material 252 is removed with tweezers or other similar device, although it will be understood by one skilled in the art that heat shrink material 252 may be removed from proximal connector 228 by any suitable means known to those skilled in the art.
- Core wire 224 is then cut 420 directly adjacent the proximal end of third proximal contact 234 such that fourth insulative element 250 and any portion of core wire 224 extending proximally from the proximal end of third proximal contact 234 is removed from proximal connector 228 .
- core wire 224 will be cut directly adjacent a proximal end of the most proximally positioned proximal contact of proximal connector 228 .
- Proximal tip 248 is then applied 422 to proximal end 256 of proximal connector 228 .
- Applying proximal tip 248 may comprise applying an adhesive, epoxy, metal, or other material such that proximal tip 248 is suitable for use on a guidewire assembly (e.g., is atraumatic).
- applying 422 proximal tip 248 to proximal connector 228 comprises applying a suitable glue or adhesive to a proximal end of core wire 224 and a proximal end of third proximal contact 234 and curing proximal tip 248 using, for example, a curing oven, solder tip, hot air, or other suitable method known to those skilled in the art for about 60 seconds at a temperature of about 140 degrees Celsius to about 160 degrees Celsius.
- joinder references do not necessarily infer that two elements are directly connected and in fixed relation to each other. It is intended that all matter contained in the above description or shown in the accompanying drawings shall be interpreted as illustrative only and not limiting. Changes in detail or structure may be made without departing from the spirit of the disclosure as defined in the appended claims.
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Abstract
Description
- This application claims the benefit of priority to U.S. Provisional Patent Application No. 62/356,761, filed Jun. 30, 2016, the entire contents of which are hereby incorporated herein by reference in their entirety.
- A. Field of the Invention
- The present disclosure relates generally to a guidewire assembly including a proximal portion configured for electrical connection to an external device. In particular, the present disclosure relates to a guidewire assembly having a proximal connector disposed on a proximal portion thereof, the proximal connector including at least one electrical contact and at least one reflowed insulative segment bonded or sealed to an adjacent electrical contact.
- B. Background
- Various diagnostic and therapeutic procedures in or on the body of a patient, such as in the circulatory system, the gastrointestinal tract, the brain vessels, the bronchial tree or the like, may be performed or facilitated by inserting a catheter into a body lumen and thereafter navigating the diagnostic or therapeutic catheter to the target site prior to, for example, delivering a medical device to the target site. To facilitate navigation of the catheter or other medical device, a guidewire is often used. The guidewire typically has a reduced diameter relative to the catheter or device; the reduced diameter aids a physician in inserting and navigating the guidewire to the target site. The catheter or device is then passed over the guidewire and guided to the target site.
- One method of maneuvering a guidewire to a target site within a patient is to place one or more position sensors on the guidewire, track the position sensors with a navigation system, and display a real-time or rendered image of the guidewire for the clinician manipulating the guidewire to view. Further, in many medical procedures, it may be desirable to monitor and/or analyze various physiological parameters within the body of a patient through a physiological data sensor. The raw signal generated by the position sensor and/or physiological data sensor located within the body may be transmitted to an external device, in which the raw signal is re-translated into locational or physiological data. The re-translated longitudinal or physiological data is then processed and the results continuously displayed on a monitor and/or saved.
- In order to power the position and/or physiological data sensor and/or to communicate signals generated by the sensor(s), some known guidewires utilize one or more cables or leads extending along an internal portion of the guidewire between the sensor and a proximal connector. Some known guidewires utilize a physical electrical connection between the proximal connector and an external device to transfer power or communicate generated signals thereto, while other known guidewires utilize a wireless connection between the proximal connector and the external device. To transfer power or generated signals to or from the proximal connector, the proximal connector includes at least one electrically isolated area for the connection to be made. The isolated area(s) are generally bonded or sealed to an insulative element so as to prevent liquid or moisture from entering the internal portion of the guidewire, contacting internal electrical components, and causing an electrical short.
- The present disclosure is directed to a guidewire assembly comprising: a guidewire having a distal portion and a proximal portion; a sensor disposed at the distal portion of the guidewire; and a proximal connector disposed at the proximal portion of the guidewire. The proximal connector comprises at least one proximal contact and at least one reflowed insulative element disposed adjacent the at least one proximal contact.
- The present disclosure is further directed to a guidewire comprising: a distal portion comprising a sensor; a shaft portion coupled to the distal portion; and a proximal connector coupled to the shaft portion. The proximal connector comprises at least one proximal contact and at least one reflowed insulative element disposed adjacent the at least one proximal contact.
- The present disclosure is further directed to a guidewire assembly obtained by a process comprising: forming a proximal connector, the proximal connector comprising a first proximal contact and a first insulative element disposed adjacent a distal end of the first proximal contact; distally advancing a heat shrink tube over the proximal connector; heating the heat shrink tube and the proximal connector to reflow the first insulative element so as to couple the first insulative element to the distal end of the first proximal contact; and removing the heat shrink tube from the proximal connector.
- The foregoing and other aspects, features, details, utilities, and advantages of the present disclosure will be apparent from reading the following description and claims, and from reviewing the accompanying drawings.
-
FIG. 1 is a diagrammatic view of a conventional system for performing one or more diagnostic or therapeutic procedures utilizing a guidewire assembly. -
FIG. 2 is a cross-sectional view of one embodiment of a guidewire assembly of the present disclosure. -
FIG. 3 is a perspective view of the guidewire assembly ofFIG. 2 . -
FIGS. 4, 4A, and 4B are a flowchart of one embodiment of a method of making a proximal connector for use in the guidewire assembly ofFIGS. 2 and 3 . -
FIGS. 5A-5E are perspective views of the proximal connector at various stages of the method illustrated inFIGS. 4, 4A, and 4B - Many medical devices, including catheters or other devices, are delivered to a target site within a patient via a guidewire assembly that includes a sensor at a distal end thereof for determining the relative position of the guidewire assembly within the patient or for relaying data relative to certain physiological parameters of the patient, such as temperature, pressure, or rate of fluid (e.g. blood) flow. To provide an electrical connection between the sensor and an external device, such as a display or monitoring device, the guidewire assembly may include a proximal connector at the proximal end thereof that includes at least one electrical contact and at least one insulative segment electrically isolating the electrical contact from the remainder of the guidewire assembly and from any other electrical contacts included in the proximal connector. Because contact between internal electrical components of the guidewire assembly and fluid or moisture should be avoided, it is generally desirable that the isolated electrical contact(s) and the insulative segment(s) adjacent thereto are sealed or bonded to one another in order to prevent such fluid or moisture contact with the internal electrical components from occurring. Further, it is also generally desirable to provide a guidewire assembly having sufficient rigidity to aid in delivery of the catheter or other medical device and having a substantially uniform longitudinal or concentric alignment between the electrical contact(s) and the insulative segment(s).
- Thus, it is desirable to provide a guidewire assembly including a sensor at a distal end thereof and a proximal connector at a proximal end thereof, wherein the proximal connector is rigid, is substantially longitudinally or concentrically aligned along a length thereof, and is sealed to prevent fluid or moisture from contacting the internal electrical components of the guidewire assembly. It is also desirable to provide methods or processes of making and using such guidewire assemblies. The present disclosure is directed to a guidewire assembly, and the process of making and using the guidewire assembly, that provides a proximal connector that is rigid, longitudinally and concentrically aligned, and sealed so as to prevent fluid or moisture from contacting internal electrical components of the guidewire assembly.
- The guidewire assemblies described herein are designed for use with a wide variety of catheters or other medical devices and implants. In one embodiment of the present disclosure, the guidewire assembly includes a sensor at a distal end thereof and a proximal connector at a proximal end thereof for electrically connecting the sensor to an external device, such as a display or monitoring device. The proximal connector includes at least one electrical contact (or proximal contact) and an insulative element positioned adjacent to the electrical contact. The material forming the insulative element is capable of being reflowed during production of the guidewire assembly so as to create a bond or seal (preferably a hermetic seal) with the adjacent electrical contact. By utilizing a reflowable material, such as nylon, to form the insulative segment, an electrical contact and adjacent insulative element are securely bonded together while also creating a seal or barrier between external fluid or moisture and internal electrical components. Further, use of a reflowable material as the insulative elements in forming the proximal connector, as compared to other conventional methods of forming a proximal connector, provides an improved longitudinal or concentric alignment along a length of the proximal connector as well as the desired rigidity of the proximal portion of the guidewire assembly. The method of making a proximal connector for use in a guidewire assembly, as described in more detail below, also provides a streamlined and more efficient method of manufacturing the proximal connector as compared to other conventional methods of manufacturing a proximal connector known in the art.
- Referring now to the Figures,
FIG. 1 illustrates one exemplary embodiment of aconventional system 100 for performing one or more diagnostic or therapeutic procedures utilizing aguidewire assembly 102. - Among other components,
system 100 includes aguidewire assembly 102, aninterface cable 104 capable of being coupled to and electrically communicating withguidewire assembly 102, and anexternal device 106, such as a signal processor, computer, or other control unit, capable of being coupled to and electrically communicating withinterface cable 104. Guidewireassembly 102 includes asensor 108, such as a positional sensor or a physiological data sensor, positioned on adistal portion 110 ofguidewire assembly 102.Sensor 108 is configured to electrically communicate withinterface cable 104 and thusexternal device 106. That is,external device 106,interface cable 104, andguidewire assembly 102 are configured such that signals generated bysensor 108 are transmitted throughguidewire assembly 102, tointerface cable 104, and toexternal device 106 so as to communicate information obtained bysensor 108, such as location, position, or physiological data, to a user.External device 106 may include, for example and without limitation, an electronic control unit (ECU), a display device, a user input device, memory, and the like. It should be understood thatsystem 100 may further include other conventional components such as, for example and without limitation, additional sensors, catheters, medical devices, coupling or connecting means, and the like. Further, it should be understood thatsystem 100 may utilize wireless transmission of a signal generated bysensor 108 toexternal device 106, such as via a transmitter or transceiver unit (not shown) adapted to wirelessly communicate via a radio frequency signal with a communication unit (not shown) arranged in connection withexternal device 106. -
FIG. 2 is a cross-sectional view of a guidewire assembly of the present disclosure, andFIG. 3 is a perspective view of the guidewire assembly ofFIG. 2 . Guidewireassembly 202 includes adistal portion 210, aproximal portion 212, and aflexible sheath 214 extending therebetween. In this particular embodiment,distal portion 210 includes adistal tip 216 coupled to a distal end of adistal spring coil 218, and anouter jacket 220 which is coupled at a distal end thereof to a proximal end ofdistal spring coil 218.Outer jacket 220 serves as a housing for asensor 208 and includes a window or opening 222 through whichsensor 208 is exposed to the outer portion ofguidewire assembly 202 and thus the medium, e.g. blood, surroundingguidewire assembly 202 when introduced into a patient.Sensor 208 may include any sensor known in the art and suitable for use within a guidewire assembly during a therapeutic or diagnostic procedure, such as and without limitation, a pressure sensor, a temperature sensor, a rate of fluid (e.g. blood) flow sensor, and or a positioning or location sensor.Flexible sheath 214 is coupled at a distal end thereof to a proximal end ofouter jacket 220 and may comprise a single tubular member as shown inFIGS. 2 and 3 or may comprise two, or three, or more flexible components coupled to one another. Further,flexible sheath 214 may be in the form of a tubular member as shown inFIGS. 2 and 3 or may be in the form of a coil spring (not shown). A core wire 224 (not shown inFIG. 3 ) extends fromproximal portion 212 throughdistal portion 210 and intodistal tip 216.Core wire 224 includes arecess 226 in whichsensor 208 is disposed.Flexible sheath 214 andcore wire 224 may be comprised of any material known in the art suitable for use in a guidewire assembly. -
Proximal portion 212 ofguidewire assembly 202 includesproximal connector 228 configured to communicate with an external device, such asexternal device 106 shown inFIG. 1 .Proximal connector 228, as illustrated inFIGS. 2 and 3 , includes a firstproximal contact 230, a secondproximal contact 232, and a thirdproximal contact 234, each of which are annular or tubular components, such as a ring electrode, longitudinally aligned with one another alongcore wire 224. First, second, and thirdproximal contacts guidewire assembly 202 by firstinsulative element 236, secondinsulative element 238, and thirdinsulative element 240, each of which are annular or tubular elements longitudinally aligned with one another as well as with first, second, and thirdproximal contacts insulative element 236 is positioned distal to and adjacent firstproximal contact 230, secondinsulative element 238 is positioned distal to and adjacent secondproximal contact 232, and thirdinsulative element 240 is positioned distal to and adjacent thirdproximal contact 234. That is, first, second, and thirdproximal contacts insulative elements proximal connector 228 may include one, two, four, five or more proximal contacts and/or insulative elements without departing from the scope of the present disclosure so long as the proximal contacts and insulative elements are arranged in an alternating configuration such that each proximal contact is insulated from one another and from the remainder of guidewire assemble 202 by at least one insulative element. - A
first transmitting cable 242, asecond transmitting cable 244, and a third transmitting cable 246 (not shown inFIG. 3 ) extend from first, second, and thirdproximal contacts sensor 208 so as to electrically couple first, second, and thirdproximal contacts sensor 208 or for transmission of power tosensor 208.Proximal connector 228 further includes an atraumaticproximal tip 248 coupled to a proximal end of thirdproximal contact 234 that closes or otherwise seals a proximal end ofguidewire assembly 202. In one embodiment,proximal tip 248, for example and without limitation, comprises an adhesive. In other embodiments,proximal tip 248 may comprise an epoxy, metal, or other material known in the art suitable for use in a guidewire assembly. - In one embodiment, first, second, and third
proximal contacts proximal contacts - First, second, and third
insulative elements guidewire assembly 202. In one particular embodiment, first, second, and thirdinsulative elements insulative elements - In accordance with various embodiments of the present disclosure,
guidewire assembly 202, as shown inFIGS. 2 and 3 , may be manufactured utilizing any number of suitable manufacturing techniques that can produce the desired structure. In one embodiment, as illustrated inFIG. 4 ,proximal connector 228 ofguidewire assembly 202 is manufactured by first providing 400proximal connector 228 comprising firstproximal contact 230, secondproximal contact 232, and thirdproximal contact 234 positioned aroundcore wire 224 as shown inFIG. 5A and as described above in detail. First, second, and thirdproximal contacts insulative element 236 is then advanced distally 402 ontoproximal connector 228 and positioned such that a distal end of firstinsulative element 236 is adjacent a proximal end of flexible sheath 214 (not shown inFIGS. 5A-5E ) and a proximal end of firstinsulative element 236 is adjacent a distal end of firstproximal contact 230, as shown inFIG. 5B . Similarly, secondinsulative element 238 is advanced distally 404 ontoproximal connector 228 and positioned such that a distal end of secondinsulative element 238 is adjacent a proximal end of firstproximal contact 230 and a proximal end of secondinsulative element 238 is adjacent a distal end of secondproximal contact 232, as shown inFIG. 5B . Thirdinsulative element 240 is then advanced distally ontoproximal connector 228 and positioned such that a distal end of thirdinsulative element 240 is adjacent a proximal end of secondproximal contact 232 and a proximal end of thirdinsulative element 240 is adjacent a distal end of thirdproximal contact 234, as shown inFIG. 5B . Afourth insulative element 250 is then advanced distally ontoproximal connector 228 and positioned such that a distal end of fourthinsulative element 250 is adjacent a proximal end of thirdproximal contact 234, as shown inFIG. 5B . As shown inFIG. 5B , each of the first, second, and thirdproximal contacts insulative elements insulative elements - One skilled in the art will appreciate, as noted above, that
proximal connector 228 may comprise, in other embodiments of the present disclosure, one, two, four, five, or more proximal contacts. It will be further appreciated by one skilled in the art that in embodiments comprising other than three proximal contacts as described above with respect toFIG. 4 , insulative elements should be positioned onproximal connector 228 in an alternating arrangement with respect to the proximal contacts such that an insulative element is present at least at the distal end ofproximal connector 228, and in some embodiments also at the proximal end ofproximal connector 228. - Once first, second, third, and fourth
insulative elements proximal connector 228, aheat shrink material 252 is advanced distally 410 overproximal connector 228 such thatheat shrink material 252 is positioned over an entirety of proximal connector 228 (i.e., aproximal end 254 ofheat shrink material 252 extends past aproximal end 256 ofproximal connector 228 and adistal end 258 of heat shrink 252 extends past adistal end 260 of proximal connector 228), as shown inFIG. 5C . Heat shrinkmaterial 252 is in the form of a hollow cylindrical tube and may be comprised of any suitable material known in the art suitable for use in a reflow process, such as polyethylene and fluorinated ethylene propylene (FEP). In one embodiment,proximal end 254 ofheat shrink material 252 extends beyondproximal end 256 ofproximal connector 228 by a minimum of 4 mm. In other embodiments,proximal end 254 ofheat shrink material 252 extends beyondproximal end 256 ofproximal connector 228 by about 4-10 mm. In yet other embodiments,proximal end 254 ofheat shrink material 252 extends beyondproximal end 256 ofproximal connector 228 by a minimum of 10 mm or more. In another embodiment,distal end 258 ofheat shrink material 252 extends beyonddistal end 260 ofproximal connector 228 by a minimum of 4 mm. Onceheat shrink material 252 is positioned over an entirety ofproximal connector 228, the placement ofheat shrink material 252 with respect toproximal connector 228 is verified 412. - After verifying 412 the placement of
heat shrink material 252 with respect toproximal connector 228, aproximal portion 262 ofheat shrink material 252 overlying fourthinsulative element 250 is heated 414 so as to tack or coupleproximal portion 262 ofheat shrink material 252 to fourthinsulative element 250. By heatingproximal portion 262 ofheat shrink material 252 over fourthinsulative element 250,heat shrink material 252 may be held in place overproximal connector 228 so as to reduce movement ofheat shrink material 252 with respect toproximal connector 228 during subsequent manufacturing ofproximal connector 228. In another embodiment (not annotated inFIG. 4 ), adistal portion 264 ofheat shrink material 252 overlying firstinsulative element 236 may be heated so as to tack or coupledistal portion 264 ofheat shrink material 252 to firstinsulative element 236. In one embodiment, for example and without limitation,heat shrink material 252 may be heated with a hot air pencil or hot air gun for a minimum of about 30 seconds at a temperature of from about 350 degrees Fahrenheit to about 400 degrees Fahrenheit. - Although described above as including the positioning of fourth
insulative element 250 onproximal connector 228 during the making or forming ofproximal connector 228, the step of positioning fourthinsulative element 250 onproximal connector 228 may be omitted in an alternative embodiment. In this particular alternative embodiment, the step of heating 414 aproximal portion 262 ofheat shrink material 252 overlying fourthinsulative element 250 is also omitted. - The entirety of
heat shrink material 252 andproximal connector 228 is then heated 416 so as to reflow first, second, third, and fourthinsulative elements heat shrink material 252 andproximal connector 228 are placed entirely within (and centered within) a hot air nozzle and heated for about 40 seconds to about 60 seconds at a temperature of from about 305 degrees Fahrenheit to about 325 degrees Fahrenheit. - Heat shrink
material 252 is then removed 418 fromproximal connector 228, as shown inFIG. 5D . In one embodiment,heat shrink material 252 is removed with tweezers or other similar device, although it will be understood by one skilled in the art that heat shrinkmaterial 252 may be removed fromproximal connector 228 by any suitable means known to those skilled in the art.Core wire 224 is then cut 420 directly adjacent the proximal end of thirdproximal contact 234 such that fourthinsulative element 250 and any portion ofcore wire 224 extending proximally from the proximal end of thirdproximal contact 234 is removed fromproximal connector 228. It will be understood by one skilled in the art that in embodiments comprising other than three proximal contacts,core wire 224 will be cut directly adjacent a proximal end of the most proximally positioned proximal contact ofproximal connector 228. -
Proximal tip 248 is then applied 422 toproximal end 256 ofproximal connector 228. Applyingproximal tip 248 may comprise applying an adhesive, epoxy, metal, or other material such thatproximal tip 248 is suitable for use on a guidewire assembly (e.g., is atraumatic). In one particular embodiment, for example and without limitation, applying 422proximal tip 248 toproximal connector 228 comprises applying a suitable glue or adhesive to a proximal end ofcore wire 224 and a proximal end of thirdproximal contact 234 and curingproximal tip 248 using, for example, a curing oven, solder tip, hot air, or other suitable method known to those skilled in the art for about 60 seconds at a temperature of about 140 degrees Celsius to about 160 degrees Celsius. - Although embodiments of this disclosure have been described above with a certain degree of particularity, those skilled in the art could make numerous alterations to the disclosed embodiments without departing from the spirit or scope of this disclosure. All directional references (e.g., upper, lower, upward, downward, left, right, leftward, rightward, top, bottom, above, below, vertical, horizontal, clockwise, and counterclockwise) are only used for identification purposes to aid the reader's understanding of the present disclosure, and do not create limitations, particularly as to the position, orientation, or use of the disclosure. Joinder references (e.g., attached, coupled, connected, and the like) are to be construed broadly and may include intermediate members between a connection of elements and relative movement between elements. As such, joinder references do not necessarily infer that two elements are directly connected and in fixed relation to each other. It is intended that all matter contained in the above description or shown in the accompanying drawings shall be interpreted as illustrative only and not limiting. Changes in detail or structure may be made without departing from the spirit of the disclosure as defined in the appended claims.
- Any patent, publication, or other disclosure material, in whole or in part, that is said to be incorporated by reference herein is incorporated herein only to the extent that the incorporated materials does not conflict with existing definitions, statements, or other disclosure material set forth in this disclosure. As such, and to the extent necessary, the disclosure as explicitly set forth herein supersedes any conflicting material incorporated herein by reference. Any material, or portion thereof, that is said to be incorporated by reference herein, but which conflicts with existing definitions, statements, or other disclosure material set forth herein will only be incorporated to the extent that no conflict arises between that incorporated material and the existing disclosure material.
Claims (20)
Priority Applications (2)
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US15/637,293 US20180000420A1 (en) | 2016-06-30 | 2017-06-29 | Proximal connector for guidewire assembly |
US17/122,610 US11969262B2 (en) | 2016-06-30 | 2020-12-15 | Proximal connector for guidewire assembly |
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US201662356761P | 2016-06-30 | 2016-06-30 | |
US15/637,293 US20180000420A1 (en) | 2016-06-30 | 2017-06-29 | Proximal connector for guidewire assembly |
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US17/122,610 Continuation US11969262B2 (en) | 2016-06-30 | 2020-12-15 | Proximal connector for guidewire assembly |
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US20180000420A1 true US20180000420A1 (en) | 2018-01-04 |
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US17/122,610 Active 2039-02-06 US11969262B2 (en) | 2016-06-30 | 2020-12-15 | Proximal connector for guidewire assembly |
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US17/122,610 Active 2039-02-06 US11969262B2 (en) | 2016-06-30 | 2020-12-15 | Proximal connector for guidewire assembly |
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Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20170354364A1 (en) * | 2016-06-09 | 2017-12-14 | Biosense Webster (Israel) Ltd. | Multi-function conducting elements for a catheter |
US20200315538A1 (en) * | 2017-12-07 | 2020-10-08 | Innovex Medical Co., Ltd. | Pressure Guide Wire |
WO2021074860A1 (en) * | 2019-10-18 | 2021-04-22 | Baylis Medical Company Inc. | Medical guidewire assembly and/or electrical connector |
US11944758B2 (en) | 2019-12-16 | 2024-04-02 | Acclarent, Inc. | Atraumatic tip assembly for guidewire |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US11173285B2 (en) * | 2018-06-28 | 2021-11-16 | Biosense Webster (Israel) Ltd. | Producing a guidewire comprising a position sensor |
Family Cites Families (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE69831142T2 (en) | 1997-03-25 | 2006-06-08 | Radi Medical Systems Ab | FEMALE CONNECTOR |
US6090052A (en) | 1997-03-25 | 2000-07-18 | Radi Medical Systems Ab | Guide wire having a male connector |
US5938624A (en) | 1997-09-10 | 1999-08-17 | Radi Medical Systems Ab | Male connector with a continous surface for a guide wire and method therefor |
ATE469600T1 (en) * | 2006-04-28 | 2010-06-15 | Radi Medical Systems | SENSOR AND GUIDE WIRE ASSEMBLY |
US8364281B2 (en) * | 2008-11-07 | 2013-01-29 | W. L. Gore & Associates, Inc. | Implantable lead |
EP2248544A1 (en) | 2009-05-05 | 2010-11-10 | ECP Entwicklungsgesellschaft mbH | Fluid pump with variable circumference, particularly for medical use |
US20120245457A1 (en) * | 2011-03-25 | 2012-09-27 | Crowley Robert J | Ultrasound imaging catheters and guidewires with non-interfering and coordinated position and orientation sensors |
EP2750862B1 (en) * | 2011-09-01 | 2016-07-06 | Covidien LP | Catheter with helical drive shaft and methods of manufacture |
US8644953B1 (en) * | 2012-08-10 | 2014-02-04 | Greatbatch Ltd. | Lead with braided reinforcement |
JP2017506090A (en) * | 2014-01-27 | 2017-03-02 | アンジオメトリックス コーポレーション | Method and apparatus for assembling an electrically stable connector |
JP2016048654A (en) | 2014-08-28 | 2016-04-07 | タイコエレクトロニクスジャパン合同会社 | Connector assembly |
-
2017
- 2017-06-29 US US15/637,293 patent/US20180000420A1/en not_active Abandoned
- 2017-06-29 EP EP17745507.8A patent/EP3457917A1/en not_active Ceased
- 2017-06-29 WO PCT/IB2017/053939 patent/WO2018002885A1/en unknown
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2020
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Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20170354364A1 (en) * | 2016-06-09 | 2017-12-14 | Biosense Webster (Israel) Ltd. | Multi-function conducting elements for a catheter |
US10905329B2 (en) * | 2016-06-09 | 2021-02-02 | Biosense Webster (Israel) Ltd. | Multi-function conducting elements for a catheter |
US12042246B2 (en) | 2016-06-09 | 2024-07-23 | Biosense Webster (Israel) Ltd. | Multi-function conducting elements for a catheter |
US20200315538A1 (en) * | 2017-12-07 | 2020-10-08 | Innovex Medical Co., Ltd. | Pressure Guide Wire |
WO2021074860A1 (en) * | 2019-10-18 | 2021-04-22 | Baylis Medical Company Inc. | Medical guidewire assembly and/or electrical connector |
US11944758B2 (en) | 2019-12-16 | 2024-04-02 | Acclarent, Inc. | Atraumatic tip assembly for guidewire |
Also Published As
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EP3457917A1 (en) | 2019-03-27 |
US11969262B2 (en) | 2024-04-30 |
WO2018002885A1 (en) | 2018-01-04 |
US20210137459A1 (en) | 2021-05-13 |
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