A field of the invention is medical devices, and particularly surgical devices. The invention provides a device that can safely deflect the esophagus during procedures. Example procedures that would benefit from the use of the device of the invention include thermal ablation of the left atrium.
Esophageal deflection is a critical step to certain surgical procedures. Catheter ablation is a procedure used to treat patients with refractory paroxysmal and persistent atrial fibrillation. Ablation changes electrical current paths in heart tissue by locally targeting cells that are supporting a problematic current path. In the example of ablation applied to treat arterial fibrillation, a common strategy is the creating of lesions at particular target locations, such as the left atrial roof, mitral isthmus, or posterior wall. One of the highest risks during the ablation procedure is damage to the esophagus. The esophagus is often very close to or in contact with the left atrium. Damage inflicted on esophageal cells during the ablation can lead to death.
A factor leading to damage and death has been the sensitivity of esophageal tissue to RF energy and/or heat, both of which can damage esophageal tissue directly and/or esophageal arteries. See, Shuraih et al, “Strategies to Prevent Esophageal Injury During Catheter Ablation of Atrial Fibrillation,” The Journal of Innovations in Cardiac Rhythm Management, 3 (2012), 719-726. Techniques employed previously include gastric acid suppression, esophageal temperature monitoring, thermal insulation of the esophagus, energy limitation, esophagus cooling, and mechanical deflection of the esophagus. Shuraih et al, supra. Shuraih et al. note that the prior techniques requirement improvement to reduce the incidence of the often fatal complication of esophageal damage during ablation.
A mechanical deflection technique proposed in the past is the deflection of the esophagus with an endoscope. Chugh et al., Mechanical Displacement of the Esophagus in Patients Undergoing Left Atrial Ablation of Atrial Fibrillation,” Heart Rhythm. 2009 March; 6(3): 319-22. An endoscopist deflected the esophagus immediately prior to ablation and then removed the endoscope. The esophagus remained deflected in a minority of the patients after the esophagus was removed. The endoscope must be removed during the ablation procedure to provide safety during the ablation energy transfer. This mechanical deflection procedure therefore does not ensure displacement of the esophagus during ablation. As noted in the publication: “Why the esophagus could not be displaced in all patients is not clear. Possible reasons include decreased laxity of attachments to surrounding structures, increased compliance of the esophageal wall resulting in distension of the esophageal lumen rather than translocation of body of the esophagus, and variations in technique. Another possibility is decreased compliance of the surrounding tissues, such as the PVs and/or their antra.” In addition, initial displacements were often lost, in “most patients in this study, the esophagus assumed its original position after the endoscope was removed, as might be expected given the elastic nature of the esophageal wall and its connective tissues. Esophageal rebound to its original position might hinder the safe delivery of radiofrequency energy. A strategy for overcoming this limitation is delivery of radiofrequency current while the esophagus is being actively displaced with the endoscope. However, there is a theoretical concern of shunting radiofrequency energy to the endoscope, which could result in thermal injury to the esophagus.”
O'Sullivan U.S. Pat. No. 8,273,016 describes an esophagus isolation catheter. The catheter has deflectable intermediate section and a straight tip or a deflectable tip section mounted at the distal end of the catheter body. Two “puller” wires are anchored proximal each other, or one puller wire, and are manipulated to create curve in the intermediate section or tip section that deflects the esophagus. This is complex to manufacture and use. Manipulation of the wire(s) also will likely provide different levels of deflection when used by different practitioners, or by the same practitioner on a different occasion. The patent also discusses limiting the outer diameter of the catheter to about 8 French, which is about 2.6 mm. A typical human esophagus has a relaxed diameter of about 2 cm. An 8 French deflection device will be easy to insert, but it will provide a small contact area with an esophagus wall during deflection. The force to achieve a deflection is concentrated in that area, and that concentrated force could create complications, after procedure discomfort, and could in an extreme case increase the likelihood of perforation.
Miller U.S. Pat. No. 7,621,908 discloses an esophageal catheter for displacing the catheter. The device includes a tube that extends through the esophagus past the diaphragm. The device is manipulated with control wires that are inserted through the tube in its lumen. The control wires have a curved portion that will displace the esophagus. The wires can be made of Nitinol and react to body temperature to have a curve when in the body. The wires can be manipulated by a practitioner to move the targeted area of an esophagus. Such manipulation can be inconsistent, and will also create relatively concentrated forces as discussed in the previous paragraph.
A preferred embodiment provides an esophageal deflection device that includes an elongate outer tube of biocompatible material having a proximal end and a distal end and a central portion therebetween. The elongate outer tube is capable of being flexed if a threshold amount of force is applied and has a curved deflection between the distal end and the central portion. The curved deflection has a stiffness sufficient to cause the esophagus to conform to the shape of the curved deflection when the elongate outer tube is inserted into the esophagus. An elongate insertion tube or rod having a distal end and a proximal end is smaller in diameter than the elongate outer tube and formed of material having a stiffness sufficient to create the threshold amount of force applied from within the elongate outer tube to at least partially straighten the curved deflection when the elongate insertion tube or rod is inserted in the deflection. A length of the elongate outer tube from a central portion to the distal end is predetermined to place the curved deflection at a targeted esophagus location near the left atrium of the heart. The curved deflection is U-shaped or is compound curve shaped and has variable stiffness sections disposed longitudinally to provide variation in stiffnesses in the longitudinal direction. The variable stiffness sections have one or more of variable material properties, variable wall thicknesses, and variable material omissions. An elongate outer tube handle is at the proximal end of the elongated outer tube forming a grip for a practitioner. An elongate insertion tube or rod handle is at the proximal end of the elongate insertion tube or rod forming a grip for a practitioner.
A preferred embodiment provides an esophageal deflection device. The device includes an elongate outer tube of biocompatible material having a proximal end and a distal end, the elongate outer tube being configured to contact walls of an esophagus, the elongate outer tube having a curved deflection between the distal end and the central portion, the elongate outer tube being flexible and resilient to maintain the curved deflection in a natural state and allow straightening of the elongate outer tube in response to force applied from within the elongate outer tube, the elongate outer tube being flexible enough to allow insertion and withdrawal from the esophagus, the curved deflection being stiffer than the esophagus such that the esophagus will conform to the shape of the curved deflection when the curved deflection is not straightened. The device also includes an elongate insertion tube or rod having a distal end and a proximal end, the elongate insertion tube being dimensioned to slide within the elongate outer tube, at least a portion of the elongate insertion tube being stiffer than the curved deflection of the elongate outer tube to create the force applied from within the elongate outer tube to at least partially straighten the curved deflection of the elongate outer tube when the portion of the elongate insertion tube is within the curved deflection of the elongate outer tube, the elongate insertion tube being sufficiently flexible to allow insertion into the esophagus while the portion of the elongate insertion tube is within the curved deflection of the elongate outer tube. The device preferably includes an elongate outer tube handle at the proximal end of the elongate outer tube forming a grip for a practitioner and an elongate insertion tube or rod handle at the proximal end of the elongate insertion tube or rod forming a grip for a practitioner. A length of the device is preferably predetermined to place the curved deflection at a targeted esophagus location near the left atrium of the heart. The curved deflection can be immediately adjacent the distal end of the elongate outer tube or separated by a straight portion of the elongate outer tube from the distal end of the elongate outer tube. The curved deflection can be U-shaped or is compound curve shaped. The elongate outer tube preferably includes bellows and the curved deflection includes bellows having different stiffness. A domed tip is preferably at the distal end of the elongate outer tube. The distal end of the elongate rod or tube can have a taper and the distal end and opening in the domed tip can be sized to permit a portion of the taper to extend through the opening the in the domed tip. The elongate outer tube and/or the insertion tube or rod can have a variable stiffness along. The device can include a depth insertion indicator and/or a radio opaque marker. The insertion tube or rod can have a lumen. Preferably, the outer diameter of the elongate outer tube is substantially matched to an esophagus inner diameter. Alternatively, an outer diameter of the elongate outer tube is at least half of an esophagus inner diameter. Alternatively, an outer diameter of the elongate outer tube is less than half of an esophagus inner diameter, the elongate outer tube further having suction ports for drawing a vacuum to draw esophagus walls into contact around the circumference of the elongate outer tube. Preferably, the device includes a plurality of temperature sensors disposed near an outermost surface of the elongate outer tube, which are preferably arranged in a three-dimensional pattern can be embedded in an outer coating of the elongate outer tube. The sensors are preferably arranged in orthogonal pairs along the device's longitudinal axis, exceeding the average length and area that the heart is in contact with the esophagus, and preferably increase in density in the region of curved deflection.
The invention also provides a method for conducting an esophageal deflection. The method includes inserting an insertion rod or tube into an elongate outer tube to straighten a curved deflection in the elongate outer tube. The method also includes inserting the elongate outer tube into an esophagus with the insertion rod to place the straightened curved deflection in a targeted region of the esophagus near the left atrium, and withdrawing the insertion rod or tube to allow the curved deflection to return to its natural shape and deflect the targeted region of the esophagus; wherein at least a portion of the elongate insertion tube is stiffer than the curved deflection of the elongate outer tube to create the force applied from within the elongate outer tube to at least partially straighten the curved deflection of the elongate outer tube The method can also include obtaining a three-dimensional heat map of the esophagus through a plurality of temperature sensors embedded near an outer surface of the elongate outer tube. The method can also include drawing a vacuum through a lumen in the insertion rod or tube. The method can include introducing fluids or gas through a lumen in the insertion rod or tube. The method can include drawing a vacuum through suction ports in the elongate outer tube to draw esophagus walls onto the circumference of the elongate outer tube. Preferably, the outer diameter of the elongate outer tube is substantially matched to an esophagus inner diameter. Alternatively, an outer diameter of the elongate outer tube is at least half of an esophagus inner diameter. Alternatively, an outer diameter of the elongate outer tube is less than half of an esophagus inner diameter, and the method includes drawing a vacuum through suction ports to draw esophagus walls into contact around the circumference of the elongate outer tube.
A preferred embodiment of the invention is an esophageal deflection device. The device includes a resilient outer elongate tube with a naturally curved section dimensioned and configured to insert into an esophagus and deflect the esophagus and another retractable tube or rod for reducing the curved section during insertion into the esophagus and allowing the naturally curved section of the elongate outer tube to return resiliently to its natural shape under control of a practitioner during a procedure to deflect the esophagus. In preferred embodiments, an insertion tube or rod slides within the outer elongate tube. The insertion tube or rod has portion that is stiffer than the elongate other tube.
The device can include additional features, such as a temperature probe, pressure/force sensor, or x-ray detectable insert desired at contact edge or along tube for feedback to user. By using a radio opaque material at the tip, cardiologists can use tools most familiar to them to identify location of indicators where the highest probability of insertion depth is necessary for specific classes of persons. This can correlate to body height, for example. Additional sensors can be used before and during a thermal ablation procedure. Temperature and flex sensor positions can be optimized for quality readings for state of esophagus in real time
Preferred devices are simple to use, even for less experienced practitioners. A device of the invention can reduce surgeon fatigue and reduce overall operation time for procedures that require or benefit from a deflection of the esophagus. The curve is created by a simple retraction of the retractable element, which allows the curved section to return to its natural curved shape and deflect the esophagus. A simply sliding movement can be monitored precisely via markings. The naturally curved section has a predetermined shape that will not diverge from the intended design shape during a procedure. The exact predetermined natural curve is replicated during use of the device in a procedure, and therefore the amount of curve will not exceed or be less than that defined by the predetermined shape.
Preferred embodiments of the invention will now be discussed with respect to experiments and drawings. Broader aspects of the invention will be understood by artisans in view of the general knowledge in the art and the description of the experiments that follows.
The elongate outer tube 100 is made of biocompatible material having a proximal end 106 and a distal end 108. An outside diameter of the elongate outer tube 100 is preferably substantially matched to an esophagus inner diameter, e.g. approximately equal to the inner diameter or 80-90-% of the inner diameter. A length from a central portion 110 to the distal end 108 is selected to place the curved deflection 104 at a targeted area of the esophagus adjacent the left atrium. The elongate outer tube 100 includes the curved deflection 104 between the distal end 108 and the central portion 110. In
The elongate outer tube 100 in experiments was formed of a thermoplastic elastomer molded over with a silicone based. Other suitable coatings include rubber or similarly compliant material. Other polymers, and mixtures of polymers could be used for optimal and varying stiffness properties including nylon, polyurethane, or polyethylene, etc. The elongate outer tube 100 is preferably a unitary, single piece design. An experimental device for demonstrating the deflection ability in in vivo testing did not use biocompatible materials and was 3D printed. The experimental materials were a mixture of TangoBlackPlus and VeroClear (which are two photopolymers) and the elongate outer tube was made using a Stratasys Objet 350 Connex3. The 3D printing allowed easy mixing of materials with different stiffness. Other experimental devices for in vivo tests were tested with a longer esophagus with a deviated shape, and the elongate outer tube was formed from a thermoplastic tubing that was thermoformed to that deviated shape.
A biomedical grade tubing can be thermoformed with the specified radius of curvature for either the U or L shape designs of the deflection curve of the elongate outer tube 100, including with bellows that are preferred to reduce the risk of kinking. Then, a silicone rubber or other compliant material can be casted onto the tubing mold. Stiffness can change longitudinally along the device to promote curvature at inflection points. This can be achieved through material mixing/layering or through alterations in geometry including changing of inner and outer diameter or material removal (i.e. precisely placed holes). Other forms of manufacturing include injection molding and material additive processes such as 3D printing. Such additive processes can produce varying material designs by layering altering mixtures of materials or by changing geometry. 3D printing can be used to customize devices before procedures where specific geometric or material mixing changes are needed, i.e., a person with irregular anatomy due to age, weight, or other, to vary the location or amount of deflection relative to the heart or other anatomical markers.
With reference to
The insertion tube or rod 102 in experiments was formed of non-biocompatible materials discussed above with respect to the elongate outer tube. It is preferably a unitary single pieced design. The insertion tube or rod provides more rigidity to the deflection device. It both strengthens the device and prevents buckling/kinking. It can have a flexible, tapered, and/or dome tip with a hole extended by a lumen from the proximal to distal end. The tip can extend beyond the elongate outer tube 100 through a hole 108b (see
Referring to
Radio opaque markers are preferably including on the elongate outer tube 100 and can also be placed on the insertion tube or rod 102. The markers can be in the region of the curved deflection 104 to assist in positioning the curved deflection 104 near the left atrium of the heart for deflection away from the heart when the insertion tube or rod 102 is within and straightening the curved deflection. The markers are placed to allow the device and its shape within the esophagus to be visible under X-ray (conveniently, cardiac ablation procedures already utilize X-ray imaging so the use of the deflection device does not add an X-ray imaging step). The markers may within a coating of the outer tube 100, for example placed at bellows in the curved deflection section 104 or throughout the length of the elongate outer tube 100.
While specific embodiments of the present invention have been shown and described, it should be understood that other modifications, substitutions and alternatives are apparent to one of ordinary skill in the art. Such modifications, substitutions and alternatives can be made without departing from the spirit and scope of the invention, which should be determined from the appended claims.
Various features of the invention are set forth in the appended claims.
The application is a continuation of prior pending U.S. application Ser. No. 16/488,453, filed Aug. 23, 2019 and claims priority under 35 U.S.C. § 120 from that application, which application was a § 371 National Phase application of PCT/US2018/021557, filed Mar. 8, 2018, which application claimed priority under 35 U.S.C. § 119 and all applicable statutes and treaties from prior U.S. provisional application Ser. No. 62/468,697, which was filed Mar. 8, 2017. All of the applications in this paragraph are incorporated by reference herein.
Number | Date | Country | |
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62468697 | Mar 2017 | US |
Number | Date | Country | |
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Parent | 16488453 | Aug 2019 | US |
Child | 18598773 | US |