Classifications

• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
  • A61F11/00—Methods or devices for treatment of the ears or hearing sense; Non-electric hearing aids; Methods or devices for enabling ear patients to achieve auditory perception through physiological senses other than hearing sense; Protective devices for the ears, carried on the body or in the hand
  • A61F11/20—Ear surgery
  • A61F11/202—Surgical middle-ear ventilation or drainage, e.g. permanent; Implants therefor
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
  • A61F11/00—Methods or devices for treatment of the ears or hearing sense; Non-electric hearing aids; Methods or devices for enabling ear patients to achieve auditory perception through physiological senses other than hearing sense; Protective devices for the ears, carried on the body or in the hand
  • A61F11/20—Ear surgery
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
  • A61F2/00—Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
  • A61F2/02—Prostheses implantable into the body
  • A61F2/18—Internal ear or nose parts, e.g. ear-drums
• • 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
  • A61M27/00—Drainage appliance for wounds or the like, i.e. wound drains, implanted drains
  • A61M27/002—Implant devices for drainage of body fluids from one part of the body to another
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
  • A61F2/00—Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
  • A61F2/02—Prostheses implantable into the body
  • A61F2/18—Internal ear or nose parts, e.g. ear-drums
  • A61F2002/183—Ear parts

Definitions

• the present invention is generally related to medical devices and apparatus.
• the invention provides systems and methods for delivering a pressure equalization tube to a tympanic membrane of an ear.
• Otitis media is among the most common diagnoses made by pediatricians. A majority of children may have at least one episode of otitis media ("earache") prior to their third birthday. Otitis media is often caused by an inability of the eustachian tube to drain fluid from the middle ear. Otitis media is often treated with antibiotics. A significant number of children exhibit recurrent episodes of otitis media and/or otitis media with effusion. Treatment of these more severe cases often involves the placement of a tympanostomy tube through the tympanic membrane to provide adequate drainage of the middle ear and reduce the likelihood of future infections. Tympanostomy tubes provide fluid communication between the middle and outer ear (e.g., pressure equalization) and typically fall out spontaneously within about a year of placement.
• Tympanostomy tube placement is among the most frequent surgical procedures performed in the pediatric population. It has been estimated that more than a million tympanostomy tubes may be placed each year, with typical patients being between about 18 months and 7 years of age at the time of the procedure. Tympanostomy tube placement is typically performed in an out-patient surgery setting under general anesthesia. The physician typically first examines the external auditory canal and tympanic membrane under microscopic visualization through a hand-held conical shaped speculum. The physician then makes an incision in the tympanic membrane (a "myringotomy”), typically using a standard, small profile scalpel which the physician advances through the conical speculum.
• myringotomy an incision in the tympanic membrane
• the physician will then place the tympanostomy tube through the tympanic membrane, typically using a basic tool for holding and advancing the tube into the myringotomy.
• the physician may then pass a suction device through the tube, into the middle ear, to aspirate fluid/effusion from the middle ear.
• tympanostomy tubes A wide variety of tympanostomy tubes is commercially available, and a still wider variety of other tubes has been proposed. Systems have also been proposed to both perform the myringotomy and deploy the tympanostomy tube with a single treatment assembly. In recent years, more complex and expensive systems have been proposed for diagnosis or treatment of the tissues of the ear, including systems using laser energy for forming a myringotomy, video systems for imaging of the ear canal, and the like. These various proposed alternatives for tympanostomy tubes and tube placement systems have met with varying degrees of acceptance. Some proposed alternatives have been overly complex, overly expensive and/or ineffective. Thus, to date, standard tubes and tube placement procedures and devices have primarily used.
• a tympanic membrane pressure equalization tube comprises a tubular body with a distal end and a proximal end and a lumen therebetween, a medial flange located at the distal end of the tube, where the medial flange comprises 3 retention elements and a space between each wing, and a lateral flange that is located at the proximal end of the tube.
• the outside diameter of the medial flange is greater than the outside diameter of the lateral flange and the diameter of the medial flange is between about 2.0 mm and about 5.0 mm and the diameter of the lateral flange is between about 1.75 mm and about 4.0 mm.
• the outside diameter of the medial flange is between about 3.0 mm and about 4.0 mm and the outside diameter of the lateral flange is between about 2.0 mm and about 3.0 mm.
• medial flange retention elements are of equal size and shape.
• the medial flange retention elements have a width of between about 0.6 mm and 1.0 mm or of about 0.8 mm.
• the medial flange retention elements have a length of between about 1.0 mm and 3.0 mm or of between about 1.8 mm and 1.9 mm.
• the lateral flange comprises two retention elements.
• the invention is a method for placing a pressure equalization tube within the tympanic membrane of a patient.
• the method comprises providing a pressure equalization tube in an uncompressed state, the pressure equalization tube having a tubular body with a distal end and a proximal end and a lumen therebetween and that has a compressed state and an uncompressed state.
• the pressure equalization tube further comprises a medial flange located at the distal end of the tubular body, the medial flange comprising 3 retention elements and a space between each retention element, and a lateral flange located at the proximal end of the tubular body.
• the outside diameter of the medial flange is greater than the outside diameter of the lateral flange and the diameter of the medial flange is between about 2.0 and 5.0 mm and the diameter of the lateral flange is between about 1.75 mm and 4.0 mm.
• the method further comprises compressing the pressure equalization tube into a compressed form wherein the medial flange retention members are longitudinally aligned with the pressure equalization tube lumen into a pressure equalization tube delivery device and do not overlap one with the other, advancing the pressure emialization tube into the tympanic membrane such that the medial flange is located medially of the tympanic membrane and the lateral flange is located laterally of the tympanic membrane and the pressure equalization tube is returned to its uncompressed form.
• the outside diameter of the medial flange is between about 3.0 and about 4.0 mm and the outside diameter of the lateral flange is between about 2.0 mm and about 3.0 mm.
• the medial flange retention elements are of equal size and shape.
• the medial flange retention elements have a width of between about 0.6 mm and 1.0 mm.
• the medial flange retention elements have a width of about 0.8 mm.
• the medial flange retention elements have a length of between about 1.0 mm and 3.0 mm.
• the medial flange retention elements have a length of between about 1.8 mm and 1.9 mm.
• the lateral flange comprises two retention elements.
• the lateral flange retention elements are of equal size and shape.
• the invention is directed to a tympanic membrane pressure equalization tube system comprising a tympanic membrane pressure equalization tube and an introducer.
• the tympanic membrane pressure equalization tube comprises a tubular body with a distal end and a proximal end and a lumen therebetween, a medial flange located at the distal end of the tubular body, said medial flange comprising two or more retention elements and a space between each retention element.
• the introducer comprises a cylindrical member with an inner surface. The inner surface has an inner surface circumference.
• the retention elements are of equal size and shape and the maximum length of each retention element is equal to the inner surface circumference of the introducer divided by the number of retention elements.
• the system comprises three retention elements and in another embodiment, the system comprises a lateral flange located at the proximal end of the tubular body.
• the invention is directed to a tympanic membrane pressure equalization tube comprising a tubular body with a distal end and a proximal end and a lumen therebetween, and a helical coil surrounding the tubular body.
• the helical coil comprises multiple raised ribs for retention of the pressure equalization tube in the tympanic membrane.
• the invention is directed to a tympanic membrane pressure equalization tube comprising a tubular body with a distal end and a proximal end and a lumen therebetween.
• the lumen of the tubular body is lined with artificial cilia to aid the transport and expulsion of effusion from the middle ear.
• the invention is directed to a tympanic membrane pressure equalization tube comprising a tubular body with a distal end and a proximal end and a lumen therebetween and a structure selected from the group consisting of a vent lumen and a wick that would aid in effusion removal during deployment of the pressure equalization tube.
• the invention is directed to a tympanic membrane pressure equalization tube comprising a tubular body with a distal end and a proximal end and a lumen therebetween, a medial flange located at the distal end of the tubular body, the medial flange comprising a cutting edge; and a lateral flange located at the proximal end of the tubular body.
• the tympanic membrane pressure equalization tube is made from a shape memory material that is pre-shaped with the cutting edge closed and centered on the medial flange and will self-dilate following deployment.
• Fig. 1 is a perspective view of a pressure equalization tube according to one embodiment of the invention.
• Fig. 2 is a side view of the pressure equalization tube of Fig. 1.
• Fig. 3 is a top view of the pressure equalization tube of Fig. 1.
• Fig. 4 is a bottom view of the pressure equalization tube of Fig. 1.
• Fig. 5 is a perspective view of a pressure equalization tube according to a second embodiment of the invention.
• Fig. 6 is a side view of the pressure equalization tube of Fig. 5.
• Fig. 7 is a side view of the pressure equalization tube of Fig. 5, from the opposite side shown in Fig. 6.
• Fig. 8 is a top view of the pressure equalization tube of Fig. 5.
• Fig. 9 is a bottom view of the pressure equalization tube of Fig. 5.
• Fig. 10 is a top view of a pressure equalization tube according to further
• Fig. 11 is a side view of the pressure equalization tube of Fig. 10.
• Fig. 12 is a cross-section view of an introducer useful for introducing a pressure equalization tube according to the invention.
• Fig. 13 is a perspective view of a pressure equalization tube according to another embodiment of the invention.
• Fig. 14 is a side view of a pressure equalization tube according to still another embodiment of the invention.
• Fig. 15 is a perspective view of a pressure equalization tube according to a further embodiment of the invention.
• Fig. 16 is a perspective view of another pressure equalization tube embodiment according to the invention.
• Fig. 17 is a side view of a pressure equalization tube according to another embodiment of the invention in its unexpanded state.
• Fig.18 is a side view of the tube of Fig. 17 in its expanded state.
• the tympanic membrane pressure equalization tube according to the invention is a grommet like device which is folded and/or compressed within the tube, and recovers its shape when delivered into the tympanic membrane.
• Embodiments of the invention are compatible for use with a suite of medical devices for visualizing the tympanic membrane, puncturing the tympanic membrane, and anesthetizing the tympanic membrane. Examples of such medical devices are shown in co- assigned U.S. Patent Application 11/749,733, the entirety of which is incorporated by reference. Accordingly, aspects of U.S. Patent Application 11/749,733 may be integrated, combined, and used in conjunction with the embodiments disclosed herein.
• Figs. 1 through 4 show a tympanic membrane pressure equalization tube 100, also referred to herein as a pressure equalization tube, a PE tube or a tympanostomy tube, according to one embodiment of the invention.
• the tube 100 is configured as a tubular body with asymmetric flanges, a medial flange 102 a lateral flange 104 and a tube lumen 106.
• the medial flange 102 has a larger diameter 102d than the lateral flange 104 diameter 104d (see Fig. 2).
• the medial flange 102 has three retention elements of equal size and shape, retention elements 108a, 108b and 108c.
• these retention elements have a width 110 of between about 0.6 mm and 1.0 mm, or about 0.80 mm, a length 112 of between about 1.0 mm and 3.0 mm, or of between about 1.8 mm and 1.9 mm, or about 1.87 mm and are spaced evenly around the
• the medial flange outside diameter 102d is between about 2.0 mm and about 5.0 mm or between about 3.0 mm and 4.0 mm or about 2.11 mm.
• the distance from the center 114 of the tube lumen 106 to the outer edge 116 of the medial flange 102 is 3.25 mm and from the center 114 of the tube lumen 106 to the inside edge 118 of the medial flange 102 is 1.65 mm.
• a second, lateral flange 104 is smaller than the medial flange 102 and is uniform in width with three retention elements 120a, 120b and 120c that are spaced 120° apart, with each notch 120a, 120b, and 120c at the same location as, or circumferentially aligned with the spaces between the medial flange retention elements 108a, 108b and 108c.
• the distance from the center 114 of the tube lumen 106 to the outside edge 122 of the lateral flange 104, the outer diameter of the lateral flange is between about 1.75 mm and about 4.0mm or between about 2.0 mm and 3.0 mm or about 2.11 mm.
• the pressure equalization tube 200 is configured as a tubular body 230 with asymmetric flanges, medial flange 202 a lateral flange 204 and a lumen 206.
• the medial flange 202 has a larger outer diameter 202d than the lateral flange 204 outer diameter 204d (see Figs. 6 and 7).
• the medial flange 202 has three equal retention elements 208a, 208b and 208c. As shown in Fig.
• these retention elements have a width 210 of between about 0.6 mm and 1.0 mm, or about 0.80 mm, a length 212 of between about 1.0 mm and 3.0 mm, or of between about 1.8 mm and 1.9 mm, or about 1.87 mm and are spaced evenly around the circumference of the tube lumen 206, that is, the wings are spaced 120° apart.
• the medial flange outside diameter 202d is between about 2.0 mm and about 5.0 mm or between about 3.0 mm and 4.0 mm or about 2.11 mm.
• the distance from the center 214 of the tube lumen 206 to the outer edge 216 of the medial flange 202 is 3.25 mm and from the center 214 of the tube lumen 206 to the inside edge 218 of the medial flange 202 is 1.65 mm.
• a second, lateral flange 204 is smaller than the medial flange 202 and is uniform in width with two notches 220a and 220b and spaced 180° apart, with notch 220a be at the same location as the spaces between the medial flange wings 208a and 208b.
• the distance from the center 214 of the tube lumen 206 to the outside edge 222 of the lateral flange 204, the outer diameter of the lateral flange is between about 1.75 mm and about 4.0 mm or between about 2.0 mm and 3.0 mm or about 2.11 mm.
• the tympanic membrane pressure equalization tube may comprise a shape memory material that can be mechanically compressed but can substantially return to an uncompressed state.
• materials that can be mechanically deformed but can return to an uncompressed state when not mechanically stressed include a number of biocompatible metals such as titanium, silver, tantalum, alloys of stainless steel, cobalt, chromium, and alumina and polymers or other pliable elastomeric materials such as polyolefms, polyurethanes, silicone rubber, PEEK, PMMA, and fluoropolymers.
• the tube 100 is often made of silicone rubber and may have an axial length of between about 2.0 mm and about 2.5 mm and in the embodiment shown in FIG.
• the axial length is about 2.2 mm.
• the thickness of each of the lateral 104 flange and the medial flange 102 is between about 0.25 mm and 0.35 mm or is approximately 0.30 mm and the flange to flange length 126 of the tube 100 is between about 1.0 mm and 2.0 mm or is about 1.6 mm.
• the tube 100 may have an inner diameter of between about 1.0 mm and about 1.5 mm, and in the embodiment shown in FIG. 2, the inner diameter is about 1.1 mm and the outer diameter may be between about 1.5 mm and 2.0 mm and is about 1.7 mm.
• the tube In order to deliver a tympanic membrane equalization tube to the tympanic membrane, the tube may be folded down and compressed into an introducer for storage until deployment into a patient's tympanic membrane.
• two- undesirable effects may occur when the tube is highly compressed and forced to contact itself. The first is that blocking may occur, that is the tacky surfaces of the tube may cause the tubes to temporarily self adhere one to the other. Blocking can deform the shape of a silicone object by having its surfaces contact one another, holding the object in something other than its natural free state. Blocking typically does not permanently change the shape of the object and the natural stresses in the object will have a tendency to overcome the blocking surface tension to restore the object to its original shape.
• the release may take a relatively long period of time (i.e. greater than 1 second). Further, the tube may become compression set, that is, the natural shape of the tube may be permanently deformed due to stress relief of the material. The stress relief can happen due to high stresses being applied for long periods of time, changing the natural unstressed shape.
• the retention elements i.e. 308a, 308b and 308c shown in Fig. 10
• the retention elements are designed to prevent touching of the edges when it they are folded down and compressed into the introducer for storage and therefore to mitigate areas of adhesion that may cause blocking.
• the relationship of the retention elements to the introducer 320 is described below.
• Figs. 10 and 11 show a tympanic membrane pressure equalization tube 300 according to a further embodiment of the invention
• Fig. 12 shows cross-sectional view of an introducer 320 for the tympanic membrane pressure equalization tube 300.
• the introducer has an inside surface 324, and outside surface 326 and an inner diameter 322.
• the tube 300 is configured as a tubular body with asymmetric flanges, a medial flange 302 a lateral flange 304 and a tube lumen 306, although tubes without a lateral flange are also contemplated according to the invention.
• the medial flange 302 has a larger diameter than the lateral flange 304.
• the medial flange 302 has three retention elements of equal size and shape, retention elements 308a, 308b and 308c, although according to the invention, the tube may include two, three, four or more retention elements. As shown in Fig.
• these retention elements have a length 312 of between about 0.6 mm and 1 mm, or about 1 mm such that when the three elements are collapsed they are smaller than the circumference of the inside surface 324 of the introducer 320 (see Fig. 12).
• the thickness 314 of the medial flange 302 is 0.305 mm. Accordingly, the length 312 of the retention elements can be calculated as follows (L):
• the maximum length 312 of the retention elements in this instance is 0.98 mm, and the length may be between about 0.6 and 1 mm.
• the retention elements are of equal size and shape and the maximum length of each retention element is equal to the circumference of the inside surface 324 of the introducer 320 divided by the number of retention elements.
• Another method to reduce retention element adhesion according to the invention is is to add a coating to the tube.
• a thin coating (0.25 ⁇ ) of parylene or other similar biocompatible coating can be applied to reduce retention element adhesion and ensure near instantaneous opening and rapid tube deployment (i.e within 1 second).
• the pressure equalization tube 400 comprises a helical tube. Surrounding the tubular body lumen 402, on the surface of the pressure equalization tube 400 is a helical coil 404 that is a raised rib wrapped in a helical spiral. The tube 400 is retained in the patient's tympanic membrane by means of the multiple raised ribs that surround the tube 400.
• the inner diameter of the pressure equalization tube is 1.1 mm or between about 0.8 and 1.4 mm
• the outer diameter is about 2.1 mm or between about 1.8 mm and 2.4 mm
• the overall length of the tube 400 is about 2.2 mm or between about 1.8 and 2.6 mm
• the helical pitch is 0.44 mm or between about 0.35 and 0.55 mm
• the tympanic membrane equalization tubes disclosed herein can include features which help recover a misplaced tympanic membrane equalization tube.
• a misplaced tympanic membrane equalization tube located distally to the tympanic membrane can be especially difficult to remove.
• Such features can include tethers attached to any portion of the tympanic membrane equalization tubes. The tethers can be grasped proximally to the tympanic membrane and used to pull the misplaced tympanic membrane equalization tube out of the ear.
• methods for inserting pressure equalization tubes into the tympanic membrane include both simple, manual methods and more complicated, automatic systems for making an incision and placing the tube into the incision.
• a manual method for inserting a pressure equaliziation tube into a tympanic membrane includes placing a speculum into the ear canal in apposition with the tympanic membrane in order to more clearly visualize the membrane. Following visualization of the tympanic membrane, a myringotomy blade is inserted into the speculum and a small incision is created in the tympanic membrane (a myringotomy) to relieve pressure caused by the excessive buildup of fluid due to infection in the middle ear. Forceps are then used to collapse the pressure equalization tube and insert it into the incision to allow external ventilation of the middle ear for an extended period of time. Suction may be applied before or after tube insertion in order to remove the fluid in the middle ear.
• the pressure equalization tube 500 shown in Fig. 14 has an open lumen 502 lined with artificial cilia 504 to aid the transport and expulsion of effusion from the middle ear.
• the artificial cilia may include microtubules and molecular motors that create waves or beating action to transport the effusion or other bodily fluids through the lumen 502 of the tube 500.
• Such cilia are described in detail in Sanchez, Timothy et al; Cilia-like Beating of Active Microtubule Bundles; Science 22 July 2011; Vol. 333 no. 6041 pp. 456- 459, or US Patent No. 6,849,910 which describes a similar mechanism for surface fluid transport using oscillatory MEMs. Both publications are incorporated by reference herein in their entirety.
• Fig. 15 shows a pressure equalization tube 600 with a vent lumen 602 and Fig. 16 shown a pressure equalization tube 620 with a wick 622 that would aid in effusion removal during deployment of the pressure equalization tubes by allowing effusion to be vented or wicked from the ear canal. Further, in the event that the physician desires to use suction to remove the effusion, an air return path is provided, breaking the effect of vacuum in a closed space.
• An internal spring loaded cam-based mechanism is located within the housing and coupled to a button.
• the method further includes triggering a mechanism which results in puncturing the tympanic membrane.
• the method involves delivering the tympanic membrane pressure equalization tube.
• the tympanic membrane pressure equalization tube that has been folded or compressed within the tube and recovers its shape into its uncompressed shape when delivered into the tympanic membrane.
• the size and shape of the medial flange retention elements are optimal for ensuring that the tympanic membrane pressure equalization tube can be inserted through a myringotomy in a tympanic membrane.
• the retention elements are longitudinally aligned with the tubular body lumen and do not overlap one with the other, limiting the cylindrical profile of the tube in the compressed state, and optimizing recovery to the perpendicular alignment of the retention elements and the tubular body lumen in the uncompressed state. Further, the size and shape of the lateral flange retention elements ensure that the lateral flange is retained on the lateral side of the tympanic membrane following delivery of the pressure equalization tube into the tympanic membrane, through the myringotomy.
• a pressure equalization tube 700 includes a cutting tube with sufficient rigidity (i.e. fabricated from a shape memory material such as nitinol or PEEK shape memory polymer) to make a myringotomy when pushed into the tympanic membrane without the use of additional delivery systems.
• the tube is pre- shaped with conventional heat/cool methods such that it is normally closed prior to use with a sharp cutter edge 702 centered on the medial flange 704 (see Fig. 17).
• the medial flange when closed is taper shaped, and will therefore self-dilate when pushed in place.
• the tube After placement, the tube will be self-anchoring, that is, the medial flange 704 will expand as a result of body heat (See Fig. 18).
• the tube medial flange dilation can be controlled with a cold mandrel inserted into the tube to keep the tube in a closed shape for safe insertion, and then allow for self-anchoring when the mandrel is removed.
• the cold mandrel can be re-inserted into the tube so that it will return to its closed shape (as shown in Fig. 17), thereby minimizing the risk of damaging the tympanic membrane from the expanded anchoring flange.

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• Health & Medical Sciences (AREA)
• Life Sciences & Earth Sciences (AREA)
• Animal Behavior & Ethology (AREA)
• Heart & Thoracic Surgery (AREA)
• Veterinary Medicine (AREA)
• Biomedical Technology (AREA)
• Otolaryngology (AREA)
• General Health & Medical Sciences (AREA)
• Engineering & Computer Science (AREA)
• Public Health (AREA)
• Vascular Medicine (AREA)
• Acoustics & Sound (AREA)
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• Ophthalmology & Optometry (AREA)
• Pulmonology (AREA)
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• Oral & Maxillofacial Surgery (AREA)
• Transplantation (AREA)
• Prostheses (AREA)
• External Artificial Organs (AREA)

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• 2013
  • 2013-03-13 US US13/800,113 patent/US9011363B2/en active Active
  • 2013-04-10 RU RU2014145020A patent/RU2014145020A/ru not_active Application Discontinuation
  • 2013-04-10 KR KR1020147031224A patent/KR102113888B1/ko not_active Expired - Fee Related
  • 2013-04-10 CA CA2869927A patent/CA2869927A1/en not_active Abandoned
  • 2013-04-10 EP EP13718264.8A patent/EP2841036B1/en active Active
  • 2013-04-10 AU AU2013246006A patent/AU2013246006A1/en not_active Abandoned
  • 2013-04-10 CN CN201380019310.1A patent/CN104244878A/zh active Pending
  • 2013-04-10 IN IN8043DEN2014 patent/IN2014DN08043A/en unknown
  • 2013-04-10 MX MX2014012237A patent/MX2014012237A/es not_active Application Discontinuation
  • 2013-04-10 WO PCT/US2013/035953 patent/WO2013155169A1/en not_active Ceased
• 2015
  • 2015-03-25 US US14/668,071 patent/US9907700B2/en active Active
• 2018
  • 2018-02-09 US US15/892,855 patent/US10835422B2/en active Active

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