The present invention relates to an introducer device for providing percutaneous access to a patient's vasculature for a transcatheter device delivery system, and, more particularly to an expandable introducer device having a folded, expandable membrane for accommodating passage of the transcatheter device delivery system therethrough.
An introducer device is used to provide percutaneous access to the vascular system of a patient and functions to permit the introduction and positioning of various minimally invasive delivery devices within the patient's vasculature. In general, making the smallest incision is the most desirable and leads to less complications, less trauma, and improved patient outcomes. Some delivery devices, however, are large and require large sheaths to accommodate and help deliver them to the desired site within the body.
In accordance with an aspect hereof, an introducer device for providing a prosthesis delivery system percutaneous access to a patient's vasculature is disclosed. The device includes a tubular membrane component having a central lumen. The tubular membrane is inserted in a folded, unexpanded state with a first diameter, and is configured to expand when a delivery device is advanced through a central lumen of the tubular membrane to an unfolded, expanded state with a second diameter larger than the first diameter.
In one aspect, the present disclosure provides an expandable introducer including an introducer hub, a seal coupled within the introducer hub, a tubular membrane defining a central lumen, the tubular membrane being coupled to the introducer hub and extending distally therefrom, and a spine attached to, partially attached to, extending through, or incorporated into an inner surface of the tubular membrane. The tubular membrane is radially-expandable from a first diameter to a second diameter larger than the first diameter in response to a device being advanced through the tubular membrane.
In another aspect hereof, and in combination with any other aspects, the disclosure provides the tubular membrane is a thin, flexible plastic tube configured to expand from a folded state to an expanded, unfolded state in response to the device being advanced therethrough.
In another aspect hereof, and in combination with any other aspects, the disclosure provides the tubular membrane is mechanically expandable.
In another aspect hereof, and in combination with any other aspects, the disclosure provides the tubular membrane comprises a polymer or nylon material of any combination thereof.
In another aspect hereof, and in combination with any other aspects, the disclosure provides the first diameter of the tubular membrane is about 1-3 mm.
In another aspect hereof, and in combination with any other aspects, the disclosure provides the second diameter of the tubular membrane is about 10-12 mm.
In another aspect hereof, and in combination with any other aspects, the disclosure provides the spine is a thin, rigid wire configured to support the tubular membrane and extends longitudinally through the tubular membrane.
In another aspect hereof, and in combination with any other aspects, the disclosure provides the spine is attached to, partially attached to, extending through, or incorporated into the inner surface of the tubular membrane.
In another aspect hereof, and in combination with any other aspects, the disclosure provides a distal end of the spine terminates proximal to a distal end of the tubular membrane.
In another aspect hereof, and in combination with any other aspects, the disclosure provides the spine extends through the entire length of the tubular membrane.
In another aspect hereof, and in combination with any other aspects, the disclosure provides the distal end of the spine tapers in a distal direction from a first thickness to a second thickness smaller than the first thickness.
In another aspect hereof, and in combination with any other aspects, the disclosure provides the spine comprises stainless steel, nitinol, and/or a rigid polymer such as polyether ether ketone (PEEK).
In another aspect hereof, and in combination with any other aspects, the disclosure provides the spine is a single spine attached to, partially attached to, extending through, or incorporated into the tubular membrane.
In another aspect hereof, and in combination with any other aspects, the disclosure provides the spine comprises two or more spines attached to, partially attached to, extending through, or incorporated into the tubular membrane.
In one aspect hereof, and in combination with any other aspects, the present disclosure provides an introducer dilator assembly comprising an introducer including an introducer hub, a tubular membrane coupled to the introducer hub and extending distally from the introducer hub, the tubular membrane having a folded state and an expanded, unfolded state, and a spine attached to, partially attached to, extending through, or incorporated into the tubular membrane and a dilator including a dilator hub, a dilator shaft coupled to the dilator hub and extending distally therefrom, and a dilator tip coupled to a distal end of the dilator shaft, wherein in an assembled configuration, the dilator shaft extends through the introducer hub and the tubular membrane such that the dilator hub is proximal of the introducer hub, the distal end of the dilator shaft is distal of a distal end of the tubular membrane, and the dilator tip extends proximally from the distal end of the dilator shaft and houses the distal end of the tubular membrane therewithin.
In another aspect hereof, and in combination with any other aspects, the disclosure provides a removable clip, wherein in the assembled configuration, the removable clip is coupled to a proximal portion of the dilator shaft between the introducer hub and the dilator hub, and prevents distal advancement of the dilator relative to the introducer.
In another aspect hereof, and in combination with any other aspects, the disclosure provides when the removable clip is removed from the assembly, the dilator may be advanced distally relative to the introducer such that the distal tip of the dilator releases the distal end of the tubular membrane.
In one aspect hereof, and in combination with any other aspects, the present disclosure provides a method comprising tracking an assembled introducer dilator assembly into a vessel, the introducer dilator assembly including an introducer including an introducer hub, a tubular membrane coupled to and extending distally from the introducer hub, and a spine attached to, partially attached to, extending through, or incorporated into the tubular membrane, and a dilator including a dilator hub, a dilator shaft coupled to the dilator hub and extending distally therefrom, and a dilator tip coupled to a distal end of the dilator shaft, advancing the assembled introducer dilator assembly until a distal end of the introducer hub is snug against the vessel to establish a hemostatic seal, advancing the dilator distally relative to the introducer to disengage the dilator tip from a distal end of the tubular membrane and allowing the distal end of the tubular membrane to be free of constraint, displacing the dilator proximally relative to the introducer such that the distal end of the dilator and the distal tip of the dilator enter a distal opening of the tubular membrane, and continuing to displace the dilator proximally relative to the introducer until the dilator is withdrawn from the introducer.
In another aspect hereof, and in combination with any other aspects, the disclosure provides the removable clip is coupled to a proximal portion of the dilator shaft between the introducer hub and the dilator hub, and prevents distal advancement of the dilator relative to the introducer.
In another aspect hereof, and in combination with any other aspects, the disclosure provides with the removable clip removed from the assembly, the dilator may be advanced distally relative to the introducer such that the distal tip of the dilator releases the distal end of the tubular membrane.
In another aspect hereof, and in combination with any other aspects, the disclosure provides the tubular membrane expands radially in response to the device being advanced distally through a proximal end of the introducer.
In another aspect hereof, and in combination with any other aspects, the disclosure provides the tubular membrane can be expanded by injecting saline through a proximal end of the assembly prior to proximally retracting the dilator.
The details of one or more aspects of the disclosure are set forth in the accompanying drawings and the description below. Other features, objects, and advantages of the techniques described in this disclosure will be apparent from the description and drawings, and from the claims.
The foregoing and other features and advantages of the present disclosure will be apparent from the following description of embodiments hereof as illustrated in the accompanying drawings. The accompanying drawings, which are incorporated herein and form a part of the specification, further serve to explain the principles of the present disclosure and to enable a person skilled in the pertinent art to make and use the embodiments of the present disclosure. The drawings may not be to scale.
It should be understood that various embodiments disclosed herein may be combined in different combinations than the combinations specifically presented in the description and accompanying drawings. It should also be understood that, depending on the example, certain acts or events of any of the processes or methods described herein may be performed in a different sequence, may be added, merged, or left out altogether (e.g., all described acts or events may not be necessary to carry out the techniques). In addition, while certain aspects of this disclosure are described as being performed by a single device or component for purposes of clarity, it should be understood that the techniques of this disclosure may be performed by a combination of devices or components associated with, for example, a delivery device. The following detailed description is merely exemplary in nature and is not intended to limit the invention of the application and uses of the invention. Furthermore, there is no intention to be bound by any expressed or implied theory presented in the preceding field of the invention, background, summary or the following detailed description.
As used in this specification, the singular forms “a”, “an” and “the” specifically also encompass the plural forms of the terms to which they refer, unless the content clearly dictates otherwise. The term “about” is used herein to mean approximately, in the region of, roughly, or around. When the term “about” is used in conjunction with a numerical range, it modifies that range by extending the boundaries above and below the numerical values set forth. In general, the term “about” is used herein to modify a numerical value above and below the stated value by a variance of 20%. It should be understood that use of the term “about” also includes the specifically recited number of value.
The terms “proximal” and “distal” herein are used with reference to the clinician using the devices. Therefore, “proximal” and “proximally” mean in the direction toward the clinician, and “distal” and “distally” mean in the direction away from the clinician.
The introducer hub 103 includes a proximal end 112, a distal end 111, and a passageway 115 extending from the proximal end 112 to the distal end 111 of the introducer hub 103. The passageway 115 is sized and shaped to accommodate a dilator shaft 201 of a dilator 200 therethrough, as explained in more detail below. The hub 103 further includes a seal 104 disposed within the passageway 115 to seal around the dilator shaft 201 and prevent blood flow out of a patient's vessel when the introducer 100 is in use. The introducer hub 103 further includes an outer surface 116 tapered in a distal direction such that the distal end 111 of the introducer hub 103 has a first diameter smaller than a second diameter of the proximal end 112 of the introducer hub 103, as shown in
In embodiments, the spine 102 is a thin, rigid wire configured to support the structure of the tubular membrane 101. In embodiments, the spine 102 is attached to, partially attached to, extending through, or incorporated into the inner surface of the tubular membrane 101 and extends longitudinally therethrough. In other embodiments, the spine 102 may be attached to, partially attached to, extending through, or incorporated into an outer surface of the tubular membrane 101. As depicted in
The removable clip 203 is a separate piece that may be coupled to the dilator shaft 201 distal of the dilator hub 204, as shown in
The dilator tip 202 is a tubular element that includes a distal end 208 coupled to the distal end 205 of the dilator shaft 201. The dilator tip 201 extends proximally from the distal end 208 attached to the dilator shaft to a proximal end 209 of the distal tip 202, and includes a cavity 211 formed between the proximal end 209 of the dilator tip 202, which is not attached to the dilator shaft 201, and the outer surface of the dilator shaft 201. The dilator tip 201 is formed of an expandable material such that the dilator tip includes a radially expanded configuration wherein the proximal end 209 is spaced from an outer surface of the dilator shaft 201 and is configured to enclose the distal end 109 of the tubular membrane 101 such that the distal end 109 of the tubular membrane 101 is disposed between the dilator shaft 201 and the dilator tip 202, as shown in
When the introducer dilator assembly 300 is inserted into the vasculature, the tubular membrane 101 is in a folded, unexpanded state.
In a step 406, the proximal end 108b of the guidewire 108 is inserted into a distal end of the central lumen 207 of the dilator shaft 201 of the dilator 200, with the dilator 200 inserted through the introducer 100 to create the introducer dilator assembly 300. The introducer dilator assembly 300 is then distally advanced over the guidewire 108 into the vessel 602 of the patient until the distal end 111 of the introducer hub 103 is snug against the vessel 602 to establish a hemostatic seal, as shown in
In steps 408, 410, 412, the dilator 200 may then be removed from the expandable introducer 100. In step 408, the removable clip 203 is removed and the dilator 200 is distally advanced through the passageway 115 of the introducer hub 103 and the central lumen 107 of the tubular membrane 101 until the dilator hub 204 is flush against the proximal end 112 of the introducer hub 103, as shown in
In some embodiments, the method may include the use of an extension tube 801 and a stopcock 802 in order to inject saline, or other fluids, into the proximal end 106 of the expandable introducer 100, as shown in
Once the dilator 200 is removed, the expandable introducer 100 and the guidewire 108 remain within the vasculature of the patient, as shown in
In a step 414, the device 601 may be advanced through the expandable introducer 100. With the distal end 108a of the guidewire 108 disposed within the vessel of the patient, the proximal end 108b of the guidewire 108 may be inserted into a distal end of a central lumen of the device 601. The device 601 may then be distally advanced over the guidewire 108 into the proximal end 106 of the expandable introducer 100 and advanced therethrough, as shown in
As the device 601 advances distally through the central lumen 107 of the tubular membrane 101, the tubular membrane 101 expands from a first diameter of a folded, unexpanded state to a second diameter larger than the first diameter of an unfolded, expanded state in response to the device 601 being advanced distally therethrough, as shown in
This skilled in the art will recognize that other steps may be included and that the order in which the steps are described are not necessarily limiting.
In some embodiments, the spine 102 of the expandable introducer 100 extends the entire length of the tubular membrane 101, as shown in
The figures described herein show the spine 102 and the tubular membrane 101 separated from each other for clarity. Similarly, the tubular membrane 101 is shown separated from the introducer hub 103, also for clarity. Those skilled in the art will understand that the spine 102 attached to, partially attached to, extending through, or incorporated into the inner surface of the membrane 101 will not have a gap therebetween, and that the tubular membrane 101 attached to the introducer hub 103 will not have a gap therebetween. Similarly, other parts attached to each other and shown in the drawings may be separated for clarity in the drawings.
It should be understood that various embodiments disclosed herein may be combined in different combinations than the combinations specifically presented in the description and accompanying drawings. It should also be understood that, depending on the example, certain acts or events of any of the processes or methods described herein may be performed in a different sequence, may be added, merged, or left out altogether (e.g., all described acts or events may not be necessary to carry out the techniques). In addition, while certain aspects of this disclosure are described as being performed by a single device or component for purposes of clarity, it should be understood that the techniques of this disclosure may be performed by a combination of devices or components associated with, for example, a medical device.
This application claims the benefit under 35 U.S.C. § 119(e) of U.S. provisional application No. 63/229,512, filed Aug. 5, 2021, the contents of which are incorporated by reference herein in their entirety.
Number | Date | Country | |
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63229512 | Aug 2021 | US |