The present invention is directed, in general, to the field of catheters. In particular, the invention relates to a catheter for cerebral angiography and neurointerventions.
Transfemoral access (TFA) has been widely used in neurointerventional procedures; it is the vascular approach most frequently used for catheterization of the supraaortic and intracranial vessels. However, TFA can lead to potentially life-threatening complications, which has sparked interest in transradial access (TRA) as a safer access option.
In a review of 19,826 consecutive patients undergoing diagnostic cerebral angiography using TFA, access-site hematoma was the most common complication overall (4.2%).
Percutaneous radial access was described by Campeau in 1989 for coronary angiography in 100 patients. Since then, a growing body of evidence suggests that TRA is safer for patients and more cost-effective.
In the 2018 ESC/EACTS guidelines on myocardial revascularization, radial access is preferred for any PCI irrespective of clinical presentation, unless there are overriding procedural considerations.
During all this years, technical innovations and specific TRA catheters for gaining access to the coronary arteries have helped to change the TFA to TRA in the cardiology field. Likewise, TRA access is showing to be a good choice for elderly patients to perform stroke thrombectomy or other kinds of neuro vascular diseases.
Though TRA has become progressively accepted for diagnostic cerebral angiography and neurointerventional procedures, there is still a need for proper specific materials to perform neurointerventions through TRA.
The known standard catheters in the field, such as Cobra catheters or Simmons catheters when used in the left vertebral artery show difficulties in its manipulation, not being able to rise in the left vertebral artery but tending to fall into the descending aorta.
This also may happen with the other supraaortic vessels depending on the anatomy of the aortic arch.
Besides, International patent application WO2020072895 discloses a cardiac catheter for angiographic procedures of a left internal mammary artery bypass graft performed using a right radial arterial approach. The catheter includes a guide catheter comprising an elongated member having an outer sheath body portion that includes (see
US2009082756A1 provides a catheter suitable for catheterization of a right coronary artery using a right transradial approach. The catheter includes a tip near its distal end, a primary curve, a secondary curve, a tertiary curve and a proximal end accessible external a catheterized body. When properly inserted, the secondary curve may rest near the junction of the bracheocephalic trunk and the right subclavian artery, and the tertiary curve may rest in the superior curve of the right subclavian artery. In addition to improved directionality, the secondary and/or tertiary curve offers additional resistance against cephalic, or upward, back-up force by providing caudal, or downward, torque to more distal portions of the catheter body. This catheter is thus designed and used for internal mammary catheterization (the artery used to perform bypass to coronary (heart arteries)) and not to catheterize brain arteries (carotids and vertebral arteries) from a radial approach as the proposed catheter for cerebral angiography and neurointerventions.
More specific catheters to perform supraaortic vessels catheterization from a TRA access are therefore needed.
To that end the present invention provides a catheter for cerebral angiography and neurointerventions.
The proposed catheter needs to perform retrogradely catheterization to supra-aortic vessels meanwhile having a contact/support to the lower aspect of the aortic arch, this will allow not only catheterize the desired vessel, it will allow the advancement of the catheter through a guidewire (once the vessel is catheterized) by having contact of the catheter in the lower aspect of the aortic arch (if the catheter does not have the contact, while trying to advance it, it will fall in the descending aorta).
The proposed catheter comprises: a proximal end, a distal end and a plurality of segments. The plurality of segments include a first curved segment, a second curved segment and a third linear segment.
The first curved segment has a curve with a first radius of curvature and is extended with a first linear segment. The second curved segment connects the first linear segment with a second linear segment and has a curve with a second radius of curvature. The curve of the first curved segment is in a different direction than the curve of the second curved segment, or in other words, the concave portion of the second curved segment faces an area delimited by the first linear segment and the second linear segment. The second linear segment has a length greater than a length of the first linear segment.
Unlike the known catheter devices in the field, in the proposed catheter the third linear segment is connected to an end of the second linear segment through a curved portion that orients the third linear segment in a direction that approaches towards the first curved segment.
In some embodiments, the curved portion comprises a radius of curvature that is smaller than the first radius of curvature.
In some embodiments, the second linear segment and the first linear segment are approximately parallel one to another.
In some embodiments, the intersection of the third linear segment and the second linear segment covers an angle of at least 160°.
Particularly, the first radius of curvature is smaller than the second radius of curvature.
The proposed catheter can have different lengths. Particularly, the total length of the catheter is between 80 cm and 150 cm. Moreover, in some embodiments, the second linear segment can have a length comprised in a range between 3-10 cm and the third linear segment can have a length comprised in a range between 70-147 cm.
The proposed catheter device enables going up in the left vertebral artery without dropping into the descending aorta while offering an improved handling and control. Likewise, the catheter provides a good torque and pushability combination.
The foregoing describes embodiments of the present invention and modifications, obvious to those skilled in the art can be made thereto, without departing from the scope of the present invention.
The previous and other advantages and features will be more fully understood from the following detailed description of embodiments, with reference to the attached figures, which must be considered in an illustrative and non-limiting manner, in which:
According to the embodiment of
As shown in the figure, a first curved segment 20 comprises a curve with a first radius of curvature and extends with a first linear segment 20A. A second curved segment 21 extends from the first segment 20 and has a curve with a second radius of curvature. The second curved segment 21 connects the first linear segment 20A with a second linear segment 22, and its curve is in a direction that is different than a direction of the curve of the first curved segment 20. More in particular, the second curved segment 21 comprises a concave portion that faces, or that is confronted with, an area/zone delimited by the first linear segment 20A and the second linear segment 22. The second linear segment 22 has a length which is larger than a length of the first linear segment 20A.
According to the proposed catheter 1, also, a third linear segment 23 is connected to an end of the second linear segment 22. Particularly, the connection is done by means of a curved portion 24 that purposely orients the third linear segment 23 in a direction that approaches towards the first curved segment 20. The radius of curvature of the curved portion 24 is particularly smaller than the first radius of curvature.
In some embodiments, the intersection of the third linear segment 23 and the second linear segment 22 covers an angle of at least 160°.
As shown in the illustrated embodiment, the second linear segment 22 and the first linear segment 20A are approximately parallel one to another. Likewise, the second radius of curvature is greater than the first radius of curvature.
In various embodiments, the overall length of the catheter 1 can be between 80 and 150 cm. The length of the second linear segment 22 can be between 3 and 10 cm. The length of the third linear segment 23 can be between 70 and 147 cm.
In some embodiments, the distal 10 or proximal 11 ends of the catheter 1, or other segments thereof, can be provided with a radiopaque element to enable visualization under fluoroscopy, or other imaging technique.
Unless otherwise indicated, all numbers expressing measurements, conditions, and so forth used in the specification and claims are to be understood as being modified in all instances by the term “about”. Accordingly, unless indicated to the contrary, the numerical parameters set forth in this specification and attached claims are approximations that can vary depending upon the desired properties sought to be obtained by the presently disclosed patient matter.
As used herein, the term “about”, when referring to a value or to an amount of a length, percentage, etc., is meant to encompass variations of in some embodiments ±10%, in some embodiments ±5%, in some embodiments ±1%, in some embodiments ±0.5%, and in some embodiments ±0.1% from the specified amount, as such variations are appropriate to perform the disclosed device.
Without further elaboration, it is believed that one skilled in the art can use the preceding description to utilize the invention to its fullest extent. The claims and embodiments disclosed herein are to be construed as merely illustrative and exemplary, and not a limitation of the scope of the present disclosure in any way. It will be apparent to those having ordinary skill in the art, with the aid of the present disclosure, that changes may be made to the details of the above-described embodiments without departing from the underlying principles of the disclosure herein. In other words, various modifications and improvements of the embodiments specifically disclosed in the description above are within the scope of the appended claims. The scope of the invention is therefore defined by the following claims and their equivalents.
Number | Date | Country | Kind |
---|---|---|---|
21382519.3 | Jun 2021 | EP | regional |
Filing Document | Filing Date | Country | Kind |
---|---|---|---|
PCT/EP2022/063840 | 5/23/2022 | WO |