EP1139916A1 - Device for placing an aortic endoprosthesis - Google Patents

Device for placing an aortic endoprosthesis

Info

Publication number
EP1139916A1
EP1139916A1 EP99959407A EP99959407A EP1139916A1 EP 1139916 A1 EP1139916 A1 EP 1139916A1 EP 99959407 A EP99959407 A EP 99959407A EP 99959407 A EP99959407 A EP 99959407A EP 1139916 A1 EP1139916 A1 EP 1139916A1
Authority
EP
European Patent Office
Prior art keywords
guide wire
wire
guidewire
guide
catheter tube
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
EP99959407A
Other languages
German (de)
French (fr)
Inventor
Mario Lachat
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Fumedica Intertrade AG
Original Assignee
Fumedica Intertrade AG
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Fumedica Intertrade AG filed Critical Fumedica Intertrade AG
Publication of EP1139916A1 publication Critical patent/EP1139916A1/en
Withdrawn legal-status Critical Current

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS 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
    • A61F2/00Filters 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
    • A61F2/95Instruments specially adapted for placement or removal of stents or stent-grafts
    • A61F2/954Instruments specially adapted for placement or removal of stents or stent-grafts for placing stents or stent-grafts in a bifurcation
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS 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
    • A61F2/00Filters 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
    • A61F2/02Prostheses implantable into the body
    • A61F2/04Hollow or tubular parts of organs, e.g. bladders, tracheae, bronchi or bile ducts
    • A61F2/06Blood vessels
    • A61F2/07Stent-grafts
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS 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
    • A61F2/00Filters 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
    • A61F2/02Prostheses implantable into the body
    • A61F2/04Hollow or tubular parts of organs, e.g. bladders, tracheae, bronchi or bile ducts
    • A61F2/06Blood vessels
    • A61F2002/065Y-shaped blood vessels
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS 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
    • A61F2/00Filters 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
    • A61F2/02Prostheses implantable into the body
    • A61F2/04Hollow or tubular parts of organs, e.g. bladders, tracheae, bronchi or bile ducts
    • A61F2/06Blood vessels
    • A61F2002/065Y-shaped blood vessels
    • A61F2002/067Y-shaped blood vessels modular

Definitions

  • the invention relates to a device for inserting aortic endoprostheses, in particular in the treatment of abdominal aortic aneurysms.
  • an endoprosthesis in the form of a coated stent, which relieves the aortic wall in the area of the aneurysm 2 (FIG. 1) from blood pressure and prevents its further expansion and tearing.
  • This stent must protrude upwards and downwards beyond the area of the aneurysm 2, i.e. Start at the top in the unstretched area of aorta 1 and lead to both pelvic arteries 3, 4.
  • the stent is usually composed of two parts, a main prosthesis 5 covering the aorta and the subsequent branch of a pelvic artery 3 and an extension 6 covering the branch of the other pelvic artery 4.
  • the object of the invention is to provide a device with which the extension can be used more easily, quickly and safely.
  • proximal and distal are intended to refer to the patient here; accordingly, the leading end of the guidewire is said to be proximal.
  • the second guide wire is spread apart from the first by 20 to 40 degrees. This condition occurs after the proximal end of the first guidewire has been inserted into the main prosthesis already inserted in the aorta.
  • a further guide which is inserted via the contralateral arteria femoralis and provided at the end with a wire loop ("lasso"). guidewire can be detected. The extension can then be inserted along this guide wire.
  • the device according to the invention can also be inserted from the outside into the aorta through a catheter tube, the catheter effecting the parallel guidance of both wires.
  • the first and second guide wires are approximately parallel. In this position, they can be withdrawn from the area of the aortic aneurysm through the iliac artery and femoral artery.
  • the material and diameter of the two connected guide wires correspond to those customary according to the prior art described above.
  • the second can be attached to the first guide wire by laser welding.
  • the ends of the guide wires are advantageously curved in an arc of 90 to 210 degrees with a radius of 2 to 20 mm. This avoids vascular lesions when inserted.
  • this is as Alignment catheter tube closed at the proximal end and provided with a tapered rounded tip. In this case, the proximal ends of the guide wires are not bent.
  • the probing of the main prosthesis and the insertion of the extension can take up to 30 minutes, this time can be reduced to 5 minutes with the new device.
  • FIG. 3 shows a device according to the invention as claimed in claim 2 in the first position of the alignment member
  • FIG. 5 shows a device according to the invention as claimed in claim 3 in the first position of the alignment member
  • FIG. 6 shows a device according to the invention according to claim 3 in the second position of the alignment member
  • FIG. 7 shows the device shown in FIG. 3 in the operating area
  • FIG. 10 shows an enlarged detail of FIG. 9 in section.
  • the first guide wire 11 of the device shown in FIG. 3 according to claim 2 is preferably about 130 to 280 cm long. It has a curvature at the proximal end 12, i.e. the end 12 preceding when inserted.
  • a preferably approximately 20 to 50 cm long second guide wire 13 is fastened with its proximal end to the wire 11 in such a way that it forms an angle of 20 to 40 degrees with the latter.
  • the attachment point 14 is about 10 to 40 cm from the proximal end 12 of the first guidewire.
  • a wire loop 16 located on a pull wire 15 wraps around the wire 11 proximal to the attachment point.
  • the wire loop preferably has a diameter of 5 to 10 mm.
  • the pull wire 15 is so long that its distal end remains accessible to the surgeon.
  • FIG. 4 shows the device according to claim 2 in the second position of the wire loop 16 acting as an alignment member. This is now distal to the attachment point 14, wraps around both guide wires in the vicinity of the distal end 17 of the second guide wire 13 and holds them in an approximately parallel orientation . In this position, the device can be withdrawn from the femoral artery without difficulty.
  • the catheter tube 18 is so long that its distal end remains accessible even after insertion into the aorta.
  • the opening 19 is preferably about 5 to 20 cm from the proximal end of the catheter tube.
  • Fig. 6 shows the same device in the second position of the catheter tube 18.
  • the catheter tube 18 is now retracted relative to the guide wires 11, 13, so that it holds in its interior in an approximately parallel orientation. In this position the device can be withdrawn from the femoral artery without difficulty.
  • FIG. 7 shows the device according to claim 2 in the first position of the wire loop 16 fastened to the puller wire 15 after insertion into the abdominal aorta 1 and slight retraction.
  • the second guide wire 13 is spread apart from the first 11 and emerges from the main prosthesis with its distal end. This end can now be easily grasped with a lasso 20, on which the displacement can finally be inserted and placed securely in the main prosthesis 5 and the pelvic artery 4.
  • the device according to claim 3 can also be used.
  • the catheter tube 18 is closed here at the proximal end with a conically rounded tip 21.
  • the proximal end of the first guidewire is not bent.
  • FIG. 10 the area around the outlet opening 19 is the one in FIG Fig. 9 shown device shown enlarged in section.
  • the first guidewire 11 and the second guidewire 13 lying in the upper area can be seen.
  • a partition 22 is also provided in the catheter tube and an outlet plug 23 for the distal end 17 of the second guidewire.

Landscapes

  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Biomedical Technology (AREA)
  • Cardiology (AREA)
  • Oral & Maxillofacial Surgery (AREA)
  • Transplantation (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Vascular Medicine (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Media Introduction/Drainage Providing Device (AREA)
  • Prostheses (AREA)

Abstract

Known devices for placing aortic endoprostheses comprise a guide wire by means of which the opening of the main prosthesis already positioned in the aneurysm is sounded prior to insertion of the extension. This is a long and risky procedure. According to the device provided for in the invention a second guide wire for the extension is fixed to the first guide wire used for the main prosthesis in such a way that said second wire can be aligned with the first. In this way the opening for receiving the extension can be sounded from the interior both rapidly and safely.

Description

Vorrichtung zum Einsetzen einer Aorten-Endoprothese Device for inserting an aortic endoprosthesis
Die Erfindung betrifft eine Vorrichtung zum Einsetzen von Aorten-Endoprothesen, insbesondere bei der Behandlung von Bauchaortenaneurys en .The invention relates to a device for inserting aortic endoprostheses, in particular in the treatment of abdominal aortic aneurysms.
Es ist bekannt, zur minimal-invasiven chirurgischen Behandlung des Bauchaortenaneurysmas eine Endoprothese in Form eines beschichteten Stents zu implantieren, die die Aortenwand im Bereich des Aneurysmas 2 (Fig. 1) vom Blutdruck entlastet und deren weitere Ausdehnung und das Zerreißen verhindert. Dieser Stent muß nach oben und unten über den Bereich des Aneurysmas 2 hinausragen, d.h. oben im ungedehnten Bereich der Aorta 1 beginnen und bis in beide Beckenarterien 3, 4 führen. Der Stent wird üblicherweise aus zwei Teilen zusammengesetzt, wobei eine Hauptprothese 5 die Aorta und den anschließenden Ast einer Beckenarterie 3 und eine Verlängerung 6 den Ast der anderen Beckenarterie 4 abdeckt. Beim Einsetzen wird zunächst auf einer Seite, z. B. rechts, die Arteria femoralis punktiert, ein Führungsdraht und nachfolgend eine Schleuse bis in die Aorta 1 geschoben und schließlich die Hauptprothese durch Zurückziehen der Schleuse freigesetzt. Danach wird durch die linke arteria femoralis ein weiterer Führungsdraht 7 (Fig. 2) zur Aorta 1 geschoben, mit dessen Ende der kurze Schenkel der Hauptprothese 5 sondiert werden muß. Dieser Vorgang ist schwierig und oft zeitraubend. Danach wird linksseitig die Verlängerung 6 mittels des weiteren Führungsdrahtes so plaziert, daß sie die Hauptprothese 5 mit der zur Haupt- prothese kontralateralen Beckenarterie 4 verbindet.For minimally invasive surgical treatment of the abdominal aortic aneurysm, it is known to implant an endoprosthesis in the form of a coated stent, which relieves the aortic wall in the area of the aneurysm 2 (FIG. 1) from blood pressure and prevents its further expansion and tearing. This stent must protrude upwards and downwards beyond the area of the aneurysm 2, i.e. Start at the top in the unstretched area of aorta 1 and lead to both pelvic arteries 3, 4. The stent is usually composed of two parts, a main prosthesis 5 covering the aorta and the subsequent branch of a pelvic artery 3 and an extension 6 covering the branch of the other pelvic artery 4. When inserting is first on one side, for. B. right, punctured the femoral artery, a guide wire and then a lock pushed into the aorta 1 and finally released the main prosthesis by pulling back the lock. Then a further guide wire 7 (FIG. 2) is pushed through the left femoral artery to the aorta 1, with the end of which the short leg of the main prosthesis 5 must be probed. This process is difficult and often time consuming. The extension 6 is then placed on the left side by means of the additional guide wire so that it connects the main prosthesis 5 with the pelvic artery 4 that is contralateral to the main prosthesis.
Aufgabe der Erfindung ist es, eine Vorrichtung anzugeben, mit der sich die Verlängerung einfacher, schneller und sicherer einsetzen läßt.The object of the invention is to provide a device with which the extension can be used more easily, quickly and safely.
Diese Aufgabe wird durch eine Vorrichtung nach dem Hauptanspruch gelöst. Die Begriffe proximal und distal sollen hier auf den Patienten bezogen sein; demgemäß wird das vorangehende Ende des Führungsdrahtes als proximal bezeichnet.This object is achieved by a device according to the main claim. The terms proximal and distal are intended to refer to the patient here; accordingly, the leading end of the guidewire is said to be proximal.
In der ersten Position des Ausrichtgliedes ist der zweite Führungsdraht vom ersten um 20 bis 40 Grad abgespreizt. Dieser Zustand stellt sich ein, nachdem das proximale Ende des ersten Führungsdrahts in die in der Aorta bereits eingesetzte Hauptprothese eingebracht wurde. Durch leichtes Zurückziehen der erfindungsgemäßen Vorrichtung erreicht man auf einfache Weise, daß das distale Ende des zweiten Führungsdrahtes durch das kurze Ende der Hauptprothese hindurchtritt und mit einem über die kontralaterale arteria femoralis eingebrachten, am Ende mit einer Drahtschlinge ("Lasso") versehenen weiteren Füh- rungsdraht erfaßt werden kann. Danach kann die Verlängerung längs dieses Führungsdrahtes eingeschoben werden. In der ersten Position kann die erfindungsgemäße Vorrichtung auch von außen durch ein Katheterrohr in die Aorta eingeschoben werden, wobei der Katheter die parallele Führung beider Drähte be- wirkt.In the first position of the alignment member, the second guide wire is spread apart from the first by 20 to 40 degrees. This condition occurs after the proximal end of the first guidewire has been inserted into the main prosthesis already inserted in the aorta. By slightly withdrawing the device according to the invention, it is easily achieved that the distal end of the second guide wire passes through the short end of the main prosthesis and is provided with a further guide which is inserted via the contralateral arteria femoralis and provided at the end with a wire loop ("lasso"). guidewire can be detected. The extension can then be inserted along this guide wire. In the first position, the device according to the invention can also be inserted from the outside into the aorta through a catheter tube, the catheter effecting the parallel guidance of both wires.
In der zweiten Position des Ausrichtgliedes sind erster und zweiter Führungsdraht annähernd parallel. In dieser Lage zueinander können sie durch die arteriae iliaca und femoralis aus dem Bereich des Aortenaneurysmas zurückgezogen werden.In the second position of the alignment member, the first and second guide wires are approximately parallel. In this position, they can be withdrawn from the area of the aortic aneurysm through the iliac artery and femoral artery.
Material und Durchmesser der beiden verbundenen Führungsdrähte entsprechen dem nach dem oben beschriebenen Stand der Technik Üblichen.The material and diameter of the two connected guide wires correspond to those customary according to the prior art described above.
Die Befestigung des zweiten am ersten Führungsdraht kann durch Laserschweißen erfolgen.The second can be attached to the first guide wire by laser welding.
Vorteilhaft sind die Enden der Führungsdrähte in einem Bogen von 90 bis 210 Grad mit einem Radius von 2 bis 20 mm gekrümmt. Dadurch lassen sich Gefäßläsionen beim Einschieben vermeiden.The ends of the guide wires are advantageously curved in an arc of 90 to 210 degrees with a radius of 2 to 20 mm. This avoids vascular lesions when inserted.
In einer anderen vorteilhaften Ausführungsform ist das als Ausrichtglied dienende Katheterrohr am proximalen Ende geschlossen und mit einer kegelförmigen abgerundeten Spitze versehen. In diesem Falle sind die proximalen Enden der Führungsdrähte nicht gebogen.In another advantageous embodiment, this is as Alignment catheter tube closed at the proximal end and provided with a tapered rounded tip. In this case, the proximal ends of the guide wires are not bent.
Durch Anbringen eines hamostatischen Ventils am distalen Ende des Katheterrohres kann unnötiger Blutverlust vermieden werden.By attaching a hamostatic valve to the distal end of the catheter tube, unnecessary blood loss can be avoided.
Während nach dem bekannten Verfahren das Sondieren der Hauptprothese und das Einsetzen der Verlängerung bis zu 30 min dauern kann, ist mit der neuen Vorrichtung eine Verkürzung dieses Zeitraums auf 5 min möglich.While, according to the known method, the probing of the main prosthesis and the insertion of the extension can take up to 30 minutes, this time can be reduced to 5 minutes with the new device.
Die Erfindung wird anhand von Zeichnungen beispielhaft weiter erläutert. Es zeigen:The invention is further illustrated by way of example with reference to drawings. Show it:
Fig. 1 eine Darstellung der Umgebung des Aneurysmas mit der eingesetzten zweiteiligen Endoprothese,1 shows the surroundings of the aneurysm with the two-part endoprosthesis used,
Fig. 2 das Sondieren nach dem Stand der Technik,2 probing according to the prior art,
Fig. 3 eine erfindungsgemäße Vorrichtung nach Anspruch 2 in der ersten Position des Ausrichtglieds;3 shows a device according to the invention as claimed in claim 2 in the first position of the alignment member;
Fig. 4 eine erfindungsgemäße Vorrichtung nach Anspruch 2 in der zweiten Position des Ausrichtglieds;4 shows a device according to the invention as claimed in claim 2 in the second position of the alignment member;
Fig. 5 eine erfindungsgemäße Vorrichtung nach Anspruch 3 in der ersten Position des Ausrichtglieds;5 shows a device according to the invention as claimed in claim 3 in the first position of the alignment member;
Fig. 6 eine erfindungsgemäße Vorrichtung nach Anspruch 3 in der zweiten Position des Ausrichtglieds;6 shows a device according to the invention according to claim 3 in the second position of the alignment member;
Fig. 7 die in Fig. 3 gezeigte Vorrichtung im Operationsgebiet;7 shows the device shown in FIG. 3 in the operating area;
Fig. 8 diese Vorrichtung in der zweiten Position des Ausrichtgliedes im Operationsgebiet;Fig. 8 this device in the second position of the Alignment member in the operating area;
Fig. 9 eine erfindungsgemäße Vorrichtung nach Anspruch 5 in der zweiten Position des Ausrichtglieds;9 shows a device according to the invention as claimed in claim 5 in the second position of the alignment member;
Fig.10 ein vergrößertes Detail von Fig. 9 im Schnitt.10 shows an enlarged detail of FIG. 9 in section.
Der erste Führungsdraht 11 der in Fig. 3 gezeigten Vorrichtung nach Anspruch 2 ist bevorzugt etwa 130 bis 280 cm lang. Am proximalen, d.h, beim Einschieben vorangehenden Ende 12 weist er eine Krümmung auf. Ein bevorzugt etwa 20 bis 50 cm langer zweiter Führungsdraht 13 ist mit seinem proximalen Ende am Draht 11 so befestigt, daß er mit diesem einen Winkel von 20 bis 40 Grad bildet. Der Befestigungspunkt 14 ist etwa 10 bis 40 cm vom proximalen Ende 12 des ersten Führungsdrahtes entfernt. Eine an einem Zugdraht 15 befindliche Drahtschlinge 16 umschlingt den Draht 11 proximal zum Befestigungspunkt. Die Drahtschlinge hat bevorzugt einen Durchmesser von 5 bis 10 mm. Der Zugdraht 15 ist so lang, daß sein distales Ende für den Operateur zugänglich bleibt.The first guide wire 11 of the device shown in FIG. 3 according to claim 2 is preferably about 130 to 280 cm long. It has a curvature at the proximal end 12, i.e. the end 12 preceding when inserted. A preferably approximately 20 to 50 cm long second guide wire 13 is fastened with its proximal end to the wire 11 in such a way that it forms an angle of 20 to 40 degrees with the latter. The attachment point 14 is about 10 to 40 cm from the proximal end 12 of the first guidewire. A wire loop 16 located on a pull wire 15 wraps around the wire 11 proximal to the attachment point. The wire loop preferably has a diameter of 5 to 10 mm. The pull wire 15 is so long that its distal end remains accessible to the surgeon.
Fig. 4 zeigt die Vorrichtung nach Anspruch 2 in der zweiten Position der als Ausrichtglied wirkenden Drahtschlinge 16. Diese befindet sich nun distal zum Befestigungspunkt 14, umschlingt beide Führungsdrähte in der Nähe des distalen Endes 17 des zweiten Führungsdrahtes 13 und hält sie in annähernd paralleler Ausrichtung. In dieser Position läßt sich die Vorrichtung ohne Schwierigkeit aus der arteria femoralis zurück- ziehen.4 shows the device according to claim 2 in the second position of the wire loop 16 acting as an alignment member. This is now distal to the attachment point 14, wraps around both guide wires in the vicinity of the distal end 17 of the second guide wire 13 and holds them in an approximately parallel orientation . In this position, the device can be withdrawn from the femoral artery without difficulty.
In Fig. 5 ist eine Vorrichtung nach Anspruch 3 mit dem Ausrichtglied in der ersten Position gezeigt. Als Ausrichtglied wirkt hier ein Katheterrohr 18, das seitlich eine Öffnung 19 aufweist, durch die der zweite Führungsdraht 13 spannungsfrei hindurchtreten kann. Das Katheterrohr 18 ist so lang, daß sein distales Ende auch nach dem Einschieben bis in die Aorta zugänglich bleibt. Die Öffnung 19 ist bevorzugt etwa 5 bis 20 cm vom proximalen Ende des Katheterrohres entfernt.5 shows a device according to claim 3 with the alignment member in the first position. A catheter tube 18, which has an opening 19 on the side through which the second guide wire 13 can pass without tension, acts as an alignment member. The catheter tube 18 is so long that its distal end remains accessible even after insertion into the aorta. The opening 19 is preferably about 5 to 20 cm from the proximal end of the catheter tube.
Fig. 6 stellt die gleiche Vorrichtung in der zweiten Position des Katheterrohres 18 dar. Das Katheterrohr 18 ist nun relativ zu den Führungsdrähten 11, 13 zurückgezogen, sodaß diese in seinem Inneren in annähernd paralleler Ausrichtung hält. In dieser Position läßt sich die Vorrichtung ohne Schwierigkeit aus der arteria femoralis zurückziehen.Fig. 6 shows the same device in the second position of the catheter tube 18. The catheter tube 18 is now retracted relative to the guide wires 11, 13, so that it holds in its interior in an approximately parallel orientation. In this position the device can be withdrawn from the femoral artery without difficulty.
In Fig. 7 ist die Vorrichtung gemäß Anspruch 2 in der ersten Position der am Zugdraht 15 befestigten Drahtschlinge 16 nach Einschieben in die Bauchaorta 1 und leichtem Zurückziehen gezeigt. Der zweite Führungsdraht 13 ist vom ersten 11 abgespreizt und tritt mit seinem distalen Ende aus der Haupt- prothese aus. Dieses Ende kann nun leicht mit einem Lasso 20 erfaßt werden, an dem sich schließlich die Verlagerung einschieben und sicher in der Hauptprothese 5 und der Beckenarterie 4 plazieren läßt.7 shows the device according to claim 2 in the first position of the wire loop 16 fastened to the puller wire 15 after insertion into the abdominal aorta 1 and slight retraction. The second guide wire 13 is spread apart from the first 11 and emerges from the main prosthesis with its distal end. This end can now be easily grasped with a lasso 20, on which the displacement can finally be inserted and placed securely in the main prosthesis 5 and the pelvic artery 4.
Fig. 8 zeigt die Vorrichtung gemäß Anspruch 2 in der zweiten Position der Drahtschlinge 16. Nach dem Einsetzen der Verlängerung 6 wurde das Lasso 20 vom zweiten Führungsdraht 13 gelöst, der Führungsdraht 11 etwas weiter eingeschoben und die Drahtschlinge 16 mittels des Zugdrahts 15 über den Befesti- gungspunkt 14 nach unten gezogen. Dadurch liegen erster und zweiter Führungsdraht annähernd parallel und können leicht durch die arteria femoralis herausgezogen werden.8 shows the device according to claim 2 in the second position of the wire loop 16. After the extension 6 has been inserted, the lasso 20 has been detached from the second guide wire 13, the guide wire 11 has been inserted somewhat further and the wire loop 16 has been pulled over the fastening by means of the pull wire 15 - Junction 14 pulled down. As a result, the first and second guidewires are approximately parallel and can easily be pulled out through the arteria femoralis.
Analog zu Fig. 7 und 8 kann auch die Vorrrichtung gemäß An- spruch 3 angewendet werden.Analogously to FIGS. 7 and 8, the device according to claim 3 can also be used.
Fig. 9 zeigt eine weitere Ausführungsform der erfindungsgemäßen Vorrichtung. Das Katheterrohr 18 ist hier am proximalen Ende mit einer kegelförmig abgerundeten Spitze 21 geschlossen. Das proximale Ende des ersten Führungsdrahtes ist dabei nicht gebogen.9 shows a further embodiment of the device according to the invention. The catheter tube 18 is closed here at the proximal end with a conically rounded tip 21. The proximal end of the first guidewire is not bent.
In Fig. 10 ist der Bereich um die Austrittsöffnung 19 der in Fig. 9 dargestellten Vorrichtung vergrößert im Schnitt gezeigt. Man erkennt den ersten Führungsdraht 11 und den im oberen Bereich darüber liegenden zweiten Führungsdraht 13. Um eine sichere Führung der Drähte zu gewährleisten, ist noch eine Trennwand 22 im Katheterrohr sowie ein Ausleitungsstopfen 23 für das distale Ende 17 des zweiten Führungsdrahtes vorgesehen. In FIG. 10, the area around the outlet opening 19 is the one in FIG Fig. 9 shown device shown enlarged in section. The first guidewire 11 and the second guidewire 13 lying in the upper area can be seen. To ensure reliable guiding of the wires, a partition 22 is also provided in the catheter tube and an outlet plug 23 for the distal end 17 of the second guidewire.
Vorrichtung zum Einsetzen einer Aorten-EndoprotheseDevice for inserting an aortic endoprosthesis
BezugszeichenlisteReference list
Aorta Aneurysma rechte Beckenarterie linke Beckenarterie Hauptprothese Verlängerung der Prothese Sonde zum Einführen der Verlängerung erster Führungsdraht proximales Ende des ersten Führungsdrahtes zweiter Führungsdraht Befestigungspunkt Zugdraht Drahtschlinge distales Ende des zweiten Führungsdrahtes Katheterrohr Öffnung des Katheterrohres Lasso kegelförmiges Ende Trennwand im Katheterrohr Ausleitungsstopfen Aorta aneurysm right pelvic artery left pelvic artery main prosthesis Extension of the prosthesis Probe for inserting the extension of the first guide wire proximal end of the first guide wire second guide wire Attachment point pulling wire Wire loop distal end of the second guide wire Catheter tube Opening of the catheter tube Lasso conical end Partition in the catheter tube Drainage plug

Claims

Vorrichtung zum Einsetzen einer Aorten-EndoprotheseDevice for inserting an aortic endoprosthesis
AnsprücheExpectations
Vorrichtung zum Einsetzen einer Gefäß-Endoprothese in ein Bauchaortenaneurysma, umfassendA device for inserting a vascular endoprosthesis into an abdominal aortic aneurysm, comprising
einen ersten geraden elastischen Führungsdraht,a first straight elastic guide wire,
einen zweiten geraden 10 bis 30 cm langen elastischen Führungsdraht, der mit seinem proximalen Ende so am ersten Führungsdraht befestigt ist, daß er mit dessen proximalem Abschnitt in spannungsfreiem Zustand einen Winkel von 20 bis 40 Grad bildet und der Befestigungspunkt 20 bis 40 cm vom proximalen Ende des ersten Führungsdrahtes entfernt ist,a second straight 10 to 30 cm long elastic guidewire, which is attached with its proximal end to the first guidewire in such a way that it forms an angle of 20 to 40 degrees with the proximal section in a tension-free state and the attachment point 20 to 40 cm from the proximal end the first guide wire is removed,
ein längs des ersten Führungsdrahtes verschiebbares Ausrichtglied, welches eine erste Position, in der beide Führungsdrähte spannungsfrei sind, und eine zweite Position, in der beide Führungsdrähte annähernd parallel zueinander ausgerichtet sind, einnehmen kann.an alignment member which is displaceable along the first guide wire and which can assume a first position in which both guide wires are free of tension and a second position in which both guide wires are aligned approximately parallel to one another.
2. Vorrichtung nach Anspruch 1, wobei das Ausrichtglied aus einem Zugdraht und einer Drahtschlinge besteht, die in der ersten Position den ersten Führungsdraht proximal und in der zweiten Position beide Führungsdrähte distal zum Befestigungspunkt umschlingt.2. The apparatus of claim 1, wherein the alignment member consists of a puller wire and a wire loop, which in the first position wraps the first guide wire proximally and in the second position both guide wires distal to the attachment point.
3. Vorrichtung nach Anspruch 1, wobei das Ausrichtglied ein den ersten Führungsdraht umgebendes Katheterrohr ist, das eine den Durchtritt des zweiten Führungsdrahts gestattende seitliche Öffnung aufweist.3. The apparatus of claim 1, wherein the alignment member is a catheter tube surrounding the first guidewire and having a side opening allowing passage of the second guidewire.
4. Vorrichtung nach einem der vorangehenden Ansprüche, d a d u r c h g e k e n n z e i c h n e t, daß die Enden der Führungsdrähte mit einem Radius von 5 bis 20 mm um 90 bis 210 Grad gekrümmt sind.4. Device according to one of the preceding claims, characterized in that the ends of the guide wires with a radius of 5 to 20 mm by 90 to 210 degrees are curved.
5. Vorrichtung nach Anspruch 3, wobei das Katheterrohr am proximalen Ende geschlossen und zu einer kegelförmigen abgerundeten Spitze ausgebildet ist.5. The device according to claim 3, wherein the catheter tube is closed at the proximal end and formed into a conical rounded tip.
6. Vorrichtung nach Anspruch 3 bis 5, wobei der erste Führungsdraht durch ein am distalen Ende des Katheterrohrs angebrachtes hämostatisches Ventil geführt wird. 6. The device of claims 3 to 5, wherein the first guide wire is passed through a hemostatic valve attached to the distal end of the catheter tube.
EP99959407A 1998-12-16 1999-12-11 Device for placing an aortic endoprosthesis Withdrawn EP1139916A1 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
DE29822381U 1998-12-16
DE29822381U DE29822381U1 (en) 1998-12-16 1998-12-16 Device for inserting an aortic endoprosthesis
PCT/EP1999/009827 WO2000035377A1 (en) 1998-12-16 1999-12-11 Device for placing an aortic endoprosthesis

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EP1139916A1 true EP1139916A1 (en) 2001-10-10

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US (1) US20010049534A1 (en)
EP (1) EP1139916A1 (en)
AU (1) AU1658500A (en)
CA (1) CA2355665A1 (en)
DE (1) DE29822381U1 (en)
WO (1) WO2000035377A1 (en)

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Also Published As

Publication number Publication date
AU1658500A (en) 2000-07-03
DE29822381U1 (en) 1999-03-18
WO2000035377A1 (en) 2000-06-22
US20010049534A1 (en) 2001-12-06
CA2355665A1 (en) 2000-06-22

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