Advanced wound site management systems and methods

• US 7,198,631 B2
• Filed: 01/23/2003
• Issued: 04/03/2007
• Est. Priority Date: 09/01/2000
• Status: Expired due to Fees

• Current Assignee: Medtronic Angiolink, Inc. (Medtronic Plc)
• Original Assignee: Medtronic Angiolink, Inc. (Medtronic Plc)
• Inventors: Bollinger, Steve, Eliasen, Kenneth Arden, Kanner, Glenn, Tallarida, Steve J.
• Primary Examiner(s): Nguyen; Anhtuan T.
• Assistant Examiner(s): Erezo; Darwin P
• Application Number:
  US10/350,268
• Publication Number:
  US 20030109890A1
• Time in Patent Office: 1,531 Days
• Field of Search: 606/139, 606/151, 606/213, 606/157, 606/148
• US Class Current: 606/139
• CPC Class Codes: A61B 17/0057 Implements for plugging an opening in the wall of a hollow or tubular organ, e.g. for sealing a vessel puncture or closing a cardiac septal defect sutures A61B17/04; closing rectum or urethra near body surface A61F2/0009
• CPC Class Codes: A61B 17/064 Surgical staples, i.e. penetrating the tissue
• CPC Class Codes: A61B 17/0644 penetrating the tissue, deformable to closed position
• CPC Class Codes: A61B 17/068 Surgical staplers , e.g. containing multiple staples or clampsstaplers containing only one staple A61B17/10; magazines or containers for staples A61B17/105; for performing anastomosis A61B17/115; staplers in general B25C5/00
• CPC Class Codes: A61B 17/0684 having a forming anvil staying above the tissue during stapling
• CPC Class Codes: A61B 17/2909 Handles
• CPC Class Codes: A61B 2017/00637 for sealing trocar wounds through abdominal wall
• CPC Class Codes: A61B 2017/00668 the implement being a tack or a staple
• CPC Class Codes: A61B 2017/0641 having at least three legs as part of one single body
• CPC Class Codes: A61B 2017/2913 cams or guiding means
• CPC Class Codes: A61B 2017/292 connection of actuating rod to handle, e.g. ball end in recess
• CPC Class Codes: A61B 2090/062 penetration depth

Abstract

An introducer having a sheath, a guide rod, and at least two wire stabilization guides being elongated members, at least a portion of which extend from an end of the sheath. The portions of the wire stabilization guides include a retention device formed on the portion of the wire stabilization guides that extend from the end of the sheath. The retention device is adapted to selectively expand outwardly, stabilizing the sheath relative to a wound site. The guide rod may be provided with one or more blood marking lumen, having a distal port, for identifying the depth of insertion into an artery or vein based on the presence or absence of pressurized blood in the lumen.

Claims

1. A medical device, comprising:

a tubular sheath having two spaced apart wire stabilization guides, the stabilization guides each comprising elongated members having at least a portion thereof extending from an end of the sheath;

a retention device formed on the portion of each of the stabilization guides extending from the end of the sheath, the retention device configured to selectively expand outwardly from the stabilization guide in at least one direction;

a wire moveably disposed within at least a portion of one of the stabilizations guides, the wire being coupled to the stabilization guide, wherein movement of the wire in a first direction causes outward expansion of the retention device; and

a guide rod sized to fit within the tubular sheath and having two slots formed along its length, at least one slot releasably holding a respective one of said wire stabilization guides.

2. A medical device according to claim 1, the retention device comprising a slit on at least two sides of the stabilization guide, wherein movement of the wire in a proximal direction causes a portion of the stabilization guide about the slit to expand outwardly.

3. A medical device according to claim 1, the retention device comprising at least one notch section, wherein movement of the wire in a proximal direction causes a portion of the stabilization guide about the notch to expand outwardly.

4. A medical device according to claim 3, the retention device comprising at least two notch sections spaced about a perimeter of the stabilization guide, wherein movement of the wire in a proximal direction causes folds at the notch sections.

5. A medical device according to claim 1, the retention device comprising at least one filament attached to the stabilization guide, wherein movement of the wire in a proximal direction causes at least a portion of the filament to expand outwardly.

6. A medical device according to claim 5, the retention device further comprising a plurality of filaments attached to the stabilization guide, wherein movement of the wire in a proximal direction causes at least a portion of each of the plurality of filaments to expand outwardly.

7. A medical device according to claim 5, wherein the at least one filament is oriented off a longitudinal axis of the stabilization guide, and wherein movement of the wire in a proximal direction causing the filament to expand outwardly.

8. A medical device according to claim 1, the retention device being capable of securing the sheath to an arterial wall to prevent transverse movement of the sheath with respect to a wound site in the arterial wall.

9. A medical device according to claim 1, wherein the wire stabilization guides being disposed opposite one another on the sheath approximately 180 degrees apart.

10. A medical device according to claim 1, wherein the wire stabilization guides are capable of being placed into a wound site in an artery or vein such that the wire stabilization guides are transverse to a long axis of the artery or vein.

11. A medical device, comprising:

a tubular sheath having two spaced apart wire stabilization guides, the stabilization guides each comprising elongated members having at least a portion thereof extending from an end of the sheath;

the sheath further comprising a plurality of tear seams formed along at least a portion of the length thereof and wherein when the sheath is approximated to a wound site and a radial force is applied to the distal end of the sheath in a direction generally perpendicular to the central axis of the sheath, the tear seams are caused to tear increasing the diameter of the sheath,

a retention device formed on the portion of each of the stabilization guides extending from the end of the sheath, the retention device configured to selectively expand outwardly from the stabilization guide in at least one direction; and

a guide rod sized to fit within the tubular sheath and having two slots formed along its length, at least one slot releasably holding a respective one of said wire stabilization guides.