NL2005619C2 - Vessel cannulation device. - Google Patents

Vessel cannulation device. Download PDF

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Publication number
NL2005619C2
NL2005619C2 NL2005619A NL2005619A NL2005619C2 NL 2005619 C2 NL2005619 C2 NL 2005619C2 NL 2005619 A NL2005619 A NL 2005619A NL 2005619 A NL2005619 A NL 2005619A NL 2005619 C2 NL2005619 C2 NL 2005619C2
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NL
Netherlands
Prior art keywords
cannula
needle
vessel
axial direction
tube
Prior art date
Application number
NL2005619A
Other languages
Dutch (nl)
Inventor
Eduard Berend Houwen
Original Assignee
Univ Groningen
Groningen Acad Ziekenhuis
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 Univ Groningen, Groningen Acad Ziekenhuis filed Critical Univ Groningen
Priority to NL2005619A priority Critical patent/NL2005619C2/en
Priority to PCT/NL2011/050717 priority patent/WO2012060694A1/en
Application granted granted Critical
Publication of NL2005619C2 publication Critical patent/NL2005619C2/en

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Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES 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
    • A61M25/00Catheters; Hollow probes
    • A61M25/0097Catheters; Hollow probes characterised by the hub
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B17/00Surgical instruments, devices or methods, e.g. tourniquets
    • A61B17/12Surgical instruments, devices or methods, e.g. tourniquets for ligaturing or otherwise compressing tubular parts of the body, e.g. blood vessels, umbilical cord
    • A61B17/122Clamps or clips, e.g. for the umbilical cord
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES 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
    • A61M25/00Catheters; Hollow probes
    • A61M25/01Introducing, guiding, advancing, emplacing or holding catheters
    • A61M25/02Holding devices, e.g. on the body
    • A61M25/04Holding devices, e.g. on the body in the body, e.g. expansible

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  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Engineering & Computer Science (AREA)
  • Biomedical Technology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • General Health & Medical Sciences (AREA)
  • Anesthesiology (AREA)
  • Hematology (AREA)
  • Pulmonology (AREA)
  • Biophysics (AREA)
  • Surgery (AREA)
  • Reproductive Health (AREA)
  • Vascular Medicine (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Medical Informatics (AREA)
  • Molecular Biology (AREA)
  • Media Introduction/Drainage Providing Device (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)

Abstract

A vessel cannulation device comprises a cannula (E), a needle (F), a fluid connection (L), a surrounding body (P) and a clamp (G), interconnected with each other by means of a main body (C) of the device (Z). The needle is slidably received in the cannula. The fluid connection is arranged for providing fluid communication between the cannula and a tube (B). In its puncturing position the needle is preventing fluid communication between the cannula and said tube. In its retracted position the needle is allowing said fluid communication. The surrounding body is partially surrounding the cannula in circumferential direction relative to the cannula with an inter-space (I) between the surrounding body and the cannula. The surrounding body has an interruption (R) in its surrounding the cannula. The clamp is arranged for squeezingly clamping the vessel and thereby closing off the vessel.

Description

P93152NL00
Title: Vessel cannulation device.
FIELD AND BACKGROUND OF THE INVENTION:
The invention relates to a vessel cannulation device.
When perfusion of tissue or an organ is in order, the afferent or efferent vessel, artery or vein (herein referred to as “vessel”) is connected to 5 tubing or a syringe. Connecting the vessel is usually done in two ways. Either the vessel is cut and a hollow cannula is inserted in the vessel, or the vessel is not severed but punctured from the side and a cannula is slid inside. The cannula is then fixed to the vessel by winding a piece of suture wire around the vessel at the point where the cannula is inside and the suture wire is tied into 10 a knot. Some cannula systems comprise a solid needle in a hollow cannula and allow the solid needle to be retracted after insertion of the cannula into the vessel: the fluid connection is then achieved. For cannulation specifically where severing of the vessel is not acceptable, there are also tools that comprise a half open puncture needle on an angled handle that, once inserted 15 through the vessel wall allow the insertion of a cannula through the half open needle after which the tool can be removed and the cannula remains. Again, the cannula is fixed to the vessel with a length of suture wire wound around the vessel and tied into a knot. These procedures require the use of at least two hands (mostly three), a separate disposable in the form of the suture wire, 20 access to all around the vessel (for winding the suture wire) and extra tools that need to be disposed of.
SUMMARY OF THE INVENTION:
It is an object of the invention to simplify the procedure of vessel 25 cannulation.
For that purpose, the invention provides a vessel cannulation device comprising a cannula, a needle, a fluid connection, a surrounding body and a 2 clamp, interconnected with each other by means of a main body of the device, wherein: - the needle has a front needle end and a rear needle end, the front needle end being arranged for puncturing a vessel; 5 - an axial direction of the device is defined to be parallel to the axial direction of the needle, a forward axial direction of the device is defined by the axial direction of the needle pointing from the rear needle end towards the front needle end, and a backward axial direction of the device is defined to be opposite to said forward axial direction; 10 - the cannula has a front cannula end pointing in said forward axial direction; - the needle is coaxially received in the cannula in such manner that the needle is axially slidable back and forth within and relative to the cannula between vessel puncturing positions of the needle and retracted positions of 15 the needle, in which vessel puncturing positions the front needle end projects from the front cannula end for puncturing the vessel, and in which retracted positions the needle is retracted, relative to said vessel puncturing positions, within the cannula in said backward axial direction; - the fluid connection is arranged for providing fluid communication 20 between the cannula and a tube, when the tube is in fluid communication with said fluid connection; - in at least one of said puncturing positions the needle is preventing fluid communication via said fluid connection between the cannula and said tube, when the tube is in fluid communication with said fluid connection; 25 - in at least one of said retracted positions the needle is allowing fluid communication via said fluid connection between the cannula and said tube, when the tube is in fluid communication with said fluid connection; - said surrounding body is partially surrounding the cannula, over a range in the axial direction of the device, in circumferential direction relative 3 to the cannula with an inter-space between the surrounding body and the cannula; - said surrounding body has a front edge in said forward axial direction and has an interruption in its surrounding the cannula, which 5 interruption is extending from the front edge in said backward axial direction over at least a subrange of said range in the axial direction of the device; and - the clamp is arranged for squeezingly clamping the vessel and thereby closing off the vessel.
Such a vessel cannulation device according to the invention requires 10 the use of only two hands and two pairs of tweezers. No extra disposables are required.
Specific embodiments of the invention are set forth in the dependent claims.
In a preferable embodiment, said inter-space, as seen in radial 15 direction relative to the cannula, is narrowing in said backward axial direction of the device.
In another preferable embodiment, said interruption, as seen in circumferential direction relative to the cannula, is narrowing in said backward axial direction of the device.
20 Furthermore, the invention may be embodied in an assembly of: - a first vessel cannulation device according to the invention; - a second vessel cannulation device according to the invention; and - an interconnecting tube; wherein the interconnecting tube is in fluid communication both 25 with the fluid connection of the first vessel cannulation device and with the fluid connection of the second vessel cannulation device for providing fluid communication between the cannula of the first vessel cannulation device and the cannula of the second vessel cannulation device.
These and other aspects of the invention will be apparent from and 30 elucidated with reference to the embodiment described hereinafter.
4 BRIEF DESCRIPTION OF THE DRAWINGS:
Further details, aspects and embodiments of the invention will be described, by way of non-limiting example only, with reference to the 5 schematic drawing, in which:
Fig. 1 shows, in perspective view, an example of an embodiment of a vessel cannulation device according to the invention;
Fig. 2 shows the device of Fig. 1 in longitudinal section;
Fig. 3 shows the device of Fig. 1 in side view; 10 Fig. 4 shows the device of Fig. 1 in another side view being opposite to that of Fig. 3;
Fig. 5 shows the device of Fig. 1 in front view; and
Fig. 6 shows the device of Fig. 1 in bottom view.
15 DETAILED DESCRIPTION:
Figs. 1-6 show a vessel cannulation device Z according to the invention. The device Z comprises a cannula E, a needle F, a fluid connection L (see Fig. 2), a surrounding body P and a clamp G, interconnected with each other by means of a main body C of the device Z. It is remarked that Figs. 1-6 20 do not show a vessel that may be connected to the device Z.
The main body C may be connected to any perfusion or syringe system via tube B. The tube B may be connected or connectable to the main body C or may be an integral part of the main body C. The main body C comprises grooves D on opposite sides of the body, that allow nesting of the 25 points of tweezers for firm grip, or any other means of holding the device.
The vessel puncturing section of the device consists of a front needle end of a solid needle F. Needle F can also be fitted with a groove on the underside of the needle to allow transportation of fluid from the puncture side out the vessel, where the outflow of fluid can then be seen as a confirmation of 30 successful puncture. Solid needle F runs through cannula E that can be either 5 a separate hollow tube or an integral part of the main body C. Cannula E opens halfway to access to tube B via space L. Solid needle F runs through cannula E and through rubber plug J in the space of main body C. Plug J seals the space around needle F so that no fluid can flow pass J out of the main body 5 C, even when needle F is slid back and forth through cannula E. At its rear needle end, needle F ends in cone A. When cone A is squeezed by tweezers it will slide in the backward axial direction of the device, away from main body C and retract needle F to allow fluid passage through E into space L and tube B.
Vessel clamp G attached to the bottom of main body C allows the 10 clamping of the vessel after puncture. Clamp G comprises space narrowing toward its closed end. Grooves H in the space of clamp G angle toward the puncture front of the body and toward the narrowing of the space. These grooves allow pulling tight of the vessel in the backward axial direction of the device. At release of tension, the vessel will slide over the grooves toward the 15 narrower part of the clamp G and grip itself tight.
The surrounding body P is partially surrounding the cannula E, over a range in the axial direction of the device Z, in circumferential direction relative to the cannula E with an inter-space I between the surrounding body P and the cannula E, wherein a dimension, measured in radial direction 20 relative to the cannula E, of said inter-space I is narrowing in said backward axial direction of the device Z. The surrounding body P has a front edge Q in said forward axial direction and an interruption R (best seen in Fig. 1) in surrounding the cannula, which interruption R is extending from the front edge Q in said backward axial direction over at least a subrange of said range 25 in the axial direction of the device Z. Hence, due to the interruption R, the inter-space I is open at the bottom towards clamp G. This inter-space I will force the vessel wall into the narrowing space when pulled over area K (see Fig. 6) towards and through the clamp G and thus form a liquid tight seal.
The configuration of the device Z can be altered from the depicted 30 longitudinal formation, to a shorter formation, with the tubing B at any angle 6 from the cannula E for cannulation the vessels that are deeply situated inside the operation site. The length of the needle F and the cannula E can be altered to suit the elasticity of the vessel under consideration. The diameters and sizes of needle F, cannula E, main body C and tubing B can also be adjusted to fit 5 any diameter, stiffness, lumen size or available excised free vessel length.
To allow puncturing of a vessel without severing the vessel, either for influx or efflux of fluid, the vessel is first dissected from surrounding tissue allowing free access to the site. Next the vessel is pulled tight with a pair of tweezers, distal to the puncture site. The main body C of the device Z is 10 gripped firmly in one of three opposing grooves D, and needle F is slided through the vessel wall into the lumen of the vessel. The needle F is slid into the vessel until the vessel tissue is in the inter-space I. Then the tweezers holding the distal part of the vessel, pulls and slides the vessel into the space H of clamp G. The cannula E is moved deeper into the vessel by the relative 15 movement of the device Z and the tweezers holding the vessel. The connection is now made. The tweezers holding the vessel can now open en squeeze the cone A (or any other means that slides back needle F) so that the needle F slides backward and opens space L via the pointy end of needle F through cannula E. Fluid can now flow from or toward the vessel and tube B.
20 The vessel cannulation device according to the invention can be used to cannulate veins, arteries or any duct in the body. The described model is suitable for vessels 2-3 mm thick, but any up or downscaling of the system is possible. The connecting vessel can either be left intact, connected on both sides, or severed distally from the puncture side, as long as enough vessel is 25 distally available for grabbing by tweezers and attachment to the clamp system. Envisioned applications are, but not limited by, organ or tissue perfusion, isolated or in situ, drug administration, tissue or organ washing, (continuous) fluid sampling or (flow, temperature, pressure or constituent) measurement, in situ perfusion rerouting and dye injection. Thus the device 30 according to the invention can be used in organ preservation and/or medication 7 (boosting), local medicine treatment and/or health and function marker measurement. Also envisioned is use in tissue and organ anatomy research, e.g. injections of dyes, isotopes, for the purpose of studying vessel anatomy in living tissue, or waxes or resins for the preservation of the internal vessel 5 structure for studying purposes.
When the vessel is left intact, the cannulation device can be removed, after which coagulation of the puncture site can take place and the anatomy is restored.

Claims (4)

1. Inrichting voor het aanbrengen van een canule in een vat, omvattende een canule (E), een naald (F), een fluïdumaansluiting (L), een omhullend lichaam (P) en een klem (G), die met elkaar verbonden zijn door middel van een hoofdlichaam (C) van de inrichting (Z), waarbij: 5. de naald (F) een voorste naalduiteinde en een achterste naalduiteinde heeft, waarbij het voorste naalduiteinde is ingericht om in een vat te prikken; - een axiale richting van de inrichting (Z) gedefinieerd is als zijnde parallel aan de axiale richting van de naald, een voorwaartse axiale richting van de inrichting gedefinieerd is door de axiale richting van de naald die gericht is 10 van het achterste naalduiteinde naar het voorste naalduiteinde, en een achterwaartse axiale richting van de inrichting gedefinieerd is als zijnde tegengesteld aan genoemde voorwaartse axiale richting; - de canule (E) een voorste canuleuiteinde gericht in genoemde voorwaartse axiale richting heeft; 15. de naald (F) coaxiaal opgenomen is in de canule op zodanige wijze dat de naald axiaal heen en weer verschuifbaar is in en ten opzichte van de canule tussen vatprikposities van de naald en teruggetrokken posities van de naald, in welke vatprikposities het voorste naalduiteinde uit het voorste canuleuiteinde steekt voor het prikken in het vat, en in welke teruggetrokken 20 posities de naald teruggetrokken is, ten opzichte van genoemde vatprikposities, in de canule in genoemde achterwaartse axiale richting; - de fluïdumaansluiting (L) is ingericht voor het verschaffen van fluïdumcommunicatie tussen de canule en een buis (B), wanneer de buis in fluïdumcommunicatie is met genoemde fluïdumaansluiting; 25. in tenminste één van genoemde vatprikposities de naald fluïdumcommunicatie verhindert via genoemde fluïdumaansluiting tussen de canule en genoemde buis, wanneer de buis in fluïdumcommunicatie is met genoemde fluïdumaansluiting; - in tenminste één van genoemde teruggetrokken posities de naald fluïdumcommunicatie toestaat via genoemde fluïdumaansluiting tussen de 5 canule en genoemde buis, wanneer de buis in fluïdumcommunicatie is met genoemde fluïdumaansluiting; - genoemd omhullend lichaam (P) deels de canule omhult, over een bereik in de axiale richting van de inrichting, in omtreksrichting ten opzichte van de canule met een tussenruimte (I) tussen het omhullend lichaam en de canule; 10. genoemd omhullend lichaam (P) een voorste rand (Q) heeft in genoemde voorwaartse axiale richting en een onderbreking (R) heeft in zijn omhullen van de canule, welke onderbreking zich uitstrekt van de voorste rand in genoemde achterwaartse axiale richting over tenminste een deelbereik van genoemd bereik in de axiale richting van de inrichting; en 15 - de klem (G) is ingericht voor het samenknijpend klemmen van het vat en daardoor afsluiten van het vat.Device for inserting a cannula into a vessel, comprising a cannula (E), a needle (F), a fluid connection (L), an envelope body (P) and a clamp (G) connected to each other by means of a main body (C) of the device (Z), wherein: 5. the needle (F) has a front needle-tip end and a rear needle-tip end, the front needle-tip end adapted to puncture into a vessel; - an axial direction of the device (Z) is defined as being parallel to the axial direction of the needle, a forward axial direction of the device is defined by the axial direction of the needle directed from the posterior needle end to the anterior needle end end, and a rearward axial direction of the device is defined as being opposite to said forward axial direction; - the cannula (E) has a front cannula end directed in said forward axial direction; 15. the needle (F) is coaxially received in the cannula in such a manner that the needle is axially reciprocally slidable in and with respect to the cannula between vessel needle positions and retracted positions of the needle, in which vessel needle positions the leading needle end protrudes from the anterior cannula end for puncturing into the vessel, and in which retracted positions the needle is retracted, relative to said vessel piercing positions, into the cannula in said rear axial direction; - the fluid connection (L) is adapted to provide fluid communication between the cannula and a tube (B) when the tube is in fluid communication with said fluid connection; 25. in at least one of said vessel puncture positions, the needle prevents fluid communication via said fluid connection between the cannula and said tube when the tube is in fluid communication with said fluid connection; in at least one of said retracted positions the needle allows fluid communication via said fluid connection between the cannula and said tube, when the tube is in fluid communication with said fluid connection; - said enveloping body (P) partially encloses the cannula, over a range in the axial direction of the device, in circumferential direction with respect to the cannula with a gap (I) between the enveloping body and the cannula; 10. said enclosing body (P) has a front edge (Q) in said forward axial direction and has an interruption (R) in its envelope of the cannula, which interruption extends from the front edge in said rear axial direction over at least one partial range of said range in the axial direction of the device; and - the clamp (G) is arranged for pinching the vessel together and thereby closing the vessel. 2. Inrichting volgens conclusie 1, waarbij genoemde tussenruimte (I), gezien in radiale richting ten opzichte van de canule (E), zich vernauwt in 20 genoemde achterwaartse axiale richting van de inrichting (Z).2. Device according to claim 1, wherein said interspace (I), viewed in radial direction with respect to the cannula (E), narrows in said rear axial direction of the device (Z). 3. Inrichting volgens conclusie 1 of 2, waarbij genoemde onderbreking (R), gezien in omtreksrichting ten opzichte van de canule (E), zich vernauwt in genoemde achterwaartse axiale richting van de inrichting (Z). 25Device according to claim 1 or 2, wherein said interruption (R), viewed in the circumferential direction relative to the cannula (E), narrows in said rear axial direction of the device (Z). 25 4. Samenstel van: - een eerste inrichting (Z) volgens een der voorgaande conclusies; - een tweede inrichting (Z) volgens een der voorgaande conclusies; en - een onderling verbindende buis (B); waarbij de onderling verbindende buis in fluïdumcommunicatie is zowel met de fluïdumaansluiting (L) van de eerste inrichting als met de fluïdumaansluiting (L) van de tweede inrichting voor het verschaffen van fluïdumcommunicatie tussen de canule (E) van de eerste inrichting en de 5 canule (E) van de tweede inrichting.Assembly of: - a first device (Z) according to any one of the preceding claims; - a second device (Z) according to any one of the preceding claims; and - an interconnecting tube (B); the interconnecting tube being in fluid communication both with the fluid port (L) of the first device and with the fluid port (L) of the second device for providing fluid communication between the cannula (E) of the first device and the cannula ( E) of the second device.
NL2005619A 2010-11-03 2010-11-03 Vessel cannulation device. NL2005619C2 (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
NL2005619A NL2005619C2 (en) 2010-11-03 2010-11-03 Vessel cannulation device.
PCT/NL2011/050717 WO2012060694A1 (en) 2010-11-03 2011-10-20 Vessel cannulation device

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
NL2005619 2010-11-03
NL2005619A NL2005619C2 (en) 2010-11-03 2010-11-03 Vessel cannulation device.

Publications (1)

Publication Number Publication Date
NL2005619C2 true NL2005619C2 (en) 2012-05-07

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Application Number Title Priority Date Filing Date
NL2005619A NL2005619C2 (en) 2010-11-03 2010-11-03 Vessel cannulation device.

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NL (1) NL2005619C2 (en)
WO (1) WO2012060694A1 (en)

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4531937A (en) * 1983-01-24 1985-07-30 Pacesetter Systems, Inc. Introducer catheter apparatus and method of use
US5626607A (en) * 1995-04-03 1997-05-06 Heartport, Inc. Clamp assembly and method of use
US5928253A (en) * 1998-03-13 1999-07-27 Cardiothoracic Systems, Inc. Integrated cannula and vascular clamp assembly
KR101033106B1 (en) * 2005-10-11 2011-05-06 코비디엔 아게 Iv catheter with in-line valve and methods related thereto

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