SI9800177A - Artificial vein - Google Patents
Artificial vein Download PDFInfo
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- SI9800177A SI9800177A SI9800177A SI9800177A SI9800177A SI 9800177 A SI9800177 A SI 9800177A SI 9800177 A SI9800177 A SI 9800177A SI 9800177 A SI9800177 A SI 9800177A SI 9800177 A SI9800177 A SI 9800177A
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES 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
- A61M1/00—Suction or pumping devices for medical purposes; Devices for carrying-off, for treatment of, or for carrying-over, body-liquids; Drainage systems
- A61M1/36—Other treatment of blood in a by-pass of the natural circulatory system, e.g. temperature adaptation, irradiation ; Extra-corporeal blood circuits
- A61M1/3621—Extra-corporeal blood circuits
- A61M1/3653—Interfaces between patient blood circulation and extra-corporal blood circuit
- A61M1/3655—Arterio-venous shunts or fistulae
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES 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
- A61M1/00—Suction or pumping devices for medical purposes; Devices for carrying-off, for treatment of, or for carrying-over, body-liquids; Drainage systems
- A61M1/14—Dialysis systems; Artificial kidneys; Blood oxygenators ; Reciprocating systems for treatment of body fluids, e.g. single needle systems for hemofiltration or pheresis
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- Health & Medical Sciences (AREA)
- Heart & Thoracic Surgery (AREA)
- Vascular Medicine (AREA)
- Biomedical Technology (AREA)
- Engineering & Computer Science (AREA)
- Anesthesiology (AREA)
- Cardiology (AREA)
- Hematology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- External Artificial Organs (AREA)
Abstract
Description
BUTUROVIČ-PONIKVAR Jadranka Ljubljana, SlovenijaBUTUROVIC-PONIKVAR Jadranka Ljubljana, Slovenia
Umetna žila (MPK: A 61 F 2/06)Artificial vein (MPK: A 61 F 2/06)
Predmet izuma je umetna žila, zlasti za trajno kratkostično povezavo arterije in vene (shunf), naprimer v roki, ciljno za ponavljajoče se priključevanje in odstranjevanje cevovodov za zvezo pacienta z dializnim aparatom.The subject of the invention is an artificial vein, in particular for the permanent short-circuiting of the artery and vein (shunf), for example in the hand, intended for the recurrent connection and removal of the patient's conduit for dialysis.
Umetna žila, njena vgraditev v pacienta za zgoraj navedeni namen in spremljajoči medicinski pojavi so nazorno opisani in slikovno predstavljeni v knjižnem delu iz leta 1995 v angl. jeziku z naslovom LONG-TERM HEMODYALISIS avtorjev N.K. Man et al. (vsi iz Pariza, Francija), izdajatelja Kluwer Academic Publishers, Dordrecht, Nizozemska, posebno v poglavju 3 z naslovom BLOOD ACCESS.The artificial vein, its incorporation into the patient for the above purpose and the accompanying medical phenomena are illustrated and illustrated in a 1995 book in English. language entitled LONG-TERM HEMODYALISIS by N.K. Man et al. (all from Paris, France), published by Kluwer Academic Publishers, Dordrecht, The Netherlands, especially in Chapter 3, entitled BLOOD ACCESS.
Gre za na primerno dolžino prirezano plastično cev kot metražni izdelek enotnega svetlega preseka, ki je iz krvnoprocesnih razlogov manjši od svetlega preseka arterije na mestu vgraditve in ne večji od svetlega preseka vene na mestu vgraditve.It is a cut length plastic tube as a single product of a single clear section, which for blood-process reasons is smaller than the clear cross-section of the artery at the site of implantation and not larger than the clear cross-section of the vein at the site of implantation.
Tokovno tehnično stanje v sklenjenem arterijsko-venskem žilnem sistemu pacienta z vgrajeno umetno žilo tu obravnavane vrste je pretežni del časa, t.j., ko pacient na dializni aparat ni priključen, in preostanek časa, t.j., ko je nanj priključen, vsakokrat drugačno.The current state of the art in a contracted arterial-venous vascular system of a patient with a built-in artificial vessel of the type discussed here is predominant in time, i.e., when the patient is not connected to the dialysis apparatus, and the rest of the time, i.e., when connected to it, is in each case different.
Računati je najmanj s tremi, na arterijo vezanimi, medsebojno neodvisnimi pragovnimi vrednostmi krvnega pretoka:At least three arterial-related, blood-independent thresholds for blood flow are counted:
(1) Z odvodom arterijske krvi v umetno žilo in po njej v veno preostali arterijski pretok ne sme pasti pod vrednost, ko bi bila preskrba s krvjo distalno od umetne žile ogrožena;(1) Removal of arterial blood into and through the artificial vein into the vein should not reduce the residual arterial flow when the supply of blood distal to the artificial vein would be compromised;
(2) Pretok arterijske krvi po umetni žili v veno mora biti v obeh stanjih, torej v stanju, ko pacient na dializni aparat ni priključen, in stanju, ko je nanj priključen, zadosten, da v njej ne pride do strjevanja krvi; in (3) Pretok arterijske krvi skozi dializni aparat mora zadoščati minimalnemu obratovalnemu pretoku za nemoteno delo dializnega aparata (ki je spet odvisen od procesnih lastnosti krvi).(2) The flow of arterial blood through an artificial vein into a vein must be in both conditions, ie in a condition when the patient is not connected to the dialysis apparatus and in a condition when it is connected to it, sufficient to prevent blood clotting in it; and (3) The flow of arterial blood through the dialysis apparatus must satisfy the minimum operating flow for the smooth operation of the dialysis apparatus (which again depends on the process properties of the blood).
Kritični, zato merodajni, pretočni člen v zgoraj navedeni tokovni shemi je igla.The critical, therefore relevant, flow member in the above flow chart is the needle.
Dejstvo je, da igla s svojo natočno omočeno prejekcijsko ploskvijo zavzame del svetlega preseka umetne žile. Da je v stanju, ko je na umetno žilo priključen dializni aparat, zadoščeno pragovni vrednosti pod (2), mora le-tej potemtakem zadostiti preostali pretočni presek umetne žile, t.j. presek med steno umetne žile in iglo.In fact, the needle, with its soaked wet projection surface, occupies part of the bright section of the artificial vein. In order for the dialysis apparatus to meet the threshold value below (2) when the dialysis apparatus is connected, the residual cross-section of the artificial vessel, i.e. the section between the wall of the artificial vein and the needle.
Ob zgornjih ugotovitvah postane samo po sebi očitno, da mora presek umetne žile iz stanja tehnike zadostiti kriterijema pod (2) in (3). Od tod sledi, da je v času, ko pacient ni priključen na dializni aparat, t.j. v pretežnem delu pacientovega življenja, svetli presek umetne žile predimenzioniran (s številnimi negativnimi posledicami za pacienta).With the above findings, it becomes apparent in itself that the cross-section of the artificial vein from the prior art must satisfy the criteria under (2) and (3). It follows that at a time when the patient is not connected to the dialysis machine, i.e. in the vast majority of the patient's life, the bright section of the artificial vein is oversized (with many negative consequences for the patient).
Ob zgornjem spoznanju si je izum zastavil za cilj, ustvariti umetno žilo, ki bo vsaj ublažila, če že ne odpravila, ugotovljeno pomanjkljivost, s katero mora živeti pacient, ki nosi umetno žilo iz stanja tehnike.In the foregoing, the invention is intended to create an artificial vein that will at least alleviate, if not eliminate, the identified deficiency with which a patient wearing an artificial vein of the prior art must live.
Navedeni cilj je po izumu dosežen z umetno žilo, ki je tako zasnovana, da ima osnovni, smotrno, a ne nujno, enoten svetli presek, v danem primeru takega, ki zadošča zgoraj navedenima kriterijama pod (2) in (3), in v bistvu kjerkoli na svoji dolžinski razsežnosti, smotrno na sredi, dušilno mesto, t.j. mesto reduciranega svetlega preseka, v danem primeru tako, ki zadošča zgoraj navedenemu kriteriju pod (2).The stated object of the invention is achieved by an artificial core designed to have a basic, expedient, but not necessarily uniform, cross-section, in the case of one which satisfies the above criteria in (2) and (3), and in essentially anywhere along its length dimension, expediently in the middle, a damping place, i the location of the reduced bright cross-section, if appropriate, which satisfies the above criterion under (2).
Razume se, da mesto reduciranega svetlega preseka umetne žile po izumu ne povzroča strujnih neregularnosti v toku krvi, predvsem zastojev in/ali vrtincev, ki bi povzročali nastanek strdkov ali kako drugače škodili krvi.It is understood that the location of the reduced clear section of the artificial vessel according to the invention does not cause current irregularities in blood flow, especially congestion and / or swirls, which would cause clots or otherwise damage the blood.
Po izumu imamo torej na voljo novo, sestavljeno umetno žilo, ki jo tvorijo prvi dolžinski odsek, predviden za prišitje k arteriji, drugi, v danem primeru dušilni, dolžinski odsek in tretji dolžinski odsek, ki je predviden za prišitje k veni.According to the invention, therefore, a new, composite artificial vein is provided, consisting of a first length section intended for sewing to the artery, a second, optionally damping, length section, and a third length section intended for sewing to a vein.
Pri tem je svetli presek drugega, t.j. dušilnega, dolžinskega odseka umetne žile ne manjši od pretočnega preseka prvega/tretjega dolžinskega odseka, zmanjšanega za natočno omočeno projekcijsko ploskev vanj zabodene odjemne/vračalne igle napeljave dializnega aparata.Here the bright cross-section of the other, i.e. of the damping, length section of the artificial vein not less than the flow cross-section of the first / third length section, reduced by the wetted projection surface of the dialysis apparatus insertion / return needles inserted therein.
Na priloženi skici je nazorno predstavljena kratkostična zveza arterije z veno pacientove roke po umetni žili iz stanja tehnike, v kateri je nakazano mesto dušenja, kakršno predvideva pričujoči izum.The accompanying drawing clearly illustrates the short-circuit connection of the artery with the vein of the patient's arm through an artificial vein of the prior art, which indicates the site of damping as contemplated by the present invention.
Po prvem izvedbenem primeru se za oblikovanje dušilnega odseka umetne žile se s pridom izkorišča po sebi znano zvezno preoblikovanje okroglega preseka umetne žile v eliptični presek le-te. Obseg konture preseka žile je konstanta. Ploščina svetlega eliptičnega preseka umetne žile je mnogokratnik ploščine svetlega okroglega preseka le-te s koeficientom, ki ustreza razmerju male osi elipse proti njeni veliki osi. Če je to razmerje naprimer enako ’/ί, je torej eliptični presek žile polovica okroglega. Pomembno pri tem je, da je zagotovljeno, da zvezni prehod okroglega preseka prvega dolžinskega odseka v eliptični presek drugega dolžinskega odseka in naprej v okroglega (v tretjem dolžinskem odseku umetne žile) ne povzroča zgoraj omenjenih strujnih neregularnosti.According to the first embodiment, the known continuous transformation of the circular section of the artificial vein into an elliptical cross section of the artificial vein is advantageously utilized to form the damping section of the artificial vein. The extent of the contour of the section of the vein is constant. The surface of a bright elliptical section of an artificial vein is a multiple of the area of the bright circular section of an artificial vein with a coefficient corresponding to the ratio of the small axis of the ellipse to its large axis. For example, if this ratio is equal to '/ ί, then the elliptical cross section of the vein is half round. Importantly, it is ensured that the continuous passage of the circular cross section of the first length section into the elliptical section of the second length section and forward in the circular (in the third length section of the artificial vein) does not cause the aforementioned current irregularities.
Po drugem izvedbenem primeru se za oblikovanje dušilnega odseka umetne žile s pridom izkorišča po sebi znana vzpostavitev okroglega preseka umetne žile manjšega premera.In another embodiment, the articulation of the smaller diameter diameter of the artificial vessel is advantageously utilized to form the damping section of the artificial vein.
Umetno žilo konstantnega preseka lahko v umetno žilo iz predhodnega odstavka pretvorimo z uporabo po sebi znanega principa stiščka.The constant-section artificial vein can be converted into the artificial vein from the preceding paragraph by the use of the known compression principle.
Po pooblastilu:Under the authority of:
Patentna pisarn^ ’ύ^Ι'.ό. Zanjo: Vinko SkubicPatent Offices ^ 'ύ ^ Ι'.ό. For her: Vinko Skubic
Claims (3)
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
SI9800177A SI9800177A (en) | 1998-06-19 | 1998-06-19 | Artificial vein |
AU43064/99A AU4306499A (en) | 1998-06-19 | 1999-06-18 | Hose for making an artificial vessel |
PCT/SI1999/000017 WO1999065559A1 (en) | 1998-06-19 | 1999-06-18 | Hose for making an artificial vessel |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
SI9800177A SI9800177A (en) | 1998-06-19 | 1998-06-19 | Artificial vein |
Publications (1)
Publication Number | Publication Date |
---|---|
SI9800177A true SI9800177A (en) | 1999-12-31 |
Family
ID=20432288
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SI9800177A SI9800177A (en) | 1998-06-19 | 1998-06-19 | Artificial vein |
Country Status (3)
Country | Link |
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AU (1) | AU4306499A (en) |
SI (1) | SI9800177A (en) |
WO (1) | WO1999065559A1 (en) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US8226592B2 (en) * | 2004-12-15 | 2012-07-24 | Rox Medical, Inc. | Method of treating COPD with artificial arterio-venous fistula and flow mediating systems |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3638649A (en) * | 1969-07-07 | 1972-02-01 | Univ Minnesota | Implantable prosthetic pass-through device |
US3882862A (en) * | 1974-01-11 | 1975-05-13 | Olga Berend | Arteriovenous shunt |
US3998222A (en) * | 1974-04-15 | 1976-12-21 | Shihata Alfred A | Subcutaneous arterio-venous shunt with valve |
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1998
- 1998-06-19 SI SI9800177A patent/SI9800177A/en not_active IP Right Cessation
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1999
- 1999-06-18 WO PCT/SI1999/000017 patent/WO1999065559A1/en active Application Filing
- 1999-06-18 AU AU43064/99A patent/AU4306499A/en not_active Abandoned
Also Published As
Publication number | Publication date |
---|---|
AU4306499A (en) | 2000-01-05 |
WO1999065559A1 (en) | 1999-12-23 |
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