CA2341414A1

CA2341414A1 - Methods and apparatus for crossing vascular occlusions

Info

Publication number: CA2341414A1
Application number: CA002341414A
Authority: CA
Inventors: Matthew R. Selmon; Charles F. Milo; Fred Co; Mark Campello; Ronald French; Amiel Aguilar
Original assignee: Individual
Current assignee: Lumend Inc
Priority date: 1998-09-30
Filing date: 1999-08-27
Publication date: 2000-04-06
Also published as: US20010000041A1; AU5590099A; US6217527B1; EP1119387A2; JP4680386B2; US6514217B1; DE69935149D1; WO2000018323A3; ATE353686T1; BR9914165A; EP1119387B1; US6221049B1; DE69935149T2; JP2002525163A; WO2000018323A2

Abstract

Methods and apparatus for crossing totally to substantially occluded blood vessels by passing a redirectable wire such as a guidewire from a relatively proximal point past the occlusion within a subintimal space formed between t he intimal layer and the adventitial layer of a blood vessel wall. The wire may be advanced to a point distal to the occlusion, and thereafter deflected bac k into the blood vesel lumen, typically using a deflecting catheter which is advanced over the guidewire after it has been positioned within the subintim al space. The deflecting catheter may include a flapper valve assembly or preformed actuator wire for redirecting the guidewire. After the guidewire i s returned to the blood vessel lumen, the deflecting catheter may be withdrawn , and the guidewire may be available for introduction of other inverventional and diagnostic catheters for performing procedures such as stenting.

Description

v wo oana~ rcrnrs~nm METHODS AND APPARATUS FOR CROSSING VASCULAR
OCCLUSIONfi FIELD OF THE INVENTION
The present ime~an relates ge~rally to medical devices, kits, and methods used in the treatment of vascular occlusions. More particularly, the invention relates to systems and procxd~s for crossing chronic occlusion in blood vessels with guidewi~s that may facilitate performance of subsequent tit ~d therapies including angioptasty, atherectomy and stenting Cardiovascular disease is a leading cause of mortality worldwide that can take on many different forms. A particularly troublesome form of cardiovascular disease results when a bGood vessel becomes totally occluded with atheroma or plaque, referred to as a cbmnic total occlusion. Until rocexitly, chronic total occlusions have usually been treated by performing a bypass procedure where an autologous or synthetic blood vessel is anastomotically attached to loc~tioc~s on the blood vessel upstream and . . ~~m of the occlusion. While hi~hty e$ective, such bypass procxdmes are quite traumatic to the patient. Rally, catheter-based intravascular procedures have been utili~d to heat chmnic total occlusions with increasing success. Catheter-based int<avascular procedures include angioplasty, atherectomy, stenting, and the like, and ara often preferred because they are much less traumatic to the patient. Before such catheter-based trcatrncnts can be performed, however, it is usually necessary to cross the occlusion with a CA 02341414 2002-02-15 p;
WO OOJ183~3 PCTNS99119~831 guidewire to provide acct far the isiterventionat . In some instances, crossing the occlusioon wrtlt a ~ can be a~omplisbed simply by pushing the guidewire th~ugb the occludon. The guidewire remains in the blood vessel lumen a~i ~ the desire; access path. In many cases, 6ovrever, the guidewire inadvateatiy peaatit~s into the subintimat sp~aoe between the iirtxa~al lays and the adventitial layer of the blood vessel as it attempts to crass the occlusion. . Once in the subiatimat space, it is very difficult and impossible in many instances to direct the guidewire back into the blood vessel lumen. In such cases, it will usually be impossible to perform the catheter-hosed ion and other procedures may have to be employs that are relatively mare ~c. Catheters and methods for forming lateral penetrations through tissue to and from blood vessels past total occlusions are described in U.S. Patent Nos. 5,443,497; 5,429,144;
5,409,0I9; 5,287,861; WO 9'I/13463; and WO 97/13471. CatHerers having side guidewire entry ports spaced proximally fibm their distal tip are also described in U.S. Patent Nos. 5,444,395; 5,413,581; 5,190,528; 5,183,4?0;
4,947,864; and 4,405,314. These and a variety of other specif c interventional and pharmaceutical taratmenbt have bees devised over the years with varying levels of success for dint a~lications.
.. ._. . _ .

CA 02341414 2002-02-15 Ii wo oona~ rcrms~nm SU1H~IARY OF T$I~ llWVCNTfON
The piavsmtion p~ovi~ methods and apparatus for aosmng subst~tis! err total abates in blood v~els. It is an object of the imret~tio~t to traverse vascular oeclusians or other biock~es formed within blood S vessels in order to provide pays ~ the placement of guidevvires or otixr irrtetventioml devices as part of an overall effort to restore or provide adequate circulario~n. It is bus t~ cross a tiaily occluded blood vessel by finding and/or creating a path with the least or relatively low resistance through or amend at least a portion of the occlusion which may include travel along orbetw~een the layers of a blood vessel wall in regions such as the subintimai space. The inveeuion fiath~ provides methods, kits, and apparatus which fadlitate aoaaing a claonic total occlusi~ in a blood vessel with a guidewire. In particular, catheters, guides, or other apparatus provided herein may be used with oonventiotwl or specialized guidewirea to direct or redirect the guidewlres $om a mbi~iraal space, or other areas betvueen the diff~t layers of a blood weasel wall, back into the blood vessel lumen. The disclosed ~ include devices formed with relatively simple construction, and may tx used in a relatively straight-forward manner.
One aspect of the invanti~ provides apparatus for crossing a vascular _ ocxlusion by directing a kad device such as a guidewire around at a least a portion of the obstruction within the blood vessel wall. A deflecting catheter may controllably deflect or direst tire guidewire through or around a vascular occlusion formal within the natural lumen of the vessel, and may direct the guidavvire within a region in bctweca the various layers of the vessel wall to completely or partially circnmv~att the blockage. The deflecting catheter may provide any combination of these controllable movements to position the guidawire in a manna that can facilitate in~ocv~eational treatments such as stdndng. Another variation of the inve~on igcludes a guidewire deflection we oan~~ pcrms~nm $Y~ ~8 a ' body formed with at least one lnmen along its la~gth, a nosooone d, a< die distal end of the catheter body having a distal aud.a l~daral apeniag. The nsgion surrounding the >aterat opening may include ~ ac~aoaat iaclinOd fix. The dial opening and the lateral opening are both in cxammtunication with the catheter body lumen. In addition, a cannula may be incdad~ hang a ~~ p~ m ~a~n with at least one passageway sact~ing that least a distal portion of the cannula. The distal end of the Hula ~sy be configured to communicate with the inclined sta~Oe adjato the lateral opening to deflect the cannula away from the longitvd~nal axis of the attlxrter body. The distal portion of the cannula may further have a ptr~-farmed abape :esiIient corn, and may be slidably positioned within the lumen of the ca~thoter body. The distal portion may have a relatively axially aligned ~gt~ton with the lurinen when the cannula is positioned within the a~heber b«ly, and a relatively curved 1 S configuration with the lumen whexi the cantata travels along the inclined and through the latmal opa~g of the deter body when the cannula is ~stally advanced through the lumen within the catheter body. The guidewire deflecdon system stay futthar cxm~pciae a guidewire configuri to Pas ~~ ~ PAY flf ~ . A variety of imaging components or markers may be also pos~ionad on various portions of the wire, caanula or catl~ta body. A hub asstmb~y mtationally secured to tix;
proximal end of the cs~ater body may be selected to controllably rotate the cansula and the eatbote~r body. .
In yet another anbodimesit of the invention, an intravascular catheter is provided having a catheter sha8 for~e~d with at least one longitudinal lumen. A nosecone may be portions at tha distil end of the csitheter sha8 having a first port in commun~aticnr with the longitudinal lumen formed with a first cross-sectional area, and a seo~dd port in ~manuaication with the ~~~~1 longitudfaal lutnm foacramed with a,eocond cmae-aectiOnal any, what the first cmss-sectional area is relatively la<Fger that the second crflss-sectional area. A cannula may be alidabty positioned within at least a portion of the longitudinal lumen of the cathctor shaft, arsi may be configured for passage . through the first port which is relatively Im~r, but not through the second port of tho nosecone which is rehirrely stndler in siu. A guidewire may be also slidably positioned within at Iesst a portion of the cannula passageway, and may be configured for passage thromgh an inclined sus~CC fomaed ad,~ac~t to the second part. The nosecone may fisth~ inchxle imaging i 0 components or cadiopaque markers that provides directional orientation.
Another embodiment of the inv~ttion provides a redirectable intravascular guidewire catheter. The cater may be formed with a catheter shaft and a guidewire deflector Evened ~ the distal end of the catheter shag.
The guidewire deflector may be formed as a nosecane assembly having a distal end port, a lateral port, and a relatively iaWnal or external flapper assembly with a deflectable cxte~nsion. The deflectable extension of the flapper assembly may have a »rst position that directs a guidewire tip through the distal end port when the guidewire tip is positioned relatively distal to tI~
deflectable extension. It may further have a second position that directs the gnidewire tip throt~h the le~l post wlu~n the tip is positioned relatively proximal to the deflectalde e~ension and advanced tbaeafter in a relatively distal direction. Additionally; a gtddewire niaY be incltEded in the catheter that is slidably positioned within the Ivm~a of the catheter shaft. A portion of the flapper assembly naay be also formed of a 8~oscopic anataria~l to provide an orientation marker for ditectionw', placement of a guidewire.
A n3directable guidttvire her is furt$or provided in accordance with the concepts of the invention comprising al~t6eter shaft, an actuator wire, and guidewire. The shaft may be fis~na~d with a first luausn and S

l Wt) t~~ ~~~~1 S second lumen each g along tix cafl~r Shaft respectively to a first dual Opening and a aeeond dial openisg. The ac~tol Wire may ba slidably positioned with the fast lamas of the cater shaft, wherein the actuator wire is formed with a ~ distal cmd m pmvida an actuated position that is biaxd towards the seoas~d.~al opening when advanced relatively distal tlunugh the first distal op~g. Fur<hm7more, the actuator wire may extend only within or beyond the ouEe: of the catheter shaft at a relatively distal or distal most end portion of the catheter shaft. The guidewire may be slidabty positioned wItbin the seoand lunarn of the catheter shaft, and may be deflected when advanced tetatively distal thraugh the second distal opening when the actuator wire is plaaad in its actuated position. In another variation of the invention, the redjraxable guidewire catheter may have a catheter shaft with a first lumen and a second lumen each extendia~g along the catheter shaft..
A one may be fwd apt the distal portion of the catheter shag, wherein the nosecone includes a distal orifice ate an intexior region formed with a sutfacx. The awirc may be formed with a distal tip that is slidably positioned with the first lumen of the catheter shaft, wherein the distal tip of the actuator wlra is redirected salty away from the longitudinal axis of tlx cattre~r shaft when advanced relatively distal along the tapered surface of the rancor and t~hrougb the nosecone orifice: The guidewire may be slidably pc~itio~d within the second lumen of the catheter d=aft, and may be defley fro~~tTye longitudinal axis of the catheter , ..
shaft by cxaitacting the acd~or wire when the guidewiie is advanced relativcty distal thtt»agh the distal orifice.
ZS Yet another variatioat of the inv~ontion provides an intravascuIar catlxter for selectively deflxtiag a guidewire that includes a catheter body fomud with a distal end and a longit~dins~l luaus formed along at (east a po~tioa of the cater body. A attp!port tube may be formed with a distal tube WO AA~li83~i PCTNS99I19S31 end that includes a aportion to accept the distal portion of a catmula.
The support tube may be slidably and rateably positioned within the longitudinal lumen of tho txer body. The cannula may inchde at least one passageway attending tiunugh at least n distal end portion of the cannula, wherein the distal pa~ation of tha cannula has a pre-farmed shape resilient curve that may commtat~te with the cus-out portion when the cannula is stidably positioned withia the conduit of the support tube. The pmxiaaal tube end of the support tube may be comiectal to a rotating assembly to rotate the support tube relative to the catlu3ba body. Another variation of the intravasa~lsr c~theta may irlcludc_ a support tube connoc~d to the distal cannula end, wherein the support tube is formed with a distal tube end section, a proximal lobo end sodion, and a backbone connecting the distal and the pmoacimal tube end suctions. The support tube or the distal canaula errd may be preformed with a p~redetermin~ed shape to deflect the distal cannula 1 S ~ away from the longitudinal axis of tax catheter body when the distal cannula end is extended proximally past the distal end of the catlu~r body.
Another aspect of the invemion provides methods for crossing a substruntially occlude blood vessel. The method may include the steps of selecting a guidewire with a deaftactable distal tip configured for placemept in a blood vessel wall, creating a longitudinal dissection plane within the blood vessel wall by inserting the gu~ire into blood vessel wall from within the blood vessel lumen 'at a proximal locati~ relativo to a vascular ocxlusion; ..
_ .
foaming a channel slang the blood vassal wall by advancing the guidewire in a relatively distal directiaa along the blood vessel wall, and selectively c~flecting the distal tip of the guidawire at a relatively distal location relative to the proximal location back into the blood vossel lumen. An interventional or diagnostic catheter may be advanood aver the deflected guidavvire from a T

we oons3~ pcrms~nm position relatively pmximst to the occlusion, through the channel, and back into the blood vessel lumen.
Other variations of the invention described herein also include metlmds where total odelusions are aroaxd by Srst forming a track or channel from a lumen in a blood vessel into a subintinial space between an intimat layer and an adventitiat layer of the blood vessel. The track may be formed so that it extends from a la~cation proximal of the total occlusion to a location which is relatively dicta! to the total occlusion, our at any positioned located therebetvveen. A passage may be the ford, firm the track back into the blood vessel lumen at the relatively distal location. In one variation of the invention, the track may be formed by advancing a wire through the blood vessel lumen into the subintitnai space by typically advancing the wire until it encounters the total occlusion. By continuing to advance the wire in a generally distal direction, it may pass into the subintimal space of the blood vessel, and may be further advararod toward a desired distal location. After the wire is located or confarmal at a point relatively distal to the total occlusion or original point of insertion, it may be typically deflected from the track or channel back i~rto the blood vessel Iumea.
In some exemplary methods descuibed herein, the wire may be deflected using a deflecting catheter. Typically, the deflecting catheter may be ~dvancxd over a proximal end of the wire aml advanced into the track . . ~~ ~ subintimal space. The wire anEi the deflecting catheter may be mani~lated so that the wire is deflected laterally through the intimal Isyer back into the blood vessel Iumen. Such detlectir~ catheters may be also useful in axially supporting the wire as it is advanced into and/or through the track, i.e. the catheter can enhance tha "p~ushability" of the wire when it is advanced forward through any resisting material. Specific designs for such deflecting catheters are described in detail below. The wire, which is initially CA 02341414 2002-02-15 II;
wo eons rcrms~nsm positioned within the track in the subialimal sp4tx, may be alternatively qrithdrawn through the de$octing cat~ber and exchanged for a second wire or . device suitable for pe~adradng throug# the ia~tt layer of the blood vessel wall back into the lumen. It will be ~prea~ed that the wires and/or deflecting and otlu"r ca~etars may be 8baly ~ over ar through ax another in a conveudoaal mat~r,witho~ departing from the scope of the invention.
Various imaging techniques may be used in accordance with the invention to detenniae when the wire andlor deflecting cadteter are positioned with respoa to a vocclusio~ so that the wire may be returned to the blood vessel lumen at a dlocation or beyond the occlusion. For example, the position dateanination can be made by tluoroscopieally imaging the blood vessel in a conventional manner.
A~rnadvely or additia~lly to such fluoroscopic imaging, intravascular imaging, e.g. intravascuiar ultrasonic imsg~8 (IWS), end a variety of optical imaging modelities, ouch as optical co~6d~enre tomography (OCT., may be employed. For example, an ultrasonic inu~pmg guidewire may be used to initially access the subintimal space aadJor may be exchanged for the wire which is used to access the subintimal . An imaging guidewire present in the subintimal spacx may readily detect the or absence of occluding naateriat within the blood vessel luc~n. The transition from detecting occluding material to the laClc of the same is a strong indication that the position of the guidewire has advanced beyond the total occlusion. The wire may be deflected far and returned towards the blood vessel lumen.
After a passageway is frmn the track err clmanel back into tlx blood vessel lumen, and a wire is in pllaas:~s the total occlusion, tile wire may .
be used as a guidewire for positioning iuttaven:ionat acai diagnostic c~t~s across the obst~tion. Interventional ca;heters are often positioned across the CA 02341414 2002-02-15 ii!
wo oons3a.3 rc~rn~nm total occlusion far ~?mg the oocl~ios, and include devices snch as angioplasty balloon cao~ebm~s, round atbaectomy cafbeba~s, dirat atlarre:ctonly cat>a~rs, and sbent P.
Another aspxt of the invention metlwds for crossing a S vascular occlusion with a deflecting wino. The wire deflecting step may include deflecting a canaula from the subl space of a blood vessel wall back irno the blood vessel lumen, and ~ passing the wire through a path defined by the caanula, typically by a lumen within the caanula. The cacmula may be advanced over the wire after the wire is disposed or advanced within the subintimal spacx, sad a cannuladeflecting step may be also included that involve: distally advancing a resiliern or preformed cwved cad portion of the caounula fi~a a cons~ini~ng lumen fomned within a ~urotmdiag catheter or sheath back inoo the blood vessel 1. Alternatively, a wino-deflstep may comprise advancing a d~leeting cathetbr ova the wire which has been advanced into the subintimal space. A cannula may then be advanced through a lateral opening of the .deflecting catheter, and penetrate through the intimal layer to define a path for the wire back into the blood vessel lumen. A wkle variety of steerable snd actively deployed cannulas may also be used is the foregoing appliaatioas..
The present invention ftuther provkles kits for crossing vascular occlusions comprising a win-deflecting asd~r having a lumen or mechanism cszpable of laterally de~loctvd~ d wire. The kit may fiether com~ise insrructioa$ setting forth any oaf the mtthods described above. Orbar m~ds and ~ fis aaconimce wide the invention, as specifically described hd~ein, may be also cor~inerl to provide nurnaous kits for many applications as in the treatment of comw~y artery and perlphaal vascular occlusions. Optionally, the kits provided herein may further comprise a wire far penetratyng into tlta subiiri>mal space aad~or beak into the wo oons~ pcrnas99nm blood vessel lumen. The kit rosy still comprise a package for containing a wire defletx~a~g , ions for its use as described in the various :methods btrain desctibed, ~d other optional devices including additional wire(s). Suitable packages include pouches, trays, tubes, boxes, and the like. The instwations may be printed on a package insert or may be printed in part or in whole on the packaging itself. The componaits of the kit within the package may be stm~iliaod by conventional procedures.
Apparatus acceding to another aspect of the invention provides wire-deflection systems. Exemplary wire-deflection. systems usually comprise a wire-deflecting catheter which includes a esthetes body and a deflecting cannula. The catheter body has a lxoximal end, a distal end; and at least one lumen extending through at least a distal portion thereof. The lumen also has a distal opening and a lateral opening. In addition, the cannula has a proximal end, a distal end, and at leant one lumen extending through a distal portion thereof. The distal portion of the cannuta may also have a prefonmed, resilient curve. The cannuta is slidably disposed within the lumen of the catheter body to assume (a) a stcaight~d configuration when the eannula is proximally retracted within the cathster body lumen and (b) a curvod configuration when the cannula is extended laterally through the lateral opening of the catheter body. In this way, the cannula can be selectively deflected through the intimal layer of the blood vessel back into the lumen of the blood vessel according to Mme of the preferable methods descn'b~ed herein. The system~may further comprise a wire configured to pass through the cannuia lumen. The wire may be a conventional guidewire or a nladified wire having a sharpened distal tip intended particularly for pra~e~dratiag the intimal layer of the blood vessel wall.
Optionally, the wire may futth~er comprise an imaging apperat~ ~ as an ultrasonic imaging means. The catheter body may include a fluoroscopically visible marker near its distal end. The marker can be configured to permit wo ooits~ rcrnrs~nm visual determination of floe royal orientation bf the distal end of the catheter body when vievvad, ~ a twn.dimansional fluoroscopic image. The catheter body will usually be xninforoed to a~hanee tarsional rigidity, and may further comprise a distal nose cone wl~ein the distal and lateral openings are defined within the nose came. The disml and of the cannula will usually be pre-formed in a smooth curve which may extend over an arc in the range from about 15 to 135 degrees, usually from about ~5 to 90 degrees. The pre-formed curve may also have a radius in the range from approximately 0.5 mm to 15 mm, usually from approximately 2 mm to 10 mm. These and other objects and advantages of the rav~on will become iriore apparent upon further consideration of the entire sp~Rcatian and drawings. Additional aspects and details of the inva~ntion will become more apparent to those skilled in the relevant are upaat review of the following detailed description of the invention set forth below.

~~~n~l BRIEF DESCRIP1ZG1N OF THE pRAW~TGS
Fig. 1 is a sche~tic illustration of a coronary artery showing ~
~y~~ ~ medical layer, and the adventitial layer.
Fig. 2 is a schcnsatic illustrations of a total occlusion within the coronary artary of Fig. 1, shown in full section.
Figs. 3A-3D illustrate the method of the present invention for crossing a total occlusion with a wire using a defecting catheter.
Fig. 3BB illustrates an ~ guidewirc advancxment step for the m~hod of Figs. 3A-3D.
I0 Fig. 4 illustrates the dial end of a deflecting catheter farmed in acxordance with the invetrtian.
Fig. 5 illustrates the distal end of another deflecting catheter useful in the methods of the present invention.
Fig. 6 illustrates the distal end of another embodiment of the invention I S that provides a deflecting catheter.
Fig. 7 illustrates a wire-deflecting catheter system formed iu accordance with the present invention.
Figs. 8-9 arc cross-sectional views of the distal end of a catheter similarly shown Fig. 9, illustrating an internal cannula in a retracted and 20 advanced configuration, respectively.
Fig. 10 is a schematic illustration of a proximal hub of a catheter for deflecting and directing a guidewire is accordance with the methods and apparatus of the invention.
Figs. 1 IA-1 IB illustrate variations for rotationally keying the 25 proximal end of catheter shafts.
Fig. 12 illustrates variations far ratationalIy keying the distal end of a wo 0arta~ rc~rms9nnm Figs. 13A-C. paovida'' illustrations of a nosecone for a guidevvire detlxtion catheter in aooordattce with the inv.
Figs. 14A-B are c-sectioooaT side views of a noeecone connected to the .distal end of a shaft with an internally positioned cannuLa and gutdewrre.
Figs. I SA-E are sia~Ii$ai aide views of a flapper mechanism positioned at the distil pc~i~n of a that controllably dews a gw~~ a distal et~d port and/or a lateral port.
Figs. 1bA-B are fed side views of external guidevvire defl~g mechanisms that are posido~ed nclatively outer to the catheter shaft body.
Figs.17 A E illuatra~e a rcfitectable guidewire catheter having a preformed actuator wire that,lckflacts a slidable guidewire positioned within an adjaoetrt lumen.
Figs. 18A-C show the distal section of a nosecone formed with a I S single orifice that may be po$itioned at the distal end of a redirectable guidewire catheter.
Fig. 19 is a simpli$e~ pe~apeerive illustration of ttadistal .per of an intrava~lar catheter than includes a support tube formed with a distal end portion for di~e~ng a plod catmula.
Fig. 20 is a simplified perspective illustration of the distal portion of an intravaseular-catheter.tltat~inc~s a support tube having a backbone for supporting the detlect3ve molvcmcnt of an internally positioned canaula.

wo ~ans~ Pcrn~n~i DETAILED DESGR~TION OB Tl~ INDENTION
Tlx~ present icrv~tion provides methods and apparatus for crossing a substaatially or totally occluded blood vessel. Each of the disclosed Embodiments may be considerod individually or in combination with other variations and aspects of the inv~on.. The nxthods and apparatus provided heroin may be useful in conmary arteries and other blood vessels with or without assistance from imaging techniqures fmm various regions within the body inching areas within or adjacent to blood vessel welts. White the some aspects of the invention may be ~ticularly applicable for the treatment of coronary artery disease, they are also useful and equally applicable in the treatment of other arteries and veins; and for other conditions including peripheral vascular diseases.
As shown in Fig. 1, for example, a relatively normal non-diseased artery (A) generally co~ises an arterial wall formed with a number of I 5 distinct layers. An innermost layer may be refacred to herein as the intimat layer (1) which includes the endothelium, the subendothelial layer, and the internal elastic lamina. A medial layer (Its of the blood vessel is located concentrically outward froar the intimat layer (I), and within another layer known as the adventitial layer (AL) which tray be considered the relatively outermost layer. Beyond the adventitial layer (AL) generally lies surrounding extravascuIar tissue. As used hercinstl~r, the region between the intimal layer (>7 and the advernitial Iayer (AL), 11Y including the medial layer (l~, will be rafen~eci to as the sublatimai apace. It is generally the subintimal space through which tlu; wires, deflecting catheteas, and other catheters of the inventia~n, will pass sit lerast in part when crossing a total of substantially occluded blood vessel. Tits guidevvires and deflecting catheters de~xibed herein may be formed of appa~a~riate dimensions for placement and travel within these rcgiona of the blood vessel wall. For most applications CA 02341414 2002-02-15 in, C
we oona~a.~ rcrnts~nm described herein, it is nwst o8xu able to bevel within the layers of the blood vessel wall, and across the inner wall of the blood vessel into the vascular lumen, without pthe outer wall region which would present additional safety cancxrns to a patient. These methods and apparatus may be of course directed to any ragiam formed between other layers of a blood vessel wall other than those particularly described above.
Fig. 2 provides an illustration of a fatal occlusion (TO) within an artery (A) such as a coronary artery. The tfltal occlusion (TO) may comprise atheroma, Plaque, thrombus, and/or othear occluding materials normally associated with cardiovascular discasE. A "total" occlusion may be described to include an obstruction consisting of occluding material that substantially blocks or occludes the entire lusnai (L) of the artery (A), or any other bleed vessel, so that blood flow through the vessel is substantially stopped or hindered. The invention may be parti~larly applicable for patients with a totally occluded artery that is not immed~iaxely life threatening sine the tissue distal to the occlusion may receive oxy~tat~ed blood from collateral arteries and circulation. However, the blood supply is usually insufficient, and it is often desirable to treat the occlusion by an intravascular intervention, such as angioplasty, atherectomy, stettting, or the like, to restore blood flow through the affected vessel. Before most of these and other interventlonai procedures can be performed, a guidewire is gesadrally placed across the occlusion. When .. a ~~, elusion preirents the placadurnt of a guidewire access the obstruction, one aspect of the invention thus provides various methods for crossing the substantially ar totally occluded blood vessel. A guidewire may be initially selected with a dble distal tip configured for placement within or in between the layers of a blood vessel wall. A longitudinal dissection plane may be careered within die blood vessel wall by inserting the guidewire ima blood vessel wall fi~ within the blood vessel lumen at a WO liAll3;iZ3 PCT/US99/19831 proximal location relative to a vaa~mr oecluano~i. A channel may be fo:med in between the layers of and along the blood vessel wall by advancing the guidewire in a relatively diatal di~acGaa along the blood vessel wall. Valour imaging procedures may be perfomned to~ identify the relative loeatiam of the S occlusion and blood v~el hmaen. For example, imaging of a coronary may be accomplished fia~n a poai~a in a vnin adjacent to the coro~ay arty.
When the relative positioning of the guddewire and the occk>sion are verified, the distal tip of the guidowlre may be a~eboetively deflected at a relatively distal location relative to the proximal loa~ion back into the blood vessel lumen Upon pla~rnent of a gnidewire across the vascular ocxlusion, interventional .
or diagnostic procedures may be subaequeatly performed over the grridewize, end more specifically, the iut~ve~ntiorrat or c catheter may be advanced over the deflected guifirm a position relatively proximal to the occlusion, through tire chmme>, and back into tire blood vessel lumen.
The distal tip of the guidewirt pray be also defected by providing the guidewirc tip with a raailiont curved. gird, and distally advancing the grudewire from a constraining lumen ir~o the blood vessel lumen.
Another aspect of the preae~ iron provides methods of crossing a vascular occlusion by controllably directing a deflectable wire into and through a blood vessel wall as descrr'bat in Figs. 3A-D. For penposes of illustration, this series of $gures may represent as upper portion of an ~ludod artery (A) as down iu F'~. 2 A wire l 0 may be advanced through the lumen (L) of an artery (A), as shown in Fig. 3A, until it encounters a total occlusion ChO). At thaot time, it may be possible for the wire 1~0 to be distally advanced through tho occlusion without deflecting into the blood vessel wall.
Should that occur, subsequent rapoaitioarog or redit~ag of the guidewire according to the methoda of the pr~eat invention may be performed, but may not be rrecxssary. Mesa us~liy, however, the wire 10 is not able to traverse a CA 02341414 2002-02-15 i~
WO 6AI18313 PCfNS99I19831 substantial occlusion by distally advancing the wire through the ohstnxtion.
The wire 10 may likely advance iato the subal space withia the naxiial layer (11~ as slwwn in Fig. 3A. Of course; the wire 10 may atso travel into or arouad at least a pardon of the total occlusion (TO) before or while it is distally advance. The i~a~al lacyer (I) and the adventitial layer (AL) togs may define a tissue plane through which the wire 10 will naturally pass as the wire is pushed distally from its prmcimal end. The wire 10 may co~inue to advance fustlurr until its tip passes beyond the distal and of the toml occlusion (TO) as shown in Fig. 3H. The tip could axially or distally advance well beyond the total occlusion to a desired location or until advancement is ceased. Although the guide:wirc 1D in Fig. 3B ie ahovva as being advanood without support, in some imtances the guidowire may however encounter sift resistance as it enters andlor passes through the space between the intimsl layer (I) and tire adventitul Layer (ALA or any other layers within a blood vessel wall. When resistar~e is tncoun;etcd, the deflection catheter 20 may be used to axially support an~i enhance the "pushability" of the gui~wirc 10 by advancing tlu over the proximal end of the guidcviire to a location,~at pno~imel of the distal tip of the guidewire as shown in Fig. 3HB. The guidewire 10 and catheter 20 may then be advanced togetlxrr or sequentially, e.g. advancing the guidewire a short distance followed by advancing the eadrd~et, as nealoid to direct the distal tip of the gaidewire, or a lateral port 22 formed in the ~th~tr, to a relatively distal location which may be paroximal to or pout the total occlusion (TO).
When the distal tip of the guidewire 10 is advanced to a desired location without additional support from the deflacting catheter 20, and is positioned beyond the total occlusion (TfJ~ the deflecting catheter may be sdover the wire 10 by coaxial introduction over the proximal encf of the wire until it appioaohas the total occlusion as shown in Fig. 38. The we e0ns3~ rc-r~nm deflectatg catbe~ 20 msy be fls~er aalvaaeed over the wire l0 until its distal tip also s beyond tba toil ooduaian (Tfl) as illusrratcd in Fig. 3C. The deflecting catheter 20 mclude~s a redirocbiag mechanism for laterally deflecting the wire 10 so dad it may pass beak in a radielly inward direction through the 'satimal layer (I) beak inZO t1x blood vessel lumen (L) when the cathettr is sequentially monad in a relatively distal direction, and a relatively pn~al direction they ~Rat~ than advancing and withd:avving the catheter 20 in a proximal diction, the guidewire 10 may be withdrawn sad advanced in a distal dinsction to ix deflected. The deflection mechanism may be selected from various t~noctiag d4wicxa an may take a variety of forms as described below. For example, as shown is Fig. 3C, a lateral port 22 is provided in the deflecting catt~a~ 20. 'l7re wire 10 may be retracted so that its distal tip lies p~roximstly of the legal port 22, and may then be advanced distally so that the wire passes latemily outwardly thmugh the port and back IS into the blood vessel lumen as shown in Fig. 3D. Various deflecting catheters and apparatus described lnrroin for directing and redirecting a guidtwire within a blood vessel wall may be selected to perform these procedures in accordance with the c~o~s of the invention.
The location and orieatabon of the deflecting cathebar and wire assembly may be monitoral in verio~ ways to cant' out the described methods for c~ossic~g a dally ooahidod Blood vessel. In particular, it may be desirable to assure that the distal tip of the wire I 0 and the port 22 or other deflecting mechanism of the erecting c~heter 20 is properly positioned beyo~ the total ooahaiion (TO) without being advaaoed excessively beyond the end of the tmal acchtsion. Typically, it may be desirable to position the ding m~ at a range from approximately 0 to 2 cm beyrond the distal end of the total axlusioa (TO), and preferably flora 0 to 0.5 cm. As discussed above, the poaibioning of the relative CA 02341414 2002-02-15 iii wo oons~ rcTnrs~ny oonnpa~ may in some im~nces be pafo~d using conv~tiomtt fluoroscopic imaging. For Vie, it may be sufficient to provide suitable radiogaque markers on the wire and/or on the deflecting mechanism of the deflecting catheter 20 to permit visual positioning and rotational orientation of the tip via fluom~py. Often, hawer~r, it may be desirable to provide ultrasonic or other iag at or near the total occlusion. A wire 10 may be thus provided with ultrasonic imaging so that the presence and the absence of the occluding material may be detectod as. the wire is advanced passod the total occlusion (TO). Alternatively, the deflecting catheter 20 may be provided with ultrasonic imaging in the fozm of a phased array located near the distal tip (not shown). Ultrasonic imaging guidewires are known to those skilled in the relevant field and are described in the patait literature as in U.S.

5,095,911, the full disclosure ofwhich is incorporated heroin by reference. In yet another alternative, an imaging guidewire may be advanced to the region of the total occlusion (TO) in a direction opposite to that of the wire 10 and catheter 20. In this way, the imaging guidewire need not advance through the total occlusion, but could still detect advancanent of the catheter and/or guidewire, particularly if ultrasonically opaque components were provided on either or both of the catheter and wire. In yet another alternative, an ultrasonic imaging cathetor or guidewire could be positioned in a vein adjacent to the arterial occlusion site, allowing ianag;ng of the entire occluded ~~ while the guidewire is adwanaed these tht~ough: Other imaging modalities may be muployed including appuatus such as optical col~rence tomography (~ (see U.S. Patent Nos. 5,321,501; 5,459,570; 5,383,467;
and 5,439,000), fluorescence imaging (see U.S. Patent Nos. 4,718,417; and 5,106,387), and Kaman ropy (WO 9?J18008):
Another desirable featum of the methods pmescribed by the t inv~tion includes the rotational positioning of the deflecting catheter 20. It wo oons3a,~ pc~rnrs~nm will be appreciated that the direction of deflection is usually selective, and it will be therefore desirable to aim the sting mechanism from the . subintimal space back toward the arteaial or blood vessel lumen (L). If the catheter 22 is providxl with ultrasonic imaging, such innaging can ba used for rotationally positioning the distal tip of the catheter. The cath~er may be rotationally rigid so that rotation of its proximal end may position the distal end of the devicx in a substantially similar maser or orientation. By detecting the presence or relative location of the blood vessel lumen (L), the deflecting port 22 or other defleGang mechanism can be properly positioned.
In an alternative embodiment, as further illustrated below, a catheter may include a rotationally specific fluoroscopic marker, preferably towards its distal end region. The marker may be such that by observing the two-dimensional image of the marker by fluoroscopic imaging, the rotational direction of the catheter tip can be determined.
Figs. 4-6 illustrate several exemplary deflecting mxhanismms for the catheters providod by the present invaation. As shown in Fig. 4, tyre distal end of a catheter 30 may have a distal port 32, a lateral port 34, and a passive deflecting mechanism 36: The passive deflecting mechanism may include a first and a second inclined guiding surface 31 and 33. The first inclined guiding surface 31 may be formed in a relatively distal position, and may be fonm~ to dirxt the proximal end of a guidewire (not shown) into the main l~~ of the catheter front the distal port 32: The gvtidewire maybe thereafter displaced relatively proximal to the catheter so that the distal end of the guidewire approaches and passes the passive deflecting mechanism 36 in a relatively proximal direction. The second indiaed guiding surface 33, which may be formod in a relatively p3r~oacimal position, may thereafter direct the distal end of the guidewire in a deflected position through the lateral port 34 when the guidewire engages the suond suttee 33 upon subsequent distal CA 02341414 2002-02-15 ", wo oons3s3 rc~rnrs~nsam advancea~c~at of the gui~vire. For mca~m~e, the ~catl~er 30 may be advanoad over the proximal end of a wire ac that tire wire passes over the distal s~uface 3 I of the deflecting mechaniun 36; and back into the main lamer of the catheter 30. In general; the car 30 is advan~aod distally in an over the wire manner relative to tha ~tudevr~re wltea the diets! tip of the guidewire is believed to lie relatively distal to a vaatadar occlusion within a blood vessel wall. The catheter 30 may be advanced over the wire so the distal tip of tl~
catheter enters the subintimal spaco and appnroaches the distal end of the guidewire. By retracting the distal end of tire wire within the lumen of catheter 30 so that its distal tip is proximal to flu deflecting mechanism 36, subsequent distal advancement of the wire dafta will engage the proximal surface 33 of the deflecting mechanism and cause the wire to be deflected laterally through laternl port 34.
Seveisl examples of active deflaaing mochanistns for redirecting a guidewire are illustrated in Figs. 5-ti. A cath~r 40 may be formed with s distal port 42 and a lateral port 44 as shown is Fig. 5. Rather than a passive deflecting mechanism, the cathate~r 40 may include an axially translatable cannula 46 having a resilient, pra.formed distal tip which may be advanced through port 44 as shown with broken lhsts. The cam~ula 46 may include a lumen which provides a guide path for the wire (not shown) why the cannula is placed in a deflected ar non-deflected p~ition. Meanwhile, the catheter 50 '" ° ' iItustrated in Fig. 6 is similar to the call~t~'40 iri'Fig. S, kept that no lateral p~ is provided. Instead, a casmula 52 bavlng a pre-formod distal end may be advanced and retractad out of a distal part 54 of the catheter 50 so that its distal end can assume a Ia~boralIy dctlecaad shoe as shown with broken lines.
It will be appreciated that these embody are intended to be ex~nplary only, and a wide varioty of other passivo and active deflecting mechanisms z1 CA 02341414 2002-02-15 m ~~5~~1~~
may be provided on ding catheters for uee itr accordance with the COnOCptS Of the prC~t ~nVentiOn.
.Referring now to Figs. 7~10, an exemplary defecting catheter 100 formed in accordance with the prhiciplea of the present invention is described in detail according to relative cathe#er suctions. As shown generally in Fig.
7, the deflecting catheter l 00 comprises a caxh~r body 102 having a distal end 104 and a proximal end 106. Catheter body 102 includes a single lumen 108, as shown in Figs: 8-10, and a deflect~ng housing 110 secured to the distal end 104 thereof. An actuator hub 112 may be secured to the proximal end 106 of catheter body 102, and an axially translatable cannula may be disposed within lumen 108. The cannula 114 may be formed with a ~ tip 116, typically formed from a metal, hard plastic, composite, or the Like, optimally being radiopaque. Alternatively or additionally, it may be desirable to provide at least one sepaxme rad~opaque marker or the cannula at or near its distal end to facilitate visuali~at~on under fluoroscopic imaging.
A
distal length I 18 of the cannuta 114 can be pre-forms with a curved shaped as shown in Figs. 7 and 9. A rationally spec~$e radiopaque marker 120 may be mounted near the distal end of catheter body 102. As illustrated; the marker has a generally U-shaped or otherwise directional configuration so that the rotational position of the distal end of the ca#heter body 102 will be apparent when the marker is observed in a two-dimensional fluoroscopic age. . . - , , .
The catheter 100 provides lataral defloction to the distal tip of the c~rmula 1 ! 4 which extends beyond the body 102 through a lateral opening 122 in the deflector housing 1 ! 0 as shown in Figa. 7-9. The deflector housing 110 also includes a distal port I24 to permit introduction of the catheter 100 over the proximal erd of a guidewire GW as illustrated in Fig. 8 with broken lines. The guidawire t3W passes t'Ismugh the distal port 124, and CA 02341414 2002-02-15 ii:
WD ~~
into the distal end of the can~mula 1 I4, and may travel thmug6 a lumen of cannula all the way to the proximal end of the catheter 100. The distal l~h i 18 of canaula 114 may be strand aad de$ecbed by axially retracting and advancing the cant~wla betw~n the configuration shown in Figs. 8 and Fig. 9, respectively. Tl~ ercmula 114 may be formed with an date diameter or cross-seodon to pemoit its pas~ge thmugh the layers of blood vessel wall sad may range firm approximately 1 F to 4 F. The c~ula 114 may be formed of From a wide range of biocotnpatible ma~isls such as polyiaride, PEEK or nitinol. Similarly, the guidewire GW should also have dima~sior~s that allow its travel thorough the relatively thin layers of a blood vessel wall, anti may range firm approxinoately 0.010 in. to 0.038 in.
The GW may be a conventional in~lar guidewire and may be formed of a variety of materials including ataidesa steel and nitinol. The distal tip of the cannula 114 may include a tis9ue penetratnng element 116 to assist the .
cannula in re-entering the lumen. of a blood vessel from within the wall region. Tlu canaula 114 should provide suffieaent sin order to tta~mit enough force to penetrate the inner bleed vessel wall but not enough so as traverse the outer vessel wall to regi~s outside of the blood vessel.
The tissue penetrating element 116 may be formed of gold-plated stainless steel, 24 platinum, or platinum iridimm alloy or other radiopaque materials.
Fig.10 provides an illustration of an actuator hub 112 com~ising a fir of coaxial, telescoping tubes 130 and 132. Tin; outer telescoping tube 132 may be connected to a proximal er~d of cannula 114, typically by an adhesive 134 or any other connective ~. A proximal fitting 136 is ftut>ter atmched to the proximal end of ~e ouoer telescoping tube 132 so that the assembly of the ca:mula 114, the tube 132, sad the fitting 136 may move together as a unit through the hemostatic fitting 140 at the proximal end of the hub 112 The hub 112 may fiuther include a ro~tauo~l fitter 142 which WO 0018323 PGTNS99/1%31 permits the cathatar body 102 to be rioted relative to the hub body. The c~nnula 114 and aver body 102 msOr be romtionaily coupled or "keyed"
together to limit or prevent relative r~on, typically by keying within the hub andlor near the distal ead, so that m~ion of the catheox body causes a like rotation of the cannula as the caZbeder is mrtadonally posidoaed withia a blood vessel. A side branch 14$ may be on hub 112 to permit perfusion andlor infusion ttnough the lumen 108 of catheter 102.
Keying at the proximal end of the catheter 100 can be achieved in a variety of ways. For example, the t~saopi~ cubes 130 and 132 can be provided with asymmetric, mating peripha~al geometries, such as oval cross-sections shown in Fig. l 1A oa iriangulmr crop-secxions shown in Fig. 11B.
Keying at the distal end can also be achieved in a number of ways, such as providing the catb~a body 102 with an asymmetric lumen 108' and the eannula 114' with a madag section, e.g. a D-shaped cross-section as illustrated in Fig. 12. The ability to limit relative rotation of the cannula within the catheter body 102 is bus since it may ensure that the curved distal length 118 is properly oriestted (usually directed radially outvvardty) why the tip 116 m~mrges through the opening 122. In use, the catheter 100 may be advaaadd over gui~dawim t3W whilo the eannula 114 is retracted as shown in Fig. 8. Orrx the afar is properly positioned, the cannula 1 I4 may be distally advanced ~ shown in Figs. 7 and 9. Distal . .. . . . ~~ :may ~ ~~ by ~y fang ~e steeve i32 in the hub 112 relative to the remainder of the lwarb so that the cannulas move forwardly within the linen 108 of the body 102. Prior to advancing ZS the cannula, the port 122 may bo properly posiHOnod so that it is dirocted inward the blood vessel ltnnen by rotating cathOter body 102, typically using the rotational hub 142. Comnndeatty, tht physician may observe the marker 120 so that the lateral port 122 can be d3raxed in the proper ~adially ~~~jt~~
inward direction. Altar tt~ cannula is advanced into the blood vessel, the guidewire GW may then be advanced distally into the lumen, the cannula t I4 may be withdrawn proximally, and the eke catheter assembly may be titan withdrawn from over the guidewire leaving the guidewire in place for introduction of other intarvartional and/or c catheters.
The deflection of a guidewire and/or casuals from within a vascular wall into the blood vessel lumen may be achieved by numerous deflecting mechanisms as described herein. For ox~tple, as shown in Figs. 13A-C, a guidewire deflection system may be formed with a deflection nosecone assembly attached to the distal end of a catheter body. The nosecone ably may be approxunateiy 0.25 in, in length, and may of course vary in shape and dimensions according to particular applications. The body (not shown) may further include a proximal portion, a longitudinal axis; and at least one lumen extending along at least a distal end portion ther~f. As shown in Fig. 13A, a nosecone 200 may be foamed with a distal opening 204, a relatively proximal and spaced apart lateral opening 206, and an inclined surface 208 adjacent to the lateral opeating. The distal opening 204 of the nosecone 200 may have a substantially circular cross-section ranging from approximately 2 F to 6 F. The lateral opening 206 may be configured with an oblong or elliptical crass-section with a relatively lateral diameter of about 0.014 - 0.050 in., and a relatively longitudinal diameter of about 0.050 -0.200 .; ~in. as shown in Fig. l 3B. The distal opening 204 and the tataral opening 2'06 may be spaced apart approximately 2-S mm, and preferably about 3 mm; or at other various distances along tire nosxone 200; and may be both in communication with the cath~etQ body lumen as shown in Fig.13C. The lateral opening 206 and adjacent inclined sut~Ce 208 may receive a cannula passing tirerathrough fivm tire cathetear body lumen. In particular, the canattla (not shown) may have art canaula surface that is configured and sized CA 02341414 2002-02-15 ,i, W~ ~1~~
for slidable auovemenot through the taLeral olxning 206 speciRcally. The cannula may be formed with at least one passageway extending through at . least a distal portion thereof. The distal end of the cannula may be configured to communicate with the inclined surface 208 adjacent to the lateral opening so as to de~Iect the caanula away from the longitudinal axis of the catheter body when the cannula is advance in a relatively distal direction.
Additionally, the distal portion of the ~ may have a pre-formed shape resilient curve, and may lx slidably positioned within the lumen of the catheter body. The ~stal cannula portion may have a relatively axially aligned configuration with the lumen when the carrots is positioned within the catheter body, and may have a relatively curved configuration with the lumen when the carrots travels along the inclined surface 208 and through the lateral opening 206 of the catheter body when the carrots is distally advanced through the lumen within the catheter body. The pre-formed shape resilient curve at the distal portion of tla; carrots may extend over an arc in the range from approximately 15 to 135 degrees, and may have a radius in the range from approximately 1 nun to 20 mm. The carrots may also include a self pen~ting distal end that includes a sharpened distal tip. Moreover, the canaula may include a radiopaque or orientation marker substantially near its distal end or along any portion thereof.
The guidewire deflection system may ~utber include a guidewire ' configured to pass thmiagh a passageway formed is!'rhe caaaula. The guidewire (not shown) may be formed with an external guidewire surface that is configured or sized for alidable movement through the distal opening 204 of the aosecorar 200, and may range from approximately 0.010 - 0.038 in.
When the guidewire is initially placed within the layers of blood vessel wall along a selected dissection plane, the distal opening 204 of the noaccone 200 may receive the proximal end of the guidewire to permit its passage 2?

CA 02341414 2002-02-15 iu wo oon~ rc~rnrs~n~~
therethmugh and along a la~ngit~inal hun~a formod within a c~aaala in the attached catheter body. The nosecone 200 may be tapered and formed with a ~t~y ocular or elliptical cross.section; or may even have a vv~ige shaped cross-section ar any othac coon that may facilitate passage in between the vessel layers along the selected disse~on plane. Moreover, a hub (not shown) may be rotationally secural to the proximal end of the catheter body to controllably rotate the canoula and the catheter body (see generally Fig.10). The hub may finrth~ include a controller connected to the cermula for controlling the slidabte movement of the cannula within the catheter body (see generally Fig. '~. After tl~ location and orientation of the distal tip of the guidewira is ascertained, the guidcwire may be deflected into the blood vessel lumen by withdrawing the c~mula and guidewire in a relatively proximal direction so at (east the distal tip of the cannula is proximal to the lateral port 206 and the inclined s~u~aCe 208. The cannula may be then advanced in a relatively distal direction so the tip of the cannula, arhich may be relatively sbarpenod, engages the inclined surface 208 adjacent to the lateral port 206. The guidewire may be advancxd distally thereafter, and relatively lateral deflection of the guidewire is thus Thieved by the deflection nosecone assembly. Additionally, the guidewire, cannula, or catheter body may also include means for imaging tissue surrounding flaw wire. The distal end of the cathefier body may include a tluoroscopically visible marker subs~ially rear its distal"chd to permit visual determination of the rotational orientation of the noseeone 200. The nosecone 200 may Iilcevvise have a variety of fluoroscopic markets.
Figs. 14A-H provide additional illustrations of an intravaseular that includes a guidewire ion as~nbly 210. The catheter may be formed with a pair of relatively inner and outer shags 212 and 214 that are coaxiatly positioned with reject to each othor. A one portion 215 may CA 02341414 2002-02-15 ", we oona~ r~c~rnrs~nm be ooanected to the distal ot~d 216 ofthe outs ciahetar shaft 214 by 1<nowa techniques in the art. Additionally, a 220 may be positioned within the c~heter that is foxed with a guidewire passageway and an external cannula surface. The cannuta 220 may be coanacted to the inner shaft 212, and may be slidably positioned within at least a portion of the longitudinal lumen 224 of the outca~ catheter abaft 214. The cannula 220 may not naxssar~y exoead within the e~ire length of the catbe~, and may be Ioc~ed wctanal to the cathaGa along scone reLtivaly proximal poz'tion. 'As shown in Fig. 14B, the distal end of the inner shaft 212 may come is contact with the proximal end of the uosecorie 215 whoa advanced distally so as to controllably Iimit the extended length of the canaula 220. The actanaI
surface of the camnula 220 may 1x aanf gnrad for selective passage of the cannula through a first or lateral port 226 but not through a second or distal port Z28 formed is the nosecone 21 S. A guidewire 230 formed with an dal s~u~Oe may be thus configured far gasmge through the distal port 228 too, and may be slidably positioned within st least a portion of the c~ula passageway. W'hm tta; ~nuia 220 is positioned relatively coaxial within the catheter, the guidewire 230 within the cannula may be directed to enter or to exit the catheba through the distal port 228. The first port 226 in the nosecone 215 may have a first transver$e cros:~.soctioc~si area, and may be in communication with a loagiduiinal lumen 224 that is defined by the inner ~ of the outer shaft 214: Tlie port 228 may also be in communication with the loag~di~nal lumen 224, wherein the socvnd port is formed with a second transverse esomonai area. The ixast c~-sectional area may be relatively larger or scnall~ than the second cross-sectional area, and are prefierably foamed with di~rent dimensions or configurations so selective pas:s~e of the 220 may be achieved.

CA 02341414 2002-02-15 ", wo oo~ns3as rcr~n98~~
A variety of imaging and ori~ddiaai markers may be also positioned along various por<iooa of the guidavvire 230, cantmla 220 andlor catheter body. In particular, tha noseoone 215 may include a radiopaque marker or imaging componentry that provi~s dua~tianal orientation of the distal portion of the catlu~a~ as tl~e re),ative di~ctioa lm which the lateral port 226 is facing. The nosocone 215 may include poets of various sizes, and may define a first port 22b as a substantially elliptical orifice and the secand port 228 as a substantially circular ark. T!x itamediate at~ea of noseoone 215 surrounding the fast port 22b may de~e an inclined surface 232 for receiving a distal canmila tip section 234 that leads to the first port.
Additional guidewire de8ectin~g, mechanisms provided in accordance with the invention are shown in Figs. 15-20. A flapptr assembly 240, as shown in Figa. I 5A-E, may be positioned at the distal portion of a catheter to controllably deflect a guidewire 242. The i~appa~ assembly 240 may be formed at the distal end of a catheter shaft to provide a redirectable intravascular guidcv~rlre cat>tetar. The ca;heter shall (not Shawn) may have a distal end, a proximal earl, a longitudinal axis, and at least one lumen extending along at least a portion of catheter abaft and the longitudinal axis of the catheter shaft. The Sapper assembly 240 may have a distal end port 244, a lateral port 246, and a flapper valve or machanism 248 with a deflectable exoension 250. The deflectable ion 250 may include a biased inclined surface which may have multiple curva~ sections. Additionally; as shown in Figs. l SA-B; the dble extension 250 may have a first position or configuration that dinxts a guidowre t~ 254 through the distal end port 244 what the guidewire tip is pa~sitlom~ed rcletively distal to the deflectable extension 250. The deflectable eion 250 may also have a second pa~ition that dirocts the guidawire tip 254 thmugh the lateral port 246 when the tip is positionod relatively proximal to the d~lectablc eotens~ion 250, and CA 02341414 2002-02-15 in wo oons3~ rcrmsm~nm advanced ~ is a relatively distal dir~ec~on~ as shown in Figs.15C-D.
The flapper valve 248 may be also form~dd with a relatively distal collar 256 ~ ~ p~itioned sub~a~ially adjacent to the distal end port 244. The distal collar 256 may be formed with a longitudinal length defined by the distaace bern the lateral port 246 aad the distal port 244. At least a paation of the flapper assembly 240, including the collar portion 256, may be formed of a fluoroscopic or radiopaque material to pa~ovide an orientation marker for directional placeaneat of the guidewire 242.
In another variation of the invadion, as shown in Fig.16A, the flapper mechanism 260 may be formed relatively e'cternally or relatively outer to the catheter body 262. The collar portion 266 of the flapper mechanism 260 may be positioned on the outer surface of the catheter body 262 along a relatively distal portion or along any otbscr saxion of the same. Furtlxrrmore, the deflectable extension.270 may be integrally formed or conaected to the collar I S 266, and may extend through a relatively distal portion of the lateral opening 264 into the interior luda~cn of the catheter body 262. Although the guidewire deflectors shown in the preceding illustt'atio~ have been depicted as sepan~te components, they may be of court integrally formed from a single piece of suitable material. In addition, as shown in Fig. 16B, a guidewire may be inserted into the interior lumen of the esthete body 262 through an opening 263 that may be formed relatively praxin~al to the flapper mechanism 260.
The guidewire may be still positianed in at least a relatively distal portion of the interior catheter lumen. A relatively rigid or stiff' manlxr 269, which may be forn~ed of stainless steel, may thus occupy a substantial proximal length of the cstlarter body lumen, to provide impmvcxl torque transmission.
Figs. 17 A-D illustrates the distal section of a redir~table guidewire cathCter. The redirectable guidevvire catl~r may comprise a catheter shaft 280 fo#nned with a first lumen 282 and a secxmd lumen 284 each actendiug wo oona~ ~crnrs~n~~
along the catheter shaft reapxtiveiy to a f rst distal opening 286 and a second distal opening 288. The cathota may include an actuator wire 290 slidabiy positioned with the first linen 282 of the esthete shaft 280. The actuator wire 290 inay be formed wide a preforriud distal end 292 to pmvide an acxiiated position that subsraoxially ext~ds or is biased towards the second distal opening 288 when advae~d relatively distal through the first distal opening 286. The secomd distal opening 288 unsay be thus obstructed or at least covered in part which will Lead to direct a guidewire 285 passing thmugh the sxond lateen 284 and distal. opening 288 away from the longitudinal axis of the her sl~ft 280. The guidewire 285 may be slidably positioned within the second lumen 284 of the catheter shaft 280, and may be deflected when advanced relatively distal through the second distal opening 288 and when the achrator wire 290 is placed in its actuated position.
As sl~wn in Fig. 17A, the actuator wire 290 rnay extend through the first distal opening 286 of the first tames 282 and may still remain within as interior distal nosocotx portion 295 of the c~ister. The distal most tip 294 of the actuator wire 290 may be formed with a flattenal portion that rests on a relatively level surface withia the noseoone pardon. Alternatively, the actuator wire 290 iiiay be configured to s~ctend outside of or beyond the outer surface of the catheter body or nosocanc portion 295 (not shown). The first distal opening 286 and/or the second oponiiig 288 may be formed at the distal most end portions of the caste= shaft 280 or at some point relatively proxianal thereof. The first and second lumens 282 and 284, which lead to their respective distal openings 286 and 288, may be formed with a variety of cross-sectional configurations and positions relative to one another. Far example, as shown in Fig. l?8, the actuator wire lumen 282 may be formed with a crescent or aro-shaped coi~~g~n~tion to guide an acriiator wire 290 Hugh. The guldewire hmien 284 array be formed with conventional CA 02341414 2002-02-15 m wo oQns3Z3 rcrrt~s~nm circular crass-section and po~sitia~d sido-by-side'reIative to the armor wire lumen 282. The actuator wire lumen 28~ may have an inner radius of about 0..017 in.; and an outer radius of about 0.014 in. The guidewire hung 284 may be also formed with a diameter of about 0.018 in. The outer diameter of S the catheter shaft 280 may be about 0.03$ in: These dimatsions may be of course varied according to particular appUcationg. At least a distal portion of the actuator wire 290 may be thus formed of a half-cylinder hypotube, as shown in Fig. 17C, far slidable movement within the actuator wire lumen 282. This configuration may further guide or direct a guidewire 285 extending from tint adjacent lumen 284. The actuator wire 290 may of course have a proximal section formed with any other type of cross-section, and may include only a distal suction that is formed with an arc-shaped region to controllably deflect the guidewire 285 is a predetermined direction.
Figs. 18A-C illustrates the distal sextion of a nasecone assembly 300 formed at the distal end of a redircctable guidcwire catheter. The catheter may be configured for crossing a subsra~ttially occluded blood vessel, and may include a catheter shaft formed with a distal portion and a longitudinal antis, and wherein the catheter shaft has a first lumen and a second lumen each extending along the catheter shaft (see generally Fig. 17B). The first and the second lumen may be also configured in a relatively side-by-side configuration along the catheter shaft. As shown in Fig. 18A, a nosecone 300 may be formed at the distal portion of tin; ~ shaft (not shown); and may include a single distal orifice 302 and an interior region 304. The interior region 304 of the nosecone 302 may be forraed with a tapered surface 306 that is shaped to contact an actuator wire 308. The actuator wire 308 may be slidably positioned with the first lumen of the cat>xter shaft. Tix distal tip of the acd~ator wire 308 may be redirected aubstaatially away from the longid~dinal axis of the catheter shaft when advec~ced relatively distal along we oQna323 PCTNS99/i983i the tapered surfax 306 of the nosxone 300 and through the nosecone orifice 302. The actuator wire 308 rnay remain within the interior region 304 of the nosecone section 300, or it m;ay extend huther away from or beyond the catheter shaft to paretrata tissue in adjoin area. A guidewire 310 may be also sIidably positioned within the sooond lumen of the ~tbetCr shaft; The guidewire 310 may be initially positioned within the seleatcd dissection plane within a blood vessel wall, and may support positioning of the catheter in an over the wire manner. R~htn the catheter is passed over the proximal portion of the guidewire and distally advanced, as shown in Fig. 18B, the guidewire 310 may travel in a relatively linear fashion along the longitudinal axis of the catheter shaft. However, when the distal end of the guidewire 310 is rehacted into the nosecone section 302, and the actuator wire 308 extended distally, subsequent advancement of the guidewix!e will result in its deflection and movement away from the catheter shaft in as askew manner. As shown in Fig. 18C, the guidewire 310 is defected away from the longitudinal axis of the catheter shaft by coning the redirected actuator wire 308 when the guidewire is advanced relaxively distal through the distal orifice 302. The orifice 302 may be formed at the distal most end of the catheter shaft or along any relatively proximal portion thereof. The catheter shaft and the nosccone 302 may be integrally formed or separately fonned and joined together by camventional techniques.
... ,. . . Fig. 19 illustrates another embodiment of the invention theft provides as intravascutar catheter for selectively ckf3ecting a guidewire. The catheter body 320 may be formed with a longitudinal lumen that includes a support tube 322 slidably and mtatably positioned within the longitudinal lumen of the catheter body. The support tube 322 may have a distal tube end sad a tutee port 324, and may also dofme a conduit that is in t~uid communication with the tube port. The distal tube end may be also fornred with a cut-out portion r.
wo oona~ rc~rros9snm 326. The catheter may also include a ca~nla 328 having a distal c~mula std, a eannula port 330 fornaed at 'its diatai rod, and at least one passageway extending through at least a distal and po~rdon d~of in fluid communication with the cantwla port. The drat port~ott of the canm~la may have a pro-fnr~ shape re,9iIiet~t cu:ve, and may be sl~lably positioned within the conduit of the support tube 322. The support tube 322 may have a longitudinal axis so that tbo distil portion of tire cannula is relatively with respect to the longitadiaal axis of the suppbit tube when the cannula 328 is positioned within the support t~ and is :vely askear wide respect to the longitudinal axis of the support tube wben the distal cannula end extends beyond the distal end of the cathCter bddy 320. A guidewire (not shown) may be positioned within at least a portion of the cnmnula passageway. When the support tube 322 aid the cannula 328 are placed in a retracted position within the cath~er body 320, the dis~l opening of the cannnla 328 within the catheter may pass over the guidewire. The catheter body 320 may be moved relatively proximally so the ~ppat tube 322 a~noends beyond the cathebar body to expose the cut-out portion 326 of the support tube. The canmila 328 within the support tube 322 may be ~ sdvanced distatty in order for the pre-formed distal cannula portion to da8ect away frora the longitudinal axis of the catheter body 320. The distsi tip of the guidewire may be thus deflected in subataatially the same as the distal portion of tire _ . ~:. ~~ when advancxd in a relatively dual direction vv~'thiii the canaula 328:
The proximal tube end of the support. tube may be also cod to a ro~ng assembly (not shown) to rotate the support tube relative to the cathe~ body.
The cutout portion 326 of the support tube 322 may be align~l in a spocific manner which guides the I diroation in whip the distal cannula po=tion is pored and extended outside of the catlu~er.

~~1 Anatl~x intravase~r provided in accordance with the iavemion is fucthsr shown in Fig. 20. T6s gay also incdnde a catheter body 340 farmed with a distri end, a cathater port 342, a lob axis, and a longitudinal lumen 8aalong at least a distal portion of the deter body in fluid comaatuucation with tire catheter port. A cannoula 348 with a distal caanula and 344 may be slidably positioned within the longitudinal lumen of the . body 340. At least one passageway spay ba formed in the cannula 348 which may provide for slidable movement of a guidewire. The passageway may be in fluid comtnunication with a canaula port formed at the distal end 344 of the cannula. The distal end 344 of the cannula may further include a support tube section 350. The support tube 3S0 may be formed with a distal tube end section 352, a proximal tube end section 354, and a backbone 356 contreettag t!u distal and the proximal tube end sxtions. The backbone 356 of the supp~tt tube 350 may include a plurality 1 S of cut-out rib sections. The removed portions of the support tube 350 may provide reduoad compression,and increased flexibility of the support tube, and may support more raspoosive deflecting movement of the distal cannula end 344. The support tube 350 may be also p~raformed with a predetermined shape to deflect the distal catst~ula end 344 away from the longitudinal axis of the catheter body 340 when the distal cannula end is extended proximally past the distal end of the catheter body. Alternatively or additionally, the distal .. .. . . . , .. . . . . .: Paula end 344 may be preformoed with'a predetern~itied~shape~ that deflects away from the longitudinal axis ofthe c:xheta body 340 end when cxtarded past the distal end of the cer body. Tlx mmanula 348 may be slidably movable within the longitudinal lumen of the over body 340. As with other ~nulas described hen, tha proximal sad of the cannula may be connected to a hub assembly that provides or aapports rotational or CA 02341414 2002-02-15 ii, wo oona~ pc°rrus~nm longitudinal movement of the casuals in either a t~elatively distal or pmxmal movement relative to the catheter body.
Wye all of the pinvelrtiaat have been described with rdcrence to the afore~ionied spplica~ions, this description of various ~ embodiments and methods shall sot be construed in a limiting sense. The aforementioned is pre~d 8or pucpots~s of illaseration and complete description that are consistent with all applicable standards. It shall be understood that all of the ink am not limited to the specific depictions, configurations or relative praporticu~a.set forth herein which depend upon a variety of eotulitionn end variables. The specification is not inte~ndcd to be exhaustive or to timut the invention to the precise forms disclosed herein. Various modifications and insubstantial changes in fotrn and detail of the particular ~nbodiments of the disclosed invention, as well as other variations of tl~ iuv~ioa, w~l be apparent to a person skilled in the art upon reference to the present disclost>re. It is therefore contemplated that the appended claims shaft cover any such ~difications, variations or equivalents as to the described embodiraeata as falling within the we spirit and scope of the invention.

Claims

WHAT IS CLAIMED IS:

1. A guidewire deflection system comprising:
a catheter body having a proximal end, a distal end, a longitudinal axis, and at least one lumen extending along the catheter body;
a nosecone formed at the distal end of the catheter body having a distal opening in communication with the catheter body lumen, a lateral opening spaced relatively proximal to the distal opening that is in communication with the catheter body lumen, and an inclined surface formed proximally adjacent to the lateral opening; and a cannula having a proximal end, a distal end, and at least one passageway extending through at least a distal portion of the cannula, wherein the distal end of the cannula is configured to deflect away from the longitudinal axis of the catheter body when the distal end thereof engages the inclined surface adjacent to the lateral opening.

2. A guidewire deflection system as recited in claim 1, wherein the distal portion of the cannula has a pre-formed shape resilient curve and is slidably positioned within the lumen of the catheter body, and wherein the distal portion has a relatively axially aligned configuration with the lumen when the cannula is positioned within the catheter body, and a relatively curved configuration with the lumen when the cannula travels along the inclined surface and through the lateral opening of the cannular body when the cannula is distally advanced through the lumen within the catheter body.

3. A guidewire deflection system as in claim 2, wherein the pro-farmed shape resilient curve at the distal portion of the cannula extends over an arc in the range from 15 to 135 degrees.

4. A guidewire deflection system as in either claim 2, wherein the pre-formed shape resilient curve has a radius in the range from 1 mm to 20 mm.

5. A guidewire deflection system as recited in claim 1, wherein the cannula is configured for slidable movement through the lateral opening.

6. A guideline deflection system as recited in claim 1, further comprising a guidewire configured to pass through the passageway of the cannula.

7. A guidewire deflection system as recited in claim 6, wherein the guidewire is configured for slidable movement through the distal opening of the nosecone.

8. A guidewire deflection system as recited in claim 6, wherein the guidewire has a sharpened distal tip.

9. A guidewire deflection system as in claim 6, wherein the guidewire comprises means for imaging tissue surrounding the ware.

10. A guidewire deflection system as in claim 1, wherein the cannula is formed with a self-penetrating distal end.

11. A guidewire deflection system as recited in claim 10, wherein the self penetrating distal end includes a sharpened distal tip.

12. A guidewire deflection system as recited in claim 1, wherein the cannula includes a radiopaque marker substantially near its distal end.

13. A guidewire deflection system as recited in claim 1, wherein the distal end of the cannula includes a radiopaque marker.

14. A guidewire deflection system as recited in claim 1, wherein the distal end of the catheter body includes a fluoroscopically visible marker substantially near its distal end to permit visual determination of the rotational orientation of the nosecone.

15. A guidewire deflection system as in claim 1, wherein the nosecone is formed with a substantially circular cross-section.

16. A guidewire deflection system as in claim 1, wherein the nosecone is formed with a wedge shaped cross-section.

17. A guidewire deflection system as in claim 1, wherein flat nosecone is formed with a substantially elliptical cross-section.

18. A guidewire deflection system as in claim 1, further comprising a hub rotationally secured to the proximal end of the catheter body to controllably rotate the cannula and the catheter body

19. A guidewire deflection system as in claim 18, wherein the hub includes a cannula controller connected to the cannula for controlling the slidable movement of the cannula within the catheter body.

20. An intravascular catheter comprising:
a catheter shaft having a distal end and a longitudinal lumen;
a nosecone positioned at the distal end of the catheter shaft having a first port in communication with the longitudinal lumen formed with a first transverse cross-sectional area, and a second port in communication with the longitudinal lumen formed with a second transverse cross-sectional area relatively smaller than the first transverse cross-sectional area;
a cannula having a passageway that is slidably positioned within at least a portion of the longitudinal lumen of the catheter shaft, and is configured for passage through the first port but not through the second port of the nosecone; and a guidewire that is slidably disposed within at least part of the cannula passageway is configured for passage through the second port.

21. An intravascular catheter as recited in claim 20, wherein the nosecone includes an imaging component that provides directional orientation.

22. An intravascular catheter as recited is claim 20, wherein the nosecone includes a radiopaque marker.

23. An intravascular catheter as recited in claim 20, wherein the nosecone defines the first port as a substantially circular orifice and the second port as a substantially elliptical orifice.

24. An intravascular catheter as recited in claim 23, wherein the nosecone further defines an inclined surface leading to the second port.

25. An intravascular catheter as recited in claim 24, wherein the nosecone defines the first port and the second port, further defines an inclined surface.

26. A redirectable intravascular guidewire catheter comprising:
a catheter shaft having a distal end, a proximal end, a longitudinal axis, and at least one lumen extending along at least a portion of catheter shaft; and a guidewire deflector formed at the distal end of the catheter shaft having a distal end port, a lateral port, and a flapper assembly with a deflectable extension having a first position that directs a guidewire tip through the distal end port when the guidewire tip is positioned relatively distal to the deflectable extension, and a second position that directs the guidewire tip through the lateral port when the tip is positioned relatively proximal to the deflectable extension and advanced thereafter in a relatively distal direction.

27. A redirectable intravascular guidewire catheter as recited in claim 26 further comprising a guidewire that is slidably positioned within the lumen of the catheter shaft.

28. A redirectable intravascular guidewire catheter as recited in claim 26, wherein at least a portion of the flapper assembly is formed of a radiopaque material to provide an orientation marker for directional placement of a guidewire.

29. A redirectable intravascular guidewire as recited in claim 26, wherein the flapper assembly is formed with a relatively distal collar that is positioned substantially adjacent to the distal end port.

30. A redirectable intravascular guidewire catheter as recited in claim 26, wherein the distal collar is includes radiopaque material.

31. A redirectable intravascular guidewire catheter as recited in claim 26, wherein the distal end of the catheter shaft is formed with an exterior surface, and wherein the relatively distal collar of the flapper valve is positioned on the exterior surface of the distal end of the catheter shaft.

32. A redirectable intravascular guidewire catheter as recited in claim 26, wherein the guidewire deflector and the catheter shaft are integrally formed.

33. A redirectable intravascular guidewire catheter as recited in claim 26, wherein the proximal end of the catheter shaft includes a stainless steel wire, and the catheter shaft is formed with an opening relatively distal to the wire for passage of a guidewire.

34. A redirectable guidewire catheter comprising:
a catheter shaft formed with a distal end, and having a first lumen and a second lumen each extending along the catheter shaft respectively to a first distal opening and a second distal opening;
an actuator wire slidably positioned within the first lumen of the catheter shaft, wherein the actuator wire is formed with a preformed distal end to provide an actuated position that is biased towards the second distal opening when advanced relatively distal through the first distal opening; and a guidewire slidably positioned within the second lumen of the catheter shaft that may be deflected when advanced relatively distal through the second distal opening and when the actuator wire is placed in its actuated position.

35. A redirectable guidewire catheter as recited in claim 34, wherein at least a portion of the actuator wire is formed of a half-cylinder hypotube.

36. A redirectable guidewire catheter as recited in claim 34, wherein the preformed distal end of the actuator wire is formed with a arc-shaped cross-section.

37. A redirectable guidewire as recited in claim 34, wherein the actuator wire extends beyond the outer of the catheter shaft.

38. A redirectable guidewire catheter comprising:
a catheter shaft formed with a distal portion and a longitudinal axis, and wherein the catheter shaft has a first lumen and a second lumen each extending within the distal portion of the catheter shaft;
a nosecone formed at the distal portion of the catheter shaft, wherein the nosecone includes a distal orifice and an interior region, and wherein the interior region of the nosecone is formed with a tapered surface and is in communication with the first and second lumens;
an actuator wire formed with a distal tip that is slidably positioned within the first lumen of the catheter shaft, wherein the distal tip of the actuator wire is redirected substantially away from the longitudinal axis of the catheter shaft when advanced relatively distal along the tapered surface of the nosecone and through the nosecone orifice; and a guidewire slidably positioned within the second lumen of the catheter shaft that may be deflected away from the longitudinal axis of the catheter shaft by contacting the redirected actuator wire when the guidewire is advanced relatively distal through the distal orifice.

39. A redirectable guidewire catheter as recited in claim 38, wherein the catheter shaft has a distal most end, and wherein the orifice is formed at the distal most end of the catheter shaft.

40. A redirectable guidewire catheter as recited in claim 39, wherein the catheter shaft and the nosecone are integrally formed.

41. A redirectable guidewire catheter as recited in claim 38, wherein the first and the second lumen are arranged in a side-by-side configuration.

42. An intravascular catheter for selectively deflecting a guidewire comprising:
a catheter body formed with a distal end and a longitudinal lumen formed along at least a portion of the catheter body;
a support tube having a distal tube end, a proximal tube end, a tube port formed at the distal tube end, and a conduit formed within the support tube in communication with the tube port, wherein the distal tube end is formed with a cut-out portion, and wherein the support tube is slidably and rotatably positioned within the longitudinal lumen of the catheter body; and a cannula having a distal cannula end, a cannula port formed at the distal cannula end, and at least one passageway extending through at least a distal end portion of the cannula that is in communication with the cannula port, wherein the distal portion of the cannula has a pre-formed shape resilient curve, and wherein the cannula is slidably positioned within the conduit of the support tube, wherein the distal end portion of the cannula is relatively aligned with respect to a longitudinal axis of the support tube when the cannula is positioned within the support tube when the distal cannula end extends beyond the distal end of the catheter body.

43. An intravascular catheter as recited in claim 42, further comprising a guidewire with a distal tip positioned within at least a portion of the cannula passageway, wherein the distal tip of the guidewire is deflected in substantially the same direction as the distal portion of the cannula.

44. An intravascular catheter as recited in claim 42, wherein the proximal tube end of the support tube is connected to a rotating assembly to rotate the support tube relative to the catheter body.

45. An intravascular catheter for selectively deflecting a guidewire comprising:
a catheter body formed with a distal end, a catheter port formed at the distal end of the catheter body, a longitudinal axis, and a longitudinal lumen extending within at least a distal portion of the catheter body in communication with the catheter port;
a cannula having a distal cannula end, a cannula port formed at the distal cannula end, and at least one passageway formed within at least a distal portion of the cannula in communication with the cannula port, wherein the cannula is slidably positioned within the longitudinal lumen of the catheter body; and a support tube connected to the distal cannula end, wherein the support tube is formed with a distal tube end section, a proximal tube end section, and a backbone connecting the distal and the proximal tube end sections, wherein the support tube is preformed with a predetermined shape to deflect the distal cannula end away from the longitudinal axis of the catheter body when the distal cannula end is extended past the distal end of the catheter body.

46. An intravascular catheter as recited in claim 45, wherein the distal cannula end is preformed with a predetermined shape that deflects away from the longitudinal axis of the distal cannula end when extended past the distal end of the catheter body.

47. An intravascular catheter as recited in claim 45, wherein the cannula is slidably movable within the longitudinal human of the catheter body.

48. An intravascular catheter as recited in claim 45, wherein the backbone of the support tube includes a plurality of cut-out rib sections.

49. A redirectable intravascular guidewire catheter comprising:
a catheter shaft having a distal end, a proximal end, a longitudinal axis, a first port formed at the distal end of the shaft, a second port spaced relatively proximal to the distal end of the shaft, and at least one lumen extending along at least a portion of the longitudinal axis of the catheter shaft in communication with the first and second ports; and a guidewire deflector formed within a distal extremity of the catheter shaft having a first surface that directs an end portion of a guidewire between the catheter shaft lumen and the first port, and a second surface that directs the end portion of the guidewire between the catheter shaft lumen and the second port.

50 The redirectable intravascular guidewire catheter as recited in claim 49, wherein the guidewire deflector includes a flapper valve having a first position that provides the first surface for contact with the guidewire, and a second position that provides the second surface for contact with the guidewire.