CN207821956U - A kind of expandable stent system - Google Patents
A kind of expandable stent system Download PDFInfo
- Publication number
- CN207821956U CN207821956U CN201720464398.3U CN201720464398U CN207821956U CN 207821956 U CN207821956 U CN 207821956U CN 201720464398 U CN201720464398 U CN 201720464398U CN 207821956 U CN207821956 U CN 207821956U
- Authority
- CN
- China
- Prior art keywords
- expandable stent
- enlarged portion
- stent system
- guiding tube
- opening
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Active
Links
Abstract
The utility model provides a kind of expandable stent system, and the normal structure of circumferencial direction can be caused damage by solving the problems, such as existing medicinal balloon during the administration.The utility model includes:Catheter main body bar;The expandable stent being at least partly inserted in inside catheter main body bar, expandable stent include enlarged portion and interconnecting piece, and opening is provided in enlarged portion;Center guiding tube is inserted in the inside of expandable stent, and the first end of center guiding tube and one end of enlarged portion connect;Handle apparatus, handle apparatus are connect with the second end of interconnecting piece and center guiding tube respectively, and the regulating switch that can be moved along the axial direction of catheter main body bar is provided on handle apparatus;Inner tube, inner tube are set to the inside of expandable stent, one end of inner tube and the open communication of enlarged portion, and the other end of inner tube is connect with handle apparatus;When regulating switch is moved along the axial direction of catheter main body bar, expandable stent is relatively moved with center guiding tube, and enlarged portion is driven to be in expansion state or contraction state.
Description
Technical field
The utility model is related to Design for Medical Device technical field more particularly to a kind of expandable stent systems.
Background technology
With the fast development of international, domestic intervention medical treatment, medical instrument is introduced into patient bore (such as blood vessel, gas
Pipe, biliary tract etc.) the various diseases of targeted therapy become more and more, especially by medical instrument targeted delivery therapeutic agent treatment office
Portion's disease is increasingly common, such as holder, conduit, foley's tube etc..
In several years in past, a large amount of interventional medical devices that target are developed.Drug stent is presently the most common target
To one of intervention therapeutic apparatus.Holder is to be coated in rack surface after mixing therapeutic agent and polymer substrate, forms an office
Portion's drug slow release system, after stenter to implant blood vessel or other inner cavities, therapeutic agent can slow release continued for several weeks or several months
Time, in addition the supporting role of holder, can effectively treat blood vessel or the narrow or occlusion of other inner cavities.However holder also has perhaps
More shortcomings, such as holder understand lasting residue in human body, and since the presence of holder needs long-term antiplatelet drug to control
It treats;Occur again it is narrow after, holder should not be implanted into again;Polymer will produce local chronic inflammatory reaction etc..
Other than holder, foley's tube is also another common target administration instrument.Foley's tube is by ball
Capsule surface coated medicament, realizes the purpose of target administration, is usually used in in-stent restenosis, lower Extremity Arterial Diseases, blood vessel point at present
The treatment of the diseases such as fork.Common foley's tube designs for single saccule, and medicinal balloon technology needs sacculus being sent to diseased region
Afterwards, (0-2min) discharges drug, targeted therapy pathological tissues or blood vessel within the of short duration time of balloon expandable, and treatment is narrow, closes
The diseases such as plug.However medicinal balloon is disadvantageous in that, since medicinal balloon needs carry out drug release in most time,
Therefore the adhesion strength of medication coat and balloon surface cannot be too strong, which results in medicinal balloon transmission process, a large amount of medicine
Object coating shedding, and the medication coat to fall off can normal tissue generation harmful effect or even generation system toxicity.
Other than medicinal balloon, now in the art there is also double-layered balloon catheter, internal layer sacculus plays expansion in two layers of sacculus
The effect of blood vessel is opened, and outer layer sacculus is made of unique microporous barrier, and the gene of therapeutic effect can will be played in process of expansion
Or drug penetrates into vascular wall, on target organ by outer layer sacculus.Double-layered balloon catheter can effectively overcome drug and convey
Loss in journey reduces the system toxicity of transmission process generation.But therapeutic agent passes through the micropore easy production of process of osmosis outward
Raw a large amount of excessive, excessive therapeutic agent can cause serious harm to distal end normal structure/tube chamber etc..In addition, double-layered balloon often needs
It internal sacculus and the pressurization of outer sacculus, overdistension to be easy to cause lancinating to damage the normal structure of circumferencial direction, increase simultaneously
Add the uncertainty of clinical efficacy.
In addition, there is also the conduits for carrying out targeted therapy to target tissue by micropin in the prior art.Micropin wraps in advance
It is rolled in sacculus, is first pushed forward conduit when treatment and adherent with pathological tissues, then dilating sacculus releases micropin, and micropin is inserted into
Deep Lesions tissue is administered treatment.The shortcomings that this instrument, is that micropin is wrapped in sacculus and is easy to puncture sacculus, and sacculus
Process of expansion is easy to cause damage and process of expansion micropin to be easy sliding in cavity circumferencial direction tissue, and positioning is extremely difficult, behaviour
It is big to make difficulty, clinical efficacy is difficult to determine.Simultaneously because micropin position inaccurate, increases the excessive risk of drug.
Utility model content
The purpose of this utility model is to provide a kind of expandable stent systems, are being administered to solve existing medicinal balloon
The problem of Cheng Zhonghui causes damage to the normal structure of circumferencial direction.
To achieve the goals above, the utility model provides a kind of expandable stent system, including:
Catheter main body bar;
The expandable stent being at least partly inserted in inside the catheter main body bar, the expandable stent include enlarged portion and with
The interconnecting piece of enlarged portion connection is provided with opening in the enlarged portion;
Center guiding tube, the center guiding tube are inserted in the inside of the expandable stent, and the center guiding tube
First end is connect with one end of the enlarged portion;
Handle apparatus, the handle apparatus are connect with the second end of the interconnecting piece and the center guiding tube respectively, and
The regulating switch that can be moved along the axial direction of the catheter main body bar is provided on the handle apparatus;
Inner tube, said inner tube are set to the inside of the expandable stent, and one end of said inner tube and the enlarged portion
Open communication, the other end of said inner tube are connect with the handle apparatus;
Wherein, when the regulating switch is moved along the axial direction of the catheter main body bar, the expandable stent with it is described
Center guiding tube relatively moves, and the enlarged portion is driven to be in expansion state or contraction state.
Wherein, the second end of the center guiding tube is connect with the regulating switch of the handle apparatus;
When the regulating switch is moved along the axial direction of the catheter main body bar, drive the center guiding tube described in
The axial direction of catheter main body bar moves, and the enlarged portion is driven to be in expansion state or contraction state.
Wherein, the interconnecting piece is connect with the regulating switch of the handle apparatus;
When the regulating switch is moved along the axial direction of the catheter main body bar, the expandable stent is driven to be led described in
The axial direction of pipe main body bar moves, and the enlarged portion is driven to be in expansion state or contraction state.
Wherein, the catheter main body bar includes:
First body of rod;
Second body of rod, one end of second body of rod are connect with first body of rod, the other end of second body of rod with
The handle apparatus connection, and the diameter of second body of rod is more than the diameter of first body of rod.
Wherein, when the enlarged portion is in expansion state, the middle section protrusion of the enlarged portion.
Wherein, the enlarged portion includes the preset quantity expanding bar being uniformly arranged around the center guiding tube, described
Interconnecting piece includes the preset quantity connecting rod being uniformly arranged around the center guiding tube, and the preset quantity expanding bar
It connects one to one with the preset quantity connecting rod, the opening is provided in each expanding bar.
Wherein, the rounded, oblong of the opening or rectangle.
Wherein, the opening is rounded, and is opened described in flush or protrusion of the one end of said inner tube with the opening
The surface of mouth.
Wherein, the opening is rounded, and the outer cover of the enlarged portion is equipped with elastomeric plastics, the elastomeric plastics pair
The position being open described in Ying Yu is provided with trepanning, and the shape of the trepanning is identical as the shape of the opening.
Wherein, one end of said inner tube and the flush of the trepanning or the surface of the prominent trepanning.
Wherein, the opening is in oblong or rectangle, and the expandable stent system further includes:
The angle regulator for being set to inside the enlarged portion and being disposed adjacent with the opening, the angular adjustment
Device is provided centrally with preset quantity sliding slot channel, and the angle regulator is run through in each sliding slot channel.
Wherein, one end of said inner tube extends to the opening along the inner cavity of the enlarged portion, and passes through the sliding slot
Channel.
Wherein, the first end of the center guiding tube is connect by guiding tube tip with one end of the enlarged portion.
Wherein, above-mentioned expandable stent system further includes:The seal wire cavity being set in the guiding tube tip.
Wherein, above-mentioned expandable stent system further includes:
One end of the micro-pipe being set to inside said inner tube, the micro-pipe extends to the opening, institute along said inner tube
The other end for stating micro-pipe is pierced by along said inner tube from the handle apparatus.
Wherein, above-mentioned expandable stent system further includes:
It is set to the range marker line on the surface of the other end of the micro-pipe.
Wherein, above-mentioned expandable stent system further includes:
The dilating sacculus being set to inside enlarged portion.
Wherein, above-mentioned expandable stent system further includes:
The balloon expandable perfusion pipe being set to inside the center guiding tube, the balloon expandable perfusion pipe is from described
The second end of center guiding tube extends to first end, and with the sacculus perfusing hole that is set to first end surfaces of center guiding tube
Connection.
Wherein, above-mentioned expandable stent system further includes:
It is set to the first end surfaces of center guiding tube and/or the development point on the enlarged portion surface.
The utility model embodiment has the advantages that:
The expandable stent system of the utility model embodiment is moved by controlling to adjust switch along the axial direction of expandable stent
It is dynamic, drive center guiding tube to be moved along the axial direction of expandable stent, and enlarged portion is driven to be in expansion state or contraction state,
When expandable stent is in expansion state, the enlarged portion of expandable stent can effectively be contacted with lesion region, at the same avoid as
Common balloon expandable process indifference caused by the normal structure of circumferencial direction is damaged, and the stability of clinical efficacy is improved.
Description of the drawings
Fig. 1 a are the first structure schematic diagram of the expandable stent system of the utility model embodiment;
Fig. 1 b are the second structural schematic diagram of the expandable stent system of the utility model embodiment;
Fig. 1 c are the first structure schematic diagram of the expandable stent system split shed of the utility model embodiment;
Fig. 1 d are expandable stent system second structural schematic diagram of split shed of the utility model embodiment;
Fig. 1 e are the third structural schematic diagram of the expandable stent system split shed of the utility model embodiment;
Fig. 2 a are the first structure schematic diagram of the expandable stent system of the utility model embodiment;
Fig. 2 b are the second structural schematic diagram of the expandable stent system of the utility model embodiment;
Fig. 3 a be the utility model embodiment expandable stent system in enlarged portion first structure schematic diagram;
Fig. 3 b be the utility model embodiment expandable stent system in enlarged portion the second structural schematic diagram;
Fig. 4 a be the utility model embodiment expandable stent system in enlarged portion third structural schematic diagram;
Fig. 4 b be the utility model embodiment expandable stent system in angle regulator first structure schematic diagram;
Fig. 4 c be the utility model embodiment expandable stent system in angle regulator the second structural schematic diagram;
Fig. 5 a be the utility model embodiment expandable stent system in guiding tube tip first structure schematic diagram;
Fig. 5 b be the utility model embodiment expandable stent system in guiding tube tip the second structural schematic diagram;
Fig. 6 a are the 5th structural schematic diagram of the expandable stent system of the utility model embodiment;
Fig. 6 b are the 6th structural schematic diagram of the expandable stent system of the utility model embodiment;
Fig. 7 is the 7th structural schematic diagram of the expandable stent system of the utility model embodiment;
Fig. 8 a are the 8th structural schematic diagram of the expandable stent system of the utility model embodiment;
Fig. 8 b be the utility model embodiment expandable stent system in micro-pipe structural schematic diagram;
Fig. 9 a are the 9th structural schematic diagram of the expandable stent system of the utility model embodiment;
Fig. 9 b are the tenth structural schematic diagram of the expandable stent system of the utility model embodiment;
Figure 10 a be the utility model embodiment expandable stent system in the first position schematic diagram that develops a little;
Figure 10 b be the utility model embodiment expandable stent system in the second position schematic diagram that develops a little;
The third place schematic diagram to develop in the expandable stent system of Figure 10 c the utility model embodiments a little;
The 4th position view to develop in the expandable stent system of Figure 10 d the utility model embodiments a little.
Specific implementation mode
The exemplary embodiment of the utility model is more fully described below with reference to accompanying drawings.Although showing this in attached drawing
The exemplary embodiment of utility model, it being understood, however, that may be realized in various forms the utility model without should be by here
The embodiment of elaboration is limited.It is to be able to be best understood from the utility model, and energy on the contrary, providing these embodiments
It is enough that the scope of the utility model is completely communicated to those skilled in the art.
The utility model embodiment, which solves existing medicinal balloon, during the administration can make the normal structure of circumferencial direction
The problem of at damage.The embodiments of the present invention provide a kind of expandable stent system, as illustrated in figs. 1A and ib, including:
Catheter main body bar 1, expandable stent 2, center guiding tube 3, handle apparatus 4 and inner tube 5.The catheter main body bar 1 includes first body of rod
11;Second body of rod 12, one end of second body of rod 12 are connect with first body of rod 11, the other end of second body of rod 12
It is connect with the handle apparatus 4, and the diameter of second body of rod 12 is more than the diameter of first body of rod 11.
Wherein, expandable stent 2 is at least partly inserted in inside the catheter main body bar 1, and the expandable stent 2 includes expansion
Portion 21 and the interconnecting piece 22 being connect with the enlarged portion 21 are provided with opening 211 in the enlarged portion 21.
The center guiding tube 3 is inserted in the inside of the expandable stent 2, and the first end of the center guiding tube 3 with
One end of the enlarged portion 21 connects, and the other end of enlarged portion 21 is connect with interconnecting piece.Specifically, the center guiding tube 3 is arranged
In the cental axial position of expandable stent 2, and the first end of center guiding tube 3 is one end far from handle apparatus 4.
Handle apparatus 4 is connect with the second end of the interconnecting piece 22 and the center guiding tube 3 respectively, and handle apparatus 4
On be provided with the regulating switch 41 that can be moved along the axial direction of the catheter main body bar 1.
Said inner tube 5 is set to the inside of the expandable stent 2, and one end 51 of said inner tube 5 and the enlarged portion 21
Opening 211 be connected to, the other end of said inner tube 5 connect with the handle apparatus 4;
Wherein, when regulating switch 41 is moved along the axial direction of the catheter main body bar 1, the expandable stent 2 with it is described
Center guiding tube 3 relatively moves, and the enlarged portion 21 is driven to be in expansion state or contraction state.
Further, as illustrated in figs. 1A and ib, the tune of the second end and the handle apparatus 4 of the center guiding tube 3
Switch 41 is saved to connect;
When the regulating switch 41 is moved along the axial direction of the catheter main body bar 1,3 edge of center guiding tube is driven
The axial direction of the catheter main body bar 1 moves, and the enlarged portion 21 is driven to be in expansion state or contraction state.
The center guiding tube 3 can slide axially relative to expandable stent 2 and catheter main body bar 1.Center guiding tube 3 is remote
The length d11 of side pole body is 5-100mm, and the length d12 of the proximal end body of rod is 30-2500mm.The distal end of the center guiding tube with
Oval tip or cone point are connected.Center guiding tube 3 from the cental axial position of expanding bar pass through after from first body of rod
It penetrates, extend to second body of rod and is connected with the regulating switch 41 on handle apparatus 4.Expanding bar and oval tip or cone
Shape tip is connected, and connecting rod extends to the cavity of handle apparatus along catheter main body bar and is connected.Pass through regulation handle
Regulating switch 41 on device 4 can pull center guiding tube that guiding tube tip is made to be slided to catheter main body bar direction in an axial direction,
Expanding bar is in that class is trapezoidal or arc-shaped expansion outward;Regulating switch on reversed regulation handle device, in being pushed axially
Heart guiding tube makes guiding tube tip distally slide, to push stretched expanding bar inwardly along in central shaft
The center guiding tube of position is shunk.Or
As shown in Figure 2 a and 2 b, the interconnecting piece 22 is connect with the regulating switch 41 of the handle apparatus 4;
When the regulating switch 41 is moved along the axial direction of the catheter main body bar 1, drive the expandable stent 2 along institute
The axial direction movement of catheter main body bar 1 is stated, and the enlarged portion 21 is driven to be in expansion state or contraction state.
Above-mentioned expanding bar can slide axially with respect to catheter main body bar 1 and center guiding tube 3.The center guiding tube 3 is remote
The length d11 of side pole body is 5-100mm, and the length d12 of the proximal end body of rod is 5-100mm.The 3 distal end body of rod of the center guiding tube from
Expanding bar cental axial position passes through to be connected with guiding tube tip 31 afterwards, and the proximal end body of rod is connected with catheter main body bar 1.Pass through tune
The regulating switch 41 for saving handle apparatus 4, can be pushed axially expanding bar and distally slide, and be in class to push expanding bar
The expansion of trapezoidal or arc.Above-mentioned regulating switch 41 is reversely adjusted, stretched expanding bar can be pulled inwardly to be guided along center
Pipe 3 is shunk.
Further, above-mentioned expandable stent 2 is in hollow structure, and the enlarged portion 21 includes equal around the center guiding tube
The preset quantity expanding bar of even setting, the interconnecting piece 22 include the preset quantity being uniformly arranged around the center guiding tube
A connecting rod, and the preset quantity expanding bar connects one to one with the preset quantity connecting rod, each expansion
The opening 211 is provided on tension rod.Connecting rod and the outer diameter of expanding bar are 0.05-10mm, and the length of expanding bar is (contraction-like
State) it is 5-100mm, the length of connecting rod is 30-2500mm.Enlarged portion 21 includes expansion state and contraction state, enlarged portion 21
When in expansion state, the middle section protrusion of the enlarged portion 21, is in class trapezium structure (as shown in Figure 1a) or arc-shaped knot
Structure (as shown in Figure 1 b), raised section maximum extension diameter d1 are 1-480mm, can be bonded with lesion region tissue tight, are expanded
The design of bar can effectively contact lesion region, while avoiding balloon expandable such as and contacting lesion region process to cavity circumference side
To normal structure caused by indifference damage, improve clinical efficacy stability.In addition, when in class trapezium structure, the enlarged portion
21 every Radical extensin bar respectively includes first segment, the second segment positioned at first segment both sides and third section, and second segment and third section
There is default angle between the first segment respectively.When enlarged portion 21 is in contraction state, each expanding bar of enlarged portion 21
In straight rod-like structure.
The material of above-mentioned expandable stent 2 is polyether block amide, nylon, polytetrafluoroethylene (PTFE), polyurethane, polyvinyl chloride, gathers
In propylene, polymethacrylates, silica gel, rubber, silicon rubber, latex, stainless steel, cochrome, Nitinol, titanium alloy
It is at least one.
Above-mentioned preset quantity can be specially 1,2,3,4 or 5 etc..Preset quantity expanding bar is around center guiding tube circumferencial direction
It is uniform or symmetrical.One end of the preset quantity expanding bar links into an integrated entity with guiding tube tip 31.
Per Radical extensin bar surface, there are one openings 211 for setting, and when expanding bar expansion is in class trapezium structure, opening is located at class
The center of trapezoidal-structure is straight active section;When expanding bar expansion is arc-shaped structure, opening is positioned at the top of arcuate structure
Point position.
Further, above-mentioned opening 211 rounded (as illustrated in figure 1 c), oblong (as shown in Figure 1 d) or rectangle be (such as
Shown in Fig. 1 e).
Microperfusion treatment can be carried out to lesion region by circular open in the utility model implementation, pass through oblong
Opening or oblong openings can carry out high dose perfusion therapy to lesion region.
Specifically, when opening 211 is rounded, circular open diameter d2 is consistent with 5 outer diameter of inner tube;Oblong openings are put down
Straight length d3 is 1-25mm, arc radius 0.05-8mm;The width d4 of oblong openings is 0.1-8mm, and straight length d5 is
1-25mm。
Further, the opening 211 is rounded, and the flush of one end 51 of said inner tube 5 and the opening 211
Or protrude the surface of the opening 211.
When opening 211 is rounded, the inner tube 5 being arranged inside enlarged portion 21 is connected to circular open, one end of inner tube 5
51 is concordant with open surfaces or stretch out, and when stretching, one end 51 of the inner tube and the vertical range on 211 surfaces of opening are 0.1-5mm.
One end 51 of inner tube 5 is 5 degree of -175 degree with the angle of expanding bar horizontal section.
Here, it for carrying out microperfusion treatment to lesion superficial layer region when being open rounded, is set inside expandable stent 2
The one end 51 for the inner tube 5 set is connected to circular open, and one end 51 of inner tube 5 is concordant with open surfaces or stretches out open surfaces 0.1-
5mm is conducive to carry out targeting positioning and microperfusion therapeutic agent to diseased region superficial layer region.One end of inner tube and expanding bar
The angle of horizontal section is 5 degree of -175 degree, and Clinical practice process can expand according to diseased region, pathological structure selection different model
Stent system progress multi-angle targeting is opened to be accurately positioned.
Preferably, as shown in Figure 3a, when being open rounded, the outer cover of the enlarged portion 21 is equipped with elastomeric plastics 6,
As shown in Figure 3b, the elastomeric plastics 6 correspond to the position of the opening 211 and are provided with trepanning 61, and the trepanning 62
Shape is identical as the shape of the opening 211.Flush or the prominent trepanning of the one end of said inner tube with the trepanning
Surface.
The elastomeric plastics 6 are high polymer elastic plastic layer.6 surface of elastomeric plastics is provided with round hole, and circle is opened
The circular open in hole and expanding bar surface is concentric, a diameter of 0.02-5mm.Elastomeric plastics thickness d 6 is 0.1-10mm, the elasticity
The length d7 of the overlay area of plastic layer be expanding bar region or be expanding bar circular open position and apart from opening 1-30mm
Position.One end 51 of inner tube 5 and 61 flush of trepanning of elastomeric plastics 6 or the surface of the prominent trepanning 61, inner tube
The vertical range of 51 protrusion of one end and high polymer elastic plastic layer is 0.1-5mm.
Above-mentioned elastomeric plastics 6 can increase enlarged portion elasticity, reduce in enlarged portion process of expansion caused by tissue wall
Damage.Meanwhile elastomeric plastics 6 can increase the friction coefficient of expanding bar, improve positioning performance when expanding bar expansion, prevent
Expanding bar generates sliding transfer after being attached to tissue wall.In addition, high polymer elastic plastic layer can also improve the bending resistance of expanding bar
Folding endurance energy improves success rate of operation of the expandable stent system when treatment height bending, Serious Stenosis etc. replicate lesion.
Above-mentioned high polymer elastic plastic layer material is polyether block amide, nylon, polytetrafluoroethylene (PTFE), polyurethane, latex, silicon
At least one of glue, rubber, silicon rubber.
As shown in fig. 4 a, high for being carried out to superficial layer lesion region when above-mentioned opening 211 is in oblong or rectangle
Density perfusion is treated, and after expanding bar expansion, lesion region tissue can be embedded in slot opening, be conducive to embedded pathological tissues
Carry out high density perfusion.
At this point, the expandable stent system further includes:Be set to inside the enlarged portion 21 and with 211 phases of the opening
The angle regulator 7 of neighbour's setting, one end of said inner tube extends to the opening along the inner cavity of the enlarged portion, and passes through
The sliding slot channel.As shown in Figure 4 b, the angle regulator 7 is provided centrally with preset quantity sliding slot channel 71, often
The angle regulator 7 is run through in a sliding slot channel 71.
The setting of angle regulator 7 is in oblong or oblong openings proximal end, 7 outer diameter of angle regulator and shape and expansion
The inner cavity of tension rod is consistent, for adjusting perfusion angle.7 center of angle regulator is equipped with the circle that 1-5 internal diameter is 0.02-6mm
Entire angle regulator 7 is run through in column type hollow runner channel 71, sliding slot channel 71, and the angle a1 with expanding bar horizontal section is
0 degree of -75 degree can carry out multi-angle perfusion therapy to embedded lesion region tissue.One end 51 of inner tube 5 is along expanding bar inner cavity
It extends to the proximal end of oblong or oblong openings and passes through sliding slot channel 71.As illustrated in fig. 4 c, one end 51 of inner tube 5 and angle
7 distal sections of regulating device are parallel or stretched out to distal end, and outreach d8 is 0.1-5mm.
It should be noted that the proximal end in the utility model embodiment refers to close to one end of handle apparatus, refer to distally
One end far from handle apparatus.
71 quantity of sliding slot channel of setting is identical as the quantity of inner tube 5 being arranged inside each expanding bar.When sliding slot channel
When 71 quantity is more than or equal to 2, at least one inner tube 5 being connected to sliding slot channel 71 can be used as pumpback pipe to make
With.It, can be to spill over embedded region normal structure week outside pumpback therapeutic process after the high density perfusion therapy for completing regional area
The therapeutic agent enclosed damages caused by reducing therapeutic agent normal tissue.
7 material of angle regulator is polyether block amide, nylon, polytetrafluoroethylene (PTFE), polyurethane, polyvinyl chloride, poly- third
At least one of alkene, polymethacrylates, stainless steel, cochrome, Nitinol, titanium alloy.
Further, the first end of center guiding tube 3 is connect by guiding tube tip 31 with one end of the enlarged portion 21.
Oval (as shown in Figure 5 a) or the taper (as shown in Figure 5 b) in the guiding tube tip 31, the first end refer to far from handle apparatus
One end, the outer diameter of the center guiding tube is 0.05-15mm, when above-mentioned guiding tube tip is oval, guiding tube tip diameter
D9 is 0.1-15mm, and when guiding tube tip is tapered, cone point angle a2 is 5-70 degree, and basal diameter d10 is 0.1-15mm.
Oval tip design can in stent system transmission process effective protection cavity organization, reduce center guiding tube
Tip is damaged in transmission process caused by tissue.Cone point, which is designed with, to be bent by height conducive to stent system, is serious narrow
Narrow equal duplication lesion, improves lesion percent of pass and success rate of operation.
Center guiding tube 3 and the material at guiding tube tip 31 be polyether block amide, nylon, polytetrafluoroethylene (PTFE), polyurethane,
At least one of polyvinyl chloride, polypropylene, polymethacrylates, stainless steel, cochrome, Nitinol, titanium alloy.
Further, as shown in figure 6 a and 6b, the expandable stent system of the utility model embodiment further includes:It is set to
Seal wire cavity 311 in the guiding tube tip 31.
Here, guidewire port can also be arranged as seal wire cavity 311, a diameter of 0.01- of guidewire port in guiding tube tip 31
10mm.The second end of center guiding tube 3 is pierced by from handle apparatus 4, as seal wire entrance.In surgical procedure, seal wire is from seal wire
Entrance penetrates, and by center guiding tube 3, and is finally pierced by from oval tip or cone point.It, can under the assistance of guiding seal wire
To further increase handling capacity of the stent system in distal end and complex lesions.
Above-mentioned catheter main body bar 1 is made of first body of rod 11 and second body of rod 12.First body of rod length d13 is 5-100mm,
Outer diameter is 0.2-30mm, and the length d14 of second body of rod is 35-2600mm, outer diameter 0.2-50mm.Catheter main body bar 1 is mostly logical
Road bar structure.Cental axial position is that proximal end guides tube passage, uniformly or symmetrical around proximal hub guiding tube circumferencial direction
1-5 connecting rod channel is distributed with.
Further, the catheter main body bar 1 can also be completely covered on expanding bar surface.As shown in fig. 7, catheter main body
Bar 1 is completely covered on expanding bar surface and is connected with guiding tube tip 31.The catheter main body pole length d15 is 45-2800mm,
Outside diameter d 16 is 0.2-50mm.
After expandable stent system is delivered to diseased region, catheter main body bar 1 is detached with guiding tube tip 31 and is withdrawn, and is released
Put expanding bar;Alternatively, expanding bar is stretched out from catheter main body bar 1, and complete subsequent expansion.Catheter main body bar 1 is to expanding bar
Covering can improve the transporting of stent system and handling, reduce transmission process because cradling piece fracture, bending, hook due to lead
The operative failure of cause.
The material of catheter main body bar 1 is polyether block amide, nylon, polytetrafluoroethylene (PTFE), polyurethane, polyvinyl chloride, poly- third
At least one of alkene, polymethacrylates, stainless steel, alloy material.
In the expandable stent system of the utility model embodiment, 5 outer diameter of inner tube is 0.02-5mm, and inner tube material is that polyethers is embedding
At least one of section amide, nylon, polytetrafluoroethylene (PTFE), polyurethane, polyvinyl chloride, polypropylene, polymethacrylates.
Further, as shown in Figure 8 a, the expandable stent system of the utility model embodiment further includes:
One end of the micro-pipe 52 being set to inside said inner tube 5, the micro-pipe 52 extends to the opening along said inner tube 5
At 211, the other end of the micro-pipe 52 is pierced by along said inner tube 5 from the handle apparatus 4.
In the utility model embodiment, it can be needed to accurately control targeted therapy depth according to clinic by above-mentioned micro-pipe,
Lesion region superficial layer, middle level, deep layer lesion region are treated.
Further, the expandable stent system of the utility model embodiment further includes:
It is set to the range marker line 53 on the surface of the other end of the micro-pipe 52.
Micro-pipe 52 can also be further arranged in stent system described in the utility model, for lesion region middle level or deep layer
Regional organization carries out micro or high density perfusion therapy.The micro-pipe 52 is arranged in inner tube 5, and inner tube 5 is canalicular channel, is used for
Micro-pipe is conveyed to expanding bar aperture position.As shown in Figure 8 b, micro-pipe 52 is made of proximal end micro-pipe 521 and distal end micro-pipe 522, distal end
Microtube length d17 is 5-80mm, and outside diameter d 18 is 0.005-3.5mm;Proximal end microtube length d19 is 30-2600mm, and outside diameter d 20 is
0.005-4.5mm.Proximal end micro-pipe 521 is pierced by along inner tube 5 from handle apparatus 4.Micro-pipe 521 surface in proximal end is equipped with range marker line
53, the depth of pathological tissues is inserted into for surgical procedure positioning micro-pipe.Distal end micro-pipe is delivered to inner tube tip by inner tube, and stretches
Go out to be inserted into middle level or deep layer lesion region.
Micro-pipe material be stainless steel, Nitinol, cochrome, platinum evanohm, platinum according in alloy, platinum, gold extremely
Few one kind.Micro-pipe has good developability under X-ray, and doctor can be helped further to position the depth that micro-pipe is inserted into tissue
Degree.
When circular open is arranged in expanding bar surface, per Radical extensin bar, the interior inner tube quantity being arranged is identical as micro-pipe quantity.
When oblong or oblong openings is arranged in expanding bar surface, per Radical extensin bar, the interior inner tube quantity being arranged is more than micro-pipe quantity,
And at least one inner tube being connected to sliding slot channel can be used as pumpback pipe.Pumpback pipe can take out perfusion liquid
It inhales, reduces damage of the therapeutic agent to irrigating region normal structure.
Further, as shown in figures 9 a and 9b, the expandable stent system of the utility model embodiment further includes:
The dilating sacculus 8 being set to inside enlarged portion 21.
Further, the expandable stent system of the utility model embodiment further includes:
The balloon expandable perfusion pipe 81 being set to inside the center guiding tube 3, the balloon expandable perfusion pipe 81
Extend to first end from the second end of the center guiding tube 3, and with the ball that is set to 3 first end surfaces of the center guiding tube
Capsule perfusing hole 82 is connected to.
Can also dilating sacculus 8 further be arranged in expanding bar region in stent system described in the utility model.Dilating sacculus 8
It is tapered for cylindrical, ellipse or sacculus both ends band when expansion.8 maximum extension outer diameter of dilating sacculus is 1-550mm, Ke Yizuo
It is closely attached on the inside of expanding bar to support, positioning performance when expanding bar expansion is further increased, especially to containing such as
When the complex lesions such as calcification point are treated, dilating sacculus can improve expanding bar opening and the attaching of lesion region tissue is imitated
Fruit prevents expanding bar expansion and position fixing process from sliding.It is provided with sacculus in the center guiding tube 3 of above-mentioned expandable stent system
Perfusion pipe 81 is expanded, for conveying balloon expandable liquid.Balloon expandable perfusion pipe 81 extends from 3 proximal port of center guiding tube
It is connected to distal end, and with the sacculus perfusing hole 82 of distal end guiding pipe surface setting.In addition, dilating sacculus 8 can be with Basilar artery
Such as blood or tissue fluid, prevent expanding bar in process of expansion because body fluid impact flow is subjected to displacement sliding.Dilating sacculus is single
Layer or multilayer material, such as at least one of silica gel, latex, rubber, silicon rubber, nylon, polyether block amide.
Further, as shown in Figure 10 a, 10b, 10c, 10d, the expandable stent system of the utility model embodiment is also wrapped
It includes:
It is set to 3 first end surfaces of center guiding tube and/or the development point 9 on 21 surface of the enlarged portion.
Stent system described in the utility model can also be further in expanding bar and guiding tube remote area setting development point
9, as shown in Figure 10 c and 10d, development point 9 can also may be used with 3 distal surface of centrally disposed guiding tube, as shown in figures 10 a and 10b
To be arranged on expanding bar surface, or it is arranged simultaneously on the surface of 3 distal end of expanding bar and center guiding tube.Development point is in X-ray
There is down good developability, the stationkeeping ability of stent system expansion and opening can be improved.
When clinic needs pair tissue contacted with expanding bar to carry out radiotherapy, the utility model can pass through past expansion
Sacculus fills and adds radioactive substance in liquid, or by way of inner tube or micro-pipe perfusion, and radioactive substance is delivered to target disease
Become tissue, radioactive substance such as, I-131, phosphorus -32 etc..
In addition, the expandable stent system of the utility model embodiment, no implantation material prolonged stay will not be brought slow in human body
Property inflammatory or thrombus reaction, and therapeutic agent delivery process, the risk that no medication coat falls off reduce system toxicity.
It should be noted that above-mentioned pathological tissues and tube chamber include at least:Cavity organization/tube chamber includes blood vessel, enteron aisle, gas
Pipe, oesophagus, the urinary tract, bile duct, common hepatic duct, ureter, vagina, nasolacrimal duct, fallopian tubal etc..
The expandable stent system of the utility model embodiment is moved by controlling to adjust switch along the axial direction of expandable stent
It is dynamic, drive center guiding tube to be moved along the axial direction of expandable stent, and enlarged portion is driven to be in expansion state or contraction state,
When expandable stent is in expansion state, the enlarged portion of expandable stent can effectively be contacted with lesion region, at the same avoid as
Common balloon expandable process indifference caused by the normal structure of circumferencial direction is damaged, and the stability of clinical efficacy is improved.
The above is only the preferred embodiment of the utility model only, is not intended to limit the utility model, all at this
Within the spirit and principle of utility model, any modification, equivalent replacement, improvement and so on should be included in the utility model
Protection domain within.
Claims (19)
1. a kind of expandable stent system, which is characterized in that including:
Catheter main body bar;
The expandable stent being at least partly inserted in inside the catheter main body bar, the expandable stent include enlarged portion and with it is described
The interconnecting piece of enlarged portion connection, is provided with opening in the enlarged portion;
Center guiding tube, the center guiding tube are inserted in the inside of the expandable stent, and the first of the center guiding tube
End is connect with one end of the enlarged portion;
Handle apparatus, the handle apparatus are connect with the second end of the interconnecting piece and the center guiding tube respectively, and described
The regulating switch that can be moved along the axial direction of the catheter main body bar is provided on handle apparatus;
Inner tube, said inner tube are set to the inside of the expandable stent, and the opening of one end of said inner tube and the enlarged portion
Connection, the other end of said inner tube are connect with the handle apparatus;
Wherein, when the regulating switch is moved along the axial direction of the catheter main body bar, the expandable stent and the center
Guiding tube relatively moves, and the enlarged portion is driven to be in expansion state or contraction state.
2. expandable stent system according to claim 1, which is characterized in that the second end of the center guiding tube with it is described
The regulating switch of handle apparatus connects;
When the regulating switch is moved along the axial direction of the catheter main body bar, drive the center guiding tube along the conduit
The axial direction of main body bar moves, and the enlarged portion is driven to be in expansion state or contraction state.
3. expandable stent system according to claim 1, which is characterized in that the tune of the interconnecting piece and the handle apparatus
Section switch connection;
When the regulating switch is moved along the axial direction of the catheter main body bar, drive the expandable stent along the conduit master
The axial direction of body rod moves, and the enlarged portion is driven to be in expansion state or contraction state.
4. expandable stent system according to claim 1, which is characterized in that the catheter main body bar includes:
First body of rod;
Second body of rod, one end of second body of rod are connect with first body of rod, the other end of second body of rod with it is described
Handle apparatus connects, and the diameter of second body of rod is more than the diameter of first body of rod.
5. expandable stent system according to claim 1, which is characterized in that when the enlarged portion is in expansion state, institute
State the middle section protrusion of enlarged portion.
6. expandable stent system according to claim 1, which is characterized in that the enlarged portion includes drawing around the center
The preset quantity expanding bar that conduit is uniformly arranged, the interconnecting piece include being preset around what the center guiding tube was uniformly arranged
Quantity connecting rod, and the preset quantity expanding bar connects one to one with the preset quantity connecting rod, Mei Gesuo
It states and is provided with the opening in expanding bar.
7. expandable stent system according to claim 1, which is characterized in that the opening rounded, oblong or rectangular
Shape.
8. expandable stent system according to claim 7, which is characterized in that the opening is rounded, and said inner tube
One end and the flush of the opening or the surface of the prominent opening.
9. expandable stent system according to claim 7, which is characterized in that the opening is rounded,
The outer cover of the enlarged portion is equipped with elastomeric plastics, and the position that the elastomeric plastics correspond to the opening is provided with
Trepanning, and the shape of the trepanning is identical as the shape of the opening.
10. expandable stent system according to claim 9, which is characterized in that one end of said inner tube and the trepanning
The surface of flush or the prominent trepanning.
11. expandable stent system according to claim 7, which is characterized in that the opening is in oblong or rectangle, institute
Stating expandable stent system further includes:
The angle regulator for being set to inside the enlarged portion and being disposed adjacent with the opening, the angle regulator
Be provided centrally with preset quantity sliding slot channel, the angle regulator is run through in each sliding slot channel.
12. expandable stent system according to claim 11, which is characterized in that one end of said inner tube is along the enlarged portion
Inner cavity extend to the opening, and pass through the sliding slot channel.
13. expandable stent system according to claim 1, which is characterized in that the first end of the center guiding tube passes through
Guiding tube tip is connect with one end of the enlarged portion.
14. expandable stent system according to claim 13, which is characterized in that further include:It is set to the guiding tip
Seal wire cavity in end.
15. expandable stent system according to claim 1, which is characterized in that further include:
One end of the micro-pipe being set to inside said inner tube, the micro-pipe extends to the opening along said inner tube, described micro-
The other end of pipe is pierced by along said inner tube from the handle apparatus.
16. expandable stent system according to claim 15, which is characterized in that further include:
It is set to the range marker line on the surface of the other end of the micro-pipe.
17. expandable stent system according to claim 1, which is characterized in that further include:
The dilating sacculus being set to inside enlarged portion.
18. expandable stent system according to claim 17, which is characterized in that further include:
The balloon expandable perfusion pipe being set to inside the center guiding tube, the balloon expandable perfusion pipe is from the center
The second end of guiding tube extends to first end, and connects with the sacculus perfusing hole for being set to first end surfaces of center guiding tube
It is logical.
19. expandable stent system according to claim 1, which is characterized in that further include:
It is set to the first end surfaces of center guiding tube and/or the development point on the enlarged portion surface.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201720464398.3U CN207821956U (en) | 2017-04-28 | 2017-04-28 | A kind of expandable stent system |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201720464398.3U CN207821956U (en) | 2017-04-28 | 2017-04-28 | A kind of expandable stent system |
Publications (1)
Publication Number | Publication Date |
---|---|
CN207821956U true CN207821956U (en) | 2018-09-07 |
Family
ID=63384847
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN201720464398.3U Active CN207821956U (en) | 2017-04-28 | 2017-04-28 | A kind of expandable stent system |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN207821956U (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN108784895A (en) * | 2017-04-28 | 2018-11-13 | 青岛智辰生物科技有限公司 | A kind of expandable stent system |
CN111096833A (en) * | 2018-10-25 | 2020-05-05 | 东莞市先健医疗有限公司 | Conveyor |
CN111632255A (en) * | 2020-04-28 | 2020-09-08 | 贵州省人民医院 | Vasodilator for cardiovascular internal medicine and preparation method thereof |
-
2017
- 2017-04-28 CN CN201720464398.3U patent/CN207821956U/en active Active
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN108784895A (en) * | 2017-04-28 | 2018-11-13 | 青岛智辰生物科技有限公司 | A kind of expandable stent system |
CN111096833A (en) * | 2018-10-25 | 2020-05-05 | 东莞市先健医疗有限公司 | Conveyor |
CN111632255A (en) * | 2020-04-28 | 2020-09-08 | 贵州省人民医院 | Vasodilator for cardiovascular internal medicine and preparation method thereof |
CN111632255B (en) * | 2020-04-28 | 2022-04-29 | 贵州省人民医院 | Vasodilator for cardiovascular internal medicine and preparation method thereof |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN108784895A (en) | A kind of expandable stent system | |
US6685672B1 (en) | Multi-balloon drug delivery catheter for angiogenesis | |
US11090467B2 (en) | Apparatus and methods for scaffolding | |
ES2300604T3 (en) | MEDICINAL DEVICE FOR THE SUPPLY OF MEDICINAL PRODUCT. | |
KR101456108B1 (en) | Catheter | |
JP4436761B2 (en) | Device with expandable potion for drug release | |
US10099040B2 (en) | Occlusion catheter system and methods of use | |
CN106390268A (en) | Expansible and infusable balloon catheter | |
EP2066388B1 (en) | Systems for local bioactive material delivery | |
US20190298983A1 (en) | Injection Port for Therapeutic Delivery | |
CN207821956U (en) | A kind of expandable stent system | |
CN106994204A (en) | Double sacculus medicine-coated balloon dilating catheters | |
US20200261695A1 (en) | Therapeutic agent delivery system with delayed activation | |
US20210236768A1 (en) | Dual lumen microcatheter | |
CN111787871A (en) | Flow control valve | |
CN205903515U (en) | Balloon dilatation catheter | |
US20050124852A1 (en) | Method and device for the treatment of incontinence | |
ES2289425T3 (en) | CATHETER FOR THE LOCAL ADMINISTRATION OF A PHARMACO. | |
CN106730264A (en) | A kind of porous foley's tube of two-chamber | |
US11400263B1 (en) | System and method for selective pressure-controlled therapeutic delivery | |
CN207575540U (en) | Double sacculus medicine-coated balloon dilating catheters | |
CN112638460B (en) | Balloon within balloon catheter systems and methods of use | |
US20170080179A1 (en) | Bilateral Frontal Sinus Device | |
CN218607684U (en) | Non-through micro catheter for local drug delivery and medical instrument comprising same | |
US20150141900A1 (en) | Method and Device for Targeted Delivery of Fluid Therapeutics |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
GR01 | Patent grant | ||
GR01 | Patent grant |