CN203315048U - Improved fallopian tube recanalization assembly - Google Patents

Improved fallopian tube recanalization assembly Download PDF

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Publication number
CN203315048U
CN203315048U CN2013203236055U CN201320323605U CN203315048U CN 203315048 U CN203315048 U CN 203315048U CN 2013203236055 U CN2013203236055 U CN 2013203236055U CN 201320323605 U CN201320323605 U CN 201320323605U CN 203315048 U CN203315048 U CN 203315048U
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China
Prior art keywords
fallopian tube
cavity
improved
seal wire
double
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Expired - Fee Related
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CN2013203236055U
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Chinese (zh)
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陶可伟
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Individual
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Individual
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Abstract

The utility model relates to an improved fallopian tube recanalization assembly. The improved fallopian tube recanalization assembly comprises a double-cavity balloon catheter and a guide wire, wherein the double-cavity balloon catheter comprises a balloon cavity and a guide wire cavity. The tail section of the guide wire cavity is inserted into or connected with a connection device which is provided with at least two end ports; at least one of the ports is a contrast agent injection end port with a control valve; meanwhile, at least one of the ports is a guide wire inlet end port, when penetrating into the end port, the guide wire can guarantee that little or no contrast agent overflows. The improved fallopian tube recanalization assembly achieves the simultaneous operation of contrast agent injection and guide wire penetrating and saves operation procedures and operation time; meanwhile, the contract agent can lubricate the guide wire to reduce the resistance of the guide wire; the double-cavity balloon catheter can steer accurately to avoid repeated steering under fluoroscopy, thereby effective avoiding the damage of the operation to a patient and reducing the radiation to a doctor and the patient.

Description

A kind of improved fallopian tube recanalization assembly
Technical field
This utility model relates to a kind of gynaecological and obstetrical instrument, particularly a kind of improved fallopian tube recanalization assembly.
Background technology
Along with social development, the sickness rate of infertility increases year by year, and fallopian tube factor shared ratio in female acyesis is the highest, accounts for 35%.Miscarriage, uterine cavity and pelvic inflammation often cause salpingemphraxis.Therefore become the important method of its treatment as noninvasive fallopian tube Interventional Salpingography.Mainly contain in the market the Gooseneck type integrated tubal re-through device of oviduct dredging suit that U.S. COOK company provides and domestic Nanjing company of Wicresoft.The former siphunculus again is comprised of pig tail catheter head and uterine neck suction cup, and seal wire is difficult to search out bight, palace fallopian tube opening after entering uterine cavity, and seal wire is detected easy damage inner membrane of uterine cavity repeatedly; Although the latter has taked the eccentric balloon technology, but because air bag section and catheter tip distance is fixing, and patient's uterine cavity degree of depth individual variation is larger, therefore in practical operation seal wire to enter the probability of bight, palace fallopian tube opening still less, and head end adopts harder leaded plastic material single hole conical design more easily to increase the weight of the damage of inner membrane of uterine cavity.
Moreover, above-mentioned two kinds of dredging conduit head ends all adopt the single hole design, when being placed in the bight, palace, the conduit head end is unfavorable for that contrast agent enters uterine cavity and observes bight, palace situation, and catheter shaft has all adopted the plastic material that hardness is higher, while causing putting pipe, because of palace body and cervical canal angle problem difficult intubation, even if insert by force the pain degree and the uterine cavity that have also increased the weight of the patient, damage.Because the existence of above-mentioned shortcoming causes operating time greatly to extend, patient and get involved the ionizing radiation that the doctor accepts the long period (often every get involved the dredging art need 1~1.5 hour), and success rate of operation descends.In sum, two kinds of main fallopian tube recanalization apparatus structure complexity in the market, complex operation, it is expensive that (external every cover is about 4000 yuan of left and right, and domestic every dredging pipe also reaches 1000 yuan of left and right), efficiency is lower, is difficult to universal in department of obstetrics and gynecology intervention field.
The inventor has applied for that on January 24th, 2013 name is called a kind of fallopian tube recanalization assembly, the patent of invention that application number is 2013100222816.A kind of fallopian tube recanalization assembly is disclosed, the catheter with double-cavity saccule and the seal wire that comprise balloon cavity and guidewire lumen, the catheter with double-cavity saccule front portion is provided with the deflection sacculus, described catheter with double-cavity saccule top is smooth circular arc, the catheter with double-cavity saccule front end has three holes, is respectively seal wire through hole and symmetrical the first liquid outlet and second liquid outlet of sidepiece on top; The terminal part jag is balloon cavity rear and guidewire lumen rear, and the end of described balloon cavity rear is fixedly connected with check valve, and described seal wire is the straight peen seal wire.The inventor further studies the effect of finding that above-mentioned fallopian tube recanalization assembly injects contrast agent and penetrates seal wire because guidewire lumen has concurrently simultaneously, make catheter tip position when deflection when squeeze into gas to balloon cavity, due to the used time of doing of gas pressure, the contrast agent in tube chamber can reflux, and pollutes; Simultaneously when being dredged art, need to adjust seal wire towards, during current operation in the perspective situation, the doctor relies on experience rotation tube chamber, yet the tube chamber outer wall is little without any sign and lumen diameter, more easily rotates 360 ° of situations that are returned to initial point, more repeatedly adjust, increased the injury of operation to human body, and all there is certain harm in perspective to doctor and patient body.
The utility model content
The purpose of this utility model is to solve above-mentioned deficiency to provide a kind of improved fallopian tube recanalization assembly.
The technical scheme that realizes this utility model purpose is: a kind of improved fallopian tube recanalization assembly, the catheter with double-cavity saccule and the seal wire that comprise balloon cavity and guidewire lumen, the catheter with double-cavity saccule front portion is provided with the deflection sacculus, have three holes, the terminal part jag is balloon cavity rear and guidewire lumen rear, the guidewire lumen rear inserts or is fixedly connected with the connecting device with at least two ports, has one in described port at least for thering is the contrast agent injection port of control valve, in described port, have at least one for seal wire, to penetrate port, when seal wire penetrates, when injecting air in the balloon cavity rear, this port keeps only having a small amount of or contrast-agent-free outflow.
Above-mentioned improved fallopian tube recanalization assembly, preferred described connecting device has two ports.
Above-mentioned improved fallopian tube recanalization assembly, preferred described contrast agent injection port is fixedly connected with flexible pipe, and the flexible pipe other end is fixedly connected with one-way valve or three-way valve.
Above-mentioned improved fallopian tube recanalization assembly, it is to offer the end face that circle and diameter are greater than the seal wire perforation of seal wire diameter 10% that preferred described seal wire penetrates port.
Above-mentioned improved fallopian tube recanalization assembly, it is rigid plastics for outside that preferred described seal wire penetrates port, the end face that middle part is soft gum elastic, the soft gum elastic at this end face middle part has the gap of scratching, and seal wire can penetrate from this gap.
Above-mentioned improved fallopian tube recanalization assembly, preferred described catheter with double-cavity saccule cross section is circular, has the circular scale labelling on pipe shaft.
Above-mentioned improved fallopian tube recanalization assembly, preferred described circular scale labelling is half circumference of labelling only, marks respectively 0 ° and 180 ° of calibration points.
Above-mentioned improved fallopian tube recanalization assembly, preferred described circular scale is labeled as from 0 ° of scale to 180 ° scale and applies the coating that one deck is different from the catheter with double-cavity saccule color.
Above-mentioned improved fallopian tube recanalization assembly, preferred described circular scale labelling is positioned at apart from catheter with double-cavity saccule top 12 ~ 15cm.
The utlity model has positive effect: (1) is at guidewire lumen tail end design connecting device, and all there is airtight measure to make when injecting air contrast agent a small amount of or without outflow, when adopting diameter to be greater than the seal wire perforation scheme of seal wire diameter 10%, owing to coordinating closely, contrast agent flows out seldom; When employing has the scheme of designated port gap gum elastic end face, elastomeric material makes other part tight closes at seal wire designated port position when penetrating state, and same contrast agent flows out seldom or without outflow; (2) divide two port operations by contrast agent and seal wire, can inject contrast agent and penetrate seal wire simultaneously, operate but not confuse in a pipe, saved program and time, and contrast agent can lubricate seal wire, reduce the seal wire running resistance; (3) it is clear and definite that the design of catheter with double-cavity saccule cross-sectional periphery scale makes the conduit steering angle, and operation accurately, is avoided repeatedly turning under Perspective Conditions, effectively reduces the injury of operation to patient, also effectively reduces doctor and the raying of patient institute.
The accompanying drawing explanation
For content of the present utility model more easily is expressly understood, below according to specific embodiment also by reference to the accompanying drawings, this utility model is described in further detail, wherein
Fig. 1 is structural representation of the present utility model.
Fig. 2 is the front view that 8 seal wires penetrate a kind of embodiment of port.
Fig. 3 is the front view that 8 seal wires penetrate the another kind of embodiment of port.
Wherein: 1 catheter with double-cavity saccule; 2 seal wires; 3 deflection sacculus; 4 balloon cavity rears; 5 guidewire lumen rears; 6 connecting devices; 7 contrast agent injection ports; 8 seal wires penetrate port; 9 flexible pipes; 10 circular scale labellings.
The specific embodiment
(embodiment 1)
See Fig. 1 and Fig. 2, the utlity model has a kind of fallopian tube recanalization assembly, the catheter with double-cavity saccule 1 and the seal wire 2 that comprise balloon cavity and guidewire lumen, catheter with double-cavity saccule 1 front portion is provided with deflection sacculus 3, top is smooth circular arc, catheter with double-cavity saccule 1 front end has three holes, is respectively seal wire through hole and symmetrical the first liquid outlet and second liquid outlet of sidepiece on top; The terminal part jag is balloon cavity rear 4 and guidewire lumen rear 5, and guidewire lumen rear 5 inserts the connecting device 6 with two ports, and in port, one is the contrast agent injection port 7 with control valve, and another penetrates port 8 for seal wire.Contrast agent injection port 7 is fixedly connected with flexible pipe 9, and flexible pipe 9 other ends are fixedly connected with one-way valve.It is rigid plastics for outside that seal wire penetrates port 8, the end face that middle part is soft gum elastic, and the soft gum elastic at this end face middle part has the gap of scratching, and seal wire 2 penetrates from this gap.Catheter with double-cavity saccule 1 cross section is circular, there is circular scale labelling 10 on pipe shaft, this is labeled as from 0 ° of scale to 180 ° scale and applies the coating that one deck is different from catheter with double-cavity saccule 1 color, and position is positioned at the catheter with double-cavity saccule 1 top 12 ~ 15cm apart from guidewire lumen, and width is 1cm.
(embodiment 2)
See Fig. 1 and Fig. 3, the utlity model has a kind of fallopian tube recanalization assembly, the catheter with double-cavity saccule 1 and the seal wire 2 that comprise balloon cavity and guidewire lumen, catheter with double-cavity saccule 1 front portion is provided with deflection sacculus 3, top is smooth circular arc, its front end has three holes, is respectively seal wire through hole and symmetrical the first liquid outlet and second liquid outlet of sidepiece on top; The terminal part jag is balloon cavity rear 4 and guidewire lumen rear 5, and guidewire lumen rear 5 is fixedly connected with the connecting device 6 with two ports, and in port, one is the contrast agent injection port 7 with control valve, and another penetrates port 8 for seal wire.Contrast agent injection port 7 is fixedly connected with flexible pipe 9, and flexible pipe 9 other ends are fixedly connected with one-way valve.Seal wire penetrates port 8 for offering circle, and diameter is greater than the end face of the seal wire perforation of seal wire diameter 10%.Catheter with double-cavity saccule 1 cross section is circular, there is circular scale labelling 10 on pipe shaft, this is labeled as from 0 ° of scale to 180 ° scale and applies the coating that one deck is different from catheter with double-cavity saccule 1 color, and position is positioned at the catheter with double-cavity saccule 1 top 12 ~ 15cm apart from guidewire lumen, and width is 1.5cm.
Above-described specific embodiment; the purpose of this utility model, technical scheme and beneficial effect are further described; institute is understood that; the foregoing is only specific embodiment of the utility model; be not limited to this utility model; all within spirit of the present utility model and principle, any modification of making, be equal to replacement, improvement etc., within all should being included in protection domain of the present utility model.

Claims (9)

1. an improved fallopian tube recanalization assembly, comprise catheter with double-cavity saccule (1) and seal wire (2) with balloon cavity and guidewire lumen, catheter with double-cavity saccule (1) front portion is provided with deflection sacculus (3), have three holes, the terminal part jag is balloon cavity rear (4) and guidewire lumen rear (5), it is characterized in that: guidewire lumen rear (5) inserts or is fixedly connected with the connecting device (6) with at least two ports, has one in described port at least for thering is the contrast agent injection port (7) of control valve, in described port, have at least one for seal wire, to penetrate port (8), when seal wire penetrates, while to balloon cavity rear (4) is middle, injecting air, this port keeps only having a small amount of or contrast-agent-free outflow.
2. improved fallopian tube recanalization assembly according to claim 1, it is characterized in that: described connecting device (6) has two ports.
3. improved fallopian tube recanalization assembly according to claim 2, it is characterized in that: described contrast agent injection port (7) is fixedly connected with flexible pipe (9), and flexible pipe (9) other end is fixedly connected with one-way valve or three-way valve.
4. improved fallopian tube recanalization assembly according to claim 1 is characterized in that: described seal wire penetrates port (8) and is greater than the end face of the seal wire perforation of seal wire diameter 10% for offering circle, diameter.
5. improved fallopian tube recanalization assembly according to claim 1, it is characterized in that: it is rigid plastics for outside that described seal wire penetrates port (8), middle part is the end face of soft gum elastic, the soft gum elastic at this end face middle part has the gap of scratching, and seal wire (2) can penetrate from this gap.
6. improved fallopian tube recanalization assembly according to claim 1 is characterized in that: described catheter with double-cavity saccule (1) cross section, for circular, has circular scale labelling (10) on pipe shaft.
7. improved fallopian tube recanalization assembly according to claim 6 is characterized in that: described circular scale labelling (10) is half circumference of labelling only, marks respectively 0 ° and 180 ° of calibration points.
8. improved fallopian tube recanalization assembly according to claim 7 is characterized in that: described circular scale labelling (10) is for applying from 0 ° of scale to 180 ° scale the coating that one deck is different from catheter with double-cavity saccule (1) color.
9. improved fallopian tube recanalization assembly according to claim 7, it is characterized in that: described circular scale labelling (10) is positioned at apart from catheter with double-cavity saccule (1) top 12~15cm.
CN2013203236055U 2013-06-04 2013-06-04 Improved fallopian tube recanalization assembly Expired - Fee Related CN203315048U (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN2013203236055U CN203315048U (en) 2013-06-04 2013-06-04 Improved fallopian tube recanalization assembly

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Application Number Priority Date Filing Date Title
CN2013203236055U CN203315048U (en) 2013-06-04 2013-06-04 Improved fallopian tube recanalization assembly

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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN105796164A (en) * 2014-12-31 2016-07-27 常州市妇幼保健院 Selective hydrotubation device

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN105796164A (en) * 2014-12-31 2016-07-27 常州市妇幼保健院 Selective hydrotubation device

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C14 Grant of patent or utility model
GR01 Patent grant
C53 Correction of patent for invention or patent application
CB03 Change of inventor or designer information

Inventor after: Xu Zhonghua

Inventor after: Tao Kewei

Inventor before: Tao Kewei

COR Change of bibliographic data

Free format text: CORRECT: INVENTOR; FROM: TAO KEWEI TO: XU ZHONGHUA TAO KEWEI

CF01 Termination of patent right due to non-payment of annual fee
CF01 Termination of patent right due to non-payment of annual fee

Granted publication date: 20131204

Termination date: 20180604