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CN2756175Y - Device for carrying out lung volume reducing operation - Google Patents

Device for carrying out lung volume reducing operation Download PDF

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Publication number
CN2756175Y
CN2756175Y CNU2004200863243U CN200420086324U CN2756175Y CN 2756175 Y CN2756175 Y CN 2756175Y CN U2004200863243 U CNU2004200863243 U CN U2004200863243U CN 200420086324 U CN200420086324 U CN 200420086324U CN 2756175 Y CN2756175 Y CN 2756175Y
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China
Prior art keywords
extensible
grasp
lung volume
volume reducing
reducing operation
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Expired - Fee Related
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CNU2004200863243U
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Chinese (zh)
Inventor
谢文愉
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Individual
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Individual
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Abstract

The utility model relates to a device for carrying out lung volume reducing operations, which is characterized in that the utility model is composed of a nickel titanium memory alloy support frame which is connected with a telescopic supporter, wherein the telescopic supporter is a sacculus which is arranged in the nickel titanium memory alloy support frame; the sacculus is made of filling type silica gel and has the diameter of 9 mm to 13 mm after filled with gas or liquid of about 0.5 to 0.8 ml; the diameter of a sphere-shaped net basket formed by the nickel titanium memory alloy support frame is 12 mm; holes with the diameter of 3 mm are arranged on both ends or one end of the sphere; the telescopic supporter is composed of memory alloy metal wires, extensible anchors and an umbrella skirt which are connected together; the umbrella skirt is attached on the memory alloy metal wires to form an umbrella-shaped structure; one side of an umbrella top is provided with the extensible anchors. The utility model eliminates the influence of severe pneumonectasis lung tissues on the whole pulmonary function and treats diffuse pneumonectasis under the condition of no operation.

Description

A kind of device of implementing lung volume reducing operation
Technical field: this utility model relates to a kind of device of implementing lung volume reducing operation, and it belongs to a kind of medical apparatus and instruments, is to be used for implementing under the internal medicine condition selectivity emphysema to subtract the device that holds treatment.
Background technology: the serious emophysematous method of medical treatment for improve patient's symptom, to prolong patient's existence all very limited, therefore, people seek a kind of new method always and treat the diffusivity emphysema for many years.Lung volume reduction surgery (LVRS) treatment diffusivity emphysema are called as nineteen nineties thoracic surgery one of the most breathtaking progress.
The mechanism that LVRS improves pulmonary function is: increase pulmonary elastic recoil, air flue conductivity, maximal expiratory flow; Lower the lung excessive expansion; Improve the respiratory muscle work efficiency.Thereby alleviate the dyspnea symptom, improve and take exercise tolerance and quality of life.
Yet also there is more limitation in LVRS: strict operative indication; There is more complication; Anesthesia and the complication relevant with anesthesia; Curative effect is difficult to prediction before the art, postoperative can't remedy because of excising the unfavorable result of too much or very few institute's curative effect that causes; High surgery cost and bigger spirit, human body misery.
Summary of the invention: the result that can improve pulmonary function based on LVRS, for solving the weak point in the above-mentioned background technology, this utility model provides a kind of device of implementing lung volume reducing operation, it can eliminate the serious lung tissue of emphysema to full influence of Pulmonary Function under the situation of motionless operation, treatment diffusivity emphysema.
For achieving the above object, this utility model adopts following technical scheme: design a kind of device of implementing lung volume reducing operation, it is characterized in that: it is connected and composed by recalled nitinol alloy stent and retractable supports.
Described retractable supports is a sacculus, and sacculus is in recalled nitinol alloy stent.
Described sacculus is the rechargeable type silica gel material; Behind the about 0.5-0.8mL of filling gas or liquid, balloon diameter is between 9mm-13mm; Its diameter of sphere net basket that described recalled nitinol alloy stent constitutes is 12mm, and there is the hole of diameter 3mm the both ends or one end of ball.
Described retractable supports is to be connected and composed by memorial alloy tinsel, extensible grasp, full skirt, is attached with full skirt on the memorial alloy tinsel and forms umbrella-shaped structure, and umbrella pushes up a side extensible grasp.
Described memorial alloy tinsel is a 2-10 root Ultimum Ti silk, and they are evenly distributed; The memorial alloy tinsel is shape in the shape of a spiral.
The full skirt that described memorial alloy tinsel outer surface covers is that the good medical material of the tissue compatibility is made; Described memorial alloy tinsel and extensible grasp can be integrative-structures.
The lever of described axis near-end and axis are integrative-structures.
Described memory alloy wire is fixed on the support, support is an axis, and the axis near-end has lever, and far-end is fixedly connected with extensible grasp, the memorial alloy tinsel that is coated with full skirt be evenly distributed on axis around, there is extensible grasp at the link place of memorial alloy tinsel and axis.
Described extensible grasp is parabolic shape when launching, extensible grasp has the 1-2 group, the extensible grasp identical outside stretching, extension of angle each other in every group; If any 2 groups of extensible grasps, the parabola direction after 2 groups of extensible grasps stretch is opposite.
Compared with prior art, the utlity model has following advantage:
1, implement under the internal medicine condition, simple to operate, no wound is painful little.
2, the wide model of indication, device is detachable, can repeat, in the hope of curative effect the best.
3, the facilities and equipments requirement is low, and the technical staff can carry out through professional training.
4, adopting the good material of histocompatibility of generally acknowledging in the present world wide---Nitinol and medical silica-gel are made, and almost have no adverse reaction, and can guarantee the persistency of placing in the body.
5, has unidirectional flap valve function under certain condition, when by intrinsic pressure the increasing of the leaf of shutoff (section) (as cough), full skirt (or sacculus) and and airway walls between moment open up a slit, allow portion gas or mucus to discharge, significantly reduce possible complication after the placement.
Description of drawings:
The utility model is described in further detail below in conjunction with implementing accompanying drawing:
Fig. 1 is that the silica gel sacculus is filling gas or liquid condition figure among the embodiment 1;
Fig. 2 is the state diagram of silica gel sacculus behind full gas or liquid among the embodiment 1;
Fig. 3 is Ultimum Ti fixed support unswollen state figure among the embodiment 1;
Fig. 4 is that the Ultimum Ti fixed support launches the back state diagram among the embodiment 1;
Fig. 5 is embodiment 1 structural representation;
Fig. 6 is embodiment 2 deployed condition structural representations;
Fig. 7 is embodiment 3 full skirt deployed condition structural representations;
Fig. 8 is embodiment 3 collapsed state structural representations;
Fig. 9 is embodiment 4 deployed condition structural representations;
Figure 10 is embodiment 4 collapsed state structural representations.
Among the figure, 1, sacculus; 2, spherical recalled nitinol alloy stent; 3, opening; 4, memorial alloy tinsel; 5, extensible grasp; 6, full skirt; 7, axis; 8, lever.
The specific embodiment:
As shown in Figure 1, the sacculus 1 of inserting in the recalled nitinol alloy stent 2, preceding in not filling (gas or liquid), sacculus 1 is a strip.
As shown in Figure 2, behind the about 0.5-0.8mL of filling gas or liquid, sacculus 1 diameter is between 9mm-13mm.Generally speaking, its wall thickness is 0.2mm, internal diameter 9.6mm, external diameter 10.0mm.In addition, additional 2mm is thick for sacculus 1 one ends, the diaphragm of diameter 2.0mm.
Fig. 3 is the state of recalled nitinol alloy stent 2 when temperature is lower than 10 ℃, and it is similarly a cylindrical shape.
As shown in Figure 4.Under the effect of body temp, recalled nitinol alloy stent 2 expands voluntarily becomes sphere, and its diameter of sphere net basket that recalled nitinol alloy stent 2 constitutes is 12mm, and the two ends of ball are the hole of diameter 3mm, and the support force of recalled nitinol alloy stent 2 is 50-60g/mm 2(30-42 ℃).During use, earlier spherical recalled nitinol alloy stent 2 is discharged in the bronchus of the target lobe of the lung (section).All footpaths the best part embeds the mucosa of bronchial wall and fixes, the opening 3 of diameter 3mm by mount proximal end is put into recalled nitinol alloy stent 2 with sacculus shown in Figure 11 again, suitably full sacculus 1 is with recalled nitinol alloy stent 2 inner chamber shutoff, be the target lobe of the lung (section), adjust sacculus 1 pressure to working standard, device is placed and is finished.
Form state at last as Fig. 5.
Embodiment 1 operation principle is as follows: above-mentioned recalled nitinol alloy stent 2 and sacculus 1 are inserted target leaf (or section) bronchus successively, the full sacculus 1 in combination back, outward appearance should be a spherical structure, utilize the Memorability of support, embed bronchial lumen, full sacculus 1 is fixed in the beaded support, thus the stifled effect of performance bolt.The lobe of the lung that gets clogged (section) withers because of wherein gas absorbed in 2-3 days gradually naturally, thereby reduce the intrathoracic volume that this lobe of the lung (section) occupies because of excessive emphysema, be beneficial to the recovery of other lobes of the lung (section) function, reach the purpose of improving patient's pulmonary function.
Above-mentioned plugging device is placed in the bronchoscopic service aisle with convergence state, utilize special release to insert target leaf (or section) bronchus, plugging device after the release launches to become aforesaid duty automatically under the body temperature condition, thus performance bronchus plugging action.This plugging device is because of the performance of material itself, can have unidirectional flap valve function, can allow by portion gas or mucus in the leaf of shutoff (section), under certain intrinsic pressure effect by sacculus with discharge with the gap that airway walls attaches mutually, reduce the complication after placing.Withered because of wherein gas absorbed in 3-5 days gradually by the lobe of the lung of shutoff (section), thereby reduce the intrathoracic volume that this lobe of the lung (section) occupies because of excessive emphysema, be beneficial to the recovery of other lobes of the lung (section) function, reach the purpose of improving patient's pulmonary function.
The structure of embodiment 2 as shown in Figure 6, the full skirt 6 of self-expanding formula bronchial occlusive device is attached to having on the spiral-shaped memorial alloy tinsel 4, the central part of full skirt 6 is axis 7, axis 7 near-ends have lever 8, it and axis 7 are integrative-structures.The far-end of axis 7 is fixedly connected with 1 group of extensible grasp 5, memorial alloy tinsel 4 also has 1 group of extensible grasp 5 with the link place of axis 7, extensible grasp 5 is that 3 memorial alloy tinsels 4 launch to be the anchor shape, be parabolic shape when wherein every memorial alloy tinsel 4 launches, extensible grasp 5 has 2 groups among the embodiment 1, the extensible grasp 5 identical outside stretching, extension of angle each other in every group; Parabola direction after 2 groups of extensible grasps 5 stretch is opposite.
Fig. 7 is embodiment 3 full skirt deployed condition structural representations.Embodiment 3 difference from Example 1 are that its full skirt 6 is on the spiral-shaped memorial alloy tinsel 4 of rightabout attached to two as shown in the figure.
Fig. 9 is embodiment 4 deployed condition structural representations.As shown in the figure, its difference from Example 2 is that its full skirt 6 is attached on three equidirectional spiral-shaped memorial alloy tinsels 4 of uniform distances.
It is the umbrella-shaped structure of 12 ± 5mm that full skirt 6 overlay films launch the back diameter; Far-end---the tinsel of the other end for exposing that the umbrella top is relative with parabola shaped outside stretching, extension, forms the anchor shape.Umbrella skeleton can be histocompatibility medical material metal or alloy preferably, and as using Ultimum Ti, then the support force of support (F) is 50-60g/mm 2(30-42 ℃).
Fig. 8 is embodiment 3 collapsed state structural representations.
Figure 10 is embodiment 4 collapsed state structural representations.
During practical operation, plugging device is placed in the service aisle of branchofiberoscope elder generation end with convergence state earlier, state when packing up such as Fig. 8 and shown in Figure 10, it arrives target leaf (or section) bronchus with tracheascope elder generation end, utilizes special applicator that plugging device is sent into target leaf (or section) bronchus.Inserting the bronchial plugging device of target leaf (or section) launches under the condition of body temperature automatically, become the anchor shape of far-end and the umbrella shape of near-end, the anchor arm that stretches around tube chamber plays the effect of being fixed in the bronchial lumen, and open umbrella-shaped structure is attached at the bronchus medial wall uniformly, plays plugging action.Be aforesaid duty, thus performance bronchus plugging action.This plugging device is because of the performance of material itself, has unidirectional flap valve function, can allow by portion gas or mucus in the leaf of shutoff (section), because of under the effect of intrinsic pressure variation of moment (as cough) by full skirt 6 with discharge with the gap that airway walls attaches mutually, to reduce the complication after placing.
It is placed in the bronchus of selecting by with self-expanding formula bronchus plugging device, utilizes the interior gas of lung to absorb naturally, progressively causes the pulmonary atelectasis of this section or inferior section in 3-5 days, eliminates the serious lung tissue of emphysema to full influence of Pulmonary Function thereby reach.

Claims (9)

1, a kind of device of implementing lung volume reducing operation, it is characterized in that: it is connected and composed by recalled nitinol alloy stent and retractable supports.
2, a kind of device of implementing lung volume reducing operation according to claim 1, it is characterized in that: described retractable supports is a sacculus, and sacculus is in recalled nitinol alloy stent.
3, a kind of device of implementing lung volume reducing operation according to claim 1, it is characterized in that: described sacculus is the rechargeable type silica gel material; Behind filling gas or the about 0.5-0.8mL of liquid, balloon diameter is between 9mm-13mm in the sacculus; Its diameter of sphere net basket that described recalled nitinol alloy stent constitutes is 12mm, and there is the hole of diameter 3mm the both ends or one end of ball.
4, a kind of device of implementing lung volume reducing operation according to claim 1, it is characterized in that: described retractable supports is to be connected and composed by memorial alloy tinsel, extensible grasp, full skirt, be attached with full skirt on the memorial alloy tinsel and form umbrella-shaped structure, umbrella pushes up a side extensible grasp.
5, a kind of device of implementing lung volume reducing operation according to claim 1 is characterized in that: described memorial alloy tinsel is a 2-10 root Ultimum Ti silk, and they are evenly distributed; The memorial alloy tinsel is shape in the shape of a spiral.
6, a kind of device of implementing lung volume reducing operation according to claim 1 is characterized in that: the full skirt that described memorial alloy tinsel outer surface covers is that the good medical material of the tissue compatibility is made; Described memorial alloy tinsel and extensible grasp can be integrative-structures.
7, a kind of device of implementing lung volume reducing operation according to claim 1, it is characterized in that: the lever of described axis near-end and axis are integrative-structures.
8, a kind of device of implementing lung volume reducing operation according to claim 1, it is characterized in that: described memory alloy wire is fixed on the support, support is an axis, the axis near-end has lever, far-end is fixedly connected with extensible grasp, the memorial alloy tinsel that is coated with full skirt be evenly distributed on axis around, there is extensible grasp at the link place of memorial alloy tinsel and axis.
9, a kind of device of implementing lung volume reducing operation according to claim 1 is characterized in that: described extensible grasp is parabolic shape when launching, and extensible grasp has the 1-2 group, the extensible grasp identical outside stretching, extension of angle each other in every group; If any 2 groups of extensible grasps, the parabola direction after 2 groups of extensible grasps stretch is opposite.
CNU2004200863243U 2004-12-06 2004-12-06 Device for carrying out lung volume reducing operation Expired - Fee Related CN2756175Y (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CNU2004200863243U CN2756175Y (en) 2004-12-06 2004-12-06 Device for carrying out lung volume reducing operation

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CNU2004200863243U CN2756175Y (en) 2004-12-06 2004-12-06 Device for carrying out lung volume reducing operation

Publications (1)

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CN2756175Y true CN2756175Y (en) 2006-02-08

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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN104622599A (en) * 2009-05-18 2015-05-20 纽姆克斯股份有限公司 Cross-sectional modification during deployment of an elongate lung volume reduction device

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9474533B2 (en) 2006-03-13 2016-10-25 Pneumrx, Inc. Cross-sectional modification during deployment of an elongate lung volume reduction device
US10188398B2 (en) 2006-03-13 2019-01-29 Pneumrx, Inc. Cross-sectional modification during deployment of an elongate lung volume reduction device
CN104622599A (en) * 2009-05-18 2015-05-20 纽姆克斯股份有限公司 Cross-sectional modification during deployment of an elongate lung volume reduction device

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C17 Cessation of patent right
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Granted publication date: 20060208

Termination date: 20101206