CN211244811U - Integrated device for draining effusion in drainage operation area - Google Patents
Integrated device for draining effusion in drainage operation area Download PDFInfo
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Abstract
本实用新型属于医疗器械领域,特别涉及一种引流术区积液的一体化装置。所述一体化装置包括:穿刺针(5),其具有针芯(5‑2)、针头(5‑3)和套管(5‑1),所述针头(5‑3)设置在所述针芯(5‑2)的端部,所述套管(5‑1)套在所述针芯(5‑2)的外部,露出所述针头(5‑3),所述套管(5‑1)的侧壁上设置有若干个侧孔(5‑1‑1);Y型连接口(6);弹性密封件(7);蝶翼装置(8);负压引流装置(4)。本实用新型首次设计了一种专门引流术区积液的一体化装置,方便用户直接使用,不用组装,提高了引流效率,加深了引流深度,不易发生阻塞。
The utility model belongs to the field of medical instruments, in particular to an integrated device for drainage of fluid in an operation area. The integrated device comprises: a puncture needle (5), which has a needle core (5-2), a needle (5-3) and a sleeve (5-1), and the needle (5-3) is arranged on the The end of the needle core (5-2), the sleeve (5-1) is sleeved on the outside of the needle core (5-2), exposing the needle (5-3), the sleeve (5-1) The side wall of ‑1) is provided with several side holes (5‑1‑1); Y-shaped connection port (6); elastic seal (7); butterfly wing device (8); negative pressure drainage device (4) . For the first time, the utility model designs an integrated device for special drainage area effusion, which is convenient for users to use directly without assembly, improves drainage efficiency, deepens drainage depth, and is not easy to be blocked.
Description
技术领域technical field
本实用新型属于医疗器械领域,特别涉及一种引流术区积液的一体化装置。The utility model belongs to the field of medical devices, in particular to an integrated device for fluid accumulation in a drainage area.
背景技术Background technique
乳腺癌患者术后,如引流不畅、皮瓣贴合欠佳,会发生术区积液现象,不利于术后伤口愈合。目前,乳腺癌外科学领域尚没有专门的工具用以解决患者术后术区积液状况,现领域内用到的技术,是借用静脉输液所用到的留置针,用其穿刺积液部位,并将留置针手动连接负压引流装置,以此将术区积液引流排出体外。但此种技术存在以下几个方面问题:Postoperative breast cancer patients, such as poor drainage and poor fit of the skin flap, will cause fluid accumulation in the surgical area, which is not conducive to postoperative wound healing. At present, there is no special tool in the field of breast cancer surgery to solve the postoperative fluid accumulation in the patient's operation area. Manually connect the indwelling needle to the negative pressure drainage device to drain the fluid in the surgical area. However, this technology has the following problems:
1、静脉穿刺输液使用的留置针,一般用于穿刺表浅血管,穿刺针头较细,一般在临床上使用20G-24G针头,延长管管径也比较细,用于引流术区积液时容易堵塞,需再次穿刺,增加患者的痛苦;1. The indwelling needle used for venipuncture and infusion is generally used to puncture superficial blood vessels. The puncture needle is relatively thin. Generally, 20G-24G needles are used in clinical practice. Blockage, need to puncture again, increase the pain of the patient;
2、现有的静脉留置针尾端通过鲁尔式接头连接负压引流装置,因现有的负压引流装置的连接管管径和鲁尔式接头不匹配,有时需多次操作才能将连接管套在鲁尔式接头上,操作费时、费力,同时因反复的牵拉,管子易折断、漏气,需重复操作,降低了患者的就医体验;2. The tail end of the existing venous indwelling needle is connected to the negative pressure drainage device through a Luer type joint. Because the diameter of the connecting pipe of the existing negative pressure drainage device does not match the Luer type joint, sometimes it takes several operations to connect the connection. The tube is sleeved on the Luer connector, which is time-consuming and labor-intensive to operate. At the same time, due to repeated pulling, the tube is easy to break and leak air. Repeated operations are required, which reduces the patient’s medical experience;
3、使用现有的留置针,积液只能从套管的尖端引流,容易引流不畅。3. Using the existing indwelling needle, the effusion can only be drained from the tip of the cannula, which is easy to drain poorly.
为了解决上述问题,提出本实用新型。In order to solve the above problems, the present invention is proposed.
实用新型内容Utility model content
本实用新型提供一种引流术区积液的一体化装置,所述一体化装置包括:The utility model provides an integrated device for drainage of fluid in the area, the integrated device includes:
穿刺针5,其具有针芯5-2、针头5-3和套管5-1,所述针头5-3设置在所述针芯 5-2的端部,所述套管5-1套在所述针芯5-2的外部,露出所述针头5-3,所述套管 5-1的侧壁上设置有若干个侧孔5-1-1;The
Y型连接口6,其具有两个侧端口a、b和尾端口c,其一侧端口a连接所述套管 5-1的尾部,另一侧端口b连接连接管3的一端;The Y-
弹性密封件7,其设置在所述Y型连接口6的尾端口c内部,弹性密封所述尾端口c;An
蝶翼装置8,其固定在所述针芯5-2的尾部且所述针芯5-2穿过所述Y型连接口 6的一侧端口a、所述尾端口c和所述弹性密封件7;The
负压引流装置4,其与所述连接管3的另一端相连。The negative
优选地,所述穿刺针5的长度为4-6cm。Preferably, the length of the
优选地,所述针头5-3内径为1.6~3.43mm、外径为2.11~4.19mm,所述套管 5-1内径为2.11~4.19mm。Preferably, the inner diameter of the needle 5-3 is 1.6-3.43 mm, the outer diameter is 2.11-4.19 mm, and the inner diameter of the cannula 5-1 is 2.11-4.19 mm.
优选地,所述连接管3的内径为4-5mm。Preferably, the inner diameter of the connecting
优选地,所述相连或连接为固定式连接。该固定式连接实现了一体化的设计,方便用户直接使用,不用组装。Preferably, the connection or connection is a fixed connection. The fixed connection realizes an integrated design, which is convenient for users to use directly without assembly.
优选地,所述Y型连接口6的一侧端口a的内径大于或者等于所述套管5-1的内径。Preferably, the inner diameter of one side port a of the Y-
优选地,所述套管5-1的尾端部分和尾端中部的旁路管道形成所述Y型连接口 6。Preferably, the tail end portion of the sleeve 5-1 and the bypass pipe in the middle portion of the tail end form the Y-
优选地,所述Y型连接口6的一侧端口a包括一段渐扩管。Preferably, one side port a of the Y-
优选地,所述针头5-3规格为8G-14G。该行业内,根据所述针头5-3规格为8G-14G即可确定所述针芯5-2和套管5-1的内径。Preferably, the specifications of the needles 5-3 are 8G-14G. In this industry, the inner diameter of the needle core 5-2 and the cannula 5-1 can be determined according to the specification of the needle 5-3 being 8G-14G.
优选地,所述负压引流装置4为负压球。Preferably, the negative
优选地,所述弹性密封件7为硅胶海绵块或树脂块。Preferably, the
优选地,所述Y型连接口6的两个侧端口a、b之间的角度大于90度。Preferably, the angle between the two side ports a and b of the Y-
本实用新型第二方面提供一种引流术区积液的方法,其使用本实用新型第一方面所述的一体化装置进行,利用所述蝶翼装置8由患者皮肤外将所述穿刺针5 整体刺入所述患者皮肤至积液区域,拉动所述蝶翼装置8将所述针芯5-2拔出,将所述套管5-1留置在所述积液区域内,所述弹性密封件7自然密封所述套管5-1,然后开启所述负压引流装置4,则所述患者积液区域内的积液通过所述套管5-1的尖端和所述套管5-1侧壁上的侧孔5-1-1流入所述套管5-1中,然后依次流过所述Y 型连接口6、所述连接管3,流入所述负压引流装置4。The second aspect of the present utility model provides a method for draining fluid in a drainage area, which uses the integrated device described in the first aspect of the present utility model, and uses the
上述操作一气呵成,减少了操作步骤,节省时间。The above operations are completed in one go, reducing the operation steps and saving time.
本实用新型第三方面提供一种第一方面所述的引流术区积液的一体化装置用于加速引流体内积液并避免发生阻塞的用途。A third aspect of the present invention provides the use of the integrated device for fluid accumulation in the drainage area described in the first aspect for accelerating fluid accumulation in the drainage fluid and avoiding obstruction.
优选地,本实用新型第三方面提供一种第一方面所述的引流术区积液的一体化装置专门用于乳腺癌术后引流术区积液的用途。Preferably, the third aspect of the present invention provides an integrated device for drainage of fluid in the first aspect, which is specially used for the drainage of fluid in the drainage area after breast cancer surgery.
上述技术方案具有以下有益效果:The above technical scheme has the following beneficial effects:
本实用新型首次设计了一种引流术区积液的一体化装置,方便用户直接使用,不用组装,避免了使用现有的静脉留置针尾端通过鲁尔式接头连接负压引流装置的引流不畅、操作繁琐等问题,同时还具有以下优点:The utility model is the first to design an integrated device for drainage of fluid in the area of drainage, which is convenient for users to use directly without assembly, and avoids the inconvenience of using the existing venous indwelling needle tail end to connect the negative pressure drainage device through a Luer joint. It also has the following advantages:
(1)因现有留置针套管管径较细,不便于人工留置侧孔,留置侧孔管子易折断,需手术操作将管子取出,增加患者痛苦的同时,也会产生负面情绪。本实用新型将穿刺针的套管内径设置为2.11~4.19mm,并在其侧壁上设置有若干个侧孔,以增加引流的效率和范围,不留有“死腔”。本实用新型的引流术区积液的一体化装置不限制仅仅专门用于乳腺癌术后引流术区积液,可以适用于任何需要体内引流液体的场合中。(1) Due to the small diameter of the existing indwelling needle cannula, it is inconvenient to artificially indwell the side hole, and the indwelling side hole tube is easy to break, requiring surgical operation to remove the tube, which increases the patient's pain and also produces negative emotions. In the utility model, the inner diameter of the cannula of the puncture needle is set to 2.11-4.19 mm, and several side holes are arranged on the side wall to increase the efficiency and range of drainage without leaving "dead space". The integrated device for drainage of fluid in the drainage area of the present invention is not limited to be exclusively used for fluid in the drainage area after breast cancer surgery, and can be applied to any occasion that requires fluid drainage in the body.
(2)优选的技术方案中,加粗了现有的穿刺针的针头,根据术区积液范围,设计8G-14G规格的针头供临床试剂操作选择,以增加引流效率。(2) In the preferred technical solution, the needle of the existing puncture needle is thickened, and the needle of 8G-14G specification is designed for clinical reagent operation selection according to the range of fluid accumulation in the operation area, so as to increase the drainage efficiency.
(3)优选的技术方案中,增加穿刺针的长度,原穿刺针长度在2.5cm左右,本实用新型将穿刺针的针头长度设计为4-6cm,以增加引流的深度。(3) In the preferred technical solution, the length of the puncture needle is increased, the original length of the puncture needle is about 2.5cm, and the length of the needle head of the puncture needle is designed to be 4-6cm in the present invention to increase the depth of drainage.
(4)优选的技术方案中,穿刺针的尾部设计Y型连接口,Y型连接口的两个侧端口之间的角度大于90度,可以增加引流效率,同时Y型角度可调节,方便装置的外部固定。(4) In the preferred technical solution, a Y-shaped connection port is designed at the tail of the puncture needle, and the angle between the two side ports of the Y-shaped connection port is greater than 90 degrees, which can increase the drainage efficiency, and at the same time, the Y-shaped angle can be adjusted, which is convenient for installation external fixation.
(5)优选的技术方案中,所述Y型连接口的一侧端口的内径大于所述套管的内径或者包括一段渐扩管,方便积液的快速流出,可以增加引流效率。(5) In the preferred technical solution, the inner diameter of one side port of the Y-shaped connection port is larger than the inner diameter of the sleeve or includes a section of gradually expanding pipe, which facilitates the rapid outflow of the effusion and can increase the drainage efficiency.
附图说明Description of drawings
图1为实施例2的引流术区积液的一体化装置示意图。FIG. 1 is a schematic diagram of an integrated device for drainage of fluid in the drainage area of Example 2. FIG.
图2为实施例2示出的另一种引流术区积液的一体化装置示意图。FIG. 2 is a schematic diagram of another integrated device for drainage of fluid in the drainage area shown in Example 2. FIG.
图3为实施例3使用实施例1所述的现有的组合引流装置和实施例2所述的“一体化”引流装置对所述模拟积液样品进行引流时,发生阻塞的概率柱状图。3 is a histogram of the probability of blockage when the simulated effusion sample is drained using the existing combined drainage device described in Example 1 and the “integrated” drainage device described in Example 2 in Example 3.
附图标记列表:List of reference numbers:
3、连接管,4、负压引流装置,5、穿刺针,5-1、套管,5-2、针芯、5-3、针头,5-1-1、侧孔,6、Y型连接口,7、弹性密封件,8、蝶翼装置。3. Connecting tube, 4. Negative pressure drainage device, 5. Puncture needle, 5-1, cannula, 5-2, needle core, 5-3, needle, 5-1-1, side hole, 6, Y type Connection port, 7. Elastic seal, 8. Butterfly wing device.
具体实施方式Detailed ways
下面通过具体实施方式进一步说明本实用新型的内容。The content of the present utility model is further described below through specific embodiments.
实施例1Example 1
现有的静脉留置针由护针帽、导管、金属楔、导管座、针管、隔离塞、针翼座、针尖保护套、延长管、大/小封管夹、直型或Y型鲁尔接头,肝素帽(1个/2 个)和/或MaxZeroTM正压无针接头(1个/2个)和/或端帽组成。Existing IV catheters consist of needle guards, catheters, metal wedges, catheter hubs, needle tubes, isolation plugs, needle wing hubs, needle tip protection sleeves, extension tubes, large/small tube closure clips, straight or Y-type luer fittings , heparin cap (1/2) and/or MaxZeroTM positive pressure needleless connector (1/2) and/or end cap.
原引流装置属于组合装置,需要现有的静脉留置针,尾端通过鲁尔式接头,通过连接管与负压引流装置连接。The original drainage device belongs to a combined device, which requires an existing venous indwelling needle, and the tail end is connected with a negative pressure drainage device through a Luer-type connector and a connecting tube.
实施例2Example 2
本实用新型提供一种引流术区积液的一体化装置,见图1,所述一体化装置包括:The utility model provides an integrated device for drainage of fluid in the area, as shown in Figure 1, the integrated device includes:
穿刺针5,其具有针芯5-2、针头5-3和套管5-1,所述针头5-3设置在所述针芯 5-2的端部,所述套管5-1套在所述针芯5-2的外部,露出所述针头5-3,所述套管 5-1的侧壁上设置有若干个侧孔5-1-1;The
Y型连接口6,其具有两个侧端口a、b和尾端口c,其一侧端口a连接所述套管 5-1的尾部,另一侧端口b连接连接管3的一端;The Y-shaped
弹性密封件7,其设置在所述Y型连接口6的尾端口c内部,弹性密封所述尾端口c;An
蝶翼装置8,其固定在所述针芯5-2的尾部且所述针芯5-2穿过所述Y型连接口 6的一侧端口a、所述尾端口c和所述弹性密封件7;The
负压装置4,其与所述连接管3的另一端相连。The
其中,所述针芯5-2和套管5-1长度均为5cm;Wherein, the length of the needle core 5-2 and the sleeve 5-1 are both 5cm;
所述针头5-3内径为3.43mm、外径为4.19mm、The inner diameter of the needle 5-3 is 3.43mm, the outer diameter is 4.19mm,
所述套管5-1内径为4.19mm,其侧壁上两侧均匀设置有共12个侧孔5-1-1;所述连接管3的内径为5mm。所述相连或连接为固定式连接。The inner diameter of the sleeve 5-1 is 4.19 mm, and a total of 12 side holes 5-1-1 are evenly arranged on both sides of the side wall; the inner diameter of the connecting
所述弹性密封件7为树脂块。所述负压装置4为负压球。The
所述Y型连接口6的一侧端口a包括一段内径为4.19mm到5mm的渐扩管。One side port a of the Y-shaped
所述Y型连接口6的另一个侧端口b和尾端口c的内径为5mm。The inner diameter of the other side port b and the tail port c of the Y-shaped
上述一体化装置的操作方法如下:The operation method of the above-mentioned integrated device is as follows:
操作时,医务人员利用所述蝶翼装置8由患者皮肤外将所述穿刺针5整体刺入所述患者皮肤至积液区域,拉动所述蝶翼装置8将所述针芯5-2拔出,将所述套管 5-1留置在所述积液区域内,所述弹性密封件7自然密封所述套管5-1,然后开启所述负压引流装置4,则所述患者积液区域内的积液通过所述套管5-1的尖端和所述套管5-1侧壁上的侧孔5-1-1流入所述套管5-1中,然后依次流过所述Y型连接口 6、所述连接管3,流入所述负压引流装置4。During operation, the medical staff uses the
图2示出的为另一种装置示意图,其中所述套管5-1的尾端部分和尾端中部的旁路管道b形成所述Y型连接口6。FIG. 2 shows a schematic diagram of another device, wherein the Y-shaped
使用时,仅所述套管5-1的前端部分刺入所述患者皮肤至积液区域内。In use, only the front end portion of the cannula 5-1 penetrates the patient's skin into the fluid accumulation area.
实施例3Example 3
针对N1-N9不同体积的乳腺癌术后模拟积液样品,本实用新型分别使用实施例1所述的原引流装置和实施例2所述的“一体化”引流装置对所述模拟积液样品进行引流,汇总操作时间如下表1所示,汇总并计算发生阻塞的概率见图3 所示。For the simulated effusion samples after breast cancer surgery with different volumes of N1-N9, the present invention uses the original drainage device described in Example 1 and the "integrated" drainage device described in Example 2 to separate the simulated effusion samples. For drainage, the operation time is summarized as shown in Table 1 below, and the probability of blockage is summarized and calculated as shown in Figure 3.
表1原引流装置和本实用新型“一体化”引流装置的操作时间Table 1 Operation time of the original drainage device and the "integrated" drainage device of the present invention
因此,本实用新型“一体化”引流装置相比于原引流装置具有更高的引流的效率,并且发生阻塞的概率大大降低。Therefore, the "integrated" drainage device of the present invention has higher drainage efficiency than the original drainage device, and the probability of blockage is greatly reduced.
以上所述,仅为本实用新型的具体实施方式,但本实用新型的保护范围并不局限于此,任何熟悉本技术领域的技术人员在本实用新型揭露的技术范围内,可轻易想到变化或替换,都应涵盖在本实用新型的保护范围之内。因此,本实用新型的保护范围应以权利要求的保护范围为准。The above are only specific embodiments of the present invention, but the protection scope of the present invention is not limited to this. Replacement should be covered within the protection scope of the present invention. Therefore, the protection scope of the present invention should be subject to the protection scope of the claims.
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