Detection device for recognizing the epidural space
11045613 · 2021-06-29
Assignee
Inventors
Cpc classification
A61B17/3401
HUMAN NECESSITIES
A61M25/01
HUMAN NECESSITIES
A61M2205/3344
HUMAN NECESSITIES
A61B5/061
HUMAN NECESSITIES
A61M2025/0089
HUMAN NECESSITIES
A61B17/3494
HUMAN NECESSITIES
A61B5/6885
HUMAN NECESSITIES
A61B2090/064
HUMAN NECESSITIES
International classification
A61B5/06
HUMAN NECESSITIES
A61M25/01
HUMAN NECESSITIES
Abstract
A detection device for recognizing the epidural space is provided. The detection device includes an upper case having a predetermined shape and a lower case coupled to the upper case to form a predetermined space part. A connection tube is provided at a predetermined position of the space part, one end of the connection tube communicates with a paracentesis needle part and the connection tube communicates with a pressure sensor for measuring pressure at a predetermined position of an outer peripheral part thereof. When the paracentesis needle part reaches the epidural space, the device allows a medicine injection catheter to be inserted into the connection tube thereby reaching the epidural space, with the connection tube and the paracentesis needle part connected to each other.
Claims
1. A detection device for recognizing an epidural space, comprising: an upper case having a predetermined shape; and a lower case coupled to the upper case to form a predetermined space part, where the lower case is removable from the upper case, wherein a connection tube is provided at a predetermined position of the predetermined space part, one end of the connection tube configured to couple with a paracentesis needle part and the other end of the connection tube having a detachable cap part, and an opening being provided at a predetermined position of an outer peripheral part of the connection tube, the opening communicating with a pressure sensor for measuring pressure, wherein the other end of the connection tube is configured to receive a medicine injection catheter when the detachable cap part is detached from the other end, wherein the upper case has fixing protrusions for fixing the paracentesis needle part, the lower case has a fixing groove part for fixing and accommodating the paracentesis needle part, and the predetermined space part further has a PCB substrate having a program embedded therein for calculating a result of the pressure sensor, wherein the fixing protrusions are protruded from the upper case toward the lower case, wherein the fixing groove part of the lower case fixes the paracentesis needle part, together with the fixing protrusions of the upper case, and wherein an outer expansion part is further removably provided on an outer surface of the one end of the connection tube to be connected to the paracentesis needle part.
2. The detection device for recognizing the epidural space according to claim 1, wherein the PCB substrate further has a LED lamp for indicating the calculation result of the pressure sensor.
3. The detection device for recognizing the epidural space according to claim 1, wherein the PCB substrate further has a travel distance sensor capable of sensing a travel distance of the medicine injection catheter.
4. The detection device for recognizing the epidural space according to claim 3, wherein the upper case is made of a diffusion PC.
5. The detection device for recognizing the epidural space according to claim 3, wherein the PCB substrate further has a LCD display window for informing a result of the travel distance sensor.
6. The detection device for recognizing the epidural space according to claim 5, wherein a power button and a reset button are further provided on one side of the upper case.
7. The detection device for recognizing the epidural space according to claim 6, wherein the one end and the other end of the connection tube protrude from the predetermined space part of the upper case and the lower case.
8. The detection device for recognizing the epidural space according to claim 7, wherein the outer expansion part is made of an elastic body.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
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DETAILED DESCRIPTION
(11) Hereinafter, the detection device for recognizing the epidural space according to the present invention will be described with reference to the accompanying drawings.
(12) As used herein, the terms “comprise”, “have” and “provided” are intended to express the presence of the features, numbers, steps, elements, parts or combinations thereof. It is not to be understood that the terms are to exclude possible presence or addition of one or more other features, numbers, steps, actions, elements, parts or combinations thereof.
(13) Also, unless otherwise defined, all terms used herein, including technical or scientific terms, have the same meaning as commonly understood by those skilled in the art to which the present invention belongs. Terms such as those defined in commonly used dictionaries are to be interpreted as having a meaning consistent with the meaning of the context in the relevant art and are not to be interpreted in an ideal or overly formal sense unless expressly defined herein.
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(15) That is, the detection device for recognizing the epidural space of the present invention is a medical device used for locating the epidural space in a state where a spine needle or an epidural needle, which are paracentesis needles, is combined therewith, as shown in
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(18) As can be seen from the drawings, the detection device for recognizing the epidural space of the present invention comprises an upper case 100 having a predetermined shape and a lower case 200, and a space part 220 formed by the coupling of the upper case 100 and the lower case 200 may accommodate a PCB substrate 300, a pressure sensor 400, a connection tube 500, a battery 600, etc., which will be described below.
(19) The upper case 100 of the detection device for recognizing the epidural space according to the present invention may have a pair of fixing protrusions 130 facing each other at predetermined positions on the outer surface thereof. The pair of fixing protrusions 130 are to stably fix a paracentesis needle part 700 to the detection device for recognition. After an engagement part 720 of the paracentesis needle part 700 is seated on the fixing groove part 210 (to be described below) of the lower case 200, the fixing protrusions 130 of the upper case 100 tightly fix the paracentesis needle part 700 from above so that the paracentesis needle part 700 is firmly coupled to the detection device for recognition.
(20) It is preferable that a power button 110 and a reset button 120 are further provided at predetermined positions on the outer surface of the upper case 100.
(21) The power button 110 may supply power to operate the PCB substrate 300, which supplies power and controls the pressure sensor 400, an LED lamp 310, an LCD display window 320 and so on for measuring the epidural space and the travel distance of a medicine injection catheter and notifying the user of the result
(22) The reset button 120 is to initialize the measurement value of the pressure sensor or the measurement result of the travel distance of the catheter 1000. A detailed description thereof will be given below.
(23) The upper case 100 may be preferably made of a material that transmits light so that the result displayed by the LCD display window 320 can be easily seen from the outside, more preferably, a diffusion PC (polycarbonate) having a light diffusion function.
(24) The lower case 200 has a shape corresponding to the upper case 100. It may have a fixing groove part 210 at a predetermined position on the edge part. As described above, the fixing groove part 210 serves to stably fix the paracentesis needle part 700, together with the fixing protrusions 130 of the upper case 100.
(25) Further, it is preferable that a heat release hole 230 for discharging the heat generated during the operation of the PCB substrate 300, the LED lamp 310, the LCD display window 320, the travel distance sensor 330, and the pressure sensor 400 accommodated in the space part 220, is provided at a predetermined position on the outer surface of the lower case 200.
(26) The upper case 100 and the lower case 200 of the present invention are illustrated as having a roughly tetragonal shape. However, this is just an exemplary illustration and it is obvious that the outer shape of the cases can be modified by those skilled in the art.
(27) The space part 220 formed by the coupling of the upper case 100 and the lower case 200 may accommodate the PCB substrate 300, the LED lamp 310, the LCD display window 320, the travel distance sensor 330, the pressure sensor 400, the connection tube 500, and the battery 600.
(28) Hereinafter, the connection tube 500, which is one of the major elements of the present invention, will be described in detail with reference to
(29) The connection tube 500 accommodated in the space part 220 may have a long cylindrical shape which has a predetermined inner diameter, and both ends and a predetermined position of the outer peripheral part of which are open.
(30) The inner diameter of the connection tube 500 is not particularly limited, but it is preferably within a range where the medicine injection catheter 1000 can pass through it.
(31) One end of the connection tube 500 may horizontally communicate with the paracentesis needle part 700 and the other end thereof may have a detachable cap part 510. In addition, an opening 530 formed at a predetermined position of the outer peripheral part communicates with the pressure sensor 400 to allow measurement of the pressure at the position where the paracentesis needle is inserted.
(32) Below a detailed explanation will be given about the pressure measurement consisting of the above elements. The paracentesis needle inserted into the skin to locate the epidural space and the connection tube 500 have been connected to each other, and the other end of the connection tube 500 has been sealed by the cap part 510. Thus, the pressure sensor 400 in communication with the opening 530 of the connection tube 500 can accurately measure the pressure at the position where the needle is inserted.
(33) Here, the cap part 510 provided at the other end of the connection tube 500 supports measuring the pressure at the position of the paracentesis needle inserted in the human body, and injecting a medicine into the epidural space with the medicine injection catheter 1000 when the epidural space has been recognized.
(34) That is, in order to locate the epidural space with no affection by the ambient pressure (atmospheric pressure), it is necessary to measure the pressure with the cap part 510 attached to the connection tube 500). However, after the epidural space is accurately located, the cap part 510 is detached from the connection tube 500 so that the medicine injection catheter 1000 can be inserted into the inner space of the connection tube 500.
(35) As described above, the detection device for recognizing the epidural space of the present invention has a connection tube 500, one end of which horizontally communicates with the paracentesis needle part 700, the other end of which has a detachable cap part 510, and which has an opening 530 at a predetermined position on the outer peripheral part that communicates with the pressure sensor 400. Thus, it is possible to not only accurately locate the epidural space, but also accurately insert the medicine injection catheter 1000 into the epidural space.
(36) In other words, in the prior art, there is no element capable of performing the same function as the connection tube 500 of the present invention. Thus, it is difficult to accurately locate the epidural space. Moreover, even if the epidural space is accurately located, it is very difficult to accurately insert the medicine injection catheter 1000 into the epidural space, because, in order to insert the medicine injection catheter 1000 into the paracentesis needle part 700, it is necessary to separate the detection device's main body from the paracentesis needle part 700 and it is highly likely that the position of the paracentesis needle part 700 will move during this process.
(37) Meanwhile, the engagement method of the cap part 510 and the connection tube 500 is not particularly limited as long as it is a fixing method capable of detachment and attachment by a physical external force. However, preferably, it may be male and female screw engagement. Given that the movement of the detection device needs to be minimized in order to prevent movement of the needle from the epidural space, male and female screw engagement is preferred. Also, it is more preferable to have packing at the cap part 510 in order to maintain airtightness.
(38) It is preferable that one end and the other end of the connection tube 500 protrude from the space part 220 of the upper case 100 and the lower case 200 by a predetermined length.
(39) Since the one end is to be physically connected to the paracentesis needle part 700 and the other end is to be connected to the cap part 510, it is preferable to design the ends such that they protrude from the space part 220 by a predetermined length in order to allow easy replacement of the needle part 700 and attachment or detachment of the cap part 510.
(40) Further, it is preferable that the outer expansion part 520 is further provided on the outer surface of one end of the connection tube 500 connected to the paracentesis needle part 700.
(41) A spine needle 710 (or an epidural needle) is generally used as the needle for detecting the epidural space. Since the spine needle 710 and the epidural needle are different from each other in their inner diameters of the engagement part 720, conventionally, each detection device for locating the epidural space has been used for each needle. However, according to the present invention, the outer expansion part 520, with which the outer diameter can be changed, is provided at one end of the connection tube 500 to be connected to the paracentesis needle part 700 so that all the needles having different inner diameters can be used with a single detection device.
(42) In one example, the outer expansion part 520 having a predetermined width and height may be provided at a predetermined position on the outer surface of one end of the connection tube 500, so that a needle having a smaller inner diameter may be coupled by press-fitting to the one end without the outer expansion part 520 being attached and a needle having a larger inner diameter may be connected via insertion of the outer expansion part 520.
(43) The outer expansion part 520 is preferably made of an elastic body whose volume can be changed by an external force, although not limited thereto.
(44) In addition, although the accompanying drawings only show the case where one outer expansion part 520 is provided, it is obvious that a plurality of outer expansion parts 520 may be provided as needed.
(45) The pressure sensor 400 communicating with the opening 530 formed at a predetermined position on the outer peripheral part of the connection tube 500 is to identify the position of muscles, at which there is no pressure change, and the position of the epidural space, at which a pressure change occurs. The specific constitution of the pressure sensor 400 is a known technology, and thus a detailed description thereof will be omitted.
(46) The PCB substrate 300 is provided on the top of the pressure sensor 400 and the LED lamp 310 and the LCD display window 320 are provided on the top of the PCB substrate 300. Also, a travel distance sensor 330 may be further provided between the connection tube 500 and the PCB substrate 300.
(47) Since the pressure difference between the muscles and the epidural space of the human body is only around 5 mbar, it is necessary to amplify the electrical signal from the pressure sensor 400 in order to inform the user of the changed pressure value.
(48) Therefore, a program for amplifying the electrical signal from the pressure sensor 400, comparing the signal with a set pressure value, and then outputting the result is embedded in the PCB substrate 300. If the measurement value of the pressure sensor 400 falls within the set pressure range, the program may perform a function of blinking the LED lamp 310 to send a signal to the user. The program may also perform a function of embodying the result value of the travel distance sensor 330 on the LCD display window 320.
(49) Below a more detailed explanation will be given about the LED lamp 310 and the LCD display window 320. When the paracentesis needle reaches the epidural space, the LED lamp 310 emits light or flashes to inform the user of the correct position of the epidural space.
(50) The LCD display window 320 serves the function of informing the travel distance of the medicine injection catheter 1000 injected into the epidural space through the inner space of the connection tube 500. After the epidural space is located, the medicine injection catheter 1000 needs to be inserted into the body to allow the injected medicine to reach the desired position. Therefore, the present invention may further have a sensor 330 for measuring the travel distance of the medicine injection catheter 1000 in order to accurately identify the travel distance and position of the medicine injection catheter 1000.
(51) The principle of measuring the travel distance of the medicine injection catheter 1000 is preferably a noncontact type. In one example, if the user inserts the medicine injection catheter 1000, a laser sensor senses and calculates the travel distance, and then displays the result on the LCD display window 320, thereby allowing the user to easily identify the length of the catheter inserted into the human body.
(52) Of course, it is obvious that a transparent window may be provided at a predetermined part of the connection tube 500 or that the connection tube 500 may be made of a transparent material, so that the travel distance of the medicine injection catheter 1000 can be perceived.
(53) Meanwhile, the reset button 120 provided at a predetermined position of the upper case 100 is a button for initializing the measurement values when the measured pressure or travel distance is to be measured again.
(54) A portable battery 600 is provided at the bottom of the connection tube 500 to supply power to all of the electrical devices inside the PCB substrate.
(55) Hereinafter, a process of locating the epidural space and injecting a medicine using the detection device for recognizing the epidural space according to the present invention, which has the above constitution, will be described.
(56) First, it is determined which part of the human body the paracentesis needle is to be inserted into in order to locate the epidural space, and then a spine needle or an epidural needle is selected accordingly.
(57) The selected needle is coupled to the detection device of the present invention, specifically, one end of the connection tube 500, and the cap part 510 is fixed to the other end. Next, the power button 110 provided at a predetermined position on the outer surface of the upper case 100 is turned on to make the detection device for recognizing the epidural space ready for operation.
(58) The needle is inserted via the designated area of the patient to detect the epidural space, with which the LED lamp 310 emits light. When the needle is positioned at the epidural space, the cap part 510 of the connection tube 500 is separated and the medicine injection catheter 1000 is inserted into a predetermined space part of the connection tube 500. Then, the medicine injection catheter 1000 is inserted up to a position determined by a preliminary examination by checking the travel distance of the medicine injection catheter 1000 displayed on the upper case 100, and the medicine is injected.
(59) While the present invention has been particularly described with reference to specific embodiments thereof, those skilled in the art will appreciate that such specific embodiments are merely preferred embodiments and that the scope of the invention is not limited thereby. It will be apparent to those skilled in the art that various changes and modifications may be made without departing from the spirit and scope of the invention. It is obvious that such modifications and variations fall within the scope of the appended claims.