JP4688853B2 - Medical dosing device - Google Patents

Description

  The present invention relates to a medical administration device used for the administration of a drug solution such as insulin.

  Conventionally, medical administration devices are often used when administering a drug solution such as insulin or a hormone preparation. In general, this type of medical administration device has an injection needle, a syringe body, and an injection button arranged in a substantially straight line, and the injection solution of a liquid medicine cartridge built in the syringe body is parallel to the injection needle. It is configured to be pushed out with an injection button. 24 and 25 show two typical conventional examples.

  24, 201 is a medical administration device body (hereinafter also referred to as a syringe body), 202 is an injection solution sucked into the medical administration device body 201, 203 is an injection button, 204 is an injection needle, and 205 is an injection. The plunger is connected to the button 203 and directly pushes out the injection 202.

  The syringe body 201 contains an injection solution 202. When administering the injection solution, the needle 204 is inserted into the skin, the injection button 203 is pushed, and the injection solution 202 in the medical administration device body 201 is pushed out. Then, the dosage of the injection solution 202 is determined while adjusting the amount by which the injection button 203 is pressed.

  That is, when the administration person (patient) pushes the injection button 203, the internal plunger 205 moves and pushes the injection solution 202 from the injection needle 204. The amount of injection solution to be administered is determined by the slide amount of the plunger 205. The administration person (patient) determines the amount of the injection solution 202 to administer, pierces the place of the skin where the injection needle 204 is injected, and pushes the injection button 203 to complete the injection. At this time, when the injection needle 204 enters the skin, the administration person (patient) must determine the insertion amount of the injection needle into the skin based on past experience and the like.

  Many of the medical administration devices used for such self-administration are mechanical and pen-type as shown in FIG. 24, but the injection button is in the same direction as when the needle was first inserted into the skin. The administration state is not stable because of pressing. On the other hand, as shown in FIG. 25, recently, in order to solve the above-mentioned problem, a portion that contacts the skin at the time of administration is provided in the vicinity of the injection needle, and the position of the injection needle and the skin is determined so as to stabilize the administration state. Some have been devised.

  In FIG. 25, 301 is a medical administration device body, 303 is an injection button, 304 is an injection needle, 306 is a skin contact portion that is applied to the skin when administering an injection solution using this conventional medical administration device, and 307 is A chemical cartridge 302 is an injection solution in the chemical cartridge 307.

  At the time of administration, the injection needle 304 is stabbed into the skin while the skin contact portion 306 is applied to the skin, the injection button 303 is pressed, and the injection solution 302 in the drug solution cartridge 307 is pushed out. The dose is determined while being adjusted by the amount pressed by the injection button 303.

  Also, in most cases, conventional medical administration devices are so-called empty in order to prevent the injection needle from being mixed with the injection solution and injecting air immediately before the injection needle is actually administered. After hitting (hereinafter, also referred to as air venting), a predetermined amount of chemical solution is administered to the human body.

  In the conventional medical administration device whose external view is shown in FIG. 24, it is possible to push the injection button or the administration button even when forgetting to attach the injection needle to the administration device body when administering the drug solution. For this reason, inadvertently pressing the injection button or the administration button may cause a problem.

  In addition, conventional medical administration devices are diagnosed by a doctor and give instructions on the amount of injection solution to be administered and an administration interval, and the administrator himself administers the drug solution according to the instructions. The administration of the administration interval is left to the administration person himself. Further, the doctor makes a diagnosis periodically, and determines the diagnosis result, the amount of the injection solution administered in the past, the injection solution amount to be newly administered from the administration interval, and gives an instruction.

  Conventionally, many of the medical administration devices used for such self-administration have been mechanical, as shown in FIG. 24 or FIG. 25, but recently, devices with electronic devices have been devised. .

  FIG. 26 and FIG. 27 show typical structural views thereof. FIG. 28 is a block diagram centering on the microprocessor. 26 is a front view, and FIG. 27 is a top view showing a partial cross section.

  In FIG. 26, 403 is a syringe body, 401 is an injection needle, 404 is a display unit, 405 is a dose setting dial for an injection solution, and 406 is an injection button.

  In FIG. 27, a cartridge 407 containing an injection solution 426 is set in the syringe body 403. The admin pulls out the injection button 406 before injection. When the injection button 406 is pulled out, the sleeve 418 and the nut 412 slide in the same direction as the injection button 406 together with the injection button 406.

  By sliding the sleeve 418, the spline part 416 of the sleeve 418 is coupled to the spline part 417 of the dose setting dial 405. The connecting portion between the sleeve 418 and the plunger 408 is not fixed in the sliding direction, but is fixed in the rotating direction. Further, the coupling portion between the sleeve 418 and the nut 412 is not fixed in the rotational direction, but is fixed in the sliding direction.

  As a result, when the user turns the dose setting dial 405, the sleeve 418 is rotated, and the plunger 408 is rotated accordingly, and the screw provided on the inner periphery of the nut 412 and the outer periphery of the plunger 408 are provided. The plunger 408 is slid by the screw thus formed. The amount of injection solution to be administered is determined by the amount by which the plunger 408 slides. If the injection button 406 is not pulled out, the sleeve 418 and the dose setting dial 405 are not coupled, and the plunger 408 does not move even if the dose setting dial 405 is rotated.

  The administration person rotates the dosage setting dial 405 to determine the amount of the injection solution to be administered, stabs the injection needle 401 at the place where the injection is performed, and pushes the injection button 406 to complete the injection. When the injection is completed, the injection button 406, the sleeve 418, and the nut 412 slide in the pushed direction. At this time, in order to detect that the injection button 406, the sleeve 418, and the nut 412 have been slid, a projection 420 is provided on the sleeve 418, and a switch 413 that is turned on or off by the projection 420 is fixed to the main body 403.

  The switch 413 is turned on when the injection button 406 is pulled out and turned off when the injection button 406 is pushed. By looking at the state of the switch 413, it is detected that the injection has been completed. The means for determining the completion of injection according to the state of the switch 413 is determined by determining the conduction state of the switch 413 using the microprocessor 425 of FIG.

  Reference numeral 417 denotes a spline portion of the setting dial 405, 419a and 419b are optical sensors, 414 is a liquid crystal display portion, 415 is a substrate, 421 is a rotating plate, and 421a is a rotating plate slit. In FIG. 28, 422 is a memory of the microprocessor 425, 423 is a calendar, 424 is a clock, and 404 is a display interface with the liquid crystal display unit 414.

  FIG. 29 is an enlarged view of a portion for detecting completion of administration. Further, when setting the amount of injection solution to be administered, the dose setting dial 405 and the sleeve 418 are rotated. The amount of injection solution to be administered is determined by the amount of movement of the plunger 408 by the rotation of the dose setting dial 405. Therefore, a method is used in which the dose setting dial 405 and the sleeve 418 are rotated and the amount of the injection solution to be administered is detected by detecting the rotation amount. Reference numeral 416 denotes a sleeve spline portion, and 417 denotes a setting dial spline portion.

  Here, for example, as shown in FIG. 30, a rotating plate 421 that rotates simultaneously with the dose setting dial 405 is provided, and the rotating plate 421 is provided with a slit 421a as shown in FIG. 31, and the light crosses the slit 421a. Two optical sensors 419a and 419b are provided. When the dose setting dial 405 rotates, the rotating plate 421 also rotates, and the slit 421a provided in the rotating plate 421 transmits or blocks light from the optical sensors 419a and 419b. Since the optical sensors 419a and 419b output an on / off signal according to the amount of light, the rotation and the rotation amount can be detected by turning on / off the outputs of the optical sensors 419a and 419b.

  The reason for using the two optical sensors 419a and 419b is that the amount of injected liquid to be administered may increase or decrease depending on the rotation direction of the dose setting dial 405. The direction of rotation is determined based on the phase difference between the on / off states of the outputs of the two optical sensors 419a and 419b, and the amount of injection solution to be administered is detected by counting the number of on / off times of the outputs of the optical sensors 419a and 419b. . As described above, the means for detecting the amount of injection solution to be administered by judging the rotation direction based on the phase difference between the outputs of the optical sensors 419a and 419b and counting the number of ON and OFF times of the outputs of the optical sensors 419a and 419b As shown in FIG. 32, a microprocessor 425 or the like is used.

  Furthermore, the time and time of administration completion, date recording or display, etc. are performed by providing a microprocessor 425 and a memory 422. Also, optical sensors 419a and 419b have been devised that use switches or the like instead of optical sensors.

  However, in the conventional medical administration device shown in FIG. 24, the injection needle 204 is inserted into the skin at the time of administration, and the injection button 203 is pressed in the same direction as the injection needle 204 is inserted into the skin. Since the injection needle 202 is administered, the injection needle 204 is further inserted deeply into the skin from the state where the injection needle 204 is first inserted into the skin, and the patient's pain increases during administration.

  In addition, as shown in FIG. 25, even in the case where the skin application portion 306 is provided in the medical administration device, the injection needle 304 is inserted into the skin while the skin contact portion 306 is applied to the skin, and the injection button 303 is set. Since the injection solution 302 is administered while pushing the injection needle 304 in the same direction as the needle pierced into the skin, the injection needle 304 is further inserted deeply into the skin from the state where the injection needle 304 was first stuck in the skin. Is as described above. This is because even if the skin contact portion 306 is provided, the actual skin is elastic, and if the syringe button 303 is actually pressed, the injection needle 304 will pierce the skin deeply by the pressed force. is there.

  In order to prevent this, it is necessary to fix the arm on the side that pushes the syringe button 303 in the air or to carefully fix it in some way during the administration. In some cases it is extremely difficult.

  And the fact that the needle penetrates deeply into the skin during administration increases the pain of the patient, which is not only physically and mentally painful, but also in some cases the patient (patient). There was a problem of having a great influence on the human body and inviting a dangerous state to life.

  Further, in the conventional medical administration device shown in FIG. 24 or FIG. 25, the injection needle is not necessarily constant, and the length varies depending on the type of the injection needle. Depending on the condition, the failure due to the injection and the burden of pain are great, which may greatly affect the human body of the administration person (patient) and lead to a life-threatening state.

  In addition, in the conventional medical administration device shown in FIG. 24, even when the injection needle is forgotten to be attached to the administration device body, the injection button or the administration button can be pressed, and thus the following problems are caused. is there.

  For example, when the injection button or the administration button is pressed without attaching the injection needle, the drug solution leaks from the tip in the direction opposite to the injection button or the administration button, as in the case of the leaked solution 221a or the backflowed solution 221b in FIG. In addition, the chemical solution flows backward in the direction of the injection button or the administration button, and further, as shown in FIG. 34, the glass tube itself containing the chemical solution is caused by the pressure generated by pressing the injection button or the administration button. Various problems have occurred, such as cracks 227 entering or rupturing, and the chemical solution leaking outside.

  In addition, in the case of administering two types of drug solutions, such as growth hormone preparations, or when dissolving and mixing a drug and a drug solution, mixing is performed after attaching an injection needle. If you forget to attach the injection needle, it is not only impossible to mix, but as mentioned above, chemical solution backflow, leakage, or cracking, rupture, etc. of the glass tube of the chemical solution cartridge will cause problems. Yes. Many of the aforementioned problems occur particularly when the patient himself administers himself.

  In the conventional medical administration device shown in FIG. 24 to FIG. 27, the possibility of an accident will be low when a doctor or a nurse administers. You may forget this if you are not always aware of the syringe bleed operation. And if you forget to vent the air, some people have a great influence on the human body, which can lead to life-threatening conditions.

  In addition, in the conventional medical administration device shown in FIG. 26 or FIG. 27, the amount of injected liquid administered can be displayed on an electronic display device. The date and time will be recorded in the memory 422, not only reducing the capacity of the memory 422 unnecessarily, but also displaying the injection volume during the air venting operation in the same way as the original injection volume. Therefore, when a doctor confirms the diagnosis result and past administration history of the administration person (patient) and decides a subsequent treatment method, there is a possibility of making an erroneous determination. If a doctor makes such a misjudgment, it may have a great influence on the human body of the administration person (patient) and may lead to a life-threatening state.

  The present invention has been made in order to solve the above-described problems of the prior art, and has an object to provide a medical administration device capable of injecting a drug solution with safety and high reliability. Yes.

  That is, the present invention has been made to solve the problems of the conventional apparatus to which the electronic apparatus as shown in FIG. 26 or FIG. 27 is added. An object of the present invention is to provide a medical administration device in which the administration liquid volume, date, and time cannot be recorded in the memory 422, and a reliable administration history can be left.

In order to achieve the above object, a medical administration device according to claim 1 of the present application includes an administration device main body having a mounting portion for mounting a chemical liquid cartridge that stores a chemical solution to be administered to a patient, and the administration device main body. An injection button which is provided on the outer peripheral surface and starts a chemical liquid administration operation when the chemical liquid in the chemical liquid cartridge is administered, and a syringe needle which administers the chemical liquid, which is disposed on the front end side of the chemical liquid cartridge, is detachably mounted A mounting part to detect, a needle stick detection part to detect that the injection needle is stuck in the skin, an injection completion detection part to detect that the injection is completed, and an injection liquid amount detection to detect the amount of injected liquid to be injected The injection liquid volume recording unit for recording the injected injection liquid volume, and the injection liquid volume detected by the injection liquid volume detection unit when the injection completion detection unit detects completion of the injection, In the liquid volume recording section And a control unit for recording, by pressing the injection button, air releasing work performed, the control unit, while the injection needle is detected that stuck to the skin at the needle stick detecting unit, wherein Only when the completion of injection is detected by the injection completion detection unit, the administered injection volume is recorded in the injection volume recording unit, and when the needle stick detection unit does not detect that the injection needle is stuck in the skin The administered injection volume is not recorded in the injection volume recording section.

Thus, the only possible to record the detected injection solution amount when simultaneously injection needle when it detects that the injection is complete is hitting the skin, history during air removal carried out by pressing the injection button is not left, the actual The history of only the administration of this product can be reliably retained, and the injection volume at the time of the air venting operation that is always performed before the administration is recorded in the memory. When confirming the diagnosis result and past administration history of the person (patient) and determining the subsequent treatment method, it is misjudged that it is administered even though it is not actually administered. Medical administration that can solve various problems such as having a great influence on the human body of the recipient (patient) and possibly causing a life-threatening state, and can further support the treatment method of the doctor more reliably Ingredients can be obtained.

  The medical administration device according to claim 2 of the present application is the medical administration device according to claim 33, wherein a calendar unit for generating current date information, a clock unit for generating current time information, The control unit detects that the injection is completed, and at the same time records the date and time when the injection is completed.

  As a result, only when the injection is detected and at the same time the injection needle is in contact with the skin, the detected injection volume, date, and time are recorded, so that there is no history of air bleeding and the actual administration time Only the history of the injection solution, date, and time are recorded in the memory at the time of the air venting operation to be performed before administration, and the memory capacity of the memory part can be reduced unnecessarily, When confirming the diagnosis results and past administration history of the patient (patient) and deciding the subsequent treatment method, a misjudgment is made that it is not actually administered but for that reason. A medical administration device capable of solving various problems such as having a great influence on the human body of the administration person (patient) and potentially causing a life-threatening state, and further assisting a doctor's treatment method. It is.

  The medical administration device according to claim 3 of the present application is the medical administration device according to claim 3, which is recorded when the amount of the injection solution to be administered and the injection is completed. And a display unit for displaying the amount of the injected solution.

  As a result, only when the injection is detected and at the same time the detected injection volume is displayed only when the injection needle is in contact with the skin, there is no history at the time of bleeding, and only the history at the time of actual administration. It can be reliably left, and the injection volume at the time of the air venting operation that is always performed before the administration is displayed, and the doctor confirms the diagnosis result of the admin (patient) and the past administration history, and the subsequent treatment When deciding the method, it is misjudged that it is not actually administered, so it has a great influence on the human body of the patient (patient), and a life-threatening state is caused. A medical administration device can be obtained that can solve various problems such as inviting, and can more reliably support a doctor's treatment method.

  Further, the medical administration device according to the invention of claim 4 of the present application is the medical administration device according to claim 3, wherein the display unit includes the injection liquid amount recorded when the injection is completed, The date and time are displayed.

  As a result, only when the injection is detected and at the same time the injection needle is in contact with the skin, the detected injection volume, date, and time are displayed, so that there is no history of air bleeding and the actual administration time. Only the history of the injection solution, date, and time are displayed during the air venting operation that must be performed before administration. In the case of determining the subsequent treatment method, it is misjudged that it is not actually administered, so that it has a great influence on the human body of the user (patient). Thus, it is possible to solve various problems such as causing a life-threatening condition, and to obtain a medical administration device that can more reliably support a doctor's treatment method.

The medical administration device according to claim 5 of the present application is the medical administration device according to claim 1, wherein the needle stick detection unit is a ring shape that slides at the same time as the needle is inserted around the injection needle. Alternatively, an arc-shaped contact detection member and a switch that operates by sliding the contact detection member are provided.
Thereby, it can detect that the injection needle is contacting skin with simple composition.

The medical administration device according to claim 6 of the present application is the medical administration device according to claim 1, wherein the needle stick detection unit includes a skin contact part that contacts a patient's skin at the time of drug administration, The switch is provided on the skin contact surface of the skin contact portion, and has a switch that operates at the same time as the injection needle pierces the skin.
Thereby, it can detect that the injection needle is contacting skin with simple composition.

(Embodiment 1)
In the first embodiment, the device is configured such that the direction in which the injection button is pressed is different from the direction in which the injection needle is inserted into the skin, so that the injection needle is further inserted deeply when the injection button is operated. It is intended to prevent it from happening.

  Hereinafter, Embodiment 1 of the present invention will be described with reference to FIGS. FIG. 1 is a perspective view showing the appearance of a medical administration device according to Embodiment 1 of the present invention, and FIG. 2 is a partially broken view of the medical administration device according to Embodiment 1 of the present invention to show the internal structure. FIG. 3 is a perspective view, and FIG. 3 shows a state in which the medical administration device according to Embodiment 1 of the present invention is actually grasped by a hand.

  In FIG. 1, 1 is a medical administration device body, 2 is an injection solution, 3 is an injection button, 4 is an injection needle, 6 is a skin contact portion, 7 is a chemical cartridge, 8 is a liquid crystal display portion, and 9 is a dose adjustment knob. It is. The injection button 3 is configured to push the injection button 3 in a direction substantially perpendicular to the direction in which the injection needle 4 extends. The direction in which the injection button 3 is pushed in is not limited to the vertical direction as long as it is not parallel to the direction in which the injection needle 4 extends, and may be any other angle as long as it is a direction that relieves pain to the patient's body.

  As a procedure for administering the injection solution, first, the drug solution cartridge 7 is set in the medical administration device body 1, the injection needle 4 is attached, and the dose adjustment knob 9 is set in the figure in order to set the amount of the injection solution 2 to be administered. Rotate right or left as indicated by the arrow. Next, the injection needle is pointed directly upward and the injection button 3 is pushed until the injection solution 2 comes out from the tip of the injection needle 4 to release air. After the air venting is completed, the medical administration device is grasped with the hand 19 as shown in FIG. 3, the injection needle 4 is inserted into the skin while the skin contact part 6 is applied to the skin of the affected area, and the injection button 3 is inserted with the index finger 18 as shown in FIG. Dosing while pushing in the direction of the arrow.

  Next, with reference to FIG. 2, a method for setting the amount of injection solution and the mechanism by which the injection solution 2 comes out from the injection needle 4 when the injection button 3 described above is pressed will be described.

  First, the method for setting the injection volume will be described. The dose adjustment knob 9 and the sleeve 10 are fixed in the rotation direction but not in the sliding direction. Further, the sleeve 10 and the plunger 15 passing through the movable piece 14 are formed as an integral member. Inside the movable piece 14, an internal thread 16 that can be engaged in the sleeve 10 and the movable piece 14 is cut, and a portion of the sleeve 10 that is contained in the movable piece 14 can be engaged in the movable piece 14. The external screw 16 is cut.

  Further, the plunger 15 is configured as a separate member from the plunger 20 in the chemical liquid cartridge 7, and is separated from the plunger 20. At the tip of the plunger 20, a plunger 21 is provided that is formed of a rubber material and is fixed to the plunger 20 so that the injection solution 2 can be pushed out in the drug solution cartridge 7. Further, the sliding amount of the movable piece 14 is configured to be always constant by regulation by the spring 17.

  Now, when the dose adjustment knob 9 is rotated in the direction in which the dose increases, the plunger 15 comes out from the movable piece 14 in the direction of the injection needle. Then, the separation distance between the plunger 15 and the plunger 20 which is separate from the plunger 15 is shortened. Further, the plunger 20 does not move unless it is pushed from the plunger 15. Since the slide amount of the movable piece 14 when the injection button 3 is pressed is always constant, the distance at which the plunger 20 of the plunger 15 is pressed becomes the injection solution amount at the time of administration. In other words, the stroke of the injection button at the time of administration is always the same regardless of the amount of injection solution to be administered, and the dose is determined by the slide amount (broad) of the plunger 15 from the movable piece 14.

  Next, a mechanism in which the injection solution 2 comes out of the injection needle 4 when the injection button 3 is pressed will be described. In FIG. 2, when the injection button 3 is pushed in the direction of the arrow, the rack 11 constituted by this and the integral member slides in the direction of the arrow. On the end surface of the rack 11 opposite to the injection button 3, a spring (injection button return portion) 17 is compressed when the injection button 3 is pressed, and is restored by elasticity when the injection button 3 is stopped. Is provided. Therefore, when the injection button 3 is stopped, the injection button 3 returns to the original position by the restoring force of the spring 17.

  A tooth mold 11 a is provided on a side surface of the rack 11, and a gear (first gear) 12 is engaged with the tooth mold 11 a and a gear 13 (second gear) is engaged with the gear 12. Is provided. Further, a tooth mold is provided on the side surface of the movable piece 14 so as to mesh with the gear 13. These rack 11, gear 12, and gear 13 constitute a pressing force transmission unit that transmits the pressing force of the injection button 3 to the plunger 15 at an angle different from the direction in which the injection needle 4 extends.

  When the injection button 3 is pressed, the rack 11 slides, the gear 12 rotates counterclockwise, and the gear 13 rotates clockwise. Then, the movable piece 14 is integrated with the plunger 15 and slides in the direction of pushing the plunger 20 and the plunger 21. Then, the plunger 21 slides in a direction to compress the injection solution 2 in the drug solution cartridge 7, and the compressed injection solution 2 is pushed out from the tip of the injection needle 4.

  In the medical administration device shown in the first embodiment, as described above, the force when the injection button 3 is pushed with the index finger 18 in the direction of the arrow in FIG. It has a structure that is not transmitted so as to penetrate deeper into the skin.

  For this reason, according to the first embodiment, at the time of administration of the drug solution, the force of pushing the injection button is prevented from being transmitted to penetrate the skin deeper than when the initial injection needle is inserted into the skin, and is in a stable state. It becomes possible to administer a drug solution.

(Embodiment 2)
In the second embodiment, when the drug solution is administered, the skin contact portion that contacts the skin of the user can be fixed by sliding in the longitudinal direction of the injection needle, so that the needle tip is independent of the type and size of the injection needle. It is possible to adjust so that the amount pierced into the skin is constant, and to reduce the pain when administering the drug solution.

  Hereinafter, Embodiment 2 of the present invention will be described with reference to FIGS. 4 is a perspective view showing the appearance of the medical administration device according to the second embodiment of the present invention, FIG. 5 is a partial cross-sectional view of the medical administration device according to the second embodiment of the present invention, and FIG. 6 is the second embodiment of the present invention. 7 is a detailed perspective view of the medical administration device according to the present invention, and FIG. 7 is a detailed view of the relationship between the injection needle and the skin contact portion of the medical administration device of the present invention.

  In FIG. 4, 31 is a medical administration device body, 32 is an injection solution, 33 is an injection button, 34 is an injection needle, 36 is a skin contact portion to be applied to the skin, 37 is a skin contact portion adjustment button, and 40 is a skin contact width adjustment. A piece (skin application area variable part, skin application width adjustment part), 41 is a skin application width adjustment button. The skin contact portion adjustment button 37 is integrated with the skin contact portion 36 and is configured to be slidable in any direction of an arrow 43.

  In FIG. 5, the skin contact portion 36 is integrated with a skin contact portion adjustment button (skin contact position variable portion) 37, so that the skin contact portion 36 and the skin contact portion adjustment button 37 can be stopped and fixed at desired positions. Further, a dowel (convex shape) 38 is provided on the skin contact portion adjustment button 37, and a concave shape 39 is provided on the side surface of the medical administration device main body 31 as a fitting fixing portion.

  Therefore, as shown in FIG. 4, the skin contact portion 36 and the skin contact portion adjustment button 37 can be changed and fixed to a desired concave position in the direction of the arrow 43 with respect to the injection needle 34, as shown in FIG. The injection needle 34 and the skin contact portion 36 can have a dimensional relationship 42 at a desired stage.

  Further, when the same type of injection needle 34 or the like is used every time during administration, the dimensional relationship 42 of the skin contact portion 36 with respect to the injection needle 34 can be changed to its optimal position and then fixed. Administration in the same state is possible, and the length of the injection needle 34 that enters the skin of the user (patient) is constant, so that reliable administration is possible.

  In FIG. 6, the skin pad width adjusting piece 40 is integrated with the skin pad width adjusting button 41, and is slid in the arrow direction 44, that is, in the downward direction in the figure, so that the skin pad 36 is made wider. At this time, when the user places the skin contact portion 36 on the skin, administration in a stable state with a better hold feeling is possible.

  For this reason, according to the second embodiment, the length that the injection needle enters the skin is made constant regardless of the type and size of the injection needle, the position of the skin contact portion can be varied, and the skin contact area is further increased. Since it can be increased, the amount that enters the skin of the injection needle does not vary even if the length varies depending on the type of injection needle, the administration state can be stabilized, and highly reliable medical administration An instrument can be provided.

  Note that the position of the skin contact portion 36 may be adjusted steplessly by enabling the skin contact portion 36 to be fixed at an arbitrary position instead of the dowel and the concave shape.

  Further, by adopting the same internal structure as in the first embodiment, the pressing direction of the injection button is made different from the direction in which the injection needle 204 is inserted into the skin, so that pain during injection is reduced. It may be.

(Embodiment 3)
This Embodiment 3 prevents the injection button or the administration button from being pressed when the injection needle is not attached to the administration device body, and the injection needle is also provided in the case of mixed drug administration. When it is not attached to the device, the drug cannot be mixed and cannot be stored in the administration device body to prevent chemical leakage, reverse flow, and cracking or rupture of the glass tube containing the chemical. It is a thing.

  Hereinafter, a third embodiment of the present invention will be described with reference to FIGS. FIG. 8 is a perspective view showing the internal structure of the medical administration device according to Embodiment 3 of the present invention with a part cut away. FIG. 9 is a perspective view for easily explaining the operation principle when the injection needle of the medical administration device according to the third embodiment is attached, and FIG. 10 is also the operation when the injection needle is not attached. It is a perspective view for demonstrating an easy-to-understand principle. FIG. 11 is a cross-sectional view of the medical administration device according to the third embodiment, partly cut away to illustrate the operation of attaching the drug cartridge of the medical administration device. FIG. 12 is a positional relationship diagram between the detection mechanism and the injection button when the injection needle is not attached to the medical administration device according to the third embodiment. FIG. 13 is a positional relationship diagram between the detection mechanism and the injection button when the injection needle is attached to the medical administration device according to the third embodiment. FIG. 14 is a positional relationship diagram between the detection mechanism and the fixing / releasing mechanism when the injection needle is not attached to the medical administration device according to the third embodiment. FIG. 15 shows a positional relationship diagram between the detection mechanism and the fixing / releasing mechanism when the injection needle is attached to the medical administration device according to the third embodiment of the present invention.

  In FIG. 8, the mechanism of injection will be briefly described. A chemical cartridge 52 is set in the main body of the administration device 66, and a disposable injection needle 51 is attached to the chemical cartridge 52. When administering to the human body, the dose setting knob 56 is adjusted to the desired dose. The plunger 55 is fixed with respect to the dose setting knob 56 in the rotational direction, but is not fixed with respect to the sliding direction. Therefore, when the dose setting knob 56 is rotated, the plunger 55 is parallel to the injection needle. It can be expanded and contracted in the direction. Now, when the dose is set to increase, the plunger 55 moves toward the tip in the same direction as the injection needle.

  Next, when the administration button 54 is pressed, the injection button integrated drive lever 57 operates in the same direction as the direction in which the injection button is pressed. A part of the side surface of the injection button integrated drive lever (injection button, rack) 57 is a gear (rack) that meshes with the gear (first gear) 60. Further, the gear (second gear) 59 meshes with the gear 60 and also meshes with the gear (rack) at the tip of the plunger 55. At the tip of the plunger 55 is a chemical solution pushing plunger 53 which is in contact with the chemical solution in the chemical solution cartridge 52. The injection button integrated drive lever 57, the gear 60, and the gear 59 constitute a drive unit for the plunger 55.

  Now, when the injection button 54 is pushed in the direction of the arrow in FIG. 8, the injection button integrated drive lever 57 rotates the gear 60 in the clockwise direction. The rotation of the gear 60 moves the plunger 55 in the longitudinal direction of the injection needle 51, that is, toward the left side in FIG. 8, while rotating the gear 59 counterclockwise. Then, the drug solution pushing plunger 53 provided at the tip of the plunger 55 can push and administer the drug solution in the drug solution cartridge 52 from the injection needle 51.

  Next, in FIG. 9, the distal end portion (L-shaped distal end portion) 58 a of the eject lever 58 is sandwiched between the resin portion 82 of the injection needle 51 and the drug solution cartridge 52. At this time, when the injection button 54 is pushed in the direction of the arrow, the injection button-integrated drive lever 57 is in a state where it can freely move in the meshing portion 61 of the eject lever 58. The eject lever 58 and the injection button integrated drive lever 57 constitute an administration operation inhibiting unit that inhibits the administration operation by pressing the injection button. The tip (detection member) 58a of the eject lever 58 is integral with the main body of the eject lever 58. When the injection needle 51 formed integrally with the resin portion 82 is attached, the spring 63 is always used. Stress is applied in the direction of the injection needle 51. The spring (spring member) 63 and the eject lever 58 constitute an injection needle mounting detector.

  Next, as shown in FIG. 10, when the injection needle 51 is removed from the drug solution cartridge 52, the portion of the eject lever 58 moves toward the injection needle 51, that is, the left side in FIG. 9 due to the stress of the spring 63. Then, the meshing portion 61 of the eject lever 58 is disengaged from the meshing portion 62 with the injection button integrated drive lever 57, and when the injection button 54 is pushed in the direction of the arrow, the meshing portion 62 is immediately released from the eject lever 58. It hits the side and cannot move freely. That is, when the injection needle 51 is removed, the injection button 54 cannot be pushed completely. As described above, in the third embodiment, it is detected whether the injection needle is attached or not at the tip 58a of the eject lever 58.

  Next, a method of setting the drug solution cartridge 52 in the administration device body 66 and storing it in the administration device body 66 will be described with reference to FIG.

  In FIG. 11, the chemical cartridge holding lid (openable door) 67 is raised upward to the state of the broken line in the figure, and the chemical cartridge 52 is inserted in the direction of the arrow in the figure. After the insertion, the chemical cartridge holding lid 67 is lowered and closed. Next, the injection needle 51 is screwed into the distal end threaded portion of the drug solution cartridge 52 with the injection needle cap 65 covered.

  Next, the projection 67 a is held and slid in the direction of the dose setting knob 56. Then, first, the rear rubber part 70 in the drug solution cartridge 52 hits the dissolving piece 72 in the administration device main body 66. Further, when the slide is carried out, the dissolving piece 72 pushes the rear rubber part 70, so that the chemical liquid 71 filled in the latter half chamber contains the separation rubber 69 and the first half chamber containing the medicine 68. Move in the direction.

  When the separation rubber 69 moves to the injection groove 77, the chemical liquid 71 flows through the injection groove (large diameter portion) 77 and flows into the medicine 68. Further, when the protrusion 67a is slid in the direction of the dose setting knob 56, all of the drug solution 71 flows into the chamber of the drug 68 from the injection groove 77, and as a result, the drug 68 and the drug solution 71 are mixed. Then, when the protrusion 67a is further slid in the direction of the dose setting knob 56, when the rear rubber portion 70 hits the separation rubber 69, it cannot slide and is fixed. This fixed structure will be described in the description of FIG. In this state, the medicinal solution cartridge 52 is stored in the administration device main body 66.

  Next, FIGS. 12 and 13 show in detail the relationship between the detection mechanism and the injection button integrated lever 57 when the injection needle is attached and when the injection needle is not attached. FIG. 12 shows a state when the injection needle is not attached, and FIG. 13 shows a state when the injection needle is attached. The “injection needle” in the description of FIGS. 12 to 15 refers to the injection needle 51 with the cap 65 covered.

  In FIG. 12A, the chemical cartridge 52 remains in a state where it is located at the tip of the slide piece 75. An eject lever 58 is positioned on the slide piece 75, and is configured to be freely movable on the slide piece 75 in parallel with the injection needle mounting direction.

  FIG. 12B is a view of FIG. 12A as viewed from below, and the slide piece 75 is provided with a slit 78 and a slit 83 that are large enough to receive the eject knob 76. Also, the eject lever 58 is provided with a slit 73 at the same position as the slit 83.

  In addition, a slit 81 having the same width is provided in the overlapping portion of the center portion of the slide piece 75 and the eject lever 58. Further, in the slit 81, the slide piece 75 and the eject lever 58 are provided. A spring 63 is provided in parallel with the slide piece 75 so as to fit within the overlapped thickness dimension. Moreover, the spring 63 is locked between the protrusion 79 protruding from the slide piece 75 and the protrusion 80 protruding from the eject lever 58 inside the slit 81. At this time, the position of the meshing portion 61 of the eject lever 58 is in a positional relationship in which the injection button integrated drive lever 57 cannot freely move in the meshing portion 61. That is, the injection button cannot be pressed.

  Next, in FIG. 13, when the injection needle is attached to the drug solution cartridge 52, the tip 58 a of the eject lever 58 is pushed to the tip of the slide piece 75. Then, the spring 63 in the slit 81 maintains its state in a compressed form from the state of FIG. On the other hand, the portion of the engaging portion 61 of the eject lever 58 has a positional relationship in which the injection button integrated lever 57 can freely move. That is, the injection button can be pressed.

  Next, the principle when the injection needle is not attached to the chemical cartridge 52, the principle that the chemical cartridge 52 cannot be accommodated in the administration device main body 66 when it is attached, and the principle that can be done will be described with reference to FIGS.

  In FIG. 14, when the injection needle is not attached to the chemical cartridge 52, the distal end portion 58 a of the eject lever 58 protrudes further toward the injection needle than the distal end of the slide piece 75. At this time, the eject knob 76 urged upward by a spring (not shown) has two slits, a slit (opening) 73 on the eject lever 58 and a slit (opening) 83 on the slide piece 75. In the penetrated state, the slide piece 75 is locked so that it cannot move in the direction of the injection needle or in the opposite direction. The eject knob 76 is arranged in a vertical direction with respect to the slide piece 75 and the eject lever 58 and is always pushed upward by a spring with respect to FIGS. 14 and 15.

  Next, in FIG. 15, when the injection needle is attached to the drug solution cartridge 52, the distal end portion 58 a of the eject lever 58 is in the same position as the distal end of the slide piece 75. In the process of screwing (attaching) the injection needle into the drug solution cartridge 52, the inside of the slit 73 of the eject lever 58 pushes the inclined portion 76a of the eject knob 76 in the direction of the arrow, so that the eject knob 76 gradually moves downward. Will be pushed down. As the injection needle is further screwed, the slit 73 on the eject lever 58 moves in a direction to further push down the inclined portion 76a of the eject knob 76. When the injection needle is completely attached to the chemical cartridge 52, the slit 73 on the eject lever 58 passes through the tip of the eject knob 76, and the eject knob 76 is positioned in the slit 83 of the slide piece 75. The slide piece 75 is locked in the direction opposite to the arrow.

  From this state, in order to store the medicinal solution cartridge 52 in the administration instrument main body 66, the medicinal solution cartridge 52 arranged on the slide piece 75 is moved while sliding in the direction of the arrow together with the slide piece 75.

  Actually, as described with reference to FIG. 11, the liquid cartridge cartridge 67 is moved in a set form in the chemical cartridge holding lid 67, but only the principle will be described here.

  Now, when the chemical cartridge 52 on the slide piece 75 is moved together with the slide piece 75 in the direction of the arrow, that is, in the right direction in FIG. 14, the slit 83 hits the inclined portion 76 a of the eject knob 76. When the slider is further moved in the direction of the arrow from this point, the eject knob 76 is pushed downward by the slide piece 75. Further, when the slide piece 75 is moved in the direction of the arrow, the eject knob 76 is moved into the slit 78 of the slide piece 75. At the same time, the front end of the eject knob 76 is fitted to the slide piece 75 so that the front end of the eject knob 76 is locked at that position so that it cannot move in the direction opposite to the arrow.

  FIG. 13A shows this state, and in order to cancel this state, a slide knob integrated with the eject knob 76 is projected outside the administration instrument body 66 as a knob. Therefore, the release operation is made possible by forcibly pushing the slide knob lightly downward with a finger.

  In addition, this is because, for example, in the case of mixing two kinds of drug solutions in the administration device main body, or when dissolving and mixing the drug and the drug solution as described in FIG. Since it cannot be stored, it cannot be mixed.

  Thus, according to the third embodiment, when the injection needle is not attached to the administration device, the injection button or the administration button cannot be pushed, and the plunger for pushing out the drug solution does not operate. In addition, in the case of an administration device for mixed drug administration, since it is configured such that mixing is not possible when the injection needle is not attached to the administration device, if the injection needle is not attached to the administration device body, the injection button is erroneously set. Alternatively, even if an administration button is pressed, it cannot be pressed, and it is possible to prevent a chemical solution leak or a chemical solution glass tube from being broken due to an erroneous operation.

(Embodiment 4)
In the fourth embodiment, in a medical administration device to which an electronic device is added, a warning display for prompting attention to perform air bleeding when an injection is performed is performed.

  The fourth embodiment of the present invention will be described below with reference to FIGS. 16 is a perspective view showing an external appearance of the medical administration device according to Embodiment 4 of the present invention before the injection needle is attached, FIG. 17 is a partial sectional view of the medical administration device of Embodiment 4, and FIG. 2 is a block diagram centering on a microprocessor 25. FIG.

  In FIG. 16, 102 is a main body cap, 103 is a medical administration device main body, 104 is a display unit, 105 is a dose setting dial, 106 is an injection button, and 127 is a speaker.

  First, it is assumed that the medical administration device is used for the first time. 16 and 17, when the main body cap 102 is removed from the medical administration device main body 103, the switch (first switch) 110 provided on the medical administration device main body 103 is turned off. At this time, all function displays displayed on the display unit 104 are all lit, and only a calendar, time, and dose are displayed after a few seconds.

  In FIG. 17, the screwing portions 109a and 109b of the medical administration device main body 103 are engaged with screws. The screwed portions 109a and 109b are rotated in the direction in which the screws are loosened, and the two screwed bodies 103a and 103b are separated from the state of one medical administration device main body 103. After the separation, the chemical cartridge is set on the screw body 103a, and the screw bodies 103a and 103b are engaged again at the portions of the screw portions 109a and 109b. It is in the form of a medical administration device 103. Then, the cartridge detection switch (second switch) 111 provided inside the medical administration device 103 is turned on from off.

  When this state is reached, the characters “Bleeding air” appear on the display unit 104 and start blinking. In synchronism with the flashing display, a sound “please bleed air” flows from the speaker 127. The administor attaches the injection needle 101, presses the injection button 106 with the injection needle 101 facing upward, and with the injection button 106 facing down until the drug solution 126 comes out of the injection needle 101. Then, the switch 113 (corresponding to the switch 413 of FIG. 32 described in the prior art) is turned on once and turned off again. The state of the switch 113 is also used to determine that the air bleeding has been completed, and the microprocessor (air bleeding display signal generation unit) 125 determines that the air bleeding has been completed.

  It should be noted that the flashing and voice announcement of the “air bleeding” character described above continues until the microprocessor 125 determines that the air bleeding has been completed. Further, the judgment of the state of the switch 110 and the switch 111, the display command to the display unit 104, and the voice announcement command are performed by the microprocessor (air bleeding voice signal generation unit) 125 of FIG. That is, the microprocessor 125, the display unit 104, and the speaker 127 constitute an air bleeding notification unit. In FIG. 18, 123 is a calendar that generates date information, and 124 is a clock that generates time information.

  Next, a state in which the drug solution cartridge 107 is already set in the medical administration device 103, that is, the second and subsequent administrations will be described. When the main body cap 102 is removed from the medical administration device 103, the switch 110 provided on the medical administration device body 103 is turned off. At this time, all function displays displayed on the display unit 104 are all lit, and only a calendar, time, and dose are displayed after a few seconds.

  Next, the display unit 104 displays the “Bleeding” character in a blinking manner, and in synchronism with this, a sound “please bleed air” flows from the speaker 127. The administor attaches the injection needle 101 and pushes the injection button 106 until the drug solution 126 comes out of the injection needle 101 with the injection needle 101 facing upward and the injection button 106 facing downward. Then, as in the case of the first time use, the microprocessor 125 looks at the state of the switch 113, and when it is judged that the air bleeding has been completed, the “air bleeding” character disappears, and further, “please air bleeding”. The announcement will stop.

  It should be noted that means for detecting the completion of injection, means for detecting the amount of injected liquid administered, means for recording the amount of injected liquid injected, detecting completion of injection, and determining the amount of injected liquid injected The means for simultaneously recording and displaying the injection volume, date, and time detected simultaneously with the detection are as described in the prior art.

  In the above description, a sign or a figure may be used for the display for prompting air bleeding in addition to the characters. In addition, the user may be urged to perform an air bleeding operation by either one of display and sound.

  Thus, according to the fourth embodiment, when the main body cap attached so as to cover the attachment portion of the injection needle body of the medical administration device main body to which the injection needle is attached is removed, the letters “air bleeding” are provided. Is displayed on the display unit, so that the drug administration person can be made aware of the air bleeding operation before the administration, and the operation of “air bleeding” can be prompted.

(Embodiment 5)
The fifth embodiment corresponds to the invention of claim 1 to claim 6, and in the medical administration device to which an electronic device is added, the amount of the injection solution to be emptied at the time of air bleeding, This makes it possible to solve the problem of memorizing without distinguishing from the original injection.

  Hereinafter, a fifth embodiment of the present invention will be described with reference to FIGS. FIG. 19 is a block diagram centering on the microprocessor 125 of the medical administration device according to the fifth embodiment of the present invention. 20 is a perspective view showing the appearance of the medical administration device according to Embodiment 5 of the present invention, FIG. 21 is a partial cross-sectional view thereof, and FIG. 22 shows the medical administration device according to another embodiment. FIG. 23 is a partial sectional view of the medical administration device of FIG.

  In FIG. 20, 102 is a needlestick attachment, 103 is a medical administration device body, 104 is a display unit, 105 is a dose setting dial, and 106 is an injection button. The needle stick attachment 102 is configured to be slidable in the direction of the injection button 106 almost at the same time as the needle 101 is inserted into the skin.

  In FIG. 21, the needle stick attachment 102 is configured to be shorter than the needle in the length direction of the needle, and slides when the needle is inserted into the skin. Switches) 109a and 109b are turned on. When the switches 109a and 109b are turned on, the microprocessor 125 determines that the injection needle is stuck in the skin.

  In addition, the administration completion detection means uses a microprocessor 125 when a switch (not shown) (corresponding to the switch 113 in FIG. 18 and the switch 413 in FIG. 32 described in the prior art) is turned on once and turned off again. It is done by letting you judge. That is, while the switches 109a and 109b are on, and only when the administration of the switch (not shown) is completed, the microprocessor 125 records the injection volume, date, and time in the memory 122. Let me judge.

  On the other hand, when the air is vented, the needle stick attachment 102 is not activated and the switches 109a and 109b are off because the injection needle 101 is directed upward and the injection button 106 is positioned downward and in the air. It remains as it is. At this time, even if the injection button 106 is pressed and the switch 113 is turned on once and turned off again to complete the administration, the switches 109a and 109b are turned off. Is determined not to be recorded in the memory 122. By doing so, only when the injection needle 101 actually pierces the skin and the administration is completed, the injection volume, date, and time are recorded in the memory 122 as a history, and the history of bleeding is not recorded. An instrument is possible. Note that either one of the switches 109a and 109b can be detected depending on the shape of the needle stick attachment.

FIG. 22 shows that these switches 109a and 109b can be integrated into one. In FIG. 22, 140 is a needlestick detection switch (third switch), 103 is a medical administration instrument body, 104 is a display unit, Reference numeral 105 denotes a dose setting dial, and 106 denotes an injection button. Needlestick detection switch 140, the administration instrument body is al provided on the skin contact surface of the skin contacting portion 141 provided so as to stably without wobbling at the time of administration.

  In FIG. 23, the needle stick detection switch 140 is turned on almost simultaneously with the time when the injection needle 101 is stuck into the skin. When the needle stick detection switch 140 is turned on, the microprocessor 125 determines that the injection needle is stuck in the skin.

  Further, the administration completion detecting means is in a state in which the switch (not shown in FIG. 19 and corresponding to the switch 113 in FIG. 18) is turned on once and turned off again, similarly to the switch 413 in FIG. 27 described in the prior art. This is done by causing the microprocessor 125 to determine when the The means for detecting the injection volume is the same as described in the prior art. That is, the injection liquid amount, date, and time are stored in the memory (injection liquid volume recording unit) 122 only when the needle stick detection switch 140 is turned on and the administration of the switch (not shown) is completed. The microprocessor (control unit) 125 is caused to make a determination so that recording is performed.

  On the other hand, when the air is released, the needle stick detection switch 140 is in an off state because the injection needle 101 is placed on the upper side and the injection button 106 is located on the lower side and in the air. At this time, even when the injection button 106 is pressed and the switch 113 is turned on once and turned off again to complete administration, the needle stick detection switch 140 is turned off. Is not recorded in the memory 122.

  By doing so, only when the injection needle pierces the skin and the administration is completed, the injection volume, date, and time are recorded in the memory 122 as a history, and the medical administration device that does not record the history at the time of bleeding is used. It becomes possible. The closer the needle stick detection switch 140 is to the injection needle 101, the more effective the detection when the injection needle 101 is applied to the skin.

  The present invention is applicable to a medical administration device used when administering an injection such as an injection solution, and does not distinguish the amount of the injection solution that is blown when the air is released from the original injection. Therefore, it is suitable for safe and reliable administration.

It is a perspective view of the medical administration device in Embodiment 1 of the present invention. It is a perspective view which fractures | ruptures and shows a part of the medical administration device. It is a perspective view showing the state where the medical administration device was actually grasped by the hand. It is a perspective view of the medical administration instrument in Embodiment 2 of this invention. It is a partial cross section figure of the medical administration device. It is a detailed perspective view of the medical administration device. It is a dimensional relationship detail drawing of the injection needle of the medical administration device of this invention, and a skin contact part. It is a perspective view which notches some medical administration devices in Embodiment 3 of the present invention, and explains an internal structure. It is a perspective view which shows the positional relationship of the administration button (or injection button) and the eject lever for demonstrating the operation | movement principle of the medical administration instrument. It is a perspective view which shows the positional relationship of the administration button (or injection button) and the eject lever for demonstrating the operation | movement principle of the medical administration instrument. It is a partial cross section figure which shows the chemical | medical solution cartridge attachment state of the medical administration instrument. It is a positional relationship figure of a detection mechanism and an injection button when not attaching an injection needle in the medical administration instrument. It is a positional relationship figure of a detection mechanism and an injection button when not attaching an injection needle in the medical administration instrument. It is a positional relationship figure of the detection mechanism and injection button when the injection needle is attached in the medical administration instrument. It is a positional relationship figure of the detection mechanism and injection button when the injection needle is attached in the medical administration instrument. FIG. 3 is a positional relationship diagram between a detection mechanism and a fixing / releasing mechanism when the injection needle is not attached in the medical administration device. FIG. 3 is a positional relationship diagram between a detection mechanism and a fixing / releasing mechanism when an injection needle is attached in the medical administration device. It is a perspective view of the medical administration device before the injection needle attachment in Embodiment 4 of this invention. It is a partial cross section figure of the medical administration device. It is a block diagram in the medical administration device. It is a block diagram for demonstrating the medical administration device. It is a perspective view of the medical administration instrument in Embodiment 5 of this invention. It is a partial cross section figure of the medical administration device. It is a perspective view of the medical administration instrument in the modification of Embodiment 5 of this invention. It is a partial cross section figure of the medical administration device. It is a perspective view which shows the conventional medical administration instrument. It is a perspective view which shows the other conventional medical administration instrument. It is a front view in the conventional medical administration device. It is a top view which shows the partial cross section in the conventional medical administration instrument. It is a block diagram for demonstrating the conventional medical administration device. It is sectional drawing which shows the means to detect the completion of administration of the conventional medical administration instrument. It is sectional drawing which shows the means to detect the amount of injection solutions of the conventional medical administration instrument. It is a side view which shows the means to detect the amount of injection solutions of the conventional medical administration instrument. It is a block diagram for demonstrating the conventional medical administration device. It is a perspective view which shows the operation state of the conventional medical administration instrument. It is a perspective view which shows the other operation state of the conventional medical administration instrument.

Claims (6)

An administration device main body having a mounting portion for mounting a liquid medicine cartridge storing a liquid medicine to be administered to a patient;
An injection button that is provided on the outer peripheral surface of the administration device main body, and activates a drug solution administration operation when administering the drug solution in the drug solution cartridge;
A mounting portion that is disposed on the front end side of the chemical liquid cartridge and detachably mounts an injection needle for administering the chemical liquid;
A needle stick detection unit for detecting that the injection needle is stuck in the skin ;
An injection completion detection unit for detecting that the injection is completed;
An injection volume detection unit for detecting the amount of injected injection;
An injection volume recording unit for recording the administered injection volume;
A controller that records the injection volume detected by the injection volume detector when the injection completion detector detects the completion of injection in the injection volume recording unit;
By pressing the injection button, the air venting operation is also performed,
While the control unit detects that the injection needle has pierced the skin in the needle puncture detection unit, the control unit determines the amount of injected liquid to be administered only when the completion of injection is detected in the injection completion detection unit. Record in the injection volume recording part,
When the needle stick detection unit does not detect that the injection needle is stuck in the skin , the administered injection volume is not recorded in the injection volume recording unit,
A medical administration device characterized by that. The medical administration device according to claim 1,
A calendar section that generates current date information;
A clock unit that generates current time information,
The control unit detects the completion of the injection and simultaneously records the date and time when the injection is completed,
A medical administration device characterized by that. The medical administration device according to claim 1,
Having a display unit for displaying an injection liquid amount when setting an injection liquid amount to be administered and an injection liquid amount recorded when the injection is completed;
A medical administration device characterized by that. The medical administration device according to claim 3,
The display unit
In addition to the injection volume recorded when the injection is completed, the date and time are displayed.
A medical administration device characterized by that. The medical administration device according to claim 1,
The needle stick detection unit
A ring-shaped or arc-shaped contact detection member that slides at the same time as the needle is stuck around the needle,
A switch operated by sliding the contact detection member,
A medical administration device characterized by that. The medical administration device according to claim 1,
The needle stick detection unit
A skin contact part that comes into contact with the patient's skin during administration of the drug solution;
A switch that is provided on the skin contact surface of the skin contact portion and that operates simultaneously with the injection needle sticking into the skin;
A medical administration device characterized by that.

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