阅读说明：本技术 传感器插入装置 (Sensor insertion device ) 是由 清水隆次 西尾章 高下雅博 于 2019-01-28 设计创作，主要内容包括：传感器插入装置(51)具备下壳体(57)、上壳体(58)、传感器基座(54)、针保持件(67)、使针保持件(67)下降的针保持件按下部(80)、以及使针保持件(67)上升的针保持件上升机构(74)。针保持件上升机构(74)具有使针保持件(67)上升的小齿轮(71)、与小齿轮(71)卡合的第一齿条(72)、以及配置于小齿轮(71)的上方的第二齿条(73)。随着上壳体(58)的下降,当第二齿条(73)到达小齿轮(71)时,小齿轮(71)通过与第二齿条(73)的卡合而使针保持件(67)上升。(The sensor insertion device (51) is provided with a lower housing (57), an upper housing (58), a sensor base (54), a needle holder (67), a needle holder pressing part (80) for lowering the needle holder (67), and a needle holder lifting mechanism (74) for lifting the needle holder (67). The needle holder lifting mechanism (74) is provided with a pinion (71) for lifting the needle holder (67), a first rack (72) engaged with the pinion (71), and a second rack (73) arranged above the pinion (71). When the second rack (73) reaches the pinion (71) as the upper housing (58) descends, the pinion (71) causes the needle holder (67) to ascend by engaging with the second rack (73).)

1. A sensor insertion device is provided with:

a lower case having an upper surface opening;

an upper case that covers the outer periphery of the lower case from above, is disposed to be slidable relative to the lower case, and is operated downward by a user when performing a needling operation;

a sensor base which is disposed in the lower case and holds a sensor for acquiring biological information;

a needle holder which is disposed above the sensor base so as to be movable up and down, and which holds a guide needle for performing acupuncture on a human body to guide the sensor into the human body; and

a needle holder lifting mechanism that lifts the needle holder holding the guide needle that has been inserted into the human body,

the needle holder lifting mechanism includes:

a pinion that raises the needle holder;

a first rack provided to the needle holder and engaged with the pinion; and

a second rack provided in the upper case and engaged with the pinion gear,

the pinion gear is engaged with the second rack to raise the needle holder as the upper housing is lowered.

2. The sensor insertion device of claim 1,

when the upper case is lowered to the vicinity of a needle punching position where the guide needle punches the human body, the pinion is engaged with a lower end portion of the second rack, and the second rack rotates the pinion to raise the needle holder together with the first rack by further lowering the upper case.

3. The sensor insertion device according to claim 1 or 2,

in a state before the needling operation, the second rack is not engaged with the pinion.

4. The sensor insertion device of any one of claims 1 to 3,

the second rack has a fixed end fixed to the upper case at an upper end side and a flexible free end provided at a lower end side.

5. The sensor insertion device of any one of claims 1 to 4,

the lower end of the second rack is inclined in a direction away from the pinion.

6. The sensor insertion device of any one of claims 1 to 5,

in the second rack, the height of the engaging teeth formed on the lower end side is lower than the height of the engaging teeth formed on the upper side of the lower end side.

7. The sensor insertion device of any one of claims 1 to 6,

the first rack is disposed so as to face upward from an upper surface of the needle holder.

8. The sensor insertion device of any one of claims 1 to 7,

the first rack engages with the pinion before and after the needling operation.

9. The sensor insertion device of any one of claims 1 to 8,

the needle holder has needle holder engaging portions at least at three locations,

the upper case has a needle holder pressing portion provided at a portion of an inner surface thereof facing the needle holder engaging portion.

10. The sensor insertion device of claim 9,

the first rack is provided between two adjacent needle holder engaging portions.

11. The sensor insertion device according to claim 9 or 10,

the guide needle is fixed between the two adjacent needle holder engaging portions on the lower surface of the needle holder.

12. The sensor insertion device of any one of claims 9 to 11,

the needle holder engaging portions are provided at three locations at equal intervals.

13. The sensor insertion device of any one of claims 1 to 12,

the lower case has a shaft support portion on an inner surface thereof that shaft-supports a shaft of the pinion gear.

14. The sensor insertion device of any one of claims 1 to 13,

the lower housing has a substantially cylindrical shape,

the needle holder lifting mechanism is disposed near a central portion of the lower housing.

15. The sensor insertion device of any one of claims 1 to 14,

the upper case has an abutting portion on an upper surface thereof against which a palm of a user abuts.

Technical Field

The present invention relates to a sensor insertion device for inserting a sensor for measuring biological information into a patient's body for continuous blood glucose measurement, for example.

Background

The conventional sensor insertion device has the following structure.

That is, the conventional sensor insertion device includes: the probe includes a lower case having an upper surface opening, an upper case covering the outer periphery of the lower case from above, a sensor base disposed in the lower case and holding a sensor, a needle holder disposed above the sensor base so as to be movable up and down and holding a guide needle of the sensor, and a needle holder lifting mechanism for lifting the needle holder.

The needle holder raising mechanism includes a spring disposed in the upper case and compressed when the upper case is pressed downward. Then, the spring releases the stored energy of the spring after lowering the needle holder, and raises the needle holder (for example, patent document 1).

Prior art documents

Patent document

Patent document 1: japanese laid-open patent publication No. 2015-509011

Disclosure of Invention

The problem with the above-described conventional example is that the patient feels a sense of discomfort when the guide needle is pulled out from the upper arm of the patient.

That is, in the conventional sensor insertion device, the guide needle is pulled out from the upper arm of the patient by releasing the stored energy of the spring, and the pulled-out guide needle abuts against the stopper and stops. At this time, the large collision sound generated by the collision of the guide needle with the stopper increases the discomfort (terrorism) of the patient.

It is therefore an object of the present invention to reduce discomfort to the patient when using a sensor insertion device.

In order to achieve the object, a sensor insertion device according to the present invention includes: a lower case having an upper surface opening; an upper case which covers the outer periphery of the lower case from above, is arranged to be slidable relative to the lower case, and is operated downward by a user when performing a needling operation; a sensor base which is disposed in the lower case and holds a sensor for acquiring biological information; a needle holder which is disposed above the sensor base so as to be movable up and down, and which holds a guide needle that is pricked into a human body to guide the sensor into the human body; and a needle holder lifting mechanism for lifting the needle holder holding the guide needle for performing the acupuncture on the human body. The needle holder lifting mechanism includes: a pinion that raises the needle holder; a first rack provided to the needle holder and engaged with the pinion; and a second rack provided in the upper case and engaged with the pinion. As the upper housing descends, the pinion gear engages with the second rack gear to raise the needle holder.

The present invention achieves the desired object by this structure.

Effects of the invention

As described above, in the present invention, after the needle is pierced by the guide needle of the needle holder, the needle holder is raised by the pinion provided in the needle holder raising mechanism, so that the impact sound caused by the spring is not generated, and the patient's discomfort (terrorism) can be reduced.

Drawings

Fig. 1 is a perspective view showing a use state of a sensor insertion device according to embodiment 1 of the present invention.

Fig. 2 is a front view showing a mounted state of the sensor base and the biological information measuring instrument of fig. 1.

Fig. 3 is a perspective view of the sensor insertion device of fig. 1.

Fig. 4 is an exploded perspective view of the sensor insertion device of fig. 1.

Fig. 5 is an exploded perspective view of the sensor insertion device of fig. 1.

Fig. 6 is an exploded perspective view of a lower housing of the sensor insertion device of fig. 1.

Fig. 7 is an exploded sectional view of the sensor insertion device of fig. 1.

Fig. 8 is a partially cut-away perspective view of a lower housing of the sensor insertion device of fig. 1.

Fig. 9 is an exploded perspective view of an upper housing of the sensor insertion device of fig. 1.

Fig. 10 is a cross-sectional view of the sensor insertion device of fig. 1.

Fig. 11 is a cross-sectional view of the sensor insertion device of fig. 1.

Fig. 12 is a partially enlarged sectional view of fig. 11.

Fig. 13 is a partially enlarged cut-away perspective view of an upper housing of the sensor insertion device of fig. 1.

Fig. 14 is a sectional view showing an operation state of the sensor insertion device of fig. 1.

Fig. 15 is a partially enlarged sectional view of fig. 14.

Fig. 16 is a sectional view showing an operation state of the sensor insertion device of fig. 1.

Fig. 17 is a partially enlarged sectional view of fig. 16.

Fig. 18 is a sectional view showing an operation state of the sensor insertion device of fig. 1.

Fig. 19 is a sectional view showing an operation state of the sensor insertion device of fig. 1.

Fig. 20 is a sectional view showing an operation state of the sensor insertion device of fig. 1.

Fig. 21 is a partially enlarged perspective view of fig. 20.

Fig. 22 is a perspective view showing a use state of a sensor insertion device according to embodiment 2 of the present invention.

Fig. 23 is a front view showing a mounted state of the sensor base and the biological information measuring device of fig. 22.

Fig. 24 is a perspective view of the sensor insertion device of fig. 22.

Fig. 25 is an exploded perspective view of the sensor insertion device of fig. 22.

Fig. 26 is a partially cut-away perspective view of the sensor insertion device of fig. 22.

Fig. 27 is a partially cut-away perspective view of the sensor insertion device of fig. 22.

Fig. 28 is an enlarged perspective view of a portion a of the sensor insertion device of fig. 26.

Fig. 29 is an enlarged perspective view of a portion B of the sensor insertion device of fig. 26.

Fig. 30 is an enlarged perspective view of a portion C of the sensor insertion device of fig. 26.

Fig. 31 is a sectional view showing an operation state of the sensor insertion device of fig. 22.

Fig. 32 is a sectional view showing an operation state of the sensor insertion device of fig. 22.

Fig. 33 is a sectional view showing an operation state of the sensor insertion device of fig. 22.

Fig. 34 is a sectional view showing an operation state of the sensor insertion device of fig. 22.

Fig. 35 is a partially cut-away perspective view showing a partially modified example of the sensor insertion device of fig. 26.

Fig. 36 is an enlarged perspective view of a portion D of the sensor insertion device of fig. 35.

Detailed Description

Hereinafter, one embodiment of the present invention will be described in detail together with the accompanying drawings.

(embodiment mode 1)

In embodiment 1, "up" and "down" indicate "up" and "down" in a use state of the sensor insertion device 1 shown in fig. 11 and the like (a state when the sensor is attached to the human body 2). The vertical direction refers to a puncture direction (a needle puncture direction, a needle withdrawal direction) of the guide needle 20 in the sensor insertion device 1.

Fig. 1 is a diagram showing a use state of the sensor insertion device 1. In fig. 1, a sensor unit 3 is attached to a part of a human body 2 together with a sensor base 4 by a sensor insertion device 1. Then, a measuring instrument (an example of a biological information measuring instrument) 5 is attached to the upper surface of the sensor base 4.

Fig. 2 shows a state in which the sensor base 4 and the measuring instrument 5 are attached to the human body 2. In fig. 2, the sensor 6 of the sensor unit 3 is left in the human body 2. Thus, the biological information of the human body 2 is detected by the sensor unit 3 and measured by the measuring instrument 5. The measurement result is transmitted from the measurement device 5 to, for example, a mobile phone (not shown).

In the present embodiment, the blood glucose level is measured as biological information, and for example, the blood glucose level of a patient is measured every 5 minutes for 1 to 2 consecutive weeks, so-called continuous blood glucose measurement is performed. This makes it possible to grasp the tendency of the patient to have a blood glucose level for a certain period of time and the blood glucose level during sleep.

As shown in fig. 3 to 10, the sensor insertion device 1 of the present embodiment includes a lower housing 7, an upper housing 8, a sensor base 4, a needle holder 26, and a needle holder lifting mechanism 30A.

The lower case 7 and the upper case 8 have a rectangular parallelepiped shape which is horizontally long in a plan view.

The lower case 7 has an upper surface opening 9 formed on the upper surface side as shown in fig. 4, and a bottom surface discharge port 10 formed on the bottom surface side for discharging the sensor unit 3 and the sensor base 4 downward as shown in fig. 7 and 8.

The upper case 8 has a lower surface opening 11 as shown in fig. 5, and covers the outer periphery of the lower case 7 from above as shown in fig. 3. Specifically, the upper case 8 and the lower case 7 each have a horizontally long rectangular parallelepiped shape in plan view, and they are stacked vertically so that the lower case 7 is disposed inside.

As shown in fig. 3, the two long side surfaces 12 of the upper case 8 disposed to face each other are provided with a grip portion 13 recessed (recessed) in a stepped manner from the outer surface side to the inner surface side from the upper side to the lower side in the center portion in the longitudinal direction. As shown in fig. 4 to 6, a slide guide portion 14 for sliding an inner protrusion protruding in a step shape from an outer surface side to an inner surface side of the grip portion 13 is provided at a portion corresponding to the grip portion 13 of the lower case 7 in accordance with the grip portion 13.

The slide guide portions 14 are provided on two long side surfaces 15 of the lower case 7, which are disposed to face each other, and are formed to protrude in a stepped manner from the inner surface from the upper side to the lower side in the center portion in the longitudinal direction. The slide guide portion 14 slides in the vertical direction (in a use state) on the front surface thereof in a state where the back surface of the grip portion 13 of the upper case 8 is in contact therewith.

By providing the grip portion 13 recessed toward the inner surface side on the long side surface 12 of the upper case 8 in this manner, the grip portion 13 does not protrude from the outer surface of the upper case 8 and has a small shape. Therefore, as shown in fig. 1, the user can easily hold the upper case 8 with the right hand. Further, since the grip 13 is provided at the center of the long side 12 of the upper case 8, it is stable, and thus the use state described later is extremely stable.

The user of the sensor insertion device 1 may be the patient himself or a third person such as a nurse or a care-giver.

The detailed shape and structure of each part will be described.

As shown in fig. 6 to 8, a tubular bacteria-proof wall 17 is provided in the lower case 7. The bacteria-proof wall 17 has an upper opening 16 and a bottom surface discharge port 10, and is provided so as to protrude from the periphery of the bottom surface discharge port 10 toward the inside of the lower case 7 so as to surround the bottom surface discharge port 10.

As described above, the sensor base 4 is disposed in the bottom surface discharge port 10 portion inside the bacteria-proof wall 17. The bacteria-proof wall 17 has a needle unit 19 held by a sensor holder 18 above the sensor base 4 inside the bacteria-proof wall. More specifically, as shown in fig. 8, the sensor holder 18 holds the needle unit 19 on the upper surface side and holds the sensor unit 3 on the lower surface side.

In this state, the sensor 6 of the sensor unit 3 is held in the guide needle 20 of the needle unit 19 (see fig. 6). When the introducer needle 20 is lowered by the needling operation, the sensor 6 is inserted into the human body 2 together with the introducer needle 20, and then only the introducer needle 20 is pulled upward. Thereby, only the sensor 6 (see fig. 2) is left in the human body 2.

The sensor base 4 is formed with a through hole 21 through which the guide pin 20 moves up and down in the inserted state.

As one of the main features of the present embodiment, as shown in fig. 8, the sensor unit 3, the sensor holder 18, the sensor base 4, the needle unit 19, and the guide needle 20 are accommodated in the bacteria-proof wall 17. In this state, as shown in fig. 7, a fungi-proofing sheet (first fungi-proofing sheet) 22 sealed so as to cover the upper opening 16 is attached to the upper opening 16 of the fungi-proofing wall 17.

As shown in fig. 7, a bottom surface 23 of the lower case 7 is attached with a bottom surface discharge port 10 sealed with a bottom surface sterilization sheet (second sterilization sheet) 24 (see fig. 5) so as to cover the bottom surface discharge port 10. The antibacterial sheet 24 has a larger area than the opening of the bottom discharge port 10 and is bonded to the bottom 23. In this way, the antimicrobial sheet 24 constitutes a part of the bottom surface 23 of the lower case 7.

That is, the fungi-proofing chamber 25 has an upper opening 16 on the upper side and a bottom outlet 10 on the lower side (an example of a lower opening of the fungi-proofing chamber 25). The upper opening 16 is sealed with the antibacterial sheet 22, and the bottom outlet 10 is sealed with the antibacterial sheet 24. Thus, the space inside the bacteria-proof wall 17 becomes the bacteria-proof chamber 25.

In a state before the sensor insertion device 1 is used, the sensor unit 3, the sensor holder 18, the sensor base 4, the needle unit 19, the guide needle 20, and the like are accommodated in the fungi-proofing chamber 25 as described above.

The space inside the bacteria-proof wall 17 is irradiated with electron beams from the outside while being sealed with the bacteria-proof sheets 22 and 24. Thereby, the sensor unit 3, the sensor holder 18, the sensor base 4, the needle unit 19, and the guide needle 20 disposed inside the bacteria-proof wall 17 are sterilized, and the sterilized state is maintained.

On the other hand, as shown in fig. 5, a cylindrical needle holder 26 having a lower surface side open is disposed in the upper case 8. The needle holder 26 is provided in the sensor insertion device 1 to be movable in the vertical direction by a needle holder lifting mechanism 30A (see fig. 7) described later. Further, an engaging arm 27 is provided between the needle holder 26 and the grip portion 13 in the upper case 8.

The engagement arm 27 engages with an engagement hole 28 (see fig. 9) formed in a side surface of the needle holder 26. When the upper case 8 is pushed down by the user during the needle puncturing operation, the needle holder 26 is lowered together with the upper case 8 due to the engagement of the engagement arms 27 with the engagement holes 28. At this time, the pinion 30 is not rotated, and is lowered together with the needle holder 26 and the upper case 8.

In detail, as will be described later, when the upper case 8 is lowered, the needle holder 26 holds the needle unit 19 (see fig. 16), and the needle holder 26 is lowered in the sensor insertion device 1 to perform the pricking operation of the guide needle 20. In the needle withdrawing operation after the needle punching operation, the needle holder 26 is raised in the sensor insertion device 1 to withdraw the guide needle 20.

In the sensor insertion device 1 of the present embodiment, a needle holder lifting mechanism 30A for lifting the needle holder 26 is provided in order to pull out the guide needle 20 (see fig. 18) inserted into the human body 2 from the human body 2.

Specifically, as shown in fig. 7 and the like, the needle holder lifting mechanism 30A includes two pinions 30 arranged so as to sandwich the needle holder 26, and racks 33 and 34 engaged with the pinions 30.

As shown in fig. 5, two pinions 30 that raise the needle holder 26 are arranged between the needle holder 26 in the upper case 8 and the short side 29 of the upper case 8.

As shown in fig. 7, a shaft support groove 32 is formed along the vertical direction of the upper case 8 inside the long side surface 12 of the upper case 8, and the shaft support groove 32 holds a shaft 31 (see fig. 9) of the pinion 30 in a state of being movable in the vertical direction. The pinion gear 30 is provided to be slidable in the vertical direction along the shaft support groove 32 when the sensor shown in fig. 11 and the like is mounted.

A rack (first rack) 33 that engages with the pinion 30 is provided along the vertical direction on the inner surface side of the upper case 8. The rack 33 is disposed on the inner surface side of the short side 29 at a portion facing the pinion 30. Further, the lower portion of the rack 33 engages with the two pinions 30 on both sides of the needle holder 26.

On the outer surface side of the needle holder 26, racks (second racks) 34 are provided along the vertical direction on both side surfaces facing the pinion 30. The two pinions 30 are engaged with the upper portion of the rack 34 on both side surfaces of the needle holder 26.

As shown in fig. 7 and the like, the racks 33, 34 are disposed so that the engaging teeth thereof face each other.

The two pinions 30 are arranged so as to be sandwiched from both sides by the racks 33 and 34, respectively, and do not rotate until the needle punching operation shown in fig. 18 is completed. When the user further operates the upper case 8 downward after the completion of the needle puncturing operation shown in fig. 18, the rack 33 is lowered relative to the needle holder 26 on the side surfaces on both sides of the needle holder 26, and the pinion 30 is rotated. When the pinion 30 rotates, the rack 34 engaged with the pinion 30 is driven by the pinion 30, and the needle holder 26 slides upward. As a result, the needle holder 26 is lifted (raised) upward by the pinions 30 on both sides, and the guide needle 20 held by the needle holder 26 is pulled out from the human body 2.

That is, the pinion 30, the rack 33, and the rack 34 constitute a needle holder lifting mechanism 30A that lifts the needle holder 26. According to this configuration, after the needling operation shown in fig. 14, by further operating the upper case 8 downward (in the needling direction of the human body 2), the needle holder 26 can be slid upward within the upper case 8.

Therefore, the user can perform the needle punching operation and the needle pulling operation using the guide needle 20 of the sensor insertion device 1 by the same operation of operating the upper case 8 downward (in the needle punching direction of the human body 2). Therefore, the convenience of use of the user can be improved.

As shown in fig. 7, the needle holder 26 is provided with a needle holding portion 36 having a cylindrical shape at a lower end side. The needle holding portion 36 is disposed to face the needle unit 19 disposed in the lower case 7. The lower end side of the needle holding portion 36 is engaged with the needle unit 19, and the needle holder 26 holds the guide needle 20 of the needle unit 19.

As described above, by providing the grip portion 13 recessed inward on the long side surface 12 of the upper case 8, the grip portion 13 is made small, and the user can easily grip the grip portion 13. In the present embodiment, pinion gears 30 are disposed in upper case 8 at positions where no grip portion 13 is formed on long side surface 12 of upper case 8, that is, at portions on both sides of grip portion 13 on long side surface 12. In this way, the pinion 30 is disposed at a position away from the recessed portion of the grip 13 of the upper case 8. Therefore, the grip portion 13 can be recessed inward as appropriate, and can be formed into a small shape that facilitates gripping of the upper case 8.

Further, engaging projections 37 are provided at four corners of the upper end side of the short side surface of the lower case 7 (see fig. 6). On the other hand, concave portions 38 are provided at four corners of the lower end side of the short side surface of the upper case 8.

As described above, when the upper case 8 is placed over the lower case 7 from above, as shown in fig. 10, the four engaging projections 37 (see fig. 6) of the lower case 7 engage with the four recesses 38 of the upper case 8.

When using the sensor insertion device 1 configured as described above, the user grips the grip portion 13 of the upper case 8 shown in fig. 3 to pick up the sensor insertion device 1, peels the antibacterial sheet 24 (see fig. 5) from the bottom surface 23 of the lower case 7, and then presses the bottom surface 23 of the lower case 7 against the human body 2.

Fig. 11 is a sectional view of the sensor insertion device 1 pressed against the human body 2, which is a sectional view of the plane a in fig. 4. Fig. 12 and 14 to 20 are cross-sectional views of the plane a of fig. 4.

Fig. 12 is an enlarged cross-sectional view of the periphery of the needle retainer 26 of fig. 11. In the upper case 8, a needle holder 26 is provided at a portion facing the upper surface of the antibacterial sheet 22. The needle holder 26 is provided with a needle holding portion 36 that engages with and holds the needle unit 19 in the bacteria-proof chamber 25 when the upper case 8 is lowered.

The lower end side of the needle holding portion 36 is disposed opposite to the upper end side of the needle unit 19 with the antibacterial sheet 22 interposed therebetween.

As shown in fig. 13, the lower end of the needle holding portion 36 is formed in a cylindrical shape that holds the outer periphery of the needle unit 19. Four blades 39 for rupturing the antibacterial sheet 22 are formed at the cylindrical lower opening edge of the needle holding portion 36.

When the user presses the upper case 8 downward from the state shown in fig. 11 with a predetermined force or more while holding the grip 13, the engagement projection 37 of the lower case 7 and the recess 38 of the upper case 8 are disengaged (see fig. 10), and the upper case 8 is pressed downward at one time. At this time, the grip 13 of the upper case 8 is guided by the slide guide 14 of the lower case 7 and moves downward (see fig. 3).

At this time, as shown in fig. 9, the engaging arms 27 of the upper case 8 engage with the engaging holes 28 of the needle holder 26 on the inner surface side of the grip 13. Thus, the needle holder 26 descends together with the upper case 8.

As shown in fig. 14 and 15, in the needle holding portion 36 of the needle holder 26, the distal end portions of the four blades 39 provided at the lower end break the antibacterial sheet 22, and the antibacterial sheet 22 is broken.

That is, in the present embodiment, the upper case 8 and the unitized lower case 7 are provided with the bacteria-proof chamber 25 therein. Therefore, since the bacteria-proof state of the bacteria-proof chamber 25 is maintained until the time of actual use, the hygiene management state can be maintained.

The needle unit 19 has a conical portion 40 (or a conical table portion) protruding upward at an upper end portion thereof. Therefore, the antibacterial sheet 22 ruptured by the blade 39 is press-fitted into the antibacterial sheet holding portion 41 provided in the needle holding portion 36 through the conical portion 40 of the needle unit 19.

When the upper case 8 is further pushed down, the needle holder 26 holds the outer surface of the needle unit 19 on the inner wall surface of the needle holding portion 36 (the inner wall surface of the sterility sheet holding portion 41) as shown in fig. 16 and 17.

In the present embodiment, in a state where the needle holding portion 36 holds the needle unit 19, the tip portion of the conical portion 40 of the needle unit 19 is inserted into the antibacterial sheet holding portion 41 of the needle holding portion 36.

Therefore, the ruptured antibacterial sheet 22 is pressed into the antibacterial sheet holding portion 41 by the conical portion 40 of the needle unit 19. In this state, the antimicrobial sheet 22 is pressed against the inner wall surface of the antimicrobial sheet holding portion 41 by the O-ring 42 provided on the side surface of the needle unit 19.

As a result, the broken antibacterial sheet 22 is held in the antibacterial sheet holding portion 41, and therefore the operation of the sensor insertion device 1 is not hindered.

When the upper case 8 is further pushed down in a state where the needle holder 26 holds the needle unit 19, the sensor unit 3 held by the sensor holder 18 is attached to the upper surface side of the sensor base 4 as shown in fig. 18.

At this time, the sensor 6 protrudes downward from the bottom surface 23 of the lower case 7 together with the guide needle 20, and the needle prick is performed by the guide needle 20. The sensor base 4 is attached to the human body 2 by an adhesive portion 43 provided on the lower surface of the sensor base 4. That is, the sensor 6 is inserted into the human body 2 together with the guide needle 20.

When the needle punching of the guide needle 20 is performed, the shaft 31 of the pinion 30 moves downward in the shaft support groove 32, and reaches the shaft support portion 35 provided in the lower case 7.

The needle pulling operation of the guide needle 20 will be described below.

In the present embodiment, as shown in fig. 7, a needle holder lifting mechanism 30A for lifting the needle holder 26 is constituted by the pinion 30, the rack 33, and the rack 34. In the needle withdrawing operation of the guide needle 20, the pinion 30 rotates by engagement with the rack 33 and the rack 34 as the upper case 8 further descends after the completion of the needle puncturing operation, and the needle holder 26 is raised. As a result, the guide needle 20 is pulled out from the human body 2.

The following is a detailed description.

After the needling operation shown in fig. 18, when the user further pushes down the upper case 8, the pinion 30 is axially supported by the shaft support portion 35 as shown in fig. 18, and thus does not further descend.

On the other hand, when the upper case 8 is further slid downward, the rack 33 inside the upper case 8 is slid downward. Therefore, the pinion 30 engaged with the rack 33 on the upper case 8 side rotates on both sides of the needle holder 26. The rotational force is transmitted to the rack 34 on the lower housing 7 side engaged with the pinion 30.

Therefore, the needle holder 26 is lifted by the upward driving force from the racks 34 disposed on both sides, and slides (rises) upward from the state of fig. 18 to the state of fig. 19.

As a result, the guide needle 20 held by the needle holder 26 is pulled out from the human body 2 and stored in the lower case 7 as shown in fig. 19. And, the sensor 6 is left in the human body 2.

The pinion 30 slides in the upper case 8 along shaft support grooves 32 on both sides, in which the shaft 31 engages, while rotating.

The force with which the pinion 30 lifts the needle holder 26 is larger than the engaging force of the engaging arm 27 of the upper case 8 with the engaging hole 28 of the needle holder 26. Therefore, the upper case 8 and the needle holder 26 are disengaged from each other, and the needle holder 26 can be raised in the upper case 8.

When the user lifts the upper case 8, as shown in fig. 20, the sensor base 4 is bonded to the human body 2 by the bonding portion 43, and therefore the sensor base 4 is separated and detached from the holding claw 44 in the bacteria-proof chamber 25.

As a result, as shown in fig. 21, the sensor base 4 is attached to the human body 2 with the sensor unit 3 held, thereby completing a series of operations.

As described above, the sensor insertion device 1 of the present embodiment includes the lower case 7, the upper case 8, the sensor base 4, the needle holder 26, and the needle holder lifting mechanism 30A. The lower case 7 has an upper surface opening 9. The upper case 8 is disposed so as to cover the outer periphery of the lower case 7 from above and to be slidable relative to the lower case, and is operated downward by the user during the needle insertion operation. The sensor base 4 is disposed in the lower case 7 and holds the sensor 6. The needle holder lifting mechanism 30A is disposed above the sensor base 4 so as to be movable up and down, and lifts the needle holder 26 holding the guide needle 20 of the sensor 6 and the needle holder 26. The needle holder raising mechanism 30A has a pinion 30, a rack 34, and a rack 33. The pinion 30 raises the needle holder 26. The rack 34 is provided on the needle holder 26 and engages with the pinion 30. The rack 33 is provided in the upper case 8 and engages with the pinion 30. As the upper case 8 descends, the pinion 30 engages with the rack 33 to raise the needle holder 26.

Therefore, after the needle holder 26 has performed the needling operation by the guide needle 20, the needle holder 26 can be raised by the pinion 30 provided in the upper case 8 by further lowering the upper case 8. As a result, the impact sound due to the spring is not generated, and the patient's discomfort (terrorism) can be reduced.

The sensor insertion device 1 of the present embodiment includes a lower case 7, an upper case 8, a bacteria-proof chamber 25, a bacteria-proof sheet 22, a bacteria-proof sheet 24, and a needle holding portion 36. The lower case 7 has an upper surface opening 9 and a bottom surface discharge port 10. The upper case 8 covers the outer periphery of the lower case 7 from above downward, is slidably disposed relative to the lower case 7, and is operated downward by the user during the needle insertion operation. The sterilization chamber 25 is provided in the lower case 7, and houses the needle unit 19 including the guide needle 20 for pricking the human body 2 and the sensor unit 3 including the sensor 6 for obtaining the blood glucose level. The antibacterial sheet 22 is attached to an upper opening of the antibacterial chamber 25. The antibacterial sheet 24 is attached to the bottom surface discharge port 10 corresponding to the lower opening of the antibacterial chamber 25. The needle holding portion 36 is provided in a portion facing the upper surface of the antibacterial sheet 22 in the upper case 8, and engages with the needle unit 19 in the antibacterial chamber 25 when the upper case 8 is lowered downward.

That is, since the upper case 8 and the unitized lower case 7 are provided with the bacteria-proof chamber therein, the bacteria-proof state of the bacteria-proof chamber is maintained until the time of actual use, and as a result, the sanitary management state can be maintained.

< appendix 1 >

The sensor insertion device of the present invention can also be determined as follows.

That is, the sensor insertion device of the first aspect of the present invention includes:

a lower case having an upper surface opening;

an upper case that covers the outer periphery of the lower case from above, is disposed to be slidable relative to the lower case, and is operated downward by a user when performing a needling operation;

a needle unit and a sensor unit disposed in the lower case;

a needle holder disposed in the upper case so as to be movable in the vertical direction;

a needle holder lifting mechanism provided to be movable in the vertical direction, the needle holder lifting mechanism including a pinion for lifting the needle holder holding the guide needle that has performed the needling action;

a discharge port of the sensor unit provided at a bottom surface of the lower case;

an engaging mechanism that is disposed on the upper case and the needle holder and engages the upper case and the needle holder when the upper case is lowered;

a first rack provided in the upper case and engaged with the pinion; and

a second rack provided to the needle holder and engaged with the pinion,

the lower case has a shaft support part for supporting a shaft of the pinion gear,

when the pinion moves downward and reaches the shaft support portion, the needle holder is raised by engagement of the pinion with the first rack and the second rack.

Sensor insertion device of second invention on the basis of the sensor insertion device of the first invention,

the shaft of the pinion reaches the shaft support portion in a state where the needle insertion operation to the human body by the guide needle is completed.

The sensor insertion device of the third invention is based on the sensor insertion device of the first or second invention,

the upper housing has a shaft supporting groove formed along a vertical direction of the upper housing, and the shaft supporting groove holds the shaft of the pinion gear.

Sensor insertion device of fourth invention on the basis of the sensor insertion device of the third invention,

the shaft of the pinion gear is disposed at a lower end portion of the shaft support groove when the upper housing is moved downward to a state where the acupuncture operation to the human body by the guide needle is completed.

A sensor insertion device of a fifth invention is based on any one of the sensor insertion devices of the first to fourth inventions,

the upper case has a rectangular parallelepiped shape that is laterally long in a plan view, and includes a grip portion that is formed on opposing long side surfaces of the upper case and is recessed in a step-like manner from above to below, and an inner protrusion that protrudes in a step-like manner at a position on an inner surface side corresponding to the grip portion,

the lower case has a slide guide portion on which the inner protruding portion of the grip portion slides, the slide guide portion being provided at a portion corresponding to the grip portion.

The sensor insertion device of the sixth invention is based on the sensor insertion device of the fifth invention,

the grip portion is provided at a central portion in a longitudinal direction from above to below on a long side surface of the upper case,

the pinion gears are disposed on both side portions of the grip portion in the upper case.

The sensor insertion device of the seventh invention on the basis of the sensor insertion device of the sixth invention,

the second rack is provided on both side surfaces of the needle holder.

The sensor insertion device of the eighth invention is based on any one of the sensor insertion devices of the fifth to seventh inventions,

the engaging mechanism includes a first engaging portion provided inside the grip portion of the upper case, and a second engaging portion provided at a portion of the needle holder facing the first engaging portion.

< appendix 2 >

The sensor insertion device of the present invention can also be determined as follows.

That is, the sensor insertion device of the eleventh aspect of the present invention includes:

a cylindrical lower case having an upper surface opening and a bottom surface discharge port;

an upper case having a lower surface opening, covering the outer periphery of the lower case from above, and configured to be slidable relative to the lower case, and operated downward by a user during a needling operation;

a sterilization chamber provided in the lower case and accommodating a needle unit including a guide needle for puncturing a human body and a sensor unit including a sensor for acquiring biological information of the human body;

a first antibacterial sheet attached to an upper opening of the antibacterial chamber;

a second antibacterial sheet attached to the bottom surface discharge port corresponding to the lower opening of the antibacterial chamber;

and a needle holding portion provided in a portion facing an upper surface of the first antimicrobial sheet in the upper case, and engaging with the needle unit in the antimicrobial chamber when the upper case is lowered downward.

The sensor insertion device of the twelfth invention on the basis of the sensor insertion device of the eleventh invention,

the needle holding portion includes a blade for breaking the first antibacterial sheet when the upper case is lowered downward.

The sensor insertion device of the thirteenth invention is based on the sensor insertion device of the twelfth invention,

the needle holding portion is cylindrical in shape that holds the outer periphery of the needle unit.

A sensor insertion device according to a fourteenth aspect of the present invention is the sensor insertion device according to the thirteenth aspect of the present invention, wherein the blade is formed at a cylindrical lower opening edge portion of the needle holding portion.

A sensor insertion device of a fifteenth invention is based on any of the sensor insertion devices of the twelfth to fourteenth inventions,

the needle unit has a cone portion or a cone frustum portion protruding upward at an upper end portion thereof,

the conical portion or the top portion of the conical table portion of the needle unit is inserted into the needle holding portion in a state where the needle unit is held by the needle holding portion.

(embodiment mode 2)

As shown in fig. 22, the sensor insertion device 51 of the present embodiment is used to attach a disc-shaped sensor base 54 holding a sensor unit 53 to a human body 52 (upper arm portion, etc.).

As shown in fig. 26, the sensor insertion device 51 is configured by a needle holder lifting mechanism 74 that lifts the needle holder 67 using a pinion 71 and two racks (a first rack 72 and a second rack 73), as in the sensor insertion device 1 of embodiment 1 described above. Further, since the needle holder 67 is raised by the pinion 71 included in the needle holder raising mechanism 74, an impact sound due to a spring is not generated, and discomfort (terrorism) to the patient can be reduced.

Hereinafter, the detailed description will be given with reference to the drawings.

In embodiment 2, "up" and "down" indicate "up" and "down" in a use state (a state when the sensor is attached to the human body 52) of the sensor insertion device 51 shown in fig. 31 and the like. The vertical direction refers to a puncture direction (a needle puncture direction and a needle withdrawal direction) of the guide needle 78 in the sensor insertion device 51.

Fig. 22 is a diagram showing a use state of the sensor insertion device 51. In fig. 22, a sensor unit 53 is attached to a part of a human body (e.g., an upper arm portion or the like) 52 together with a sensor base 54 by a sensor insertion device 51. Then, a measuring instrument 55 (an example of a biological information measuring instrument) is attached to the upper surface of the sensor base 54 (see fig. 23).

Fig. 23 shows a state in which the sensor base 54 and the measuring instrument 55 are attached to the human body (upper arm) 52. In fig. 23, a sensor 56 included in a sensor unit 53 is left in a human body 52. Thus, the biological information of the human body 52 is detected by the sensor 56 and measured by the measuring device 55. The measurement result is transmitted from the measurement device 55 to, for example, a mobile phone (not shown).

In the present embodiment, the blood glucose level is measured as the biological information, and for example, the blood glucose level of the patient is measured every 5 minutes for 1 to 2 weeks, so-called continuous blood glucose measurement is performed. This makes it possible to grasp the tendency of the patient to have a blood glucose level for a certain period of time and the blood glucose level during sleep.

As shown in fig. 24 to 27, the sensor insertion device 51 includes a lower housing 57, an upper housing 58, a sensor base 54, a needle holder 67, and a needle holder lifting mechanism 74.

As shown in fig. 25, lower case 57 has a cylindrical shape, and an upper surface opening 59 is provided on the upper surface side of the cylindrical shape, and a bottom surface discharge port 60 for discharging sensor base 54 downward is provided on the lower surface side.

As shown in fig. 25, the sensor base 54 is a substantially cylindrical member, and holds the sensor unit 53 including the sensor 56 of fig. 23 inside.

As shown in fig. 25, the upper case 58 has a cylindrical shape with a closed upper surface side and an open lower surface side, and has a lower surface opening 61. The upper case 58 is covered from above so as to cover the outer peripheral surface of the lower case 57 (see fig. 24).

That is, the upper case 58 has a cylindrical shape like the lower case 57, and they are covered so as to be overlapped with each other. A grip 62 that is gripped by a user is provided on the outer peripheral surface of the upper case 58. The upper surface portion 63 of the upper case 58 is provided with an abutting portion 64 against which the palm of the user abuts during use. A cylindrical slide guide portion 65 is provided on the outer peripheral surface of the lower case 57 at a portion corresponding to the grip portion 62 of the upper case 58.

Therefore, when the user uses the sensor insertion device 51, the grip portion 62 of the upper case can be gripped with five fingers of the left hand, for example, in a state where the palm of the right hand is brought into contact with the contact portion 64 of the upper case, for example. Therefore, the use state described later can be made extremely stable.

The user of the sensor insertion device 51 may be the patient himself or a third person such as a nurse or a care-giver.

The detailed shape and structure of each part will be described.

As shown in fig. 25, a sensor base 54 that holds the sensor 56 (see fig. 23), a base holder 66 that holds the sensor base 54, and a needle holder 67 that covers the base holder 66 are arranged in the lower case 57. A skin tape 68 for sticking the sensor base 54 to the human body 52 is provided on the lower surface of the sensor base 54.

Fig. 26 and 27 show the sensor insertion device 51 not in use (before sensor mounting).

As shown in fig. 27, the sensor base 54 is inserted from the lower side of the base holder 66. Fig. 27 shows a state in which the skin tape 68 is removed to explain the states of the sensor base 54 and the base holder 66.

Three base engaging portions 69 of the base holder 66 provided at substantially equal angular intervals along the outer peripheral portion thereof are engaged with first engaging claws 70 provided at substantially equal angular intervals at the middle portion of the lower case 57 (see fig. 26 a and 28). The outer peripheral surface of the base holder 66 is covered with a needle holder 67. The needle holder 67, the base holder 66, and the sensor base 54 are held at the middle portion of the lower case 57, and slide downward from the middle position when attached to the patient.

The needle holder 67 has a substantially disk shape and is provided in the lower case 57 so as to be movable in the vertical direction (insertion direction). As shown in fig. 26, a pinion 71, a first rack 72, and a second rack 73 constituting a needle holder lifting mechanism 74 for lifting the needle holder 67 are arranged on the upper surface side of the needle holder 67.

The needle holder lifting mechanism 74 is disposed near the center of the lower case 57 and the needle holder 67. To describe in more detail, the pinion 71 is provided in the vicinity of the central axis of the cylindrical lower housing 57 and the substantially disk-shaped needle holder 67.

The pinion 71 is coupled to shafts 75 extending from both left and right ends of the gear portion.

The shaft 75 is provided as a rotation shaft of the pinion 71, and its longitudinal direction is arranged in a state orthogonal to the central axis of the lower case 57. Both ends of the shaft 75 are pivotally supported by shaft supporting portions 76 provided on the inner surface of the lower case 57. Therefore, the pinion 71 rotates in the middle of the lower case 57 while being pivotally supported by the shaft support portion 76.

A first rack 72 having a substantially quadrangular prism shape is engaged with the pinion 71. The first rack 72 is provided so as to protrude upward from the upper surface of the needle holder 67. In the state before use shown in fig. 27, the first rack 72 engages with the pinion 71 below the gear portion.

As shown in fig. 31, the first rack 72 has an upper portion of the needle unit 77 embedded in a lower portion thereof. Further, below the first rack 72, a guide needle 78 held by a needle unit 77 protrudes from the lower surface side of the sensor base 54.

The guide needle 78 includes a sensor 56 for measuring biological information (blood glucose level, etc.) inside the needle.

As shown in fig. 26, in the pinion 71, a second rack 73 having a substantially quadrangular prism shape is disposed on the side opposite to the first rack 72 and above the pinion 71.

The second rack 73 has a fixed end fixed to the top surface of the upper case 58 on the upper end side and a flexible free end on the lower end side. Therefore, the lower end side of the second rack 73 is movable radially outward from the central axis of the upper case 58. The second rack 73 is disposed so as to be sandwiched from both the left and right sides with respect to the pinion 71 together with the first rack 72. That is, in a state where the upper housing 58 is lowered (see fig. 32 and 33), the first rack 72 and the second rack 73 are disposed such that the respective engaging teeth face each other, and the pinion 71 is disposed therebetween. Therefore, the second rack 73 engages with the pinion 71 on the side opposite to the first rack 72.

Thus, the needle holder lifting mechanism 74 is disposed near the central axis of the lower case 57 and the needle holder 67. Therefore, the needle holder 67 having completed the needling operation can be stably lifted. The needle pulling operation will be described later.

The needle holder 67 is provided with needle holder engaging portions 79 at three (a plurality of) locations at equal angular intervals along the outer peripheral portion of the upper surface thereof. Further, a needle holder pressing portion 80 is provided on an inner surface of the upper case 58 at a portion facing the needle holder engaging portion 79 (see fig. 26B and 29).

That is, since the needle holder pressing portion 80 engages with the needle holder engaging portion 79, the needle holder 67 is pressed (slid) downward when the upper housing 58 is lowered.

As shown in fig. 31, a lower housing engagement portion 81 is provided on an upper outer periphery of the lower housing 57. The lower housing engagement portion 81 is engaged with an upper housing engagement claw 82 provided at a lower portion of the inner periphery of the upper housing 58 (see fig. 26C and 30).

When using the sensor insertion device 51 configured as described above, the user holds the upper case 58 and picks up the sensor insertion device 51, and presses the bottom surface discharge port 60 of the lower case 57 against the human body 52 as shown in fig. 31. Fig. 31 to 34 show cross-sectional views of the sensor insertion device 51.

The needling operation of the guide needle 78 is performed as follows.

Specifically, the user presses the upper case 58 downward (toward the human body 52) from the state shown in fig. 31. At this time, when the upper case 58 is pressed with a predetermined force or more, the lower case engaging portion 81 and the upper case engaging claw 82 are disengaged (see fig. 30), and the upper case 58 is released from being held by the lower case 57. Therefore, the upper case 58 is pressed downward at one time. The grip portion 62 (outer peripheral surface) of the upper case 58 is guided by the slide guide portion 65 (outer peripheral surface) of the lower case 57 and moves downward (see fig. 24).

At this time, as shown in fig. 29, the needle holder engaging portion 79 is pressed downward by the needle holder pressing portion 80 on the upper case 58 side, and the needle holder 67 descends together with the upper case 58, pressing the base holder 66 downward.

Thus, in the base holder 66, the three outer peripheral base engaging portions 69 are disengaged from the first engaging claws 70, and the holding of the base holder 66 with respect to the lower case 57 is released. Therefore, as the needle holder 67 held by the upper housing 58 is lowered, the base holder 66 and the sensor base 54 are lowered at a time.

That is, the engaging force between the needle holder pressing portion 80 on the upper case 58 side and the needle holder engaging portion 79 on the needle holder 67 side is greater than the engaging force between the base engaging portion 69 on the base holder 66 side and the first engaging claw 70 on the lower case 57 side.

Thus, the engagement of the base holder 66 with the lower case 57 can be released and the base holder 66 can be lowered while the engagement of the needle holder pressing portion 80 on the upper case 58 side with the needle holder engaging portion 79 on the needle holder 67 side is maintained.

When the needle holder 67 is lowered, the first rack 72 fixed to the upper surface of the needle holder 67 shifts from the state shown in fig. 31 to the state shown in fig. 32 while rotating the engaged pinion 71 counterclockwise. Specifically, the pinion 71 moves from the lower end portion to the upper end portion of the first rack 72 while rotating counterclockwise.

In the state before the needling operation shown in fig. 31, the pinion gear 71 engages with the first rack 72 and does not engage with the second rack 73.

At this time, as shown in fig. 32, the guide needle 78 protrudes downward from the bottom surface discharge port 60 of the lower case 57 and pierces the human body 52. The sensor 56 guided by the introducer needle 78 is inserted into the human body 52 along with the introducer needle 78.

At this time, as shown in fig. 32, the base holder 66 is held by the lower case 57 by the base engaging portion 69 engaging with the second engaging claw 83 of the lower case 57. The sensor base 54 is attached to the human body 52 by the adhesive force of the skin tape 68 attached to the lower surface side.

At this time, as shown in fig. 32, the first rack 72 is engaged with the pinion 71 at the upper side thereof. The pinion 71 is engaged with the first rack 72 by lowering the lower end of the second rack 73.

That is, when the needling operation shown in fig. 32 is completed, the pinion 71 is engaged with both the first rack 72 and the second rack 73, and the preparation for the needle withdrawing operation described later is completed.

In this state, the needling operation of the guide needle 78 is completed.

Next, the needle pulling operation of the guide needle 78 will be described.

In the present embodiment, as shown in fig. 26, a needle holder lifting mechanism 74 for lifting the needle holder 67 is constituted by the pinion 71, the first rack 72, and the second rack 73. In the needle withdrawing operation of the guide needle 78, as the upper housing 58 is further lowered after the completion of the needling operation, the pinion 71 is rotated clockwise by the engagement with the first rack 72 and the second rack 73, and the needle holder 67 is raised. As a result, the guide needle 78 is pulled out from the human body 2.

The needle pulling operation will be specifically described below.

When the user further pushes down the upper case 58 from the state in which the needling operation shown in fig. 32 is completed, the engagement between the needle holder pushing portion 80 and the needle holder engaging portion 79 is released, and the upper case 58 is lowered relative to the needle holder 67 and the lower case 57.

Thereby, the second rack 73 fixed to the upper case 58 moves downward, engages with the pinion 71 from the lower end (free end side), and rotates the pinion 71 clockwise. The rotational force is transmitted to the first rack 72 via the pinion 71. As a result, as shown in fig. 33, the first rack 72 rises. Therefore, the needle holder 67 to which the first rack 72 is fixed is lifted by the clockwise rotation of the pinion 71, and slides (rises) upward.

As a result, the guide needle 78 held by the needle holder 67 is pulled out from the human body 52 with the sensor 56 being left in the human body 52, and is stored in the needle storage portion 84 provided in the base holder 66. Therefore, the guide pin 78 protruding from the bottom surface discharge port 60 of the lower case 57 is housed in the lower case 57. Also, the sensor 56 is left in the human body 52.

When the user picks up the upper case 58, as shown in fig. 34, the sensor base 54 is adhered to the human body 52 by the adhesive force of the skin tape 68, and therefore the sensor base 54 is separated from the base holder 66 and remains on the surface of the human body 52. Thereby, the sensor base 54 is discharged from the bottom surface discharge port 60 of the lower case 57 together with the sensor 56.

As a result of the above operation, as shown in fig. 34, the sensor base 54 is attached to the human body 52 with the sensor 56 inserted into the human body 52.

This completes a series of operations (the needle puncturing operation and the needle removing operation) performed by the sensor insertion device 51.

Therefore, the user can perform the needle punching operation and the needle pulling operation using the sensor insertion device 51 and the guide needle 78 by the same operation of operating the upper case 58 downward (in the needle punching direction of the human body 52). Therefore, the convenience of use of the user can be improved.

At this time, the guide needle 78 pulled out from the human body 52 is accommodated in the needle accommodating portion 84 provided in the base holder 66, and is protected by the base holder 66. That is, the base holder 66 serves as a cover body covering the bottom surface discharge port 60, and the guide pin 78 is covered by the base holder 66. Thus, the user or another person will not come into inadvertent contact with the introducer needle 78, taking into account the risk of blood infection.

As described above, in the sensor insertion device 51 of the present embodiment, after the needle insertion operation into the human body 52 is performed by the guide needle 78, the needle holder 67 is raised by the pinion 71 provided in the lower case 57. This can avoid the occurrence of impact sound caused by a spring during the conventional needle withdrawing operation, and can reduce discomfort (terrorism) to the patient.

In the sensor insertion device 51 of the present embodiment, as shown in fig. 26 and 31, the pinion 71, the first rack 72, and the second rack 73 constituting the needle holder lifting mechanism 74 are disposed in the vicinity of the central axis of the cylindrical lower case 57 and in the vicinity of the central axis of the needle holder 67. Therefore, the needle holder 67 receives the lifting force of the needle holder lifting mechanism 74 near the central axis thereof, and therefore the needle holder 67 can be lifted stably with good balance.

As a result, the needle pulling operation can be stably performed.

In the sensor insertion device 51 of the present embodiment, as shown in fig. 31, the lower end side of the second rack 73 fixed to the upper case 58 is formed as a free end having flexibility. Therefore, when the second rack 73 descends and comes into contact with the pinion 71, the distal end side of the second rack 73 is bent in a direction away from the pinion 71, and therefore the second rack 73 can be appropriately engaged with the pinion 71.

As a result, the needle pulling operation can be stably performed.

In the sensor insertion device 51 of the present embodiment, as shown in fig. 26, needle holder engaging portions 79 are provided at three locations on the upper surface of the needle holder 67. The first rack 72 is provided between the two adjacent needle holder engagement portions 79.

Therefore, during the needle punching operation, the first rack 72 is disposed between the two adjacent needle holder engagement portions 79, and therefore can be lowered in a stable state. Therefore, the first rack 72, which is lowered in a stable state, rotates the pinion 71, so that a stable needling operation can be performed.

In the sensor insertion device 51 of the present embodiment, as shown in fig. 31, the needle unit 77 that holds the guide needle 78 is fixed between the two adjacent needle holder engagement portions 79 on the lower surface of the needle holder 67. More specifically, the guide pin 78 is disposed directly below the first rack 72.

Therefore, during the needle punching operation, the needle unit 77 also descends in a stable state directly below the first rack 72 that descends in a stable state. As a result, stable needling operation can be performed.

In the sensor insertion device 51 of the present embodiment, the needle holder engagement portions 79 of the needle holder 67 are provided at three locations at equal angular intervals along the outer peripheral portion of the needle holder 67. That is, the needle holder engagement portion 79 is arranged so as to form a regular triangle.

Therefore, since the three needle holder engagement portions 79 press the needle holder 67 at equal angular intervals, a more stable needling operation can be performed.

In the sensor insertion device 51 of the present embodiment, as shown in fig. 26, the upper case 58 has a cylindrical shape with an open lower surface, and the upper surface portion 63 of the upper case 58 is formed with the contact portion 64 against which the palm of the user comes into contact.

Therefore, the user can press the upper case 58 with the palm which is easy to apply force during the needling action and the needle pulling action, and thus the needling action and the needle pulling action can be performed stably.

As shown in fig. 35D and 36, the second rack 73 may be configured such that the lower end side thereof is inclined toward the side opposite to the pinion 71, that is, the side away from the pinion 71.

That is, the second rack 73 is inclined away from the pinion 71 as going downward.

According to this configuration, the lower end side of the second rack 73 is inclined in the direction away from the pinion 71, and therefore the lower end side of the second rack 73 can be gradually engaged with the pinion 71.

As a result, since the second rack 73 and the pinion gear 71 can be appropriately engaged with each other, the needle extracting operation can be stably performed.

Further, the height of the engagement teeth formed on the lower end side of the second rack 73 may be made lower than the height of the engagement teeth formed above the second rack 73.

According to this configuration, the lower end side of the second rack 73 is engaged with the pinion 71 from the low-height engaging teeth, so that the lower end side of the second rack 73 can be gradually engaged with the pinion 71.

As a result, as described above, since the second rack 73 and the pinion gear 71 can be appropriately engaged with each other, the needle extracting operation can be stably performed.

As described above, the sensor insertion device 51 of the present embodiment includes the lower case 57, the upper case 58, the sensor base 54, the needle holder 67, and the needle holder lifting mechanism 74. The lower case 57 has an upper surface opening portion 59. The upper case 58 is disposed so as to cover the outer periphery of the lower case 57 from above and to be slidable relative to the lower case, and is operated downward by the user during the needle insertion operation. The sensor base 54 is disposed in the lower case 57 and holds a sensor 56 for acquiring biological information. The needle holder 67 is disposed above the sensor base 54 so as to be movable up and down, and holds a guide needle 78 that punctures a needle into a human body to guide the sensor 56 into the human body. The needle holder lifting mechanism 74 lifts the needle holder 67 that holds the guide needle that has been inserted into the human body. The needle holder raising mechanism 74 has a pinion 71, a first rack 72, and a second rack 73. The pinion 71 raises the needle holder 67. The first rack 72 is provided to the needle holder 67 and engages with the pinion 71. The second rack 73 is provided in the upper case 58 and engages with the pinion 71. As the upper housing 58 descends, the pinion 71 engages with the second rack 73 to raise the needle holder 67.

That is, in the sensor insertion device 51 of the present embodiment, after the needle insertion is performed by the guide needle 78 of the needle holder 67, the upper case 58 is further operated downward, and the needle holder 67 is raised by the pinion 71, the first rack 72, and the second rack 73 included in the needle holder raising mechanism 74. Therefore, the impact sound due to the spring is not generated, and the discomfort (terrorism) of the patient can be reduced.

Industrial applicability

The present invention is expected to be effectively used as a sensor insertion device for inserting a sensor for measuring biological information into the body of a patient, for example, for continuous blood glucose measurement.

Description of reference numerals:

1 sensor insertion device

2 human body

3 sensor unit

4 sensor base

5 measuring instrument (biological information measuring instrument)

6 sensor

7 lower casing

8 upper shell

9 upper surface opening part

10 bottom outlet (lower opening of antibacterial chamber)

11 lower surface opening part

12 long side

13 grip part

14 sliding guide part

15 long side surface

16 upper opening part

17 bacteria-proof wall

18 sensor holder

19-needle unit

20 guide needle

21 through hole

22 antibacterial sheet (first antibacterial sheet)

23 bottom surface

24 antibacterial sheet (second antibacterial sheet)

25 bacteria-proof room

26-needle holder

27 snap arm

28 clamping hole

29 short side

30 pinion

30A needle holder raising mechanism

31 axle

32-shaft supporting groove

33 Rack (first rack)

34 Rack (second rack)

35 shaft support part

36 needle holder

37 engaging projection

38 recess

39 blade

40 conical part

41 antibacterial sheet holding part

42O-shaped ring

43 adhesive part

44 holding claw

51 sensor insertion device

52 human body

53 sensor unit

54 sensor base

55 measuring apparatus

56 sensor

57 lower casing

58 upper shell

59 upper surface opening part

60 bottom surface discharge outlet

61 lower surface opening part

62 gripping part

63 upper surface part

64 abutting part

65 sliding guide

66 base holder

67 needle holder

68 skin adhesive tape

69 base engaging part

70 first engaging claw

71 pinion gear

72 first rack

73 second rack

74 needle holder raising mechanism

75 axle

76 shaft support part

77 needle unit

78 guide needle

79 needle holder engaging portion

80 needle holder pressing part

81 lower housing engaging part

82 upper case engaging claw

83 second engaging claw

84 needle receiving portion.