JP6333935B2 - Medical medical device and medical treatment tool - Google Patents

Description

  The present invention relates to a medical treatment apparatus used for treatment in a medical field such as dentistry or medical department, and a medical treatment tool constituting the medical treatment apparatus.

  For example, medical treatment tools used for dental treatment and root canal treatment in the dentistry field include handpieces such as air turbine handpieces and micromotor handpieces controlled by the medical device main body, ultrasonic waves, etc. There are a scaler handpiece for cleaning teeth by vibration, a laser handpiece connected to a treatment laser generator through a waveguide, and the like, and an appropriate medical treatment tool is used according to the purpose of the treatment.

  Since such a medical treatment tool needs to be replaced as the patient to be treated changes, the driving conditions such as parameters suitable for each medical treatment tool must be input each time the replacement is performed. There was a problem of not becoming. For such a problem, Patent Document 1 discloses a medical medical device that reads and controls a driving condition suitable for a replaced medical treatment tool.

  Specifically, the medical medical device described in Patent Document 1 has a communication function in a medical treatment tool (handpiece), and is provided with an identification body that stores identification information of the medical treatment tool. Since the device main body reads the identification information, the medical treatment tool can be driven and controlled under an appropriate drive condition, so there is no need to individually set a plurality of drive conditions for the medical treatment tool at the time of connection. Further, the history of sterilization processing can be stored on the medical device main body side, and it can be determined whether the medical treatment tool has been sterilized by reading the identification information.

  However, in the medical treatment apparatus described in Patent Document 1, since the sterilized untreated medical instrument and the medical device main body can be connected, the next patient in which the connected sterilized untreated medical instrument is replaced. There was a risk of being used.

JP 2004-41587 A

  In view of the above problems, an object of the present invention is to provide a medical treatment apparatus and a medical treatment tool that can prevent a sterilized untreated medical treatment tool from being used for the next patient who has been replaced. To do.

The present invention provides a medical treatment instrument having an identification information storage unit for storing unique identification information, and a medical instrument provided with a reading unit that is detachably connectable to the medical treatment instrument and reads the identification information. A medical medical device configured with an apparatus main body, which stores a sterilization information storage unit that stores sterilization information regarding sterilization processing of the medical treatment tool, and reads the sterilization information of the medical treatment tool. A sterilization process determination unit that determines whether the sterilization process is performed or not, a use regulation unit that regulates the use of the medical treatment tool based on a determination result of the sterilization process by the sterilization process determination unit, and the medical treatment A use detecting unit for detecting the use of the surgical treatment tool, and a use notification unit for notifying the use of at least the used medical surgical tool for each of the medical surgical tools based on a detection result of the use detection unit. Provided, said The medical treatment instrument includes a surgical instrument side connection portion that connects to a main body side connection portion provided in the medical device main body, and at least one of the medical treatment instrument or the medical device main body includes the use restriction. A connection obstruction portion that functions as a portion and forms a connection prevention shape that prevents connection between the main body side connection portion and the surgical instrument side connection portion is provided.

The present invention is also a medical treatment tool that is detachably attached to the medical device main body, the sterilization processing information storage unit storing sterilization processing information related to the sterilization processing, and the sterilization processing information of the medical treatment tool. use restricting portion for restricting the use based on the sterilization untreated determination result by the sterilization process determination unit determines whether or sterilization untreated sterilization treated Nde read and, the main body-side connecting portion provided in the medical device body A surgical instrument side connection part to be connected to the surgical instrument side connection part, functioning as the use restricting part and forming a connection obstacle part forming a connection prevention shape for preventing connection with the main body side connection part al is, the use detector for detecting that it has been used in the treatment, based on the detection result of said use detection unit, characterized in that the use notification section for notifying the use is provided.

  The medical instrument refers to a medical instrument that can be removed from the medical device body and sterilized. For example, a dental air turbine handpiece, a micromotor handpiece, an air motor handpiece, a scaler handpiece, a laser Includes treatment handpieces, root canal treatment handpieces, oral surgery handpieces, and the like.

  The medical device main body is a control device that controls driving of the connected medical treatment tool, and is a dental chair unit connected to a tube that supplies a medium such as electricity, air, and water to the medical treatment tool. And a dental chair unit having a motor that can be connected to the medical treatment tool at the tip of the dental tube, an instrument for an assistant separate from the dental chair unit, and a portable home visit Includes medical equipment, laser therapy equipment, etc.

The above-mentioned identification information is read when the identification information is read from the medical treatment tool connected to the medical device body, or from the medical treatment tool not in contact with the medical device body. Including the case of reading. When the medical treatment tool and the medical device main body are in contact with each other, the identification information is read through an electric circuit or a communication circuit. A communication function using magnetic force, a communication function using magnetic force, a communication function using light like a barcode or QR code (registered trademark), a case of reading by a communication function using image recognition, and the like.
Note that the identification information is information for identifying each medical treatment instrument, for example, a serial number. Further, the identification information may include other information such as the sterilization information and information on the use time.

  Examples of the sterilization include sterilization using an autoclave that sterilizes in a high-temperature and high-pressure environment, sterilization using ethylene oxide gas, immersion sterilization soaking in a sterilizing solution such as peracetic acid, plasma using low-temperature plasma. Including sterilization treatment, radiation sterilization treatment that sterilizes by irradiating radiation such as gamma rays and electron beams.

  Forming the above-described connection prevention shape means forming a connection prevention shape that is a physical obstacle to the connection between the medical device body and the medical treatment tool, or the medical device body and the medical device. Even when the surgical instrument is connected, it includes a case where the shape of the main body side connection part and the surgical instrument side connection part is deformed when a shape that cannot maintain the connection state is formed.

Specifically, at least one of the main body side connection part or the surgical instrument side connection part is caused to protrude a protruding piece that prevents connection, or at least one connection part of the main body side connection part or the surgical instrument side connection part , And when the concave portion and the convex portion respectively provided in the main body side connection portion or the surgical instrument side connection portion are connected by fitting, the convex portion is prevented from being inserted into the concave portion. As described above, by projecting the projecting piece toward the recess direction of the concave portion, by pivoting the connection obstacle portion provided at a position other than the main body side connection portion and the treatment instrument side connection portion around a predetermined position It includes that the connection failure part is disposed at a position for preventing connection. That is, any shape may be used as long as it can prevent connection with the main body side connection portion or the surgical instrument side connection.
When the protruding piece protrudes to a position where connection is prevented, the protruding direction of the protruding piece may be the longitudinal axis direction of the medical treatment tool, or may be a radial direction or an oblique direction. .

  Restricting the above-mentioned use includes blocking the transmission of a drive signal from the medical device body to the medical treatment tool, stopping the supply of a working medium such as air or electricity, and the like on the medical device body. It also includes the case where the control of the medical treatment tool provided by the control unit provided, the physical or electrical invalidation of the operation switch, and the control of the transmission of the driving force to the medical treatment tool are included.

  The use notification unit may be provided in any place as long as it is provided so that the use of each medical treatment tool can be notified for each medical treatment tool. For example, the medical device main body When it is provided in a holder for holding the medical treatment tool provided in the case, or when it is provided in the medical treatment tool, a display part provided in the medical device main body is included.

  The above-mentioned notification includes a case of always informing the use notification unit corresponding to the used medical treatment tool, a case of detecting and notifying an electric signal received by receiving a use command, and the notification The method includes, for example, notification by light such as lighting or blinking of an LED, display of the used medical treatment instrument on the display unit, notification by sound or vibration, and the like.

According to the present invention, based on the determination result of whether the medical treatment tool connected to the medical device body when the patient is replaced is sterilized or unsterilized, When the medical device main body is to be connected, the connection failure part forms the connection prevention shape based on the sterilization information, thereby connecting the medical treatment tool and the medical device main body. Therefore, it is possible to reliably prevent physical connection between the surgical instrument side connection portion and the main body side connection portion, and the sterilization-untreated treatment for the post-change patient who is the next patient who has been changed. The medical treatment tool can be prevented from being used, and the problem of contamination on the medical device main body side can be prevented.
In addition, when the change detection unit is provided, it is possible to detect that the patient has changed, and when the patient has changed, the medical treatment tool connected to the medical device body is sterilized or sterilized. Whether it is unprocessed can be determined. Based on the determination result, the connection failure unit can block the connection, and the use restriction unit can regulate the connection between the medical treatment tool that has not been sterilized by the patient after the replacement and the medical device body. . Therefore, the practitioner can use only the sterilized medical treatment tool for the treatment.

Also, a use detection unit for detecting the use of the medical treatment tool, and a use for notifying the use of at least the used medical treatment tool for each medical treatment tool based on the detection result of the use detection unit Since the notification unit is provided, only the medical treatment tool actually used for the treatment is notified, so only the notified medical treatment tool needs to be sterilized. It becomes obvious at a glance.

  Moreover, since use can be alert | reported for every medical treatment tool, when performing the treatment of another patient, the said medical treatment tool which should be replaced | exchanged can be determined easily. Therefore, the practitioner can clearly and easily determine the medical treatment tool to be replaced, and can perform a smooth treatment.

  In addition, in the case where the use notification unit is provided in the holder part of the medical treatment tool, if the configuration is such that a lamp or the like is turned on or blinking for each medical treatment tool to be replaced, When performing the treatment for the next patient, the lamps that are turned on or blinking are always in the field of view, so that it is necessary to sterilize only the medical instrument that has been used once. It is possible to reliably refrain from reusing the surgical instrument.

  As an aspect of the present invention, the medical treatment tool includes an identification body including the identification information storage unit, and the reading unit reads the identification information from the adjacent identification body in a non-contact manner. can do.

  The identifier is an identifier having a communication function with the reading unit. The communication function includes, for example, a communication function using radio waves such as RFID, a communication function using infrared rays, and a magnetic force. A communication function using a light, a communication function using light such as a barcode or QR code (registered trademark), a communication function using image recognition, and the like.

  According to the present invention, it is possible to prevent the medical device body and the medical device from coming into contact when the medical device to be connected to the medical device body has not been sterilized. Therefore, the medical device main body can be prevented from being contaminated.

  Specifically, by providing the reading unit and the identification body, the medical device body can read the identification information without making contact with the medical treatment tool. Therefore, when the medical device body includes a sterilization determination unit, the medical device body reads the sterilization information corresponding to the identification information without contacting the medical treatment tool, It is possible to determine whether the medical treatment tool is sterilized or unsterilized.

  Thus, since it is not necessary to contact the medical treatment instrument and the medical device main body when determining the sterilization treatment, the medical treatment tool to be connected to the medical device main body should be sterilized. Even if it is not treated, it is possible to prevent the medical device body from being contaminated by connecting the medical treatment tool that has not been sterilized to the medical device body.

As also aspects of this invention, the use restricting portion may be characterized by prohibiting the operation of the medical practitioner instrument by the operation signal sent to the medical device body or al the medical practitioner tool.
The operation signal is a drive signal for driving the medical treatment tool, an operation signal for causing the medical treatment tool to perform a predetermined operation command, or a signal for stopping supply of a medium such as irradiation light or cooling water. It is a supply signal for a working medium such as electricity, water, air, light, etc. that is accompanied by some operation or drive according to an operation signal for the medical treatment instrument.

  The prohibition of the above-described operation means that the input signal for operating the medical treatment instrument is physically blocked, for example, the transmission of an electric signal based on the operation of the operation switch of the medical treatment instrument is prevented. This includes preventing transmission of electrical signals from the medical device body to the medical instrument.

  According to the present invention, for example, when it is determined that the medical treatment tool has not been sterilized, a drive signal is not transmitted from the medical device body to the medical treatment tool, and driving of the medical treatment tool is restricted. Is done. Therefore, it is possible to prevent the practitioner from performing the treatment using the medical treatment tool used for another patient by mistake.

Moreover, as an aspect of the present invention, an exchange detection unit that detects the exchange of the medical treatment tool, and a restriction release unit that releases the use restriction of the medical treatment tool by the use restriction unit based on the sterilization information. It can be characterized by being provided.
The replacement of the medical treatment tool described above means that the medical treatment tool has been removed from the medical device body, or that the medical treatment tool connected to the medical device body is another medical device. Including replacement with a surgical instrument.

  According to the present invention, since the use restriction can be released by replacing the medical treatment tool whose use is restricted with a sterilized medical treatment tool, the medical treatment tool that a practitioner can use for the treatment is described above. It can be recognized that it is connected to the medical device body. Therefore, the practitioner can concentrate on the treatment without worrying about whether or not the medical treatment tool has been replaced after the change of the patient.

  In addition, as an aspect of the present invention, a sterilization processing number storage unit that stores the number of sterilization processes in which the sterilization process is performed is provided. It can be characterized by restricting the use of the tool.

The number of sterilization treatments includes the number of sterilization treatments and the number of sterilization treatments calculated based on the case where the sterilization treatment is performed under predetermined conditions.
The above-mentioned calculated number of sterilization treatments is determined in advance for the number of sterilization treatments calculated by providing a load coefficient based on the difference in sterilization treatment temperature and sterilization treatment time with respect to the standard sterilization conditions, or for predetermined sterilization treatment conditions. The number of sterilization treatments obtained by adding the number of sterilization treatments, the number of sterilization treatments calculated based on the integrated value of the number of sterilization treatments and taking into account deterioration of the medical treatment tool.

By this invention, it can prevent using the said medical treatment tool deteriorated by the sterilization process for a treatment.
For example, when the medical treatment tool is sterilized using an autoclave, the medical treatment tool is placed under high temperature and high pressure conditions for a predetermined time. Thus, by repeating the sterilization treatment of the medical treatment tool, consumables such as a motor and an O-ring used for the medical treatment tool gradually deteriorated and may not be usable during the treatment. .

  However, the use restriction unit restricts the use of the medical treatment tool based on the sterilization information and the number of sterilization treatments, so that the medical treatment tool exceeds a predetermined number of sterilization treatments. Since the use of the medical treatment tool can be restricted in some cases, it is possible to prevent the driving of the medical treatment tool from being stopped during the treatment. Therefore, the practitioner can perform the operation with peace of mind.

  Further, as an aspect of the present invention, a replacement determination unit that determines whether or not the medical treatment tool needs to be replaced based on the number of times of sterilization, and a predetermined notification based on a determination result of the replacement determination unit A replacement notification unit.

The replacement of the medical treatment tool described above includes replacement of the medical treatment tool main body, replacement of consumable parts constituting the medical treatment tool such as a motor and an O-ring provided therein, and the like. .
Determining whether or not the above replacement is necessary is, for example, a case where the limit value of the number of integrated sterilization processes stored in advance in the identification unit is compared with the number of integrated sterilization processes, or the sterilization process information When the judgment is made by comparing the cumulative sterilization number of times calculated from the value obtained by multiplying or adding the desired coefficient to the limit value of the cumulative sterilization number, the operator decides within the range of the limit value of the cumulative sterilization number. The case where the determination is made in comparison with the number of integration processing performed includes the case where it is determined that the number of integration processing has exceeded a predetermined value.

  The predetermined notification based on the determination result of the replacement determination unit described above means that a sound such as a buzzer or a melody is emitted or the light is flashed or lit when the medical treatment tool needs to be replaced. In addition to notifying by display on the display unit or the like, for example, displaying the allowable number of times of processing until replacement is required as a character on the display unit and notifying, etc. is included. In particular, the necessity of replacement can be recognized by adopting a configuration that performs a predetermined operation different from the case where it is determined that the medical treatment tool has not been sterilized.

  According to the present invention, even if the medical treatment tool has been sterilized, the practitioner can recognize that the medical treatment tool should be replaced before the treatment, so that it can be replaced with a usable medical treatment tool. it can. Thereby, it is possible to perform the treatment smoothly without exchanging the medical treatment tool during the treatment, and to prevent the patient from feeling uneasy.

  In addition, when the treatment temperature and time of the autoclave can be set to the optimum treatment temperature and time according to the medical treatment tool, the criteria for determining the durability of the medical treatment tool may change depending on the treatment conditions. However, by providing the sterilization processing number processing unit, according to the sterilization processing conditions, since it can be converted into the sterilization processing number based on the reference sterilization processing number, the sterilization conditions are different. In addition, the number of times that the medical treatment tool has been sterilized can be calculated. Thereby, for example, by comparing and determining the limit number of times of sterilization treatment of the medical treatment tool stored in advance in the identification information and the cumulative number of sterilization treatment, it is possible to inform the necessity of replacement of the medical treatment tool, The practitioner can grasp the replacement time of the medical treatment tool.

  In this way, even when sterilized under various sterilization conditions, the replacement timing of the medical instrument can be determined based on a predetermined standard. For example, the medical instrument is recommended by a contractor. Even when the sterilization process takes longer than the sterilization conditions to be performed, the practitioner can accurately grasp the replacement time of the medical treatment tool, and the sterilization apparatus is close to the replacement time. It can be replaced in advance with a medical treatment tool that can be safely treated.

Moreover, as an aspect of the present invention, the sterilization determination unit can determine whether the sterilization process is performed or the sterilization process is performed by comparing and determining the timing of the sterilization process and the use timing of the medical treatment tool.
According to the present invention, it is possible to determine whether the medical treatment tool is sterilized or unsterilized based on the use time of the medical treatment tool and the sterilization time.
For example, by comparing and determining the time during which the medical treatment tool is sterilized and the time when the medical treatment tool is used to finish the treatment, the use time and the sterilization time of the medical treatment tool can be determined later. Can be accurately determined.

  That is, when the medical instrument that has not been sterilized after use is connected to the medical device body, the medical tool that has been used after sterilization is connected to the medical device body However, since it can be determined that the medical treatment tool has not been sterilized, use of the medical treatment tool that has not been sterilized can be reliably regulated.

  In addition, for example, in the case of comparing and determining the date and time of the sterilization treatment and the date and time of the medical treatment tool, the sterilization treatment is performed after use of the medical treatment tool. Although it is determined that it is possible, it is possible to determine when it is necessary to sterilize again because the time has passed since the sterilization process, and it is possible to prevent reuse of the medical instrument. Can do.

Further, as an aspect of the present invention, a change detection unit that detects a change of a patient who is a target of a treatment is provided, and the change detection unit detects a change of the patient based on pre-operation information of a patient after the next change. Can be detected.
The post-substitution patient refers to a patient who performs a procedure next to a patient who has completed the procedure.

Detecting the patient turn described above, detecting the end of the patient's treatment,
For example, detecting the completion of medical preparations for the patient who is the next patient after the change. More specifically, it includes reception of an elevation signal of a dental chair unit, image recognition of a patient's face, etc., switching of patient chart information, a combination thereof, and the like.

  The pre-treatment information refers to, for example, information related to the completion of the post-substitution patient treatment preparation after the patient's treatment. , Information based on medical record information of the post-substitution patient, information based on detection of the weight of the post-substitution patient, information based on a change in mass on the chair, information based on the rise of the chair, Includes information based on reception.

  According to the present invention, it is possible to determine whether the medical treatment tool is sterilized or unsterilized before the treatment of the post-substitution patient, so that the non-sterilized medical treatment tool is used for the post-substitution patient. Can be prevented. Therefore, the practitioner can safely operate the patient after the change.

As another aspect of the present invention, the alternation detection unit can detect the alternation of the patient based on the end information of the patient's treatment.
The term “end information” refers to information related to the completion of the patient's treatment. For example, information based on a chair lowering operation signal, information based on patient mass detection, information based on reception of a treatment end signal by the practitioner, and electronic medical record Detecting that the patient has been closed, and recognizing the movement of the patient getting off the medical chair with a camera.

According to the present invention, it is possible to determine whether the medical treatment tool has been sterilized or not yet sterilized after the patient's treatment is completed and before the replacement patient is treated. Thus, since the use of the sterilized untreated medical device can be surely regulated before the operation of the post-substitution patient, it is a case where the medical treatment tool is forgotten to be removed from the medical device body. However, it is possible to more reliably prevent the use of the sterilized untreated medical treatment tool.
Moreover, since it can replace | exchange for the said medical treatment tool which can be used for a treatment before the said treatment of a patient after a change, the practitioner can perform the treatment of the said post-change patient smoothly.

ADVANTAGE OF THE INVENTION By this invention, the medical treatment apparatus and medical treatment tool which can prevent that the medical treatment tool without a sterilization process used for the next patient who changed are provided can be provided.

1 is a schematic perspective view of a medical medical device. Schematic explanatory drawing of the instrument for dental care. The block diagram of a medical treatment system. The block diagram of RFID and a reader. Explanatory drawing of identification information, use detection information, and process temperature information. The flowchart of the whole treatment. The flowchart of a connection process. The flowchart of a connection process. Explanatory drawing of the patient replacement part in other embodiment.

FIG. 1 is a schematic perspective view of the medical medical device 1, and FIG. 2 is a schematic explanatory view of the dental medical instrument 20 in a state in which the connection between the handpiece 30 and the connection unit 40 is released. FIG. 2A shows a side view of the handpiece 30 and the connection unit 40 in a state where the dental instrument 20 is disassembled, and FIG. 2B shows a rear end face of the handpiece 30. A rear view is shown, and FIG. 2C is a front view showing the front end surface of the connection unit 40. FIG. 2A shows a partial cross section of the handpiece side connecting portion 34 that is the rear end portion of the handpiece 30 and the unit side connecting portion 43 that is the tip portion of the connecting unit 40.
Further, the direction in which the handpiece 30 is located along the longitudinal direction of the dental care instrument 20 (left side in FIG. 2) is the front, and the direction in which the connection unit 40 is present (right side in FIG. 2) is the rear.

  FIG. 3 shows a block diagram of the medical treatment apparatus 1, and FIG. 4 shows an explanatory view of the dental care instrument 20. Specifically, FIG. 4 shows a block diagram of the RFID tag 50 provided in the handpiece 30 constituting the dental care instrument 20 and the RFID reader / writer 60 provided in the connection unit 40.

  FIG. 5 is an explanatory diagram of the usage detection information U and the processing temperature information H. Specifically, FIG. 5A shows the content of the identification information L, and FIG. 5B shows the content of the usage detection information U. FIG. 5C shows the contents of the processing temperature information H.

6 to 8 show flowcharts of patient treatment using the medical treatment apparatus 1. FIG. 6 shows an overall flowchart of the treatment, and FIGS. 7 and 8 show flowcharts for identifying the handpiece 30 using the RFID tag 50.
FIG. 9 is an explanatory diagram of the medical device main body 10 that determines a change of a patient by another method.

As shown in FIG. 1, the medical medical device 1 includes a chair unit 70 including a medical device main body 10 and a plurality of dental medical instruments 20.
As shown in FIG. 2, the dental treatment instrument 20 has a configuration in which a handpiece 30 arranged on the distal end side and a connection unit 40 connected to the handpiece 30 and the medical device main body 10 can be detachably coupled. It is. The connection unit 40 is connected to a connection tube 42 connected to the medical device main body 10.

As shown in FIGS. 1 and 3, the chair unit 70 includes a medical chair 71 on which a patient to be treated is seated, a suction device such as saliva and cooling water, and a device for gargleing. 72, an assistant holder 73 for arranging a bachyme syringe such as saliva in the oral cavity, and a foot controller 74 connected to the medical chair 71.
The medical chair 71 is configured such that the back seat can be tilted and the seat surface can be raised and lowered, and a weight sensor 71 a capable of measuring the weight of the patient seated on the medical chair 71 is provided therein.

The foot controller 74 includes a pedal 74a for operating the driving of the dental care instrument 20 by the practitioner's foot.
Note that the pedal 74a is configured to detect the depression and the depression amount.

  As shown in FIGS. 1 and 3, the medical device main body 10 performs operations such as operation setting of the dental medical instrument 20, various notification operation settings, and operation of raising and lowering the medical chair 71. An operation panel 13 to be performed, a holder 14 for holding a dental care instrument 20 located below the front of the operation panel 13, a monitor 15 provided on the back side of the operation panel 13, and a side portion of the operation panel 13 A tray table 16 and a main body side notification device 17 for notification based on a predetermined operation. Inside the operation panel 13, a processing device control unit 11 composed of a CPU and a ROM, and a processing device control unit 11 are provided. And a main body side storage device 12 connected thereto.

  As shown in FIG. 3, the processing device control unit 11 includes a handpiece identification determination unit 11a, a main body side communication control unit 11b, an information reading control unit 11c, a sterilization processing determination unit 11d, a use determination unit 11e, A drive control unit 11f, a main body side notification operation processing unit 11g, a patient change detection unit 11h, a connection determination unit 11i, a connection notification operation control unit 11j, and an exchange determination unit 11k are provided.

  The handpiece identification determination unit 11a compares the identification information L for identifying the handpiece 30 with the handpiece information I stored in the handpiece information storage unit 12a described later, and the handpiece 30 connected to the connection unit 40 is medical. It is a determination part which determines whether the apparatus main body 10 can drive.

  The main body side communication control unit 11 b is a control unit that controls communication between the handpiece 30 and the connection unit 40. Specifically, reception of information such as identification information L transmitted from the handpiece 30 and usage detection information U that is information related to the use of the handpiece 30 is controlled, and handpiece identification is performed with respect to the handpiece 30. Transmission of the determination result determined by the determination unit 11a is controlled.

  The information reading control unit 11c controls reading of driving conditions such as parameters relating to driving control of the handpiece 30 from a driving control information storage unit 12b described later. In the driving conditions, parameters such as the rotation limit number of the motor corresponding to each handpiece 30 are recorded as the driving conditions.

The sterilization processing determination unit 11d is a determination unit that determines whether or not the handpiece 30 is sterilized based on the sterilization processing information O.
The usage determination unit 11e is a determination unit that performs a determination process as to whether or not the handpiece 30 can be used for the treatment based on the sterilization processing information O and the usage detection information U received from the handpiece 30.

The drive control unit 11f controls the operation of the handpiece 30 according to the drive conditions read by the information read control unit 11c and the determination results of the sterilization processing determination unit 11d, the use determination unit 11e, and the replacement determination unit 11k. It is.
Specifically, the drive control unit 11f controls the input signal transmitted to the handpiece 30 when the pedal 74a of the foot controller 74 is operated by the practitioner's foot according to the drive control condition. For example, if the handpiece 30 has been sterilized, the driving is controlled according to the driving conditions, and if the handpiece 30 has not been sterilized, the driving signal is cut off.

The main body side notification operation processing unit 11 g is a control unit that reads the notification operation program and controls the notification operation of the main body side notification device 17 .
The patient change detection unit 11 h is a detection unit that detects a change of a patient sitting on the medical chair 71. Specifically, a change in mass measured by the weight sensor 71a is measured, and it is detected whether or not the patient has changed based on the change.

  The connection determination unit 11i indicates that the handpiece-side connection unit 34 of the handpiece 30 and the unit-side connection unit 43 formed at the tip of the connection unit 40 have approached a predetermined distance, or that the handpiece 30 and the connection unit 40 Is a determination unit that performs determination processing to determine that the connection between the handpiece 30 and the connection unit 40 has been released.

  Specifically, information obtained from an approach detection sensor 435 described later is analyzed to determine whether the handpiece 30 and the connection unit 40 are approaching, connecting / disconnecting. Whether or not the handpiece 30 connected to the connection unit 40 has been replaced is determined in cooperation with the handpiece identification determination unit 11a.

The connection notification operation control unit 11j receives the determination result of the connection determination unit 11i, and controls a predetermined notification operation performed according to the determination result.
Whether or not the replacement determination unit 11k should replace the handpiece 30 by comparing and determining the sterilization processing number calculated by the sterilization processing number calculation unit 51h and the sterilization processing limit number stored in the replacement reference information storage unit 12c described later. Judgment processing is performed.

  The main body side storage device 12 is configured by an HDD, an SSD, or the like, and includes a handpiece information storage unit 12a that stores handpiece information I that is information of the handpiece 30, and a drive control that stores driving conditions of the handpiece 30. An information storage unit 12b, an exchange reference information storage unit 12c that stores the number of sterilization treatment limits that is the maximum number of times that the handpiece 30 that can be connected to the medical device main body 10 can be sterilized, and a notification operation performed based on each operation A notification setting storage unit 12d that stores an operation program, and an approach notification operation storage unit 12e that stores an operation program of a notification operation performed based on the approach between the handpiece 30 and the connection unit 40 are provided.

As shown in FIG. 1, the operation panel 13 is an input unit that is installed on the front side of the tray table 16 and performs a predetermined operation input, and includes a touch screen, a pointing stick, a switch, or the like. An appropriate input device such as a mouse may be provided.
As shown in FIG. 1, the holder 14 provided on the front side of the operation panel 13 is a handpiece holder in which a dental treatment instrument 20 is arranged.

  As shown in FIG. 1, the monitor 15 is a display unit provided on the back side of the operation panel 13. For example, the monitor 15 includes medical record information such as a patient's sex, age, and last treatment date, and an X-ray imaging apparatus (not shown). An X-ray image relating to a tooth to be treated that has been imaged and generated, a tooth image captured by an intraoral camera (not shown), and the like are displayed.

Tray table 16 is a tray table having a flat plane 16a that is recessed slightly in comparison with the outer frame on the upper surface inside the practitioner, such as the handpiece 30 and switching Kezuko device 5 before connecting to the connection unit 40 in the plane 16a A tool functioning as a component of the operation panel 13 can be placed.

The main body side notification device 17 corresponding to the notification unit and the approach notification unit reads the notification program stored in the notification setting storage unit 12d under the control of the main body side notification operation processing unit 11g and the connection notification operation control unit 11j. This is a notification device that performs a predetermined notification operation.
Specifically, a holder light output unit 17a that visually informs by turning on or blinking an LED lamp by a control process such as the main body side notification operation processing unit 11g is provided at an appropriate position of the holder 14 for each of various handpieces. In addition, a main body side sound output unit 17b that is an output unit that outputs a sound such as a buzzer or sound and a main body side notification monitor 17c that displays a determination result are installed on the left side of the operation panel 13 when the monitor 15 is viewed from the front. Yes.

  Further, as shown in FIG. 2A, the dental treatment instrument 20 includes a connection unit 40 connected to the chair unit 70 via the connection tube 42, and a handpiece 30 corresponding to the medical treatment tool. Are detachably connected.

  The RFID tag 50 is attached to the handpiece-side connecting portion 34 which is a connecting portion of the handpiece 30 connected to the connecting unit 40, and the RFID reader is connected to the unit-side connecting portion 43 which is a connecting portion of the connecting unit 40 connected to the handpiece 30. A writer 60 is provided.

Incidentally, RFID reader-writer 60, be provided in place of the operation panel 13 or the holder 14 such medical device body 10 of the medical device body 10 is not provided on the unit side connection portion 43 is a connection part of the connection unit 40 good.

  Further, in this embodiment, since it is an example of a micromotor handpiece, the handpiece 30 is connected to the motor unit, but other connection joints are used in the air turbine handpiece and other handpieces. Needless to say. The motor unit and other connection joints are collectively referred to as a connection unit 40. In this embodiment, a description will be given based on a micromotor handpiece, but there are various handpieces 30. Furthermore, what connected the various handpieces 30 to the connection unit 40 is generically expressed as an instrument.

  As shown in FIG. 2A, the handpiece 30 corresponding to the medical treatment tool is a head that grips a gripping portion 31 that has a small diameter toward the tip, and a cutting tool 5 that is positioned at the tip of the gripping portion 31. The handpiece side notification unit 33 is provided on the peripheral surface of the rear end side of the grip portion 31 gripped by fingers.

  The handpiece-side notification unit 33 corresponding to the notification unit and the approach notification unit is a notification unit that performs a notification operation that is executed based on a program that is read under the control of the HP notification operation control unit 51f. It is comprised with the handpiece side light output part 33a which alert | reports by lighting or blinking.

  In the present embodiment, the notification is performed by turning on the handpiece-side notification unit 33, but the configuration is not necessarily limited to this configuration. For example, a configuration for notification by sound or vibration may be used, or a combination thereof. There may be.

  As shown in FIG. 2A, the rear end portion of the handpiece 30 is provided with a handpiece-side connection portion 34 that is connected to the distal end portion of the connection unit 40 in the connected state with the connection unit 40. A concave portion 34a that forms a cylindrical space into which the unit side insertion portion 432 can be inserted is formed inside.

  A first drive transmission shaft 311 that is connected to an output shaft 41, which will be described later, is provided at the central portion of the recess 34a in a connected state in which the handpiece 30 and the connection unit 40 are connected.

  The first drive transmission shaft 311 is configured to be rotatable by connecting to an output shaft 41 that rotates as a micromotor (not shown) provided in the connection unit 40 rotates. The transmission shaft 311 can transmit the rotation of the micromotor to the head unit 32 through a plurality of gears (not shown). As a result, the cutting tool 5 held at the tip of the head portion 32 can be rotated.

As shown in FIG. 2A, the handpiece-side connection portion 34 corresponding to the treatment instrument-side connection portion includes a handpiece connection surface 341 formed on the rear end side of the handpiece 30 and an inner peripheral surface of the recess 34a. Are formed of a handpiece inner wall 342, a handpiece outer wall 343 that forms the outer peripheral surface of the handpiece 30, and a positioning projection 344 that protrudes rearward from the handpiece connection surface 341.
As shown in FIG. 2B, the handpiece inner wall 342 constitutes an inner peripheral surface of a recess 34 a that forms a cylindrical space inside the grip portion 31 and has a circular cross section having a predetermined diameter.

The handpiece outer wall 343 is a cylindrical outer peripheral surface that has a diameter larger than the inner diameter of the handpiece inner wall 342 and is formed at the rear end portion of the handpiece 30.
The positioning convex part 344 is a projecting part formed in a substantially rectangular parallelepiped shape projecting rearward from the first drive transmission shaft 311 in the longitudinal direction.

Further, the handpiece 30 is an active RFID that can communicate information in a non-contact manner between the handpiece inner wall 342 and the handpiece outer wall 343 and in the vicinity of the positioning convex portion 344 of the handpiece 30. A tag 50 is provided.
A protruding mechanism 35 in which the columnar body moves back and forth along the longitudinal direction of the handpiece 30 can also be provided between the handpiece inner wall 342 and the handpiece outer wall 343.

  The protrusion mechanism 35 corresponding to the connection failure part is a protrusion mechanism that functions as a notification operation part, and is housed inside the handpiece-side connection part 34 in a state where the handpiece 30 is sterilized. In addition, as a result of the determination process by the sterilization determination unit 11d and the use determination unit 11e, when the handpiece 30 is determined to be unsterilized, the columnar body protrudes backward under the control of the protrusion control unit 51i described later. is there.

  As shown in FIG. 4, the RFID tag 50 corresponding to the identifier includes an RFID control unit 51 that reads a predetermined program and controls the operation of the handpiece 30, an RFID storage unit 52 that stores predetermined information, and a connection unit 40, a communication antenna 53 for communicating with 40, a battery 54 that is a heat-resistant rechargeable battery, a timer 55 that is a clock that counts the date and time, and a temperature measurement unit that measures the temperature outside the handpiece 30 56.

  The RFID control unit 51 includes a CPU, a ROM, and a RAM, and includes a temperature reading unit 51a, a time reading unit 51b, a reading control unit 51c, a communication control unit 51d, an information update control unit 51e, and an HP notification. It comprises an operation control unit 51f, a treatment detection unit 51g, and a sterilization processing number calculation unit 51h. In the case where the protrusion mechanism 35 is provided, the protrusion control unit 51 i is included as a configuration of the RFID control unit 51.

The temperature reading unit 51 a is a control unit that performs reading control of the temperature outside the handpiece 30 measured by the temperature measurement unit 56.
The time reading unit 51b is a control unit that performs reading control of the time (date and time) measured by the time measuring unit 55 when a predetermined situation occurs. Specifically, the time reading unit 51b detects the start and end of driving of the handpiece 30, the connection and disconnection of the handpiece 30 and the connection unit 40, or the temperature measured by the temperature reading unit 51a. When the temperature reaches a predetermined temperature, time reading control is performed.

  The reading control unit 51c controls the reading of information stored in the RFID storage unit 52 and the transmission of a transmission signal for transmitting the read information to the medical device main body 10 to the communication control unit 51d.

  The communication control unit 51d is a control unit that controls communication between the handpiece 30 and the connection unit 40, similarly to the main body side communication control unit 11b. Specifically, a read command transmitted from the connection unit 40 is received, and transmission processing for transmitting the identification information L, the usage detection information U, and the like to the connection unit 40 is controlled.

  The information update control unit 51e is a control unit that controls the temperature read by the temperature reading unit 51a and the time read by the time reading unit 51b to update the information written in the sterilization processing information O and the usage detection information U. is there.

H P JOURNAL intellectual operation control unit 51f by receiving the judgment result of the use determination unit 11e, a control unit for controlling the predetermined notification operation based on the reception result.
The treatment detection unit 51g is a control unit that performs control to receive a drive signal based on the operation of the chair unit 70 and to transmit a read command for reading time from the time measuring unit provided in the RFID tag 50 to the communication control unit 51d.

Sterilization count calculation output portion 51h, in a case of the handpiece 30 was sterilized by autoclaving, with the timing unit 55 measures the "processing temperature 121 ° C.", the processing time measured by the temperature measuring unit 56 is "processing time When the time exceeds 20 minutes, the number of times that the handpiece 30 has been sterilized is calculated as one, and the number of times of sterilization is calculated. .

  The protrusion control part 51i is a control part that constitutes the RFID control part 51, and receives the determination results of the sterilization process determination part 11d and the use determination part 11e, thereby causing the protrusion mechanism 35 to protrude toward the connection unit 40. It is a control part which controls operation | movement or the accommodation operation | movement of the protrusion mechanism 35 which protruded. The protruding mechanism will be omitted because it will be described in detail in Japanese Patent Application No. 2015-155925 filed by the present applicant.

  As shown in FIG. 4, the RFID storage unit 52 is a storage unit that stores information regarding the handpiece 30 including the RFID tag 50, and an identification information storage unit 52 a that stores identification information L that identifies the handpiece 30, Sterilization processing information storage unit 52b for storing sterilization processing information regarding sterilization processing, and usage detection information storage for storing usage detection information U including information related to usage when the use of handpiece 30 is detected and time information corresponding to this information. The unit 52c and a sterilization processing number storage unit 52d for storing the number of sterilization processings.

Here, based on FIG. 5, the identification information L, the sterilization processing information O, and the usage detection information U will be briefly described.
The identification information L is information for the medical device body 10 to identify each handpiece 30, and as shown in FIG. 5A, the serial number of the handpiece is written in the left frame, and next to it. Contains information about the date of manufacture and location. Note that the handpiece information I stored in the handpiece information storage unit 12 a is configured to store driving conditions based on the serial number of the handpiece 30.

  The usage detection information U is information that records the date and time of the start and end of use of the handpiece 30. As shown in FIG. 5B, the time item and the action item correspond to each other. Are lined up. More specifically, the time item includes a year / month / day column and a time column, which are vertically arranged in time series. The contents of the operation corresponding to each time are described next to the time item, and as the contents, any of “drive start”, “drive end”, “connect”, “disconnect” is described. Yes.

  The sterilization information O records the time when the predetermined temperature is reached, the temperature, and the fact that the sterilization process has been performed. As shown in FIG. 5C, the time item corresponds to the temperature item. Are lined up. The time item is composed of a year / month / day column and a time column, which are vertically arranged in a time series, and the temperature with respect to the time is described on the side. If the temperature is 121 ° C. and the time in excess of 20 minutes, it is described as sterilized.

  In this embodiment, the time reading unit 51b is configured to perform time reading control when the temperature reaches a predetermined temperature. However, by always reading the time, the time and temperature are always or periodically read. It is good also as a structure which enumerates.

The communication antenna 53 is a communication unit that transmits and receives a relative distance from the RFID reader / writer 60 within a range of several meters to several centimeters based on communication processing of the communication control unit 53b.
The battery 54 is a rechargeable battery that supplies power to the RFID tag 50 and the handpiece-side notification unit 33 provided on the handpiece 30, and is a heat-resistant battery that can supply power even when the handpiece 30 is autoclaved. Have sex. The battery 54 is configured to be rechargeable by connecting the handpiece 30 and the connection unit 40.

As shown in FIG. 2, the connection unit 40 is a connection body that integrally forms the dental treatment instrument 20 by being connected to the rear end of the handpiece 30, and the tip of the handpiece 30 is included therein. a micromotor (not shown) for causing the switching Kezuko tool 5 that is removably attached to the portion rotationally driven, incorporates an output shaft 41 for transmitting rotation to the tip coupled to the distal end side of the micromotor Yes. Further, the output shaft 41 is connected to the first drive transmission shaft 311 in a connected state with the handpiece 30 so that the rotational driving force of the micromotor can be transmitted to the first drive transmission shaft 311.

  In addition, at the rear end of the connection unit 40, an irradiation power supply connected to a lead wire for driving power supply to a micromotor built in the connection unit 40 or a light guide path of a light source for irradiation of an affected area provided at the front end of the handpiece 30. A connecting tube 42 that houses a lead wire for use is connected. The rear end of the connection tube 42 is connected to the medical device main body 10, and the drive of the connection unit 40 is controlled by the drive control unit 11 f via a drive power supply lead wire.

As shown in FIG. 3, the distal end portion of the connection unit 40 includes a unit-side connection portion 43 that is connected to the handpiece-side connection portion 34 in a connected state with the handpiece 30.
The unit side connection portion 43 corresponding to the main body side connection portion is a unit connection end surface 431 that is a connection surface with the handpiece 30 and a cylindrical unit side that protrudes from the center portion of the unit connection end surface 431 toward the distal end direction. An insertion portion 432, a unit outer wall 433 that forms the outer peripheral surface of the connection unit 40, a positioning recess 434 that is disposed at a position facing the positioning projection 344 in the connected state, and an approach used to detect the approach of the handpiece 30 It comprises a detection sensor 435.

  As shown in FIG. 2 (a), the unit-side insertion portion 432 is a cylindrical tubular body that protrudes in the front end direction with the same length as the depth of the concave portion 34a provided in the grip portion 31, and has an inner diameter in a sectional view. Forms a circle that is one or more times larger than the first drive transmission shaft 311, and forms a circle that is slightly smaller in outer diameter than the handpiece inner wall 342. In addition, an output shaft 41 that is connected to the first drive transmission shaft 311 in the connected state with the handpiece 30 is disposed in the central portion of the internal space formed in the unit side insertion portion 432.

The unit outer wall 433 is an outer peripheral surface formed on the distal end side of the connection unit 40, and the diameter thereof is substantially the same as that of the handpiece outer wall 343. That is, in the connected state of the handpiece 30 and the connection unit 40, the rear end surface of the handpiece 30 and the front end surface of the connection unit 40 are formed flush with each other.
As shown in FIG. 2C, the positioning concave portion 434 is a fitting hole that can be fitted to the positioning convex portion 344 formed above the unit connection end surface 431.

The proximity detection sensor 435 is an proximity detection sensor provided at a position on the unit connection end surface 431 facing the positioning recess 434 when the unit connection end surface 431 is viewed from the front (see FIG. 2C). By irradiating infrared rays from the element and receiving the reflected light by the light receiving element, it is possible to detect the approach, connection, or release of the handpiece connection surface 341 that is the connection surface of the handpiece 30.
Further, the approach of the handpiece 30 may be detected using the strength of the communication signal between the RFID tag 50 and the RFID reader / writer 60 instead of the approach detection sensor 435.

  The unit connection end surface 431 is disposed at a position facing the positioning convex portion 344, and moved so as to connect the handpiece side connecting portion 34 and the unit side connecting portion 43, thereby fitting the positioning convex portion 344. Match. Thereby, the radial positioning of the handpiece 30 and the connection unit 40 can be performed.

Further, an RFID reader / writer 60 is provided between the unit-side insertion portion 432 and the unit outer wall 433 at a position facing the RFID tag 50 in the connected state.
As shown in FIG. 4, the RFID reader / writer 60 corresponding to the reading unit includes an RW communication antenna 61 that transmits and receives information to and from the RFID tag 50.

  The RW communication antenna 61 is a communication antenna that can transmit to and receive from the communication antenna 53 configuring the RFID tag 50.

In this embodiment, the communication form between the RW communication antenna 61 and the communication antenna 53 is a radio wave system in which radio waves are communicated between the two antennas. In this case, a modulator and a double tone modulator may be provided as necessary.
Further, the communication form between the RW communication antenna 61 and the communication antenna 53 is not limited to this form. For example, an electromagnetic wave that is communicated by mutual induction by providing a coil between both antennas and applying a high frequency between the two coils. A coupling method or an electromagnetic induction method may be used.

The patient's treatment using the medical treatment apparatus 1 having such a configuration will be described based on the flowchart shown in FIG.
As preparation for the treatment, the medical diagnostic apparatus 1 is turned on, and patient information of a patient to be examined first is read and displayed on the monitor 15. When the first patient sits on the medical chair 71, the weight change on the medical chair 71 is measured by the weight sensor 71a under the control of the patient change detection unit 11h.

  The practitioner takes out the sterilized handpiece 30 from the sterilization bag in front of the patient sitting on the medical chair 71 and brings the handpiece 30 close to the connection unit 40. Thereby, the medical device main body 10 can detect the handpiece 30 (step s1).

  More specifically, the practitioner brings the handpiece side connection portion 34 closer to the unit side connection portion 43 in order to connect the handpiece 30 and the connection unit 40. Thus, the signal from the RFID tag 50 provided on the handpiece 30 is received by the RFID reader / writer 60 provided on the connection unit 40, and the signal from the RFID tag 50 is received from the RFID reader / writer 60 to the RFID tag 50. A transmission command such as an identification signal is issued.

  In response to this transmission command, the reading control unit 51c stores identification information L stored in the identification information storage unit 52a, sterilization processing information O stored in the sterilization processing information storage unit 52b, and usage stored in the use detection information storage unit 52c. Read control with the detection information U is performed. Then, identification information L, sterilization processing information O, and use detection information U are transmitted from the communication antenna 53 toward the RW communication antenna 61 under the control of the communication control unit 51d. Based on the fact that the RFID reader / writer 60 has received the identification information L, it is determined whether the handpiece 30 can be driven and controlled by the medical device body 10.

Here, the process of determining whether the handpiece 30 can be driven by the medical device main body 10 will be briefly described with reference to FIGS. 7 and 8.
When the connection unit 40 receives the identification information L transmitted from the handpiece 30 (step t1), the handpiece information I stored in the handpiece information storage unit 12a is read under the control of the information reading control unit 11c. Then, the handpiece 30 determines that the serial number of the identification information L and the serial number stored in the handpiece information I are collated by the handpiece identification determination unit 11a to find out whether there is a match. 10 determines whether it can be driven (step t2).

  If it is determined that the handpiece 30 can be driven by the medical device main body 10 as a result of the determination by the handpiece identification determination unit 11a (step t2: Yes), the handpiece identification determination is performed by the control of the main body side communication control unit 11b. The determination result determined by the unit 11a is transmitted to the handpiece 30 (step t3A).

  By receiving the determination result determined by the handpiece identification determination unit 11a (step t3B), the HP notification operation control unit 51f lights the handpiece side notification unit 33 in blue based on the determination result (step t4). ) End the connection determination step. Thereby, without connecting the handpiece 30 and the connection unit 40, the practitioner can know that the handpiece 30 can be connected to the medical device main body 10 and driven and controlled.

  On the other hand, when it is determined by the determination process of the handpiece identification determination unit 11a that the handpiece 30 cannot be driven by the medical device main body 10 (step t2: No), the handpiece is connected via the RW communication antenna 61. The determination result of the identification determination unit 11a is transmitted to the communication antenna 53 (step t5A). Then, based on the reception of the determination result by the communication antenna 53 (step t5B), the handpiece-side notification unit 33 is lit in orange under the control of the HP notification operation control unit 51f (step t6).

  Accordingly, it is understood that the practitioner cannot drive and control the handpiece 30 with the medical device main body 10 without connecting the handpiece 30 and the connection unit 40. Therefore, the connection operation between the handpiece 30 and the connection unit 40 can be stopped, or the practitioner connects the handpiece 30 to the medical device main body 10 by calling the driving condition of the handpiece 30 from, for example, the network. Drive control.

Next, the sterilization processing information O transmitted from the RFID tag 50 and the use detection information U are compared and determined to determine whether the handpiece 30 can be used (step s2).
The determination as to whether or not the handpiece 30 can be used is performed by reading information on whether or not the handpiece 30 has been sterilized from the sterilization processing information O and identifying the state of the handpiece 30 and detecting the use. The end time of use (or time of disconnection) immediately before storing in the information U is compared with the time for performing the sterilization processing stored in the sterilization processing information O, and the sterilization processing is performed after the handpiece 30 is used. And a usability determination step for determining whether or not.

  Specifically, in the sterilization information reading process, under the control of the sterilization process determination unit 11d, the “sterilization process” that is the content of the sterilization process item corresponding to the earliest sterilization process time described in the sterilization process information O is read. , Identifying that the handpiece 30 has been sterilized.

In the next use availability determination step, the latest use end time stored in the use detection information U is compared with the latest sterilization end time stored in the sterilization processing information O under the control of the use determination unit 11e. Determine.
Specifically, under the control of the use determination unit 11e, the latest use end time (14:52 on January 10, 2015) stored in the use detection information U and the latest use stored in the sterilization information O are stored. The sterilization end time (January 10, 2015, 16:52) is read and compared, and it is determined that the handpiece 30 has been sterilized after use (step s2: Yes).

  Along with this determination result (step s2: Yes), the notification program stored in the notification setting storage unit 12d is read under the control of the main body side notification operation processing unit 11g, and the notification program is executed. As a result, “use of the handpiece” is displayed on the main body side notification monitor 17c and the monitor 15, and the HP notification operation control unit 51f based on the determination result being transmitted to the handpiece 30 controls the handpiece side. The notification unit 33 is lit in green. Thereby, the practitioner can recognize that the handpiece 30 has been sterilized, and the handpiece 30 can be connected to the connection unit 40.

In this embodiment, identification of the sterilization state of the handpiece 30 and determination of whether or not sterilization processing has been performed after use of the handpiece 30 are performed in this order. The determination as to whether or not sterilization has been completed after use may be made first.
In addition, when it is determined that the sterilization process has not been performed by the sterilization process determination, only the sterilization process determination can be performed. This eliminates unnecessary processing and reduces the load on the CPU.

  When the practitioner connects the handpiece 30 and the connection unit 40, the connection between the handpiece 30 and the connection unit 40 is determined from the information obtained from the proximity detection sensor 435 provided in the connection unit 40 under the control of the connection determination unit 11i. While detecting (step s3), the drive condition suitable for the handpiece 30 is read from the exchange reference | standard information storage part 12c based on the serial number of the identification information L of the connected handpiece 30 by control of the drive control part 11f (step S3). Step s4).

  As a result, a drive signal corresponding to the amount of depression of the pedal 74a provided in the chair unit 70 is controlled in accordance with the read drive conditions, and is supplied to the handpiece 30 via the drive power supply lead wire built in the connection tube 42. The cutting tool 5 transmitted and attached to the tip of the handpiece 30 rotates (step t5). Thereby, the practitioner can perform a desired treatment on the patient.

  In addition, the treatment detection unit 51g that has received the drive signal based on the depression operation of depressing the pedal 74a performs control to transmit a reading command for reading time from the time measuring unit 55 to the communication control unit 51d. When the RFID reader / writer 60 receives the reading command, the time reading unit 51b and the information update control unit 51e record the driving time read from the time measuring unit 55 in the usage detection information U, and update the usage detection information U sequentially. (Step s6). The use detection information U is updated during the treatment (step s7: No).

  When the practitioner completes the desired treatment for the patient and the practitioner removes his / her foot from the pedal 74a (step s7: Yes), the treatment detection unit 51g detects that the drive signal has been stopped for a predetermined time, and the drive signal Is recorded as the treatment end time in the use detection information U.

  When the patient who has finished the treatment descends from the medical chair 71, it is recognized that the patient has descended from the mass change of the weight sensor 71a measured by the control of the medical device main body 10h (step s8: Yes). Thereafter, when the patient who is the target of the next operation is not seated on the medical chair 71 and the power to the medical device body 10 is turned off (step s9: Yes), the operation is completed. In addition, when the power supply of the medical device main body 10 cannot be turned off (step s9: No), it is continuously detected whether the patient has been changed by the control of the medical device main body 10h (step s8: No).

  On the other hand, when the next patient is seated on the medical chair 71, it is recognized that the next patient is seated on the medical chair 71 due to the mass change of the weight sensor 71a measured by the control of the medical device body 10h (step s8: Yes), the information obtained from the proximity detection sensor 435 is analyzed to detect whether the handpiece 30 is connected to a plurality of connection units 40 (step s10).

  In the present embodiment, the change of the patient is detected when the next patient is seated. However, the change of the patient may be detected when the patient who has finished the treatment has descended from the medical chair 71.

  When the handpiece 30 is not connected to the connection unit 40 (step s10: No), the handpiece 30 that has been sterilized in front of the patient sitting on the medical chair 71 is taken out of the sterilization bag, and the handpiece 30 is removed. Is brought close to the connection unit 40, and the medical device main body 10 detects the handpiece 30 (step s1).

  On the other hand, when the handpiece 30 is connected to any one of the connection units 40 (step s10: Yes), the sterilization time of the handpiece 30 connected to the connection unit 40 And use time are compared and determined by the control of the use determination unit 11e to determine whether sterilization has been completed (step s11).

  That is, when the handpiece 30 connected to the connection unit 40 is not used for the previous patient's treatment, it is determined that the handpiece 30 has been sterilized by the use determination unit 11e (step s11: Yes). ), The driving conditions of the handpiece 30 connected to the connection unit 40 can be read and used for treatment (step s4).

  Moreover, when it determines with the handpiece 30 which is going to connect to the connection unit 40 being unsterilized (step s2: No), the handpiece 30 connected to the connection unit 40 is used for the previous patient. If it is determined that the sterilization is not yet processed (step s11: No), the drive signal to the handpiece 30 is electrically cut off by the control of the drive control unit 11f (step s12).

  Further, under the control of the main body side notification operation processing unit 11g, the holder light output unit 17a is lit red and a buzzer is emitted from the main body side audio output unit 17b. Further, information indicating that the handpiece 30 cannot be used is displayed on the main body side notification monitor 17c or the monitor 15 (step s13).

  Furthermore, the determination results of the sterilization processing determination unit 11d and the use determination unit 11e are transmitted to the communication antenna 53 via the RW communication antenna 61, and the HP notification operation control unit 51f that receives this determination result controls the handpiece side. The notification unit 33 is lit red (step s13).

  By these operations, the practitioner can grasp that the handpiece 30 connected to the connection unit 40 or to be connected has not been sterilized since the previous use, and the patient has not been sterilized. It is possible to reliably prevent the handpiece 30 from being used.

In the blocking and notification operations of these drive signals, the medical device body 10 detects the connection state between the connection unit 40 and the handpiece 30 by analyzing information obtained from the proximity detection sensor 435 under the control of the connection determination unit 11i. If the connection unit 40 and the handpiece 30 are still connected (step s14: No), the notification operation is repeated (step s13 ).

  In a state where such a drive signal is cut off, it is detected by the control of the connection determination unit 11i that the handpiece 30 and the connection unit 40 have been removed based on information from the approach detection sensor 435 (step S1). s14: Yes), the interruption of the drive signal to the handpiece 30 is released by the control of the drive control unit 11f. Therefore, when the practitioner connects the sterilized handpiece 30 to the connection unit 40 (step s3), the sterilized handpiece 30 can be driven and controlled by the medical device body 10 (step s5). ).

  When it is determined that the handpiece 30 to be connected to the connection unit 40 has not been sterilized (step s2: No), the handpiece-side connecting portion 34 is moved back and forth along the longitudinal direction of the handpiece 30. By providing a protrusion mechanism 35 that moves the cylindrical body (see FIG. 2), the connection between the handpiece 30 and the connection unit 40 can be reliably prevented.

More specifically, when it is determined by the determination processing of the sterilization processing determination unit 11d and the use determination unit 11e that the handpiece 30 cannot be used for treatment (step s2: No), the communication antenna 53 receives the determination result. Based on the above, the protrusion control unit 51i performs control to cause the protrusion mechanism 35 to protrude rearward (step s12). Thereby, when it is going to connect the handpiece side connection part 34 and the unit side connection part 43, connection can be obstructed by the protrusion mechanism 35, and the connection of the handpiece 30 and the connection unit 40 can be controlled. .
Note that the use control of the handpiece 30 by the drive control by the drive control unit 11f and the protrusion of the protrusion mechanism 35 can be released by sterilizing the handpiece 30 with an autoclave.

Further, since the RFID tag 50 provided in the handpiece 30 includes the heat-resistant battery 54, the handpiece 30 can be autoclaved alone.
If the handpiece 30 was sterilized in an autoclave, the control information update control unit 51e and a sterilization number calculation output section 51h, and stored in sterilized count storage unit 52d calculates the sterilization accumulated number.

The accumulated number of sterilization treatments stored in the sterilization treatment number storage unit 52d can be used as a basis for determining whether to replace the handpiece 30.
More specifically, under the control of the replacement determination unit 11k, the handpiece 30 is determined by comparing the sterilization processing limit number stored in the replacement reference information storage unit 12c with the sterilization processing integration number stored in the sterilization processing number storage unit 52d. Processing for determining whether or not to replace is performed.

  If it is determined that the handpiece 30 needs to be replaced, the drive signal of the handpiece 30 is electrically interrupted by the control of the drive control unit 11f and the control of the main body side notification operation processing unit 11g. The holder light output unit 17a blinks yellow and a warning sound is emitted from the main body side audio output unit 17b. Further, information indicating that the handpiece 30 should be replaced is displayed on the main body side notification monitor 17c or the monitor 15.

  Thereby, the practitioner can recognize that the number of sterilization treatments of the handpiece 30 has exceeded the sterilization treatment limit number. Further, by using a different warning from that when the handpiece 30 is not sterilized after use, that is, by changing the lighting pattern of the holder light output unit 17a and the warning sound pattern from the main body side audio output unit 17b, It can be appreciated that 30 is not sterilized and needs to be replaced.

  The medical diagnostic apparatus 1 having such a configuration is detachably connectable to the handpiece 30 having the identification information storage unit 52a that stores the unique identification information L of the handpiece 30, and is identifiable. 52e for storing the sterilization processing information O related to the sterilization processing of the handpiece 30 and the change of the patient to be treated is detected. A sterilization process determination unit 11d that reads the sterilization process information O of the handpiece 30 and determines whether the sterilization process has been performed or not yet sterilized based on the patient shift detection unit 11h, and the change detection by the patient change detection unit 11h, and a sterilization process determination With the use restriction unit for restricting the use of the handpiece 30 based on the result of the sterilization unprocessed determination by the part 11d It is possible to prevent the handpiece 30 of the sterilization unprocessed used for post-reversal patients with the following patients replacement.

  More specifically, by providing the patient change detection unit 11h and the sterilization determination unit 11d, it is possible to detect that the patient has changed, and the handpiece 30 connected to the medical device main body 10 when the patient is changed is sterilized. It can be determined whether it has been treated or unsterilized. Since the drive signal is stopped by the control of the drive control unit 11f based on the determination result and the use of the untreated sterilized handpiece 30 for the patient after the change can be restricted, the practitioner can only use the sterilized handpiece 30. Can be used for treatment.

  Further, the handpiece 30 includes an RFID tag 50 including an identification information storage unit 52a, and the RFID reader / writer 60 reads the identification information L from the adjacent RFID tag 50 in a non-contact manner, whereby the medical device main body. When the handpiece 30 scheduled to be connected to 10 has not been sterilized, the sterilization state can be determined without bringing the medical device body 10 and the handpiece 30 into contact with each other. Therefore, it is possible to prevent the medical device body 10 from being contaminated.

  Specifically, the RFID reader / writer 60 is provided in the medical device main body 10 and the RFID tag 50 is provided in the handpiece 30, so that the medical device main body 10 reads the identification information L without contacting the handpiece 30. Can do. Therefore, under the control of the information reading control unit 11c and the sterilization processing determination unit 11d provided in the medical device main body 10, the medical device main body 10 does not contact the handpiece 30 and sterilization processing information O corresponding to the identification information L is obtained. Can be determined whether the handpiece 30 has been sterilized or not yet sterilized.

  As described above, since it is not necessary to bring the handpiece 30 and the medical device main body 10 into contact for the determination of the sterilization treatment, the handpiece 30 to be connected to the medical device main body 10 has not been sterilized. However, it is possible to prevent the handpiece 30 from being connected to the medical device main body 10 and to prevent the medical device main body 10 from being contaminated.

  In addition, the drive control unit 11f is characterized by prohibiting the operation of the handpiece 30 by blocking the drive signal sent from the medical device body 10 to the handpiece 30. When it is determined that the process is to be performed, the drive signal from the medical device main body 10 to the handpiece 30 is not transmitted, and the driving of the handpiece 30 is restricted. Therefore, it is possible to prevent the practitioner from performing an operation using the handpiece 30 used for another patient by mistake.

  The medical device main body 10 is provided with a unit side connection portion 43, and the handpiece 30 is provided with a handpiece side connection portion 34 connected to the unit side connection portion 43, and at least one of the medical device main body 10 is provided with a unit. The protrusion mechanism 35 which forms the connection prevention shape which prevents the connection of the side connection part 43 and the handpiece side connection part 34 can be provided. Thereby, when it is going to connect the sterilization-untreated handpiece 30 and the medical device main body 10, the handpiece 30 and the medical device are formed by the protruding mechanism 35 that forms a connection prevention shape based on the sterilization processing information O. The connection with the main body 10 can be prevented, and the physical connection between the handpiece side connection portion 34 and the unit side connection portion 43 can be reliably prevented.

  Thus, by providing the protrusion mechanism 35, the practitioner cannot physically connect the untreated sterilized handpiece 30 to the medical device main body 10. Therefore, the use of the unsterilized untreated handpiece 30 for other patients can be surely restricted, and the problem of contamination can be prevented.

  In addition, the patient change detection unit 11h detects whether the handpiece 30 has been sterilized or not sterilized before the operation of the patient after the change by detecting the change of the patient based on the sitting of the patient after the next change to be changed. Since the determination can be made, it is possible to prevent the use of the sterilized untreated handpiece 30 for the patient after the change. Therefore, the practitioner can safely treat the patient after the change.

In addition, the patient change detection unit 11h is configured to detect the change of the patient based on the end information of the operation based on the patient getting out of the medical chair 71, so that the patient change after the patient's operation is completed. Before the treatment, it can be determined whether the handpiece 30 has been sterilized or not yet sterilized. As a result, since the use of a non-sterilized medical device can be reliably controlled before the operation of the patient after the replacement, even if it is forgotten to remove the handpiece 30 from the medical device body 10, it is not sterilized. The use of the processing handpiece 30 can be prevented more reliably.
Furthermore, since the handpiece 30 that can be used for the treatment can be confirmed before the treatment of the patient after the change, the practitioner can smoothly perform the treatment of the patient after the change.

  Further, a treatment detection unit 51g that detects the use of the handpiece 30 and a holder light output unit 17a that notifies at least the use of the used handpiece 30 for each handpiece 30 based on the detection result of the treatment detection unit 51g. Since only the holder light output unit 17a of the holder 14 that holds the handpiece 30 actually used for the treatment is notified by being provided in the holder 14, only the notified handpiece 30 may be sterilized. Therefore, the object to be sterilized becomes clear at a glance.

  Moreover, since use can be alert | reported for every handpiece 30, the handpiece 30 which should be replaced | exchanged before performing another patient's treatment can be determined easily. Therefore, the practitioner can clearly and easily determine the handpiece 30 to be replaced, and can perform a smooth treatment.

  Moreover, the holder light output part 17a is a structure which is provided in the holder part of the handpiece 30, and lights or blinks a lamp etc. for every handpiece 30 which should be replaced | exchanged. As a result, the practitioner can recognize that only the handpiece 30 that has been used once has to be sterilized because the lit or blinking lamp is always in the field of view when performing the treatment for the next patient. The reuse of the handpiece 30 can be reliably avoided.

  In addition, a connection determination unit 11 i that detects replacement of the handpiece 30 based on information obtained by the proximity detection sensor 435 and a drive control unit 11 f that releases use restriction of the handpiece 30 are provided. Thus, the use restriction can be released by exchanging the use-restricted handpiece 30 with a sterilized handpiece 30. Thereby, the practitioner can recognize that the handpiece 30 that can be used for the treatment is connected to the medical device body 10. Therefore, the practitioner can concentrate on the treatment without worrying about whether or not the handpiece 30 has been replaced after the change of the patient.

  Further, a sterilization process number storage unit 52d that stores the number of sterilization processes that have been sterilized is provided, and the drive control unit 11f regulates the use of the handpiece 30 based on the sterilization process information O and the number of sterilization processes. By using the feature, it is possible to prevent the handpiece 30 that has deteriorated due to the sterilization treatment from being used for the treatment.

  More specifically, when the handpiece 30 is sterilized using an autoclave, the handpiece 30 is kept under a high temperature and high pressure condition for a predetermined time. There was a risk that it could deteriorate and become unusable during the treatment.

  However, when the drive control unit 11f is configured to restrict the use of the handpiece 30 based on the sterilization processing information O and the number of sterilization processes, the handpiece 30 can be used when the handpiece 30 exceeds the predetermined number of sterilization processes. The use of the handpiece 30 can be restricted and the driving of the handpiece 30 can be prevented from stopping during the treatment. Therefore, the practitioner can perform the operation with peace of mind.

  Further, by providing a replacement determination unit 11k that determines whether or not the handpiece 30 needs to be replaced based on the number of times of sterilization, and a monitor 15 that performs predetermined notification based on the determination result of the replacement determination unit 11k, Even if the piece 30 has been sterilized, the practitioner can recognize that the handpiece 30 should be replaced before the operation, and can replace the handpiece 30 with a usable one. Thereby, it is possible to perform the treatment smoothly without exchanging the handpiece 30 during the treatment, and it is possible to prevent the patient from feeling uneasy.

  Moreover, when it is set as the structure which can set the processing temperature and processing time of an autoclave to the optimal processing temperature and time according to the handpiece 30, the judgment criteria of durability of the handpiece 30 change according to these processing conditions. However, since the number of sterilization treatment times 51h is provided, the number of sterilization treatments can be converted into the number of sterilization treatments based on the standard number of sterilization treatments according to the sterilization treatment conditions. Even if the sterilization conditions are different, the number of times the handpiece 30 has been sterilized can be calculated according to a predetermined standard. Thereby, for example, the limit number of sterilization processes of the handpiece 30 stored in advance in the replacement reference information storage unit 12c and the integrated value of the calculated number of sterilization processes can be compared and determined to notify the necessity of replacement of the handpiece 30. The practitioner can grasp the replacement time of the handpiece 30.

  As described above, even when sterilization is performed under various sterilization conditions, the replacement time of the handpiece 30 can be determined based on a predetermined standard. Even when sterilization is performed over a longer period of time, the practitioner can accurately grasp the replacement time of the handpiece 30, and a sterilization apparatus with a near replacement time can be safely operated. The piece 30 can be replaced in advance.

  In addition, the sterilization processing determination unit 11d compares and determines the sterilization time and the use time of the handpiece 30 to determine whether the sterilization process has been performed or not yet sterilized, thereby determining the use time of the handpiece 30 and the sterilization process. It is possible to determine whether the handpiece 30 has been sterilized or not yet sterilized on the basis of the time of the above, and to accurately determine the front and back of the use time of the handpiece 30 and the sterilization time.

  That is, the handpiece 30 that has not been sterilized after use is connected to the medical device main body 10, or the handpiece 30 that has been used after sterilization is connected to the medical device main body 10. Since it can be determined that the piece 30 has not been sterilized, use of the handpiece 30 that has not been sterilized can be reliably regulated.

  In addition, for example, in the case of comparing and determining the date and time of the sterilization process and the date and time of the handpiece 30, the sterilization process is performed after the handpiece 30 is used, that is, it is determined that the sterilization process is completed and usable. However, since the time has passed since the sterilization process, it can be determined whether the sterilization process is necessary again, and the reuse of the handpiece 30 can be prevented.

In the correspondence between the configuration of the present invention and the above-described embodiment, the medical treatment tool corresponds to the handpiece 30.
The reading unit corresponds to the RFID reader / writer 60,
The shift detection unit corresponds to the patient shift detection unit 11h,
The use restriction unit corresponds to the drive control unit 11f,
The identifier corresponds to the RFID tag 50,
The main body side connection portion corresponds to the unit side connection portion 43,
The surgical instrument side connection portion corresponds to the handpiece side connection portion 34,
The connection obstacle corresponds to the protruding mechanism 35,
The use detection unit corresponds to the treatment detection unit 51g,
The usage notification unit and the replacement notification unit correspond to the holder light output unit 17a and the handpiece side notification unit 33 ,
The exchange detection unit corresponds to the connection determination unit 11i,
The restriction release unit corresponds to the drive control unit 11f,
The replacement determination unit corresponds to the replacement determination unit 11k. However, the present invention is not limited to the configuration of the above-described embodiment, and many embodiments can be obtained.

  For example, the usage notification unit and the replacement notification unit correspond to the holder light output unit 17a, but the monitor 15, the main body side audio output unit 17b that is an output unit that outputs sound such as a buzzer or sound, and the determination result May be handled by the main body side notification monitor 17c.

  In addition, as the usage notification unit and the replacement notification unit, a configuration for notifying that the handpiece 30 has been used or needs to be replaced by vibrating the handpiece 30 to be used after the change of the patient is detected. It may be.

  In this embodiment, the number of sterilization treatments is configured to count the number of sterilization treatments when the sterilization treatment conditions exceed the standard sterilization treatment conditions. Handpiece 30 based on the number of sterilization treatments calculated by providing a load coefficient based on the difference between them, the number of sterilization treatments obtained by adding a predetermined number of times to a predetermined sterilization treatment condition, and the integrated value of the number of sterilization treatments The number of sterilization treatments calculated in consideration of the deterioration of the liquid may be used.

In this embodiment, the sterilization process is a sterilization process using an autoclave that is sterilized in a high-temperature and high-pressure environment. However, the sterilization process does not necessarily need to be an autoclave. Immersion sterilization treatment for immersing in a solution, plasma sterilization treatment using low-temperature plasma, radiation sterilization treatment for sterilization by irradiating radiation such as gamma rays or electron beams may be used.
Even when these sterilization treatments are used, the number of sterilization treatments can be calculated by the sterilization treatment number calculation unit 51h based on the reference value in each sterilization treatment.

  Further, in this embodiment, the change of the patient is detected based on the mass change measured by the weight sensor 71a. However, the present invention is not limited to this embodiment, and the end of the patient's treatment is detected, What is necessary is just to detect that the medical preparation of the patient after a change which is a patient's next patient is completed.

  For example, as shown in FIG. 9, an image capturing camera 75 that captures an image of a patient's face may be provided above the medical chair 71 to recognize the patient's face and the like. By providing the image capturing camera 75 in this way, it is possible to detect whether the patient has changed by capturing the patient seated on or away from the medical chair 71.

  In addition, captured image data can be stored as patient information. Then, when the patient is seated on the medical chair 71 from the next time onward, it is possible to detect whether the patient has changed by collating the newly captured image with the image recorded in the patient information and searching for the feature points.

  In addition to the above, the change of the patient is detected based on reception of the raising / lowering signal of the medical chair 71, switching of the patient's medical chart information, detection of the weight of the patient after the change, and reception of the treatment start / end signal by the practitioner. Various configurations can be adopted.

  In the present embodiment, the RFID tag 50 is configured to have a communication function with the RFID reader / writer 60. However, the communication function is not limited to RFID, and a communication function using radio waves in the same manner as RFID, A communication function using infrared rays, a communication function using magnetic force, a communication function using light such as a barcode or a QR code (registered trademark), a communication function using image recognition, and the like may be used.

  In the present embodiment, the RFID tag 50 is used as an identification body. However, any configuration may be used as long as the identification information L can be communicated. Each of the medical instruments may include a resistor, a coil, a capacitor, or the like having different specific values that are provided in advance for each of the medical instruments. When these identification bodies are used, an identification signal is transmitted to the medical device main body 10 via an electric wire or the like arranged in the connection tube 38. In addition, as the reading unit, the handpiece 30 can be identified by the handpiece identification determination unit 11 a provided in the medical device body 10.

  Furthermore, the RFID reader / writer 60 can be provided on the tray table 16. Thereby, the medical device main body 10 can be identified without contacting the handpiece 30 placed on the flat surface 16a with the connection unit 4040, and it can be determined whether the handpiece 30 is sterilized without removing it from the bag. .

  In addition, as an example of a medical device according to the present invention, a dental device has been described as an example. However, the present invention is not limited to a dental device, and is also used as a medical device for oral surgery, otolaryngology, obstetrics / gynecology, ophthalmology, etc. it can.

DESCRIPTION OF SYMBOLS 1 Medical treatment apparatus 10 Medical equipment main body 17a Holder light output part 11d Sterilization process determination part 11g Drive control part 11i Connection determination part 11h Replacement detection part 11k Replacement determination part 20 Dental instrument 30 Handpiece 34 Handpiece Side connection unit 35 Projection mechanism 40 Connection unit 43 Unit side connection unit 435 Approach detection sensor 50 RFID tag 51g Use detection unit 52a Identification information storage unit 52b Sterilization process information storage unit 52d Sterilization process number storage unit 60 RFID reader / writer L Identification information O Sterilization information U Use detection information

Claims (13)

A medical treatment instrument having an identification information storage unit that stores unique identification information, and a medical device body that is detachably connectable to the medical treatment instrument and includes a reading unit that reads the identification information A medical medical device comprising:
A sterilization process information storage unit for storing sterilization process information related to the sterilization process of the medical treatment instrument;
A sterilization process determination unit that reads the sterilization process information of the medical treatment tool and determines whether it has been sterilized or unprocessed;
Based on the determination result of the sterilization unprocessed by the sterilization determination unit, a use regulation unit that regulates use of the medical treatment tool,
A use detector for detecting the use of the medical instrument;
Based on the detection result of the use detection unit, a use notification unit that notifies at least the use of the used medical treatment tool for each medical treatment tool is provided,
The medical treatment tool is:
A surgical instrument side connection portion connected to a main body side connection portion provided in the medical device main body is provided,
At least one of the medical treatment tool or the medical device main body,
A medical medical device provided with a connection obstacle part that functions as the use restricting part and forms a connection prevention shape that prevents connection between the main body side connection part and the surgical instrument side connection part. The medical treatment tool is:
An identification body comprising the identification information storage unit is provided,
The reading unit is
The medical diagnosis apparatus according to claim 1, wherein the identification information is read in a non-contact manner from the identification object that is in proximity. The use restriction unit is
Medical care apparatus according to claim 1 or claim 2 to inhibit the operation of the medical practitioner instrument by the operation signal sent to the medical device body or al the medical practitioner tool. An exchange detection unit for detecting exchange of the medical treatment tool;
The medical treatment apparatus according to any one of claims 1 to 3 , further comprising a restriction release unit that releases use restriction of the medical treatment tool by the use restriction unit based on the sterilization information. . A sterilization processing number storage unit for storing the number of sterilization processing performed the sterilization processing,
The use restriction unit is
The medical treatment apparatus according to any one of claims 1 to 4 , wherein use of the medical treatment tool is regulated based on the sterilization information and the number of sterilization processes. A replacement determination unit that determines whether or not replacement of the medical treatment tool is necessary based on the number of times of sterilization;
The medical treatment apparatus according to claim 5 , wherein use of the medical treatment tool is regulated based on the sterilization information and a determination result of the replacement determination unit. The sterilization determination unit
The medical treatment according to any one of claims 1 to 6 , wherein the sterilization treatment time and the use time of the medical treatment tool are compared and determined to determine whether the sterilization treatment is performed or not. apparatus. A medical treatment tool that is detachably attached to a medical device body,
A sterilization process information storage unit for storing sterilization process information related to the sterilization process;
The use restricting portion for restricting the use on the basis of the sterilization process information reading Nde the sterilization unprocessed by the sterilization process determination unit determines whether or sterilization untreated sterilization processed determination result of the medical treatment device,
A surgical instrument side connection portion connected to a main body side connection portion provided in the medical device main body is provided,
In the surgical instrument side connection part,
The use and function as restricting portions, connection failure portion forming a connection preventing shape for preventing the connection between the body-side connecting part is provided, et al is,
A use detection unit that detects that the treatment has been used;
A medical treatment tool provided with a use notification unit that notifies use based on a detection result by the use detection unit . Provided with identifying object with the identification information storage unit you store individual identification information,
The medical treatment tool according to claim 8 , wherein the identification information is read into the medical device body in a non-contact manner by an approach of a reading unit provided in the medical device body. The use restriction unit is
Medical practitioner tool according to claim 9 for inhibiting the operation of the medical practitioner instrument by the operation signal to be sent to the medical device body or al the medical practitioner tool. Based on the sterilization detection by the sterilizing detection unit which detects that performing the sterilization treatment, medical treatment tool according to <br/> claim 9 or 10 using restriction is released. A sterilization processing number storage unit is provided for storing the number of sterilization processing performed the sterilization processing,
The use restriction unit is
Medical practitioner tool according to any one of the sterilization process information and the sterilization claims use of the medical practitioner tool is Ru is regulated based on the number of times to claim 9 or claim 11. The medical treatment according to claim 12 , wherein a predetermined notification is performed based on a determination result of a replacement determination unit that determines whether or not the medical treatment tool needs to be replaced based on the number of times of sterilization. Ingredients.

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