WO2011108179A1 - Capsule drug delivery device - Google Patents
Capsule drug delivery device Download PDFInfo
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- WO2011108179A1 WO2011108179A1 PCT/JP2011/000171 JP2011000171W WO2011108179A1 WO 2011108179 A1 WO2011108179 A1 WO 2011108179A1 JP 2011000171 W JP2011000171 W JP 2011000171W WO 2011108179 A1 WO2011108179 A1 WO 2011108179A1
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- WIPO (PCT)
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- unit
- capsule
- information
- imaging
- comparison
- Prior art date
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- 239000002775 capsule Substances 0.000 title claims abstract description 111
- 238000012377 drug delivery Methods 0.000 title description 3
- 239000003814 drug Substances 0.000 claims abstract description 154
- 229940079593 drug Drugs 0.000 claims abstract description 131
- 238000012545 processing Methods 0.000 claims abstract description 96
- 238000003384 imaging method Methods 0.000 claims description 183
- 238000012795 verification Methods 0.000 claims description 99
- 238000004891 communication Methods 0.000 claims description 28
- 238000009825 accumulation Methods 0.000 abstract description 2
- 239000003795 chemical substances by application Substances 0.000 abstract 5
- 230000037406 food intake Effects 0.000 abstract 2
- 238000000034 method Methods 0.000 description 24
- 201000010099 disease Diseases 0.000 description 20
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 20
- 230000008569 process Effects 0.000 description 17
- 238000003745 diagnosis Methods 0.000 description 14
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- 230000006870 function Effects 0.000 description 8
- 230000005540 biological transmission Effects 0.000 description 6
- 238000012790 confirmation Methods 0.000 description 5
- 238000002347 injection Methods 0.000 description 5
- 239000007924 injection Substances 0.000 description 5
- 230000008859 change Effects 0.000 description 4
- 238000002591 computed tomography Methods 0.000 description 4
- 239000003550 marker Substances 0.000 description 4
- 230000003287 optical effect Effects 0.000 description 4
- 238000002600 positron emission tomography Methods 0.000 description 4
- 238000001514 detection method Methods 0.000 description 3
- 238000001647 drug administration Methods 0.000 description 3
- 230000006872 improvement Effects 0.000 description 3
- 241000167880 Hirundinidae Species 0.000 description 2
- 239000003153 chemical reaction reagent Substances 0.000 description 2
- 238000003780 insertion Methods 0.000 description 2
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- 238000007689 inspection Methods 0.000 description 2
- 230000003340 mental effect Effects 0.000 description 2
- 230000001629 suppression Effects 0.000 description 2
- 210000001015 abdomen Anatomy 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000001839 endoscopy Methods 0.000 description 1
- 210000001035 gastrointestinal tract Anatomy 0.000 description 1
- 238000005286 illumination Methods 0.000 description 1
- 238000001727 in vivo Methods 0.000 description 1
- 230000010354 integration Effects 0.000 description 1
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- 210000000214 mouth Anatomy 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- 239000004065 semiconductor Substances 0.000 description 1
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- 238000003325 tomography Methods 0.000 description 1
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Images
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B1/00—Instruments for performing medical examinations of the interior of cavities or tubes of the body by visual or photographical inspection, e.g. endoscopes; Illuminating arrangements therefor
- A61B1/04—Instruments for performing medical examinations of the interior of cavities or tubes of the body by visual or photographical inspection, e.g. endoscopes; Illuminating arrangements therefor combined with photographic or television appliances
- A61B1/041—Capsule endoscopes for imaging
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M31/00—Devices for introducing or retaining media, e.g. remedies, in cavities of the body
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M31/00—Devices for introducing or retaining media, e.g. remedies, in cavities of the body
- A61M31/002—Devices for releasing a drug at a continuous and controlled rate for a prolonged period of time
Definitions
- the present invention relates to a capsule-type dosing device that dispenses when it is orally injected and moves through a body cavity to reach the affected area, and includes a large-scale medical diagnostic apparatus and dosing timing for specifying the affected area position in advance.
- the present invention relates to a technique for simplifying handling by eliminating the need for a patient-mounted extracorporeal device for determination and a wireless transceiver for transmitting and receiving verification information.
- the doctor specifies that the capsule position has been reached based on the information wirelessly transmitted from the orally-administered capsule to the extracorporeal device, and that the doctor has reached the affected part. It is known to give a medication instruction after confirmation and realize medication.
- the medication position specifying device 31 uses a medical diagnostic device such as an X-ray CT device, MRI, PET, an X-ray observation device, an ultrasonic observation device, and a bed 33 or a detector 33 for acquiring image information. have.
- a medical diagnostic device such as an X-ray CT device, MRI, PET, an X-ray observation device, an ultrasonic observation device, and a bed 33 or a detector 33 for acquiring image information. have.
- the medication operation by the medication position specifying device 31 will be described.
- the patient P of the medication position specifying device 31 attaches the extracorporeal device 35 to the abdomen with a belt under the instruction of the doctor, attaches the three-dimensional marker 40 to the extracorporeal device 35, and lies on the bed 32.
- the doctor moves the bed 32 into a detector (gantry) 33 by a PC (personal computer) 34 and operates the detector 33 to perform X-ray imaging of the patient P.
- the image information obtained by photographing is taken into the PC 34 and subjected to predetermined processing, and then displayed on the display monitor 34a. In the displayed image, the spherical bodies 44, 45, 46, and 47 of the three-dimensional marker 40 are also displayed.
- the doctor makes an in-vivo diagnosis based on the display image, identifies the affected part X and the position of the affected part X that require medication, and records the position information of the affected part X from the PC 34 to the memory 53 in the external device 35 attached to the patient.
- the three-dimensional marker 40 is then removed from the extracorporeal device 35 and the patient P swallows the medication capsule 10. Thereafter, the patient P may leave the medical institution (however, the extracorporeal device 35 remains worn).
- the medication capsule 10 moves inside the body while transmitting radio waves to the outside by the information transmitting unit 12.
- the transmitted radio wave is received by the extracorporeal receiving unit 50 built in the extracorporeal device 35 attached to the patient and sent to the determining unit 51.
- the determination unit 51 calculates the position of the medication capsule 10 relative to the extracorporeal device 35 based on the reception level and reception direction of the transmitted radio wave, and is recorded in the memory 53 and the calculated location information of the medication capsule 10.
- the position information of the affected part X is compared, and if both match, a release signal is transmitted to the inside of the body via the extracorporeal transmission unit 52.
- the transmitted release signal is received by the receiving unit 15 in the medication capsule 10, and the medicine A in the reservoir 13 is released by the control unit 16. That is, the medicine A is released at the position of the affected part X specified by the specifying device 31, and the medicine is directly administered to the affected part X.
- Reference numeral 17 denotes a battery.
- a capsule medication system shown in FIGS. 9A and 9B is also disclosed.
- the patient P first undergoes endoscopy at a medical institution.
- the doctor makes a diagnosis based on the image obtained by the specifying device (endoscopic device) 100, and specifies the position of the affected part requiring medication.
- the PC 109 converts the image data of the specified affected part, and records the converted data in the intracapsule memory 131 of the medication capsule 130 by data transmission between the wireless transmission unit 136 and the intracapsule reception unit 135.
- the patient P then swallows the medication capsule 130.
- the patient may leave the medical facility after swallowing the capsule.
- the medication capsule 130 moves while imaging the patient's body by the imaging unit 91.
- the acquired captured image is sent to the capsule determination unit 133.
- the movement amount detection unit 132 sends the movement amount information to the in-capsule determination unit 133.
- the in-capsule determination unit 133 processes the movement amount information of the medication capsule 130 that has been sent.
- the determination unit 133 determines that the medication capsule 130 has reached the vicinity of the affected part, and notifies the control unit 16 In response to this, the control unit 16 releases the medicine A. Since the release of the medicine is controlled inside the medication capsule 130, the patient P does not need to wear an extracorporeal device, and the patient P has a high degree of freedom.
- 92 is an objective lens
- 93 is an image sensor
- 94 is an LED for illumination.
- a CT Computer Tomography
- an X-ray observation apparatus an MRI (Magnetic Resonance)
- MRI Magnetic Resonance
- Imaging PET (Positron Emission Tomography)
- ultrasonic tomographic observation apparatus ultrasonic tomographic observation apparatus
- endoscope apparatus and other medical diagnostic apparatuses are used.
- these apparatuses are too large and have difficulty in use.
- a heavy burden is imposed. In particular, when it takes a long time for the capsule to reach the affected area, the burden is large.
- the endoscope apparatus includes an endoscope apparatus main body 101, a body cavity insertion section 102, an image acquisition apparatus 103, an operation section 104, a light source apparatus 105, an image processor apparatus 106, a display monitor 107, a mouthpiece 108, and an insertion amount detection.
- This is a large-scale device including a device 108a, a PC (personal computer) 109, and a wireless transmission unit 136.
- the medication capsule 130 also has a complicated structure such as the capsule determination unit 133, the capsule reception unit 135, the capsule memory 131, the movement amount detection unit 132, the timer circuit 134, the movement distance measurement unit 111, and the integration unit 137. is doing.
- the image information serving as a comparison reference is transferred and stored in the in-capsule memory 131, so that the extracorporeal device may be removed, and the burden on the patient is reduced.
- the in-capsule memory 131 it is necessary to provide the wireless transmission unit 136 in the medication position specifying device 100 and to provide the in-capsule reception unit 135 in the medication capsule 130. That is, the structure is large and the operational burden is large.
- FIG. 9 is a combination of units each provided independently of the endoscope apparatus 100, the PC 109, the wireless transmission unit 136, and the medication capsule 130. All of the conventional examples are called “capsule dosing systems” and are literally systems. The system exchanges information through a complicated route.
- the present invention has been created in view of such circumstances, and includes a large-scale medical diagnostic apparatus for specifying an affected part position and storing the specified affected part position in a capsule, and an extracorporeal apparatus for determining a medication timing.
- An object of the present invention is to provide a capsule-type dosing device that can be made unnecessary, simplify handling, and simplify the internal structure of the capsule.
- the present invention solves the above problems by taking the following measures.
- the capsule-type dosing device according to the present invention has the following components. In this section, it is possible to refer to FIG. 1 in the case of Example 1 described later.
- the present invention It is equipped with a capsule that can be moved through the body cavity that is orally injected to reach the affected area in the body,
- the capsule includes a drug holding unit, an imaging unit, an imaging signal processing unit, a collation information storage unit, a comparison unit, and a drug release unit.
- the drug holding unit holds a drug to be administered to an affected part in the body cavity or an affected part in the vicinity of the body cavity,
- the imaging unit is configured to be able to generate a first imaging signal by capturing an original on which collation information related to characteristics of the affected part is posted before the capsule is orally introduced into the living body.
- the imaging signal processing unit After the capsule is orally injected into the living body, the inside of the body cavity leading to the affected area is continuously or intermittently photographed to photograph the second imaging signal,
- the imaging signal processing unit generates the verification information from the first imaging signal and the image information from the second imaging signal,
- the verification information storage unit stores the verification information,
- the comparison unit compares the verification information stored in the verification information storage unit with the image information generated by the imaging signal processing unit, When the comparison determination result between the image information and the collation information is coincident in the comparison unit, the drug release unit releases the drug from the drug holding unit toward the affected part.
- the imaging unit is a means for capturing an image of an affected part in the body and acquiring an imaging signal.
- the imaging unit accumulates a signal charge corresponding to the amount of incident light, photoelectrically converts it, and outputs it.
- the drug holding unit is means for holding a drug to be released to the affected part in advance in the capsule.
- the drug release unit is a means that operates according to a control signal when the capsule reaches the affected part and releases the drug from the drug holding part toward the affected part.
- the capsule itself has a function of determining that the capsule has reached the affected area.
- An imaging signal processing unit for converting the imaging signal acquired by the imaging unit into image information is required, but this is not provided outside the capsule but is included in the capsule-type dispensing device itself.
- a verification information storage unit that stores the verification information in advance It is a requirement that the comparison unit for comparing the image information with the collation information is also provided in the capsule-type dispensing device itself, not outside the capsule.
- the form of storing verification information in the verification information storage unit is simple. That is, information obtained by photographing with an imaging unit incorporated in the capsule and signal-processed by the imaging signal processing unit incorporated in the capsule is used as collation information. Before the capsule is placed orally, the capsule-type dosing device is turned on, the imaging unit, the imaging signal processing unit, and the verification information storage unit are started, and then the original with the verification source information is taken and the verification source Information is taken in, and further image processing is performed to generate verification information, which is stored in the verification information storage unit. Accumulation of the collation information in the collation information storage unit is extremely simple as compared with a method of acquiring collation information using a large-scale medical diagnostic apparatus in the case of the prior art.
- the verification source information in the original includes the previously captured image data of the disease of the person or similar patient, color information that can identify the disease, reaction color information of the affected area in the state where the reagent has been added in advance, and the size of the disease It is preferable to obtain information such as information on a disease, information on the shape of a disease and the like, which are relatively easily available.
- the capsule-type dosing device may be stored in a fixed manner (ROM specification).
- Such collation information is obtained using a large-scale medical diagnostic apparatus such as an X-ray CT apparatus, an endoscopic apparatus, an MRI, a PET, an X-ray observation apparatus, and an ultrasonic tomography observation apparatus as in the prior art. It is not something to get.
- This is image information photographed and generated via an image capturing unit and an image signal processing unit included in the simple capsule-type dispensing device itself.
- the present invention eliminates the need for a medical diagnostic device that is large in order to obtain collation information and an extracorporeal device that is attached to the patient to determine the arrival of the affected part of the capsule. .
- the present invention eliminates the need for a large-scale medical diagnostic apparatus for acquiring the collation information, and wirelessly accumulates the collation information in the collation information storage unit built in the capsule. Does not require a transceiver.
- a patient-mounted extracorporeal device that determines the arrival of the affected part position of the capsule and transmits a release signal required in the prior art, and a large scale for obtaining the verification information and specifying the affected part position
- a medical diagnostic device and a wireless transceiver for storing verification information in a verification information storage unit with a built-in capsule are not necessarily required.
- the original image in which the verification source information is captured is captured by the imaging unit in advance to generate the first imaging signal, and the imaging signal processing unit performs image processing on the first imaging signal, thereby verifying the verification information.
- the generated verification information is stored in the verification information storage unit.
- the second imaging signal acquired by the imaging unit when the capsule moves through the body cavity is converted into image information by the imaging signal processing unit and passed to the comparison unit.
- the comparison unit compares the image information sent from the imaging signal processing unit with the verification information read from the verification information storage unit.
- the comparison unit activates the drug release unit to release the drug held in the drug holding unit toward the affected part during a period in which the comparison determination results indicate coincidence.
- a large-scale medical diagnostic apparatus for acquiring collation information or specifying the position of an affected part, a wireless transceiver for accumulating collation information in a collation information storage unit built in the capsule, It does not require a patient-mounted extracorporeal device that determines whether the affected area has reached the position or transmits a release signal, and can be handled easily. Inspection personnel who judge image matching are also unnecessary.
- a series of procedures relating to direct administration of a drug to the affected area such as acquisition and holding of verification information, drug delivery, imaging of a body cavity / affected area, signal processing, image information verification, drug release, etc. Since it is configured so that it can be performed completely, an extracorporeal device worn by the patient, a large-scale medical diagnostic device, and a wireless transmitter / receiver for transmitting / receiving collation information become unnecessary, and handling is simplified correspondingly.
- FIG. 1 is a block diagram showing a configuration of a capsule-type dispensing device according to Embodiment 1 of the present invention.
- FIG. 2 is a block diagram showing the configuration of the capsule-type dosing device according to the second embodiment of the present invention.
- FIG. 3 is a flowchart showing the processing of the capsule dosing device according to the second embodiment of the present invention.
- FIG. 4 is a block diagram showing the configuration of a capsule-type dispensing device in Embodiment 3 of the present invention.
- FIG. 5 is a block diagram showing a configuration of a capsule-type dispensing device according to Embodiment 4 of the present invention.
- FIG. 6 is a flowchart showing processing of the capsule dosing device according to the fourth embodiment of the present invention.
- FIG. 1 is a block diagram showing a configuration of a capsule-type dispensing device according to Embodiment 1 of the present invention.
- FIG. 2 is a block diagram showing the configuration of the capsule-type dosing
- FIG. 7 is a configuration diagram of a capsule-type dispensing device according to Embodiment 5 of the present invention. It is the 1st figure showing the example of a capsule medication system in the prior art. It is a 2nd figure which shows the example of a capsule dosing system in a prior art. It is a 3rd figure which shows the example of a capsule dosing system in a prior art. It is a 4th figure which shows the example of a capsule dosing system in a prior art. It is a 1st figure which shows the example of a capsule dosing system of another aspect in a prior art. It is a 2nd figure which shows the example of the capsule dosing system of another aspect in a prior art.
- the capsule-type dosing device of the present invention having the above configuration ⁇ 1> can be further advantageously developed in the following embodiment.
- the capsule further includes a first information input unit.
- the first information input unit is configured to be able to input additional verification information to be added to the verification information or to update the verification information before the capsule is orally injected into the living body, and the verification information storage unit The collation information obtained by adding the additional collation information input to the first information input unit is stored.
- the first information input unit is activated in advance to store the latest verification information in the verification information storage unit.
- FIG. 2 it is possible to refer to FIG. 2 in the case of Example 2 described later.
- the latest and current patient information that is suitable for collation should be collated with respect to the collation information to be collated with the image information obtained by the imaging unit and the imaging signal processing unit while the capsule is moving around the body cavity or the affected part. It is possible to use additional or updated verification information corresponding to the disease. As a result, the timing at which the drug release unit should release the drug toward the affected part can be determined with higher accuracy.
- ⁇ 3 When using the capsule-type dosing device, the purpose and conditions of treatment and diagnosis are generally different for each patient.
- the purpose and conditions of treatment and diagnosis such as the type of disease in the affected area, the degree and condition of the disease, the surrounding situation of the affected area, the distance and speed of movement of the capsule to the affected area, the size of the capsule, the amount and strength of the drug used, and the patient It varies from patient to patient. Therefore, it is desirable to set the operation mode in the imaging unit and the operation mode in the imaging signal processing unit in accordance with the purpose and conditions of treatment and diagnosis for each patient.
- a second information input unit capable of setting modes relating to the operation of the imaging unit and the imaging signal processing unit is further provided. It goes without saying that the second information input unit is also built in the capsule.
- the second information input unit may be configured to have the function of the first information input unit of ⁇ 2 >>. In this section, it is possible to refer to FIG. 2 in the case of Example 2 described later.
- the second information input unit sets the operation mode in the imaging unit and / or the operation mode in the imaging signal processing unit for the purpose and condition of treatment and diagnosis. Set according to the change of.
- both the imaging unit and the imaging signal processing unit can be set to an operation mode suitable for the purpose and condition of treatment and diagnosis for each patient.
- the accuracy of drug release through image matching can be made higher.
- ⁇ 4 The capsule-type dosing device administers the drug to the affected area, but it is desirable to be able to visually grasp the actual state of the drug administration, not just the drug administration. That is.
- image information at least when the comparison determination result of the comparison unit indicates coincidence is important for diagnosis / treatment.
- the image information acquired and generated by the imaging unit / imaging signal processing unit is notified from the capsule to the outside.
- a wireless communication unit is provided. Needless to say, this wireless communication unit is also incorporated in the capsule.
- the image information does not necessarily have to be from the initial stage of oral injection, and may be from at least the point of coincidence determination by the comparison unit. In this section, it is possible to refer to FIG. 4 in the case of Example 3 described later.
- the timing of notification to the outside is when the comparison determination result matches, and notification is not performed until that time, so that power consumption can be suppressed.
- ⁇ 5 Regarding the function of the wireless communication unit configured as described in ⁇ 4> above, it is preferable to further notify the background of the comparison determination by the comparison unit and the comparison determination result to the outside. This makes it possible to easily confirm the success or failure of direct administration of the drug to the affected area.
- ⁇ 6> In the configurations of ⁇ 4> and ⁇ 5 >> with the wireless communication unit added, the imaging resolution is coarsened to reduce power consumption during the period when the comparison determination result indicates inconsistency, and the imaging is performed during the period when the result indicates coincidence. It is conceivable that image information with a large amount of information is notified externally by a wireless communication unit with a fine resolution. In this section, it is possible to refer to FIG. 5 in the case of Example 4 described later.
- Such a configuration can be expected to improve the accuracy of confirmation of the medication result through high definition of the medication image to be notified to the outside while suppressing power consumption.
- FIG. 1 is a block diagram showing the configuration of a capsule-type dosing device in Embodiment 1 of the present invention.
- reference numeral 20 denotes a capsule which is orally introduced into a living body and can move through a body cavity from an oral cavity to an affected area where a medicine is to be administered in the living body.
- the capsule 20 has a shape in which both ends of the cylinder are hemispherical.
- Reference numeral 1 denotes an imaging unit that images a body cavity from the time of oral injection to the affected part.
- the imaging unit 1 includes a CCD image sensor, a MOS image sensor, or the like that accumulates a signal charge corresponding to the amount of incident light, photoelectrically converts it, and outputs it. .
- An imaging signal processing unit 2 generates image information from the imaging signal acquired by the imaging unit 1.
- Reference numeral 3 denotes a collation information storage unit composed of a semiconductor memory or the like that accumulates collation information related to the characteristics of the affected part to which a drug is to be administered. The collation information is acquired and generated by the imaging unit 1 and the imaging signal processing unit 2.
- a comparison unit 4 compares the image information obtained by the imaging signal processing unit 2 with the collation information stored in the collation information storage unit 3 and outputs a comparison determination result.
- Reference numeral 5 denotes a drug holding unit that holds in advance a drug to be administered to an affected part in a body cavity or an affected part in the vicinity of the body cavity.
- Reference numeral 6 denotes a medicine supply unit that supplies medicine to the medicine holding unit 5.
- Reference numeral 7 denotes a drug release unit that releases the drug from the drug holding unit 5 toward the affected area when the comparison determination result by the comparison unit 4 shows a match.
- the imaging unit 1, the imaging signal processing unit 2, the collation information storage unit 3, the comparison unit 4, the drug holding unit 5, the drug supply unit 6, and the drug release unit 7 are built in the capsule 20.
- the imaging unit 1 is built in the capsule 20 in a state in which the outside (body cavity, affected part) can be imaged by the imaging unit 1.
- the drug release unit 7 has a function of releasing the drug in the drug holding unit 5 to the outside of the capsule 20.
- the imaging unit 1 captures the verification source information from the original on which the verification source information related to the affected part to which the drug is to be administered before oral administration, and generates a first imaging signal.
- the output side of the imaging signal processing unit 2 is connected to the collation information storage unit 3 and the comparison unit 4.
- the imaging signal processing unit 2 generates verification information by performing signal processing on the first imaging signal acquired by the imaging unit 1 before the capsule oral injection, and sends the generated verification information to the verification information storage unit 3.
- the verification information storage unit 3 stores the verification information that has been sent.
- a second imaging signal is generated and transmitted to the imaging signal processing unit 2 by capturing the surroundings continuously or intermittently while moving through the body cavity in the living body.
- the imaging signal processing unit 2 generates image information from the second imaging signal and sends the generated image information to the comparison unit 4.
- the output side of the verification information storage unit 3 is connected to the comparison unit 4 so that the verification information sent out by the imaging signal processing unit 2 is sent to the comparison unit 4 while moving in the body cavity after oral injection. It has become.
- the drug supply unit 6 is configured to supply a drug to the drug holding unit 5 by injection or the like, and the drug release unit 7 removes the drug from the drug holding unit 5 when receiving a comparison coincidence signal from the comparison unit 4. It is configured to discharge toward (affected part).
- the output side of the comparison unit 4 is connected to the medicine discharge unit 7.
- the medicine Prior to the oral administration of the capsule-type dosing device, the medicine is replenished to the medicine holding section 5 using the medicine replenishing section 6.
- the capsule-type dispensing device When the capsule-type dispensing device is turned on, the medicine holding unit 5 is in a state of holding the replenished medicine, and the imaging unit 1, the imaging signal processing unit 2, and the verification information storage unit 3 are activated.
- the activated capsule-type dosing device prompts the person in charge of the dosing and shows the collation source information (information relating to the characteristics of the affected area, which is necessary for specifying the affected area) to be collated by the imaging unit 1.
- the first image signal is generated by photographing the original.
- the imaging unit 1 sends the generated first imaging signal to the imaging signal processing unit 2.
- the imaging signal processing unit 2 performs image processing on the first imaging signal to generate verification information, and sends the generated verification information to the verification information storage unit 3.
- the verification information storage unit 3 stores the received verification information.
- the collation information is information relating to the affected area to which the drug is to be administered, and is data in which the characteristics of the affected area of the drug administration target are recorded, and is data for specifying the affected area.
- collation information the image information of the affected part of the person or similar patient previously photographed, the color information that can identify the affected part, the reaction color information of the affected part in the state where the reagent has been added in advance, the information on the size of the affected part, the affected part Information on the shape of the object.
- a large-scale medical diagnostic apparatus as in the prior art is not used.
- the patient is prompted and the capsule-type dosing device is orally introduced into the patient (hereinafter referred to as a living body).
- the inserted capsule 20 moves in the body cavity of the living body toward the affected part.
- the imaging unit 1 continuously or intermittently captures the inside of the body cavity, and images the second imaging signal obtained by the imaging. It is sent to the signal processing unit 2.
- the imaging signal processing unit 2 performs image processing on the received second image signal to generate image information.
- the comparison unit 4 takes in the image information from the imaging signal processing unit 2 and the collation information from the collation information storage unit 3, and compares the two pieces of information taken in each other.
- the comparison unit 4 generates a comparison determination result indicating that the comparison determination result indicates coincidence, and generates a comparison determination result indicating that when the comparison determination result indicates disagreement, and outputs the comparison determination result to the drug release unit 7.
- the drug release unit 7 that has received the comparison determination result indicating inconsistency enters an inactive state and does not release the drug held in the drug holding unit 5.
- the drug release unit 7 that has received the comparison determination result indicating coincidence determines that the capsule has reached the affected area, enters an active state, and releases the drug held in the drug holding unit 5 toward the affected area.
- an extracorporeal device worn by a patient is not required as in the prior art.
- the comparison unit 4 makes a comparison determination as to whether or not part or all of the image information matches the collation information (image information). Further, when the collation information is information indicating the color and the size of the disease, the comparison unit 4 relates to the information regarding the color and size of the imaging region included in the image information and the color and size of the disease included in the collation information. Compare and judge information.
- the verification information is disease shape information
- the comparison unit 4 compares and determines the shape of the imaging region included in the image information and the shape of the disease included in the verification information.
- the collation information is information related to the size of the affected area, the following determination is made. That is, when the size of the imaging region in the image information is larger than the size of the disease in the verification information, it is determined that both pieces of information match.
- the collation information stored in the collation information storage unit 3 may be one or more of a plurality of pieces of information (information on the color and size of the imaging region described above).
- the comparison unit 4 performs a comparison process using a plurality of pieces of information.
- the initial collation information may be stored in the collation information storage unit 3 in advance at the manufacturing stage.
- the drug supply unit 6 and the drug release unit 7 may have a common route. Alternatively, if the medicine holding part 5 itself is of a cartridge type, the medicine replenishing part 6 may be omitted.
- a process for capturing an original on which verification source information is posted and generating a first imaging signal, a process for generating a first verification signal by processing the first imaging signal, and a body cavity A process of moving the capsule 20 to the affected part, a process of photographing a body cavity or the vicinity of the affected part to generate a second imaging signal, a process of generating image information by signal processing the second imaging signal, A series of procedures related to direct administration of a drug to an affected area including a process for comparing and determining image information and verification information and a drug release control process based on the comparison determination result are self-contained in a capsule-type dosing device Is done.
- a large-scale medical diagnostic apparatus for acquiring collation information or specifying the position of an affected part, a wireless transceiver for accumulating collation information in a collation information storage unit built in the capsule,
- a patient-mounted extracorporeal device that determines whether or not the affected part has reached the position or transmits a release signal is not required, and the handling thereof is very simple. Inspection personnel to determine image match are not required.
- Not requiring a medical diagnostic device eliminates the need for the patient to lie in bed. It also reduces the physical and mental burden on the patient. The patient is not restrained at a predetermined place, and may leave the treatment room after the capsule 20 is orally introduced. There is no need for a patient-mounted extracorporeal device.
- the medication process of the present embodiment described above is a self-contained process inside the capsule 20, the time lag of drug release is small because of comparison from comparison and comparison, and the accuracy of direct administration of the drug to the affected area is high. It will be expensive.
- an information input unit is further added to the configuration of the first embodiment.
- the information input unit is provided to input additional verification information for addition or update, and to set operation modes of the imaging unit and the imaging signal processing unit.
- FIG. 2 is a block diagram showing the configuration of the capsule-type dosing device according to the second embodiment of the present invention.
- the configuration unique to the present embodiment is the information input unit 8 as described above.
- the information input unit 8 inputs additional or updated verification information to the verification information storage unit 3 and sets an operation mode for the imaging unit 1 and the imaging signal processing unit 2.
- the output side of the information input unit 8 is connected to the collation information storage unit 3, the imaging unit 1, and the imaging signal processing unit 2.
- the information input unit 8 is built in the capsule 20.
- Other configurations are the same as those in the first embodiment, and thus description thereof is omitted.
- the information input unit 8 in the second embodiment corresponds to the first and second information input units in claims 2 and 3.
- the capsule-type dispensing device When starting to use the capsule-type dispensing device, the capsule-type dispensing device prompts the person in charge of medication to input additional verification information to the information input unit 8.
- the additional verification information is information that is as recent as possible and corresponds to the current disease of the patient.
- the capsule-type dosing device prompts the person in charge of medication to cause the information input unit 8 to set the operation mode in the imaging unit 1 and the operation mode in the imaging signal processing unit 2.
- the operation mode is adapted to the purpose and condition of treatment and diagnosis for each patient.
- FIG. 3 is a flowchart showing the above operation.
- the capsule-type dosing device prompts the person in charge of medication and causes the information input unit 8 to input additional verification information corresponding to the latest disease and the current disease of the patient.
- the input additional verification information is stored in the verification information storage unit 3.
- the operation mode in the imaging unit 1 and the imaging signal processing unit 2 is then set from the information input unit 8.
- the process proceeds to the normal operation described in the first embodiment.
- the additional collation information that is acquired or added earlier is added to the collation information acquired in the operation of the first embodiment (corresponding to the latest and the current disease of the patient). (Additional or updated collation information) is added and stored in the collation information storage unit 3.
- the comparison unit 4 compares the verification information with the image information.
- the imaging unit 1 and the imaging signal processing unit 2 are set to the operation mode (the optimal operation mode corresponding to the current treatment and diagnosis purpose and change of conditions for the patient) input to the information input unit 8. . Therefore, when the capsule 20 moves in the body cavity or in the vicinity of the affected area, the quality of the image information obtained by the imaging unit 1 and the imaging signal processing unit 2 is optimal for the purpose and conditions of treatment and diagnosis for the patient. Furthermore, the collation between the image information and the collation information to which the additional collation information is added also corresponds to the current disease of the patient, and the collation accuracy is sufficiently high. By synergizing the effects described above, the timing of the timing at which the drug release unit 7 releases the drug toward the affected part becomes more accurate. Other operations are the same as in the case of the first embodiment, and a description thereof will be omitted.
- capsule-type dosing devices are used in the body, it is difficult to supply drive power from the outside, and batteries are generally used as drive sources. Therefore, it is desirable to suppress power consumption as much as possible.
- the power is turned on immediately before use, and the power is turned off during storage. At the start of use, the purpose of use is clear. Input of the verification information for addition or update by the information input unit 8 is suitable when the power is turned on.
- the operation mode setting performed from the information input unit 8 to the imaging unit 1 and the imaging signal processing unit 2 corresponds to a change in the purpose and condition of the current treatment and diagnosis for the patient. In this case, the operation of the battery is continued. It is desirable to take time into account.
- the destination point is obtained by optimizing the operation mode of the imaging unit 1 and the imaging signal processing unit 2 and additionally storing optimal verification information in the verification information storage unit 3.
- Application of the optimal operating conditions up to and improvement of the recognition accuracy of the dosing position can be achieved.
- the information input unit 8 inputs the additional verification information to the verification information storage unit 3 and sets the operation mode for the imaging unit 1 and the imaging signal processing unit 2.
- the information input unit 8 may be a unit (first information input unit) having a function of only inputting additional verification information to the verification information storage unit 3 or imaging. It may be a unit (second information input unit) having a function of only setting the operation mode in the unit 1 and the imaging signal processing unit 2.
- a wireless communication unit is further added to the configuration of the first embodiment.
- the wireless communication unit is provided to wirelessly notify the image information acquired by imaging, the background of comparison determination by the comparison unit, and the comparison determination result to the outside.
- FIG. 4 is a block diagram showing the configuration of a capsule-type dispensing device in Embodiment 3 of the present invention.
- a configuration unique to the present embodiment is the wireless communication unit 9 as described above.
- the wireless communication unit 9 is activated when the comparison determination result by the comparison unit 4 indicates a match, wirelessly transmits the image information acquired and generated by the imaging unit 1 and the imaging signal processing unit 2 to the outside of the body, and the comparison unit The process of comparison determination by 4 and the comparison determination result are wirelessly transmitted to the outside of the body.
- the output side of the comparison unit 4 and the output side of the imaging signal processing unit 2 are connected to the wireless communication unit 9.
- the wireless communication unit 9 is built in the capsule 20. Other configurations are the same as those in the first embodiment, and thus description thereof is omitted.
- the comparison unit 4 transmits a comparison determination result indicating coincidence to the medicine release unit 7 and also transmits a comparison determination result indicating coincidence to the wireless communication unit 8.
- the wireless communication unit 9 that has received the comparison determination result indicating coincidence wirelessly transmits the image information generated by the imaging signal processing unit 2 to the outside of the body, and the background of the comparison determination by the comparison unit 4 and the comparison determination result to the outside of the body. Send it wirelessly.
- the state in which the medicine is released toward the affected area is also image information.
- the wirelessly transmitted image information, the history of comparison determination and the comparison determination result are stored in an external memory via a receiving unit and a memory control unit (not shown) installed outside. Other operations are the same as in the case of the first embodiment, and a description thereof will be omitted.
- Example 4 In the fourth embodiment of the present invention, the following configuration is further added to the configuration of the third embodiment. That is, in Example 4, there is a relationship between the comparison unit 4 and the imaging unit 1 and between the comparison unit 4 and the imaging signal processing unit 2, and in a period in which the comparison determination result of the comparison unit 4 shows a mismatch. The control is made so that the imaging resolution is coarsened and the imaging resolution is fined during a period of coincidence.
- FIG. 5 is a block diagram showing the configuration of the capsule-type dosing device according to the fourth embodiment of the present invention.
- the same reference numerals as in FIG. 4 of the third embodiment denote the same components.
- the imaging unit 1 and the imaging signal processing unit 2 operate in a low resolution mode during a period in which the comparison determination result received from the comparison unit 4 does not match, and in a high resolution mode during a period indicating the match. It is configured to work with.
- the comparison unit 4 is configured to send the comparison determination result to the imaging unit 1 and the image signal processing unit 2. Since other configurations are the same as those in the third embodiment, the description thereof is omitted.
- the comparison unit 4 initially outputs a signal indicating mismatch as a comparison determination result to the imaging unit 1 and the image signal processing unit 2.
- the imaging unit 1 and the image signal processing unit 2 set a low resolution mode in which the imaging resolution is coarsened and power consumption is reduced.
- the comparison unit 4 matches the image information from the imaging signal processing unit 2 and the verification information from the verification information storage unit 3, the comparison unit 4 sends a signal indicating a match as a comparison determination result to the wireless communication unit 9 and the imaging unit 1. Output to the imaging signal processing unit 2.
- the operation mode is switched to the high resolution mode in which the imaging resolution is increased.
- the image information acquired and generated by the imaging unit 1 and the image signal processing unit 2 (image information when the collation is established) becomes high definition.
- This image information is supplied to the wireless communication unit 9.
- the wireless communication unit 9 wirelessly transmits high-definition image information to the outside. At this time, it is desirable that the history of comparison determination and the comparison determination result are also transmitted. Other operations are the same as in the case of the third embodiment, and a description thereof will be omitted.
- FIG. 6 is a flowchart showing the above operation.
- a normal operation is performed, and a determination is made in the comparison unit 4 in the process.
- the normal operation is repeated in the period in which the comparison determination result indicates a mismatch, but the operation mode of the imaging unit 1 and the image signal processing unit 2 is switched to the high resolution mode in the period in which the comparison determination result indicates a match.
- it is possible to satisfy both suppression of power consumption and acquisition of high-definition image information. Acquisition of high-definition image information leads to an improvement in the accuracy of confirmation of medication results.
- the resolution is set to be high in order to increase the quality of the image information when the verification is established, but instead, the quality of the image information is increased by increasing the number of frames per unit time. It may be high. That is, in this modified example, the imaging unit 1 and the imaging signal processing unit 2 operate in a mode in which the number of frames per unit time is small during the period in which the comparison determination result received from the comparison unit 4 indicates a mismatch, In the period shown, it is configured to operate in a mode with a large number of frames per unit time. Image information with a large number of frames per unit time is information with a large amount of information. In this case as well, both the suppression of power consumption and the acquisition of high-quality image information can be satisfied, leading to an improvement in the accuracy of confirmation of medication results.
- the operation mode when the comparison determination result comes to coincide may be set to a mode with a high resolution and a large number of frames per unit time.
- FIG. 7 is a configuration diagram of a capsule-type dispensing device according to Embodiment 5 of the present invention.
- a light source 18 that irradiates a subject and an optical lens 11 are disposed in front of the capsule 20, and an imaging unit 1 is disposed behind the light source 18.
- the optical lens 11 forms an optical image of a subject on the imaging unit 1, and the imaging unit 1 accumulates signal charges corresponding to the amount of incident light, photoelectrically converts them, and outputs them.
- a drug replenishment unit 6 and a drug release unit 7 are arranged in the rear part of the capsule 20, and a drug holding unit 5 is arranged in front of the capsule 20. Further, the following are appropriately arranged in the capsule 20. That is, a CPU 19 that controls the entire capsule dosage unit, an imaging signal processing unit 2 that converts the output of the imaging unit 1 into image information, and a memory 3a as a verification information storage unit 3 that stores verification information used for image comparison.
- the comparison unit 4 that compares the image information output from the imaging signal processing unit 2 with the collation information output from the memory 3a and outputs the comparison determination result, the information input unit 8 that designates the operation to the CPU 19, and the imaging signal
- a wireless communication unit 9 that communicates information output from the processing unit 2 and the comparison unit 4 to the outside and a battery 21 are arranged in the capsule 20.
- solid lines connecting the blocks indicate signal / data lines, and broken lines indicate control lines.
- the capsule-type dosing device configured as described above operates using the built-in battery 21 as a power source.
- the drug is supplied from the drug supply unit 6 to the drug holding unit 5.
- the CPU 19 controls the medicine supply unit 6 and the medicine holding unit 5 to change them from the medicine supply state to the holding state.
- the CPU 19 prompts the person in charge of medication to input the latest collation information corresponding to the current disease of the patient to be used for the image comparison to the information input unit 8 and captures the acquired additional collation information in the memory 3a.
- the CPU 19 prompts the person in charge of medication to capture the original image on which the verification source data is described, thereby acquiring the first imaging signal and processing the acquired first imaging signal to generate verification information.
- the CPU 19 adds the additional verification information captured by the information input unit 8 to the verification information generated by the signal processing unit 2, and then stores the verification information in the memory 3a. Further, the CPU 19 adjusts the number of images to be captured per unit by controlling the imaging unit 1, the imaging signal processing unit 2, and the light source 18 based on the operating conditions input from the information input unit 8. Further, the CPU 19 sets the operation state of each block based on the operation condition, and then shifts to the normal operation state. Thereby, the output from the imaging unit 1 is converted into image information by the imaging signal processing unit 2 and output.
- the comparison unit 4 compares the image information from the imaging signal processing unit 2 with the collation information from the memory 3a, and determines whether or not these pieces of information match. The determination content is sent to the CPU 19.
- the CPU 19 controls the drug release unit 7 to release the drug held in the drug holding unit 5, and the CPU 19 activates the wireless communication unit 9 to perform communication. .
- the wireless communication unit 9 transmits the information of the process determined by the comparison unit 4 and the image information transmitted to the outside of the body using wireless communication.
- the medicine can be directly administered to the affected area where the image information acquired by photographing matches the collation information.
- it eliminates the need for extracorporeal devices worn by patients, large-scale medical diagnostic devices, and wireless transceivers for sending and receiving verification information, simplifying handling, and reducing physical and mental burdens on patients.
- the capsule-type dosing device of the present invention is a series of items related to direct administration of a drug to the affected area, such as acquisition and holding of collation information, drug delivery, imaging of a body cavity / affected area, signal processing, image information collation, drug release, etc.
- the procedure can be performed in a self-contained manner, and there is no need for extracorporeal devices attached to the patient, large-scale medical diagnostic devices, and wireless transceivers for sending and receiving verification information. This is useful for medical cameras such as capsule cameras.
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Abstract
The disclosed invention includes a drug agent retaining unit, an image capture unit, an image capture signal processing unit, a query information accumulation unit, a comparison unit, and a drug agent release unit, housed within a capsule that is capable of moving within a body cavity. The image capture unit is configured to be capable of photographing an original, query information concerning characteristics of an affected part being included therein, and generating a first image capture signal, prior to the ingestion of the capsule, as well as photographing the body cavity and photographing a second image capture signal after the ingestion of the capsule. The image capture signal processing unit respectively generates query information from the first image capture signal and image information from the second image capture signal. The comparison unit compares the query information and the image information. When the comparison determination result of the comparison unit denotes a match, the drug agent release unit releases the drug agent from the drug agent retaining unit.
Description
本発明は、経口投入されて体腔(たいこう)内を移動し患部に至ると投薬を行うカプセル型投薬装置にかかわり、あらかじめ患部位置を特定しておくための大掛かりな医療診断装置や投薬タイミングを決定するための患者装着の体外装置や照合情報の送受信のための無線送受信機を不要化して、取り扱いを簡易化するための技術に関する。
The present invention relates to a capsule-type dosing device that dispenses when it is orally injected and moves through a body cavity to reach the affected area, and includes a large-scale medical diagnostic apparatus and dosing timing for specifying the affected area position in advance. The present invention relates to a technique for simplifying handling by eliminating the need for a patient-mounted extracorporeal device for determination and a wireless transceiver for transmitting and receiving verification information.
体内の患部に直接投薬するカプセル型投薬装置としては、経口投入した投薬用カプセルから体外装置に向けて無線送信される情報に基づいてカプセル位置を特定し、カプセルが患部に達したことを医師が確認した上で投薬指示を出し、投薬を実現するものが知られている。
As a capsule-type dosing device that directly administers to the affected part in the body, the doctor specifies that the capsule position has been reached based on the information wirelessly transmitted from the orally-administered capsule to the extracorporeal device, and that the doctor has reached the affected part. It is known to give a medication instruction after confirmation and realize medication.
図8A~図8Dは従来のカプセル投薬システムの一例を示す(特許文献1参照)。その概要は次のとおりである。投薬位置特定装置31は、X線CT装置、MRI、PET、X線観察装置、超音波観測装置等の医療診断装置を利用しており、さらには寝台32や画像情報取得のための検出器33を有している。以下、投薬位置特定装置31による投薬動作を説明する。
8A to 8D show an example of a conventional capsule dosing system (see Patent Document 1). The outline is as follows. The medication position specifying device 31 uses a medical diagnostic device such as an X-ray CT device, MRI, PET, an X-ray observation device, an ultrasonic observation device, and a bed 33 or a detector 33 for acquiring image information. have. Hereinafter, the medication operation by the medication position specifying device 31 will be described.
投薬位置特定装置31の患者Pは医師の指示のもと腹部にベルトで体外装置35を装着し、体外装置35に三次元マーカ40を取り付け、寝台32上に横になる。医師はPC(パーソナルコンピュータ)34によって寝台32を検出器(ガントリー)33内に移動させ、検出器33を作動させて患者PのX線撮影を行う。撮影で得られた画像情報をPC34に取り込み、所定の処理を行った上で表示モニタ34aに表示させる。表示された画像には三次元マーカ40の各球状体44,45,46,47も表示されている。医師は表示画像に基づいて体内の診断を行い、投薬が必要な患部Xと患部Xの位置の特定を行い、さらに患部Xの位置情報をPC34から患者装着の体外装置35内のメモリ53に記録させる。患部Xの位置情報のメモリ53への記録が完了すると、次いで三次元マーカ40を体外装置35から取り外し、患者Pは投薬用カプセル10を嚥下する。このあと、患者Pは医療機関を離れても構わない(ただし体外装置35は装着したままとする)。投薬用カプセル10は情報送信部12により電波を体外に送信しながら体内を移動する。送信された電波は患者装着の体外装置35に内蔵の体外受信部50で受信され、判断部51に送られる。判断部51は送られてきた電波の受信レベルおよび受信方向等に基づいて、体外装置35に対する投薬用カプセル10の位置を算出し、算出した投薬用カプセル10の位置情報とメモリ53に記録されている患部Xの位置情報とを比較して、両者が一致したら体外送信部52を介して放出信号を体内に向けて送信する。送信された放出信号は投薬用カプセル10内の受信部15で受信され、制御部16によってリザーバ13内の薬剤Aが放出される。つまり、特定装置31で特定した患部Xの位置にて薬剤Aの放出が行われ、患部Xに対する直接的な投薬となる。17は電池である。
The patient P of the medication position specifying device 31 attaches the extracorporeal device 35 to the abdomen with a belt under the instruction of the doctor, attaches the three-dimensional marker 40 to the extracorporeal device 35, and lies on the bed 32. The doctor moves the bed 32 into a detector (gantry) 33 by a PC (personal computer) 34 and operates the detector 33 to perform X-ray imaging of the patient P. The image information obtained by photographing is taken into the PC 34 and subjected to predetermined processing, and then displayed on the display monitor 34a. In the displayed image, the spherical bodies 44, 45, 46, and 47 of the three-dimensional marker 40 are also displayed. The doctor makes an in-vivo diagnosis based on the display image, identifies the affected part X and the position of the affected part X that require medication, and records the position information of the affected part X from the PC 34 to the memory 53 in the external device 35 attached to the patient. Let When the recording of the position information of the affected part X in the memory 53 is completed, the three-dimensional marker 40 is then removed from the extracorporeal device 35 and the patient P swallows the medication capsule 10. Thereafter, the patient P may leave the medical institution (however, the extracorporeal device 35 remains worn). The medication capsule 10 moves inside the body while transmitting radio waves to the outside by the information transmitting unit 12. The transmitted radio wave is received by the extracorporeal receiving unit 50 built in the extracorporeal device 35 attached to the patient and sent to the determining unit 51. The determination unit 51 calculates the position of the medication capsule 10 relative to the extracorporeal device 35 based on the reception level and reception direction of the transmitted radio wave, and is recorded in the memory 53 and the calculated location information of the medication capsule 10. The position information of the affected part X is compared, and if both match, a release signal is transmitted to the inside of the body via the extracorporeal transmission unit 52. The transmitted release signal is received by the receiving unit 15 in the medication capsule 10, and the medicine A in the reservoir 13 is released by the control unit 16. That is, the medicine A is released at the position of the affected part X specified by the specifying device 31, and the medicine is directly administered to the affected part X. Reference numeral 17 denotes a battery.
別の態様として、図9A,図9Bに示すカプセル投薬システムも開示されている。患者Pは、まず医療機関で内視鏡検査を受ける。医師は特定装置(内視鏡装置)100で得られた画像を元に診断を行い、投薬の必要な患部の位置を特定する。PC109は特定した患部の画像データを変換し、無線送信部136とカプセル内受信部135との間のデータ伝送により、変換されたデータを投薬用カプセル130のカプセル内メモリ131に記録する。次いで、患者Pは投薬用カプセル130を嚥下する。患者はカプセルを嚥下したあとは、医療機関を離れても構わない。投薬用カプセル130は、撮像部91により患者の体内を撮像しながら移動する。取得された撮像画像はカプセル内判断部133に送られる。移動量検出部132は、移動量情報をカプセル内判断部133に送る。カプセル内判断部133は、送られてきた投薬用カプセル130の移動量情報を処理する。判断部133は、撮像部91により撮像された画像がカプセル内メモリ131の画像と類似している場合には、患部の近傍に投薬用カプセル130が達したと判断して、その旨を制御部16に送る。制御部16は、これを受けて薬剤Aの放出を行う。投薬用カプセル130の内部で薬剤の放出の制御を行うため、患者Pは体外装置を装着する必要がなく、患者Pの自由度は高い。92は対物レンズ、93は撮像素子、94は照明用のLEDである。
As another aspect, a capsule medication system shown in FIGS. 9A and 9B is also disclosed. The patient P first undergoes endoscopy at a medical institution. The doctor makes a diagnosis based on the image obtained by the specifying device (endoscopic device) 100, and specifies the position of the affected part requiring medication. The PC 109 converts the image data of the specified affected part, and records the converted data in the intracapsule memory 131 of the medication capsule 130 by data transmission between the wireless transmission unit 136 and the intracapsule reception unit 135. The patient P then swallows the medication capsule 130. The patient may leave the medical facility after swallowing the capsule. The medication capsule 130 moves while imaging the patient's body by the imaging unit 91. The acquired captured image is sent to the capsule determination unit 133. The movement amount detection unit 132 sends the movement amount information to the in-capsule determination unit 133. The in-capsule determination unit 133 processes the movement amount information of the medication capsule 130 that has been sent. When the image captured by the imaging unit 91 is similar to the image in the in-capsule memory 131, the determination unit 133 determines that the medication capsule 130 has reached the vicinity of the affected part, and notifies the control unit 16 In response to this, the control unit 16 releases the medicine A. Since the release of the medicine is controlled inside the medication capsule 130, the patient P does not need to wear an extracorporeal device, and the patient P has a high degree of freedom. 92 is an objective lens, 93 is an image sensor, and 94 is an LED for illumination.
図8A~図8Dの従来例の場合、患者の体内において薬剤を投与すべき位置をあらかじめ特定しておくための投薬位置特定装置31としてCT(Computer Tomography)、X線観測装置、MRI(Magnetic Resonance Imaging)、PET(Positron Emission Tomography)、超音波断層観測装置、内視鏡装置等の医療診断装置が用いられるが、これらの装置はいずれも大掛かり過ぎて使用容易性に難点がある。また、患者は医療診断装置に備え付けられたベッド等に固定されるので、大きな負担を強いられる。特に、患部にカプセルが到達するまで長い時間がかかる場合は、負担が大きい。
In the case of the conventional example shown in FIGS. 8A to 8D, a CT (Computer Tomography), an X-ray observation apparatus, an MRI (Magnetic Resonance) are used as a dosing position specifying device 31 for specifying in advance a position where a drug should be administered in the body of a patient. Imaging, PET (Positron Emission Tomography), ultrasonic tomographic observation apparatus, endoscope apparatus, and other medical diagnostic apparatuses are used. However, these apparatuses are too large and have difficulty in use. In addition, since the patient is fixed to a bed or the like provided in the medical diagnosis apparatus, a heavy burden is imposed. In particular, when it takes a long time for the capsule to reach the affected area, the burden is large.
図9A、図9Bの従来例の場合、患部位置特定のためにやはり大掛かりな内視鏡装置を必要としている。内視鏡装置は、内視鏡装置本体101、体腔内への挿入部102、画像取得装置103、操作部104、光源装置105、画像プロセッサ装置106、表示モニタ107、マウスピース108、挿入量検出装置108a、PC(パソコン)109、および無線送信部136を伴う大掛かりなものである。投薬用カプセル130においても、カプセル内判断部133、カプセル内受信部135、カプセル内メモリ131、移動量検出部132、タイマ回路134、移動距離計測部111、積算部137などの複雑な構造を有している。
In the case of the conventional example of FIGS. 9A and 9B, a large-scale endoscope apparatus is still necessary for specifying the position of the affected area. The endoscope apparatus includes an endoscope apparatus main body 101, a body cavity insertion section 102, an image acquisition apparatus 103, an operation section 104, a light source apparatus 105, an image processor apparatus 106, a display monitor 107, a mouthpiece 108, and an insertion amount detection. This is a large-scale device including a device 108a, a PC (personal computer) 109, and a wireless transmission unit 136. The medication capsule 130 also has a complicated structure such as the capsule determination unit 133, the capsule reception unit 135, the capsule memory 131, the movement amount detection unit 132, the timer circuit 134, the movement distance measurement unit 111, and the integration unit 137. is doing.
図9A、図9Bの従来例においては、比較基準となる画像情報をカプセル内メモリ131に転送格納するので、体外装置は取り外してもよく、患者の負担は軽減される。しかし、カプセル内メモリ131に転送するために、投薬位置特定装置100に無線送信部136を設けておく必要があるとともに、投薬用カプセル130にカプセル内受信部135を設けておく必要がある。つまり、構造が大掛かりになっているとともに、操作上の負担が大きい。
In the conventional example of FIGS. 9A and 9B, the image information serving as a comparison reference is transferred and stored in the in-capsule memory 131, so that the extracorporeal device may be removed, and the burden on the patient is reduced. However, in order to transfer to the in-capsule memory 131, it is necessary to provide the wireless transmission unit 136 in the medication position specifying device 100 and to provide the in-capsule reception unit 135 in the medication capsule 130. That is, the structure is large and the operational burden is large.
図8A~図8Dの従来例は、投薬位置特定装置31、PC34、体外装置35、三次元マーカ40および投薬用カプセル10の、それぞれが単独的に提供されるユニットを組み合わせたものである。図9の従来例は、内視鏡装置100、PC109、無線送信部136および投薬用カプセル130の、それぞれが単独的に提供されるユニットを組み合わせたものである。いずれの従来例も“カプセル投薬システム”と称されるもので、文字通りのシステムとなっている。そのシステムは、複雑な経路で情報のやり取りを行うものである。
8A to 8D is a combination of units each provided with the medication position specifying device 31, the PC 34, the extracorporeal device 35, the three-dimensional marker 40, and the medication capsule 10 independently. The conventional example of FIG. 9 is a combination of units each provided independently of the endoscope apparatus 100, the PC 109, the wireless transmission unit 136, and the medication capsule 130. All of the conventional examples are called “capsule dosing systems” and are literally systems. The system exchanges information through a complicated route.
本発明は、このような事情に鑑みて創作したものであり、患部位置を特定し特定した患部位置をカプセル内に記憶させるための大掛かりな医療診断装置や投薬タイミングを決定するための体外装置を不要化して取り扱いを簡易化し、カプセルの内部構造を簡素化することが可能なカプセル型投薬装置を提供することを目的としている。
The present invention has been created in view of such circumstances, and includes a large-scale medical diagnostic apparatus for specifying an affected part position and storing the specified affected part position in a capsule, and an extracorporeal apparatus for determining a medication timing. An object of the present invention is to provide a capsule-type dosing device that can be made unnecessary, simplify handling, and simplify the internal structure of the capsule.
本発明は、次のような手段を講じることにより上記の課題を解決する。
The present invention solves the above problems by taking the following measures.
《1》本発明によるカプセル型投薬装置は、以下の構成要素を有している。なお、本項においては後述する実施例1の場合の図1を参照することが可能である。
<< 1 >> The capsule-type dosing device according to the present invention has the following components. In this section, it is possible to refer to FIG. 1 in the case of Example 1 described later.
本発明は、
経口投入されて生体内の患部に至る体腔を移動可能なカプセルを備え、
前記カプセルは、薬剤保持部と、撮像部と、撮像信号処理部と、照合情報蓄積部と、比較部と、薬剤放出部とを備えており、
前記薬剤保持部は、前記体腔にある患部または前記体腔の近傍にある患部に投与すべき薬剤を保持し、
前記撮像部は、前記カプセルが前記生体に経口投入される前には、前記患部の特徴に関する照合情報が掲載された原本を撮影して第1の撮像信号を生成可能に構成される一方、前記カプセルが前記生体に経口投入された後は前記患部に至る前記体腔の内部を連続または断続して撮影して第2の撮像信号を撮影し、
前記撮像信号処理部は、前記第1の撮像信号から前記照合情報を、前記第2の撮像信号から画像情報をそれぞれ生成し、
前記照合情報蓄積部は前記照合情報を蓄積し、
前記比較部は、前記照合情報蓄積部に蓄積された前記照合情報と前記撮像信号処理部で生成された前記画像情報とを比較し、
前記薬剤放出部は、前記比較部において前記画像情報と前記照合情報との比較判定結果が一致を示すと、前記薬剤保持部から前記薬剤を前記患部に向けて放出させる。 The present invention
It is equipped with a capsule that can be moved through the body cavity that is orally injected to reach the affected area in the body,
The capsule includes a drug holding unit, an imaging unit, an imaging signal processing unit, a collation information storage unit, a comparison unit, and a drug release unit.
The drug holding unit holds a drug to be administered to an affected part in the body cavity or an affected part in the vicinity of the body cavity,
The imaging unit is configured to be able to generate a first imaging signal by capturing an original on which collation information related to characteristics of the affected part is posted before the capsule is orally introduced into the living body. After the capsule is orally injected into the living body, the inside of the body cavity leading to the affected area is continuously or intermittently photographed to photograph the second imaging signal,
The imaging signal processing unit generates the verification information from the first imaging signal and the image information from the second imaging signal,
The verification information storage unit stores the verification information,
The comparison unit compares the verification information stored in the verification information storage unit with the image information generated by the imaging signal processing unit,
When the comparison determination result between the image information and the collation information is coincident in the comparison unit, the drug release unit releases the drug from the drug holding unit toward the affected part.
経口投入されて生体内の患部に至る体腔を移動可能なカプセルを備え、
前記カプセルは、薬剤保持部と、撮像部と、撮像信号処理部と、照合情報蓄積部と、比較部と、薬剤放出部とを備えており、
前記薬剤保持部は、前記体腔にある患部または前記体腔の近傍にある患部に投与すべき薬剤を保持し、
前記撮像部は、前記カプセルが前記生体に経口投入される前には、前記患部の特徴に関する照合情報が掲載された原本を撮影して第1の撮像信号を生成可能に構成される一方、前記カプセルが前記生体に経口投入された後は前記患部に至る前記体腔の内部を連続または断続して撮影して第2の撮像信号を撮影し、
前記撮像信号処理部は、前記第1の撮像信号から前記照合情報を、前記第2の撮像信号から画像情報をそれぞれ生成し、
前記照合情報蓄積部は前記照合情報を蓄積し、
前記比較部は、前記照合情報蓄積部に蓄積された前記照合情報と前記撮像信号処理部で生成された前記画像情報とを比較し、
前記薬剤放出部は、前記比較部において前記画像情報と前記照合情報との比較判定結果が一致を示すと、前記薬剤保持部から前記薬剤を前記患部に向けて放出させる。 The present invention
It is equipped with a capsule that can be moved through the body cavity that is orally injected to reach the affected area in the body,
The capsule includes a drug holding unit, an imaging unit, an imaging signal processing unit, a collation information storage unit, a comparison unit, and a drug release unit.
The drug holding unit holds a drug to be administered to an affected part in the body cavity or an affected part in the vicinity of the body cavity,
The imaging unit is configured to be able to generate a first imaging signal by capturing an original on which collation information related to characteristics of the affected part is posted before the capsule is orally introduced into the living body. After the capsule is orally injected into the living body, the inside of the body cavity leading to the affected area is continuously or intermittently photographed to photograph the second imaging signal,
The imaging signal processing unit generates the verification information from the first imaging signal and the image information from the second imaging signal,
The verification information storage unit stores the verification information,
The comparison unit compares the verification information stored in the verification information storage unit with the image information generated by the imaging signal processing unit,
When the comparison determination result between the image information and the collation information is coincident in the comparison unit, the drug release unit releases the drug from the drug holding unit toward the affected part.
撮像部は体内において患部を撮影し撮像信号を取得するための手段であり、入射光量に応じた信号電荷を蓄積し光電変換して出力する。薬剤保持部は、患部に対して放出すべき薬剤をカプセル内であらかじめ保持しておく手段である。薬剤放出部は、カプセルが患部に達したときに制御信号により動作して薬剤保持部から薬剤を患部に向けて放出する手段である。
The imaging unit is a means for capturing an image of an affected part in the body and acquiring an imaging signal. The imaging unit accumulates a signal charge corresponding to the amount of incident light, photoelectrically converts it, and outputs it. The drug holding unit is means for holding a drug to be released to the affected part in advance in the capsule. The drug release unit is a means that operates according to a control signal when the capsule reaches the affected part and releases the drug from the drug holding part toward the affected part.
さらに、カプセルが患部に達したことの判定の機能をカプセル自体の内部に持たせる。撮像部で取得された撮像信号を画像情報に変換するための撮像信号処理部が必要となるが、これをカプセルの外部に設けるのではなく、当該カプセル型投薬装置自体が有している。カプセル型投薬装置自体において、撮像部、撮像信号処理部によって取得生成した画像情報を患部に関する照合情報と比較することもポイントで、そのためには、照合情報をあらかじめ蓄積しておく照合情報蓄積部と、画像情報を照合情報と比較するための比較部とが、これもカプセルの外部ではなく当該カプセル型投薬装置自体に備えられていることを要件とする。
Furthermore, the capsule itself has a function of determining that the capsule has reached the affected area. An imaging signal processing unit for converting the imaging signal acquired by the imaging unit into image information is required, but this is not provided outside the capsule but is included in the capsule-type dispensing device itself. In the capsule-type dosing device itself, it is also important to compare the image information acquired and generated by the imaging unit and the imaging signal processing unit with the verification information about the affected part. For this purpose, a verification information storage unit that stores the verification information in advance It is a requirement that the comparison unit for comparing the image information with the collation information is also provided in the capsule-type dispensing device itself, not outside the capsule.
加えて、照合情報蓄積部への照合情報の蓄積の形態は、簡易なものとなっている。それは、カプセルに内蔵の撮像部によって撮影されたうえで、同じくカプセルに内蔵の撮像信号処理部によって信号処理された情報を照合情報とするものである。カプセルを経口投入する前に、カプセル型投薬装置に電源を入れ、撮像部、撮像信号処理部、照合情報蓄積部を起動したうえで、照合元情報が写っている原本の撮影を行って照合元情報を取り込み、さらに画像処理を行って照合情報を生成し、これを照合情報蓄積部に蓄積する。この照合情報の照合情報蓄積部への蓄積は、従来技術の場合の大掛かりな医療診断装置を用いて照合情報を取得する方式に比べてきわめて簡単なものとなっている。この点にも本発明のポイントがある。原本にある照合元情報としては、以前に撮影された本人または類似患者の疾患の画像データや、疾患が特定できる色情報、事前に試薬を投入した状態における患部の反応色情報、疾患の大きさの情報、疾患の形状の情報等など入手が比較的容易なものが好ましい。なお、電源投入時に取り込むことに代えて、カプセル型投薬装置の製造段階で固定的に格納するのでもよい(ROM仕様)。
In addition, the form of storing verification information in the verification information storage unit is simple. That is, information obtained by photographing with an imaging unit incorporated in the capsule and signal-processed by the imaging signal processing unit incorporated in the capsule is used as collation information. Before the capsule is placed orally, the capsule-type dosing device is turned on, the imaging unit, the imaging signal processing unit, and the verification information storage unit are started, and then the original with the verification source information is taken and the verification source Information is taken in, and further image processing is performed to generate verification information, which is stored in the verification information storage unit. Accumulation of the collation information in the collation information storage unit is extremely simple as compared with a method of acquiring collation information using a large-scale medical diagnostic apparatus in the case of the prior art. This is also the point of the present invention. The verification source information in the original includes the previously captured image data of the disease of the person or similar patient, color information that can identify the disease, reaction color information of the affected area in the state where the reagent has been added in advance, and the size of the disease It is preferable to obtain information such as information on a disease, information on the shape of a disease and the like, which are relatively easily available. In place of taking in when the power is turned on, the capsule-type dosing device may be stored in a fixed manner (ROM specification).
このような照合情報は、なにも従来技術のような、X線CT装置、内視鏡装置、MRI、PET、X線観測装置、超音波断層観測装置等の大掛かりな医療診断装置を用いて取得するものではない。当該簡易なカプセル型投薬装置自体が有している撮像部および画像信号処理部を経由して撮影・生成された画像情報である。
Such collation information is obtained using a large-scale medical diagnostic apparatus such as an X-ray CT apparatus, an endoscopic apparatus, an MRI, a PET, an X-ray observation apparatus, and an ultrasonic tomography observation apparatus as in the prior art. It is not something to get. This is image information photographed and generated via an image capturing unit and an image signal processing unit included in the simple capsule-type dispensing device itself.
まとめると、照合情報の取得と保持、患部に直接投与すべき薬剤を患部まで運ぶ機能、患部に至るまでの消化管などの体腔ないし患部付近の撮影、撮像で取得した撮像信号の信号処理、信号処理で得た画像情報の照合、比較判定結果が肯定的となった際に薬剤を放出する機能など、患部への薬剤の直接の投与に関係する一連の手順をカプセル型投薬装置(投薬用カプセル)自体において自己完結的に遂行するように構成されている。すなわち、従来技術にみられた、情報を複雑な経路でやり取りするシステムの構築という発想から脱却している。
In summary, acquisition and retention of collation information, the function of transporting drugs that should be administered directly to the affected area, imaging of body cavities such as the digestive tract leading to the affected area or the vicinity of the affected area, signal processing of the imaging signal acquired by imaging, signal A series of procedures related to direct administration of drugs to the affected area, such as collation of image information obtained by processing, and the function of releasing drugs when the result of comparison and determination becomes affirmative. ) Is self-contained in itself. In other words, it is a departure from the idea of constructing a system for exchanging information through a complicated route, as seen in the prior art.
本発明は、図8A~図8Dの従来例と比較すると、照合情報を取得するのに大掛かりな医療診断装置とカプセルの患部位置到達を判断するのに患者に装着する体外装置とが不要となる。また、本発明は、図9A、図9Bの従来例と比較すると、照合情報を取得するのに大掛かりな医療診断装置が不要となり、照合情報をカプセル内蔵の照合情報蓄積部に蓄積するのに無線の送受信機を必要としない。
Compared with the conventional example of FIGS. 8A to 8D, the present invention eliminates the need for a medical diagnostic device that is large in order to obtain collation information and an extracorporeal device that is attached to the patient to determine the arrival of the affected part of the capsule. . Compared with the conventional example of FIGS. 9A and 9B, the present invention eliminates the need for a large-scale medical diagnostic apparatus for acquiring the collation information, and wirelessly accumulates the collation information in the collation information storage unit built in the capsule. Does not require a transceiver.
すなわち、本発明では、従来技術で必要とされたカプセルの患部位置到達を判断したり放出信号を送信したりする患者装着の体外装置や、照合情報を取得したり患部位置を特定するための大掛かりな医療診断装置や、照合情報をカプセル内蔵の照合情報蓄積部に蓄積するための無線の送受信機は必ずしも必要でなくなる。
That is, in the present invention, a patient-mounted extracorporeal device that determines the arrival of the affected part position of the capsule and transmits a release signal required in the prior art, and a large scale for obtaining the verification information and specifying the affected part position Such a medical diagnostic device and a wireless transceiver for storing verification information in a verification information storage unit with a built-in capsule are not necessarily required.
この構成においては、まずあらかじめ撮像部によって照合元情報が写っている原本の撮影を行って第1の撮像信号を生成し、撮像信号処理部が第1の撮像信号を画像処理することで照合情報を生成し、生成した照合情報を照合情報蓄積部に蓄積しておく。カプセルが体腔を移動する際に撮像部が取得する第2の撮像信号は、撮像信号処理部で画像情報に変換され、比較部に渡される。比較部では撮像信号処理部から送られてくる画像情報と照合情報蓄積部から読み出した照合情報とを比較する。比較部は比較判定結果が一致を示す期間では薬剤放出部を起動させて薬剤保持部に保持されている薬剤を患部に向けて放出させる。
In this configuration, first, the original image in which the verification source information is captured is captured by the imaging unit in advance to generate the first imaging signal, and the imaging signal processing unit performs image processing on the first imaging signal, thereby verifying the verification information. And the generated verification information is stored in the verification information storage unit. The second imaging signal acquired by the imaging unit when the capsule moves through the body cavity is converted into image information by the imaging signal processing unit and passed to the comparison unit. The comparison unit compares the image information sent from the imaging signal processing unit with the verification information read from the verification information storage unit. The comparison unit activates the drug release unit to release the drug held in the drug holding unit toward the affected part during a period in which the comparison determination results indicate coincidence.
以上のように、照合情報の取得と保持、患部への移動、体腔ないし患部付近の撮影、第1、第2の撮像信号の信号処理、信号処理により得られる照合情報と画像情報との比較判定、比較判定結果に基づいた薬剤放出、といった一連の手順が自己完結的に遂行される。したがって、従来技術のように照合情報を取得したり患部位置を特定するための大掛かりな医療診断装置や、照合情報をカプセル内蔵の照合情報蓄積部に蓄積するための無線の送受信機や、カプセルの患部位置到達を判断したり放出信号を送信したりする患者装着の体外装置を必要とせず、簡易に取り扱うことが可能となっている。画像一致を判断する検査要員も不要となる。
As described above, acquisition and holding of verification information, movement to an affected area, imaging of a body cavity or the vicinity of an affected area, signal processing of first and second imaging signals, and comparison determination between verification information obtained by signal processing and image information A series of procedures such as drug release based on the comparison determination result is performed in a self-contained manner. Therefore, as in the prior art, a large-scale medical diagnostic apparatus for acquiring collation information or specifying the position of an affected part, a wireless transceiver for accumulating collation information in a collation information storage unit built in the capsule, It does not require a patient-mounted extracorporeal device that determines whether the affected area has reached the position or transmits a release signal, and can be handled easily. Inspection personnel who judge image matching are also unnecessary.
本発明によれば、照合情報の取得と保持、薬剤運搬、体腔・患部の撮影、信号処理、画像情報の照合、薬剤放出など、患部への薬剤の直接の投与に関係する一連の手順を自己完結的に遂行可能に構成してあるので、患者装着の体外装置や大掛かりな医療診断装置や照合情報の送受信のための無線送受信機が不要となり、その分、取り扱いが簡便化する。
According to the present invention, a series of procedures relating to direct administration of a drug to the affected area such as acquisition and holding of verification information, drug delivery, imaging of a body cavity / affected area, signal processing, image information verification, drug release, etc. Since it is configured so that it can be performed completely, an extracorporeal device worn by the patient, a large-scale medical diagnostic device, and a wireless transmitter / receiver for transmitting / receiving collation information become unnecessary, and handling is simplified correspondingly.
上記した《1》の構成の本発明のカプセル型投薬装置は、次のような実施の形態においてさらに有利に展開することが可能である。
The capsule-type dosing device of the present invention having the above configuration <1> can be further advantageously developed in the following embodiment.
《2》患部を判定するときの基準となる照合情報については、なるべく最新の、そして患者の現在の疾患に対応した照合情報であることが望ましい。そこで、前記カプセルは第1の情報入力部をさらに備える。前記第1の情報入力部は、前記カプセルが前記生体に経口投入される前に前記照合情報に追加するまたは前記照合情報を更新する追加照合情報を入力可能に構成され、前記照合情報蓄積部は前記第1の情報入力部に入力された前記追加照合情報を加えた前記照合情報を蓄積する。
<< 2 >> The reference information used as a reference when determining the affected part is preferably the latest reference information corresponding to the current disease of the patient. Therefore, the capsule further includes a first information input unit. The first information input unit is configured to be able to input additional verification information to be added to the verification information or to update the verification information before the capsule is orally injected into the living body, and the verification information storage unit The collation information obtained by adding the additional collation information input to the first information input unit is stored.
カプセル型投薬装置が使用開始されるとき、前もって第1の情報入力部を起動して最新の照合情報を照合情報蓄積部に蓄積することとする。なお、本項においては後述する実施例2の場合の図2を参照することが可能である。
When the capsule-type dosing device starts to be used, the first information input unit is activated in advance to store the latest verification information in the verification information storage unit. In this section, it is possible to refer to FIG. 2 in the case of Example 2 described later.
このように構成すれば、カプセルが体腔ないし患部付近を移動中に撮像部および撮像信号処理部で得た画像情報に対して照合すべき照合情報について、照合する上で相応しい、最新かつ患者の現在の疾患に対応した、追加または更新の照合情報を用いることが可能となる。ひいては、薬剤放出部が薬剤を患部に向けて放出すべきタイミングの割り出しをより高精度なものにすることが可能になる。
With this configuration, the latest and current patient information that is suitable for collation should be collated with respect to the collation information to be collated with the image information obtained by the imaging unit and the imaging signal processing unit while the capsule is moving around the body cavity or the affected part. It is possible to use additional or updated verification information corresponding to the disease. As a result, the timing at which the drug release unit should release the drug toward the affected part can be determined with higher accuracy.
《3》当該カプセル型投薬装置を使用するに当たっては、その都度の患者ごとに治療や診断の目的や条件が様々に異なるのが一般的である。患部の疾患の種類、疾患の程度・状態、患部の周辺状況、患部までのカプセル移動距離・移動速度、カプセルのサイズ、薬剤使用量・強度、患者の容態など、治療や診断の目的や条件は患者ごとに様々に変化する。したがって、撮像部における動作モードや撮像信号処理部における動作モードは、その都度の患者ごとの治療や診断の目的や条件に合わせて設定することが望ましい。そこで、この治療や診断の目的や条件の変化に対応させるべく、さらに、撮像部と撮像信号処理部の動作に関するモードを設定可能な第2の情報入力部を備えているように構成する。この第2の情報入力部もカプセルに内蔵されていることはいうまでもない。応用として、第2の情報入力部は上記《2》の第1の情報入力部の機能を兼ね備えたものに構成してもよい。なお、本項においては後述する実施例2の場合の図2を参照することが可能である。
<< 3 >> When using the capsule-type dosing device, the purpose and conditions of treatment and diagnosis are generally different for each patient. The purpose and conditions of treatment and diagnosis, such as the type of disease in the affected area, the degree and condition of the disease, the surrounding situation of the affected area, the distance and speed of movement of the capsule to the affected area, the size of the capsule, the amount and strength of the drug used, and the patient It varies from patient to patient. Therefore, it is desirable to set the operation mode in the imaging unit and the operation mode in the imaging signal processing unit in accordance with the purpose and conditions of treatment and diagnosis for each patient. Therefore, in order to cope with changes in the purpose and conditions of the treatment and diagnosis, a second information input unit capable of setting modes relating to the operation of the imaging unit and the imaging signal processing unit is further provided. It goes without saying that the second information input unit is also built in the capsule. As an application, the second information input unit may be configured to have the function of the first information input unit of << 2 >>. In this section, it is possible to refer to FIG. 2 in the case of Example 2 described later.
このように構成すれば、当該カプセル型投薬装置の使用開始に当たり、第2の情報入力部において、撮像部における動作モードの設定または/および撮像信号処理部における動作モードを治療や診断の目的や条件の変化に対応させて設定する。こうすることにより、撮像部、撮像信号処理部のいずれもその都度の患者ごとの治療や診断の目的や条件に合った動作モードに設定することができる。その結果として、画像照合を通じての薬剤放出の精度をより高精度なものにすることが可能になる。
According to this configuration, at the start of use of the capsule-type dispensing device, the second information input unit sets the operation mode in the imaging unit and / or the operation mode in the imaging signal processing unit for the purpose and condition of treatment and diagnosis. Set according to the change of. By doing so, both the imaging unit and the imaging signal processing unit can be set to an operation mode suitable for the purpose and condition of treatment and diagnosis for each patient. As a result, the accuracy of drug release through image matching can be made higher.
《4》当該カプセル型投薬装置は患部への薬剤の投与を行うものであるが、単に薬剤投与に止まらずに、その薬剤投与の実際の様子を視覚的に把握できるようにしておくことは望ましいことである。撮像部・撮像信号処理部によって取得生成された画像情報のうち、少なくとも比較部の比較判定結果が一致を示すときの画像情報は診断・治療にとって重要である。このときの画像情報を保持するには、カプセル内の照合情報蓄積部に取得した画像情報を記憶させておくことが考えられる。しかし、体内を移動して体外へ排出されたカプセルを回収して、そこから画像情報を取り出すことはできないことではないが、困難性を伴うものである(排出経路に難あり)。そこで、取得した画像情報を外部の記憶手段に送って記憶させることを考える。すなわち、撮像部・撮像信号処理部によって取得生成された画像情報をカプセルから外部に通知することとする。そのための手段として無線通信部を設けることとする。この無線通信部もカプセルに内蔵されていることはいうまでもない。画像情報については、必ずしも経口投入の初期からのものとする必要はなく、少なくとも比較部による一致判定の時点からのものであればよい。なお、本項においては後述する実施例3の場合の図4を参照することが可能である。
<< 4 >> The capsule-type dosing device administers the drug to the affected area, but it is desirable to be able to visually grasp the actual state of the drug administration, not just the drug administration. That is. Of the image information acquired and generated by the imaging unit / imaging signal processing unit, image information at least when the comparison determination result of the comparison unit indicates coincidence is important for diagnosis / treatment. In order to hold the image information at this time, it is conceivable to store the acquired image information in the collation information storage unit in the capsule. However, it is not impossible to recover capsules that have been moved out of the body and discharged out of the body, and image information cannot be extracted therefrom, but it is difficult (the discharge route is difficult). Therefore, consider acquiring acquired image information and storing it in an external storage means. That is, the image information acquired and generated by the imaging unit / imaging signal processing unit is notified from the capsule to the outside. For this purpose, a wireless communication unit is provided. Needless to say, this wireless communication unit is also incorporated in the capsule. The image information does not necessarily have to be from the initial stage of oral injection, and may be from at least the point of coincidence determination by the comparison unit. In this section, it is possible to refer to FIG. 4 in the case of Example 3 described later.
この構成においては、比較判定結果の一致時の患部の画像情報を外部に通知するので、投薬結果の成否判断が容易となる。また、外部への通知のタイミングは比較判定結果の一致時であって、それまでは通知は行わないので、電力消費を抑制することが可能となる。
In this configuration, since the image information of the affected part at the time of coincidence of the comparison determination results is notified to the outside, it is easy to determine the success or failure of the medication result. In addition, the timing of notification to the outside is when the comparison determination result matches, and notification is not performed until that time, so that power consumption can be suppressed.
《5》上記《4》の構成の無線通信部の機能について、さらに、前記比較部による比較判定の経緯および比較判定結果を外部に通知するように構成することが好ましい。これにより、患部に対する薬剤の直接的投与の成否を容易に確認することが可能になる。
<< 5 >> Regarding the function of the wireless communication unit configured as described in <4> above, it is preferable to further notify the background of the comparison determination by the comparison unit and the comparison determination result to the outside. This makes it possible to easily confirm the success or failure of direct administration of the drug to the affected area.
《6》無線通信部が付加された上記《4》,《5》の構成において、比較判定結果が不一致を示す期間では撮像の解像度を粗くして消費電力を抑え、一致を示す期間では撮像の解像度を細かくした上で、その情報量の大きい画像情報を無線通信部によって外部通知することが考えられる。なお、本項においては後述する実施例4の場合の図5を参照することが可能である。
<6> In the configurations of <4> and << 5 >> with the wireless communication unit added, the imaging resolution is coarsened to reduce power consumption during the period when the comparison determination result indicates inconsistency, and the imaging is performed during the period when the result indicates coincidence. It is conceivable that image information with a large amount of information is notified externally by a wireless communication unit with a fine resolution. In this section, it is possible to refer to FIG. 5 in the case of Example 4 described later.
このように構成すれば、消費電力を抑制しながら、外部に通知する投薬時の画像を高精細にすることを通じて投薬結果の確認の精度の向上が期待できる。
Such a configuration can be expected to improve the accuracy of confirmation of the medication result through high definition of the medication image to be notified to the outside while suppressing power consumption.
《7》無線通信部が付加された上記《4》,《5》の構成の場合に、上記《6》に代えて、比較判定結果が不一致を示す期間では単位時間当たりのフレーム数を少なくして消費電力を抑え、一致を示す期間では単位時間当たりのフレーム数を多くした上で、その情報量の大きい画像情報を無線通信部によって外部通知することが考えられる。
<7> In the case of the above configurations <4> and <5> to which a wireless communication unit is added, instead of the above <6>, the number of frames per unit time is reduced during the period in which the comparison determination result indicates a mismatch. Thus, it is conceivable that the power consumption is reduced and the number of frames per unit time is increased during a period of coincidence, and image information having a large amount of information is externally notified by the wireless communication unit.
このように構成すれば、消費電力を抑制しながら、外部に通知する投薬時の画像を高品質にすることを通じて投薬結果の確認の精度の向上が期待できる。
With this configuration, it is expected that the accuracy of confirmation of the medication result can be improved by improving the quality of the medication image notified to the outside while suppressing power consumption.
以下、図面を参照して本発明のカプセル型投薬装置の実施例について説明する。
Hereinafter, embodiments of the capsule-type dosing device of the present invention will be described with reference to the drawings.
(実施例1)
図1は本発明の実施例1におけるカプセル型投薬装置の構成を示すブロック図である。図1において、20は生体に経口投入されて口腔から生体内で薬剤を投与すべき患部に至る体腔を移動可能なカプセルである。このカプセル20は、円筒の両端をそれぞれ半球状にした形状を有している。1は経口投入時から患部に至る体腔を撮影する撮像部であって、撮像部1は入射光量に応じた信号電荷を蓄積して光電変換して出力するCCDイメージセンサやMOSイメージセンサなどからなる。2は撮像部1によって取得された撮像信号から画像情報を生成する撮像信号処理部である。3は薬剤を投与すべき患部の特徴に関する照合情報を蓄積する半導体メモリなどからなる照合情報蓄積部である。照合情報は、撮像部1と撮像信号処理部2とによって取得生成される。4は撮像信号処理部2による画像情報と照合情報蓄積部3における照合情報とを比較して比較判定結果を出力する比較部である。5は、体腔にある患部または体腔の近傍にある患部に対して投与すべき薬剤をあらかじめ保持しておく薬剤保持部である。6は薬剤保持部5に対して薬剤を補給する薬剤補給部である。7は比較部4による比較判定結果が一致を示すときに薬剤保持部5から薬剤を患部に向けて放出する薬剤放出部である。撮像部1、撮像信号処理部2、照合情報蓄積部3、比較部4、薬剤保持部5、薬剤補給部6および薬剤放出部7はカプセル20に内蔵されている。撮像部1は、撮像部1によって外部(体腔、患部)を撮影可能な状態でカプセル20に内蔵されている。薬剤放出部7は、薬剤保持部5の薬剤をカプセル20の外部に放出する機能を有している。さらに撮像部1は、経口投入前には薬剤を投与すべき患部に関する照合元情報が掲載されている原本からその照合元情報を撮影して第1の撮像信号を生成するものである。撮像信号処理部2の出力側は照合情報蓄積部3と比較部4とに接続されている。撮像信号処理部2は、カプセル経口投入前に撮像部1が取得した第1の撮像信号を信号処理することで照合情報を生成し、生成した照合情報を照合情報蓄積部3に送出する。照合情報蓄積部3は送られてきた照合情報を蓄積する。また、撮像部1が経口投入後に生体内体腔を移動中に連続または断続して周囲を撮影することで第2の撮像信号を生成して撮像信号処理部2に送出する。撮像信号処理部2は、第2の撮像信号から画像情報を生成し、生成した画像情報を比較部4に送出する。照合情報蓄積部3の出力側は比較部4に接続されており、経口投入後の生体内体腔を移動中においては、撮像信号処理部2が送出する照合情報が比較部4に送られるようになっている。 Example 1
FIG. 1 is a block diagram showing the configuration of a capsule-type dosing device inEmbodiment 1 of the present invention. In FIG. 1, reference numeral 20 denotes a capsule which is orally introduced into a living body and can move through a body cavity from an oral cavity to an affected area where a medicine is to be administered in the living body. The capsule 20 has a shape in which both ends of the cylinder are hemispherical. Reference numeral 1 denotes an imaging unit that images a body cavity from the time of oral injection to the affected part. The imaging unit 1 includes a CCD image sensor, a MOS image sensor, or the like that accumulates a signal charge corresponding to the amount of incident light, photoelectrically converts it, and outputs it. . An imaging signal processing unit 2 generates image information from the imaging signal acquired by the imaging unit 1. Reference numeral 3 denotes a collation information storage unit composed of a semiconductor memory or the like that accumulates collation information related to the characteristics of the affected part to which a drug is to be administered. The collation information is acquired and generated by the imaging unit 1 and the imaging signal processing unit 2. A comparison unit 4 compares the image information obtained by the imaging signal processing unit 2 with the collation information stored in the collation information storage unit 3 and outputs a comparison determination result. Reference numeral 5 denotes a drug holding unit that holds in advance a drug to be administered to an affected part in a body cavity or an affected part in the vicinity of the body cavity. Reference numeral 6 denotes a medicine supply unit that supplies medicine to the medicine holding unit 5. Reference numeral 7 denotes a drug release unit that releases the drug from the drug holding unit 5 toward the affected area when the comparison determination result by the comparison unit 4 shows a match. The imaging unit 1, the imaging signal processing unit 2, the collation information storage unit 3, the comparison unit 4, the drug holding unit 5, the drug supply unit 6, and the drug release unit 7 are built in the capsule 20. The imaging unit 1 is built in the capsule 20 in a state in which the outside (body cavity, affected part) can be imaged by the imaging unit 1. The drug release unit 7 has a function of releasing the drug in the drug holding unit 5 to the outside of the capsule 20. Further, the imaging unit 1 captures the verification source information from the original on which the verification source information related to the affected part to which the drug is to be administered before oral administration, and generates a first imaging signal. The output side of the imaging signal processing unit 2 is connected to the collation information storage unit 3 and the comparison unit 4. The imaging signal processing unit 2 generates verification information by performing signal processing on the first imaging signal acquired by the imaging unit 1 before the capsule oral injection, and sends the generated verification information to the verification information storage unit 3. The verification information storage unit 3 stores the verification information that has been sent. In addition, after the imaging unit 1 is orally injected, a second imaging signal is generated and transmitted to the imaging signal processing unit 2 by capturing the surroundings continuously or intermittently while moving through the body cavity in the living body. The imaging signal processing unit 2 generates image information from the second imaging signal and sends the generated image information to the comparison unit 4. The output side of the verification information storage unit 3 is connected to the comparison unit 4 so that the verification information sent out by the imaging signal processing unit 2 is sent to the comparison unit 4 while moving in the body cavity after oral injection. It has become.
図1は本発明の実施例1におけるカプセル型投薬装置の構成を示すブロック図である。図1において、20は生体に経口投入されて口腔から生体内で薬剤を投与すべき患部に至る体腔を移動可能なカプセルである。このカプセル20は、円筒の両端をそれぞれ半球状にした形状を有している。1は経口投入時から患部に至る体腔を撮影する撮像部であって、撮像部1は入射光量に応じた信号電荷を蓄積して光電変換して出力するCCDイメージセンサやMOSイメージセンサなどからなる。2は撮像部1によって取得された撮像信号から画像情報を生成する撮像信号処理部である。3は薬剤を投与すべき患部の特徴に関する照合情報を蓄積する半導体メモリなどからなる照合情報蓄積部である。照合情報は、撮像部1と撮像信号処理部2とによって取得生成される。4は撮像信号処理部2による画像情報と照合情報蓄積部3における照合情報とを比較して比較判定結果を出力する比較部である。5は、体腔にある患部または体腔の近傍にある患部に対して投与すべき薬剤をあらかじめ保持しておく薬剤保持部である。6は薬剤保持部5に対して薬剤を補給する薬剤補給部である。7は比較部4による比較判定結果が一致を示すときに薬剤保持部5から薬剤を患部に向けて放出する薬剤放出部である。撮像部1、撮像信号処理部2、照合情報蓄積部3、比較部4、薬剤保持部5、薬剤補給部6および薬剤放出部7はカプセル20に内蔵されている。撮像部1は、撮像部1によって外部(体腔、患部)を撮影可能な状態でカプセル20に内蔵されている。薬剤放出部7は、薬剤保持部5の薬剤をカプセル20の外部に放出する機能を有している。さらに撮像部1は、経口投入前には薬剤を投与すべき患部に関する照合元情報が掲載されている原本からその照合元情報を撮影して第1の撮像信号を生成するものである。撮像信号処理部2の出力側は照合情報蓄積部3と比較部4とに接続されている。撮像信号処理部2は、カプセル経口投入前に撮像部1が取得した第1の撮像信号を信号処理することで照合情報を生成し、生成した照合情報を照合情報蓄積部3に送出する。照合情報蓄積部3は送られてきた照合情報を蓄積する。また、撮像部1が経口投入後に生体内体腔を移動中に連続または断続して周囲を撮影することで第2の撮像信号を生成して撮像信号処理部2に送出する。撮像信号処理部2は、第2の撮像信号から画像情報を生成し、生成した画像情報を比較部4に送出する。照合情報蓄積部3の出力側は比較部4に接続されており、経口投入後の生体内体腔を移動中においては、撮像信号処理部2が送出する照合情報が比較部4に送られるようになっている。 Example 1
FIG. 1 is a block diagram showing the configuration of a capsule-type dosing device in
薬剤補給部6は薬剤保持部5に対して薬剤を注入等により補給するものとして構成され、薬剤放出部7は比較部4から比較一致の信号を受け取ったときに薬剤保持部5の薬剤を外部(患部)に向けて放出するものとして構成されている。比較部4の出力側は薬剤放出部7に接続されている。
The drug supply unit 6 is configured to supply a drug to the drug holding unit 5 by injection or the like, and the drug release unit 7 removes the drug from the drug holding unit 5 when receiving a comparison coincidence signal from the comparison unit 4. It is configured to discharge toward (affected part). The output side of the comparison unit 4 is connected to the medicine discharge unit 7.
次に、上記のように構成された本実施例のカプセル型投薬装置の動作を説明する。カプセル型投薬装置を経口投入するに先立って、薬剤補給部6を用いて薬剤を薬剤保持部5に補給する。カプセル型投薬装置の電源を投入すると、薬剤保持部5は補給された薬剤を保持する状態になるとともに、撮像部1、撮像信号処理部2、照合情報蓄積部3が起動される。起動したカプセル型投薬装置は、投薬担当者を促して、撮像部1により照合の元になる照合元情報(患部の特徴に関する情報であって、患部を特定するのに必要となる情報)が写っている原本の撮影を実施させて第1の撮像信号を生成する。撮像部1は生成した第1の撮像信号を撮像信号処理部2に送出する。撮像信号処理部2は、第1の撮像信号を画像処理することで照合情報を生成し、生成した照合情報を照合情報蓄積部3に送出する。照合情報蓄積部3は、受け取った照合情報を蓄積する。照合情報は、薬剤を投与すべき患部に関する情報であって、薬剤投与対象の患部の特徴が記録されたデータであり患部を特定するデータとなる。照合情報としては、以前に撮影された本人または類似患者の患部の画像情報や、患部を特定できる色情報、事前に試薬を投入した状態における患部の反応色情報、患部の大きさの情報、患部の形状の情報等である。この照合情報の取得と蓄積の過程では、従来技術のような大掛かりな医療診断装置は用いていない。また、患者装着の体外装置や無線送受信機も必要でない。
Next, the operation of the capsule-type dispensing device of the present embodiment configured as described above will be described. Prior to the oral administration of the capsule-type dosing device, the medicine is replenished to the medicine holding section 5 using the medicine replenishing section 6. When the capsule-type dispensing device is turned on, the medicine holding unit 5 is in a state of holding the replenished medicine, and the imaging unit 1, the imaging signal processing unit 2, and the verification information storage unit 3 are activated. The activated capsule-type dosing device prompts the person in charge of the dosing and shows the collation source information (information relating to the characteristics of the affected area, which is necessary for specifying the affected area) to be collated by the imaging unit 1. The first image signal is generated by photographing the original. The imaging unit 1 sends the generated first imaging signal to the imaging signal processing unit 2. The imaging signal processing unit 2 performs image processing on the first imaging signal to generate verification information, and sends the generated verification information to the verification information storage unit 3. The verification information storage unit 3 stores the received verification information. The collation information is information relating to the affected area to which the drug is to be administered, and is data in which the characteristics of the affected area of the drug administration target are recorded, and is data for specifying the affected area. As collation information, the image information of the affected part of the person or similar patient previously photographed, the color information that can identify the affected part, the reaction color information of the affected part in the state where the reagent has been added in advance, the information on the size of the affected part, the affected part Information on the shape of the object. In the process of acquiring and accumulating the collation information, a large-scale medical diagnostic apparatus as in the prior art is not used. In addition, there is no need for a patient-mounted extracorporeal device or a wireless transceiver.
次に、患者を促してカプセル型投薬装置を患者(以下、生体という)に経口投入する。投入されたカプセル20は生体の体腔内を患部に向かって移動するが、その移動中に、撮像部1は体腔内部を連続または断続して撮影し、撮影により得られる第2の撮像信号を撮像信号処理部2に送出する。撮像信号処理部2は受け取った第2の画像信号の画像処理を行って画像情報を生成する。カプセル20の移動中に、比較部4は、撮像信号処理部2から画像情報を、照合情報蓄積部3から照合情報をそれぞれ取り込み、取り込んだ両情報を相互比較する。比較部4は、比較判定結果が一致を示すとそのことを示す比較判定結果を、不一致を示すとそのことを示す比較判定結果を生成し、これら比較判定結果を薬剤放出部7に出力する。不一致を示す比較判定結果を受け取った薬剤放出部7はインアクティブ状態となり薬剤保持部5に保持されている薬剤を放出しない。一方、一致を示す比較判定結果を受け取った薬剤放出部7は、カプセルが患部に到達したと判断してアクティブ状態となり、薬剤保持部5に保持されている薬剤を患部に向けて放出する。ここでの比較判定の過程では、従来技術のように患者装着の体外装置は必要でない。
Next, the patient is prompted and the capsule-type dosing device is orally introduced into the patient (hereinafter referred to as a living body). The inserted capsule 20 moves in the body cavity of the living body toward the affected part. During the movement, the imaging unit 1 continuously or intermittently captures the inside of the body cavity, and images the second imaging signal obtained by the imaging. It is sent to the signal processing unit 2. The imaging signal processing unit 2 performs image processing on the received second image signal to generate image information. While the capsule 20 is moving, the comparison unit 4 takes in the image information from the imaging signal processing unit 2 and the collation information from the collation information storage unit 3, and compares the two pieces of information taken in each other. The comparison unit 4 generates a comparison determination result indicating that the comparison determination result indicates coincidence, and generates a comparison determination result indicating that when the comparison determination result indicates disagreement, and outputs the comparison determination result to the drug release unit 7. The drug release unit 7 that has received the comparison determination result indicating inconsistency enters an inactive state and does not release the drug held in the drug holding unit 5. On the other hand, the drug release unit 7 that has received the comparison determination result indicating coincidence determines that the capsule has reached the affected area, enters an active state, and releases the drug held in the drug holding unit 5 toward the affected area. In this comparison and determination process, an extracorporeal device worn by a patient is not required as in the prior art.
比較部4における画像情報と照合情報との比較処理の詳細は次のとおりである。照合情報が画像情報である場合、比較部4は画像情報の一部または全部と照合情報(画像情報)とが一致するか否かの比較判断を行う。また、照合情報が色および疾患の大きさを示す情報である場合、比較部4は画像情報に含まれる撮影部位の色、大きさに関する情報と、照合情報に含まれる疾患の色、大きさに関する情報とを比較判断する。照合情報が疾患の形状情報である場合、比較部4は画像情報に含まれる撮影部位における形状と照合情報に含まれる疾患の形状とを比較判断する。ここで照合情報が患部の大きさに関する情報である場合、以下のように判断する。すなわち、画像情報における撮影部位の大きさが照合情報における疾患の大きさよりも大きいときは、両情報が一致すると判断する。
Details of the comparison processing between the image information and the collation information in the comparison unit 4 are as follows. When the collation information is image information, the comparison unit 4 makes a comparison determination as to whether or not part or all of the image information matches the collation information (image information). Further, when the collation information is information indicating the color and the size of the disease, the comparison unit 4 relates to the information regarding the color and size of the imaging region included in the image information and the color and size of the disease included in the collation information. Compare and judge information. When the verification information is disease shape information, the comparison unit 4 compares and determines the shape of the imaging region included in the image information and the shape of the disease included in the verification information. Here, when the collation information is information related to the size of the affected area, the following determination is made. That is, when the size of the imaging region in the image information is larger than the size of the disease in the verification information, it is determined that both pieces of information match.
照合情報蓄積部3に蓄積される照合情報は、複数の情報(上述した撮影部位の色、大きさに関する情報等)のうちの1つ以上であればよい。なお複数の情報を用いる場合は、比較部4は、複数の情報で比較処理を行う。また照合情報蓄積部3への初期の照合情報の格納は、製造段階等でのあらかじめの格納でもよい。薬剤補給部6と薬剤放出部7とは、その経路を共通にしてもよい。あるいは、薬剤保持部5自体をカートリッジ方式とすれば、薬剤補給部6はなくてもよい。
The collation information stored in the collation information storage unit 3 may be one or more of a plurality of pieces of information (information on the color and size of the imaging region described above). When a plurality of pieces of information are used, the comparison unit 4 performs a comparison process using a plurality of pieces of information. The initial collation information may be stored in the collation information storage unit 3 in advance at the manufacturing stage. The drug supply unit 6 and the drug release unit 7 may have a common route. Alternatively, if the medicine holding part 5 itself is of a cartridge type, the medicine replenishing part 6 may be omitted.
以上をまとめると、照合元情報が掲載された原本を撮影して第1の撮像信号を生成する処理と、第1の撮像信号を信号処理して照合情報を生成して保持する処理と、体腔内でカプセル20を患部に移動させる処理と、体腔ないし患部付近を撮影して第2の撮像信号を生成する処理と、第2の撮像信号を信号処理することで画像情報を生成する処理と、画像情報と照合情報とを比較判定する処理と、比較判定結果に基づいた薬剤の放出制御処理と、を含む患部への薬剤の直接の投与に関係する一連の手順がカプセル型投薬装置において自己完結される。したがって、従来技術のように照合情報を取得したり患部位置を特定するための大掛かりな医療診断装置や、照合情報をカプセル内蔵の照合情報蓄積部に蓄積するための無線の送受信機や、カプセルの患部位置到達を判断したり放出信号を送信したりする患者装着の体外装置を必要とせず、その取り扱いは非常に簡易なものとなる。画像一致を判断する検査要員は不要である。医療診断装置を要しないことは、患者がベッドに横たわっている必要性をなくなる。患者の肉体的、精神的負担を軽減することにもなる。患者は所定の場所に拘束されることがなく、カプセル20の経口投入後、治療室から出て行ってもかまわない。患者装着の体外装置も必要でなくなる。
In summary, a process for capturing an original on which verification source information is posted and generating a first imaging signal, a process for generating a first verification signal by processing the first imaging signal, and a body cavity A process of moving the capsule 20 to the affected part, a process of photographing a body cavity or the vicinity of the affected part to generate a second imaging signal, a process of generating image information by signal processing the second imaging signal, A series of procedures related to direct administration of a drug to an affected area including a process for comparing and determining image information and verification information and a drug release control process based on the comparison determination result are self-contained in a capsule-type dosing device Is done. Therefore, as in the prior art, a large-scale medical diagnostic apparatus for acquiring collation information or specifying the position of an affected part, a wireless transceiver for accumulating collation information in a collation information storage unit built in the capsule, A patient-mounted extracorporeal device that determines whether or not the affected part has reached the position or transmits a release signal is not required, and the handling thereof is very simple. Inspection personnel to determine image match are not required. Not requiring a medical diagnostic device eliminates the need for the patient to lie in bed. It also reduces the physical and mental burden on the patient. The patient is not restrained at a predetermined place, and may leave the treatment room after the capsule 20 is orally introduced. There is no need for a patient-mounted extracorporeal device.
以上説明した本実施例の投薬処理は、カプセル20の内部における自己完結的な処理であるので、撮像から比較、比較一致から薬剤放出のタイムラグが小さく、患部への薬剤の直接的投与の精度が高いものとなる。
Since the medication process of the present embodiment described above is a self-contained process inside the capsule 20, the time lag of drug release is small because of comparison from comparison and comparison, and the accuracy of direct administration of the drug to the affected area is high. It will be expensive.
(実施例2)
本発明の実施例2では、実施例1の構成にさらに情報入力部が追加されている。情報入力部は、追加または更新するための追加照合情報が入力されるとともに、撮像部、撮像信号処理部の動作モードを設定するために設けられる。 (Example 2)
In the second embodiment of the present invention, an information input unit is further added to the configuration of the first embodiment. The information input unit is provided to input additional verification information for addition or update, and to set operation modes of the imaging unit and the imaging signal processing unit.
本発明の実施例2では、実施例1の構成にさらに情報入力部が追加されている。情報入力部は、追加または更新するための追加照合情報が入力されるとともに、撮像部、撮像信号処理部の動作モードを設定するために設けられる。 (Example 2)
In the second embodiment of the present invention, an information input unit is further added to the configuration of the first embodiment. The information input unit is provided to input additional verification information for addition or update, and to set operation modes of the imaging unit and the imaging signal processing unit.
図2は本発明の実施例2におけるカプセル型投薬装置の構成を示すブロック図である。図2において、実施例1の図1におけるのと同じ符号は同一の構成要素を指している。本実施例に特有の構成は、上述したように情報入力部8である。情報入力部8は、照合情報蓄積部3に追加または更新の照合情報を入力するとともに、撮像部1および撮像信号処理部2に動作モードの設定を行うものである。情報入力部8の出力側は照合情報蓄積部3と撮像部1と撮像信号処理部2とに接続されている。情報入力部8はカプセル20に内蔵されている。その他の構成については、実施例1の場合と同様であるので、説明を省略する。なお、実施例2においける情報入力部8は、請求項2、3における第1、第2の情報入力部に相当する。
FIG. 2 is a block diagram showing the configuration of the capsule-type dosing device according to the second embodiment of the present invention. In FIG. 2, the same reference numerals as those in FIG. 1 of the first embodiment indicate the same components. The configuration unique to the present embodiment is the information input unit 8 as described above. The information input unit 8 inputs additional or updated verification information to the verification information storage unit 3 and sets an operation mode for the imaging unit 1 and the imaging signal processing unit 2. The output side of the information input unit 8 is connected to the collation information storage unit 3, the imaging unit 1, and the imaging signal processing unit 2. The information input unit 8 is built in the capsule 20. Other configurations are the same as those in the first embodiment, and thus description thereof is omitted. The information input unit 8 in the second embodiment corresponds to the first and second information input units in claims 2 and 3.
次に、上記のように構成された本実施例のカプセル型投薬装置の動作を説明する。カプセル型投薬装置の使用を開始するに際して、カプセル型投薬装置は、投薬担当者を促して情報入力部8に追加照合情報を入力させる。追加照合情報としては、なるべく最新の、そして患者の現在の疾患に対応した情報とする。さらにまた、カプセル型投薬装置は、投薬担当者を促して情報入力部8に撮像部1における動作モードや撮像信号処理部2における動作モードを設定させる。その動作モードは、その都度の患者ごとの治療や診断の目的や条件に合ったものとする。
Next, the operation of the capsule-type dispensing device of the present embodiment configured as described above will be described. When starting to use the capsule-type dispensing device, the capsule-type dispensing device prompts the person in charge of medication to input additional verification information to the information input unit 8. The additional verification information is information that is as recent as possible and corresponds to the current disease of the patient. Furthermore, the capsule-type dosing device prompts the person in charge of medication to cause the information input unit 8 to set the operation mode in the imaging unit 1 and the operation mode in the imaging signal processing unit 2. The operation mode is adapted to the purpose and condition of treatment and diagnosis for each patient.
図3は上記の動作を示すフローチャートである。カプセル型投薬装置の電源を投入するとプログラムによる動作が開始される。まずはカプセル型投薬装置は、投薬担当者を促して、情報入力部8に最新かつ患者の現在の疾患に対応した追加照合情報を入力させる。入力された追加照合情報は照合情報蓄積部3に格納される。追加照合情報の入力が完了すると、次いで、情報入力部8から撮像部1および撮像信号処理部2における動作モードの設定がなされる。この動作モードの設定が完了すると、実施例1で説明した通常の動作へと進む。
FIG. 3 is a flowchart showing the above operation. When the power of the capsule-type dispensing device is turned on, the operation by the program is started. First, the capsule-type dosing device prompts the person in charge of medication and causes the information input unit 8 to input additional verification information corresponding to the latest disease and the current disease of the patient. The input additional verification information is stored in the verification information storage unit 3. When the input of the additional verification information is completed, the operation mode in the imaging unit 1 and the imaging signal processing unit 2 is then set from the information input unit 8. When the setting of the operation mode is completed, the process proceeds to the normal operation described in the first embodiment.
上述したように実施例2では、第1の実施例の動作で取得される照合情報に、先に取得されるまたは追加される追加照合情報追加照合情報(最新かつ患者の現在の疾患に対応した追加または更新の照合情報)が加えられたうえで、照合情報格納部3に格納される。カプセル20が体腔を移動する状態では、比較部4は、この照合情報と画像情報とを比較する。
As described above, in the second embodiment, the additional collation information that is acquired or added earlier is added to the collation information acquired in the operation of the first embodiment (corresponding to the latest and the current disease of the patient). (Additional or updated collation information) is added and stored in the collation information storage unit 3. In a state where the capsule 20 moves through the body cavity, the comparison unit 4 compares the verification information with the image information.
また、撮像部1および撮像信号処理部2は、情報入力部8に入力された動作モード(患者に対する現在の治療や診断の目的や条件の変化に対応した最適の動作モード)に設定されている。そのため、カプセル20が体腔ないし患部付近を移動する際には、撮像部1および撮像信号処理部2で得た画像情報の品質はその患者に対する治療や診断の目的や条件に最適のものとなる。さらに、その画像情報と追加照合情報が追加された照合情報との照合もその患者の現在の疾患に相応したものとなり、その照合の精度は充分に高いものとなる。以上説明した効果が相乗されることにより、薬剤放出部7が薬剤を患部に向けて放出するタイミングの割り出しはより高精度なものとなる。その他の動作については、実施例1の場合と同様であるので説明を省略する。
In addition, the imaging unit 1 and the imaging signal processing unit 2 are set to the operation mode (the optimal operation mode corresponding to the current treatment and diagnosis purpose and change of conditions for the patient) input to the information input unit 8. . Therefore, when the capsule 20 moves in the body cavity or in the vicinity of the affected area, the quality of the image information obtained by the imaging unit 1 and the imaging signal processing unit 2 is optimal for the purpose and conditions of treatment and diagnosis for the patient. Furthermore, the collation between the image information and the collation information to which the additional collation information is added also corresponds to the current disease of the patient, and the collation accuracy is sufficiently high. By synergizing the effects described above, the timing of the timing at which the drug release unit 7 releases the drug toward the affected part becomes more accurate. Other operations are the same as in the case of the first embodiment, and a description thereof will be omitted.
カプセル型投薬装置は、体内で使用される関係上、駆動電源を外部から供給することはむずかしく駆動源として電池が使用されるのが一般的である。したがって、消費電力はできる限り抑制することが望ましい。電源投入は使用直前とし、保管中は電源をオフ状態にしておくものとする。使用開始に際しては、使用目的が明確になっている。情報入力部8による追加または更新の照合情報の入力は、電源投入時が適している。
Since capsule-type dosing devices are used in the body, it is difficult to supply drive power from the outside, and batteries are generally used as drive sources. Therefore, it is desirable to suppress power consumption as much as possible. The power is turned on immediately before use, and the power is turned off during storage. At the start of use, the purpose of use is clear. Input of the verification information for addition or update by the information input unit 8 is suitable when the power is turned on.
また、電池駆動の場合、動作継続時間に制限がある。情報入力部8から撮像部1および撮像信号処理部2へ行う動作モードの設定は、患者に対する現在の治療や診断の目的や条件の変化に対応したものとするが、その場合に電池の動作継続時間を加味することが望ましい。
In addition, in the case of battery drive, there is a limit to the operation duration. The operation mode setting performed from the information input unit 8 to the imaging unit 1 and the imaging signal processing unit 2 corresponds to a change in the purpose and condition of the current treatment and diagnosis for the patient. In this case, the operation of the battery is continued. It is desirable to take time into account.
以上のように本実施例によれば、撮像部1および撮像信号処理部2の動作モードの最適化と、照合情報蓄積部3への最適な照合情報の追加蓄積とを行うことにより、目的地点までの最適動作条件の適用と投薬位置の認識精度の向上をともに達成することができる。
As described above, according to the present embodiment, the destination point is obtained by optimizing the operation mode of the imaging unit 1 and the imaging signal processing unit 2 and additionally storing optimal verification information in the verification information storage unit 3. Application of the optimal operating conditions up to and improvement of the recognition accuracy of the dosing position can be achieved.
上記の説明においては、情報入力部8は、照合情報蓄積部3に追加照合情報を入力するとともに、撮像部1および撮像信号処理部2に動作モードの設定を行うものとした。しかしながら、情報入力部8はこのような構成に代えて、照合情報蓄積部3に追加照合情報を入力するだけの機能を備えたもの(第1の情報入力部)であってもよいし、撮像部1および撮像信号処理部2へ動作モードの設定を行うだけの機能を備えたもの(第2の情報入力部)であってもよい。
In the above description, the information input unit 8 inputs the additional verification information to the verification information storage unit 3 and sets the operation mode for the imaging unit 1 and the imaging signal processing unit 2. However, instead of such a configuration, the information input unit 8 may be a unit (first information input unit) having a function of only inputting additional verification information to the verification information storage unit 3 or imaging. It may be a unit (second information input unit) having a function of only setting the operation mode in the unit 1 and the imaging signal processing unit 2.
(実施例3)
本発明の実施例3は、実施例1の構成にさらに無線通信部が追加されている。無線通信部は、撮像によって取得された画像情報と、比較部による比較判定の経緯および比較判定結果とを外部に無線で通知するために設けられる。 (Example 3)
In the third embodiment of the present invention, a wireless communication unit is further added to the configuration of the first embodiment. The wireless communication unit is provided to wirelessly notify the image information acquired by imaging, the background of comparison determination by the comparison unit, and the comparison determination result to the outside.
本発明の実施例3は、実施例1の構成にさらに無線通信部が追加されている。無線通信部は、撮像によって取得された画像情報と、比較部による比較判定の経緯および比較判定結果とを外部に無線で通知するために設けられる。 (Example 3)
In the third embodiment of the present invention, a wireless communication unit is further added to the configuration of the first embodiment. The wireless communication unit is provided to wirelessly notify the image information acquired by imaging, the background of comparison determination by the comparison unit, and the comparison determination result to the outside.
図4は本発明の実施例3におけるカプセル型投薬装置の構成を示すブロック図である。図3において、実施例1の図1におけるのと同じ符号は同一の構成要素を指している。本実施例に特有の構成は、上述したように無線通信部9である。無線通信部9は、比較部4による比較判定結果が一致を示すときに起動され、撮像部1および撮像信号処理部2によって取得生成された画像情報を体外に向けて無線送信するとともに、比較部4による比較判定の経緯および比較判定結果を体外に向けて無線送信するように構成されている。比較部4の出力側および撮像信号処理部2の出力側は無線通信部9に接続されている。無線通信部9はカプセル20に内蔵されている。その他の構成については、実施例1の場合と同様であるので、説明を省略する。
FIG. 4 is a block diagram showing the configuration of a capsule-type dispensing device in Embodiment 3 of the present invention. In FIG. 3, the same reference numerals as those in FIG. 1 of the first embodiment denote the same components. A configuration unique to the present embodiment is the wireless communication unit 9 as described above. The wireless communication unit 9 is activated when the comparison determination result by the comparison unit 4 indicates a match, wirelessly transmits the image information acquired and generated by the imaging unit 1 and the imaging signal processing unit 2 to the outside of the body, and the comparison unit The process of comparison determination by 4 and the comparison determination result are wirelessly transmitted to the outside of the body. The output side of the comparison unit 4 and the output side of the imaging signal processing unit 2 are connected to the wireless communication unit 9. The wireless communication unit 9 is built in the capsule 20. Other configurations are the same as those in the first embodiment, and thus description thereof is omitted.
次に、上記のように構成された本実施例のカプセル型投薬装置の動作を説明する。比較部4は比較判定結果が一致を示すとき、薬剤放出部7に一致を示す比較判定結果を送出するとともに、無線通信部8に一致を示す比較判定結果を送出する。一致を示す比較判定結果を受け取った無線通信部9は、撮像信号処理部2が生成した画像情報を体外に向けて無線送信するとともに、比較部4による比較判定の経緯および比較判定結果を体外に向けて無線送信する。薬剤が患部に向けて放出されている様子も画像情報となる。無線送信されてくる画像情報と比較判定の経緯および比較判定結果は、外部に設置されている図示しない受信部とメモリ制御部とを介して外部メモリに格納される。その他の動作については、実施例1の場合と同様であるので説明を省略する。
Next, the operation of the capsule-type dispensing device of the present embodiment configured as described above will be described. When the comparison determination result indicates coincidence, the comparison unit 4 transmits a comparison determination result indicating coincidence to the medicine release unit 7 and also transmits a comparison determination result indicating coincidence to the wireless communication unit 8. The wireless communication unit 9 that has received the comparison determination result indicating coincidence wirelessly transmits the image information generated by the imaging signal processing unit 2 to the outside of the body, and the background of the comparison determination by the comparison unit 4 and the comparison determination result to the outside of the body. Send it wirelessly. The state in which the medicine is released toward the affected area is also image information. The wirelessly transmitted image information, the history of comparison determination and the comparison determination result are stored in an external memory via a receiving unit and a memory control unit (not shown) installed outside. Other operations are the same as in the case of the first embodiment, and a description thereof will be omitted.
体内を移動して体外へ排出されたカプセルを回収して、画像情報や比較判定の経緯および比較判定結果を取り出すことはむずかしい(排出経路に難あり)。しかし、本実施例のように無線で送受信するように構成してあれば、患部に対する薬剤の直接的投与の成否を容易に確認することができる。この場合に、外部へ無線通信するのは比較判定結果が一致を示す状態であって、不一致を示す状態では通知は行わない。これにより電力消費が抑制されて、電池駆動による動作継続時間を長くすることが可能となる。
It is difficult to collect the capsules that have moved through the body and discharged outside the body, and to retrieve the image information, the background of the comparison determination, and the comparison determination result (the discharge route is difficult). However, if it is configured to transmit and receive wirelessly as in the present embodiment, the success or failure of direct administration of the drug to the affected area can be easily confirmed. In this case, wireless communication to the outside is in a state in which the comparison determination result indicates coincidence, and notification is not performed in a state in which disagreement is present. As a result, power consumption is suppressed, and the operation continuation time by battery driving can be extended.
(実施例4)
本発明の実施例4では、実施例3の構成にさらに次の構成が追加されている。すなわち、実施例4では、比較部4と撮像部1との間、および比較部4と撮像信号処理部2との間に関係性をもたせ、比較部4の比較判定結果が不一致を示す期間では撮像の解像度を粗くし、一致を示す期間では撮像の解像度を細かくする制御を行うように構成したものである。 Example 4
In the fourth embodiment of the present invention, the following configuration is further added to the configuration of the third embodiment. That is, in Example 4, there is a relationship between thecomparison unit 4 and the imaging unit 1 and between the comparison unit 4 and the imaging signal processing unit 2, and in a period in which the comparison determination result of the comparison unit 4 shows a mismatch. The control is made so that the imaging resolution is coarsened and the imaging resolution is fined during a period of coincidence.
本発明の実施例4では、実施例3の構成にさらに次の構成が追加されている。すなわち、実施例4では、比較部4と撮像部1との間、および比較部4と撮像信号処理部2との間に関係性をもたせ、比較部4の比較判定結果が不一致を示す期間では撮像の解像度を粗くし、一致を示す期間では撮像の解像度を細かくする制御を行うように構成したものである。 Example 4
In the fourth embodiment of the present invention, the following configuration is further added to the configuration of the third embodiment. That is, in Example 4, there is a relationship between the
図5は本発明の実施例4におけるカプセル型投薬装置の構成を示すブロック図である。図5において、実施例3の図4におけるのと同じ符号は同一構成要素を指している。本実施例においては、撮像部1と撮像信号処理部2とは、比較部4から受け取った比較判定結果が不一致を示す期間では低い解像度のモードで動作し、一致を示す期間では高い解像度のモードで動作するように構成されている。以上の制御を実施するために比較部4はその比較判定結果を撮像部1と画像信号処理部2とに送出するように構成されている。その他の構成については、実施例3と同様であるので説明を省略する。
FIG. 5 is a block diagram showing the configuration of the capsule-type dosing device according to the fourth embodiment of the present invention. In FIG. 5, the same reference numerals as in FIG. 4 of the third embodiment denote the same components. In the present embodiment, the imaging unit 1 and the imaging signal processing unit 2 operate in a low resolution mode during a period in which the comparison determination result received from the comparison unit 4 does not match, and in a high resolution mode during a period indicating the match. It is configured to work with. In order to carry out the above control, the comparison unit 4 is configured to send the comparison determination result to the imaging unit 1 and the image signal processing unit 2. Since other configurations are the same as those in the third embodiment, the description thereof is omitted.
次に、上記のように構成された本実施例のカプセル型投薬装置の動作を説明する。比較部4は当初は比較判定結果として不一致を示す信号を撮像部1と画像信号処理部2とに出力する。この状態において撮像部1と画像信号処理部2とでは、撮像の解像度を粗くして消費電力を抑える低解像度モードが設定される。比較部4において撮像信号処理部2からの画像情報と照合情報蓄積部3からの照合情報とが一致すると、比較部4は比較判定結果として一致を示す信号を無線通信部9と撮像部1と撮像信号処理部2とに出力する。一致を示す比較判定結果を受け取った信号撮像部1と撮像信号処理部2とでは、動作モードが撮像の解像度を高くする高解像度モードに切り替えられる。これにより、撮像部1と画像信号処理部2とで取得・生成される画像情報(照合成立時の画像情報)は高精細となる。この画像情報が無線通信部9に供給される。無線通信部9は高精細な画像情報を外部に無線送信する。このとき、比較判定の経緯および比較判定結果も送信されることが望ましい。その他の動作については、実施例3の場合と同様であるので説明を省略する。
Next, the operation of the capsule-type dispensing device of the present embodiment configured as described above will be described. The comparison unit 4 initially outputs a signal indicating mismatch as a comparison determination result to the imaging unit 1 and the image signal processing unit 2. In this state, the imaging unit 1 and the image signal processing unit 2 set a low resolution mode in which the imaging resolution is coarsened and power consumption is reduced. When the comparison unit 4 matches the image information from the imaging signal processing unit 2 and the verification information from the verification information storage unit 3, the comparison unit 4 sends a signal indicating a match as a comparison determination result to the wireless communication unit 9 and the imaging unit 1. Output to the imaging signal processing unit 2. In the signal imaging unit 1 and the imaging signal processing unit 2 that have received the comparison determination result indicating coincidence, the operation mode is switched to the high resolution mode in which the imaging resolution is increased. Thereby, the image information acquired and generated by the imaging unit 1 and the image signal processing unit 2 (image information when the collation is established) becomes high definition. This image information is supplied to the wireless communication unit 9. The wireless communication unit 9 wirelessly transmits high-definition image information to the outside. At this time, it is desirable that the history of comparison determination and the comparison determination result are also transmitted. Other operations are the same as in the case of the third embodiment, and a description thereof will be omitted.
図6は上記の動作を示すフローチャートである。まずは通常動作を行い、その過程で比較部4での判断が行われる。比較判定結果が不一致を示す期間では、通常動作を繰り返すが、比較判定結果が一致を示す期間では、撮像部1および画像信号処理部2の動作モードが高解像度モードに切り替えられる。以上の結果として、消費電力の抑制と高精細画像情報の取得とをともに満たすことができる。高精細画像情報の取得は、投薬結果の確認精度の向上につながる。
FIG. 6 is a flowchart showing the above operation. First, a normal operation is performed, and a determination is made in the comparison unit 4 in the process. The normal operation is repeated in the period in which the comparison determination result indicates a mismatch, but the operation mode of the imaging unit 1 and the image signal processing unit 2 is switched to the high resolution mode in the period in which the comparison determination result indicates a match. As a result of the above, it is possible to satisfy both suppression of power consumption and acquisition of high-definition image information. Acquisition of high-definition image information leads to an improvement in the accuracy of confirmation of medication results.
上記では照合成立時の画像情報の品質を高いものにするのに、解像度を高く設定するように構成したが、これに代えて、単位時間当たりのフレーム数を多くすることにより画像情報の品質を高くするのでもよい。すなわち、この変形例では、撮像部1と撮像信号処理部2とは、比較部4から受け取った比較判定結果が不一致を示す期間では、単位時間当たりのフレーム数が少ないモードで動作し、一致を示す期間では、単位時間当たりのフレーム数が多いモードで動作するように構成されている。単位時間当たりのフレーム数が多い画像情報は、情報量の大きい情報である。この場合も、消費電力の抑制と高品質画像情報の取得とをともに満たすことができ、投薬結果の確認精度の向上につながる。
In the above, the resolution is set to be high in order to increase the quality of the image information when the verification is established, but instead, the quality of the image information is increased by increasing the number of frames per unit time. It may be high. That is, in this modified example, the imaging unit 1 and the imaging signal processing unit 2 operate in a mode in which the number of frames per unit time is small during the period in which the comparison determination result received from the comparison unit 4 indicates a mismatch, In the period shown, it is configured to operate in a mode with a large number of frames per unit time. Image information with a large number of frames per unit time is information with a large amount of information. In this case as well, both the suppression of power consumption and the acquisition of high-quality image information can be satisfied, leading to an improvement in the accuracy of confirmation of medication results.
なお、応用として、比較判定結果が一致を示すようになったときの動作モードとして、高解像度かつ単位時間当たりのフレーム数が多いモードに設定するように構成してもよい。
It should be noted that as an application, the operation mode when the comparison determination result comes to coincide may be set to a mode with a high resolution and a large number of frames per unit time.
(実施例5)
本発明の実施例5は上述した実施例よりも詳しくカプセル型投薬装置を説明するものである。図7は本発明の実施例5のカプセル型投薬装置の構成図である。カプセル20の前方部に被写体を照射する光源18と光学レンズ11とが配置され、その後方に撮像部1が配置されている。光学レンズ11は被写体の光学像を撮像部1に結像させるものであり、撮像部1は入射光量に応じた信号電荷を蓄積し光電変換して出力するものである。カプセル20の後方部には薬剤補給部6と薬剤放出部7とが配置され、その前方に薬剤保持部5が配置されている。さらにカプセル20内には、以下のものが適宜に配置されている。すなわち、当該カプセル型投薬装置の全体を制御するCPU19、撮像部1の出力を画像情報に変換する撮像信号処理部2、画像比較に使用する照合情報を蓄積する照合情報蓄積部3としてのメモリ3a、撮像信号処理部2から出力される画像情報とメモリ3aから出力される照合情報とを比較してその比較判定結果を出力する比較部4、CPU19に動作指定を行う情報入力部8、撮像信号処理部2と比較部4とから出力される情報を外部に通信する無線通信部9、および電池21がカプセル20内に配置されている。図において、ブロック間を結ぶ実線は信号・データのラインを示し、波線は制御ラインを示している。 (Example 5)
Embodiment 5 of the present invention describes a capsule-type dispensing device in more detail than the above-described embodiment. FIG. 7 is a configuration diagram of a capsule-type dispensing device according to Embodiment 5 of the present invention. A light source 18 that irradiates a subject and an optical lens 11 are disposed in front of the capsule 20, and an imaging unit 1 is disposed behind the light source 18. The optical lens 11 forms an optical image of a subject on the imaging unit 1, and the imaging unit 1 accumulates signal charges corresponding to the amount of incident light, photoelectrically converts them, and outputs them. A drug replenishment unit 6 and a drug release unit 7 are arranged in the rear part of the capsule 20, and a drug holding unit 5 is arranged in front of the capsule 20. Further, the following are appropriately arranged in the capsule 20. That is, a CPU 19 that controls the entire capsule dosage unit, an imaging signal processing unit 2 that converts the output of the imaging unit 1 into image information, and a memory 3a as a verification information storage unit 3 that stores verification information used for image comparison. The comparison unit 4 that compares the image information output from the imaging signal processing unit 2 with the collation information output from the memory 3a and outputs the comparison determination result, the information input unit 8 that designates the operation to the CPU 19, and the imaging signal A wireless communication unit 9 that communicates information output from the processing unit 2 and the comparison unit 4 to the outside and a battery 21 are arranged in the capsule 20. In the figure, solid lines connecting the blocks indicate signal / data lines, and broken lines indicate control lines.
本発明の実施例5は上述した実施例よりも詳しくカプセル型投薬装置を説明するものである。図7は本発明の実施例5のカプセル型投薬装置の構成図である。カプセル20の前方部に被写体を照射する光源18と光学レンズ11とが配置され、その後方に撮像部1が配置されている。光学レンズ11は被写体の光学像を撮像部1に結像させるものであり、撮像部1は入射光量に応じた信号電荷を蓄積し光電変換して出力するものである。カプセル20の後方部には薬剤補給部6と薬剤放出部7とが配置され、その前方に薬剤保持部5が配置されている。さらにカプセル20内には、以下のものが適宜に配置されている。すなわち、当該カプセル型投薬装置の全体を制御するCPU19、撮像部1の出力を画像情報に変換する撮像信号処理部2、画像比較に使用する照合情報を蓄積する照合情報蓄積部3としてのメモリ3a、撮像信号処理部2から出力される画像情報とメモリ3aから出力される照合情報とを比較してその比較判定結果を出力する比較部4、CPU19に動作指定を行う情報入力部8、撮像信号処理部2と比較部4とから出力される情報を外部に通信する無線通信部9、および電池21がカプセル20内に配置されている。図において、ブロック間を結ぶ実線は信号・データのラインを示し、波線は制御ラインを示している。 (Example 5)
以上のように構成されたカプセル型投薬装置は、内蔵された電池21を電源として動作する。使用される前に薬剤補給部6から薬剤保持部5へ薬剤が補給される。そのうえで電源が投入されると、CPU19は薬剤補給部6および薬剤保持部5を制御して、これらを薬剤補給状態から保持状態に変化させる。またCPU19は、投薬担当者を促して画像比較に使用する最新かつ患者の現在の疾患に対応した追加照合情報を情報入力部8に入力させて取り込んだうえで、取り込んだ追加照合情報をメモリ3aに格納する。さらにCPU19は、投薬担当者を促して照合元データが記載された原本を撮影することで第1の撮像信号を取得しさらに取得した第1の撮像信号を信号処理することで照合情報を生成させる。さらにCPU19は、信号処理部2で生成させた照合情報に、情報入力部8で取り込んだ追加照合情報を加えたうえでその照合情報をメモリ3aに格納する。さらにCPU19は、情報入力部8から入力される動作条件に基づいて、撮像部1と撮像信号処理部2と光源18とを制御することで、撮影する画像の単位当たりの枚数を調整する。さらにCPU19は、上記動作条件に基づいて各ブロックの動作状態を設定したうえで、通常動作状態に移行する。これにより撮像部1からの出力は撮像信号処理部2で画像情報に変換されて出力される。比較部4は、撮像信号処理部2からの画像情報とメモリ3aからの照合情報とを比較して、それらの情報が一致するか否かの一致判定を行う。判定内容はCPU19に送られる。比較部4が一致と判断する場合、CPU19は薬剤放出部7を制御して薬剤保持部5に保持されている薬剤を放出させ、さらに、CPU19は、無線通信部9を起動させて通信を行う。無線通信部9は送られてくる比較部4が一致と判断した過程の情報と画像情報とを無線を使用して体外に送信する。
The capsule-type dosing device configured as described above operates using the built-in battery 21 as a power source. Before being used, the drug is supplied from the drug supply unit 6 to the drug holding unit 5. Then, when the power is turned on, the CPU 19 controls the medicine supply unit 6 and the medicine holding unit 5 to change them from the medicine supply state to the holding state. Further, the CPU 19 prompts the person in charge of medication to input the latest collation information corresponding to the current disease of the patient to be used for the image comparison to the information input unit 8 and captures the acquired additional collation information in the memory 3a. To store. Further, the CPU 19 prompts the person in charge of medication to capture the original image on which the verification source data is described, thereby acquiring the first imaging signal and processing the acquired first imaging signal to generate verification information. . Further, the CPU 19 adds the additional verification information captured by the information input unit 8 to the verification information generated by the signal processing unit 2, and then stores the verification information in the memory 3a. Further, the CPU 19 adjusts the number of images to be captured per unit by controlling the imaging unit 1, the imaging signal processing unit 2, and the light source 18 based on the operating conditions input from the information input unit 8. Further, the CPU 19 sets the operation state of each block based on the operation condition, and then shifts to the normal operation state. Thereby, the output from the imaging unit 1 is converted into image information by the imaging signal processing unit 2 and output. The comparison unit 4 compares the image information from the imaging signal processing unit 2 with the collation information from the memory 3a, and determines whether or not these pieces of information match. The determination content is sent to the CPU 19. When the comparison unit 4 determines that they match, the CPU 19 controls the drug release unit 7 to release the drug held in the drug holding unit 5, and the CPU 19 activates the wireless communication unit 9 to perform communication. . The wireless communication unit 9 transmits the information of the process determined by the comparison unit 4 and the image information transmitted to the outside of the body using wireless communication.
本実施例のカプセル型投薬装置によれば、実施例1~4で説明したように、撮影で取得した画像情報が照合情報と一致する患部に対して薬剤を直接的に投与することができるとともに、患者装着の体外装置や大掛かりな医療診断装置や照合情報の送受信のための無線送受信機を不要化し、取り扱いを簡便化し、さらに患者の肉体的、精神的負担を軽減することができる。
According to the capsule-type dosing device of the present embodiment, as described in the first to fourth embodiments, the medicine can be directly administered to the affected area where the image information acquired by photographing matches the collation information. In addition, it eliminates the need for extracorporeal devices worn by patients, large-scale medical diagnostic devices, and wireless transceivers for sending and receiving verification information, simplifying handling, and reducing physical and mental burdens on patients.
本発明のカプセル型投薬装置は、照合情報の取得と保持、薬剤運搬、体腔・患部の撮影、信号処理、画像情報の照合、薬剤放出など、患部への薬剤の直接の投与に関係する一連の手順を自己完結的に遂行可能であり、患者装着の体外装置や大掛かりな医療診断装置や照合情報の送受信のための無線送受信機が不要で取り扱いが簡便であり、患者の肉体的、精神的負担が軽減されるもので、カプセルカメラなどの医療カメラに有用である。
The capsule-type dosing device of the present invention is a series of items related to direct administration of a drug to the affected area, such as acquisition and holding of collation information, drug delivery, imaging of a body cavity / affected area, signal processing, image information collation, drug release, etc. The procedure can be performed in a self-contained manner, and there is no need for extracorporeal devices attached to the patient, large-scale medical diagnostic devices, and wireless transceivers for sending and receiving verification information. This is useful for medical cameras such as capsule cameras.
1 撮像部
2 撮像信号処理部
3 照合情報蓄積部
3a メモリ
4 比較部
5 薬剤保持部
6 薬剤補給部
7 薬剤放出部
8 情報入力部
9 無線通信部
11 光学レンズ
18 光源
19 CPU
20 カプセル
21 電池 DESCRIPTION OFSYMBOLS 1 Imaging part 2 Imaging signal processing part 3 Collation information storage part 3a Memory 4 Comparison part 5 Drug holding part 6 Drug supply part 7 Drug release part 8 Information input part 9 Wireless communication part 11 Optical lens 18 Light source 19 CPU
20capsules 21 batteries
2 撮像信号処理部
3 照合情報蓄積部
3a メモリ
4 比較部
5 薬剤保持部
6 薬剤補給部
7 薬剤放出部
8 情報入力部
9 無線通信部
11 光学レンズ
18 光源
19 CPU
20 カプセル
21 電池 DESCRIPTION OF
20
Claims (7)
- 経口投入されて生体内の患部に至る体腔を移動可能なカプセルを備え、
前記カプセルは、薬剤保持部と、撮像部と、撮像信号処理部と、照合情報蓄積部と、比較部と、薬剤放出部とを備えており、
前記薬剤保持部は、前記体腔にある患部または前記体腔の近傍にある患部に投与すべき薬剤を保持し、
前記撮像部は、前記カプセルが前記生体に経口投入される前には、前記患部の特徴に関する照合元情報が掲載された原本を撮影して第1の撮像信号を生成可能に構成される一方、前記カプセルが前記生体に経口投入された後は前記患部に至る前記体腔の内部を連続または断続して撮影して第2の撮像信号を撮影し、
前記撮像信号処理部は、前記第1の撮像信号から照合情報を、前記第2の撮像信号から画像情報をそれぞれ生成し、
前記照合情報蓄積部は前記照合情報を蓄積し、
前記比較部は、前記照合情報蓄積部に蓄積された前記照合情報と前記撮像信号処理部で生成された前記画像情報とを比較し、
前記薬剤放出部は、前記比較部において前記画像情報と前記照合情報との比較判定結果が一致を示すと、前記薬剤保持部から前記薬剤を前記患部に向けて放出させる、
カプセル型投薬装置。 It is equipped with a capsule that can be moved through the body cavity that is orally injected to reach the affected area in the body,
The capsule includes a drug holding unit, an imaging unit, an imaging signal processing unit, a collation information storage unit, a comparison unit, and a drug release unit.
The drug holding unit holds a drug to be administered to an affected part in the body cavity or an affected part in the vicinity of the body cavity,
While the imaging unit is configured to be able to generate a first imaging signal by photographing an original on which collation source information related to the characteristics of the affected part is posted before the capsule is orally injected into the living body, After the capsule is orally injected into the living body, the inside of the body cavity leading to the affected area is continuously or intermittently photographed to photograph a second imaging signal,
The imaging signal processing unit generates verification information from the first imaging signal and image information from the second imaging signal,
The verification information storage unit stores the verification information,
The comparison unit compares the verification information stored in the verification information storage unit with the image information generated by the imaging signal processing unit,
When the comparison result between the image information and the collation information is coincident in the comparison unit, the drug release unit releases the drug from the drug holding unit toward the affected part.
Capsule type dosing device. - 前記カプセルは第1の情報入力部をさらに備え、
前記第1の情報入力部は、前記カプセルが前記生体に経口投入される前に前記照合情報に追加するまたは前記照合情報を更新する追加照合情報を入力可能に構成され、
前記照合情報蓄積部は前記第1の情報入力部に入力された前記追加照合情報を加えた前記照合情報を蓄積する、
請求項1に記載のカプセル型投薬装置。 The capsule further includes a first information input unit,
The first information input unit is configured to be able to input additional verification information to be added to the verification information or to update the verification information before the capsule is orally injected into the living body,
The verification information storage unit stores the verification information added with the additional verification information input to the first information input unit;
The capsule-type dosing device according to claim 1. - 前記カプセルは、第2の情報入力部をさらに備え、
前記第2の情報入力部は、前記カプセルが前記生体に経口投入される前に前記撮像部と前記撮像信号処理部との動作モードに関する情報が入力可能に構成され、
前記撮像部と前記撮像信号処理部とは、前記第2の情報入力部に入力された情報に基づいて前記動作モードが設定可能に構成されている、
請求項1に記載のカプセル型投薬装置。 The capsule further includes a second information input unit,
The second information input unit is configured to be able to input information about operation modes of the imaging unit and the imaging signal processing unit before the capsule is orally injected into the living body.
The imaging unit and the imaging signal processing unit are configured such that the operation mode can be set based on information input to the second information input unit.
The capsule-type dosing device according to claim 1. - 前記カプセルは無線通信部をさらに備え、
前記無線通信部は、前記比較部において前記画像情報と前記照合情報との比較判定結果が一致を示すと、前記撮像信号処理部が生成した前記画像情報を外部に無線送信するように構成されている、
請求項1に記載のカプセル型投薬装置。 The capsule further includes a wireless communication unit,
The wireless communication unit is configured to wirelessly transmit the image information generated by the imaging signal processing unit to the outside when the comparison determination result between the image information and the verification information indicates a match in the comparison unit. Yes,
The capsule-type dosing device according to claim 1. - 前記無線通信部は、さらに、前記比較部による比較判定の経緯および比較判定結果を外部に無線送信するように構成されている、
請求項4に記載のカプセル型投薬装置。 The wireless communication unit is further configured to wirelessly transmit the background of the comparison determination by the comparison unit and the comparison determination result to the outside.
The capsule-type dosing device according to claim 4. - 前記比較部は、前記比較判定結果を前記撮像部と前記画像信号処理部とに送出するように構成され、
前記撮像部と前記画像信号処理部とは、前記比較部から受け取った前記比較判定結果が不一致を示す期間では低い解像度のモードで動作し、一致を示す期間では高い解像度のモードで動作するように構成されている、
請求項4に記載のカプセル型投薬装置。 The comparison unit is configured to send the comparison determination result to the imaging unit and the image signal processing unit,
The imaging unit and the image signal processing unit operate in a low resolution mode during a period in which the comparison determination result received from the comparison unit indicates a mismatch, and operate in a high resolution mode during a period in which the comparison indicates a match. It is configured,
The capsule-type dosing device according to claim 4. - 前記比較部は、前記比較判定結果を前記撮像部と前記画像信号処理部とに送出するように構成され、
前記撮像部と前記画像信号処理部とは、前記比較部から受け取った前記比較判定結果が不一致を示す期間では単位時間当たりのフレーム数の少ないモードで動作し、一致を示す期間では単位時間当たりのフレーム数の多いモードで動作するように構成されている、
請求項4に記載のカプセル型投薬装置。 The comparison unit is configured to send the comparison determination result to the imaging unit and the image signal processing unit,
The imaging unit and the image signal processing unit operate in a mode in which the number of frames per unit time is small during a period in which the comparison determination result received from the comparison unit indicates a mismatch, and per unit time in a period indicating a match. It is configured to operate in a mode with a large number of frames,
The capsule-type dosing device according to claim 4.
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Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN111227769A (en) * | 2020-01-20 | 2020-06-05 | 张源一 | Endoscopic capsule, camera shooting mechanism thereof and medicine discharging control method |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
TWM448255U (en) * | 2012-08-23 | 2013-03-11 | Morevalued Technology Co Let | Capsule endoscopy device |
WO2016079840A1 (en) * | 2014-11-20 | 2016-05-26 | オリンパス株式会社 | Capsule endoscope system, capsule endoscope, capsule endoscope wireless communication method, and program |
CN105833418B (en) * | 2016-03-15 | 2022-04-22 | 南京航空航天大学 | Blood vessel treatment device of dosing based on piezoelectricity drive |
Citations (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2004261522A (en) * | 2003-03-04 | 2004-09-24 | Olympus Corp | Capsule type medical device |
JP2005102851A (en) * | 2003-09-29 | 2005-04-21 | Olympus Corp | Medication capsule, capsule type medical device, capsule type medical device system and control method |
JP2005334331A (en) * | 2004-05-27 | 2005-12-08 | Olympus Corp | Capsule dosing system |
JP2006061399A (en) * | 2004-08-26 | 2006-03-09 | Hitachi Ltd | Inspection capsule and inspection system |
JP2007021039A (en) * | 2005-07-20 | 2007-02-01 | Olympus Corp | Body cavity introduction device and body cavity introduction device placement system |
JP2007523703A (en) * | 2004-02-28 | 2007-08-23 | チョンクイン ジンシャン サイエンス アンド テクノロジー(グループ) カンパニー リミテッド | Medical wireless capsule endoscope system |
JP2008237640A (en) * | 2007-03-28 | 2008-10-09 | Fujifilm Corp | Capsule endoscope, capsule endoscope system, and capsule endoscope operation control method |
JP2008256515A (en) * | 2007-04-04 | 2008-10-23 | Hoya Corp | Chart deterioration detecting method |
JP2009045193A (en) * | 2007-08-20 | 2009-03-05 | Hoya Corp | Capsule endoscope and miniaturized medical device for organ diagnosis |
JP2009172287A (en) * | 2008-01-28 | 2009-08-06 | Fujifilm Corp | Capsule endoscope, capsule endoscope operation control method, and information management apparatus |
JP2009225933A (en) * | 2008-03-21 | 2009-10-08 | Fujifilm Corp | Capsule endoscope system, and capsule endoscope motion control method |
JP2009273676A (en) * | 2008-05-15 | 2009-11-26 | Hoya Corp | Endoscope apparatus capable of detecting color unevenness |
JP2009273684A (en) * | 2008-05-15 | 2009-11-26 | Hoya Corp | Endoscope apparatus capable of detecting color unevenness |
-
2010
- 2010-03-01 JP JP2010044036A patent/JP2011177339A/en active Pending
-
2011
- 2011-01-14 WO PCT/JP2011/000171 patent/WO2011108179A1/en active Application Filing
Patent Citations (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2004261522A (en) * | 2003-03-04 | 2004-09-24 | Olympus Corp | Capsule type medical device |
JP2005102851A (en) * | 2003-09-29 | 2005-04-21 | Olympus Corp | Medication capsule, capsule type medical device, capsule type medical device system and control method |
JP2007523703A (en) * | 2004-02-28 | 2007-08-23 | チョンクイン ジンシャン サイエンス アンド テクノロジー(グループ) カンパニー リミテッド | Medical wireless capsule endoscope system |
JP2005334331A (en) * | 2004-05-27 | 2005-12-08 | Olympus Corp | Capsule dosing system |
JP2006061399A (en) * | 2004-08-26 | 2006-03-09 | Hitachi Ltd | Inspection capsule and inspection system |
JP2007021039A (en) * | 2005-07-20 | 2007-02-01 | Olympus Corp | Body cavity introduction device and body cavity introduction device placement system |
JP2008237640A (en) * | 2007-03-28 | 2008-10-09 | Fujifilm Corp | Capsule endoscope, capsule endoscope system, and capsule endoscope operation control method |
JP2008256515A (en) * | 2007-04-04 | 2008-10-23 | Hoya Corp | Chart deterioration detecting method |
JP2009045193A (en) * | 2007-08-20 | 2009-03-05 | Hoya Corp | Capsule endoscope and miniaturized medical device for organ diagnosis |
JP2009172287A (en) * | 2008-01-28 | 2009-08-06 | Fujifilm Corp | Capsule endoscope, capsule endoscope operation control method, and information management apparatus |
JP2009225933A (en) * | 2008-03-21 | 2009-10-08 | Fujifilm Corp | Capsule endoscope system, and capsule endoscope motion control method |
JP2009273676A (en) * | 2008-05-15 | 2009-11-26 | Hoya Corp | Endoscope apparatus capable of detecting color unevenness |
JP2009273684A (en) * | 2008-05-15 | 2009-11-26 | Hoya Corp | Endoscope apparatus capable of detecting color unevenness |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN111227769A (en) * | 2020-01-20 | 2020-06-05 | 张源一 | Endoscopic capsule, camera shooting mechanism thereof and medicine discharging control method |
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