1. Field of the Disclosure
The present disclosure relates to a capsule medical device guide system that guides a capsule medical device introduced into a subject.
2. Description of the Related Art
In the related art, a capsule medical device has been developed. The capsule medical device is introduced into a subject and obtains various kinds of information about the inside of the subject, or administers a medical agent or the like into the subject. For example, a capsule endoscope formed to have such a size as to allow itself to be introduced into a digestive tract of a subject is known.
The capsule endoscope includes an imaging function and a wireless communication function inside a capsule-shaped casing. The capsule endoscope is swallowed by a subject and performs capturing while moving through the inside of a digestive tract by means of peristaltic movement or the like. The capsule endoscope then sequentially and wirelessly transmits image data of images of the inside of an organ of the subject (hereinafter also referred to as an in-vivo image). The wirelessly transmitted image data are received by a receiving device provided outside the subject and obtained by an image display device such as a workstation to be subjected to a predetermined image process. Consequently, the in-vivo image of the subject can be displayed in the form of a still image or a motion image.
In recent years, a guide system that guides, by means of a magnetic field, a capsule endoscope introduced into a subject has been proposed. For example, JP 2010-17554 A discloses a guide system that guides a capsule endoscope by means of a magnetic field. Specifically, a permanent magnet is provided inside the capsule endoscope, and a magnetic field generating unit such as an electromagnet and a permanent magnet is provided in a guide device. A liquid such as water is then introduced into a digestive tract (e.g., stomach) of a subject, and the capsule endoscope is caused to float in the liquid. In this state, the capsule endoscope is guided by a magnetic field generated by the magnetic field generation unit. The guide system is provided with a display device that receives image data obtained by the capsule endoscope and displays an in-vivo image. This allows a user to operate the guidance for the capsule endoscope using an operation input unit provided on the guide device with reference to the in-vivo image displayed on the display device.
There is a need for a capsule medical device guide system that allows a user to easily recognize that a capsule medical device is separated from a boundary of a liquid when the capsule medical device is guided in the liquid introduced into a subject.
A capsule medical device guide system according to one aspect of the present disclosure is configured to guide a capsule medical device that captures inside a subject into which a liquid is introduced, and may include: a guide unit configured to guide the capsule medical device by a magnetic field; a position detecting unit configured to detect positional information of the capsule medical device; a display unit configured to display information relating to the capsule medical device within the subject; a scale displayed on the display unit and representing a position of the capsule medical device within the subject; a mark representing, on the scale, an area where the magnetic field is capable of guiding the capsule medical device; a first indicator representing, on the scale, a boundary position of a range in the area where the capsule medical device is capable of being guided; a second indicator representing, on the scale, a current position of the capsule medical device; and a control unit configured to control positions of the first indicator and the second indicator on the scale based on the positional information detected by the position detecting unit.
The above and other objects, features, advantages and technical and industrial significance of this disclosure will be better understood by reading the following detailed description of presently preferred embodiments of the disclosure, when considered in connection with the accompanying drawings.
Hereinafter, a capsule medical device guide system according to an embodiment of the present disclosure will be described with reference to the drawings. In the following description, a capsule endoscope that is orally introduced into a subject to capture the inside of the subject (inside of a lumen) is described as an example of a capsule medical device that is guided in the capsule medical device guide system according to the present embodiment. However, the present disclosure is not limited by this embodiment. In other words, the present disclosure can be applied to guidance for various capsule-shaped medical devices such as, for example, a capsule endoscope that moves through, while capturing, the inside of a lumen ranging from an esophagus to an anus of a subject, a capsule medical device that delivers a medical agent or the like into a subject, and a capsule medical device including a pH sensor that measures pH within a subject.
In the following description, a shape, a size, and a positional relation are only schematically illustrated in each drawing to such an extent that contents of the present disclosure can be understood. Therefore, the present disclosure is not limited only to the shape, the size, and the positional relation represented in each drawing. In the drawings, identical elements are provided with the same reference signs.
The capsule endoscope 10 is introduced into an organ of a subject together with a predetermined liquid by means of oral ingestion or the like, moves through the inside of a digestive tract, and is eventually discharged to the outside of the subject. During this time, the capsule endoscope 10 floats in the liquid within the organ of the subject such as a stomach, and captures the inside of the subject to sequentially generate image data of in-vivo images while being guided by the magnetic field MG. The capsule endoscope 10 then wirelessly transmits the image data.
The capsule-shaped casing 100 is an outer casing formed to have such a size as to allow itself to be introduced into an organ of a subject. The capsule-shaped casing 100 has a tubular casing 101 and dome-shaped casings 102, 103, and is configured such that both opening ends of the tubular casing 101 are closed by the dome-shaped casings 102, 103. The tubular casing 101 is a colored casing that is substantially opaque to visible light. On the other hand, each of the dome-shaped casings 102, 103 is a dome-like optical member that is transparent to light having a predetermined wavelength band such as visible light. As illustrated in
The imaging unit 11A has an illumination unit 12A such as an LED, an optical system 13A such as a condenser lens, and an image sensor 14A such as a CMOS image sensor or a CCD. The illumination unit 12A emits illumination light such as white light to an imaging field of the image sensor 14A and illuminates a subject within the imaging field through the dome-shaped casing 102. The optical system 13A collects reflected light from the imaging field at an imaging surface of the image sensor 14A to form an image. The image sensor 14A converts, into an electrical signal, the reflected light (optical signal) from the imaging field received at the imaging surface, and outputs the electrical signal as an image signal.
In the same way as the imaging unit 11A, the imaging unit 11B has an illumination unit 12B such as an LED, an optical system 13B such as a condenser lens, and an image sensor 14B such as a CMOS image sensor or a CCD. The imaging unit 11B captures a subject within an imaging field through the dome-shaped casing 103.
As illustrated in
The control unit 15 controls operation of each of the imaging units 11A, 11B and operation of the wireless communication unit 16 and controls input and output of a signal between these components. More specifically, the control unit 15 causes the image sensor 14A to capture a subject within the imaging field illuminated with the illumination unit 12A, and causes the image sensor 14B to capture a subject within the imaging field illuminated with the illumination unit 12B. The control unit 15 then performs a predetermined signal process on an image signal output from each of the image sensors 14A, 14B. The control unit 15 further causes the wireless communication unit 16 to sequentially and wirelessly transmit the above-mentioned image signals in time series.
The wireless communication unit 16 includes an antenna 16a for transmitting a wireless signal. The wireless communication unit 16 obtains, from the control unit 15, an image signal of an in-vivo image generated by each of the imaging units 11A, 11B that have captured a subject, and performs a modulation process or the like on the image signal to generate a wireless signal. The wireless communication unit 16 then transmits the generated wireless signal via the antenna 16a.
The power unit 17 is a power storage unit such as a button type battery and a capacitor, and has a switch unit such as a magnetic switch and an optical switch. When the power unit 17 is configured to have the magnetic switch, an on/off state of a power source is switched by a magnetic field applied from the outside. In the on state, power in the power storage unit is appropriately supplied to each component of the capsule endoscope 10, that is, the imaging units 11A, 11B, the control unit 15, and the wireless communication unit 16. In the off state, the power unit 17 stops supplying power to each component of the capsule endoscope 10.
The permanent magnet 18 enables the magnetic field MG generated by a magnetic field generating unit 25 to guide the capsule endoscope 10. The permanent magnet 18 is arranged to be fixed within the capsule-shaped casing 100 so that a magnetization direction is inclined to the long axis La. In
Referring again to
The receiving unit 21 includes a plurality of receiving antennas 21a and sequentially receives wireless signals from the capsule endoscope 10 via these receiving antennas 21a. The receiving unit 21 selects an antenna having the highest reception electric field intensity from among these receiving antennas 21a, and performs a demodulation process or the like on a wireless signal from the capsule endoscope 10 received via the selected antenna. The receiving unit 21 thus extracts an image signal from the wireless signal and outputs the image signal to the display unit 23.
The position detecting unit 22 detects the position of the capsule endoscope 10 within a subject based on intensity of a wireless signal received by the receiving unit 21, and generates and outputs information about the position of the capsule endoscope 10. Hereinafter, the information about the position of the capsule endoscope 10 is simply referred to as positional information. For instance, as disclosed in JP 2007-283001 A, the position of the capsule endoscope 10 can be obtained in such a manner that an initial value of the position is appropriately set, and a process of calculating an estimate value of the position by means of the Gauss-Newton method is repeated until a shift amount between the calculated estimate value and a previous estimate value becomes equal to or less than a predetermined value. Alternatively, the position of the capsule endoscope 10 may be calculated in such a manner that a coil that generates a high-frequency magnetic field is provided in the capsule endoscope 10, and the magnetic field generated by this coil is detected outside a subject.
The display unit 23 has various displays such as a liquid crystal display. The display unit 23 displays an in-vivo image that is based on an image signal input from the receiving unit 21, positional information of the capsule endoscope 10, and various other types of information.
The operation input unit 24 accepts input of various types of information such as guide instruction information for guiding the capsule endoscope 10 and setting information for setting various modes for the guide device 20. The guide instruction information is information for controlling the position and a posture of the capsule endoscope 10 to be subjected to guide operation. The guide instruction information specifically includes information about translation operation, tilt angle changing operation, and azimuth angle changing operation or the like. The translation operation translates the capsule endoscope 10 in a horizontal direction or a vertical direction. The tilt angle changing operation changes a tilt angle of the long axis La of the capsule endoscope 10 with respect to the vertical direction. The azimuth angle changing operation changes an azimuth angle that is an angle around a vertical axis of a field of the capsule endoscope 10, i.e., respective fields of the imaging units 11A, 11B which will be described later. The operation input unit 24 inputs, to the control unit 26, these items of information that have been input and accepted.
The operation input unit 24 is realized by, for example, a joystick, a console including various buttons and various switches, and an input device such as a keyboard. In the first embodiment, joysticks illustrated in
As illustrated in
As illustrated in
As illustrated in
As illustrated in
As illustrated in
As illustrated in
The back surface of the joystick 31 is provided with the up button 34U and the down button 34B. When the up button 34U is pressed as represented by an arrow Y15j in
When guide instruction information corresponding to pressing operation of each of the arrows Y15j, Y16j for the up button 34U and the down button 34B is input from the operation input unit 24 to the control unit 26, the control unit 26 calculates, based on this guide instruction information, a guide direction and a guide amount of the distal end of the capsule endoscope 10 on the absolute coordinate system in association with the pressed button. The control unit 26 changes a magnetic field generated by the magnetic field generating unit 25 so that the capsule endoscope 10 is translated in the vertical direction in accordance with the calculated guide direction and guide amount. For example, when the up button 34U is pressed, the magnetic field generating unit 25 weakens intensity of the magnetic field MG and reduces magnetic attracting force that acts on the permanent magnet 18 provided in the capsule endoscope 10. Consequently, the capsule endoscope 10 is elevated as represented by the arrow Y15. On the other hand, when the down button 34B is pressed, the magnetic field generating unit 25 strengthens intensity of the magnetic field MG and increases magnetic attracting force that acts on the permanent magnet 18 provided in the capsule endoscope 10. Consequently, the capsule endoscope 10 is lowered as represented by the arrow Y16.
In addition to these joysticks 31, 32, the operation input unit 24 may further have an input device including various operation buttons and a keyboard or the like.
The magnetic field generating unit 25 generates a magnetic field for changing, relative to a subject, the position, the tilt angle, and the azimuth angle of the capsule endoscope 10 introduced into the subject. A configuration of the magnetic field generating unit 25 is not particularly limited as long as the magnetic field MG, a magnetic gradient of which can be controlled by the control unit 26, can be formed in an area on the bed 20a on which a subject is placed. More specifically, the magnetic field generating unit 25 may include an electromagnet, or the magnetic field generating unit 25 may include a permanent magnet and a drive unit that changes a position or a direction of the permanent magnet.
The control unit 26 includes the guide control unit 261 and a display control unit 262. The guide control unit 261 controls operation of the magnetic field generating unit 25. The display control unit 262 controls a display form of an image and various types of information displayed on the display unit 23.
The guide control unit 261 controls the magnetic field generating unit 25 in a guide mode that depends on a signal input from the operation input unit 24 based on positional information of the capsule endoscope 10 input from the position detecting unit 22 and guide instruction information input from the operation input unit 24. The capsule endoscope 10 is thus guided to a position desired by a user. The guide mode includes a water bottom mode, an underwater mode, and a water surface mode. In the water bottom mode, the capsule endoscope 10 is guided while in contact with a bottom of a liquid introduced into an organ of a subject. In the underwater mode, the capsule endoscope 10 is guided while floating in a liquid. In the water surface mode, the capsule endoscope 10 is guided while floating on a surface of a liquid. Hereinafter, a surface, the inside, and a bottom of a liquid introduced into a subject are described as a water surface, underwater, and a water bottom, respectively. The liquid as used herein also includes a liquid other than water (e.g., saline or the like).
The display control unit 262 generates a screen with a predetermined format including an in-vivo image that is based on an image signal received by the receiving unit 21, positional information of the capsule endoscope 10, and various other types of information. The display control unit 262 causes the display unit 23 to display the screen.
The storage unit 27 includes a storage medium and a writing reading device. The storage medium, such as a flash memory or a hard disk, saves information in a rewritable manner. The writing reading device writes and reads information to and from the storage medium. The storage unit 27 stores image data of an in-vivo image group of a subject that is based on an image signal transmitted from the capsule endoscope 10. The storage unit 27 also stores information such as various programs and various parameters that is used by the control unit 26 to control each component of the guide device 20.
The operation information display area m5 is an area on which a posture diagram m8 and a posture diagram m9 are displayed. The posture diagram m8 indicates the posture of the capsule endoscope 10 on a vertical plane, and the posture diagram m9 indicates the posture of the capsule endoscope 10 on a horizontal plane. On each of the posture diagrams m8, m9, a plurality of directions in which the capsule endoscope 10 can be guided is indicated by arrows. When there is operation input for guiding the capsule endoscope 10 in any of the directions, a display color of an arrow corresponding to the input direction among these arrows is changed. This assists a user to perform the guide operation.
Guide instruction information input from the operation input unit 24 is reflected in a control signal that is output when the guide control unit 261 controls the magnetic field generating unit 25. Therefore, the posture of the capsule endoscope 10 displayed on each of the posture diagrams m8, m9 can be considered to be substantially the same as the posture of the actual capsule endoscope 10 in a subject.
The positional information display area m6 includes a scale m10 and various marks. The scale m10 indicates the position in the Z direction. The various marks are displayed on the scale m10. More specifically, a working area lower limit mark m11, a working area upper limit mark m12, a water bottom mark m13, and a capsule current position mark m14 are displayed on the scale m10. The working area lower limit mark m11 indicates a lower limit position of an area in which the magnetic field MG capable of guiding the capsule endoscope 10 exists, that is, a working area. The working area upper limit mark m12 indicates an upper limit position of the working area. The water bottom mark m13 serves as a first indicator indicating a position of a bottom of a liquid introduced into an organ of a subject. The capsule current position mark m14 serves as a second indicator indicating a current position of the capsule endoscope 10.
Next, an examination method using the capsule medical device guide system 1 will be described.
In the first embodiment, the capsule endoscope 10 is designed so as to have a specific gravity less than a specific gravity of the liquid W and float on the liquid W while the guidance by the magnetic field generating unit 25 is not performed. In this case, owing to a balance between buoyancy of the capsule endoscope 10 with respect to the liquid W, gravity that acts on the capsule endoscope 10, and magnetic attracting force applied by the magnetic field generating unit 25, the capsule endoscope 10 can be stopped at a desired position within the liquid W to allow the inside of the organ ST to be observed.
When the subject is examined by the capsule medical device guide system 1, as illustrated in
In step S10, when a signal including an instruction to start guiding the capsule endoscope 10 is input from the operation input unit 24 to the control unit 26, each component of the guide device 20 starts operating. More specifically, the receiving unit 21 starts the operation to receive a wireless signal transmitted from the capsule endoscope 10, extract an image signal from the wireless signal, and output the image signal to the display unit 23. The position detecting unit 22 starts the operation to detect the position of the capsule endoscope 10 and output positional information. The display unit 23 starts, as illustrated in
The control unit 26 starts obtaining the positional information of the capsule endoscope 10 output from the position detecting unit 22, and starts the control to cause the display unit 23 to display the position of the capsule endoscope 10. More specifically, in the positional information display area m6 illustrated in
In the subsequent step S11, the control unit 26 sets the guide mode of the capsule endoscope 10 to the water bottom mode in which the guidance is performed while a part of the capsule endoscope 10 is in contact with the water bottom WB.
In step S12, the control unit 26 resets a coordinate value ZBT in the Z direction indicating a position of the water bottom WB. Accordingly, as illustrated in
In the subsequent step S13, the guide control unit 261 performs the control to guide the capsule endoscope 10 toward the water bottom WB. Specifically, the guide control unit 261 causes the magnetic field generating unit 25 to generate such a magnetic field that magnetic attracting force applied to the permanent magnet 18 provided inside the capsule endoscope 10 is strengthened.
In step S14, the control unit 26 sets, as the coordinate value ZBT of the water bottom WB, a minimum value Zmin reached by the coordinate value ZCP of the capsule endoscope 10 after the coordinate value ZBT is reset in step S12. Consequently, as illustrated in
In step S15, the control unit 26 determines whether the capsule endoscope 10 reaches the water bottom WB. When the coordinate value ZCP of the capsule endoscope 10 does not change even though a magnetic field that guides the capsule endoscope 10 in a −Z direction is generated by the magnetic field generating unit 25, the capsule endoscope 10 is determined to reach the water bottom WB as illustrated in
When the capsule endoscope 10 does not reach the water bottom WB (step S15: No), the operation of the guide device 20 returns to step S13. On the other hand, when the capsule endoscope 10 reaches the water bottom WB (step S15: Yes), the control unit 26 then determines whether a signal designating the underwater mode is input from the operation input unit 24 (step S16).
When the signal designating the underwater mode is not input (step S16: No), the guide control unit 261 performs, in accordance with guide instruction information input from the operation input unit 24, the control to guide the capsule endoscope 10 at the water bottom WB while feeding back positional information of the capsule endoscope 10 (step S17). More specifically, the tilt angle and the azimuth angle of the capsule endoscope 10 are changed while a part of the capsule endoscope 10 is in contact with the water bottom WB.
On the other hand, when the signal designating the underwater mode is input (step S16: Yes), the guide control unit 261 performs the guide control to cause the capsule endoscope 10 to float from the water bottom WB and stand still underwater (step S18). More specifically, magnetic attracting force for the capsule endoscope 10 is temporarily weakened to cause the capsule endoscope 10 to float from the water bottom WB, and the magnetic attracting force is adjusted so that the gravity, the buoyancy, and the magnetic attracting force that act on the capsule endoscope 10 are balanced.
After this guide control causes the capsule endoscope 10 to float from the water bottom WB, as illustrated in
At this time, a user visually recognizes that the capsule current position mark m14 is separated from the water bottom mark m13, whereby the user can easily grasp that the capsule endoscope 10 has floated from the water bottom WB. Therefore, the guide operation for the capsule endoscope 10 using the operation input unit 24 can be started after it is confirmed that the capsule endoscope 10 has floated from the water bottom WB and stood still underwater.
In the subsequent step S19, the guide control unit 261 performs, in accordance with guide instruction information input from the operation input unit 24, the control to guide the capsule endoscope 10 underwater while feeding back positional information of the capsule endoscope 10. After the guidance in the underwater mode is started, if the minimum value Zmin of the coordinate value ZCP of the capsule endoscope 10 is updated, the coordinate value ZBT of the water bottom may be or may not be updated in accordance with the minimum value Zmin. For example, in a case where the inner wall of the organ ST is inclined, and the capsule endoscope 10 moves to a deeper position, the minimum value Zmin of the coordinate value ZCP can be updated.
In the subsequent step S20, the control unit 26 determines whether a signal including an instruction to end the guidance for the capsule endoscope 10 is input from the operation input unit 24.
When the signal including the instruction to end the guidance is not input (step S20: No), the control unit 26 then determines whether a signal designating the water bottom mode is input from the operation input unit 24 (step S21). The water bottom mode is selected, for example, when the guidance for the capsule endoscope 10 is performed all over again underwater. When the signal designating the water bottom mode is input (step S21: Yes), the operation of the guide device 20 returns to step S12. On the other hand, when the signal designating the water bottom mode is not input (step S21: No), the operation of the guide device 20 returns to step S19.
In step S20, when the signal including the instruction to end the guidance is input (step S20: Yes), the control unit 26 resets the coordinate value ZBT of the water bottom WB (step S22). After that, the operation of the guide device 20 is ended.
As described above, according to the first embodiment, both the water bottom mark m13 indicating the position of the water bottom WB and the capsule current position mark m14 indicating the current position of the capsule endoscope 10 are simultaneously displayed on the positional information display area m6. Therefore, the user can easily recognize that the capsule endoscope 10 is separated from the water bottom WB by observing the positional information display area m6.
In addition, according to the first embodiment, the minimum value Zmin of the coordinate value ZCP of the capsule endoscope 10 is set as the coordinate value ZBT of the water bottom. Therefore, the coordinate value ZBT of the water bottom can be accurately obtained.
Next, a second embodiment of the present disclosure will be described.
A configuration of a capsule medical device guide system according to the second embodiment is similar to that of the first embodiment. A method for determining the coordinate value ZBT of the water bottom WB is different from that of the first embodiment.
In step S30 subsequent to step S11, the control unit 26 resets the coordinate value ZBT in the Z direction indicating the position of the water bottom WB. Accordingly, as illustrated in
In step S31, the guide control unit 261 performs the control to guide the capsule endoscope 10 toward the water bottom WB. The subsequent steps S15 to S17 are similar to those of the first embodiment.
In step S16, when the signal designating the underwater mode is input from the operation input unit 24 to the control unit 26 (step S16: Yes), the control unit 26 sets a current coordinate value ZCP of the capsule endoscope 10 as the coordinate value ZBT of the water bottom WB (step S32). At this time, as illustrated in
In the subsequent step S33, the guide control unit 261 performs the guide control to cause the capsule endoscope 10 to float from the water bottom WB and stand still underwater. After this guide control causes the capsule endoscope 10 to float from the water bottom, in the display unit 23, as illustrated in
As described above, according to the second embodiment, the coordinate value ZCP of the capsule endoscope 10 obtained when the water bottom mode is changed to the underwater mode is set as the coordinate value ZBT of the water bottom WB. Therefore, the coordinate value ZBT of the water bottom WB does not need to be updated in accordance with the change of the coordinate value ZCP of the capsule endoscope 10, and the process can be simplified.
First Variation
Next, a first variation of the above-mentioned first and second embodiments will be described.
The control unit 26A further includes a determination unit 263 in addition to the guide control unit 261 and the display control unit 262. Operation of the guide control unit 261 and operation of the display control unit 262 are similar to those of the first embodiment.
The determination unit 263 determines, based on positional information of the capsule endoscope 10 output from the position detecting unit 22, a contact state of the capsule endoscope 10 with respect to a boundary surface of the liquid W introduced into the subject as illustrated in
When the determination unit 263 determines that the capsule endoscope 10 is separated from the water bottom WB, the display control unit 262 causes the display unit 23 to display, as a determination result, a notification indicating that the capsule endoscope 10 has floated from the water bottom WB. For example, as illustrated in
As described above, according to the first variation, a user can more easily recognize that the capsule endoscope 10 is separated from the water bottom WB within the subject.
Second Variation
Next, a second variation of the above-mentioned first and second embodiments will be described.
In the above-mentioned first and second embodiments, when the guidance for the capsule endoscope 10 is started, the guide mode is automatically set (refer to steps S10 and S11 in
Third Variation
Next, a third variation of the above-mentioned first and second embodiments will be described.
In the above-mentioned first and second embodiments, when the guide mode is set to the water bottom mode, the capsule endoscope 10 is guided to the water bottom WB by means of the automatic control performed by the guide control unit 261. However, the capsule endoscope 10 may be guided to the water bottom WB by means of manual operation by a user for the operation input unit 24. In this case, the guide control unit 261 performs, in accordance with guide instruction information input from the operation input unit 24, the control to guide the capsule endoscope 10 to the water bottom WB while feeding back positional information of the capsule endoscope 10.
In this case, in the same way as the first embodiment, the coordinate value ZBT of the water bottom WB may be updated along with the minimum value Zmin of the coordinate value ZCP of the capsule endoscope 10 as illustrated in
Fourth Variation Next, a fourth variation of the above-mentioned first and second embodiments will be described.
The above-mentioned first and second embodiments have described the guide control for the capsule endoscope 10 performed when the water bottom mode is changed to the underwater mode. However, similar control may be performed when the water surface mode is changed to the underwater mode.
More specifically, the capsule endoscope 10 is designed so as to have a specific gravity greater than the specific gravity of the liquid W and sink in the liquid W while the guidance by the magnetic field generating unit 25 is not performed.
In the guide device 20, after the guidance for the capsule endoscope 10 is started, the guide mode is set to the water surface mode. Then, a coordinate value ZSF representing a position of the water surface WS is reset, and the guide control to elevate the capsule endoscope 10 to the water surface WS is performed. At this time, as illustrated in
As the coordinate value ZSF of the water surface WS, a maximum value Zmax of the coordinate value ZCP of the capsule endoscope 10 after the reset of the coordinate value ZSF is set. Alternatively, as the coordinate value ZSF of the water surface WS, the coordinate value ZCP of the capsule endoscope 10 obtained when the water surface mode is changed to the underwater mode after the capsule endoscope 10 reaches the water surface WS may be set.
After the capsule endoscope 10 reaches the water surface WS, when the capsule endoscope 10 is sunk underwater and subjected to the guide control, a user visually recognizes that the capsule current position mark m14 is separated from the water surface mark m16 in the positional information display area m6, whereby the user can easily grasp that the capsule endoscope 10 has sunk from the water surface WS.
In addition, as a further variation, similar display control can be performed when the capsule endoscope 10 is brought into contact with a lateral inner wall of the organ ST, and then capsule endoscope 10 is separated from the inner wall and caused to float underwater. In this case, the display unit 23 only needs to display a mark (side surface mark) representing a position of the lateral inner wall kept in contact with the capsule endoscope 10 and the capsule current position mark m14 representing the position of the capsule endoscope 10. The user visually recognizes a positional relation between the side surface mark and the capsule current position mark m14, whereby the user can easily grasp whether the capsule endoscope 10 is separated from the lateral inner wall and floats underwater.
Fifth Variation
Next, a fifth variation of the above-mentioned first and second embodiments will be described.
In the above-mentioned first and second embodiments, the magnetic field generating unit 25 that generates a magnetic field to be applied to the permanent magnet 18 provided inside the capsule endoscope 10 is used as a guide unit for the capsule endoscope 10. However, a guide method for the capsule endoscope is not limited to the method using a magnetic field. For example, the capsule endoscope may be guided in such a manner that a propeller is provided in the capsule endoscope and thrust force of the propeller is controlled. Alternatively, the capsule endoscope may be guided in such a manner that an ultrasound motor is provided in the capsule endoscope and drive force of the ultrasound motor is controlled.
The above-mentioned first and second embodiments and first to fifth variations of these embodiments are merely examples for performing the present disclosure, and the present disclosure is not limited to these embodiments and variations. In the present disclosure, a plurality of components disclosed in the first and second embodiments and each of the first to fifth variations can be appropriately combined so as to form various disclosures. It is obvious from the above description that the present disclosure can be variously modified according to a specification or the like, and can further include various other embodiments within a scope of the present disclosure.
According to the present disclosure, a position of a capsule medical device within a subject and a boundary position of a range in which the capsule medical device is capable of being guided within the subject are displayed on a display unit. Therefore, a user can easily recognize that the capsule medical device is separated from a boundary of a liquid.
Additional advantages and modifications will readily occur to those skilled in the art. Therefore, the disclosure in its broader aspects is not limited to the specific details and representative embodiments shown and described herein. Accordingly, various modifications may be made without departing from the spirit or scope of the general inventive concept as defined by the appended claims and their equivalents.
Number | Date | Country | Kind |
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2014-167962 | Aug 2014 | JP | national |
This application is a continuation of PCT international application Ser. No. PCT/JP2015/062658 filed on Apr. 27, 2015 which designates the United States, incorporated herein by reference, and which claims the benefit of priority from Japanese Patent Applications No. 2014-167962, filed on Aug. 20, 2014, incorporated herein by reference.
Number | Date | Country | |
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Parent | PCT/JP2015/062658 | Apr 2015 | US |
Child | 15285777 | US |