A portable imaging device for cerebral hematoma localization
Through the matrix multi-channel design and flexible detection unit of the portable cerebral hematoma positioning imaging device, the absorption rate and scattering characteristics of near-infrared light are used to solve the problems of inaccurate cerebral hematoma positioning and noise interference in the existing technology, and achieve rapid, Accurate cerebral hematoma localization and imaging provide effective diagnosis and treatment reference for first aid.
Patent Information
- Application Number
- CN202411546893.X
- Authority / Receiving Office
- CN · China
- Patent Type
- Patents(China)
- Current Assignee / Owner
- Filing Date
- 2024-11-01
- Publication Date
- 2025-01-21
- Estimated Expiration
- 2044-11-01
AI Technical Summary
The existing cerebral hematoma positioning imaging devices are difficult to achieve rapid injury inspection outside the hospital, and cannot provide sufficient diagnostic and treatment reference data for first aid, and the detection range and accuracy are limited, so noise interference cannot be eliminated.
It adopts a portable cerebral hematoma positioning imaging device, adopts a matrix multi-channel design, combines the body's integrated detection unit and an external flexible detection unit, and uses the absorption rate and scattering characteristics of near-infrared light to achieve rapid positioning and imaging of cerebral hematoma and remove noise interference. , improve detection accuracy.
It achieves rapid positioning and imaging of cerebral hematoma, improves the quality of injury classification, improves first aid efficiency, and can provide accurate position reference for first aid treatment.
Smart Images

Figure CN119033338B_ABST
Abstract
Description
Technical Field
[0001] The invention relates to the technical field of cerebral hematoma positioning imaging, in particular to a portable cerebral hematoma positioning imaging device. Background Art
[0002] Cerebral hematoma is usually caused by craniocerebral trauma, which can lead to impaired consciousness and rapidly progress to brain herniation, thus endangering life. Early detection of life-threatening cerebral hematoma and preliminary characterization and positioning, providing reference for rescue personnel and rational selection of treatment methods are urgent issues to be addressed in out-of-hospital treatment sites such as disaster relief and battlefield treatment. Currently commonly used methods such as ultrasound and CT cannot achieve rapid injury assessment of cerebral hematoma victims out of hospital due to technical limitations, cost control, and large-scale equipment, and cannot provide sufficient diagnostic and treatment reference data for on-site emergency treatment.
[0003] In addition, in disaster emergency rescue and battlefield first aid, cerebral hematoma caused by exogenous trauma is a common secondary lesion of brain injury. After the blood vessels in the brain or between the brain tissue and the skull rupture, blood accumulates in the brain or between the brain and the skull, which compresses the brain tissue, increases intracranial pressure, and endangers the patient's life. The incidence of intracranial hematoma accounts for about 10% of closed craniocerebral injuries and 40% to 50% of severe craniocerebral injuries, and is higher in special scenarios. Intracranial hematoma can be roughly divided into epidural hematoma, subdural hematoma, and intracranial hematoma.
[0004] Rapid diagnosis and treatment of cerebral hematoma is of great significance to improving the survival rate of patients. Existing detection methods mainly include CT, ultrasound, MRI, etc. CT and MRI are not suitable for emergency rescue and battlefield first aid scenarios because of their large size and inability to be carried by one person. Ultrasound is limited by the scattering of sound waves by the skull and cannot effectively detect the entire brain.
[0005] The absorption rate and scattering characteristics of near-infrared light in cerebral hematoma and normal brain tissue are different. The higher the hemoglobin concentration, the higher the absorption rate of near-infrared light. By measuring the intensity of scattered light in a specific area, the degree of blood enrichment at that location can be determined. Combined with the pre-recorded basic detection data and trauma conditions, the positioning detection of cerebral hematoma can be achieved.
[0006] At present, the disclosed technologies include Inftrascanner 1000 / 2000 brain hematoma scanner, and publication number CN104434034B discloses "a handheld near-infrared brain hematoma detection device". However, the brain hematoma positioning imaging device in the prior art has only single-channel detection, and the detection target area is limited. Each detection is limited to a range of about 3 cm long and 1 cm wide. The accuracy of the detection target area is limited, and the noise interference of the skin, skull, etc. on the near-infrared light cannot be eliminated. It can only qualitatively detect whether the hematoma in the target area is negative or positive, and cannot provide accurate position reference for timely diagnosis and treatment such as puncture drainage, craniotomy and other emergency measures. In addition, the detection head and the host are integrated into one design, which cannot cope with all detection areas. It is inconvenient to detect when the patient's head cannot move to cooperate. Summary of the invention
[0007] The purpose of the present invention is to provide a portable cerebral hematoma positioning imaging device, which increases the portability and practicality of the device, adopts matrix multi-channel coverage, combination of target channel and background noise channel, graphical fitting of detection data, integrated detection unit group and flexible flexible detection unit combination technical means, to achieve rapid positioning and imaging of cerebral hematoma, improve the quality of triage, improve treatment efficiency and make disposal decisions.
[0008] To achieve the above-mentioned objectives, the present invention provides a portable cerebral hematoma positioning imaging device, comprising a main unit, a shell being provided on the outside of the main unit, a non-slip rubber sleeve being provided on the surface of the shell, a display being provided on the upper surface of the main unit, a control system being provided inside the main unit, a main body integrated detection unit being connected to the lower surface of the main unit, two groups of external flexible detection units being provided on one side of the main unit, and the two groups of external flexible detection units being connected to the main unit via connecting lines.
[0009] Preferably, the control system includes a modular modular battery, a power management mainboard, a signal control processing mainboard, a function button mainboard and a first flexible printed circuit. The signal control processing mainboard is arranged on the lower surface of the display, and the signal control processing mainboard is connected to the function button mainboard through the first flexible printed circuit. The power management mainboard is arranged under the function button mainboard, and the modular modular battery is connected to the side of the power management mainboard away from the function button mainboard.
[0010] Preferably, the main body integrated detection unit includes a three-pole detection bracket, a three-pole detection bracket shell, a second flexible printed circuit, a first photoelectric conversion IC chip, a first output light LED, an output optical fiber and a first receiving optical fiber. The second flexible printed circuit is arranged inside the three-pole detection bracket shell. The upper end of the second flexible printed circuit is connected to the signal control processing main board, and the lower end of the second flexible printed circuit is divided into three-pole branch circuits, and the three-pole branch circuits extend to the inside of the three-pole detection bracket shell, respectively.
[0011] Preferably, the center of the lower end of the second flexible printed circuit is connected to the first emitting light LED, and each of the three-pole branch circuits is provided with two first photoelectric conversion IC chips, which are distributed in a circle and are in three groups. Each group of two first photoelectric conversion IC chips are respectively connected to the lower end of the second flexible printed circuit, and the lower end of each group of two first photoelectric conversion IC chips is connected to the first receiving optical fiber. The lower end of the first emitting light LED is connected to the emitting optical fiber, and the three first photoelectric conversion IC chips close to the first emitting light LED are used to collect noise signal data of skin and skull tissue, and the three first photoelectric conversion IC chips far from the first emitting light LED are used to collect actual signal data after the noise data is removed.
[0012] Preferably, the outside of the six first optical fibers and the outer surface of the output optical fiber are covered with silicone contacts, and the silicone contacts are respectively molded with the first optical fibers and the output optical fiber inserts, and the silicone contacts are arranged at the bottom end of the outer shell of the three-pole detection bracket.
[0013] Preferably, the signal control processing main board is connected to the external flexible detection unit through the connecting line, and the external flexible detection unit includes a silicone body, a built-in flexible printed circuit board, a second photoelectric conversion IC chip, a second output light LED and a second receiving optical fiber. The built-in flexible printed circuit board is arranged inside the silicone body, and a plug is arranged at one end of the built-in flexible printed circuit board, and the plug is arranged at the other end of the connection line where the connecting line is connected to the host.
[0014] Preferably, two groups of second photoelectric conversion IC chips and one group of second output light LEDs are respectively arranged inside the silicone body, the two groups of second photoelectric conversion IC chips and one group of second output light LEDs are respectively connected to the built-in flexible printed circuit board, the lower surfaces of the two groups of second photoelectric conversion IC chips are connected to the second receiving optical fiber, and the second photoelectric conversion IC chip has the same function as the first photoelectric conversion IC chip.
[0015] Preferably, the lower surfaces of the two groups of the second photoelectric conversion IC chips are connected to the second receiving optical fiber, the outer surfaces of the two groups of the second receiving optical fiber are covered with separate receiving contacts, and the lower part of the second output light LED is connected to a transmitting optical fiber, and the outer surface of the transmitting optical fiber is covered with a separate transmitting contact.
[0016] Therefore, the present invention adopts the above-mentioned portable cerebral hematoma positioning imaging device, which has the following technical effects:
[0017] (1) The use of a detachable external flexible detection unit increases the applicability and portability of the device, providing all-round coverage detection inspection when the application scenario is complex and the patient's head is inconvenient to move;
[0018] (2) The device adopts a matrix 3+2 multi-channel design, with a total of 5 groups and 10 channels. Each group contains two detection channels. One is a noise channel, which detects the background noise data of tissues such as the skull and skin. The other is a target signal data detection channel. In signal processing, the noise data of the noise channel is removed from the target signal data to make the target signal more accurate. Among them, 3 groups of channels are set in the integrated detection unit of the main body, evenly distributed around the circumference, which can cover all detection areas within a 70mm circumference and can cope with most cerebral hematoma scenarios.
[0019] (3) The device uses the different absorption rates and scattering characteristics of near-infrared light in cerebral hematoma and normal brain tissue. By judging the degree of blood enrichment at that location and combining it with the pre-recorded basic detection data and trauma situation, it can intuitively provide a relatively accurate location reference for emergency treatment plans.
[0020] The technical solution of the present invention is further described in detail below through the accompanying drawings and embodiments. BRIEF DESCRIPTION OF THE DRAWINGS
[0021] Figure 1 It is a structural schematic diagram of an embodiment of a portable cerebral hematoma localization imaging device of the present invention;
[0022] Figure 2 It is a cross-sectional view of a host of an embodiment of a portable cerebral hematoma localization imaging device of the present invention;
[0023] Figure 3 It is a cross-sectional view of a body integrated detection unit of an embodiment of a portable cerebral hematoma positioning imaging device of the present invention;
[0024] Figure 4 It is a cross-sectional view of an external flexible detection unit of an embodiment of a portable cerebral hematoma positioning imaging device of the present invention;
[0025] Figure 5 The present invention is a schematic diagram of a portable cerebral hematoma localization imaging device embodiment.
[0026] Reference numerals
[0027] 1. Host; 11. Shell; 12. Anti-slip rubber sleeve; 4. Display; 5. Control system; 51. Modular battery; 52. Power management main board; 53. Signal control processing main board; 54. Function button main board; 55. First flexible printed circuit; 6. Main body integrated detection unit; 61. Three-pole detection bracket shell; 62. Second flexible printed circuit; 63. First photoelectric conversion IC chip; 64. First emitting light LED; 66. Emitting optical fiber; 67. First receiving optical fiber; 7. External flexible detection unit; 71. Silicone body; 72. Built-in flexible printed circuit; 73. Second photoelectric conversion IC chip; 74. Second emitting light LED; 75. Second receiving optical fiber; 76. Plug; 77. Transmitting optical fiber; 8. Connecting wire; 9. Silicone contact; 10. Separate receiving contact; 13. Separate transmitting contact. DETAILED DESCRIPTION
[0028] The technical solution of the present invention is further described below through the accompanying drawings and embodiments.
[0029] Unless otherwise defined, the technical terms or scientific terms used in the present invention should be understood by people with ordinary skills in the field to which the present invention belongs. The words "first", "second" and similar words used in the present invention do not indicate any order, quantity or importance, but are only used to distinguish different components. "Include" or "comprise" and similar words mean that the elements or objects appearing before the word include the elements or objects listed after the word and their equivalents, without excluding other elements or objects. "Connect" or "connected" and similar words are not limited to physical or mechanical connections, but may include electrical connections, whether direct or indirect. "Up", "down", "left", "right" and the like are only used to indicate relative positional relationships. When the absolute position of the described object changes, the relative positional relationship may also change accordingly.
[0030] like Figure 1 As shown, a portable cerebral hematoma positioning imaging device includes a host 1. A shell 11 is provided on the outside of the host 1. The shell 11 is used to integrate and install various components. An anti-slip rubber sleeve 12 is provided on the surface of the shell 11. The function of the anti-slip rubber sleeve 12 is to prevent the user from losing the device when operating in a non-hospital environment. A display 4 is provided on the upper surface of the host 1, a control system 5 is provided inside the host 1, a main body integrated detection unit 6 is connected to the lower surface of the host 1, and two sets of external flexible detection units 7 are provided on one side of the host 1. The two sets of external flexible detection units 7 are connected to the host 1 through a connecting line 8.
[0031] like Figure 2As shown, the control system 5 includes a modular battery 51, a power management mainboard 52, a signal control processing mainboard 53, a function button mainboard 54, a first flexible printed circuit 55 and the signal control processing mainboard 53 are arranged on the lower surface of the display screen, and the image and data information processed by the signal control processing mainboard 53 are displayed through the display 4. The signal control processing mainboard 53 is connected to the function button mainboard 54 through the first flexible printed circuit 55, and the function of the function button mainboard 54 is to integrate the operation button. A power management mainboard 52 is arranged below the function button mainboard 54, and a modular battery 51 is connected to the side of the power management mainboard 52 away from the function button mainboard 54. The function of the power management mainboard 52 is to distribute the power provided by the modular battery 51 to each power unit according to preset requirements.
[0032] like Figure 3 As shown, the main body integrated detection unit 6 includes a three-pole detection bracket housing 61, a second flexible printed circuit 62, a first photoelectric conversion IC chip 63, a first emitting light LED 64, an emitting optical fiber 66 and a first receiving optical fiber 67. The three-pole detection bracket housing 61 is a three-pole detection bracket three-pole detection bracket housing 61, and a second flexible printed circuit 62 is arranged inside the three-pole detection bracket housing 61. The upper end of the second flexible printed circuit 62 is connected to the signal control processing main board 53, which is used to receive the light signal after tissue scattering, and convert it into an electrical signal and send it to the signal control processing main board 53. The lower end of the second flexible printed circuit 62 is divided into three-pole branch circuits, which extend to the three-pole bracket of the three-pole detection bracket housing 61 and the inside of the three-pole detection bracket housing 61.
[0033] The center of the lower end of the second flexible printed circuit 62 is connected to the first light emitting LED 64. Two first photoelectric conversion IC chips 63 are arranged on each branch circuit of the three-pole branch circuit, which are distributed in a circle and the number is 3 groups. Figure 5 As shown, they are photoelectric conversion IC-A1, A2, B1, B2, C1, and C2, and each group of two first photoelectric conversion IC chips 63 are connected to the lower end of the second flexible printed circuit 62, and each group of two first photoelectric conversion IC chips 63 are connected to the lower end of the first receiving optical fiber 67, and the lower end of the first output light LED 64 is connected to the output optical fiber 66. The three first photoelectric conversion IC chips 63 close to the first output light LED 64 are used to collect noise signal data of skin and skull tissue, and the three first photoelectric conversion IC chips 63 far away from the first output light LED 64 are used to collect actual signal data after removing noise data. The outer surfaces of the six first receiving optical fibers 67 and the outer surfaces of the output optical fibers 66 are coated with silicone contacts 9, and the silicone contacts 9 are respectively molded with the first receiving optical fibers 67 and the output optical fibers 66, and the silicone contacts 9 are arranged at the bottom end of the three-pole detection bracket housing 61.
[0034] like Figure 4As shown, the signal control processing mainboard 53 is connected to the external flexible detection unit 7 through the connecting line 8. The function of the external flexible detection unit 7 is to be used in some local areas where the detection area is small and it is inconvenient to use the integrated detection unit. The external flexible detection unit 7 includes a silicone body 71, a built-in flexible printed circuit board 72, a second photoelectric conversion IC chip 73, a second emitting light LED 74, and a second receiving optical fiber 75. The silicone body 71 is provided with a built-in flexible printed circuit board 72. One end of the built-in flexible printed circuit board 72 is provided with a plug 76. The plug 76 can be set at the other end of the connection line 8 where it is connected to the host 1.
[0035] Two sets of second photoelectric conversion IC chips 73 and a set of second light emitting LEDs 74 are arranged inside the silicone body 71. Figure 5 , two groups of second photoelectric conversion IC chips 73 are marked as a1, b1, a2, and b2 respectively; the two groups of second photoelectric conversion IC chips 73 and a group of second light emitting LEDs 74 are connected to the built-in flexible printed circuit board 72 respectively. The lower surface of each second photoelectric conversion IC chip 73 is connected to a second receiving optical fiber 75, and the second photoelectric conversion IC chip 73 has the same function as the first photoelectric conversion IC chip 63. The lower surfaces of the two groups of second photoelectric conversion IC chips 73 are connected to second receiving optical fibers 75, and the outer surfaces of the two groups of second receiving optical fibers 75 are covered with separate receiving contacts 10, and the lower part of the second light emitting LED 74 is connected to a transmitting optical fiber 77, and the outer surface of the transmitting optical fiber 77 is covered with a separate transmitting contact 13.
[0036] The present invention will be further described below through specific implementation modes.
[0037] Embodiment 1
[0038] Reference Figure 5 As shown, in this embodiment, if the patient's head is in a space that is easy to detect, the detection unit provided by the main body detection unit can be used for detection directly, and the ends of the three groups of detection units are placed in the target area of the injured head, and are adjusted so that the ends of the detection units are in contact with the scalp tissue. After the enabling function is started, the first output light LED 64 emits a near-infrared light source, which is refracted and scattered by the tissue and then emitted. The signal is captured by the first photoelectric IC chip and sent to the signal processing mainboard. The mainboard built-in program can determine the hematoma condition of the area through which the light path passes based on the comparison operation of the incident light and the output light. The three-channel detection range covers a circular area, which is fitted into an image by the built-in software and displayed on the screen of the host 1 for reference in diagnosis and treatment.
[0039] Embodiment 2
[0040] Reference Figure 5As shown, in this embodiment, if the patient's head is in a space that is not easy to detect, an external flexible detection unit 7 can be used. The patch of the external flexible detection unit 7 is placed on the target area of the patient to be tested. After the enabling function is started, the second output light LED 74 emits a near-infrared light source, which is refracted and scattered by the tissue and then emitted. The signal is captured by the second photoelectric conversion IC chip 73 and sent to the signal processing mainboard. The built-in program of the mainboard can determine the hematoma condition of the area through which the light path passes based on the comparison operation of the incident light and the output light. The detection range covers a circular area, which is fitted into an image by the built-in software and displayed on the screen of the host 1 for reference in diagnosis and treatment.
[0041] Therefore, the following beneficial effects are achieved by using the above-mentioned portable cerebral hematoma localization imaging device:
[0042] (1) The use of a detachable external flexible detection unit increases the applicability and portability of the device, providing all-round coverage detection inspection when the application scenario is complex and the patient's head is inconvenient to move;
[0043] (2) The device adopts a matrix 3+2 multi-channel design, with a total of 5 groups and 10 channels. Each group contains two detection channels. One is a noise channel, which detects the background noise data of tissues such as the skull and skin. The other is a target signal data detection channel. In signal processing, the noise data of the noise channel is removed from the target signal data to make the target signal more accurate. Among them, 3 groups of channels are set in the integrated detection unit of the main body, evenly distributed around the circumference, which can cover all detection areas within a 70mm circumference and can cope with most cerebral hematoma scenarios.
[0044] (3) The device uses the different absorption rates and scattering characteristics of near-infrared light in cerebral hematoma and normal brain tissue. By judging the degree of blood enrichment at that location and combining it with the pre-recorded basic detection data and trauma situation, it can intuitively provide a relatively accurate location reference for emergency treatment plans.
[0045] Finally, it should be noted that the above embodiments are only used to illustrate the technical solution of the present invention rather than to limit it. Although the present invention has been described in detail with reference to the preferred embodiments, those skilled in the art should understand that they can still modify or replace the technical solution of the present invention with equivalents, and these modifications or equivalent replacements cannot cause the modified technical solution to deviate from the spirit and scope of the technical solution of the present invention.
Claims
1. A portable cerebral hematoma localization imaging device, characterized in that: The device comprises a host, wherein a shell is provided on the outside of the host, a non-slip rubber sleeve is provided on the surface of the shell, a display is provided on the upper surface of the host, a control system is provided inside the host, a body integrated detection unit is connected to the lower surface of the host, and two groups of external flexible detection units are provided on one side of the host, and the two groups of external flexible detection units are connected to the host through connecting lines; The main body integrated detection unit includes a three-pole detection bracket shell, a second flexible printed circuit, a first photoelectric conversion IC chip, a first emitting light LED, an emitting optical fiber and a first receiving optical fiber. The second flexible printed circuit is arranged inside the three-pole detection bracket shell. The upper end of the second flexible printed circuit is connected to the signal control processing main board. The lower end of the second flexible printed circuit is divided into three-pole branch circuits, and the three-pole branch circuits extend to the inside of the three-pole detection bracket shell respectively. The center of the lower end of the second flexible printed circuit is connected to the first emitting light LED. Each of the three-pole branch circuits is provided with two first photoelectric conversion IC chips, which are distributed in a circle and the number is 3 groups. Each group of two first photoelectric conversion IC chips is respectively connected to the lower end of the second flexible printed circuit. Each group of two first photoelectric conversion IC chips is connected to the first receiving optical fiber at the lower end. The lower end of the first emitting light LED is connected to the emitting optical fiber. The three first photoelectric conversion IC chips close to the first emitting light LED are used to collect noise signal data of skin and skull tissues, and the three first photoelectric conversion IC chips far away from the first emitting light LED are used to collect actual signal data after removing noise data.
2. A portable cerebral hematoma localization imaging device according to claim 1, characterized in that: The control system includes a modular battery, a power management mainboard, a signal control processing mainboard, a function button mainboard and a first flexible printed circuit. The signal control processing mainboard is arranged on the lower surface of the display. The signal control processing mainboard is connected to the function button mainboard through the first flexible printed circuit. The power management mainboard is arranged below the function button mainboard, and the modular battery is connected to the side of the power management mainboard away from the function button mainboard.
3. A portable cerebral hematoma localization imaging device according to claim 2, characterized in that: The outside of the six first receiving optical fibers and the outer surface of the output optical fibers are covered with silicone contacts, and the silicone contacts are respectively molded with the first receiving optical fibers and the output optical fiber inserts, and the silicone contacts are arranged at the bottom end of the three-pole detection bracket housing.
4. The portable cerebral hematoma localization imaging device according to claim 3, characterized in that: The signal control processing main board is connected to the external flexible detection unit through the connecting line. The external flexible detection unit includes a silicone body, a built-in flexible printed circuit board, a second photoelectric conversion IC chip, a second output light LED and a second receiving optical fiber. The built-in flexible printed circuit board is arranged inside the silicone body. A plug is arranged at one end of the built-in flexible printed circuit board, and the plug is arranged at the other end of the connection line where the connecting line is connected to the host.
5. The portable cerebral hematoma localization imaging device according to claim 4, characterized in that: Two groups of second photoelectric conversion IC chips and one group of second output light LEDs are respectively arranged inside the silicone body, the two groups of second photoelectric conversion IC chips and one group of second output light LEDs are respectively connected to the built-in flexible printed circuit board, the lower surfaces of the two groups of second photoelectric conversion IC chips are connected to the second receiving optical fiber, and the second photoelectric conversion IC chip has the same function as the first photoelectric conversion IC chip.
6. The portable cerebral hematoma localization imaging device according to claim 5, characterized in that: The lower surfaces of the two groups of the second photoelectric conversion IC chips are connected to the second receiving optical fiber, and the outer surfaces of the two groups of the second receiving optical fiber are covered with separate receiving contacts. The lower part of the second output light LED is connected to a transmitting optical fiber, and the outer surface of the transmitting optical fiber is covered with a separate transmitting contact.
Citation Information
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A handheld near-infrared brain hematoma injury detection device
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