Wearable intraocular pressure monitoring device

Through jet method design and wireless transmission technology, the accuracy and convenience of the wearable intraocular pressure monitoring device are achieved, and the measurement error and discomfort problems of traditional methods are solved, allowing patients to independently monitor and remotely analyze intraocular pressure.

CN120240954AInactive Publication Date: 2025-07-04THE THIRD MEDICAL CENT OF THE CHINESE PEOPLES LIBERATION ARMY GENERAL HOSPITAL
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Patent Information

Application Number
CN202510432952.9
Authority / Receiving Office
CN · China
Patent Type
Applications(China)
Current Assignee / Owner
Filing Date
2025-04-08
Publication Date
2025-07-04
Estimated Expiration
Not applicable · inactive patent

AI Technical Summary

Technical Problem

Traditional intraocular pressure measurement methods may cause measurement errors and patient discomfort, and existing contactless equipment requires professional operation, limiting intraocular pressure monitoring in daily life.

Method used

The wearable intraocular pressure monitoring device designed by jet method can uniformly distribute pressure on the corneal surface through the branched air duct of the micro fan, and combine it with intraocular pressure monitoring sensors and wireless data transmission to achieve autonomous patient monitoring.

Benefits of technology

Reduces measurement errors and improves monitoring accuracy and convenience, and patients can independently monitor intraocular pressure and analyze data remotely.

✦ Generated by Eureka AI based on patent content.

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Abstract

The invention relates to the technical field of medical instruments, and discloses a wearable intraocular pressure monitoring device which comprises a lens body, the corneal pressure of a patient is monitored by adopting an air injection method, and an air outlet pipe with branches is arranged at the output end of a micro fan; the air outlets of the air outlet pipes are aligned with the top ends of the left side and the right side of a single eye of a patient wearing the lens body so that pressure can be more evenly distributed on the surface of the cornea, and therefore measurement errors possibly caused by too large single-point pressure are reduced, and meanwhile the intraocular pressure monitoring sensor located on the inner side of the lens body is matched so that the cornea pressure of the patient can be monitored; the monitored data are transmitted to a signal processing unit in a hollow shell in the middle above the front end of the mirror body, then controlled by a main controller located in the hollow shell, and sent to a terminal through wireless transmission units on the left side and the right side of the front end face of the mirror body, so that a patient and a doctor can remotely check and analyze the data conveniently; and the monitoring convenience is improved.
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Description

Technical Field

[0001] The present invention relates to the technical field of medical devices, and particularly to a wearable intraocular pressure monitoring device. Background Art

[0002] Intraocular pressure monitoring is an important means for diagnosing and managing ophthalmic diseases such as glaucoma. Traditional intraocular pressure measurement methods mainly include contact and non-contact methods. Contact measurement usually uses devices such as Goldmann applanation tonometer or Tono-Pen, while non-contact measurement usually uses a pneumatic tonometer.

[0003] Currently, intraocular pressure monitoring technology is an important part of the diagnosis and treatment of ophthalmic diseases. Traditional intraocular pressure measurement methods usually involve directly contacting the cornea with pneumatic or mechanical devices. These methods may cause discomfort to patients and may cause measurement errors in some cases. For example, single-point contact measurement may lead to inaccurate measurement results due to the asymmetry of the corneal shape or excessive local pressure. Although existing non-contact intraocular pressure measurement devices reduce patient discomfort, they may require patients to be in a specific posture for measurement and need to be operated by professionals in a hospital or clinic, which limits intraocular pressure monitoring in patients' daily lives. Summary of the Invention

[0004] (1) Technical Problems to be Solved

[0005] In view of the deficiencies of the prior art, the present invention provides a wearable intraocular pressure monitoring device. The present invention uses the jet method to monitor the corneal pressure of patients. A branch-shaped air outlet pipe is provided at the output end of the micro fan. The air outlet of the air outlet pipe is aligned with the top ends on the left and right sides of a single eye of the patient after wearing the lens body, so as to distribute the pressure more evenly on the corneal surface, thereby reducing the measurement error that may be caused by excessive single-point pressure. At the same time, in cooperation with the intraocular pressure monitoring sensor inside the lens body, the corneal pressure of the patient can be monitored, and the monitored data is transmitted to the signal processing unit inside the middle hollow shell above the front end of the lens body, and then controlled by the main controller in the same hollow shell. The data is sent to the terminal through the wireless transmission units on the left and right sides of the front end face of the lens body, which is convenient for patients and doctors to remotely view and analyze the data, improving the convenience of monitoring.

[0006] (2) Technical Solutions

[0007] To solve the above technical problems, the present invention provides the following technical solution: A wearable intraocular pressure monitoring device, including a lens body, the rear of the top ends on both left and right sides of the lens body are rotatably connected with counterweight temple arms, a silica gel layer is fixedly connected to the outer side of the counterweight temple arms, a battery compartment is fixedly connected to the middle of the top of the lens body, micro fans are fixedly connected to both left and right sides of the top of the lens body, an air outlet pipe is fixedly connected to the output end of the micro fans, a monitoring compartment is opened on the rear end face of the lens body, an intraocular pressure monitoring sensor is fixedly connected to the lower side in the front of the lens body, a hollow shell is fixedly connected to the middle above the front end face of the lens body, a main controller is arranged on the left side inside the hollow shell, a signal processing unit is arranged on the right side inside the hollow shell, a wireless transmission unit is fixedly connected to the middle of both left and right sides of the front end face of the lens body, an LED light strip is fixedly connected to the rear edge inside the lens body, and an adhesive layer is arranged between the surface of the LED light strip and the rear edge inside the lens body. The wind blown out by the air outlet pipe can distribute the pressure more evenly on the corneal surface, thereby reducing the measurement error that may be caused by excessive single-point pressure, and facilitating the remote viewing and analysis of data by patients and doctors, improving the convenience of monitoring.

[0008] Preferably, the micro fans, the intraocular pressure monitoring sensor, the main controller, the signal processing unit, the wireless transmission unit, and the LED light strip are all electrically connected to the battery compartment, and the micro fans, the intraocular pressure monitoring sensor, the main controller, the signal processing unit, the wireless transmission unit, and the LED light strip are all connected to the battery compartment by wires.

[0009] Preferably, the main controller is electrically connected to the intraocular pressure monitoring sensor, the signal processing unit, and the wireless transmission unit, and the wireless transmission unit is wirelessly connected to the terminal through Bluetooth. It can supply power to electronic components such as the micro fans, the intraocular pressure monitoring sensor, the main controller, the signal processing unit, the wireless transmission unit, and the LED light strip that require electric energy to drive. A rechargeable battery is arranged in the battery compartment, and it can be detached from the charging wire after charging, improving the comfort of the patient's wearing to a certain extent.

[0010] Preferably, the intraocular pressure monitoring sensor is fixed at the front end position inside the monitoring compartment opened on the rear end face of the lens body. The number of monitoring compartments opened on the rear end face of the lens body is two groups, and the monitoring compartments are distributed on both left and right sides of the rear end face of the lens body. The number of intraocular pressure monitoring sensors in a single group of monitoring compartments on the rear end face of the lens body is two, and the intraocular pressure monitoring sensors are distributed at the lower left and right sides of the front end of a single group of monitoring compartments, which can monitor the two top ends of the patient's cornea, increasing the monitoring range, and at the same time avoiding the situation that the corneal shape of some people may not be completely symmetrical, resulting in deviation of subsequent results.

[0011] Preferably, the air outlet pipe is provided with two air outlet ends, and the end of the air outlet pipe away from the micro fan is fixed at the left and right positions above the front end face of the lens body. The number of the micro fans and the air outlet pipes is two groups. The micro fans are fixed at the top positions of the lens body near the left and right sides of the battery compartment, and the air outlet ends of the air outlet pipes away from the micro fans are fixed at the left and right sides above a single monitoring compartment. The air outlet of the air outlet pipe is aligned with the top ends of the left and right sides of a single eye after the patient wears the lens body, so as to distribute the pressure more evenly on the corneal surface, thereby reducing the measurement error that may be caused by excessive single-point pressure.

[0012] Preferably, the shape of the weighted temple is L-shaped, and the overall weight of the weighted temple is the same as the total weight of the lens body, the micro fan, the intraocular pressure monitoring sensor, the main controller, the signal processing unit, and the wireless transmission unit. The overall weight of the weighted temple is the same as the overall weight of the lens body, making it more stable and not easy to slide when worn, thereby improving the measurement accuracy.

[0013] Preferably, the silicone layer covers the surface of the weighted temple, and the thickness of the silicone layer covering the surface of the weighted temple is 2 mm. The material of the silicone layer is hydrogenated silicone rubber. The setting of the silicone layer not only provides a soft touch for the patient's skin, but also greatly reduces the skin indentation or allergy phenomenon that may be caused by long-term wearing due to its good elasticity and breathability.

[0014] Preferably, the overall shape of the LED light strip is U-shaped. LED lamp beads are arranged inside the LED light strip, and the distance between the LED lamp beads is 1.5 cm. The soft light design of the LED light strip can reduce the measurement error caused by insufficient light, ensuring the accuracy of the intraocular pressure monitoring data.

[0015] Preferably, through grooves communicating with each other are formed between the two monitoring compartments on the rear end face inside the lens body and at the bottom of the battery compartment. The wires arranged between the intraocular pressure monitoring sensor and the battery compartment and between the LED light strip and the battery compartment are all located in the through grooves. The induction of the wires can keep the monitoring compartment clean and tidy, and at the same time avoid the obstruction of the wires from preventing the intraocular pressure monitoring sensor from monitoring the corneal pressure of the patient.

[0016] Compared with the prior art, the present invention provides a wearable intraocular pressure monitoring device, having the following

[0017] Beneficial effects:

[0018] 1. Compared with the prior art, the present invention monitors the corneal pressure of patients by means of the jet method. A wind outlet pipe with branches is provided at the output end of the micro fan. The air outlets of the wind outlet pipe are aligned with the top ends on the left and right sides of a single eye after the patient wears the lens body, distributing the pressure more evenly on the corneal surface, thereby reducing the measurement error that may be caused by excessive single-point pressure. Moreover, since the shape of some people's corneas may not be completely symmetrical, the bilateral air outlet design can better adapt to this asymmetry, ensuring the accuracy of the measurement results. At the same time, in cooperation with the intraocular pressure monitoring sensor inside the lens body, it can monitor the corneal pressure of the patient and transmit the monitored data to the signal processing unit inside the middle hollow shell above the front end of the lens body, and then be controlled by the main controller also located in the hollow shell, and the data is sent to the terminal through the wireless transmission units on the left and right sides of the front end face of the lens body, facilitating remote viewing and analysis of the data by patients and doctors and improving the convenience of monitoring.

[0019] 2. Compared with the prior art, through the designed counterweight temple and silicone layer, the present invention avoids the overall weight of the lens body being too high, which not only affects the discomfort of the patient when wearing but also causes the problem of the lens body tilting forward. The overall weight of the counterweight temple is the same as that of the lens body, making it more stable and less likely to slide when worn, thereby improving the measurement accuracy. The setting of the silicone layer not only provides a soft touch for the patient's skin, but also its good elasticity and breathability greatly reduce the skin indentation or allergic phenomena that may be caused by long-term wearing.

[0020] 3. Compared with the prior art, the LED light strip designed in the present invention adopts a soft light design, which fully considers the irritation problem that may be caused to the eyes when performing intraocular pressure monitoring in low-light or dark environments. The soft light LED light strip can provide uniform and soft light, effectively avoiding the discomfort of the eyes caused by direct or reflected strong light, ensuring that patients can perform comfortable intraocular pressure measurement under any lighting conditions. At the same time, this soft light design can also reduce the measurement error caused by insufficient light, ensuring the accuracy of the intraocular pressure monitoring data. BRIEF DESCRIPTION OF THE DRAWINGS

[0021] Figure 1 is a schematic diagram of the overall structure of the present invention;

[0022] Figure 2 is a three-dimensional structure schematic diagram of the overall rotation of the present invention by 180 degrees horizontally;

[0023] Figure 3 is a longitudinal sectional structure schematic diagram of the lens body of the present invention;

[0024] Figure 4 is a longitudinal sectional structure schematic diagram of the hollow shell of the present invention;

[0025] Figure 5Schematic diagram of the overall structure of the LED light strip of the present invention;

[0026] Figure 6 Schematic longitudinal sectional structure diagram of the counterweight temple of the present invention.

[0027] Wherein: 1, lens body; 2, silica gel layer; 3, battery compartment; 4, micro fan; 5, air outlet pipe; 6, hollow shell; 7, wireless transmission unit; 8, monitoring compartment; 9, intraocular pressure monitoring sensor; 10, LED light strip; 11, main controller; 12, signal processing unit; 13, adhesive layer; 14, counterweight temple. Specific embodiments

[0028] Next, the technical solutions in the embodiments of the present invention will be clearly and completely described in conjunction with the accompanying drawings in the embodiments of the present invention. Obviously, the described embodiments are only a part of the embodiments of the present invention, rather than all the embodiments. Based on the embodiments of the present invention, all other embodiments obtained by those of ordinary skill in the art without creative efforts shall fall within the protection scope of the present invention.

[0029] Embodiment 1:

[0030] Please refer to Figures 1 - 4 as shown:

[0031] A wearable intraocular pressure monitoring device includes a lens body 1. The middle of the top of the lens body 1 is fixed with a battery compartment 3 by screws. The left and right sides of the top of the lens body 1 are fixed with micro fans 4 by screws. The output end of the micro fan 4 is connected to an air outlet pipe 5 through a flange. A monitoring compartment 8 is opened on the rear end face of the lens body 1. The intraocular pressure monitoring sensor 9 is fixed to the lower side of the front of the lens body 1 by screws. The main controller 11 is arranged on the left side inside the hollow shell 6, and the signal processing unit 12 is arranged on the right side inside the hollow shell 6. The wireless transmission unit 7 is fixed to the middle of the left and right sides of the front end face of the lens body 1 by screws.

[0032] In this embodiment: The wind blown out by the air outlet pipe 5 can distribute the pressure more evenly on the corneal surface, thereby reducing the measurement error that may be caused by excessive single-point pressure, and facilitating remote viewing and analysis of data by patients and doctors, improving the convenience of monitoring.

[0033] In an alternative embodiment: The micro - fan 4, the intraocular pressure monitoring sensor 9, the main controller 11, the signal processing unit 12, the wireless transmission unit 7, and the LED light bar 10 are all electrically connected to the battery compartment 3, and the micro - fan 4, the intraocular pressure monitoring sensor 9, the main controller 11, the signal processing unit 12, the wireless transmission unit 7, and the LED light bar 10 are all connected to the battery compartment 3 by wires. The main controller 11 is electrically connected to the intraocular pressure monitoring sensor 9, the signal processing unit 12, and the wireless transmission unit 7, and the wireless transmission unit 7 is wirelessly connected to the terminal via Bluetooth.

[0034] In this embodiment: It can supply power to electronic components such as the micro - fan 4, the intraocular pressure monitoring sensor 9, the main controller 11, the signal processing unit 12, the wireless transmission unit 7, and the LED light bar 10 that require electrical energy for driving. A rechargeable battery is provided in the battery compartment 3, which can be detached from the charging cable after charging, improving the comfort of the patient's wearing to a certain extent.

[0035] In an alternative embodiment: The intraocular pressure monitoring sensor 9 is fixed at the front - end position inside the monitoring compartment 8 opened on the rear - end face of the lens body 1. The number of the monitoring compartments 8 opened on the rear - end face of the lens body 1 is two groups, and the monitoring compartments 8 are distributed on the left and right sides of the rear - end face of the lens body 1. The number of the intraocular pressure monitoring sensors 9 in a single group of the monitoring compartments 8 on the rear - end face of the lens body 1 is two, and the intraocular pressure monitoring sensors 9 are distributed at the lower - left and lower - right positions at the front end of a single group of the monitoring compartments 8.

[0036] In this embodiment: It can monitor the two top ends of the patient's cornea, increasing the monitoring range and avoiding the situation where the corneal shape of some people may not be completely symmetrical, resulting in deviation of subsequent results.

[0037] In an alternative embodiment: The air outlet pipe 5 has two air - outlet ends, and the end of the air outlet pipe 5 far from the micro - fan 4 is fixed at the left and right positions above the front - end face of the lens body 1. The number of both the micro - fan 4 and the air outlet pipe 5 is two groups. The micro - fan 4 is fixed at the top positions of the lens body 1 near the left and right sides of the battery compartment 3, and the air - outlet ends of the air outlet pipe 5 far from the micro - fan 4 are fixed at the left and right positions above a single group of the monitoring compartments 8.

[0038] In this embodiment: The air - outlet of the air outlet pipe 5 is aligned with the left and right top ends of a single eye after the patient wears the lens body 1, distributing the pressure more evenly on the corneal surface, thereby reducing the measurement error that may be caused by excessive single - point pressure.

[0039] Embodiment Two:

[0040] Please refer to Figure 1 、 Figure 2 and Figure 6 as shown:

[0041] On the rear sides of the tops of the left and right sides of the lens body 1, a counterweight temple 14 is connected through a rotating shaft. The outer side of the counterweight temple 14 is covered and fixed by a silica gel layer 2. The shape of the counterweight temple 14 is L-shaped, and the overall weight of the counterweight temple 14 is the same as the total weight of the lens body 1, the micro fan 4, the intraocular pressure monitoring sensor 9, the main controller 11, the signal processing unit 12, and the wireless transmission unit 7.

[0042] In this embodiment: The overall weight of the counterweight temple 14 is the same as the overall weight of the lens body 1, making it more stable and less likely to slide during wearing, thus improving the accuracy of measurement.

[0043] In an alternative embodiment: The silica gel layer 2 covers the surface of the counterweight temple 14, and the thickness of the silica gel layer 2 covering the surface of the counterweight temple 14 is 2 mm. The material of the silica gel layer 2 is hydrogenated silicone rubber.

[0044] In this embodiment: The setting of the silica gel layer 2 not only provides a soft touch for the patient's skin, but its good elasticity and breathability also greatly reduce the skin indentation or allergy phenomena that may be caused by long-term wearing.

[0045] Embodiment Three:

[0046] Please refer to Figure 2 and Figure 5 as shown: At the rear edge inside the lens body 1, an LED light strip 10 is connected through an adhesive layer 13. The overall shape of the LED light strip 10 is U-shaped. LED lamp beads are arranged inside the LED light strip 10, and the distance between the LED lamp beads is 1.5 cm.

[0047] In this embodiment: The soft light design of the LED light strip 10 can reduce the measurement error caused by insufficient light, ensuring the accuracy of the intraocular pressure monitoring data.

[0048] In an alternative embodiment: Through holes are provided in a penetrating manner between two groups of monitoring bins 8 on the rear end face inside the lens body 1 and at the bottom of the battery bin 3. The wires arranged between the intraocular pressure monitoring sensor 9 and the battery bin 3 and between the LED light strip 10 and the battery bin 3 are all located in the through holes.

[0049] In this embodiment: The arrangement of the wires can keep the inside of the monitoring bin 8 clean and tidy, and at the same time avoid the obstruction of the wires from preventing the intraocular pressure monitoring sensor 9 from monitoring the corneal pressure of the patient.

[0050] Working principle: Before use, insert the charging cable into the charging port provided at the top of the battery bin 3 in the middle of the top of the lens body 1 to charge the battery in the battery bin 3. After charging is completed, it can be used normally.

[0051] In use, open the weighted temple 14 and wear it together with the lens body 1 in front of the patient's eyes. The silicone layer 2 on the surface of the weighted temple 14 contacts the skin around the patient's ear. After wearing, turn on the intraocular pressure monitoring sensor 9 and the LED light bar 10 in the monitoring chamber 8 opened at the rear end of the lens body 1. At the same time, turn on the micro fans 4 on the left and right sides at the top of the lens body 1. The micro fans 4 compress the outside air and blow the air into the monitoring chamber 8 inside the lens body 1 through the air outlet pipe 5. At this time, the flexible air blows towards the corneal surface of the patient's eyes. The intraocular pressure monitoring sensor 9 monitors the patient's intraocular pressure condition and transmits the data to the signal processing unit 12 inside the hollow shell 6 in the middle above the front end of the lens body 1. Then, it is controlled by the main controller 11 also in the hollow shell 6, and the data is sent to the terminal through the wireless transmission unit 7 on the left and right sides of the front end face of the lens body 1. At the same time, the LED light bar 10 is attached to the edge of the detection chamber opened inside the lens body 1. The light generated by the LED light bar 10 prevents the intraocular pressure monitoring sensor 9 from being difficult to accurately monitor the patient's intraocular pressure data under poor lighting conditions. After the patient wears it for the specified time, the lens body 1 can be removed.

[0052] Although the embodiments of the present invention have been shown and described, for those of ordinary skill in the art, it can be understood that various changes, modifications, substitutions, and variations can be made to these embodiments without departing from the principles and spirit of the present invention. The scope of the present invention is defined by the appended claims and their equivalents.

Claims

1. A wearable intraocular pressure monitoring device, comprising a lens body (1), characterized in that: The top rear of both left and right sides of the lens body (1) is rotatably connected with counterweight temple arms (14). A silica gel layer (2) is fixedly connected to the outer side of the counterweight temple arms (14). A battery compartment (3) is fixedly connected to the middle of the top of the lens body (1). Miniature air blowers (4) are fixedly connected to the left and right sides of the top of the lens body (1). An air outlet pipe (5) is fixedly connected to the output end of the miniature air blower (4). A monitoring compartment (8) is formed on the rear end face of the lens body (1). An intraocular pressure monitoring sensor (9) is fixedly connected to the lower front side inside the lens body (1). A hollow shell (6) is fixedly connected above the middle of the front end face of the lens body (1). A main controller (11) is arranged on the left side inside the hollow shell (6). A signal processing unit (12) is arranged on the right side inside the hollow shell (6). A wireless transmission unit (7) is fixedly connected to the middle of the left and right sides of the front end face of the lens body (1). An LED light strip (10) is fixedly connected to the rear edge inside the lens body (1). An adhesive layer (13) is arranged between the surface of the LED light strip (10) and the rear edge inside the lens body (1).

2. The wearable intraocular pressure monitoring device according to claim 1, characterized in that: The miniature air blowers (4), intraocular pressure monitoring sensors (9), main controller (11), signal processing unit (12), wireless transmission unit (7), and LED light strip (10) are all electrically connected to the battery compartment (3), and the miniature air blowers (4), intraocular pressure monitoring sensors (9), main controller (11), signal processing unit (12), wireless transmission unit (7), and LED light strip (10) are all connected to the battery compartment (3) by wires.

3. The wearable intraocular pressure monitoring device according to claim 1, characterized in that: The main controller (11) is electrically connected to the intraocular pressure monitoring sensor (9), signal processing unit (12), and wireless transmission unit (7), and the wireless transmission unit (7) is wirelessly connected to the terminal via Bluetooth.

4. The wearable intraocular pressure monitoring device according to claim 1, wherein: The intraocular pressure monitoring sensor (9) is fixed at the front end position inside the monitoring compartment (8) formed on the rear end face of the lens body (1). The number of monitoring compartments (8) formed on the rear end face of the lens body (1) is two groups, and the monitoring compartments (8) are distributed on the left and right sides of the rear end face of the lens body (1). The number of intraocular pressure monitoring sensors (9) in a single group of monitoring compartments (8) on the rear end face of the lens body (1) is two, and the intraocular pressure monitoring sensors (9) are distributed at the lower front left and right positions of a single group of monitoring compartments (8).

5. The wearable intraocular pressure monitoring device according to claim 1, characterized in that: The air outlet pipe (5) has two air outlet ends, and the end of the air outlet pipe (5) far from the miniature air blower (4) is fixed at the left and right positions above the front end face of the lens body (1). The number of both the miniature air blowers (4) and the air outlet pipes (5) is two groups. The miniature air blowers (4) are fixed at the top positions of the lens body (1) near the left and right sides of the battery compartment (3), and the air outlet ends of the air outlet pipes (5) far from the miniature air blowers (4) are fixed at the left and right sides above a single group of monitoring compartments (8).

6. The wearable intraocular pressure monitoring device according to claim 1, wherein: The counterweight temple arms (14) are in the shape of an L, and the overall weight of the counterweight temple arms (14) is the same as the total weight of the lens body (1) and the miniature air blowers (4), intraocular pressure monitoring sensors (9), main controller (11), signal processing unit (12), and wireless transmission unit (7).

7. The wearable intraocular pressure monitoring device according to claim 1, characterized in that: The silica gel layer (2) covers the surface of the weighted temple (14), and the thickness of the silica gel layer (2) covering the surface of the weighted temple (14) is 2 mm. The material of the silica gel layer (2) is hydrogenated silicone rubber.

8. The wearable intraocular pressure monitoring device according to claim 1, characterized in that: The overall shape of the LED strip (10) is U-shaped. LED beads are arranged inside the LED strip (10), and the distance between the LED beads is 1.5 cm.

9. The wearable intraocular pressure monitoring device according to claim 1, characterized in that: Through slots that communicate with each other are provided between the two groups of monitoring bins (8) on the rear end face inside the lens body (1) and at the bottom of the battery bin (3). The wires provided between the intraocular pressure monitoring sensor (9) and the battery bin (3) and between the LED strip (10) and the battery bin (3) are all located in the through slots.

Citation Information

Patent Citations

  • System, Method, and Apparatus for Controlling Environment Surrounding Eye

    CN113749610A

  • Wearable display device

    CN113825351A

  • Glaucoma postoperative rehabilitation eye shield

    CN117814996A

  • Non-contact intraocular pressure meter and measuring method

    CN119033329A

  • Head-mounted intraocular pressure measuring equipment based on VR design

    CN221533710U