This application is a National Stage of International Application No. PCT/FR2018/051326, filed Jun. 7, 2018, which claims priority to French Patent Application No. 1854106, filed May 17, 2018, the entire disclosures of which are hereby incorporated by reference in their entirety for all purposes.
The present invention relates to a device and a method for the automatic determination of the subjective ocular refraction of a patient, as well as a booth equipped with such a device.
Ocular refraction is the change of direction of a light ray that passes through different media in the eye. This ray ultimately converges on the retina, that is to say on the layer of cells that line the bottom of the eyeball and which is intended to transform light energy into nerve impulses that are then decoded by the brain in the form of images.
Ocular refraction is used to determine abnormalities in the vision (ametropia) of a person (hereinafter referred to as the “patient”). The ametropias of an eye are defined by the position of the light rays entering the eye, which are deflected in relation to the retina. Depending on the position of these rays, the eye is considered myopic, normal or hypermetropic. In addition, when light rays describe a surface on the retina instead of a point, the eye is astigmatic.
To determine the ocular refraction of a patient, an automatic refractometer (or “auto-refractometer”) is generally used to measure a theoretical refraction called objective refraction, which defines an objective correction for each of the patient's eyes.
However, since the condition of a patient's eyes may vary over time, the results provided by an automatic refractometer are variable over time. Muscular and neurosensory phenomena such as accommodation can also cause these results to vary. Thus, during an ophthalmological examination or consultation, in particular with a view to prescribing corrective lenses adapted to the patient, the ophthalmologist (or another vision professional such as an orthoptist, optometrist or optician) determines the subjective ocular refraction of the patient, requiring the patient's participation.
The eye care professional (ophthalmologist, orthoptist, optometrist or optician for example) usually uses an automatic refractor to do this. An automatic refractor typically consists of an ocular device with two eyepieces to be placed in front of the patient's eyes, a management unit configured to take corrective lenses from a supply and position them in the eyepieces, and a control interface that is used by the eye care professional to operate the management unit. During this examination, different combinations of corrective lenses are placed in the eyepieces, and the patient checks, by looking at a target through the ocular device, whether the lens or lenses presented allow a clear view of the target.
The eye care professional generally has to perform a large number of successive tests before being able to determine a comfortable vision correction for the patient. Such an examination is therefore takes a significant amount of time.
FR 3 050 922 discloses a method for reducing the duration of an examination of the subjective ocular refraction of a patient. This method, whose aim is to control an automatic refractor, is characterised by a step of the determination of an accommodative profile indicating a capacity of the eye to accommodate excessively or not, and a step of generation of at least one selection command identifying corrective lenses to be successively positioned in the ocular device in order to subject the eye to several successive refractive tests, wherein the selection command depends on the accommodative profile determined. This method enables the automatic determination of a set of tests by identifying corrective lenses to be positioned in the ocular device, thus reducing the duration of the examination.
However, during the examination eye tests are always performed in the usual way. In particular:
This method, although partially automated, still requires the intervention of an operator, usually an eye care professional, which has drawbacks especially in terms of cost and availability.
The present invention provides a device for the automatic determination of at least the subjective ocular refraction of a patient. It concerns a device comprising:
According to the invention:
The central unit is preferably configured to generate a prescription comprising a prescription for spectacles for the patient, adapted to the subjective ocular refraction thus determined.
In the context of the present invention, the term “direct” detection and/or transmission of gestural indications (or indications generated in the form of gestures) means the detection without the intervention of a third party (such as an operator, in particular an eye care professional) of these gestural indications and the transmission of these gestural indications to the central unit of the device, also without the intervention of a third party.
Thus, thanks to the simultaneous automatic generation of instructions to the patient (via the instruction generation system) with a view in particular to the conduct of one or more eye tests, and the direct detection and taking into account of the patient's responses (expressed in the form of gestures) during this or these eye tests (via the interface system), this device does not require the intervention of an operator, such as an eye care professional, to perform the necessary eye test(s) at the central unit of the device to determine the subjective ocular refraction of the patient. Simply by collaborating with the patient, without the intervention of a third party (such as an operator), this device thus makes it possible to automatically determine the subjective ocular refraction of the patient and to automatically generate a prescription where necessary, which brings advantages in particular in terms of cost and availability and makes it possible to remedy the aforementioned drawbacks.
Advantageously, the said device comprises, in addition, at least one of the following elements:
Moreover, in a particular embodiment, the device also comprises a transmission element configured to transmit the prescription remotely to a user.
In addition, in a preferred embodiment, the instruction generation system comprises a voice output unit.
In the context of the present invention:
In a first embodiment, the interface system comprises at least one manual actuating element. This manual actuating element is configured to be manually operated by the patient. This may include one or more actuating elements such as buttons. It can also be a joystick. In this first embodiment, the indications in the form of gestures thus represent manual actuations of the manual actuating element.
In addition, in a second embodiment, the interface system comprises a system for automatic detection of patient gestures. In this second embodiment, the indications (in the form of gestures) represent gestures, in particular movements of one or both hands, which are detected automatically and directly by the said automatic gesture detection system (and transmitted to the central unit).
Moreover, in a particular embodiment, the said device comprises, in addition:
Within the framework of the present invention, the various components (and in particular the automatic refractor, the central unit, the data acquisition unit, the instruction generation system and the interface system, as well as the automatic refractometer and the frontofocometer, as the case may be) of the device may be connected together in different ways, in order to communicate and transmit data and/or commands in particular.
Thus, advantageously:
The present invention also relates to a booth for automatic determination of the subjective ocular refraction of a patient (and preferably for generation of a prescription).
According to the invention, said booth is at least partially closed and comprises at least one seat for a patient and a device for automatic determination of the subjective ocular refraction of a patient as specified above.
Advantageously, the various elements (of the said device for automatic determination of the subjective ocular refraction) are arranged in the booth in such a way that they are accessible, if necessary, from the patient's seat.
The present invention further concerns a method for automatic determination of the subjective ocular refraction of a patient, by means of a device such as the aforementioned one, which comprises at least:
According to the invention, the said method comprises:
The said process advantageously also comprises at least one data input step, which is implemented prior to the generation step.
The generation and testing steps preferably use a fog test.
In addition, in a preferred embodiment, the test step consists of displaying letter Es with branches with different orientations, which can be easily and simply recognised, especially by populations of illiterate individuals.
The invention will be better understood, and the other purposes, details, characteristics and advantages of the invention will appear more clearly in the following detailed explanatory description of the embodiments of the invention given as a purely by way of a illustrative and non-exhaustive example, with reference to the attached schematic drawings. In these drawings:
Device 1, shown schematically in
This device 1 usually comprises:
The data input unit 11 can comprise any type of element or usual means of inputting data, such as for example a keyboard associated with a screen or a touch screen.
According to the invention, said device 1 further comprises:
According to the invention, the interface system 14 is configured to detect, directly, indications generated by the patient in the form of gestures, and preferably in manual form, at least during an eye test, and to transmit these detected indications (in the form of gestures) directly to central unit 9 via a link 15.
In addition, according to the invention, central unit 9 comprises a control element 16 which is configured:
Central unit 9 also comprises a processing element 17 configured to generate a prescription. This prescription comprises, in particular, a prescription for corrective lenses of spectacles for the patient, whose correction is adapted to the subjective ocular refraction determined by control element 16.
Said device 1 also comprises a recording element 18 which is configured to record at least the prescription (and possibly the objective ocular refraction) generated by processing element 17, on a storage medium 18A, internal or external (to central unit 9), of any usual type, for example a USB key.
Additionally and/or alternatively, device 1 comprises a printing element (or printer) 19. This printing element 19 is configured to print on paper the prescription generated by processing element 17 (or simply the subjective ocular refraction) and received via a link 20. Thus, immediately after the examination, the patient will have a prescription in the form of a paper document, allowing them to obtain spectacles adapted to their vision.
Furthermore, in a special embodiment, device 1 comprises, additionally and/or alternatively, a transmission element 21. This transmission element 21 is configured to transmit (in particular remotely via the Internet) the prescription, generated by processing element 17 (or simply the subjective ocular refraction) and received via a link 22, to a user, for example a healthcare professional.
Thus, device 1 is able to perform a teletransmission of the prescription and/or subjective ocular refraction.
In a preferred embodiment, the instruction generation system 12 comprises a conventional voice output unit, comprising a loudspeaker 31 (
In the context of the present invention:
In a first embodiment, interface system 14 comprises at least one manual actuating element 23. This manual actuating element 23 is configured to be manually operated by the patient. In particular, this may be one or more actuating elements such as buttons, e.g. pushbuttons or rotary knobs, as shown for example in
In addition, in a second embodiment, interface system 14 comprises a detection system 26 (
Furthermore, in a particular embodiment, device 1 comprises a voice command system (not shown) that allows the patient to provide said device 1 (and in particular central unit 9) with indications in vocal form, especially during an eye test.
Furthermore, in a preferred embodiment, said device 1 also comprises, as shown in
Moreover, in a particular embodiment, said device 1 comprises, in addition, as shown in
Within the framework of the present invention, the various components (and in particular automatic refractor 2, central unit 9, data input unit 11, instruction generation system 12 and interface system 14, as well as, where appropriate, automatic refractometer 27 and frontofocometer 29) of device 1 can be connected together in different ways, in order to communicate and transmit data and/or commands in particular.
In a first embodiment, shown in
In the example of
In the example shown in
In addition, in the two embodiments of
In addition, in a second embodiment, shown in
In this second embodiment, device 1 also comprises a device 42 of the “HUB” or “Switch” type, which connects via connectors 36, e.g. of the RJ45 type, the nanocomputer 33 of the interface system 14 to the central unit 9.
In addition, in a third embodiment (not shown), at least some of the elements of device 1 communicate with each other via wireless (or “wifi”) communication.
In a preferred application, represented in
The various elements of the said device 1 and in particular automatic refractor 2, interface system 14, automatic refractometer 27 and frontofocometer 29 are arranged in such a way as to be accessible from the patient seat 44.
Automatic refractometer 27 and frontofocometer 29 can be optional in a simplified embodiment.
By way of illustration, data input unit 11, for example a keyboard 45 combined with a display 46, can be arranged at the entrance to booth 43, as shown in the example in
In the example shown, booth 43 comprises within it:
A PR method for automatic determination of the subjective ocular refraction of a patient is described below, with reference to
This PR method comprises:
Steps E1 to E4 of the PR method are described in more detail below.
In the data input step E1, the patient inputs (using the data input unit 11) data about themselves, including age, which will be used by central unit 9 to determine subjective ocular refraction.
In a particular embodiment, the following can be envisaged:
In the data input step E1, in a preferred embodiment, the patient is also asked, via instruction generation system 12, to perform a measurement using automatic refractometer 27 to measure the objective ocular refraction RO of their eyes.
As an alternative, especially where device 1 is without an automatic refractometer 27, the patient can also be asked to enter (via the data input unit 11) the objective ocular refraction of their eyes if they know it.
In the data input step E1, in a preferred but not exclusive embodiment, the patient is also asked, via the instruction generation system 12, to place their spectacles in the frontofocometer 29 so that the latter automatically measures the lens corrections of their spectacles.
The subsequent generation step E2, implemented by the central unit 9, consists of automatically generating at least one eye test, using in particular the age of the patient, their objective ocular refraction RO and their optical correction range measured with a frontofocometer 29.
The eye test(s) are determined by central unit 9 to present different combinations of corrective lenses to the patient based on the objective ocular refraction RO. The patient looks at displays 25 controlled by central unit 9 through eyepiece device 3 fitted with these corrective lenses, and provides indications as to their vision via interface system 14 in test step E3.
Based on these patient indications, central unit 9 then determines an RB refraction (or fog refraction) and derives the subjective RF ocular refraction in processing step E4.
In a preferred embodiment, generation step E2 uses a fog test. Naturally, other types of tests can be carried out by device 1 in the context of the present invention.
Preferably, the fog test consists of making displays (viewed by the patient through the corrective lenses presented in eyepiece device 3) of letter Es, with branches of the E displayed in four different orientations, i.e. to the right, downwards, to the left and upwards. Four E's of different orientations are planned to be displayed, with the RO correction of the patient and E's of 2/10 in ocular device 3. The patient views these displays through the corrective lenses arranged in the ocular device 3. The vision is gradually brightened (and made possible) by gradually removing fog.
Preferably, with the fog technique, device 1 performs the test on only one eye to determine the RB refraction. By convention, the right eye is used, unless measurement with automatic refractometer 27 is impossible on the right eye.
In test step E3, to guide the patient, the instruction generation system 12 can emit (in sub-step E3A) the following voice message to the patient: “The following reading test is called the fog test. It is used to accurately determine your correction. Your vision will be deliberately blurred through the spectacles, and will then gradually become clearer. We will display letter Es with branches in four different orientations as follows. To the right, down, left and up. At the beginning, it will be totally impossible for you to respond and then we will gradually clear your vision by removing the fog. The most important thing for this test is to respond only when you can guess the direction of the E. When you do this, use the directional joystick to tell us the direction of the E, i.e. up, down, right, left”. This directional joystick corresponds to joystick 25 described above.
By way of illustration, the method of calculation of the RB refraction is as follows, wherein the RB refraction is obtained starting from the RO refraction to which +4 dioptres are added.
The four possible E′s are displayed, then corrective lenses of the RO+4 dioptre are integrated into the ocular device 3 of the automatic refractor. A single E of size 2/10 is displayed, and the orientation is changed after each response. In this case:
Central unit 9 determines the RB refraction using the following expression: RB=refraction making it possible to read 2/10−1.25 (sphere dioptres).
Once the RB refraction has been determined for one eye, central unit 9 can either determine the RB refraction for the other eye in the same way or perform the following calculations:
Finally, processing step E4, implemented by central unit 9, includes the automatic determination of the subjective ocular RF refraction.
Central unit 9 calculates the subjective ocular refraction RF from the RB refraction determined as described above.
To do this, central unit 9 takes into account the accommodation value Δ (such as Δ=RB−RO) of the patient, as follows, to determine the subjective ocular refraction RF:
Test step E4 also consists of generating a prescription P from this subjective RF ocular refraction. More specifically, central unit 9 determines the prescription P to be entered on the prescription, as follows:
Finally, the prescription P is provided to the patient, for example by being printed by print element 19. Prescription P can also be transmitted remotely to a third party, for example to a healthcare professional, using transmission element 21.
Device 1 can also be set up to issue an alert message advising the patient to consult an eye care professional in an emergency if their visual acuity is too low.
The method described above is therefore a method for the automated determination of the subjective ocular refraction of a patient, using an algorithm (integrated into central unit 9) and an analysis by artificial intelligence of the combination of objective refraction data measured automatically using, in particular, an automatic refractometer 27, the patient's age, their optical correction range measured using a frontofocometer 29 and their responses collected by central unit 9, wherein the various elements of the device 1 are controlled automatically by central unit 9, wherein central unit 9 presents in the eyepieces 4A and 4B of ocular device 3 a series of adapted corrective lenses, wherein the eye test(s) are implemented with vocal guidance of the patient by a synthesised voice (via the instruction generation system 12) and comprising a collection of responses using interface system 14.
Number | Date | Country | Kind |
---|---|---|---|
1854106 | May 2018 | FR | national |
Filing Document | Filing Date | Country | Kind |
---|---|---|---|
PCT/FR2018/051326 | 6/7/2018 | WO |
Publishing Document | Publishing Date | Country | Kind |
---|---|---|---|
WO2019/220023 | 11/21/2019 | WO | A |
Number | Name | Date | Kind |
---|---|---|---|
4105303 | Guyton | Aug 1978 | A |
5914772 | Dyer | Jun 1999 | A |
20060023163 | Foster | Feb 2006 | A1 |
20090153796 | Rabner | Jun 2009 | A1 |
20130339043 | Bakar | Dec 2013 | A1 |
20140129259 | Seriani | May 2014 | A1 |
20150070650 | Seriani | Mar 2015 | A1 |
20150150446 | Park et al. | Jun 2015 | A1 |
20160310000 | Meneghini | Oct 2016 | A1 |
20170329154 | Liang | Nov 2017 | A1 |
Number | Date | Country |
---|---|---|
3050922 | Nov 2017 | FR |
Entry |
---|
International Search Report mailed Feb. 2, 2019, issued in corresponding International Application No. PCT/FR2018/051326, filed Jun. 7, 2018, 3 pages. |
Written Opinion of the International Searching Authority mailed Feb. 2, 2019, issued in corresponding International Application No. PCT/FR2018/051326, filed Jun. 7, 2018, 7 pages. |
Written Opinion of the International Searching Authority mailed Feb. 2, 2019, issued in corresponding International Application No. PCT/FR2018/051326, filed Jun. 7, 2018, 5 pages. |
International Preliminary Report on Patentability mailed Nov. 17, 2020, issued in corresponding International Application No. PCT/FR2018/051326, filed Jun. 7, 2018, 1 page. |
Number | Date | Country | |
---|---|---|---|
20210212560 A1 | Jul 2021 | US |