Embodiments relate to an applanation tonometry apparatus for the measurement of intraocular pressure, and a case for the transport and use of the apparatus.
Intraocular pressure (IOP) is a physiological parameter routinely measured by eye care professionals. Elevated IOP is the most important risk factor in primary open angle glaucoma (POAG) which, combined with normal tension glaucoma (NTG), is the second leading cause of irreversible blindness in the United States. Patients with POAG and NTG have the same characteristic optic neuropathy (cupping) and visual field loss, but in NTG the IOPs have never been found to be elevated. Elevated IOP is also found in patients with ocular hypertension (OHT), but not the neuropathy or field changes. The only current treatment for POAG, NTG and OHT is reduction of IOP.
The instrument that is the reference standard for IOP measurement is the Goldmann applanation tonometer, used worldwide by ophthalmologists for over 50 years. This instrument functions to flatten part of the cornea to measure eye pressure, wherein the pressure within the eye is determined by how much force is needed to flatten the cornea.
Glaucoma management, which is so dependent on IOP, would benefit greatly by the acquisition of more IOP data. Essentially all IOP measurements are obtained on visits to the ophthalmologist's office—usually one measurement during typical office hours, and rarely more than one visit every two or three months. In glaucoma management, there is no parallel to the ubiquitous monitoring by diabetic patients of capillary blood glucose or by arterial hypertensive patients of blood pressure and heart rate. For these conditions, adjuncts in patient care increase the volume of measurements during clinic hours as well as extend the monitoring beyond the eight hours that the clinic is open.
Measurement of IOP at different times of the day usually yields different readings, sometimes highest at night. However, there is considerable variability in the diurnal pattern between individuals. Differences in IOP throughout the day are of special interest. In some POAG patients, despite treatment which results in normal IOPs (measured in the ophthalmologist's office), cupping and field loss can progress. In NTG, cupping occurs and can progress in the presence of IOP within the normal statistical limits (measured in the ophthalmologist's office). In OHT, over time, cupping and field loss can develop. The question in these cases is whether the progression (in POAG and NTG) and development (in OHT) of glaucoma damage is due to elevated IOP at times of the day when they cannot be measured in the ophthalmologist's office.
The disadvantages for both patients and medical personnel of an institutional site in measuring diurnal IOP led to the idea of home tonometry, which Posner noted in 1965, having patients use a Maklakoff type tonometer (Eye & Ear Nose Throat Mon 1965, 44: 64-66). Jensen and Maumenee (Am J Ophthalmol 1976, 76: 929-932) and later Alpar (Glaucoma 1983, 5: 130-132) had a family member measure the patient's IOP with the Schiotz tonometer.
A more recent approach to measuring diurnal IOP in the home environment introduced the concept of self-tonometry. Two technically sophisticated instruments, both hand-held and based on the applanation principle of the Goldmann tonometer, have been studied. In Zeimer and Wilenski's instrument (IEEE Trans Biomed Eng 1982, 29: 178-183), the IOP endpoint is detected by a photodiode array optical device instead of the signature pattern recognition used in Goldmann tonometry. Draeger and group used a microprocessor controlled optical sensor (see Groenhoff et al., Int Ophthalmol 1992, 16: 299-303). Both showed promise in the hands of their inventors, but others have found the correlation of patient measurements and ophthalmologist measurements using the Goldmann tonometer problematic, and also found that these devices can be moderately difficult to use. What may be most significant is the limited interest in these instruments since their invention in the 1980's, despite the concurrent heightened awareness of the potential importance of diurnal IOP.
As would be expected, self-tonometry with non-contact tonometers (see Stewart et al., Ann Ophthalmol 1991, 23: 177-182; Carenini et al., Int Ophthalmol 1992, 16: 295-297) that have been shown to be less reliable than the Goldmann method in the hands of ophthalmologists has met with a general lack of professional interest. Finally, the Tono-Pen®, based on the McKay-Marg applanation principle, is used by some ophthalmologists' technicians for IOP screening. While it has occasionally been used for self-tonometry (see Kupin et al., Am J Ophthalmol 1993, 116: 643-644), it is not easy to apply to oneself, and an ophthalmologist would not depend on measurements with a screening instrument as a basis for clinical decisions.
In one embodiment, a case for transportation and use of an applanation tonometry apparatus includes a housing including a base and a wall structure extending upwardly therefrom, the housing sized to receive the applanation tonometry apparatus therein. A lid is pivotally connected to an upper rim of the wall structure, the lid having a closed position overlying the housing and an open position rotated away from the housing, the lid supporting the applanation tonometry apparatus in the open position. A handle is pivotally connected to the lid and has a stored position within the lid and a use position rotated away from the lid, the handle supporting the lid in the open position by engagement with a support surface.
In another embodiment, a case for transportation and use of an applanation tonometry apparatus includes a housing including a base and a wall structure extending upwardly therefrom, the housing sized to receive the applanation tonometry apparatus therein. A lid is pivotally connected to an upper rim of the wall structure, the lid having a closed position overlying the housing and an open position rotated away from the housing approximately 180 degrees from the closed position, the lid supporting the applanation tonometry apparatus in the open position. A handle is pivotally connected to an outer surface of the lid and has a stored position within the lid and a use position rotated away from the lid, the handle including telescoping legs for supporting the lid in the open position by engagement with a support surface.
In one embodiment, an applanation tonometry system includes a housing including a base and a wall structure extending upwardly therefrom, and an applanation tonometry apparatus disposed within the housing, the apparatus having a base plate. A lid is pivotally connected to an upper rim of the wall structure, the lid having a closed position overlying the housing and an open position rotated away from the housing. A handle is pivotally connected to the lid and having a stored position within the lid and a use position rotated away from the lid, the handle supporting the lid in the open position by engagement with a support surface. For use, the apparatus is raised vertically from the housing and rotated approximately 180 degrees in a generally horizontal plane to align with the lid in the open position, the lid supporting the applanation tonometry apparatus in the open position.
As required, detailed embodiments of the present invention are disclosed herein; however, it is to be understood that the disclosed embodiments are merely exemplary of the invention that may be embodied in various and alternative forms. The figures are not necessarily to scale; some features may be exaggerated or minimized to show details of particular components. Therefore, specific structural and functional details disclosed herein are not to be interpreted as limiting, but merely as a representative basis for teaching one skilled in the art to variously employ the present invention.
Embodiments are directed to an applanation tonometry apparatus for measurement of intraocular pressure (IOP). Referring first to
With continuing reference to
The wiring for each component described above preferably runs to a single cable connector and then to a power supply (not shown), wherein the wiring is preferably minimized and the transformers simplified for home use. Apparatus 10 is designed for portability in that it is light, compact and easy to use in a user's home environment, or other location outside of a physician's office. Lightweight materials, such as aluminum and plastics, can be used to construct base 12, joystick 14 and guide plate 16, support 18, and chin-forehead rest 46, and compactness can be achieved with telescoping vertical supports of chin/forehead rest 46. Apparatus 10 can be used with ease for testing the IOP of either the left or right eye.
The adjustment of tonometer tip 42 could be automated to obtain the endpoint applanation pattern. Proximity devices could be used to detect the presence of the eye as the tonometer tip 42 is applied to the cornea. Once the tip 42 is in contact with the cornea, image recognition software could use stepper motors to move the tonometer 40 through its 3-axes of movement (up and down, right and left, toward and away) until the applanation pattern is centered and the endpoint pattern is reached.
Additionally, external monitoring can be accomplished by viewing output from video camera 30 on an additional video monitor. The applanation pattern image being viewed by the user can then be simultaneously viewed by the physician, and is helpful for teaching users how to use the apparatus 10. Self-tonometry data can also be recorded to provide a direct, valid, verifiable, highly dependable assessment of the reliability of use of the apparatus 10 at home or another location outside of the office. A video recorder can be provided in communication with the video camera 30, and the output of a microprocessor analyzed to provide the applanation pattern images and the IOP readings, respectively, for subsequent assessment of the applanation endpoint patterns users obtain at home. The recording could be activated by the user's pressure on sensors (not shown) provided in the chin-forehead rest 46. Data recording during self-tonometry could include the day, time, a still image of the applanation endpoint pattern, and the IOP.
Prior to initiating testing using apparatus 10 described above, dye (for example, fluorescein) and anesthetic (for example, benoxinate, Fluorox, Ocusoft, Inc.) drops may be instilled in the user's test eye. The dye allows for easier viewing of the tear meniscus between the cornea and the tonometer tip 42, and the anesthetic numbs the surface of the eye to ensure that the user does not feel any discomfort during testing.
When using apparatus 10, the user takes position in contact with chin-forehead rest 46, and moves the joystick 14 with one hand for course positioning to bring the tonometer tip 42 close to the test eye, aligning the tip 42 by looking directly at it such that it appears symmetric. Using the joystick 14, the user then brings the tonometer tip 42 into contact with his/her cornea. As the tonometer tip 42 applanates (flattens) the cornea of the test eye, the user views the applanation pattern (typically green in color) on one video monitor 28 with the observing eye. Next, the user manipulates the joystick 14 to adjust the tonometer tip 42 position to center the applanation pattern on the monitor 28. Finally, with the other hand, the user manipulates the tonometer dial 44 to obtain the applanation endpoint pattern for IOP measurement as described below. The user will then remove the tonometer tip 42 from the cornea using the joystick 14 and repeat the procedure on the other eye.
In addition to self-tonometry, the applanation tonometry apparatus can be configured to enable tonometry by another, such as a caretaker. In the embodiment depicted in
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The apparatus described herein provides a diagnostic tool that will enable ophthalmologists to obtain a vastly increased volume of user IOP information throughout 24 hours. This could greatly improve medical control of IOP, the primary risk factor of glaucoma.
While exemplary embodiments are described above, it is not intended that these embodiments describe all possible forms of the invention. Rather, the words used in the specification are words of description rather than limitation, and it is understood that various changes may be made without departing from the spirit and scope of the invention. Additionally, the features of various implementing embodiments may be combined to form further embodiments of the invention.
This application claims the benefit of U.S. provisional Application No. 61/643,505 filed May 7, 2012, the disclosure of which is incorporated in its entirety by reference herein.
Number | Date | Country | |
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61643505 | May 2012 | US |