METHOD FOR PROVIDING CONTROL DATA FOR A LASER OF A TREATMENT APPARATUS
20230372155 · 2023-11-23
Inventors
Cpc classification
International classification
Abstract
The invention relates to a method for providing control data for a laser (18) of a treatment apparatus (10) for the correction of a cornea (26), including ascertaining (S10) an effect of a deformation of the cornea (26) on preset corneal parameters by means of a corneal deformation model, wherein the cornea (26) can be modeled in a deformed and non-deformed state by the corneal deformation model, wherein values of preset corneal parameters in the non-deformed state of the cornea (26) are varied and the effect of this variation on values of the corneal parameters in the deformed state of the cornea (26) is ascertained for determining the effect of the deformation; determining (S12) the most important corneal parameters for a treatment and/or deformation of the cornea (26) depending on a magnitude of the ascertained effect; adapting (S14) at least one preset fit function as the compensation function of the deformation to the values of the most important corneal parameters; calculating (S16) a deformation-corrected treatment value by means of the compensation function; and providing (S18) the deformation-corrected treatment value for the treatment apparatus (10).
Claims
1. A method for providing control data for a laser of a treatment apparatus for the correction of a cornea of a human or animal eye, wherein the method comprises the following steps performed by at least one control device: ascertaining an effect of a deformation of the cornea on preset corneal parameters by means of a corneal deformation model, wherein the cornea can be modeled in a deformed state and a non-deformed state by the corneal deformation model, wherein values of multiple preset corneal parameters in the non-deformed state of the cornea are varied and the effect of this variation on values of the corneal parameters in the deformed state of the cornea is ascertained for determining the effect of the deformation; determining the most important corneal parameters for a treatment and/or deformation of the cornea depending on a magnitude of the ascertained effect; adapting one or multiple respectively preset fit functions to the values of the most important corneal parameters, wherein the one adapted fit function provides a compensation function for compensating for the deformation or the multiple adapted fit functions are composed to the compensation function; calculating a deformation-corrected treatment value by means of the compensation function and preoperative values of the most important corneal parameters; and providing the deformation-corrected treatment value as control data for the treatment apparatus.
2. The method according to claim 1, wherein the corneal deformation model is based on the Euler-Bernoulli beam theory.
3. The method according to claim 1, wherein the values of the preset corneal parameters are varied within respectively preset ranges of values for determining the effect of the deformation, wherein the ranges of values comprise respective default values of the respective corneal parameter.
4. The method according to claim 1, wherein the preset fit function is a polynomial function, in particular a second order polynomial.
5. The method according to claim 1, wherein the adapted fit functions of the most important corneal parameters are multiplied by or summed with each other for the compensation function.
6. The method according to claim 1, wherein a planned refractive power correction and/or a planned lenticule diameter are adapted by the compensation function.
7. The method according to claim 1, wherein a deformation of the cornea, which is generated by a contact element, is compensated for by means of the compensation function, and/or wherein a deformation of the cornea, which is generated upon closing the cornea after removal of a lenticule from the cornea, is compensated for by means of the compensation function.
8. A control device that is formed to perform a method according to claim 1.
9. A treatment apparatus with at least one eye surgical laser for the separation of a lenticule with predefined interfaces from a human or animal eye by cavitation bubbles and with at least one control device according to claim 8.
10. The treatment apparatus according to claim 9, wherein the at least one eye surgical laser is suitable to emit laser pulses in a wavelength range between 300 nm and 1400 nm, at a respective pulse duration between 1 fs and 1 ns, and a repetition frequency of greater than 10 kHz.
11. The treatment apparatus according to claim 9, wherein the control device comprises at least one storage device for at least temporary storage of at least one control dataset, wherein the control dataset or datasets include(s) control data for positioning and/or for focusing individual laser pulses in the cornea; and includes at least one beam device for beam guidance and/or beam shaping and/or beam deflection and/or beam focusing of a laser beam of the laser.
12. A computer program including commands that cause the control device according to claim 8 to execute the method.
13. A non-transitory computer-readable medium, on which the computer program according to claim 12 is stored.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
[0034] Further features of the invention are apparent from the claims, the figures and the description of figures. The features and feature combinations mentioned above in the description as well as the features and feature combinations mentioned below in the description of figures and/or shown in the figures alone are usable not only in the respectively specified combination, but also in other combinations without departing from the scope of the invention. Thus, implementations are also to be considered as encompassed and disclosed by the invention, which are not explicitly shown in the figures and explained, but arise from and can be generated by separated feature combinations from the explained implementations. Implementations and feature combinations are also to be considered as disclosed, which thus do not comprise all of the features of an originally formulated independent claim. Moreover, implementations and feature combinations are to be considered as disclosed, in particular by the implementations set out above, which extend beyond or deviate from the feature combinations set out in the relations of the claims.
[0035]
[0036]
[0037]
[0038]
[0039]
[0040]
[0041]
[0042]
[0043] In the figures, identical or functionally identical elements are provided with the same reference characters.
DETAILED DESCRIPTION
[0044]
[0045] Furthermore,
[0046] The illustrated laser 18 can preferably be a photodisruptive and/or ablative laser, which is formed to emit laser pulses in a wavelength range between 300 nm and 1400 nm, preferably between 700 nm and 1200 nm, at a respective pulse duration between 1 fs and 1 ns, preferably between 10 fs and 10 ps, and a repetition frequency of greater than 10 kHz, preferably between 100 kHz and 100 MHz. Optionally, the control device 20 additionally comprises a storage device (not illustrated) for at least temporary storage of at least one control dataset, wherein the control dataset or datasets include(s) control data for positioning and/or for focusing individual laser pulses in the cornea. The position data and/or focusing data of the individual laser pulses, that is the lenticule geometry of the lenticule 12 to be separated, are generated based on predetermined control data, in particular from a previously measured topography and/or pachymetry and/or the morphology of the cornea or of the optical visual disorder correction to be generated.
[0047] For determining the visual disorder data, which can for example indicate a value in diopters, suitable examination data for describing the visual disorder can be received by the control device 20 from a data server or the examination data can be directly input into the control device 20.
[0048] Further, a contact element 28 can be provided, which can belong to the treatment apparatus 10. Alternatively, the contact element 28 can also be provided separately from the treatment apparatus 10. The contact element 28, which can also be referred to as patient interface or fixing system, serves to fix the eye or the cornea 26 for the treatment. Hereto, the contact element 28 can comprise a plano-concave lens, which is adapted to the cornea 26 for fixing. By fixing by means of the contact element 28, however, it can occur that the cornea 26 deforms and thus the geometry of the lenticule 12 does no longer have the originally planned dimensions. Therefore, it can occur that a planned refractive power value or refractive power value to be corrected for example deviates from an achieved refractive power value after the treatment with the treatment apparatus 10.
[0049] In
[0050] For illustrating the corneal deformation model, the deformation of the volume body of the cornea 26 is shown for the deformation by the contact element 28 in
[0051] Herein,
[0052] Thus, a radius of curvature of a respectively central corneal surface 34 can preferably be described by means of the corneal deformation model according to the formula
[0053] wherein it provides the radius of curvature of the central corneal surface 34 before the deformation (r.sub.cent,pre). Therein, r.sub.ca describes the radius of curvature of the anterior corneal surface 30 and rip describes the radius of curvature of the posterior corneal surface 32. The variable q describes a relative position of the central corneal surface 34 to the neutral corneal surface 36, wherein q can take a value between 0 and 1.
[0054] In similar manner, a position in z-direction, which is dependent on the radial position, can also be described to the radius of curvature, wherein the z-direction extends in the direction of the optical axis. It can be described for the respective central corneal surface 34 with the formula
[0055] wherein r.sub.X describes a radial position starting from the center of the cornea 26 and dcc describes a central thickness of the cornea 26 at the highest point or inflection point of the cornea 26.
[0056] Upon the deformation of the cornea 26 by the contact element 28, it can be provided in the corneal deformation model that the radius of curvature of the anterior corneal surface 30 is adapted to a radius of curvature of the contact element 28. This situation is for example illustrated in
[0057] In
[0058] In the deformation of the cornea 26 by closing the area of the lenticule 12, it can be provided in the corneal deformation model that the radius of curvature of the anterior interface 16 is adapted to a radius of curvature of the anterior interface 14 such that the cornea 26 according to
[0059] In
[0060] On the x-axis of
[0061] For determining the graphic shown in
[0062] In corresponding manner, further corneal parameters can also be varied except for the radius of curvature of the anterior corneal surface r.sub.ca 30, as for example illustrated in
[0063] Returning to the method diagram of
[0064] After determining the most important corneal parameters for the treatment and/or deformation, one or multiple respectively preset fit functions can be adapted to the values of the ascertained most important corneal parameters in a step S14, to determine a compensation function, which can be provided for compensating for the deformation, in particular the refractive power correction. As illustrated in
[0065] In this example, a first polynomial function can have been adapted to
[0066] This compensation function can then be provided to the treatment apparatus 10, in particular to the control device 20, for compensating for the deformation to perform a deformation-corrected refractive power correction.
[0067] Thus, a deformation-corrected treatment value can be calculated by means of the compensation function in a step S16, in that preoperative values of the most important corneal parameters are substituted into the compensation function and thus the deformation-corrected treatment value is generated. In this example, the deformation-corrected treatment value is the refractive power correction, which is to be ascertained by the compensation function. In order to correct the originally planned refractive power correction for the deformation to be expected, the preoperative values of the most important corneal parameters, which are r.sub.ca and k.sub.cap in this example, can be ascertained from predetermined examination data, wherein they can be substituted into the ascertained compensation function. Thus, both the influence of the corneal parameter r.sub.ca and k.sub.cap upon deformation of the cornea 26 on the refractive power correction can be compensated for by the compensation function, in particular at the same time, which provides an improved deformation correction since the most important corneal parameters are taken into account in the compensation function. In corresponding manner, a compensation function with the most important corneal parameters can also be ascertained for the further corneal parameters R.sub.cap, TZ and further corneal parameters, wherein the deformation can then be compensated for also for these corneal parameters in corresponding manner.
[0068] Finally, the thus obtained deformation-corrected treatment values can be provided as control data for the treatment apparatus 10, in particular the control device 12, in a step S18.
[0069] Overall, the examples show how a simple and fast compensation for deformation effects can be achieved by means of the compensation function.