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Methods and systems for treating presbyopia are provided. In accordance with an embodiment, by way of example only, a method of treating presbyopia of an eye includes ablating the stroma to form a final ablated shape in the stroma, the final ablated shape including a central zone defined by a concav

Methods and systems for treating presbyopia are provided. In accordance with an embodiment, by way of example only, a method of treating presbyopia of an eye includes ablating the stroma to form a final ablated shape in the stroma, the final ablated shape including a central zone defined by a concavity having a central zone depth and a central zone diameter, the central zone depth and the central zone diameter each selected to provide the cornea with a near-vision add power after the epithelium is regenerated over the stroma.

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1. A method of treating presbyopia of an eye, the method comprising: determining a presbyopia-correcting refractive power for the eye by determining an ametropic-correcting prescription for the eye; andablating a stroma of a cornea of the eye to form a final ablated shape in the stroma, the final ab

1. A method of treating presbyopia of an eye, the method comprising: determining a presbyopia-correcting refractive power for the eye by determining an ametropic-correcting prescription for the eye; andablating a stroma of a cornea of the eye to form a final ablated shape in the stroma, the final ablated shape including a central zone defined by a concavity having a central zone depth (d), a central zone diameter (D), and a radius of curvature (R) in a range of about 3 mm to about 20 mm, the central zone depth and the central zone diameter each selected to provide a near-vision add power between 1.0 Diopters and 3.5 Diopters after the epithelium is regenerated over the stroma; wherein d=D2÷8R, D=Φ√{square root over (%)}, where % is an optimal percentage of light passing through a near vision zone of the cornea and (1) is an average photopic pupil diameter of a patient who is 45 years or older, the optimal percentage being between about 20% and about 60% andR=Δn÷ΔP where ΔP is a desired near vision add power and Δn is a difference in refractive index between the epithelium and the stroma. 2. The method of claim 1, further comprising excising tissue from the stroma around the central zone to form a ring-shaped outer zone, the ring-shaped outer zone having an outer zone diameter and an outer zone depth, each selected to provide the cornea with the near-vision add power after the epithelium is regenerated. 3. The method of claim 1, wherein ablating the stroma results in the central zone having the central zone diameter in a range of about 1.5 millimeters to about 3.5 millimeters and having the central zone depth in a range of about 10 μm to about 300 μm. 4. The method of claim 1, wherein the near-vision add power is 1.0 Diopter, the central zone diameter is in a range of about 1.0 mm to 3.0 mm, and the central zone depth is in a range of about 6 μm to about 50 μm. 5. The method of claim 1, wherein the near-vision add power is 1.5 Diopter, the central zone diameter is in a range of about 1.0 mm to 3.0 mm, and the central zone depth is in a range of about 8 μm to about 75 μm. 6. The method of claim 1, wherein the near-vision add power is 2.0 Diopter, the central zone diameter is in a range of about 1.0 mm to 3.0 mm, and the central zone depth is in a range of about 11 μm to about 100 μm. 7. The method of claim 1, wherein the near-vision add power is 2.5 Diopter, the central zone diameter is in a range of about 1.0 mm to 3.0 mm, and the central zone depth is in a range of about 14 μm to about 125 μm. 8. The method of claim 1, wherein the near-vision add power is 3.0 Diopter, the central zone diameter is in a range of about 1.0 mm to 3.0 mm, and the central zone depth is in a range of about 17 μm to about 180 μm. 9. The method of claim 1, wherein the near-vision add power is 3.5 Diopter, the central zone diameter is in a range of about 1.0 mm to 3.0 mm, and the central zone depth is in a range of about 21 μm to about 210 μm. 10. The method of claim 1, further comprising the step of removing a portion of an epithelium of the cornea of the eye to expose an anterior surface of the stroma. 11. The method of claim 1, wherein ablating the stroma comprises photoaltering the stroma to expose a posterior surface of epithelium that is located anterior relative to the stroma. 12. A system for treating presbyopia of an eye having an epithelium, a cornea, and a stroma, the system comprising: a laser configured to provide a laser beam along an optical path;a support for positioning an eye for presbyopic treatment in the optical path of the laser beam;a processor in operable communication with the laser; anda computer readable medium including instructions that, when executed, cause the processor to (1) determine a laser target surface on the eye and (2) provide commands to the laser to ablate a surface of the stroma to form a final ablated shape in the stroma, wherein the final ablated shape includes a central zone defined by a concavity having a central zone depth (d), a central zone diameter (D), and a radius of curvature (R) in a range of about 3 mm to about 20 mm, and the central zone depth and the central zone diameter in combination provide the cornea with a near-vision add power between 1.0 Diopters and 3.5 Diopters after the epithelium is regenerated over the stroma; wherein d=D2÷8R, D=φ√{square root over (%)}, where % is an optimal percentage of light passing through a near vision zone of the cornea and φ is an average photopic pupil diameter of a patient who is 45 years or older, the optimal percentage being between about 20% and about 60%, andR=Δn÷ΔP, where ΔP is a desired near vision add power and Δn is a difference in refractive index between the epithelium and the stroma. 13. The system of claim 12, wherein the computer readable medium comprises instructions that, when executed, cause the processor to provide commands to the laser to remove a portion of the epithelium to expose an anterior surface of the stroma. 14. The system of claim 12, wherein the computer readable medium comprises instructions that, when executed, cause the processor to provide commands to the laser to form a flap. 15. The system of claim 12, wherein the computer readable medium comprises instructions that, when executed, cause the processor to provide commands to the laser to excise tissue from the stroma around the central zone to form a ring-shaped outer zone, the ring-shaped outer zone having an outer zone diameter and an outer zone depth. 16. The system of claim 12, wherein the computer readable medium comprises instructions that, when executed, cause the processor to provide commands to the laser to excise tissue from the stroma to form the central zone having a central zone diameter in a range of about 1.0 millimeters to about 2.5 millimeters and a central zone depth in a range of about 0.6 μm to about 88 μm. 17. The system of claim 12, further comprising a wavefront measurement subsystem in operable communication with the processor, the wavefront measurement subsystem configured to generate wavefront data for one or more measured aberrations of the eye for use by the system to provide an ametropic-correcting prescription. 18. The system of claim 12, wherein the near-vision add power is 2.0 Diopter, the central zone diameter is in a range of about 1.0 mm to 3.0 mm, and the central zone depth is in a range of about 11 μm to about 100 μm. 19. The system of claim 12, wherein the near-vision add power is 2.5 Diopter, the central zone diameter is in a range of about 1.0 mm to 2.5 mm, and the central zone depth is in a range of about 14 μm to about 125 μm.