43 results about "Corneal surgery" patented technology

Optical coherence tomography (OCT) is used to map the surface elevation and thickness of the cornea. The OCT maps are used to plan laser procedures for the treatment of an irregular, opacified or weakened cornea, and in the treatment of refractive errors. In the excimer laser phototherapeutic keratectomy (PTK) procedure, the OCT data is used to plan a map of ablation depth needed to restore a smooth optical surface. In the excimer laser photorefractive keratectomy procedure, OCT mapping of epithelial thickness is used to achieve clean laser epithelial removal. In femtosecond laser anterior keratoplasty procedure, OCT data is used to plan the depth of femtosecond laser dissection to remove an anterior layer of the cornea, leaving a smooth recipient bed of uniform thickness to receive a disk of donated corneal tissue. The linkage of an OCT system to a precise laser surgical system enables the performance of new procedures that are safer, less invasive and produce faster visual recovery than conventional surgical procedures.

An intraocular light probe has a mask or shield affixed at its distal end thereof which forms a directed light beam for intraocular illumination of target tissues or intraocular application of therapeutic light. The mask or shield serves to more fully focus, intensify and direct the beam toward the target tissues. The mask or shield also helps direct light away from other tissues and away from the eyes of the surgeon. This lessens unwanted glare. By placing a light probe beneath a surgical instrument such as a phacoemulsifier or vitrector, laser, cutting instrument (e.g., scissors or knife), forceps or probe/manipulator, whether as part of or separate from an infusion sleeve, a mask or shield effect is created. This has the same benefits of directing the beam toward target tissues, away from other tissues and away from the eyes of the surgeon. The mask or shield is opaque or semi-opaque and made of a soft, semi-rigid or rigid material. The shield can be rigid enough to serve as the shaft of an instrument with a probe or manipulator at its distal tip. It may also be reflective on the side adjacent to the fiber bundle to help direct, magnify, and intensify the beam of light. The shape of the shield can be flat, curved or circular with an opening along one side. The mask/shield can be removed from the fiberoptic light for sterilization. The device of the invention is preferably introduced into the eye via the primary or side-port incision to provide intraocular cross-lighting of tissues during surgical procedures such as cataract surgery, corneal surgery, vitrectomy, intraocular lens implantation, refractive surgery, glaucoma surgery and vitreo/retinal surgery.

In a control program, according to which a laser-beam spot is guided, while being controlled with respect to position and time, over a cornea to be corrected photorefractively, so as to ablate a predetermined ablation profile therefrom, the effect of the angle between the laser earn and the corneal surface on the energy density of the laser-beam spot incident on the corneal surface and/or on the fraction of the laser-beam energy incident on the corneal surface which is reflected away, is taken into account when generating the control program.

A laser-based method and apparatus for corneal surgery. The present invention is intended to be applied primarily to ablate organic materials, and human cornea in particular. The invention uses a laser source which has the characteristics of providing a shallow ablation depth (0.2 microns or less per laser pulse), and a low ablation energy density threshold (less than or equal to about 10 mJ/cm.sup.2), to achieve optically smooth ablated corneal surfaces. The preferred laser includes a laser emitting approximately 100-50,000 laser pulses per second, with a wavelength of about 198-300 nm and a pulse duration of about 1-5,000 picoseconds. Each laser pulse is directed by a highly controllable laser scanning system. Described is a method of distributing laser pulses and the energy deposited on a target surface such that surface roughness is controlled within a specific range. Included is a laser beam intensity monitor and a beam intensity adjustment means, such that constant energy level is maintained throughout an operation. Eye movement during an operation is corrected for by a corresponding compensation in the location of the surgical beam. Beam operation is terminated if the laser parameters or the eye positioning is outside of a predetermined tolerable range. The surgical system can be used to perform surgical procedures including removal of corneal scar, making incisions, cornea transplants, and to correct myopia, hyperopia, astigmatism, and other corneal surface profile defects.

The present invention is directed to a solution for measuring geometric parameters in the eye which are required for calculating the refractive power of intraocular lenses. The device according to the invention for axial length measurement which acquires axial length, anterior corneal radii, anterior chamber depth, and other parameters in the anterior eye segment includes a control unit, a first measuring device for determining axial length, and an additional measuring device which acquires a plurality of structures in the anterior segment (such as the cornea, anterior chamber, and lens) and which has at least one illumination unit and at least one image recording unit. By determining additional partial-distance parameters of the anterior eye segments, the IOL can be calculated with high precision even after refractive surgery in which the natural relationship between the radii of the anterior and posterior corneal surfaces is extensively altered by corneal surgery.

A system for visualizing an eye of a patient during corneal surgery includes a processor and a first and second camera in signal communication with the processor. The cameras are positionable for focusing on a cornea positioned for surgery. A first and a second display and optics therefor are in signal communication with the processor and are positionable for viewing through a first and a second eyepiece of a stereo microscope, respectively. Software is resident on the processor for receiving a first and second corneal image from the first and second cameras, for processing the received first and second images for display, and for transmitting the processed first and second images to the first and the second displays, respectively, via the display optics. The displays can then be viewed by a surgeon through the microscope at least during the surgery.

A system for visualizing an eye of a patient during corneal surgery includes a processor and a first and second camera in signal communication with the processor. The cameras are positionable for focusing on a cornea positioned for surgery. A first and a second display and optics therefor are in signal communication with the processor and are positionable for viewing through a first and a second eyepiece of a stereo microscope, respectively. Software is resident on the processor for receiving a first and second corneal image from the first and second cameras, for processing the received first and second images for display, and for transmitting the processed first and second images to the first and the second displays, respectively, via the display optics. The displays can then be viewed by a surgeon through the microscope at least during the surgery.

“Universal improvement” of vision is achieved by effectively changing the shape of the anterior refracting surface of the cornea to an ideal “turtleback” shape, on which is imposed the necessary curvature adjustment to achieve correction of distance vision. In accordance with one embodiment, the cornea is actually formed to the turtleback shape through corneal surgery, preferably laser ablation surgery. In accordance with a second embodiment, a contact lens with the desired distance corrected ideal turtleback shape on its anterior surface is positioned over the cornea.

A method for surface ablation of cornea tissue comprising the steps of (i) providing a laser source that is adapted to generate and transmit focused pulsed laser energy, the laser source including a delivery head that is adapted to direct the laser energy to a target structure of an eye, (ii) disposing the delivery head a spaced distance from the target eye structure, and (iii) transmitting the laser energy to the target eye structure, whereby the surface of the eye structure tissue is primarily, more preferably, solely ablated.

Diffuse lamellar keratitis or DLK is a recently recognised post-surgical condition involving an inflammation that occurs in laser corneal surgery patients. This condition is typically associated with the LASIK surgical procedure (Laser Assisted In Situ Keratomileusis). The cause is presently unknown. the present invention provides a sterilization apparatus, which may be a retrofitting of the existing sterilizer, which reduces the occurrence of DLK and also methods for maintaining the sterilizer to reduce the occurrence of DLK.

Devices, systems, surgical kits and methods for corneal surgery, preferably using femto-laser assisted, corneal tattooing. The corneal tattoos are formed with one or more viscous opaque substances such as pasty substances of different colors to match eye colors of different patients.

The present invention provides a novel pharmaceutical agent for recovering corneal sensitivity after corneal surgery and improving symptoms of dry eye. This pharmaceutical agent is useful for improving decreased corneal sensitivity and dry eye associated with corneal neurodegeneration such as post-cataract operation, post-LASIK operation, post-PRK operation, postkeratoplasty operation, neuroparalytic keratopathy, corneal ulcer, diabetic keratopathy and the like, since it contains a Rho protein inhibitor.

Methods and apparatus are configures to measure an eye without contacting the eye with a patient interface, and these measurements are used to determine alignment and placement of the incisions when the patient interface contacts the eye. The pre-contact locations of one or more structures of the eye can be used to determine corresponding post-contact locations of the one or more optical structures of the eye when the patient interface has contacted the eye, such that the laser incisions are placed at locations that promote normal vision of the eye. The incisions are positioned in relation to the pre-contact optical structures of the eye, such as an astigmatic treatment axis, nodal points of the eye, and visual axis of the eye.

A compound represented by formula (1), or a pharmaceutically acceptable salt thereof is effective as a therapeutic agent or a prophylactic agent for a corneal disease or sensory nerve damage due to corneal surgery, and as a regeneration accelerator for corneal sensory nerves:

wherein R¹ represents a hydrogen atom or a carboxyl group, R² represents a hydrogen atom or a hydroxy group, R³ represents a hydrogen atom or a carboxyl group, and R⁴ represents a hydrogen atom or a hydroxy group.

The present invention provides a new type of pharmaceutical agent that recovers corneal sensitivity after corneal surgery or improves the condition of dry eye. Application of a somatostatin receptor agonist is expected to provide an improvement effect on decreased corneal sensitivity after cataract surgery or LASIK surgery, decreased corneal sensitivity and dry eye associated with corneal neurodegeneration such as neuroparalytic keratopathy, corneal ulcer, diabetic keratopathy and the like.

A blade for corneal surgery for separating a corneal epithelium in a flap shape, includes: upper and lower blade surfaces; and an edge surface connecting the upper and lower blade surfaces, the edge surface having a height of 1 to 70 μm and a connecting portion with each of the upper and lower blade surfaces having a curved surface.

This invention provides a corneal surgery risk evaluation method and system thereof. Utilizing a mechanical numerical model to evaluate stress differences before corneal surgery and after, and further providing a suggested surgical path and risk after surgery. The evaluation method, comprising: measuring Intraocular pressure (IOP); inputting geometric parameters and material parameters of multi-layer of corneal; constructing a first corneal numerical model; constructing a second corneal numerical model with at least one cutting path character; evaluating whether the cutting path character should be re-constructed or not.

A time domain-optical coherence tomography (TD-OCT) technology is adopted to carry out high resolution imaging on a human cornea; the thickness of the human cornea can be accurately measured by usinga quick zoom lens; through the moving distance of a reference arm, the optical path difference between the front surface and the rear surface of a cornea can be calculated, thus the refractivity of the cornea can be calculated by ZEMAX optical simulation software; and the method is noncontact and is used to measure the thickness and refractivity of a cornea. The method can measure the thickness and refractivity of a cornea in a human body, the measurement is noncontact, high precision, and nondestructive; moreover, after a corneal surgery, the thickness and refractivity of corneas can be tracked, and at the same time, a preoperative detection device and method are provided for a refractive surgery.

A corneal surgery apparatus for correcting a refractive error by ablating corneal tissue with a laser beam, being capable of finding a correction pattern optimum for a patient to ensure precise correction, and a method of determining correction data. The apparatus includes units for inputting refractive power data on a trial contact lens, converting the refractive power data to obtain ablation data, controlling an ablation amount of the corneal tissue based on the ablation data, storing the refractive power data corresponding to each contact lens, and revising the refractive power data. The method includes processes for obtaining a correction value made with a contact lens based on of an ophthalmic examination, selecting a contact lens based on the value and converting the refractive power data on the selected contact lens into the ablation data for correcting the refractive error if the trial use of the contact lens results favorably.