The present invention relates to a fastening device for fixing an intraocular lens having protruding support elements in the eye of a patient.
The invention further relates to a kit of parts comprising an intraocular lens having protruding support elements and at least one fastening device which can be connected to one of the protruding support elements.
Cataracts are one of the most common diseases of the human eye in old age. By implanting an artificial lens instead of the cloudy natural lens, around 90% of patients can restore 50% to 100% of their visual performance. Cataract surgery is therefore the most common surgery on the human eye. In Germany alone, around 600,000 of this type of surgery are carried out every year.
In cataract surgery, the cloudy natural lens is removed and an artificial intraocular lens (IOL) with suitable refractive power is inserted. While in the past the entire natural lens was removed, it is now common practice to leave the posterior and lateral lens capsules in the eye.
In addition to the lens part providing the refractive power, the artificial intraocular lens usually has protruding support elements, so-called “haptics”, which are intended to be supported in the area of the ciliary sulcus in order to keep the IOL centered in the area of the lens capsule. Although this works well in most cases, in cases with capsular bag injuries or in cases with a weak suspension apparatus of the lens capsule it can happen that the IOL cannot be implanted in the intended place or does not remain in the lens capsule bag and slips and/or tilts, which is of course to be regarded as unacceptable.
In cases with capsular bag defects during cataract surgery, ophthalmic surgeons currently use two treatment options. With the method called “Iris fixation of IOL implant”, however, relatively large incisions have to be made in the cornea. The risks of this method are damage to the cornea and the iris and, in the long term, the formation of glaucoma. Impaired pupillary response is another disadvantage of this method. For this reason, the “sulcus-trans-scleral IOL suture fixation” method is increasingly being practiced in order to be able to reproduce the desired visual acuity in aphakic patients or patients whose eyes have insufficient capsule support. With this surgical technique, the sclera has to be partially unfolded and then sutured again in order to sew the haptics of IOLs to parts of the sclera. This technique is surgically demanding and carries a certain risk of introcular bleeding. In addition, this procedure can also result in tilting, decentering and/or slipping of the IOL into the vitreous space. A major disadvantage of this method is that IOLs with thick haptics cannot be implanted because of the unacceptably high decentration rate, although IOLs with thick haptics are increasingly preferred by ophthalmic surgeons because of the possibility of simpler injection techniques.
Yokrat Ton et al. published in 2007 an anchoring device for an intraocular lens that anchors in the ciliary sulcus. This device and the associated type of fixation were identified as effective in the animal model.
The present invention aims to create a fastening device for fixing a intraocular lens that comprises protruding support elements in the eye of a patient, which allows a better and more reliable fixing of an intraocular lens in the human eye and which in particular allows a tilted and/or slipped intraocular lens to be permanently repositioned, e.g. in a revision surgery, or to implant an artificial intraocular lens primarily safely against slipping and/or tilting.
To achieve this object, the fastening device according to the invention comprises at least one tip which is suitable for penetrating the human ciliary body and preferably also for penetrating the human sclera and which is or can be connected to a protruding support element.
Because a fastening device is connected to the haptics, which is provided with a tip for penetrating anatomical structures of the eye in the area of the lens or the lens capsule, the artificial intraocular lens cannot only be fixed by the haptics, which serve as pure support elements, which are elastically supported on the sulcus. Rather, the haptics and thus the intraocular lens can be pinned to anatomical structures of the eye using a type of needle, so that subsequent slipping or tilting of the intraocular lens can practically be ruled out. Other important advantages of this method are the possibility of using all types of open-loop haptics (regardless of the material and thickness of the haptics) and of course the better centering of the IOL, which is an important problem with the “Sulcus-trans-scleral IOL suture fixation” method.
In connection with the present invention, penetration means that the tip can penetrate from the inside through the ciliary body or the sclera. The tip does not have the strength to pierce said anatomical structures itself. Rather, it is provided that said structures are pierced or perforated with special needles or lances in order to grip the tip with a special tool from the outside and pull it out through the pierced opening. The fastening device according to the invention is preferably designed in one piece with the protruding support elements, i.e. the haptics, that is to say that the artificial intraocular lens is already produced with the fastening device according to the invention on the protruding support elements.
The fastening device according to the invention is primarily intended as a medical product for ophthalmological revision surgery, but can also be used in the primary care of cataract patients and can be attached to the haptics of intraocular lenses to supplement them before being used. For this purpose, the fastening device according to the invention has a connecting structure for connecting the fastening device to a protruding support element of the intraocular lens, as corresponds to a preferred embodiment of the present invention. The connecting structure is preferably designed as a hinge-like openable clamping region into which a protruding support element can be inserted and clamped. The tip is then passed through the ciliary sulcus or the sclera and appropriately anchored.
According to a preferred embodiment of the present invention, the connecting structure is made of a different material than the at least one tip. In this way, the two essential regions of the fastening device according to the invention—the tip and the connecting structure—can be produced from materials that are adapted in each case in order to best serve their respective purpose.
For better anchoring of the tip in the ciliary sulcus or in the sclera, the fastening device according to the invention can preferably be developed in such a way that the at least one tip has at least one barbed hook. In this way the tip is self-locking and allows the surgery to be performed quickly.
According to a preferred embodiment of the present invention, the fastening device has two tips which are connected to one another via a common cavity extending within in the two tips. With this particular and preferred embodiment of the present invention, the fastening device according to the invention can be sewn to the eye if both tips are passed through the mentioned anatomical structures and a thread is drawn through the common cavity in the two tips, which is then suitably knotted.
In order to be able to grasp and manipulate the fastening device according to the invention reliably and without damaging it during surgery, the fastening device has, adjacent to the connecting structure, at the end of the fastening device opposite the tip, a holding region for engagement by surgical tweezers, as in correspondence to a preferred embodiment of the present invention. The holding region is preferably made of a different material than the connecting structure and/or the tip and can therefore be designed with regard to the material according to the requirements of stability and toughness for multiple gripping during surgery.
The surgical tool according to the invention for manipulating the fastening device according to the invention comprises a shaft and a coupling for the tip so that the surgeon can insert the surgical tool into the eye through the perforation that was previously created in the sclera, grasp the tip of the fastening device intraocularly and pull it with the shaft out through the perforation.
The invention is explained in more detail below with reference to an exemplary embodiment shown in the drawing. In the drawings
In
In the side view of the fastening device 1 according to the invention according to
In the following figures, the same or equivalent parts are provided with the same reference numerals.
In
In
The individual steps of the surgical method made possible by the invention are shown in
In a first step (
Filing Document | Filing Date | Country | Kind |
---|---|---|---|
PCT/AT2018/000101 | 12/27/2018 | WO | 00 |