Suprachoroidal space pressurizing balloon in high myopia macular region and implanting device thereof
Technical Field
The invention relates to the technical field of ophthalmology, in particular to a suprachoroidal space pressurizing balloon in a high myopia macular region and an implanting device thereof.
Background
High myopia macular degeneration such as macular hole, macular retinal detachment and the like is one of the main causes of blindness at present, and the current treatment methods include vitrectomy, posterior scleral compression (reinforcement) surgery and the like. Vitreous surgery is a procedure in which vitreous traction is removed and the inner limiting membrane is removed to promote the amelioration of macular degeneration, and posterior scleral compression (reinforcement) is a procedure in which compression is performed from behind the sclera to promote the amelioration of macular degeneration. The vitreous resection operation cannot prevent the growth of the axis of the eye, the postoperative lesion may recur, and some lesions cannot be solved by the vitreous resection operation alone. Posterior scleral compression (reinforcement) surgery has problems of lack of compression materials, unstable effect, complications, and the like. The suprachoroidal hyaluronic acid injection is a method for rhegmatogenous retinal detachment, in which hyaluronic acid is injected into the suprachoroidal space at the site of the peripheral fissure, forming a compression ridge, thus acting as a therapeutic agent, and is currently used in a relatively small number. Aiming at the defects of a vitrectomy operation and a posterior sclera pressurization (reinforcement) operation, the invention designs a suprachoroidal space pressurization balloon in a high-myopia macular region and an implantation device thereof, and the purposes of shortening the axis of the eye and treating macular degeneration are achieved by jacking from the suprachoroidal space.
Disclosure of Invention
Aiming at the defects in the prior art, the invention aims to provide a suprachoroidal space pressurizing balloon in a high myopia macular region and an implanting device thereof.
In order to realize the purpose, the invention is realized by the following technical scheme: high myopia macular district choroid epicoele pressurization sacculus and implantation device thereof, including pressurization sacculus and implantation ware, the pressurization sacculus is located inside the front end of implantation ware, the pressurization sacculus include sacculus body, soft silicone tube and screw thread injection mouth, the one end of sacculus body is connected through soft silicone tube and screw thread injection mouth and is connected, screw thread injection mouth and syringe cooperation.
Preferably, the balloon body is a foldable balloon, the diameter of the balloon is about 1mm-10mm, the cross section of the balloon is oval or oblate, and the thickness of the balloon is about 0.2mm-5mm.
Preferably, the soft silica gel tube has a length of about 20-50mm and an inner diameter of 0.1-0.6mm.
Preferably, the implanter comprises a balloon mounting cavity with a cylindrical or flat-cylindrical top end, a positioning light source, a liquid injection balloon, an injection rod of a body part, an optical fiber and an injection port at the tail end, wherein a pressurizing balloon is arranged in the balloon mounting cavity. The injection bag is wound at the front end of the implanter and is provided with 1-10 side holes, a cavity of the injection bag is communicated with a tail end injection port, and the injection port is connected with an injector injected with normal saline or ringer's solution or viscoelastic agent. When the device enters the suprachoroidal space from the sclera, the injection liquid can flow out from the tail end injection port through the injection sac to cause the local choroidal separation, so that the implantation of the device is facilitated. The positioning light source is positioned at the top end of the implanter and connected with the optical fiber, and the top end of the implanter can be positioned in the operation. The push-injection rod is arranged in contact with the pressurizing saccule, the pressurizing saccule is pushed out by the push-injection rod after the push-injection rod is implanted in place, and the push-out mode can be rotary or direct push-injection.
Preferably, a filling liquid such as silicone oil, physiological saline, ringer's solution, heavy water, viscoelastic agent, etc. is injected into the end of the soft silicone tube.
The invention has the beneficial effects that: the foldable balloon is reasonable in structural design, the foldable balloon is adopted, implantation of the foldable balloon is facilitated, positioning is accurate, the treatment effect is exact, the adopted implantation device is convenient to open and withdraw, the foldable balloon is more convenient and reliable to use, pain of a patient is reduced, the working efficiency of a doctor is improved, and the foldable balloon is high in practicability.
Drawings
The invention is described in detail below with reference to the drawings and the detailed description;
FIG. 1 is a schematic structural view of the present invention;
FIG. 2 is a schematic view of the configuration of the pressurizing balloon of the present invention;
reference numerals: A. pressurizing the balloon; b, implanting into an apparatus; 1. a balloon body; 2. a soft silicone tube; 3. a threaded injection port; 5. positioning a light source; 6. an auxiliary injection port; 7. injecting a liquid bag; 8. a push injection rod; 9. an optical fiber.
Detailed Description
In order to make the technical means, the creation characteristics, the achievement purposes and the effects of the invention easy to understand, the invention is further explained by combining the specific embodiments.
Referring to fig. 1-2, the following technical solutions are adopted in the present embodiment: the suprachoroidal space pressurizing balloon in the high myopia macular region and the implanting device thereof comprise a pressurizing balloon A and an implanter B, wherein the pressurizing balloon A is positioned inside the front end of the implanter B, the pressurizing balloon A comprises a balloon body 1, a soft silicone tube 2 and a thread injection port 3, and one end of the balloon body 1 is connected with the thread injection port 3 through the soft silicone tube 2; the threaded injection port 3 is matched with an injector.
It is worth noting that the balloon body 1 is a foldable balloon, the balloon body 1 is circular or quasi-circular after being unfolded, the diameter is about 1mm-10mm, the cross section is oval or oblate, and the thickness is about 0.1mm-5mm.
It is noted that the length of the soft silicone tube 2 is about 20-50mm, and the inner diameter is 0.1-0.6mm.
It is worth noting that the implanter B comprises a cylindrical sacculus arranging cavity at the top end, a positioning light source 5, an injection sac 7, a push injection rod 8 of a body part, an optical fiber 9 and an injection port 6 at the tail end, wherein a pressurizing sacculus A is arranged in the sacculus arranging cavity, the injection port 6 is arranged at the tail end of the implanter B, and the injection port 6 is connected with an injector filled with physiological saline or ringer's solution or viscoelastic agent; the injection bag 7 is wrapped at the front end of the implanter B and is provided with 1-10 side holes, the injection bag 7 is provided with a cavity communicated with the tail end injection port 6, the positioning light source 5 is connected with the optical fiber 9, and the injection rod 8 is arranged in contact with the pressurizing balloon A. The liquid injection bag is annularly sleeved at the top end of the implanter, and a pipe is led from the back to inject liquid through the injection port 6, so that the main purpose is to separate the suprachoroidal space and the implanter can conveniently enter the eye. After the point light source is positioned under the yellow spots, the folding sacculus is pushed out, the implanter is withdrawn, liquid is injected into the sacculus, the sacculus is opened, and the fixation is good.
In addition, the end of the soft silicone tube 2 is injected with filling liquid, such as silicone oil, normal saline, ringer's solution, heavy water, viscoelastic agent, and the like.
The balloon body of the specific embodiment is unfolded to be round, the diameter is about 1mm-10mm, the cross section is oval or oblate, the thickness is about 0.1mm-5mm, and the balloon can be folded. One end of the saccule is connected with a soft silicone tube, the length is about 20-50mm, and the inner diameter is 0.1-0.6mm. The end of the silicone tube is connected with an injection screw. The material of the implant can be metal, hard polymer material such as PMMA, etc. The material of the pressurizing saccule can be silica gel or other high polymer materials.
When the foldable balloon implanting device is used, the implanting device is used for assisting in implantation, the front end of the implanting device is a balloon mounting cavity and can fix the foldable balloon in the balloon mounting cavity, and the implanting device is hollow. The normal saline or the ringer's solution flows out from the side hole (1-10) of the front end injection sac to cause the local choroid to be separated, and the implanter and the sac are guided to submerge to the suprachoroidal space of the macular area. The positioning light source is used to identify the location reached by the balloon.
After implantation, the saccule is pushed out of the implanter and flattened to the suprachoroidal space in the macular region, the implanter is taken out, filling liquid such as silicone oil, normal saline, ringer's solution, heavy water, viscoelastic and the like is injected from the tail end of the silica gel hose to a proper height, the silica gel hose is tied and sutured on the sclera wall, the rest part is cut off, and finally, the sclera and conjunctiva are sutured.
The foregoing shows and describes the general principles and broad features of the present invention and advantages thereof. It will be understood by those skilled in the art that the present invention is not limited to the embodiments described above, which are described in the specification and illustrated only to illustrate the principle of the present invention, but that various changes and modifications may be made therein without departing from the spirit and scope of the present invention, which fall within the scope of the invention as claimed. The scope of the invention is defined by the appended claims and equivalents thereof.