Deep vein thrombosis modeling device and method
A technology for deep vein thrombosis and modeling, which is applied in veterinary surgery, medical science, veterinary instruments, etc., can solve the problems of high failure rate of modeling experiments, high experience requirements, and increased mortality, so as to improve thrombus formation. rate, reduce the chance of infection, and avoid the effects of excessive blood loss
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no. 1 example
[0065] In this embodiment, the deep vein thrombosis modeling device includes a scraper assembly and a main head 30, the scraper assembly includes an implanted tube 10 and a scraper disposed at the front end of the implanted tube 10, the Inserting the tube piece 10 can push the scraping piece to the modeling site of the blood vessel, and the main head 30 is located outside the body. The main head 30 is provided with a driving piece, and the output end of the driving piece is connected to the outside of the body. The implanted tube 10 is connected in a transmission. When the implanted tube 10 drives the rotary scraper to be inserted into the animal, the driving member drives the rotary scraper in the blood vessel by driving the implanted tube 10 to rotate. Rotating so that the scraper causes mechanical damage to the inner wall of the blood vessel during the rotating process, so that the blood vessel forms a thrombus at the modeling site. Specifically, in order to drive the inser...
no. 2 example
[0081] In order to further improve the modeling efficiency and success rate, the deep vein thrombosis modeling device is also provided with a drug delivery member, and the drug delivery member can deliver the coagulation-promoting drug to the modeling site to further promote modeling The site of thrombosis, specifically, the drug delivery element includes a drug-loaded balloon and a drug coating at least partially covering the outer surface of the drug-loaded balloon, the drug coating comprising a carrier and a drug loaded on the carrier. For procoagulant drugs, the carrier can be selected from the prior art, preferably polyethylene glycol. When the balloon body 20 is placed in the modeling site, the procoagulant drug can be detached from the carrier and dispersed in the blood.
[0082] The difference between this embodiment and Embodiment 1 is that the drug-carrying function of the balloon body 20 can also be achieved in the following manner. At least one sealing membrane 70 ...
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