The current use of sutures to complete vascular anastomosis is time consuming, which can lead to exposing a patient to additional bacteria in the air during surgery. This can lead to an increased time for recovery. The current practice of suture focused end-to-end vascular anastomosis is imperfect and prone to leakage which requires additional blood, more doctor's time, more time in the operating room, and extends costs to patients and insurance companies. Expense driven partially by current practice leads to some patients not being able to afford or receive necessary life-improving or life-saving operations.
The current use of sutures to complete vascular anastomosis requires an average of 20 minutes per connection, which can lead to exposing a patient to bacteria in the air during surgery. A lengthy time during surgery weakens the patient's health, and creates a lengthy time for healing. The current practice of suture focused end-to-end vascular anastomosis is imperfect and prone to leakage which requires additional blood, more doctor's time, more time in the operating room, and extends costs to patients and insurance companies. Expense driven partially by current practice leads to some patients not being able to afford or receive necessary life-improving or life-saving operations. Problems related to the current practice can also cause complications including death.
The present invention takes on average under two minutes to complete sutureless end-to-end vascular anastomosis, saving an average of 18 minutes per connection during any surgery. Healing time is reduced significantly. Use of the sutureless end-to-end vascular anastomosis significantly reduces the likelihood of leakage. The cumulative benefit reduces patient time in the operating room, reduces medical staff time in operating room, opens up more time for additional surgeries or other uses of operating rooms generally, reduces costs to patients, and reduces costs to insurance companies. Considering a combination of time savings and cost savings, more patients will arguably be able to afford and receive necessary life-improving or life-saving operations.
Other current sutureless end-to-end anastomosis devices have more parts, are more complicated, and are made of materials that are not absorbable by the human body. The present invention consists of only three simple parts that are more easily and speedily assembled, made with materials that are absorbable by the human body, and does not use materials such as glue which can pose additional problems for a patient.
The present invention is made of material that can be absorbed by the human body and does not therefore need to be removed. This promotes faster and more effective healing. The preferred embodiment has three simple and easy to use parts, and takes on average less than two minutes to assemble.
The preferred embodiment of the present invention comprises three pieces when assembled. An exterior bell 10, and interior bell 12, and a locking ring 14. A key 16 is used to slide the vein over barbed ends 18 and 20 of exterior bell 10 and interior bell 12.
Referring now to the Figures, a key 16 is shown. Key 16 has an expander 22 which is inserted into the open end of a severed vein or artery. As expander 22 is pressed further into the end of a central vein, the vein diameter is increased and further pressing of key 16 into the vein results in the vein being expanded and bent back as the vein encounters curved wall 24. By placing exterior bell 10 over an end of a severed vein or artery and extending the vein through the bell so that a portion of the vein extends beyond the end of the bell, key 16 may be used by the other hand of the surgeon to expand the vein and bend it back over itself so that expander 22 may be inserted into the end of a barbed portion 26 of the end of exterior bell 10. The vein can then be slid off of the expander 22 and on to the barbs so that the vein is retained on exterior bell 10. Locking ring 14 will have already been placed on interior bell 12 before the vein is attached. In some embodiments, a split locking ring may be used that does not require prior placement. Key 16 is now used to expand the other end of the severed vein in the same manner and is used to locate the portion of the vein extending out of the end of interior bell 12 on to a barbed portion 28 of interior bell 12. Each end of the vein is now attached to a bell. Exterior bell 10 has a larger diameter and is sized so that the end of interior bell 12 will slid into the end of exterior bell 10. When the two bells are interconnected, locking ring 14 is pushed and snapped over ribs 30 on the outside of exterior bell 10 until locking ring 14 encounters a shoulder 32 on interior bell 12. The locking ring 14 is tightened only enough to ensure that there will be no leakage. Teeth 34 on locking ring 14 engage ribs 30 on the outside of exterior bell 10 to lock the two bells together in positive engagement thereby completing the sutureless end-to-end vascular anastomosis.
This application claims priority to U.S. Provisional Patent Application 61/927,873 filed Jan. 15, 2014.