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In-Stent Restenosis: A Case Study

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A 78 year old female with hypertension appear with stable angina pectoris. An angiogram of the left anterior descending coronary artery revealed a lesion near the bifurcation vessel. The lesion was bifurcated with a ballon catheter and an endeavor drug eluting stent was deployed in the blood vessel. The patient left without any complications on a medical therapy. Ten months later, the angiogram of the patient revealed a Grade IV Stent Fracture and a substantial in-stent restenosis (Appendix 1). Problem Description: We believe that the endeavor stent failed and led to a substantial in-stent restenosis because the 316L stainless steel material used in the stent, wasn’t strong enough to bear the radial load in the struts. Additionally, we believe that the standard PC + zatrolimus drug on the endeavor …show more content…

Firstly, the main function of the implanted stent is to prevent arteries from clogging back up and allowing blood to flow through. Secondly, we believe that our implant material should be fatigue resistant because it experience pulsatile flow due to the presence of a pulsatile blood pressure. The implant should be stronger in radial than shear because the implant will have to withstand significant amount of force from the fatty deposits of the vessels. Additionally, the implant should have minimum reactivity with blood constituents because we don’t want to induce unnecessary thrombosis or any sort of inflammation. Thirdly, we believe that class 1 biomaterial are ideal for our implant because our material requires failure loads of 10-50 times the body weights, meaning it has to be extremely strong. Furthermore, we believe that our material should have extremely high resistance to compressive deformation as well as little reactivity with the environment, in order to accomplish the necessary

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