1.Is Thalidomide Safe and Effective for the Inhibition of Neointima Hyperplasia?.
Korean Circulation Journal 2004;34(4):343-345
No abstract available.
Hyperplasia*
;
Neointima*
;
Thalidomide*
2.Is Thalidomide Safe and Effective for the Inhibition of Neointima Hyperplasia?.
Korean Circulation Journal 2004;34(4):343-345
No abstract available.
Hyperplasia*
;
Neointima*
;
Thalidomide*
3.Experimental Study of the Histologic Findings of the Neoendothelialization according to Length of Polytetrafluoroethylene in Rabbit.
Kwang Suk LEE ; Ki Hoon KANG ; Kyu Ho KYON
Journal of Korean Orthopaedic Research Society 1998;1(2):174-187
The purpose of this study was to investigate the patency rates and the histologic findings of neoendothelialization according to the length of implanted polytetrafluoroethylene (PTFE) with an internal diameter of 3mm. Under the operating microscope, grafts of 8 and 24mm in length were implanted in the right carotid arteries of thirty rabbits by interrupted end-to-end microanastomosis. They were divided into two groups according to the length of implanted PTFE. Each group had fifteen rabbits. All implanted grafts were 25micro meter in fibril length and 0.39mm in wall thickness. Three grafts per group were harvested at 1, 2, 4, 8, and 12 weeks after implantation and all grafts were observed for patency rates and the histologic findings with a light microscope and scanning electron microscope. In conclusion, there was no difference in patency rates according to the length of implanted PTFE. However, the formation of neointima and subintimal tissue was delayed and incomplete in the longer implanted PTFE group.
Carotid Arteries
;
Neointima
;
Polytetrafluoroethylene*
;
Rabbits
;
Transplants
4.The Histologic Study of the Neoendothelialization of Polytetrafluoroethylene as an Arterial Substitute in Rabbit.
Kwang Suk LEE ; Ki Hoon KANG ; Kyu Ho KYON
The Journal of the Korean Orthopaedic Association 1998;33(7):1909-1920
The purpose of this study was to investigate the patency rates and the histologic findings of neoen- dothelialization according to the length of implanted polytetrafluoroethylene (PTFE) with an internal diameter of 3 mm. Under the operating microscope, grafts of 8 and 24 mm in length were implanted in the right carotid arteries of thirty rabbits by interrupted end-to-end microanastomosis. They were divided into two groups according to the length of implanted PTFE. Each group compised fifteen rabbits. All implanted grafts were 25 pm in fibril length and 0.39 mm in wall thickness. Three grafts per group were harvested at 1, 2, 4, 8, and 12 weeks after implantation respectively and all grafts were observed for patency rates and the histologic findings with light microscope and scanning electron microscope. In conclusion, there was no difference in patency rates according to the length of implanted PTFE and histologically the formation of neointima and subintimal tissue was delayed and incomplete in longer implanted PTFE.
Carotid Arteries
;
Neointima
;
Polytetrafluoroethylene*
;
Rabbits
;
Transplants
5.A Case of Neointimal Calcification in a Drug-Eluting Stent.
Young June YANG ; Jaemin SHIM ; Jung Sun KIM ; Young Guk KO ; Donghoon CHOI ; Yangsoo JANG ; Myeong Ki HONG
Korean Journal of Medicine 2011;81(1):98-101
Neointimal hyperplasia is the main mechanism of stent restenosis. Therefore, drug-eluting stents have replaced bare metal stents because there is less neointima and scar formation. Recently, some cases of stent restenosis after using a bare metal stent were found to involve calcification, not neointimal hyperplasia, and regarded as de novo atherosclerosis. We report unusual circular calcification inside a drug-eluting stent, which we called neointimal calcification.
Atherosclerosis
;
Cicatrix
;
Drug-Eluting Stents
;
Hyperplasia
;
Neointima
;
Stents
6.A Case of Neointimal Calcification in a Drug-Eluting Stent.
Young June YANG ; Jaemin SHIM ; Jung Sun KIM ; Young Guk KO ; Donghoon CHOI ; Yangsoo JANG ; Myeong Ki HONG
Korean Journal of Medicine 2011;81(1):98-101
Neointimal hyperplasia is the main mechanism of stent restenosis. Therefore, drug-eluting stents have replaced bare metal stents because there is less neointima and scar formation. Recently, some cases of stent restenosis after using a bare metal stent were found to involve calcification, not neointimal hyperplasia, and regarded as de novo atherosclerosis. We report unusual circular calcification inside a drug-eluting stent, which we called neointimal calcification.
Atherosclerosis
;
Cicatrix
;
Drug-Eluting Stents
;
Hyperplasia
;
Neointima
;
Stents
7.The Effects of Local Radiation using Ho-166 Balloon on Porcine Coronary Restenosis.
Korean Circulation Journal 2000;30(9):1139-1148
BACKGROUND: Restenosis remains one of major clinical problems in the coronary intervention. The effects of local radiation using radioactive balloon loaded with Ho-166 on coronary restenosis in the porcine model were observed. METHODS: Overdilation injury was performed in porcine coronary arteries using control balloon [Group I, n=, left anterior descending artery (LAD)=, left circumflex artery (LCX)=, right coronary artery (RCA)=] and Ho-166 loaded polyurethane-coating balloon [Group II; n=0, 21.98.1 mCi (20 Gy at 0.5 mm in depth), LAD=, LCX=, RCA=] at 5 atm for 3 min. Follow-up quantitative coronary angiogram (QCA) and histopathologic findings were compared at 4 weeks after balloon injury between two groups. RESULTS: Acute or late thrombotic arterial occlusion was not observed in both groups. Diameter stenosis measured by QCA was not different between two groups (Group I: 11.61.6%, II: 7.68.4%, P=.44). On histopathologic study, injury score, external and internal elastic lamina area, and media area were not different between two groups. Neointimal area and histopathologic area stenosis were significantly higher in Group I (0.320.86mm2, 20.677.01%) than those of Group II (0.150.26mm2, 12.032.44%). By immunocytochemistry, proliferating cell nuclear antigen indices in neointima and media were 8.244.44%, 7.972.46% in Group I, and 7.172.25%, 5.471.44% in Group II, which were not different between two groups(P=.587, 0.089). CONCLUSION: Local radiation using Ho-166 balloon is effective in reducing neointimal proliferation in a porcine model.
Arteries
;
Constriction, Pathologic
;
Coronary Restenosis*
;
Coronary Vessels
;
Follow-Up Studies
;
Immunohistochemistry
;
Neointima
;
Proliferating Cell Nuclear Antigen
8.An Experimental Study on the Influence of New Spiral Stent(Hanaro) on the Vascular Structures.
Myung Kwan LIM ; Jae Hyung PARK ; Jin Wook CHUNG ; Yoong Ki JEONG ; Myeong Cherl KOOK ; Jung Wook SEO
Journal of the Korean Radiological Society 1996;34(6):745-756
PURPOSE: The purpose of this study was to evaluate basic experimental data for the clinical application of a self-expandable stainless steel intravascular Hanaro spiral stent. MATERIALS AND METHODS: For evaluation of thephysical properties of the Hanaro stent, hoop strength, radioopacity, longitudinal flexibility, and foreshortening were measured. Twelve intravascular Hanaro spiral stents were placed in the infrarenal abdominal aorta (n=6) and comon iliac artery (n=6) in six mongrel dogs. Angiography and light microscopic examination were performed after one, two and eight months of placement of the stents. RESULTS: The stent had good radioopacity and was deployed with minimal foreshortening. Hoop strength of a 6mm-interval bend was found to be superior to that of 8mm- and 10mm-bend stent. On angiography the patency rate and thrombosis rate were 100% and 0% in the abdominal aorta and 50% and 50% in the common iliac artery, respectively. Minimal corrosion was seen in all stents, and they appearedto be biocompatible. The stent wires were covered with well-developed neointima which after one month had mostly fibroblast and collagen tissue; the thickness of the neointima increased gradually during a period of eightmonths. At the end of that period, collagen fibres in the neointima were denser and showed a more paralled configuration than at one month. CONCLUSION: The Hanaro stent has good physical properties and also has a high patency rate, and good biocompatibilities. The stent may therefore be reliably and safely deployed in the humanvascular system.
Angiography
;
Animals
;
Aorta, Abdominal
;
Atherosclerosis
;
Collagen
;
Corrosion
;
Dogs
;
Iliac Artery
;
Neointima
;
Pliability
;
Stainless Steel
;
Stents
;
Thrombosis
9.Effect of Stents Coated with Artemisinin or Dihydroartemisinin in a Porcine Coronary Restenosis Model.
Suyoung JANG ; Myung Ho JEONG ; Kyung Seob LIM ; In Ho BAE ; Jun Kyu PARK ; Dae Sung PARK ; Jae Won SHIM ; Jung Ha KIM ; Hyun Kuk KIM ; Doo Sun SIM ; Young Joon HONG ; Youngkeun AHN ; Jung Chaee KANG
Korean Circulation Journal 2017;47(1):115-122
BACKGROUND AND OBJECTIVES: Artemisinin and dihydroartemisinin are drugs used to treat malaria. These drugs suppress inflammatory reactions. The aim of this study was to examine the anti-intima hyperplasia effect of a novel drug-eluting stent with artemisinin or dihydroartemisinin in a porcine coronary restenosis model. MATERIALS AND METHODS: Pigs were randomized into four groups; in the first, the coronary arteries (20 pigs, a total of 40 coronary arteries, with 10 coronary arteries in each group) was implanted with bare metal stents (BMS, n=10); the second group was given polymer-coated stents (PCS, n=10); the third group was treated with artemisinin-eluting stents (AES, n=10); and the fourth group was given dihydroartemisinin-eluting stents (DAES, n=10). Histopathologic analysis was performed 28 days after stenting. RESULTS: The injury and fibrin scores among the four groups were not significantly different. However, the internal elastic lamina, lumen area, and neointima area were significantly different. Moreover, the percent area of stenosis (46.2±18.66% in BMS vs. 89.4±10.92% in PCS vs. 83.3±17.07% in AES vs. 36.7±11.20% in DAES, p<0.0001) and inflammation score (1.0 [range: 1.0-1.0] vs. 3.0 [range: 2.25-3.0] vs. 3.0 [range: 1.0-3.0] vs. 2.0 [range: 1.75-3.0] in BMS, PCS, AES, and DAES, respectively; p<0.001) were markedly decreased in the DAES group compared to the PCS group. CONCLUSION: DES, which uses a natural substance, dihydroartemisinin, showed a neointima and inflammatory suppressive effect in a porcine coronary restenosis model.
Constriction, Pathologic
;
Coronary Restenosis*
;
Coronary Vessels
;
Drug-Eluting Stents
;
Fibrin
;
Hyperplasia
;
Inflammation
;
Malaria
;
Neointima
;
Stents*
;
Swine
10.Influence of Dexamethasone: Coated Nitinol Stent on Neointimal Formation in the Canine Great Vessel Model.
Hyun Ki YOON ; Kil Sun PARK ; Sung Gwon KANG ; Sang soo PARK ; Tae Hyung KIM ; Kyu Bo SUNG ; Ho Young SONG
Journal of the Korean Radiological Society 2001;44(4):433-440
PURPOSE: To evaluate the effect of dexamethasone(DM) and polyurethane(PU)-coated nitinol stent on neointimal formation in the canine great vessels. MATERIALS AND METHODS: Thirty-six nitinol wire stents were implanted in the abdominal aorta and inferior vena cava(IVC) of six dogs. In each animal, six different types of stent (NC, non-coated; PU, polyurethane coated; DM, DM and polyurethane coated) were serially positioned in permutationally possible order in the aorta below the renal arteries and in the IVC below the renal veins. For DM stent an in-vitro drug release test was performed to determine the stability of DM release. The thickness of the intima and media of the aorta and of the intima of the IVC were measured three (n=3) or six months (n=3) after stent placement at and between the wires. RESULTS: In the in-vitro study, 25% of DM was released during the first week, and the subsequent release rate was 3 microgram/day for 6 months. The intima-to-media ratio of DM-stented aorta was less than in aortas where PU or NC stents were used (p<0.05). The neointima thickness of DM stent in the IVC was less than that of PU stent (p<0.05). These differences were less prominent between the wires than at them, and there was no significant difference between the three-and six-month groups (p>0.05). CONCLUSION: In this canine great vessel model, newly designed DM-coated nitinol stent decreased neointimal formation.
Animals
;
Aorta
;
Aorta, Abdominal
;
Dexamethasone*
;
Dogs
;
Neointima
;
Polyurethanes
;
Renal Artery
;
Renal Veins
;
Stents*