Endovascular creation of an in vivo bifurcation aneurysm model in rabbits

被引:101
作者
Cloft, HJ
Altes, TA
Marx, WF
Raible, RJ
Hudson, SB
Helm, GA
Mandell, JW
Jensen, ME
Dion, JE
Kallmes, DF
机构
[1] Univ Virginia, Hlth Sci Ctr, Dept Radiol, Charlottesville, VA 22903 USA
[2] Univ Virginia, Hlth Sci Ctr, Dept Neurosurg, Charlottesville, VA 22903 USA
[3] Univ Virginia, Hlth Sci Ctr, Dept Pathol, Charlottesville, VA 22903 USA
关键词
aneurysm; carotid; cerebral; therapy; animals; carotid arteries; therapeutic blockade;
D O I
10.1148/radiology.213.1.r99oc15223
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
PURPOSE: To develop a rabbit model of an intracranial bifurcation aneurysm to test new endovascular therapies. MATERIALS AND METHODS: An experimental aneurysm model was created in rabbits by means of endovascular balloon occlusion of the left common carotid artery, which created an aneurysm at the bifurcation formed by the aortic arch and the brachiocephalic trunk. A total of 18 aneurysms were created. In eight rabbits, the aneurysms were incubated with intraluminal elastase to induce degeneration of the elastic laminae. The animals were followed Up with angiography for as long as 3 months. The animals were sacrificed at various times, and histologic evaluation of the aneurysm was performed. RESULTS: Ten aneurysms created without elastase infusion were ail very small or completely closed at 1-3 months. Six aneurysms created with elastase infusion had long-term patency (two were patent at 1 month and four, at 3 months). The elastase aneurysms had a mean width of 3 mm (range, 2-3.5 mm) and a mean length of 5 mm (range, 3-7 mm). Histologic evaluation revealed destruction of the normal elastin layers, which allowed the artery to become aneurysmal. CONCLUSION: This aneurysm model re-created the hemodynamic forces and size of human cerebral bifurcation aneurysms and maintained the integrity of the endothelium. The creation of the aneurysms was rapid, reliable, and reproducible.
引用
收藏
页码:223 / 228
页数:6
相关论文
共 22 条
  • [1] Abruzzo T, 1998, AM J NEURORADIOL, V19, P1309
  • [2] ANGELLJAMES JE, 1974, ACTA ANAT, V87, P283
  • [3] ELASTASE-INDUCED EXPERIMENTAL ANEURYSMS IN RATS
    ANIDJAR, S
    SALZMANN, JL
    GENTRIC, D
    LAGNEAU, P
    CAMILLERI, JP
    MICHEL, JB
    [J]. CIRCULATION, 1990, 82 (03) : 973 - 981
  • [4] THE CANINE TAIL ARTERY AS A MODEL FOR CEREBRAL ANEURYSM STUDIES
    BOYCE, TT
    ROACH, MR
    [J]. CANADIAN JOURNAL OF PHYSIOLOGY AND PHARMACOLOGY, 1989, 67 (01) : 34 - 39
  • [5] Cawley CM, 1996, AM J NEURORADIOL, V17, P1761
  • [6] CHAVIS TD, 1994, ANN M AM SOC NEUR NA
  • [7] TREATMENT OF EXPERIMENTAL ANEURYSMS USING COLLAGEN-COATED MICROCOILS
    DAWSON, RC
    KRISHT, AF
    BARROW, DL
    JOSEPH, GJ
    SHENGELAIA, GG
    BONNER, G
    [J]. NEUROSURGERY, 1995, 36 (01) : 133 - 139
  • [8] Dawson RC, 1996, AM J NEURORADIOL, V17, P853
  • [9] GRAVES VB, 1990, AM J NEURORADIOL, V11, P249
  • [10] ELECTROTHROMBOSIS OF SACCULAR ANEURYSMS VIA ENDOVASCULAR APPROACH .1. ELECTROCHEMICAL BASIS, TECHNIQUE, AND EXPERIMENTAL RESULTS
    GUGLIELMI, G
    VINUELA, F
    SEPETKA, I
    MACELLARI, V
    [J]. JOURNAL OF NEUROSURGERY, 1991, 75 (01) : 1 - 7