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Molecular MR imaging of human thrombi in a swine model of pulmonary embolism using a fibrin-specific contrast agent
被引:41
作者:
Spuentrup, Elmar
Katoh, Marcus
Buecker, Arno
Fausten, Bernd
Wiethoff, Andrea J.
Wildberger, Joachim E.
Haage, Patrick
Parsons, Edward C., Jr.
Botnar, Rene M.
Graham, Philip B.
Vettelsehoss, Manfred
Guenther, Rolf W.
机构:
[1] Rhein Westfal TH Aachen, Dept Diagnost Radiol, Aachen, Germany
[2] Rhein Westfal TH Aachen, Dept Thorac & Cardiovasc Surg, Aachen, Germany
[3] EPIX Pharmaceut, Cambridge, MA USA
[4] Univ Hosp Witten Herdecke, Helios Klinikum Wuppertal, Dept Diagnost & Intervent Radiol, Wuppertal, Germany
[5] Harvard Univ, Beth Israel Deaconess Med Ctr, Sch Med, Dept Med,Cardiovasc Div, Boston, MA 02215 USA
[6] Tech Univ Munich, Dept Nucl Med, D-8000 Munich, Germany
关键词:
magnetic resonance imaging;
molecular imaging;
thrombosis;
embolism;
pulmonary vessel;
contrast;
D O I:
10.1097/RLI.0b013e31804fa154
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:
Objective: Molecular targeted MR imaging of human clots material in a model of pulmonary embolism using a fibrin-specific magnetic resonance imaging contrast agent (EP-2104R, EPIX Pharmaceuticals, Cambridge, MA). Material and Methods: Fresh ex vivo engineered thrombi (human blood) and human clots removed from patients were delivered in 11 swine. Molecular MR imaging with a 3D gradient-echo [3D fast field echo (3DFFE)] sequence and a navigator-gated and cardiac-triggered 3D inversion-recovery black-blood gradient-echo sequence (IR) was performed before thrombus delivery, after thrombus delivery but before contrast media application, and 2 hours after i.v. administration of 4 mu mol/kg EP-2104R. MR images were analyzed by 2 investigators and contrast-to-noise ratio (CNR) was assessed. Thrombi were removed for assessment of gadolinium (Gd) concentration. Results: Only after contrast media application were pulmonary emboli [freshly engineered thrombi (n = 23) and human clot material removed from patients (n = 25)] visualized as white foci on MR images. CNR was 13 +/- 3 (ex vivo engineered clot) and 22 +/- 9 (patient clot material) for the fast field echo (FFE)-sequence and 29 +/- 9 (ex vivo engineered clot) and 43 +/- 18 (patient clot material) for the IR-sequence, respectively. A high Gd concentration in the clots was found (82 +/- 43 mu M for the freshly engineered and 247 +/- 44 mu M for the clots removed from patients, respectively). Conclusions: EP-2104R allows for molecular MR imaging of human clot material in the pulmonary vessels of a swine model.
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页码:586 / 595
页数:10
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