Detection of renal artery stenosis using 30 phase contrast MR angiography and dynamic perfusion imaging.

Citation
S. Miller et al., Detection of renal artery stenosis using 30 phase contrast MR angiography and dynamic perfusion imaging., ROFO-F RONT, 170(2), 1999, pp. 163-167
Citations number
29
Categorie Soggetti
Radiology ,Nuclear Medicine & Imaging
Journal title
ROFO-FORTSCHRITTE AUF DEM GEBIET DER RONTGENSTRAHLEN UND DER BILDGEBENDEN VERFAHREN
ISSN journal
09366652 → ACNP
Volume
170
Issue
2
Year of publication
1999
Pages
163 - 167
Database
ISI
SICI code
0936-6652(199902)170:2<163:DORASU>2.0.ZU;2-M
Abstract
Purpose: To assess renal artery stenosis (RAS) by 3D phase contrast (PC) MR angiography and dynamic perfusion imaging of the kidneys. Methods: On a st andard 1.0 T MR imaging system (Magnetom Expert, Siemens), 32 patients with angiographically proven unilateral RAS were examined using a 3D PC sequenc e (TR 40 ms/TE 9 ms/venc 30 cm/s). An ECG-gated Turbo-FLASH 2D sequence (TR 4.5 ms/TE 2.2 ms/TIeff. 400 ms) was applied to study the first pass of a p aramagnetic contrast agent (0.1 mmol Gd-DTPA/kg) through the kidneys. Signa l intensity (SI) over time curves of the renal cortex were obtained and eva luated considering temporal relation and percentage of maximum SI compared to the aorta and normal kidneys. Analysis of the MRA was performed by two i ndependent blinded readers. The gold-standard DSA was interpreted by consen sus reading of two experienced radiologists. Results: RAS was detected by 3 0 PC MRA with a sensitivity of 93% and specificity of 81% (ppv 82%, npv 93% , accuracy 87%, kappa = 0.61). Maximum SI in RAS was significantly decrease d (p < 0.001-0.0001). A temporally delayed enhancement of 1.5 +/- 1.3 s was found for RAS >75% (p < 0.002) but not for RAS < 75% (p > 0.1). Conclusion s: 30 PC MRA is capable of detecting RAS in a high percentage of patients. Dynamic perfusion imaging of the kidneys, applied additionally, can confirm the diagnosis and give valuable information about the hemodynamic relevanc e of RAS in suspected unilateral disease.