TY - JOUR
T1 - In-vitro validation, with histology, of intravascular ultrasound in renal arteries
AU - Leertouwer, Trude C.
AU - Gussenhoven, Elma J.
AU - Van Jaarsveld, Brigit C.
AU - Van Overhagen, Hans
AU - Bom, Nicolaas
AU - Man in'T Veld, Arie J.M.I.
PY - 1999/1/1
Y1 - 1999/1/1
N2 - Objective. To investigate the feasibility of using intravascular ultrasound to characterize normal and diseased renal arteries. Materials and methods. Forty-four renal artery specimens from 21 humans, removed at autopsy, were studied with intravascular ultrasound in vitro. From each vascular specimen, two to four sets of corresponding intravascular ultrasound images and histologic sections were subjected to qualitative analysis. The renal arterial wall was considered normal by intravascular ultrasound when the wall thickness (intima and media) was 0.5 mm or less. On intravascular ultrasound imaging, a distinction was made between bright lesions with or without peripheral shadowing (i.e. calcification). Histological sections were examined and fibromuscular lesions were scored with or without calcifications. Quantitative analysis of a multitude of intravascular ultrasound cross-sections (interval 5 mm) included assessment of the lumen area, vessel area, plaque area and percentage area obstructed. The target site (smallest lumen area) was compared with a reference site (largest lumen area before the first major side branch). Results. Of the 130 corresponding intravascular ultrasound images and histologic sections analysed, 55 were normal and 75 presented a bright lesion on ultrasound; in 31 lesions, peripheral shadowing was involved. The sensitivity of the intravascular ultrasound in detecting calcifications was 87%, and the specificity was 89%. Lumen area reduction at the target site was associated with vessel and plaque area enlargement in eight specimens, with plaque area enlargement in 12 specimens and with a vessel area reduction in 21 specimens.
AB - Objective. To investigate the feasibility of using intravascular ultrasound to characterize normal and diseased renal arteries. Materials and methods. Forty-four renal artery specimens from 21 humans, removed at autopsy, were studied with intravascular ultrasound in vitro. From each vascular specimen, two to four sets of corresponding intravascular ultrasound images and histologic sections were subjected to qualitative analysis. The renal arterial wall was considered normal by intravascular ultrasound when the wall thickness (intima and media) was 0.5 mm or less. On intravascular ultrasound imaging, a distinction was made between bright lesions with or without peripheral shadowing (i.e. calcification). Histological sections were examined and fibromuscular lesions were scored with or without calcifications. Quantitative analysis of a multitude of intravascular ultrasound cross-sections (interval 5 mm) included assessment of the lumen area, vessel area, plaque area and percentage area obstructed. The target site (smallest lumen area) was compared with a reference site (largest lumen area before the first major side branch). Results. Of the 130 corresponding intravascular ultrasound images and histologic sections analysed, 55 were normal and 75 presented a bright lesion on ultrasound; in 31 lesions, peripheral shadowing was involved. The sensitivity of the intravascular ultrasound in detecting calcifications was 87%, and the specificity was 89%. Lumen area reduction at the target site was associated with vessel and plaque area enlargement in eight specimens, with plaque area enlargement in 12 specimens and with a vessel area reduction in 21 specimens.
KW - Atherosclerosis
KW - Intervention
KW - Renal artery obstruction
KW - Renovascular hypertension
KW - Ultrasonography
KW - Validation studies
UR - http://www.scopus.com/inward/record.url?scp=0032971307&partnerID=8YFLogxK
U2 - 10.1097/00004872-199917020-00012
DO - 10.1097/00004872-199917020-00012
M3 - Article
C2 - 10067797
AN - SCOPUS:0032971307
VL - 17
SP - 271
EP - 277
JO - Journal of Hypertension
JF - Journal of Hypertension
SN - 0263-6352
IS - 2
ER -