In vivo elastographic investigation of ethanol-induced hepatic lesions

被引:22
作者
Hoyt, K
Forsberg, F
Merritt, CRB
Liu, JB
Ophir, J
机构
[1] Thomas Jefferson Univ, Dept Radiol, Philadelphia, PA 19107 USA
[2] Drexel Univ, Sch Biomed Engn Sci & Hlth Syst, Philadelphia, PA 19104 USA
[3] Univ Texas, Sch Med, Dept Radiol, Houston, TX 77030 USA
关键词
elastography; strain imaging; ultrasound; animal model; ethanol; hepatic lesions;
D O I
10.1016/j.ultrasmedbio.2005.01.017
中图分类号
O42 [声学];
学科分类号
070206 [声学]; 082403 [水声工程];
摘要
Ethanol-induced hepatic lesions were investigated in swine for in vivo use as a strain imaging animal model. Lesions (n = 25) were induced by injecting ethanol (doses 0.33 to 2.0 mL) directly into the surgically exposed liver at depths of 12, 15 or 25 mm. Lesions were imaged with a modified HDI 1000 scanner (Philips Medical Systems, Bothell, WA, USA). The elastograms (n = 91) characterized lesions as being areas harder than the surrounding soft hepatic tissue. Elastographic lesion sizes and the corresponding injected ethanol dose used to induce the lesions were shown to be statistically significant (r(2) = 0.22; p = 0.029) using a linear regression analysis. Additionally, lesion depth was shown to be statistically insignificant (r(2) < 0.12; p > 0.10) when regressed against elastographic lesion size. An analysis of elastographic and gross pathology lesion sizes indicated no correlation (r(2) < 0.01; p = 0.973). Subsequently, lesion types were sorted by size and regression lines were computed from quasilinear regions of the corresponding run charts. Trend lines indicate a four-to-three size relationship between the selected elastographic and pathology lesion sizes. Comparison of elastogram lesion sizes from two independent observers using a paired t-test resulted in no statistically significant difference (p = 0.14). In conclusion, ethanol-induced hepatic lesions in swine is a suitable animal model for evaluation of strain-based imaging systems, due to the ease of generation and repeatability. (c) 2005 World Federation for Ultrasound in Medicine & Biology.
引用
收藏
页码:607 / 612
页数:6
相关论文
共 25 条
[1]
In vivo breast tumor detection using transient elastography [J].
Bercoff, J ;
Chaffai, S ;
Tanter, M ;
Sandrin, L ;
Catheline, S ;
Fink, M ;
Gennisson, JL ;
Meunier, M .
ULTRASOUND IN MEDICINE AND BIOLOGY, 2003, 29 (10) :1387-1396
[2]
Elastography imaging of small animal oncology models: A feasibility study [J].
Bilgen, M ;
Srinivasan, S ;
Lachman, LB ;
Ophir, J .
ULTRASOUND IN MEDICINE AND BIOLOGY, 2003, 29 (09) :1291-1296
[3]
METHODS FOR ESTIMATION OF SUBSAMPLE TIME DELAYS OF DIGITIZED ECHO SIGNALS [J].
CESPEDES, I ;
HUANG, Y ;
OPHIR, J ;
SPRATT, S .
ULTRASONIC IMAGING, 1995, 17 (02) :142-171
[4]
REDUCTION OF IMAGE NOISE IN ELASTOGRAPHY [J].
CESPEDES, I ;
OPHIR, J .
ULTRASONIC IMAGING, 1993, 15 (02) :89-102
[5]
A freehand elastographic imaging approach for clinical breast imaging: System development and performance evaluation [J].
Doyley, MM ;
Bamber, JC ;
Fuechsel, F ;
Bush, NL .
ULTRASOUND IN MEDICINE AND BIOLOGY, 2001, 27 (10) :1347-1357
[6]
Elastography of breast lesions: Initial clinical results [J].
Garra, BS ;
Cespedes, EI ;
Ophir, J ;
Spratt, SR ;
Zuurbier, RA ;
Magnant, CM ;
Pennanen, MF .
RADIOLOGY, 1997, 202 (01) :79-86
[7]
In vivo real-time freehand palpation imaging [J].
Hall, TJ ;
Zhu, YN ;
Spalding, CS .
ULTRASOUND IN MEDICINE AND BIOLOGY, 2003, 29 (03) :427-435
[8]
Freehand ultrasound elastography of breast lesions:: Clinical results [J].
Hiltawsky, KM ;
Krüger, M ;
Starke, C ;
Heuser, L ;
Ermert, H ;
Jensen, A .
ULTRASOUND IN MEDICINE AND BIOLOGY, 2001, 27 (11) :1461-1469
[9]
Elastographic imaging of the normal canine prostate in vitro [J].
Kallel, F ;
Price, RE ;
Konofagou, E ;
Ophir, J .
ULTRASONIC IMAGING, 1999, 21 (03) :201-215
[10]
Krouskop T A, 1987, J Rehabil Res Dev, V24, P1