Phase III multicenter trial comparing the efficacy of 2% dodecafluoropentane emulsion (EchoGen) and sonicated 5% human albumin (Albunex) as ultrasound contrast agents in patients with suboptimal echocardiograms

被引:85
作者
Grayburn, PA
Weiss, JL
Hack, TC
Klodas, E
Raichlen, JS
Vannan, MA
Klein, AL
Kitzman, DW
Chrysant, SG
Cohen, JL
Abrahamson, D
Foster, E
Perez, JE
Aurigemma, GP
Panza, JA
Picard, MH
Byrd, BF
Segar, DS
Jacobson, SA
Sahn, DJ
DeMaria, AN
机构
[1] Univ Texas, SW Med Ctr, Echocardiog Labs, Div Cardiol, Dallas, TX 75216 USA
[2] Johns Hopkins Univ, Med Ctr, Baltimore, MD 21218 USA
[3] Deaconess Nashoba Hosp, Ayer, MA USA
[4] Thomas Jefferson Univ, Philadelphia, PA 19107 USA
[5] Tufts Univ New England Med Ctr, Boston, MA 02111 USA
[6] Cleveland Clin Fdn, Cleveland, OH 44195 USA
[7] Bowman Gray Med Ctr, Winston Salem, NC USA
[8] Oklahoma Cardiovasc & Hypotens Ctr, Oklahoma City, OK USA
[9] Vet Affairs Med Ctr, E Orange, NJ USA
[10] Orange Cty Heart Inst & Res Ctr, Orange, CA USA
[11] Univ Calif San Francisco, San Francisco, CA 94143 USA
[12] Washington Univ, Med Ctr, St Louis, MO USA
[13] Univ Massachusetts, Med Ctr, Worcester, MA USA
[14] NIH, Bethesda, MD 20892 USA
[15] Massachusetts Gen Hosp, Boston, MA 02114 USA
[16] Vanderbilt Univ, Nashville, TN USA
[17] Indiana Univ, Indianapolis, IN 46204 USA
[18] Res Hlth Inc, Houston, TX USA
[19] Univ Oregon, Hlth Sci Ctr, Portland, OR USA
[20] Univ Calif San Diego, San Diego, CA 92103 USA
关键词
D O I
10.1016/S0735-1097(98)00219-8
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives. This study was performed to compare the safety and efficacy of intravenous 2% dadecafluoropentane (DDFP) emulsion (EchoGen) with that of active control (sonicated human albumin [Albunex]) for left ventricular (LV) cavity opacification in adult patients with a suboptimal echocardiogram. Background. The development of new fluorocarbon-based echocardiographic contrast agents such as DDFP has allowed opacification of the left ventricle after peripheral venous injection. We hypothesized that DDFP was clinically superior to the Food and Drug Administration-approved active control. Methods. This was a Phase III, multicenter, single blind, active controlled trial. Sequential intravenous injections of active control and DDFP were given 30 min apart to 254 patients with a suboptimal echocardiogram, defined as one in which the endocardial borders mere not visible in at least two segments in either the apical two- or four-chamber views. Studies were interpreted in blinded manner by two readers and the investigators. Results. Full or intermediate LV cavity opacification was more frequently observed after DDFP than after active control (78% vs. 31% for reader A; 69% vs. 34% for reader B; 83% vs. 55% for the investigators, p < 0.0001). LV cavity opacification scores were higher with DDFP (2.0 to 2.5 vs. 1.1 to 1.5, p < 0.0001). Endocardial border delineation was improved by DDFP in 88% of patients versus 45% with active control (p < 0.001). Similar improvement was seen for duration of contrast effect, salvage of suboptimal echocardiograms, diagnostic confidence and potential to affect patient management. There was no difference between agents in the number of patients with adverse events attributed to the test agent (9% for DDFP vs. 6% for active control, p = 0.92). Conclusions. This Phase ill multicenter trial demonstrates that DDFP is superior to sonicated human albumin for LV cavity opacification, endocardial border definition, duration of effect, salvage of suboptimal echocardiograms, diagnostic confidence and potential to influence patient management. The two agents had similar safety profiles.
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收藏
页码:230 / 236
页数:7
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