F-18-fluorodeoxyglucose positron emission tomography imaging-assisted management 2002 of patients with severe left ventricular dysfunction and suspected coronary disease: A randomized, controlled trial (PARR-2)

被引:323
作者
Beanlands, Rob S. B.
Nichol, Graham
Huszti, Ella
Humen, Dennis
Racine, Normand
Freeman, Michael
Gulenchyn, Karen Y.
Garrard, Linda
deKemp, Robert
Guo, Ann
Ruddy, Terrence D.
Benard, Francois
Lamy, Andre
Iwanochko, Robert M.
机构
[1] Univ Ottawa, Inst Heart, Natl Cardiac PET Ctr, Div Cardiol, Ottawa, ON K1Y 4K7, Canada
[2] London Hlth Sci Ctr, Div Cardiol, London, ON, Canada
[3] Univ Toronto, St Michaels Hosp, Div Cardiol, Toronto, ON M5B 1W8, Canada
[4] Univ Toronto Hlth Sci Network, Toronto Hosp, Div Cardiol, Toronto, ON, Canada
[5] Hamilton Hlth Sci, ES Garnett Mem PET Ctr, Dept Nucl Med, Hamilton, ON, Canada
[6] Hamilton Hlth Sci, Div Cardiac Surg, Hamilton, ON, Canada
[7] McGill Univ, Dept Biostat & Epidemiol, Montreal, PQ, Canada
[8] Montreal Heart Inst, Div Cardiol, Montreal, PQ H1T 1C8, Canada
[9] CHU Sherbrooke, Div Nucl Med, Sherbrooke, PQ J1K 2R1, Canada
[10] Univ Washington, Harborview Ctr Prehosp Emergency Care, Seattle, WA 98195 USA
基金
加拿大健康研究院;
关键词
D O I
10.1016/j.jacc.2007.09.006
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives We conducted a randomized trial to assess the effectiveness of F-18-fluorodeoxyglucose (FDG) positron emission tomography (PET)-assisted management in patients with severe ventricular dysfunction and suspected coronary disease. Background Such patients may benefit from revascularization, but have significant perioperative morbidity and mortality. F-18-fluorodeoxyglucose PET can detect viable myocardium that might recover after revascularization. Methods Included were patients with severe left ventricular (LV) dysfunction and suspected coronary disease being considered for revascularization, heart failure, or transplantation work-ups or in whom PET was considered potentially useful. Patients were stratified according to recent angiography or not, then randomized to management assisted by FDG PET (n = 218) or standard care (n = 212). The primary outcome was the composite of cardiac death, myocardial infarction, or recurrent hospital stay for cardiac cause, within 1 year. Results At 1 year, the cumulative proportion of patients who had experienced the composite event was 30% (PET arm) versus 36% (standard arm) (relative risk 0.82, 95% confidence interval [CI] 0.59 to 1.14; p = 0.16). The hazard ratio (HR) for the composite outcome, PET versus standard care, was 0.78 (95% Cl 0.58 to:1.1; p = 015); for patients that adhered to PET recommendations for revascularization, revascularization work-up, or neither, HR = 0.62 (95% Cl 0.42 to 0.93; p = 0.019); in those without recent angiography, for cardiac death, HR = 0.4 (95% Cl 0.17 to 0.96; p = 0.035). Conclusions This study did not demonstrate a significant reduction in cardiac events in patients with LV dysfunction and suspected coronary disease for FDG PET-assisted management versus standard care. In those who adhered to PET recommendations and in patients without recent angiography, significant benefits were observed. The utility of FDG PET is best realized in this subpopulation and when adherence to recommendations can be achieved. (J Am Coll Cardiol 2007;50:2002-:12) (c) 2007 by the American College of Cardiology Foundation.
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收藏
页码:2002 / 2012
页数:11
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