Comparison between left ventricular electromechanical mapping and radionuclide perfusion imaging for detection of myocardial viability

被引:85
作者
Kornowski, R [1 ]
Hong, MK [1 ]
Leon, MB [1 ]
机构
[1] Cardiol Res Fdn, Washington Hosp Ctr, Washington, DC USA
关键词
mapping; ventricles; myocardium; ischemia;
D O I
10.1161/01.CIR.98.18.1837
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background-A novel 3-dimensional left ventricular (LV) mapping system uses low-intensity magnetic field energy to determine the location of sensor-tipped electrode catheters within the LV. Using this system, we sought to distinguish between infarcted, ischemic, and normal myocardium by comparing LV electromechanical mapping data with myocardial perfusion imaging studies. Methods and Results-Unipolar voltage potentials and local endocardial shortening (LS) were measured in 18 patients (mean age, 58+/-12 years) with symptomatic chronic angina having reversible and/or fixed myocardial perfusion defects on single photon emission computed tomography imaging studies using Tl-201 at rest and Tc-99m-sestamibi after adenosine stress. Overall, a significant difference in voltage potentials and LS values was found between groups (P<0.001 for each comparison by ANOVA). The average voltage potentials (14.0+/-2.0 mV) and LS values (12.5+/-2.8%) were highest when measured in myocardial segments (n=56) with normal perfusion and lowest (7.5+/-3.4 mV and 3.4+/-3.4%) when measured in myocardial segments with fixed perfusion defects (n=20) (P<0.0001). Myocardial segments with reversible perfusion defects (n=66) had intermediate voltage amplitudes (12.0+/-2.8 mV, P=0.048 versus normal and P=0.005 versus fixed segments) and LS values (10.3+/-3.7%, P=0.067 versus normal and P=0.001 versus fixed segments). Conclusions-in patients with myocardial ischemia, LV mapping, compared with myocardial perfusion imaging, shows (1) mild reduction of endocardial voltage potentials and LS in segments with reversible perfusion defects and (2) profound electromechanical impairment in segments with fixed perfusion defects. Thus, such an LV mapping procedure may allow the detection on-line of myocardial viability in the catheterization laboratory.
引用
收藏
页码:1837 / 1841
页数:5
相关论文
共 11 条
[1]   Nonfluoroscopic, in vivo navigation and mapping technology [J].
BenHaim, SA ;
Osadchy, D ;
Schuster, I ;
Gepstein, L ;
Hayam, G ;
Josephson, ME .
NATURE MEDICINE, 1996, 2 (12) :1393-1395
[2]   Identification of viable myocardium [J].
Bonow, RO .
CIRCULATION, 1996, 94 (11) :2674-2680
[3]   EFFECT OF NITROGLYCERIN ON THE ELECTRICAL CHANGES OF EARLY OR SUBENDOCARDIAL ISCHEMIA EVALUATED BY MONOPHASIC ACTION-POTENTIAL RECORDINGS [J].
DONALDSON, RM ;
TAGGART, P ;
SWANTON, H ;
FOX, K ;
RICKARDS, AF ;
NOBLE, D .
CARDIOVASCULAR RESEARCH, 1984, 18 (01) :7-13
[4]   STUDY OF THE ELECTRO-PHYSIOLOGICAL EFFECTS OF EARLY OR SUBENDOCARDIAL ISCHEMIA WITH INTRACAVITARY ELECTRODES IN THE DOG [J].
DONALDSON, RM ;
TAGGART, P ;
NASHAT, F ;
ABED, J ;
RICKARDS, AF ;
NOBLE, D .
CLINICAL SCIENCE, 1983, 65 (06) :579-588
[5]   LONG-TERM RECORDING OF MONOPHASIC ACTION-POTENTIALS FROM HUMAN ENDOCARDIUM [J].
FRANZ, MR .
AMERICAN JOURNAL OF CARDIOLOGY, 1983, 51 (10) :1629-1634
[6]   LOCALIZATION OF REGIONAL MYOCARDIAL ISCHEMIA BY RECORDING OF MONOPHASIC ACTION-POTENTIALS [J].
FRANZ, MR ;
FLAHERTY, JT ;
PLATIA, EV ;
BULKLEY, BH ;
WEISFELDT, ML .
CIRCULATION, 1984, 69 (03) :593-604
[7]  
Gepstein L, 1997, CIRCULATION, V96, P3672
[8]  
Gepstein L, 1997, CIRCULATION, V95, P1611
[9]   Preliminary animal and clinical experiences using an electromechanical endocardial mapping procedure to distinguish infarcted from healthy myocardium [J].
Kornowski, R ;
Hong, MK ;
Gepstein, L ;
Goldstein, S ;
Ellahham, S ;
Ben-Haim, SA ;
Leon, MB .
CIRCULATION, 1998, 98 (11) :1116-1124
[10]   CELLULAR ELECTROPHYSIOLOGICAL MARKER OF IRREVERSIBLE ISCHEMIC MYOCARDIAL INJURY [J].
MCGEE, J ;
SINGER, DH ;
TENEICK, RE ;
KLONER, R ;
BELIC, N ;
REIMER, K ;
ELSON, J .
AMERICAN JOURNAL OF PHYSIOLOGY, 1978, 235 (05) :H559-H568