Myocardial Reperfusion Improves Ventricular Isovolumic Relaxation in Patients with Acute Myocardial Infarction

被引:0
作者
Liu, Chun-Peng [1 ]
Hu, Wei-Chih [2 ]
Wang, Jia-Jung [3 ]
Mar, Guang-Yuan [1 ]
机构
[1] Kaohsiung Vet Gen Hosp, Dept Internal Med, Kaohsiung, Taiwan
[2] Chung Yuan Christian Univ, Dept Biomed Engn, Chungli, Taiwan
[3] I Shou Univ, Dept Biomed Engn, Kaohsiung, Taiwan
来源
2009 3RD INTERNATIONAL CONFERENCE ON BIOINFORMATICS AND BIOMEDICAL ENGINEERING, VOLS 1-11 | 2009年
关键词
acute myocardial infarction (AMI); thrombolysis; percutaneous coronary intervention (PCI); diastolic function; time constant; PLASMINOGEN-ACTIVATOR; TRIAL; STREPTOKINASE; PERFORMANCE; MORTALITY; INDEX;
D O I
暂无
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
The study aimed to investigate the effects of thrombolytic therapy and percutaneous coronary intervention (PCI) on the time constant of left ventricular (LV) isovolumic relaxation. Of 38 patients with acute myocardial infarction (AMI) recruited in the work, 26 patients (treated group) received intravenously thrombolytic therapy within 12 hours after the AM! event, and 12 patients (controlled group) received PCI at fifth or sixth day after the AMI event. LV pressure was measured with Millar catheters during diagnostic catheterization both at first week after admission and at 3-month follow-up. We found that in the patients with the thrombolytic therapy, the time constant of the isovolumic relaxation significantly decreases from 50.1 +/- 11.0 ms measured at the first week to 44.2 +/- 8.8 ms measured at the 3-month follow-up (p<0.05). In contrast, the time constant measured from the patients with PCI is significantly increased from 46.3 +/- 8.4 at the first week to 63.1 +/- 15.9 ms at the 3-month follow-up (p<0.05). In addition, the time constant was considerably smaller in the treated patients than in the controlled patients three months after occurrence of AMI (p<0.001). In conclusion, myocardial microvessels early reopened by the thrombolysis may dominantly contribute to the improvement in LV diastolic function, suggesting that the thrombolytic therapy may play a more progressive role in the AMI-related treatment as PCI equipment is not available.
引用
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页码:2831 / +
页数:3
相关论文
共 17 条
[1]  
[Anonymous], 1988, Lancet, V1, P545
[2]  
[Anonymous], 1986, LANCET, V1, P397
[3]   EFFECTS OF LATE ADMINISTRATION OF TISSUE-TYPE PLASMINOGEN-ACTIVATOR ON LEFT-VENTRICULAR REMODELING AND FUNCTION AFTER MYOCARDIAL-INFARCTION [J].
BONADUCE, D ;
PETRETTA, M ;
VILLARI, B ;
BREGLIO, R ;
CONFORTI, G ;
MONTEMURRO, MV ;
LANZILLO, T ;
MORGANO, G .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 1990, 16 (07) :1561-1568
[4]   LEFT-VENTRICULAR EJECTION FRACTION MAY NOT BE USEFUL AS AN END-POINT OF THROMBOLYTIC THERAPY COMPARATIVE TRIALS [J].
CALIFF, RM ;
HARRELSONWOODLIEF, L ;
TOPOL, EJ .
CIRCULATION, 1990, 82 (05) :1847-1853
[5]   THE WESTERN WASHINGTON RANDOMIZED TRIAL OF INTRACORONARY STREPTOKINASE IN ACUTE MYOCARDIAL-INFARCTION - A 12-MONTH FOLLOW-UP REPORT [J].
KENNEDY, JW ;
RITCHIE, JL ;
DAVIS, KB ;
STADIUS, ML ;
MAYNARD, C ;
FRITZ, JK .
NEW ENGLAND JOURNAL OF MEDICINE, 1985, 312 (17) :1073-1078
[6]   Estimation of the left ventricular relaxation time constant τ requires consideration of the pressure asymptote [J].
Langer, SFJ ;
Habazettl, H ;
Kuebler, WM ;
Pries, AR .
PHYSIOLOGICAL RESEARCH, 2005, 54 (06) :601-610
[7]  
NORRIS RM, 1988, LANCET, V1, P104
[8]   A NEW APPROACH TO INSITU LEFT-VENTRICULAR VOLUME CLAMPING IN DOGS [J].
OHTANI, M ;
NIKOLIC, SD ;
GLANTZ, SA .
AMERICAN JOURNAL OF PHYSIOLOGY, 1991, 261 (04) :H1335-H1343
[9]   Serial changes and prognostic implications of a Doppler-derived index of combined left ventricular systolic and diastolic myocardial performance in acute myocardial infarction [J].
Poulsen, SH ;
Jensen, SE ;
Nielsen, JC ;
Moller, JE ;
Egstrup, K .
AMERICAN JOURNAL OF CARDIOLOGY, 2000, 85 (01) :19-25
[10]   VOLUME LOADING SLOWS LEFT-VENTRICULAR ISOVOLUMIC RELAXATION RATE - EVIDENCE OF LOAD-DEPENDENT RELAXATION IN THE INTACT DOG HEART [J].
RAFF, GL ;
GLANTZ, SA .
CIRCULATION RESEARCH, 1981, 48 (06) :813-824