TY - JOUR
T1 - Dissociation between global and regional systolic and diastolic ventricular function during coronary occlusion and reperfusion
AU - Verani, Mario S.
AU - Bolli, Roberto
AU - Tadros, Sameh
AU - Myers, Mary Lee
AU - Neto, Salvador Borges
AU - Jain, Avanindra
AU - Phillips, Le Anna
AU - Roberts, Robert
N1 - Funding Information:
From the Section of Cardiology, College of Medicine. Supported in part by grant-in-aid 65G225 from the Association, Texas AtEliate, Austin, Tex., and a Research Neto) funded by Conselho National de Deeenvolvimcm Tecnologico (CNPq) Brazil. Received for publication March 5,1987; requests: Mario S. Verani, M.D., Baylor College Hospital, 6535 Fannin F-905, Houston, TX
Copyright:
Copyright 2018 Elsevier B.V., All rights reserved.
PY - 1987/10
Y1 - 1987/10
N2 - Indexes of giobal ventricular function such as the ejection fraction (EF) and the peak diastolic filling rate (PDFR) are often used to assess the effects of coronary recanalization in patients with myocardial infarction. In this investigation we assessed the relationship between these global indexes and directly measured indexes of regional function during 15 minutes of coronary occlusion followed by 120 minutes of reperfus on in 22 open-chest dogs. A computerizod nuclear cardiac probe was used to assess EF and PDFR. Indexes of regional function were measured by Doppler ultrasonic wall-thickening probes. During coronary occlusion, paradoxical systolic thinning occurred and the EF and PDFR decreased an average of 31.6% and 24.4%, respectively. During reperfusion the EF and PDFR improved rapidly and at 60 minutes were similar to baselline. Systolic wall thickening improved more gradually and remained abnormal throughout reperfusion. Likewise, indexes of diastolic function (mean rate to half end-diastolic thinning and late diastolic thinning fraction) recovered slowly and remained abnormal throughout reperfusion (78% and 69.7%, respectively). The correlation between the rate of change of giobal and regional function was poor during both coronary occlusion and reperfusion. Thus, during coronary occlusion the global and regional indexes of ventricular function undergo directionally similar changes. However, during coronary reperfusion the global indexes do not reflect the slow recovery of the stunned myocardium.
AB - Indexes of giobal ventricular function such as the ejection fraction (EF) and the peak diastolic filling rate (PDFR) are often used to assess the effects of coronary recanalization in patients with myocardial infarction. In this investigation we assessed the relationship between these global indexes and directly measured indexes of regional function during 15 minutes of coronary occlusion followed by 120 minutes of reperfus on in 22 open-chest dogs. A computerizod nuclear cardiac probe was used to assess EF and PDFR. Indexes of regional function were measured by Doppler ultrasonic wall-thickening probes. During coronary occlusion, paradoxical systolic thinning occurred and the EF and PDFR decreased an average of 31.6% and 24.4%, respectively. During reperfusion the EF and PDFR improved rapidly and at 60 minutes were similar to baselline. Systolic wall thickening improved more gradually and remained abnormal throughout reperfusion. Likewise, indexes of diastolic function (mean rate to half end-diastolic thinning and late diastolic thinning fraction) recovered slowly and remained abnormal throughout reperfusion (78% and 69.7%, respectively). The correlation between the rate of change of giobal and regional function was poor during both coronary occlusion and reperfusion. Thus, during coronary occlusion the global and regional indexes of ventricular function undergo directionally similar changes. However, during coronary reperfusion the global indexes do not reflect the slow recovery of the stunned myocardium.
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U2 - 10.1016/0002-8703(87)90776-9
DO - 10.1016/0002-8703(87)90776-9
M3 - Article
C2 - 2959131
AN - SCOPUS:0023203475
SN - 0002-8703
VL - 114
SP - 687
EP - 695
JO - American heart journal
JF - American heart journal
IS - 4 PART 1
ER -