TY - JOUR
T1 - Early Treatment of Acute Myocardial Infarction With Intravenous Streptokinase
T2 - A High-Risk Syndrome
AU - Koren, Gideon
AU - Luria, Myron H.
AU - Weiss, Avraham T.
AU - Kriwisky, Michael
AU - Mosseri, Morris
AU - Lotan, Chaim
AU - Applebaum, David
AU - Welber, Sima
AU - Sapoznikov, Dan
AU - Ben David, Yosef
AU - Hasin, Yonathan
AU - Gotsman, Mervyn S.
PY - 1987/2
Y1 - 1987/2
N2 - Fifty-one successive patients treated with intravenous streptokinase 1.7 ±0.8 (mean ± SD) hours after onset of symptoms of acute myocardial infarction were evaluated during a three-month posthospital follow-up period. Coronary angiography was performed four to nine days after the initial hospital admission. Twenty-eight patients had a second late angiogram. Forty-one patients had successful reperfusion but only 25% of all patients were without significant clinical cardiovascular manifestations during this period. Postmyocardial infarction angina pectoris occurred in 21 patients, an abnormal stress test result was present in 28 patients, eight patients developed congestive heart failure, and five patients had reinfarction. An intervention with percutaneous transluminal coronary angioplasty or coronary artery bypass graft was performed in 15 (37%) of 41 reperfused patients. A significantly higher intervention rate was present in patients treated with streptokinase within one hour following the onset of symptoms. Early reocclusion (within three months of the infarct) was noted in patients with 60% or more residual stenosis in their infarct-related coronary artery. These patients also had a significantly greater incidence of angina pectoris. Our findings indicate that early thrombolytic therapy of acute myocardial infarction preserves myocardium, and since the infarct-related artery is patent, but narrowed, the jeopardized area is responsible for a high-risk syndrome with an increased likelihood of ischemic symptoms. An early aggressive approach may be indicated, especially for patients with greater than 60% residual stenosis in their infarct-related coronary artery.
AB - Fifty-one successive patients treated with intravenous streptokinase 1.7 ±0.8 (mean ± SD) hours after onset of symptoms of acute myocardial infarction were evaluated during a three-month posthospital follow-up period. Coronary angiography was performed four to nine days after the initial hospital admission. Twenty-eight patients had a second late angiogram. Forty-one patients had successful reperfusion but only 25% of all patients were without significant clinical cardiovascular manifestations during this period. Postmyocardial infarction angina pectoris occurred in 21 patients, an abnormal stress test result was present in 28 patients, eight patients developed congestive heart failure, and five patients had reinfarction. An intervention with percutaneous transluminal coronary angioplasty or coronary artery bypass graft was performed in 15 (37%) of 41 reperfused patients. A significantly higher intervention rate was present in patients treated with streptokinase within one hour following the onset of symptoms. Early reocclusion (within three months of the infarct) was noted in patients with 60% or more residual stenosis in their infarct-related coronary artery. These patients also had a significantly greater incidence of angina pectoris. Our findings indicate that early thrombolytic therapy of acute myocardial infarction preserves myocardium, and since the infarct-related artery is patent, but narrowed, the jeopardized area is responsible for a high-risk syndrome with an increased likelihood of ischemic symptoms. An early aggressive approach may be indicated, especially for patients with greater than 60% residual stenosis in their infarct-related coronary artery.
UR - http://www.scopus.com/inward/record.url?scp=84942003441&partnerID=8YFLogxK
U2 - 10.1001/archinte.1987.00370020057036
DO - 10.1001/archinte.1987.00370020057036
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C2 - 3813740
AN - SCOPUS:84942003441
SN - 0003-9926
VL - 147
SP - 237
EP - 240
JO - Archives of Internal Medicine
JF - Archives of Internal Medicine
IS - 2
ER -