B. Eick et al., SUCCESSFUL TREATMENT OF A LARGE INTRACORO NARY THROMBUS WITH UROKINASE AND A CHIMERICAL MONOCLONAL PLATELET-AGGREGATION INHIBITOR, Deutsche Medizinische Wochenschrift, 122(22), 1997, pp. 709-715
History and clinical findings: 7 days after an operation for intervert
ebral disc prolapse a 43-year-old man was referred with the clinical a
nd ECG signs of an acute posterior wall myocardial infarction. Investi
gations: Creatine kinase (CK) activity was raised to 204 U/l (myocardi
al-specific isoenzyme CKMB of 23.6 U/l, 11.6% of total) and glutamatic
-oxalate transferase (GOT) activity to 37 U/l. Emergency cardiac cathe
terisation, performed 4 hours after renewed onset of precordial pain s
howed no abnormal findings in the right coronary artery, despite the E
CG signs, but a definite filling defect in the anterior interventricul
ar branch which on intravascular ultrasound was an echo-dense noncalci
fied structure. Treatment and course: After percutaneous transluminal
coronary angioplasty in the area of the obstructing structure al free-
floating mass was identified in the proximal part of the anterior inte
rventricular branch, most likely a thrombus. Intercoronary thrombolysi
s was therefore undertaken with urokinase (bolus of 1 mill. IU) togeth
er with the chimerical mono-clonal antibody c7E3, which inhibits plate
let aggregation by blocking the platelet glycoprotein surface receptor
IIb/IIIa. Coronary angiography 12 hours later revealed almost complet
e dissolution of the previously obstructing mass. Conclusion: Combinin
g the platelet aggregation inhibitor c7E3 with a thrombolytic agent is
an alternative treatment to the current management of intracoronary t
hrombi. Intravascular ultrasound is a suitable method for demonstratin
g angiographically inconspicious or unclear but pathogenetically signi
ficant vessel changes.