PREDICTIVE VALUE OF URINARY THROMBOXANE A2 METABOLITES IN EARLY DIAGNOSIS OF ACUTE MYOCARDIAL INFARCTION
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The aim of this study is to determine the predictive value of urinary thromboxane A2 metabolites in early diagnosis of AM! (Acute Myocardial Infarction) and to compare its sensitivity and specificity with other measures used to diagnose AM! as ECG (Electrocardiogram) CKMB (creatinine lcinase-MB ) , LDH (lactate dehycirogenase) , and myoglobin. The present work was performed on 52 individuals . They were divided into 3 groups ; group 1(30 patients suffering from AM!) , group II (12 patients suffering from unstable angina) , and group DI (10 healthy individuals as a control group). Single urine sample was obtained from every patient as well as control subjects 6 hours from the onset of chest pain for quantitative estimation of 1-2,3 dinor-TXB, in urine. Two blood samples were obtained from every patient and control subjects , one within 6 hours after the onset of chest pain for estimation of serum myoglobin and CKMB. The second blood sample was obtained 24 hours after the onset of chest pain for estimation of serum levels of LDH to confirm the diagnosis. ECG was performed for all patients and control subjects 6 and 24 hours after the onset of chest pain. It was found that urinary 1-2,3 dinor-TXB2 , within 6 hours from the onset of chest pain , was elevated in all AMI patients except one (96.7%). In unstable angina group, it is elevated in all patients except two with levels much less than those of AMI group. All control subjects had normal urinary 1-2,3 dinor-TXI32. A positive interrelationship was found between 1-2,3 dinor-1'X82 , CKMB , and myoglobin measured within 6 hours after the onset of chest pain. In diagnosing AMI , urinary 1-2,3 dinor-Tashowed sensitivity of 96.7% , specificity of 91.7% , positive predictive value (PPV) of 96.7% , negative predictive value (NPP) of 91.7% , and accuracy of 95.2%. this very high degree of sensitivity and specificity indicated that urinary 1-2,3 dinor-DCEt2 measurement is a sensitive and specific method for early diagnosis of AMI. It is also a very rapid test, cost effective, detected in urine early in the course of AM1 and is not affected by anti-platelet drugs or muscular injury. Moreover , its sensitivity, specificity, PPV , NPP , and accuracy are higher than that of CKMB and myoglobin in early diagnosis of AMI.