Enzymatic estimation of myocardial infarct size when early creatine kinase values are not available. 1983

J L Smith, and H D Ambos, and H K Gold, and J E Muller, and W K Poole, and D S Raabe, and R E Rude, and E Passamani, and E Braunwald, and B E Sobel, and R Roberts

Estimates of myocardial infarct (MI) size based on plasma creatine kinase (CK) are used widely for prognosis and in the assessment of therapy designed to salvage ischemic myocardium. However, if the initial plasma CK activity is elevated, MI size will be underestimated. To determine the impact of loss of early CK values on estimates of MI size and to develop a procedure to compensate for it, estimates of MI size based on complete and incomplete MB and total CK time-activity curves from 120 patients (experimental group) were compared. Estimates of MI size based on data inclusion intervals beginning at 24, 12, 8, and 4 hours before peak CK were 11, 14, 23, and 47% smaller than values based on complete CK curves, but the correlation was good between complete and incomplete estimates of MI size at any given interval, with r values ranging from 0.91 to 0.98. The derived correction factors were then prospectively applied to a new population (n = 25) with complete CK curves to compensate for purposely omitted early CK values. The corrected estimates of MI size were within 7% of those based on the complete CK curves. Similar results were obtained for transmural and nontransmural and anterior or inferior MI. Thus, if peak plasma CK is known, underestimation of MI size can be compensated for despite the unavailability of early CK values. Since greater than 90% of patients present before plasma CK has reached its peak (24 hours), MI size can be obtained in nearly all patients. Thus, being able to correct for unavailable early CK values makes MI size a more widely applicable endpoint for use in clinical trials and patient management.

UI MeSH Term Description Entries
D008722 Methods A series of steps taken in order to conduct research. Techniques,Methodological Studies,Methodological Study,Procedures,Studies, Methodological,Study, Methodological,Method,Procedure,Technique
D009203 Myocardial Infarction NECROSIS of the MYOCARDIUM caused by an obstruction of the blood supply to the heart (CORONARY CIRCULATION). Cardiovascular Stroke,Heart Attack,Myocardial Infarct,Cardiovascular Strokes,Heart Attacks,Infarct, Myocardial,Infarction, Myocardial,Infarctions, Myocardial,Infarcts, Myocardial,Myocardial Infarctions,Myocardial Infarcts,Stroke, Cardiovascular,Strokes, Cardiovascular
D011446 Prospective Studies Observation of a population for a sufficient number of persons over a sufficient number of years to generate incidence or mortality rates subsequent to the selection of the study group. Prospective Study,Studies, Prospective,Study, Prospective
D003402 Creatine Kinase A transferase that catalyzes formation of PHOSPHOCREATINE from ATP + CREATINE. The reaction stores ATP energy as phosphocreatine. Three cytoplasmic ISOENZYMES have been identified in human tissues: the MM type from SKELETAL MUSCLE, the MB type from myocardial tissue and the BB type from nervous tissue as well as a mitochondrial isoenzyme. Macro-creatine kinase refers to creatine kinase complexed with other serum proteins. Creatine Phosphokinase,ADP Phosphocreatine Phosphotransferase,ATP Creatine Phosphotransferase,Macro-Creatine Kinase,Creatine Phosphotransferase, ATP,Kinase, Creatine,Macro Creatine Kinase,Phosphocreatine Phosphotransferase, ADP,Phosphokinase, Creatine,Phosphotransferase, ADP Phosphocreatine,Phosphotransferase, ATP Creatine
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D000368 Aged A person 65 years of age or older. For a person older than 79 years, AGED, 80 AND OVER is available. Elderly
D013997 Time Factors Elements of limited time intervals, contributing to particular results or situations. Time Series,Factor, Time,Time Factor

Related Publications

J L Smith, and H D Ambos, and H K Gold, and J E Muller, and W K Poole, and D S Raabe, and R E Rude, and E Passamani, and E Braunwald, and B E Sobel, and R Roberts
June 1985, American heart journal,
J L Smith, and H D Ambos, and H K Gold, and J E Muller, and W K Poole, and D S Raabe, and R E Rude, and E Passamani, and E Braunwald, and B E Sobel, and R Roberts
April 1980, Clinical cardiology,
J L Smith, and H D Ambos, and H K Gold, and J E Muller, and W K Poole, and D S Raabe, and R E Rude, and E Passamani, and E Braunwald, and B E Sobel, and R Roberts
January 1986, The American journal of cardiology,
J L Smith, and H D Ambos, and H K Gold, and J E Muller, and W K Poole, and D S Raabe, and R E Rude, and E Passamani, and E Braunwald, and B E Sobel, and R Roberts
January 1998, American heart journal,
J L Smith, and H D Ambos, and H K Gold, and J E Muller, and W K Poole, and D S Raabe, and R E Rude, and E Passamani, and E Braunwald, and B E Sobel, and R Roberts
October 1978, Clinical chemistry,
J L Smith, and H D Ambos, and H K Gold, and J E Muller, and W K Poole, and D S Raabe, and R E Rude, and E Passamani, and E Braunwald, and B E Sobel, and R Roberts
June 1974, Deutsche medizinische Wochenschrift (1946),
J L Smith, and H D Ambos, and H K Gold, and J E Muller, and W K Poole, and D S Raabe, and R E Rude, and E Passamani, and E Braunwald, and B E Sobel, and R Roberts
December 1977, Circulation research,
J L Smith, and H D Ambos, and H K Gold, and J E Muller, and W K Poole, and D S Raabe, and R E Rude, and E Passamani, and E Braunwald, and B E Sobel, and R Roberts
December 1965, Polski tygodnik lekarski (Warsaw, Poland : 1960),
J L Smith, and H D Ambos, and H K Gold, and J E Muller, and W K Poole, and D S Raabe, and R E Rude, and E Passamani, and E Braunwald, and B E Sobel, and R Roberts
May 2006, Journal of cardiovascular medicine (Hagerstown, Md.),
J L Smith, and H D Ambos, and H K Gold, and J E Muller, and W K Poole, and D S Raabe, and R E Rude, and E Passamani, and E Braunwald, and B E Sobel, and R Roberts
December 1983, British heart journal,
Copied contents to your clipboard!