Literature DB >> 6693639

Patterns of creatine kinase release during acute myocardial infarction after nonsurgical reperfusion: comparison with conventional treatment and correlation with infarct size.

H Blanke, D von Hardenberg, M Cohen, H Kaiser, K R Karsch, J Holt, H Smith, P Rentrop.   

Abstract

Coronary arteriography and biplane ventriculography were performed in 51 patients during the acute (mean of 6.6 hours after onset of symptoms) and chronic (1 to 3 months after admission) phase of myocardial infarction. Twenty-four patients were treated in a conventional manner. In 27 patients, reperfusion was achieved with intracoronary streptokinase after 24 +/- 20 minutes of infusion. Peak creatine kinase and cumulative creatine kinase release were derived from serial creatine kinase measurements. Ejection fraction and the length of the akinetic or dyskinetic segments were calculated in the chronic phase. The time interval between onset of symptoms and peak creatine kinase was significantly shorter for the streptokinase-treated patients as compared with the conventionally treated patients (13.5 +/- 5.3 versus 22.9 +/- 7.4 hours, p = 0.0001). Significant linear correlations were obtained for both streptokinase-treated and control patients, relating: 1) peak creatine kinase value to both length of the noncontracting segment and ejection fraction in the chronic phase, and 2) cumulative creatine kinase release to both length of the noncontracting segment and ejection fraction in the chronic phase. Patients treated with streptokinase experienced a relatively greater release of enzyme for a given infarct size as compared with those treated in a conventional manner. The difference in enzyme release between the two groups increased as infarct size increased. These observations may be explained by enhanced washout of enzyme from the infarct zone, secondary to reperfusion after intracoronary streptokinase therapy.(ABSTRACT TRUNCATED AT 250 WORDS)

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Year:  1984        PMID: 6693639     DOI: 10.1016/s0735-1097(84)80242-9

Source DB:  PubMed          Journal:  J Am Coll Cardiol        ISSN: 0735-1097            Impact factor:   24.094


  7 in total

1.  Prediction of spontaneous coronary reperfusion in myocardial infarction.

Authors:  F W Verheugt; F C Visser; E E van der Wall; M J van Eenige; J C Res; J P Roos
Journal:  Postgrad Med J       Date:  1986-11       Impact factor: 2.401

2.  Effect of hyaluronidase on mortality and morbidity in patients with early peaking of plasma creatine kinase MB and non-transmural ischaemia. Multicentre investigation for the limitation of infarct size (MILIS).

Authors:  R Roberts; E Braunwald; J E Muller; C Croft; H K Gold; T D Hartwell; A S Jaffe; S M Mullin; C Parker; E R Passamani
Journal:  Br Heart J       Date:  1988-10

3.  Are enzymatic tests good indicators of coronary reperfusion?

Authors:  H A Bosker; A van der Laarse; V M Cats; A V Bruschke
Journal:  Br Heart J       Date:  1992-02

4.  A randomised dose ranging study of recombinant tissue plasminogen activator in acute myocardial infarction.

Authors:  A J McNeill; J S Shannon; S R Cunningham; D J Flannery; N P Campbell; M M Khan; G C Patterson; S W Webb; A A Adgey
Journal:  Br Med J (Clin Res Ed)       Date:  1988-06-25

5.  Effect of nifedipine on enzymatically estimated infarct size in the early phase of acute myocardial infarction.

Authors:  L J Walker; G MacKenzie; A A Adgey
Journal:  Br Heart J       Date:  1988-04

6.  Ten year mortality in relation to original size of myocardial infarct: results from the Gothenburg metoprolol study.

Authors:  J Herlitz; B W Karlson; A Hjalmarson
Journal:  Br Heart J       Date:  1994-03

7.  Enzyme estimates of infarct size correlate with functional and clinical outcomes in the setting of ST-segment elevation myocardial infarction.

Authors:  Aslan T Turer; Kenneth W Mahaffey; Dianne Gallup; W Douglas Weaver; Robert H Christenson; Nathan R Every; E Magnus Ohman
Journal:  Curr Control Trials Cardiovasc Med       Date:  2005-08-23
  7 in total

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