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  • Myocardial infarction  (2)
  • Myokardinfarkt  (2)
  • Aggressive anticoagulation  (1)
  • 1
    ISSN: 1432-0584
    Keywords: Intracoronary stenting ; Aggressive anticoagulation ; Subacute occlusion ; Bleeding complication ; Prothrombin fragment 1+2
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Patients with intracoronary stent implantation are treated with aggressive anticoagulant and antiplatelet therapy consisting of high-dose heparin, phenprocoumon, acetylsalicylic acid, dipyridamole, and the infusion of dextran to prevent a subacute thrombotic occlusion of the stented segment. In an effort to optimize this treatment by reducing both imminent bleeding complications and subacute thrombotic occlusion, the concentrations of prothrombin fragment 1+2 (F1+2) were determined after intracoronary Palmaz-Schatz stent implantation in 19 consecutive patients. The F1+2 concentrations after stent implantation and before the initiation of oral anticoagulant therapy (OAT) were 0.35 nm/l and 0.25–0.53 nm/l (median and 25th–75th percentile), versus 0.74 nm/l and 0.52–0.78 nm/l, in healthy subjects and 0.61 nm/l and 0.30–1.02 nm/l in 15 patients with ongoing proximal DVT. Nine days after initiation of OAT, F1+2 concentrations in both patient groups had not yet reached levels observed in patients with OAT in the stable state (0.16 nm/l, 0.12–0.26 nm/l;n=76;P〈0.0001 compared with healthy subjects; INR 2.0–4.5). Despite an INR greater than 2.0, accompanying heparinization was terminated on day 9. In two stented patients a minor bleeding complication arose after the removal of the arterial catheter. Subacute thrombotic occlusions were not observed. Since F1+2 concentrations did not exceed the upper limit of normal range (1.11 nm/l) in any of the 19 patients, the therapeutic regimen was not changed. Monitoring F1+2 may thus be helpful in introducing a more individual treatment if aggressive anticoagulation has to be performed.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1432-1440
    Keywords: Creatine kinase, isoenzymes ; Creatin kinase, isoenzyme-MB ; Antibodies, inhibiting ; Kinetic enzyme activity determination ; Myocardial infarction ; Creatinkinase-Isoenzyme ; Creatinkinase-Isoenzym MB ; Antikörper, inhibierende ; Enzymaktivitäts-Bestimmung, kinetische ; Myokardinfarkt
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Zusammenfassung Es wird über eine neue Methode zur quantitativen Bestimmung der Creatinkinase MB-Aktivität im Serum berichtet. Die Methode beruht auf einer direkten Messung der Aktivität der Creatin-kinase-Untereinheit B nach Hemmung der Aktivität der Creatinkinase-Untereinheit M durch inhibierende Antikörper und benötigt zur Durchführung 15 min. Bei allen 83 untersuchten Patienten mit klinisch gesichertem Myokardinfarkt konnten zwischen der 6. und 28. Stunde nach Infarkteintritt Creatinkinase MB-Aktivität gemessen werden. Der Creatinkinase MB-Anteil zum Zeitpunkt der höchsten Creatinkinase-Gesamtaktivität betrug 6–17%, im Mittel 8%. Diese Methode ermöglicht daher in der Notfalldiagnostik eine Differentialdiagnose unklarer Creatinkinase-Gesamtaktivitäts-Erhöhungen.
    Notes: Summary A new method for the determination of creatine kinase-MB activity in the serum is presented. The principle of this method is the direct measurement of the activity of creatine kinase M subunits by inhibiting antibodies. The total test procedure takes 15 min. In the sera of all the 83 patients tested, who have clinically proven myocard infarction, creatine kinase-MB activity can be measured between the 6th and 28th hour after infarction. At the time of maximum total creatine kinase activity the percentage of creatine kinase-MB activity is between 6 and 17%, the mean value being 8%. In cases of emergency this method can be used for the differential diagnosis of elevated total creatine kinase activities of unknown origin.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Journal of molecular medicine 56 (1978), S. 449-456 
    ISSN: 1432-1440
    Keywords: CK-isoenzymes ; Myocardial infarction ; Disappearance rate constant ; CK-Isoenzyme ; Myokardinfarkt ; Eliminationskonstante
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Zusammenfassung Wir untersuchten die Kinetik der Gesamtaktivität der Creatinkinase und die des Isoenzyms CK-MB bei 83 Patienten mit gesichertem Myokardinfarkt in Serienmessungen in 2–6 stündlichen Abständen. Die Aktivität des Isoenzyms CK-MB wurde mit der immunologischen Inhibitionsmethode bestimmt. Isoenzym CK-MB war bei allen Patienten nachweisbar. Die maximale CK-MB Aktivität betrug im Mittel 65 U/l (Bereich: 9-241 U/l). Der mittlere prozentuale CK-MB Aktivitätsanteil an der Gesamtaktivität lag zum Zeitpunkt der maximalen CK-MB Aktivität bei 13,2% (Bereich: 3,4–21,7%). Das Maximum der CK-MB Aktivität wird im Mittel 17,4 h (Bereich: 3,0–32,5 h) nach Beginn der akuten Schmerzsymptomatik erreicht. Es liegt damit 1,4 h vor dem Gipfel der CK-Gesamtaktivität. Die Berechnung der Eliminationskonstante (n=31) für die CK-MB Aktivität ergab bei einer sehr starken individuellen Streuung einen Mittelwert von 9,3×10−4 U/min, entsprechend einer Halbwertszeit von 12,5 h (CK-Gesamt: 15,5 h). Die Bestimmung der CK-MB Aktivität hat somit meist nur innerhalb von 48 h nach einem fraglich cardialen Ereignis diagnostische Wertigkeit. Da der Nachweis von Isoenzym CK-MB im Serum nicht im strengen Sinne spezifisch für eine Herzmuskelschädigung ist, ist es sinnvoll, die Höhe des prozentualen CK-MB Aktivitätsanteiles als differentialdiagnostischen Parameter zu benutzen. Bis zu 36 h nach Myokardinfarkt liegt dieser Wert bei 80% der Patienten über 6%.
    Notes: Summary We investigated the activity kinetics of CK-total and CK-MB in 83 patients with proven myocardial infarctions. Serial serum samples were taken at intervals of 2–6 h. The activity of isoenzym CK-MB was determined by means of the immunological inhibition method. CK-MB activity was determined in all patients. The mean peak activity of CK-MB was 65 U/l (range: 9-241 U/l). At the time of peak CK-MB activity the mean percentage CK-MB activity was 13.2% (range: 3.4–21.7%). The CK-MB activity reached its peak at 17.4 h (range: 3.0–32.5 h) after the onset of retrosternal pain. This is 1.4 h after peak CK-total activity. The mean disappearance rate constant for CK-MB (n=31) was found to be 9.3×10−4 U/min with a large individual variation. This value corresponds to a half life of 12.5 h (CK-total: 15.5 h). The determination of CK-MB activity is therefore only of diagnostic significance within 48 h of possible myocardial occurrence. Moreover, isoenzyme CK-MB is not found exclusively in myocardium. For this reason it is better to use the percentage CK-MB activity in the differential diagnosis of myocardial infarction. With 80% of the patients this value is greater than 6% within 36 h of proven myocardial infarction.
    Type of Medium: Electronic Resource
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