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Analyse von QRST-Integral und QT-Dispersion mittels „Body surface potential mapping” bei Patienten mit malignen ventrikulären Arrhythmien

Analysis of QRST integral and QT dispersion by body surface potential mapping in patients with malignant ventricular arrhythmias

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Zusammenfassung

Bei 74 Patienen wurde in einer retrospektiven Analyse der Wert des „Body surface potential mapping” (BSPM) im Vergleich zum 12-Kanal-EKG zur Erfassung von Repolarisationsstörungen bei Patienten mit koronarer Herzkrankheit und ohne kardiale Grunderkrankung untersucht. Bei Patienten mit idiopathischem Kammerflimmern (n=13) war sowohl die Anzahl von Extrema im QRST-Integralmap signifikant höher als in der Kontrollgruppe (n=18; 3,15±0,99 gegen 2,17±0,51, p<0,001) als auch die QT-Dispersion signifikant größer (0,10±0,03 gegen 0,07±0,01, p<0,001) Mittels QT-Dispersion im 12-Kanal-EKG war kein Unterschied zwischen beiden Gruppen nachweisbar. Bei Patienten mit koronarer Herzerkrankung (KHK) waren die Anzahl Extrema im QRST-Integralmap und QT-Dispersion ebenfalls höher als in der Kontrollgruppe, es fanden sich jedoch keine signifikanten Unterschiede zwischen den Patienten mit plötzlichem Herztod (n=22) und ohne stattgehabte, maligne, ventrikuläre Arrhythmie (n=21).

Das BSPM erfaßt Störungen der Repolarisation mit größerer Sensitivität als das 12-Kanal-EKG und erfaßt somit eine mögliche Ursache lebensbedrohlicher Arrhythmien bei Patienten ohne kardiale Grunderkrankung. Ein eventueller Nutzen zur Risikoerkennung bei Patienten mit KHK muß noch gezeigt werden.

Summary

In a retrospective analysis in 74 patients with coronary artery disease or no obvious heart disease, the value of “body surface potential mapping” for the identification of repolarization abnormalities was investigated compared to the standard 12-lead ECG. In patients with idiopathic ventricular fibrillation the number of extrema in the QRST integral map was significantly higher than in the control group (3.15±0.99 vs. 2.17±0.51, p<0.001) and the QT dispersion was also higher (0.10±0.03 vs. 0.07±0.01, p<0.001), whereas there was no difference between either group in the 12-lead ECG QT dispersion. In patients with coronary artery disease the number of extrema in the QRST integral map and QT dispersion were also higher compared to the control group, but there were no significant differences between patients with or without aborted sudden cardiac death.

In conclusion, BSPM identifies repolarization abnormalities not detected by 12-lead ECG, thereby identifying a potential reason for cardiac arrest in patients without overt heart disease. The usefulness of this technique for risk stratification in patients with coronary artery disease remains to be elucidated.

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Literatur

  1. Ahnve S, Helmers C, Lundman T, Rehnqvist N, Sjögren A (1980) QTc intervals in acute myocardial infarction: first-year prognostic implications. Clin Cardiol 3:303–308

    Article  PubMed  CAS  Google Scholar 

  2. Ahnve S (1985) Correction of the QT interval for heart rate: reviews of different formulas and the use of Bazett’s formula in myocardial infarction, Am Heart J 109:568–574

    Article  PubMed  CAS  Google Scholar 

  3. Barr C, Naas A, Freeman M, Lang C, Struthers A (1994) QT dispersion and sudden unexpected death in chronic heart failure. Lancet 343:327–329

    Article  PubMed  CAS  Google Scholar 

  4. Brugada P, Brugada J (1992) Right bundle branch block, persistent ST segment elevation and sudden cardiac death: A distinct clinical and electrocardiographic syndrome. J Am Coll Cardiol 20:1391–1396

    PubMed  CAS  Google Scholar 

  5. Buja G, Meneghello M, Bellotto F (1989) Isolated episode of exercise-related ventricular fibrillation in a healthy athlete. Intern J Cardiol 24:121–123

    Article  CAS  Google Scholar 

  6. Dambrink J-H, SippensGroenewegen A, van Gilst W, Peels K, Grimbergen C, Kingma J (1995) Association of left ventricular remodeling and nonuniform electrical recovery expressed by nondipolar QRST integral map patterns in survivors of a first anterior myocardial infarction. Circulation 92:300–310

    PubMed  CAS  Google Scholar 

  7. Das G (1990) QT interval and repolarisation time in patients with intraventricular conduction delay. J Electrocardiol 23:49–52

    Article  PubMed  CAS  Google Scholar 

  8. Day C, McComb J, Campbell R (1990) QT dispersion: an indication of arrhythmia risk in patients with long QT intervals. Br Heart J 63:342–344

    Article  PubMed  CAS  Google Scholar 

  9. Gardner M, Montague T, Armstrong C, Horácek B, Smith E (1986) Vulnerability to ventricular arrhythmia: assessment by mapping of body surface potential. Circulation 73:684–692

    PubMed  CAS  Google Scholar 

  10. Glancy J, Garrat C, Woods K, de Bono D (1995) QT dispersion and mortality after myocardial infarction. Lancet 345:945–948

    Article  PubMed  CAS  Google Scholar 

  11. Green L, Abildskov J (1995) Clinical applications of body surface potential mapping. Clin Cardiol 18:245–249

    Article  PubMed  CAS  Google Scholar 

  12. Horwitz L (1995) Current clinical utility of body surface mapping. J Invas Cardiol 9:265–274

    Google Scholar 

  13. Hubley-Kozey C, Mitchell L, Gardner M, Warren J, Penney C, Smith E, Horácek M (1995) Spatial features in body-surface potential maps can identify patients with a history of sustained ventricular tachycardia. Circulation 92:1825–1838

    PubMed  CAS  Google Scholar 

  14. Leitch J, Basta M, Dobson A (1995) QT dispersion does not predict early ventricular fibrillation after acute myocardial infarction. PACE 18:45–48

    PubMed  CAS  Google Scholar 

  15. Lux R, Green L, MacLeod R, Taccardi B (1994) Assessment of spatial and temporal characteristics of ventricular repolarisation. J Electrocardiol 27 Suppl:100–105

    Article  PubMed  Google Scholar 

  16. Merri M, Benhorin J, Alberti M, Locati E, Moss A (1989) Electrocardiographic quantitation of ventricular repolarization. Circulation 80:1301–1308

    PubMed  CAS  Google Scholar 

  17. Mitchell L, Hubley-Kozey C, Smith E, Wyse D, Duff H, Gillis A, Horácek B (1992) Electrocardiographic body surface mapping in patients with ventricular tachycardia. Circulation 86: 383–393

    PubMed  CAS  Google Scholar 

  18. Perkiömäki J, Koistinen M, Yli-Mäyry S, Huikuri H (1995) Dispersion of QT interval in patients with and without susceptibility to ventricular tachyarrhythmias after previous myocardial infarction. J Am Coll Cardiol 26: 174–179

    Article  PubMed  Google Scholar 

  19. Pye M, Quinn A, Cobbe S (1994) QT interval dispersion: a non-invasive marker of susceptibility to arrhythmia in patients with sustained ventricular arrhythmias? Br Heart J 71:511–514

    Article  PubMed  CAS  Google Scholar 

  20. Schwartz P, Wolf S (1978) QT Interval Prolongation as predictor of sudden death in patients with myocardial infarction. Circulation 57:1074–1077

    PubMed  CAS  Google Scholar 

  21. SippensGroenewegen A, Spekhorst H, van Hemel N, Kingma J, Hauer R, de Bakker J, Grimbergen C, Janse M, Dunning A (1994) Value of body surface mapping in localizing the site of origin of ventricular tachycardia in patients with previous myocardial infraction. J Am Coll Cardiol 24:1708–1724

    Article  PubMed  CAS  Google Scholar 

  22. Taylor G, Crampton R, Gibson R, Stebbins P, Waldman M, Beller G (1981) Prolonged QT interval at onset of acute myocardial infarction in predicting early phase ventricular tachycardia. Am Heart J 102:16–24

    Article  PubMed  CAS  Google Scholar 

  23. Tsunakawa H, Nishiyama G, Kusahana Y, Harumi K (1989) Identification of suspectibility to ventricular tachycardia after myocardial infarction by nondipolarity of QRST area maps. J Am Coll Cardiol 14:1530–1536

    Article  PubMed  CAS  Google Scholar 

  24. Ward D (1988) Prolongation of the QT interval as an indicator of risk of a cardiac event. Eur Heart J 9 Suppl G: 139–144

    PubMed  Google Scholar 

  25. Wheelan K, Mukharji J, Rude R, Poole W, Gustafson N, Thomas L, Strauss H, Jaffe A, Muller J, Roberts R, Croft C, Passamani E, Willerson J (1986) Sudden death and its relation to QT interval prolongation after acute myocardial infarction: two-year follow-up. Am J Cardiol 57:745–750

    Article  PubMed  CAS  Google Scholar 

  26. Zareba W, Moss A, le Cessie S (1994) Dispersion of ventricular repolarisation and arrhythmic cardiac death in coronary artery disease. Am J Cardiol 74: 550–553

    Article  PubMed  CAS  Google Scholar 

  27. Kadish AH (1995) The effects of gender on cardiac electrophysiology and arrhythmias. In: Zipes D, Jalife J (ed) Cardiac electrophysiology: from cell to bedside (second edition). Saunders Company, Philadelphia: 1268–1275

    Google Scholar 

  28. Macfarlane PW, McLaughlin SC, Devine B, Yang TF (1994) Effects of age, sex and race on ECG interval measurements. J Electrocardiol 27 (suppl): 14–19

    Article  PubMed  Google Scholar 

  29. Moss AJ (1993) Measurement of the QT interval and the risk associated with QTc prolongation: a review. Am J Cardiol 72:23B-25B

    Article  PubMed  CAS  Google Scholar 

  30. Rautaharju PM, Warren JW, Calhoun HP (1990) Estimation of QT prolongation. A persistent, avoidable error in computer electrocardiography. J Electrocardiol 23 (suppl):111–117

    Article  PubMed  Google Scholar 

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Stellbrink, C., Stegemann, E., Killmann, R. et al. Analyse von QRST-Integral und QT-Dispersion mittels „Body surface potential mapping” bei Patienten mit malignen ventrikulären Arrhythmien. Herzschr Elektrophys 8, 107–112 (1997). https://doi.org/10.1007/BF03042497

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