Heart rate variability during the acute phase of myocardial infarction
| Autor: | P. Stroder, C. Signorini, Giancarlo Casolo, M. Zucchini, F. Calzolari, S Lazzerini, A. Sulla, E. Balli |
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| Rok vydání: | 1992 |
| Předmět: |
Male
medicine.medical_specialty Myocardial Infarction Hemodynamics Autonomic Nervous System Sudden death Ventricular Function Left Heart Rate Physiology (medical) Internal medicine Heart rate medicine Humans Heart rate variability Angina Unstable Myocardial infarction medicine.diagnostic_test business.industry Unstable angina Coronary Care Units Arrhythmias Cardiac Heart Middle Aged medicine.disease Surgery Tissue Plasminogen Activator Ambulatory Electrocardiography Ambulatory Cardiology Female Cardiology and Cardiovascular Medicine business Electrocardiography |
| Zdroj: | Circulation. 85:2073-2079 |
| ISSN: | 1524-4539 0009-7322 |
| DOI: | 10.1161/01.cir.85.6.2073 |
| Popis: | BACKGROUND After acute myocardial infarction (AMI), several abnormalities of the autonomic control to the heart have been described. Heart rate (HR) variability has been used to explore the neural control to the heart. A low HR variability count measured 7-13 days after AMI is significantly related to a poor outcome. Little information is available on HR variability early after AMI and its relation to clinical and hemodynamic data. METHODS AND RESULTS We studied 54 consecutive patients (42 men and 12 women; mean age, 60.4 +/- 11 years) with evidence of AMI by collecting the 24-hour HR SD from Holter tapes recorded on day 2 or 3. We also measured HR variability in 15 patients with unstable angina and in 35 age-matched normal subjects. HR variability was lower in AMI than in unstable angina patients (57.6 +/- 21.3 versus 92 +/- 19 msec; p less than 0.001) and controls (105 +/- 12 msec; p less than 0.001). Also, HR variability was greater in non-Q-wave than in Q-wave AMI (p less than 0.0001) and in recombinant tissue-type plasminogen activator-treated patients with respect to the rest of the group (p less than 0.02). No difference was found for infarct site. HR variability was significantly related to mean 24-hour HR, peak creatine kinase-MB, and left ventricular ejection fraction (all p less than 0.0001). Patients belonging to Killip class greater than I or who required the use of diuretics or digitalis had lower counts (p less than 0.004, p less than 0.001, and p less than 0.024, respectively). Six patients died within 20 days after admission to the hospital. In these patients, HR variability was lower than in survivors (31.2 +/- 12 versus 60.9 +/- 20 msec; p less than 0.001), and a value less than 50 msec was significantly associated with mortality (p less than 0.025). CONCLUSIONS HR variability during the early phase of AMI is decreased and is significantly related to clinical and hemodynamic indexes of severity. The causes for the observed changes in HR variability during AMI may be reduced vagal and/or increased sympathetic outflow to the heart. It is suggested that early measurements of HR variability during AMI may offer important clinical information and contribute to the early risk stratification of patients. |
| Databáze: | OpenAIRE |
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