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J Am Coll Cardiol, 2000; 35:1470-1477
© 2000 by the American College of Cardiology Foundation
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CLINICAL STUDIES

Distinct hemodynamic profiles in patients with vasovagal syncope: a heterogeneous population

Win-Kuang Shen, MD, FACC*, Phillip A. Low, MD{dagger}, Robert F. Rea, MD, FACC*, Christine M. Lohse, BS{ddagger}, David O. Hodge, MS{ddagger} and Stephen C. Hammill, MD, FACC*

* Division of Cardiovascular Diseases and Internal Medicine, Mayo Clinic and Mayo Foundation, Rochester, Minnesota, USA
{dagger} Peripheral Neuropathy Research Laboratory, Mayo Clinic and Mayo Foundation, Rochester, Minnesota, USA
{ddagger} Section of Biostatistics, Mayo Clinic and Mayo Foundation, Rochester, Minnesota, USA

Manuscript received April 22, 1999; revised manuscript received November 11, 1999, accepted January 7, 2000.

Reprint requests and correspondence: Dr. Win-Kuang Shen, Division of Cardiovascular Diseases and Internal Medicine, Mayo Clinic, 200 First Street Southwest, Rochester, Minnesota 55905

OBJECTIVE

The objective was to investigate mechanisms of vasovagal syncope by identifying laboratory techniques that characterize cardiovascular profiles in patients with vasovagal syncope.

BACKGROUND

The triggering mechanisms of vasovagal syncope are complex. The patient population is likely heterogeneous. We hypothesized that distinct hemodynamic profiles are definable with provocative maneuvers.

METHODS

Three groups of subjects were matched for age and gender: 16 patients with a history of syncope and an inducible vasovagal response during passive tilt table testing (70°, 45 min, group I), 16 with a history of syncope, negative passive tilt table testing but positive isoproterenol tilt table testing (0.05 µg/kg per min, 70°, 10 min, group II), and 16 control subjects. Beat-to-beat hemodynamic functions were determined noninvasively by photoplethysmography and impedance cardiography.

RESULTS

At baseline, hemodynamic functions were not different among the three groups (supine). In response to tilt before any symptoms developed, total peripheral resistance decreased 9% ± 14% in group I from baseline supine to tilt position but increased 27% ± 18% in group II and 28% ± 17% in controls (p < 0.001). Responses to isoproterenol were not significantly different between group II and controls in supine position. In response to tilt during isoproterenol infusion before any symptoms developed, total peripheral resistance decreased 24% ± 20% in group II and increased 20% ± 48% in controls (p = 0.002).

CONCLUSIONS

Group I patients may have impaired ability to increase vascular resistance during orthostatic stress. The inability to overcome isoproterenol-induced vasodilatation during tilt is important in triggering a vasovagal response in group II patients. These data suggest that the population with vasovagal response is heterogeneous. Distinct hemodynamic profiles in response to various provocative maneuvers are definable with noninvasive, continuous monitoring techniques.

Abbreviations and Acronyms
  BP = blood pressure
  CO = cardiac output
  DBP = diastolic blood pressure
  HR = heart rate
  MBP = mean blood pressure
  SBP = systolic blood pressure
  SV = stroke volume
  TPR = total peripheral resistance
  Z = thoracic impedance




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