Long-term pharmacological therapy for vasovagal syncope guided by acute head-up tilt testing resulted in 94% of patients remaining symptom-free compared to 0% in those with an ineffective acute response.
Cohort (n=54)
Randomized
No
Does HUT-guided pharmacological therapy prevent recurrent syncope in patients with vasovagal syncope?
Pharmacological therapy guided by acute drug testing during a head-up tilt test is highly effective in preventing recurrent vasovagal syncope.
Absolute Event Rate: 94% vs 0%
p-value: p=<0.01
The purpose of this study was to determine the efficacy of long-term pharmacological therapy selected on the basis of a head-up tilt test (HUT) in patients in whom reproducibility of the HUT response was demonstrable in the initial study. The HUT (80 degrees upright) was performed for 15 min with or without an infusion of isoproterenol (0.01-0.03 microgram/kg per min) in 54 patients with recurrent unexplained syncope. When vasovagal syncope was induced (positive response), the HUT was repeated to examine the test reproducibility. Vasovagal syncope was induced in 24 patients during HUT alone, and in 30 patients during the HUT with isoproterenol. Acute reproducibility was observed in 49/54 (91%) patients. In the tilt-positive patients, HUT was repeated after an intravenous administration of propranolol (0.1 mg/kg) or disopyramide (1 mg/kg) (acute test). Propranolol proved effective in 21 (80%) of 26 patients, and disopyramide in 13 (56%) of 23 patients. Thereafter, evaluation was done on the long-term clinical follow-up of the pharmacological intervention selected on the basis of the acute test in the 34 patients in whom the HUT could not induce vasovagal syncope after the oral administration of the pharmacological agent (propranolol 60 mg/day, disopyramide 300 mg/day). Thirty-two of 34 patients (94%) did not develop syncopal attacks during a 44 +/- 12-month period. Thus, in patients with unexplained syncope, HUT appears to have a high degree of acute reproducibility, and the acute drug response guided by HUT may be used to develop an effective long-term pharmacological therapy.
Nakagawa et al. (Thu,) conducted a cohort in Vasovagal syncope (n=54). HUT-guided pharmacological therapy (propranolol or disopyramide) vs. Patients with ineffective acute drug response on HUT was evaluated on Freedom from recurrent symptoms (syncope or presyncope) (p=<0.01). Long-term pharmacological therapy for vasovagal syncope guided by acute head-up tilt testing resulted in 94% of patients remaining symptom-free compared to 0% in those with an ineffective acute response.
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