Key result
Cardiac deceleration capacity was significantly higher in patients with vasovagal syncope than controls and independently associated with syncope (OR 1.518; 95% CI 1.301-1.770; P=0.0001).
Why the study?
Increased parasympathetic activity is thought to contribute to vasovagal syncope, but direct measurements of vagal control are difficult.
Does cardiac deceleration capacity (DC) measured by 24-hour ECG discriminate patients with vasovagal syncope from healthy controls?
Case-Control (n=226)
Does cardiac deceleration capacity (DC) measured by 24-hour ECG discriminate patients with vasovagal syncope from healthy controls?
Odds Ratio: 1.518 (95% CI 1.301–1.77)
Absolute Event Rate: 9.6% vs 6.5%
p-value: p=0.0001
Cardiac deceleration capacity >7.5 ms may serve as a useful non-invasive tool to monitor cardiac vagal activity and diagnose vasovagal syncope, especially when tilt table testing is negative.
DC >7.12 ms may aid noninvasive vagal assessment in vasovagal syncope; leaves open prospective validation before diagnostic adoption.
Background: Increased parasympathetic activity is thought to play important roles in syncope events of patients with vasovagal syncope (VVS). However, direct measurements of the vagal control are difficult. The novel deceleration capacity (DC) of heart rate measure has been used to characterize the vagal modulation. This study aimed to assess vagal control in patients with VVS and evaluate the diagnostic value of the DC in VVS. Methods: Altogether, 161 consecutive patients with VVS (43±15 years; 62 males) were enrolled. Tilt table test was positive in 101 and negative in 60 patients. Sixty-five healthy subjects were enrolled as controls. DC and heart rate variability in 24-hour ECG, echocardiogram, and biochemical examinations were compared between the syncope and control groups. Results: DC was significantly higher in the syncope group than in the control group (9.6±3.3 versus 6.5±2.0 ms, P <0.001). DC was similarly increased in patients with VVS with a positive and negative tilt table test (9.7±3.5 and 9.4±2.9 ms, P =0.614). In multivariable logistic regression analyses, DC was independently associated with syncope (odds ratio=1.518 [95% CI, 1.301–1.770]; P =0.0001). For the prediction of syncope, the area under curve analysis showed similar values when comparing single DC and combined DC with other risk factors ( P =0.1147). From the receiver operator characteristic curves for syncope discrimination, the optimal cutoff value for the DC was 7.12 ms. Conclusions: DC>7.5 ms may serve as a good tool to monitor cardiac vagal activity and discriminate VVS, particularly in those with negative tilt table test.
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Zheng et al. (2020) conducted a case-control in Vasovagal syncope (n=226). Cardiac deceleration capacity vs. Healthy controls was evaluated on Syncope (OR 1.518, 95% CI 1.301-1.770, p=0.0001). Cardiac deceleration capacity was significantly higher in patients with vasovagal syncope than controls and independently associated with syncope (OR 1.518; 95% CI 1.301-1.770; P=0.0001).
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