Key result
P&S monitoring successfully differentiated syncope into 3 distinct subtypes (VVS-PE, VVS-HR, and VVS-PN) in 2,727 cardiology patients to facilitate more precise therapy.
Observational (n=2,727)
P&S monitoring can noninvasively differentiate subtypes of vasovagal syncope based on autonomic responses, which may help guide more precise therapy.
Autonomic profiling may help tailor vasovagal syncope management; leaves open whether.
Syncope is difficult to definitively diagnose, even with tilt-table testing and beat-to-beat blood pressure measurements, the gold-standard. Both are qualitative, subjective assessments. There are subtypes of syncope associated with autonomic conditions for which tilt-table testing is not useful. Heart rate variability analyses also include too much ambiguity. Three subtypes of syncope are differentiated: vasovagal syncope (VVS) due to parasympathetic excess (VVS-PE), VVS with abnormal heart rate response (VVS-HR), and VVS without PE (VVS-PN). P&S monitoring (ANSAR, Inc., Philadelphia, PA) differentiates subtypes in 2727 cardiology patients (50.5% female; average age: 57 years; age range: 12-100 years), serially tested over four years (3.3 tests per patient, average). P&S monitoring noninvasively, independently, and simultaneously measures parasympathetic and sympathetic (P&S) activity, including the normal P-decrease followed by an S-increase with head-up postural change (standing). Syncope, as an S-excess (SE) with stand, is differentiated from orthostatic dysfunction (e.g., POTS) as S-withdrawal with stand. Upon standing, VVS-PE is further differentiated as SE with PE, VVS-HR as SE with abnormal HR, and VVS-PN as SE with normal P- and HR-responses. Improved understanding of the underlying pathophysiology by more accurate subtyping leads to more precise therapy and improved outcomes.
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DePace et al. (2018) conducted an observational in Syncope (n=2,727). P&S monitoring was evaluated on Differentiation of syncope subtypes. P&S monitoring successfully differentiated syncope into 3 distinct subtypes (VVS-PE, VVS-HR, and VVS-PN) in 2,727 cardiology patients to facilitate more precise therapy.
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