DESCRIPTION OF TIME-DOMAIN-BASED AND FREQUENCY-DOMAIN-BASED MEASURES OF HEART-RATE-VARIABILITY IN INDIVIDUALS TAKING ANTIARRHYTHMICS, BETA-BLOCKERS, CALCIUM-CHANNEL BLOCKERS, AND OR ANTIHYPERTENSIVE DRUGS AFTER SUDDEN CARDIAC-ARREST
Mj. Cowan et al., DESCRIPTION OF TIME-DOMAIN-BASED AND FREQUENCY-DOMAIN-BASED MEASURES OF HEART-RATE-VARIABILITY IN INDIVIDUALS TAKING ANTIARRHYTHMICS, BETA-BLOCKERS, CALCIUM-CHANNEL BLOCKERS, AND OR ANTIHYPERTENSIVE DRUGS AFTER SUDDEN CARDIAC-ARREST, Journal of electrocardiology, 26, 1993, pp. 1-13
Concomitant drug therapies after sudden cardiac arrest and their poten
tial effect of altering heart rate variability (HRV) represent confoun
ding factors in interpreting the outcome of nonpharmacologic therapies
on HRV. The purpose of this study is to describe a broad spectrum of
time-domain and frequency-domain measurements of HRV in 50 individuals
after sudden cardiac arrest. Some of the individuals were taking anti
arrhythmics (n = 9), beta blockers (n = 13), calcium channel blockers
(n = 10), nitrates (n = 8), cardiac glycosides (n = 10), and/or antihy
pertensives (n = 12). Heart rate variability was measured using a Holt
er recorder for 24 hours and the SpaceLabs FT2000 Monitoring System (R
edmond, WA). In those individuals taking antiarrhythmic drugs, the pow
er density within the low-frequency range (.016-.04 Hz) was significan
tly decreased (P = .001) compared to those not taking antiarrhythmics
(n = 41). However, 78% of the people taking antiarrhythmics also had c
ongestive heart failure (New York Heart Association functional classes
II and III), which also decreased HRV. Those individuals taking beta
blockers tended to have slower heart rates (P < .01). The association
between beta blocker use and HRV was positive, but not statistically s
ignificant except for the increased power density in the low-frequency
range (P < .05). In general, the relationships between HRV and drug t
herapy-calcium channel blockers, antihypertensives, cardiac glycosides
, or nitrates-were not statistically significant.