Hypertonic saline solution may enhance cardiac conduction via the fast
inward sodium channel and alter transmembrane Ca++ conductance via th
e sodium-calcium exchanger, Evidence suggests that both Ca++ conductan
ce and myocardial conduction velocity may affect ventricular defibrill
ation, Since hypertonic saline solution solutions (ie, sodium bicarbon
ate) may be administered to patients who have conditions that often re
quire ventricular defibrillation (ie, cardiac arrest or hypovolemic sh
ock), we studied the effect of hypertonic saline solution on the defib
rillation threshold (DFT) in 16 pentobarbital-anesthetized domestic fa
rm swine (20 to 30 kg). Defibrillation was performed using two interfa
ced epicardial electrode patches. DFTs were determined at baseline and
during treatment phase, Pigs were randomly assigned to treatment cons
isting of either hypertonic saline solution (6 mmol/kg load, 2.0 to 3.
0 mmol/kg infusion) to maintain serum sodium concentrations 10 to 15 m
mol/L above baseline or control (D5W given in equal volume), DFT value
s (joules) that predicted 50% success were modeled from a best-fit his
togram, Hypertonic saline solution did not change DFT values from base
line values (10.2+/-4.3 vs 10.8+/-7.0, respectively). Likewise, placeb
o (D5W) did not change DFT values from baseline values (10.1+/-4.5 vs
11.3+/-4.3). During treatment phase, DFT values were 99+/-28% of basel
ine values in the hypertonic saline solution group and 116+/-23% of ba
seline values in the D5W groups (p=0.21). The administration of hypert
onic saline solution also did not affect ventricular conduction veloci
ty, right ventricular action potential duration, or right ventricular
effective refractory period, These data indicate that hypertonic salin
e solution does not appreciably affect defibrillation efficacy or elec
trical treatment of ventricular fibrillation.