Clinical Study

Suitability, Efficacy, and Safety of Vernakalant for New Onset Atrial Fibrillation in Critically Ill Patients

Table 3

Hemodynamic changes during treatment.

ParametersAll ( )Responders ( )Nonresponders ( ) value

Maximum HR—1/min
 At baseline 127 (70–163)128 (75–160)115 (70–163)0.39
 After 10 minutes112 (60–146)111 (70–140)113 (60–146)0.55
 After 30 minutes105 (61–155)92 (64–146)110 (61–155)0.43
 After 60 minutes99 (69–139)89 (70–130)110 (69–139)0.47
 After 120 minutes95 (70–158)89 (70–146)107 (74–158)0.26
NA requirements
 At baseline11 (34%)6 (35%)5 (33%)1.00
 Dose—mcg/kg/min0.00 (0.00–0.10)0.00 (0.00–0.05)0.00 (0.00–0.10)0.82
MAP
 At baseline 67 (54–90)65 (54–86)68 (62–90)0.11
 After 10 minutes73 (57–103)72 (57–92)75 (62–103)0.58
 After 30 minutes77 (55–103)72 (55–88)84 (59–103)0.02
 After 60 minutes70 (54–101)70 (54–101)75 (55–96)0.19
 After 120 minutes72 (60–106)71 (60–85)76 (62–106)0.04
Lactate—mmol/L
 At baseline 1.1 (0.6–2.1)1.0 (0.6–2.1)1.1 (0.8–1.6)0.92
 After 120 minutes1.2 (0.6–3.1)1.1 (0.6–3.1)1.3 (0.9–1.5)0.79
SvO2—%
 At baseline 63 (49–75)64 (51–75)60 (49–75)0.22
 After 120 minutes65 (48–75)63 (48–75)65 (55–72)0.75

HR: heart rate; MAP: mean arterial pressure; NA: noradrenaline. Results are given as median (minimum–maximum) or numbers (percentages). Groups were compared with Fisher’s exact test or the Mann-Whitney test, as appropriate.