Skip to main content
. 2009 May 19;13(3):R75. doi: 10.1186/cc7890

Table 4.

Results: safety

Dexmedetomidine Haloperidol P
ICU mortality, n 0 0 1.00
Hospital mortality, n 0 1 0.31
QTc interval prior to study drug, sec: mean (95% CI) 0.411 (0.384 to 0.438) 0.426 (0.395 to 0.457) 0.41
QTc interval while on study drug, sec: mean (95% CI) 0.395 (0.365 to 0.425) 0.446 (0.423 to 0.457) 0.0061
Patients with abnormal QTc interval (> 0.440 sec) while on study drug: % 40 40 1.00
Patients with longer QTc interval than baseline while on study drug: % 30 70 0.07
Arrhythmia while on study drug: % 20 20 1.00
Patients requiring norepinephrine* infusion while on study drug: % 80 50 0.16
Patients newly requiring norepinephrine or a 20% increase in norepinephrine* infusion in the 8 hours after commencement of study drug: % 20 20 1.00
Of patients requiring norepinephrine, proportion of the time while on study drug receiving norepinephrine: mean (95%CI) 59.8 (17.9 to 100.0) 34.4 (0.0 to 87.1) 0.37
Of patients requiring norepinephrine, level of infusion (μg/min) while on study drug: mean (95%CI) 2.51 (0.07 to 4.90) 3.97 (0.00 to 11.07) 0.55
Any adverse event attributed to the study drug: % 0 10** 0.31
Patients requiring reintubation: n, % 0 0 1.00

* norepinephrine was the only inotropic or vasopressor medication used in any study patient

** excessive prolongation of the QTc interval, necessitating drug discontinuation

CI = confidence interval; ICU = intensive care unit; QTc = QT interval corrected for heart rate.