LORAZEPAM AND MIDAZOLAM IN THE INTENSIVE-CARE UNIT - A RANDOMIZED, PROSPECTIVE, MULTICENTER STUDY OF HEMODYNAMICS, OXYGEN-TRANSPORT, EFFICACY, AND COST
Ac. Cernaianu et al., LORAZEPAM AND MIDAZOLAM IN THE INTENSIVE-CARE UNIT - A RANDOMIZED, PROSPECTIVE, MULTICENTER STUDY OF HEMODYNAMICS, OXYGEN-TRANSPORT, EFFICACY, AND COST, Critical care medicine, 24(2), 1996, pp. 222-228
Objectives: To evaluate and compare the clinical efficacy, impact on h
emodynamic and oxygen transport variables, safety profiles, and cost e
fficiency of sedation and anxiolysis with lorazepam vs. continuous inf
usion of midazolam in critically ill, intensive care unit patients. De
sign: Multicenter, prospective, randomized, open-label study. Setting:
Teaching hospitals. Patients: Ninety five critically ill, mechanicall
y ventilated patients with fiberoptic pulmonary artery catheters in pl
ace were randomly assigned to receive short term (8 hrs) sedation with
either intermittent intravenous injection lorazepam (group A, n = 50)
or continuous intravenous infusion midazolam (group B, n = 45) titrat
ed to clinical response. Measurements and Main Results: The severity o
f illness, demographic characteristics, levels of anxiety and agitatio
n, hemodynamic parameters, oxygen transport variables, quality of seda
tion, nursing acceptance, and laboratory chemistries reflecting drug s
afety were recorded. There were no significant differences with regard
to demographic data, hemodynamic and oxygen transport variables, or l
evels of anxiety and agitation between the two groups at baseline, 5 m
ins, 30 mins, and 4 and 8 hrs after administration of sedation. There
were no significant differences in the quality of sedation or anxiolys
is. Midazolam treated patients used significantly larger amounts of dr
ug for similar levels of sedation and anxiolysis (14.4 +/- 1.2 mg/8 hr
s vs. 1.6 +/- 0.1 mg/8 hrs, p = .001). Both drugs were safely administ
ered and patient and nurse satisfaction was similar. Conclusions: Seda
tion and anxiolysis with lorazepam or midazolam in critically ill pati
ents is safe and clinically effective. Hemodynamic and oxygen transpor
t variables are similarly affected by both drugs. The dose of midazola
m required for sedation is much larger than the dose of lorazepam requ
ired for sedation, and midazolam is therefore less cost efficient.