J. Weindler et al., Low-dose oral clonidine as premedication before intraocular surgery in retrobulbar anesthesia, EUR J OPTHA, 10(3), 2000, pp. 248-256
PURPOSE. We investigated whether low-dosed oral clonidine premedication bef
ore elective intraocular surgery in retrobulbar anesthesia is effective in
terms of anxiolysis, sedation, stable hemodynamics, lower intraocular press
ure and perioperative endocrine stress response.
METHODS. In a prospective, randomised, double-blind study, 44 patients sche
duled for elective intraocular surgery received either 0.15 mg clonidine (n
=22) or a matched placebo (n=22) orally 60 minutes before retrobulbar anest
hesia. The main study parameters were sedation, anxiolysis, hemodynamics an
d intraocular pressure. Additionally, mediators of endocrine stress respons
es were measured five times, in 13 patients after clonidine and 12 after pl
acebo.
RESULTS. After clonidine 86% of the patients showed sedation and after plac
ebo 90.9% showed no sedation (p<0.01). Clonidine produced effective anxioly
sis (Erlanger-Anxiety-Scale: 31.6 +/- 2.6 points vs. 38.1 +/- 8.5 points) b
efore the operation (p<0.01). Systolic blood pressure was significantly low
er after clonidine. Effects on mean and diastolic blood pressure were small
but statistically significant. Norepinephrine and cortisole plasma concent
rations were significantly lower after clonidine. Intraocular pressure was
significantly lower too (p<0.05). No clinically relevant adverse effects we
re observed e.g. inappropriate sedation, hypotension (<100 mmHg), bradycard
ia (<50 bpm) or hypoxemia (SpO(2)<90%).
CONCLUSIONS. Oral low-dose clonidine produces light sedation, significant a
nxiolysis and stable hemodynamics, and attenuates the endocrine response to
perioperative stress. Thus, clonidine seems sufficient to increase patient
comfort for intraocular surgery and might even offer clinically worthwhile
benefits such as stable hemodynamics and a reduced response to perioperati
ve stress.