Author/Authors :
Mireskandari, Mohammad Otorhinolaryngology Research Center - Tehran University of Medical Sciences, Tehran, Iran , Makarem, Jalil Department of Anesthesia and Intensive Care - Imam Khomeini Hospital Complex - Tehran University of Medical Sciences, Tehran, Iran , Saedi, Babak Otorhinolaryngology Research Center - Tehran University of Medical Sciences, Tehran, Iran , Jafarzadeh, Afshin Department of Anesthesia and Intensive Care - Imam Khomeini Hospital Complex - Tehran University of Medical Sciences, Tehran, Iran , Karvandian, Kasra Department of Anesthesia and Intensive Care - Imam Khomeini Hospital Complex - Tehran University of Medical Sciences, Tehran, Iran , Eftekhar, Negar Department of Anesthesia and Intensive Care - Imam Khomeini Hospital Complex - Tehran University of Medical Sciences, Tehran, Iran , Samadi, Shahram Department of Anesthesia and Intensive Care - Imam Khomeini Hospital Complex - Tehran University of Medical Sciences, Tehran, Iran , Majedi, Hossein Department of Anesthesia and Intensive Care - Imam Khomeini Hospital Complex - Tehran University of Medical Sciences, Tehran, Iran , Amali, Amin Otorhinolaryngology Research Center - Tehran University of Medical Sciences, Tehran, Iran , Toosi, Roja Otorhinolaryngology Research Center - Tehran University of Medical Sciences, Tehran, Iran , Naghavi, Batool Otorhinolaryngology Research Center - Tehran University of Medical Sciences, Tehran, Iran , Vosoughi, Fardis Otorhinolaryngology Research Center - Tehran University of Medical Sciences, Tehran, Iran
Abstract :
Background: The aim of this study was to assess the quality of the surgical field,
amount of blood loss, and duration of surgery following induced hypotension with
labetalol, nitroglycerin, and high dose propofol in patients undergoing FESS under
general anesthesia.
Methods: One hundred and eight patients scheduled for FESS under general
anesthesia were recruited in this randomized trial and were allocated to one of the
three study groups: 1) Nitroglycerine (NTG) group: nitroglycerine with a dose of 2-
5 μg/kg/min was administered; 2) Labetalol (LAB) group: an IV bolus dose of
labetalol (20 mg) was injected at first and then IV infusion of labetalol at a rate of 1-
2 mg/min; 3) High dose propofol plus normal saline (0.5-1 ml/min) group.
Hemodynamic variables and the amount of bleeding were recorded intraoperatively
and the surgeons' satisfaction was asked following each surgery considering the
surgical field quality using a 5-item Likert scale.
Results: The average blood loss (ml) in patients in the LAB group was significantly
less than patients in NTG and high dose propofol groups (127 ml vs 198 and 145 ml,
respectively) (p- value=0.001) and the surgeons expressed greater satisfaction with
the surgical field quality in the LAB group (p- value=0.001).
Conclusion: Labetalol infusion may be a safe and effective method for induction of
controlled hypotension to provide a comparatively bloodless field. High dose
propofol may be a second choice if labetalol is not available.
Keywords :
Propofol , Nitroglycerine , Labetalol , Induced hypotension , Functional endoscopic sinus surgery