Abstract

Objective To compare the efficacy of different doses of dexmedetomidine for sedation in patients with Parkinson′s disease(PD) undergoing deep brain stimulation(DBS) surgery. Methods Seventy-five patients of both sexes with PD, of American Society of Anesthesiologists physical status Ⅱ or Ⅲ, aged 48-72 yr, with body mass index of 18-24 kg/m2, undergoing elective DBS surgery, were divided into 3 groups(n=25 each) using a random number table method: different doses of dexmedetomidine groups(D1-3 groups). Dexmedetomidine was intravenously infused in a loading dose of 0.5 μg/kg at 10 min before local infiltration anesthesia with 0.25 % ropivacaine 10-20 ml, followed by an infusion of 0.3, 0.5 and 0.8 μg·kg-1·h-1 in D1-3 groups, respectively.The infusion of dexmedetomidine was suspended during neurological test, the patients were awakened, and dexmedetomidine was infused at 0.3, 0.5 and 0.8 μg·kg-1·h-1 until the end of the surgery after the test.Bispectral index(BIS) value was recorded immediately before anesthesia(T0), immediately after administration prior to wake-up(T1) and during neurological test(T2). The wake-up time and adverse reactions such as requirement for rescue analgesics, pulse oxygen saturation(SpO2)<90% and snoring were recorded. Results Compared with group D1, the requirement for rescue analgesics and BIS value at T1, 2 were significantly decreased in D2 and D3 groups, and the wake-up time was significantly prolonged, and the incidence of SpO2<90% and snoring was increased in group D3 (P<0.05 or 0.01). Compared with group D2, the requirement for rescue analgesics and BIS value at T1 were significantly decreased, the wake-up time was prolonged, and the incidence of SpO2<90% and snoring was increased in group D3(P<0.05 or 0.01). Conclusion Dexmedetomidine 0.5 μg·kg-1·h-1 can produce good sedative efficacy and safety for DBS surgery in patients with PD. Key words: Dose-response relationship, drug; Dexmedetomidine; Conscious sedation; Parkinson disease; Electric stimulation

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