Lymphatic venous anastomosis could be applied on patients suffering from limb lymphedema after surgery or radiotherapy. The particular pathophysiology leads unconventional fluid treatment strategy and changes in urine output. Hemodynamic monitors shows the benefits in perianesthetic care in fluid maintenance and decrease postanesthetic complication. Invasive hemodynamic monitors, such as arterial line and FlowTrac, have risks of hematoma, infection, nerve injury in puncture site. In this study, photoplethysmography is applied comparing with conventional mean arterial pressure for perianesthetic hemodynamic optimization in bispectral index (BIS)-guided target-controlled infusion sedation on lymphatic venous anastomosis.
After allocation, patients would be assigned to Standard group or ClearSight group. All patients will be sedative with BIS-guided Propofol/Alfentanil Target-Controlled Infusion. The BIS will be maintained between 40-70 with electromyography(EMG) \< 30%. Ce(effect site concentration) of Propofol is adjusted according to BIS score. Ce of Alfentanil is adjusted between 15-75 ng/ml. Patients have spontaneous respiration during the procedure with O2 simple mask. If the oxygen saturation by pulse oximetry(SpO2) \< 95%, prescribe chin lift first. Nasopharyngeal airways is given if chin lift can not improve the saturation. Crystalloid, usually Lactate Ringer, is infused with the rate 4ml/kg/hr. The goal of Standard group is to maintain mean arterial pressure(MAP) \> 60%. If MAP \< 60%, 3ml/kg crystalloid is challenged in 10 minutes. If MAP still less than 60% after the second fluid challenge, Ephedrine 4-8mg iv is prescribed. ClearSight group is to maintain stroke volume(SV). If SV decreases more than 10%, 3ml/kg crystalloid is challenged in 10 minutes. If MAP still less than 60% after the second fluid challenge, Ephedrine 4-8mg iv is prescribed.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
DOUBLE
Enrollment
200
Use radial arterial line to monitor mean arterial pressure
Use Edwards EV1000 Clinical Platform NI with ClearSight finger sleeve to monitor SV(stroke volume)
Maximal MAP fluctuation
In standard group, MAP(mean arterial pressure measured from arterial line), maximum minus minimum
Time frame: after induction until recovery from anesthesia, assessed up to 24 hours
Maximal change of SVV
In ClearSight group, SVV(stroke volume variation measured from ClearSight), maximum minus minimum
Time frame: after induction until recovery from anesthesia, assessed up to 24 hours
Urine output
urine output ml/kg/h
Time frame: after induction until recovery from anesthesia, assessed up to 24 hours
Creatinine
Creatinine (serum)
Time frame: preanesthesia and 24 hours postanesthesia
Acute kidney injury
use AKIN/RIFLE criteria
Time frame: Loss of kidney function that develops within 7 days after surgery
Total fluid volume (ml)
In both groups, total crystalloid fluid volume used during anesthesia
Time frame: after induction until recovery from anesthesia, assessed up to 24 hours
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