the hypothesis is that Dexmedetomidine seems to decrease incidence of post-operative delirium . one possible mechanism is that Dex have a minor influence on cognition, since it has no effect on GABA receptor,another is that Dex could induce a sleep similar to natural sleep, thereby decreasing sleep deprivation and circadian rhythm disorder in post-operative patients. In this study , investigators devise the two different sedatives(Dexmedetomidine and Propofol)'influence on postoperative delirium in hip fracture elderly participants under spinal anesthesia
With a complex etiology, delirium is usually caused by various peri-operative stimuli on basis of predisposing factors, including senility, hypoxia and hypotension, pain, drug (such as pethidine, benzodiazepine, anticholinergic, and drug withdrawal), complications prior to surgery, post-operative sleep disorder. As for the mechanism of delirium, the commonly accepted hypothesis includes the decreased central cholinergic neurons function and the inflammation of central nervous system. Most of the hip fracture patients are senile, suffering generally from many complications with exposure to many drugs, and poor in nutritional status with decreased cognitive function even before the surgery in some of them, all of which are risk factors for post-operative delirium. Systematic review suggests that incidence of POD in patients undergoing elective hip arthroplasty is up to 4-53.3%. It is of great importance, therefore, to explore the effective approaches to lower POD incidence in senile patients with operation on hip fracture. Dexmedetomidine Hydrochloride is a novel highly-selective α2 adrenergic receptor agonist, and its selectivity to α2 receptor is 8 times of that of clonidine. It has multiple functions including sedation, anti-anxiety, hypnosis, analgesia and sympathetic blockade, with a wide application prospect for peri-operative patients. Researches suggest that Dex applied peri-operatively may stabilize blood pressure and heart rate, control intra-operative stress, and decrease post-operative side reactions such as nausea, vomiting, restlessness, delirium and chills. Moreover, advantages of Dex also include analgesia and reduction of opioid usage. Clinical pharmacological characteristics of Dex suggest its possible function to decrease post-operative delirium. Meanwhile, Dex seems to have a minor influence on cognition, since it has no effect on GABA receptor. Another important feature of it is that Dex induces a sleep similar to natural sleep, thereby decreasing sleep deprivation and circadian rhythm disorder in post-operative patients, and decreasing incidence of post-operative delirium. Researches evaluating the capability of Dex to decrease delirium incidence are focused on ICU sedation post to operation. Riker et al compared the sedative effect between Dex and midazolam in patients with severe mechanical ventilation, revealing a lower delirium incidence in Dex than in midazolam (54.0% vs 76.6%) in patients maintained with the same depth of sedation. Systematic review concludes that Dex in effective to prevent and treat post-operative delirium in ICU patients. In this study ,the investigators devise the two different sedatives (Dexmedetomidine and Propofol)'influence on postoperative delirium in hip fracture elderly participants under spinal anesthesia
Dexmedetomidine is given to patients during spinal anesthesia at the dose of 0.5 μg/kg,adjusted the dose to keep BIS between 70-80 until 30 minutes before the end of surgery
Propofol is given with an initial ratio of 2-10mg/kg/h, when the operation starts,adjust the propofol's dose to keep BIS between 70-80 before the end of surgery
occurrence of postoperative delirium in postoperative 72 hours
Evaluation of delirium is performed by trained investigational assistant who does not know the randomization of patients. Follow up is carried out before operation and at 9Am and 3Pm during post-operative day 1-3 (POD1-3). During follow up, RASS (Richmond Agitation-Sedation Scale, RASS) is used firstly to evaluate sedation of the patients, and for those with ARSS \>-4 (-3~+4), the Confusion Assessment Method (CAM) is adopted for evaluation. A case consistent with delirium standard at any time point during follow up is determined to be delirium positive. Diagnosis should be confirmed for a CAM-positive patient by a psychological expert based on DSM-V standard
Time frame: patient enrolled will be evaluated at 9Am and 3Pm during post-operative day 1-3 (POD1-3).At any time point above,delirium is detected,then the patient will be diagnosed as postoperative delirium. All patients enrolled is Non-delirium before surgery。
Consumption of analgesic
the patients will receive patient-controlled intravenous analgesia,record the consumption of intravenous analgesia in the 48 postoperative hours
Time frame: record the data of comsumption of analgeisic at 48 hours after operation
Times of intra-operative occurrence of hypotension, bradycardia, hypertension and tachycardia that need treatment.
assess the adverse effect of anaesthetic
Time frame: during the operation
Score of quality of post-operative sleeping
Score of sleeping quality is evaluated based on the some questions during follow up
Time frame: quality of sleeping will be assessed at 9Am during post-operative day 1-3
Hospital stay
the duration from the day of operation to the date meeting discharge criteria as determined by doctor in charge
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Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
SINGLE
Enrollment
1,000
Time frame: record the days of hospital stay at the 30 days after surgery
Post-operative complications besides delirium
complications besides delirium ,such as vomiting,nausea,hypotention,hypertention,bradycardia
Time frame: observe and evaluate complications at the 30 days after surgery
Mortality up to day 30 post to operation
Data for 30-day survival is collected through telephone follow up by the assistant.
Time frame: the data will be collected after 30 days of operation
pain score
describe severity of the pain the patient feel using Numerical Rating Scale (NRS)
Time frame: Pain score will be evaluated at time point of operation, 1,6,24, 48 hours after operation, using NRS score