Result The static pain score of group KF1 and group KF2 during first 12 hours was significantly lower than that of group F( P< 0 05),which became similar after 12 hours.
And side effects such as nausea and vomiting were recorded. Resuls. The percentage of patients with pain score less than 2 at 4hr,8hr,24hr and 48hr was 100%, 77. 5%, 80% and 90% , respectively, And no side effects occurred.
GroupⅠcontinuous infused low concentration remifentanil after operation instantly,and groupⅡinfused normal saline. The changes of hemodynamics,SPO_2,respiratory rate,visual analogue pain score and Sedative score at 1 hour,2 hour,4 hour,8 hour,16 hour,24 hour,48 hour and 72 hour after operation and the side effects all were recorded.
There were no obvious differences in the static pain score and the adverse effects between group KF1 and group KF2.And there was no illusion occurred in three groups.
① Comparison of analgesic integrals of rats in each group: Analgesic integral of Ⅰ phase in allied-decoction group of 40 g/kg was lower significantly than that in model group (82.1±9.8, 95.3±8.7, t=3.17, P < 0.05).
① At 4,12,24 and 48 hours after operation, the analgesia scores in the PCEA group and the intravenous continuous analgesia group were significantly lower than those in the intramuscular analgesia group(t =2.106 to 11.886,P< 0.05),the analgesic effect was better in the PCEA group than in the intravenous continuous analgesia group.
Results: In Group I and Ⅱ, the analgesic scores were (1.25±1.10) and (1.75±1.12) respectively. The remission rates of pain were 85% and 75% respectively.
Objective. To observe the effect of continuous intravenous drip of fentanyl on relief pain after surgery. Method. First,forty postoperative patients (ASA grade Ⅰ - Ⅲ )were given fentanyl 30ug -50ug for a loading dose and then continuous infusion of 20ug - 25ug/hr was administered. The scores for pain and sedation were assessed 4hr,8hr,24hr and 48hr after operation,respectively. And side effects such as nausea and vomiting were recorded. Resuls. The percentage of patients with pain score less than 2 at 4hr,8...
Objective: To evaluate the efficacy and safety of continuous constant epidural infusion morphine combined with 0.125% Bupivcaine for postoperative analgesia after thoracic surgery. Method: One hundred patients scheduled for thoracic surgery under general anesthesia were randomly allocated to one of both groups respectively: CCEA group (n = 50) and intramuscular analgesia group (IM group n = 50). Pain scores .sedation scores and patients satisfaction scores toward analgesia were recorded, and HR, MAP, RR, Sp...
Objective To compare the analgesic effect and motor block of ropivacaine with bupivacaine at low concentration in laboring parturient using patient controlled epidural analgesia(PCEA) Methods Fifty two ASA physical statusⅠ orⅡ full term primiparous parturients were randomized to receive 0 1% ropivacaine fentanyl(n=26) or 0 075% bupivacaine fentanyl(n=26) using a prospective double blind design Basal infusion 6ml/h were supplemented with patient controlled boluses (2ml/h) every 10 min as re...