CLINICAL STUDY OF THE EFFICIENCY AND SAFETY OF PATIENT CONTROLLED ANALGESIA WITH LORNOXICAM IN SCHOOL CHILDREN
Hong Liu
Abstract
Hong Liu
Abstract
Objective:To assess the analgesic effect and safety of patient controlled analgesia(PCA) with lornoxicam in patient compared with tramadol. Methods: 60 patients undergoing surgical treatments of gluteus muscle contracture with epidural analgesia and ketamine anesthesia were randomly divided into two groups: group L received PCA with lornoxicam and group T received PCA with tramadol. At the end of operation, 0.15mg/kg lornoxicam was injected as starting dose, 0.3mg/kg lornoxicam was diluted to 100ml with normal saline into PCA pump in group L, and 1mg/kg tramadol was injected as starting bolus dose, 10mg/kg tramadol was diluted to 100ml with normal saline into PCA pump in Group T. The subjects received PCA at the following dosages: bolus dose = 2ml; background infusion = 5ml/h. Lockout was for 15 minutes. After PCA had been started, pain scores,global impression score and side effects were assessed at 1h, 4h, 8h, 12h, 20h. Results: There was no difference in pain scores and global impression scores for PCA between the two groups( P 0.05). Lornoxicam caused fewer adverse effects than tramadol( P 0.01). There was no difference in changes of hepatic, renal functions and coagulation before and after PCA( P 0.05).Conclusions: These results indicate that using Lornoxicam via PCA is an effective and safe method to control postoperative pain as well as tramadol in children.
A significance statement is not available in the OpenAlex record.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
Objective:To assess the analgesic effect and safety of patient controlled analgesia(PCA) with lornoxicam in patient compared with tramadol. Methods: 60 patients undergoing surgical treatments of gluteus muscle contracture with epidural analgesia and ketamine anesthesia were randomly divided into two groups: group L received PCA with lornoxicam and group T received PCA with tramadol. At the end of operation, 0.15mg/kg lornoxicam was injected as starting dose, 0.3mg/kg lornoxicam was diluted to 100ml with normal saline into PCA pump in group L, and 1mg/kg tramadol was injected as starting bolus dose, 10mg/kg tramadol was diluted to 100ml with normal saline into PCA pump in Group T. The subjects received PCA at the following dosages: bolus dose = 2ml; background infusion = 5ml/h. Lockout was for 15 minutes. After PCA had been started, pain scores,global impression score and side effects were assessed at 1h, 4h, 8h, 12h, 20h. Results: There was no difference in pain scores and global impression scores for PCA between the two groups( P 0.05). Lornoxicam caused fewer adverse effects than tramadol( P 0.01). There was no difference in changes of hepatic, renal functions and coagulation before and after PCA( P 0.05).Conclusions: These results indicate that using Lornoxicam via PCA is an effective and safe method to control postoperative pain as well as tramadol in children.
Key concepts: Lornoxicam, Medicine, Tramadol, Anesthesia, Saline, Bolus (digestion), Patient-controlled analgesia, Dose