INCLEN XIX CHINA

 
                         

 

RESEARCH AND TRAINING FOR IMPROVING

EQUITY, EFFICIENCY AND QUALITY IN HEALTH CARE

 
 

 

 


  Dr. Li Lei M.D., M.Sc.

 

 

ORAL PRESENTATION  35

 

ACUPOINT INJECTION WITH 0.9% SALINE FOR THE PREVENTING NAUSEA AND VOMITING AFTER TOTAL ABDOMINAL HYSTERECTOMY

Li Lei, MD1, Supranee  Niruthisard, MD2 Somjai Wangsuphachart, MD3, Somrat Lertmaharit 4

1  Department of Nuclear Medicine, Kunming Medical College,  Kunming, Yanna, P.R. of China

2  Department of Anesthesiology, Faculty of Medicine, Chulalongkorn University, Thailand

3   Department of Radiology and Clinical Epidemiology Unit, Faculty of Medicine, Chulalongkorn  University, Thailand

4   Department of Preventive and Social Medicine, Faculty of Medicine, Chulalongkorn University, Thailand

 

Objective: To study the effectiveness of  acupoint injection with 0.9% saline at the four acupoints (both side of PC-6 and ST-36) for the prevention of nausea and vomiting after total abdominal hysterectomy (TAH) under general anesthesia (GA).

Design: A prospective, randomized, double-blinded, placebo-controlled trial.

Setting: This protocol was approved by Faculty of Medicine, Chulalongkorn University ethics committee, and informed consent was obtained from all patients in King Chulalongkorn Memorial Hospital, Thai Red Cross Society.

Participants: ASA physical status I-III, aging 20-60 years, weighing between 45-80 Kg, no carcinoma,  scheduling for total abdominal hysterectomy under general anesthesia. Sixty two cases entered the study, sixty one patients finished the study, one case was excluded for operative accidence. The eligible patients were allocated into two groups by block randomization, placebo group was 31 cases, acupoint group was 30 cases.

Interventions: Both groups of patients were under the standard general anesthesia and total abdominal hysterectomy. At the end of the operation, muscle relaxant was reversed, the patient was extubated,  the patient in the study group received acupoint injection with 0.9% saline 2 ml into each PC-6 and 3 ml into each ST-36, while the control group did not get any injection. Then identical adhesive tapes were applied to the acupoints before patient was transferred to the recovery room.

Outcome measures: Efficacy was assessed by measuring complete response rate (no nausea, no vomiting and no rescue antiemetics) in both groups for the first 24 hours after the  operation as primary  outcome, while the number of retching and vomiting as well as antiemetic rescue used within 24 hours in both groups were the secondary outcomes. 

Results:  1. There was no statistical significant difference in the complete response rate( % ) between the two groups ( 43.3% in acupoint group, while 35.5% in control group ). 95% CI of  the difference is between - 0.167  to  0.323. 2.  However, the number of  vomiting in  acupoint group was significantly less than control group (P =0.024) in first 24 hours, especially during 6-24 hours (P = 0.005). 

Conclusion: Acupoint injection with normal saline does not reduce the overall incidence of  post operative nausea and vomiting in 24 hours after total abdominal hysterectomy under general anesthesia. However it does reduce the severity and intensity of PONV in terms of  number of  retching and vomiting in first 24 hours after the operation.

Key words: Acupoint injection, 0.9% saline, total abdominal hysterectomy, general anesthesia, postoperative nausea and vomiting.