Intestinal paralysis after gastrointestinal surgery
Conditions
Interventions
Experimental group
:The experimental group received percutaneous acupoint electrical stimulation + standard nursing
control group:The control group only received standard nursing. The first postoperative exhaust time of the two groups was counted.
Sponsors
Weifang People's Hospital
Eligibility
Sex/Gender
All
Age
20 Years to 60 Years
Inclusion criteria
Inclusion criteria: 1. Age 20-70 years old; 2. It was pathologically confirmed as gastric adenocarcinoma, and the preoperative clinical stage was cT1-4NxM0; 3. Preoperative heart, lung, liver, kidney function can tolerate surgery; 4. Preoperative ASA score was grade I-III; 5. Selective laparoscopic radical gastrectomy was performed with Roux-en-Y anastomosis; 6. No opioids were used for postoperative analgesia; 7. Patients and their families can understand the study protocol and are willing to participate in the study, and sign informed consent.
Exclusion criteria
Exclusion criteria: 1. Gastric adenocarcinoma accompanied by distant metastasis, or concurrent with other abdominal organs of the primary malignant tumor; 2. Patients or family members requested to withdraw from the trial. 3. Patients with perforation, obstruction, bleeding, etc. requiring emergency surgical resection; 4. History of abdominal surgery; 5. Long-term oral laxatives, antilaxatives or other patients that affect exhaust and defecation; 6. Combined with mental or psychological illness.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| First postoperative exhaust time; | — |
Secondary
| Measure | Time frame |
|---|---|
| Time of first defecation;Time of first fluid intake Time of first fluid intake;Resume normal eating times;Short-term postoperative complications (mainly including anastomotic fistula, anastomotic bleeding, and intestinal obstruction);Postoperative hospital stay; | — |
Countries
China
Contacts
Public ContactZhai Shengyong
Weifang People's Hospital
Outcome results
None listed