Perioperative anxiety and pain management in female patients undergoing abdominal surgery
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Patients under general anesthesia who are scheduled to undergo gynecological abdominal surgery; 2. ASA classification grades 1 to 3; 3. Age equal to or greater than 18 years old; 4. The patient voluntarily participated in this study.
Exclusion criteria
Exclusion criteria: 1. Those with functional disorders of important organs such as the heart, liver, lungs and kidneys; 2. Have contraindications for TEAS, such as having implanted electrophysiological devices in the body, local skin damage at electrostimulated acupoints, or being infected; 3. People with communication disorders; 4. Implantable intrathoracic devices, such as pacemakers, defibrillators or any other surgical implants; 5. Those who take drugs or have been using sedatives or anesthetics for a long time; 6. Currently participating in other project researchers.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Postoperative Nausea and Vomiting; | — |
Secondary
| Measure | Time frame |
|---|---|
| Anxiety Visual Analogue Scale;Postoperative pain numerical score;Intraoperative propofol dosage;Intraoperative remifentanil dosage;Intraoperative sufentanil dosage;Anal exhaust;Get out of bed;Evaluation of the three-level recovery status of gastrointestinal function after surgery;Length of stay;Score of the 40-item recovery Quality Rating Scale; | — |
Countries
China
Contacts
Chongqing Traditional Chinese Medicine Hospital