Early postoperative pain in patients undergoing laparoscopic cholecystectomy
Conditions
Interventions
C Group:Classical Music Therapy
B Group:blank control
I Group :Individualized music therapy
Sponsors
Huzhou Center Hospital
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1. ASAI~II; 2. Age 18~65 years old; 3. First time undergoing abdominal surgery; 4. Subjects voluntarily participate in this study and sign the informed consent form.
Exclusion criteria
Exclusion criteria: 1. The skin of the proposed music treatment area is damaged, red, swollen, infected, etc.; 2. Tinnitus, arrhythmia, etc. before surgery; 3. Patients with artificial devices such as pacemakers; 4. History of previous major abdominal surgery; 5. Chronic pain, neuropathic pain, long-term use of painkillers or other psychotropic drugs; 6. Morbidly obese (body mass index (BMI) > 35 kg/m^2); 7. Combined with psychiatric and neurological diseases, infections, severe anxiety, severe insomnia, severe cardiovascular and cerebrovascular diseases, liver and kidney dysfunction, hematopoietic system diseases, etc.; 8. Unwilling to join the group and unable to complete the pilot plan.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Postoperative 6h VAS pain score; | — |
Secondary
| Measure | Time frame |
|---|---|
| Preoperative 24h and postoperative 24h sleep indices;Neutrophil to lymphocyte ratio (NLR);Number of postoperative remedial analgesia, and use of analgesic drugs;VAS pain scores at 24h preoperatively and 24h postoperatively;Postoperative 24h nausea and vomiting score (PONV score);Patient Satisfaction Score (1-10);Anxiety score (STAI-S scale) 24h preoperatively and 24h postoperatively;24h preoperative and 24h postoperative 15-item quality of recovery score (QOR15 scale); | — |
Countries
China
Contacts
Public ContactHe Huanzhong
Huzhou Center Hospital
Outcome results
None listed