Postoperative gastrointestinal dysfunction
Conditions
Interventions
Lumbar square muscle block group (Group Q):The patient underwent a postoperative ultrasound-guided lumbar-square muscle block
Transversus abdominis fascia plane block group (Group T):The patient underwent a postoperative ultrasound-guided transversus abdominis myofascial planar block
Sponsors
Jiangsu Provincial People's Hospital Suqian Hospital
Eligibility
Sex/Gender
Female
Age
18 Years to 40 Years
Inclusion criteria
Inclusion criteria: 1. patients who underwent cesarean section; 2. aged 18-40 years; 3. American Society of Anesthesiologists (ASA) class I-II; 4. those who voluntarily participated in this study and signed the relevant informed consent form.
Exclusion criteria
Exclusion criteria: 1. Patients with a history of mental illness, alcoholism, drug abuse, or chronic pain; 2. Patients with severe cardiac, hepatic, or renal dysfunction; 3. Patients with a history of prior gastrointestinal surgery; 4. Patients with allergies to intraoperative-related medications; and 5. Any other condition that, in the opinion of the investigator, makes it inappropriate to participate in this trial.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Postoperative I-FEED score; | — |
Secondary
| Measure | Time frame |
|---|---|
| Time to first postoperative bowel movement;Nausea and vomiting score;Postoperative pain VAS score;Quality of Recovery QoR-15 score;Systemic Immunoinflammatory Index;number of analgesic pump compressions;number of postoperative pain remedies (score >=4, flurbiprofenate 100 mg IV);number of gastroretentive remedies (>=5 points, gastroretentive 10 mg IV); | — |
Countries
China
Contacts
Public ContactLiu Jingying
Jiangsu Provincial People's Hospital Suqian Hospital
Outcome results
None listed