Postpartum pain and depression
Conditions
Interventions
ES+SF group :Esketamine + sufentanil
group B:Butorphanol + sufentanil
NS+SF group :normal saline + sufentanil
Sponsors
Lishui People's Hospital
Eligibility
Sex/Gender
Female
Age
18 Years to 45 Years
Inclusion criteria
Inclusion criteria: 1. Aged 18 to 45 years, American Society of Anesthesiologists (ASA) class II,BMI = 37 weeks); 5. Planned cesarean section under combined lumbar and rigid anesthesia with postoperative self-administered intravenous analgesia; 6. The patients or their family members were informed about the medications used in this study and voluntarily signed the informed consent forms to participate in this research.
Exclusion criteria
Exclusion criteria: 1.Complicated with hypertension, severe heart disease, impaired liver and kidney function, diabetes, eclampsia, preeclampsia, placental abruption, etc.; 2.Abnormal blood coagulation function and contraindications to spinal anesthesia; 3.Use of sedative or analgesic drugs within 2 hours before surgery; 4.Allergy to the study drug; 5.History of alcohol or drug dependence; 6.Complicated with mental system diseases and chronic pain diseases before surgery; 7.Complicated with COVID-19 infection. 8.Those with incomplete data or interrupted follow-up.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Uterine Contraction Pain Score(VAS-U);Incision Resting Pain Score(VAS-R);Incision Movement Pain Score(VAS-P); | — |
Secondary
| Measure | Time frame |
|---|---|
| Depression score;times of PCIA;The times of rescue analgesia;Maternal Satisfaction Score;First Push PCIA Time;The proportion of patients who receive analgesic drug rescue; | — |
Countries
China
Contacts
Public ContactDai Hong
Lishui People's Hospital
Outcome results
None listed