Perioperative quality of recovery
Conditions
Interventions
Control group:Conventional opioid anesthesia strategy
Experimental group:Esketamine is used for anesthetic induction and maintenance of combined cervical plexus block
Sponsors
Shanxi Bethune Hospital
Eligibility
Sex/Gender
All
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: 1. Age 18-65 years old; 2. American Society of Anesthesiologists (ASA) grade I-II; 3. Body mass index 18.5-30 kg/m^2; 4. Patients who underwent elective partial thyroidectomy and agreed to use a postoperative analgesic pump.
Exclusion criteria
Exclusion criteria: 1. Patients with retrosternal goiter or perioperative lymph node dissection; 2. Patients who are allergic or contraindicated to esketamine or any NMDA receptor antagonist; 3. Patients with severe cardiovascular and cerebrovascular diseases or liver and kidney insufficiency; 4. Patients with a history of hyperthyroidism; 5. Female patients who are pregnant, lactating, or planning to become pregnant; 6. Patients with a history of mental illness; Patients with a history of substance abuse or dependence; 7. Patients who are unable to follow the postoperative follow-up, cooperate with the study plan, or refuse to participate.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 15-item quality of recovery scale score; | — |
Secondary
| Measure | Time frame |
|---|---|
| Anesthesia awakening time and extubation time;Self-rating anxiety scale score;Self-rating depression scale score;Incidence and severity of nausea and vomiting;Incidence of adverse reactions;visual analog scale of pain score;15-item quality of recovery scale score; | — |
Countries
China
Contacts
Public ContactZhang Jianwen
Shanxi Bethune Hospital
Outcome results
None listed