Analgesia after uterine fibroid arterial embolization
Conditions
Interventions
Experimental group:Paravertebral block via T12
Control group:None
Sponsors
Department of Anesthesiology, the Second Affiliated Hospital of Suzhou University
Eligibility
Sex/Gender
Female
Age
18 Years to 60 Years
Inclusion criteria
Inclusion criteria: 1.Women aged 18~60 years; 2. ASA ?-?; 3.Patients with MRI reports confirming the diagnosis of uterine fibroids; 4.Symptomatic uterine fibroids with surgical indications; 5.Refuse hysterectomy and voluntarily undergo uterine artery embolization; 6.There are no obvious abnormalities in liver and kidney function examination, no obvious abnormalities in coagulation function, no history of allergy to non steroidal anti-inflammatory drugs, and no history of addiction to sedatives.
Exclusion criteria
Exclusion criteria: 1.Patients with contraindications of regional anesthesia, such as puncture site infection, coagulation dysfunction, severe organ dysfunction and inability to tolerate regional block, etc; 2.Inability to cooperate with treatment and assessment, such as mental disorders, dementia, etc.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Postoperative sufentanil consumption; | — |
Secondary
| Measure | Time frame |
|---|---|
| The press numbers of intraoperative PCIA ;The maximum intraoperative pain score;The pain score immediately after surgery;Postoperative pain score;The maximum pain score within 24h after surgery;The incidence of intraoperative remedial analgesia;The incidence of postoperative remedial analgesia; | — |
Countries
China
Contacts
Public ContactYong Ni
The Second Affiliated Hospital of Soochow University
Outcome results
None listed