Atrial Fibrillation
Conditions
Interventions
conscious sedation :This is a non-interventional retrospective cohort study without experimental interventions.
deep sedation or general anesthesia:This is a non-interventional retrospective cohort study without experimental interventions.
Sponsors
Fuwai Hospital Shenzhen, Chinese Academy of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to 95 Years
Inclusion criteria
Inclusion criteria: 1. Aged 18–95 years on the day of surgery; 2.BMI >=18 kg/m^2; 3.Diagnosed with paroxysmal atrial fibrillation or persistent atrial fibrillation by 12-lead ECG or 24-hour Holter monitoring; 4.Undergoing catheter ablation for atrial fibrillation; 5.Patients receiving combined propofol and dexmedetomidine during atrial fibrillation catheter ablation were assigned to the DS group; 6.Patients receiving combined fentanyl and midazolam during atrial fibrillation catheter ablation were assigned to the CS group; 7.Complete medical record data available to enable assessment of the primary and secondary endpoints;
Exclusion criteria
Exclusion criteria: 1.Incomplete medical record data; 2.Patients who do not meet the inclusion criteria;
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Postoperative hypotension; | — |
Secondary
| Measure | Time frame |
|---|---|
| Operation duration;ncidence of hypotension;Postoperative nausea and vomiting (PONV): use of metoclopramide within 24 hours postoperatively;Length of hospital stay;Hospitalization cost; | — |
Countries
China
Contacts
Public ContactLinlin Chen
Fuwai Hospital Shenzhen, Chinese Academy of Medical Sciences
Outcome results
None listed