Burn
Conditions
Interventions
Experimental group:Propofol combined with alfentanil
Sponsors
Shenzhen Children's Hospital
Eligibility
Sex/Gender
All
Age
0.5 Years to 3 Years
Inclusion criteria
Inclusion criteria: 1. Children who are scheduled to undergo burn dressing change under intravenous anesthesia, aged 6 months to 3 years, ASA I-II grade; 2. The burn area is 5%-30%, and the depth is second degree; 3. Those who change dressings for burns for the first time; 4. Parents or guardians agree to participate in this researcher.
Exclusion criteria
Exclusion criteria: 1. Severe liver and kidney dysfunction; 2. Lung disease and reduced respiratory reserve; 3. Hypersensitivity to opioids or (and) proteins; 4. Patients with neurological diseases such as epilepsy who need to take long-term sedative and antispasmodic drugs and other genetic metabolic diseases; 5. Dressing time exceeds 30 minutes; 6. Parents or guardians do not agree to participate in this researcher.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Average arterial blood pressure;Oxygen saturation;Heart rate;Depth of sedation;Transcutaneous carbon dioxide value;Pain score; | — |
Secondary
| Measure | Time frame |
|---|---|
| Awakening time;Satisfaction of operating physician; | — |
Countries
China
Contacts
Public ContactChen Fang
Shenzhen Children's Hospital
Outcome results
None listed