Pediatric bronchopneumonia
Conditions
Interventions
Shallow sedation group:BIS: 50~60
Deep sedation group:BIS: 25~35
Sponsors
the First People's Hospital of Nantong
Eligibility
Sex/Gender
All
Age
5 Years to 12 Years
Inclusion criteria
Inclusion criteria: 1.The clinical treatment was ineffective, and the diagnosis of pediatric pneumonia was confirmed through biochemical indicators and X-ray examination; 2.Presence of symptoms including cough, sputum production, and wheezing; 3.Male or female, aged 5 to 12 years; 4.No history of allergic reaction to the investigational drug;
Exclusion criteria
Exclusion criteria: 1.Combined with significant cardiopulmonary insufficiency; 2.Clinically significant deviations from established laboratory ranges; 3.Presence of a preexisting respiratory tract malformation; 4.Presence of acute or severe bronchial asthma; 5.Incomplete clinical data; 6.History of repeated anesthesia;
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Percent of lung consolidation area; | — |
Secondary
| Measure | Time frame |
|---|---|
| Systemic Inflammation Response Index(SIRI);University of Michigan sedation scale(UMSS);Bispectral Index;Incidence rate of postoperative adverse events;Systemic Immune-inflammation Index (SII);Aggregate Index of Systemic Inflammation (AISI);Total Hospital Stay; | — |
Countries
China
Contacts
Public ContactGu Yi
the First People's Hospital of Nantong
Outcome results
None listed