Diaphragmatic dysfunction
Conditions
Interventions
Observational group:None
Sponsors
Jiangsu Cancer Hospital
Eligibility
Sex/Gender
All
Age
18 Years to 79 Years
Inclusion criteria
Inclusion criteria: 1. Aged >=18 years and <80 years; 2. Provided written informed consent prior to study enrollment; 3. Classified as American Society of Anesthesiologists (ASA) Physical Status (PS) Grade II to III; 4. Body mass index (BMI) ranging from 18.5 to 30 kg/m^2; 5. Scheduled to undergo video-assisted thoracoscopic (VATS) lung resection under general anesthesia.
Exclusion criteria
Exclusion criteria: 1. Aged >=80 years; 2. Previous history of thoracic surgery; 3. Patients unable to participate in the study due to physical conditions; 4. Presence of severe vital organ failure; 5. Pregnant or lactating female patients; 6. Patients with diaphragmatic excursion (DE) <=1 cm on preoperative diaphragmatic ultrasonography, indicating potential preoperative diaphragmatic dysfunction; 7. History of respiratory tract infection within 4 weeks preoperatively; 8. Patients currently participating in other clinical trials; 9. Patients who refused to participate in this study; 10. Patients with inadequate ultrasonographic visualization of the diaphragm, precluding acquisition of valid diaphragmatic function measurement data.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Point-of-Care Ultrasound (POCUS) Measurement Indices of the Diaphragm; | — |
Secondary
| Measure | Time frame |
|---|---|
| EIT measure outcome;Chest Drain Duration;PPCs within 7 days after surgery;Visual Analogue Scale (VAS) score for postoperative pain;length of stay after surgery;ICU Length of Stay; | — |
Countries
China
Contacts
Public ContactHe Jianhua
Jiangsu Cancer Hospital
Outcome results
None listed