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Effect of Furosemide atomization on lung injury after thoracoscopic heart valve surgery

Effect of Furosemide atomization on lung injury after thoracoscopic heart valve surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500101146
Enrollment
Unknown
Registered
2025-04-21
Start date
2023-10-23
Completion date
Unknown
Last updated
2025-04-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Valvular heart disease

Interventions

Blank control group (Group C):no-intervention
Furosemide atomization Group (M group):At the beginning of the operation, the nebulizer, anesthesia circuit and ultrasonic atomizer were connected through T-shaped tube and atomized inhalation was per

Sponsors

The First Affiliated Hospital of Guangxi Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Age 18-65 years old; 2. ASA grade III~IV; 3. Cardiac function grade I to III; 4. Ethical, sign informed consent.

Exclusion criteria

Exclusion criteria: 1. The patient is currently taking immunosuppressant drugs or complicated with diabetes, chronic respiratory diseases, severe liver and kidney dysfunction, immune diseases, and blood diseases; 2. in the active infection stage (leukocyte 10 x 10^9/L); 3. Preoperative ultrasound indicated severe pulmonary hypertension or left ventricular dysfunction: left ventricular ejection fraction (LVEF) 70 mm, cardiothoracic ratio > 0.7; 4. BMI > 35 kg/m^2; 5. Preoperative poor pulmonary oxygenation, blood oxygen saturation < 90%, blood oxygen saturation < 95% when inhaling pure oxygen; 6. People with known allergies to furosemide

Design outcomes

Primary

MeasureTime frame
Lowest murray lung injury score within 6 hours after surgery;Incidence of lung injury 6h after surgery;

Secondary

MeasureTime frame
Internal environmental parameters include arterial blood gas, crystal osmotic pressure, CVP and lactic acid;Respiratory parameters included peak airway pressure, PEEP and dynamic lung compliance;Cell counts in bronchoalveolar lavage fluid(BALF);NO content in BALF;TNF-a content in BALF;Interleukin-6 content in BALF;Interleukin-1ß content in BALF;Intercellular adhesion molecule-1 (ICAM1) content in BALF;Angiopoietin-2 content in BALF;Content of alveolar surface active protein D (SP-D) in BALF;TNF-a content in venous blood;NO content in venous blood;IL-6 content in venous blood;IL-1ß content in venous blood;ICAM1 content in venous blood;Content of pulmonary alveolar surface active protein-D in venous blood;Vascular blood angiopoietin-2 content;Time of postoperative ventilator assistance;ICU stay;Postoperative recovery time (postoperative to discharge time);hospital stays;Secondary intubation rate;Demand for non-invasive ventilation in general wards after surgery;Serious adverse events after surgery;Oxygenation index;Chest radiograph;echocardiography;C-reactive protein;Systemic inflammatory index;Neutrophil/lymphocyte ratio;Platelet/lymphocyte ratio;Urea nitrogen/serum protein ratio;

Countries

China

Contacts

Public ContactQi Mao

The First Affiliated Hospital of Guangxi Medical University

644826829@qq.com+86 152 4068 4649

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026