Acute Lung Injury, Smoke Inhalation Injury
Conditions
Keywords
Smoke Inhalation Injury, Acute Lung Injury, Heparin
Brief summary
This study aims to examine the effects of nebulized heparin on the clinical outcomes in adult patients suffering smoke inhalation injury. Patients will be randomized to receive nebulized heparin or an equal volume of normal saline for 14 days and the incidence of acute lung injury will be compared in either group.
Detailed description
Adult patients who suffered smoke inhalation injury and who are candidates for elective intubation, have evidence of bronchial burn by fiberoptic bronchoscopy, have no evidence of acute lung injury and no more than 24 hours since inhalation injury will be included. Patients will be randomized into 2 groups: Group A (Intervention): Patients will receive 5000 IU heparin mixed with 3 ml saline and nebulized every 4 hours until they are extubated or until 14 days have elapsed whichever is earlier. Group B (Control): Patients will receive 4 ml of normal saline nebulized every 4 hours until they are extubated or until 14 days have elapsed whichever is earlier. The primary end point is the VFDs.
Interventions
DRUGHeparin
Heparin sodium (Generic, 5000 IU/ml ampoules)
OTHERNormal Saline
0.9% sodium chloride solution (normal saline)
Sponsors
Ain Shams University
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
1\. Adult patients indicated for elective intubation: * History of being trapped in a house or industrial fire. * Production of carbonaceous sputum. * Perioral facial burns affecting nose, lips, mouth, or throat . * Altered level of consciousness at any time after the incident and including confusion. * Symptoms of respiratory distress including a sense of suffocation, choking, breathlessness, and wheezing or discomfort affecting the eyes or throat, including irritation of the mucosal membranes. * Signs of respiratory distress including stertorous or labored breathing, and tachypnea or auscultatory abnormalities, including crepitations or rhonchi. * Hoarseness or loss of voice. 2. Evidence of bronchial burn by bronchoscopy to assess severity of inhalational trauma * NO injury: absence of carbonaceous deposits, erythema, oedema, brochorrhea, or obstruction. * Mild injury: minor patchy areas of erythema or carbonaceous deposits in proximal or distal bronchi. * Moderate injury: moderate degree of erythema, carbonaceous deposits, bronchorrhea, or bronchial obstructions. * Sever injury: sever inflammation with friability, copious carbonaceous deposits, bronchorrhea, or obstruction. * Massive injury: evidence of mucosal sloughing, necrosis or endoluminal obliteration. 3\. No evidence of acute lung injury at presentation (either by radiology or ABG) * Radiological findings: Normal lung without increased interstitial markings, ground glass opacification, or consolidation. * ABG findings : PaO2/ Fio2 \> 300. 4. Time between inhalational injury and intubation not longer than 24 hours.
Exclusion criteria
1. Burn injury \> 24 hours. 2. History of pulmonary diseases. 3. Pregnancy or breast feeding. 4. History of allergy to heparin or HIT. 5. History or laboratory evidence of coagulopathy. 6. Burns area \> 50% of total body surface area. -
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| VFDs | 28 days | Number of days free of mechanical ventilation |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| ICU-free days | 28 days | Number of days free from ICU and alive |
| Duration of mechanical ventilation | 28 days | Time from institution to termination of mechanical ventilation |
| Mortality | 28 days | Survival to ICU discharge |
| Side effects | 28 days | Occurrence of heparin-induced adverse effects, e.g., thrombocytopenia, abnormal bleeding |
| P/F ratio | 14 days | PaO2/FiO2 |
Countries
Egypt
Outcome results
None listed