Bronchoscopy-guided tissue sampling is a central technique in many diseases including diagnosing and staging lung cancers, diagnosing interstitial lung diseases, and acute and/or chronic rejections following lung transplantation. Confocal fluorescence microscopy is a novel technique used for real-time microscopic imaging of proximal and distal airways, microvessels, and inflammatory cells. We hypothesize that confocal fluorescence microscopy images of airways and alveolar structures during standard bronchoscopy could help recognize and classify the presence or absence of acute or chronic rejection in lung transplant recipients.
Bronchoscopy-guided tissue sampling is a central technique in many diseases including diagnosing and staging lung cancers, diagnosing interstitial lung diseases, and acute and/or chronic rejections following lung transplantation. Confocal fluorescence microscopy is a novel technique used for in vivo microscopic imaging of proximal and distal airways including bronchial and alveolar walls, microvessels, and inflammatory cells. We hypothesize that confocal fluorescence microscopy images of bronchiolar and alveolar structures during standard bronchoscopy could help recognize and classify the presence or absence of acute or chronic rejection in lung transplant recipients. The objectives and outcomes of this study are: 1. To assess the safety of confocal microscopy imaging in pediatric patients 2. To create diagnostic criteria for fibered confocal fluorescence microscopy image interpretation of acute and chronic rejections following lung transplantation 3. To determine the sensitivity and specificity of confocal imaging in these patient groups compared to the transbronchial biopsies 4. Correlate confocal images to FEV1 results 5. Correlate with CXRs and/or CT images
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
DIAGNOSTIC
Masking
NONE
-Alveolar imaging
Boston Children's Hospital
Boston, Massachusetts, United States
Sensitivity and specificity of confocal imaging in these patient groups compared to the transbronchial biopsies
Correlate confocal images to histolopathologic findings of acute rejection, chronic rejection, and no evidence of rejection
Time frame: One year
Number of participants with adverse events
Monitor for serious adverse events
Time frame: One year
Correlation of confocal images with FEV1 results
Measure the degree of fibrosis/collagen by confocal imaging and compare to FEV1 values
Time frame: One year
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