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Lung transplant recipients undergo bronchoscopy with biopsies for clinical indications and for surveillance in the diagnosis of acute rejection using standard transbronchial forceps. It is recognized that standard forceps biopsies underestimate the presence or degree of airway rejection due to crush artifact and sample size. Transbronchial cryobiopsies have been shown in the literature to provide larger samples without crush artifact in a safe fashion in lung cancer patients. The aim of this study is to determine if transbronchial cryobiopsy is superior to standard transbronchial forceps biopsies in regards to sample size, architecture and the diagnosis of early rejection in lung transplant recipients which if discovered earlier may improve survival.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Cryoprobe biopsy | Active Comparator | All patients enrolled will undergo standard forceps biopsies followed by cryoprobe biopsies and results will be compared |
|
| Forceps Biopsy | Active Comparator | All patients enrolled will undergo standard forceps biopsies followed by cryoprobe biopsies and results will be compared |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Cryoprobe biopsy | Procedure |
| ||
| Forceps Biopsy |
| Measure | Description | Time Frame |
|---|---|---|
| Differences in size of biopsy specimen and architectural preservation of the airways/alveoli (ie degree of crush artifact) | Direct measurements of pathologic specimens from the forceps and cryoprobe will be compared. In addition, amount of crush artifact will alse be directly measured and compared utilizing pathology software which measures area of viable tissue. | From date of study enrollment until the patient is 2 years post lung transplant |
| Measure | Description | Time Frame |
|---|---|---|
| Diagnostic yield (ie presence of acute cellular rejections (ACR), chronic rejection, lymphocytic bronchiolitis and infection) | Each specimen will be independently reviewed by a lung transplant pathology physician to determine the presence or absence of rejection and results compared. All data will be available to the transplant team in the event any rejection is found, it will be acted upon immediately as per the transplant teams protocol. |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Lonny Yarmus | Johns Hopkins University | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Johns Hopkins Hospital | Baltimore | Maryland | 21287 | United States |
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| From date of study enrollment until the patient is 2 years post lung transplant |