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| Name | Class |
|---|---|
| NeuroCure Clinical Research Center, Charite, Berlin | OTHER |
| Department of Infectiology and Pneumonology, Charite, Berlin | UNKNOWN |
| University of Giessen | OTHER |
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Stroke patients frequently suffer from stroke associated pneumonia. Pathophysiologically speaking, dysphagia and central nervous system (CNS)-injury induced immunosuppression largely contribute to the risk for pneumonia. In mouse models for stroke, the self-cleaning mechanisms of the lung are also affected by stroke, possibly further contributing to this risk.
The investigators designed a pilot-study to examine the structural and functional integrity of the self-cleaning mechanisms of the lung in stroke patients.
Survival and functional outcome of stroke is strongly depending on the occurence of pneumonia (stroke-associated pneumonia, SAP). Early diagnose and treatment of SAP is paramount in the treatment of stroke patients. While dysphagia strongly contributes to its pathogenesis, recent years have also shown a strong risk-modulation by CNS injury induced immunosuppression, making stroke patients more susceptible to SAP. Additionally, murine models of stroke showed changes in mucociliary clearance as possible contributors to SAP. It remains unclear, whether structural integrity and mucociliary clearance of the respiratory epithel change in stroke patients, and whether these changes might contribute to the occurence of SAP.
Therefore, the investigators designed this exploratory observational pilot-study to examine the structural and functional integrity of respiratory epithel in severely affected stroke patients and correlate these findings to immune phenotyping and occurence of SAP. The investigators will conduct bronchoscopy in severely affected stroke patients to collect histological samples in order to evaluate multiple tissue predictors, as well as perform optical coherence tomography to examine ciliary kinetics in-vivo. The investigators will furthermore perform serum and plasma immune phenotyping, record occuring pneumonias and correlate these data in order to identify possible predictors of pneumonia.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| stroke |
| ||
| control |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| bronchoscopy | Diagnostic Test | Patients will undergo bronchoscopy to sample respiratory tissue in different heights in order to analyze mucociliary clearance |
|
| Measure | Description | Time Frame |
|---|---|---|
| Mucociliary Clearance | - number of cilia (scanning electron microscopy) | at time of bronchoscopy (within 2 weeks after acute ischemic stroke) |
| Mucociliary Clearance | - activity of cilia given as frequency (in-vivo optical coherence tomography) | at time of bronchoscopy (within 2 weeks after acute ischemic stroke) |
| Measure | Description | Time Frame |
|---|---|---|
| Occurence of stroke-associated pneumonia | Pneumonia is defined according to the consensus recommendations (Smith et al., Stroke 2015) | 7 days after stroke |
| Activity of autonomous nervous system |
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Inclusion Criteria:
Exclusion Criteria:
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The population of the observational cohort consists of severely affected stroke patients, which require diagnostic or therapeutic bronchoscopy, from within out academic stroke center (mostly from the interdisciplinary neurological-neurosurgical intensive care unit). The control group will consist of neurologically healthy individuals presenting for standard bronchoscopy for any reason, i.e. diagnostic exclusion of malignoma. These will be recruited from an academic pneumologic center. Our center is located in the metropolitan area of Berlin. Due to the exploratory, "pilot" characteristics of this study, there will be no targeted inclusion in terms of age or gender, but we aim for a representative sample.
| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Andreas Meisel, Prof. Dr. med. | Contact | +49 30 450 560026 | andreas.meisel@charite.de | |
| Benjamin Hotter, Dr. med. | Contact | +49 30 450 639729 | benjamin.hotter@charite.de |
| Name | Affiliation | Role |
|---|---|---|
| Andreas Meisel, Prof. Dr. med. | Charite University, Berlin, Germany | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| NeuroCure Clinical Research Center (NCRC), Charité | Recruiting | Mitte | 10117 | Germany |
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| ID | Term |
|---|---|
| D000083242 | Ischemic Stroke |
| ID | Term |
|---|---|
| D020521 | Stroke |
| D002561 | Cerebrovascular Disorders |
| D001927 | Brain Diseases |
| D002493 | Central Nervous System Diseases |
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| ID | Term |
|---|---|
| D001999 | Bronchoscopy |
| ID | Term |
|---|---|
| D003948 | Diagnostic Techniques, Respiratory System |
| D019937 | Diagnostic Techniques and Procedures |
| D003933 | Diagnosis |
| D004724 | Endoscopy |
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| University of Luebeck |
| OTHER |
| Labor Berlin - Charité Vivantes GmbH | UNKNOWN |
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Concentration of Cortisol, Adrenaline and Noradrenaline in blood and heart frequency variability
| at time of bronchoscopy (within 2 weeks after acute ischemic stroke) |
| Activity of immune System - Concentration of cytokines | Concentration of cytokines (IL-6, IL-13 and more) in blood | at time of bronchoscopy (within 2 weeks after acute ischemic stroke) |
| Activity of immune System - Concentration of inflammatory markers | Concentration of inflammatory markers (PCT, CRP) in blood | at time of bronchoscopy (within 2 weeks after acute ischemic stroke) |
| Activity of immune System - Expression of HLA-DR | Expression of Human Leukocyte Antigens (HLA)-DR on monocytes in antigens/cell | at time of bronchoscopy (within 2 weeks after acute ischemic stroke) |
| Structural changes in respiratory tissue (nasal, tracheal and bronchial) - Autophagy | Intensity of fluorescence of Light chain (LC) 3b protein, Aurora A and Human enhancer of filamentation (HEF)1 | at time of bronchoscopy (within 2 weeks after acute ischemic stroke) |
| Structural changes in respiratory tissue (nasal, tracheal and bronchial) - Apoptosis | Intensity of fluorescence of TUNEL | at time of bronchoscopy (within 2 weeks after acute ischemic stroke) |
| Structural changes in respiratory tissue (nasal, tracheal and bronchial) - Increase of secretory cells | Expression levels of surfactant protein, Muc5a, SPDEF, Foxa3 | at time of bronchoscopy (within 2 weeks after acute ischemic stroke) |
| D009422 |
| Nervous System Diseases |
| D014652 | Vascular Diseases |
| D002318 | Cardiovascular Diseases |
| D003949 | Diagnostic Techniques, Surgical |
| D019060 | Minimally Invasive Surgical Procedures |
| D013514 | Surgical Procedures, Operative |
| D013510 | Pulmonary Surgical Procedures |
| D019616 | Thoracic Surgical Procedures |