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recruitment difficulties
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Pulmonary embolism is a frequent and recurrent pathology, especially in the elderly. It is often preventable, with high mortality and morbidity, making it a major public health issue. The clinical presentation of pulmonary embolism is non-specific and very highly variable, ranging from asymptomatic thrombus diagnosed incidentally to sudden death. The current diagnosis of pulmonary embolism is based on several diagnostic techniques, mainly non-invasive, which should be used sequentially.
We propose to sample the volatile organic compounds using a device that allows them to be trapped on polymer cartridges. Sampling will be performed under monitoring of respiratory pressure and a capnograph to collect alveolar and upper respiratory tract air separately without contamination of the oral cavity or sinuses.
This exploratory metabolic analysis will be non-targeted (analysis of all molecules detectable without a priori).
The main objective of the study is to identify specific metabolic profiles to predict the results of ventilation-perfusion pulmonary tomoscintigraphy in subjects undergoing this examination for suspected acute pulmonary embolism.
Secondary purposes :
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Presence of pulmonary embolism | ≥ 1 noninfused and normoventilated segment(s) by pulmonary tomoscintigraphy |
| |
| No pulmonary embolism | Pulmonary perfusion without anomaly (segmental or sub-segmental) by pulmonary tomoscintigraphy |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Pulmonary embolism diagnosis by nuclear medicine imaging | Other | nuclear medicine imaging |
|
| Measure | Description | Time Frame |
|---|---|---|
| quantitative comparison of metabolic profiles | The quantitative variables compared between the two "contributive" groups are the relative quantities of volatile organic compounds (metabolites) detected by chromatographic techniques coupled with mass spectrometry in exhaled air samples. | Metabolites are collected immediately before pulmonary tomoscintigraphy |
| Measure | Description | Time Frame |
|---|---|---|
| Wells score or revised Geneva score | The first secondary outcome consists of the primary outcome (quantitative metabolic variables) to which are added quantitative variables of clinical probability score for pulmonary embolism (Wells score or revised Geneva score). | Clinical scores are collected immediately before pulmonary tomoscintigraphy |
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Inclusion Criteria:
Exclusion Criteria:
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Consecutive patients presenting to the Nuclear Medicine Department of our hospital for a pulmonary ventilation-perfusion tomoscintigraphy will be proposed to participate in the study
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| Name | Affiliation | Role |
|---|---|---|
| Arnaud Agin, PhD | University Hospital, Strasbourg, France | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| University Hospital, Strasbourg, france | Strasbourg | 67000 | France |
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| ID | Term |
|---|---|
| D011655 | Pulmonary Embolism |
| D004194 | Disease |
| ID | Term |
|---|---|
| D008171 | Lung Diseases |
| D012140 | Respiratory Tract Diseases |
| D004617 | Embolism |
| D016769 | Embolism and Thrombosis |
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Exhaled breath (volatile organic compounds trapped on polymer cartridges)
| number and location of deficient segments on ventilation-perfusion pulmonary tomoscintigraphy. |
number and location of deficient segments on ventilation-perfusion pulmonary tomoscintigraphy. |
| day 1 |
| D014652 |
| Vascular Diseases |
| D002318 | Cardiovascular Diseases |
| D010335 | Pathologic Processes |
| D013568 | Pathological Conditions, Signs and Symptoms |