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Between 10 and 15% of critically ill patients require platelet transfusion within their intensive care unit (ICU).
Platelets (PLT) are given to prevent bleeding in thrombocytopenic patients or to treat bleeding as part of massive transfusion or in bleeding thrombocytopenic patients.
International and local guidelines (American Association of Blood Banks-AABB) are mainly based on experts' opinion. The efficacy of PLT transfusion in the ICU setting remains poorly studied and unknown and the administration of PLT may be associated with adverse effects including an increased risk of hospital acquired infection. Finally, the short PLT shelve-life may be responsible for inventory issues. Altogether, this makes very important to improve the evidence that support PLT transfusion in ICU patients.
This is a multicentre prospective observational study that aims to first determine PLT transfusion efficacy and to identify the parameters associated with transfusion efficacy and to analyse the compliance with international (and local) guidelines of PLT transfusion in ICU patients.
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| Measure | Description | Time Frame |
|---|---|---|
| platelet transfusion efficacy | corrected count platelet increment | between 18 hours and 28 days after transfusion |
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Inclusion Criteria:
Exclusion Criteria:
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Patients admitted to intensive care and receiving platelet transfusion whatever the reason for it.
| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| AUBRON Cécile | Contact | +33 2 98 34 78 59 | cecile.aubron@chu-brest.fr |
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| CHU d'Angers | Recruiting | Angers | 49100 | France |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 37759268 | Derived | Reizine F, Le Marec S, Le Meur A, Consigny M, Berteau F, Bodenes L, Geslain M, McQuilten Z, Le Niger C, Huntzinger J, Seguin P, Thibert JB, Simon D, Reignier J, Egreteau PY, Tadie JM, Huet O, Asfar P, Ehrmann S, Aubron C. Prophylactic platelet transfusion response in critically ill patients: a prospective multicentre observational study. Crit Care. 2023 Sep 27;27(1):373. doi: 10.1186/s13054-023-04650-z. |
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All collected data that underlie results in a publication
Data will be available after the publication of result and ending three years maximum following the last visit of the last patient
Data access requests will be reviewed by the internal committee of Brest UH. requestors will be required to sign and complete a data access agreement
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| ID | Term |
|---|---|
| D016638 | Critical Illness |
| ID | Term |
|---|---|
| D020969 | Disease Attributes |
| D010335 | Pathologic Processes |
| D013568 | Pathological Conditions, Signs and Symptoms |
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| CHRU de Brest | Recruiting | Brest | 29609 | France |
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| CH des Pays de Morlaix | Recruiting | Morlaix | 29 672 | France |
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| CHU de Nantes | Recruiting | Nantes | 44093 | France |
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| CHU de Rennes | Recruiting | Rennes | 35033 | France |
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| CHU de Tours | Recruiting | Tours | 37044 | France |
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| Chba Site de Vannes | Recruiting | Vannes | 56 017 | France |
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