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| Name | Class |
|---|---|
| Johannes Gutenberg University Mainz | OTHER |
| University Hospital Greifswald | OTHER |
| University Hospital Dresden | OTHER |
| University Hospital, Aachen |
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Patients treated with Vitamin K antagonists (VKA) or direct oral anticoagulants as Rivaroxaban, Apixaban, Edoxaban or Dabigatran, who experience severe bleeding and/or need urgent interventions/operations that cannot wait are included in this registry, or during emergency operations.
The Registry will offer the opportunity to evaluate the effects of reversal agents as PCC, aPCC, rVIIa, specific antidots in e.g. severe bleeding patients treated with oral anticoagulants.
By collecting case reports from several university hospitals and clinics, different treatment strategies in clinical practice will be observed and evaluated, and may serve as a comprehensive information resource for the safe management with DOA, but also with the long-term anticoagulation based on coumarin derivatives in the near future.
The current objective of this registry is to:
Document the clinical course and outcome of various clinical bleeding events associated with DOA or VKA in patients with severe life-threatening bleeding making intervention necessary
Document the clinical course and outcome of urgent surgical interventions within 24 hours after admission in patients under DOA or VKA treatment.
Characterisation of therapeutic strategies in stopping acute life-threatening bleeding including following agents and methods:
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| DOA | Expected number of patients estimated by study duration N= 90 patients treated with direct oral anticoagulants (DOA) with acute bleeding N= 40 patients treated with direct oral anticoagulants (DOA) with urgent surgical intervention | ||
| VKA | Expected number of patients estimated by study duration N= 90 treated with vitamin K antagonists (VKA) with acute bleeding N= 40 patients treated with vitamin K antagonists (VKA) with urgent surgical intervention |
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| Measure | Description | Time Frame |
|---|---|---|
| Primary Outcome | Primary observation points (for all patients): In hospital mortality up to 30 days after admission Secondary observation points (group of patients with life threatening bleeding under oral anticoagulation)
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| Measure | Description | Time Frame |
|---|---|---|
| Secondary Outcome | Secondary observation points (group of patients with acute surgery under oral anticoagulation)
|
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Patient Eligibility
a) Bleeding patients:
Anticoagulated patients with DOA or VKA with clinically overt major bleeding according to a specified ISTH definition for non-surgical patients:
OR b) Acute surgical need Patients treated with DOA or VKA and who need urgent operation which cannot wait (< 24 h after last intake of drug)
AND
with or without reversal agent use (e.g. PCC, aPCC, rVIIa) (and/or haemodialysis for dabigatran)
AND
provides informed consent after the acute event
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Expected number of patients estimated by study duration
N= 90 patients treated with direct oral anticoagulants (DOA) with acute bleeding N= 90 treated with vitamin K antagonists (VKA) with acute bleeding
N= 40 patients treated with direct oral anticoagulants (DOA) with urgent surgical intervention N= 40 patients treated with vitamin K antagonists (VKA) with urgent surgical intervention
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Cardioangiology Center Bethanien (CCB) | Frankfurt am Main | 60389 | Germany |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 32605708 | Background | Lindhoff-Last E, Herrmann E, Lindau S, Konstantinides S, Grottke O, Nowak-Goettl U, Lucks J, Zydek B, Heymann CV, Birschmann I, Sumnig A, Beyer-Westendorf J, Schellong S, Meybohm P, Greinacher A. Severe Hemorrhage Associated With Oral Anticoagulants. Dtsch Arztebl Int. 2020 May 1;117(18):312-319. doi: 10.3238/arztebl.2020.0312. | |
| 35491419 |
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| ID | Term |
|---|---|
| D006470 | Hemorrhage |
| ID | Term |
|---|---|
| D010335 | Pathologic Processes |
| D013568 | Pathological Conditions, Signs and Symptoms |
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| OTHER |
| Goethe University | OTHER |
| University Hospital Schleswig-Holstein | OTHER |
| Vivantes Netzwerk für Gesundheit GmbH | OTHER |
| Ruhr University of Bochum | OTHER |
| Technische Universität Dresden | OTHER |
| Städtisches Klinikum Dresden-Friedrichstadt | UNKNOWN |
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If possible, left-over from plasma samples ("retention sample") should be used to perform further analyses as drug concentrations. Retention samples of very low volume would suffice for HPLC (information on collection method needed) to assess plasma concentrations of anticoagulants in these patients.
| open |
| Pfeilschifter W, Lindhoff-Last E, Alhashim A, Zydek B, Lindau S, Konstantinides S, Grottke O, Nowak-Gottl U, von Heymann C, Birschmann I, Beyer-Westendorf J, Meybohm P, Greinacher A, Herrmann E; RADOA-Registry Investigators (Reversal Agent use in patients treated with Direct Oral Anticoagulants or vitamin K antagonists Registry). Intracranial bleeding under vitamin K antagonists or direct oral anticoagulants: results of the RADOA registry. Neurol Res Pract. 2022 May 2;4(1):16. doi: 10.1186/s42466-022-00183-y. |