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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 patients needing urgent interventions/operations or in 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 | N= 130 patients treated with direct oral anticoagulants (DOAC) with acute bleeding N= 65 patients treated with direct oral anticoagulants (DOAC) with urgent surgical intervention |
| |
| VKA | N= 130 patients treated with vitamin K antagonists (VKA) with acute bleeding N= 65 patients treated with vitamin K antagonists (VKA) with urgent surgical intervention |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Urgent surgery which can not be postponed to the next 24 hrs | Procedure | The urgent surgical intervention is not part of the registry protocol. The intervention is the acute event that leads to enrollment in the registry. It might be e.g. the surgical treatment of a trauma, fall, acute abdomen, appendicitis or anything else. |
| Measure | Description | Time Frame |
|---|---|---|
| In hospital mortality up to 30 days after admission | Death rate (number of deaths) | up to 30 days after hospital admission |
| Measure | Description | Time Frame |
|---|---|---|
| Stop of bleeding defined according to the treating physicians | Decission according to the treating physicians | up to 30 days after hospital admission |
| Fatality rate caused by unstoppable bleeding |
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Inclusion Criteria:
Group a) Bleeding patients:
OR
Group b) Acute surgical need patients
Exclusion Criteria for Group a and b:
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Expected number of patients estimated by study duration
N= 130 patients treated with direct oral anticoagulants (DOA) with acute bleeding N= 130 treated with vitamin K antagonists (VKA) with acute bleeding
N= 65 patients treated with direct oral anticoagulants (DOA) with urgent surgical intervention N= 65 patients treated with vitamin K antagonists (VKA) with urgent surgical intervention
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| Name | Affiliation | Role |
|---|---|---|
| Edelgard Lindhoff-Last, Prof. | CCB Studienzentrum GmbH | Principal Investigator |
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| 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. |
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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.
|
Death rate (number of deaths)
| up to 30 days after hospital admission |
| Use versus no use of reversal agents - difference in outcome? | documentation of use of reversal agents in eCRF | up to 30 days after hospital admission |
| Definition of supportive measures being effective in stopping bleeding | documentation of supportive measures in eCRF | up to 30 days after hospital admission |
| Effectiveness of dialysis vs. no dialysis in case of dabigatran accumulation associated with bleeding | time frame until stop of bleeding | up to 30 days after hospital admission |
| Causality assessment: Relation of SAE to anticoagulant medication | Decission according to the treating physicians | up to 30 days after hospital admission |
| Blood loss, number of transfusions necessary | documentation of supportive measures in eCRF | up to 30 days after hospital admission |
| Satisfaction of surgeon during and after surgery concerning bleeding | Decission according to the treating physicians | up to 30 days after hospital admission |
| Use versus no use of reversal agents - difference in blood loss and number of transfusions | documentation of supportive measures in eCRF | up to 30 days after hospital admission |
| Delay in performance of surgery due to anticoagulation | time Frame documented in eCRF | up to 30 days after hospital admission |
| ID | Term |
|---|---|
| D006470 | Hemorrhage |
| ID | Term |
|---|---|
| D010335 | Pathologic Processes |
| D013568 | Pathological Conditions, Signs and Symptoms |
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