Stumpfes Bauchtrauma Flashcards

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3
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Epi

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4
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Kinder vs Erw

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5
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Bauchtrauma Pattern

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6
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WElchje Organe betroffen

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7
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Erste Schritte?

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8
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Zeichen fuer intraabd Verletzung

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9
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GCS plus Vitalparameter

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10
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Welcher Index ist relevant?

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11
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Welche Schritt

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Zugang und Labor, und was fuer Labor?

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12
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FAST inludes?

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13
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Problem mit Fast

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14
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Was ist das E-FAST sign

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Im M Mode Sandy Beach vs Barcode

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15
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I CT Abd entspricht

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16
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Was ist die PECARN Prediction Rule?

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17
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NOM Algo? bei Milz oder Leber Verleztung Verdacht

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18
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NOM nach haemodynamischen Status

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19
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Wann ist NOM nicht mehr indiziert

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20
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Versagen NOM wie haeufig?

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21
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Versagen NOM - wann?

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22
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NOM Nachsorge

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23
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Naechster Schritt

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24
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Naechster Schritt?

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26
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Pt die nach Transfusion nicht stabilisiern dann

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27
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Zusammenfassung?

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28
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TXA Indikationen

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The use of tranexamic acid (TXA) in pediatric trauma is guided by emerging evidence and expert consensus, aiming to reduce hemorrhage and improve outcomes. While specific guidelines can vary by institution and region, here are general principles and recommendations based on current understanding and practice:

Pediatric Trauma Guidelines for TXA Use

Indications
- Severe Trauma: TXA is indicated for pediatric patients with significant hemorrhage or those at risk of significant bleeding due to traumatic injuries.
- Evidence of Hemorrhagic Shock: TXA is recommended for children presenting with signs of hemorrhagic shock (e.g., hypotension, tachycardia, altered mental status).
- High-Risk Situations: Situations such as major blunt or penetrating trauma with expected high blood loss.

Dosage and Administration
- Loading Dose: Administer 15 mg/kg intravenously (IV) over 10 minutes. The maximum single dose should not exceed 1 gram.
- Maintenance Dose: Follow the loading dose with an infusion of 2 mg/kg per hour IV over 8 hours. The maximum total dose should not exceed 1 gram over the 8-hour period.

Timing
- Early Administration: TXA should be administered as soon as possible, ideally within 3 hours of injury. Evidence from adult studies suggests that early administration (within 1 hour) is associated with better outcomes. Delayed administration (beyond 3 hours) may be less effective and could potentially be harmful.

Contraindications
- Known Hypersensitivity: Patients with known hypersensitivity to TXA should not receive it.
- Active Thromboembolic Disease: Patients with active thromboembolic conditions such as deep vein thrombosis, pulmonary embolism, or history of recent stroke.
- Renal Impairment: Caution in severe renal impairment; dosage adjustments may be required.

Precautions
- Thromboembolic Risk: Monitor patients closely for signs of thrombosis, especially in those with a history or risk factors for thromboembolic events.
- Seizures: High doses or rapid administration may increase the risk of seizures.

Side Effects
- Common: Nausea, vomiting, diarrhea.
- Serious: Seizures, thromboembolic events, hypersensitivity reactions.

Monitoring
- Hemodynamic Status: Continuous monitoring of vital signs and perfusion.
- Bleeding: Monitor for signs of ongoing bleeding and response to treatment.
- Renal Function: Assess renal function, particularly in patients receiving prolonged therapy or with pre-existing renal conditions.

Evidence and Guidelines
- The use of TXA in pediatric trauma is supported by extrapolation from adult data and limited pediatric studies. The CRASH-2 trial in adults demonstrated a significant reduction in mortality with TXA use in trauma patients.
- The Pediatric Trauma Society and other pediatric critical care bodies may provide specific guidelines and protocols tailored to pediatric populations.

Recommendations from Expert Bodies
- Pediatric Trauma Society (PTS): Advocates for the consideration of TXA in pediatric trauma with significant hemorrhage.
- Advanced Trauma Life Support (ATLS) for Children: Supports the early use of TXA in the management of pediatric trauma with significant bleeding.

Conclusion
While the guidelines for TXA use in pediatric trauma are based on growing evidence, ongoing research and clinical trials will continue to refine these recommendations. Clinicians should integrate these guidelines with clinical judgment and individual patient circumstances to optimize outcomes.