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Antifibrinolytic and Adjunct Hemostatic Agents: The Pediatric Extracorporeal Membrane Oxygenation Anticoagulation
Katie M Moynihan1,2,3,4,5,6,7,8,9,10,11,12,13,14, Lindsay M Ryerson4,5, Jennifer Le6
1Department of Cardiology, Boston Children's Hospital, Boston, MA.
Insights
Evidence for antifibrinolytics and hemostatic agents in pediatric extracorporeal membrane oxygenation (ECMO) is limited. Further research is needed to establish safe and effective usage strategies for these critical treatments.
Area of Science:
- Pediatric critical care medicine
- Hematology
- Extracorporeal life support
Background:
- Extracorporeal membrane oxygenation (ECMO) is a life-support measure for neonates and children with severe cardiorespiratory failure.
- Bleeding and thrombotic complications are significant challenges during pediatric ECMO.
- Antifibrinolytic and hemostatic agents are often considered to manage these complications, but evidence is scarce.
Purpose of the Study:
- To establish consensus on the use of antifibrinolytics and adjunct hemostatic agents in pediatric ECMO patients.
- To provide evidence-based recommendations and expert consensus statements for managing bleeding and thrombotic issues.
- To inform the Pediatric ECMO Anticoagulation CollaborativE consensus conference.
Main Methods:
- A systematic literature search was conducted across major databases (PubMed, EMBASE, Cochrane Library) from 1988 to 2021.
- A modified Delphi process involving 48 experts was used to develop recommendations and consensus statements.
- Evidence quality was assessed using GRADE, and risk of bias was evaluated using the Quality in Prognosis Studies tool.
Main Results:
- The study identified sparse and inconclusive evidence for antifibrinolytics (epsilon-aminocaproic acid, tranexamic acid), recombinant factor VII activated (rFVIIa), and topical hemostatic agents (THAs).
- One weak recommendation and three consensus statements were generated.
- Consensus was defined as greater than 80% agreement among experts.
Conclusions:
- Current evidence supporting the use of antifibrinolytics, rFVIIa, and THAs in pediatric ECMO is limited and inconclusive.
- Significant research is required to determine optimal and safe strategies for employing these agents.
- Further studies are essential to guide clinical practice in managing hemostatic complications during pediatric ECMO.
Objectives:
To derive systematic-review informed, modified Delphi consensus regarding antifibrinolytic and adjunct hemostatic agents in neonates and children supported with extracorporeal membrane oxygenation (ECMO) for the Pediatric ECMO Anticoagulation CollaborativE consensus conference.
Data Sources:
A structured literature search was performed using PubMed, EMBASE, and Cochrane Library (CENTRAL) databases from January 1988 to May 2021.
Study Selection:
Use of antifibrinolytics (epsilon-aminocaproic acid [EACA] or tranexamic acid), recombinant factor VII activated (rFVIIa), or topical hemostatic agents (THAs).
Data Extraction:
Two authors reviewed all citations independently, with a third independent reviewer resolving conflicts. Eleven references were used for data extraction and informed recommendations. Evidence tables were constructed using a standardized data extraction form.
Measurements And Main Results:
Risk of bias was assessed using the Quality in Prognosis Studies tool. The evidence was evaluated using the Grading of Recommendations Assessment, Development, and Evaluation system. Forty-eight experts met over 2 years to develop evidence-based recommendations and, when evidence was lacking, expert-based consensus statements for the management of bleeding and thrombotic complications in pediatric ECMO patients. A web-based modified Delphi process was used to build consensus via the Research And Development/University of California Appropriateness Method. Consensus was defined as greater than 80% agreement. One weak recommendation and three consensus statements are presented.
Conclusions:
Evidence supporting recommendations for administration of antifibrinolytics (EACA or tranexamic acid), rFVIIa, and THAs were sparse and inconclusive. Much work remains to determine effective and safe usage strategies.
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