SSC Subcommittee on Pediatric and Neonatal Thrombosis and Hemostasis

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The Subcommittee is focused on addressing clinical and scientific issues in pediatric (including neonatal) thrombosis and hemostasis.

If you are interested in the subcommittee and want to follow its activity, please click "join community" to participate.


Mandate
  • To address issues in area of thrombosis in children and neonates.
  • To address issues in area of hemostasis in children and neonates.
  • To develop clinical standards for evaluation of children and neonates suffering from hemostasis and thrombosis problems.
  • To develop clinical research standards recommendations in children and neonates with hemostatic and thrombotic issues.
  • To develop international collaboration using registries, cooperative cohort studies, clinical trials or other appropriate methods in rare hemostasis and thrombosis problems in children and neonates.
  • To generate, publish and distribute reports and recommendations relating to pediatric and neonatal laboratory methods, standards and patient care.
  • To collaborate with other SSCs in appropriate situations.
  • To engage diverse, international, inter-disciplinary, inter-professional participation and representation at all stages of career, in all Pediatric/Neonatal SSC activities and initiatives.

Role

The following are the ongoing activities and responsibilities of the Subcommittee.

  • Educational Program: To continue to provide latest updates to all stakeholder communities (specialists, primary care providers, patients/parents, etc.) on diagnosis, treatment, outcomes, and prevention of disorders pediatric thrombosis and hemostasis, as well as latest recommendations, standards, guidelines/guidances, and research opportunities. 
  • Joint SSC Work: To continue to collaborate with other SSC chairs to promote crossover work, including for example physiologic inhibitors and thrombophilia, control of anticoagulation, and women’s health.
  • Position Papers: To continue to generate position papers to define current status in pediatric thrombosis & hemostasis and related research as well as to generate clinical guidance papers.
  • Working Parties: Groups of experts (hematologists and non-hematologists) have been assembled to further develop position papers relating to a variety of pediatric thrombosis & hemostasis issues.
  • Cooperative Registry and Cohort Study Initiation and Support: Promoting international collaboration to develop/maintain registries and cohort studies for rare pediatric thrombosis and hemostasis issues. Recent examples include the IPTN, AT registry, and severe PC registry.

If you are a member of the Society and would like to know how to participate in the work of this group, please join the group to receive updates on activity or submit an Expression of Interest Form to the Chairman or any of the Co-Chairmen. We would be pleased to learn of your interest.

Leadership

  • Chair - Madhvi Rajpurkar
  • Co-chair - Alessandra Bosch-Spiteri
  • Co-chair - Ernest Amankwah
  • Co-chair - Laura Avila
  • Co-chair - Sophie Jones
  • Co-chair - Christine Sabapathy 
  • Co-chair - Hale Ören
  • Co-chair - Lakshmi Srivaths
  • Co-chair - Hilary Whitworth 

Working Parties

Task Force

  • Cross-Network Data Harmonization and Data Sharing in Pediatric Thrombosis Research (Co-Leads: Julie Jaffray, Christine Sabapathy)

Projects

    Official Communications:

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    Announcements

    • Open for Public Comment: Diagnosing and evaluating women and girls with hemophilia

      Per the Guidelines and Guidance (G&G) Committee process for guidance manuscripts, draft manuscripts go through a public comment period and G&G Committee review and approval before submitting the manuscript to the Journal of Thrombosis and Haemostasis (JTH).

       

      The G&G Committee would like to announce that the guidance manuscript titled, " The Diagnosis and Evaluation of Women and Girls with Hemophilia and Hemophilia Carriers: Guidance from the SSC of the ISTH," is now open for public comment. Note: This manuscript is confidential and in draft form.

       

      Please click here to submit your comments by Thursday, February 19, 2026.

    • Save the Date: An Educational Day on Pediatric Hemostasis will be held on Friday, July 10, 2026!

      Save the Date:

      An Educational Day on Pediatric Hemostasis and Thrombotic Disorders will be held on Friday, July 10, 2026, ahead of the ISTH Annual Congress in Paris. Additional details regarding the venue and agenda will be shared in due course.

      This educational initiative is being conducted in coordination with the French Society on Thrombosis and Hemostasis(Club des Pédiatres en Hémostase – Société Française de Thrombose et d'Hémostase [SFTH]), the International Pediatric Thrombosis Network (IPTN), and the Pediatric and Neonatal Subcommittee of the SSC of the ISTH. The program will focus on contemporary topics in pediatric bleeding and thrombotic disorders and is intentionally designed to complement, and not duplicate, the Pediatric/Neonatal SSC scientific session.

      We look forward to your future participation.

      With best regards,
      Madhvi

    • Your participation in the DengueCBDR study is being requested

      Dear Colleagues,

      On behalf of the Hemostasis Working Party of the Pediatric/Neonatal Thrombosis and Haemostasis Subcommittee, we are pleased to invite your center to participate in a collaborative research initiative entitled “International Registry of Dengue Infection in Congenital Bleeding Disorders (DengueCBDR).” This study has been approved by the International Society on Thrombosis and Haemostasis.

      Patients with congenital bleeding disorders are at increased risk of bleeding complications during dengue virus infection due to thrombocytopenia, platelet dysfunction, vascular leakage, and coagulopathy. Despite the clinical importance of this issue, there is currently a lack of comprehensive international registry data addressing bleeding manifestations, management strategies, and outcomes in this vulnerable population.

      The primary objective of this study is to evaluate bleeding complications, management approaches, clinical outcomes, and associated complications in patients with congenital bleeding disorders—such as hemophilia, von Willebrand disease, and platelet disorders—who are affected by dengue infection. Your participation would make a valuable contribution to improving the understanding and management of bleeding in this clinical context.

       To facilitate data collection, the study group has developed a REDCap-based electronic data capture system for patient registration. The full study proposal in English is available upon request for centers interested in participating.

      Should you require further information or wish to express interest in joining this international registry, please contact Nongnuch.sir@mahidol.ac.th. or fill in your contact information https://docs.google.com/forms/d/e/1FAIpQLSdY8BM1O5nTQHJoSuW-Knm_EXBSaer5oh34JuuSNhLTqvrSUw/viewform?usp=header

      We would be honored to collaborate with your institution on this important initiative.

      Yours sincerely,

      Nongnuch Sirachainan MD

      On behalf of the Hemostasis Working Party

      Pediatric/Neonatal Thrombosis and Haemostasis Subcommittee

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    Community Admins

    Children's Hospital of Michigan / Wayne State University/Central Michigan University
    United States