Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2025 Apr;12(4):e304-e311.
doi: 10.1016/S2352-3026(25)00029-8.

Rising to the challenge: an international Delphi consensus study on fetal and neonatal alloimmune thrombocytopenia

Affiliations
Review

Rising to the challenge: an international Delphi consensus study on fetal and neonatal alloimmune thrombocytopenia

Romy Pothof et al. Lancet Haematol. 2025 Apr.

Abstract

Fetal and neonatal alloimmune thrombocytopenia (FNAIT) is a condition in which a fetus is at risk for severe thrombocytopenia, possibly resulting in intracranial haemorrhage, due to maternal alloantibodies formed against human platelet antigens (HPAs). Currently, no FNAIT screening programme exists. Pregnancies at risk of FNAIT are identified in individuals who have previously given birth to a child with FNAIT. Management of the condition differs depending on the country. A panel of experts in obstetrics, neonatology, paediatrics, laboratory and transfusion medicine, haematology, health technology assessments, and population screening-related administration who are members of the FNAIT Modified Delphi Expert Group from Europe, the USA, Canada, and Australia, were invited to participate in this study. This Delphi study included three rounds of online questionnaires, which were formulated by professionals from the Dutch FNAIT centre of expertise in collaboration with co-authors, and one live meeting in Leiden, the Netherlands in April, 2023. Funding for the live meeting in Leiden was obtained from the Dutch Research Council. The final questionnaire had 35 statements on current management and a possible antenatal FNAIT screening programme. Answer options were: agree, disagree, neither agree or disagree, and not sufficient knowledge. Consensus threshold was set at 80%. After three rounds of questionnaires, consensus was reached on 25 (71%) of 35 statements. The experts agreed on the use of anti-HPA-1a antibody levels to identify high-risk FNAIT pregnancies, although a cutoff value was not defined. The panel achieved consensus on the design of a cost-effective screening programme based only on anti-HPA-1a antibody level measurement. International differences were observed in case of two aspects: addition of corticosteroids to intravenous immunoglobulins and delivery mode in FNAIT pregnancies. This Delphi study facilitated sharing of international knowledge, which enabled clarification of local policies related to perceived standards of care.

PubMed Disclaimer

Conflict of interest statement

Declaration of interests EJTV declares a PhD grant from Johnson&Johnson; and trial funding from Johnson&Johnson and Rallybio. JB declares support for the present manuscript from David and Elizabeth Sherman, Josephine Lawrence Hopkins Foundation; received research support via contributions to the Platelet Disorders Support Association; declares consulting fees from Janssens, UCB, Argenx, RallyBio; declares participation in a Data Safety Monitoring Board or Advisory Board for UCB for rozanolixizumab; and is a Medical Advisory Board Chair of Platelet Disorder Support Association (ended almost 3 years ago) and the executive committee secretary of the Childrens Cancer and Blood Foundation. BRC received consulting fees from Rallybio; received one honorarium from Chinese Society of Blood Transfusion, Blood Center of Zhejiang Province and Zhejiang Society of Blood Transfusion; and received meeting registration fee from ISBT 2024. HT received consulting fees from Janssen Pharmaceuticals; and declares participation in a Data Safety Monitoring Board or Advisory Board for Janssen Pharmaceuticals. MdH received consulting fees from Johnson&Johnson; and received honorarium as a speaker for Bio-Rad. All other authors declared no competing interests.

Substances

LinkOut - more resources