Evidence map›Paper›PMID 41862209›Full record

ArticleAmerican journal of perinatology2026

Study Design of the Global Prospective Hemolytic Disease of the Fetus and Newborn Registry (GERANIUM).

May Lee Tjoa, Ashley Orillion, Raymond Mankoski, Nida Imran, Carol Mao, Alexis Krumme, Sylvie Van Hoorde, Blanca Linares-Rivas Rico, Yosuke Komatsu

Registry-linked trialAbstract readClinical Trial Protocol
In one paragraph

Article in American journal of perinatology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT07194070 (Global Prospective Hemolytic Disease of the Fetus and Newborn Registry), which is not on this map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT07194070 recruitingnot on this map

Global Prospective Hemolytic Disease of the Fetus and Newborn Registry

Typeobservational_patient_registrySponsorJanssen Research & Development, LLCRan2025 to 2030Enrolled175ConditionsHemolytic Disease of the Fetus and NewbornArmsStandard of Care
3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

May Lee TjoaJohnson & Johnson, Cambridge, Massachusetts, United States.
Ashley OrillionJohnson & Johnson, Horsham, Pennsylvania, United States.
Raymond MankoskiThe NemetzGroup, Boston, Massachusetts, United States.
Nida ImranJohnson & Johnson, Horsham, Pennsylvania, United States.
Carol MaoJohnson & Johnson, Horsham, Pennsylvania, United States.
Alexis KrummeJohnson & Johnson, Horsham, Pennsylvania, United States.
Sylvie Van HoordeJohnson & Johnson, Beerse, Belgium.
Blanca Linares-Rivas RicoJohnson & Johnson, Madrid, Spain.
Yosuke KomatsuJohnson & Johnson, Spring House, Pennsylvania, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: Hemolytic disease of the fetus and newborn (HDFN) is a rare and serious immune-mediated condition that can result in poor fetal and neonatal outcomes. During pregnancy, monitoring with middle cerebral artery Doppler ultrasound and intrauterine transfusions (IUTs) are the current standard of care, although intravenous immunoglobulin (IVIg) has been adopted in some centers to attempt to delay the onset of fetal anemia. Significant gaps remain in understanding the safety and effectiveness of current HDFN management, both during pregnancy and in neonates and children. We present the design of the Global Prospective Hemolytic Disease of the Fetus and Newborn Registry (GERANIUM; ClinicalTrials.gov Identifier: NCT07194070), a study that will provide real-world, prospective, longitudinal data on management, clinical course, and outcomes of HDFN from the antenatal period up to 2 years after birth. Study Design: GERANIUM is a prospective, observational study enrolling alloimmunized pregnant individuals (aged ≥18 years) before 24 weeks of gestational age who are at high risk for HDFN based on previous obstetric history. This study will enroll approximately 175 participants across multiple global sites. Data collected during pregnancy include fetal loss, frequency and severity of HDFN, treatment patterns, as well as effectiveness and adverse outcomes of IUTs and other interventions. Following birth, infants will be followed for the first 2 years of life, with documentation of HDFN sequelae, including treatments, growth, and development. Impact on the parents and children will be assessed using validated participant- and observer-reported outcome measures. Conclusion: The GERANIUM registry will provide prospective, contemporaneous data on current management of HDFN and associated outcomes. Key Points: · HDFN can result in fetal loss or poor long-term outcomes.. · IUT and IVIg can be associated with serious complications.. · Impacts of HDFN on patients' quality of life are unclear.. · GERANIUM will provide contemporaneous data on HDFN care.. · Prospective data for mothers/infants will be collected..

Indexed as

Erythroblastosis, FetalImmunoglobulins, IntravenousRegistriesBlood Transfusion, IntrauterineFemaleHumansInfant, NewbornMiddle Cerebral ArteryObservational Studies as TopicPregnancyProspective StudiesResearch DesignImmunoglobulins, Intravenous

Identifiers

PMID41862209
PMCPMC13581419

What Socratic holds

Textmetadata
Read underepoch 390

Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.