Evidence map›Paper›PMID 39532115›Full record

ArticleAmerican journal of perinatology2025

Identifying Hemolytic Disease of the Fetus and Newborn within a Large Integrated Health Care System.

Fagen Xie, Michael J Fassett, Jiaxiao M Shi, Vicki Y Chiu, Theresa M Im, Sunhea Kim, Nana A Mensah, Nehaa Khadka, Daniella Park, Carol Mao and 3 more

Abstract read
In one paragraph

Article in American journal of perinatology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Article
  2. Article
  3. 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

13 authors.

Fagen XieDepartment of Research and Evaluation, Kaiser Permanente Southern California, Pasadena, California.ORCID 0000-0002-1565-0490
Michael J FassettDepartment of Obstetrics and Gynecology, Kaiser Permanente West Los Angeles Medical Center, Los Angeles, California.
Jiaxiao M ShiDepartment of Research and Evaluation, Kaiser Permanente Southern California, Pasadena, California.
Vicki Y ChiuDepartment of Research and Evaluation, Kaiser Permanente Southern California, Pasadena, California.
Theresa M ImDepartment of Research and Evaluation, Kaiser Permanente Southern California, Pasadena, California.
Sunhea KimDepartment of Research and Evaluation, Kaiser Permanente Southern California, Pasadena, California.
Nana A MensahDepartment of Research and Evaluation, Kaiser Permanente Southern California, Pasadena, California.
Nehaa KhadkaDepartment of Research and Evaluation, Kaiser Permanente Southern California, Pasadena, California.
Daniella ParkDepartment of Research and Evaluation, Kaiser Permanente Southern California, Pasadena, California.
Carol MaoJanssen Global Services LLC, a Johnson & Johnson company, Horsham, Pennsylvania.
Matthew MolaeiJanssen Global Services LLC, a Johnson & Johnson company, Horsham, Pennsylvania.
Iris LinJanssen Scientific Affairs LLC, a Johnson & Johnson company, Horsham, Pennsylvania.
Darios GetahunDepartment of Research and Evaluation, Kaiser Permanente Southern California, Pasadena, California.ORCID 0000-0003-3610-8841

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This study aims to identify hemolytic disease of the fetus and newborn (HDFN) pregnancies using electronic health records (EHRs) from a large integrated health care system.A retrospective cohort study was performed among pregnant patients receiving obstetrical care at Kaiser Permanente Southern California health care system between January 1, 2008, and June 30, 2022. Using structured (diagnostic/procedural codes, medication, and laboratory records) and unstructured (clinical notes analyzed via natural language processing) data abstracted from EHRs, we extracted HDFN-specific "indicators" (maternal positive antibody test and abnormal antibody titer, maternal/infant HDFN diagnosis and blood transfusion, hydrops fetalis, infant intravenous immunoglobulin [IVIG] treatment, jaundice/phototherapy, and first administrated Rho[D] Immune Globulin) to identify potential HDFN pregnancies. Chart reviews and adjudication were then performed on select combinations of indicators for case ascertainment. HDFN due to ABO alloimmunization alone was excluded. The HDFN frequency and proportion of each combination were fully analyzed.Among the 464,711 eligible pregnancies, a total of 136 pregnancies were confirmed as HDFN pregnancies. The percentage of the HDFN-specific indicators ranged from 0.02% (infant IVIG treatment) to 34.53% (infant jaundice/phototherapy) among the eligible pregnancies, and 32.35% (infant IVIG treatment) to 100% (maternal positive antibody test) among the 136 confirmed HDFN pregnancies. Four combination groups of four indicators, four combination groups of five indicators, and the unique combination of six indicators showed 100% of HDFN pregnancies, while 80.88% of confirmed HDFN pregnancies had the indicator combination of maternal positive antibody test, maternal/infant HDFN diagnosis, and infant jaundice/phototherapy.We successfully identified HDFN pregnancies by leveraging a combination of medical indicators extracted from structured and unstructured data that may be used in future pharmacoepidemiologic studies. Traditional indicators (positive antibody test results, high titers, and clinical diagnosis codes) alone did not accurately identify HDFN pregnancies, highlighting an unmet need for improved practices in HDFN coding. · A case ascertainment method was developed to identify HDFN from structured and unstructured data.. · The method used in this study may be used in future pharmacoepidemiologic studies.. · The study highlighted an unmet need for improved practices in HDFN coding..

Indexed as

Delivery of Health Care, IntegratedErythroblastosis, FetalAdultCaliforniaElectronic Health RecordsFemaleHumansImmunoglobulins, IntravenousInfant, NewbornPhototherapyPregnancyRetrospective StudiesImmunoglobulins, Intravenous

Identifiers

PMID39532115
PMCPMC12020509

What OpenQuestion holds

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LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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 OpenQuestion graph.