Evidence map›Paper›PMID 33173174›Full record

ArticlePediatric research2021

Prediction of ABO hemolytic disease of the newborn using pre- and perinatal quantification of maternal anti-A/anti-B IgG titer.

Grethe R Krog, Mette L Donneborg, Bo M Hansen, Henriette Lorenzen, Frederik B Clausen, Kristian V Jensen, Anette Kjærbye-Thygesen, Per Albertsen, Finn Ebbesen, Thomas Bergholt and 2 more

Abstract read
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Article in Pediatric research, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
3.3field-weighted citation impact, top 8% of its field
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

8 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
  2. The Diagnostic Potential of the L Score for ABO Hemolytic Disease of the Newborn: Insights from a Cross-Sectional Study.Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion · 2024
    Article
  3. End-tidal carbon monoxide concentrations measured within 48 hours of birth predict hemolytic hyperbilirubinemia.Journal of perinatology : official journal of the California Perinatal Association · 2024
    Article
  4. Article
  5. Article
  6. Article
  7. Laboratory Monitoring of Mother, Fetus, and Newborn in Hemolytic Disease of Fetus and Newborn.Transfusion medicine and hemotherapy : offizielles Organ der Deutschen Gesellschaft fur Transfusionsmedizin und Immunhamatologie · 2021
    Review
  8. Hemolytic Disease of the Newborn: A Review of Current Trends and Prospects.Pediatric health, medicine and therapeutics · 2021
    Review
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

12 authors at 6 institutions in 1 country.

Grethe R KrogDepartment of Clinical Immunology, Copenhagen University hospital, Capital Region, Denmark. grethe.risum.krog@regionh.dk.ORCID http://orcid.org/0000-0002-9663-8476
Mette L DonneborgDepartment of Pediatrics, Aalborg University Hospital, North Region, Denmark.
Bo M HansenDepartment of Pediatrics, Herlev Hospital, Capital Region, Denmark.
Henriette LorenzenFaculty of Health, University College Copenhagen, Capital Region, Denmark.
Frederik B ClausenDepartment of Clinical Immunology, Copenhagen University hospital, Capital Region, Denmark.
Kristian V JensenDepartment of Neonatal Intensive Care, Hvidovre Hospital, Capital Region, Denmark.
Anette Kjærbye-ThygesenDepartment of Gynecological Obstetrics, Hvidovre Hospital, Capital Region, Denmark.
Per AlbertsenDepartment of Pediatrics, Nordsjællands Hospital, Capital Region, Denmark.
Finn EbbesenDepartment of Pediatrics, Aalborg University Hospital, North Region, Denmark.
Thomas BergholtInstitute of Clinical Medicine, University of Copenhagen, Capital Region, Denmark.
Mette K SmedMaternity Ward, Copenhagen University hospital, Capital Region, Denmark.
Morten H DziegielDepartment of Clinical Immunology, Copenhagen University hospital, Capital Region, Denmark.
Copenhagen University Hospital · DKUniversity of Copenhagen · DKAalborg University Hospital · DKHvidovre Hospital · DKNordsjællands Hospital · DKUniversity College Copenhagen · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHemolysis in fetus/newborns is often caused by maternal antibodies. There are currently no established screening procedures for maternal ABO antibodies harmful to fetus/newborn. We investigated the clinical significance, and predictive value of maternal anti-A/B titer for hyperbilirubinemia in ABO-incompatible newborns.

methodsWe conducted a case-control study of blood group O mothers and their ABO-compatible (O) vs. -incompatible (A/B) newborns receiving phototherapy, and of ABO-incompatible newborns receiving phototherapy vs. no phototherapy. Newborn data and treatment modalities were recorded, and total serum bilirubin and hemoglobin were measured. Maternal anti-A/B immunoglobulin-γ (IgG) titers were measured prenatally and perinatally, and negative and positive predictive values (NPV, PPV) were calculated to assess the risk of developing hyperbilirubinemia requiring phototherapy.

resultsWe found a significantly higher maternal IgG antibody titer in the case group (p < 0.001). Maternal anti-A/B titers at first trimester had modest predictive values: NPV = 0.82 and PPV = 0.65 for neonatal hyperbilirubinemia; titers at birth improved the predictive values: NPV = 0.93 and PPV = 0.73. Newborn hemoglobin was significantly lower in incompatibles compared to compatibles (p = 0.034). Furthermore, increased anti-A/B IgG production during pregnancy was associated with hyperbilirubinemia and hemolysis in incompatible newborns.

conclusionsThere was a significant association between maternal anti-A/B IgG titer and hyperbilirubinemia requiring treatment. IMPACT: Maternal anti-A/B IgG titer in the first trimester and at birth is predictive of hemolytic disease of the ABO-incompatible newborn. Increased IgG anti-A/B production throughout pregnancy in mothers to ABO-incompatible newborns developing hyperbilirubinemia contrasts a constant or reduced production in mothers to newborns not developing hyperbilirubinemia. Screening tools available in most immunohematology laboratories can identify clinically important IgG anti-A/B. Use of maternal samples taken at birth yielded NPV = 0.93 and PPV = 0.73.

Indexed as

Infant, Newborn, DiseasesABO Blood-Group SystemAdultAutoantibodiesBlood Group IncompatibilityCase-Control StudiesErythroblastosis, FetalFemaleHumansHyperbilirubinemia, NeonatalImmunoglobulin GInfant, NewbornMalePhototherapyPregnancyABO Blood-Group SystemAutoantibodiesImmunoglobulin G

Identifiers

PMID33173174
OpenAlexW3102991022

What OpenQuestion holds

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Registered trials

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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.