Evidence map›Paper›PMID 40208211›Full record

ArticleTransfusion2025

Several features of newborns following intrauterine intravascular blood transfusion for fetal hemolytic disease caused by anti-D alloimmunization.

Altay Babacan, Selenay Sevinc Sarklioglu, Kerem Cavus, Serdar Ümit Sarici

Abstract read
In one paragraph

Article in Transfusion, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Altay BabacanDepartment of Pediatrics, Ufuk University Faculty of Medicine, Ankara, Turkey.ORCID https://orcid.org/0000-0002-1508-1056
Selenay Sevinc SarkliogluDepartment of Genetic Medicine, Weill Cornell Medicine, New York, USA.
Kerem CavusDepartment of Emergency Medicine, Ufuk University, Faculty of Medicine, Ankara, Turkey.
Serdar Ümit SariciDepartment of Pediatrics, Ufuk University, Faculty of Medicine, Ankara, Turkey.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundEarly detection and intervention for fetal hemolytic disease are essential to prevent severe complications. This study evaluates the antenatal and postnatal clinical and laboratory characteristics of newborns who underwent intrauterine intravascular transfusion due to anti-D-induced hemolytic disease. STUDY DESIGN AND

methodsTwenty newborns who received intrauterine transfusions between 18 and 35 weeks of gestation were included. Data on maternal history, transfusion frequency, birth anthropometrics, ABO blood group, D typing, laboratory findings, morbidities, and hospitalization duration were analyzed.

resultsThirteen cases (65%) had anti-D antibody titers ≥1:1024. Intrauterine transfusions were administered once in 55% of cases, twice in 15%, and three or more times in 30%, with a mean gestational age of 29.6 ± 2.3 weeks. The mean birth weight and gestational age were 2478.7 ± 222.03 g and 35.6 ± 2.08 weeks, respectively. Severe hyperbilirubinemia requiring treatment was present in 50% of newborns, while 50% exhibited anemia-related complications. Hypoxic-ischemic encephalopathy and intracranial hemorrhage were observed in 55% and 45% of cases, respectively. Exchange transfusions were required in 65% (once) and 10% (twice) of cases. All newborns received standard hemolytic disease treatments, including high-intensity phototherapy (94.3 ± 22.4 h), infusion therapy (packed red cell transfusions, 10 mL/kg, 8 ± 2 times), and intravenous immunoglobulin (0.5-1 g/kg, 6 ± 1 times).

conclusionNewborns with anti-D-alloimmunization-induced hemolytic disease requiring intrauterine transfusion demand intensive neonatal care to manage anemia, hyperbilirubinemia, hypoxic-ischemic encephalopathy, and intracranial hemorrhage.

Indexed as

Blood Transfusion, IntrauterineErythroblastosis, FetalIsoantibodiesAdultFemaleHumansInfant, NewbornMalePregnancyRetrospective StudiesRho(D) Immune GlobulinIsoantibodiesRHO(D) antibodyRho(D) Immune Globulinhemolytic disease of the fetushemolytic disease of the newbornintrauterine blood transfusionnewborn

Identifiers

PMID40208211
PMCPMC12088306

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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.