Evidence map›Paper›PMID 39707247›Full record

ArticleBMC pregnancy and childbirth2024

Hemolytic disease of the fetus and newborn and Rhesus alloimmunization in Latin American countries: a scoping review.

Mário Dias Corrêa Júnior, Salvador Espino Y Sosa, Milene Fernandes, Lais do Carmo, Renato Watanabe de Oliveira, Gabriela Kanevsky

Abstract readScoping Review
In one paragraph

Article in BMC pregnancy and childbirth, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. Article
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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

6 authors.

Mário Dias Corrêa JúniorDepartment of Obstetrics and Gynecology, Minas Gerais Federal University, Campus Health, Av. Prof. Alfredo Balena, 190 - Santa Efigênia, Belo Horizonte, MG, 30130-100, Brazil. correajr@gmail.com.
Salvador Espino Y SosaClinical Research Department, Instituto Nacional de Perinatologia Isidro Espinosa de los Reyes, Mexico City, Mexico.
Milene FernandesRWE and Late Phase, CTI Clinical Trial & Consulting Services, Lisbon, Portugal.
Lais do CarmoHEOR LATAM, Janssen-Cilag, São Paulo, Brazil.
Renato Watanabe de OliveiraRWE LATAM, Janssen-Cilag, São Paulo, Brazil.
Gabriela KanevskyImmunology LATAM, Janssen, Mendoza, Buenos Aires, CP (1428), 1259, Argentina. GKanevsk@ITS.JNJ.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHemolytic disease of the fetus and newborn (HDFN) is a condition due to maternal blood group antibodies targeting antigens in fetal red blood cells, with significant prenatal/perinatal morbidity and mortality. Severe HDFN cases are often associated with alloimmunization against Rhesus D (RhD) or Kell antigens. Information about HDFN epidemiology and treatment in Latin American countries is limited. This review aims to identify and synthesize the available evidence on the epidemiology and management of HDFN in this region.

methodsIn July 2023, EMBASE, PubMed, LILACS, and other databases were searched for articles reporting epidemiology, treatment, prenatal and perinatal outcomes, and patient journey of HDFN cases in Latin American countries. A snowball search of cross-references and gray literature complemented the initial search. Publications in English, Spanish, and Portuguese were reviewed. Data were extracted using a defined template and charted in tables.

resultsWe reviewed five guidelines and 19 observational studies from Brazil, Chile, Mexico, Argentina, Colombia, Panamá, Paraguay, and Peru. HDFN due to Rh alloimmunization ranged from 0.5 to 5 per 1000 live births, and anti-D remains the most frequent alloantibody type for severe HDFN. The perinatal mortality rate of HDFN is approximately 1.3-1.6 per 100,000 live births, and fetal deaths can reach 30% among patients treated with intrauterine transfusions. Up to 47% of alloimmunized pregnancies were referred to reference centers only during the third trimester. About 60% of eligible pregnancies received anti-D IgG prophylaxis.

conclusionsAlthough estimates in LATAM countries are scarce and lack standardized measures, we observed that the incidence, morbidity, and mortality of HDFN in this region are problematic. RhD alloimmunization was reported in approximately up to 70% of severe HDFN cases, despite anti D HDFN being largely preventable.

Indexed as

Erythroblastosis, FetalRh IsoimmunizationFemaleHumansInfant, NewbornIsoantibodiesLatin AmericaPregnancyRh-Hr Blood-Group SystemIsoantibodiesRh-Hr Blood-Group SystemAnemiaErythroblastosisFetalHemolyticInfantLatin AmericaNewbornRh alloimmunization

Identifiers

PMID39707247
PMCPMC11660609

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