Evidence map›Paper›PMID 40737630›Full record

ArticleUltrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology2025

Is parvovirus B19 infection upsurge in 2023-2024 associated with adverse pregnancy outcome?

S Prasad, A Khalil, Y Yinon, N Regev, R Brawura-Biskupski-Samaha, M Massoud, N Mazanowska, F G Sileo, F Prefumo, P Kosinski and 3 more

Abstract readMulticenter Study
In one paragraph

Article in Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the 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.

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

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

13 authors.

S Prasad *Fetal Medicine Unit, St George's University Hospitals NHS Foundation Trust, University of London, London, UK.ORCID 0000-0003-2329-4470
A Khalil *Fetal Medicine Unit, St George's University Hospitals NHS Foundation Trust, University of London, London, UK.ORCID 0000-0003-2802-7670
Y YinonDepartment of Obstetrics and Gynecology, Sheba Medical Center, Faculty of Medical and Health Sciences, Tel Aviv University, Tel Aviv, Israel.ORCID 0000-0003-0702-370X
N RegevDepartment of Obstetrics and Gynecology, Sheba Medical Center, Faculty of Medical and Health Sciences, Tel Aviv University, Tel Aviv, Israel.
R Brawura-Biskupski-SamahaDepartment of Obstetrics, Perinatology and Neonatology, Centre of Postgraduate Medical Education, Warsaw, Poland.ORCID 0000-0001-5784-873X
M MassoudDepartment of Obstetrics and Gynaecology, University Hospitals Lyon, Lyon, France.
N MazanowskaDepartment of Obstetrics and Gynecology, Institute of Mother and Child, Warsaw, Poland.
F G SileoPrenatal Medicine Unit, Obstetrics and Gynaecology Unit, Department of Medical and Surgical Sciences for Mother, Child and Adult, University of Modena and Reggio Emilia, Modena, Italy.ORCID 0000-0001-7380-0576
F PrefumoObstetrics and Gynecology Unit, IRCCS Istituto Giannina Gaslini, Genova, Italy.ORCID 0000-0001-7793-714X
P KosinskiDepartment of Obstetrics, Perinatology, Gynecology and Reproductive Medicine, Medical University of Warsaw, Warsaw, Poland.ORCID 0000-0003-3812-7560
J Morales RoselloDepartment of Obstetrics and Gynecology, La Fe University and Polytechnic Hospital, Valencia, Spain.
F D'AntonioCenter for Fetal Care and High-Risk Pregnancy, Department of Obstetrics and Gynecology, University "G. d'Annunzio" of Chieti-Pescara, Chieti, Italy.
Collaborators

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveA surge in parvovirus B19 infections has been reported in 2023-2024 across Europe and the USA, raising concerns about the associated perinatal risks. The aim of this study was to compare perinatal outcomes following maternal parvovirus B19 infection during the 2023-2024 period with those from a pre-2023 cohort.

methodsThis multicenter, retrospective cohort study compared perinatal outcomes in women with maternal parvovirus B19 infection according to whether infection occurred pre-2023 (2012-2022) or between 2023 and 2024. Pregnant women with confirmed parvovirus B19 infection were eligible for inclusion. Cases were excluded if they had incomplete records, an ongoing pregnancy, coinfection with cytomegalovirus or Epstein-Barr virus, pre-existing structural or genetic abnormality, immune fetal hydrops or a maternal serology result not indicative of parvovirus B19 infection. The primary outcome was perinatal mortality, which was defined as intrauterine fetal death ≥ 20 weeks' gestation or neonatal death ≤ 28 days after delivery. The secondary outcomes were persistent fetal anemia requiring more than one intrauterine transfusion (IUT) and a composite adverse perinatal outcome (CAPO), defined as the presence of one or more adverse outcomes, including perinatal mortality, pregnancy loss < 20 weeks, new-onset structural anomaly and termination of pregnancy owing to parvovirus-related morbidity. Differences between the two groups were assessed using standard statistical tests, and a generalized linear mixed model was used to identify predictors of perinatal mortality in the 2023-2024 cohort.

resultsFollowing exclusions, 140 cases from pre-2023 and 175 cases from 2023-2024 were analyzed. The rate of fetal hydrops at presentation was similar across the two groups (22.9% in pre-2023 vs 23.4% in 2023-2024; P = 0.905). The rates of perinatal mortality (6.4% in pre-2023 vs 8.0% in 2023-2024; P = 0.294) and CAPO (17.9% in pre-2023 vs 21.7% in 2023-2024; P = 0.395) were not significantly different between groups, but the proportion of fetuses with persistent fetal anemia requiring a second IUT was significantly higher in the 2023-2024 cohort (46.0% vs 19.4%; P = 0.011). For the 2023-2024 cohort, fetal hydrops at presentation was an independent predictor of perinatal mortality (adjusted odds ratio, 10.91 (95% CI, 1.89-63.07); P = 0.007).

conclusionIn this multicenter collaboration, we report perinatal outcomes following maternal parvovirus B19 infection during the recent upsurge and compare them with those of a historical cohort. Although perinatal mortality and CAPO rates were similar between cohorts, cases in the recent surge (2023-2024) required more prenatal interventions, including the need for more than one IUT. Early identification and monitoring remain essential to mitigate adverse perinatal outcomes following maternal parvovirus B19 infection. © 2025 The Author(s). Ultrasound in Obstetrics & Gynecology published by John Wiley & Sons Ltd on behalf of International Society of Ultrasound in Obstetrics and Gynecology.

Indexed as

Erythema InfectiosumParvoviridae InfectionsParvovirus B19, HumanPregnancy Complications, InfectiousAdultEuropeFemaleFetal DeathHumansInfant, NewbornPerinatal MortalityPregnancyPregnancy OutcomeRetrospective StudiesUnited States2023–2024 outbreakadverse pregnancy outcomesfetal anemiafifth diseasehydrops fetalisintrauterine transfusionmaternal infectionparvovirus B19perinatal mortalitypregnancy outcomesslapped‐cheek syndrome

Identifiers

PMID40737630
PMCPMC12401498

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.