Evidence map›Paper›PMID 35512490›Full record

Observational studyPlacenta2022

The clinical impact of maternal COVID-19 on mothers, their infants, and placentas with an analysis of vertical transfer of maternal SARS-CoV-2-specific IgG antibodies.

J D Ward, C Cornaby, T Kato, R C Gilmore, D Bunch, M B Miller, R C Boucher, J L Schmitz, F A Askin, L R Scanga

Open access · greenAbstract readObservational Study
In one paragraph

Observational study in Placenta, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
3.1field-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

7 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
  2. Observational
  3. Article
  4. Review
  5. Article
  6. Article
  7. 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

10 authors at 2 institutions in 1 country.

J D WardUniversity of North Carolina School of Medicine, Department of Pathology and Laboratory Medicine, Chapel Hill, NC, USA. Electronic address: jeremy.ward@unchealth.unc.edu.
C CornabyImmunology, Histocompatibility and Immunogenetics Laboratories/McLendon Clinical Laboratories UNC Hospitals, Chapel Hill, NC, USA.
T KatoUniversity of North Carolina School of Medicine, Marisco Lung Institute/UNC Cystic Fibrosis Center, Chapel Hill, NC, USA.
R C GilmoreUniversity of North Carolina School of Medicine, Marisco Lung Institute/UNC Cystic Fibrosis Center, Chapel Hill, NC, USA.
D BunchUniversity of North Carolina School of Medicine, Department of Medicine, Division of Nephrology and Hypertension, Chapel Hill, NC, USA.
M B MillerUniversity of North Carolina School of Medicine, Department of Pathology and Laboratory Medicine, Chapel Hill, NC, USA; Clinical Microbiology and Molecular Microbiology Laboratories, University of North Carolina Health Care, Chapel Hill, NC, USA.
R C BoucherUniversity of North Carolina School of Medicine, Marisco Lung Institute/UNC Cystic Fibrosis Center, Chapel Hill, NC, USA.
J L SchmitzUniversity of North Carolina School of Medicine, Department of Pathology and Laboratory Medicine, Chapel Hill, NC, USA; Immunology, Histocompatibility and Immunogenetics Laboratories/McLendon Clinical Laboratories UNC Hospitals, Chapel Hill, NC, USA.
F A AskinUniversity of North Carolina School of Medicine, Department of Pathology and Laboratory Medicine, Chapel Hill, NC, USA.
L R ScangaUniversity of North Carolina School of Medicine, Department of Pathology and Laboratory Medicine, Chapel Hill, NC, USA. Electronic address: lori.scanga@unchealth.unc.edu.
University of North Carolina at Chapel Hill · USUniversity of North Carolina Health Care · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionThe effect of SARS-CoV-2 severity or the trimester of infection in pregnant mothers, placentas, and infants is not fully understood.

methodsA retrospective, observational cohort study in Chapel Hill, NC of 115 mothers with SARS-CoV-2 and singleton pregnancies from December 1, 2019 to May 31, 2021 via chart review to document the infants' weight, length, head circumference, survival, congenital abnormalities, hearing loss, maternal complications, and placental pathology classified by the Amsterdam criteria.

resultsOf the 115 mothers, 85.2% were asymptomatic (n = 37) or had mild (n = 61) symptoms, 13.0% had moderate (n = 9) or severe (n = 6) COVID-19, and 1.74% (n = 2) did not have symptoms recorded. Moderate and severe maternal infections were associated with increased C-section, premature delivery, infant NICU admission, and were more likely to occur in Type 1 (p = 0.0055) and Type 2 (p = 0.0285) diabetic mothers. Only one infant (0.870%) became infected with SARS-CoV-2, which was not via the placenta. Most placentas (n = 63, 54.8%) did not show specific histologic findings; however, a subset showed mild maternal vascular malperfusion (n = 26, 22.6%) and/or mild microscopic ascending intrauterine infection (n = 28, 24.3%). The infants had no identifiable congenital abnormalities, and all infants and mothers survived. DISCUSSION: Most mothers and their infants had a routine clinical course; however, moderate and severe COVID-19 maternal infections were associated with pregnancy complications and premature delivery. Mothers with pre-existing, non-gestational diabetes were at greatest risk of developing moderate or severe COVID-19. The placental injury patterns of maternal vascular malperfusion and/or microscopic ascending intrauterine infection were not associated with maternal COVID-19 severity.

Indexed as

COVID-19Pregnancy Complications, InfectiousPremature BirthFemaleHumansImmunoglobulin GInfantInfectious Disease Transmission, VerticalMothersPlacentaPregnancyRetrospective StudiesSARS-CoV-2Immunoglobulin GMaternal COVID-19Maternal diabetesMaternal vascular malperfusionSARS-CoV-2SARS-CoV-2 antibodies

Identifiers

PMID35512490
PMCPMC9057562
OpenAlexW4225291634

What OpenQuestion holds

Textmetadata
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.