Am J Perinatol
DOI: 10.1055/a-2253-5665
Review Article

Optimal Delivery Management for the Prevention of Early Neonatal SARS-CoV-2 Infection: Systematic Review and Meta-analysis

Christina S. Chan*
1   Division of Neonatal-Perinatal Medicine, Department of Pediatrics, University of Texas, Southwestern Medical Center, Dallas, Texas
,
Juin Yee Kong*
2   Department of Neonatology, Kandang Kerbau Women's and Children's Hospital, Singapore
,
Rehena Sultana
3   Department of Quantitative Medicine, Centre for Quantitative Medicine, Duke-NUS Medical School, Singapore
,
Vatsala Mundra
4   School of Medicine, University of Texas, Southwestern Medical Center, Dallas, Texas
,
Kikelomo L. Babata
1   Division of Neonatal-Perinatal Medicine, Department of Pediatrics, University of Texas, Southwestern Medical Center, Dallas, Texas
,
Kelly Mazzarella
1   Division of Neonatal-Perinatal Medicine, Department of Pediatrics, University of Texas, Southwestern Medical Center, Dallas, Texas
,
Emily H. Adhikari
5   Department of Obstetrics and Gynecology, University of Texas, Southwestern Medical Center, Dallas, Texas
,
Kee Thai Yeo
2   Department of Neonatology, Kandang Kerbau Women's and Children's Hospital, Singapore
,
Jean-Michel Hascoët
6   Department of Pediatrics, Division of Neonatology, Lorraine University, DevAH, CHRU-Nancy, France
,
Luc P. Brion
1   Division of Neonatal-Perinatal Medicine, Department of Pediatrics, University of Texas, Southwestern Medical Center, Dallas, Texas
› Author Affiliations
Funding L.P.B. has received funding from the National Institutes of Health, from the Gerber Foundation, and from the Children's Medical Center Foundation in Dallas, TX for unrelated research.

Abstract

Objective Delivery management interventions (DMIs) were recommended to prevent delivery-associated transmission of maternal SARS-CoV-2 (severe acute respiratory syndrome coronavirus 2) to infants without evidence of effect on early neonatal SARS-CoV-2 infection (ENI) and neonatal death <28 days of life (ND). This systematic review describes different DMI combinations and the frequency of ENI and ND.

Study Design Individual patient data were collected from articles published from January 1, 2020 to December 31, 2021 from Cochrane review databases, Medline, and Google Scholar. Article inclusion criteria were: documented maternal SARS-CoV-2 polymerase chain reaction (PCR)-positive status 10 days before delivery or symptomatic at delivery with a positive test within 48 hours, known delivery method, and known infant SARS-CoV-2 PCR result. Primary outcomes were ENI (positive PCR at 12 hours to 10 days) and ND. All characteristics were pooled using the DerSimonian–Laird inverse variance method. Primary outcome analyses were performed using logit transformation and random effect. Pooled results were expressed as percentages (95% confidence intervals). Continuity correction was applied for all pooled results if any included study has 0 event.

Results A total of 11,075 publications were screened. 117 publications representing 244 infants and 230 mothers were included. All publications were case reports. ENI and ND were reported in 23.4% (18.2–29.18) and 2.1% (0.67–4.72) of cases, respectively. Among cases with available information, DMIs were reported for physical environment (85–100%), delivery-specific interventions (47–100%), and infant care practices (80–100%). No significant comparisons could be performed between different DMI combinations due to small sample size.

Conclusion The evidence supporting any DMI in SARS-CoV-2-infected mothers to prevent ENI or ND is extremely limited. Limitations of this meta-analysis include high risk of bias, small sample size, and large confidence intervals. This identifies the need for multinational database generation and specific studies designed to provide evidence of DMI guidelines best suited to prevent transmission from mother to neonate.

Key Points

  • In this review we analyzed 2 years of maternal SARS-CoV-2 published cases.

  • We assessed association of delivery management interventions with infant SARS-CoV-2 infection.

  • We found no evidence supporting any DMI for that purpose.

Data Availability Statement

The datasets generated during and/or analyzed during the current study are available from the corresponding author on reasonable request.


* Authors contributed equally.


Supplementary Material



Publication History

Received: 25 May 2023

Accepted: 22 January 2024

Accepted Manuscript online:
24 January 2024

Article published online:
19 February 2024

© 2024. Thieme. All rights reserved.

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