# Maternal and neonatal outcomes following SARS-CoV-2 infection in an unvaccinated pregnant cohort: A trimester-specific analysis

**Authors:** Rozhan Khezri, Kamran Ebrahimi, Saeedeh Askari, Shayesteh Jahanfar, Fateme Darvish Motevalli, Kourosh Javdani Esfehani

PMC · DOI: 10.1371/journal.pone.0341647 · PLOS One · 2026-02-23

## TL;DR

This study shows that unvaccinated pregnant women infected with SARS-CoV-2 in their third trimester face higher risks of preterm birth and worse neonatal outcomes.

## Contribution

The study reveals trimester-specific risks of SARS-CoV-2 infection in unvaccinated pregnant women, emphasizing heightened vulnerability in the third trimester.

## Key findings

- Third-trimester SARS-CoV-2 infection was associated with a 26.4% preterm birth rate, significantly higher than in earlier trimesters.
- Neonates born to mothers infected in the third trimester had lower APGAR scores at 1 and 5 minutes compared to other trimesters.
- Fever was more prevalent in third-trimester infections, but no vertical transmission or neonatal deaths were observed.

## Abstract

Adverse pregnancy outcomes are significant public health issues in developing countries. This study aims to evaluate the trimester-specific impact of COVID-19 infection on maternal and neonatal outcomes in a cohort of unvaccinated Iranian women. A multi-center cross-sectional study was conducted between March 21, 2020, and March 21, 2021, involving 217 unvaccinated pregnant women with RT-PCR-confirmed SARS-CoV-2 infection who delivered in hospitals across three counties in Northwest Iran. Participants were stratified by the trimester of COVID-19 diagnosis: first (n = 20), second (n = 87), and third (n = 110). Data on demographics, as well as maternal, obstetric, and neonatal outcomes, were extracted from the National Health System. Statistical analyses included ANOVA, Chi-square, Fisher’s exact and Kruskal-Wallis tests, with post-hoc Bonferroni corrections. A significant association was found between the trimester of infection and the rate of PTB (p = 0.028). Women infected in the third trimester had a substantially higher PTB rate (26.4%) compared to those infected in the second (11.5%) and first (15.0%) trimesters. Neonatal outcomes also varied significantly; APGAR scores at 1 and 5 minutes were lowest in the third-trimester infection group (8.16 ± 0.78 and 8.39 ± 0.80, respectively) compared to the first (9.08 ± 0.88 and 9.03 ± 0.90) and second (8.45 ± 0.71 and 8.79 ± 0.83) trimesters (p < 0.001 for both). Fever was significantly more prevalent in the third trimester (33.6%) than in the first (10.0%, p = 0.013). No vertical transmission or neonatal deaths were recorded. This study demonstrates a clear trimester-specific risk gradient for SARS-CoV-2 infection in unvaccinated pregnant women. Infection during the third trimester was associated with a significantly increased odds of PTB and lower neonatal APGAR scores(1,5). These findings underscore the critical vulnerability of late pregnancy to COVID-19 complications and highlight the importance of trimester-specific vigilance, enhanced antenatal surveillance, and robust vaccination advocacy for pregnant women.

## Linked entities

- **Diseases:** SARS-CoV-2 (MONDO:0100096), COVID-19 (MONDO:0100096)

## Full-text entities

- **Diseases:** myalgia (MESH:D063806), stillbirth (MESH:D050497), nausea and vomiting (MESH:D020250), uterine irritability (MESH:D014591), neonatal disease (MESH:D007232), miscarriage (MESH:D000022), endothelial (MESH:D005642), infectious diseases (MESH:D003141), sepsis (MESH:D018805), preterm labor (MESH:D007752), death (MESH:D003643), sore throat (MESH:D010612), hypertension (MESH:D006973), neonatal death (MESH:D066087), placental insufficiency (MESH:D010927), thrombotic (MESH:D013927), cough (MESH:D003371), Infection (MESH:D007239), PTB (MESH:D047928), chill (MESH:D023341), COVID-19 (MESH:D000086382), placental damage (MESH:D010922), fatigue (MESH:D005221), chest pain (MESH:D002637), pneumonia (MESH:D011014), hypercoagulability (MESH:D019851), overweight (MESH:D050177), respiratory (MESH:D012131), nausea (MESH:D009325), anosmia (MESH:D000857), vomiting (MESH:D014839), hypoxia (MESH:D000860), respiratory distress syndrome (MESH:D012128), Fever (MESH:D005334), dysgeusia (MESH:D004408), headache (MESH:D006261), inflammation (MESH:D007249), GERD (MESH:D005764), preeclampsia (MESH:D011225), dyspnea (MESH:D004417), pulmonary complications (MESH:D008171)
- **Chemicals:** oxygen (MESH:D010100)
- **Species:** Homo sapiens (human, species) [taxon 9606], Severe acute respiratory syndrome coronavirus 2 (no rank) [taxon 2697049]

## Full text

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## References

31 references — full list in the complete paper: https://tomesphere.com/paper/PMC12928596/full.md

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Source: https://tomesphere.com/paper/PMC12928596