Association between maternal coronavirus disease 2019 and transient tachypnea of the newborn: a single-center study

Article information

Clin Exp Pediatr. 2023;66(11):493-500

Publication date (electronic) : 2023 October 24

doi : https://doi.org/10.3345/cep.2023.00563

Sung Hee Lee, MD¹, Ju Hyun Jin, MD¹, Jong Ha Yoo, MD², Shin Won Yoon, MD^,1

¹Department of Pediatrics, National Health Insurance Service Ilsan Hospital, Goyang, Korea

²Department of Laboratory Medicine, National Health Insurance Service Ilsan Hospital, Goyang, Korea

Corresponding author: Shin Won Yoon, MD. Department of Pediatrics, National Health Insurance Service Ilsan Hospital, 100 Ilsan-ro, Ilsandon-gu, Goyang 10444, Korea Email: swyoon@nhimc.or.kr

Received 2023 April 13; Revised 2023 August 16; Accepted 2023 August 18.

Abstract

Introduction

Since December 2019, as severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) became a pandemic, the number of pregnant women infected with SARS-CoV-2 also increased [1]. Some studies raised concerns regarding the possibility of vertical transmission while others reported that the risk is almost negligible [2-5]. There are limited analyses regarding coronavirus disease 2019 (COVID-19) on maternal and neonatal clinical features but outcomes are unclear [6-8]. Korean guidelines recommend the isolation of neonates either in a negative pressure room or in a private room at the neonatal intensive care unit (NICU) when negative pressure rooms are unavailable [9]. However, this policy delays mother-infant bonding and makes breastfeeding difficult. The Centers for Disease Control and Prevention (CDC) and the World Health Organization recommend rooming-in for breastfeeding with no need for separation of mothers and neonates [10,11]. A few studies have reported adverse neonatal outcomes of COVID-19 infected mothers; however, these associations are still unclear [7,8,12]. Currently, limited data with small sample sizes are available regarding the risk of perinatal infection and neonatal outcomes of infants born to COVID-19 infected mothers in Korea [1,13,14]. A recent Korean National Mother-Child Cohort study on neonatal outcomes discovered a possible association of COVID-19 mothers with increased NICU admission [15]. However, this association is not clear since the isolation policy may have affected admission. Moreover, the detailed clinical respiratory outcome was not presented in the data.

This study aimed to compare the clinical outcomes of neonates born to mothers who had COVID-19 during pregnancy with those born to mothers who did not. In addition, by providing information on the clinical outcomes of newborns, we seek to secure a basis for re-examining the current national neonatal infection response guidelines for COVID-19.

Methods

2. Study population

This single-center retrospective study was conducted in neonates born to mothers with COVID-19 from February 2021 to March 2022 at the National Health Insurance Service (NHIS) Ilsan Hospital, a COVID-19 designated hospital. A total of 556 neonates were born during this period, with 156 born to mothers with COVID-19 (Fig. 1). Among the 156 neonates, 113 were born to mothers with COVID-19 within 2 weeks of delivery. For the 1:2 matched case-control analysis, neonates under 35 weeks gestational age (GA) were excluded, and 103 neonates born to infected mothers were assigned to the case group and 206 to the control group. The control group comprised neonates with matched GA born to mothers without COVID-19 at NHIS Ilsan Hospital during the same period. COVID-19 was confirmed by a positive result in the OP/NP swab reverse transcription quantitative real-time PCR (RT-PCR).

Fig. 1.

Flow chart of study participants. A total of 103 neonates (≥35 weeks’ GA) born to mothers infected with SARS-CoV-2 within 2 weeks of delivery were matched to 206 GA-matched neonates in the control group. GA, gestational age; COVID-19, coronavirus disease 2019; SARSCoV-2, severe acute respiratory syndrome coronavirus 2.

Results

1. Clinical characteristics of SARS-CoV-2 infected mothers

Table 1 presents the clinical characteristics of the 99 mothers infected with SARS-CoV-2 who were confirmed RT-PCR positive within 2 weeks of delivery. The average fetal exposure to maternal COVID-19 infection was approximately 5 days. Only 12 mothers (12.12%) had been vaccinated against SARS-CoV-2 during pregnancy. Seventy-nine mothers (79.8%) exhibited symptoms such as fever, cough, sputum, and anosmia, and 15 (15.15%) were diagnosed with pneumonia, as confirmed by chest radiography. Regarding the severity of the disease, 2 mothers (2.02%) infected with COVID-19 required oxygen therapy, 3 (3.03%) required HFNC, and none required invasive ventilator care. Five mothers (5.05%) were diagnosed with hypertension, and 14 (14.14%) had GDM. PROM (3.03%) and preterm labor (4.04%) occurred, but no fetal distress. Placental pathology was performed in 14 mothers, and abnormal findings such as infarction, thrombosis, or inflammation were identified in 11 (78.57%).

Table 1.

Clinical characteristics of mothers with COVID-19 (N=99)

2. Clinical characteristics of neonates born to SARS-CoV-2 infected mothers

Table 2 shows the neonatal clinical characteristics obtained by matching the case and control groups at a 1:2 ratio according to GA at delivery. A total of 103 neonates with late preterm or term birth (GA ≥ 35 weeks) were included in the case group, and 206 in the control group were matched.

Table 2.

Clinical characteristics of neonates (≥35 weeks’ GA) born to mothers with COVID-19 versus GA-matched controls

The mean GA of the case group was 38.45±1.27 weeks, with the majority (88.4%) were born full-term. The mean birth weight was 3,120.95±397.19 g, and 94.2% weighed ≥2,500 g. Four infants (3.94%) were SGA, 58 (56.3%) were male, and 4 pairs (7.8%) were twins. The mean Apgar scores were 7 and 9 at 1 and 5 minutes, respectively. All neonates in the case group were admitted to the NICU for isolation, while 30% of the control group needed NICU admission (P<0.001). The cesarean section (C-section) rate was higher in the case group compared to the control group (91.26% vs. 40.29%, P<0.001).

All neonates had negative RT-PCR results from OP/NP swabs taken at 24 hours and repeated at 48 hours. In the antibody test, 15 neonates (14.85%) tested positive for IgG, but none tested positive for IgM.

3. Outcomes of neonates born to SARS-CoV-2 infected mothers

Table 3 shows the outcomes obtained by matching the case and control groups at a 1:2 ratio according to GA at delivery. There were significant differences between the 2 groups regarding length of stay (P=0.020), TTN (P<0.001), use of noninvasive ventilation (P=0.040), and supplemental oxygen (P=0.022). There was no significant difference between the 2 groups for RDS, MAS, use of invasive ventilation, or duration of respiratory support.

Table 3.

Outcomes of neonates (≥35 weeks’ GA) born to mothers with COVID-19 versus GA-matched controls

4. Logistic regression analyses of outcomes neonates born to mothers with COVID-19 adjusted for covariates.

Table 4 shows the univariate and multivariate logistic regression analysis of the association between SARS-CoV-2 infected mothers and neonatal respiratory outcomes. The risk of TTN (OR, 3.53; 95% CI, 1.83–6.80; adjusted OR [AOR], 3.69; 95% CI, 1.69–8.07), use of noninvasive respiratory ventilator (OR, 2.06; 95% CI, 1.09–3.89; AOR, 2.28; 95% CI, 1.05–4.97), and supplemental oxygen (OR, 3.06; 95% CI, 1.13–8.28; AOR, 4.83; 95% CI, 1.46–15.95) significantly increased after adjusting for covariates, including maternal age, obstetric complications (hypertension and GDM), mode of delivery, birth weight, sex, and SGA.

Table 4.

Uni- and multivariate logistic regression analyses of respiratory outcomes of neonates (≥35 weeks’ GA) born to mothers with COVID-19 versus GA-matched controls

Discussion

The NHIS Ilsan Hospital, a designated COVID-19 hospital, has the most experience in delivering infected mothers with COVID-19 in Korea. To our knowledge, this single-center study included the largest Korean cohort of neonates born to mothers with COVID-19. Among the 113 neonates born to 106 mothers with COVID-19, none tested positive for SARS-CoV-2; however, adverse outcomes with an increased risk of TTN were associated with maternal COVID-19 infection.

In a previous systematic review of 201 neonates, 4 (2.4%) were reported to have confirmed SARS-CoV-2 infection during the first 48 hours of life [6]. In a retrospective cohort analysis conducted at a single center in New York, 2 of 101 neonates had indeterminate test results for SARS-CoV-2 nasopharyngeal swabs [17]. There was no evidence of vertical or antenatal transmission of SARS-CoV-2 infection in our study, as many previous articles have shown [2,3].

Several studies have revealed that maternal COVID-19 infection increases the risk of adverse neonatal outcomes, but these associations remain unclear [6,7,18]. This largest single-center study in Korea is comparable to a nationwide cohort study in Sweden [7], in which 2,323 infants delivered by SARs-CoV-2 positive mothers exhibited a significant association with admission to the neonatal unit (OR, 1.47), RDS (OR, 2.4), any respiratory disorder (OR, 1.42), and hyperbilirubinemia (OR, 1.47) after matching for maternal characteristics [7]. In England, another national cohort study restricted to full-term pregnancies (GA ≥37 weeks) reported no significant differences in neonatal adverse outcomes but a higher likelihood of longer postnatal hospital stay (21.1% compared with 12.6%; AOR, 1.61) [8]. A recent Korean multicenter retrospective cohort study conducted in 15 hospitals included 62 newborns [1]. They focused on the findings that the severity of the disease in pregnant women infected with SARS-CoV-2 did not affect neonatal outcomes [1]. Our study highlighted the short-term neonatal respiratory outcomes of mothers with COVID-19. A 1:2 case-control matched analysis showed significant differences between the 2 groups in the length of stay (P=0.020), TTN (P<0.001), use of noninvasive ventilation (P=0.040), and oxygen supplement (P=0.022).

Over 91% of the study group underwent C-section. As we know, C-section has the potential to increase the risk of TTN, and infants delivered by planned C-section without labor are more likely to develop respiratory distress [19]. At our institution, elective cesarean delivery was preferred due to strong infection control restrictions. During the early era of the epidemic in China, C-sections were performed to reduce the risk of intrapartum transmission. A meta-analysis of 1,100 pregnancies, reported a high cesarean rate of 85% [20]. Severity of maternal infection may increase obstetric decisions to deliver, but with the low vertical transmission rate, there is no need for an elective C-section because of COVID-19 itself. Because cesarean deliveries are associated with increased neonatal morbidity, the decision to deliver by C-section should be carefully considered [21].

Our study found that maternal COVID-19 infection was still associated with a higher risk of TTN after controlling for other factors that may affect neonatal outcomes, including C-section. The multivariate regression analysis showed that neonates of mothers with COVID-19 were 3.69 times more likely to have TTN, 2.28 times more likely to use noninvasive ventilation, and 4.83 times more likely to require oxygen supplementation than neonates of mothers without COVID-19. Given the possibility of an increase incidence of respiratory symptoms, close monitoring of these neonates is recommended.

A possible mechanism for increased respiratory distress in infants born to SARS-CoV-2 infected mother is related to altered levels of proinflammatory cytokines in pregnant women infected with SARS-CoV-2 [22]. Zhu et al. [23] reported a high prevalence of respiratory distress among clinical symptoms in neonates born to mothers with COVID-19, which is attributed to the findings that elevated maternal concentrations of cytokines, such as interleukin-6, interleukin-1β, and tumor necrosis factor-alpha affect fetal development resulting in abnormalities, including bronchopulmonary dysplasia and brain damage. Potential adverse effects on newborns of SARS-CoV-2 infected mothers with hypoxemia and immunopathogenesis need to be examined further.

A previous prospective cohort study and systematic review reported that maternal COVID-19 infection may be associated with a high prevalence of preterm birth [24,25]. A retrospective case-control study in China found a significantly higher preterm birth rate (22.2%) in neonates born to mothers with COVID-19 than in the control group [18]. In a cohort of 255 neonates from 11 hospitals in Massachusetts, worsening of maternal illness led to preterm delivery and caused adverse outcome of infants [12]. In our study cohort, 3.9% were born with low birth weight, and 11.7% were born prematurely. All included pregnant women were in the third trimester and diagnosed within 2 weeks before delivery; therefore, COVID-19 infection affecting prematurity or intrauterine growth retardation could not be evaluated in this study. As our study cohort mainly comprised late preterm or full-term neonates (91 out of 103 infants were born at 37 weeks or more GA), we did not examine the association of preterm risks.

The CDC recommend COVID-19 vaccination at any point during pregnancy [26]. In Korea, COVID-19 vaccination was initiated on October 18, 2020, but the vaccination rate was poor among pregnant women due to a lack of consensus. Only 12.1% of COVID-19 positive mothers were vaccinated, which was too small to observe a significant effect on maternal disease severity.

Maternal IgG antibodies to SARS-CoV-2 (including neutralizing anti-SARS-CoV-2 adaptive antibodies) are known to cross the placenta after infection with COVID-19 during pregnancy, with or without symptoms [27,28]. It has been reported that infection occurring more than 2 months prior to delivery enables efficient transfer of maternal SARS-CoV-2 IgG across the placenta in a prospective observational study [29], but the efficiency between the timing of maternal SARS-CoV-2 and the transfer of immunity across the placenta remains unclear. Antibody tests were performed in 87 mothers and 101 infants. Due to recent (≤2 weeks of delivery) infection in the mother, IgG antibodies were detected at birth in only 15 of 101 infants and 27 of 87 mothers. The protective effect of maternal antibodies crossing the placenta in newborns requires further research based on accumulated data.

The strict isolation policy implemented at our institution may not be generalizable. Mothers were under a stringent policy in which the neonate was isolated from the mother until the mother was free from quarantine, which ranged from 10 to 7 days according to updated guidelines. Increased hospital days in the study group do not necessarily represent the actual clinical severity of infants, as the majority of NICU admissions were done as a precautionary measure to closely monitor the neonatal condition or to isolate the infant until the PCR result was confirmed negative. Hospital days was also influenced by their mothers’ discharge plans.

Moreover, according to the hospital isolation policy, expressed milk was not allowed to leave the isolation room, and all items in the isolation room had to be discarded. Temporary separation may be inevitable for mothers when symptoms are severe; however, the benefits of breastfeeding and mother-infant contact should be considered when implementing guidelines. In a retrospective cohort study at a single center in New York, no clinical evidence of perinatal transmission was identified, despite most newborns rooming-in and directly breastfeeding [17]. In a nationwide study by the Spanish Society of Neonatology Registry, skin-to-skin contact after delivery, rooming-in with the mother, and breastfeeding have been documented in a high proportion of neonates without adverse events [30]. Our data of zero detection of SARS-CoV-2 RNA in breast milk adds to the current suggestion that transmission of SARS-CoV-2 via breast milk is unlikely. We highly recommend breastfeeding after discharge, and it was confirmed that 57.8% of patients were breastfeeding at the one-month outpatient follow-up.

The long-term outcomes in neonates born to mothers with COVID-19 remain unknown. A recent cohort study of 18,355 offspring with SARS-CoV-2 exposure in utero, showed that infants may be at higher risk for neurodevelopmental disorders at 12 months of age [31]. In addition to SARS-CoV-2, several reports have suggested that activation of maternal immunity due to exposure to other microbial infections in utero, may have long-term effects on the development of offspring [32,33].

SARS-CoV-2 recognizes and binds to the angiotensin-converting enzyme 2 (ACE2) receptor, causing severe hypoxemia. In pregnant women with SARS-CoV-2 infection, ACE2 insufficiency and placental hypoxia can have adverse effects on mothers and their fetuses [34]. Several studies have shown that pregnant women have more susceptibility to severe illness from SARS-CoV-2 infection than non-pregnant women [22,33]. Therefore, pregnancy and perinatal complications, including preeclampsia, fetal death, preterm birth, intrauterine growth retardation, and respiratory distress, are likely to occur in SARS-CoV-2 infected mothers and their newborns [34].

Through the placental pathology of SARS-CoV-2 infected pregnant women, it was confirmed that viral infection caused a variety of placental conditions, such as increases in intervillous or subvillous fibrin, thrombi in vessels, and multifocal infarctions [34,35]. In our study, 14 placental pathologies were reviewed, 8 of which showed intervillous infarction or thrombus presenting with hypoxia. Clinical fetal distress was not observed in our study; however, a larger sample size is required to establish an association between placental pathology and perinatal complications or long-term risks.

Matching the control group by GA to assess the risk of late preterm or term infants born to mothers with COVID-19 was a strength of this study. However, this study has some limitations. First, our results span the eras of alpha and delta variants to the omicron variant of SARS-CoV-2; but we did not examine differences between the variants. Second, the findings of our study may not be generalizable, as it was a single-center study. Thirdly, there may be a subjective bias for infants born to mothers with COVID-19 with respiratory symptoms. Finally, since the participants in our study were infected mothers within 2 weeks of delivery and newborns over 35 weeks of GA, we could not determine how SARS-CoV-2 infection in the first and second trimesters affects newborns. Further large multicenter research on the effect of maternal COVID-19 infection including long-term outcomes of neonates, is needed.

In conclusion, our study shows the possibility of an increase in the incidence of TTN in neonates born to mothers infected with COVID-19, close monitoring for respiratory symptoms after delivery is recommended.

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