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. 2021 Sep 16;155(3):450–454. doi: 10.1002/ijgo.13916

Fetal pulmonary artery Doppler evaluation in pregnant women after recovery from COVID‐19

Ezgi Turgut 1,, Sule Goncu Ayhan 1, Deniz Oluklu 1, Eda Ozden Tokalioglu 1, Ozlem Moraloglu Tekin 1, Dilek Sahin 1
PMCID: PMC9087611  PMID: 34499751

Abstract

Objective

To evaluate fetal lung development using pulmonary artery Doppler in pregnant women who had recovered from COVID‐19.

Methods

The prospective case–control study included 41 pregnant women who had recovered from COVID‐19 and 43 healthy pregnant women (control group). All the women in the study group had been diagnosed with COVID‐19 and had completed a quarantine period.

Results

The demographic data of patients were similar in the groups (P > 0.05). Main pulmonary artery peak systolic velocity was higher and pulsatility indices were lower in pregnant women who recovered from COVID‐19 compared to the controls (P < 0.001, P = 0.001). Acceleration time, ejection time, and acceleration/ejection time ratio (PATET) of the fetal MPA Doppler were significantly decreased in pregnant women who recovered from COVID‐19 (P < 0.001, P = 0.036, and P = 0.002, respectively). The patients who had recovered from COVID‐19 were divided into two groups: those treated with expectant management and those treated in hospital. The pulmonary artery acceleration time and PATET ratio were significantly lower in the group treated in the hospital (P = 0.023 and P = 0.045, respectively).

Conclusion

Detailed Doppler evaluations of the pulmonary artery may help in evaluating the fetal adverse effects of COVID‐19 disease.

Keywords: COVID‐19, fetal Doppler ultrasound, pregnancy, pulmonary artery Doppler

Synopsis

Detailed Doppler evaluations of the pulmonary artery may help in evaluating the fetal adverse effects of COVID‐19 disease.

1. INTRODUCTION

Inadequate lung development leads to neonatal complications, with high mortality and morbidity, especially respiratory distress syndrome (RDS) in newborns. 1 In contrast to amniotic fluid testing, a Doppler exam is a non‐invasive method to assess fetal lung maturation. 2 , 3 , 4 Determining fetal pulmonary artery blood flow acceleration time, ejection time, and acceleration/ejection time ratio (PATET) is a new approach for monitoring pulmonary artery pressure. 2 , 3 Previous studies showed that the acceleration time was negatively correlated with pulmonary artery systolic pressure. 5 , 6

The COVID‐19 pandemic has spread rapidly worldwide, with adverse pregnancy outcomes, including maternal multisystemic organ damage, with hypercoagulation, hypoxia, and an excessive inflammatory response, reported in infected individuals. 7 , 8 , 9 , 10 The aforementioned adverse effects can explain reported complications, such as early pregnancy loss and fetal growth retardation, caused by COVID‐19. 11 , 12 , 13 Although the mechanisms underlying placental transmission of COVID‐19 and its associated effects on fetal organs are not clear, fetal vascular malperfusion is the most common finding in placental pathology. 14 , 15 Fetal vascular malperfusion may lead to incomplete maturation of fetal lungs and increased pulmonary artery pressure. The aim of the present study was to evaluate the development of fetal lungs using pulmonary artery Doppler in pregnant women who had recovered from COVID‐19.

2. MATERIALS AND METHODS

The present study was conducted at Ankara City Hospital between February 1, 2021, and June 30, 2021. The prospective case–control study included 41 pregnant women who had recovered from COVID‐19 and 43 healthy pregnant women (control group). All the women in the study group had been diagnosed with COVID‐19 by a reverse transcription polymerase chain reaction test and had completed a quarantine period. The quarantine period was 14 days for those discharged from the hospital and patients who were followed up at home. Women with a history of multifetal pregnancies, fetal structural anomalies, and maternal systemic diseases were excluded. In the control group, pregnant women with symptoms associated with COVID‐19 infection (e.g. a fever, cough, sore throat, or myalgia) were not included.

Written informed consent was obtained from all participants. Approval for the study was obtained from the Turkish Ministry of Health and Medical Research Ethics Department of the hospital (decision number E2‐21‐380).

Gestational age was determined by the last menstrual period or first trimester crown–rump length. All Doppler measurements were performed at 28–40 weeks of gestation by the same maternal fetal medicine specialist using a Voluson S10 ultrasound machine C1‐5‐RS convex probe (1.75–4.95 MHz; General Electric Healthcare). The fetal cardiac four‐chamber view was obtained first and then the fetal main pulmonary artery (MPA) was visualized. The pulmonary valves and the bifurcation of the right and left branches of the pulmonary artery were identified. The measurements were obtained by placing the cursor between the valve and the bifurcation of pulmonary artery. When a specific MPA Doppler pattern was obtained, 4 systolic/diastolic (S/D) ratio, resistance index (RI), pulsatility index, and peak systolic velocity (PSV) values were measured by manual or automatic tracing. 16 Acceleration time and ejection time were measured by a manual trace. Acceleration time is the time from the onset of flow to the maximum flow of the PSV and ejection time is the time from the beginning to the end of ventricular systole. The PATET ratio was calculated. 16 , 17

In the Doppler measurements, the mean values of three consecutive cardiac cycles were used.

Statistical analysis was enforced using IBM SPSS Statistics 17.0 (IBM Corp., Armonk, NY, USA). Descriptive statistics were given as mean ± standard deviation for numerical data with normal distribution or median and minimum–maximum values for numerical data that do not follow a normal distribution. The normality of the variables was tested with both Shapiro–Wilk and Kolmogorov–Smirnov tests. Groups were compared with the Student t‐test and Mann–Whitney U‐test. A type‐1 error less than 0.05 was considered statistically significant.

3. RESULTS

The present study included 41 patients who recovered from COVID‐19 and 43 control cases. Table 1 shows the demographics of the study population. The maternal baseline characteristics of the two groups were similar. The clinical features of COVID‐19 are shown in Table 2. The mean gestational age at the time of the COVID‐19 diagnosis was 16.1 weeks (range 5–30 weeks), and 12 (29%) of the patients had been hospitalized. All the hospitalized patients received treatment with low‐molecular weight heparin. Only one patient received lopinavir‐ritonavir therapy.

TABLE 1.

Baseline data and characteristics of the groups a

Controls (n = 43) Recovered from COVID‐19 (n =41) P value
Maternal age (years) 27.4 ± 4.8 28.6 ± 5.5 0.342
BMI (kg/m2) 28.5 ± 7.0 27.8 ± 4.1 0.477
Nulliparity 19 (44.2) 16 (39) 0.230
Gestational age at ultrasound assessment (weeks) 32.0 ± 0.7 32.3 ± 4.3 0.823
BPD (weeks) 32.9 ± 3.9 32.7 ± 4.1 0.903
AC (weeks) 31.6 ± 5.9 31.3 ± 6.1 0.801
FL (weeks) 32.0 ± 3.9 31.8 ± 4.1 0.854
EFW (g) 2053 ± 785 2015 ± 814 0.872
DVP (mm) 50.9 ± 11.7 50.6 ± 10.8 0.907

Abbreviations: AC, abdominal circumference; BMI, body mass index; BPD, biparietal diameter; DVP, deepest vertical pocket; EFT, estimated fetal weight; FL, femur length.

a

Values are given as as number (percentage) or mean ± SD.

TABLE 2.

Clinical characteristics of COVID‐19 a

Variables Values
Gestational age at diagnosis (weeks) 16.1 (5–30)
Admission to hospital 12 (29)
COVID‐19 therapy 12 (29)
Low‐molecular weight heparin 12 (29)
Lopinavir‐ritonavir 1 (2)
a

Values are given as number (percentage) or median (interquartile range).

The findings of the Doppler assessments are shown in Table 3. The MPA‐PSV was higher and the pulsatility index was lower in the pregnant women who had recovered from COVID‐19 compared to the controls (P < 0.001 and P = 0.001, respectively). The acceleration time, ejection time, and PATET ratio of the fetal MPA were significantly decreased in the pregnant women who had recovered from COVID‐19 (P < 0.001, P = 0.036, and P = 0.002, respectively). The patients who had recovered from COVID‐19 were divided into two groups: those treated with expectant management and those treated in hospital. When the pulmonary artery Doppler data in these groups were compared, the pulmonary artery S/D ratio, acceleration time, and PATET ratio were significantly lower in the group treated in the hospital (P = 0.049, P = 0.023, and P = 0.045).

TABLE 3.

Fetal Doppler assesment a

Controls (n = 43) Recovered from COVID‐19 (n = 41) P value
PA PSV 53.5 ± 11.8 66.8 ± 16.7 <0.001
PA S/D 7.1 ± 1.1 6.6 ± 1.6 0.082
PA PI 2.2 ± 0.2 1.8 ± 0.5 0.001
PA RI 0.8 ± 0.01 1.0 ± 0.4 0.565
PA AT 57.2 ± 9.8 44.9 ± 13.4 <0.001
PA ET 215.0 ± 35.8 198.9 ± 40.5 0.036
PATET 0.27 ± 0.06 0.23 ± 0.07 0.002

Abbreviations: AT, acceleration time; ET, ejection time; PA, pulmonary artery; PATET, acceleration/ejection time ratio; PI, pulsatility index; PSV, peak systolic velocity; S/D, systolic/diastolic ratio.

a

Values are given as mean ± SD. Statistically significant data (P < 0.05) is written in bold.

4. DISCUSSION

In the present study, low MPA pulsatility index, acceleration time, and ejection time values and low PATET ratios were found in the pregnant women who had recovered from COVID‐19 compared to the values in the control group. In addition, the pulmonary artery S/D ratio, acceleration time, and PATET ratio were significantly lower in the group treated in the hospital.

During fetal lung maturation, pulmonary impedance decreases, and pulmonary artery flow increases, with the ejection flow reaching a peak in mid‐systole. In contrast, the ejection flow peaks earlier in patients with high pulmonary impedance. As a result, the acceleration time and PATET ratio decrease, as reported in earlier studies. 5 , 6 , 18 A study that investigated the relationship between the PATET ratio and surfactant/albumin ratio revealed an inverse relationship between the PATET ratio and neonatal respiratory distress. 18 In another study, the PATET ratio was lower in infants diagnosed with RDS. 5 Büke et al. 2 investigated the relationship between the fetal PATET ratio and neonatal transient tachypnea. In their study, the PATET ratio had a negative predictive value of 96%, sensitivity of 83.3%, and specificity of 82.7% in detecting transient tachypnea. In the present study, both the PATET ratio and acceleration time were decreased in the patients who had recovered from COVID‐19. The PATET ratio and acceleration time were significantly lower in the symptomatic patients who required hospitalization. It is believed that these findings might be a reflection of the adverse effects of maternal COVID‐19 infection on the fetal lung.

In a study on 756 fetuses that used fetal MPA Doppler to predict neonatal RDS, the PATET ratio was decreased in fetuses that developed RDS. In contrast to the present findings, they reported that the MPA pulsatility index was increased, and the PSV was decreased, in fetuses that developed RDS. Importantly, in the present study, the ability of the pulsatility index and RI to predict the development of RDS appeared to have lower sensitivity and specificity compared to that of the PATET ratio. 16 On the other hand, Lindsley et al. 19 observed no differences in fetal pulmonary artery PSV, S/D ratio, pulsatility index, and RI value of preterm newborns with RDS versus those without RDS. Further studies are needed to shed light on the importance of the PSV, S/D ratio, pulsatility index, and RI in fetal lung maturation (Table 4).

TABLE 4.

Comparison of fetal pulmonary artery Doppler data according to treatment approach of patients recovered from COVID‐19 a

Expectant management (n = 29) Treatment in hospital (n = 12) P value
PA PSV 68.5 ± 18.6 62.8 ± 10.7 0.436
PA S/D 7.1 ± 1.1 6.6 ± 1.6 0.049
PA PI 1.7 ± 0.6 2.0 ± 0.4 0.185
PA RI 1.06 ± 0.5 0.95 ± 0.4 0.488
PA AT 48.1 ± 13.4 37.1 ± 10.3 0.023
PA ET 203.3 ± 38.6 188.2 ± 44.6 0.250
PATET 0.24 ± 0.07 0.20 ± 0.07 0.045

Abbreviations: AT, acceleration time; ET, ejection time; PA, pulmonary artery; PATET, acceleration/ejection time ratio; PI, pulsatility index; PSV, peak systolic velocity; S/D, systolic/diastolic ratio.

a

Values are given as mean ± SD. Statistically significant data (P < 0.05) is written in bold.

Fetal distress and preterm birth are common obstetrical complications of COVID‐19. Fetal pulmonary status has become an important issue. 11 , 12 , 13 , 20 , 21 In a review on neonatal complications in newborns (n = 67), RDS or pneumonia was observed in 18% (n = 12), low birth weight in 13% (n = 9), asphyxia in 2% (n = 1), and perinatal death in 3% (n = 2) of the newborns. Despite strict infection control and prevention procedures during the birth and separation of the mother and newborn, four newborns, three of whom had pneumonia, were positive for COVID‐19, and vertical transmission could not be excluded. 22 However, there is insufficient evidence to support vertical transmission of COVİD‐19. 23 Previous research showed that the virus disrupted fetomaternal perfusion by causing placental injury, including villitis, inflammation, and arteriopathy. 24 , 25 It was therefore hypothesized that COVID‐19 infection‐related events, such as increased levels of cytokines, maternal hypoxia, and impaired coagulation cascades, may have negative effects on fetal pulmonary circulation, including placental malperfusion. 7 , 11 , 13

The present study has strengths and weaknesses. It was a prospective single‐center study, with a standard follow‐up protocol. However, the cases were not evaluated with respect to vertical transmission. In addition, neonatal outcomes could not be presented as they were delivered at different centers.

In conclusion, COVID‐19 causes more severe disease in pregnant women compared with non‐pregnant women. 20 , 21 Many studies have been conducted on fetal adverse effects, 14 , 15 , 20 , 21 but many questions about fetal consequences remain unanswered. COVID‐19 infection can have a negative impact on placental tissues and fetal organs. 24 , 25 Further studies are needed to clarify the impact of maternal COVID‐19 infection on fetal lung development.

CONFLICTS OF INTEREST

The authors have no conflicts of interest.

AUTHOR CONTRIBUTIONS

ET, SGA, and DS conceived the study. ET, EOT, and DO performed the statistical analysis. The management of the trial was overseen by ET, SGA, DS, and OMT. ET drafted the manuscript. All authors contributed to the approved the final manuscript.

Turgut E, Ayhan SG, Oluklu D, Tokalioglu EO, Tekin OM, Sahin D. Fetal pulmonary artery Doppler evaluation in pregnant women after recovery from COVID‐19. Int J Gynecol Obstet. 2021;155:450–454. 10.1002/ijgo.13916

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