Acessibilidade / Reportar erro

Screening for coronavirus disease 2019 in pregnant women admitted for delivery: an observational study

SUMMARY

OBJECTIVE:

The aim of this study was to examine the impact of symptom-based screening on the prevalence and outcomes of neonatal coronavirus disease 2019 in pregnant women admitted for delivery.

METHODS:

A retrospective observational study was conducted from June to August 2020 at Gonzaga Mota of Messejana Hospital, Fortaleza, CE, Brazil. All pregnant women were screened for coronavirus disease 2019 based on symptoms. Reverse transcription-polymerase chain reaction or immunology assays for severe acute respiratory syndrome coronavirus 2 were performed when a patient reported a symptom. All newborns of symptomatic patients were submitted for Reverse transcription-polymerase chain reaction. Newborns were divided into groups according to the Reverse transcription-polymerase chain reaction results to identify the relationship between maternal symptoms and neonatal coronavirus disease 2019.

RESULTS:

A total of 55 (55/1,026, 5.4%) and 50 (50/1,026, 4.8%) pregnant women reported symptoms and had a positive confirmatory test, respectively. The most common symptom of coronavirus disease 2019 among the pregnant women with positive confirmatory test was cough (n=23, 46%). Seven newborns (7/50, 14%) of symptomatic mothers had positive Reverse transcription-polymerase chain reaction. Upon birth, no newborn had serious complications.

CONCLUSION:

Universal screening of pregnant women admitted for delivery can reduce the perinatal transmission of coronavirus disease 2019. Symptom-based screening can be an alternative for regions with a low prevalence of the disease where a better allocation of financial resources is necessary.

Keywords
COVID-19; Obstetric delivery; Newborn; Perinatal care; SARS-CoV-2; Infectious disease transmission

INTRODUCTION

The first case of a severe acute respiratory syndrome caused by a new coronavirus, later called severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), was identified in December 2019 in Wuhan, Hubei Province, China. Coronavirus disease 2019 (COVID-19) has spread rapidly across the world, prompting the World Health Organization (WHO) to declare a pandemic status on March 11, 202011. Gheblawi M, Wang K, Viveiros A, Nguyen Q, Zhong JC, Turner AJ, et al. Angiotensin-converting enzyme 2: SARS-CoV-2 receptor and regulator of the renin-angiotensin system: celebrating the 20th anniversary of the discovery of ACE2. Circ Res. 2020;126(10):1456-74. https://doi.org/10.1161/CIRCRESAHA.120.317015
https://doi.org/10.1161/CIRCRESAHA.120.3...
,22. Wu YC, Chen CS, Chan YJ. The outbreak of COVID-19: an overview. J Chin Med Assoc. 2020;83(3):217-20. https://doi.org/10.1097/JCMA.0000000000000270
https://doi.org/10.1097/JCMA.00000000000...
. At the end of January 2021, COVID-19 infected more than 98 million people and was responsible for more than 2.1 million deaths worldwide33. World Health Organization. WHO coronavirus disease (COVID-19) dashboard. Geneva: World Health Organization; 2021. [cited on Jan 26, 2021]. Available from: https://covid19.who.int/
https://covid19.who.int/...
.

Clinically, COVID-19 has a wide range of disease manifestations that have been identified in five different cases: asymptomatic (1.2%), mild to moderate (80.9%), severe (13.8%), critical (4.7%), and mortality (2.3%). Young adults of reproductive age are the most affected, but the highest mortality occurs in the elderly population and those with comorbidities such as obesity, hypertension, diabetes, and other chronic diseases44. Jin Y, Yang H, Ji W, Wu W, Chen S, Zhang W, et al. Virology, epidemiology, pathogenesis, and control of COVID-19. Viruses. 2020;12(4):372. https://doi.org/10.3390/v12040372
https://doi.org/10.3390/v12040372...
. The number of COVID-19 cases among pregnant women is still uncertain. Studies performed with pregnant women at the time of delivery revealed that the prevalence of COVID-19 ranged from 0.43 to 19.8%55. Díaz-Corvillón P, Mönckeberg M, Barros A, Illanes SE, Soldati A, Nien JK, et al. Routine screening for SARS CoV-2 in unselected pregnant women at delivery. PLoS One. 2020;15(9):e0239887. https://doi.org/10.1371/journal.pone.0239887
https://doi.org/10.1371/journal.pone.023...

6. Biasucci G, Cannalire G, Raymond A, Capra ME, Benenati B, Vadacca G, et al. Safe perinatal management of neonates born to SARS-CoV-2 positive mothers at the epicenter of the italian epidemic. Front Pediatr. 2020;8:565522. https://doi.org/10.3389/fped.2020.565522
https://doi.org/10.3389/fped.2020.565522...

7. Ferrazzi E, Beretta P, Bianchi S, Cetin I, Guarnerio P, Locatelli A, et al. SARS-CoV-2 infection testing at delivery: a clinical and epidemiological priority. J Matern Fetal Neonatal Med. 2022;35(12):2417-19. https://doi.org/10.1080/14767058.2020.1788532
https://doi.org/10.1080/14767058.2020.17...

8. Gagliardi L, Danieli R, Suriano G, Vaccaro A, Tripodi G, Rusconi F, et al. Universal severe acute respiratory syndrome coronavirus 2 testing of pregnant women admitted for delivery in 2 Italian regions. Am J Obstet Gynecol. 2020;223(2):291-2. https://doi.org/10.1016/j.ajog.2020.05.017
https://doi.org/10.1016/j.ajog.2020.05.0...

9. Massarotti C, Adriano M, Cagnacci A, Gorlero F, Gustavino C, Vallerino G, et al. Asymptomatic SARS-CoV-2 infections in pregnant patients in an Italian city during the complete lockdown. J Med Virol. 2021;93(3):1758-60. https://doi.org/10.1002/jmv.26458
https://doi.org/10.1002/jmv.26458...
-1010. Ochiai D, Kasuga Y, Iida M, Ikenoue S, Tanaka M. Universal screening for SARS-CoV-2 in asymptomatic obstetric patients in Tokyo, Japan. Int J Gynaecol Obstet. 2020;150(2):268-9. https://doi.org/10.1002/ijgo.13252
https://doi.org/10.1002/ijgo.13252...
. This large variation in the prevalence of SARS-CoV-2 infection at the time of delivery depends on the area studied, type of screening performed, number of tests performed, period studied, and gestational risk1111. Cronin S, Piacquadio M, Brendel K, Goldberg A, Goldberg M, White C, et al. RE: universal SARS-CoV-2 testing on admission to the labor and delivery unit: low prevalence among asymptomatic obstetric patients. Infect Control Hosp Epidemiol. 2021;42(7):908-9. https://doi.org/10.1017/ice.2020.382
https://doi.org/10.1017/ice.2020.382...
.

The impact of COVID-19 on pregnant women is still poorly understood. Initially, based on the respiratory physiology of a pregnant woman, maternal immune response during pregnancy, and experience of other severe acute respiratory syndromes, it was believed that SARS-CoV-2 infection in the perigestational period could lead to more serious cases1212. Liu H, Wang LL, Zhao SJ, Kwak-Kim J, Mor G, Liao AH. Why are pregnant women susceptible to COVID-19? An immunological viewpoint. J Reprod Immunol. 2020;139:103122. https://doi.org/10.1016/j.jri.2020.103122
https://doi.org/10.1016/j.jri.2020.10312...
. Current evidence indicates that the morbidity and mortality of COVID-19 among pregnant women are similar to those of non-pregnant women. However, some authors have identified high mortality among pregnant women with COVID-19, suggesting that factors such as a higher prevalence of comorbidities, ethnic differences, and poor quality of obstetric care may contribute to a more severe development of the disease1313. Brandt JS, Hill J, Reddy A, Schuster M, Patrick HS, Rosen T, et al. Epidemiology of coronavirus disease 2019 in pregnancy: risk factors and associations with adverse maternal and neonatal outcomes. Am J Obstet Gynecol. 2021;224(4):389.e1-9. https://doi.org/10.1016/j.ajog.2020.09.043
https://doi.org/10.1016/j.ajog.2020.09.0...

14. Zambrano LD, Ellington S, Strid P, Galang RR, Oduyebo T, Tong VT, et al. Update: characteristics of symptomatic women of reproductive age with laboratory-confirmed SARS-CoV-2 infection by pregnancy status - United States, January 22-October 3, 2020. MMWR Morb Mortal Wkly Rep. 2020;69(44):1641-7. https://doi.org/10.15585/mmwr.mm6944e3
https://doi.org/10.15585/mmwr.mm6944e3...
-1515. Takemoto MLS, Menezes MO, Andreucci CB, Nakamura-Pereira M, Amorim MMR, Katz L, et al. The tragedy of COVID-19 in Brazil: 124 maternal deaths and counting. Int J Gynaecol Obstet. 2020;151(1):154-6. https://doi.org/10.1002/ijgo.13300
https://doi.org/10.1002/ijgo.13300...
.

The risk of neonatal COVID-19 is due to possible vertical transmission, maternal transmission after delivery, or even transmission from the health team involved in the care of the mother-child binomial. Current knowledge about neonatal COVID-19 is still limited to a small number of cases, which indicate a favorable clinical course with few symptoms and low morbidity and mortality. However, identification of pregnant women infected with SARS-CoV-2 at the time of delivery is important in order to enforce safety and isolation measures1616. Vardhelli V, Pandita A, Pillai A, Badatya SK. Perinatal COVID-19: review of current evidence and practical approach towards prevention and management. Eur J Pediatr. 2021;180(4):1009-31. https://doi.org/10.1007/s00431-020-03866-3
https://doi.org/10.1007/s00431-020-03866...
.

The goal of this study was to evaluate the impact of a symptom-based screening protocol on the prevalence and outcomes of neonatal COVID-19.

METHODS

This was a retrospective observational study conducted from June 2020 to August 2020 at Gonzaga Mota of Messejana Hospital, Fortaleza, CE, Brazil. The inclusion criterion was admission for delivery during the study period. Exclusion criteria were loss of follow-up and non-agreement to participate in the study. During this period, all pregnant women admitted for delivery were screened for COVID-19 clinical symptoms such as cough, dyspnea, abnormalities in smell and taste, hyporexia, fever, diarrhea, and headache at any time during pregnancy. Pregnant women with a history or occurrence of any symptoms were immediately isolated and referred for laboratory investigation at the time of childbirth. A single swab collection from the posterior oropharynx and nasopharynx was performed when the pregnant woman was between the 3rd and 10th days after the onset of symptoms, and then a reverse transcriptase polymerase chain reaction (RT-PCR) assay was conducted for SARS-CoV-2 (Bio-Manguinhos, Rio de Janeiro, RJ, Brazil; Instituto de Biologia Molecular do Paraná, Curitiba, PR, Brazil; Mobius Life Science, Pinhais, PR, Brazil). On the contrary, the immunology assay (rapid test) was performed from the 7th day after the onset of symptoms (Wondfo One Step COVID-19 rapid test kits, Guangzhou, China).

In all newborns of symptomatic pregnant women, clinical conditions at birth were assessed, and, if possible, prompt clamping of the umbilical cord within 1 min of life was suggested, while skin-to-skin contact was not indicated. The nasopharyngeal swab to perform RT-PCR was conducted in children after initial care at birth or up to 48 h of life1717. Agência Nacional de Vigilância Sanitária. Nota técnica GVIMS/GGTES/ANVISA Nº 07/2020. 2020. [cited on Nov 30, 2020]. Available from: https://www.anvisa.gov.br/segurancadopaciente/index.php/alertas/item/nota-tecnica-gvims-ggtes-anvisa-n-07-2020
https://www.anvisa.gov.br/segurancadopac...
. Bathing a newborn was done if birth was by vaginal delivery. After birth, asymptomatic newborns of symptomatic pregnant women with favorable maternal conditions stayed isolated with the mother in the rooming-in until hospital discharge, with maternal hygiene care guidelines and by wearing a mask and maintaining 2 m between the binomials. If the newborns had symptoms (fever, cough, difficulty in breathing and/or tachypnea, hypoactivity, and food refusal), they were referred to the neonatal unit in intensive or intermediate care and remained in isolation until symptoms had been resolved and the mothers could be accommodated in room1818. Sociedade Brasileira de Pediatria. Recomendações para Assistência ao Recém-Nascido na sala de parto de mãe com COVID-19 suspeita ou confirmada. 2020. [cited on Nov 30, 2020]. Available from: https://www.sbp.com.br/fileadmin/user_upload/22422b-NAlerta-Assist_RN_SalaParto_de_mae_com_COVID-19.pdf
https://www.sbp.com.br/fileadmin/user_up...
.

Newborns of symptomatic pregnant women were divided into two groups based on the result of the RT-PCR after birth (RT-PCR SARS-CoV-2 positive and RT-PCR SARS-CoV-2 negative) to identify the possible relationship between any maternal symptom and a positive neonatal COVID-19.

Data were analyzed using IBM SPSS Statistics for Windows, version 25.0 (Armonk, NY: IBM Corp.). In addition, descriptive statistics were performed on symptomatic pregnant women. The mean (± standard deviation) and median (interquartile ranges) were used for continuous variables. Differences in the distribution of maternal and neonatal characteristics were assessed using the chi-square or Fisher’s exact tests for categorical variables and the Mann-Whitney U test for continuous variables. p=0.05 was found to be statistically significant. The study was approved by the Ethic Committee of the University of Fortaleza (CAAE number 34594620.9.0000.5052/approval number 4.147.638) and conducted within ethical principles and rules, with a free and informed consent form signed by all participants.

RESULTS

During the time of the study (June to August 2020), 1,026 pregnant women were admitted for delivery. A total of 55 (55/1,026, 5.4%) pregnant women reported a history or presence of symptoms related to COVID-19. On the contrary, 50 (50/1,026, 4.8%) pregnant women had a positive confirmatory test (Figure 1). The median age of these symptomatic pregnant women was 23 years (interquartile range [IQR]: 20 to 28.2 years). The most common symptom of COVID-19 among the 50 pregnant women with positive confirmatory tests was cough (n=23, 46%), followed by coryza (n=16, 32%), ageusia (n=16, 32%), anosmia (n=15, 30%), headache (n=12, 24%), fever (n=11, 22%), sore throat (n=11, 22%), myalgia (n=9, 18%), nasal obstruction (n=8, 16%), diarrhea (n=8, 16%), fatigue (n=5, 10%), dyspnea (n=4, 8%), and adynamia (n=2, 4%) (Table 1).

Figure 1.
Patients’ flowchart. From June to August 2020, 1,026 pregnant women were admitted for delivery. A total of 55 pregnant women reported a history or symptoms related to coronavirus disease 2019. Additionally, 50 pregnant women had a positive confirmatory test. Thirty-one pregnant women tested positive for coronavirus disease 2019. Moreover, 7/50 newborns from symptomatic mothers had a positive reverse transcriptase polymerase chain reaction for severe acute respiratory syndrome coronavirus 2. Five were neonates of mothers with positive coronavirus disease 2019 laboratory investigation, and two were neonates of pregnant women with negative coronavirus disease 2019 laboratory investigation. There was no significant difference between these groups in the prevalence of neonatal coronavirus disease 2019.
Table 1.
Characteristics of pregnant women with symptoms for coronavirus disease 2019 and their newborns.

Of the total symptomatic pregnant women submitted to the laboratory, 31 tested positive for COVID-19 (31/50, 62%) (Figure 1). Based on the interval between the onset of symptoms and admission for delivery, 26 patients were investigated using RT-PCR, with 5 positive tests (5/26, 19.2%), and 40 patients underwent immunological testing, with 28 positive cases (28/40, 70%). Moreover, 7 of the 50 newborns from symptomatic mothers had a positive RT-PCR for SARS-CoV-2, and 6 swabs were obtained immediately at birth and 1 after 36 h of life. Five were neonates of mothers with positive COVID-19 laboratory tests (two positive RT-PCR and three positive immunologic tests), and two were neonates of pregnant women with negative COVID-19 laboratory tests (one negative RT-PCR and one negative RT-PCR and immunological test) (Figure 1 and Table 2).

Table 2.
Clinical and laboratory characteristics of newborns with reverse transcriptase polymerase chain reaction positive for coronavirus disease 2019.

The overall median birth weight was 3,290 g (IQR: 3,037–3,650 g) and the median APGAR score at the 1st and 5th min was 8 (IRQ: 8–9) and 9 (IRQ: 9–9), respectively. There was no substantial difference between maternal and neonatal variables compared to groups of positive and negative newborns for SARS-CoV-2 RT-PCR (Table 1). Upon birth, no newborn had serious complications. One newborn had mild respiratory distress, while another (male) had mild respiratory distress associated with fever at 36 h of life, and bilateral hydronephrosis was diagnosed and transferred to a tertiary hospital during the investigation (Table 2).

DISCUSSION

The effect of COVID-19 on pregnant women and newborns is still poorly understood. Apparently, vertical transmission is an unusual phenomenon. However, there is a risk of transmission during the neonatal period, particularly during breastfeeding and in the care of the newborn by healthcare professionals and family members. Some studies suggest that pregnant women should be universally screened at the time of admission for delivery. Some authors recommend screening based on symptoms or pregnancy risk1919. Tanacan A, Erol SA, Turgay B, Anuk AT, Secen EI, Yegin GF, et al. The rate of SARS-CoV-2 positivity in asymptomatic pregnant women admitted to hospital for delivery: experience of a pandemic center in Turkey. Eur J Obstet Gynecol Reprod Biol. 2020;253:31-4. https://doi.org/10.1016/j.ejogrb.2020.07.051
https://doi.org/10.1016/j.ejogrb.2020.07...
,2020. Chandrasekharan P, Vento M, Trevisanuto D, Partridge E, Underwood MA, Wiedeman J, et al. Neonatal resuscitation and postresuscitation care of infants born to mothers with suspected or confirmed SARS-CoV-2 infection. Am J Perinatol. 2020;37(8):813-24. https://doi.org/10.1055/s-0040-1709688
https://doi.org/10.1055/s-0040-1709688...
.

The main findings of our study showed that at the beginning of the COVID-19 pandemic and in the face of financial and laboratory constraints, symptom-based screening of pregnant women admitted to a low-risk hospital for delivery was a decision that did not seem to worsen perinatal outcomes. However, our study has several limitations. First, the lack of a control group that underwent universal screening did not allow comparison of perinatal outcomes with symptom-based screening. The other limitation was the lack of diagnostic criteria for perinatal SARS-CoV-2 transmission, which were not defined at the time of the pandemic.

At the beginning of December 2020, the countries with the highest number of confirmed cases of COVID-19 were the USA (15.4 million), India (9.7 million), and Brazil (6.6 million), with a total of 46,435, 7,022, and 31,099 cases, respectively, per million inhabitants33. World Health Organization. WHO coronavirus disease (COVID-19) dashboard. Geneva: World Health Organization; 2021. [cited on Jan 26, 2021]. Available from: https://covid19.who.int/
https://covid19.who.int/...
. The overall prevalence of symptomatic SARS-CoV-2 infection has remained uncertain. Oran et al.2121. Oran DP, Topol EJ. Prevalence of asymptomatic SARS-CoV-2 infection: a narrative review. Ann Intern Med. 2020;173(5):362-7. https://doi.org/10.7326/M20-3012
https://doi.org/10.7326/M20-3012...
estimated that about 55–60% of people infected with SARS-CoV-2 had any symptoms. However, the authors highlighted the inconsistency of the data in the literature, as the percentage of symptomatic patients in the studies ranged from 7 to 93.7%.

Universal screening showed that about one-third of pregnant women with COVID-19 were symptomatic when they were admitted for delivery. However, the proportion of pregnant women infected with SARS-CoV-2 with symptoms was highly variable. A study conducted in Chile between April and June 2020 found that 56.8% of pregnant women (37/583) with COVID-19 at delivery were symptomatic55. Díaz-Corvillón P, Mönckeberg M, Barros A, Illanes SE, Soldati A, Nien JK, et al. Routine screening for SARS CoV-2 in unselected pregnant women at delivery. PLoS One. 2020;15(9):e0239887. https://doi.org/10.1371/journal.pone.0239887
https://doi.org/10.1371/journal.pone.023...
, while another four studies, carried out in three different countries [Japan, Spain, and the USA (Southern California and Brooklyn, New York, NY)] with fewer participants, found no symptomatic pregnant women with RT-PCR for SARS-CoV-21010. Ochiai D, Kasuga Y, Iida M, Ikenoue S, Tanaka M. Universal screening for SARS-CoV-2 in asymptomatic obstetric patients in Tokyo, Japan. Int J Gynaecol Obstet. 2020;150(2):268-9. https://doi.org/10.1002/ijgo.13252
https://doi.org/10.1002/ijgo.13252...
.

Also, the Centers for Disease Control and Prevention (CDC) described that the most commonly reported signs and symptoms were cough (50.3%), headache (42.7%), muscle aches (36.7%), and fever (32%) among pregnant women with COVID-19. In the review study by Amaral et al.2222. Amaral WND, Moraes CL, Rodrigues APDS, Noll M, Arruda JT, Mendonça CR. Maternal coronavirus infections and neonates born to mothers with SARS-CoV-2: a systematic review. Healthcare. 2020;8(4):511. https://doi.org/10.3390/healthcare8040511
https://doi.org/10.3390/healthcare804051...
, cough (44.4%) and nausea (10.2%) were the most frequent symptoms among pregnant women affected by COVID-19, while in the study by Elshafeey et al.2323. Elshafeey F, Magdi R, Hindi N, Elshebiny M, Farrag N, Mahdy S, et al. A systematic scoping review of COVID-19 during pregnancy and childbirth. Int J Gynaecol Obstet. 2020;150(1):47-52. https://doi.org/10.1002/ijgo.13182
https://doi.org/10.1002/ijgo.13182...
, these symptoms were fever (67.3%) and cough (65.7%). In our study, we found that, in addition to cough and coryza, taste and smell abnormalities were often reported by pregnant women with COVID-19.

The rate of perinatal transmission at our institution was 16.1% (5/31), similar to that described by Biasucci et al.66. Biasucci G, Cannalire G, Raymond A, Capra ME, Benenati B, Vadacca G, et al. Safe perinatal management of neonates born to SARS-CoV-2 positive mothers at the epicenter of the italian epidemic. Front Pediatr. 2020;8:565522. https://doi.org/10.3389/fped.2020.565522
https://doi.org/10.3389/fped.2020.565522...
(13.3%), and higher than that described by Corvillon et al.55. Díaz-Corvillón P, Mönckeberg M, Barros A, Illanes SE, Soldati A, Nien JK, et al. Routine screening for SARS CoV-2 in unselected pregnant women at delivery. PLoS One. 2020;15(9):e0239887. https://doi.org/10.1371/journal.pone.0239887
https://doi.org/10.1371/journal.pone.023...
(5.4%). Shah et al.2323. Elshafeey F, Magdi R, Hindi N, Elshebiny M, Farrag N, Mahdy S, et al. A systematic scoping review of COVID-19 during pregnancy and childbirth. Int J Gynaecol Obstet. 2020;150(1):47-52. https://doi.org/10.1002/ijgo.13182
https://doi.org/10.1002/ijgo.13182...
described a classification system and case description for SARS-CoV-2 infection in pregnant women, fetuses, and neonates. Based on the proposal by Shah et al.2323. Elshafeey F, Magdi R, Hindi N, Elshebiny M, Farrag N, Mahdy S, et al. A systematic scoping review of COVID-19 during pregnancy and childbirth. Int J Gynaecol Obstet. 2020;150(1):47-52. https://doi.org/10.1002/ijgo.13182
https://doi.org/10.1002/ijgo.13182...
6/7 cases of COVID-19 in our observational study can be categorized as neonatal infection acquired intrapartum (detection of the virus by PCR in a nasopharyngeal swab at birth and not at 24–48 h). Interestingly, there were two cases of perinatal COVID-19 in neonates of mothers who tested negative for SARS-CoV-2, which can be due to a mother’s false-negative RT-PCR or neonatal transmission shortly after delivery.

Current data indicate an association between COVID-19 and a risk of preterm birth and low birth weight1414. Zambrano LD, Ellington S, Strid P, Galang RR, Oduyebo T, Tong VT, et al. Update: characteristics of symptomatic women of reproductive age with laboratory-confirmed SARS-CoV-2 infection by pregnancy status - United States, January 22-October 3, 2020. MMWR Morb Mortal Wkly Rep. 2020;69(44):1641-7. https://doi.org/10.15585/mmwr.mm6944e3
https://doi.org/10.15585/mmwr.mm6944e3...
,1515. Takemoto MLS, Menezes MO, Andreucci CB, Nakamura-Pereira M, Amorim MMR, Katz L, et al. The tragedy of COVID-19 in Brazil: 124 maternal deaths and counting. Int J Gynaecol Obstet. 2020;151(1):154-6. https://doi.org/10.1002/ijgo.13300
https://doi.org/10.1002/ijgo.13300...
,2222. Amaral WND, Moraes CL, Rodrigues APDS, Noll M, Arruda JT, Mendonça CR. Maternal coronavirus infections and neonates born to mothers with SARS-CoV-2: a systematic review. Healthcare. 2020;8(4):511. https://doi.org/10.3390/healthcare8040511
https://doi.org/10.3390/healthcare804051...
,2424. Shah PS, Diambomba Y, Acharya G, Morris SK, Bitnun A. Classification system and case definition for SARS-CoV-2 infection in pregnant women, fetuses, and neonates. Acta Obstet Gynecol Scand. 2020;99(5):565-8. https://doi.org/10.1111/aogs.13870
https://doi.org/10.1111/aogs.13870...
,2525. Cavalcante MB, Cavalcante CTMB, Sarno M, Barini R, Kwak-Kim J. Maternal immune responses and obstetrical outcomes of pregnant women with COVID-19 and possible health risks of offspring. J Reprod Immunol. 2021;143:103250. https://doi.org/10.1016/j.jri.2020.103250
https://doi.org/10.1016/j.jri.2020.10325...
. However, in our study, all newborns with perinatal COVID-19 were born at term and with adequate weight. This result is justified by the fact that our maternity care serves low-risk pregnancies. All neonates evolved without serious complications. Two newborns developed respiratory distress, which may be due to COVID-19 or adaptation of the fetal circulation to neonatal or newborn transient tachypnea, in addition to neonatal infection, as one of these children had a positive urine culture and was diagnosed with bilateral hydronephrosis.

CONCLUSION

Universal screening of pregnant women admitted for delivery is the best way to reduce the risk of perinatal transmission of COVID-19. At the beginning of the COVID-19 pandemic, still in a scenario without vaccination coverage and with financial and laboratory restrictions, as well as the low morbidity of COVID-19 in the neonatal period, it was necessary to carry out a selective screening. The observed results suggest that screening only symptomatic pregnant women at the time of admission for delivery in low-risk maternity was the correct alternative for regions with a low prevalence of the disease and where a better allocation of financial resources was needed.

REFERENCES

  • 1.
    Gheblawi M, Wang K, Viveiros A, Nguyen Q, Zhong JC, Turner AJ, et al. Angiotensin-converting enzyme 2: SARS-CoV-2 receptor and regulator of the renin-angiotensin system: celebrating the 20th anniversary of the discovery of ACE2. Circ Res. 2020;126(10):1456-74. https://doi.org/10.1161/CIRCRESAHA.120.317015
    » https://doi.org/10.1161/CIRCRESAHA.120.317015
  • 2.
    Wu YC, Chen CS, Chan YJ. The outbreak of COVID-19: an overview. J Chin Med Assoc. 2020;83(3):217-20. https://doi.org/10.1097/JCMA.0000000000000270
    » https://doi.org/10.1097/JCMA.0000000000000270
  • 3.
    World Health Organization. WHO coronavirus disease (COVID-19) dashboard. Geneva: World Health Organization; 2021. [cited on Jan 26, 2021]. Available from: https://covid19.who.int/
    » https://covid19.who.int/
  • 4.
    Jin Y, Yang H, Ji W, Wu W, Chen S, Zhang W, et al. Virology, epidemiology, pathogenesis, and control of COVID-19. Viruses. 2020;12(4):372. https://doi.org/10.3390/v12040372
    » https://doi.org/10.3390/v12040372
  • 5.
    Díaz-Corvillón P, Mönckeberg M, Barros A, Illanes SE, Soldati A, Nien JK, et al. Routine screening for SARS CoV-2 in unselected pregnant women at delivery. PLoS One. 2020;15(9):e0239887. https://doi.org/10.1371/journal.pone.0239887
    » https://doi.org/10.1371/journal.pone.0239887
  • 6.
    Biasucci G, Cannalire G, Raymond A, Capra ME, Benenati B, Vadacca G, et al. Safe perinatal management of neonates born to SARS-CoV-2 positive mothers at the epicenter of the italian epidemic. Front Pediatr. 2020;8:565522. https://doi.org/10.3389/fped.2020.565522
    » https://doi.org/10.3389/fped.2020.565522
  • 7.
    Ferrazzi E, Beretta P, Bianchi S, Cetin I, Guarnerio P, Locatelli A, et al. SARS-CoV-2 infection testing at delivery: a clinical and epidemiological priority. J Matern Fetal Neonatal Med. 2022;35(12):2417-19. https://doi.org/10.1080/14767058.2020.1788532
    » https://doi.org/10.1080/14767058.2020.1788532
  • 8.
    Gagliardi L, Danieli R, Suriano G, Vaccaro A, Tripodi G, Rusconi F, et al. Universal severe acute respiratory syndrome coronavirus 2 testing of pregnant women admitted for delivery in 2 Italian regions. Am J Obstet Gynecol. 2020;223(2):291-2. https://doi.org/10.1016/j.ajog.2020.05.017
    » https://doi.org/10.1016/j.ajog.2020.05.017
  • 9.
    Massarotti C, Adriano M, Cagnacci A, Gorlero F, Gustavino C, Vallerino G, et al. Asymptomatic SARS-CoV-2 infections in pregnant patients in an Italian city during the complete lockdown. J Med Virol. 2021;93(3):1758-60. https://doi.org/10.1002/jmv.26458
    » https://doi.org/10.1002/jmv.26458
  • 10.
    Ochiai D, Kasuga Y, Iida M, Ikenoue S, Tanaka M. Universal screening for SARS-CoV-2 in asymptomatic obstetric patients in Tokyo, Japan. Int J Gynaecol Obstet. 2020;150(2):268-9. https://doi.org/10.1002/ijgo.13252
    » https://doi.org/10.1002/ijgo.13252
  • 11.
    Cronin S, Piacquadio M, Brendel K, Goldberg A, Goldberg M, White C, et al. RE: universal SARS-CoV-2 testing on admission to the labor and delivery unit: low prevalence among asymptomatic obstetric patients. Infect Control Hosp Epidemiol. 2021;42(7):908-9. https://doi.org/10.1017/ice.2020.382
    » https://doi.org/10.1017/ice.2020.382
  • 12.
    Liu H, Wang LL, Zhao SJ, Kwak-Kim J, Mor G, Liao AH. Why are pregnant women susceptible to COVID-19? An immunological viewpoint. J Reprod Immunol. 2020;139:103122. https://doi.org/10.1016/j.jri.2020.103122
    » https://doi.org/10.1016/j.jri.2020.103122
  • 13.
    Brandt JS, Hill J, Reddy A, Schuster M, Patrick HS, Rosen T, et al. Epidemiology of coronavirus disease 2019 in pregnancy: risk factors and associations with adverse maternal and neonatal outcomes. Am J Obstet Gynecol. 2021;224(4):389.e1-9. https://doi.org/10.1016/j.ajog.2020.09.043
    » https://doi.org/10.1016/j.ajog.2020.09.043
  • 14.
    Zambrano LD, Ellington S, Strid P, Galang RR, Oduyebo T, Tong VT, et al. Update: characteristics of symptomatic women of reproductive age with laboratory-confirmed SARS-CoV-2 infection by pregnancy status - United States, January 22-October 3, 2020. MMWR Morb Mortal Wkly Rep. 2020;69(44):1641-7. https://doi.org/10.15585/mmwr.mm6944e3
    » https://doi.org/10.15585/mmwr.mm6944e3
  • 15.
    Takemoto MLS, Menezes MO, Andreucci CB, Nakamura-Pereira M, Amorim MMR, Katz L, et al. The tragedy of COVID-19 in Brazil: 124 maternal deaths and counting. Int J Gynaecol Obstet. 2020;151(1):154-6. https://doi.org/10.1002/ijgo.13300
    » https://doi.org/10.1002/ijgo.13300
  • 16.
    Vardhelli V, Pandita A, Pillai A, Badatya SK. Perinatal COVID-19: review of current evidence and practical approach towards prevention and management. Eur J Pediatr. 2021;180(4):1009-31. https://doi.org/10.1007/s00431-020-03866-3
    » https://doi.org/10.1007/s00431-020-03866-3
  • 17.
    Agência Nacional de Vigilância Sanitária. Nota técnica GVIMS/GGTES/ANVISA Nº 07/2020. 2020. [cited on Nov 30, 2020]. Available from: https://www.anvisa.gov.br/segurancadopaciente/index.php/alertas/item/nota-tecnica-gvims-ggtes-anvisa-n-07-2020
    » https://www.anvisa.gov.br/segurancadopaciente/index.php/alertas/item/nota-tecnica-gvims-ggtes-anvisa-n-07-2020
  • 18.
    Sociedade Brasileira de Pediatria. Recomendações para Assistência ao Recém-Nascido na sala de parto de mãe com COVID-19 suspeita ou confirmada. 2020. [cited on Nov 30, 2020]. Available from: https://www.sbp.com.br/fileadmin/user_upload/22422b-NAlerta-Assist_RN_SalaParto_de_mae_com_COVID-19.pdf
    » https://www.sbp.com.br/fileadmin/user_upload/22422b-NAlerta-Assist_RN_SalaParto_de_mae_com_COVID-19.pdf
  • 19.
    Tanacan A, Erol SA, Turgay B, Anuk AT, Secen EI, Yegin GF, et al. The rate of SARS-CoV-2 positivity in asymptomatic pregnant women admitted to hospital for delivery: experience of a pandemic center in Turkey. Eur J Obstet Gynecol Reprod Biol. 2020;253:31-4. https://doi.org/10.1016/j.ejogrb.2020.07.051
    » https://doi.org/10.1016/j.ejogrb.2020.07.051
  • 20.
    Chandrasekharan P, Vento M, Trevisanuto D, Partridge E, Underwood MA, Wiedeman J, et al. Neonatal resuscitation and postresuscitation care of infants born to mothers with suspected or confirmed SARS-CoV-2 infection. Am J Perinatol. 2020;37(8):813-24. https://doi.org/10.1055/s-0040-1709688
    » https://doi.org/10.1055/s-0040-1709688
  • 21.
    Oran DP, Topol EJ. Prevalence of asymptomatic SARS-CoV-2 infection: a narrative review. Ann Intern Med. 2020;173(5):362-7. https://doi.org/10.7326/M20-3012
    » https://doi.org/10.7326/M20-3012
  • 22.
    Amaral WND, Moraes CL, Rodrigues APDS, Noll M, Arruda JT, Mendonça CR. Maternal coronavirus infections and neonates born to mothers with SARS-CoV-2: a systematic review. Healthcare. 2020;8(4):511. https://doi.org/10.3390/healthcare8040511
    » https://doi.org/10.3390/healthcare8040511
  • 23.
    Elshafeey F, Magdi R, Hindi N, Elshebiny M, Farrag N, Mahdy S, et al. A systematic scoping review of COVID-19 during pregnancy and childbirth. Int J Gynaecol Obstet. 2020;150(1):47-52. https://doi.org/10.1002/ijgo.13182
    » https://doi.org/10.1002/ijgo.13182
  • 24.
    Shah PS, Diambomba Y, Acharya G, Morris SK, Bitnun A. Classification system and case definition for SARS-CoV-2 infection in pregnant women, fetuses, and neonates. Acta Obstet Gynecol Scand. 2020;99(5):565-8. https://doi.org/10.1111/aogs.13870
    » https://doi.org/10.1111/aogs.13870
  • 25.
    Cavalcante MB, Cavalcante CTMB, Sarno M, Barini R, Kwak-Kim J. Maternal immune responses and obstetrical outcomes of pregnant women with COVID-19 and possible health risks of offspring. J Reprod Immunol. 2021;143:103250. https://doi.org/10.1016/j.jri.2020.103250
    » https://doi.org/10.1016/j.jri.2020.103250
  • Funding: none.

Publication Dates

  • Publication in this collection
    17 July 2023
  • Date of issue
    2023

History

  • Received
    25 Apr 2023
  • Accepted
    26 Apr 2023
Associação Médica Brasileira R. São Carlos do Pinhal, 324, 01333-903 São Paulo SP - Brazil, Tel: +55 11 3178-6800, Fax: +55 11 3178-6816 - São Paulo - SP - Brazil
E-mail: ramb@amb.org.br