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Erschienen in: BMC Pregnancy and Childbirth 1/2021

Open Access 02.04.2021 | COVID-19 | Research article

The association between SARS-CoV-2 infection and preterm delivery: a prospective study with a multivariable analysis

verfasst von: Oscar Martinez-Perez, Pilar Prats Rodriguez, Marta Muner Hernandez, Maria Begoña Encinas Pardilla, Noelia Perez Perez, Maria Rosa Vila Hernandez, Ana Villalba Yarza, Olga Nieto Velasco, Pablo Guillermo Del Barrio Fernandez, Laura Forcen Acebal, Carmen Maria Orizales Lago, Alicia Martinez Varea, Begoña Muñoz Abellana, Maria Suarez Arana, Laura Fuentes Ricoy, Clara Martinez Diago, Maria Jesus Janeiro Freire, Macarena Alférez Alvarez-Mallo, Cristina Casanova Pedraz, Onofre Alomar Mateu, Cristina Lesmes Heredia, Juan Carlos Wizner de Alva, Rut Bernardo Vega, Montserrat Macia Badia, Cristina Alvarez Colomo, Antonio Sanchez Muñoz, Laia Pratcorona Alicart, Ruben Alonso Saiz, Monica Lopez Rodriguez, Maria del Carmen Barbancho Lopez, Marta Ruth Meca Casbas, Oscar Vaquerizo Ruiz, Eva Moran Antolin, Maria Jose Nuñez Valera, Camino Fernandez Fernandez, Albert Tubau Navarra, Alejandra Maria Cano Garcia, Carmen Baena Luque, Susana Soldevilla Perez, Irene Gastaca Abasolo, Jose Adanez Garcia, Maria Teulon Gonzalez, Alberto Puertas Prieto, Rosa Ostos Serna, Maria del Pilar Guadix Martin, Monica Catalina Coello, Elena Ferriols Perez, Africa Caño Aguilar, Maria Luisa De la Cruz Conty, Jose Antonio Sainz Bueno, Spanish Obstetric Emergency Group

Erschienen in: BMC Pregnancy and Childbirth | Ausgabe 1/2021

Abstract

Background

To determine whether severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2, the cause of COVID-19 disease) exposure in pregnancy, compared to non-exposure, is associated with infection-related obstetric morbidity.

Methods

We conducted a multicentre prospective study in pregnancy based on a universal antenatal screening program for SARS-CoV-2 infection. Throughout Spain 45 hospitals tested all women at admission on delivery ward using polymerase-chain-reaction (PCR) for COVID-19 since late March 2020. The cohort of positive mothers and the concurrent sample of negative mothers was followed up until 6-weeks post-partum. Multivariable logistic regression analysis, adjusting for known confounding variables, determined the adjusted odds ratio (aOR) with 95% confidence intervals (95% CI) of the association of SARS-CoV-2 infection and obstetric outcomes. Main outcome measures: Preterm delivery (primary), premature rupture of membranes and neonatal intensive care unit admissions.

Results

Among 1009 screened pregnancies, 246 were SARS-CoV-2 positive. Compared to negative mothers (763 cases), SARS-CoV-2 infection increased the odds of preterm birth (34 vs 51, 13.8% vs 6.7%, aOR 2.12, 95% CI 1.32–3.36, p = 0.002); iatrogenic preterm delivery was more frequent in infected women (4.9% vs 1.3%, p = 0.001), while the occurrence of spontaneous preterm deliveries was statistically similar (6.1% vs 4.7%). An increased risk of premature rupture of membranes at term (39 vs 75, 15.8% vs 9.8%, aOR 1.70, 95% CI 1.11–2.57, p = 0.013) and neonatal intensive care unit admissions (23 vs 18, 9.3% vs 2.4%, aOR 4.62, 95% CI 2.43–8.94, p <  0.001) was also observed in positive mothers.

Conclusion

This prospective multicentre study demonstrated that pregnant women infected with SARS-CoV-2 have more infection-related obstetric morbidity. This hypothesis merits evaluation of a causal association in further research.
Hinweise

Supplementary Information

The online version contains supplementary material available at https://​doi.​org/​10.​1186/​s12884-021-03742-4.

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Abkürzungen
OR
Odds ratio
aOR
Adjusted odds ratio
NICU
Neonate intensive care unit
PCR
Polymerase-chain-reaction
PROM
Premature rupture of membranes at term
PPROM
Premature rupture of membranes at term

Key message

This prospective multicentre study revealed that pregnant women infected with SARS-CoV-2 have more infection-related obstetric morbidity (Preterm birth, premature rupture of membranes at term and neonatal intensive care unit admissions).

Background

Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), identified in December 2019, is the cause of the illness named COVID-19 [1, 2]. With more than 249,000 confirmed cases and more than 28,700 deaths by 20th August 2020, Spain remains one of the European countries most severely affected by the ongoing COVID-19 pandemic [3, 4]. Spain also established a universal screening programme for pregnancies in light of the higher disease exposure. We observed that obstetric intervention may influence the clinical course of the disease [57]. The cohort of pregnant women assembled through this programme lends itself to evaluation of concerns about obstetric outcomes.
The majority of non-pregnant patients with SARS-CoV-2 infection have uncomplicated or mild illness (81%), some will develop severe illness associated with cytokine-mediated inflammation phenomena such as IL-6 associated with the need for mechanical ventilation [8]. Initial studies have reported similar involvement in pregnant patients [9]. The inflammatory mediators associated SARS-CoV-2 infection have previously been related to poor perinatal outcomes [10, 11]. This background naturally leads to the question as to whether SARS-CoV-2 infection affects pregnancy adversely.
We hypothesised that SARS-CoV-2 infection in pregnancy, compared to non-infection, would increase infection-related obstetric morbidity including preterm birth and premature rupture of membranes which in turn would increase the admissions of the neonate to intensive care units. We tested the hypothesis in a multivariable logistic regression analysis, adjusting for the effect of known confounding variables.

Methods

This was a multicentre prospective study of consecutive cases of SARS-CoV-2 infection in a pregnancy cohort registered by the Spanish Obstetric Emergency group in 45 hospitals [12]. The registry’s objective updates were approved by the coordinating hospital’s Medical Ethics Committee on March 23rd, 2020 (reference number: PI 55/20); each collaborating center subsequently obtained protocol approval locally. The registry protocol is available in ClinicalTrials.gov, identifier: NCT04558996, and in Additional File 1. A complete list of the centers contributing to the study is provided in Supplementary Table 1, Additional File 2. Upon recruitment, given the contagiousness of the disease and the lack of personal protection equipment, mothers consented by either signing a document (Additional File 3), when possible, or by giving permission verbally which was recorded in the patient’s chart. A specific database was designed for recording information regarding SARS-CoV-2 infection in pregnancy. Data were entered by the lead researcher for each center after delivery, with a follow-up of 6-weeks postpartum in order to detect complications or symptomatic infections. We developed an analysis plan using recommended contemporaneous methods and followed existing guidelines for reporting our results (Supplementary Table 2, Additional File 2) [13].

Infected group

We included infected obstetric patients detected by routine screening for SARS-CoV-2 infection, which was carried out in every pregnant at admission on delivery ward during the study period from the 23rd of March to the 31st of May 2020 (Fig. 1). SARS-CoV-2 infection was diagnosed by positive double-sampling polymerase-chain-reaction (PCR) from nasopharyngeal swabs. All identified cases were included in the study, irrespective of clinical signs and symptoms or the result of another serological test. In those cases, with a clinical presentation of SARS-CoV-2 infection, it was classified following the WHO division for adults: mild symptoms, mild-moderate pneumonia, severe pneumonia and septic shock [14].

Non-infected comparison group

Non-infected patients were those defined by a negative PCR in the routine screening carried out in every pregnant at admission on delivery ward. Among these PCR negative mothers, each center identified 2–3 pregnancies delivered immediately before and/or after delivery of each SARS-CoV-2 infected mother (Fig. 1). This method of identifying mothers not exposed to SARS-CoV-2 infection was deployed to adjusted for center conditions at the time of delivery and decreased the risk of bias.

Study information

Hospitals collected the encoded information in two separate phases: during the enrolment period that occurred at the time of the SARS-CoV-2 test during pregnancy and within 6 weeks after birth. Information regarding the demographic characteristics of each pregnant woman, comorbidities and current obstetric history was extracted from the clinical history and from the interview with the patient; subsequently, age and race were categorized following the classification used by the CDC [15]. Definitions of obstetric conditions followed international criteria [1618]. Perinatal events, medical and obstetric complications were recorded. Preterm deliveries were classified as spontaneous onset (including those resulting from a PPROM), induced labour/C-section due to PPROM and iatrogenic (not associated with PPROM). Patients were followed until six weeks postpartum. Neonatal events were recorded until 14 days postpartum. Recorded variables are listed in Supplementary Table 1, Additional File 1. A total of 33 dropout cases were recorded from the beginning of the registry; the reasons were incomplete information in the registry database, did not participate in the six-week postpartum follow-up and/or voluntary withdrawal of the patient.

Data analysis

We estimated that a sample size of 246 SARS-CoV-2 positive pregnancies with a ratio 1:3 of negative pregnancies would detect a 6% difference in proportions between groups with a power of 80% at a significance level of 5%, assuming a 7% event rate of preterm deliveries in the non-infected group [19]. This level of event rate also permitted us to build logistic regression models without overfitting using the 10:1 event per variable rule.
For the descriptive analysis of the data, absolute and relative frequencies were used in the case of categorical variables and means and ranges in the case of quantitative variables. The possible association of both the characteristics of the patients and the outcomes collected with SARS-CoV-2 infection was analysed using the Pearson’s Chi-square test or Fisher’s exact test and the Mann-Whitney U test (after checking the absence of normality of the data using the Kolmogorov-Smirnov test). Statistical tests were two-sided and were performed with SPSS V.20 (IBM Inc., Chicago, Il, USA); statistically significant associations were considered to exist when the p value was less than 0.05.
For computing measures of association of the outcomes of interest that were statistically significant in the univariate analysis (and with enough number of events) with SARS-CoV-2 infection, the influence of known and suspected measured confounding factors was controlled for multivariable logistic regression modelling in order to derive adjusted odds ratios (aOR) with 95% confidence intervals (95% CI). Models were built for each outcome separately, incorporating a range of independent variables appropriate for the adjustment of the association between SARS-CoV-2 infection and that outcome. The selection process for variables was driven by causal knowledge for the adjustment of confounding, based on previous findings and clinical constraints [11, 1418]. Besides SARS-CoV-2 positivity, the preterm delivery model included Ethnicity [categorized as white European, Latin American and other ethnic groups (black non-Hispanic, Asian non-Hispanic and Arab)], multiple pregnancy, in vitro fertilization, gestational hypertensive disorders (moderate or severe preeclampsia and HELLP), miscarriage risk and clinical and ultrasound prematurity screening; the spontaneous preterm delivery model included ethnicity (categorized as above), multiple pregnancy, miscarriage risk and clinical and ultrasound prematurity screening; the premature rupture of membranes at term (PROM) model included multiple pregnancy, miscarriage risk, cough, obesity (BMI > 30 kg/m2) and smoking [categorized as smokers (actual and ex-smokers) and non-smokers]; the preterm premature rupture of membranes (PPROM) model included multiple pregnancy and miscarriage risk; and the neonate intensive care unit (NICU) admission model included multiple pregnancy, gestational hypertensive disorders and clinical and ultrasound prematurity screening as independent variables.
A complete list of the final set of covariates is provided with each model in the results section. The modelling was conducted after excluding cases with missing data. A prematurity screening program was not established in all participating hospitals and that variable had 11.3% of missing values, whereas the remaining variables had less than 1.2% of missing values. Regression analyses were carried out using lme4 package in R, version 3.4 (RCoreTeam, 2017) [20].

Results

One thousand and nine (1009) patients were analysed. 246 pregnant women in the infected group and 763 in the non-infected group. Of the 246 positive cases, 88.6% (n = 218) were asymptomatic at delivery while 11.4% (n = 28) were symptomatic. Of the asymptomatic women, 44 (20.2%) had previously presented symptoms and 174 (79.8%) were totally asymptomatic. On the other hand, of the pregnant women who showed symptoms at the time of delivery, 24 (85.7%) cases corresponded to mild symptoms (being the most prevalent, cough 33.3%, and anosmia 20.8%, followed by fatigue/discomfort, fever and dyspnoea), 2 (7.1%) pregnant women presented mild-moderate pneumonia and another 2 (7.1%) pregnant women had developed severe pneumonia. No case of septic shock or maternal death was recorded in pregnant women with SARS-CoV-2 infection included in the study.
The demographic characteristics, comorbidities and current obstetric history of the positive cohort and the subsample of negative patients concurrent in time deliveries (246 vs 763) are shown in Table 1. The only variable in which statistically significant differences were observed was ethnicity, being significantly higher the proportion of Latin American women in the infected cohort compared to the non-infected group (p <  0.001; OR = 2.85, 95% CI: 1.96–4.15), while the opposite was true for White European patients (p < 0.001, OR = 0.49, 95% CI: 0.36–0.67).
Table 1
Demographic characteristics, comorbidities and current obstetric history of the study participants (n = 1009)
 
Infected Group
Non-Infected Group
p-value
 
Number
246
763
  
Maternal characteristics
 Maternal age (years; mean/range)
32.6 (18–45)
32.5 (18–49)
0.671
 
 Age Range
  18–24
28 (11.5%)
70 (9.2%)
0.309
 
  25–34
114 (46.3%)
400 (52.8%)
0.097
 
  35–49
101 (41.1%)
287 (37.9%)
0.335
 
 Ethnicity
  White European
158 (64.2%)
600 (78.9%)
< 0.001*
0.49 (0.36–0.67)
  Latino Americans
59 (24.0%)
76 (10.0%)
< 0.001*
2.85 (1.96–4.15)
  Black non-Hispanic
8 (3.3%)
11 (1.4%)
0.100
 
  Asian non-Hispanic
4 (1.6%)
18 (2.4%)
0.494
 
  Arab
17 (6.9%)
55 (7.2%)
0.875
 
 Nulliparous
82 (38.5%)
254 (37.4%)
0.775
 
 Smoking a
35 (14.2%)
94 (12.3%)
0.436
 
Maternal comorbidities
 Obesity (BMI > 30 kg/m2)
33 (13.7%)
119 (16.8%)
0.255
 
 Cardiovascular comorbidities
  Chronic Heart Failure b
3 (1.2%)
7 (1.0%)
0.744
 
  Pre-pregnancy HBP
3 (1.2%)
6 (0.9%)
0.587
 
 Pulmonary comorbidities
  Chronic Pulmonary Disease (not asthma)
1 (0.4%)
1 (0.1%)
0.445
 
  Asthma
4 (1.7%)
25 (3.5%)
0.144
 
 Hematologic comorbidities
  Chronic Blood Disease
1 (0.4%)
4 (0.6%)
1.000
 
  Thrombophilia
3 (1.2%)
13 (1.8%)
0.546
 
  Antiphospholipid Syndrome
0 (0.0%)
1 (0.1%)
1.000
 
 Chronic kidney disease
0 (0.0%)
2 (0.3%)
1.000
 
 Chronic liver disease
3 (1.2%)
2 (0.3%)
0.097
 
 Rheumatic disease
1 (0.4%)
7 (1.0%)
0.397
 
 Diabetes mellitus
1 (0.4%)
10 (1.5%)
0.305
 
 Depressive syndrome
2 (0.8%)
8 (1.1%)
0.680
 
Current obstetric history
 Gestational age at enrolment (weeks+days; mean/range)
38 + 1 (27–42)
38 + 6 (21–42)
< 0.001
 
 Multiple pregnancy
6 (2.4%)
31 (4.1%)
0.239
 
 In Vitro Fertilization
15 (6.1%)
27 (3.5%)
0.081
 
 Haemoglobin < 10 g/dL
6 (2.5%)
39 (5.4%)
0.065
 
 Platelets < 100,000/μL
3 (1.2%)
2 (0.3%)
0.104
 
 Pregnancy-induced hypertension c
12 (4.9%)
34 (4.8%)
0.962
 
 Gestational diabetes
17 (7.0%)
61 (8.4%)
0.476
 
 Intrauterine growth restriction
13 (5.3%)
27 (3.8%)
0.303
 
 High Risk Preeclampsia Screening
8 (3.7%)
38 (5.8%)
0.230
 
 High-risk Chromosomal Abnormality Screening
4 (1.7%)
18 (2.6%)
0.428
 
 Clinical and Ultrasound Prematurity Screening
5 (2.3%)
21 (3.3%)
0.461
 
 Miscarriage risk
11 (4.5%)
17 (2.2%)
0.062
 
Data are shown as n (% of total), except where otherwise indicated
OR: odds ratio; CI: confidence interval; BMI: Body Mass Index; HBP: High Blood Pressure
*Statistically significant differences: OR and 95% CI were estimated
a Current smoker and ex-smoker
b Including Congenital Heart Disease, not Hypertension
c Hypertension + preeclampsia
When the possible association of perinatal and neonatal events with SARS-CoV-2 infection was analysed by univariate and multivariable logistic regression using complete case analyses (without imputation for missing values) (Tables 2 and 3), twice as many deliveries with less than 37 weeks of gestation were observed in the infected cohort (13.8%) than in the negative group (6.7%) (p = 0.002), with an adjusted OR equal to 2.12 (95% CI: 1.32–3.36), although no statistically significant differences had been observed in the clinical and ultrasound screening for prematurity between both groups (p = 0.461) (Table 1). Among preterm deliveries, iatrogenic preterm delivery (not associated with PPROM) was practically four times more frequent in infected by SARS-CoV-2 pregnant women than in the non-infected group (4.9% vs 1.3%, p = 0.001), while the occurrence of spontaneous preterm deliveries was not affected by SARS-CoV-2 infection status (p = 0.760, adjusted OR = 1.10, 95% CI: 0.57–2.06) (Table 3). In the positive group, symptomatic SARS-CoV-2 infection were present in 5 (42%) out of 12 iatrogenic preterm deliveries, while this was the case in only 3 (20%) out of 15 spontaneous preterm deliveries.
Table 2
Maternal and neonatal outcomes of the study participants (n = 1009)
 
Infected Group
Non-Infected Group
p-value
Number
246
763
 
Perinatal outcome
 Gestational age at delivery (weeks+days; mean/range)
38 + 4 (27–42)
39 + 0 (23–42)
0.010
 Type of delivery
  Cesarean
55 (22.4%)
143 (18.7%)
0.214
  Eutocic
170 (69.1%)
506 (66.3%)
0.419
  Instrumental
21 (8.5%)
114 (14.9%)
0.010
 Preterm deliveries (< 37 weeks of gestational age)
34 (13.8%)
51 (6.7%)
0.001
  Spontaneous delivery (including PPROM)
15 (6.1%)
36 (4.7%)
0.390
  Induced/Elective C-section due to PPROM
7 (2.8%)
5 (0.7%)
0.012
  Iatrogenic delivery (no PPROM)
12 (4.9%)
10 (1.3%)
0.001
   Causes of preterm iatrogenic delivery:
   COVID-19 mild symptoms
3/12
0/10
 
   Pneumonia
3/12
0/10
 
   Severe preeclampsia
4/12
1/10
0.323
 PROM
39 (15.8%)
75 (9.8%)
0.009
 PPROM
11 (4.5%)
15 (2.0%)
0.031
  Gestational age at PPROM (weeks+days; mean/range)
33 + 5 (28–36)
33 + 6 (28–36)
0.610
Medical and obstetrical complications
 Admitted in ICU
5 (2.0%)
2 (0.3%)
0.011
  Days in ICU (mean/range)
9.5 (6–14)
2 (2–2)
 
Obstetrical complications
 Hemorrhagic events
10 (4.1%)
34 (4.5%)
0.794
  Abruptio placentae
2 (0.8%)
1 (0.1%)
0.149
  Postpartum hemorrhage
8 (3.3%)
33 (4.3%)
0.459
 Gestational hypertensive disorders
11 (4.5%)
44 (5.8%)
0.436
  Severe preeclampsia
6 (2.4%)
3 (0.4%)
0.008
   Admitted in ICU
2/6
0/3
 
   Invasive ventilation
0/6
0/7
 
  Moderate preeclampsia
5 (2.0%)
41 (5.4%)
0.025
Neonatal data
 Apgar 5 score < 7
5 (2.0%)
8 (1.1%)
0.325
 Umbilical artery pH < 7.10
6 (3.0%)
24 (3.8%)
0.608
 Admitted in NICU
23 (9.3%)
18 (2.4%)
0.001
  Days in NICU (mean/range)
13.8 (1–48)
10.7 (2–26)
0.379
   Cause of NICU admission:
   Prematurity
15/23
12/18
 
   Respiratory distress
2/23
6/18
 
 Neonatal COVID-19 PCR testing within the first 48 h
196 (79.7%)
0 (0.0%)
 
Stillbirth
3 (1.2%)
1 (0.1%)
0.047
Neonatal mortality
0 (0.0%)
1 (0.1%) a
1.000
6 weeks mother follow-up
 Mastitis
1 (0.4%)
1 (0.1%)
0.428
14 days neonate follow-up
 Readmission due to COVID-19
0 (0.0%)
0 (0.0%)
 
Data are shown as n (% of total), except where otherwise indicated
COVID-19: Coronavirus disease 2019; PROM: Premature rupture of membranes; PPROM: Preterm Premature Rupture of Membranes; ICU: Intensive care unit; NICU: Neonatal intensive care unit
a Prematurity causes, gestational age at delivery was 24 weeks
Table 3
Odds ratio and adjusted odds ratio for obstetric outcomes associated with SARS-CoV-2 exposure in pregnancy
  
Outcomes
Preterm delivery
Spontaneous preterm delivery
PROM
PPROM
NICU admission
Univariate analysis (OR)
 SARS-CoV-2 positive
2.23
1.31
1.72
2.33
4.27
  95% CI
1.41–3.54
0.69–2.39
1.14–2.62
1.06–5.15
2.26–8.05
  p-value
0.001
0.390
0.009
0.031
0.001
Multivariate analysis (aOR)
 SARS-CoV-2 positive
2.12
1.10
1.70
2.26
4.62
  95% CI
1.32–3.36
0.57–2.06
1.11–2.57
0.99–4.98
2.43–8.94
  p-value
0.002
0.760
0.013
0.045
< 0.001
 In Vitro Fertilization
2.37
  95% CI
0.97–5.16
  p-value
0.041
 Miscarriage Risk
2.61
4.19
2.69
  95% CI
0.92–6.42
1.35–10.88
0.42–9.91
  p-value
0.050
0.006
0.198
Ethnicity
 Latin American vs White European
2.11 (1.04–4.09)
 Other Ethnic Groups vs White European
0.38 (0.06–1.27)
  p-value
0.031 and 0.188
 Multiple pregnancy
1.86*10−7
3.72
  95% CI
0.00 – .
1.02–10.73
  p-value
0.981
0.025
 Gestational Hypertensive Disorders
3.63
  95% CI
1.28–8.91
  p-value
0.008
OR Odds Ratio
aOR adjusted Odds Ratio
95% CI 95% Confidence Interval
PROM Premature Rupture of Membranes at term
PPROM Preterm Premature Rupture of Membranes
NICU Neonatal Intensive Care Unit
Multivariable logistic regression used for each outcome as dependent variable and COVID-19 exposure in pregnancy and known/suspected confounding variables as independent variables (see Methods for details)
-- Variables not included or not held in the multivariate model
Similarly, a higher risk of premature rupture of membranes, at term (PROM) and preterm (PPROM), was observed in the infected group (p = 0.009 and p = 0.031, respectively) (Table 2). In the case of PROM, the finding of multivariable logistic regression was consistent with the above result, with a 70% increase of occurrence in infected patients compared to non-infected (adjusted OR = 1.70, 95% CI: 1.11–2.57) (Table 3).
No maternal deaths were recorded in the 1009 patients in the study, but there were intrauterine fetal deaths, with the proportion of these being considerably higher in patients in the positive group than in the subsample of negative patients (1.2% vs 0.1%, p = 0.047) (Table 2).
When the information regarding the neonate was analysed (Tables 2 and 3), those born to mothers with SARS-CoV-2 infection were admitted to the NICU significantly more often than those born to non-infected mothers (p < 0.001, adjusted OR = 4.62, 95% CI: 2.43–8.94). Prematurity and respiratory distress were the main causes of NICU admission (Table 2), while none of these admissions were due to SARS-CoV-2 infection in newborns. In 189 (76.8%) of the SARS-CoV-2 infection cases, a PCR analysis was performed on nasopharyngeal and/or oropharyngeal samples of the newborns; 147 were performed during the first 12 h of life, three of which were positive, and another 42 were performed until 48 h of life, all resulting negative. The 3-initial positive newborns were retested at 48 h, with final negative results.

Discussion

Main findings

Through a multicentre prospective study, we analysed the relationship between SARS-CoV-2 exposure and infection-related obstetric outcomes. We found, using multivariable models adjusting for confounding factors, that the pregnant women with SARS-CoV-2 infection had more preterm births, premature rupture of membranes at term and NICU admissions compared to the pregnant woman who were not exposed.

Strengths and weaknesses

Ours is a study with a group of positive mothers carried out during a difficult pandemic situation whose continuing objective is to investigate the influence of SARS-CoV-2 infection on delivery and the puerperium. We wish to obtain the best epidemiological information in the shortest possible time with a follow-up 6 weeks after delivery. Patient recruitment continues in our registry and this is an initial analysis. Our work is one of the first multicentre prospective studies to analyse the relationship between SARS-CoV-2 infection and prematurity. The relationship that we establish with premature rupture of membranes raises future lines of research.
The most important limitation of our work is the inability to compare infected patients with uninfected patients from the beginning due to the lack of diagnostic tests and the health sector crisis that occurred. When a screening system was established, there were not as many patients with severe symptoms and the number of events reduced the ability to analyse some effects of symptomatic SARS-CoV-2 infection. Many cases of obstetric severe preeclampsia, haemorrhage, pulmonary thromboembolism and abruptio occurred mainly in the months of March and April before many centres started screening programmes and the cohort study began, so no distinction has been made between the different clinical presentations of the disease. We could not do a multivariable analysis of such conditions.
No serological test was performed on patients who had a negative PCR test, either because the tests were not available at the time of recruitment or because they did not have a proven sensitivity. In some cases, these patients may have already had the disease. No serology was performed during those months on asymptomatic PCR-positive patients to confirm their disease and immune response. Our study is best understood if the results are interpreted under this premise and therefore our group continues to recruit patients to seek more associations, explanations and causations. This work reflects the conditions of patients with SARS-CoV-2 infection at the time of delivery and the puerperium. It has not analysed the course of the disease during pregnancy, nor has it recorded late abortions, vertical transmission, or causes of intrauterine mortality.
In addition, we acknowledge as a limitation the absence of the complete cohort screened from analysis. In this sense our study has a hybrid design. The PCR negative comparison group was a subsample of the screen negative cohort from all 45 hospitals that had PCR positive mothers. The concurrent method applied for selection of non-infected cohort allowed for a comparison unaffected by difference in time of exposure and outcome assessment.

Comparison with other studies

The symptoms of the patients in our study do not differ from those already published [21, 22]. Although most did not have any symptoms, we did find an increase in obstetric pathology in these patients, which in our opinion indicates that in the pregnant woman with asymptomatic SARS-CoV-2 infection there is a specific obstetric pathology that needs to be recognised. In the same way as other authors, we have also found a demographic factor, such as ethnicity, that increases the possibility that a patient has SARS-CoV-2 infection [15, 23]. It is necessary to know if there is a component of genetic susceptibility or if there are social factors that explain this association. There are already studies that relate this situation to less access to healthcare resources or the possibility of confinement which complies with healthcare measures [24].
Patients with SARS-CoV-2 infection are at increased risk of preterm delivery associated with increased iatrogenic preterm delivery. The explanation for this risk is the need to end the pregnancy due to maternal diseases, such as severe pre-eclampsia and pneumonia, which are more frequent in these patients and lead to more labour inductions. A unique and novel finding in our study is the association between premature rupture of membranes at term and SARS-CoV-2 infection. PROM may result in immediate risks and subsequent problems including maternal or neonatal infection [25]. One of the possible explanations we found for this association is the activation of a series of mediators and biochemical pathways of inflammation in the premature rupture of membranes and premature delivery that are also found in SARS-CoV-2 infection, such as macrophages or IL-6 [26]. The studies demonstrating the influence of IL-6 on preterm delivery are a strong basis for studying this association [27]. Cytokines are vital in regulating immunological and inflammatory responses. Among them, IL-6 is of major importance because there is evidence that circulating IL-6 levels are closely linked to the severity of the SARS-CoV-2 infection [28]. There are already treatments that are indicated based on these findings [29].
We observed a significant increase in the stillbirth rate in the univariate analysis alone. The role of inflammation mediators in these deaths could be the subject of a line of research because it is known that women without SARS-CoV-2 infection who have a pregnancy loss, have significantly higher amniotic fluid IL-6 concentration levels than those with a normal outcome [30]. We found no differences in mortality or early or late neonatal morbidity related to SARS-CoV-2 exposure in our study, unlike reports from other series [31, 32]. .There is a higher risk that the children of SARS-CoV-2 infection mothers enter the NICU, with prematurity being one of the determining factors. All newborns were followed for at least 14 days by the different neonatology units of the participating hospitals, without any case of neonatal SARS-CoV-2 infection being detected in that period.
To date, there has been indirect evidence on placental involvement which would explain our findings [33, 34]. Our results derived using multivariable analyses confirm those of the cases series published at the beginning of the pandemic that described preterm deliveries and premature rupture of the membranes [21, 31, 35].

Conclusion

Pregnant SARS-CoV-2 infection patients are a population at risk of suffering preterm deliveries, and the disease has an impact on NICU admissions. Premature rupture of membranes at term and preterm are more frequent in patients with SARS-CoV-2 infection.

Acknowledgements

Authors thank José Montes (Effice Research) for his support with the statistics, Professor Khalid Khan (Department of Preventive Medicine and Public Health, University of Granada) and Dr. Mar Gil Mina (Hospital Universitario de Torrejón) for their scientific advice, and Meisys for their support with the manuscript writing.

Declarations

All procedures were approved by the Drug Research and Clinical Research Ethics Committee of the Puerta de Hierro University Hospital (Madrid, Spain) on 23rd March 2020 (protocol registration number, 55/20); each collaborating center subsequently obtained protocol approval locally (Ethics Committees of the participant hospitals, listed in the Supplementary Table 1 of the Additional File 2). Upon recruitment, mothers consented to participate in the study by either signing a document, when possible, or by giving permission verbally which was recorded in the patient’s chart in the electronic clinical recording system. The possibility of verbal consent was approved by the Ethics Committees during the first three months of the pandemic, given the contagiousness of the disease and the lack of personal protection equipment; afterwards, written consent (using the Patient Consent Form, Additional File 3) was collected from every patient who had previously given permission verbally.
Not Applicable.

Competing interests

The authors declare that they have no competing interests.
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Metadaten
Titel
The association between SARS-CoV-2 infection and preterm delivery: a prospective study with a multivariable analysis
verfasst von
Oscar Martinez-Perez
Pilar Prats Rodriguez
Marta Muner Hernandez
Maria Begoña Encinas Pardilla
Noelia Perez Perez
Maria Rosa Vila Hernandez
Ana Villalba Yarza
Olga Nieto Velasco
Pablo Guillermo Del Barrio Fernandez
Laura Forcen Acebal
Carmen Maria Orizales Lago
Alicia Martinez Varea
Begoña Muñoz Abellana
Maria Suarez Arana
Laura Fuentes Ricoy
Clara Martinez Diago
Maria Jesus Janeiro Freire
Macarena Alférez Alvarez-Mallo
Cristina Casanova Pedraz
Onofre Alomar Mateu
Cristina Lesmes Heredia
Juan Carlos Wizner de Alva
Rut Bernardo Vega
Montserrat Macia Badia
Cristina Alvarez Colomo
Antonio Sanchez Muñoz
Laia Pratcorona Alicart
Ruben Alonso Saiz
Monica Lopez Rodriguez
Maria del Carmen Barbancho Lopez
Marta Ruth Meca Casbas
Oscar Vaquerizo Ruiz
Eva Moran Antolin
Maria Jose Nuñez Valera
Camino Fernandez Fernandez
Albert Tubau Navarra
Alejandra Maria Cano Garcia
Carmen Baena Luque
Susana Soldevilla Perez
Irene Gastaca Abasolo
Jose Adanez Garcia
Maria Teulon Gonzalez
Alberto Puertas Prieto
Rosa Ostos Serna
Maria del Pilar Guadix Martin
Monica Catalina Coello
Elena Ferriols Perez
Africa Caño Aguilar
Maria Luisa De la Cruz Conty
Jose Antonio Sainz Bueno
Spanish Obstetric Emergency Group
Publikationsdatum
02.04.2021
Verlag
BioMed Central
Erschienen in
BMC Pregnancy and Childbirth / Ausgabe 1/2021
Elektronische ISSN: 1471-2393
DOI
https://doi.org/10.1186/s12884-021-03742-4

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