Keywords
SARS-CoV-2 - pregnancy - COVID-19 - screening
Since identification of the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2)
and associated coronavirus disease 2019 (COVID-19) in early 2020, infection has reached
pandemic levels and has strained health care delivery systems worldwide. Although
not currently seen as a group at high risk for complications from COVID-19,[1] the care of pregnant women and their newborns involves many areas of outpatient
and inpatient care in the peripartum period. Early experiences from a hospital system
in New York in mid-March 2020 supported the concept of universal screening of women
admitted for delivery, and the results of universal screening of 215 women from this
same hospital system were recently published, noting a 13.5% prevalence of asymptomatic,
SARS-CoV-2 infection.[2]
[3] In developing plans for maternity care at Kaiser Permanente Southern California
(KPSC) during the COVID-19 pandemic, the inclusion of universal testing on admission
for delivery was seen as a key concept, allowing for (1) rapid determination of the
woman's SARS-CoV-2 status, (2) risk-appropriate use of personal protective equipment
(PPE), and (3) timely and appropriate neonatal testing, rooming practices, and care.
The objective of this study was to estimate the prevalence of SARS-CoV-2 infection
through universal screening of a large ethnically diverse population of pregnant women
admitted for labor and delivery in the KPSC health care system.
Materials and Methods
Women admitted to obstetrical units for delivery in all 15 KPSC hospitals between
April 6 and May 11, 2020 were universally offered SARS-CoV-2 testing on admission.
Following KPSC standard protocol, a single swab collection from both the posterior
oropharynx and nasopharynx was obtained and tested for SARS-CoV-2. If the anticipated
admission-delivery interval was less than 24 hours, the sample was processed without
the use of transport media at the local medical center laboratory using the Abbott
IDNOW COVID-19 assay (Abbott Diagnostics Scarborough, Inc., Scarborough, ME)[4] according to manufacturer's specifications. Initial samples with an “invalid” result
were repeated immediately, and if valid, the second result used for this analysis.
For estimated admission-delivery interval greater than 24 hours, the sample was placed
in transport media and processed at one of two KPSC regional reference laboratories
using the Roche cobas 6800 real-time polymerase chain reaction SARS-CoV-2 assay (Roche
Diagnostics, Indianapolis, IN).[5] All neonates born to women with confirmed COVID-19 infection were tested at 24 hours
of life with a single oropharyngeal/nasopharyngeal combination swab using the Roche
test platform. Electronic health records (EHR) were used to obtain information on
maternal age, race/ethnicity (categorized as non-Hispanic white, non-Hispanic black,
Hispanic, Asian/Pacific Islander, and other/mixed racial/ethnic groups) timing of
prenatal care initiation (early or after the first trimester), parity (nullipara or
multipara), gravida (0, 1, and ≥2), smoking during pregnancy (yes/no), maternal pre-pregnancy
body mass index (kg/m2) measured routinely at first antenatal visit, gestational age based on clinical estimates
obtained from perinatal EHR records and maternal comorbidities (pregestational hypertension,
diabetes, asthma, and chronic obstructive pulmonary disease), and evidence of COVID-19
through the time of hospital discharge.
Statistical Analysis
Differences in the distribution of maternal and infant characteristics were assessed
using the Chi-square test for categorical variables and Student's t-test for continuous variables. The prevalence of SARS-CoV-2 infection in women admitted
for delivery was calculated from the number of women tested positive during labor
after the implementation of universal testing per 100 women tested. All analyses were
performed using SAS software version 9.4 (SAS Institute, Cary, NC) by two of the authors
(D.G. and V.C.). This study was approved by the institutional review board of KPSC
with waiver of informed consent.
Results
The cohort was comprised of 3,963 pregnant women admitted to labor and delivery units
after the universal screening for SARS-CoV-2 was instituted ([Table 1]). A total of 40 (1.00%) women declined testing or had no result, leaving 3,923 (99.00%)
women with results for analysis. Out of those women who were tested for SARS-CoV-2,
17 women had a positive test, resulting in an 0.43% (95% confidence interval [CI]:
0.23–0.63%) prevalence of SARS-CoV-2 infection in the population studied. All women
who tested positive were asymptomatic at the time of admission. One woman developed
a headache attributed to clinical COVID-19 on postpartum day 3. Of the women who tested
negative, 24 had fever on admission and none of those women developed COVID-19 infection
during the following 14 days. No neonates had positive SARS-CoV-2 test results at
24 hours of life.
Table 1
Study cohort and SARS-CoV-2 test status from April 6 to May 11, 2020
|
Number (%)
|
|
Total deliveries
|
3,963 (100.00)
|
|
Number of SARS-CoV-2 tests done
|
3,923 (99.00)
|
|
Abbott
|
2,692 (68.62%, 95% CI: 66.87–70.37%)
|
|
Roche
|
1,229 (31.33%, 95% CI: 28.74–33.92%)
|
|
Outside laboratory
|
2 (0.05%, 95% CI: 0.01–0.18%)
|
|
Number declined or no result
|
40 (1.00)
|
|
Number tested positive
|
17 (0.43%, 95% CI: 0.23–0.63%)
|
|
Abbott
|
8 (0.30%, 95% CI: 0.09–0.51%)
|
|
Roche
|
8 (0.65%, 95% CI: 0.20–1.10%)
|
|
Outside laboratory
|
1 (0.03%, 95% CI: 0.00–0.14%)
|
Abbreviations: CI, confidence interval; SARS-CoV-2, severe acute respiratory syndrome
coronavirus 2.
Demographic characteristics of the study cohort are shown in [Table 2]. Over half of the women delivered during the study period were from Hispanic racial-ethnic
background (51.2%) followed by non-Hispanic white (23.5%), non-Hispanic black (7.7%),
Asian/Pacific Islander (15.0%), and Other/Mixed (1.8%) racial-ethnic background. There
were no significant differences in demographic characteristics between women with
positive test results and the remainder of the cohort.
Table 2
Characteristics based on SARS-COV-2 test results
|
Characteristics
|
Total deliveries
n = 3,923
|
SARS-CoV-2 test result
|
p-Values
|
|
Negative
n = 3,906
|
Positive
n = 17
|
|
Maternal age, year mean (SD)
|
31.2 (5.29)
|
31.2 (5.29)
|
33.2 (5.46)
|
0.145
|
|
Maternal age, n (%)
|
|
|
|
0.390
|
|
15–24 years
|
463 (11.80)
|
462 (11.83)
|
1 (5.88)
|
|
|
25–29 years
|
992 (25.29)
|
990 (25.35)
|
2 (11.76)
|
|
|
30–34 years
|
1,375 (35.05)
|
1,368 (35.02)
|
7 (41.18)
|
|
|
≥ 35 years
|
1,093 (27.86)
|
1,086 (27.80)
|
7 (41.18)
|
|
|
Race/ethnicity, n (%)
|
|
|
|
0.807
|
|
Hispanic
|
2,009 (51.21)
|
1,999 (51.18)
|
10 (58.82)
|
|
|
Non-Hispanic White
|
921 (23.48)
|
918 (23.50)
|
3 (17.65)
|
|
|
Non-Hispanic Black
|
301 (7.67)
|
300 (7.68)
|
1 (5.88)
|
|
|
Non-Hispanic Asian/Pacific Islander
|
587 (14.96)
|
585 (14.98)
|
2 (11.76)
|
|
|
Other/mixed
|
72 (1.84)
|
71 (1.82)
|
1 (5.88)
|
|
|
Unknown
|
33 (0.84)
|
33 (0.84)
|
0 (0.00)
|
|
|
Pre-pregnancy BMI, n (%)
|
|
|
|
0.981
|
|
< 18.5 kg/m2
|
30 (0.76)
|
30 (0.77)
|
0 (0.00)
|
|
|
18.5–24.9 kg/m2
|
857 (21.85)
|
854 (21.86)
|
3 (17.65)
|
|
|
25.0–29.9 kg/m2
|
596 (15.19)
|
593 (15.18)
|
3 (17.65)
|
|
|
30.0–34.9 kg/m2
|
363 (9.25)
|
362 (9.27)
|
1 (5.88)
|
|
|
35.0+ kg/m2
|
269 (6.86)
|
268 (6.86)
|
1 (5.88)
|
|
|
Missing
|
1,808 (46.09)
|
1,799 (46.06)
|
9 (52.94)
|
|
|
Smoking during pregnancy, n (%)
|
118 (3.01)
|
118 (3.02)
|
0 (0.00)
|
0.467
|
|
Early prenatal care initiation, n (%)
|
3,281 (83.63)
|
3,270 (83.72)
|
11 (64.71)
|
0.100
|
|
Gravidity, n (%)
|
|
|
|
0.530
|
|
0–1
|
1,162 (29.62)
|
1,159 (29.67)
|
3 (17.65)
|
|
|
2
|
1,129 (28.78)
|
1,124 (28.78)
|
5 (29.41)
|
|
|
≥ 3
|
1,519 (38.72)
|
1,510 (38.66)
|
9 (52.94)
|
|
|
Parity, n (%)
|
|
|
|
0.315
|
|
Nullipara
|
1,663 (42.39)
|
1,656 (42.40)
|
7 (41.18)
|
|
|
Multipara
|
2,012 (51.28)
|
2,002 (51.26)
|
10 (58.82)
|
|
|
Gestational age at admission (wk), mean (SD)
|
38.6 (2.21)
|
38.6 (2.20)
|
37.9 (4.41)
|
0.701
|
|
Comorbidities[a], n (%)
|
556 (14.17)
|
554 (14.18)
|
2 (11.76)
|
0.775
|
Abbreviations: BMI, body mass index; SARS-CoV-2, severe acute respiratory syndrome
coronavirus 2; SD, standard deviation.
a Comorbidities are pregestational hypertension and diabetes as well as asthma and
chronic obstructive pulmonary disease.
Discussion
Principal Findings and Results
In this population-based observational study of women presenting for labor and delivery
at the KPSC health care system, 99.0% of eligible patients were screened for SARS-COV-2
infection. This number represents a substantial success of our implementation of universal
screening. The calculated prevalence of a positive test for SARS-CoV-2 infection was
0.43%, an estimate much lower than the 15.4% reported by Sutton et al.[3] They reported a prevalence of 13.5% asymptomatic and 1.9% symptomatic positive COVID-19
infection. Prevalence in our study is also lower than the recent report by Vintzileos
et al,[6] finding SARS-CoV-2 infection in 19.9% (34% symptomatic and 66% asymptomatic) of
161 women tested on admission to labor and delivery at NYU Winthrop Hospital.
Clinical Implications
As Southern California and New York City have different population densities, travel
influx, and differing timelines for public health interventions to reduce the spread
of COVID-19, this lower rate of asymptomatic disease in our study population may represent
the effects of these differences. Pregnant women may also be adhering more strictly
to COVID-19 prevention guidelines, resulting in a lower rate of infection. Additionally,
this low prevalence of SARS-CoV-2 infection can inform the development of plans for
cohorting of pregnant COVID-19 patients as well as PPE optimization strategies.
The racial/ethnic composition of our study cohort is similar to that of the overall
pregnant population in KPSC ([Table 3]). Although our study was not designed to show racial/ethnic disparities in positive
test results, there were more positive test results in women 30 or more years of age
(82.36%) compared with women who tested negative (62.82%).
Table 3
Race/ethnicity distribution of study population and KPSC births in 2019 (age 15–45
years)
|
Race/ethnicity
|
Study population
n = 3,963 (%)
|
KPSC births in 2019[a]
n = 41,430 (%)
|
|
Hispanic
|
2,030 (51.22)
|
21,368 (51.58)
|
|
Non-Hispanic White
|
926 (23.37)
|
10,066 (24.30)
|
|
Non-Hispanic Black
|
308 (7.77)
|
2,994 (7.23)
|
|
Asian/Pacific Islander
|
592 (14.94)
|
6,056 (14.62)
|
|
Other/multiple
|
74 (1.87)
|
754 (1.82)
|
|
Unknown
|
33 (0.83)
|
192 (0.46)
|
Abbreviation: KPSC, Kaiser Permanente Southern California.
a Kaiser Permanente Southern California pregnant population delivered in 2019.
The absence of positive test results in this small group of neonates (n = 17) delivered to asymptomatic, SARS-CoV-2 positive women is reassuring (95% CI:
0.00–19.51%). Reports of 38 Chinese women with COVID-19 infection also have shown
no vertical transmission.[7]
[8]
[9]
[10] Several case reports of potential vertical transmission, however, have also been
reported,[11]
[12] and maternal disease severity is a potential risk factor for vertical transmission.[13] It would follow that no neonatal infections were found in our cohort of asymptomatic
mothers suggesting that the likelihood of vertical or intrapartum transmission of
SARS-CoV-2 is low.
Strengths and Limitations
The strengths of our study are the ability to implement a universal SARS-CoV-2 screening
program with nearly universal acceptance of testing by a large and ethnically diverse
population. Concerns regarding the accuracy of SARS-CoV-2, however, remain. All available
COVID-19 tests have been approved only under Emergency Use Authorization by the United
States Food and Drug Administration (FDA). Consequently, traditional information regarding
clinical test performance (sensitivity, specificity, positive, and negative predictive
values) is not currently available. Both the Abbott and Roche assays reportedly have
good analytical sensitivity with limits of detection of 125 genome equivalents/mL
and 0.004 (target 2) to 0.007 (Target 1) TCID50/mL, respectively.[4]
[5] The KPSC Laboratory Care Delivery System has performed limited interplatform reproducibility
testing with <1% discordance when performed on samples collected within 48 hours of
one another.
Conclusion
Universal SARS-CoV-2 screening in a large diverse cohort of pregnant women at the
time of delivery in Southern California demonstrated very low prevalence of infection,
allowing for risk-appropriate maternal and neonatal care as well as informing PPE
use. As the COVID-19 pandemic continues to evolve, further studies are needed to provide
community-specific data to guide obstetrical care and general public health measures.
