Skip to main content
PLOS ONE logoLink to PLOS ONE
. 2020 Dec 10;15(12):e0238409. doi: 10.1371/journal.pone.0238409

Universal screening for SARS-CoV-2 infection among pregnant women at Elmhurst Hospital Center, Queens, New York

Sheela Maru 1,2,3,*, Uday Patil 3,4, Rachel Carroll-Bennett 2,3, Aaron Baum 1, Tracy Bohn-Hemmerdinger 2,3, Andrew Ditchik 2,3, Michael L Scanlon 1, Parvathy Krishnan 3,4, Kelly Bogaert 2,3, Carson Woodbury 2,3, Duncan Maru 1,3,4,5, Lawrence Noble 3,4, Randi Wasserman 3,4, Barry Brown 2,3, Rachel Vreeman 1, Joseph Masci 3,5
Editor: Rogelio Cruz-Martinez6
PMCID: PMC7728244  PMID: 33301498

Abstract

Background

Universal screening for SARS-CoV-2 infection on Labor and Delivery (L&D) units is a critical strategy to manage patient and health worker safety, especially in a vulnerable high-prevalence community. We describe the results of a SARS-CoV-2 universal screening program at the L&D Unit at Elmhurst Hospital in Queens, NY, a 545-bed public hospital serving a diverse, largely immigrant and low-income patient population and an epicenter of the global pandemic.

Methods and findings

We conducted a retrospective cross-sectional study. All pregnant women admitted to the L&D Unit of Elmhurst Hospital from March 29, 2020 to April 22, 2020 were included for analysis. The primary outcomes of the study were: (1) SARS-CoV-2 positivity among universally screened pregnant women, stratified by demographic characteristics, maternal comorbidities, and delivery outcomes; and (2) Symptomatic or asymptomatic presentation at the time of testing among SARS-CoV-2 positive women.

A total of 126 obstetric patients were screened for SARS-CoV-2 between March 29 and April 22. Of these, 37% were positive. Of the women who tested positive, 72% were asymptomatic at the time of testing. Patients who tested positive for SARS-CoV-2 were more likely to be of Hispanic ethnicity (unadjusted difference 24.4 percentage points, CI 7.9, 41.0) and report their primary language as Spanish (unadjusted difference 32.9 percentage points, CI 15.8, 49.9) than patients who tested negative.

Conclusions

In this retrospective cross-sectional study of data from a universal SARS-Cov-2 screening program implemented in the L&D unit of a safety-net hospital in Queens, New York, we found over one-third of pregnant women testing positive, the majority of those asymptomatic. The rationale for universal screening at the L&D Unit at Elmhurst Hospital was to ensure safety of patients and staff during an acute surge in SARS-Cov-2 infections through appropriate identification and isolation of pregnant women with positive test results. Women were roomed by their SARS-CoV-2 status given increasing space limitations. In addition, postpartum counseling was tailored to infection status. We quickly established discharge counseling and follow-up protocols tailored to their specific social needs. The experience at Elmhurst Hospital is instructive for other L&D units serving vulnerable populations and for pandemic preparedness.

Introduction

New York City (NYC) has been a global epicenter of the SARS-CoV-2 outbreak, accounting for 17% of confirmed cases in the United States, as of April 25, 2020 [1]. In the initial response, SARS-CoV-2 testing in NYC focused on symptomatic individuals at testing centers or emergency departments and hospitalized patients [2]. Asymptomatic infected individuals may contribute substantially to transmission, including in hospital settings [39]. The fraction of SARS-CoV-2 infections in NYC that are asymptomatic–a key parameter for epidemiological models that forecast rates of infection, hospitalization, and death–is unknown. Moreover, much of the available data is not stratified by socio-demographic characteristics, which is critical to understand health disparities [10].

Labor and delivery (L&D) wards were some of the first places where universal screening for SARS-CoV-2 was instituted in the US. On March 29, 2020, the L&D Unit at Elmhurst Hospital in Queens, NYC instituted universal screening in order to manage care and isolation of admitted patients. The primary objective of this study was to describe the prevalence of SARS-CoV-2 infection, stratified by socio-demographic data, and symptom presentation among universally screened pregnant women. We explain the rationale, implications, and significance of screening in this public hospital caring for a severely affected and vulnerable population.

Methods

Study design and setting

We retrospectively reviewed medical charts of all pregnant women who were universally screened for SARS-CoV-2 on admission to the L&D Unit at Elmhurst Hospital. Elmhurst Hospital is a 545-bed public hospital that serves a diverse, largely immigrant and low-income patient population. The hospital serves about 134,000 patients per year and performs 2,200 deliveries annually [11]. The hospital has been hard hit by the pandemic, caring for 2,920 known COVID-19 cases as of May 4, 2020 [12].

Participants and data collection

We included all pregnant women admitted to the L&D Unit at Elmhurst Hospital from March 29, 2020 to April 22, 2020. This time period was selected as it comprised the ‘surge’ of cases in NYC. Study size was limited by the time period. Demographic and clinical data were extracted from the electronic medical record (EPIC) both using a data extraction tool (SlicerDicer) and manually, then de-identified manually and assigned a random study number. SARS-CoV-2 testing was performed using nasopharyngeal swabs and the results were from BioReference Laboratories and the Elmhurst Hospital Laboratory (Cepheid Rapid PCR). Primary outcomes were SARS-CoV-2 test result (positive/negative/invalid) and the presence of SARS-CoV-2 symptoms on admission. Demographic data included age, ethnicity, primary language, marital status (‘not married’ includes single and divorced statuses), health insurance status (public, private and uninsured), and zip code. Race was not included due to the poor quality of the data in the medical record. Clinical data included SARS-CoV-2 test result, SARS-CoV-2 symptoms, gestational age at delivery (divided into term and preterm), mode of delivery (vaginal delivery includes assisted vaginal deliveries), comorbidities, and length of stay. The comorbidities we assessed were as follows: hypertensive disorders (chronic hypertension, gestational hypertension, preeclampsia, superimposed preeclampsia), pre-pregnancy maternal obesity, asthma or pulmonary disease, diabetes (pre-gestational and gestational), infectious disease (HIV, hepatitis B), depression or anxiety, and other significant maternal disease including heart, kidney, or thyroid disease.

Statistical analysis

We describe SARS-CoV-2 test positivity and the symptom status at admission among positive patients. Test positivity is stratified by sociodemographic characteristics, maternal comorbidities, and delivery outcomes. Demographic characteristics, maternal comorbidities, and delivery outcomes of patients who tested positive versus negative for SARS-CoV-2 were compared using 2-sided unpaired t-tests, with unadjusted differences and 95% confidence intervals (CI) reported.

Ethical approval

This study was approved by the Institutional Review Board at the Icahn School of Medicine at Mount Sinai, IRB-20-03424, and approved by NYC Health + Hospitals.

Results

One hundred percent of admissions to the L&D Unit during the study period were tested. Two women had invalid test results and were excluded from analysis. Among the remaining 124 women, the mean age was 30.2 years, 78 (62.9%) were Hispanic, 26 (20.1%) were Asian, and 112 (90.3%) had public insurance. 78.3% of patients who tested positive for SARS-CoV-2 identified their ethnicity as Hispanic compared to 53.9% of patients who tested negative, a significant difference of 24.4 percentage points (95% CI: 7.9, 41.0). Similarly, 73.9% of patients who tested positive for SARS-CoV-2 self-reported their primary language as Spanish compared to 41.0% of patients who tested negative, a significant difference of 32.9 percentage points (95% CI: 15.8, 49.9). There was not a statistically significant difference in other demographic characteristics or rates of maternal comorbidities between patients who tested positive versus negative for SARS-CoV-2 (Table 1).

Table 1. SARS-CoV-2 test results among 124 obstetrical patients admitted to labor and delivery, by demographic characteristics.

Variable SARS-CoV-2 Positive No. (%) SARS-CoV-2 Negative No. (%) Unadjusted Difference (CI)
Total Number 46 78 --
Age (years)
< median (30 years) 20 (43.5%) 43 (55.1%) -11.6 (-30.1, 6.7)
> median (30 years) 26 (56.5%) 35 (44.9%)
Ethnicity
Hispanic 36 (78.3%) 42 (53.9%) 24.4 (7.9, 41.0)
Not Hispanic 10 (21.7%) 36 (46.2%)
Primary Language
Spanish 34 (73.9%) 32 (41.0%) 32.9 (15.8, 49.9)
Other 12 (26.1%) 46 (59.0%)
Marital status
Married 19 (41.3%) 36 (46.2%) -4.8 (-23.2, 13.5)
Not Married 27 (58.7%) 42 (53.9%)
Insurance status
Public 43 (93.5%) 69 (88.5%) 5.0 (-5.2, 15.3)
Other 3 (6.5%) 9 (11.5%)
Comorbidities
orb 26 (56.5%) 35 (44.9%) 11.6 (-6.8, 30.1)
None 20 (43.5%) 43 (55.1%)
Current or Prior Smoker
Yes 2 (4.4%) 5 (6.4%) -2.1 (-10.2, 6.1)
No 44 (95.7%) 73 (93.6%)

Forty-six of 124 (37.1%) screened pregnant women had a positive SARS-CoV-2 test. Of those, 33 (71.7%) were asymptomatic and 13 (28.3%) were symptomatic (Fig 1). Of those women who were symptomatic, the median number of symptoms on admission was 2, with the most common symptoms fever and cough. Other symptoms that were reported by patients in this cohort included body aches, sore throat, shortness of breath or difficulty breathing, headache, and runny nose. The presence of symptoms did not appear to be related to the mode of delivery or associated with preterm delivery. Of note, during our study period there were no maternal deaths.

Fig 1. SARS-CoV-2 symptoms on admission and test results among 126 obstetrical patients presenting for delivery.

Fig 1

Among 38 SARS-CoV-2 positive women who delivered by the time of data collection, 35 (92.1%) had a term delivery and 25 (65.8%) had a vaginal delivery. This was similar to 74 SARS-CoV-2 negative women who delivered by the time of data collection, among whom 78 (87.8%) had a term delivery and 49 (66.2%) had a vaginal delivery. A significantly greater percentage of women who tested positive for SARS-CoV-2 had a length of stay greater than or equal to 48 hours compared to women who tested negative (45.7% vs 25.6%, unadjusted difference of 20.0 percentage points, 95% CI: 2.3, 37.7) (Table 2).

Table 2. SARS-CoV-2 test results among 124 obstetrical patients admitted to labor and delivery, by delivery outcome.

Variable SARS-CoV-2 Positive No. (%) SARS-CoV-2 Negative No. (%) Unadjusted Difference (CI)
Total Number 46 78 --
Gestational Age a,b
Term 35 (92.1%) 65 (87.8%) 4.3 (-7.3, 15.9)
Preterm 3 (7.9%) 9 (12.2%)
Mode of Delivery b
Vaginal 25 (65.8%) 49 (66.2%) 0.4 (-18.5, 19.3)
Cesarean 13 (34.2%) 25 (33.8%)
Length of Stay
≥48 hours 21 (45.7%) 20 (25.6%) 20.0 (2.3, 37.7)
<48 hours 25 (54.4%) 58 (74.4%)

a At time of delivery.

b Excludes 12 patients who were still pregnant at the time of data collection.

Seventy-eight of the screened women resided in one of 4 zip-codes, with the remaining residing across 29 distinct zip-codes. The NYC Department of Health and Mental Hygiene reported that, as of April 22, 2020, these 4 zip-codes had a SARS-CoV-2 test-positive rate of 59% to 79% for the general population [9]. In our data, women residing in these top four zip-codes had a test-positive rate of 30.4%.

Discussion

Our study represents one of the few published studies of universal screening for SARS-CoV-2. We found that over one third of pregnant women tested positive for SARS-CoV-2 at the L&D Unit at Elmhurst. Selection bias may have been present as pregnant women with SARS-CoV-2 infection or symptoms may have been more likely to present for admission. However, this is significantly higher than results published from universal screening conducted at L&D Units in other NYC hospitals [8,13,14]. A study among 215 pregnant women at New York-Presbyterian Allen Hospital and Columbia University Irving Medical Center found that 15% tested positive for SARS-CoV-2, and another among 161 pregnant women at NYU Winthrop Hospital found that 20% tested positive for SARS-CoV-2.

The higher rate of infection at Elmhurst Hospital is likely secondary to the demographics of the surrounding population. Over 200,000 Queens residents live in crowded homes, and 70,000 in severely crowded homes [15]. Recent data from NYC show a lower rate of infection for non-hospitalized Hispanic patients compared with Black or White patients; however, these data on race and ethnicity that come from laboratory reports were noted to be only 40% complete. Our universal screening data show significantly higher rates of infection among Hispanics compared to non-Hispanics, which is more consistent with data among all hospitalized patients in NYC [16]. Gaps in data are likely obscuring disparities.

The cross-sectional association we observed between test-positivity and Hispanic ethnicity and Spanish as a primary language may be confounded by patients' socioeconomic status. At Elmhurst Hospital we serve a largely immigrant (foreign-born), resource-poor population. The primary language of Spanish likely indicates the patient was not born in the USA or is a first-degree descendant of Latin American immigrants (although there may be exceptions). Both of these characteristics are common in our patient population. Additionally, Spanish as a preferred language may indicate barriers to seeking or utilizing healthcare, which may affect co-morbidities and infection rates.

When looking at mode of delivery and gestational age at delivery, no significant difference in either of these was noted between the SARS-CoV-2 positive and negative mothers. SARS-CoV-2 status was not an indication for cesarean section or for preterm induction of labor.

The increased length of stay in the symptomatic patients is likely secondary to the severity of illness being greater in symptomatic patients. In order to warrant admission for SARS-Cov-2 symptoms typically maternal fever had to be accompanied by either maternal or fetal tachycardia, shortness of breath or decreased oxygen saturation on room air, or concerning findings on chest X-ray for possible pneumonia. Patients who did not meet these criteria, and had normal vital signs apart from fever, and reassuring fetal testing were typically assessed in our triage area and discharged home rather than admitted. These patients who were not admitted would not have been included in this cohort. The criteria for discharge among symptomatic patients included normalization of vital signs, specifically remaining afebrile and having oxygen saturation of over 95% consistently on room air both at rest and with ambulation.

Our first Obstetric SARS-CoV-2 case was March 15. Early in the pandemic, when we tested based on symptoms and history alone, several obstetric patients were admitted for birth asymptomatic and were later readmitted with severe COVID-19 infection. We were concerned about the likely spread to staff and other patients within our unit from pre-symptomatic and asymptomatic women. At the same time, our hospital was quickly becoming the epicenter of cases in the US, and all available physical space was required to care for COVID-19 patients. A large part of the postpartum unit was needed for non-obstetric COVID-19 care, and we suddenly had limited capacity to isolate positive postpartum women and those with unknown status. Upon this structural change, we began universal screening of pregnant women with planned or unplanned admission. One limitation of our study was the use of two different test types for universal screening. We were initially using BioReference Laboratory tests which returned in several days, and as rapid tests became available we switched to the Cepheid Rapid PCR. These tests likely had different sensitivities and specificities (though we were not provided with this information) and may have affected our screening results.

SARS-CoV-2 screening fundamentally shifted the way we roomed, counseled, and followed women (Fig 2). Cohorting women by SARS-CoV-2 infection status allowed us to most safely use the restricted space. Several walls were built to further partition the space in the triage, labor, and postpartum areas in order to ensure separation of SARS-CoV-2 positive women and those of unknown status from women known to be negative. In the early days of the pandemic, SARS-CoV-2 positive mothers were roomed separately from their infants, however, this procedure was reconsidered as the volume of known SARS-CoV-2 positive mothers increased with universal screening. Given limited physical space and staff to isolate all infants and considering the importance of simulating the home-environment during the postpartum hospitalization to promote safe infant care and breastfeeding, we proceeded with shared decision making with SARS-CoV-2 positive mothers around rooming-in with their infants. Severe overcrowding of housing is a challenge where most of our mothers live, making isolation of a baby and mother in the home-setting infeasible for most. We educated women on appropriate PPE use, breastfeeding, and social distancing measures that families could utilize upon discharge home. We postponed postpartum maternal vaccinations for SARS-CoV-2 positive women to eliminate any confusion between vaccine-related fever and COVID-19 symptoms (those who were SARS-CoV-2 negative received routine postpartum vaccination). Additionally, upon discharge we provided infected and PUI (Person Under Investigation) mothers with surgical facemasks and single-use Tempa-DOT thermometers, as the pharmacies in the surrounding zip-codes had none available. Our clinicians actively followed our infected and PUI mothers via phone after discharge, screening for symptoms and access to thermometers and acetaminophen.

Fig 2. Strategies employed by the labor and delivery unit at Elmhurst Hospital during the initial phase of the SARS-CoV-2 outbreak.

Fig 2

We found high rates of asymptomatic SARS-CoV-2 infection among pregnant women; these screening data and our experience at a large public hospital at the epicenter of the nation’s pandemic are instructive. In future epidemics, it may be prudent to look at L&D screening numbers early on, as pregnant women continue to seek essential care despite social distancing measures and also represent the general young and healthy community population. Additionally, this experience illustrates a nimble response to an acute shortage of space and PPE for hard-hit vulnerable communities.

Supporting information

S1 Data

(XLSX)

Acknowledgments

We would like to acknowledge the staff of Obstetrics and Gynecology and Pediatrics at Elmhurst Hospital who cared for our community under stress, the women who showed such bravery during pregnancy and delivery in the face of the pandemic, and the COVID-19 Unit for Research at Elmhurst for the timely research support.

Data Availability

All relevant data are within the paper and its Supporting Information files.

Funding Statement

The authors received no specific funding for this work.

References

Decision Letter 0

Rogelio Cruz-Martinez

Transfer Alert

This paper was transferred from another journal. As a result, its full editorial history (including decision letters, peer reviews and author responses) may not be present.

16 Jun 2020

PONE-D-20-14679

Universal screening for SARS-CoV-2 infection among pregnant women at Elmhurst Hospital Center, Queens, New York

PLOS ONE

Dear Dr. Maru,

Thank you for submitting your manuscript to PLOS ONE. After careful consideration, we feel that it has merit but does not fully meet PLOS ONE’s publication criteria as it currently stands. Therefore, we invite you to submit a revised version of the manuscript that addresses the points raised during the review process.

This very-well written manuscript add interesting information regarding the clinical relevance of universal screening for SARS2-Covid infection in pregnant women. The authors aimed to assess the incidence of SARS2-Covid infection according to the socio-demographic data. I believe that this information is relevant for clinicians attending pregnant women in this pandemic era and thus, the manuscript could be suitable for publication in this Journal after including all the reviewer´s corrections.

Please submit your revised manuscript by Jul 31 2020 11:59PM. If you will need more time than this to complete your revisions, please reply to this message or contact the journal office at plosone@plos.org. When you're ready to submit your revision, log on to https://www.editorialmanager.com/pone/ and select the 'Submissions Needing Revision' folder to locate your manuscript file.

Please include the following items when submitting your revised manuscript:

  • A rebuttal letter that responds to each point raised by the academic editor and reviewer(s). You should upload this letter as a separate file labeled 'Response to Reviewers'.

  • A marked-up copy of your manuscript that highlights changes made to the original version. You should upload this as a separate file labeled 'Revised Manuscript with Track Changes'.

  • An unmarked version of your revised paper without tracked changes. You should upload this as a separate file labeled 'Manuscript'.

If you would like to make changes to your financial disclosure, please include your updated statement in your cover letter. Guidelines for resubmitting your figure files are available below the reviewer comments at the end of this letter.

If applicable, we recommend that you deposit your laboratory protocols in protocols.io to enhance the reproducibility of your results. Protocols.io assigns your protocol its own identifier (DOI) so that it can be cited independently in the future. For instructions see: http://journals.plos.org/plosone/s/submission-guidelines#loc-laboratory-protocols

We look forward to receiving your revised manuscript.

Kind regards,

Rogelio Cruz-Martinez, Ph.D.

Academic Editor

PLOS ONE

Journal Requirements:

When submitting your revision, we need you to address these additional requirements.

1. Please ensure that your manuscript meets PLOS ONE's style requirements, including those for file naming. The PLOS ONE style templates can be found at https://journals.plos.org/plosone/s/file?id=wjVg/PLOSOne_formatting_sample_main_body.pdf and https://journals.plos.org/plosone/s/file?id=ba62/PLOSOne_formatting_sample_title_authors_affiliations.pdf

2. We note that you have indicated that data from this study are available upon request. PLOS only allows data to be available upon request if there are legal or ethical restrictions on sharing data publicly. For information on unacceptable data access restrictions, please see http://journals.plos.org/plosone/s/data-availability#loc-unacceptable-data-access-restrictions.

In your revised cover letter, please address the following prompts:

a) If there are ethical or legal restrictions on sharing a de-identified data set, please explain them in detail (e.g., data contain potentially identifying or sensitive patient information) and who has imposed them (e.g., an ethics committee). Please also provide contact information for a data access committee, ethics committee, or other institutional body to which data requests may be sent.

b) If there are no restrictions, please upload the minimal anonymized data set necessary to replicate your study findings as either Supporting Information files or to a stable, public repository and provide us with the relevant URLs, DOIs, or accession numbers. Please see http://www.bmj.com/content/340/bmj.c181.long for guidelines on how to de-identify and prepare clinical data for publication. For a list of acceptable repositories, please see http://journals.plos.org/plosone/s/data-availability#loc-recommended-repositories.

We will update your Data Availability statement on your behalf to reflect the information you provide.

Additional Editor Comments (if provided):

I strongly suggest including the socio-economic status and if possible the number of persons per households of the studied population in order to evaluate if hyspanic ethnicity and Spanish as a primary language are or not confounder associated factors. 

[Note: HTML markup is below. Please do not edit.]

Reviewers' comments:

Reviewer's Responses to Questions

Comments to the Author

1. Is the manuscript technically sound, and do the data support the conclusions?

The manuscript must describe a technically sound piece of scientific research with data that supports the conclusions. Experiments must have been conducted rigorously, with appropriate controls, replication, and sample sizes. The conclusions must be drawn appropriately based on the data presented.

Reviewer #1: Yes

Reviewer #2: Partly

**********

2. Has the statistical analysis been performed appropriately and rigorously?

Reviewer #1: Yes

Reviewer #2: No

**********

3. Have the authors made all data underlying the findings in their manuscript fully available?

The PLOS Data policy requires authors to make all data underlying the findings described in their manuscript fully available without restriction, with rare exception (please refer to the Data Availability Statement in the manuscript PDF file). The data should be provided as part of the manuscript or its supporting information, or deposited to a public repository. For example, in addition to summary statistics, the data points behind means, medians and variance measures should be available. If there are restrictions on publicly sharing data—e.g. participant privacy or use of data from a third party—those must be specified.

Reviewer #1: Yes

Reviewer #2: No

**********

4. Is the manuscript presented in an intelligible fashion and written in standard English?

PLOS ONE does not copyedit accepted manuscripts, so the language in submitted articles must be clear, correct, and unambiguous. Any typographical or grammatical errors should be corrected at revision, so please note any specific errors here.

Reviewer #1: Yes

Reviewer #2: Yes

**********

5. Review Comments to the Author

Please use the space provided to explain your answers to the questions above. You may also include additional comments for the author, including concerns about dual publication, research ethics, or publication ethics. (Please upload your review as an attachment if it exceeds 20,000 characters)

Reviewer #1: Comments to the Author:

The study by Dr. Maru et al. describes the prevalence of SARS-COV-2 infection among pregnant patients that were admitted to a L&D room, at the epicenter of the COVID-19 pandemia in USA. The authors add very valuable information regarding the spectrum of COVID-19 disease in this population; they also address demographic characteristics to their findings.

I have some suggestions and questions:

1. Line 91: past tense. “The primary objective of this study was to describe”.

2. Line 111: In Methods: could you describe were the swabs were taken (nasopharyngeal, oropharyngeal, etc)?

3. Line 116: Comorbidities: could you describe which comorbidities were assessed?

4. Line 133: Table 1. Title: Were all the patients presenting for delivery? You report 12 still pregnant patients. Table 1 per se: Comorbidities (No.) means the number of comorbidities, then you report 1+, this means all the patients had 2 or more comorbidities or had at least one? Could you be more clear? If you wish to express it as yes / none, in the results text you may describe the comorbidities and the presence of more than 1, and may be usefull in this scenario to eliminate the Word (No.) in the table.

5. Line 140: Results: Concerning the symptomatic patients, could you be more thorough about the symptoms? Was the presence of symptoms related to the mode of delivery/preterm delivery? Any fatalities?

6. Line 148: Results: I don´t understand the variable primary language (Spanish) and its relationship with positivity testing: does this mean these patients were not born in USA or are first degree descedants of latin american inmigrants, and this relates these characteristics with positivity? Is there a way you could you be more elaborate?

7. Lines 149-151: Results: could you add the ORs to the description?

8. In discussion: I would like you to remark that the mode of delivery and preterm delivery were not related to SARS-COV-2 positivity (findings contrary to the descriptions in China and other places outside USA). Was the length of stay greater in the symptomatic patients due to the severity of illness? Was the criteria for discharge different in this population?

9. Line 204: Discussion: Which kind of facemasks? (surgical, isolation, dental, etc).

10. Figure 2: In SARS-CoV-2 positive line, in the row counseling, mother wears which kind of mask?

In line SARS-CoV-2 negative row counseling, you counseled normal postpartum vaccination?

In line Person Under Investigation, row Health worker PPE, in the other interaction, which kind of mask was used? The same for the mother.

11. Minor Observations: language and readibility lines 58-62, line 103, line 109, line 190, line 203, Table 2: line SARS-CoV-2 positive row Counseling, line PUI row Counseling and Follow-up, line 226.

12. Minor Observations: please correct references 9, 11-13.

Reviewer #2: I have read the article Universal screening for SARS-CoV-2 infection among pregnant women at Elmhurst Hospital Center, Queens, New York.

This is a cross-sectional study evaluating the universal screening of SARS-CoV-2 among obstetric population attending a reference center from NY.

The article is well writting, the topic is adequate for the situation we are going through and it is highly relevant.

Although, the study is a cross-sectional, it seems in the analysis to be an analytical cross-sectional. The authors use two main outcomes, the first is the positive SARS-CoV-2 infection, and the second the presence of symptoms. It does not seem right. If this is an analytical cross-sectional, all population is supposed to be screened at arrival in which exposure and outcome are measured at the same time. As judged by your diagram, it seems that the exposures were symptomatic and asymptomatic pregnant, in which the main outcome would be the positive or negative test.

About reporting:

Title and abstracts are adequate. Mention of the study design as well as informative and balanced summary are present. Although, the study design is not adequate.

Background/rationale is adequate. Nevertheless, the objective only describes the population and outcome of interest (it seems that the original idea of the authors was to assess only population and outcome as a descriptive cross-sectional and not an analytical in which exposures are also measures). In this sense. If the authors intended to perform only a descriptive cross-sectional, all statistical inference in beyond the capability of the design and the odds ratios should be taken out. Statistical inferences like odds ratio, are meant only for analytical studies in which there are two groups of exposures (exposed and controls).

Study design: The PECOS is compatible with an analytical cross-sectional study as judged by the analysis and results, but not by the objective.

Population: All pregnant women attending the hospital

Exposure: symptomatic

Controls: asymptomatic

Outcome: positive rt-PCR for SARS-CoV-2

Participants: Study design and setting have repetitive information with participants and data collection.

Variables: Please, clearly define all outcomes, exposures, potential confounders. Describe all variables and definitions.

Data sources: adequate.

Study size: please describe the study size or if not calculated, reasons for not doing it.

Biases: please describe potential biases that addresses selection bias, recall bias, and so.

Statistical methods: If this is an analytical cross-sectional, odds ratios are adequate. If this is a descriptive cross-sectional, odds ratios should be taken out.

About results:

Participants are described. All the initial description as well as the first table are compatible with Population and outcome, adequately describing the data. In this case, odds ratio is inadequate. After table 1, data are now divided by population, exposed to symptoms or no symptoms, and those deriving in positive or negative PCR as the main outcome.

Define the study design adequately first and then proceed to the analysis.

The rest of the results are adequate.

Discussion. Please, add strengths and limitations. Please discuss as a limitation the use of rapid test for SARS-CoV-2 compared to non-rapid tests.

Please describe the possible reasons for the higher prevalence of positive tests among the Spanish speaking community.

Figure 2 and all its description is beyond the objective and scope of the manuscript. Please remove figure 2 and the surrounding discussion.

Discussion seems adequate, the problem is that the discussion is compatible with a descriptive cross-sectional study in which only population and outcome are assessed at the same time. This differs from the results as they seem to be derived from an analytical study.

Please add any findings

General comments:

Please use prevalence instead of incidence. Incidence implies a time period and this is not quite compatible with a cross-sectional study. It would be better to say prevalence.

The study design differs in the main objective, methods, the way results are presented, and conclusion. Please, choose one design and analyze the data according to it.

**********

6. PLOS authors have the option to publish the peer review history of their article (what does this mean?). If published, this will include your full peer review and any attached files.

If you choose “no”, your identity will remain anonymous but your review may still be made public.

Do you want your identity to be public for this peer review? For information about this choice, including consent withdrawal, please see our Privacy Policy.

Reviewer #1: Yes: Rosa Villalobos-Gómez

Reviewer #2: No

[NOTE: If reviewer comments were submitted as an attachment file, they will be attached to this email and accessible via the submission site. Please log into your account, locate the manuscript record, and check for the action link "View Attachments". If this link does not appear, there are no attachment files.]

While revising your submission, please upload your figure files to the Preflight Analysis and Conversion Engine (PACE) digital diagnostic tool, https://pacev2.apexcovantage.com/. PACE helps ensure that figures meet PLOS requirements. To use PACE, you must first register as a user. Registration is free. Then, login and navigate to the UPLOAD tab, where you will find detailed instructions on how to use the tool. If you encounter any issues or have any questions when using PACE, please email PLOS at figures@plos.org. Please note that Supporting Information files do not need this step.

Decision Letter 1

Rogelio Cruz-Martinez

18 Aug 2020

Universal screening for SARS-CoV-2 infection among pregnant women at Elmhurst Hospital Center, Queens, New York

PONE-D-20-14679R1

Dear Dr. Maru,

We’re pleased to inform you that your manuscript has been judged scientifically suitable for publication and will be formally accepted for publication once it meets all outstanding technical requirements.

Within one week, you’ll receive an e-mail detailing the required amendments. When these have been addressed, you’ll receive a formal acceptance letter and your manuscript will be scheduled for publication.

An invoice for payment will follow shortly after the formal acceptance. To ensure an efficient process, please log into Editorial Manager at http://www.editorialmanager.com/pone/, click the 'Update My Information' link at the top of the page, and double check that your user information is up-to-date. If you have any billing related questions, please contact our Author Billing department directly at authorbilling@plos.org.

If your institution or institutions have a press office, please notify them about your upcoming paper to help maximize its impact. If they’ll be preparing press materials, please inform our press team as soon as possible -- no later than 48 hours after receiving the formal acceptance. Your manuscript will remain under strict press embargo until 2 pm Eastern Time on the date of publication. For more information, please contact onepress@plos.org.

Kind regards,

Rogelio Cruz-Martinez, Ph.D.

Academic Editor

PLOS ONE

Acceptance letter

Rogelio Cruz-Martinez

3 Dec 2020

PONE-D-20-14679R1

Universal screening for SARS-CoV-2 infection among pregnant women at Elmhurst Hospital Center, Queens, New York

Dear Dr. Maru:

I'm pleased to inform you that your manuscript has been deemed suitable for publication in PLOS ONE. Congratulations! Your manuscript is now with our production department.

If your institution or institutions have a press office, please let them know about your upcoming paper now to help maximize its impact. If they'll be preparing press materials, please inform our press team within the next 48 hours. Your manuscript will remain under strict press embargo until 2 pm Eastern Time on the date of publication. For more information please contact onepress@plos.org.

If we can help with anything else, please email us at plosone@plos.org.

Thank you for submitting your work to PLOS ONE and supporting open access.

Kind regards,

PLOS ONE Editorial Office Staff

on behalf of

Dr Rogelio Cruz-Martinez

Academic Editor

PLOS ONE


Articles from PLoS ONE are provided here courtesy of PLOS

RESOURCES