Keywords
obstetrics - COVID-19 - SARS-CoV-2 - protocols - labor and delivery - antepartum fetal
surveillance
Recently, a novel coronavirus severe acute respiratory syndrome-coronavirus-2 (SARS-CoV-2)
causing the clinical disease novel coronavirus disease 2019 (COVID-19) has been declared
a worldwide pandemic, with 3 million cases and 200,000 deaths.[1]
[2] The first case reported in the United States occurred in early March.[3] The United States has had 1,171,510 confirmed cases and 68,279 deaths as of May
5, 2020.[4] In late March, hospitals in New York City (NYC) were faced with a surge of cases
and by May 5, New York State had 313,636 cases and 24,717 deaths with more than half
of the cases (171,723) and confirmed deaths (13,684) occurring in NYC.[5]
[6] In just 4 weeks, one NYC hospital saw a 40-fold increase in COVID-19 infection among
their maternity patients.[7] As knowledge of the disease evolved, rapid changes in hospital practices were necessary.
While the pandemic appears to be plateauing in NYC, the virus is affecting other regions
of the United States, and in the coming months, there remains a risk of a second wave
in cases.
Recent data from a systematic review of COVID-19 during pregnancy highlighted the
outcomes of 51 cases and stresses the importance of additional studies exploring the
implications of SARS-CoV-2 infection in pregnancy, as well as the rationale-driving
obstetric interventions.[8] A report from NYC described 43 SARS-CoV-2 infected pregnant women, including seven
diagnosed prior to adoption of universal SARS-CoV-2 polymerase chain reaction (PCR)
testing.[9] In this study, 9% of the women developed severe disease, and almost 5% had critical
disease. This data are consistent with reports from Wuhan where there was an 8% risk
of severe disease in pregnant women.[10] Given the lack of data, the relatively immunocompromised state of pregnancy, and
the potential for severe disease, further understanding of COVID-19 clinical management,
as well as hospital level preparation for its control are crucial.
In the United States, both expert opinion and advice from professional societies have
guided the clinical management of COVID-19.[11]
[12]
[13] Guidance on cesarean delivery, prevention of postpartum hemorrhage, and collection
of biospecimens have come from obstetrical centers with experience in prior coronavirus
outbreaks.[14] An overview of COVID-19 in pregnant women proposed a framework for the unique complexities
and logistics in managing this disease in obstetrics.[15] Finally, public health agencies have provided guidance on how to modify practices
during this pandemic.[16] To date, the literature is limited on how hospitals are providing obstetric care
and have responded to COVID-19. As the threat of the disease remains, hospitals, practitioners,
and health systems may benefit from the real-world information gained by centers that
have been at the forefront of the pandemic.
Herein, we report a survey of members of the NYC Maternal-Fetal Medicine (MFM) Research
Consortium across four health systems during the peak of the pandemic. The survey
aims to elucidate the practices put into place to guide patient care after four weeks
managing SARS-CoV-2 infections in obstetrical patients. Given the dynamic nature of
this disease, practices changed quickly as new issues arose, and our goal was to report
our experience to other obstetrical providers, hospitals, and leaders as they formulate
their own local-practices in managing the pandemic.
Materials and Methods
This was an internet-based survey conducted with four sites participating in the NYC
MFM Research Consortium during the SARS-CoV-2 pandemic. The NYC MFM Research Consortium
was formed in 2017 and in March to April 2020, decided to focus solely on COVID-19-related
research. We developed a survey that focused on practices and procedures around the
following domains: (1) screening for COVID-19 in patients presenting to labor and
delivery; (2) management of SARS-CoV-2 infected and noninfected patients undergoing
labor and delivery; (3) management of SARS-CoV-2 PCR positive and negative antepartum
inpatients; (4) management of neonates of SARS-CoV-2-positive and -negative patients;
(5) antepartum fetal surveillance for COVID-19 inpatients; and (6) obstetrical interventions
in the COVID-19 patient. Given the nature of the pandemic and our desire to conduct
the survey in real-time, we did not perform pretesting for survey validation.
Surveys were administered via Redcap.[17] Participants were either MFM specialists, or obstetrical service or labor and delivery
directors, and received no incentives. Because we wanted to capture practice patterns
during the height of the pandemic, the survey time spanned from April 14, 2020 through
April 17, 2020. A member of each Consortium site completed 118 questions over six
survey pages/screens. Redcap allowed us to check for survey completeness, and respondents
were able to review and correct their answers as needed.
Given the small number of centers involved, we did not weight the responses, and did
not adjust for nonrepresentative samples. We did not plan to perform a statistical
analysis and limited this manuscript to the survey responses. The Institutional Review
Board of Mount Sinai Health System approved this survey.
Results
Four centers agreed to participate in the survey, and all participants completed the
survey in its entirety. [Table 1] presents the characteristics of the hospitals surveyed. All the hospitals are tertiary
referral centers located in different regions in NYC, representing a diverse patient
population. Site 1 included only one hospital within its health system, while the
other three sites included two hospitals within their system. In two of the sites,
the majority of patients were non-Hispanic Whites, while in the other two, the majority
were Hispanic. During the study, the prevalence of SARS-CoV-2 infected women presenting
to labor and delivery ranged from 8 to 46%.
Table 1
Characteristics of hospitals surveyed
Hospital
|
Site 1
|
Site 2
|
Site 3
|
Site 4
|
Number of total deliveries in 2019
|
4,600
|
5,210
|
13,597
|
10,678
|
Race/ethnicity distribution[a] (%)
|
Non-Hispanic White 36
|
Non-Hispanic White 6
|
Non-Hispanic White 60
|
Non-Hispanic White 52
|
Non-Hispanic Black 16
|
Non-Hispanic Black 29
|
Non-Hispanic Black 10
|
Non-Hispanic Black 7
|
Hispanic 54
|
Hispanic 43
|
Hispanic 18
|
Hispanic 18
|
Asian 5
|
Asian 4
|
Asian 10
|
Asian 21
|
Number of SARS-CoV-2 (+) deliveries that occurred during survey time
|
32
|
40
|
67
|
30
|
a Sites provided estimates of race/ethnicity.
Personal Protective Equipment
All sites reported having adequate personal protective equipment (PPE) available,
and required staff to wear surgical masks at all times. In SARS-CoV-2 PCR negative
or persons under investigation (PUI), most sited limited N95 (N95) respirator use
to procedures with a risk of intubation and during the second stage of labor. Only
one center required full PPE for care of a PUI or SARS-CoV-2 PCR negative patient.
All sites screened patients for COVID-19 using clinical history and temperature on
presentation to labor and delivery. Most sites performed universal nasopharyngeal
PCR for SARS-CoV-2 on admission, or 24 to 48 hours prior to a scheduled admission,
although, since the time of survey completion, all four sites adopted this procedure.
The majority of sites also screened the patient's support person using clinical symptoms
and temperature checks during admission. One center performed SARS-CoV-2 PCR testing
for all support persons either on admission to labor and delivery (L&D), or 24 to
48 hours prior to a scheduled admission.
Practices and Procedures for SARS-CoV-2 PCR Negative or Persons under Investigation
Most sites made changes to their procedures and protocols forSARS-CoV-2 negative and
PUI ([Table 2]). Early in the pandemic, centers prohibited a support person. This policy was changed,
and by the time of the survey, all sites, allowed only one support person. All sites
recommended early epidural placement to reduce chance of general anesthesia in the
case of emergency cesarean. Nitrous oxide analgesia was suspended in the one site
where it was available. Most sites continued to perform delayed cord clamping. No
sites used oxygen for nonreassuring fetal heart rate tracing (NRFHT), and most sites
continued to use carboprost for the management of postpartum hemorrhage (PPH). All
centers also continued to use nonsteroidal anti-inflammatory drugs (NSAIDS). During
the postpartum period, most centers cohorted patients based on SARS-CoV-2 status.
All centers allowed rooming in of newborns. All sites had a nursery available for
newborns of SARS-CoV-2-negative mothers. No sites tested newborns and the majority
of sites continued to perform circumcisions. All sites continued to make lactation
consultation available. All sites encouraged early discharge if appropriate (at 24 hours
for vaginal deliveries or 48 hours for cesarean deliveries) and performed a phone
follow-up shortly after discharge.
Table 2
Labor and delivery/postpartum practices and procedures for SARS-CoV-2 negative or
person under investigation
Practices and procedures
|
Site 1
|
Site 2
|
Site 3
|
Site 4
|
All
|
Only one support person allowed
|
Yes
|
Yes
|
Yes
|
Yes
|
4/4
|
Early epidural recommended
|
Yes
|
Yes
|
Yes
|
Yes
|
4/4
|
Nitrous oxide suspended[a]
|
N/A
|
N/A
|
Yes
|
N/A
|
1/4
|
All cesareans performed in an AIIR OR
|
No
|
No
|
No
|
No
|
0/4
|
O2 for NRFHRT
|
No
|
No
|
No
|
No
|
0/4
|
carboprost for PPH
|
Yes[b]
|
Yes
|
Yes
|
Yes
|
4/4
|
NSAID used
|
Yes
|
Yes
|
Yes
|
Yes
|
4/4
|
Cohorting patients based on SARS-CoV-2 status
|
Yes
|
No
|
Yes
|
Yes
|
3/4
|
Offering early discharge to all patients
|
Yes
|
No
|
Yes
|
Yes
|
3/4
|
Phone follow-up for patients discharged early
|
Yes
|
Yes
|
Yes
|
Yes
|
4/4
|
Abbreviations: AIIR, airborne infection isolation room (also known as negative pressure
room); N/A, not available; NRFHRT, nonreassuring fetal heart rate tracing; NSAID,
nonsteroidal anti-inflammatory drug; OR, operating room; PPH, postpartum hemorrhage;
SARS-CoV-2, severe acute respiratory syndrome-coronavirus-2.
a Nitrous oxide used in only one center.
b Only used in known negatives.
Practices and Procedures forSARS-CoV-2 PCR Positive Patients
In SARS-CoV-2-positive pregnancies, most sites changed policies to attempt to limit
virus exposure ([Table 3]). When available, all sites performed vaginal deliveries in an airborne infection
isolation room (AIIR, also known as negative pressure room). Most sites performed
cesarean deliveries in a standard operating room (OR; without negative pressure) on
L&D. One site performed all SARS-CoV-2-positive cesareans in a negative pressure room
in the main OR. Most centers suspended cord blood banking. Most centers protected
nursing staff by limiting direct patient contact and some centers placed intravenous
(IV) pumps and tubing outside of the room. Most centers discharged patients with a
2-week course of prophylactic heparin or enoxaparin. Unlike for SARS-CoV-2 negative
patients, the majority of sites did not use carboprost for the management of PPH in
SARS-CoV-2-positive patients. Starting at 23 weeks, most centers would give corticosteroids
for fetal lung maturity and magnesium sulfate for SARS-CoV-2 patient with signs or
symptoms of preterm labor or preeclampsia. The majority of centers continued rooming
in of neonates. Universally, newborn testing occurred at 24 hours; however, one center
repeated testing at 48 hours if the initial test was negative. Most centers cohorted
newborns of SARS-CoV-2-positive mothers in the neonatal intensive care unit (NICU)
or the newborn nursery. No site routinely isolated newborns in the hospital for 14
days.
Table 3
Labor and delivery/postpartum practices and procedures for SARS-CoV-2 PCR-positive
patients
Practices and procedures
|
Site 1
|
Site 2
|
Site 3
|
Site 4
|
All
|
If available, vaginal delivery performed in an AIIR room on L&D
|
Yes
|
Yes
|
Yes
|
Yes
|
4/4
|
Vaginal delivery performed in an AIIR room in the main OR
|
No
|
No
|
No
|
No
|
0/4
|
Cesarean performed in standard OR on L&D
|
Yes
|
Yes
|
Yes
|
Yes[a]
|
3/4
|
Cesarean performed in an AIIR room on L&D
|
No
|
No
|
No
|
No[a]
|
3/3
|
Cesarean performed in standard room in the main OR
|
No
|
Yes
|
No
|
No
|
1/4
|
Cesarean performed in an AIIR room in the main OR
|
No
|
No
|
No
|
Yes
|
1/4
|
Critically ill delivered in an AIIR in main OR
|
No
|
No
|
Yes
|
Yes
|
2/4
|
Cord blood banking collection suspended
|
No
|
N/A
|
Yes
|
Yes
|
2/3
|
Labor nurse in and out of room
|
Yes
|
Yes
|
Yes
|
Yes
|
4/4
|
IV pumps and tubing outside of room
|
Yes
|
No
|
Yes
|
No
|
2/4
|
Modified PPE procedure to accommodate urgent cesarean
|
Yes[b]
|
Yes
|
No
|
No
|
1/4
|
carboprost used
|
No
|
Yes
|
No
|
No
|
1/4
|
NSAID used
|
Yes[c]
|
Yes
|
Yes
|
Yes
|
3/4
|
Thromboprophylaxis for 2 weeks postpartum[e]
|
Yes
|
Yes[d]
|
Yes
|
No
|
3/4
|
Abbreviations: AIIR, airborne infection isolation room (also known as negative pressure
room); IV, intravenous; L&D, labor and delivery; N/A, not applicable; NSAID, nonsteroidal
anti-inflammatory drug; OR, operating room; PCR, polymerase chain reaction; PPE, personal
protective equipment; SARS-CoV-2, severe acute respiratory syndrome-coronavirus-2;
VTE, venous thromboembolism.
a Yes, only if negative pressure in main OR unavailable, then perform with HEPA filter.
b Case by case
c Use caution in ordering NSAIDs for symptomatic postpartum patients with novel coronavirus
disease 2019 (COVID-19) infection and/or asymptomatic COVID-19 with chronic kidney
disease.
d Sometimes
e Sites used either heparin or enoxaparin for thromboprophylaxis.
Antepartum Fetal Surveillance in SARS-CoV-2 PCR-Positive Hospitalized Patients
There was less consensus on antepartum fetal surveillance in COVID-19 patients. For
example, there was variability in the level of fetal testing for a COVID-19, non-ICU
patient, with a viable fetus. One site would do no testing until 34 weeks, and another
would start at 24 weeks ([Table 4]). One site would not start testing until 26 weeks. When patients were admitted to
the ICU, but not intubated, half of the respondents performed daily non-stress tests
(NSTs) while half performed only daily fetal heart (FH) tone checks. One site had
an obstetrical ICU and performed continuous monitoring for all ICU patients, regardless
of their clinical status. For ICU patients who were intubated with viable fetuses,
half of the sites monitored by FHs check, while the other half performed an NST. In
a patient with a fetus beyond 24 weeks of gestation that was decompensating, half
of the centers would perform a FH check, while one center would do an NST, and one
would not monitor the fetus. For half of the sites, after 34 weeks, the risks of continued
expectant management of a patient with COVID-19 seemed to outweigh the risks of prematurity,
and these centers would forgo testing and recommend delivery.
Table 4
Comments on antepartum fetal surveillance for COVID-19 pregnant women
Clinical scenario
|
Site 1
|
Site 2
|
Site 3
|
Site 4
|
23–33[6] weeks of GA: mother stable
|
N/A
|
<26 FH checks, >26 weeks daily NST
|
None until 34 weeks
|
Daily NST starting at 24 weeks
|
23–33[6] weeks of GA: mother in the ICU, not intubated
|
Continuous
|
<26 weeks FH checks, >26 weeks daily NST
|
None until 34 weeks
|
Daily NST starting at 24 weeks
|
23–33[6] weeks of GA: mother in the ICU, intubated
|
Continuous
|
<28 weeks FH checks, >28 weeks daily NST
|
None until 34 weeks
|
Daily NST starting at 24 weeks.
|
23–33[6] weeks of GA: mother in the ICU, decompensating
|
Continuous
|
<28 weeks FH checks, >28 weeks daily NST
|
None until 34 weeks
|
Daily NST starting at 28 weeks
|
34+ weeks of GA: mother in the ICU, not intubated
|
Continuous
|
Deliver
|
Deliver
|
Deliver
|
34+ weeks of GA: mother in the ICU, intubated
|
Continuous
|
Deliver
|
Deliver
|
Deliver
|
34+ weeks of GA: mother in the ICU, decompensating
|
Continuous
|
Deliver
|
Deliver
|
Deliver
|
Abbreviations: COVID-19, novel coronavirus disease 2019; FH, fetal heart; GA, gestational
age; ICU, intensive care unit; NST, non-stress test; N/A, not answered.
Obstetrical Interventions for SARS-CoV-2-Positive Patients
In a critically ill COVID-19 patient, all centers would perform an emergent cesarean
for worsening maternal status starting at 24 weeks. For worsening fetal status, the
majority would perform an emergent cesarean starting at 28 weeks. There was less consensus
on emergent delivery for fetal indications at less than 28 weeks, as only half of
the sites would intervene, and only under certain circumstances after shared decision
making with the patient. For an unstable COVID-19 in the ICU, most centers would deliver
the patient, if possible, in an AIIR room in the main OR. Half of the centers would
deliver a patient with COVID-19 symptoms who is otherwise stable and with reassuring
fetal status between 34 to 36 weeks. Seventy five percent of the sites would deliver
a stable COVID-19 patient with reassuring fetal status between 37 to 39 weeks. Finally,
most sites were using novel COVID-19 treatments and recommending thromboprophylaxis
([Table 5]).
Table 5
Use of novel COVID-19 treatments and adjunctive therapy
|
[Table 1]
|
[Table 2]
|
[Table 3]
|
[Table 4]
|
All
|
Azithromycin
|
Yes
|
No
|
Yes
|
Yes
|
3/4
|
Hydroxychloroquine
|
Yes
|
Yes
|
Yes
|
Yes
|
4/4
|
Remdesivir
|
Yes
|
No
|
Yes
|
Yes
|
3/4
|
Monoclonal antibody
|
Yes
|
No
|
Yes
|
Yes
|
3/4
|
Plasmapheresis
|
No
|
No
|
Yes
|
Yes
|
2/4
|
Outpatient thromboprophylaxis[a] SARS-CoV-2-positive patients
|
Yes
|
Yes
|
Yes
|
No
|
3/4
|
Prone ventilation
|
No
|
Yes
|
No
|
Yes
|
2/4
|
Abbreviations: COVID-19, novel coronavirus disease 2019; SARS-CoV-2, severe acute
respiratory syndrome-coronavirus-2.
a Sites used either heparin or enoxaparin for thromboprophylaxis.
Discussion
Here we report on the obstetrical practices and protocols from four academic medical
centers in NYC at the height of the COVID-19 pandemic. All sites made changes to their
practices that were consistent with public health recommendations and practical for
local circumstances. There appeared to be agreement with screening and testing for
COVID-19, as well as L&D protocols for SARS-CoV-2-positive patients, particularly
involving use of PPE, and medication use such as corticosteroids, magnesium sulfate,
carboprost, and thromboprophylaxis, as well as procedures for newborn testing. We
found less consensus with respect to inpatient antepartum fetal surveillance.
While we were unable to document specific practice changes from weeks 1 to 4, there
was evidence of independent changes in practice by the time of the survey and after.
For example, very early in the pandemic, hospitals prohibited support persons from
accompanying laboring patients. This policy changed by the time the survey was performed.
Additionally, at the time of the survey, only half the centers were doing universal
testing. As of this writing, all centers have adopted this policy. Knowledge of SARS-CoV-2
status may affect downstream decisions, and identifying infected patients allows for
appropriate cohorting and protection of staff. If a center elects a strategy of selective
testing, a broader list of inclusion criteria including common obstetrical complications
that may be confused with COVID-19 (i.e., preeclampsia and chorioamnionitis) is advised.[18]
[19] One site with a high prevalence of COVID-19 found testing of support persons valuable
because it guided which visitors could stay to support the patient, while limiting
risk for other patients and staff. While there was less consensus with respect to
inpatient antepartum fetal surveillance, all sites reported establishing a clear policy
that delineated at what gestational age to start and what patients would be candidates
for testing. This is useful when counseling both patients and other members of the
health care team.
Strengths and Limitations
Our study has several strengths. We surveyed leaders of obstetrical units in NYC immersed
in the development and testing of new protocols in an early epicenter of the pandemic.
We document the practices put into place after 4 weeks of planning and caring for
pregnant COVID-19 patients. The sites surveyed also cared for a large diverse patient
population. Finally, we were able to demonstrate how sites independently arrived at
similar conclusions in certain areas while differing practices in others. We also
acknowledge several limitations that could introduce bias. This survey included only
large, urban centers with access to robust resources. One site had an obstetrical
ICU, an uncommon practice model nationally. This may make some of the protocols less
generalizable to smaller centers. Additionally, resources varied at different sites
and so consensus on areas such as negative pressure operating rooms or delivery rooms
could not be obtained.
Conclusion
Several expert commentaries have provided guidance on PPE, procedures during L&D,
and management of common obstetrical issues during the pandemic.[20]
[21]
[22] A recent Cochrane review aimed at compiling international guidelines related to
COVID-19 during pregnancy. [23] This group found international consensus in a few important areas, including which
pregnant women should wear a mask or respirator, and how centers were managing support
persons in asymptomatic women.[23] Less consensus was noted with respect to antepartum fetal surveillance in COVID-19
patients, or whether COVID-19 was a contraindication to antenatal steroids for fetal
lung maturity. To our knowledge, this is the first survey to document obstetrical
protocols and procedures put into place at multiple centers within an urban setting
during the COVID-19 pandemic, and that specifically surveyed policies on inpatient
antepartum fetal surveillance and corticosteroids for fetal lung maturity. While we
are not able to say whether the protocols mentioned here represent “the best practices,”
they do represent practices that were developed over time to best care for patients,
and at the same time to protect health care workers. Ultimately, our hope is that
sharing policies such as SARS-CoV-2 universal testing on patients in labor or scheduled
for delivery, cohorting patients, antepartum fetal surveillance, and obstetrical interventions
will help simplify and direct care for a COVID-19 obstetrical patients.