The Zambian Preterm Birth Prevention Study ( ZAPPS ) : Cohort characteristics at enrollment [ version 2 ; peer review : 2 approved ]

Background:Sub-Saharan Africa bears a disproportionate burden of preterm birth and other adverse outcomes. A better understanding of the demographic, clinical, and biologic underpinnings of these adverse outcomes is urgently needed to plan interventions and inform new discovery. Methods:The Zambian Preterm Birth Prevention Study (ZAPPS) is a prospective observational cohort established at the Women and Newborn Hospital (WNH) in Lusaka, Zambia. We recruit pregnant women from district health centers and the WNH and offer ultrasound examination to determine eligibility. Participants receive routine obstetrical care, lab testing, midtrimester cervical length measurement, and serial fetal growth monitoring. At delivery, we assess gestational age, birthweight, vital status, and sex and assign a delivery phenotype. We collect blood, urine, and vaginal swab specimens at scheduled visits and store them in an on-site biorepository. In September 2017, enrollment of the ZAPPS Phase 1 – the subject of this report – was completed. Phase 2 – which is limited to HIV-uninfected women – reopened in January 2018. Results:Between August 2015 and September 2017, we screened 1784 women, of whom 1450 (81.2%) met inclusion criteria and were enrolled. The median age at enrollment was 27 years (IQR 23–32) and thee median gestational age was 16 weeks (IQR 13–18). Among parous women (N=866; 64%), 21% (N=182) reported a prior Open Peer Review


Introduction
Preterm birth is a global challenge impacting both developed and developing countries 1,2 . It contributes to approximately 35% of neonatal and 75% of perinatal mortality each year 3,4 . Further, preterm infants who survive are at an elevated risk of long-term respiratory, cardiovascular, gastrointestinal, and neurodevelopmental morbidities. These complications may affect subsequent health, growth, psychosocial functioning, and even economic capacity of these individuals 5-7 .
The greatest burden of mortality and morbidity from preterm births occur in low-and middle-income countries (LMICs) 8 . Of an estimated 14.9 million preterm births globally each year, 13.6 million (91%) occur in LMICs 1 . Preterm birth rates are as low as 5% in some European countries and as high as 18% in some African countries 1 , precisely where the resources to prevent preterm birth and manage preterm infants are least developed. In Zambia, for example, the preterm birth rate is estimated to be 13% 1 . Each year there are 77,600 preterm births and 6,800 infant deaths due to preterm birth complications 9 .
The burden of maternal HIV infection is also high in many LMIC settings, where it has been associated with a 50% increased risk of preterm birth 10 . Although the increasing availability of maternal antiretroviral therapy has led to dramatic reductions in pediatric HIV incidence 11 , it does not seem to reduce HIV-attributable preterm birth in this population. In fact, antiretroviral drug exposure may in fact increase the risk of preterm birth among some HIV-infected gravidas 12-14 .
Preterm birth can result from many different etiological entities. Approximately one-third of preterm deliveries are indicated because of pre-eclampsia, hemorrhage, abnormal placentation, intra-uterine growth restriction, oligohydramnios, or multi-fetal gestation. Spontaneous preterm labor is implicated in about 40% of preterm births; another 25% are related to preterm prelabor rupture of the membranes 15-17 . The underlying causes of spontaneous preterm birth in HIV-infected and HIV-uninfected populations are not well understood. Although several maternal and newborn interventions (e.g. antenatal corticosteroids, neonatal resuscitation, and kangaroo mother care) can reduce the complications of preterm birth, prevention is key. Much remains to be discovered about the risk factors, causes, and pathophysiology of preterm delivery, and how to prevent its occurrence.

Study design
The Zambian Preterm Birth Prevention Study (ZAPPS) aims to establish a well-characterized pregnancy cohort to better understand the risk factors associated with preterm birth and other adverse birth outcomes in a LMIC setting. The cohort was established to be a local resource to the University of Zambia School of Medicine and to contribute to general scientific knowledge around the biology of pregnancy and parturition.

ZAPPS enrolls pregnant women at the Women and Newborn
Hospital of the University Teaching Hospital (UTH) in Lusaka, Zambia into a prospective antenatal cohort. The UTH is the province's only tertiary referral center, serving a primary catchment population of approximately 2 million people. The Women and Newborn Hospital receives referrals for high-risk pregnancies, including those with complex medical histories, history of prior preterm birth, stillbirth, or pregnancy loss, and has a very busy labor ward with approximately 18,000 deliveries per year 18 . Study participants are recruited from the UTH and five nearby high-volume Lusaka district health clinics. We established this cohort with the aim to better characterize demographic determinants, biomedical causes, and underlying pathophysiologic mechanisms associated with adverse birth outcomes in Lusaka, Zambia. Through the Global Alliance to Prevent Prematurity and Stillbirth, we collaborate with a consortium of international scientists, many of whom are also working in LMIC countries, in order to advance our understanding of the causes of preterm delivery. This study was designed in accordance with the Strengthening The Reporting of Observational Studies in Epidemiology (STROBE) guidelines 19 .

Study participants
Pregnant women who meet the following criteria are eligible for enrollment in ZAPPS: (1) 18 years of age or older; (2) viable intrauterine singleton or twin pregnancy; (3) presentation to antenatal care prior to 20 weeks' gestation if HIV-uninfected or 24 weeks' if HIV-infected; (4) residing within Lusaka with no plans to relocate during the study follow-up period; (4) willing to provide written, informed consent; (5) willing to allow participation of their infant(s) in the study; (6) willing to be followed up at home for birth outcomes if necessary. Initially, all pregnant women with a gestational age ≥ 20 weeks by a standard algorithm 20 were excluded; however, this criterion was extended

Amendments from Version 1
In this revision we have clarified the study objectives and outcomes and explained the role of the biorepository in our overarching goals, but noting that the primary purpose of this paper is to describe the baseline clinical characteristics of our cohort population. We have also expanded our description of study methods, maternal and neonatal clinical assessments, and specimen collection and storage protocols. We have also made updates to Table 1 due to a data cleaning exercise that resulted in minor shifts in distributions of some women across groups of variables. This version now reports gestational age at enrollment for all participants. We also describe the limitation of missingness in some of our baseline variables, particularly point-ofcare test results such as hemoglobin and syphilis. Since our study is integrated with routine care at the clinical sites, for several casesparticularly in the early conduct of the study-we did not repeat routine tests previously performed at government clinics and failed to document these results on our study forms. Finally, we have added an explicit description of the two phases of the ZAPPS cohort -Phase 1, which this paper describes and for which recruitment closed in September 2017, and Phase 2, which commenced enrollment in January 2018 and is ongoing at this time.

REVISED
to ≥24 weeks for HIV-infected women following a protocol amendment in July 2016 to align this group with related, ongoing clinical trials at this site (NCT03297216, NCT02970552).
In September 2017, enrollment of the ZAPPS Phase 1 -the subject of this report -was completed and enrollment paused as we amended the protocol to focus on HIV-uninfected women only. Phase 2 reopened enrollment in January 2018.

Primary objective
The primary objective of this study is to establish a wellcharacterized cohort of pregnant women and their infants -and an accompanying specimen biorepository -with follow-up through delivery and up to 42 days postpartum. Our overarching goal is to create a resource in Zambia to better elucidate the biological mechanisms leading to preterm delivery in an effort to identify new strategies for early detection and prevention.

Outcomes
The primary outcome of the ZAPPS cohort study is preterm birth, defined as birth prior to 37 weeks completed gestation. The secondary outcomes are: (33) delivery prior to 34 weeks completed gestation and (34) low birth weight, defined as infants weighing less than 2500 grams at delivery.

Study procedures
Potential participants are identified at an early antenatal visit. Community educators approach participants who may be preliminarily eligible by gestational age criteria based on reported last menstrual period and fundal height. Potentially eligible women are escorted to the UTH study clinic. After an information session, a sonographer performs an ultrasound examination to determine fetal viability and gestational age estimation either by crown rump length (if <14 weeks) 21 or fetal biometry (if ≥14 weeks) measurements 22 . Women deemed eligible for study participation and choosing to participate are administered an informed consent in the language of their choice: English, Nyanja, or Bemba. While screening and enrollment procedures may occur on the same day, women could return on a subsequent day for enrollment to allow time to consider the risks and benefits of study participation and to discuss the study with their family.
Clinical care and follow-up Study participants receive routine antenatal care at the ZAPPS study clinic at the UTH, with visits scheduled at enrollment, 24 weeks, 32 weeks, and 36 weeks of gestation, according to standard of care in Zambia. Additionally, women are asked to return to the clinic for a postpartum visit, typically 6 weeks after delivery (Table 1).
After enrollment, all participants return for universal cervical length evaluation between 20 and 24 weeks' gestation. Those with a short cervix by transvaginal ultrasound, defined as <2.5 cm 23 , then attend additional visits scheduled at 28 and 32 weeks' gestation for repeat cervical length ultrasounds and are referred to a study physician at the UTH for further counseling and follow-up. All participants undergo an additional fetal biometry ultrasound, performed at 32 weeks' gestation. Each study sonographer is trained using curricula adapted from the INTERGROWTH-21 21,24 and Cervical Length Education and Review (CLEaR) program for cervical length measurements. All biometry parameters are measured twice and then averaged. Cervical length -measured three times over a period of 3 to 5 minutes -is first measured by transabdominal ultrasound; those whose transabdominal cervical length is <3.5cm or not measurable then undergo transvaginal measurement 25,26 .
At each antenatal care visit, study nurses perform a vital sign assessment and a physical exam, which includes maternal height and weight; mid-upper arm circumference measurement; fundal height measurement; assessment for pallor, edema, and abdominal tenderness; fetal heart rate assessment; and cervical exam as clinically indicated. We use point-of-care tests for HIV, anemia, malaria, syphilis, and urinary tract infection, and provide tetanus toxoid injection(s), iron, folate, malaria intermittent preventive treatment, and de-worming treatment in accordance with local standards of care. Participants with pre-existing or new HIV diagnoses are counseled and referred to appropriate antiretroviral therapy and prevention of mother-to-child transmission services. At the postpartum visit, study nurses assess maternal and infant interval complications, perform maternal and infant physical exams, assess infant feeding and general well-being, and provide health education counselling. The Edinburgh Postnatal Depression Screen is self-administered by participants at 24 weeks and again at the postpartum visit. Participants who screen positive are referred for further care at the UTH outpatient psychiatric clinic.
Throughout the study, study nurses assess participants' past medical and obstetrical history and current pregnancy signs and symptoms. Participants are asked specifically if they have ever been diagnosed with high blood pressure, heart disease, diabetes, HIV/AIDS, tuberculosis, or any other chronic illness. Study staff carefully screen participants at each study visit for the presence of adverse or serious adverse events. Participants are referred to the appropriate higher level care provider at the UTH for any adverse events identified that require medical care beyond the scope of the study nurses' practice.
To maximize retention, locator information on all participants is collected at screening and reviewed at each subsequent encounter. All participants are informed during the consent process that their locator sources will be used to contact them if they do not attend their scheduled study visits. Missed visits are identified by an electronic database that tracks expected and actual visits. If a participant misses a scheduled visit, study staff follow standardized procedures to attempt to contact the participant through the following mechanisms: (1) phone contact with the participant directly, (2) phone contact with other contacts provided on the participant's locator information, and (3) home visits.

Data collection and management
Clinical data: After enrollment, study staff collect medical, antenatal, and HIV history data (as applicable) through intervieweradministered questionnaires and review of participants' Extended to <24 weeks for HIV-infected in July 2016 † Additional visits for participants with short cervix * Birth weight, birth length, head circumference, foot length, physical and neuromuscular maturity medical records. At the time of delivery, or at first contact postpartum, detailed information is collected about the clinical course of the participant's delivery and delivery outcomes for both the mother and infant(s). This allows clinical phenotyping of all adverse birth outcomes. Shortly after delivery and prior to hospital discharge, the study team documents assessment of infant vital signs, weight, length, head circumference, complete physical exam, and of neuromuscular maturity using the New Ballard Score 27 . If the infant requires admission to the neonatal intensive care unit, the newborn assessment is done after the infant is deemed stable by the pediatrician.
Biological specimen collection: Trained study nurses collect maternal specimens at enrollment, 24-week, and 32-week visits, as well as at delivery (Table 1) following approved standard operating procedures to ensure quality and uniformity. While the 24-and 32-week study visits are scheduled according to gestational age, in the event that a participant misses her appointment, specimens may be collected as soon as possible once she returns to clinic. Trained study nurses collect maternal specimens pre-delivery as well as placenta and cord blood specimens immediately following delivery. All specimens are stored and transferred in insulated containers with continuous temperature monitoring to the on-site lab by clinic staff within two hours of collection. Study lab staff process all specimens according to assay manufacturers' instructions, analyzing some specimens immediately per standard antenatal care guidelines and storing others for later study-related analyses (Table 1). HIV-1 plasma viral loads are performed for participants identified as HIVinfected at enrollment. Lab staff follow strict quality protocols for maternal blood processing to produce aliquots of whole blood, serum, plasma, and buffy coat for storage in barcoded cryotubes. All specimens are stored at -80° C in temperature-controlled freezer systems equipped with continuous temperature monitoring and text message notification of temperature deviations. The UTH serves as the primary biorepository for stored specimens, with redundancy at a central project repository in Seattle, Washington and at the University of North Carolina at Chapel Hill in Chapel Hill, NC.

Ethical considerations
The ZAPPS protocol was developed in consultation with a local community advisory board to ensure study procedures are acceptable in the communities from which participants would be recruited. The study and its protocol revisions undergo continuing ethical review by the relevant research ethics authorities at the University of Zambia School of Medicine (Reference number: 016-04-14) and the University of North Carolina School of Medicine (Study number: 14-2113). Participation in all study activities is voluntary, and each participant provides written, informed consent prior to enrollment.
To address the minimal risks associated with participation in this non-interventional study, all study personnel have been trained on standard operating procedures to protect participant privacy and confidentiality. Staff receive protection of human research participants training prior to conducting any study activities and every two years thereafter. Key research staff members complete Good Clinical Practice or Good Clinical Laboratory Practice training, as applicable. All study-related and unrelated adverse events and social harms are graded using the National Institute of Health's Division of AIDS Table for Grading the Severity of Adult and Pediatric Adverse Events. All adverse events are reported to regulatory authorities, according to their individual guidelines.
All participants in this study may benefit from enhanced health education and close clinical monitoring. The knowledge generated from this observational study regarding maternal risk factors and neonatal outcomes of preterm birth are expected to outweigh the risks of participation. Conclusions drawn from this knowledge may inform future clinical trials on the prevention of adverse birth outcomes in low-resource settings, which may in turn enable policymakers worldwide to make informed decisions regarding effective interventions for the improvement of maternal-neonatal health.

Characteristics of cohort at enrollment
Between August 2015 and September 2017, 1784 women were recruited and screened from local antenatal clinics by ZAPPS study staff. Among them, 1450 (81.3%) met inclusion criteria and were enrolled. Of the 334 not enrolled, 274 (82%) were at advanced gestational age on ultrasound, 7 (2%) were less than 18 years old, 12 (4%) were unwilling to provide informed consent, 5 (1%) were unwilling to remain in the study area, and 36 (11%) were not enrolled for other reasons.

Discussion
The underlying pathological processes responsible for activation of the common parturition pathway in preterm labor, preterm prelabor rupture of membranes, and preterm delivery are incompletely understood. A comprehensive investigation of these processes could help define clinical signs and biological markers of high-risk pregnancies and allow the development and application of early preventive interventions targeted to those women at highest risk. Our cohort study will describe the frequency, predictors, and potential confounders of preterm birth and other adverse outcomes in HIV-infected and uninfected women. Our biorepository is being established in parallel to investigate biological correlates of these outcomes.
Future planned analyses of the ZAPPS cohort data will investigate frequency and determinants of the following adverse birth outcomes, both individually and in composite: preterm birth (delivery <37 weeks), very preterm birth (delivery <34 weeks), stillbirth, low birthweight (<2500g), very low birthweight (<1500g), small for gestational age (<10%ile), and very small for gestational age (<3%ile). We will define birthweight-forage according to INTERGROWTH-21 st standards 24 . We will distinguish spontaneous preterm deliveries from providerindicated preterm deliveries and investigate the prevalence and distribution of preterm phenotypes 28 , both within our cohort and relative to other studies 29 . Specimens stored at our UTH laboratory will be used for study-related analyses to identify inflammatory markers (e.g., chemokines, cytokines), microbiome community states, metabolic analytes, proteins, hormones, transcripts, and various infectious factors that may be predict adverse birth outcomes. As nearly one-fourth of our cohort was HIVinfected at enrollment, we will conduct specific analyses within this population to better understand the effect of both HIV and antiretroviral therapy on adverse birth outcomes.
Gestational age can be estimated by patient report of the last normal menstrual period (LMP), ultrasound biometry 24,30 , or a combination of the two 20 . Our experience in Zambia is that the LMP is an imprecise measure that artificially inflates the actual rate of preterm birth in the population 31 , and that it may in fact introduce bias 32 . We chose to establish gestational age by ultrasound alone in this cohort.
The strength of ZAPPS is found in its size (nearly 1500 participants enrolled to date) and its design (a prospective antenatal cohort enrolling in early pregnancy). We note that our cohort is at risk of attrition, a well-known challenge of antenatal cohorts, as well as biases of selective participation contributing to a cohort not fully representative of the general population. We enroll pregnant women in the nation's capital of Lusaka, and we have specifically prioritized the enrollment of HIVinfected women, relaxing the eligibility criteria for gestational age at enrollment for this population. This over-representation of HIV-infected participants in our cohort will enhance our ability to investigate epidemiologic and mechanistic associations of HIV and preterm birth. We acknowledge substantial missingness of key point-of-care results (hemoglobin, syphilis, and malaria) as another important limitation to our cohort. Since our study is integrated with routine care at clinical sites, several participants-particularly in the early conduct of the study-did not undergo repeat testing at the study clinic if they had recently done so at the clinic from which they were recruited. This has been rectified in Phase 2 of the cohort.
In summary, we have established a well-characterized antenatal cohort in Lusaka, Zambia that benefits from ultrasound gestational age dating, longitudinal clinical assessments, biological specimen collection and storage, and careful classification of birth and neonatal outcomes (including phenotyping of all preterm births and stillbirths). The knowledge gained from this study has the potential to drive future research in preterm birth and other adverse birth outcomes, to inform the development of novel preventive therapies and treatments, and to influence clinical care and health policy worldwide.

Collaboration
The ZAPPS study is part of the Preventing Preterm Birth Initiative of the Global Alliance to Prevent Prematurity and Stillbirth (GAPPS). The Zambia cohort is co-led by the University of Zambia and the University of North Carolina at Chapel Hill. Study findings will be made available through appropriate local channels, including academic and public health research symposia. Our primary purpose is as a shared resource and we invite collaborators with high-impact ideas to apply for access to data and stored specimens from the ZAPPS study as well as other sites in the GAPPS biorepository network. Potential collaborators are invited to contact GAPPS directly (info@gapps.org) or the ZAPPS principal investigators: Jeffrey Stringer (jeffrey_stringer@ med.unc.edu) and Bellington Vwalika (bvwalika@unza.zm).

Data availability
De-identified individual patient data underlying Table 2

Results:
There is some redundancy in the results text when looking at the table and vice versa. Not sure how the authors can handle this. In conformity with data and specimen collection as described in methods, advised to also detail the specimens collected so far? Table 2: Education-too many categories. Can collapse. GA missing on 22 women-how were they included? BMI-Typo, should be 13.5 not 13-5 Discussion: Again can be realigned with the results presentation.

If applicable, is the statistical analysis and its interpretation appropriate? Partly
Are all the source data underlying the results available to ensure full reproducibility?

Yes
Are the conclusions drawn adequately supported by the results? Partly cohort. We mention the biorepository, but that is not the primary aim of this paper. We have clarified the role of the biorepository throughout the abstract and manuscript, but note that the purpose of this paper is primarily to describe the clinical characteristics of our population.
The second paragraph in the discussion section (lines 268-280) details the outcomes to be studied in future analyses. We think it would be confusing to bring that detail into the methods of this paper as these analyses have not yet been conducted and we have not included any outcomes in this baseline cohort description. We have attempted to clarify this in said paragraph.

Methods:
Clinical care and followup/ Data collection and management: Overall lacks specificity in discussion for e.g. what particular medical history and exam is done? How is size, neuromuscular maturity assessed? Is there a window of collection? Who does it? What's the training? What is the quality control? How are the specimens stored? What particular tests are anticipated? What is meant by temperature-controlled? 'analyzing some specimens immediately per standard antenatal care guidelines and storing others for later studyrelated analyses"can be unpacked.
We have added / clarified the following: Lines 146-149: "At each antenatal care visit, study nurses perform a vital sign assessment and a physical exam, which includes maternal height and weight; mid-upper arm circumference measurement; fundal height measurement; assessment for pallor, edema, and abdominal tenderness; fetal heart rate assessment; and cervical exam as clinically indicated."

1.
Lines 161-163: "Participants are asked specifically if they have ever been diagnosed with high blood pressure, heart disease, diabetes, HIV/AIDS, tuberculosis, or any other chronic illness."

2.
Lines 180-183: "Shortly after delivery and prior to hospital discharge, the study team documents assessment of infant vital signs, weight, length, head circumference, complete physical exam, and of neuromuscular maturity via the New Ballard Score."

3.
Lines 187-189: "While the 24-and 32-week study visits are scheduled according to gestational age, in the event that a participant misses her appointment, specimens may be collected as soon as possible once she returns to clinic."
Lines 186-187: "following approved standard operating procedures to ensure quality and uniformity."

6.
Lines 275-280: Possible protocol-related tests anticipated are described in the discussion section: "Specimens stored at our UTH laboratory will be used for study-related analyses to identify inflammatory markers (e.g., chemokines, cytokines), microbiome community states, metabolic analytes, proteins, hormones, transcripts, and various infectious factors that may be predict adverse birth outcomes."

7.
Lines 191-204: "All specimens are transferred in insulated containers with continuous temperature monitoring to the on-site lab" … "All specimens are stored at -80ᵒ C in temperature-controlled freezer systems equipped with continuous temperature monitoring and text message notification of temperature deviations."

8.
Line 199: We have added a reference to Table 1, which delineates exactly which tests are performed immediately and we discuss which types of study-related testing may be 9.
performed in the future in the Discussion as outlined above.

Results:
There is some redundancy in the results text when looking at the table and vice versa. Not sure how the authors can handle this. We prefer to retain some redundancy between Table 1 and the Results section. Many journals require this (e.g., JAMA). The description of key baseline characteristics of our cohort in the Results section is not meant to be exhaustive, but rather to highlight key data that appear in Table 1.
In conformity with data and specimen collection as described in methods, advised to also detail the specimens collected so far? While specimens have been collected, given this is a baseline paper of cohort characteristics at enrollment, we have not presented data on the total numbers of specimens that have been collected to date. This will be addressed in a future publication. We have collapsed this to: "None", "0-12 years", and "≥12 years" GA missing on 22 women-how were they included? Thank you for noting this. After additional data cleaning since our first submission of this manuscript, we have now been able to assign entry gestational age for each cohort participant.
BMI-Typo, should be 13.5 not 13-5 We have corrected this to "18.5" from "18-5" Discussion:Again can be realigned with the results presentation. Thank you. We feel that as a result of these suggested revisions, the discussion and results section are now more closely aligned.

Preterm Birth Prevention Study (ZAPPS: Cohort characteristics at enrollment)"
Overall the study is important to understand the dynamics of preterm birth in a sub-saharan developing country, with intent to plan interventions.
I have the following comments: -Abstract: Methods -should read as 'the Zambian Preterm Birth Prevention study (ZAPPS) is an observational study, of a prospective antenatal cohort ……….' Results-this cohort is 1450 participants and is not clear is this the entire cohort or a subset as the protocol mentions the enrollment to be estimated at 4000, so is recruitment still ongoing? This needs to be clarified. Discussion -also add the primary objective of the ZAPPS study, as stated below Page 3 Primary objective -should also include the primary objective of the study as stated in the protocol Primary outcome measure -Rate of preterm births per 100 person years, incidence rate of preterm birth (delivery <37 weeks' gestation) Page 4 Clinical care and follow up It is stated that after enrollment women return for cervical length evaluation between 20 and 24 weeks and those with a short cervix have additional visits at 28 and 32-in table 1 the ultrasound is at 34 and not 32 weeks. It is important to mention if this is standard of care for all patients at this site or only for those with previous preterm birth. Page 6 mentions that this is a non-interventional study.
No mention is made of the maternal depression screen at 24 and 42 weeks.
Page 4 Biological specimen collection Study nurses collected maternal specimens at enrollment -and these were point of care tests for HIV, anemia, syphilis and UTI. The results section has a reasonably large number of missing information on some of the parameters. Page 5 table 1 What were the vaginal and rectal swab tests for?

Page 6
Results section Table 2-the missing numbers of participates with data on Syphilis is 107, Haemoglobin at enrollment 424 and malaria is 302, this needs to be explained by the authors. Patients with malaria, low haemoglobin and syphilis are at risk for preterm birth, so missing data will influence results for the ZAPPS study. This should be discussed by the authors as a study limitation if these figures are correct.
This comment does not influence this paper as it for those recruited up to Sept 2017.
Of note is that the protocol for ZAPPS has been amended in Feb 2018 to exclude women with HIV. So eventually will there be separate analysis for the women who are included in this manuscript vs those recruited later?

Is the work clearly and accurately presented and does it cite the current literature? Yes
Is the study design appropriate and is the work technically sound? Yes

Are sufficient details of methods and analysis provided to allow replication by others? Partly
If applicable, is the statistical analysis and its interpretation appropriate? Not applicable Are all the source data underlying the results available to ensure full reproducibility? Yes

Are the conclusions drawn adequately supported by the results? Yes
Results-this cohort is 1450 participants and is not clear is this the entire cohort or a subset as the protocol mentions the enrollment to be estimated at 4000, so is recruitment still ongoing? This needs to be clarified. Recruitment is indeed ongoing, but under a slightly revised protocol. This is a description of the cohort established under the original protocol only. The original estimated enrollment of 4000 has been amended to 2000 on the ClinicalTrials.gov website.
Discussion-also add the primary objective of the ZAPPS study, as stated below Our primary objective in the protocol reads as follows: "to establish a cohort of 2,000 pregnant women and their infants, following them through delivery and up to 42 days postpartum." We have revised the language in the Discussion of the abstract to reflect that original wording (lines 31-32).

Page 3
Primary objective -should also include the primary objective of the study as stated in the protocol Our primary objective in the protocol reads as follows: "to establish a cohort of 2,000 pregnant women and their infants, following them through delivery and up to 42 days postpartum. We will recruit and enroll 2,000 women and their newborn infants in Zambia." We have revised the language in our "Primary objective" section to reflect this wording (lines 106-110).
Primary outcome measure -Rate of preterm births per 100 person years, incidence rate of preterm birth (delivery <37 weeks' gestation) Thank you for noting this inconsistency. The primary outcome as stated in the most recent protocol is as follows: "The primary outcome is preterm birth, defined as birth prior to 37 weeks completed gestation. The secondary outcomes are (1) delivery prior to 34 weeks completed gestation and (2) low birth weight, defined as less than 2500 grams." We have added an "Outcomes" section to the Methods of this paper to address this omission (lines 111-118).

Page 4 Clinical care and follow up
It is stated that after enrollment women return for cervical length evaluation between 20 and 24 weeks and those with a short cervix have additional visits at 28 and 32-in table 1 the ultrasound is at 34 and not 32 weeks. It is important to mention if this is standard of care for all patients at this site or only for those with previous preterm birth. Page 6 mentions that this is a non-interventional study. We have revised the text to the following: "After enrollment, all participants return for universal cervical length evaluation between 20 and 24 weeks' gestation. Those with a short cervix by transvaginal ultrasound, defined as <2.5 cm, then attend additional visits scheduled at 28 and 32 weeks' gestation for repeat cervical length ultrasounds and are referred to a study physician at the UTH for further counseling and follow-up" (lines 135-139). The additional visits at 28 and 34 weeks' for cervical length ultrasound are only for those women with short cervix. This is explained also in the footnote to Table 1. Biometry ultrasound at 32 weeks is performed for all participants.
No mention is made of the maternal depression screen at 24 and 42 weeks. Thank you for pointing this out. The following sentence has been added to the section on Clinical care & follow-up: "The Edinburgh Postnatal Depression Screen is self-administered by participants at 24 weeks and again at the postpartum visit. Participants who screen positive are referred to outpatient psychiatric care" (lines 157-159). In addition, "Maternal depression screen" appears in Table 1 at 24 weeks and 42 days postpartum.

Page 4 Biological specimen collection
Study nurses collected maternal specimens at enrollment -and these were point of care tests for HIV, anemia, syphilis and UTI. The results section has a reasonably large number of missing information on some of the parameters. Since our study is integrated with routine care at the clinical sites, for several cases-particularly in the early conduct of the study-we did not repeat routine tests previously performed at government clinics and failed to document these results on our study forms. This is a limitation of the study that we have described in our Discussion (lines 295-299). We also note that it has been rectified in Phase 2 of the cohort (line 299).

Page 5 table 1
What were the vaginal and rectal swab tests for? Vaginal and rectal swabs are collected for specimen storage for future protocol-related testing. No real-time tests are currently being performed on these swabs. We have clarified this in Table 1. Table 2-the missing numbers of participates with data on Syphilis is 107, Haemoglobin at enrollment 424 and malaria is 302, this needs to be explained by the authors. Patients with malaria, low haemoglobin and syphilis are at risk for preterm birth, so missing data will influence results for the ZAPPS study. This should be discussed by the authors as a study limitation if these figures are correct. These figures are correct. As we note above, since our study is integrated with routine care at the clinical sites, for several cases-particularly in the early conduct of the study-we did not repeat routine tests previously performed at government clinics and failed to document these results on our study forms. This is a limitation of the study that we have described in our Discussion (lines 295-299). We also note that it has been rectified in Phase 2 of the cohort (line 299).

Page 6 Results section
This comment does not influence this paper as it for those recruited up to Sept 2017. Of note is that the protocol for ZAPPS has been amended in Feb 2018 to exclude women with HIV. So eventually will there be separate analysis for the women who are included in this manuscript vs those recruited later? That is correct. Given the amended protocol has revised key inclusion / exclusion criteria, the next phase of the ZAPPS cohort has not been described in this baseline manuscript. We have added an explicit description of the two phases of the ZAPPS cohort in the Methods section (lines 102-104).
Competing Interests: No competing interests were disclosed.