- 1Unidade de Clínica Tropical—Global Health and Tropical Medicine (GHTM), Instituto de Higiene e Medicina Tropical (IHMT), Universidade NOVA de Lisboa, Lisboa, Portugal
- 2Department of Pediatrics, Hospital Dr. Ayres de Menezes, São Tomé, Sao Tome and Principe
- 3Department of Obstetrics & Gynecology, Hospital Dr. Ayres de Menezes, São Tomé, Sao Tome and Principe
- 4CEAUL, NOVA Medical School/Faculdade de Ciências Médicas, Universidade NOVA de Lisboa, Lisboa, Portugal
- 5Faculdade de Medicina de Lisboa, Universidade de Lisboa, Lisboa, Portugal
Background: Neonatal mortality reduction is a global goal, but its factors are seldom studied in most resource-constrained settings. This is the first study conducted to identify the factors affecting perinatal and neonatal deaths in Sao Tome & Principe (STP), the smallest Central Africa country.
Methods: Institution-based prospective cohort study conducted at Hospital Dr. Ayres Menezes. Maternal-neonate dyads enrolled were followed up after the 28th day of life (n = 194) for identification of neonatal death-outcome (n = 22) and alive-outcome groups (n = 172). Data were collected from pregnancy cards, hospital records and face-to-face interviews. After the 28th day of birth, a phone call was made to evaluate the newborn's health status. Crude odds ratios and corresponding 95% confidence intervals were obtained. A p value <0.05 was considered statistically significant.
Results: The mean gestational age of the death-outcome and alive-outcome groups was 36 (SD = 4.8) and 39 (SD = 1.4) weeks, respectively. Death-outcome group (n = 22) included sixteen stillbirths, four early and two late neonatal deaths. High-risk pregnancy score [cOR 2.91, 95% CI: 1.18–7.22], meconium-stained fluid [cOR 4.38, 95% CI: 1.74–10.98], prolonged rupture of membranes [cOR 4.84, 95% CI: 1.47–15.93], transfer from another unit [cOR 6.08, 95% CI:1.95–18.90], and instrumental vaginal delivery [cOR 8.90, 95% CI: 1.68–47.21], were factors significantly associated with deaths. The odds of experiencing death were higher for newborns with infectious risk, IUGR, resuscitation maneuvers, fetal distress at birth, birth asphyxia, and unit care admission. Female newborn [cOR 0.37, 95% CI: 0.14–1.00] and birth weight of more than 2,500 g [cOR 0.017, 95% CI: 0.002–0.162] were found to be protective factors.
Conclusion: Factors such as having a high-risk pregnancy score, meconium-stained amniotic fluid, prolonged rupture of membranes, being transferred from another unit, and an instrumental-assisted vaginal delivery increased 4– to 9–fold the risk of stillbirth and neonatal deaths. Thus, avoiding delays in prompt intrapartum care is a key strategy to implement in Sao Tome & Principe.
Introduction
The first 28 days of life—the neonatal period—are the most vulnerable days for a child's survival (1, 2). Even nowadays, a significant number of babies die before birth, never having the chance to take their first breath (1, 2). The terminology used depends on the time of death. Perinatal mortality includes stillbirths and early neonatal deaths (ENND), indicating the death of a live newborn before the age of seven completed days (1). Late neonatal deaths (LNNDs) are those that occur after 7 days to 28 completed days of birth (2).
Globally, perinatal mortality accounts for three-fourths of deaths during the neonatal period (3, 4). More than half of the cases of stillbirths occur when pregnant women are in labor, and these deaths are directly related to the lack of skilled care at this critical time (5, 6). On the other hand, the largest contributors to neonatal mortality (ENND plus LNND) are complications of preterm birth, birth asphyxia, infection, and congenital malformations although they can differ depending on the country context (7).
Only in the last two decades, mainly after Lawn et al. published article titled “4 million neonatal deaths: When? Where? Why?” (8), attention started to be given to the neonatal period in developing countries although stillbirths are still invisible and missing from the Sustainable Development Goals (SDG) agenda (5, 9, 10). It urges to highlight that stillbirths and newborn deaths account for twice as many deaths as malaria and human immunodeficiency virus (HIV) infection combined but have received much less awareness and funding in these resource-constrained countries (8, 9).
Understanding the causes of stillbirths (fetal deaths) is also complex, as there are many promoting and interacting factors (11). In most low –to medium—income countries (LMICs), it is difficult to determine the exact reason for the stillbirth; therefore, the cause of death is often classified as “unexplained” (5). The definition of stillbirth used in this study was the WHO/ICD (for international comparison and reporting) as a baby born without any signs of life at or after 28 weeks of gestation or at least 1,000 g in birth weight (9, 12). Intrapartum stillbirth was defined as a dead-born fetus where intrauterine death occurred after the onset of labor and before birth (fresh stillbirth) (9). Antepartum stillbirth is a dead born fetus where intrauterine death occurs before the onset of labor (macerated stillbirth) (9). Researchers report that different risk factors for fetal death, such as maternal factors (advanced maternal age, high pre-pregnancy body mass index, smoking, low socioeconomic status), obstetric history (grand multiparity, previous stillbirth), antepartum factors (fewer than four antenatal visits, fetal growth restriction, maternal anemia, maternal fever and infections, antepartum hemorrhage, hypertension), and intrapartum factors (preterm birth, extremes of neonatal birth weight, cesarean delivery, operative vaginal delivery, and assisted breech delivery), are all factors that have been reported in various studies as causes of stillbirths (6, 11, 13–16).
Sao Tome & Principe (STP) is a LMIC with low HIV/AIDS prevalence and a malaria pre-elimination phase (17, 18). On the other hand, perinatal and neonatal mortality rates are considered a public health problem, given that neonatal deaths account for approximately 43% of all under5 deaths (19). At the time this study was initiated in 2016, there was an annual rate of 22 stillbirths and 22 newborn deaths per 1,000 livebirths (19). There is an established antenatal care (ANC) service in STP, with a 98% rate of women seen at least once by a skilled health provider during pregnancy and a 95.4% rate of deliveries occurring in health units (18). There is no health insurance policy in the country or any private maternity units. In STP, there are three to four obstetricians, one anesthesiologist and one to two general doctors who provide care to the neonates (20). There are no neonatologists in the country. The midwives in the labor ward are responsible for the initial resuscitation of normal deliveries, and doctors from the pediatric department are called to the labor ward to attend babies in distress.
The HAM maternity unit has a facility-based clinical care unit for ill newborn babies, but there is no neonatal or child intensive care unit in the country.
We are aware that the concept of knowing what works in terms of reducing perinatal and neonatal mortality is complicated by a huge diversity of country contexts and of determinants of maternal and neonatal health (21–24). However, according to Lawn and other authors, identifying and addressing avoidable causes of neonatal death is possible even in poorly functioning health systems, justifying our current study (8, 9). Answering—why, when, and where—newborns die in Sao Tome & Principe will enable the design of appropriate planning to prevent this major public health problem since, for appropriate prevention of fetal and newborn mortality, data pertaining to its determinants are important.
To the best of our knowledge, this is the first study to assess perinatal and neonatal deaths in STP, and it was undertaken within the context of a broader project on neonatal adverse birth outcomes (ABOs) and other maternal problems in this LMIC (25–31).
Therefore, we conducted a prospective cohort study to identify the most important factors associated with death among newborns delivered at HAM.
Materials and methods
Study design and period
An institution-based prospective cohort study was conducted at Hospital Dr. Ayres de Menezes (HAM) for mother-neonate dyads followed up until the 28th day after delivery (neonatal period). Recruitment of participants (mother-newborn dyad) occurred from July 2016 to November 2018.
Setting
The archipelago of Sao Tome & Principe is one of the smallest sub-Saharan African (SSA) countries, with approximately 200.000 inhabitants and a total land surface of approximately 1,001 km2 on two islands (Sao Tome and a smaller island named Principe) (17, 18). As a tertiary healthcare facility, HAM receives the most complicated cases from facilities in lower levels of care. The Neonatal Care Unit (NCU) receives high-risk babies delivered within the institution and referrals from other health facilities or from home with a total capacity to admit six babies. This unit, like others in SSA settings, is basic and able to manage simple neonatal complications such as hypothermia, feeding problems and sepsis suspicion. Although NCU was rebuilt in 2016, there is still a lack of continuous positive airway pressure therapy, surfactant therapy and enteric feeding for assisting sick babies.
Study population and follow-up
All mother-neonate dyads admitted to the HAM maternity unit for childbirth constituted the source population whereas the study populations were selected neonates delivered in the HAM maternity unit during the study period. During the study period, 4,540 deliveries were recorded, corresponding to 450 cesarean deliveries and 3,740 normal vaginal births.
The inclusion criteria for participants were as follows: (1) all neonates delivered at HAM with a gestational age of 28 weeks or more and (2) newborns who were born outside the hospital but were later admitted at HAM within the first 12 h of life. A total of 535 newborns were initially enrolled.
The exclusion criteria included the following: (1) all neonates delivered at HAM with a gestational age of less than 28 weeks, (2) newborns whose mothers had no antenatal pregnancy card, (3) newborns whose mothers had cognitive impairment. The newborn was also excluded if his health status was unknown at his twenty-eight days of life.
Consenting participants in the sample were followed up (mother-newborn dyad) throughout their stays until hospital discharge. The survival status of neonates after discharge was ascertained by making a follow-up mobile phone call at the end of the neonatal period. Those who could not be reached by phone after four attempts in different weeks were taken as nonrespondents, and the mother-newborn dyad was excluded. A flowchart of participation in the study is shown in Figure 1.
Sampling method
This is a substudy undertaken to estimate adverse birth outcomes (ABOs) and related risk factors in the country.
The sample size initially calculated for the broader project, using Raosoft® (http://www.raosoft.com/samplesize.html), was based on the formula for sample size and margin of error from the software, reaching the minimum sample size of S = 355, with 355 (95%) and 579 (99%) interval confidence. The original study included 537 mother-neonate dyads enrolled based on the following assumptions: two-sided 95% confidence level, power of 80% to detect an odds ratio of at least two for ABO. Since the sample size was not calculated for present outcomes, to assess perinatal and neonatal deaths, a power analysis was performed, varying from 77% to 87% for outcomes such as gestational age (GA < 37) for this study. In this study, 194 mother-neonate dyads were included. Participants were selected through random sampling. Each morning, from the pile of motherś medical folders, every second interval folder was selected and then carried on requesting contentment for enrollment. To guarantee a sample with few biases and effects by means of confounding variables, the study was conducted in different months (two weeks every two other months), avoiding seasonal interference (rain season and malaria period). Women were interviewed only after the delivery, although the invitation and consent were obtained during her admission to the maternity unit before birth (live birth or stillbirth).
Selection of groups: death and alive neonatal outcome
A total of 194 mother-neonate dyads were included and were divided into two groups according to the newborn status (alive vs. dead) at the end of the neonatal period. Newborns who died before the 28th day of life (death-outcome group with stillbirths included; n = 22) were compared with newborns alive at the 28th day of life (alive-outcome group; n = 172) concerning maternal, antepartum, and intrapartum characteristics.
Study variables
The dependent variables for the study were death (stillbirth and neonatal—early and late-death) and live newborns.
For neonates who died at home after discharge, probable causes of death were assigned by the principal investigator (pediatrician) using the International Statistical Classification of Diseases and Related Health Problems ICD-11 coding. For neonates who died in the HAM, the cause of death was assigned by physicians, who work in the hospital, and confirmed by the principal investigator.
The independent variables tested in this study included factors grouped into five categories: (1) newborns' maternal sociodemographic factors (age, educational status, occupation, marital status, partner's education, and residence); (2) preconception factors (previous contraceptive utilization), plus current obstetric condition (gravidity, parity, previous abortion and stillbirth, previous cesarean section and preceding birth interval); (3) ANC service (number of visits, gestational age at first ANC visit, obstetric ultrasound, number of fetuses in the ultrasound) plus antepartum factors as positive ANC screenings [high-pregnancy risk score, maternal anemia as hemoglobin concentration <11 g/dl, bacteriuria, hyperglycemia, Rh incompatibility, intestinal parasitic infection (IPI), malaria, HIV, syphilis, hepatitis B virus and sickle cell]; (4) health facility-related factors (being transferred from another unit, who assisted the delivery and partograph use) plus intrapartum factors as mode of delivery and complications (fetal malpresentation (32), umbilical cord complication (33), prolonged rupture of membranes (PROM) (34, 35), meconium-stained amniotic fluid (36), postpartum hemorrhage as bleeding >500 ml, preeclampsia defined as hypertension ≥140/90 mmHg and proteinuria in dipsticks in women who were normotensive at ANC, and obstructed labor (37); (5) newborns characteristics as (gestational age, sex, birth weight) and complications [intrauterine growth restriction (IUGR), congenital anomalies, infectious risk, neonatal resuscitation, fetal distress at birth, birth asphyxia and admission at NCU] (38–40).
Data collection
Data on antepartum, intrapartum, and postpartum characteristics of participants were gathered and collected from ANC pregnancy cards, obstetric maternal and newborn clinical records. For antepartum data, relevant details of the perinatal history and antenatal period were collected systematically from the ANC pregnancy card. Intrapartum data were collected from labor follow-up sheets, delivery summaries and maternal medical records. Postpartum data were abstracted from newborn birth charts and/or newborn medical records if admitted to the NCU.
Maternal sociodemographic characteristics were supplemented with a structured administered questionnaire through a face-to-face interview of the mothers 12–24 h after delivery, similar to other studies from LMICs (41).
Data quality alive-outcome group
The questionnaires were administered in Portuguese, the country national language. The questionnaire was pretested at HAM one month before data collection in 23 mothers, and modification was made based on the pretest result, mainly adjusting terminology for more culturally friendly terms. Womeńs consent to participate in the study was obtained at the time of admission at HAM, but the interview was held after a woman was stabilized and ready to be discharged. Continuous follow-up and supervision of data collection were made by the supervisors. The collected data were checked daily for completeness. The principal investigator (pediatrician) executed and was responsible for all main activities as follows: (1) obtaining consent and enrollment of the participants, (2) data collection from antenatal cards plus maternal clinical and newborns' records, (3) newborns' clinical observation (for diagnosis confirmation), (4) face-to-face interviews, (5) administering all phone interviews and (6) data collection entry into the database.
Data management
The anonymity and safety of the participants were ensured. Data were secured in a confidential and private location. Participants were referred to by identification numbers, and the informed consent forms were kept separate from the questionnaires. Both could only be linked by a coding sheet available only to the principal investigator.
Data analysis
Data were entered into the QuickTapSurvey app (©2010–2021 Formstack), and the dataset was exported to Excel for cleaning and further analysis using the Statistical Package for the Social Sciences for Windows, version 25.0 (IBM Corp. Released 2017. IBM SPSS Statistics for Windows, Version 25.0. Armonk, NY: IBM Corp.) and Stata 15.0 (StataCorp. 2017. Stata Statistical Software: Release 15. College Station, TX: StataCorp LLC). All data were checked for completeness and accuracy by the principal investigator and a qualified biostatistician.
Descriptive statistics, namely, frequencies and percentages were estimated. For binary variables, crude odds ratios estimates with 95% confidence intervals (95% CI) were obtained from corresponding contingency tables, and for categorical variables with more than two categories, exact logistic regression was used. In this study, the neonatal death-outcome group was coded as 1, and the neonatal alive-outcome group was coded as 0. The proportion of missing data ranged from 0.8 to 10% across variables, and missing values higher than 10% were described in the analysis. A level of significance α = 0.05 was considered.
Results
A total of 194 newborns were followed up during their first 28 days of life. In this study, the newborn's mean gestational age (GA) was 38.86 weeks with a standard deviation (SD) of 2.26 (minimum 28–maximum 42 weeks). The death-outcome group (n = 22) had a mean GA and birth weight of 36 (SD = 4.83) and 2,515 (SD = 997) g, respectively, while their counterparts (172 in the alive-outcome group) had 39 (SD = 1.41) weeks and 3,209 (SD = 507) g, respectively. The mean maternal age was 27.14 years, with a SD of 6.86 (minimum 15–maximum 43) years old. The mean maternal age for the death-outcome group and alive-outcome group was 30.73 (SD = 7.45) and 26.68 (SD = 6.66) years, respectively.
The death-outcome group under-study included 16 stillbirths (72.7%), four (18%) ENND and two (9%) LNND. Stillbirths were 69% intrapartum stillbirths (fresh stillbirths), and 31% were antepartum stillbirths (macerated stillbirths). Stillbirth characteristics are further described in Supplementary Additional File S1, and the early and late neonatal deaths (ENND and LNND) are described in Supplementary Additional File S2.
The maternal characteristics as well as antepartum, intrapartum, and postpartum factors for the total of the participants and for the death-outcome group vs. the alive-outcome group are described in Tables 1, 2.
Table 1. Univariable analysis of perinatal and neonatal deaths among newborns admitted at HAM, Sao Tome & Principe (n = 194; death-outcome group = 22 and alive-outcome group = 172).
Table 2. Univariable logistic regression analysis of neonatal deaths among newborns who were live births n = 178 [death-outcome group: 6 and alive-outcome group: 172].
There were no maternal deaths in this study, with a total of 2 maternal near-misses occurring in the stillbirths' motherś death-outcome group numbers 5 and 11 that needed hysterectomy intervention due to atonic uterus with major obstetric hemorrhage.
Factors associated with perinatal and neonatal deaths
Crude odds ratios were estimated to assess the association of perinatal and neonatal deaths with several characteristics (Tables 1, 2). Results of this analysis showed that meconium-stained amniotic fluid, prolonged rupture of membranes, transfer from another unit, and instrumental vaginal delivery were significantly associated with perinatal and neonatal deaths.
Sociodemographic factors
A maternal secondary education level (cOR 0.162, 95% CI 0.46–0.566, p = 0.002) and a babýs father secondary education level (cOR 0.140, 95% CI 0.029–0.67, p = 0.006) were found to be protective factors for perinatal and neonatal deaths.
Antepartum factors
The odds of perinatal and neonatal deaths were three times higher among mothers classified as having a high-pregnancy risk (cOR 2.91, 95% CI 1.18–7.22, p = 0.017). Mothers without hemoglobin test during the ANC follow-up had a higher risk of having a perinatal and neonatal death (cOR 5.68, 95% CI 1.89–17.05, p = 0.004) than those without anemia.
Health facility-related factors
The odds of perinatal and neonatal deaths were six times higher among mothers transferred from another unit compared to those directly admitted at HAM maternity (cOR 6.08, 95% CI 1.95–18.90, p = 0.004).
Intrapartum factors
PROM as well as meconium-stained amniotic fluid were other intrapartum factors, with the odds of deaths being almost five times higher for newborns whose mothers had a PROM (cOR 4.84, 95% CI 1.47–15.93, p = 0.016), and four times higher for those with a meconium-stained amniotic fluid (cOR 4.38, 95% CI 1.74–10.98, p = 0.002).
For the mode of delivery, having an instrumental assisted delivery was associated with an eightfold higher risk of perinatal and neonatal death (cOR 8.90, 95% CI 1.68–47.21, p = 0.020).
Newborns' factors
Newborns with intrauterine growth restriction had a twenty-one-fold higher risk of death (cOR 21.13, 95% CI 4.82–92.59, p < 0.001), and newborns with an infectious risk had almost sevenfold higher odds of dying (cOR 6.61, 95% CI 2.57–16.98, p < 0.001). Regarding newborn characteristics, female neonates (cOR 0.38, 95% CI 0.14–1.00, p = 0.044) and birth weight greater than 2,500 g and lower than 3,999 g (cOR 0.017, 95% CI 0.002–0.162, p < 0.001), and greater than 4,000 g (cOR 0.028, 95% CI 0.001–0.564, p = 0.034) were protective factors against perinatal and neonataldeaths.
Postpartum characteristics were only assessed for a total of six death-outcome group since sixteen stillbirths were not further included for analysis. Performance of neonatal resuscitation, fetal distress at birth (APGAR score at first-minute inferior to seven), birth asphyxia, and admission to the neonatal care unit were all related to an increased risk for neonatal death (Table 2).
Discussion
In this prospective cohort study, the main aim was to identify associated factors with perinatal and neonatal death. The most vulnerable period for death—partum, early or late neonatal period—and to identify where they die—in the maternity, at home or in the pediatric ward—was also possible as we were able to follow newborns up until their 28th day of life. In this study, we found that 90% died in HAM maternity before the 7th day of life, that is, during the perinatal period, with mainly being stillborn (73%). The magnitude of stillbirths observed in this study (3%) is in line with the studies conducted in Nigeria (4.8%) (49) and Tanzania (3.5%) (50) and lower compared with studies from Ethiopia (6.7%) (51). Most stillbirths were intrapartum deaths, as also identified in LMICs similar to STP, and most could have been prevented (52, 53).
Thus, this study indicates a probability of a stillbirth in 30 per 1,000 liverbirths, and a probability of neonatal death rate of 11 per 1,000 livebirths. The value found for the perinatal mortality is two times higher than the rates estimated for the country (18, 19).
In this study, intrapartum characteristics, such as pregnant women with meconium-stained amniotic fluid, prolonged rupture of membranes, and instrumental vaginal delivery, were the main factors significantly associated with perinatal and neonatal death. Health facility-related factors, as pregnant women transferred from another unit were also at a significant risk.
High-pregnancy risk score notification was the only antepartum factor significantly associated with perinatal and neonatal deaths. For newborns, experiencing fetal distress at birth, needing resuscitation maneuvers, having birth asphyxia and admission to the neonatal unit were identified as high-risk factors for death. Being a female newborn and having a birth weight greater than 2,500 grams were found to be protective factors.
Odds of experiencing death were identified as four times higher among newborns from mothers with meconium-stained amniotic fluid. This finding is consistent with studies from Ethiopia (6, 54) and Yemen (13) that also reported higher rates of fetal death due to intrauterine passage of meconium into amniotic fluid and a fivefold increase in perinatal mortality compared with low-risk patients with clear amniotic fluid (55). Meconium-stained amniotic fluid is associated with fetal distress since the fetus, in response, inhales the meconium, which in turn leads to airway obstruction, surfactant dysfunction and pneumonitis, which leads to loss of the fetus (6).
PROM was also a significant factor associated with neonatal deaths in this study, showing fivefold higher odds for the death-outcome group. This association was also identified in other studies from low-resource constrained countries reporting one-third of stillbirths occurring during labor as a result of prolonged labor or obstructed labor not attended to promptly (38, 39, 41, 56, 57). The reason for this might be because PROM is a risk factor for early-onset neonatal sepsis as well as a high risk of fetal distress, respiratory distress syndrome, intraventricular hemorrhage, and death (34, 35, 58). In this study we found an overall prevalence of PROM of 8.1%, which is in accordance with the global incidence that ranges from approximately 5% to 10% of all deliveries in the world (59, 60).
Lack of emergency obstetric care (EmOC) is well-known to increase the risk of neonatal mortality, as laboring mothers with complications cannot immediately receive appropriate health services, such as access to a cesarean section (39). In this study, mothers who needed to be transferred from another health unit for delivery at HAM had a sixfold higher risk of having a neonatal death outcome than mothers directly admitted at HAM. Half the mothers who were transferred from the death-outcome group had to do a 60 -kilometer journey that took approximately two to three hours until reaching HAM maternity in the capital city. Distance from a health facility with EmOC and the considerable travel times are well-known barriers and influential factors of birth adverse outcomes also found in other studies in sub-Saharan Africa (58, 61).
In this study, the overall rate of 3.1% of instrumental assisted vaginal birth deliveries was found to be lower compared to 17% of births by cesarean section and 79.9% of normal vaginal deliveries. Instrumental-assisted deliveries are an effective intervention for deliveries complicated by prolonged labor or fetal distress but are also related to adverse outcomes since fetal distress or cephalopelvic disproportion are more frequently the motive to use this technique. Therefore, the ninefold higher risk of death outcome found in this study, similar to other researchers reporting (14, 62, 63), relates to late appropriate intrapartum care intervention with subsequently higher rates of fetal distress and risk of an intrapartum stillbirth.
Antenatal care health services in STP follow a high-risk stratification for each pregnancy and, in this study, this notification of a high-risk pregnancy in the pregnant women antenatal pregnancy card was significantly associated with a threefold higher risk for fetal and neonatal death than alive-outcome group. High-pregnancy risk was operationally defined as one or more of the following according to STP national practice, namely, age as inferior to 15 years old or superior to 35, grand multipara, previous history of a stillbirth or early neonatal death, previous cesarean section, and previous hemorrhagic complication. This is consistent with other studies that reported higher rates of perinatal and neonatal mortality with extreme maternal ages and previous adverse obstetric history (grand multipara, previous stillbirth, or early neonatal death) (1, 13). However, in this study, we could not find a statistically significant difference between groups when each of these variables were independently analyzed.
Regarding the newborns' characteristics, the overall sex ratio at birth was 52.6% for males and 47.4% for females. The death rate was higher in male neonates (72%) than in the female death-outcome group (27.3%), with female sex being a protective factor. Sex variations are frequently reported, with a highly consistent pattern of excess male mortality across different populations and income groups (64). Male infants are more vulnerable to fetal and early neonatal death, with most studies reporting no gender difference in mortality after 7 days of age (64). This sex difference may be explained by a sex-specific difference in the growth and function of male and female placentae, making boys more vulnerable to different adverse outcomes (64–66).
Birth weights of more than 2,500 g were protective factors for death outcome in this study. This finding is comparable with different research on other African countries that associates a birth weight of less than 2,500 g (LBW) with higher rates of stillbirth and neonatal death (1). Additionally, the odds of experiencing death were 21 times higher for babies with IUGR or fetal growth restriction defined, in this study, as a term LBW (birthweight <2,500 g and gestational age ≥37 weeks) (46). Low birth weight is a worldwide recognized important multifaceted public health problem since LBW infants are 20 times more likely to develop complications and die than normal weight infants (6, 67).
We found that the odds of death were six times higher for newborns with maternal infectious risk. This finding is in agreement with previous studies conducted in SSA, as neonatal infectious risk is linked to amniotic fluid contamination that can cause intrapartum fetal infection or early postpartum neonatal infection with sepsis complicated with septic shock and multiple organ dysfunction, in which both are the most common causes of death in the perinatal period (38, 47). Infection is an important cause of stillbirth and neonatal death in LMICs, although there is a lack of overall information regarding the organisms involved, the types of transmission, and the mechanisms of death in these constrained countries (68). In Sao Tome & Principe, malaria and syphilis are no longer an infection-burden and cause of stillbirth or neonatal death; therefore, other bacterial and viral maternal infections should be linked to stillbirth and ENND (68). In STP, there are no means to establish a neonatal infection through blood cultures; that is, neonatal infection is based only on clinical signs with no bacteriological documentation. Additionally, nothing is known about the rate of vertical transmission of Streptococcus Group B (GBS) from colonized mothers at birth in the country. Therefore, there is a current gap in the knowledge, capability of making diagnosis and prevention and treatment of neonatal infections in STP. For instance, a study from Ethiopia (68) detected that the rate of vertical transmission of GBS from colonized mothers at birth was as high as 45.02% due to term PROM, PROM ≥18 h before delivery and mothers having fever during labor. Detecting the risk for vertical transmission of GBS and implementing prevention methods such as adequate intrapartum administration of antibiotics are recognized as easy and affordable practices for reducing mortality due to infectious causes and should be implemented in the country along with culture techniques (47).
All four congenital major malformations detected in this study resulted in a perinataldeath, although due to the low number of newborns enrolled it was not possible to establish a statistically significant difference. Congenital malformations are known to be associated with poor outcomes for newborns, and 10%–20% of stillbirths are attributed to intrinsic fetal anomalies (57). Studies from Zimbabwe (69), Ethiopia (1) and Yemen (13) found that congenital anomalies among stillbirths were associated with a 5-fold (69), 34-fold (1) and 40-fold (13) higher risk than those among live births. Another important consideration regarding congenital anomalies is the type of malformation, since some, such as neural tube defects, are preventable and can be reduced by 30 to 50% by folic acid supplementation in pregnant women and have been estimated to cause 29% of deaths related to congenital anomalies in LMICs (4). In this study, three out of the four major anomalies were neural tube defects, highlighting the need to enhance proper supplementation to preconceptional women in the country.
In this study, we were not able to find a higher risk associated with newborn gestational age. The high rate of stillbirths found in our study as well as the low number of preterm babies enrolled (5.6%) explain the lack of association. Stillbirths are among the most common pregnancy-related adverse outcomes worldwide, but they differ between low- and high-income countries. In high-income countries, most stillbirths occur early in the preterm period, whereas in low-resource constrained countries, most occur in term or in late preterm births, as found in our study (70). Additionally, the neonatal deathis higher in babies born between 37 and 38 weeks of gestation than in those born between 39 and weeks (4).
From stillbirths in this study, 69% occurred during the intrapartum period, in accordance with other studies from LMICs (5). These intrapartum stillbirths mean that intrauterine death occurred after the onset of labor and before birth (fresh stillbirth). We can also guess that some of them could be early neonatal deaths, as there are known barriers and difficulties in these contexts to establish whether a fetus or motionless newborn is living or dead after its delivery. For instance, information on some Apgar scores in these death-outcome group was not recorded, perhaps because of lack of time, especially when the neonates had to be rushed to receive resuscitation maneuvers. Studies from SSA highlight that it is very frequent that some depressed but living fetuses with a possible heartbeat do not receive resuscitation maneuvers and are prompt classified as stillbirths (1, 70). This is supported by a systematic review of sixteen hospitals and community-based perinatal mortality studies (71, 72).
In this study, newborns who needed resuscitation maneuvers were at a 16-fold higher risk of dying. Additionally, the odds of neonatal death from fetal distress at birth and birth asphyxia were 36 and 55 times higher, respectively. These results are in line with studies conducted in Cameroon (34) and Ethiopia (39) as well as published literature that suggests that lower APGAR scores are associated with severe multiorgan damage resulting in brain damage, lung dysfunction, cardiomyopathy, renal failure, hepatic failure, necrotizing enterocolitis and consequently death (73). Previous studies conducted by the authors, that compared outcomes between adolescent pregnant girls and older counterparts identified that adverse outcomes imputable to adolescent births were fetal distress and performance of neonatal resuscitation maneuvers, highlighting the risks surrounding this period among deliveries at HAM maternity unit (25, 26).
Perinatal asphyxia can be caused by factors grouped according to whether they are before birth (antepartum risk actors), during birth (intrapartum risk factors), or after birth (postpartum or fetal risk factors) (48, 73). Nonetheless, the single most important predictor is, undoubtedly, the quality of intrapartum care during labor and delivery.
The most important aspect of this study for public health is that it identifies potential characteristics that predispose newborns to life-threatening conditions, which is critical to address the underlying causes and provide prompt interventions by various stakeholders in the healthcare system (74).
This study allows us to perceive how to answer our question “when, where and why do newborns die in STP?” as “when”: mostly during labor, “where”: in uterus and “why”: mainly due to fetal distress and intrapartum-related deaths probably due to low quality and constraints of care during labor and delivery. Ending preventable stillbirths and neonatal deaths does not necessarily require new or innovative interventions. Most modifiable risk factors identified in this study can be addressed and prevented with timely, quality care during childbirth, including ongoing intrapartum monitoring and opportune intervention in case of complications (5). Some interventions, such as cardiotocography to monitor a baby's well-being in the womb by measuring contractions, are estimated to reduce the rate of infant deaths around the time of birth by 80% (75). Thus, according to this study results, the priority for STP is to prevent stillbirths through proper fetal surveillance, therefore, measures such as, the implementation of simple techniques in all maternity units, namely foetal heart rate monitoring and to provide algorithms to deliver prompt interventions when needed are essential.
In summary, the findings of this study will be useful to health policymakers and program developers in implementing appropriate interventions to achieve the newborn health post-2015 Sustainable Development Goals of no more than 12 neonatal deaths per 1,000 live births in Sao Tome & Principe by 2030 (76).
Strengths and limitations
In this study, the researcher retrieved maternal and neonatal data directly from ANC cards and maternity registers to limit recall bias. The selection of the death-outcome group and alive-outcome group was based on the records of maternal and neonatal registers; therefore, it is less likely that this study has misclassification biases both in the exposure and death-outcome group ‒alive-outcome group categories (44, 67).
Regarding the limitations, this is a relatively small study aiming to identify factors associated with perinatal and neonatal deaths in Sao Tome & Principe with a cohort of 194 newborns that were followed up until 28th days of age, 22 died and 172 survived. Thus, this study results cannot be generalized.
Another limitation is that some of the variables mentioned in the univariable analysis had wide confidence intervals and high odds ratios due to the low number of newborns in the death-outcome group enrolled in this study.
Nonetheless, the current study can assist Sao Tome & Principe policy makers and stakeholders in designing new policies for the country to improve maternal and neonatal health outcomes.
Conclusions
Perinatal mortality is a major public health problem in Sao Tome & Principe, as reinforced by this study, indicating a probability of a stillbirth in 30 per 1,000 liverbirths, and a probability of neonatal death rate of 11 per 1,000 livebirths, values higher than the rates estimated for the country.
Complications such as a high-risk pregnancy score, meconium-stained amniotic fluid, prolonged rupture of membranes, being transferred from another unit, and an instrumental-assisted vaginal delivery increased the risk of stillbirth and neonatal death between 4– and 9–fold, and 90% of all these deaths occurred in the perinatal period.
Newborns with an infectious risk, intrauterine growth restriction, fetal distress at birth, who needed resuscitation maneuvers, birth asphyxia, and those admitted to the neonatal unit had a 3- to 55-fold higher risk for dying than the alive-outcome group. Female newborn and birth weight of more than 2,500 g were found to be protective factors.
Thus, the priority for STP is to prevent stillbirths through proper fetal surveillance. Measures such as, the implementation of simple techniques in all maternity units, namely fetal heart rate monitoring and to provide algorithms to deliver prompt interventions when needed will improve perinatal and neonatal outcomes and survival in Sao Tome & Principe.
Data availability statement
The original contributions presented in the study are included in the article/Supplementary Material, further inquiries can be directed to the corresponding author.
Ethics statement
The study complies with the Declaration of Helsinki and was approved and consented to by the Ministry of Health of Sao Tome & Principe and by the main board of Hospital Dr. Ayres de Menezes, since at the time the study protocol was submitted there was no ethics committee in STP. Only recently has the country's National Ethics Committee been appointed. Previously, study analysis and approval were performed by dedicated ethics oversight bodies, such as the Ministry of Health of Sao Tome & Principe and the main board of the Hospital Dr. Ayres de Menezes, and both approved this study.
Moreover, all methods in our study were performed in accordance with the relevant guidelines and regulations in practice.
Written informed consent was obtained from all participants after the purpose of the research was explained orally by the researcher. Approval by the participantś parents or legal guardians was asked in the case of adolescents under 16 years of age or for illiterate women.
The participants or their legal representatives also consented to have the results of this research work to be published. Participation in the survey was voluntary, as participants could decline to participate at any time during the study.
The studies involving humans were approved by dedicated ethics oversight bodies such as the Ministry of Health of Sao Tome and Principe and by the main board of Hospital Dr. Ayres de Menezes. The studies were conducted in accordance with the local legislation and institutional requirements. Written informed consent for participation in this study was provided by the participants’ legal guardians/next of kin.
Author contributions
AV: Conceptualization, Formal Analysis, Funding acquisition, Investigation, Methodology, Project administration, Writing – original draft. SS: Resources, Visualization, Writing – review & editing. NB: Resources, Visualization, Writing – review & editing. MA: Data curation, Formal Analysis, Software, Writing – review & editing. AP: Formal Analysis, Methodology, Software, Supervision, Validation, Writing – review & editing. FP: Conceptualization, Methodology, Supervision, Writing – review & editing. MM: Conceptualization, Methodology, Supervision, Writing – review & editing.
Funding
The author(s) declare financial support was received for the research, authorship, and/or publication of this article.
AV was supported by the Fundação para a Ciência e Tecnologia (FCT) (https://www.fct.pt/index.phtml.pt/), grant number SFRH/BD/117037/2016.
Acknowledgments
A special remark for the late Professor João Luís Baptista MD PhD—AV research cosupervisor—a great man who was a thinker and a fighter for Africás improvement of public health. We are indebted to all the women who participated in the study. The authors would like to thank Elizabeth Carvalho and the (1) medical team and nurses of Hospital Dr. Ayres de Menezes Maternity unit for their support, especially to the chief-nurse Paulina Oliveira; and (2) Ana Sequeira, Rita Coelho, Ana Margalha, Ana Castro, Alexandra Coelho, and Inês Gomes for field support. We would like to acknowledge Instituto Camões, I.P. for logistic assistance in STP.
Conflict of interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Publisher's note
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.
Supplementary material
The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fped.2024.1335926/full#supplementary-material
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Keywords: neonatal mortality, perinatal mortality, stillbirth, neonatal death, Sao Tome & Principe
Citation: Vasconcelos A, Sousa S, Bandeira N, Alves M, Papoila AL, Pereira F and Machado MC (2024) Factors associated with perinatal and neonatal deaths in Sao Tome & Principe: a prospective cohort study. Front. Pediatr. 12:1335926. doi: 10.3389/fped.2024.1335926
Received: 9 November 2023; Accepted: 2 February 2024;
Published: 16 February 2024.
Edited by:
Tina Marye Slusher, University of Minnesota Twin Cities, United StatesReviewed by:
Drucilla Jane Roberts, Harvard Medical School, United StatesNeamin Tesfay, Ethiopian Public Health Institute, Ethiopia
© 2024 Vasconcelos, Sousa, Bandeira, Alves, Papoila, Pereira and Machado. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Alexandra Vasconcelos YWxleGFuZHJhdmFzY0BnbWFpbC5jb20=