Skip to main content

ORIGINAL RESEARCH article

Front. Public Health, 09 February 2023
Sec. Public Health Policy
This article is part of the Research Topic Addressing Contemporary Public Health Challenges in Ghana for Improved Outcomes: Getting to SDG 3 View all 12 articles

Maternal factors and child health conditions at birth associated with preterm deaths in a tertiary health facility in Ghana: A retrospective analysis

\nSeth Kwaku Afagbedzi
Seth Kwaku Afagbedzi1*Yakubu AlhassanYakubu Alhassan1Deda Ogum AlangeaDeda Ogum Alangea2Henrietta TaylorHenrietta Taylor3
  • 1Department of Biostatistics, School of Public Health, University of Ghana, Accra, Ghana
  • 2Department of Population, Family and Reproductive Health, School of Public Health, University of Ghana, Accra, Ghana
  • 3Paediatric Department, 37 Military Hospital, Accra, Ghana

Background: Preterm birth continues to be a leading cause of death for children under the age of 5 globally. This issue carries significant economic, psychological, and social costs for the families affected. Therefore, it is important to utilize available data to further research and understand the risk factors for preterm death.

Objective: The objective of this study was to determine maternal and infant complications that influence preterm deaths in a tertiary health facility in Ghana.

Methods: A retrospective analysis of data on preterm newborns was conducted at the neonatal intensive care unit of Korle Bu Teaching Hospital (KBTH NICU) in Ghana, covering the period January 2017 to May 2019. Pearson's Chi-square test of association was used to identify factors that were significantly associated with preterm death after admission at the NICU. The Poisson regression model was used to determine the risk factors of preterm death before discharge after admission to the NICU.

Results: Of the 1,203 preterm newborns admitted to the NICU in about two and half years, 355 (29.5%) died before discharge, 7.0% (n = 84) had normal birth weight (>2.5 kg), 3.3% (n = 40) had congenital anomalies and 30.5% (n = 367) were born between 34 and 37 gestational week. All 29 preterm newborns between the 18–25 gestational week died. None of the maternal conditions were significant risk factors of preterm death in the multivariable analysis. The risk of death at discharge was higher among preterm newborns with complications including hemorrhagic/hematological disorders of fetus (aRRR: 4.20, 95% CI: [1.70–10.35], p = 0.002), fetus/newborn infections (aRRR: 3.04, 95% CI: [1.02–9.04], p = 0.046), respiratory disorders (aRRR: 13.08, 95% CI: [5.50–31.10], p < 0.001), fetal growth disorders/restrictons (aRRR: 8.62, 95% CI: [3.64–20.43], p < 0.001) and other complications (aRRR: 14.57, 95% CI: [5.93–35.77], p < 0.001).

Conclusion: This study demonstrate that maternal factors are not significant risk factors of preterm deaths. Gestational age, birth weight, presence of complications and congenital anomalies at birth are significantly associated with preterm deaths. Interventions should focus more on child health conditions at birth to reduce the death of preterm newborns.

Introduction

Preterm birth, since 2016, has been identified as the leading cause of under 5 mortality globally (1, 2). Previously, pneumonia was the leading cause of death with more than half of deaths before age 5 years, but the main cause of death has now shifted to prematurity (3). This shift in epidemiology of infant mortality from pneumonia to preterm birth, should increase concern for and investment into addressing prematurity (1). As at 2010, more than 60% of preterm births occurred in south Asia and Sub-Sahara Africa (SSA) (4), which increased to 81.1% in 2016 (5). Moreover, the highest rates of preterm deaths have been recorded in West Africa at ~16 per 1,000 live births (1).

Prematurity not only contributes directly to neonatal deaths globally but also increases the risk of death from other causes (6). These causes are multifactorial, including infant biological and medical conditions, such as birthweight, gestational age, (710), congenital anomalies, birth complications (2, 3), respiratory problems, jaundice, sepsis, necrotizing enterocolitis, intrapartum asphyxia, seizures, bleeding disorders among others (11, 12). Preterm babies are more affected by these factors because they are physiologically and metabolically less mature than term infants (13). Maternal factors such as age, hypertensive disorders, height, pre-gestational diabetes and pre-eclampsia also increase the risk of preterm deaths (12, 14, 15). Preterm births are not only associated with deaths but also with high economic, psychological, and social costs incurred by affected families (16, 17).

Risk factors of preterm births, which also contribute to a large proportion of preterm deaths (18), have been less explored in low-to-middle-income (LMIC) settings compared to high income countries (HIC). Thus, they are poorly understood and may be totally different in the former (1). It has been projected that if current trends continue in preterm births among other causes of death, SSA will record about 60% of the under-five deaths even in 2030 (3). Prematurity has also been found as one of the top five causes of neonatal deaths in Ghana (19, 20). As at 2010, the estimated preterm birth rate for the country was 14.5 per 100 live births, which reduced to 12 per 100 live births in 2019 with over 8,000 deaths per year (21, 22). It is obvious Ghana has fallen short of its target to reduce the NMR to 21 per 1,000 live births in 2018. This is indicated in an estimated rate of 24 deaths per 1,000 live births in the Ghana National Newborn Health Strategy and Action Plan for 2014–2018 (20). Addressing the national burden of preterm-related neonatal and child mortality is crucial to achieve the SDG 3.2. This study seeks to explore maternal and infant factors influencing preterm births and deaths in the nation's largest tertiary referral hospital. The current analysis offers the opportunity to utilise routine data which is readily available to answer pertinent questions on preterm birth and death with relatively less resources.

Methods

Data source

A retrospective analysis of secondary data on preterm infants was conducted at the neonatal intensive care unit of the Korle Bu Teaching Hospital (KBTH NICU) in Ghana. Data extraction forms were used to collect data from folders from the pediatric department, the admission and discharge book at the nurse's desk, including copies of death certificates covering the period January 2017 to May 2019. All medical records of preterm infants pronounced dead on arrival at KBTH NICU, and those on preterm infants with incomplete data were excluded. Korle Bu Teaching Hospital NICU is a tertiary referral centre that is equipped with 20 incubators, 20 cots, and 10 radiant warmers. The unit manages ~2,500 newborns annually with about 10 new admissions each day. Preterm babies account for 50–60% of all new admissions. About 80% of the newborns admitted at the unit are referred from the KBTH labor wards and obstetric theatre. The rest are referred from peripheral hospitals. Data extraction span over 5 weeks with the support of five research assistants.

Outcome measure

The primary dependent variable for this study was the discharge outcome at NICU among preterm births, that is whether the preterm infant was dead or alive before discharge from NICU. Preterm infant deaths before discharge were confirmed from the duplicates of death certificates kept at NICU.

Exposure variables

Exposure variables were subdivided into maternal, delivery-related, and infant factors. Maternal factors included sociodemographic characteristics of the preterm infant's mother such as age, occupation, marital status, educational status, religion, parity, and HIV status of mother as well as maternal medical conditions. The place of delivery (whether at KBTH or other facilities), mode of delivery (either by caesarian section or vaginal delivery), and whether any resuscitation was done in an attempt to stabilize the newly delivered preterm infant, constituted delivery-related factors. Infant factors including sex of infant, gestational age in weeks at birth, birth weight, as well as the presence or absence of congenital anomalies and complications were also assessed.

Birth complications in the preterm newborns were categorized using the WHO's International Classification of Diseases (ICD-11) for Mortality and Morbidity Statistics (Version: 04 / 2019) (23). The categories included hemorrhagic/hematological disorders of the fetus, fetus/newborn infections [this is based on clinical evaluation and lab tests (cultures, CRP)], respiratory disorders, fetal growth disorders, and others (digestive system disorders, transitory endocrine/metabolic disorders, disturbances of temperature regulation, neurological disorders and, genitourinary system disorders). Gestational age at delivery were categorized as extreme preterm (< 28 weeks), very preterm (28 to < 32 weeks), moderate preterm (32 to < 34 weeks), and late preterm (34 to < 37 weeks). Also, the infant's birth weight in kilograms (kg) was categorized as normal (>2.5 kg), low birth weight (< 2.5–1.5 kg), very low birth weight (< 1.5–1.0 kg), and extremely low birth weight (< 1.0 kg).

Data analysis

The data extracted from the medical records were cleaned, coded, and entered into a Microsoft excel 2016 spreadsheet and exported into Stata IC version 16 (Stata Corp, College Station, TX, US) for final analysis. Descriptive statistics including frequencies, proportions, mean, and standard deviation were were used to describe the maternal and child characteristics by gestational age at bith. The line plot was also used to describe the preterm outcome after admission at NICU by the completed gestational age at birth in weeks.

Pearson's Chi-square test of association was used to identify factors that were significantly associated with preterm outcomes after admission at the NICU. The Poisson regression model was used to determine the risk factors of preterm death before discharge after admission to the NICU. The variance inflation factor (VIF) was used to assess multicollinearity. The final multivariable model had a average VIF of 2.66 (range: 1.07–7.08) below the threshold of 10. The deviance and Pearson's goodness of fit test were both non-significant with p-values of 1.000 indicating the model is appropriate. The statistical significance for the study was set at a p-value of 0.05.

Missingness and completeness of data used for analysis

Medical records of a total of 1,274 preterm newborns admitted into the NICU of Korle-Bu Teaching Hospital during the years 2017 (n = 387, 30.4%), 2018 (n = 618, 48.5%), and 2019 (n = 269, 21.1%) were reviewed. Due to missingness on some very important variables in the study, a total of 1,203 observations with complete information were used for the analysis of this study, 359 (29.8%) from 2017, 577 (48.0%) from 2018, and 267 (22.2%) from 2019 records (Figure 1).

FIGURE 1
www.frontiersin.org

Figure 1. Flow chart of data extraction, showing missingness and final data used for analysis.

Results

Descriptive characteristics of study participants

The average age of the 1,203 mothers whose newborns were admitted to the NICU was 30.0 (±6.4) years with most (n = 568, 47.2%) of them in the age range 30–39 years. A few 3.9% (n = 47) had no formal education whilst 18.7% (n = 225) of them had a tertiary level of education. One thousand and six (83.6%) were married and 54.0% (n = 650) of them had given birth to only one child. Fifteen (1.25%) of the mothers were HIV positive. The majority (n = 1,057, 87.9%) of the preterm newborns were delivered at Korle-Bu Teaching Hospital, with over a third (n = 323, 37.3%) of the births through cesarean section. About half (n = 583, 48.5%) of the mothers had no maternal medical conditions. Among the 38 with maternal infectious diseases, hepatitis B was the common with 17, followed by syphilis with 12, urinary tract infection with 5 and 4 with candidiasis. About 50.5% of the preterm infants were males. Of the 1,207 preterm newborns admitted to the NICU, 15.9% (n = 192) of them had no complications and 42.8% of them required resuscitation. Less than a tenth (n = 84, 7.0%) were born with normal birth weight (>2.5 kg), 3.3% had congenital anomalies and about a third (n = 367, 30.5%) were born at 34 to 37 weeks (Table 1).

TABLE 1
www.frontiersin.org

Table 1. Descriptive characteristics of child, maternal and delivery-related factors by gestational age at birth.

Table 1 also shows the descriptive characteristics of the participants by the gestational age at birth. The gestational age at birth of the newborns varied significantly across some of the characteristics including mode of delivery, maternal condition, complication of child at NICU admission, resusicitation, birthweight and presence of congenital anormaly (Table 1).

Outcome of care among preterm newborns admitted at the NICU

Of the 1,203 preterm newborns admitted at the NICU, 29.5% (n = 355) died before discharge. Marital status [χ2(2) = 7.2, p-value = 0.028] was significantly associated with outcome at discharge with higher mortality among single mothers (40.5%) compared to co-habiting (23.0%) and married mothers (29.3%). Also, place of delivery [χ2(1) = 10.72, p-value = 0.001] was a significant factor with higher mortality among mothers who delivered elsewhere (41.1%) compared to those who delivered in Korle-Bu (27.9%). Mode of delivery [χ2(1) = 3.9, p-value = 0.048] was associated with outcome at discharge with higher mortality among vaginal delivery (32.4%) compared to caesarean section delivery (27.1%). Death at discharge from NICU was also higher among preterm newborns who were resuscitated (38.8%) compared to the non-resuscitated (22.5%) [χ2(1) = 37.7, p-value < 0.001]. Mortality at discharge from NICU was higher among preterm births newborns with lower birthweight [χ2(3) = 314.2, p-value < 0.001]. Also, mortality at discharge from NICU was higher among newborns with congenital anomaly [χ2(1) = 10.5, p-value = 0.001]. Gestational weeks at birth was also associated with moratlity at NICU discharge [χ2(3) = 245.6, p-value < 0.001] were the factors that significantly influenced the outcome of preterm infants at the KBTH NICU (Table 2).

TABLE 2
www.frontiersin.org

Table 2. Prevalence and association between death before discharge and demographic characteristics among preterm newborns admitted at the NICU.

Completed gestational age in weeks at birth and Preterm outcome after admission at NICU

Figure 2 shows the oucomes dead and alive outcomes before the discharge of preterm newborns admitted to the NICUby their completed gestational age in weeks at birth. All 29 preterm newborns with gestational age < 26 weeks died. Only 2 (7.7%) of the 26 newborns during the 26th gestational week survived whilst 43.0% (n = 34/79) of the newborns during the 28th gestational week survived. On the other hand, mortality were 17.1% and 15.9% among the newborns on the 35 and 36th week, respectively. The proportion of preterm newborns surviving at each gestational age increased steeply between 27 and 28th gestational weeks (from 14.7 to 43%) then increased steadily to 32nd gestational weeks before levelling from 34 to 36th gestational weeks. Proportionately more preterm before the 29th gestational weeks died than survive (57% of preterm die at 28 weeks). Half of the preterm newborns born between the 29 and 30th gestational week survived.

FIGURE 2
www.frontiersin.org

Figure 2. Preterm outcome by the week of birth.

Risk factors of death before discharge among preterm newborns admitted at the NICU

Table 3 shows the unadjusted and adjusted Poisson regression model of risk factors of death outcome among NICU admitted preterm newborns. From the adjusted Poisson model, maternal conditions were not significant risk factors of preterm death. The risk of death at discharge was significantly higher among new borns with with complications including hemorrhagic/hematological disorders of the fetus (aRRR: 4.20, 95% CI: [1.70–10.35], p = 0.002), fetus/newborn infections (aRRR: 3.04, 95% CI: [1.02–9.04], p = 0.046), respiratory disorders (aRRR: 13.08, 95% CI: [5.50–31.10], p < 0.001), fetal growth disorders (aRRR: 8.62, 95% CI: [3.64–20.43], p < 0.001) and other complications (aRRR: 14.57, 95% CI: [5.93–35.77], p < 0.001).

TABLE 3
www.frontiersin.org

Table 3. Risk factors of death before discharge among preterm newborns admitted at the NICU.

Compared to those with normal weight at birth, the risk of death at discharge was significantly higher among those with very low birth weight (aRRR: 2.27, 95% CI: [1.22–4.23], p = 0.010) and those with extreme low birth weight (aRRR: 3.15, 95% CI: 1.68–5.88], p < 0.001).

The risk of death at discharge in admitted preterm newborns with congenital anomalies was over twice the risk in preterm with no congenital anomaly (aRR: 2.18, 95% CI: [1.52–3.12], p < 0.001). Compared to late/moderate preterm newborns, the adjusted risk of death was significantly higher among the very preterm newborns (aRR: 1.41, 95% CI: [1.11–1.79], p = 0.005) and the extreme preterm newborns (aRR: 1.87, 95% CI: [1.43–2.46], p < 0.001) (Table 3).

Discussion

Three out of every ten preterm newborns (29.5%) admitted to the NICU died before discharge. The risk of death among these preterm newborns decreases as their gestational age increases. Those who were born extremely preterm (< 32 weeks gestation), had a higher risk of death compared to those born late preterm. Risk of mortality was higher among preterm new-borns with birth weight below 1.5 kg. The risk of death before discharge among preterm babies admitted at NICU was higher for babies with neonatal co-morbidities such as Haemorrhagic /haematological disorders of foetus, foetus/new-born infections, Respiratory disorders, Fetal growth disorders. The existence of complications and congenital anomalies at birth among preterm newborns increased the risk of death. The study, however, found that maternal conditions were not significant risk factors of death at the NICU.

Preterm birth remains a major cause of perinatal, neonatal, and infant mortality (3, 18, 24). The current study found that preterm birth accounted for about one-third of the deaths recorded over a two and quarter year period (January, 2017–April, 2019) at just one facility. A similar prevalence (26%) was reported by an earlier study that assessed neonatal deaths from 2003 to 2009 in northern Ghana (25). Even higher prevalence rates were recorded in South-East Nigeria (46.1%) for the period 2009 to 2013 (8) and 67.7% in South Africa (26). While significant progress has been made in reducing infection-related deaths among children generally, successes have been slow among neonates and more especially among preterms (4). In 2017, Ghana the Maternal Health Survey using a nationally representative sample, estimated neonatal mortality for the 5-year period preceding the survey as 25 deaths per 1,000 live births. The report indicated a very high uptake (98%) of antenatal care (ANC) from a skilled provider among pregnant women with about four out of five of them having four or more ANC visits (27). However, the uptake of ANC must be complemented with quality of care to mitigate neonatal deaths. Adu-Bonsaffoh et al. (14), recently reported that poor antenatal care among other factors predicted the incidence of preterm delivery in the same facility used for this study (28). Moreover, factors that predict preterm birth evidently account for a large proportion of preterm mortality (18). Also a cause for concern, is the preterm births that could have been avoided in low and middle-income countries (LMIC) as it has been found that about 14.2% of provider-initiated preterm birth in LIMC were not medically indicated (15).

Neonatal mortality has long been known to be associated with gestational age, with decreasing mortality in infants as gestational weeks approach full-term (10, 13, 2931). Findings from this study corroborate these earlier reports because the risk of death among the preterm newborns decreased with increasing gestational age, with those extremely preterm having a higher risk of death compared to those born late preterm. D'Onofrio et al. (28), reported similar findings in their study that extreme preterm birth with a gestational period of 23–27 weeks was a predictor of infant mortalityClick or tap here to enter text.. Jacob et al. (2015), also found that mortality at lower gestational ages was most commonly attributed to extreme preterm birth with the attendant complications (32). About three out of four babies born at 24 weeks of gestation do not survive, one out of three babies die at 25 weeks of gestation and one out of four babies dies at 26 weeks of gestation before discharge from the hospital (33). The risk of death among these preterm newborns significantly increased with the presence of congenital anomalies and complications including hemorrhagic/hematological disorders of the fetus, respiratory disorders, and fetal growth disorders. Preterm birth complications is one of the three leading causes of death worldwide (3). Hyperglycemia occurring on the first day of life in extremely preterm infants (34), increased severity of respiratory failure (35), necrotizing enterocolitis, intraventricular hemorrhage in extreme to very preterm population (32, 36, 37), and birth asphyxia (25) have also been implicated as predictors of preterm deaths. Fetal and newborn infections however, did not siginificantly increase the risk of mortality. This supports earlier observations of significant reductions in infection-related deaths among children (4). These findings do not however, eliminate infection from the causes of preterm deaths as some studies have found its association with the latter (19, 36, 37).

Birth weight was also negatively associated with death in NICU. A very low birth weight (1.0 to < 1.5 kg) and extremely low birth weight (< 1.0 kg) significantly increased the risk of preterm death. Earlier findings have also indicated low birth weight (LBW) as a predictor of death in the first 24 hours after birth (38). Extremely low birth weight is significantly associated with death in the first 6 days after birth (7) and neonatal death before discharge from the health facility (26). A meta analysis of empirical data from 12 randomized controlled trials conducted in 10 low-to-middle-income countries revealed that maternal supplementation with multiple micronutrients (a minimum of 1 recommended dietary allowance of multiple micronutrients), compared to iron–folic acid (IFA) supplementation alone during pregnancy, increased birthweight thereby, protecting one in ten infants from LBW (39). Maternal micronutrient supplementation (MMS) also reduces fetal growth restriction, prematurity, and neonatal mortality (40, 41). In Ghana, it has also been found that MMS reduces the risk of LBW compared to IFA supplementation alone (42). Moreover, the WHO has also indicated that there is high-certainty evidence that MMS reduces the risk of having LBW neonates compared with IFA supplements only, which is the standard care. However, MMS barely improved other fetal and neonatal outcomes including preterm birth rates. Hence, WHO has not yet recommended MMS for pregnant women. More research is required to ascertain if MMS will improve other neonatal outcomes, and how the micronutirents can be best combined into a single supplement (43). Furthermore, careful consideration must be given to the cultural setting as the economic situation, cultural representations of motherhood, and the unpredictable demands of the pregnant body could influence pregnancy food practices (44).

While birth weight is highly correlated with gestational age, studies that controlled for body size have reported a consistent relationship between prematurity and increased risk of morbidity and mortality (45). More robust survival predictive models based on a combination of gestational age and birth weight still predicts poorer outcomes for preterms classified as small for gestational age (SGA) compared to normal weight or term births (46).

Kangaroo mother care (KMC) is another intervention is being explored to improve the survival of low birthweight and preterm infants though the uptake is slow in low-to-middle-income countries (4749). There is evidence of its integration into healthcare facilities providing newborn care for LBW in Ghana with designated wards in some hospitals (50, 51). This intervention is increasingly being implemented/scaled-up in different parts of the country.

Maternal factors and delivery conditions were not significant risk factors of preterm death before discharge from NICU in the current study. This supports the earlier findings of Iyoke et al. that survival was not dependent on maternal risk factors in a retrospective review of singleton preterm and term births from 2009 to 2013 in a teaching hospital in Nigeria (52). Contrary findings have also been reported by Bayou and Berhan, who found that obstructed labor, malpresentation, antepartum hemmorrhage and hypertensive disorders of pregnancy were significant predictors of high perinatal mortality (53). Additionally, Adu-Bonsaffoh et al., indicated that maternal age, hypertensive disorders and preterm rupture of membranes were associated with preterm birth in the same facility the current study was conducted (14). The limited data from the records reviewed in this study did not allow for the effect of maternal lifestyle factors including smoking and alcohol intake to be assessed although they have been implicated in literature as influencing preterm births and some negative neonatal outcomes (5456).

There is the need for further research into interventions that are safe, effective, and scalable in limited-resource settings, where most preterm-associated infant mortality occurs (5). It might be useful to focus on hospital care related interventions delivered during labour and birth, which have been found to be most effective in reducing neonatal deaths. The KMC and the use of antenatal corticosteroids can avert about half and one third of preterm-related deaths, respectively (57, 58). Also, low and middle-income countries should improve their availability and quality of data on preterm births as recommended by the WHO in the framework of the Global Strategy for Women's, Children's and Adolescents' Health (59, 60). Currently, most of the data available are from facility-based research studies, which were often conducted in tertiary facilities and are largely not nationally representative (5) as is the case for this study. Efforts in this post-2015 era should advance beyond just promoting child survival to reducing child morbidity and ensuring healthy development. It is crucial that as child survival improves, children are not left with impairments (3).

Study limitations

Although the study design adequately answered the study objective, the retrospective record review employed did not allow for some relevant clinical indicators of preterm birth implicated in literature, such as maternal lifestyle factors including smoking and alcohol intake, medications used by mothers during pregnancy, and record of antenatal care among others to be assessed. For the same reason, a very important predictor of preterm outcome such as single/multiple birth was not extracted. Furthermore, authors are unable to report on other method of determining gestational age and its possible impact on preterm classification.the data used in this study was obtained from just one tertiary facility. Hence the sample is not nationally representative and findings cannot be generalized for the country.Since the data was extracted from hospital records, issues of missingness of information on specific characteristics was common. This was evident from the flow chart in Figure 1 where 71 observation did not have data on key variables. Also, the method of measurement of information such as gestational age at birth may vary from one record to the other. Also, the issue of complete omission of information of some records cannot be ignored given that past records of hard copies spanning over a 3 years were reviewed.

Conclusion

This study demonstrate that maternal factors are not significant risk factors of preterm deaths. Gestational age, birth weight, presence of complications and congenital anomalies at birth are significantly associated with preterm deaths. Interventions delivered during labour and birth including kangaroo mother care and the use of antenatal corticosteroids should be scaled up to ensure nationwide coverage so as to reduce preterm deaths. Additionally, further research involving national level data on preterm deaths and associated causes is recommended.

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 studies involving human participants were reviewed and approved by Korle Bu Teaching Hospital, Institutional Review Board, IRB No: KBTH-IRB/00010/2019. Written informed consent from the participants' legal guardian/next of kin was not required to participate in this study in accordance with the national legislation and the institutional requirements.

Author contributions

HT conceived the study, prepared the data collection guide, and collected the data. HT and DOA researched the literature. SKA and YA were involved in the data analysis and result interpretations. SKA wrote the first draft of the manuscript. All authors reviewed, proofread, and approved the final version of the manuscript.

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.

References

1. Lawn JE, Kinney M. Preterm birth: now the leading cause of child death worldwide. Sci Transl Med. (2014) 6:263ed. doi: 10.1126/scitranslmed.aaa2563

PubMed Abstract | CrossRef Full Text | Google Scholar

2. UN Inter-agency Group for Child Mortality Estimation. Levels and Trends in Child Mortality: Report 2017. New York (2017).

Google Scholar

3. Liu L, Oza S, Hogan D, Perin J, Rudan I, Lawn JE, et al. Global, regional, and national causes of child mortality in 2000-13, with projections to inform post-2015 priorities: An updated systematic analysis. Lancet. (2015) 3856:430–40. doi: 10.1016/S0140-6736(14)61698-6

PubMed Abstract | CrossRef Full Text | Google Scholar

4. Blencowe H, Cousens S, Oestergaard MZ, Chou D, Moller A-B, Narwal R, et al. National, regional, and worldwide estimates of preterm birth rates in the year 2010 with time trends since 1990 for selected countries: a systematic analysis and implications. Lancet. (2012) 3792:2162–72. doi: 10.1016/S0140-6736(12)60820-4

PubMed Abstract | CrossRef Full Text | Google Scholar

5. Chawanpaiboon S, Vogel JP, Moller A-B, Lumbiganon P, Petzold M, Hogan D, et al. Global, regional, and national estimates of levels of preterm birth in 2014: a systematic review and modelling analysis. Lancet Glob Health. (2019) 7:e37–46. doi: 10.1016/S2214-109X(18)30451-0

PubMed Abstract | CrossRef Full Text | Google Scholar

6. Lawn JE, Kerber K, Enweronu-Laryea C, Cousens S. 3.6 million neonatal deaths—what is progressing and what is not? Sem Perinatol. (2010) 34:371–386. doi: 10.1053/j.semperi.2010.09.011

PubMed Abstract | CrossRef Full Text | Google Scholar

7. Castro ECM, de Leite ÁJM, de Almeida MFB, Guinsburg R. Perinatal factors associated with early neonatal deaths in very low birth weight preterm infants in Northeast Brazil. BMC Pediatr. (2014) 14:312. doi: 10.1186/s12887-014-0312-5

PubMed Abstract | CrossRef Full Text | Google Scholar

8. Iyoke CA, Lawani OL, Ezugwu EC, Ilechukwu G, Nkwo PO, Mba SG, et al. Prevalence and perinatal mortality associated with preterm births in a tertiary medical center in South East Nigeria. Int J Womens Health. (2014) 6:881. doi: 10.2147/IJWH.S72229

PubMed Abstract | CrossRef Full Text | Google Scholar

9. Chen A, Feresu SA, Barsoom MJ. Heterogeneity of preterm birth subtypes in relation to neonatal death. Obstet Gynecol. (2009) 114:516–22. doi: 10.1097/AOG.0b013e3181b473fc

PubMed Abstract | CrossRef Full Text | Google Scholar

10. Marchant T, Willey B, Katz J, Clarke S, Kariuki S, Kuile Ft, et al. Neonatal mortality risk associated with preterm birth in East Africa, adjusted by weight for gestational age: individual participant level meta-analysis. PLoS Med 9:e1001292. doi: 10.1371/journal.pmed.1001292

PubMed Abstract | CrossRef Full Text | Google Scholar

11. Kunle-Olowu OE, Peterside O, Adeyemi OO. Prevalence and outcome of preterm admissions at the neonatal unit of a tertiary health Centre in Southern Nigeria. Open J Pediatr. (2014) 4:67–75. doi: 10.4236/ojped.2014.41009

CrossRef Full Text | Google Scholar

12. Schmiegelow C, Minja D, Oesterholt M, Pehrson C, Suhrs HE, Boström S, et al. Factors associated with and causes of perinatal mortality in northeastern Tanzania. Acta Obstet Gynecol Scand. (2012) 91:1061–8. doi: 10.1111/j.1600-0412.2012.01478.x

PubMed Abstract | CrossRef Full Text | Google Scholar

13. Engle WA. Morbidity and mortality in late preterm and early term newborns: a continuum. Clin Perinatol. (2011) 38:493–516. doi: 10.1016/j.clp.2011.06.009

PubMed Abstract | CrossRef Full Text | Google Scholar

14. Adu-Bonsaffoh K, Gyamfi-Bannerman C, Oppong SA, Seffah JD. Determinants and outcomes of preterm births at a tertiary hospital in Ghana. Placenta. (2019) 79:62–7. doi: 10.1016/j.placenta.2019.01.007

PubMed Abstract | CrossRef Full Text | Google Scholar

15. Vogel JP, Lee ACC, Souza JP. Maternal morbidity and preterm birth in 22 low- and middle-income countries: a secondary analysis of the WHO Global Survey dataset. BMC Pregnancy Childbirth. (2014) 14:56. doi: 10.1186/1471-2393-14-56

PubMed Abstract | CrossRef Full Text | Google Scholar

16. Petrou S, Abangma G, Johnson S, Wolke D, Marlow N. Costs and health utilities associated with extremely preterm birth: evidence from the EPICure study. Value Health. (2009) 12:1124–34. doi: 10.1111/j.1524-4733.2009.00580.x

PubMed Abstract | CrossRef Full Text | Google Scholar

17. Bérard A, Le Tiec M, De Vera MA. Study of the costs and morbidities of late-preterm birth. Arch Dis Childhood-Fetal Neonatal Edition. (2012) 97:F329–34. doi: 10.1136/fetalneonatal-2011-300969

PubMed Abstract | CrossRef Full Text | Google Scholar

18. Basso O, Wilcox A. Mortality risk among preterm babies: immaturity versus underlying pathology. Epidemiology. (2010) 21:521–7. doi: 10.1097/EDE.0b013e3181debe5e

PubMed Abstract | CrossRef Full Text | Google Scholar

19. Siakwa M, Laryea KDT, Ankobil A, Dare S, Ebu N. A five-year neonatal mortality trend in a Ghanaian Teaching Hospital after the implementation of strategies to achieve the Millenium Development Goal (MDG) 4. Int J Paediatr Child Health. (2014) 2:43–9.

Google Scholar

20. Ministry of Health. Ghana National Newborn Health Strategy and Action Plan 2014-2018: A Road Map to Reduce Neonatal Deaths Nationwide. Accra (2014).

Google Scholar

21. Every Preemie Scale. Ghana: Profile of Preterm and Low Birth Weight Prevention and Care. Connecticut (2019)

Google Scholar

22. UNICEF. Maternal and Newborn Health Disparities: Ghana, Accra: UNICEF.

Google Scholar

23. World Health Organization. ICD-11 for Mortality and Morbidity Statistics (Version: 04/2019). (2019). Geneva: World Health Organization.

Google Scholar

24. Khashu M, Narayanan M, Bhargava S, Osiovich H. Perinatal outcomes associated with preterm birth at 33 to 36 weeks' gestation: a population-based cohort study. Pediatrics. (2009) 123:109–13. doi: 10.1542/peds.2007-3743

PubMed Abstract | CrossRef Full Text | Google Scholar

25. Welaga P, Moyer CA, Aborigo R, Adongo P, Williams J, Hodgson A, et al. Why Are Babies Dying in the First Month after Birth? A 7-Year Study of Neonatal Mortality in Northern Ghana. PLoS ONE. (2013) 8:e58924. doi: 10.1371/journal.pone.0058924

PubMed Abstract | CrossRef Full Text | Google Scholar

26. Hoque M, Haaq S, Islam R. Causes of neonatal admissions and deaths at a rural hospital in KwaZulu-Natal, South Africa. S Afr J Epidemiol Infect. (2011) 26:26–9. doi: 10.1080/10158782.2011.11441416

CrossRef Full Text | Google Scholar

27. GSS GHS and ICF. Ghana Maternal Health Survey 2017: Key Indicators Report. Accra, Ghana: GSS (2018).

Google Scholar

28. D'Onofrio BM, Class QA, Rickert ME, Larsson H, Långström N, Lichtenstein P, et al. Preterm Birth and Mortality and Morbidity. JAMA Psychiatry. (2013) 70:1231. doi: 10.1001/jamapsychiatry.2013.2107

PubMed Abstract | CrossRef Full Text | Google Scholar

29. Melamed N, Klinger G, Tenenbaum-Gavish K, Herscovici T, Linder N, Hod M, et al. Short-term neonatal outcome in low-risk, spontaneous, singleton, late preterm deliveries. Obstet Gynecol. (2009) 114:253–60. doi: 10.1097/AOG.0b013e3181af6931

PubMed Abstract | CrossRef Full Text | Google Scholar

30. Tomashek KM, Shapiro-Mendoza CK, Davidoff MJ, Petrini JR. Differences in mortality between late-preterm and term singleton infants in the United States, 1995–2002. J Pediatr. (2007) 151:450–6. doi: 10.1016/j.jpeds.2007.05.002

PubMed Abstract | CrossRef Full Text | Google Scholar

31. Johanzon M, Ödesjö H, Jacobsson B, Sandberg K, Wennerholm UB. Extreme Preterm Birth: Onset of Delivery and its Effect on Infant Survival and Morbidity. Obstetr Gynecol. (2008) 111:42–50. doi: 10.1097/01.AOG.0000295866.97499.35

PubMed Abstract | CrossRef Full Text | Google Scholar

32. Jacob J, Kamitsuka M, Clark RH, Kelleher AS, Spitzer AR. Etiologies of NICU Deaths. Pediatrics. (2015) 135:e59–65. doi: 10.1542/peds.2014-2967

PubMed Abstract | CrossRef Full Text | Google Scholar

33. DelormeP, Goffinet F, Ancel PY, Foix-L'Hélias L, Langer B, Lebeaux C, et al. Cause of preterm birth as a prognostic factor for mortality. Obstetr Gynecol. (2016) 127:40–8. doi: 10.1097/AOG.0000000000001179

PubMed Abstract | CrossRef Full Text | Google Scholar

34. Alexandrou G, Skiöld B, Karlén J, Tessma MK, Norman M, Adén U, et al. Early hyperglycemia is a risk factor for death and white matter reduction in preterm infants. Pediatrics. (2010) 125:e584–91. doi: 10.1542/peds.2009-0449

PubMed Abstract | CrossRef Full Text | Google Scholar

35. Ambalavanan N, Van Meurs KP, Perritt R, Carlo WA, Ehrenkranz RA, Stevenson DK, et al. Predictors of death or bronchopulmonary dysplasia in preterm infants with respiratory failure. J Perinatol. (2008) 28:420–6. doi: 10.1038/jp.2008.18

PubMed Abstract | CrossRef Full Text | Google Scholar

36. Berrington JE, Hearn RI, Bythell M, Wright C, Embleton ND. Deaths in preterm infants: changing pathology over 2 decades. J Pediatr. (2012) 160:49–53.e1. doi: 10.1016/j.jpeds.2011.06.046

PubMed Abstract | CrossRef Full Text | Google Scholar

37. Schindler T, Koller-Smith L, Lui K, Bajuk B, Bolisetty S. Causes of death in very preterm infants cared for in neonatal intensive care units: a population-based retrospective cohort study. BMC Pediatr. (2017) 17:59. doi: 10.1186/s12887-017-0810-3

PubMed Abstract | CrossRef Full Text | Google Scholar

38. Castro ECM, de Madeiro Leite ÁJ, Guinsburg R. Mortality in the first 24h of very low birth weight preterm infants in the Northeast of Brazil. Revista Paulista de Pediatria (English Edition). (2016) 34:106–13. doi: 10.1016/j.rppede.2015.12.008

PubMed Abstract | CrossRef Full Text | Google Scholar

39. Fall CHD, Fisher DJ, Osmond C, Margetts BM. Multiple micronutrient supplementation during pregnancy in low-income countries: A meta-analysis of effects on stillbirths and on early and late neonatal mortality. Food Nutr Bull. (2009) 30:S533–46. doi: 10.1177/15648265090304S408

PubMed Abstract | CrossRef Full Text | Google Scholar

40. West Jr KP, Shamim AA, Labrique AB, Ali H, Shaikh S, Mehra S, et al. Efficacy of antenatal multiple micronutrient (MM) vs iron-folic acid (ifa) supplementation in improving gestational and postnatal viability in rural Bangladesh: the JiVitA-3 Trial. FASEB J. (2013) 27:6. doi: 10.1096/fasebj.27.1_supplement.358.6

CrossRef Full Text | Google Scholar

41. Ronsmans C, Fisher DJ, Osmond C, Margetts BM, Fall CHD. Multiple micronutrient supplementation during pregnancy in low-income countries: A meta-analysis of effects on stillbirths and on early and late neonatal mortality. Food Nutr Bull. (2010) 30:S547–55. doi: 10.1177/15648265090304S409

PubMed Abstract | CrossRef Full Text | Google Scholar

42. Adu-Afarwuah S, Lartey A, Okronipa H, Ashorn P, Zeilani M, Peerson JM, et al. Lipid-based nutrient supplement increases the birth size of infants of primiparous women in Ghana. Am J Clin Nutr. (2015) 101:835–46. doi: 10.3945/ajcn.114.091546

PubMed Abstract | CrossRef Full Text | Google Scholar

43. WHO. WHO recommendation on multiple micronutrient supplementation during pregnancy. The WHO Reproductive Health Library. (2018). Geneva: WHO.

Google Scholar

44. de-Graft Aikins A. Food Beliefs and Practices During Pregnancy in Ghana: Implications for Maternal Health Interventions. Health Care Women Int. (2014) 35–9:954–972. doi: 10.1080/07399332.2014.926902

PubMed Abstract | CrossRef Full Text | Google Scholar

45. Friedrich L, Stein RT, Pitrez PM, Corso AL, Jones MH. Reduced lung function in healthy preterm infants in the first months of life. Am J Respir Crit Care Med. (2006) 173:442–7. doi: 10.1164/rccm.200503-444OC

PubMed Abstract | CrossRef Full Text | Google Scholar

46. Draper ES, Manktelow B, Field DJ, James D. Prediction of survival for preterm births by weight and gestational age: retrospective population based study. BMJ. (1999) 3197:1093. doi: 10.1136/bmj.319.7217.1093

PubMed Abstract | CrossRef Full Text | Google Scholar

47. Conde-Agudelo A, Díaz-Rossello JL. Kangaroo mother care to reduce morbidity and mortality in low birthweight infants. Cochr Database Syst Rev. (2016) 2016:CD002771. doi: 10.1002/14651858.CD002771.pub4

PubMed Abstract | CrossRef Full Text | Google Scholar

48. Simmons LE, Rubens CE, Darmstadt GL, Gravett MG. Preventing Preterm Birth and Neonatal Mortality: Exploring the Epidemiology, Causes, and Interventions. Semin Perinatol. (2010) 34:408–15. doi: 10.1053/j.semperi.2010.09.005

PubMed Abstract | CrossRef Full Text | Google Scholar

49. Shrivastava SR, Shrivastava PS, Ramasamy J. Utility of kangaroo mother care in preterm and low birthweight infants. S Afr Family Pract. (2013) 55:340–4. doi: 10.1080/20786204.2013.10874373

PubMed Abstract | CrossRef Full Text | Google Scholar

50. Bergh A-M, Manu R, Davy K, Van Rooyen E, Asare GQ, Awoonor-Williams J, et al. Progress with the Implementation of Kangaroo Mother Care in Four Regions in Ghana. Ghana Med J. (2013) 47:57–63.

PubMed Abstract | Google Scholar

51. Bergh A-M, Manu R, Davy K, van Rooyen E, Asare GQ, Williams JKA, et al. Translating research findings into practice – the implementation of kangaroo mother care in Ghana. Implement Sci. (2012) 7:75. doi: 10.1186/1748-5908-7-75

PubMed Abstract | CrossRef Full Text | Google Scholar

52. Iyoke C, Lawani L, Ezugwu E, Ilo K, Ilechukwu G, Asinobi I, et al. Maternal risk factors for singleton preterm births and survival at the University of Nigeria Teaching Hospital, Enugu, Nigeria. Niger J Clin Pract. (2015) 18:744. doi: 10.4103/1119-3077.158141

PubMed Abstract | CrossRef Full Text | Google Scholar

53. Bayou G, Berhan Y. Perinatal mortality and associated risk factors: a case control study. Ethiop J Health Sci. (2012) 22:153–62.

PubMed Abstract | Google Scholar

54. Been JV, Millett C. Reducing the global burden of preterm births. Lancet Glob Health. (2019) 7:e414. doi: 10.1016/S2214-109X(19)30059-2

PubMed Abstract | CrossRef Full Text | Google Scholar

55. Odendaal HJ, Steyn DW, Elliott A, Burd L. Combined effects of cigarette smoking and alcohol consumption on perinatal outcome. Gynecol Obstet Invest. (2009) 67:1–8. doi: 10.1159/000150597

PubMed Abstract | CrossRef Full Text | Google Scholar

56. Strandberg-Larsen K, Grønbæk M, Andersen AMN, Andersen PK, Olsen J. Alcohol drinking pattern during pregnancy and risk of infant mortality. Epidemiology. (2009) 20:884–91. doi: 10.1097/EDE.0b013e3181bbd46c

PubMed Abstract | CrossRef Full Text | Google Scholar

57. Bhutta ZA, Das JK, Bahl R, Lawn JE, Salam RA, Paul VK, et al. Can available interventions end preventable deaths in mothers newborn babies, and stillbirths, and at what cost? Lancet. (2014) 3840:347–70. doi: 10.1016/S0140-6736(14)60792-3

PubMed Abstract | CrossRef Full Text | Google Scholar

58. WHO and UNICEF. Every Newborn: An Action Plan to End Preventable Deaths. (2014). Geneva, Switzerland: World Health Organization.

Google Scholar

59. WHO. The Global Strategy for Women's, Children's and Adolescents' Health (2016-2030).” Every Woman Every Child, Italy. (2016). Geneva, Switzerland: World Health Organization, 1–108.

Google Scholar

60. Tunçalp, Ö, Were W. M., MacLennan C., Oladapo O. T., Gülmezoglu A. M., Bahl R. Quality of care for pregnant women and newborns—the WHO vision. BJOG. (2015) 122:1045–49. doi: 10.1111/1471-0528.13451

PubMed Abstract | CrossRef Full Text | Google Scholar

Keywords: preterm birth, maternal factors, child health conditions at birth, preterm death, newborn, Ghana

Citation: Afagbedzi SK, Alhassan Y, Alangea DO and Taylor H (2023) Maternal factors and child health conditions at birth associated with preterm deaths in a tertiary health facility in Ghana: A retrospective analysis. Front. Public Health 11:1108744. doi: 10.3389/fpubh.2023.1108744

Received: 26 November 2022; Accepted: 23 January 2023;
Published: 09 February 2023.

Edited by:

Delanyo Dovlo, Ghana College of Physicians and Surgeons, Ghana

Reviewed by:

Dan Yedu Quansah, Lausanne University Hospital, Switzerland
Michal Fried, National Institutes of Health (NIH), United States

Copyright © 2023 Afagbedzi, Alhassan, Alangea and Taylor. 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: Seth Kwaku Afagbedzi, yes safagbedzi@gmail.com

Disclaimer: 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.