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Original research
Prospective cohort study of mortality in very low birthweight infants in a single centre in the Eastern Cape province, South Africa
  1. Isabel A Michaelis1,
  2. Ingeborg Krägeloh-Mann2,
  3. Ncomeka Manyisane1,
  4. Mikateko C Mazinu3,
  5. Esme R Jordaan3
  1. 1Paediatrics, Walter Sisulu University, Mthatha, Eastern Cape, South Africa
  2. 2Children's Hospital, Neuropaediatrics, Developmental Neurology, Social Paediatrics, Eberhard Karls University Tübingen Faculty of Medicine, Tübingen, Baden-Württemberg, Germany
  3. 3Biostatistics unit, South African Medical Research Council, Tygerberg, Western Cape, South Africa
  1. Correspondence to Dr Isabel A Michaelis; isabel.michaelis{at}


Background Neonatal mortality is a major contributor worldwide to the number of deaths in children under 5 years of age. The primary objective of this study was to assess the overall mortality rate of babies with a birth weight equal or below 1500 g in a neonatal unit at a tertiary hospital in the Eastern Cape Province, South Africa. Furthermore, different maternal-related and infant-related factors for higher mortality were analysed.

Methods This is a prospective cohort study which included infants admitted to the neonatal wards of the hospital within their first 24 hours of life and with a birth weight equal to or below 1500 g. Mothers who consented answered a questionnaire to identify factors for mortality.

Results 173 very low birth weight (VLBW) infants were recruited in the neonatal department between November 2017 and December 2018, of whom 55 died (overall mortality rate 32.0%). Twenty-three of the 44 infants (53,5%) with a birth weight below 1000 g died during the admission. One hundred and sixty-one mothers completed the questionnaire and 45 of their babies died.

Main factors associated with mortality were lower gestational age and lower birth weight. Need for ventilator support and sepsis were associated with higher mortality, as were maternal factors such as HIV infection and age below 20 years.

Conclusion This prospective study looked at survival of VLBW babies in an underprivileged part of the Eastern Cape of South Africa. Compared with other public urban hospitals in the country, the survival rate remains unacceptably low. Further research is required to find the associated causes and appropriate ways to address these.

  • neonatology
  • mortality

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What is known about the subject?

  • The perinatal mortality rate in sub-Saharan Africa is about 30 per 1000 live births. Preterm and very low birthweight (VLBW) infants account for a large number of neonatal deaths. Although South Africa is considered an upper-middle-income country by the World Bank, survival of VLBW varies greatly dependent on resources. Survival of VLBW infants in studies from South Africa are about 75%.

What this study adds?

  • Survival of VLBW infants fulfilling inclusion criteria for the study was 68%. Survival for VLBW babies in our setting is lower than in other South African urban settings.


Despite improved survival rates of neonates worldwide, the survival of preterm and low birthweight babies is still a challenge, especially in middle- and low-income countries.1–4

In 2018, WHO described a worldwide increase of babies born prematurely over the last two decades. The incidence has been estimated between 5% and 18% of all life births.5 6 The prevalence of babies born with a very low birth weight (VLBW) varies between different countries. For example, in one South African study, the prevalence was 3%, while in the USA it lies between 1.23% and 1.43%.7–9 Furthermore, prematurity and low birth weight have been identified as the leading causes of mortality in children less than 5 years of age.5 10–12 It is also well known that neonatal mortality for VLBW infants varies considerably among high-income and low-middle income countries: a mortality rate of 15% is found in the USA,13 20% by the Vermont Oxford network,14 29.1% in Iran,3 28.2% in South Korea,11 32% in the Eastern Mediterranean Region15 and 24.6% in India.16 Some single centres worldwide show a lower mortality rate with 9.5%, 12.4%, 13.0% and 17.2% in single centres in Singapore, Taiwan, Hong-Kong, Saudi-Arabia, respectively.14 17–19

In South Africa, neonatal mortality accounted for 32% of the under 5 mortality rate.4 20 21 A recent study illustrated survival rates of VLBW neonates between different hospitals in the Western Cape Province of South Africa characterised by unrestricted or restricted resources.22 The team found a significant difference with a survival rate of 84.4% and 70.4%, respectively.22 Kalimba and Ballot23 studied the survival rate of extremely low birth weight (ELBW) babies (babies weighing less than 1000 g at birth) born between 2006 and 2010 in Johannesburg and found that only 25.6% of babies born with a birth weight of less than 900 g survived their hospital stay, with birth weight and gestational age being the strongest predictors for survival. A newer retrospective cross-sectional South African study found an overall survival rate in VLBW babies (500–1499 g) of 75.7%.24

However, there are also other known contributory factors, which can be divided into neonate-related or maternal-related risk factors. Examples of neonate-related risk factors studied in the literature include low Apgar scores, hyaline membrane disease (HMD), intubation and mechanical ventilation, sepsis and haemodynamic instability.25 26 Maternal or obstetric risk factors include eclampsia, alcohol consumption, smoking, low socioeconomic status, scarce antenatal care and human immuno deficiency virus (HIV) infection.18 23 27 28 Several studies suggest an increased risk of premature labour in mothers taking antiretroviral treatment (ART) for HIV infection during pregnancy,29–32 while others did not find a relationship.33 This is noteworthy, as 30.8% of pregnant women in South Africa tested positive for HIV in 2015, and are put on treatment as soon as the infection is diagnosed.34 35

The primary aim of this study was to research neonatal mortality of VLBW infants admitted to the neonatal unit in a hospital in a mixed urban and rural setting in the Eastern Cape Province of South Africa. Second, the association between death and different maternal and neonatal factors were explored.


Frere Hospital is a large (885 beds) public tertiary hospital in East London in the Eastern Cape Province in South Africa, with a seven-bed paediatric intensive care unit (PICU), which cares for neonates and paediatric medical and surgical patients. Because of this very limited PICU access, babies with a weight below 1000 g are not provided with invasive ventilatory support due to poor survival. These babies will receive surfactant if needed and continuous positive airway pressure (CPAP) ventilation is available for six infants in the high care neonatal unit, which can cater for 12 infants altogether. This high care ward is constantly above capacity, often having to care for up to 20 infants, when there is only adequate space for the above-mentioned 12 neonates. Infants with a birth weight over 1000 g will be taken to PICU and receive invasive ventilation if needed and if space is available for them. Stable neonates with a weight of more than 1000 g are referred to the general nursery ward, where they receive kangaroo mother care (KMC) in the ward and, if necessary, intravenous fluids and/or antibiotics and oxygen. Once clinically stable, off oxygen support, tolerating full enteral feeds and weighing more than 1500 g, infants will be transferred to the KMC ward until mothers are competent in caring for their baby and the weight has increased to at least 1700 g. Some stable babies might be transferred to their regional hospital once their weight has reached 1500 g.

Frere Hospital is the tertiary neonatal and obstetric referral centre for obstetric units and for surrounding district hospitals in the middle part of the Eastern Cape Province. Some referrals centres are more than 300 km away. These areas were deprived of adequate infrastructure during the Apartheid regimen and are still one of the most under-resourced and insufficiently managed parts of South Africa.

Materials and methods

This was a prospective cohort study. All babies born at the hospital, or admitted within the first 24 hours of life into the neonatal unit, with a birth weight equal or below 1500 g and without any life-threatening malformations were included. Neonates who were admitted to the neonatal ward or PICU beyond 24 hours of life were excluded as it was not possible to get sufficient information on those mother–infant pairs. Mothers were then approached for consent to include their data. The recruitment period lasted from December 2017 to November 2018.

After receiving written consent from the mothers, data concerning mother and child during the prenatal, perinatal and neonatal period were collected from the maternal and neonatal case records, as well as from a questionnaire filled in with the mother (see online supplemental file). The babies were followed up until discharge or death. All babies received standard care during this period, as outlined above.

Supplemental material

Gestational age was determined by either an early ultrasound or by applying the Ballard gestational age scoring system. It is estimated that about 70% of the babies admitted to our neonatal wards will have had their gestational age assessed by early ultrasound. The different variables were defined as follows: a persistent ductus arteriosus as identified by echocardiogram; HMD by the presence respiratory distress; fractional inspired oxygen requirement above 40% followed by a confirmatory blood gas and typical X-ray signs; sepsis as clinical signs confirmed with a positive blood, urine or cerebrospinal fluid culture and/or raised C reactive protein taken at least 24 hours apart; normal weight gain was determined when weight loss after birth did not exceed more than 10% and birth weight was regained within 10–14 days of life; intracranial haemorrhage (ICH) was diagnosed with cranial ultrasound, which was only performed in clinically unstable infants with the clinical suspicion of ICH; resuscitation at birth included mask or invasive ventilation with or without cardiac compressions and medication.

Patient and public involvement

The patients, being mother–newborn pairs, were not involved in the study design. Every new-born admitted in our wards during the study period was assessed for inclusion in our study, no recruitment from the patient’s side was necessary. The results of this study are verbally communicated to the mothers and/or caretakers.

Statistical analysis

Demographic data are presented as frequencies (percentages) for categorical data, and as means (SD) for continuous data. To test for association between the outcome variable (mortality) and the predictor variables, a log binomial regression model was used. In order to investigate the relationship between hypertension and mortality in babies in more detail, a multiple regression model was used, adjusting for IUGR and gestational age. The standard for significance for all analyses was a p<0.05. Data were analysed using STATA V.15.


During the study period, 4342 babies were born in the hospital, 4210 of these were live births and 231 (5.3%) were born with a birth weight between 500 g and 1500 g. Of those 231 VLBW infants, only 173 met the inclusion criteria for the study. Of those, 55 died during admission, resulting in an overall mortality rate of 31.8% (95% CI 25.2% to 39.2%) for VLBW infants admitted to our unit.

One hundred and sixty-one of the 173 VLBW infants were successfully recruited (caregivers gave informed consent) during the study period. Forty-five (28.0%) of those babies died before discharge and 116 (72.0%) were discharged home or referred to a peripheral hospital if they had reached a weight above 1500 g. Forty-four of the 161 babies were born with a birth weight below 1000 g, of those 23 (53,5%) did not survive until discharge. For an overview of recruitment and numbers of participants, see figure 1. All 116 babies discharged from hospital received a follow-up date for the high-risk clinic.

Figure 1

Flow diagram of recruitment numbers of cohort. VLBW: very low birth weight. d/c : discharged


The maternal age ranged between 14 and 46 years. Fifty-eight (36.0%) mothers had HIV infection diagnosed before or during the pregnancy or at birth. Thirty-nine of them (67.2%) had been on ART at delivery for more than 4 weeks. Sixteen (27.6%) mothers had been on ART for less than 4 weeks or were not on treatment at all when giving birth, and their babies were thus considered at high risk for HIV transmission and treated accordingly. For other variables please see table 1.

Table 1

Maternal demographic variables

Of the 161 babies included in the study, 96 were female (59.7%). Almost all HIV exposed babies (n=58) tested negative for HIV infection at birth with a negative birth HIV-PCR (n=55; 94.8%). Three babies, who died a few hours after birth, did not receive an HIV-PCR at birth and their status is therefore unknown. For other variables please see table 2.

Table 2

Infant demographics variables

Factors associated with in hospital mortality

Maternal associated factors for the univariate model:

Univariate regression analysis was used to examine the association between mortality and associated individual factors. Associated factors of infants dying while still in hospital were higher in babies of teenage mothers, mothers with illnesses and mothers on medication. Maternal hypertension and pre-eclampsia were associated with decreased mortality in the babies. Education level of the mother and other socioeconomic status factors were not significantly related to a higher mortality risk during admission in our study, with employment status only showing a trend towards significance (table 3).

Table 3

Significant univariate associations between VLBW infant mortality and maternal-related factors

Other illnesses included malignancies, epilepsy, mental health disorders. Medication included all other medication besides ART Most maternal factors that were not significantly associated with mortality in the regression analysis are not shown in this table.

Neonatal-associated factors:

There were many significant neonatal-associated factors related to infant mortality, such as low gestational age (p<0.01), low birth weight (p<0.01), IUGR (p<0.01) and the need for resuscitation at birth (p<0.01) or during the hospital stay (p=0.01). Male gender was not associated with higher mortality risk (p=0.94; RR=1.0; 95% CI 0.7 to 1.5) (table 4).

Table 4

Significant univariate associations between infant mortality and infant-related factors of VLBW infants

Multiple regression analysis

As could be seen in the univariate analysis, maternal hypertension was associated with decreased mortality in the babies. However, when adjusting for IUGR and gestational age in the multiple regression analysis, no significant association was found for maternal hypertension (p=0.28; RR=0.88; 95% CI 0.70 to 1.11), as shown in table 5.

Table 5

Results of maternal and infant factors in multiple regression analysis


The prevalence of VLBW infants of all live birth in this single hospital study in the Eastern Cape province between December 2017 and November 2018 was 5.4%. This figure lies within the prevalence of 3%–7% reported worldwide,3 13 but is likely elevated due to the referrals from obstetric units and surrounding district hospitals.

Almost 32% of admitted VLBW neonates with inclusion criteria died before discharge. For infants with a birth weight of 1000 g or less this number rose to 60%, while the chance for survival of infants weighing 1000 g and up to 1500 g at birth was higher, with a mortality rate of 18.5%. Thus, the overall mortality rate is higher than the reported average of approximately 25% in major cities in South Africa,24 36 37 and much higher than in the hospitals with much greater resources from the Western Cape province.22 It is also much higher than in most hospitals in high-income countries where mortality rates for VLBW infants are as low as 9.5%–17.2%.14 17–19 38 39 The high mortality in our setting is most likely due to the scarcity of skilled healthcare workers, limited infrastructures, as well as a patient overloaded, resource-restricted system, as described.4 The data support that although South Africa is considered an upper-middle-income country by the World Bank, survival of VLBW varies greatly dependent on resources.22

Consistent with other studies examining the causes of mortality in VLBW babies, birth weight and low gestational age were predictors of neonatal mortality in our study population.18 23 26 35 Complications of prematurity, such as the development of HMD and the associated need for surfactant replacement therapy with ventilation was associated with a significantly increased risk of mortality, as reported in previous research.3 22 23 26 Other studies have shown that CPAP and/or surfactant replacement therapy reduce mortality in VLBW and/or preterm neonates with HMD.22 40 Unavailability of PICU beds and overcrowding in our high care unit with low nurse-infants’ ratio could explain why we were unable to find this benefit in our cohort.

Interestingly, our study did not find that the wide range of maternal factors found in other studies increasing in-hospital mortality of infants, including lack of antenatal care, maternal primiparity, mode of delivery or complications thereof.23 27 28 32

Although a substantial percentage (36%) of the babies were born to HIV infected mothers, and 13.8% (n=8) of those had not received any ART before giving birth, all HIV-PCR done were negative. This is encouraging, but further research is needed to investigate HIV transmission rates in VLBW babies in low-resource settings.34 35

There are several limitations to this study. Even though this was a prospective study, data collection was not exhaustive and some prenatal variables could not be explored due to lack of information. Also, due to staff shortage, ultrasound of the head was not performed routinely, but only in clinically suspicious situations, and thus intracranial pathologies might have been missed. Furthermore, this is a single hospital-based study, therefore, the number of VLBW cases is limited.


Our cohort shows a higher in-hospital mortality of VLBW infants compared with some other urban hospitals in South Africa. These findings indicate that the survival of VLBW and especially ELBW babies are still unacceptably low in this resource restricted public hospital. This is most likely caused by numerous factors, many of which have also been implicated in similar studies, but need to be further investigated in future research and appropriately addressed.



  • Contributors IM’ contribution consisted of funding acquisition, study design, investigation, data curation, supervision and drafting the initial manuscript. NM contributed to study design, investigation, data curation and reviewing the manuscript. IK-M contributed to supervision, writing and reviewing the final manuscript. MM contributed to data curation and data analysis. EJ contributes to data curation and data analysis and writing and reviewing the final manuscript.

  • Funding This work was supported by the South African Medical Research Council (SAMRC) Fund, grant number (086/2017). The sponsorship of the SAMRC Pilot Grant serves to encourage clinicians in rural South Africa to engage in research.

  • Competing interests None declared.

  • Patient consent for publication Not required.

  • Ethics approval Walter Sisulu University Human Research Ethics Committee 086/2017.

  • Provenance and peer review Not commissioned; externally peer reviewed.

  • Data availability statement All data relevant to the study are included in the article or uploaded as online supplemental information. The existing data are deidentified participants data of mother and infant. Data will be available from

  • Supplemental material This content has been supplied by the author(s). It has not been vetted by BMJ Publishing Group Limited (BMJ) and may not have been peer-reviewed. Any opinions or recommendations discussed are solely those of the author(s) and are not endorsed by BMJ. BMJ disclaims all liability and responsibility arising from any reliance placed on the content. Where the content includes any translated material, BMJ does not warrant the accuracy and reliability of the translations (including but not limited to local regulations, clinical guidelines, terminology, drug names and drug dosages), and is not responsible for any error and/or omissions arising from translation and adaptation or otherwise.

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