# A retrospective cohort study of premature neonatal mortality rates and contributing factors in a tertiary referral NICU in Addis Ababa, Ethiopia from 2022 to 2023

**Authors:** Gregory C. Valentine, Krystle M. Perez, Olivia C. Brandon, Sharla Rent, Gal Barbut, Merhawit Abadi, Gesit Metaferia, Redeat Workneh, Mahlet Abayneh

PMC · DOI: 10.1016/j.cegh.2025.102118 · Clinical epidemiology and global health · 2025-07-31

## TL;DR

This study examines why premature babies die in a hospital in Ethiopia, finding that lung issues and infections are major causes, with unexpected high rates of lung bleeding.

## Contribution

The study identifies pulmonary hemorrhage as a significant but underreported cause of mortality in premature neonates in Ethiopia.

## Key findings

- 22.1% of premature neonates in the study died, with extremely low birthweight neonates having 84% mortality.
- Respiratory distress syndrome was the leading cause of death (67.7%), followed by sepsis (39.5%) and pulmonary hemorrhage (25%).
- Pulmonary hemorrhage deaths were associated with higher cesarean delivery and antenatal corticosteroid use.

## Abstract

Prematurity remains the leading contributor for neonatal death globally, with Ethiopia having the 4th highest incidence of neonatal deaths. Clarifying specific contributors of prematurity-related neonatal death is critical to improve outcomes.

We evaluated neonatal causes of death among premature neonates at St. Paul’s Hospital Millennium Medical College’s (SPHMMC) neonatal intensive care unit (NICU).

Through a retrospective electronic database, we evaluated mortality outcomes for neonates <37 weeks’ gestation admitted to SPHMMC NICU from February 2022–May 2023, excluding those with congenital anomalies. Logistic regression models assessed the association between variables and outcomes.

Of 1033 premature neonates included in the analysis, 228 (22.1 %) died. Mortality was inversely related to birthweight with extremely low birthweight neonates (≤1000g) having 84 % mortality. The top 3 causes of prematurity-related mortality included respiratory distress syndrome (67.7 %, 159/228), sepsis (39.5 %, 90/228), and pulmonary hemorrhage (25.0 %, 57/228). Neonates that died from pulmonary hemorrhage had higher antenatal corticosteroids (ACS) exposure (66.7 % vs 36.7 %, p < 0.001), less chorioamnionitis (29.5 % vs 55.5 %, p = 0.004), and higher cesarean section delivery (71.9 % vs 53.1 %, p = 0.02). Notably, there were no associations between mortality and ACS exposure or lack thereof in the overall cohort in multivariate models.

While respiratory distress syndrome and sepsis are commonly reported findings of premature mortality, surprisingly, 25 % of premature newborns died from pulmonary hemorrhage at SPHMMC NICU. Further investigations are needed to clarify the causes and contributing factors leading to premature death and to determine whether pulmonary hemorrhage is an underreported, underrecognized contributor to prematurity-related mortality globally.

## Linked entities

- **Diseases:** respiratory distress syndrome (MONDO:0009971)

## Full-text entities

- **Genes:** PTBP1 (polypyrimidine tract binding protein 1) [NCBI Gene 5725] {aka HNRNP-I, HNRNPI, HNRPI, PTB, PTB-1, PTB-T}, PRPH2 (peripherin 2) [NCBI Gene 5961] {aka AOFMD, AVMD, CACD2, DS, MDBS1, RDS}
- **Diseases:** infection (MESH:D007239), infants (MESH:D063766), coagulopathy (MESH:D001778), Respiratory Distress Syndrome (MESH:D012128), Intrauterine Growth Restriction (MESH:D005317), ACS (MESH:C565152), pre-eclampsia (MESH:D011225), neonatal death (MESH:D066087), death (MESH:D003643), sepsis (MESH:D018805), chorioamnionitis (MESH:D002821), Extremely Low Birthweight (MESH:D001724), neurodevelopmental disabilities (MESH:D007859), Newborn (MESH:D006475), asphyxia (MESH:D001237), Hypoxic Ischemic Encephalopathy (MESH:D020925), congenital anomalies (MESH:D000013), Preterm (MESH:D047928), related (MESH:D019973), Prematurity (MESH:C536271), Pulmonary hemorrhage (MESH:D006470)
- **Chemicals:** steroids (MESH:D013256), dexamethasone (MESH:D003907), ACS (-), MDG (MESH:D000245), vitamin K (MESH:D014812)
- **Species:** Homo sapiens (human, species) [taxon 9606], Human immunodeficiency virus 1 (no rank) [taxon 11676]

## Full text

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## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12311812/full.md

## References

39 references — full list in the complete paper: https://tomesphere.com/paper/PMC12311812/full.md

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Source: https://tomesphere.com/paper/PMC12311812