Evidence map›Paper›PMID 42806374›Full record

ArticleTropical medicine and health2026

In-hospital mortality and associated factors among term neonates with documented perinatal asphyxia in eastern Democratic Republic of the Congo: a retrospective cohort study.

Joseph Ntagerwa Ntaganzibwa, Francisca Isia Nanci, Benjamin Ntaligeza Mashukano, Serge Mushamuka Zigabe, Germain Mudumbi Zabaday, Eliezer Rhuderhekuguma Kulimushi, Samuel Ndinaye, David Bahati Bashomeka, Grâce Mushagalusa Bavurhe, Christian Cito Shabani and 7 more

Abstract read
In one paragraph

Article in Tropical medicine and health, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

17 authors.

Joseph Ntagerwa NtaganzibwaFaculty of Medicine, Université Catholique de Bukavu, Bukavu, Democratic Republic of the Congo.
Francisca Isia NanciFaculty of Medicine, Université Catholique de Bukavu, Bukavu, Democratic Republic of the Congo.
Benjamin Ntaligeza MashukanoFaculty of Medicine, Université Catholique de Bukavu, Bukavu, Democratic Republic of the Congo.
Serge Mushamuka ZigabeFaculty of Medicine, Université Catholique de Bukavu, Bukavu, Democratic Republic of the Congo.
Germain Mudumbi ZabadayFaculty of Medicine, Université Catholique de Bukavu, Bukavu, Democratic Republic of the Congo.
Eliezer Rhuderhekuguma KulimushiFaculty of Medicine, Université Catholique de Bukavu, Bukavu, Democratic Republic of the Congo.
Samuel NdinayeFaculty of Medicine, Université Catholique de Bukavu, Bukavu, Democratic Republic of the Congo.
David Bahati BashomekaFaculty of Medicine, Université Catholique de Bukavu, Bukavu, Democratic Republic of the Congo.
Grâce Mushagalusa BavurheFaculty of Medicine, Université Catholique de Bukavu, Bukavu, Democratic Republic of the Congo.
Christian Cito ShabaniFaculty of Medicine, Université Catholique de Bukavu, Bukavu, Democratic Republic of the Congo.
Joy-Arsène BwemaFaculty of Medicine, Université Catholique de Bukavu, Bukavu, Democratic Republic of the Congo.
Lucie Nshobole CebweruFaculty of Medicine, Université Catholique de Bukavu, Bukavu, Democratic Republic of the Congo.
Elysée Akonkwa BirereFaculty of Medicine, Université Catholique de Bukavu, Bukavu, Democratic Republic of the Congo.
Bel'Ange Assongo WabiwaFaculty of Medicine, Université Catholique de Bukavu, Bukavu, Democratic Republic of the Congo.
Walter BinjaFaculty of Medicine, Université Catholique de Bukavu, Bukavu, Democratic Republic of the Congo.
Oreste BattistiFaculty of Medicine, Université Catholique de Bukavu, Bukavu, Democratic Republic of the Congo.
Richard Mbusa KambaleFaculty of Medicine, Université Catholique de Bukavu, Bukavu, Democratic Republic of the Congo. richkambale7@gmail.com.ORCID https://orcid.org/0000-0002-6545-2441

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPerinatal asphyxia remains an important contributor to neonatal mortality and neurodevelopmental impairment, particularly in resource-limited settings, yet contemporary evidence from eastern Democratic Republic of the Congo (DRC) is scarce. We assessed the hospital burden, clinical severity, and factors associated with in-hospital mortality among affected neonates admitted to a tertiary neonatal intensive care unit (NICU).

methodsWe conducted a retrospective cohort study at the Hôpital Provincial Général de Référence de Bukavu, eastern DRC, including neonates with documented perinatal asphyxia admitted between January 2021 and December 2025. Diagnosis was based on an integrated assessment of perinatal, clinical, neurological, and, when available, biochemical findings documented by the attending NICU pediatrician. Hospital-detected incidence was estimated among inborn neonates. Prognostic analyses were restricted to term neonates and used logistic regression, with Firth penalization for multivariable analysis because of the limited number of deaths.

resultsAmong 2,333 NICU admissions, 257 neonates (11.0%) had documented perinatal asphyxia, of whom 60 (23.3%) died. Among 183 inborn cases, the hospital-detected incidence proportion was 20.9 per 1,000 livebirths (95% CI 18.0-24.2). The primary prognostic analysis included 153 term neonates, of whom 27 (17.6%) died. Among 121 neonates with documented Sarnat-Sarnat staging, mortality increased from 4.5% in stage I to 15.3% in stage II and 32.5% in stage III (global exact p=0.018). Lower birth weight and outborn status were associated with mortality in univariable analyses. In the Firth multivariable model (n=99; 16 deaths), Sarnat-Sarnat stage remained associated with mortality overall, although adjusted estimates were highly imprecise.

conclusionsDocumented perinatal asphyxia was associated with substantial in-hospital mortality in this tertiary NICU, with mortality increasing across recorded encephalopathy stages. Lower birth weight and outborn status emerged as additional prognostic signals in exploratory univariable analyses. Given the limited number of deaths and substantial imprecision of adjusted estimates, these findings should be considered hypothesis-generating and require confirmation in larger prospective studies.

Indexed as

Democratic Republic of the CongoNeonatal encephalopathyNeonatal mortalityNewborn healthPerinatal asphyxia

Identifiers

PMID42806374
PMCPMC13617873

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.