Evidence map›Paper›PMID 41632759›Full record

ArticlePloS one2026

Assessing the validity of post-discharge readmission and mortality as a composite outcome among newborns in Uganda.

Abhroneel Ghosh, Vuong Nguyen, J Mark Ansermino, Yashodani Pillay, Angella Namala, Joseph Ngonzi, Nathan Kenya-Mugisha, Niranjan Kissoon, Matthew O Wiens

Abstract read
In one paragraph

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

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

9 authors.

Abhroneel GhoshIndian Statistical Institute, Kolkata, West Bengal, India.ORCID https://orcid.org/0009-0008-3809-2189
Vuong NguyenInstitute for Global Health, BC Children's and Women's Hospital, Vancouver, British Columbia, Canada.
J Mark AnserminoInstitute for Global Health, BC Children's and Women's Hospital, Vancouver, British Columbia, Canada.
Yashodani PillayInstitute for Global Health, BC Children's and Women's Hospital, Vancouver, British Columbia, Canada.
Angella NamalaJinja Regional Referral Hospital, Jinja City, Uganda.
Joseph NgonziDept of Obstetrics and Gynaecology, Mbarara University of Science and Technology, Mbarara, Uganda.ORCID https://orcid.org/0000-0001-5253-9516
Nathan Kenya-MugishaWalimu, Kampala, Uganda.
Niranjan KissoonInstitute for Global Health, BC Children's and Women's Hospital, Vancouver, British Columbia, Canada.
Matthew O WiensInstitute for Global Health, BC Children's and Women's Hospital, Vancouver, British Columbia, Canada.ORCID https://orcid.org/0000-0002-3287-5181

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundComposite outcomes, which include mortality and readmission rates, are often used in risk prediction models following hospital discharge when event rates for the primary outcome of interest, mortality, are low. However, greater readmission rates may result in reduced mortality making interpretation of the composite outcome difficult. We assess the usefulness of a composite outcome of post-discharge readmission and mortality as a target outcome in this context.

methodsThis was a secondary analysis of data collected among mothers and their newborn(s) admitted for delivery at two regional referral hospitals in Uganda. Six-week post-discharge mortality (all-cause) and readmission in newborn infants were analyzed using a competing risk framework. The Sub distribution Hazard Ratios (SHRs) were compared across predictor variables to examine the relationship between the two outcomes.

resultsA total of 6040 newborns with complete six-week follow-up were enrolled, of whom 50.6% were male and 64% of mothers delivered via caesarean section. Thirty-five (0.58%) infants died within the six-week follow-up period and 241 (3.99%) were readmitted. Of the 206 predictors, 81 had a consistent association with both outcomes. These include a higher weight (SHRs: 0.14, 0.68) and length of the baby (SHRs: 0.85, 0.91). However, 125 variables depicted an association in opposing directions which may be linked to social and financial barriers to care-seeking. These include a travel time to the hospital of greater than 1 hour (SHRs: 1.4, 0.28).

conclusionWhile mortality is unequivocally a negative outcome, readmission may be a positive outcome, reflecting health seeking, or a negative outcome, reflecting recurrent illness. This directional dichotomy is reflected to varying degrees within different variables. When using a composite outcome for a prediction model, caution should be exercised to ensure that the model identifies individuals at risk of the intended outcomes of interest, rather than merely the proxies used to represent those outcomes. Identifying predictors with a consistent relationship for both outcomes may yield a more optimized and less biased prediction model for use in clinical care.

Indexed as

Infant MortalityPatient DischargePatient ReadmissionAdultFemaleHumansInfant, NewbornMaleUganda

Identifiers

PMID41632759
PMCPMC12867235

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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.