Evidence map›Paper›PMID 41932702›Full record

ArticleBMJ open2026

Synthetic data-augmented machine learning for 30-day readmission prediction in patients with chronic conditions: a retrospective real-world study.

Todd Brothers, Keyuri Adhikari, Maryam Ramazani, Ahmed Imtiaz, Mohammad Al-Mamun

Abstract read
In one paragraph

Article in BMJ open, 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

What it found

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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

5 authors.

Todd BrothersPharmacy Practice, University of Rhode Island - College of Pharmacy, Kingston, Rhode Island, USA.ORCID http://orcid.org/0000-0003-1799-7233
Keyuri AdhikariPharmaceutical Systems and Policy, West Virginia University, Morgantown, West Virginia, USA.
Maryam RamazaniIndustrial and Management Systems Engineering, West Virginia University, Morgantown, West Virginia, USA.
Ahmed ImtiazIndustrial and Management Systems Engineering, West Virginia University, Morgantown, West Virginia, USA.
Mohammad Al-MamunPharmaceutical Systems and Policy, West Virginia University, Morgantown, West Virginia, USA mohammad.almamun@hsc.wvu.edu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesTo develop and evaluate an explainable machine learning framework enhanced with synthetic data generation to predict unplanned 30-day hospital readmissions among patients with chronic obstructive pulmonary disease (COPD), heart failure (HF) and type 2 diabetes mellitus (T2DM), and to identify key clinical and social predictors of readmission.

designA retrospective cohort study using electronic health record data incorporating both structured variables and information extracted from unstructured clinical notes. Synthetic data were generated using advanced resampling and deep learning-based techniques to address outcome imbalance and improve model training.

settingIntensive care unit and general ward admissions at a single tertiary academic medical centre included in the MIMIC-IV (Medical Information Mart for Intensive Care IV) database.

participantsAdult patients (≥18 years) were admitted with a primary diagnosis of COPD (n=14 050), HF (n=7097) or T2DM (n=12 735) between 2008 and 2019, with complete 30-day follow-up and no in-hospital mortality during the index admission. PRIMARY AND SECONDARY OUTCOME MEASURES: The primary outcome was unplanned all-cause hospital readmission within 30-days of discharge. Predictors were drawn from six domains, including demographics, comorbidities, clinical acuity, therapies, behavioural factors and care continuity. Predictive performance was evaluated using multiple machine learning methods and fivefold cross-validation, with model interpretability assessed using established goal and local explanation approaches.

resultsEnsemble-based machine learning models demonstrated the strongest predictive performance across all three disease cohorts. Key predictors of readmission included higher illness severity, greater comorbidity burden, medication non-adherence, gaps in preventive care and limited social support. Models incorporating synthetic data augmentation showed improved discrimination compared with models trained on original data alone.

conclusionsAn explainable synthetic-data driven framework incorporating clinical, behavioural and social data can support prediction of 30-day readmissions among patients with common chronic conditions using routinely available electronic health record data.

Indexed as

Diabetes Mellitus, Type 2Heart FailureMachine LearningPatient ReadmissionPulmonary Disease, Chronic ObstructiveAgedChronic DiseaseElectronic Health RecordsFemaleHumansMaleMiddle AgedPredictive Learning ModelsRetrospective StudiesChronic DiseaseElectronic Health RecordsMachine Learning

Identifiers

PMID41932702
PMCPMC13052753

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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.