Toward Predicting 30-Day Readmission Among Oncology Patients: Identifying Timely and Actionable Risk Factors

Author:

Hwang Sy1,Urbanowicz Ryan12,Lynch Selah2,Vernon Tawnya3,Bresz Kellie3,Giraldo Carolina34,Kennedy Erin5,Leabhart Max3,Bleacher Troy3,Ripchinski Michael R.3,Mowery Danielle L.126ORCID,Oyer Randall A.3ORCID

Affiliation:

1. Institute for Biomedical Informatics, University of Pennsylvania, Philadelphia, PA

2. Department of Biostatistics, Epidemiology, & Informatics, University of Pennsylvania, Philadelphia, PA

3. Ann B. Barshinger Cancer Institute (ABBCI), University of Pennsylvania, Philadelphia, PA

4. Osteopathic Medicine, Philadelphia College of Osteopathic Medicine, Philadelphia, PA

5. Department of Nursing, University of Pennsylvania, Philadelphia, PA

6. Abramson Cancer Center, University of Pennsylvania, Philadelphia, PA

Abstract

PURPOSE Predicting 30-day readmission risk is paramount to improving the quality of patient care. In this study, we compare sets of patient-, provider-, and community-level variables that are available at two different points of a patient's inpatient encounter (first 48 hours and the full encounter) to train readmission prediction models and identify possible targets for appropriate interventions that can potentially reduce avoidable readmissions. METHODS Using electronic health record data from a retrospective cohort of 2,460 oncology patients and a comprehensive machine learning analysis pipeline, we trained and tested models predicting 30-day readmission on the basis of data available within the first 48 hours of admission and from the entire hospital encounter. RESULTS Leveraging all features, the light gradient boosting model produced higher, but comparable performance (area under receiver operating characteristic curve [AUROC]: 0.711) with the Epic model (AUROC: 0.697). Given features in the first 48 hours, the random forest model produces higher AUROC (0.684) than the Epic model (AUROC: 0.676). Both models flagged patients with a similar distribution of race and sex; however, our light gradient boosting and random forest models were more inclusive, flagging more patients among younger age groups. The Epic models were more sensitive to identifying patients with an average lower zip income. Our 48-hour models were powered by novel features at various levels: patient (weight change over 365 days, depression symptoms, laboratory values, and cancer type), hospital (winter discharge and hospital admission type), and community (zip income and marital status of partner). CONCLUSION We developed and validated models comparable with the existing Epic 30-day readmission models with several novel actionable insights that could create service interventions deployed by the case management or discharge planning teams that may decrease readmission rates over time.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

General Medicine

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