Early machine learning prediction of hospitalized patients at low risk of respiratory deterioration or mortality in community-acquired pneumonia: Derivation and validation of a multivariable model

Yewande E. Odeyemi, Amos Lal, Erin F. Barreto, Allison M. Lemahieu, Hemang Yadav, Ognjen Gajic, Phillip Schulte

Research output: Contribution to journalArticlepeer-review

Abstract

Current prognostic tools for pneumonia predominantly focus on mortality, often neglecting other crucial outcomes such as the need for advanced respiratory support. The objective of this study was to develop and validate a tool that predicts the early risk of non-occurrence of respiratory deterioration or mortality. We conducted a single-center, retrospective cohort study involving hospitalized adult patients with community-acquired pneumonia (CAP) and acute hypoxic respiratory failure from January 2009 to December 2019 (n = 4379). We employed the gradient boosting machine (GBM) learning to create a model that estimates the likelihood of patients requiring advanced respiratory support (high-flow nasal cannula [HFNC], non-invasive mechanical ventilation [NIMV], and invasive mechanical ventilation [IMV]) or mortality during hospitalization. This model utilized readily available data, including demographic, physiologic, and laboratory data, sourced from electronic health records and obtained within the first 6 h of admission. Out of the cohort, 890 patients (25.2%) either required advanced respiratory support or died during their hospital stay. Our predictive model displayed superior discrimination and higher sensitivity (cross-validation C-statistic = 0.71; specificity = 0.56; sensitivity = 0.72) compared to the pneumonia severity index (PSI) (C-statistic = 0.65; specificity = 0.91; sensitivity = 0.24; P value < 0.001), while maintaining a negative predictive value (NPV) of approximately 0.85. These data demonstrate that our machine-learning model predicted the non-occurrence of respiratory deterioration or mortality among hospitalized CAP patients more accurately than the PSI. The enhanced sensitivity of this model holds the potential for reliably excluding low-risk patients from pneumonia clinical trials.

Original languageEnglish (US)
Pages (from-to)337-345
Number of pages9
JournalBiomolecules and Biomedicine
Volume24
Issue number2
DOIs
StatePublished - Mar 11 2024

Keywords

  • Community-acquired pneumonia (CAP)
  • advanced respiratory support
  • machine learning
  • mortality
  • predictive modeling

ASJC Scopus subject areas

  • General Biochemistry, Genetics and Molecular Biology
  • General Medicine

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