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Randomized Controlled Trial
. 2024 Sep;19(9):802-811.
doi: 10.1002/jhm.13391. Epub 2024 May 26.

Prognostic clinical decision support for pneumonia in the emergency department: A randomized trial

Affiliations
Randomized Controlled Trial

Prognostic clinical decision support for pneumonia in the emergency department: A randomized trial

Derek J Williams et al. J Hosp Med. 2024 Sep.

Abstract

Background: Hospitalization rates for childhood pneumonia vary widely. Risk-based clinical decision support (CDS) interventions may reduce unwarranted variation.

Methods: We conducted a pragmatic randomized trial in two US pediatric emergency departments (EDs) comparing electronic health record (EHR)-integrated prognostic CDS versus usual care for promoting appropriate ED disposition in children (<18 years) with pneumonia. Encounters were randomized 1:1 to usual care versus custom CDS featuring a validated pneumonia severity score predicting risk for severe in-hospital outcomes. Clinicians retained full decision-making authority. The primary outcome was inappropriate ED disposition, defined as early transition to lower- or higher-level care. Safety and implementation outcomes were also evaluated.

Results: The study enrolled 536 encounters (269 usual care and 267 CDS). Baseline characteristics were similar across arms. Inappropriate disposition occurred in 3% of usual care encounters and 2% of CDS encounters (adjusted odds ratio: 0.99, 95% confidence interval: [0.32, 2.95]). Length of stay was also similar and adverse safety outcomes were uncommon in both arms. The tool's custom user interface and content were viewed as strengths by surveyed clinicians (>70% satisfied). Implementation barriers include intrinsic (e.g., reaching the right person at the right time) and extrinsic factors (i.e., global pandemic).

Conclusions: EHR-based prognostic CDS did not improve ED disposition decisions for children with pneumonia. Although the intervention's content was favorably received, low subject accrual and workflow integration problems likely limited effectiveness. Clinical Trials Registration: NCT06033079.

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Conflict of interest statement

Conflict of Interest Disclosures (includes financial disclosures): Derek Williams reports in-kind research support from BioMerieux for unrelated work; Judith Martin receives funding to the University from: Merck, Sharp and Dome, National Institutes of Health, Centers for Disease Control and Prevention and Moderna for unrelated work; Carlos Grijalva reports consultancy fees from Pfizer, Merck, and Sanofi-Pasteur; and grants from Campbell Alliance/Syneos Health and Sanofi for unrelated work. Robert Freundlich reports stock in 3M and consulting from Oak Hill Clinical Informatics for unrelated work. Matthew Weinger consults for Fresenius Kabi USA and is the PI on an investigator-initiated grant from Merck for unrelated work.

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