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ePneumonia: Development of an Electronic Clinical Decision Support System for Community-Onset Pneumonia

ePneumonia: Development of an Electronic Clinical Decision Support System for Community-Onset Pneumonia

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03358342
Enrollment
10000
Registered
2017-11-30
Start date
2017-11-22
Completion date
2019-12-31
Last updated
2020-10-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pneumonia

Brief summary

The investigators plan to further develop a prototype, evidence-based, electronic clinical decision support system (CDSS) for pneumonia care (ePneumonia) with interoperability across Electronic Health Records in order to improve clinical outcomes and reduce healthcare resource utilization. The specific aims of this study are to evaluate the usability of ePneumonia adapted for Cerner and its impact on clinical, patient-centered and healthcare resource utilization outcomes in a stepped-wedge implementation study in 16 hospital emergency departments (EDs) across the Intermountain Healthcare integrated health system.

Detailed description

Since the launch of a paper-based pneumonia care process model in 1994, decision support for pneumonia care has been under continuous development at Intermountain. Studies published in 2001 and 2006 demonstrated decreased mortality using paper-based methods. An electronic pneumonia Clinical Decision Support System was later developed in the original Intermountain computing environment and implemented in 4 regional emergency departments (ED) in 2011. This tool featured a novel mortality predictor and real-time synthesis of clinical data to guide diagnosis, risk stratification, admission triage and guideline-concordant treatment. An outcome study published in 2015 demonstrated reduction in mortality with tool use compared to usual care. Most recently, Intermountain researchers led by study co-Investigator, Dr. Brandon Webb, developed an innovative tool to predict risk of drug-resistant bacteria and demonstrated its potential to improve antibiotic use and outcomes. The investigators have entered a robust phase of additional development and adaptation of ePneumonia into the Cerner Electronic Health Record (EHR) system. The objective of this study is to advance development of an evidence-based, electronic CDSS for pneumonia care with interoperability across EHRs in order to improve clinical outcomes and reduce healthcare resource utilization. The specific aim of this study is to evaluate the usability of ePneumonia and its associated impact on clinical, patient-centered and healthcare resource utilization outcomes in a stepped-wedge implementation study in 16 hospital EDs in the Intermountain Healthcare integrated health system. * Hypothesis #1: Healthcare providers will affirm ePneumonia usability, lack of interference with clinical workflow and only minor unintended consequences of use. * Hypothesis #2: In patients with community-onset pneumonia, ePneumonia use will improve clinical and patient-centered outcomes and decrease healthcare resource utilization. One year of baseline clinical outcome data will be gathered for all 16 emergency departments. The first of 6 clusters of ED's will begin prospective data collection in January 2018, with the remaining coming on at 2 month intervals until ePneumonia has been deployed at all sites. An additional 1 year of data collection will be continued through 2019.

Interventions

OTHERePneumonia CDS

ePneumonia clinical decision support system for community-onset pneumonia

Sponsors

Intermountain Health Care, Inc.
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* All patients ≥ 18 years who are identified by either (2a) ICD-10 codes for pneumonia; or acute respiratory failure or sepsis with secondary pneumonia codes or (2b) clinician completion of ePneumonia for Cerner. * Intermountain Healthcare physicians working in the 16 ED's

Exclusion criteria

* Patients without radiographic confirmation of pneumonia * subsequent episodes of pneumonia within the study period, so as not to over-represent patients with recurrent pneumonia caused by recurrent aspiration or structural lung disease, and * immunosuppressed patients, such as those with AIDS.

Design outcomes

Primary

MeasureTime frameDescription
30 day all-cause mortality30 daysmortality within 30 days of initial ED visit

Secondary

MeasureTime frameDescription
Accuracy of Drug Resistance in Pneumonia (DRIP) score within the ePneumonia logic to predict Multi-Drug Resistant (MDR) pathogens30 daysSensitivity, specificity, positive and negative predictive values for DRIP score versus identified pathogens
Antibiotic utilization rates, in terms of appropriateness of spectrum30 daysAntibiotic utilization rates, in terms of appropriateness of spectrum versus identified pneumonia pathogen
Rate of secondary hospital admission within 7 days for ED patients whose initial disposition was outpatient care7 daysRate of secondary hospital admission within 7 days for ED patients whose initial disposition was outpatient care
Matching of patient disposition from the ED with ePneumonia recommendationEnd of initial ED visit, <24 hours after ED arrivalePneumonia use will increase simple agreement between patient disposition from the ED with ePneumonia recommendation based on illness severity
Length of stayDuration of hospital stay, censored at 90 daysePneumonia use will shorten length of stay measured in hours
Healthcare providers will affirm ePneumonia usability, lack of interference with clinical workflow and only minor unintended consequences of use3 year study durationQualitative outcome based on provider surveys
Direct costsDuration of hospital stay, censored at 90 daysePneumonia use will produce lower direct costs (total and variable)

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 12, 2026