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Sustainable deimplementation of continuous pulse oximetry monitoring in children hospitalized with bronchiolitis:
Christopher P Bonafide1,2,3,4, Rui Xiao5, Amanda C Schondelmeyer6,7,8
1Section of Hospital Medicine, Children's Hospital of Philadelphia, Children's Hospital of Philadelphia Hub for Clinical Collaboration, 3500 Civic Center Blvd, Philadelphia, PA, 19104, USA. bonafide@chop.edu.
Insights
The Eliminating Monitor Overuse (EMO) trial investigates strategies to reduce the overuse of continuous pulse oximetry in children with bronchiolitis. This study aims to find the best methods for sustaining deimplementation of unnecessary medical practices.
Area of Science:
- Pediatric hospital medicine
- Health services research
- Deimplementation science
Background:
- Continuous pulse oximetry monitoring for bronchiolitis is often overused, despite guidelines recommending it only for specific circumstances.
- Guideline-discordant practices persist, highlighting a need for effective deimplementation strategies.
- Previous pilot studies showed initial reductions in overuse but lacked data on long-term sustainment.
Purpose of the Study:
- To compare two deimplementation strategies for reducing overuse of continuous pulse oximetry in pediatric bronchiolitis patients.
- To evaluate the effectiveness of strategies targeting unlearning versus unlearning combined with substitution.
- To identify mechanisms driving sustained practice change in deimplementation.
Main Methods:
- A hybrid type III effectiveness-deimplementation trial using a longitudinal cluster-randomized design.
- Randomization of 16-19 hospitals to either educational outreach with audit/feedback or the same plus an EHR-integrated clinical pathway decision support tool.
- Primary outcome: sustainment of deimplementation (reduction in overuse) in non-oxygen-dependent bronchiolitis patients; secondary outcomes include equity, cost, fidelity, routinization, and institutionalization.
Main Results:
- Data collection and analysis are ongoing as part of the Eliminating Monitor Overuse (EMO) trial.
- The study is designed to provide rigorous comparative data on deimplementation strategy effectiveness.
- Hypothesized mechanisms of routinization and institutionalization will be tested.
Conclusions:
- The EMO trial will provide critical insights into sustaining deimplementation of overused medical practices.
- Findings will inform best practices for reducing unnecessary monitoring in pediatric care.
- The study aims to advance the science of deimplementation and improve care for pediatric lung disease.
Background:
Methods of sustaining the deimplementation of overused medical practices (i.e., practices not supported by evidence) are understudied. In pediatric hospital medicine, continuous pulse oximetry monitoring of children with the common viral respiratory illness bronchiolitis is recommended only under specific circumstances. Three national guidelines discourage its use for children who are not receiving supplemental oxygen, but guideline-discordant practice (i.e., overuse) remains prevalent. A 6-hospital pilot of educational outreach with audit and feedback resulted in immediate reductions in overuse; however, the best strategies to optimize sustainment of deimplementation success are unknown.
Methods:
The Eliminating Monitor Overuse (EMO) trial will compare two deimplementation strategies in a hybrid type III effectiveness-deimplementation trial. This longitudinal cluster-randomized design will be conducted in Pediatric Research in Inpatient Settings (PRIS) Network hospitals and will include baseline measurement, active deimplementation, and sustainment phases. After a baseline measurement period, 16-19 hospitals will be randomized to a deimplementation strategy that targets unlearning (educational outreach with audit and feedback), and the other 16-19 will be randomized to a strategy that targets unlearning and substitution (adding an EHR-integrated clinical pathway decision support tool). The primary outcome is the sustainment of deimplementation in bronchiolitis patients who are not receiving any supplemental oxygen, analyzed as a longitudinal difference-in-differences comparison of overuse rates across study arms. Secondary outcomes include equity of deimplementation and the fidelity to, and cost of, each deimplementation strategy. To understand how the deimplementation strategies work, we will test hypothesized mechanisms of routinization (clinicians developing new routines supporting practice change) and institutionalization (embedding of practice change into existing organizational systems).
Discussion:
The EMO trial will advance the science of deimplementation by providing new insights into the processes, mechanisms, costs, and likelihood of sustained practice change using rigorously designed deimplementation strategies. The trial will also advance care for a high-incidence, costly pediatric lung disease.
Trial Registration:
ClinicalTrials.gov, NCT05132322 . Registered on November 10, 2021.
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