Reducing length of antibiotics for children with ear infections: protocol for a cluster-randomized trial in the USA

Author:

Keith Amy1ORCID,Jenkins Timothy C23,O'Leary Sonja45,Stein Amy B1ORCID,Katz Sophie E6ORCID,Newland Jason7ORCID,Rinehart Deborah J18ORCID,Gilbert Aiden1,Dodd Sherry7,Terrill Cindy M7,Frost Holly M145ORCID

Affiliation:

1. Center for Health Systems Research, Denver Health & Hospital Authority, Denver, CO 80201, USA

2. Division of Infectious Diseases, Department of Medicine, Denver Health & Hospital Authority, Denver, CO 80204, USA

3. Division of Infectious Diseases, Department of Medicine, University of Colorado School of Medicine, Aurora, CO 80045, USA

4. Department of General Pediatrics, Denver Health Medical Center, Denver, CO 80204, USA

5. Department of General Pediatrics, University of Colorado School of Medicine, Aurora, CO 80045, USA

6. Division of Infectious Diseases, Department of Pediatrics, Vanderbilt University Medical Center, Nashville, TN 37232, USA

7. Division of Infectious Diseases, Department of Pediatrics, Washington University in St. Louis, St. Louis, MO 63110, USA

8. Division of General Internal Medicine, Department of Medicine, University of Colorado School of Medicine, Aurora, CO 80045,, USA

Abstract

Aim: Preventing unnecessarily long durations of antibiotic therapy is a key opportunity to reduce antibiotic overuse in children 2 years of age and older with acute otitis media (AOM). Pragmatic interventions to reduce durations of therapy that can be effectively scaled and sustained are urgently needed. This study aims to fill this gap by evaluating the effectiveness and implementation outcomes of two low-cost interventions of differing intensities to increase guideline-concordant antibiotic durations in children with AOM. Methods: The higher intensity intervention will consist of clinician education regarding guideline-recommended short durations of antibiotic therapy; electronic health record (EHR) prescription field changes to promote prescribing of recommended short durations; and individualized clinician audit and feedback on adherence to recommended short durations of therapy in comparison to peers, while the lower intensity intervention will consist only of clinician education and EHR changes. We will explore the differences in implementation effectiveness by patient population served, clinician type, clinical setting and organization as well as intervention type. The fidelity, feasibility, acceptability and perceived appropriateness of the interventions among different clinician types, patient populations, clinical settings and intervention type will be compared. We will also conduct formative qualitative interviews with clinicians and administrators and focus groups with parents of patients to further inform the interventions and study. The formative evaluation will take place over 1.5 years, the interventions will be implemented over 2 years and evaluation of the interventions will take place over 1.5 years. Discussion: The results of this study will provide a framework for other healthcare systems to address the widespread problem of excessive durations of therapy for AOM and inform national antibiotic stewardship policy development. Clinical Trial Registration : NCT05608993 ( ClinicalTrials.gov )

Publisher

Becaris Publishing Limited

Subject

Health Policy

Reference31 articles.

1. Epidemiology of acute otitis media in the postpneumococcal conjugate vaccine era;Kaur R;Pediatrics,2017

2. Prevalence of inappropriate antibiotic prescriptions among US ambulatory care visits, 2010–2011;Fleming-Dutra KE;JAMA,2016

3. Antibiotic prescribing in ambulatory pediatrics in the United States;Hersh AL;Pediatrics,2011

4. Short-course antibiotics for acute otitis media;Kozyrskyj A;The Cochrane database of systematic reviews.,2010

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