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N/A N=26,139 Other

Using Electronically Derived Automated Reports of Appropriate Antibiotic Use to Inform Stewardship Interventions

Community-acquired Pneumonia · Acute Otitis Media · Pharyngitis

Enrolled (actual)
26,139
Serious AEs
Results posted
Nov 2025
Primary outcome: Primary: Guideline-concordant Antibiotic Use for Adults With Pharyngitis — 1458; 2477 Participants

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Quasi experimental intervention (Other)
Age
Pediatric, Adult, Older Adult
Sex
All
Sponsor
Children's Hospital of Philadelphia
Primary completion
Jun 2024

Outcome Measures

OutcomeResultp-value
PRIMARY
Guideline-concordant Antibiotic Use for Adults With Pharyngitis
1458; 2477
PRIMARY
Guideline-concordant Antibiotic Use for Children With Acute Otitis Media
6154; 6287
PRIMARY
Guideline-concordant Antibiotic Use for Adults With Community-acquired Pneumonia
204; 242
PRIMARY
Guideline-concordant Antibiotic Use for Children With Community-acquired Pneumonia
213; 308
SECONDARY
Guideline-concordant Antibiotic Choice for Adults Hospitalized With Community Acquired Pneumonia
268; 302
SECONDARY
Guideline-concordant Antibiotic Duration for Adults Hospitalized With Community Acquired Pneumonia
230; 261
SECONDARY
30-day Community Acquired Pneumonia-related Outpatient Revisits (Emergency Department, Urgent Care, or Primary Care) in Adults
0; 0
SECONDARY
30-day Readmissions for Community Acquired Pneumonia in Adults
13; 6
SECONDARY
Guideline-concordant Antibiotic Choice for Pediatric Community Acquired Pneumonia
394; 362
SECONDARY
Guideline-concordant Antibiotic Duration for Pediatric Community Acquired Pneumonia
221; 322
SECONDARY
28-day Community Acquired Pneumonia-related Outpatient Revisits (Emergency Department, Urgent Care, or Primary Care) in Children
13; 20
SECONDARY
28-day Readmissions for Pediatric Community Acquired Pneumonia
8; 14
SECONDARY
Guideline-concordant Decision to Prescribe Antibiotics for Adult Pharyngitis
1464; 2492
SECONDARY
Guideline-concordant Antibiotic Choice Adult Pharyngitis
27; 160
SECONDARY
Guideline-concordant Antibiotic Duration for Adult Pharyngitis
31; 175
SECONDARY
30-day Pharyngitis Outpatient Revisits (Emergency Department, Urgent Care, or Primary Care) in Adults
291; 578
SECONDARY
30-day Deep Neck Space Infection Admission
0; 1
SECONDARY
Guideline-concordant Decision to Prescribe Antibiotics for Pediatric Acute Otitis Media
9935; 8547
SECONDARY
Guideline-concordant Antibiotic Choice for Pediatric Acute Otitis Media
7498; 6828
SECONDARY
Guideline-concordant Antibiotic Duration for Pediatric Acute Otitis Media
7565; 7281
SECONDARY
28-day Acute Otitis Media-related Outpatient Revisits (Emergency Department, Urgent Care, or Primary Care)
891; 756
SECONDARY
28-day Mastoiditis or Intracranial Infection Admissions
0; 0
SECONDARY
Guideline-concordant Decision to Not Prescribe Antibiotics for Pediatric Acute Otitis Media
284; 292
SECONDARY
Guideline-concordant Decision to Not Prescribe Antibiotics for Adult Pharyngitis
1432; 2312

Summary

The main goal of this study is to use automated electronic reports to assess and improve guideline-concordant antibiotic use for: 1) adult inpatients with community-acquired pneumonia; 2) pediatric inpatients with community-acquired pneumonia; 3) adult outpatients with acute pharyngitis; and 4) pediatric outpatients with acute otitis media.

Eligibility Criteria

Patient Inclusion Criteria:

  • Diagnosis of one of four conditions based on ICD-10 diagnostic codes.

Patient Exclusion Criteria:

  • Presence of specific complex chronic conditions
  • Use of immunocompromising medications
  • Transfer from another health facility.

Clinician Inclusion Criteria:

  • Prescribing clinicians (including attending physicians, fellows, residents, nurse practitioners, and physician assistants) at one of the participating outpatient practices or inpatient units.
  • Age ≥ 18 years old
  • Employed by one of the participating sites

Clinician Exclusion Criteria:

  • Volunteers or other non-employee hospital staff
  • Limited English proficiency
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT06027593). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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