Clinical Trials Logo

Clinical Trial Summary

Children with pneumonia presenting to the emergency department at Monroe Carell Jr. Children's Hospital at Vanderbilt or Children's Hospital of Pittsburgh will be potentially eligible for study. During intervention periods, providers caring for enrolled children will be presented with a detailed decision support strategy that emphasizes management in accordance with national guideline recommendations. The anticipated study duration is 24 months and, as this study does not include direct contact with enrolled subjects, there is no anticipated follow up.


Clinical Trial Description

Pneumonia is the most common serious infection in childhood. In the United States (US), pneumonia accounts for 1-4% of all emergency department (ED) visits in children (3-28 per 1,000 US children per year) and ranks among the top 3 reasons for pediatric hospitalization with >100,000 hospitalizations per year (15-22 per 100,000 US children per year). Pneumonia also accounts for more days of antibiotic use in US children's hospitals than any other condition. Emergency care for childhood pneumonia, including hospitalization rates, varies widely across the nation. A study examining hospital admission rates at 35 US children's hospitals from 2009-12 showed marked differences in severity-adjusted pneumonia hospital admission rates (median 31%; range 19-69%). Provider preferences and inaccurate risk perceptions contribute to these differences in hospitalization rates. Within the Intermountain Healthcare System in Utah, Dean et al. exposed large differences in admission rates (range 38-79%) among 18 individual ED providers providing care for >2,000 adults with pneumonia. Differences were not explained by patient characteristics or illness severity and higher rates of hospitalization did not reduce hospital readmissions or mortality. In another multicenter study of 472 adults with pneumonia at <4% risk of 30-day mortality estimated using objective severity scores, providers overestimated the risk of mortality in 5% of outpatients (range across institutions 0-12%) and 41% of inpatients (range across institutions 36-48%). These studies suggest that risk perceptions are often inaccurate, and potentially lead to unnecessary or prolonged hospitalizations and intensive therapies. Similar studies have not been performed in children because no valid prognostic tools exist to reliably predict pediatric pneumonia severity. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06033079
Study type Interventional
Source Vanderbilt University Medical Center
Contact
Status Completed
Phase N/A
Start date November 20, 2020
Completion date November 30, 2022

See also
  Status Clinical Trial Phase
Completed NCT04217980 - Severe Pneumonia Diagnostic in Pediatric Population by Lung Ultrasonography and Procalcitonin N/A
Terminated NCT03929484 - A Feasibility Study Evaluating a Novel Mask (Nasal Reservoir Cannula) N/A
Active, not recruiting NCT04923035 - Paediatric Pneumococcal Pneumonia in Malaysia Prior to and During Pneumococcal Conjugate Vaccine (PCV) Implementation
Completed NCT03710759 - Effect of Assisted Autogenic Drainage In Children Suffering From Pneumonia N/A
Recruiting NCT02669654 - Effectiveness Trial of Day-care vs. Usual Care of Severe Pneumonia & Malnutrition in Children Phase 4
Recruiting NCT03446534 - The Norwegian Antibiotics for Pneumonia in Children Study Phase 4
Enrolling by invitation NCT05826873 - Discharge Stewardship in Children's Hospitals N/A
Recruiting NCT03612362 - Impact of Improved "Injera" Baking Stove Use on Childhood Acute Respiratory Infection Prevention in Northwest Ethiopia N/A
Completed NCT06174454 - Clinical Efficacy of Respiratory Pediatric Physiotherapy on a Child With Hospital Treated Pneumonia N/A
Completed NCT03760419 - Improving CarE for Community Acquired Pneumonia 1 N/A
Completed NCT06154876 - Effect Of Cough Assist Device On Hemodynamic Status And Oxygen Saturation For Ventilated Children N/A
Terminated NCT03067558 - Acute Respiratory Infection Diagnostic Aids (ARIDA) Controlled Accuracy Evaluation Protocol N/A