Intermittent Versus Continuous Pulse Oximetry Monitoring of Infants Admitted for Bronchiolitis

Not Applicable

Completed

Conditions: Bronchiolitis
Hypoxia

Interventions: Other: Continuous pulse oximetry monitoring
Device: Intermittent pulse oximetry monitoring

Registration Number: NCT01014910

Lead Sponsor: Children's Mercy Hospital Kansas City

Brief Summary: Bronchiolitis is a lower respiratory tract infection (LRTI) syndrome cause by different types of viruses and occurs in young children. Although bronchiolitis is a widespread and fairly common illness in children, pediatricians vary significantly in how it is treated. This includes how children are monitored for their oxygen status when not receiving supplemental oxygen. Studies suggest that continuous pulse oximetry measurement of children admitted to the hospital with bronchiolitis regardless of use of supplemental oxygen prolongs their hospital stay. This increases the cost of care for these patients and increases their risk of hospital-associated complications.

This study is a randomized trial of continuous pulse oximeter use in patients admitted with bronchiolitis versus transitioning patients not requiring oxygen to intermittent pulse oximetry monitoring. The investigators hypothesize that this will decrease length of stay as well as associated costs of care and number of medical interventions performed in the hospital.

Detailed Description: Background: Bronchiolitis is a lower respiratory tract infection (LRTI) syndrome caused by different viruses. It is the most common LRTI in children under 24 months old, accounting for approximately 90,000 hospitalizations annually and costing over $700 million in children under 12 months. Health care providers vary in diagnosis and management, however. In 2006 the American Academy of Pediatrics (AAP) released guidelines for bronchiolitis management in an effort to standardize clinical practice. Part of these guidelines recommends patients admitted to the hospital receive supplemental oxygen if they are persistently hypoxic, which is defined as pulse oximeter readings persistently below 90%. However, this recommendation is based on expert opinion.

Research has previously shown healthy infants routinely experience brief episodes of decreased oxygen levels while sleeping without significant health effects. Other studies demonstrate no relationship between short intervals of transient or mildly decreased oxygen levels and long-term mental or developmental delays. Furthermore, children with bronchiolitis remain hospitalized longer without any appreciable improvement in the course or outcome of their illness when continuously monitored for oxygen level.

Widespread pulse oximeter use has increased hospitalization rates over 250%, and close monitoring increases length of stay for children who otherwise could be discharged home. The 2006 guidelines discourage continuous pulse oximetry monitoring in children not requiring supplemental oxygen, but health care providers routinely ignore this recommendation. No studies have assessed the impact of more strictly adhering to the practices recommended by the AAP.

Research Procedures: This is a randomized control study and is a multi-site collaboration with University of Missouri Children's Hospital in Columbia, Missouri. Children admitted to the study sites with bronchiolitis will be batch randomized (i.e. randomized separately at each site) to undergo either continuous pulse oximetry monitoring throughout the entire hospitalization or receive intermittent monitoring when not on supplemental oxygen. Patients will additionally receive all care standard to the management of their illness. Of note, the proposed intervention is the recommended standard of care for oxygen monitoring compared to the general practice used at both study sites. Researchers will then review charts after discharge for length of stay, number of medical interventions performed, diagnostic testing completed, and treatments provided. Cost of stay for patients in each group will be estimated and compared as well. Patients will be involved in the study for their entire admission.

Recruitment & Eligibility

Status: COMPLETED

Sex: All

Target Recruitment: 161

Inclusion Criteria

Children less than or equal to 24 months old with a history of term delivery (gestational age ≥37 weeks) admitted with a presumptive diagnosis of bronchiolitis
Bronchiolitis will be defined as an episode of wheezing or increased work of breathing associated with signs of an upper respiratory tract infection experienced by a patient
Enrollment within 24 hours of admission

Exclusion Criteria

History of severe cardiac or pulmonary illness, including but not limited to bronchopulmonary dysplasia, chronic lung disease, asthma/reactive airway disease, congenital heart disease, heart failure, and cardiothoracic surgery
History of home albuterol use for asthma or reactive airway disease
History of use of bronchodilator with successful patient response to the medication
Use of corticosteroids within the past two weeks up to day of admission
Use of antibiotics after admission for suspected pneumonia or similar pulmonary disease
History of premature birth (<37 weeks gestation)
History of receiving palivizumab (anti-RSV antibody)
Diagnosis of chronic immune deficiency, hematologic dyscrasia, or cancer
Chronic treatment with immunosuppressants
Parents/guardians unable to give informed consent in English
Need for PICU transfer at any point during illness
Transfer from an outside institution where patient was hospitalized for ≥12 hours
Previous enrollment in this study
Pediatric attending refuses to comply with study protocol

Study & Design

Study Type: INTERVENTIONAL

Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Continuous pulse oximetry monitoring	Continuous pulse oximetry monitoring	Patients will receive continuous pulse oximetry monitoring throughout their hospital stay regardless of their need for supplemental oxygen.
Intermittent pulse oximetry monitoring	Intermittent pulse oximetry monitoring	Patients will receive pulse oximetry monitoring during vital signs checks (every 4 hours) and as indicated clinically when not on supplemental oxygen. When patients require supplemental oxygen they will be continuously monitored by pulse oximetry until their oxygen requirement has resolved.

Primary Outcome Measures

Name	Time	Method
Length of Stay in the Hospital	Summarized from admission to hospital discharge

Secondary Outcome Measures

Name	Time	Method
Clinical Deterioration Necessitating Transfer to Higher Level of Care	Summarized from admission to hospital discharge

Trial Locations

Locations (4): University of Missouri Children's Hospital
🇺🇸
Columbia, Missouri, United States
Children's Mercy Hospital
🇺🇸
Kansas City, Missouri, United States
Christus Santa Rosa Children's Hospital
🇺🇸
San Antonio, Texas, United States
Hasbro Children's Hospital
🇺🇸
Providence, Rhode Island, United States