Oxygen Saturation Monitoring in Bronchiolitis
Primary Purpose
Bronchiolitis
Status
Completed
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Intermittent oxygen monitoring
Continuous oxygen monitoring
Sponsored by
About this trial
This is an interventional supportive care trial for Bronchiolitis focused on measuring Bronchiolitis, Length of Hospital Stay, Clinical Trial, Oxygen Saturation Monitoring
Eligibility Criteria
Children admitted to the general pediatric inpatient unit (GPIU) with bronchiolitis will be eligible if their clinical status is stable and not at high risk of deterioration
Inclusion Criteria:
- Clinical diagnosis of bronchiolitis as determined by the attending physician.
- First episode of acute bronchiolitis.
- Age: 4 weeks to 24 months.
- Clinical status stable for 6 hours
- Parent consent
Exclusion Criteria:
- Known risk factors for clinical deterioration including chronic medical condition; premature birth (<35weeks), history of apnea, weight < 4kg, receiving morphine
- Patient on heated high flow oxygen at enrolment
- ICU admission on current admission
- No telephone available
Sites / Locations
- McMaster Children's Hospital
- Trillium Health Partners (Credit Valley Site)
- Lakeridge Health Oshawa
- Children's Hospital of Eastern Ontario
- North York General Hospital
- Hospital for Sick Children
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Experimental
Arm Label
Continuous oxygen monitoring
Intermittent oxygen monitoring
Arm Description
Oxygen saturation will be measured continuously through the child's hospital stay until discharge.
Oxygen saturation will be measured intermittently, every 4 hours, through the child's hospital stay until discharge.
Outcomes
Primary Outcome Measures
Length of hospital stay from randomization on the inpatient unit to discharge from hospital
Secondary Outcome Measures
Duration of oxygen supplementation from randomization to discontinuation of supplementation
Number of medical interventions performed from time of randomization to hospital discharge
Time from randomization to meeting hospital discharge criteria
Length of hospital stay from inpatient unit admission to hospital discharge
Parent anxiety
Parents will rate their level of anxiety at the current time (state anxiety) and generally (trait anxiety) from the adult State Trait Anxiety Inventory questionnaire during the hospital stay.
Number of parent work days missed from randomization to 15 days after discharge
Nursing satisfaction
The attending nurse will be asked to complete a 10 mm visual analogue scale (VAS) to measure their satisfaction with the quality of monitoring.
PICU admission after randomization
PICU consultation after admission
Unscheduled return to care within 15 days of discharge
Mortality
Cost-Effectiveness
Cost-effectiveness will be measured by the incremental cost-effectiveness ratio (ICER), a ratio defined by the incremental difference in costs between treatment arms and the incremental difference in length of stay.
Full Information
NCT ID
NCT02947204
First Posted
October 20, 2016
Last Updated
March 20, 2020
Sponsor
The Hospital for Sick Children
Collaborators
Canadian Institutes of Health Research (CIHR), Children's Hospital of Eastern Ontario
1. Study Identification
Unique Protocol Identification Number
NCT02947204
Brief Title
Oxygen Saturation Monitoring in Bronchiolitis
Official Title
Intermittent vs. Continuous Oxygen Saturation Monitoring in Infants Hospitalized for Bronchiolitis: A Randomized Controlled Trial
Study Type
Interventional
2. Study Status
Record Verification Date
March 2020
Overall Recruitment Status
Completed
Study Start Date
November 2016 (Actual)
Primary Completion Date
May 2019 (Actual)
Study Completion Date
May 2019 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
The Hospital for Sick Children
Collaborators
Canadian Institutes of Health Research (CIHR), Children's Hospital of Eastern Ontario
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The investigators will conduct a study around the best way to monitor infants hospitalized with bronchiolitis, the most common lung infection and a leading reason for hospitalization in infants. Infants with bronchiolitis have breathing difficulties and are provided supplemental oxygen if their oxygen levels are low. However, there is uncertainty regarding how to best monitor oxygen levels. A probe placed on the hand or foot can be used to monitor oxygen levels all the time (continuous oxygen monitoring) or just every 4-6 hours (intermittent oxygen monitoring). Research has suggested that placing infants with bronchiolitis on continuous monitoring results in unnecessary use of oxygen and infants staying longer in hospital. However, due to the lack of high quality research, its unclear which strategy is best and practice varies. The objective of this study is to conduct high quality research across hospitals to determine whether intermittent compared to continuous oxygen monitoring will reduce the length of hospital stay in infants hospitalized with bronchiolitis. The investigators will also compare safety and cost. The results of this study will inform bronchiolitis practice standards and the best use of health care resources.
Detailed Description
BACKGROUND This research protocol focuses on bronchiolitis, a leading cause of infant hospitalization and cumulative expense for the health care system. Supportive management, such as oxygen supplementation and monitoring, is the major focus of care, as active medical treatment is not effective. Oxygen saturation monitoring may be performed on an intermittent (e.g. every 4-6hrs) or continuous basis for stable infants hospitalized with bronchiolitis. Observational studies find that the use of continuous monitoring is associated with overuse of supplemental oxygen and longer hospital stay. Based on this low quality evidence, practice guidelines state that clinicians may choose not to use continuous monitoring and practice variation exists due to a lack of RCTs.
SPECIFIC AIMS Primary: To determine if intermittent vs continuous oxygen saturation monitoring will reduce length of hospital stay in infants with bronchiolitis. Secondary: To determine differences in other outcomes - effectiveness, safety, acceptability, and cost.
METHODOLOGY Design: multi-centre, pragmatic, parallel group, 1:1, two arm superiority RCT. Population: Previously healthy infants (4 weeks-2 years) hospitalized with bronchiolitis who are clinically stable, will be recruited from children's and community hospitals in Ontario, Canada.
Interventions: Randomization to intermittent (every 4hrs) or continuous oxygen saturation monitoring. In keeping with local and national clinical practice guidelines, an acceptable oxygen saturation target of ≥ 90% will be used for both groups.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Bronchiolitis
Keywords
Bronchiolitis, Length of Hospital Stay, Clinical Trial, Oxygen Saturation Monitoring
7. Study Design
Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Investigator
Allocation
Randomized
Enrollment
219 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Continuous oxygen monitoring
Arm Type
Active Comparator
Arm Description
Oxygen saturation will be measured continuously through the child's hospital stay until discharge.
Arm Title
Intermittent oxygen monitoring
Arm Type
Experimental
Arm Description
Oxygen saturation will be measured intermittently, every 4 hours, through the child's hospital stay until discharge.
Intervention Type
Other
Intervention Name(s)
Intermittent oxygen monitoring
Other Intervention Name(s)
Intermittent
Intervention Description
Oxygen saturation and vital signs will be measured intermittently at a frequency of every 4 hours by the bedside nurse through the child's hospital stay until discharge. Vital signs will be completed every 4 hours.
Intervention Type
Other
Intervention Name(s)
Continuous oxygen monitoring
Other Intervention Name(s)
Continuous
Intervention Description
Oxygen saturation will be measured continuously through the child's hospital stay until discharge. Vital signs will be completed every 4 hours.
Primary Outcome Measure Information:
Title
Length of hospital stay from randomization on the inpatient unit to discharge from hospital
Time Frame
1 month
Secondary Outcome Measure Information:
Title
Duration of oxygen supplementation from randomization to discontinuation of supplementation
Time Frame
1 month
Title
Number of medical interventions performed from time of randomization to hospital discharge
Time Frame
1 month
Title
Time from randomization to meeting hospital discharge criteria
Time Frame
1 month
Title
Length of hospital stay from inpatient unit admission to hospital discharge
Time Frame
1 month
Title
Parent anxiety
Description
Parents will rate their level of anxiety at the current time (state anxiety) and generally (trait anxiety) from the adult State Trait Anxiety Inventory questionnaire during the hospital stay.
Time Frame
1 month
Title
Number of parent work days missed from randomization to 15 days after discharge
Time Frame
15 days after discharge
Title
Nursing satisfaction
Description
The attending nurse will be asked to complete a 10 mm visual analogue scale (VAS) to measure their satisfaction with the quality of monitoring.
Time Frame
1 month
Title
PICU admission after randomization
Time Frame
1 month
Title
PICU consultation after admission
Time Frame
1 month
Title
Unscheduled return to care within 15 days of discharge
Time Frame
15 days after discharge
Title
Mortality
Time Frame
15 days after discharge.
Title
Cost-Effectiveness
Description
Cost-effectiveness will be measured by the incremental cost-effectiveness ratio (ICER), a ratio defined by the incremental difference in costs between treatment arms and the incremental difference in length of stay.
Time Frame
15 days after discharge.
10. Eligibility
Sex
All
Minimum Age & Unit of Time
4 Weeks
Maximum Age & Unit of Time
24 Months
Accepts Healthy Volunteers
No
Eligibility Criteria
Children admitted to the general pediatric inpatient unit (GPIU) with bronchiolitis will be eligible if their clinical status is stable and not at high risk of deterioration
Inclusion Criteria:
Clinical diagnosis of bronchiolitis as determined by the attending physician.
First episode of acute bronchiolitis.
Age: 4 weeks to 24 months.
Clinical status stable for 6 hours
Parent consent
Exclusion Criteria:
Known risk factors for clinical deterioration including chronic medical condition; premature birth (<35weeks), history of apnea, weight < 4kg, receiving morphine
Patient on heated high flow oxygen at enrolment
ICU admission on current admission
No telephone available
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Sanjay Mahant
Organizational Affiliation
The Hospital for Sick Children
Official's Role
Principal Investigator
Facility Information:
Facility Name
McMaster Children's Hospital
City
Hamilton
State/Province
Ontario
ZIP/Postal Code
L8N 2Z5
Country
Canada
Facility Name
Trillium Health Partners (Credit Valley Site)
City
Mississauga
State/Province
Ontario
ZIP/Postal Code
L5B 1B8
Country
Canada
Facility Name
Lakeridge Health Oshawa
City
Oshawa
State/Province
Ontario
ZIP/Postal Code
L1G 2B9
Country
Canada
Facility Name
Children's Hospital of Eastern Ontario
City
Ottawa
State/Province
Ontario
ZIP/Postal Code
K1H 8L1
Country
Canada
Facility Name
North York General Hospital
City
Toronto
State/Province
Ontario
ZIP/Postal Code
M2K 1E1
Country
Canada
Facility Name
Hospital for Sick Children
City
Toronto
State/Province
Ontario
ZIP/Postal Code
M5G 1X8
Country
Canada
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
33646286
Citation
Mahant S, Wahi G, Bayliss A, Giglia L, Kanani R, Pound CM, Sakran M, Kozlowski N, Breen-Reid K, Arafeh D, Moretti ME, Agarwal A, Barrowman N, Willan AR, Schuh S, Parkin PC; Canadian Paediatric Inpatient Research Network (PIRN). Intermittent vs Continuous Pulse Oximetry in Hospitalized Infants With Stabilized Bronchiolitis: A Randomized Clinical Trial. JAMA Pediatr. 2021 May 1;175(5):466-474. doi: 10.1001/jamapediatrics.2020.6141.
Results Reference
derived
PubMed Identifier
29678995
Citation
Mahant S, Wahi G, Giglia L, Pound C, Kanani R, Bayliss A, Roy M, Sakran M, Kozlowski N, Breen-Reid K, Lavigne M, Premji L, Moretti ME, Willan AR, Schuh S, Parkin PC. Intermittent versus continuous oxygen saturation monitoring for infants hospitalised with bronchiolitis: study protocol for a pragmatic randomised controlled trial. BMJ Open. 2018 Apr 20;8(4):e022707. doi: 10.1136/bmjopen-2018-022707.
Results Reference
derived
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Oxygen Saturation Monitoring in Bronchiolitis
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