CareBEST
Low-value care, and variation in practice for children hospitalized with bronchiolitis – a multicentric prospective observational study
Participating Sites and National Principal Investigator
Dr. Olivier Drouin
Quebec
CHU Sainte-Justine (Montreal)
Dr. Olivier Drouin
Montreal Children’s Hospital (Montreal)
Dr. Patricia Li & Dr. Evelyn Constantin
CHU de Quebec l‘Universite de Laval (Quebec City)
Dr. Josée Anne Gagnon
Hôpital Maisonneuve-Rosemont (Montreal)
Dr. Marc-André Turcot
Centre hospitalier Cité-de-la-Santé (Laval)
Dr. Camille Bédard
British Columbia
BC Children’s Hospital (Vancouver)
Dr. Matthew Carwana
Nova Scotia
IWK Health Centre (Halifax)
Drs. Sarah Manos & Kristina Krmpotic
Ontario
McMaster Children’s Hospital (Hamilton)
Dr. Gita Wahi
Children's Hospital London Health Sciences Centre (London)
Dr. Breanna Chen
The Hospital for Sick Children (Toronto)
Drs. Peter Gill & Sanjay Mahant
Children’s Hospital of Eastern Ontario (Ottawa)
Drs. Melanie Buba & Maria Karaceper
Kingston Health Sciences Centre (Kingston)
Dr. Anupam Seghal
Lakeridge Health (Oshawa)
Dr. Mahmoud Sakran
Alberta
Alberta Children’s Hospital (Calgary)
Dr. Michelle Bailey
Stollery Children’s Hospital (Edmonton)
Dr. Karen Forbes
What Do We Want To Know?
Low-value care is defined as the use of a health service, such as treatments and investigations, for which the harms or costs outweigh the benefits. We are studying the use of 6 low-value healthcare services in children aged 1 to 12 months hospitalized with bronchiolitis to better understand the use of low-value care, and how this differs between different patients, doctors, and hospitals.
The treatments of interest are:
respiratory virus testing
chest x-rays
continuous pulse oximetry
short-acting beta-agonists
systemic corticosteroids
antibiotics
Our questions are:
How frequently used are the 6-low value care services?
How much variability is there in the use of low-value care services between different patients, doctors, and hospitals?
How do family characteristics (like race and ethnicity, socioeconomic status, language) contribute to differences and disparities in bronchiolitis care?
How Are We Doing It?
We are collecting data from medical charts on the care and treatments patients received while admitted for bronchiolitis. We are also collecting questionnaire data from parents to know more about the family’s characteristics, their perspectives and experiences with the care received for bronchiolitis, and a follow-up questionnaire that will help us know if additional visits to the hospital happened in the 30 days after a child’s discharge.
How Can I Participate?
We are recruiting parents of children aged 1 to 12 months old and hospitalized with bronchiolitis in 15 hospitals across Canada.
If you are approached for the study, you will be asked to complete questionnaires while you are at the hospital with your child. You will be recontacted by phone or email 30-days after your child is discharged to complete the follow-up questionnaire. Both questionnaires should not take longer than 5-10 minutes.
How Is The Project Going?
We are currently wrapping up participant recruitment across sites, and confirming our next step: either continuing recruitment in some sites to reach our original targets, or supplementing recruitment with retrospective data collection.