Join us on Saturday June 29, 2019 at the Yarmouth Dooleys for the Annual Cystic Fibrosis Canada Fundraiser!
Tickets can be purchased at the door for $15.
The day will feature a musical performance by Cameron Nickerson, Craig Goodwin, Sounds of Colour and Shannon Malone and Curt Leblanc.
New International Guidelines on Mental Health in CF
Cystic Fibrosis Canada’s Virtual Education Program for Patients and Caregivers
Depression and Anxiety in CF with Dr. Alexandra Quittner
On May 5, 2015, Cystic Fibrosis Canada hosted its second educational webinar in our Virtual Education Program for Patients and Caregivers. Dr. Alexandra Quittner provided an overview of mental health in CF and the recently developed guidelines for screening for mental health issues in North America and Europe. Dr. Quittner earned her Ph.D. in Clinical Psychology from the University of Western Ontario and is currently Professor of Psychology and Pediatrics at the University of Miami.
In her presentation, Dr. Quittner focused on the results of The International Depression/Anxiety Epidemiological Study (TIDES) and the new international guidelines on mental health in CF that were developed as a result. The 9-year study included sites in the U.S. and 8 European countries and, with 6,088 CF patients and 4,102 parents screened, was the largest study of its kind conducted for a chronic illness. The aim was to determine the extent to which CF patients and parent caregivers experience symptoms of depression and anxiety. The team discovered that both patients and parents experienced higher levels of depression and anxiety than the general population, and when a parent was depressed or anxious, their teen was also more likely to be depressed or anxious.
Based on this data, a large, international committee co-chaired by Dr. Quittner, has developed international guidelines on mental health in CF. Among their recommendations, the committee suggests annual screening and ongoing education for all CF patients beginning at age 12 and also recommends offering screening to parents of children with CF from the time of the child’s birth to 17 years of age.
To learn more, please watch Dr. Quittner’s full presentation here.