Prevalence of Depression among Caregivers of Indian Children with Cystic Fibrosis
Javeed Iqbal Bhat1, Wasim Ahmad Wani2, Bashir A Charoo2
1Department of Pediatrics, Sher-i-Kashmir Institute of Medical Sciences, Srinagar, Jammu and Kashmir, 190011, India. drjaveediqbal@gmail.com.
Insights
High rates of depression in caregivers of children with cystic fibrosis negatively impact child health. Parental depression is linked to increased respiratory issues and stunting in children with CF.
Area of Science:
- Pediatric Health
- Mental Health
- Chronic Illness Care
Background:
- Cystic fibrosis (CF) presents significant challenges for affected children and their families.
- Caregiver mental health is crucial for managing chronic pediatric conditions.
- Understanding caregiver depression in CF is vital for holistic patient care.
Purpose of the Study:
- To determine the prevalence of depression among caregivers of children with cystic fibrosis (CF).
- To assess the impact of caregiver depression on the health and well-being of children with CF.
Main Methods:
- A cross-sectional study involving 41 parents of children with CF at a tertiary care hospital.
- The Centre for Epidemiological Studies Depression Scale (CES-D) was used to screen for depression (cut-off score ≥16).
- Outcomes measured included child growth and respiratory exacerbations.
Main Results:
- Over half (51.4%) of caregivers scored above the clinical cut-off for depression (mean CES-D score 22.0).
- Children of depressed caregivers experienced significantly more respiratory exacerbations (3.83 vs. 2.18 episodes).
- Stunting was more prevalent in children with high caregiver depression scores (15 vs. 7).
Conclusions:
- Caregiver depression is highly prevalent in pediatric cystic fibrosis cases.
- Parental depression significantly impairs the health and well-being of children with CF.
- Lower socioeconomic and educational status were associated with higher rates of caregiver depression.
Objective:
To study the prevalence of depression among caregivers of children with cystic fibrosis and its impact on the health and well being of these children.
Methods:
This cross-sectional study was conducted in a tertiary care hospital from September 2015 through August 2016. Forty one parents of children receiving treatment at the Cystic fibrosis (CF) clinic were approached to be part of the study. Six families declined the request resulting in 85% recruitment rate. The Centre for Epidemiological Studies Depression Scale (CES-D) was used to assess depression score among caregivers. The CES-D provides clinical cut-off scores of ≥16 that help in identifying persons at risk for depression. CES-D was completed by the parent closely associated with care of the affected child. Main outcome measure was to find the number of caregivers of patients who has score of ≥16 on CES-D scale, and its effect on growth and respiratory exacerbations of the affected child.
Results:
A total of 23 fathers and 12 mothers participated in the study. The mean age of male and female caregivers was 30.9 ± 5.4 and 27.8 ± 4.7 y respectively. Eighteen (51.4%) caregivers scored above the clinical cut-off on the CES-D in the index study with mean score of 22.0 ± 4.0. The mean CES-D score among non-depressive caregivers was 7.76 ± 4.2. Significant negative association was found between parental depression and child's health. Children with high parental CES-D score suffered significantly more respiratory exacerbations (3.83 ± 1.2 episodes) in last six months than parents with low CES-D score (2.18 ± 1.28 episodes) (p value = 0.00). Similarly, stunting was more commonly seen in patients with high caregiver CES-D score (15 vs. 7; P value = 0.01).
Conclusions:
A very high prevalence of caregiver depression was found in cystic fibrosis, which negatively impacted care and well being of the affected patients. Depression was more common in families with poor economic and education level.
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