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Updated: Jun 13, 2025

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Depression and Its Determinants Among Patients With Sickle Cell Disease: A Cross-Sectional Study
Bhuwan Dahit1, Madhusudan Subedi1, Ajay Kumar Rajbhandari1
1Patan Academy of Health Sciences Lalitpur Nepal.
Depression affects over a third of sickle cell disease (SCD) patients, with age and complications being key risk factors. Early diagnosis and treatment are crucial for this vulnerable population.
Area of Science:
- Medical Research
- Hematology
- Psychiatry
Background:
- Depression is a significant concern in sickle cell disease (SCD) patients, often overlooked and inadequately treated.
- Underdiagnosis and undertreatment of depression in SCD can lead to adverse health outcomes.
Purpose of the Study:
- To determine the prevalence of depression among individuals with SCD.
- To identify sociodemographic, clinical, and psychological factors associated with depression in SCD patients.
Main Methods:
- A cross-sectional study was conducted in Nepal involving 358 SCD patients aged over 13.
- Depression was assessed using the Beck Depression Inventory (BDI).
- Logistic regression analysis was employed to identify determinants of depression.
Main Results:
- The prevalence of depression was 36.31% in the studied SCD population.
- Age (40-49 years), SCD complications, and genetic counseling were associated with increased depression risk.
- Lower middle-class status, pain crises, moderate self-esteem, and discrimination were linked to decreased depression likelihood.
Conclusions:
- Depression is highly prevalent in patients with SCD.
- Sociodemographic, clinical, and psychological factors significantly influence depression in SCD.
- There is an urgent need for early screening and intervention for depression in SCD patients.
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