Sickle Cell Disease-Related Stigma: Quantitative Assessment From India
| dc.contributor.author | Parikipandla, Sridevi et al.. | |
| dc.date.accessioned | 2025-10-17T10:45:10Z | |
| dc.date.available | 2025-10-17T10:45:10Z | |
| dc.date.issued | 2025 | |
| dc.description.abstract | This multisite cross-sectional study quantitatively assessed stigma related to sickle cell disease (SCD) in India using the Indian Council of Medical Research-SCD Stigma Scale for India among 208 adult patients and 184 caregivers. Approximately 27% of patients and 41% of caregivers reported severe or very severe stigma. ‘Familial & reproductive’, ‘illness burden’ and ‘perceived blame & social judgement’ stigma domains contributed significantly. Ordinal logistic regression analysis identified pain episodes in patients (AOR = 1.199, p = 0.013) and caregiver gender (AOR = 0.300, p = 0.016) and income (AOR = 0.999, p = 0.048) as significant factors associated with stigma severity. The findings underscore a substantial psychosocial burden and highlight the need for culturally grounded, multilevel interventions integrated into SCD care programs to address stigma comprehensively. | |
| dc.identifier.citation | Babu, B. V., Sharma, Y., Sridevi, P., Surti, S. B., Bal, M., Bhat, D., Sarmah, J., Ranjit, M., & Jena, R. K. (2025). Sickle cell disease-related stigma: Quantitative assessment from India. Pediatric Blood Cancer, Advance online publication. https://doi.org/10.1002/pbc.32116 | |
| dc.identifier.uri | http://ctuap.ndl.gov.in/handle/123456789/108 | |
| dc.language.iso | en | |
| dc.title | Sickle Cell Disease-Related Stigma: Quantitative Assessment From India | |
| dc.type | Article |
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