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A social profile of deaths related to sickle cell disease in India

A case for an ethical policy response

Bibliographic Data

ID22071806
AuthorsSangeeta Chattoo (0000-0002-7689-9716, University of York, corresponding author), Dipty Jain (0000-0002-8628-4977, Council of Scientific and Industrial Research), Nidhi Nashine (Indira Gandhi Government Medical College & Hospital), Rajiv K Singh (0000-0002-7951-202X), Rajan Singh
Year2023
Volume11
Pages1265313-1265313
Publication date2023-12-21
Peer ReviewedYes
Open AccessYes
TypeARTICLE
VenueFrontiers in Public Health (JOURNAL)
Journal identifiersISSN: 2296-2565 • E-ISSN: 2296-2565
PublisherFrontiers Media SA (PUBLISHER • CH)
DOI10.3389/fpubh.2023.1265313
PMID38179555
OpenAlexW4390057281
LanguageEN
Citations received2
References cited31

India accounts for 14.5 percent of the global SCD newborns, roughly over 42,000 a year, second to sub-Saharan Africa. Despite the availability of cheap diagnostic and treatment options, SCD remains a largely neglected disease within healthcare policy and practice. Epidemiological modeling based on small, often dated, regional studies (largely from sub-Saharan Africa) estimate that between 50 and 90 percent of affected children will/die before the age of 5 years. This premise, coupled with targets of reducing under 5 mortality (SDG 4), privileges public health interventions for screening and prevention of new births, undermining investments in long-term health and social care. This paper presents a retrospective, descriptive analysis of the socio-demographic profile of 447 patients diagnosed with sickle cell or sickle-beta thalassemia, who died following admission at a tertiary care entre in India. We used anonymized hospital records of 3,778 sickle cell patients, admitted in pediatric and adult/medical wards between January 2016 and February 2021. A majority of hospital deaths occurred in the second and third decades of life, following a hospital admission for a week. The overall mortality during 2016–2019 was 14% with little gender difference over time. Contrary to our expectations, the number of hospital deaths did not increase during the first year of the COVID-19 pandemic, between 2020 and 2021. The conclusion highlights the importance of longitudinal, socio-demo-graphic data on deaths as providing important insights for identifying ethical policy interventions focused on improving SCD outcomes over time, reducing inequities in access to care, and preventing what might be considered “excess” deaths

Disease · Disease burden · Family medicine · Health care · Pandemic · Psychological intervention · Public health · Demography · Global Maternal and Child Health · Hemoglobinopathies and Related Disorders · Iron Metabolism and Disorders · Medicine · Nursing · Epidemiology · Pediatrics

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Unique citing works2
Citations per year1
Citation span2024 - 2025 (2)
Citation velocityrecent
Highly citedNo
Citation typesNeutral: 2

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