Newborn Screening Boosts India’s Fight Against Sickle Cell Disease

CURRENT AFFAIRS: Newborn Screening India 2025, Sickle Cell Disease Screening, ICMR SCD Study, Tribal Health SCD, Genetic Counselling India, Hydroxyurea Therapy, SCD Carrier Rate India, Preventive Health Newborns, Inherited Blood Disorders India

Newborn Screening Boosts India’s Fight Against Sickle Cell Disease

Newborn screening changing health outcomes

Newborn Screening Boosts India’s Fight Against Sickle Cell Disease: In recent years, India has taken serious steps to tackle sickle cell disease (SCD), especially in areas where it is most common. One major move has been screening newborns for early signs of the disorder. From 2019 to 2024, the Indian Council of Medical Research (ICMR) ran a study across seven major centres. Over 63,000 newborns were tested in tribal and high-risk regions. The results revealed that 11.4% were carriers, and 0.9% had SCD. These numbers make it clear that early detection can save lives.

Why early diagnosis matters?

Sickle cell disease is genetic, which means a child is born with it. If not caught early, it can cause severe anaemia, infections, and even strokes in children. Screening right after birth helps identify babies at risk, so doctors can act quickly. With early treatment, children have a better chance at growing up healthy. In fact, the study found that early intervention has reduced mortality from 20–30% to under 5% in some areas.

Support doesn’t stop at diagnosis

Babies who tested positive were not just identified—they received comprehensive care. Doctors provided penicillin to prevent infections, folic acid to help red blood cells, and hydroxyurea therapy to reduce disease severity. This kind of care helps the body manage the symptoms better and reduces emergency visits and hospital stays.

Empowering families with knowledge

One key part of the programme was genetic counselling. When parents understand what SCD is, they’re better prepared. Counsellors guided families about risks in future pregnancies, what symptoms to look out for, and how to manage the condition. This is especially helpful in communities where awareness is still growing.

Regional gaps in screening

The ICMR study also highlighted how SCD prevalence varies from one region to another. While some tribal areas showed high carrier rates, others had fewer cases. This kind of data helps in targeting health services more effectively. But there are still challenges, like lack of infrastructure and awareness in remote locations.

Looking forward

The success of this study is just the beginning. To make a real difference, screening needs to be expanded, especially in rural and tribal belts. With continued investment in public health, education, and access to treatment, India can significantly reduce the burden of SCD over time.

Static GK Fact: Sickle cell disease is most commonly found in tribal communities in states like Maharashtra, Odisha, Chhattisgarh, and Madhya Pradesh. The Government of India launched a National Sickle Cell Anaemia Elimination Mission in 2023 to address this issue.

Static Usthadian Current Affairs Table

Topic Detail
Study conducted by Indian Council of Medical Research (ICMR)
Study years 2019 to 2024
Number of newborns tested Over 63,000
Carrier rate found 11.4%
SCD diagnosis rate 0.9%
States with high SCD prevalence Maharashtra, Odisha, Chhattisgarh, Madhya Pradesh
Treatments provided Penicillin, folic acid, hydroxyurea
Mortality drop due to early care From 20–30% to under 5%
Launched Mission National Sickle Cell Anaemia Elimination Mission (2023)
Importance of screening Prevents severe complications in infancy
Newborn Screening Boosts India’s Fight Against Sickle Cell Disease
  1. India screened over 63,000 newborns between 2019–2024 for Sickle Cell Disease (SCD) in high-risk areas.
  2. ICMR’s multi-centre study revealed 11.4% were carriers and 0.9% had SCD.
  3. Early diagnosis of SCD helps prevent anaemia, infections, and strokes in infants.
  4. Newborn screening can reduce mortality from 30% to under 5%, as per the ICMR study.
  5. Penicillin and folic acid are provided to prevent infections and support red blood cell health.
  6. Hydroxyurea therapy is used to manage and reduce SCD complications.
  7. Genetic counselling was offered to help families understand future risks and management.
  8. SCD is a genetic disorder, meaning children inherit it from parents at birth.
  9. The National Sickle Cell Anaemia Elimination Mission was launched in 2023.
  10. High prevalence of SCD is found in tribal communities in Maharashtra, Odisha, Chhattisgarh, and MP.
  11. ICMR targeted screening in tribal and remote regions with highest disease burden.
  12. Tribal areas showed regional variation in SCD carrier rates, helping in better resource allocation.
  13. Preventive health measures included not just screening but long-term care and education.
  14. The study emphasized the importance of health infrastructure in remote areas.
  15. Genetic counselling empowered families to plan future pregnancies wisely.
  16. Lack of awareness and infrastructure still challenges universal SCD screening.
  17. Early intervention significantly reduced emergency visits and hospitalisation.
  18. Inherited blood disorders like SCD require lifetime management and awareness.
  19. India’s public health approach now focuses on prevention and early detection.
  20. Expanding newborn screening nationwide can drastically reduce India’s SCD burden over time.

Q1. Which organization conducted the large-scale newborn screening for Sickle Cell Disease in India between 2019 and 2024?


Q2. What percentage of newborns were found to be carriers of Sickle Cell Disease in the ICMR study?


Q3. Which of the following treatments is not commonly used in managing Sickle Cell Disease in newborns?


Q4. What was one key impact of early intervention for SCD-positive newborns in the study?


Q5. In which year did the Indian government launch the National Sickle Cell Anaemia Elimination Mission?


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