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. 2025 Apr;92(4):405-408.
doi: 10.1007/s12098-024-05392-8. Epub 2025 Jan 4.

Unveiling the Burden of Sickle Cell Anemia: A Pilot Study Validating Dried Blood Spots for Newborn Screening

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Unveiling the Burden of Sickle Cell Anemia: A Pilot Study Validating Dried Blood Spots for Newborn Screening

Madhu Latha Karra et al. Indian J Pediatr. 2025 Apr.

Abstract

This hospital-based cross-sectional study aimed to screen newborns for sickle cell anemia immediately after birth and validate dried blood spot (DBS) samples against conventional venous blood samples (CBS) for hemoglobin variant analysis by HPLC. Among 751 newborns, 2.93% were found to have sickle cell trait. Hemoglobin variants were analyzed in both DBS and CBS samples, showing good agreement with 100% sensitivity and 100% specificity. Passing Bablok regression indicated minimal proportional bias, while Bland-Altman analysis showed a bias of 0.67, but the line of equality within the 95% CI of the bias indicated acceptable minimal systematic bias. The concordance correlation coefficient was 0.91 (p < 0.0001), Pearson's ρ (precision measure) was 0.967, and Cohen's kappa statistics gave a weighted kappa of 0.93, confirming no significant differences between the two methods. This study supports DBS as a reliable method for universal neonatal screening for sickle cell disease, demonstrating its potential for widespread clinical use.

Keywords: Anemia; Dried blood spots; HbS; Method comparison; Method validation; Newborn screening; Sickle cell disease; Sickle cell trait.

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Conflict of interest statement

Declarations. Conflict of Interest: None.

References

    1. Piel FB, Hay SI, Gupta S, Weatherall DJ, Williams TN. Global burden of sickle cell anaemia in children under five, 2010–2050: modelling based on demographics, excess mortality, and interventions. PLoS Med. 2013;10:e1001484. - DOI - PubMed - PMC
    1. Robitaille N, Delvin EE, Hume HA. Newborn screening for sickle cell disease: a 1988–2003 Quebec experience. Paediatr Child Health. 2006;11:223–7. - DOI - PubMed - PMC
    1. Colah RB, Mehta P, Mukherjee MB. Newborn screening for sickle cell disease: Indian experience. Int J Neonatal Screen. 2018;4:31. - DOI - PubMed - PMC
    1. Hockham C, Bhatt S, Colah R, et al. The spatial epidemiology of sickle-cell anemia in India. Sci Rep. 2018;8:17685. - DOI - PubMed - PMC
    1. Mookken T. Universal implementation of newborn screening in India. Int J Neonatal Screen. 2020;6:24. - DOI - PubMed - PMC

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