Prospective Newborn Screening for Sickle Cell Disease and Other Inherited Blood Disorders in Central Malawi.

Int J Public Health · 2021 · PMC8284589 · PMID 34335138

Europe PMC DOI

hedged sentence

0.1000

closest p · 2.0× alpha

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boldest claim

The sentences

did not reach statistical significancep = 0.1so close (0.05 < p ≤ 0.1)

The presence of SCT appeared to be inversely associated with G6PD trait in males; 22.1% (97/439) of male infants without SCT had G6PD deficiency, while 16.7% (35/209) of SCT males were G6PD deficient, however, these estimates did not reach statistical significance ( p = 0.1) ( Table 3 ).

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