PT  - JOURNAL ARTICLE
AU  - Tim R. Randolph
AU  - Austin Le
AU  - Jeffrey DeMond
TI  - A Modified Sodium Metabisulfite Method to Distinguish Sickle Cell Disease from Sickle Cell Trait for Use in Underdeveloped Countries
AID  - 10.29074/ascls.119.002030
DP  - 2019 Jan 01
TA  - American Society for Clinical Laboratory Science
PG  - ascls.119.002030
4099  - http://hwmaint.clsjournal.ascls.org/content/early/2019/10/09/ascls.119.002030.short
4100  - http://hwmaint.clsjournal.ascls.org/content/early/2019/10/09/ascls.119.002030.full
AB  - The objective of this study was to develop a simple, inexpensive, and rapid confirmatory test using a sodium metabisulfite microscopic method to distinguish AS from SS genotype in patients testing positive for hemoglobin S. Equal volumes of de-identified EDTA blood and 2% sodium metabisulfite were mixed, placed on a microscope slide with coverslip, and observed for sickling at 30-minute intervals over 3 hours. Sickle cells were enumerated/200 RBCs under 100x oil immersion and placed into 4 Likert categories (1+-4+) based on degree of sickling. In AS samples, 2+ and 3+ sickle cells rose most rapidly while 4+ sickle cells showed the steepest rise in the SS samples. Based on these data the number of 4+ sickle cells were counted every 30-minutes over 3 hours in 5 AS and 28 SS samples at 37 degrees Celsius. Mean number of 4+ sickle cells in AS samples were 4.75/200 at 2 hours and 17.75/200 at 3 hours whereas SS samples yielded 78.29/200 at 2 hours and 115.43/200 at 3 hours. Two-hour incubation showed a statistical difference (P=0.00024) between groups in the shortest time and may be used to distinguish SS from AS genotypes. More testing is needed to determine cutpoints to distinguish genotype.