2021
DOI: 10.1039/d0lc01235a
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Emerging point-of-care technologies for anemia detection

Abstract: Anemia, characterized by low blood hemoglobin level, affects about 25% of the world's population with the heaviest burden borne by women and children. Anemia leads to impaired cognitive development in...

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Cited by 30 publications
(20 citation statements)
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“…In SCD, sickle RBCs are vulnerable to shear flow stress and hemolysis, which triggers release of microvesicles and cell-free hemoglobin. [79][80][81] We postulate that hemolysis leads to a decreased surface-to-volume ratio and disrupted cytoskeletal network in RBCs in SCD, which translates to observed enhanced microcapillary occlusion. In addition, in sickle RBCs, BCAM/Lu binds to the LN alpha 5 chain.…”
Section: Discussionmentioning
confidence: 99%
“…In SCD, sickle RBCs are vulnerable to shear flow stress and hemolysis, which triggers release of microvesicles and cell-free hemoglobin. [79][80][81] We postulate that hemolysis leads to a decreased surface-to-volume ratio and disrupted cytoskeletal network in RBCs in SCD, which translates to observed enhanced microcapillary occlusion. In addition, in sickle RBCs, BCAM/Lu binds to the LN alpha 5 chain.…”
Section: Discussionmentioning
confidence: 99%
“…An approach that may offer a compromise to advocates of PBM and those of limited testing is to use of point-of-care hemoglobin screening with formal laboratory testing only in those who screen as anemic [38]. There are a number of minimally invasive and non-invasive devices that could perform this in a cost-effective fashion [39]. Future research could look at the impact of a more broad perioperative anemia screening program in all surgical patients.…”
Section: Discussionmentioning
confidence: 99%
“…Nearly 7% of the people in the world carry hemoglobin gene variants. Most prevalent hemoglobin variants are the recessive β-globin gene mutations, βS or S, βC or C, and βE or E 2,3 .Genetic disorders, such as SCD, are among the major causes for anemia [4][5][6][7] .…”
Section: Sickle Cell Diseasementioning
confidence: 99%