Literature DB >> 27571128

Discontinuation of Folic Acid Supplementation in Young Patients With Sickle Cell Anemia.

Giang-Kim T Nguyen1, Angela Lewis, Carol Goldener, Brenda Reed, Robin Yates Dulman, Elizabeth Yang.   

Abstract

Folic acid (FA) is commonly prescribed for patients with sickle cell anemia, but evidence for the efficacy of this practice is lacking. We stopped FA supplementation and measured red blood cell folate levels after discontinuation of FA in 72 patients with clinically severe forms of sickle cell disease. We compared hemoglobin and reticulocyte counts before and after FA discontinuation in 51 of those patients, the majority of whom were on hydroxyurea. No patients had red blood cell folate levels below normal and no significant difference in hemoglobin levels (P=0.18) or reticulocyte counts (P=0.37) was found before and after FA discontinuation.

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Year:  2017        PMID: 27571128     DOI: 10.1097/MPH.0000000000000675

Source DB:  PubMed          Journal:  J Pediatr Hematol Oncol        ISSN: 1077-4114            Impact factor:   1.289


  2 in total

1.  Folic acid supplementation in children with sickle cell disease: study protocol for a double-blind randomized cross-over trial.

Authors:  Brock A Williams; Heather McCartney; Erin Adams; Angela M Devlin; Joel Singer; Suzanne Vercauteren; John K Wu; Crystal D Karakochuk
Journal:  Trials       Date:  2020-06-29       Impact factor: 2.279

2.  The relation between regular outpatient follow-up and frequency of emergency department visits in sickle cell pediatric patients.

Authors:  Abeer F Ismail; Raghad A Tarawah; Zainab Y Azzouni; Lojain T Alharbi; Raghad M Altayyar
Journal:  Saudi Med J       Date:  2020-12       Impact factor: 1.484

  2 in total

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