Literature DB >> 31227564

Hydroxyurea Use for Sickle Cell Disease Among Medicaid-Enrolled Children.

David C Brousseau1, Troy Richardson2, Matt Hall2, Angela M Ellison3, Samir S Shah4, Jean L Raphael5, David G Bundy6, Staci Arnold7.   

Abstract

BACKGROUND: Recent publications should have resulted in increased hydroxyurea usage in children with sickle cell disease (SCD). We hypothesized that hydroxyurea use in children with SCD increased over time and was associated with decreased acute care visits.
METHODS: This was a secondary analysis of the Truven Health Analytics-IBM Watson Health MarketScan Medicaid database from 2009 to 2015. The multistate, population-based cohort included children 1 to 19 years old with an International Classification of Diseases, Ninth or 10th Revision diagnosis of SCD between 2009 and 2015. Changes in hydroxyurea were measured across study years. The primary outcome was the receipt of hydroxyurea, identified through filled prescription claims. Acute care visits (emergency department visits and hospitalizations) were extracted from billing data.
RESULTS: A mean of 5138 children each year were included. Hydroxyurea use increased from 14.3% in 2009 to 28.2% in 2015 (P < .001). During the study period, the acute-care-visit rate decreased from 1.20 acute care visits per person-year in 2009 to 1.04 acute care visits per person-year in 2015 (P < .001); however, the drop in acute care visits was exclusively in the youngest and oldest age groups and was not seen when only children enrolled continuously from 2009 to 2015 were analyzed.
CONCLUSIONS: There was a significant increase in hydroxyurea use in children with SCD between 2009 and 2015. However, in 2015, only ∼1 in 4 children with SCD received hydroxyurea at least once. Increases in hydroxyurea were not associated with consistently decreased acute care visits in this population-based study of children insured by Medicaid.
Copyright © 2019 by the American Academy of Pediatrics.

Entities:  

Mesh:

Substances:

Year:  2019        PMID: 31227564     DOI: 10.1542/peds.2018-3285

Source DB:  PubMed          Journal:  Pediatrics        ISSN: 0031-4005            Impact factor:   7.124


  13 in total

Review 1.  Revisiting fetal hemoglobin inducers in beta-hemoglobinopathies: a review of natural products, conventional and combinatorial therapies.

Authors:  Mandrita Mukherjee; Motiur Rahaman; Suman Kumar Ray; Praphulla Chandra Shukla; Tuphan Kanti Dolai; Nishant Chakravorty
Journal:  Mol Biol Rep       Date:  2021-11-25       Impact factor: 2.316

Review 2.  Considerations for the future: current and future treatment paradigms with mineralocorticoid receptor antagonists-unmet needs and underserved patient cohorts.

Authors:  Murray Epstein
Journal:  Kidney Int Suppl (2011)       Date:  2022-03-18

3.  Impact of hydroxyurea dose and adherence on hematologic outcomes for children with sickle cell anemia.

Authors:  Susan E Creary; Chase Beeman; Joseph Stanek; Kathryn King; Patrick T McGann; Sarah H O'Brien; Robert I Liem; Jane Holl; Sherif M Badawy
Journal:  Pediatr Blood Cancer       Date:  2022-04-04       Impact factor: 3.838

Review 4.  Changing the Clinical Paradigm of Hydroxyurea Treatment for Sickle Cell Anemia Through Precision Medicine.

Authors:  Min Dong; Patrick T McGann
Journal:  Clin Pharmacol Ther       Date:  2020-10-08       Impact factor: 6.875

5.  Impact of Medicaid expansion on access and healthcare among individuals with sickle cell disease.

Authors:  Mariam Kayle; Jhaqueline Valle; Susan Paulukonis; Jane L Holl; Paula Tanabe; Dustin D French; Ravi Garg; Robert I Liem; Sherif M Badawy; Marsha J Treadwell
Journal:  Pediatr Blood Cancer       Date:  2020-03-08       Impact factor: 3.167

6.  Opioid Prescription Filling Trends Among Children with Sickle Cell Disease After the Release of State-Issued Guidelines on Pain Management.

Authors:  Susan E Creary; Deena J Chisolm; Sharon K Wrona; Jennifer N Cooper
Journal:  Pain Med       Date:  2020-10-01       Impact factor: 3.750

7.  HABIT efficacy and sustainability trial, a multi-center randomized controlled trial to improve hydroxyurea adherence in youth with sickle cell disease: a study protocol.

Authors:  Arlene Smaldone; Deepa Manwani; Banu Aygun; Kim Smith-Whitley; Haomiao Jia; Jean-Marie Bruzzese; Sally Findley; Joshua Massei; Nancy S Green
Journal:  BMC Pediatr       Date:  2019-10-15       Impact factor: 2.567

8.  GSTM1 and Liver Iron Content in Children with Sickle Cell Anemia and Iron Overload.

Authors:  Latika Puri; Jonathan M Flanagan; Guolian Kang; Juan Ding; Wenjian Bi; Beth M McCarville; Ralf B Loeffler; Aaryani Tipirneni-Sajja; Martha Villavicencio; Kristine R Crews; Claudia M Hillenbrand; Jane S Hankins
Journal:  J Clin Med       Date:  2019-11-05       Impact factor: 4.241

Review 9.  Administrative data identify sickle cell disease: A critical review of approaches in U.S. health services research.

Authors:  Scott D Grosse; Nancy S Green; Sarah L Reeves
Journal:  Pediatr Blood Cancer       Date:  2020-09-17       Impact factor: 3.838

10.  Hydroxyurea Optimization through Precision Study (HOPS): study protocol for a randomized, multicenter trial in children with sickle cell anemia.

Authors:  Emily R Meier; Susan E Creary; Matthew M Heeney; Min Dong; Abena O Appiah-Kubi; Stephen C Nelson; Omar Niss; Connie Piccone; Maa-Ohui Quarmyne; Charles T Quinn; Kay L Saving; John P Scott; Ravi Talati; Teresa S Latham; Amanda Pfeiffer; Lisa M Shook; Alexander A Vinks; Adam Lane; Patrick T McGann
Journal:  Trials       Date:  2020-11-27       Impact factor: 2.279

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.