Literature DB >> 30900800

Hydroxyurea use among children with sickle cell anemia.

Sarah L Reeves1,2, Hannah K Jary1, Jennifer P Gondhi1, Jean L Raphael3, Lynda D Lisabeth2,4, Kevin J Dombkowski1.   

Abstract

This study describes hydroxyurea use among children ages 1 to 17 with sickle cell anemia (SCA) enrolled in at least one year of Medicaid in six states from 2005 to 2012. Administrative claims were used to summarize the number of days' supply of hydroxyurea dispensed by state and year. A total of 7963 children with SCA contributed 22 424 person-years. Among person-years with greater than 30 days of hydroxyurea, only 18% received at least 300 days of hydroxyurea, which varied by state. Following updated recommendations for all children with SCA to be offered hydroxyurea, strategies to increase hydroxyurea adherence among this population are needed.
© 2019 Wiley Periodicals, Inc.

Entities:  

Keywords:  Medicaid; administrative claims; hydroxyurea; sickle cell anemia

Mesh:

Substances:

Year:  2019        PMID: 30900800      PMCID: PMC6529195          DOI: 10.1002/pbc.27721

Source DB:  PubMed          Journal:  Pediatr Blood Cancer        ISSN: 1545-5009            Impact factor:   3.167


  11 in total

1.  Monitoring toxicity, impact, and adherence of hydroxyurea in children with sickle cell disease.

Authors:  Amanda M Brandow; Julie A Panepinto
Journal:  Am J Hematol       Date:  2011-08-03       Impact factor: 10.047

2.  Adherence to hydroxyurea therapy in children with sickle cell anemia.

Authors:  Courtney D Thornburg; Agustin Calatroni; Marilyn Telen; Alex R Kemper
Journal:  J Pediatr       Date:  2009-11-01       Impact factor: 4.406

3.  An analysis of inpatient pediatric sickle cell disease: Incidence, costs, and outcomes.

Authors:  Laura M Bou-Maroun; Fabien Meta; Curtis J Hanba; Andrew D Campbell; Gregory A Yanik
Journal:  Pediatr Blood Cancer       Date:  2017-08-12       Impact factor: 3.167

Review 4.  Medication adherence among pediatric patients with sickle cell disease: a systematic review.

Authors:  Kathleen E Walsh; Sarah L Cutrona; Patricia L Kavanagh; Lori E Crosby; Chris Malone; Katie Lobner; David G Bundy
Journal:  Pediatrics       Date:  2014-11-17       Impact factor: 7.124

5.  Pain Management for Sickle Cell Disease in the Pediatric Emergency Department: Medications and Hospitalization Trends.

Authors:  Chantel Cacciotti; Sarah Vaiselbuh; Eleny Romanos-Sirakis
Journal:  Clin Pediatr (Phila)       Date:  2016-10-23       Impact factor: 1.168

Review 6.  Hydroxyurea for sickle cell anemia: what have we learned and what questions still remain?

Authors:  Patrick T McGann; Russell E Ware
Journal:  Curr Opin Hematol       Date:  2011-05       Impact factor: 3.284

7.  Prevalence and treatment of depression in children and adolescents with sickle cell disease: a retrospective cohort study.

Authors:  Jeanette M Jerrell; Avnish Tripathi; Roger S McIntyre
Journal:  Prim Care Companion CNS Disord       Date:  2011

8.  Hydroxyurea adherence and associated outcomes among Medicaid enrollees with sickle cell disease.

Authors:  Sean D Candrilli; Sarah H O'Brien; Russell E Ware; Milap C Nahata; Eric E Seiber; Rajesh Balkrishnan
Journal:  Am J Hematol       Date:  2011-02-15       Impact factor: 10.047

9.  Pneumococcal vaccination coverage among children with sickle cell anemia, sickle cell trait, and normal hemoglobin.

Authors:  Sarah L Reeves; Hannah K Jary; Jennifer P Gondhi; Mary Kleyn; Abram L Wagner; Kevin J Dombkowski
Journal:  Pediatr Blood Cancer       Date:  2018-06-15       Impact factor: 3.167

10.  Impact of hydroxyurea on clinical events in the BABY HUG trial.

Authors:  Courtney D Thornburg; Beatrice A Files; Zhaoyu Luo; Scott T Miller; Ram Kalpatthi; Rathi Iyer; Phillip Seaman; Jeffrey Lebensburger; Ofelia Alvarez; Bruce Thompson; Russell E Ware; Winfred C Wang
Journal:  Blood       Date:  2012-08-22       Impact factor: 22.113

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  4 in total

1.  Pediatric Orphan Drug Indications: 2010-2018.

Authors:  Lauren Kimmel; Rena M Conti; Anna Volerman; Kao-Ping Chua
Journal:  Pediatrics       Date:  2020-03-03       Impact factor: 7.124

2.  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

3.  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

4.  Improving Preventive Care for Children With Sickle Cell Anemia: A Quality Improvement Initiative.

Authors:  Michael D Cabana; Anne Marsh; Marsha J Treadwell; Peggy Stemmler; Michael Rowland; M A Bender; Neha Bhasin; Jong H Chung; Kathryn Hassell; N F Nik Abdul Rashid; Trisha E Wong; Naomi S Bardach
Journal:  Pediatr Qual Saf       Date:  2020-12-28
  4 in total

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