Literature DB >> 29767446

Hydroxycarbamide adherence and cumulative dose associated with hospital readmission in sickle cell disease: a 6-year population-based cohort study.

Jifang Zhou1, Jin Han1,2,3, Edith A Nutescu1, Victor R Gordeuk3, Santosh L Saraf3, Gregory S Calip1,4.   

Abstract

Sickle cell disease (SCD) is a congenital haemoglobinopathy that causes frequent acute care/emergency room visits and hospital admissions for affected individuals. Evidence from population-based studies demonstrating the role of hydroxycarbamide (HC, also termed hydroxyurea) in reducing hospital readmission rates is limited. Our objective was to describe the use of HC and its association with acute care utilization and readmission rates using a large, nationally-representative US health insurance claims database over a 6-year period between 2009 and 2014. We identified 20 721 SCD-related inpatient and acute care encounters. Patients had been exposed to HC within 6 months prior to admission in 4263 (21%) of SCD-related admission events. HC use was more common among children aged 10-17 years and young adults aged 18-29 years. HC was associated with lower 30-day all-cause readmission rates in adults treated with average daily doses ≥1 g (odds ratio [OR], 0·72, 95% confidence interval [CI] 0·52-0·99) and doses of 0·5-1 g (OR, 0·73, 95% CI 0·57-0·93), compared to HC treatment with average daily doses of <0·5 g; adherence to HC with proportion of days covered of ≥0·80 was also associated with significantly lower 30-day all-cause readmission risks (OR, 0·59, 95% CI 0·41-0·84). Optimal therapeutic dosing and adherence to HC treatment significantly reduces 30-day readmissions among patients with SCD.
© 2018 John Wiley & Sons Ltd.

Entities:  

Keywords:  acute care; adherence; epidemiology; hydroxycarbamide; readmission; sickle cell disease

Mesh:

Substances:

Year:  2018        PMID: 29767446      PMCID: PMC6037608          DOI: 10.1111/bjh.15396

Source DB:  PubMed          Journal:  Br J Haematol        ISSN: 0007-1048            Impact factor:   6.998


  41 in total

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Review 2.  Sickle Cell Disease.

Authors:  Frédéric B Piel; Martin H Steinberg; David C Rees
Journal:  N Engl J Med       Date:  2017-04-20       Impact factor: 91.245

3.  Risk Factors for 30-Day Readmission in Adults with Sickle Cell Disease.

Authors:  Max A Brodsky; Mark Rodeghier; Maureen Sanger; Jeannie Byrd; Brandi McClain; Brittany Covert; Dionna O Roberts; Karina Wilkerson; Michael R DeBaun; Adetola A Kassim
Journal:  Am J Med       Date:  2017-01-05       Impact factor: 4.965

4.  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

5.  Safety of hydroxyurea in children with sickle cell anemia: results of the HUG-KIDS study, a phase I/II trial. Pediatric Hydroxyurea Group.

Authors:  T R Kinney; R W Helms; E E O'Branski; K Ohene-Frempong; W Wang; C Daeschner; E Vichinsky; R Redding-Lallinger; B Gee; O S Platt; R E Ware
Journal:  Blood       Date:  1999-09-01       Impact factor: 22.113

6.  Hydroxyurea prescription, availability and use for children with sickle cell disease in Italy: Results of a National Multicenter survey.

Authors:  Raffaella Colombatti; Giovanni Palazzi; Nicoletta Masera; Lucia Dora Notarangelo; Elisa Bonetti; Piera Samperi; Angelica Barone; Silverio Perrotta; Elena Facchini; Maurizio Miano; Giovanni Carlo Del Vecchio; Maria Elena Guerzoni; Paola Corti; Federica Menzato; Simone Cesaro; Maddalena Casale; Paolo Rigano; Gian Luca Forni; Giovanna Russo; Laura Sainati
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7.  An empirical basis for standardizing adherence measures derived from administrative claims data among diabetic patients.

Authors:  Sudeep Karve; Mario A Cleves; Mark Helm; Teresa J Hudson; Donna S West; Bradley C Martin
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8.  Risk factors for hospital readmission within 30 days: a new quality measure for children with sickle cell disease.

Authors:  Melissa J Frei-Jones; Joshua J Field; Michael R DeBaun
Journal:  Pediatr Blood Cancer       Date:  2009-04       Impact factor: 3.167

9.  Hydroxyurea for treatment of severe sickle cell anemia: a pediatric clinical trial.

Authors:  A Ferster; C Vermylen; G Cornu; M Buyse; F Corazza; C Devalck; P Fondu; M Toppet; E Sariban
Journal:  Blood       Date:  1996-09-15       Impact factor: 22.113

10.  Clinical and hematologic effects of hydroxyurea in children with sickle cell anemia.

Authors:  S Jayabose; O Tugal; C Sandoval; P Patel; D Puder; T Lin; P Visintainer
Journal:  J Pediatr       Date:  1996-10       Impact factor: 4.406

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  6 in total

1.  Patient-Reported Outcomes and Economic Burden of Adults with Sickle Cell Disease in the United States: A Systematic Review.

Authors:  Soyon Lee; Diana K Vania; Menaka Bhor; Dennis Revicki; Seye Abogunrin; Grammati Sarri
Journal:  Int J Gen Med       Date:  2020-07-07

2.  Increased acute care utilization in a prospective cohort of adults with sickle cell disease.

Authors:  Sophie Lanzkron; Jane Little; Joshua Field; Joseph Ryan Shows; Hang Wang; Rebecca Seufert; Jasmine Brooks; Ravi Varadhan; Carlton Haywood; Mustapha Saheed; Chiung Yu Huang; Brandi Griffin; Steven Frymark; Allie Piehet; Derek Robertson; Marc Proudford; Adrienne Kincaid; Charles Green; Lorri Burgess; Marcus Wallace; Jodi Segal
Journal:  Blood Adv       Date:  2018-09-25

3.  A Multidimensional Electronic Hydroxyurea Adherence Intervention for Children With Sickle Cell Disease: Single-Arm Before-After Study.

Authors:  Susan Creary; Deena Chisolm; Joseph Stanek; Jane Hankins; Sarah H O'Brien
Journal:  JMIR Mhealth Uhealth       Date:  2019-08-08       Impact factor: 4.773

4.  Medical and Non-medical Costs of Sickle Cell Disease and Treatments from a US Perspective: A Systematic Review and Landscape Analysis.

Authors:  Zachary Baldwin; Boshen Jiao; Anirban Basu; Joshua Roth; M A Bender; Zizi Elsisi; Kate M Johnson; Emma Cousin; Scott D Ramsey; Beth Devine
Journal:  Pharmacoecon Open       Date:  2022-04-26

Review 5.  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

6.  Beta2-Adrenergic Receptor Polymorphisms and Haplotypes Associate With Chronic Pain in Sickle Cell Disease.

Authors:  Ellie H Jhun; Nilanjana Sadhu; Xiaoyu Hu; Yingwei Yao; Ying He; Diana J Wilkie; Robert E Molokie; Zaijie Jim Wang
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  6 in total

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