Literature DB >> 19880135

Adherence to hydroxyurea therapy in children with sickle cell anemia.

Courtney D Thornburg1, Agustin Calatroni, Marilyn Telen, Alex R Kemper.   

Abstract

OBJECTIVES: To assess adherence to hydroxyurea therapy in children with sickle cell anemia (SCA), evaluate the association between adherence and hematologic profile, and identify barriers and facilitators of adherence. STUDY
DESIGN: Children with SCA (n=75) receiving hydroxyurea were recruited for a single-institution cross-sectional study. The primary outcome was association between treatment adherence and percent fetal hemoglobin (HbF).
RESULTS: Good adherence was estimated at 82% with visual analog scale, 84% with Morisky score, 85% with medical provider report, 77% with clinic visits, and 49% on the basis of pharmacy refills. Increase in HbF was moderately associated with good adherence as measured with the parent/proxy Morisky score (r=-0.39; 95% CI, -0.58-0.17; P < .01) and prescription refills (r=0.39; 95% CI, 0.16-0.57; P < .01). The number of pharmacy refills and the Morisky score explained 23% of the variation in HbF response.
CONCLUSIONS: Adherence was > or =75% with 4 of 5 measures. Pharmacy refills and the Modified Morisky Scale may be used to identify children at high risk for poor response because of non-adherence and children with good adherence with poor response because of individual pharmacodynamics. Future research should prospectively compare adherence measures and evaluate methods to improve treatment adherence. Copyright 2010 Mosby, Inc. All rights reserved.

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Year:  2009        PMID: 19880135      PMCID: PMC3901082          DOI: 10.1016/j.jpeds.2009.09.044

Source DB:  PubMed          Journal:  J Pediatr        ISSN: 0022-3476            Impact factor:   4.406


  22 in total

1.  Parental health beliefs and compliance with prophylactic penicillin administration in children with sickle cell disease.

Authors:  V Elliott; S Morgan; S Day; L S Mollerup; W Wang
Journal:  J Pediatr Hematol Oncol       Date:  2001-02       Impact factor: 1.289

2.  Structured telephone-based outreach using nonmedical personnel can improve adherence to comprehensive care in families of children with sickle cell disease.

Authors:  M Patik; L Phillips; B Kladny; A Captain; E Gettig; L Krishnamurti
Journal:  Am J Hematol       Date:  2006-06       Impact factor: 10.047

3.  Hydroxyurea in children with sickle cell disease: impact on splenic function and compliance with therapy.

Authors:  N F Olivieri; E P Vichinsky
Journal:  J Pediatr Hematol Oncol       Date:  1998 Jan-Feb       Impact factor: 1.289

4.  Long-term hydroxyurea therapy for infants with sickle cell anemia: the HUSOFT extension study.

Authors:  Jane S Hankins; Russell E Ware; Zora R Rogers; Lynn W Wynn; Peter A Lane; J Paul Scott; Winfred C Wang
Journal:  Blood       Date:  2005-10-01       Impact factor: 22.113

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

Review 6.  Hydroxyurea for children with sickle cell disease.

Authors:  Matthew M Heeney; Russell E Ware
Journal:  Pediatr Clin North Am       Date:  2008-04       Impact factor: 3.278

7.  Patient compliance and the conduct and interpretation of therapeutic trials.

Authors:  R B Haynes; R Dantes
Journal:  Control Clin Trials       Date:  1987-03

8.  Chemical and functional analysis of hydroxyurea oral solutions.

Authors:  Matthew M Heeney; Matthew R Whorton; Thad A Howard; Christina A Johnson; Russell E Ware
Journal:  J Pediatr Hematol Oncol       Date:  2004-03       Impact factor: 1.289

9.  A pilot study of hydroxyurea to prevent chronic organ damage in young children with sickle cell anemia.

Authors:  Courtney D Thornburg; Natalia Dixon; Shelly Burgett; Nicole A Mortier; William H Schultz; Sherri A Zimmerman; Melanie Bonner; Kristina K Hardy; Agustin Calatroni; Russell E Ware
Journal:  Pediatr Blood Cancer       Date:  2009-05       Impact factor: 3.167

10.  Hydroxyurea therapy lowers transcranial Doppler flow velocities in children with sickle cell anemia.

Authors:  Sherri A Zimmerman; William H Schultz; Shelly Burgett; Nicole A Mortier; Russell E Ware
Journal:  Blood       Date:  2007-04-11       Impact factor: 22.113

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  53 in total

1.  Effect of communication style and physician-family relationships on satisfaction with pediatric chronic disease care.

Authors:  Matthew P Swedlund; Jayna B Schumacher; Henry N Young; Elizabeth D Cox
Journal:  Health Commun       Date:  2011-11-11

2.  Feasibility of web-based technology to assess adherence to clinic appointments in youth with sickle cell disease.

Authors:  Avani C Modi; Lori E Crosby; Janelle Hines; Dennis Drotar; Monica J Mitchell
Journal:  J Pediatr Hematol Oncol       Date:  2012-04       Impact factor: 1.289

3.  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

4.  Do difficulties in swallowing medication impede the use of hydroxyurea in children?

Authors:  ElShadey Bekele; Courtney D Thornburg; Amanda M Brandow; Mukta Sharma; Arlene M Smaldone; Zhezhen Jin; Nancy S Green
Journal:  Pediatr Blood Cancer       Date:  2014-04-17       Impact factor: 3.167

5.  Greater number of perceived barriers to hydroxyurea associated with poorer health-related quality of life in youth with sickle cell disease.

Authors:  Arlene Smaldone; Deepa Manwani; Nancy S Green
Journal:  Pediatr Blood Cancer       Date:  2019-04-02       Impact factor: 3.167

6.  National trends in hospitalizations for sickle cell disease in the United States following the FDA approval of hydroxyurea, 1998-2008.

Authors:  Maureen M Okam; Shimon Shaykevich; Benjamin L Ebert; Alan M Zaslavsky; John Z Ayanian
Journal:  Med Care       Date:  2014-07       Impact factor: 2.983

Review 7.  Systematic and Meta-Analytic Review: Medication Adherence Among Pediatric Patients With Sickle Cell Disease.

Authors:  Kristin Loiselle; Jennifer L Lee; Lauren Szulczewski; Sarah Drake; Lori E Crosby; Ahna L H Pai
Journal:  J Pediatr Psychol       Date:  2015-09-18

8.  Decreased fetal hemoglobin over time among youth with sickle cell disease on hydroxyurea is associated with higher urgent hospital use.

Authors:  Nancy S Green; Deepa Manwani; Mahvish Qureshi; Karen Ireland; Arpan Sinha; Arlene M Smaldone
Journal:  Pediatr Blood Cancer       Date:  2016-08-30       Impact factor: 3.167

9.  Feasibility trial for primary stroke prevention in children with sickle cell anemia in Nigeria (SPIN trial).

Authors:  Najibah A Galadanci; Shehu Umar Abdullahi; Leah D Vance; Abdulkadir Musa Tabari; Shehi Ali; Raymond Belonwu; Auwal Salihu; Aisha Amal Galadanci; Binta Wudil Jibir; Halima Bello-Manga; Kathleen Neville; Fenella J Kirkham; Yu Shyr; Sharon Phillips; Brittany V Covert; Adetola A Kassim; Lori C Jordan; Muktar H Aliyu; Michael R DeBaun
Journal:  Am J Hematol       Date:  2017-06-15       Impact factor: 10.047

10.  Preventive Care Delivery to Young Children With Sickle Cell Disease.

Authors:  David G Bundy; John Muschelli; Gwendolyn D Clemens; John J Strouse; Richard E Thompson; James F Casella; Marlene R Miller
Journal:  J Pediatr Hematol Oncol       Date:  2016-05       Impact factor: 1.289

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