Literature DB >> 27225236

Adherence to hydroxyurea medication by children with sickle cell disease (SCD) using an electronic device: a feasibility study.

Susumu Inoue1, Gergana Kodjebacheva2, Tammy Scherrer3, Gary Rice4, Matthew Grigorian4, Jeremy Blankenship2, Nkechi Onwuzurike3.   

Abstract

Adherence to hydroxyurea (HU) is a significant modifying factor in sickle cell vaso-occlusive pain. We conducted a study using an electronic medication container-monitor-reminder device (GlowCap™) to track adherence and determine whether use of this device affected rates of HU adherence. Subjects were regular attendees to our clinic. They were given a 37-item questionnaire and were asked to use a GlowCap containing HU. When the device cap is opened, it makes a remote "medication taken" record. The device also provides usage reminder in the form of lights and alarm sounds if the cap opening is delayed. Nineteen subjects participated in the survey, and 17 in the intervention phase. Of the 17, 12 had reliable adherence data. Seventeen caregivers of patients and two patients completed the survey. Two most common barriers to adherence identified were lack of reminders and absence of medicine home delivery. The intervention component of this study, which used both the electronic (GlowCap) method and medication possession ratio showed that the median adherence rate for the 12 patients evaluated was 85 %. The GlowCap device accurately kept a record of adherence rates. This device may be an effective tool for increasing HU medication adherence.

Entities:  

Keywords:  Hydroxyurea; Medication adherence; Sickle cell disease

Mesh:

Substances:

Year:  2016        PMID: 27225236     DOI: 10.1007/s12185-016-2027-x

Source DB:  PubMed          Journal:  Int J Hematol        ISSN: 0925-5710            Impact factor:   2.490


  25 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.  The rationale for using hydroxycarbamide in the treatment of sickle cell disease.

Authors:  David C Rees
Journal:  Haematologica       Date:  2011-04       Impact factor: 9.941

3.  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

4.  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

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 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

Review 7.  Hydroxyurea for the treatment of sickle cell disease: efficacy, barriers, toxicity, and management in children.

Authors:  John J Strouse; Matthew M Heeney
Journal:  Pediatr Blood Cancer       Date:  2012-04-19       Impact factor: 3.167

8.  Compliance with penicillin prophylaxis in patients with sickle cell disease.

Authors:  S J Teach; K A Lillis; M Grossi
Journal:  Arch Pediatr Adolesc Med       Date:  1998-03

Review 9.  Interplay between coagulation and vascular inflammation in sickle cell disease.

Authors:  Erica Sparkenbaugh; Rafal Pawlinski
Journal:  Br J Haematol       Date:  2013-04-18       Impact factor: 6.998

10.  Screening for noncompliance among patients with hypertension: is self-report the best available measure?

Authors:  T S Inui; W B Carter; R E Pecoraro
Journal:  Med Care       Date:  1981-10       Impact factor: 2.983

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  9 in total

1.  Hydroxyurea Initiation Among Children With Sickle Cell Anemia.

Authors:  Sarah L Reeves; Hannah K Jary; Jennifer P Gondhi; Jean L Raphael; Lynda D Lisabeth; Kevin J Dombkowski
Journal:  Clin Pediatr (Phila)       Date:  2019-05-21       Impact factor: 1.168

2.  Intentional and unintentional nonadherence to hydroxyurea among people with sickle cell disease: a qualitative study.

Authors:  Jason R Hodges; Shannon M Phillips; Sarah Norell; Chinonyelum Nwosu; Hamda Khan; Lingzi Luo; Sherif M Badawy; Allison King; Paula Tanabe; Marsha Treadwell; Lucia Rojas Smith; Cecelia Calhoun; Jane S Hankins; Jerlym Porter
Journal:  Blood Adv       Date:  2020-09-22

3.  Feasibility of an mHealth self-management intervention for children and adolescents with sickle cell disease and their families.

Authors:  Shannon Phillips; Julie Kanter; Martina Mueller; Amy Gulledge; Kenneth Ruggiero; Mary Johnson; Teresa J Kelechi
Journal:  Transl Behav Med       Date:  2021-04-07       Impact factor: 3.626

4.  Patient-Centered eHealth Interventions for Children, Adolescents, and Adults With Sickle Cell Disease: Systematic Review.

Authors:  Sherif M Badawy; Robert M Cronin; Jane Hankins; Lori Crosby; Michael DeBaun; Alexis A Thompson; Nirmish Shah
Journal:  J Med Internet Res       Date:  2018-07-19       Impact factor: 5.428

5.  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

6.  A Stress and Pain Self-management mHealth App for Adult Outpatients With Sickle Cell Disease: Protocol for a Randomized Controlled Study.

Authors:  Miriam O Ezenwa; Yingwei Yao; Molly W Mandernach; David A Fedele; Robert J Lucero; Inge Corless; Brenda W Dyal; Mary H Belkin; Abhinav Rohatgi; Diana J Wilkie
Journal:  JMIR Res Protoc       Date:  2022-07-29

7.  Barriers to hydroxyurea use from the perspectives of providers, individuals with sickle cell disease, and families: Report from a U.S. regional collaborative.

Authors:  Marsha J Treadwell; Lisa Du; Neha Bhasin; Anne M Marsh; Theodore Wun; M A Bender; Trisha E Wong; Nicole Crook; Jong H Chung; Shannon Norman; Nicolas Camilo; Judith Cavazos; Diane Nugent
Journal:  Front Genet       Date:  2022-08-26       Impact factor: 4.772

Review 8.  Disparities in hypertension and cardiovascular disease in blacks: The critical role of medication adherence.

Authors:  Keith C Ferdinand; Kapil Yadav; Samar A Nasser; Helene D Clayton-Jeter; John Lewin; Dennis R Cryer; Fortunato Fred Senatore
Journal:  J Clin Hypertens (Greenwich)       Date:  2017-08-30       Impact factor: 3.738

9.  Factors Influencing Motivation and Engagement in Mobile Health Among Patients With Sickle Cell Disease in Low-Prevalence, High-Income Countries: Qualitative Exploration of Patient Requirements.

Authors:  David-Zacharie Issom; André Henriksen; Ashenafi Zebene Woldaregay; Jessica Rochat; Christian Lovis; Gunnar Hartvigsen
Journal:  JMIR Hum Factors       Date:  2020-03-24
  9 in total

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