Literature DB >> 30636474

Healthcare utilization and hydroxyurea adherence in youth with sickle cell disease.

Sherif M Badawy1,2, Alexis A Thompson1,2, Jane L Holl1,3, Frank J Penedo4, Robert I Liem1,2.   

Abstract

BACKGROUND: Sickle cell disease (SCD) complications lead to poor health-related quality of life (HRQOL) and increased healthcare utilization in this population, which could be mitigated with hydroxyurea therapy; however, adherence is suboptimal. We assessed the relationship of healthcare utilization to hydroxyurea adherence and HRQOL amongst youth with SCD.
METHODS: Thirty-four patients with SCD (median age 14 years, IQR 12-18) on hydroxyurea participated in this cross-sectional study and completed Morisky Adherence Scale 8-items and Patient Reported Outcomes Measurement Information System (PROMIS®) HRQOL measures. A medical chart review was conducted to assess healthcare utilization.
RESULTS: Participants with more frequent hospitalizations and emergency room (ER) visits and longer length of stay (LOS) had significantly lower fetal hemoglobin (rs=-0.44; rs=-0.45; rs=-0.46, p < 0.05) and mean corpuscular volume (rs=-0.47; rs=-0.42; rs=-0.48, p < 0.05), respectively. More frequent hospitalizations and ER visits and longer LOS correlated significantly with worse fatigue (rs=0.51; rs=0.41; rs=0.53, p < 0.05), pain (rs=0.41; rs=0.38; rs=0.47, p < 0.05), physical function mobility (rs=-0.67; rs=-0.59; rs=-0.67, p < 0.05), depression (rs=0.38; rs=0.31; rs=0.42, p < 0.05), and social isolation (rs=0.76; rs=0.76; rs=-0.84, p < 0.05), respectively.
CONCLUSIONS: We conclude that increased healthcare utilization in youth with SCD is associated with low adherence to hydroxyurea and worse HRQOL domain scores. It is important emphasize the clinical benefits of high adherence to hydroxyurea, particularly among youth with SCD. Future longitudinal studies are warranted to assess the directionality of these relationships, and may reveal modifiable behavioral factors associated with early changes in hydroxyurea adherence levels.

Entities:  

Keywords:  Sickle cell disease; adherence; healthcare utilization; hydroxyurea; quality of life

Mesh:

Substances:

Year:  2019        PMID: 30636474     DOI: 10.1080/08880018.2018.1505988

Source DB:  PubMed          Journal:  Pediatr Hematol Oncol        ISSN: 0888-0018            Impact factor:   1.969


  17 in total

1.  Association between clinical outcomes and metformin use in adults with sickle cell disease and diabetes mellitus.

Authors:  Sherif M Badawy; Amanda B Payne
Journal:  Blood Adv       Date:  2019-11-12

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

Review 3.  Clinical trial considerations in sickle cell disease: patient-reported outcomes, data elements, and the stakeholder engagement framework.

Authors:  Sherif M Badawy
Journal:  Hematology Am Soc Hematol Educ Program       Date:  2021-12-10

4.  Digital behavioural interventions for people with sickle cell disease.

Authors:  Sherif M Badawy; Robert M Cronin; Robert I Liem; Tonya M Palermo
Journal:  Cochrane Database Syst Rev       Date:  2021-04-27

5.  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

6.  Quality of life in pre-adolescent children with sickle cell disease in Brazil.

Authors:  Claudia Di Lorenzo Oliveira; Shannon Kelly; Cesar de Almeida-Neto; Anna Barbara Carneiro-Proietti; Fabiana Chagas Camargos Piassi; Tassila Salomon; Miriam V Flor-Park; Claudia Maximo; Daniela Werneck Rodrigues; Rosimere Afonso Mota; Carolina Miranda Teixeira; Paula Loureiro; Ester Cerdeira Sabino; Brian Custer
Journal:  Pediatr Hematol Oncol       Date:  2019-09-06       Impact factor: 1.969

7.  Comparing the Effectiveness of Education Versus Digital Cognitive Behavioral Therapy for Adults With Sickle Cell Disease: Protocol for the Cognitive Behavioral Therapy and Real-time Pain Management Intervention for Sickle Cell via Mobile Applications (CaRISMA) Study.

Authors:  Sherif M Badawy; Kaleab Z Abebe; Charlotte A Reichman; Grace Checo; Megan E Hamm; Jennifer Stinson; Chitra Lalloo; Patrick Carroll; Santosh L Saraf; Victor R Gordeuk; Payal Desai; Nirmish Shah; Darla Liles; Cassandra Trimnell; Charles R Jonassaint
Journal:  JMIR Res Protoc       Date:  2021-05-14

8.  Development of the InCharge Health Mobile App to Improve Adherence to Hydroxyurea in Patients With Sickle Cell Disease: User-Centered Design Approach.

Authors:  Nicole M Alberts; Sherif M Badawy; Jerlym S Porter; Jane S Hankins; Jason Hodges; Jeremie H Estepp; Chinonyelum Nwosu; Hamda Khan; Matthew P Smeltzer; Ramin Homayouni; Sarah Norell; Lisa Klesges
Journal:  JMIR Mhealth Uhealth       Date:  2020-05-08       Impact factor: 4.773

9.  The relationship between frequency and severity of vaso-occlusive crises and health-related quality of life and work productivity in adults with sickle cell disease.

Authors:  Avery A Rizio; Menaka Bhor; Xiaochen Lin; Kristen L McCausland; Michelle K White; Jincy Paulose; Savita Nandal; Rashid I Halloway; Lanetta Bronté-Hall
Journal:  Qual Life Res       Date:  2020-01-13       Impact factor: 4.147

10.  Habit Strength, Medication Adherence, and Habit-Based Mobile Health Interventions Across Chronic Medical Conditions: Systematic Review.

Authors:  Sherif M Badawy; Richa Shah; Usman Beg; Mallorie B Heneghan
Journal:  J Med Internet Res       Date:  2020-04-28       Impact factor: 5.428

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