Hydroxyurea Adherence for Personal Best in Sickle Cell Treatment (HABIT) efficacy trial: Community health worker support may increase hydroxyurea adherence of youth with sickle cell disease

Author:

Green Nancy S.1ORCID,Manwani Deepa2,Aygun Banu3ORCID,Appiah‐Kubi Abena3,Smith‐Whitley Kim45,Castillo Yina1,Soriano Lucy1,Jia Haomiao6,Smaldone Arlene M.6

Affiliation:

1. Department of Pediatrics, Division of Hematology, Oncology and Stem Cell Transplantation Columbia University Irving Medical Center New York New York USA

2. Department of Pediatrics, Division of Hematology, Oncology and Cellular Therapy Albert Einstein College of Medicine New York New York USA

3. Department of Pediatrics Division of Hematology, Oncology and Cellular Therapy, Cohen Children's Medical Center New York New York USA

4. Division of Hematology Children's Hospital of Philadelphia Philadelphia Pennsylvania USA

5. Pfizer, Inc. New York New York USA

6. School of Nursing Columbia University Irving Medical Center New York New York USA

Abstract

AbstractDespite disease‐modifying effects of hydroxyurea on sickle cell disease (SCD), poor adherence among affected youth commonly impedes treatment impact. Following our prior feasibility trial, the “Hydroxyurea Adherence for Personal Best in Sickle Cell Treatment (HABIT)” multi‐site randomized controlled efficacy trial aimed to increase hydroxyurea adherence for youth with SCD ages 10–18 years. Impaired adherence was identified primarily through flagging hydroxyurea‐induced fetal hemoglobin (HbF) levels compared to prior highest treatment‐related HbF. Eligible youth were enrolled as dyads with their primary caregivers for the 1‐year trial. This novel semi‐structured supportive, multidimensional dyad intervention led by community health workers (CHW), was augmented by daily tailored text message reminders, compared to standard care during a 6‐month intervention phase, followed by a 6‐month sustainability phase. Primary outcomes from the intervention phase were improved Month 6 HbF levels compared to enrollment and proportion of days covered (PDC) for hydroxyurea versus pre‐trial year. The secondary outcome was sustainability of changes up to Month 12. The 2020–2021 peak coronavirus disease 2019 (COVID‐19) pandemic disrupted enrollment and clinic‐based procedures; CHW in‐person visits shifted to virtual scheduled interactions. We enrolled 50 dyads, missing target enrollment. Compared to enrollment levels, both HbF level and PDC significantly ‐ but not sustainably ‐ improved within the intervention group (p = .03 and .01, respectively) with parallel increased mean corpuscular volume (MCV) (p = .05), but not within controls. No significant between‐group differences were found at Months 6 or 12. These findings suggest that our community‐based, multimodal support for youth–caregiver dyads had temporarily improved hydroxyurea usage. Durability of impact should be tested in a trial with longer duration of CHW‐led and mobile health support.

Publisher

Wiley

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