Patterns and Predictors of Hydroxyurea Use Among Californians Living With Sickle Cell Disease

被引:0
作者
Rushing, Melinda [1 ]
Horiuchi, Sophia [4 ]
Kayle, Mariam [5 ]
Reeves, Sarah L. [1 ,2 ]
Glaros, Alexander K. [3 ]
Paulukonis, Susan [4 ]
机构
[1] Univ Michigan, Susan B Meister Child Hlth Evaluat & Res Ctr, Dept Pediat, Ann Arbor, MI USA
[2] Univ Michigan, Dept Epidemiol, Sch Publ Hlth, Ann Arbor, MI USA
[3] Cent Michigan Univ, Childrens Hosp Michigan, Detroit, MI USA
[4] Publ Hlth Inst, Tracking Calif Program, Oakland, CA USA
[5] Duke Univ, Sch Nursing, Durham, NC USA
关键词
sickle cell disease; hydroxyurea; medication adherence; MEDICATION ADHERENCE; PEDIATRIC-PATIENTS; UNITED-STATES; ADULTS; CARE; TRANSITION; ANEMIA; HYDROXYCARBAMIDE; ADOLESCENTS; BARRIERS;
D O I
10.1097/MPH.0000000000003027
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Hydroxyurea is the primary disease-modifying therapy for sickle cell disease (SCD), yet adherence is low. Our objective was to identify patterns and predictors of hydroxyurea adherence among Medicaid enrollees with SCD. Children and adults with SCD who received Medicaid benefits between 2009 and 2018 in California were included. Monthly hydroxyurea possession ratios were calculated using filled hydroxyurea prescriptions. Group-based trajectory modeling was applied to identify hydroxyurea possession trajectories and multinomial logistic regression modeling to evaluate predictors of hydroxyurea possession group membership: prior acute care visits due to VOCs, prescriber specialty, and participant sex and age. 713 participants (48% in the 0 to 17 age group, 50% male) had 3 distinct hydroxyurea possession groups: persistently high (n=263, 37%), moderate to low (n=253, 35%), and low to no possession (n=197, 28%). The 18 to 24 and 25+ age groups had greater odds of being in the moderate to low (OR: 2.62, 1.70) and low to no (OR: 3.60, 2.45) than the persistently high possession group compared with the 0 to 17 age group when adjusted for prior VOCs. Children had greater odds of being in the persistently high hydroxyurea possession group compared with young adults and adults, suggesting there are protective factors at this age that promotes better hydroxyurea adherence.
引用
收藏
页码:169 / 176
页数:8
相关论文
共 47 条
[1]   Long-Term Medication Adherence Trajectories to Direct Oral Anticoagulants and Clinical Outcomes in Patients With Atrial Fibrillation [J].
An, Jaejin ;
Bider, Zoe ;
Luong, Tiffany Q. ;
Cheetham, T. Craig ;
Lang, Daniel T. ;
Fischer, Heidi ;
Reynolds, Kristi .
JOURNAL OF THE AMERICAN HEART ASSOCIATION, 2021, 10 (21)
[2]   Healthcare utilization and hydroxyurea adherence in youth with sickle cell disease [J].
Badawy, Sherif M. ;
Thompson, Alexis A. ;
Holl, Jane L. ;
Penedo, Frank J. ;
Liem, Robert I. .
PEDIATRIC HEMATOLOGY AND ONCOLOGY, 2018, 35 (5-6) :297-308
[3]   Adherence to hydroxyurea, health-related quality of life domains, and patients' perceptions of sickle cell disease and hydroxyurea: a cross-sectional study in adolescents and young adults [J].
Badawy, Sherif M. ;
Thompson, Alexis A. ;
Lai, Jin-Shei ;
Penedo, Frank J. ;
Rychlik, Karen ;
Liem, Robert I. .
HEALTH AND QUALITY OF LIFE OUTCOMES, 2017, 15
[4]  
Bemrich-Stolz C J, 2015, Int J Hematol Ther, V1, DOI 10.15436/2381-1404.15.003
[5]   Purposeful selection of variables in logistic regression [J].
Bursac, Zoran ;
Gauss, C. Heath ;
Williams, David Keith ;
Hosmer, David W. .
SOURCE CODE FOR BIOLOGY AND MEDICINE, 2008, 3 (01)
[6]   Transition for Adolescents and Young Adults With Sickle Cell Disease in a US Midwest Urban Center: A Multilevel Perspective on Barriers, Facilitators, and Future Directions [J].
Calhoun, Cecelia ;
Luo, Lingzi ;
Baumann, Ana A. ;
Bauer, Anna ;
Shen, Evelyn ;
McKay, Virginia ;
Hooley, Cole ;
James, Aimee ;
King, Allison A. .
JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY, 2022, 44 (05) :E872-E880
[7]   Hydroxyurea adherence and associated outcomes among Medicaid enrollees with sickle cell disease [J].
Candrilli, Sean D. ;
O'Brien, Sarah H. ;
Ware, Russell E. ;
Nahata, Milap C. ;
Seiber, Eric E. ;
Balkrishnan, Rajesh .
AMERICAN JOURNAL OF HEMATOLOGY, 2011, 86 (03) :273-277
[8]  
CHARACHE S, 1992, BLOOD, V79, P2555
[9]   EFFECT OF HYDROXYUREA ON THE FREQUENCY OF PAINFUL CRISES IN SICKLE-CELL-ANEMIA [J].
CHARACHE, S ;
TERRIN, ML ;
MOORE, RD ;
DOVER, GJ ;
BARTON, FB ;
ECKERT, SV ;
MCMAHON, RP ;
BONDS, DR ;
ORRINGER, E ;
JONES, S ;
STRAYHORN, D ;
ROSSE, W ;
PHILLIPS, G ;
PEACE, D ;
JOHNSONTELFAIR, A ;
MILNER, P ;
KUTLAR, A ;
TRACY, A ;
BALLAS, SK ;
ALLEN, GE ;
MOSHANG, J ;
SCOTT, B ;
STEINBERG, M ;
ANDERSON, A ;
SABAHI, V ;
PEGELOW, C ;
TEMPLE, D ;
CASE, E ;
HARRELL, R ;
CHILDERIE, S ;
EMBURY, S ;
SCHMIDT, B ;
DAVIES, D ;
KOSHY, M ;
TALISCHYZAHED, N ;
DORN, L ;
PENDARVIS, G ;
MCGEE, M ;
TELFER, M ;
DAVIS, A ;
CASTRO, O ;
FINKE, H ;
PERLIN, E ;
SITEMAN, J ;
GASCON, P ;
DIPAOLO, P ;
GARGIULO, S ;
ECKMAN, J ;
BAILEY, JH ;
PLATT, A .
NEW ENGLAND JOURNAL OF MEDICINE, 1995, 332 (20) :1317-1322
[10]   ENHANCE-(Electronic Hydroxyurea Adherence): A Protocol to Increase Hydroxyurea Adherence in Patients with Sickle Cell Disease [J].
Creary, Susan ;
Chisolm, Deena J. ;
O'Brien, Sarah H. .
JMIR RESEARCH PROTOCOLS, 2016, 5 (04)