Adherence to hydroxyurea and clinical outcomes among children with sickle cell anemia

被引:4
|
作者
Reeves, Sarah L. [1 ,2 ,6 ]
Dombkowski, Kevin J. [1 ]
Peng, Hannah K. [1 ]
Phan, Hanna [1 ,3 ]
Kolenic, Giselle [4 ]
Creary, Susan E. [5 ]
Madden, Brian [1 ]
Lisabeth, Lynda D. [2 ]
机构
[1] Univ Michigan, Dept Pediat, Susan Meister Child Hlth Evaluat & Res CHEAR Ctr B, Ann Arbor, MI USA
[2] Univ Michigan, Dept Epidemiol, Sch Publ Hlth, Ann Arbor, MI USA
[3] Univ Michigan, Coll Pharm, Ann Arbor, MI USA
[4] Univ Michigan, Dept Biostat, Sch Publ Hlth, Ann Arbor, MI USA
[5] Ohio State Univ, Ctr Child Hlth Equ & Outcomes Res, Dept Pediat, Nationwide Childrens Hosp, Columbus, OH USA
[6] 2800 Plymouth Rd,NCRC Bldg 16,Rm G027W, Ann Arbor, MI 48109 USA
关键词
acute care; hydroxyurea; sickle cell disease; YOUNG-CHILDREN; CARE UTILIZATION; DISEASE; IMPACT; PAIN; INTERVENTIONS; MANAGEMENT; MEDICATION; EDUCATION;
D O I
10.1002/pbc.30332
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objective: Hydroxyurea lowers the incidence of vaso-occlusive pain crises (VOC) and acute chest syndrome (ACS) among children with sickle cell anemia (SCA). Our objective was to assess the relationship between levels of adherence to hydroxyurea and clinical outcomes among children and adolescents with SCA.Methods: This retrospective cohort study included Medicaid data (2005-2012) from Florida, Illinois, Louisiana, Michigan, South Carolina, and Texas. The study population consisted of children 1-17 years old with SCA enrolled in Medicaid for 3 years. Among children that initiated hydroxyurea, the medication possession ratio (MPR) was calculated as the proportion of days covered by hydroxyurea. Six months after initiation of hydroxyurea, clinical outcomes were assessed through the end of the study period: numbers of VOC-related inpatient admissions and emergency department visits, and encounters for ACS. Multivariable Poisson models were used to predict outcomes by MPR quartile adjusting for previous healthcare utilization, state, and age.Results: Hydroxyurea was initiated by 515 children. The median MPR was 0.53 (interquartile range = 0.3-0.8). The annual median number of visits was 0.0 for ACS, 1.3 for VOC-related emergency department, and 1.4 for VOC-related inpatient admissions. For each outcome, the highest quartile of MPR had the lowest predicted count; this difference was significant for ACS visits when compared with the lowest quartile of MPR.Conclusion: This study demonstrated a high level of adherence (>75%) was essential to achieve a lower incidence of common negative clinical outcomes. Further, moderate and severe hydroxyurea nonadherence may be more common than previously appreciated among children, emphasizing the importance of developing and testing innovative strategies to increase adherence.
引用
收藏
页数:6
相关论文
共 50 条
  • [1] Comment on: "Adherence to hydroxyurea and clinical outcomes among children with sickle cell anemia"
    Dar, Marrium Sultan
    [J]. PEDIATRIC BLOOD & CANCER, 2023, 70 (10)
  • [2] Reply to: Comment on: "Adherence to hydroxyurea and clinical outcomes among children with sickle cell anemia"
    Reeves, Sarah L.
    Dombkowski, Kevin J.
    Peng, Hannah K.
    Phan, Hanna
    Kolenic, Giselle
    Creary, Susan E.
    Madden, Brian
    Lisabeth, Lynda
    [J]. PEDIATRIC BLOOD & CANCER, 2023,
  • [3] Impact of hydroxyurea dose and adherence on hematologic outcomes for children with sickle cell anemia
    Creary, Susan E.
    Beeman, Chase
    Stanek, Joseph
    King, Kathryn
    McGann, Patrick T.
    O'Brien, Sarah H.
    Liem, Robert, I
    Holl, Jane
    Badawy, Sherif M.
    [J]. PEDIATRIC BLOOD & CANCER, 2022, 69 (06)
  • [4] Adherence to Hydroxyurea Therapy in Children with Sickle Cell Anemia
    Thornburg, Courtney D.
    Calatroni, Agustin
    Telen, Marilyn
    Kemper, Alex R.
    [J]. JOURNAL OF PEDIATRICS, 2010, 156 (03): : 415 - 419
  • [5] Hydroxyurea Initiation Among Children With Sickle Cell Anemia
    Reeves, Sarah L.
    Jary, Hannah K.
    Gondhi, Jennifer P.
    Raphael, Jean L.
    Lisabeth, Lynda D.
    Dombkowski, Kevin J.
    [J]. CLINICAL PEDIATRICS, 2019, 58 (13) : 1394 - 1400
  • [6] Hydroxyurea use among children with sickle cell anemia
    Reeves, Sarah L.
    Jary, Hannah K.
    Gondhi, Jennifer P.
    Raphael, Jean L.
    Lisabeth, Lynda D.
    Donnbkowski, Kevin J.
    [J]. PEDIATRIC BLOOD & CANCER, 2019, 66 (06)
  • [7] Clinical and hematologic effects of hydroxyurea in children with sickle cell anemia
    Jayabose, S
    Tugal, O
    Sandoval, C
    Patel, P
    Puder, D
    Lin, T
    Visintainer, P
    [J]. JOURNAL OF PEDIATRICS, 1996, 129 (04): : 559 - 565
  • [8] IMPROVED ADHERENCE TO HYDROXYUREA IN CHILDREN WITH SICKLE CELL ANEMIA UTILIZING TEXT MESSAGES
    Estepp, Jeremie
    Johnson, Margery
    Smeltzer, Matthew
    Winter, Bryan
    Carroll, Yvonne
    Hankins, Jane
    [J]. PEDIATRIC BLOOD & CANCER, 2013, 60 : S23 - S23
  • [9] Impact of Hydroxyurea on Perioperative Management and Outcomes in Children With Sickle Cell Anemia
    Hayashi, Masanori
    Calatroni, Agustin
    Herzberg, Brittany
    Ross, Allison K.
    Rice, Henry E.
    Thornburg, Courtney
    [J]. JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY, 2011, 33 (07) : 487 - 490
  • [10] Effect of hydroxyurea in sickle cell anemia:: A clinical trial in children and teenagers with severe sickle cell anemia and sickle cell β-thalassemia
    Koren, A
    Segal-Kupershmit, D
    Zalman, L
    Levin, C
    Abu Hana, M
    Palmor, H
    Luder, A
    Attias, D
    [J]. PEDIATRIC HEMATOLOGY AND ONCOLOGY, 1999, 16 (03) : 221 - 232