Paternal Stress and Child Outcomes in Youth with Sickle Cell Disease

被引:4
|
作者
Moody, Kendall L. [1 ]
机构
[1] Howard Univ, Sch Social Work, Howard Pl NW, Washington, DC 20059 USA
关键词
parent psychosocial functioning; quality of life; sickle cell disease; stress; QUALITY-OF-LIFE; PARENTING STRESS; CHRONIC ILLNESS; ATTITUDES; IMPACT;
D O I
10.1093/jpepsy/jsab059
中图分类号
B844 [发展心理学(人类心理学)];
学科分类号
040202 ;
摘要
Objective The objective of this study was to investigate the relationship between parental stress and health-related quality of life (HRQOL) among children with sickle cell disease (SCD). Methods A cross-sectional correlational survey research design was used for this quantitative study. One hundred-fifty patients between the ages of 8-17years old and their caregivers were enrolled from an outpatient comprehensive sickle cell program within a hospital setting. Patients completed the Pediatric Quality of Life Scale 3.0 SCD Module, whereas parents completed the Parental Stress Scale and demographic information questionnaire. Multiple regression analysis was used to determine if parental stress scores predicted the HRQOL of children diagnosed with SCD after controlling for demographic variables. Results The sample included 150 patients (median age: 12years old; female: 52%) who were diagnosed with SCD along with 150 of their caregivers. Higher levels of parental stress predicted lower HRQOL scores (p < .001). Conclusion As parents reported elevated levels of stress related to caring for their child with SCD, patients reported worsening HRQOL. More evidence is needed in order to determine, which constructs of parental stress had a significant impact on HRQOL. It may be helpful for healthcare workers to be aware of familial influences of reduced HRQOL among children diagnosed with SCD. Parents reporting increased stress related to raising their child with SCD may benefit from additional support and resources.
引用
收藏
页码:1140 / 1147
页数:8
相关论文
共 50 条
  • [21] Opportunities to improve outcomes in sickle cell disease
    Mehta, Satyen R.
    Afenyi-Annan, Araba
    Byrns, Patricia J.
    Lottenberg, Richard
    AMERICAN FAMILY PHYSICIAN, 2006, 74 (02) : 303 - 310
  • [22] Outcomes of Splenectomy in Children with Sickle Cell Disease
    Soh, Peter B.
    Siddiqui, Abdul H.
    BLOOD, 2014, 124 (21)
  • [23] Perinatal outcomes of sickle cell disease in pregnancy
    Kuo, Kelly
    Caughey, Aaron B.
    AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 2016, 214 (01) : S314 - S314
  • [24] Abortions Outcomes of People with Sickle Cell Disease
    Wade, Sydney A.
    Chen, Erin Y.
    Lanzkron, Sophie M.
    Burke, Anne E.
    Pecker, Lydia H.
    BLOOD, 2023, 142
  • [25] Contemporary outcomes of sickle cell disease in pregnancy
    Kuo, Kelly
    Caughey, Aaron B.
    AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 2016, 215 (04) : 505.e1 - 505.e5
  • [26] Inflammatory Bowel Disease in a Child with Sickle Cell Anemia
    Alqoaer, Khaled
    Ahmed, Mohammed M.
    Alhowaiti, Efteraj S.
    CASE REPORTS IN PEDIATRICS, 2014, 2014
  • [27] The effect of hydroxyurea on vasculopathy in a child with sickle cell disease
    Helton, KJ
    Wang, WC
    Wynn, LW
    Khan, RB
    Steen, RG
    AMERICAN JOURNAL OF NEURORADIOLOGY, 2002, 23 (10) : 1692 - 1696
  • [28] Fat Embolism Syndrome in a Child with Sickle Cell Disease
    Maroni, Arielle
    Dauger, Stephane
    Chomton, Maryline
    JOURNAL OF PEDIATRICS, 2019, 214 : 236 - 236
  • [29] Clostridium difficile Sepsis in a Child With Sickle Cell Disease
    Babbit, Christopher J.
    Romansky, Stephen G.
    INFECTIOUS DISEASES IN CLINICAL PRACTICE, 2006, 14 (02) : 112 - 113
  • [30] Transplanting the child with sickle cell disease, are we prepared?
    Stewart, DM
    Mattox, S
    Miller, C
    Steed, MG
    BIOLOGY OF BLOOD AND MARROW TRANSPLANTATION, 2006, 12 (02) : 148 - 148