Cognitive functioning, patient health communication, and worry mediate pain predictive effects on health-related quality of life in youth with sickle cell disease

被引:12
|
作者
Varni, James W. [1 ]
Panepinto, Julie A. [2 ]
机构
[1] Texas A&M Univ, Coll Med, Dept Pediat, Dept Landscape Architecture & Urban Planning,Coll, College Stn, TX 77843 USA
[2] Med Coll Wisconsin, Dept Pediat Hematol Oncol Bone Marrow Transplanta, Childrens Hosp Wisconsin, Childrens Res Inst, Milwaukee, WI 53226 USA
基金
美国国家卫生研究院;
关键词
cognition; health communication; health-related quality of life; pain; PedsQL; sickle cell disease; MULTIDIMENSIONAL FATIGUE SCALE; GENERIC CORE SCALES; BEHAVIOR RATING INVENTORY; GASTROINTESTINAL SYMPTOMS; WORKING-MEMORY; RELIABILITY; CHILDREN; PEDSQL(TM); FEASIBILITY; VALIDITY;
D O I
10.1002/pbc.28680
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objectives The objective was to investigate the serial mediating effects of perceived cognitive functioning, patient health communication, and disease-specific worry in the relationship between pain and overall generic health-related quality of life (HRQOL) in youth with sickle cell disease (SCD) from the patient perspective. Methods The pain, cognitive functioning, communication and worry scales from the Pediatric Quality of Life Inventory (PedsQL) Sickle Cell Disease Module and the PedsQL Multidimensional Fatigue Scale, and the PedsQL 4.0 Generic Core Scales were completed in a multisite national study by 233 youth with SCD of ages 5-18. Hierarchical multiple regression and serial multiple mediator model analyses were conducted to test the mediating effects of perceived cognitive functioning, health communication, and disease-specific worry as intervening variables in the association between the pain predictor variable and overall generic HRQOL. Results Pain predictive effects on overall generic HRQOL were serially mediated by cognitive functioning, health communication, and disease-specific worry. In predictive analytics models utilizing hierarchical multiple regression analyses with age and gender demographic covariates, pain, cognitive functioning, health communication, and worry accounted for 65% of the variance in patient-reported overall generic HRQOL (P < .001), representing a large effect size. Conclusions Perceived cognitive functioning, patient health communication, and disease-specific worry explain in part the mechanism of pain predictive effects on overall generic HRQOL in youth with SCD. Identifying SCD-specific pain, perceived cognitive functioning, health communication, and disease-specific worry as predictor variables of overall generic HRQOL from the patient perspective may inform clinical interventions and future patient-centered clinical research.
引用
收藏
页数:8
相关论文
共 50 条
  • [21] Pain catastrophizing is associated with poorer health-related quality of life in pediatric patients with sickle cell disease
    Bakshi, Nitya
    Lukombo, Ines
    Belfer, Inna
    Krishnamurti, Lakshmanan
    JOURNAL OF PAIN RESEARCH, 2018, 11 : 947 - 953
  • [22] Health-Related Quality of Life in Children With Sickle Cell Disease Using the Child Health Questionnaire
    Wrotniak, Brian H.
    Schall, Joan I.
    Brault, Megan E.
    Balmer, Dorene F.
    Stallings, Virginia A.
    JOURNAL OF PEDIATRIC HEALTH CARE, 2014, 28 (01) : 14 - 22
  • [23] Sickle cell disease health-related quality of life questionnaire project.
    Werner, Ellen M.
    Treadwell, Marsha
    Hassell, Kathryn
    Keller, San
    Levine, Roger
    BLOOD, 2006, 108 (11) : 953A - 953A
  • [24] Health-related quality of life in patients with sickle cell disease in Saudi Arabia
    Anwar E. Ahmed
    Ahmed S. Alaskar
    Ahmad M. Al-Suliman
    Abdul-Rahman Jazieh
    Donna K. McClish
    Majid Al Salamah
    Yosra Z. Ali
    Hafiz Malhan
    May Anne Mendoza
    Abdulrahman O. Gorashi
    Mohamed E. El-toum
    Wala E. El-toum
    Health and Quality of Life Outcomes, 13
  • [25] Health-related quality of life in sickle cell disease: Past, present, and future
    Panepinto, Julie A.
    Bonner, Melanie
    PEDIATRIC BLOOD & CANCER, 2012, 59 (02) : 377 - 385
  • [26] HEALTH-RELATED QUALITY OF LIFE OF SICKLE CELL DISEASE PATIENTS AND FAMILIES IN COLOMBIA
    Romero, M.
    Sanabria, M.
    Huerfano, L. M.
    VALUE IN HEALTH, 2016, 19 (03) : A96 - A96
  • [27] Health-related quality of life in children with sickle cell disease: a concept analysis
    Al Nasiri, Yusra
    Al Mawali, Adhra
    JOURNAL OF CONTEMPORARY MEDICAL SCIENCES, 2019, 5 (01): : 59 - 63
  • [28] Parental report of health-related quality of life in children with sickle cell disease
    Palermo, TM
    Schwartz, L
    Drotar, D
    McGowan, K
    JOURNAL OF BEHAVIORAL MEDICINE, 2002, 25 (03) : 269 - 283
  • [29] Impact of poverty and sickle cell disease on the health-related quality of life of children
    Panepinlo, Julie A.
    Foerster, Lisa M.
    Sabnis, Svapna
    Pajewski, Nicholas
    Hoffrnann, Raymond
    BLOOD, 2007, 110 (11) : 33A - 33A
  • [30] Health-related quality of life in patients with sickle cell disease in Saudi Arabia
    Ahmed, Anwar E.
    Alaskar, Ahmed S.
    Al-Suliman, Ahmad M.
    Jazieh, Abdul-Rahman
    McClish, Donna K.
    Al Salamah, Majid
    Ali, Yosra Z.
    Malhan, Hafiz
    Mendoza, May Anne
    Gorashi, Abdulrahman O.
    El-Toum, Mohamed E.
    El-Toum, Wala E.
    HEALTH AND QUALITY OF LIFE OUTCOMES, 2015, 13