Communication during childhood cancer: Systematic review of patient perspectives

被引:70
作者
Lin, Beryl [1 ,2 ]
Gutman, Talia [1 ,3 ]
Hanson, Camilla S. [1 ,3 ]
Ju, Angela [1 ,3 ]
Manera, Karine [1 ,3 ]
Butow, Phyllis [4 ]
Cohn, Richard J. [2 ,5 ]
Dalla-Pozza, Luciano [6 ]
Greenzang, Katie A. [7 ]
Mack, Jennifer [7 ]
Wakefield, Claire E. [2 ,5 ]
Craig, Jonathan C. [1 ,3 ]
Tong, Allison [1 ,3 ]
机构
[1] Univ Sydney, Sch Publ Hlth, Sydney, NSW, Australia
[2] Univ New South Wales, Sch Womens & Childrens Hlth, Sydney, NSW, Australia
[3] Childrens Hosp Westmead, Ctr Kidney Res, Westmead, NSW, Australia
[4] Univ Sydney, Psychooncol Cooperat Res Grp, Sch Psychol, Sydney, NSW, Australia
[5] Sydney Childrens Hosp, Kids Canc Ctr, Randwick, NSW, Australia
[6] Childrens Hosp Westmead, Canc Ctr Children, Sydney, NSW, Australia
[7] Dana Farber Canc Inst, Dana Farber Boston Childrens Canc & Blood Disorde, Boston, MA 02115 USA
基金
英国医学研究理事会;
关键词
adolescent; cancer; child; communication; decision making; patient; qualitative; HEALTH-CARE PROFESSIONALS; SHARED DECISION-MAKING; ACUTE LYMPHOBLASTIC-LEUKEMIA; YOUNG PEOPLES EXPERIENCES; INFORMED-CONSENT; CHILDRENS PARTICIPATION; PEDIATRIC-PATIENTS; CULTURAL-DIFFERENCES; QUALITATIVE RESEARCH; PARENTS EXPERIENCES;
D O I
10.1002/cncr.32637
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Effective communication is challenging in childhood cancer, where decisions carry unpredictable and life-threatening implications. We aimed to describe patients' experiences of communicating with clinicians during treatment of childhood cancer. A systematic review of qualitative studies to April 2019 was performed. Eligible studies included patients diagnosed with cancer at age <= 18 years and reported their perspectives of communicating with clinicians during treatment of childhood cancer. Data were extracted from primary studies for thematic synthesis. From 101 articles across 25 countries involving 1870 participants who were diagnosed with cancer between ages 3 to 18 years, we identified 6 themes: 1) rendered invisible and powerless (displaced and undermined by adult authority; betrayed and distrustful; feeling neglected; helpless and intimidated; disempowered by lack of information); 2) fear and worry for the future (paralyzed by devastating news; uncertainty, anticipation, and dread; broaching intimate and private topics); 3) burdened with responsibility (pressured and unprepared; balancing external expectations; protecting hope); 4) therapeutic patient-provider relationships (emotional support and encouragement; validated personhood and companionship); 5) safety in trust (truthfulness and transparency; prepared by awareness and understanding; reassured by reliable expertise; depending on adults for protection and difficult decisions; security in expressing opinions and needs); and 6) empowerment and assertive agency (right to individual knowledge and choice; control over own life; partnership and respect; enhancing capacity for self-management). During treatment of childhood cancer, patients gain a sense of respect, safety, and control when they feel clinicians address their information and developmental needs. However, communication that is perceived to be parent-centered can be disempowering. Promoting child agency and partnership may improve care and outcomes for children with cancer.
引用
收藏
页码:701 / 716
页数:16
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