Interventions for promoting participation in shared decision-making for children and adolescents with cystic fibrosis

被引:23
|
作者
Malone, Helen [1 ]
Biggar, Susan [2 ]
Javadpour, Sheila [3 ]
Edworthy, Zai [4 ]
Sheaf, Greg [5 ]
Coyne, Imelda [1 ]
机构
[1] Trinity Coll Dublin, Sch Nursing & Midwifery, 24 DOlier St, Dublin 2, Ireland
[2] AHPRA, Melbourne, Vic, Australia
[3] Our Ladys Childrens Hosp, Dept Resp Med, Dublin, Ireland
[4] Temple St Childrens Univ Hosp, Dept Psychol, Dublin, Ireland
[5] Trinity Coll Dublin, Lib, Dublin, Ireland
关键词
CHRONIC DISEASE TREATMENT; PATIENT-CENTERED CARE; I CHANGE ADHERENCE; OF-LIFE MEASURE; HEALTH-CARE; IMPROVING TRANSITION; RAISE EXPECTATIONS; SELF-MANAGEMENT; QUALITY; VALIDATION;
D O I
10.1002/14651858.CD012578.pub2
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Shared decision-making is important in child and adolescent healthcare because there is growing international recognition of children and young people's rights to be included in decisions that affect them. In order for young people to participate effectively in shared decision-making they need to develop the skills of engagement with healthcare professionals and confidence in interacting with them. They also need to learn how to manage their condition and treatments on their own when they move into adulthood. Children and young peoplewho participate in shared decision-making in healthcare are likely to bemore informed, feelmore prepared, and experience less anxiety about the unknown. Significant improvements in cystic fibrosis (CF) survival over recent decades, due to improved therapies and better management of care, means that young people with CF are routinely transitioning to adult healthcare where increasing emphasis on self-management brings greater complexity in decision-making. We need to know what interventions are effective in promoting shared decision-making for young people with CF. Objectives To assess the effectiveness of interventions that promote participation in shared decision-making for children and adolescents (aged between four and 18 years) with CF. Search methods We searched the Cochrane Cystic Fibrosis and Genetic Disorders Group's Cystic Fibrosis Trials Register, compiled from electronic database searches and handsearches of journals and conference abstract books. We also searched the reference lists of articles and reviews addressing shared decision-making. Date of most recent search: 12 March 2019. We searched PubMed, CINAHL (EBSCO), Embase (Elsevier), PsycINFO (EBSCO), WHO ICTRP, ASSIA (ProQuest), ERIC (ProQuest), ProQuest Dissertations and Theses, and ClinicalTrials.gov. We contacted study authors with published relevant research in shared decision-making for adults to ask if they were aware of any published or ongoing studies on the promotion of the intervention for children or adolescents (or both) with CF. Date of most recent search: 19 March 2019. Selection criteria We planned to include randomised controlled trials (RCTs) (but not cross-over RCTs) of interventions promoting shared decision-making for children and adolescents with CF aged between four and 18 years, such as information provision, booklets, two-way interaction, checking understanding (by the participant), preparation to participate in a healthcare decision, decision-aids, and training interventions or educational programs. We planned to include interventions aimed at children or adolescents (or both), parents or healthcare professionals or any combination of these groups provided that the focus was aimed at promoting shared decision-making for children and adolescents with CF. Data collection and analysis Two authors independently reviewed papers identified in the searches. Main results No eligible RCTs were identified for inclusion in this systematic review. Authors' conclusions We were unable to identify RCTs with evidence which would support healthcare policy-making and practice related to implementation of shared decision-making for children and adolescents (aged between four and 18 years) with CF). We hope that having identified this gap in research, awareness will increase amongst researchers of the need to design high-quality shared decision-making interventions for young people with CF, perhaps adapted from existing models for adults, and to test these interventions and children's preferences in RCTs. It is also important to target health professionals with evidence-based education programmes on shared decision-making and a need for international consensus on addressing the variability in education programmes.
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页数:38
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