Published literature

Publications

Published children's palliative care research: browsable, searchable and filterable by the same taxonomy as researchers, groups and guides.

This library is curated by The Siden Research Team as part of the TRENDS in Pediatric Palliative Care newsletter and library. Learn more about TRENDS and The Siden Research Team and subscribe to read their monthly expert commentaries on their website.

Showing onlyReview/Synthesis×Clear all

Showing 26–43 of 43 publications

Can the Ethical Best Practice of Shared Decision-Making lead to Moral Distress?
Prentice T, Gillam L · Journal of bioethical inquiry · 2018 · DOI: 10.1007/s11673-018-9847-8
When healthcare professionals feel constrained from acting in a patient's best interests, moral distress ensues. The resulting negative sequelae of burnout, poor retention rates, and ultimately poor patient care are well recognized across healthcare providers.…
Information needs of young people with cerebral palsy and their families during the transition to adulthood: a scoping review
Matthew F, Debra S, Cunningham Charles E, Willem G · Journal of Transition Medicine · 2018 · DOI: 10.1515/jtm-2018-0003
The transition to adulthood is a developmental phase which occurs as young people move from adolescence into adulthood. Young people with disabilities, including cerebral palsy (CP), and their families have reported challenges during the transition to adulthoo…
The under reporting of recruitment strategies in research with children with life-threatening illnesses: A systematic review
Hudson B, Oostendorp L, Candy B, Vickerstaff V, Jones L, Lakhanpaul M, Bluebond-Langner M, Stone P · Palliative Medicine · 2017 · DOI: 10.1177/0269216316663856
Opportunities for Palliative Care in Public Health
De Lima L, Pastrana T · Annu Rev Public Health · 2016 · DOI: 10.1146/annurev-publhealth-032315-021448
In May 2014, the World Health Assembly, of the World Health Organization (WHO), unanimously adopted a palliative care (PC) resolution, which outlines clear recommendations to the United Nations member states, such as including PC in national health policies an…
The AAP Resilience in the Face of Grief and Loss Curriculum
Serwint J, Bostwick S, Burke A, Church A, Gogo A, Hofkosh D, King M, Linebarger J, McCabe M, Moon M, Osta A, Rana D, Sahler O, Smith K, Rivera F, Baldwin C · Pediatrics. · 2016
What are the limits of parental authority? Pediatric bioethics and the law
Johnson L, Steuer K, Campbell A, Baker J · Journal of Pain and Symptom Management · 2016
Objectives * Distinguish between the "best interest standard" and "the harm principle" in the evaluation of familial medical decision making in pediatrics and analyze the strengths and weaknesses of each. * Identify key legal cases in pediatrics and explain th…
Inclusion of children with disabilities in mainstream child development research
Feldman M, M. B, A. S, and Luckasson R · Disability & Society · 2012 · DOI: 10.1080/09687599.2012.748647
This study investigated whether children with disabilities are excluded from mainstream child development research. Fifteen per cent of 533 articles from Child Development and Developmental Psychology (1996?2010) were randomly selected. The exclusion rate was …
Family caregiving for persons with heart failure at the intersection of heart failure and palliative care: a state-of-the-science review
Nicholas Dionne-Odom J, Hooker S, Bekelman D, Ejem D, McGhan G, Kitko L, Str�mberg A, Wells R, Astin M, Metin Z, Mancarella G, Pamboukian S, Evangelista L, Buck H, Bakitas M, Hooker S, Metin Z, Pamboukian S, Buck H · Heart Failure Reviews · DOI: 10.1007/s10741-017-9597-4
Many of the 23 million individuals with heart failure (HF) worldwide receive daily, unpaid support from a family member or friend. Although HF and palliative care practice guidelines stipulate that support be provided to family caregivers, the evidence base to…
← PreviousPage 2 of 2