Parent and physician perspectives on quality of care at the end of life in children with cancer. - Test2 - elhamkhani - TriplyDB

Parent and physician perspectives on quality of care at the end of life in children with cancer.

Parent and physician perspectives on quality of care at the end of life in children with cancer.

http://www.wikidata.org/entity/Q53279623

about

Establishing psychosocial palliative care standards for children and adolescents with cancer and their families: An integrative review Understanding death with limited experience in life: dying children's and adolescents' understanding of their own terminal illness and death Systematic review of psychosocial morbidities among bereaved parents of children with cancer Cross-cultural adaptation of an innovative approach to learning about difficult conversations in healthcare.Palliative care in the pediatric ICU: challenges and opportunities for family-centered practice Supportive medical care for children with acute lymphoblastic leukemia in low- and middle-income countries.Paediatric palliative home care by general paediatricians: a multimethod study on perceived barriers and incentives.When to stop? Decision-making when children's cancer treatment is no longer curative: a mixed-method systematic review.Trends in the aggressiveness of end-of-life care for Korean pediatric cancer patients who died in 2007-2010.Patient involvement in informed consent for pediatric phase I cancer research.Absorbing information about a child's incurable cancer.Availability of palliative care services for children with cancer in economically diverse regions of the world.Factors that distinguish symptoms of most concern to parents from other symptoms of dying children.Differences in parent-provider concordance regarding prognosis and goals of care among children with advanced cancer.Long-term psychosocial outcomes among bereaved siblings of children with cancer Symptoms in children with advanced cancer: child and nurse reports Understanding bereavement: what every oncology practitioner should know.Communication about the risks and benefits of phase I pediatric oncology trials.Does emotional intelligence predict breaking bad news skills in pediatric interns? A pilot study Health Care Reform and Concurrent Curative Care for Terminally Ill Children: A Policy Analysis "I was able to still be her mom"--parenting at end of life in the pediatric intensive care unit Ensuring pain relief for children at the end of life.Considerations about hastening death among parents of children who die of cancer.Pediatric Oncology Palliative Care: Experiences of General Practitioners and Bereaved Parents Bereaved parents and siblings offer advice to health care providers and researchers.Conducting end-of-life studies in pediatric oncology.Challenges to participation in paediatric palliative care research: a review of the literature.Looking beyond where children die: determinants and effects of planning a child's location of death.Parents' views of cancer-directed therapy for children with no realistic chance for cure A Curriculum to Improve Residents' End-of-Life Communication and Pain Management Skills During Pediatrics Intensive Care Rotation: Pilot Study.Adherence to medication: A nation-wide study from the Children's Cancer Hospital, Egypt.The Development of a Pediatric Inpatient Experience of Care Measure: Child HCAHPS Symptom profiles in children with advanced cancer: Patient, family caregiver, and oncologist ratings.Trends in End-of-Life Care in Pediatric Hematology, Oncology, and Stem Cell Transplant Patients Palliative Care as a Standard of Care in Pediatric Oncology Palliative care in adolescents and young adults with cancer.Pediatric palliative care provision around the world: a systematic review.Parental perceptions of end-of-life care on paediatric intensive care units: a literature review.Parental decision making for children with cancer at the end of life: a meta-ethnography.Paediatric end-of-life care needs in Switzerland: current practices, and perspectives from parents and professionals. A study protocol.

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Parent and physician perspectives on quality of care at the end of life in children with cancer.

http://www.wikidata.org/entity/Q53279623

description

2005 nî lūn-bûn

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2005年学术文章

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2005年学术文章

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2005年學術文章

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Parent and physician perspecti ...... life in children with cancer.

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Parent and physician perspecti ...... life in children with cancer.

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Parent and physician perspecti ...... life in children with cancer.

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Parent and physician perspecti ...... life in children with cancer.

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Parent and physician perspecti ...... life in children with cancer.

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JCO.2005.04.010

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Journal of Clinical Oncology

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Parent and physician perspecti ...... life in children with cancer.

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Brian Turner

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Caron Moore

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Holcombe E Grier

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Jan Watterson

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Jane C Weeks

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Jennifer W Mack

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Joanne M Hilden

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Joanne Wolfe

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10.1200/JCO.2005.04.010

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2005-09-19T00:00:00Z

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quality of care