"Trying to be a good parent" as defined by interviews with parents who made phase I, terminal care, and resuscitation decisions for their children.
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Establishing psychosocial palliative care standards for children and adolescents with cancer and their families: An integrative reviewAims and tasks in parental caregiving for children receiving palliative care at home: a qualitative study.The under reporting of recruitment strategies in research with children with life-threatening illnesses: A systematic reviewWhen to stop? Decision-making when children's cancer treatment is no longer curative: a mixed-method systematic review.Decision making by parents of children with incurable cancer who opt for enrollment on a phase I trial compared with choosing a do not resuscitate/terminal care optionThe development of an instrument that can identify children with palliative care needs: the Paediatric Palliative Screening Scale (PaPaS Scale): a qualitative study approach.Long-term psychosocial outcomes among bereaved siblings of children with cancerSpirituality in childhood cancer care.An emerging field of research: challenges in pediatric decision makingRegoaling: a conceptual model of how parents of children with serious illness change medical care goals.The parent perspective: "being a good parent" when making critical decisions in the PICU.Meaning making during parent-physician bereavement meetings after a child's death.Practical communication guidance to improve phase 1 informed consent conversations and decision-making in pediatric oncologyIntense parenting: a qualitative study detailing the experiences of parenting children with complex care needsChanges in siblings after the death of a child from cancer.Patient- and Family-Centered Care as an approach to reducing disparities in asthma outcomes in urban African American children: A review of the literature.Parent-clinician communication intervention during end-of-life decision making for children with incurable cancer."I was able to still be her mom"--parenting at end of life in the pediatric intensive care unitFamily Conferences in the Neonatal ICU: Observation of Communication Dynamics and ContributionsReceipt of Life-Sustaining Treatments for Taiwanese Pediatric Patients Who Died of Cancer in 2001 to 2010: A Retrospective Cohort Study.Good-parent beliefs of parents of seriously ill childrenParent's Perspectives on the End-of-life Care of their Child with Cancer: Indian Perspective.Problems and hopes perceived by mothers, fathers and physicians of children receiving palliative care.Parent perceptions of early prognostic encounters following children's severe traumatic brain injury: 'locked up in this cage of absolute horror'.Palliative Care as a Standard of Care in Pediatric OncologyUsing qualitative methods to evaluate a family behavioral intervention for type 1 diabetes.Pediatric palliative care-when quality of life becomes the main focus of treatment.Parental decision making for children with cancer at the end of life: a meta-ethnography.Palliative care for children with cancer.The complexity of consenting to clinical research in phase I pediatric cancer studies."Being a good patient" during times of illness as defined by adolescent patients with cancer.Paediatric end-of-life care needs in Switzerland: current practices, and perspectives from parents and professionals. A study protocol.Experiences of Pediatric Oncology Patients and Their Parents at End of Life: A Systematic Review.Pediatric advance care planning (pACP) for teens with cancer and their families: Design of a dyadic, longitudinal RCCT.Prognostic disclosures over time: Parental preferences and physician practices.Participation in a clinical trial for a child with cancer is burdensome for a minority of children.Why Do Parents Want to Know their Child's Carrier Status? A Qualitative Study.When health care professionals say "more" and parents say "enough"A randomized clinical trial of adolescents with HIV/AIDS: pediatric advance care planning.Parenting in the face of childhood life-threatening conditions: The ordinary in the context of the extraordinary.
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P2860
"Trying to be a good parent" as defined by interviews with parents who made phase I, terminal care, and resuscitation decisions for their children.
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on 05 October 2009
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
"Trying to be a good parent" a ...... decisions for their children.
@en
"Trying to be a good parent" a ...... decisions for their children.
@nl
type
label
"Trying to be a good parent" a ...... decisions for their children.
@en
"Trying to be a good parent" a ...... decisions for their children.
@nl
prefLabel
"Trying to be a good parent" a ...... decisions for their children.
@en
"Trying to be a good parent" a ...... decisions for their children.
@nl
P2093
P2860
P356
P1476
"Trying to be a good parent" a ...... decisions for their children.
@en
P2093
Brent Powell
Deo Kumar Srivastava
Joann Harper
Judy Hicks
Linda L Oakes
Nancy K West
Sheri L Spunt
Wayne L Furman
P2860
P304
P356
10.1200/JCO.2008.20.0204
P407
P577
2009-10-05T00:00:00Z