What we don't know about how we decide

Virtual Mentor

Volumn 12, Issue 7, 2010, Pages 586-589

  Feudtner, Chris ^a,b  

^a CHILDREN S HOSPITAL OF PHILADELPHIA   (United States)

^b UNIVERSITY OF PENNSYLVANIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 84891363056     PISSN: 19377010     EISSN: None     Source Type: Journal    
DOI: 10.1001/virtualmentor.2010.12.7.oped1-1007     Document Type: Article

References (8)

1. National Institutes of Health. Regulations and ethical guidelines. http://ohsr.od.nih.gov/guidelines/index.html. Accessed May 24, 2010.
2. Rapoport A. Addressing ethical concerns regarding pediatric palliative care research. Arch Pediatr Adolesc Med. 2009;163(8):688-691.
3. Dickinson HO, Parkinson KN, Ravens-Sieberer U, et al. Self-reported quality of life of 8-12-year-old children with cerebral palsy: a cross-sectional European study. Lancet. 2007;369(9580):2171-2178.
4. Westgren N, Levi R. Quality of life and traumatic spinal cord injury. Arch Phys Med Rehabil. 1998;79(11):1433-1439.
5. Beauchamp TL, Childress JF. Principles of Biomedical Ethics. 5th ed. New York, NY: Oxford University Press; 2001.
6. Ross LF. Children, Families, and Health Care Decision Making. Oxford: Oxford University Press; 1998.
7. Towle A, Godolphin W. Framework for teaching and learning informed shared decision making. BMJ. 1999;319(7212):766-771.
8. Robinson A, Thomson R. Variability in patient preferences for participating in medical decision making: implication for the use of decision support tools. Qual Health Care. 2001;10 Suppl 1:i34-i38.