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Caring for the Child With Cancer at the Close of Life
Amy J. Markowitz, JD;
Stephen J. McPhee, MD
JAMA. 2005;293:1382.
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| Since this article does not have an abstract, we have provided the first 150 words of the full text and any section headings. |
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On November 3, 2004, Drs Hurwitz, Duncan, Wolfe,1 introduced Frank, a 13-year-old with acute lymphoblastic leukemia (ALL), his mother, and Dr L, his oncologist. Frank had been diagnosed about 4 years prior to his interview in August 2003. Although approximately 25% of children with cancer ultimately die of their disease, the authors note that in the early course of a patients illness, it is often impossible to determine whether the disease will be cured by cancer-directed treatment. If it becomes apparent that there are no longer any options for potentially curative therapy, the patient, family, and oncology team face enormous medical, psychological, and spiritual challenges. Optimal palliative care for children requires that the physician and caregiving team engage the patient and family in discussions of their hopes and fears and provide solace and support for emotional and physical pain.
For 7 weeks . . . [Full Text of this Article]
THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES
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An Official American Thoracic Society Clinical Policy Statement: Palliative Care for Patients with Respiratory Diseases and Critical Illnesses
Lanken et al.
Am. J. Respir. Crit. Care Med. 2008;177:912-927.
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