Communication about prognosis between parents and physicians of children with cancer: parent preferences and the impact of prognostic information.

@article{Mack2006CommunicationAP,
  title={Communication about prognosis between parents and physicians of children with cancer: parent preferences and the impact of prognostic information.},
  author={Jennifer W Mack and Joanne Wolfe and Holcombe E. Grier and Paul D. Cleary and Jane C. Weeks},
  journal={Journal of clinical oncology : official journal of the American Society of Clinical Oncology},
  year={2006},
  volume={24 33},
  pages={
          5265-70
        }
}
  • J. Mack, J. Wolfe, +2 authors J. Weeks
  • Published 20 November 2006
  • Medicine
  • Journal of clinical oncology : official journal of the American Society of Clinical Oncology
PURPOSE Concerns about the harms of prognostic information, including distress and loss of hope, cause some physicians to avoid frank disclosure. We aimed to determine parent preferences for prognostic information about their children with cancer and the results of receiving such information. PATIENTS AND METHODS We surveyed 194 parents of children with cancer (overall response rate, 70%), treated at the Dana-Farber Cancer Institute and Children's Hospital (Boston, MA) and the children's… 

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References

SHOWING 1-10 OF 57 REFERENCES
Understanding of prognosis among parents of children who died of cancer: impact on treatment goals and integration of palliative care.
TLDR
Considerable delay exists in parental recognition that children have no realistic chance for cure, but earlier recognition of this prognosis by both physicians and parents is associated with a stronger emphasis on treatment directed at lessening suffering and greater integration of palliative care.
Parent and physician perspectives on quality of care at the end of life in children with cancer.
  • J. Mack, J. Hilden, +5 authors J. Wolfe
  • Medicine
    Journal of clinical oncology : official journal of the American Society of Clinical Oncology
  • 2005
TLDR
For parents of children who die of cancer, doctor-patient communication is the principal determinant of high-quality physician care.
Cancer patient preferences for communication of prognosis in the metastatic setting.
TLDR
Most metastatic cancer patients want detailed prognostic information but prefer to negotiate the extent, format, and timing of the information they receive from their oncologists.
Preferences for Participation in Treatment Decision Making and Information Needs of Parents of Children With Cancer: A Pilot Study
TLDR
The results showed that parents had systematic preferences about TDM, preferring collaborative followed by passive and active roles, and that parents as a group do not have uniform information needs.
'Hitting You Over the Head': Oncologists' Disclosure of Prognosis to Advanced Cancer Patients
TLDR
Oncologists' reluctance to disclose prognosis and preserve patient hope are held in check by their need to ensure that patients have 'realistic expectations' about therapy, and ways to enhance the communication process are recommended.
The dynamics of change: cancer patients' preferences for information, involvement and support.
TLDR
Situational factors, such as change in disease status, may alter a patient's preferences for information and involvement, and it is needed to match the provision of information and support to the expressed needs of patients.
Prognostic Disclosure to Patients with Cancer near the End of Life
TLDR
To evaluate how often physicians favor communicating frank survival estimates to patients with terminal cancer who request them, a cohort of all patients with cancer admitted to five outpatient hospices in Chicago, Illinois, during 130 consecutive days in winter and spring 1996 is assembled.
Relationship between cancer patients' predictions of prognosis and their treatment preferences.
TLDR
Patients with metastatic colon and lung cancer overestimate their survival probabilities and these estimates may influence their preferences about medical therapies, according to patient and physician estimates of the probability of 6-month survival.
Parents' recollection of the initial communication of the diagnosis of cystic fibrosis.
TLDR
Parents learning the diagnosis of cystic fibrosis are receiving a kind of lecture, which contains more information than they can possibly assimilate, and impairment of early comprehension and retention of information about CF is unavoidable.
...
1
2
3
4
5
...