Abstract
Objective
Informing the child about his/her diagnosis and treatment plan is essential; research has shown that it is related to the patient's quality of life and adherence to medication.
Methods
For 7 months during 2008 (February – September), two study-specific questionnaires were constructed and administered to 304 parents of children diagnosed with cancer at the Children's Cancer Hospital, Egypt (CCHE).
Results
Among the 313 eligible parents of children diagnosed with cancer, 304 (97%) answered the first, and 281 (92%) answered the second questionnaire. We found that nearly three quarters (72%) of the parents had their child's cancer diagnosis communicated by the physician. Among the 72%, the rate of the children present with the parent or parents during the disease disclosure conversation was 39 percent (n = 85/219). The majority of the children were in the age group 5–18 years (55%).
Conclusions
Our findings indicate that cancer disclosure at the Children's Cancer Hospital is to a certain degree common, yet even when disclosure does take place; it is mainly in the absence of the child. Moreover, the information provided during the conversation may not be fully comprehended by the parent or the child due to the physician's misleading use of terms when disclosing the disease. Therefore, better practice should be developed for disease disclosure, and proper communication should be established between the patients and the provider; patient autonomy should also have an influence in the clinical practice.
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