Medication risk communication with cancer patients in a Middle East cancer care setting
- PMID: 27175061
- PMCID: PMC4854243
- DOI: 10.2147/PPA.S99718
Medication risk communication with cancer patients in a Middle East cancer care setting
Abstract
Purpose: Cancer treatments are frequently associated with adverse effects, but there may be a cultural reluctance by care providers to be forthcoming with patients regarding these risks for fear of promoting nonadherence. Conversely, research in a number of countries indicates high levels of patient desire for this information. We sought to explore cancer patient experiences, satisfaction, and preferences for medication risk communication in a Middle East care setting.
Methods: We developed and administered a ten-item questionnaire (Arabic and English) to a convenience sample of consenting adult patients receiving treatment at the National Center for Cancer Care and Research in Qatar.
Results: One hundred and forty-three patients were interviewed. Most (88%) stated that the level of side effect information they received was sufficient, with physicians (86%) followed by pharmacists (39%) as the preferred sources. The majority (97%) agreed that knowing about possible side effects would help them recognize and manage the reaction, and 92% agreed that it would help them understand how to minimize or prevent the risks. Eighteen percent indicated that this information would make them not want to take treatment. Two-thirds (65%) had previously experienced intolerance to their cancer treatment regimen.
Conclusion: Most patients surveyed expressed preference for the details of possible side effects they may encounter in their treatment. However, one in five considered such information a factor for nonadherence, indicating the need for patient-specific approaches when communicating medication risks.
Keywords: Middle East; cancer treatment; risk communication.
Figures
References
-
- Belvedere O, Minisini A, Ramello M, Sobrero A, Grossi F. Information given to cancer patients on diagnosis, prognosis and treatment: the clinical oncologist’s perspective. Eur J Cancer. 2004;40(12):1850–1854. - PubMed
-
- Mallinger JB, Griggs JJ, Shields CG. Patient-centered care and breast cancer survivors’satisfaction with information. Patient Educ Couns. 2005;57(3):342–349. - PubMed
-
- Haris KA. The informational needs of patients with cancer and their families. Cancer Pract. 1998;6(1):39–46. - PubMed
LinkOut - more resources
Full Text Sources
Other Literature Sources
