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Increasing numbers of cancer patients in recent years due to the improvement of diagnostic and therapeutic tools and the reduction of hospital days that transit patient care in short-term hospital structures has significantly increased their problems and informational needs. Providing cancer patients with the best possible information is consistently a point of concern for cancer nurses worldwide. Systematic, documented and personalized information is associated with a better understanding of the nature of the disease, an increase in patient autonomy, active participation in decision-making, compliance with the care plan, reduction of stress and improvement of patients’ quality of life. However, informational needs often remain unsatisfied across the disease trajectory, exacerbated by the fact that cancer patients seek and are entitled to more information. Factors that affect the adequacy of patients’ information are lack of structured information with the use of educational / informational material, lack of knowledge about the full picture of the disease complicated by cultural factors and the insufficient healthcare professionals’ training in communication techniques. Healthcare professionals, scientific societies, volunteer associations and other healthcare organizations, recognizing the contribution of information as a necessary element of the care plan, have contributed to its wider availability through publications, brochures, guidelines, websites, and other similar practices. The purpose of this article was to describe the most important sources of information available to healthcare professionals, patients and their families, as well as to describe the structures and services that support cancer patients.
|Κατηγορία:||Volume 60, N 1|
|Συγγραφείς:||Theocharis Ι. Konstantinidis , Ourania Govina|