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Medical and psychosocial challenges in caring for adolescent and young adult patients with cancer

机译:照顾青少年和年轻成人癌症患者的医学和社会心理挑战

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Over the last five years there have been tremendous changes in the care of adolescent and young adult cancer patients in Australia, generally accepted as 15-25 years old. There has been recognition that the needs of adolescent and young adults with cancer are different from both adults and younger children, and warrant specialised services. A cancer diagnosis during this period of transition has the potential to significantly impact upon many areas of normal development including physical, psychological, social, sexual, educational and financial domains. Relatively little is known about the basic biology, genetic, epidemiologic, therapeutic and economic factors that affect incidence, disease outcomes and cancer related quality of life in this population. This paper explores the medical and psychosocial needs for these patients and summarises the recent progress of the Youth Cancer program in Australia, which has led to the development of this new subspeciality and the creation of youth cancer services.
机译:在过去的五年中,澳大利亚的青少年和成年癌症患者的护理发生了巨大变化,通常被认为是15-25岁。已经认识到,青少年和年轻人患癌症的需要与成年人和年幼的孩子都不同,因此需要专门的服务。在这一过渡时期的癌症诊断可能会严重影响正常发展的许多领域,包括身体,心理,社会,性,教育和经济领域。对于影响该人群的发病率,疾病结局和癌症相关生活质量的基本生物学,遗传,流行病学,治疗和经济因素知之甚少。本文探讨了这些患者的医疗和心理需求,并总结了澳大利亚青年癌症计划的最新进展,该计划导致了这一新的专业发展,并创建了青年癌症服务。

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