European Journal of Cancer Supplements · 2014 · 236 citations · 51 references
NursingOncologyCancer Survivorship CareCancer Symptom ManagementSelf-management SupportCancer SurvivorshipPsychosocial RehabilitationSupportive Care In CancerSurvivorship Care PlanningSymptom ManagementSymptom ReportingCancer-related Psychological DistressPopulation Cancer RegistriesPsychological Symptom DistressPsychosocial TreatmentSurvivorshipSurvivorship Quality Of LifeSurvivorship Symptom ManagementTransition From Treatment To Survivorship
The number of cancer survivors has increased steadily, yet they continue to face disease‑ and treatment‑related problems. This paper reviews key physical and psychosocial health issues in cancer survivors, including pain, fatigue, distress, and work participation, and discusses self‑management, e‑Health, lifestyle promotion, HRQoL assessment, and registry use. The authors synthesize current evidence and outline strategies for self‑management, e‑Health interventions, lifestyle promotion, HRQoL assessment, and registry‑based research to guide practice. Key findings emphasize that symptoms cluster interdependently, interventions should be evidence‑based and tailored, low‑cost self‑management and e‑Health approaches are suitable for most survivors, and greater focus is needed on dissemination, cost‑effectiveness, and vulnerable groups.
The population of cancer survivors has grown steadily over the past several decades. Surviving cancer, however, is not synonymous with a life free of problems related to the disease and its treatment. In this paper we provide a brief overview of selected physical and psychosocial health problems prevalent among cancer survivors, namely pain, fatigue, psychological distress and work participation. We also address issues surrounding self-management and e-Health interventions for cancer survivors, and programmes to encourage survivors to adopt healthier lifestyles. Finally, we discuss approaches to assessing health-related quality of life in cancer survivors, and the use of cancer registries in conducting psychosocial survivorship research. We highlight research and practice priorities in each of these areas. While the priorities vary per topic, common themes that emerged included: (1) Symptoms should not be viewed in isolation, but rather as part of a cluster of interrelated symptoms. This has implications for both understanding the aetiology of symptoms and for their treatment; (2) Psychosocial interventions need to be evidence-based, and where possible should be tailored to the needs of the individual cancer survivor. Relatively low cost interventions with self-management and e-Health elements may be appropriate for the majority of survivors, with resource intensive interventions being reserved for those most in need; (3) More effort should be devoted to disseminating and implementing interventions in practice, and to evaluating their cost-effectiveness; and (4) Greater attention should be paid to the needs of vulnerable and high-risk populations of survivors, including the socioeconomically disadvantaged and the elderly.
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N.K. Aaronson, Sam H. Ahmedzai, Bengt Bergman et al. · JNCI Journal of the National Cancer Institute · 1993 · 16K citations
The Patient-Reported Outcomes Measurement Information System (PROMIS)
David Cella, Susan Yount, Nan Rothrock et al. · Medical Care · 2007 · 3.1K citations
Pharmacy, Health Services Administration, Health Assessment +16