2005
DOI: 10.1081/cnv-50482
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The Epidemiology of Cancer Pain

Abstract: We identified 28 epidemiological surveys by applying a sensitive search in Medline and CancerLit databases, supplemented by hand searches. Only two surveys enrolled more than 10,000 patients with cancer. The remaining were hospital or clinic-based surveys of at most a few hundred patients. Fourteen surveys were conducted in the United States. The majority of the remaining studies were conducted in Europe (Finland, France, Germany, UK/Ireland). No single survey identified a prevalence of any type of pain below … Show more

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Cited by 220 publications
(64 citation statements)
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“…In addition, the term "consultation service" is not used homogeneously in the context of the palliative care [2,16,17,22,23]. The distribution of diagnosed cancer entities and the high relevance of cancer pain we found is similar to what was reported in other studies [8,23,24], as were the recommendations that were made. However, we are unable to specify from our data whether and how the recommendations were implemented [25].…”
Section: Discussionsupporting
confidence: 75%
“…In addition, the term "consultation service" is not used homogeneously in the context of the palliative care [2,16,17,22,23]. The distribution of diagnosed cancer entities and the high relevance of cancer pain we found is similar to what was reported in other studies [8,23,24], as were the recommendations that were made. However, we are unable to specify from our data whether and how the recommendations were implemented [25].…”
Section: Discussionsupporting
confidence: 75%
“…Interventions at the end of life can also be helpful for both patients and their partners. We know that caregivers of patients in hospice experience high levels of distress (Haley, LaMonde, Han, Narramoer, & Schonwetter, 2001) and that patients sometimes experience uncontrolled pain (Goudas, Bloch, Gialeli‐Goudas, Lau, & Carr, 2005). A three‐session, in‐home intervention plus hospice care compared with hospice alone resulted in significant improvements in caregivers’ self‐efficacy for managing patient pain and other symptoms; however, patients did not report improvements in pain control or quality of life (Keefe et al., 2005).…”
Section: Cancermentioning
confidence: 99%
“…(2005) reported a moderate level of agreement for pain rated by patients with advanced cancer and by physicians during the last week of life. Pain is recognised as a substantial burden for patients with cancer (Goudas et al. 2005), and the definition of palliative care addresses the need for pain control at the end of life (EAPC 1998).…”
Section: Discussionmentioning
confidence: 99%