2020
DOI: 10.1016/j.euf.2019.10.014
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Distress and Quality of Life Among Patients with Advanced Genitourinary Cancers

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Cited by 14 publications
(7 citation statements)
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“…An elevated risk of suicide in patients with sensory impairment [13] and some cancers, especially in the first 6 months after diagnosis of malignancy, is well documented [14]. Furthermore, the prevalence of distress and impairment of quality of life have been highlighted in many types of cancer [15]. In Oregon and Washington, most patients who used assisted suicide had cancer or terminal illnesses leading to loss of autonomy, dignity and quality of life [16].…”
Section: Discussionmentioning
confidence: 99%
“…An elevated risk of suicide in patients with sensory impairment [13] and some cancers, especially in the first 6 months after diagnosis of malignancy, is well documented [14]. Furthermore, the prevalence of distress and impairment of quality of life have been highlighted in many types of cancer [15]. In Oregon and Washington, most patients who used assisted suicide had cancer or terminal illnesses leading to loss of autonomy, dignity and quality of life [16].…”
Section: Discussionmentioning
confidence: 99%
“…Ho et al further considered fatigue as a potential intervention target because fatigue may lead to depression (19). A mini-review reported that the prevalence of distress among patients with renal, bladder and prostate cancer were 20%, 12% and 30%, respectively (20). Another study found that the prevalence of depression, anxiety and post-traumatic stress disorder among patients with newly diagnosed bladder or renal cancer was 77.5%, 69.3% and 25.2%, respectively (21).…”
Section: Discussionmentioning
confidence: 99%
“…[11] Outpatients with H&N cancer in the Netherlands reported satisfaction with their nurse's knowledge and attention to concerns when a distress screening and follow-up intervention was implemented, [8] and evidence supports promoting screening and psychosocial interventions among patients with urological cancers. [12] Furthermore, Riedl et al [7] observed that oncology patients were more likely to engage in screening if the results of said screening were then incorporated into their individual care plan. Indeed, it has become well recognized that, on its own, distress screening is not effective in achieving truly patient-centred care; patients need their HCPs to be supported and upskilled to address their distress scores with them, then further assess, assist, and refer for evidence-based care where indicated.…”
Section: Introductionmentioning
confidence: 99%
“…The screening process is perceived to be highly acceptable, helpful in facilitating communication about patient issues, increasing awareness of the assistance available, and enhancing clinician-patient rapport [11] . Outpatients with H&N cancer in the Netherlands reported satisfaction with their nurse's knowledge and attention to concerns when a distress screening and follow-up intervention was implemented, [8] and evidence supports promoting screening and psychosocial interventions among patients with urological cancers [12] . Furthermore, Riedl et al [7] observed that oncology patients were more likely to engage in screening if the results of said screening were then incorporated into their individual care plan.…”
Section: Introductionmentioning
confidence: 99%