Literature DB >> 14681951

Prostate cancer patients' support and psychological care needs: Survey from a non-surgical oncology clinic.

Kathleen Lintz1, Clare Moynihan, Suzanne Steginga, Andy Norman, Ros Eeles, Robert Huddart, David Dearnaley, Maggie Watson.   

Abstract

While there are numerous uncertainties surrounding prostate cancer's detection and treatment, more research focusing on the psychological needs of prostate patients is required. This study investigated the support and psychological care needs of men with prostate cancer. Patients were approached during urological oncology clinics and asked to complete the: Support Care Needs Survey (SCNS), Support Care Preferences Questionnaire, EORTC QLQ-C30 (Version 3) Measure plus Prostate Module, and the Hospital Anxiety and Depression Scale (HADS). Of the 249 patients meeting study entry criteria, there was an 89% response rate resulting in a cohort of 210 patients. The data showed that significant unmet need exists across a number of domains in the areas of psychological and health system/information. The more commonly reported needs were 'fears about cancer spreading (44%),' 'concerns about the worries of those close to you (43%),' and 'changes in sexual feelings (41%).' Half of all patients reported some need in the domain of sexuality, especially men younger than 65 years. Needs were being well met in the domain of patient care and support. A significant number of patients reported having used or desiring support services, such as information about their illness, brochures about services and benefits for patients with cancer (55%), a series of talks by staff members about aspects of prostate cancer (44%), and one-on-one counselling (48%). Quality of life (QoL) was most negatively impacted in those who: were < or =65 years old, had been diagnosed within one year, or had metastatic disease. Men < or =65 had decreased social functioning, greater pain, increased sleep disturbance, and were more likely to be uncomfortable about being sexually intimate. Patients recently diagnosed had increased fatigue, more frequent urination, greater disturbance of sleep, and were more likely to have hot flushes. Those with advanced disease scored lower on 12 out of 15 QoL categories. PSA level had no effect on QoL or anxiety/depression scores. Men with advanced disease had greater levels of depression and those < or =65 years old were more likely to be anxious. Although most men with prostate cancer seem to function quite well, a substantial minority report areas of unmet need that may be targets for improving care. Copyright 2003 John Wiley & Sons, Ltd.

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Year:  2003        PMID: 14681951     DOI: 10.1002/pon.702

Source DB:  PubMed          Journal:  Psychooncology        ISSN: 1057-9249            Impact factor:   3.894


  67 in total

1.  Assessing longitudinal quality of life in prostate cancer patients and their spouses: a multilevel modeling approach.

Authors:  Lixin Song; Laurel L Northouse; Thomas M Braun; Lingling Zhang; Bernadine Cimprich; David L Ronis; Darlene W Mood
Journal:  Qual Life Res       Date:  2010-10-08       Impact factor: 4.147

Review 2.  The decision-related psychosocial concerns of men with localised prostate cancer: targets for intervention and research.

Authors:  Suzanne K Steginga; Emma Turner; Jenny Donovan
Journal:  World J Urol       Date:  2008-06-12       Impact factor: 4.226

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4.  Initial evaluation of the validity and reliability of the culturally adapted Spanish CaSUN (S-CaSUN).

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5.  The Effects of Social Support on Health-Related Quality of Life of Patients with Metastatic Prostate Cancer.

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Journal:  J Cancer Educ       Date:  2016-06       Impact factor: 2.037

6.  The EORTC Quality of Life Questionnaire for patients with prostate cancer: EORTC QLQ-PR25. Validation study for Spanish patients.

Authors:  J I Arraras; E Villafranca; F Arias de la Vega; P Romero; M Rico; M Vila; G Asín; V Chicata; M A Domínguez; N Lainez; A Manterola; E Martínez; M Martínez
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7.  The relationship of quality of life and distress in prostate cancer patients compared to the general population.

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8.  Determinants and implications of cancer patients' psychosocial needs.

Authors:  N Ernstmann; M Neumann; O Ommen; M Galushko; M Wirtz; R Voltz; M Hallek; H Pfaff
Journal:  Support Care Cancer       Date:  2009-03-13       Impact factor: 3.603

9.  Patient and clinician communication of self-reported insomnia during ambulatory cancer care clinic visits.

Authors:  Mary Lou Siefert; Fangxin Hong; Bianca Valcarce; Donna L Berry
Journal:  Cancer Nurs       Date:  2014 Mar-Apr       Impact factor: 2.592

10.  The effectiveness of the Screening Inventory of Psychosocial Problems (SIPP) in cancer patients treated with radiotherapy: design of a cluster randomised controlled trial.

Authors:  Anna P B M Braeken; Lilian Lechner; Francis C J M van Gils; Ruud M A Houben; Daniëlle Eekers; Ton Ambergen; Gertrudis I J M Kempen
Journal:  BMC Cancer       Date:  2009-06-09       Impact factor: 4.430

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