Literature DB >> 16529976

How satisfied are head and neck cancer (HNC) patients with the information they receive pre-treatment? Results from the satisfaction with cancer information profile (SCIP).

C D Llewellyn1, M McGurk, J Weinman.   

Abstract

Recent UK government recommendations state that high quality information must be provided for cancer patients. The objectives of this study were firstly, to explore how satisfied head and neck cancer (HNC) patients were with information provided about their illness and treatment, in order to identify areas of improvement. Secondly, to assess the extent to which satisfaction with information before treatment was predictive of long-term outcomes. Patients completed the satisfaction with information profile (SCIP), the Hospital Anxiety and Depression Scale (HADS) and the SF-12 Health Survey (SF-12v2) before treatment (n=82), 1 month after the end of treatment (n=68) and 6-8 months later (n=50). Patients were generally satisfied with information, however key areas of improvement were identified, such as the provision of information about support groups, where to go for financial advice and the long-term affects of treatment on ability to work, physical functioning and QoL. Satisfaction with information before treatment was predictive of depression and Mental Component Summary scores (HR-QoL) 6-8 months after the end of treatment. This study highlights the need for tailored information provision and the impact on longitudinal outcomes of satisfying patient's needs for information prior to treatment.

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Year:  2006        PMID: 16529976     DOI: 10.1016/j.oraloncology.2005.11.013

Source DB:  PubMed          Journal:  Oral Oncol        ISSN: 1368-8375            Impact factor:   5.337


  24 in total

1.  'What will I be like' after my diagnosis of head and neck cancer?

Authors:  S N Rogers; E S Hogg; W K A Cheung; L K L Lai; P Jassal; D Lowe; A Kanatas
Journal:  Eur Arch Otorhinolaryngol       Date:  2014-07-22       Impact factor: 2.503

2.  Satisfaction with information and unmet information needs in men and women with cancer.

Authors:  Hermann Faller; Uwe Koch; Elmar Brähler; Martin Härter; Monika Keller; Holger Schulz; Karl Wegscheider; Joachim Weis; Anna Boehncke; Bianca Hund; Katrin Reuter; Matthias Richard; Susanne Sehner; Carina Szalai; Hans-Ulrich Wittchen; Anja Mehnert
Journal:  J Cancer Surviv       Date:  2015-05-09       Impact factor: 4.442

3.  Satisfaction with information and its association with illness perception and quality of life in Indonesian breast cancer patients.

Authors:  Aulia Iskandarsyah; Cora de Klerk; Dradjat R Suardi; Monty P Soemitro; Sawitri S Sadarjoen; Jan Passchier
Journal:  Support Care Cancer       Date:  2013-06-18       Impact factor: 3.603

4.  The use of health related quality of life data to produce information sheets for patients with head and neck cancer.

Authors:  S N Rogers; E S Hogg; W K A Cheung; L K L Lai; P Jassal; D Lowe
Journal:  Ann R Coll Surg Engl       Date:  2015-07       Impact factor: 1.891

5.  Patient and staff assessment of an audiovisual education tool for head and neck radiation therapy.

Authors:  Lyndon Morley; Alison McAndrew; Karen Tse; Peter Rakaric; Bernard Cummings; Angela Cashell
Journal:  J Cancer Educ       Date:  2013-09       Impact factor: 2.037

Review 6.  The relation between information provision and health-related quality of life, anxiety and depression among cancer survivors: a systematic review.

Authors:  O Husson; F Mols; L V van de Poll-Franse
Journal:  Ann Oncol       Date:  2010-09-24       Impact factor: 32.976

7.  Patient experience of the acute post-surgical period following total laryngectomy during the COVID-19 era.

Authors:  Laura-Jayne Watson; David Hamilton; Joanne M Patterson
Journal:  Int J Lang Commun Disord       Date:  2022-04-11       Impact factor: 2.909

8.  Is the Satisfaction with Cancer Information Profile (SCIP) valid for tailoring information for patients with head and neck cancer?

Authors:  Matthew C Hankins; Carrie D Llewellyn
Journal:  BMC Cancer       Date:  2008-06-06       Impact factor: 4.430

9.  Psychological management for head and neck cancer patients: United Kingdom National Multidisciplinary Guidelines.

Authors:  G Humphris
Journal:  J Laryngol Otol       Date:  2016-05       Impact factor: 1.469

10.  Exploring experiences of cancer care in Wales: a thematic analysis of free-text responses to the 2013 Wales Cancer Patient Experience Survey (WCPES).

Authors:  Michael Bracher; Dame Jessica Corner; Richard Wagland
Journal:  BMJ Open       Date:  2016-09-02       Impact factor: 2.692

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