Cargando…
Patient satisfaction with GP-led melanoma follow-up: a randomised controlled trial
BACKGROUND: There are no universally accepted guidelines for the follow-up of individuals with cutaneous melanoma. Furthermore, to date, there have been no randomised controlled trials of different models of melanoma follow-up care. This randomised controlled trial was conducted to evaluate the effe...
Autores principales: | , , , , , |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2010
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2869159/ https://www.ncbi.nlm.nih.gov/pubmed/20461089 http://dx.doi.org/10.1038/sj.bjc.6605638 |
_version_ | 1782181097232138240 |
---|---|
author | Murchie, P Nicolson, M C Hannaford, P C Raja, E A Lee, A J Campbell, N C |
author_facet | Murchie, P Nicolson, M C Hannaford, P C Raja, E A Lee, A J Campbell, N C |
author_sort | Murchie, P |
collection | PubMed |
description | BACKGROUND: There are no universally accepted guidelines for the follow-up of individuals with cutaneous melanoma. Furthermore, to date, there have been no randomised controlled trials of different models of melanoma follow-up care. This randomised controlled trial was conducted to evaluate the effects of GP-led melanoma follow-up on patient satisfaction, follow-up guideline compliance, anxiety and depression, as well as health status. METHODS: A randomised controlled trial of GP-led follow-up of cutaneous melanoma was conducted over a period of 1 year with assessment by self-completed questionnaires and review of general practice-held medical records at baseline and 12 months later. It took place in 35 general practices in North-east Scotland. Subjects were 142 individuals (51.4% women 48.6% men; mean (s.d.) age 59.2 (15.2) years previously treated for cutaneous melanoma and free of recurrent disease. The intervention consisted of protocol-driven melanoma reviews in primary care, conducted by trained GPs and supported by centralised recall, rapid access pathway to secondary care and a patient information booklet. The main outcome measure was patient satisfaction measured by questionnaire. Secondary outcomes were adherence to guidelines, health status measured by Short Form-36 and the Hospital Anxiety and Depression Scale. RESULTS: There were significant improvements in 5 out of 15 aspects of patient satisfaction during the study year in those receiving GP-led melanoma follow-up (all P⩽0.01). The intervention group was significantly more satisfied with 7 out of 15 aspects of care at follow-up after adjustment for potential confounders. There was significantly greater adherence to guidelines in the intervention group during the study year. There was no significant difference in health status or anxiety and depression between intervention and control groups at either baseline or outcome. CONCLUSIONS: GP-led follow-up is feasible, engenders greater satisfaction in those patients who receive it, permits closer adherence to guidelines and does not result in adverse effects on health status or anxiety and depression when compared with traditional hospital-based follow-up for melanoma. |
format | Text |
id | pubmed-2869159 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-28691592011-05-11 Patient satisfaction with GP-led melanoma follow-up: a randomised controlled trial Murchie, P Nicolson, M C Hannaford, P C Raja, E A Lee, A J Campbell, N C Br J Cancer Clinical Study BACKGROUND: There are no universally accepted guidelines for the follow-up of individuals with cutaneous melanoma. Furthermore, to date, there have been no randomised controlled trials of different models of melanoma follow-up care. This randomised controlled trial was conducted to evaluate the effects of GP-led melanoma follow-up on patient satisfaction, follow-up guideline compliance, anxiety and depression, as well as health status. METHODS: A randomised controlled trial of GP-led follow-up of cutaneous melanoma was conducted over a period of 1 year with assessment by self-completed questionnaires and review of general practice-held medical records at baseline and 12 months later. It took place in 35 general practices in North-east Scotland. Subjects were 142 individuals (51.4% women 48.6% men; mean (s.d.) age 59.2 (15.2) years previously treated for cutaneous melanoma and free of recurrent disease. The intervention consisted of protocol-driven melanoma reviews in primary care, conducted by trained GPs and supported by centralised recall, rapid access pathway to secondary care and a patient information booklet. The main outcome measure was patient satisfaction measured by questionnaire. Secondary outcomes were adherence to guidelines, health status measured by Short Form-36 and the Hospital Anxiety and Depression Scale. RESULTS: There were significant improvements in 5 out of 15 aspects of patient satisfaction during the study year in those receiving GP-led melanoma follow-up (all P⩽0.01). The intervention group was significantly more satisfied with 7 out of 15 aspects of care at follow-up after adjustment for potential confounders. There was significantly greater adherence to guidelines in the intervention group during the study year. There was no significant difference in health status or anxiety and depression between intervention and control groups at either baseline or outcome. CONCLUSIONS: GP-led follow-up is feasible, engenders greater satisfaction in those patients who receive it, permits closer adherence to guidelines and does not result in adverse effects on health status or anxiety and depression when compared with traditional hospital-based follow-up for melanoma. Nature Publishing Group 2010-05-11 2010-05-11 /pmc/articles/PMC2869159/ /pubmed/20461089 http://dx.doi.org/10.1038/sj.bjc.6605638 Text en Copyright © 2010 Cancer Research UK https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material.If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Clinical Study Murchie, P Nicolson, M C Hannaford, P C Raja, E A Lee, A J Campbell, N C Patient satisfaction with GP-led melanoma follow-up: a randomised controlled trial |
title | Patient satisfaction with GP-led melanoma follow-up: a randomised controlled trial |
title_full | Patient satisfaction with GP-led melanoma follow-up: a randomised controlled trial |
title_fullStr | Patient satisfaction with GP-led melanoma follow-up: a randomised controlled trial |
title_full_unstemmed | Patient satisfaction with GP-led melanoma follow-up: a randomised controlled trial |
title_short | Patient satisfaction with GP-led melanoma follow-up: a randomised controlled trial |
title_sort | patient satisfaction with gp-led melanoma follow-up: a randomised controlled trial |
topic | Clinical Study |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2869159/ https://www.ncbi.nlm.nih.gov/pubmed/20461089 http://dx.doi.org/10.1038/sj.bjc.6605638 |
work_keys_str_mv | AT murchiep patientsatisfactionwithgpledmelanomafollowuparandomisedcontrolledtrial AT nicolsonmc patientsatisfactionwithgpledmelanomafollowuparandomisedcontrolledtrial AT hannafordpc patientsatisfactionwithgpledmelanomafollowuparandomisedcontrolledtrial AT rajaea patientsatisfactionwithgpledmelanomafollowuparandomisedcontrolledtrial AT leeaj patientsatisfactionwithgpledmelanomafollowuparandomisedcontrolledtrial AT campbellnc patientsatisfactionwithgpledmelanomafollowuparandomisedcontrolledtrial |