Literature DB >> 16438812

Palliative care in primary care: a study to determine whether patients and professionals agree on symptoms.

Gail Ewing1, Margaret Rogers, Stephen Barclay, Janet McCabe, Anna Martin, Malcolm Campbell, Chris Todd.   

Abstract

BACKGROUND: Difficulties in managing symptoms of palliative care patients at home have been identified, yet there has been no investigation of agreement on symptom assessment in primary care. Lack of agreement between patients' and primary care professionals' symptom assessments may be contributing to difficulties in symptom control. AIM: To investigate agreement on symptom assessments between patients at home and GPs and district nurses. DESIGN OF STUDY: Prospective, self-completed, structured symptom assessments.
SETTING: Routine contacts with adult palliative care patients estimated to be in their last year of life.
METHOD: Patient and professional symptom assessments were obtained using CAMPAS-R, a comprehensive and reliable measure validated for palliative care in the community. Prevalence of reported symptoms was calculated in patient-professional pairs. Intraclass correlation techniques (ICCs) and percentage agreement were used to determine how well symptom assessments of patients and professionals agreed.
RESULTS: Anxiety and depression were significantly more likely to be reported by professionals, and GPs over-identified nausea, vomiting and constipation. Professionals assessed emotional symptoms as more severe than patients. Agreement on scoring of physical symptoms was better, although this was at least partially due to agreement on absence of symptoms. Unlike previous reports, pain scores recorded by doctors in this study, were not significantly different from patients.
CONCLUSION: This quick and easy to complete assessment tool, CAMPAS-R, has potential for monitoring quality of palliative care symptom control at home.

Entities:  

Mesh:

Year:  2006        PMID: 16438812      PMCID: PMC1821417     

Source DB:  PubMed          Journal:  Br J Gen Pract        ISSN: 0960-1643            Impact factor:   5.386


  33 in total

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Journal:  Soc Sci Med       Date:  2003-01       Impact factor: 4.634

6.  Correlation of patient and caregiver ratings of cancer pain.

Authors:  S A Grossman; V R Sheidler; K Swedeen; J Mucenski; S Piantadosi
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7.  Symptomatology of cancer patients in palliative care: content validation of self-assessment questionnaires against medical records.

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8.  Pain and its treatment in outpatients with metastatic cancer.

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9.  Multicentre study of cancer pain and its treatment in France.

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10.  Palliative care at home: an audit of cancer deaths in Grampian region.

Authors:  D G Millar; D Carroll; J Grimshaw; B Watt
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  10 in total

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3.  Quality of life: what does it mean for general practice?

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Review 4.  The psychometric properties of cancer multisymptom assessment instruments: a clinical review.

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5.  Association between patient-reported symptoms and nurses' clinical impressions in cancer patients admitted to an acute palliative care unit.

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6.  Impact of tracheostomy placement on anxiety in mechanically ventilated adult ICU patients.

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7.  Health care providers underestimate symptom intensities of cancer patients: a multicenter European study.

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8.  Clinical effectiveness of online training in palliative care of primary care physicians.

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9.  Is breathlessness what the professional says it is? Analysis of patient and professionals' assessments from a German nationwide register.

Authors:  Steffen T Simon; Nadine Altfelder; Bernd Alt-Epping; Claudia Bausewein; Vera Weingärtner; Raymond Voltz; Christoph Ostgathe; Lukas Radbruch; Gabriele Lindena; Friedemann Nauck
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10.  Provider Perceptions of Quality of Life, Neurocognition, Physical Well-being, and Psychosocial Health in Patients with Primary Immunodeficiency/Immune Dysregulation Conditions.

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  10 in total

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