Literature DB >> 23678854

Effectiveness of a specialized outpatient palliative care service as experienced by patients and caregivers.

Gesa Groh1, Birgit Vyhnalek, Berend Feddersen, Monika Führer, Gian Domenico Borasio.   

Abstract

OBJECTIVES: In Germany since 2007 patients with advanced life-limiting diseases are eligible for Specialized Outpatient Palliative Care (SOPC). To provide this service, SOPC teams have been established as a new facility in the health care system. The objective of this study was to evaluate the effectiveness of one of the first SOPC teams based at the Munich University Hospital.
METHODS: All patients treated by the SOPC team and their primary caregivers were eligible for this prospective nonrandomized study. The main topics of the surveys before and after involvement of the SOPC team were: for patients, the assessment of symptom burden (Minimal Documentation System for Palliative Medicine, MIDOS), satisfaction with quality of palliative care (Palliative Outcome Scale, POS), and quality of life (McGill Quality of Life Questionnaire, MQOL); for caregivers, burden of care (Häusliche Pflegeskala, home care scale, HPS), anxiety and depression (Hospital Anxiety and Depression Scale, HADS), and quality of life (Quality of Life in Life-Threatening Illness-Family Carer Version, QOLLTI-F).
RESULTS: Of 100 patients treated between April and November 2011, 60 were included in the study (median age 67.5 years, 55% male, 87% oncological diseases). In 23 of 60 patients, only caregivers could be interviewed. The median interval between the first and second interview was 2.5 weeks. Quality of life increased significantly in patients (p<0.05) and caregivers (p<0.001), as did the patients' perception of quality of palliative care (POS, p<0.001), while the caregivers' psychological distress and burden of care significantly decreased (HADS, p<0.001; HPS, p<0.001).
CONCLUSIONS: The involvement of an SOPC team leads to a significant improvement in the quality of life of patients and caregivers and can lower the burden of home care for the caregivers of severely ill patients.

Entities:  

Mesh:

Year:  2013        PMID: 23678854     DOI: 10.1089/jpm.2012.0491

Source DB:  PubMed          Journal:  J Palliat Med        ISSN: 1557-7740            Impact factor:   2.947


  19 in total

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Journal:  J Pain Symptom Manage       Date:  2018-02-08       Impact factor: 3.612

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5.  Specialized home palliative care for adults and children: differences and similarities.

Authors:  Gesa Groh; Berend Feddersen; Monika Führer; Gian Domenico Borasio
Journal:  J Palliat Med       Date:  2014-06-13       Impact factor: 2.947

6.  Improving patient knowledge of palliative care: A randomized controlled intervention study.

Authors:  Elissa Kozlov; M Carrington Reid; Brian D Carpenter
Journal:  Patient Educ Couns       Date:  2016-12-21

7.  Illness and end-of-life experiences of children with cancer who receive palliative care.

Authors:  Erica C Kaye; Courtney A Gushue; Samantha DeMarsh; Jonathan Jerkins; April Sykes; Zhaohua Lu; Jennifer M Snaman; Lindsay Blazin; Liza-Marie Johnson; Deena R Levine; R Ray Morrison; Justin N Baker
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8.  A multicountry assessment in Eurasia: Alignment of physician perspectives on palliative care integration in pediatric oncology with World Health Organization guidelines.

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Review 9.  The Palliative Outcome Scale (POS) applied to clinical practice and research: an integrative review.

Authors:  Fernanda Capella Rugno; Marysia Mara Rodrigues do Prado De Carlo
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10.  Defining the Boundaries of Palliative Care in Pediatric Oncology.

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Journal:  J Pain Symptom Manage       Date:  2019-12-12       Impact factor: 3.612

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