Literature DB >> 22265127

The Catalonia World Health Organization demonstration project for palliative care implementation: quantitative and qualitative results at 20 years.

Xavier Gómez-Batiste1, Carmen Caja, Jose Espinosa, Ingrid Bullich, Marisa Martínez-Muñoz, Josep Porta-Sales, Jordi Trelis, Joaquim Esperalba, Jan Stjernsward.   

Abstract

Catalonia (Spain) has a total population of 7.3 million citizens for whom the National Health Service (NHS) provides health care that is free at the point of access. The prevalence of terminally ill patients is between 30,100 and 39,600. Twenty years ago, the World Health Organization (WHO), in collaboration with the Catalan Department of Health and the Catalan Institute of Oncology, began a demonstration project (WHO Demonstration Project) in palliative care (PC) with the aim of implementing specialist PC services, generating experience in this field, identifying areas for improvement, and introducing educative procedures (clinical and nonclinical). Over the past 20 years, 237 PC clinical services (72 home care support teams, 49 hospital support teams, 60 units with 742 dedicated beds, 50 outpatient clinics, and six psychosocial support teams) have been implemented. In the five years since the previous evaluation, 57 new clinical services (15 new hospital support teams, 36 outpatient clinics, and six psychosocial support teams among others) and four nonclinical services (education, research, WHO Collaborating Center, and planning) have been implemented. During the year 2010, a total of 46,200 processes were undertaken for the care of 23,100 patients, of whom 12,100 (52%) had cancer and 11,000 (48%) had other chronic advanced diseases. The overall yearly costs are around €52,568,000, with an overall savings of €69,300,000 (€2275 per patient, net savings to the NHS of €16,732,000). In the last five years, three qualitative evaluations and a benchmarking process have been performed to identify weak points and inequities in care provision among districts. Systematic assessments indicate high cost-effectiveness of care as well as high levels of satisfaction by patients and their relatives, thus reinforcing the principle that access to PC under the auspices of the NHS at the end of life is a basic human right.
Copyright © 2012 U.S. Cancer Pain Relief Committee. Published by Elsevier Inc. All rights reserved.

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Year:  2012        PMID: 22265127     DOI: 10.1016/j.jpainsymman.2011.05.006

Source DB:  PubMed          Journal:  J Pain Symptom Manage        ISSN: 0885-3924            Impact factor:   3.612


  13 in total

Review 1.  Palliative Care for the Seriously Ill.

Authors:  Amy S Kelley; R Sean Morrison
Journal:  N Engl J Med       Date:  2015-08-20       Impact factor: 91.245

2.  Palliative care team visits. Qualitative study through participant observation.

Authors:  Maria Del Mar Alfaya Góngora; Maria José Bueno Pernias; César Hueso Montoro; Plácido Guardia Mancilla; Rafael Montoya Juárez; Maria Paz García Caro
Journal:  Colomb Med (Cali)       Date:  2016-03-30

3.  Does a regional comprehensive palliative care program improve pain in outpatient cancer patients?

Authors:  Tatsuya Morita; Kazuki Sato; Mitsunori Miyashita; Akemi Yamagishi; Yoshiyuki Kizawa; Yasuo Shima; Hiroya Kinoshita; Satoshi Suzuki; Yutaka Shirahige; Takuhiro Yamaguchi; Kenji Eguchi
Journal:  Support Care Cancer       Date:  2014-04-05       Impact factor: 3.603

4.  Questions and answers on the Belgian model of integral end-of-life care: experiment? Prototype? : "Eu-euthanasia": the close historical, and evidently synergistic, relationship between palliative care and euthanasia in Belgium: an interview with a doctor involved in the early development of both and two of his successors.

Authors:  Jan L Bernheim; Wim Distelmans; Arsène Mullie; Michael A Ashby
Journal:  J Bioeth Inq       Date:  2014-08-16       Impact factor: 1.352

Review 5.  Integrated palliative care in the Spanish context: a systematic review of the literature.

Authors:  Eduardo Garralda; Jeroen Hasselaar; José Miguel Carrasco; Karen Van Beek; Naouma Siouta; Agnes Csikos; Johan Menten; Carlos Centeno
Journal:  BMC Palliat Care       Date:  2016-05-13       Impact factor: 3.234

6.  Trends of Do-Not-Resuscitate consent and hospice care utilization among noncancer decedents in a tertiary hospital in Taiwan between 2010 and 2014: A Hospital-based observational study.

Authors:  Hsiao-Ting Chang; Ming-Hwai Lin; Chun-Ku Chen; Pesus Chou; Tzeng-Ji Chen; Shinn-Jang Hwang
Journal:  Medicine (Baltimore)       Date:  2016-11       Impact factor: 1.889

7.  The Impact of Hospice Care on Survival and Healthcare Costs for Patients with Lung Cancer: A National Longitudinal Population-Based Study in Taiwan.

Authors:  Jui-Kun Chiang; Yee-Hsin Kao; Ning-Sheng Lai
Journal:  PLoS One       Date:  2015-09-25       Impact factor: 3.240

8.  PROLONG: a cluster controlled trial to examine identification of patients with COPD with poor prognosis and implementation of proactive palliative care.

Authors:  Ria G Duenk; Yvonne Heijdra; Stans C Verhagen; Richard P N R Dekhuijzen; Kris C P Vissers; Yvonne Engels
Journal:  BMC Pulm Med       Date:  2014-04-02       Impact factor: 3.317

9.  Case conferences between general practitioners and specialist teams to plan end of life care of people with end stage heart failure and lung disease: an exploratory pilot study.

Authors:  Geoffrey Mitchell; Jianzhen Zhang; Letitia Burridge; Hugh Senior; Elizabeth Miller; Sharleen Young; Maria Donald; Claire Jackson
Journal:  BMC Palliat Care       Date:  2014-05-05       Impact factor: 3.234

10.  Implementing the first regional hospice palliative care program in Ontario: the Champlain region as a case study.

Authors:  José Pereira; Jocelyne Contant; Gwen Barton; Christopher Klinger
Journal:  BMC Palliat Care       Date:  2016-07-26       Impact factor: 3.234

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