4 results on '"hospice team"'
Search Results
2. Exploring Oral Literacy in Communication With Hospice Caregivers.
- Author
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Wittenberg-Lyles, Elaine, Goldsmith, Joy, Oliver, Debra Parker, Demiris, George, Kruse, Robin L., and Van Stee, Stephanie
- Subjects
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ORAL communication , *LITERACY , *HOSPICE care , *CAREGIVERS , *ANXIETY , *QUALITY of life - Abstract
Abstract: Context: Low oral literacy has been identified as a barrier to pain management for informal caregivers who receive verbal instructions on pain medication and pain protocols. Objectives: To examine recorded communication between hospice staff and informal caregivers and explore caregiver experiences. Methods: Using transcripts of interactions (n = 47), oral literacy features were analyzed by examining the generalized language complexity using the Flesch-Kincaid grading scale and the dialogue interactivity defined by talking turns and interaction time. Means for longitudinal follow-up measures on caregiver anxiety, quality of life, perception of pain management, knowledge and comfort providing pain medication, and satisfaction were examined to explore their relationship to oral literacy. Results: Communication between team members and caregivers averaged a fourth-grade level on the Flesch-Kincaid scale, indicating that communication was easy to understand. Reading ease was associated (r = 0.67, P < 0.05) with caregiver understanding of and comfort with pain management. Perceived barriers to caregiver pain management were lower when sessions had increased use of passive sentences (r = 0.61, P < 0.01), suggesting that passive voice was not an accurate indicator of language complexity. Caregiver understanding and comfort with administering pain medications (r = −0.82, P < 0.01) and caregiver quality of life (r = −0.49, P < 0.05) were negatively correlated with dialogue pace. Conclusion: As the grade level of talk with caregivers and hospice teams increased, associated caregiver anxiety increased. Caregivers with higher anxiety also experienced greater difficulty in understanding pain medication and its management. Specific adjustments that hospice teams can make to improve caregiver experiences are identified. [Copyright &y& Elsevier]
- Published
- 2013
- Full Text
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3. Palliative medicine in Mediterranean countries: different approaches, same philosophy
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Antonio Noguera-Tejedor, Carlos Centeno, Matteo Moroni, John Y. Rhee, Maria Caterina Pallotti, Guido Biasco, and Pallotti MC, Noguera-Tejedor A, Rhee JY, Moroni M, Biasco G, Centeno C.
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Cross-Cultural Comparison ,0301 basic medicine ,Palliative care ,MEDLINE ,Medicine (miscellaneous) ,Symptom assessment ,03 medical and health sciences ,Nursing ,Humans ,Medicine ,Palliative Medicine ,palliative care ,030109 nutrition & dietetics ,Oncology (nursing) ,business.industry ,General Medicine ,Caregiver support ,Service model ,Cross-cultural studies ,hospital support team ,Medical–Surgical Nursing ,Hospice Care ,Italy ,hospice team ,Spain ,Spiritual care ,business - Abstract
Despite the fact that Italy and Spain are culturally similar, there are important differences in palliative care services development. For example, Italy has a greater proportion of hospice teams compared with Spain, while Spain has a greater proportion of hospital support teams.1 Noting these differences, we decided to compare a major palliative care service model from each country: the Seragnoli Hospice Foundation (FHS), Italy, and the Palliative Care Support Team (PCST) at the Clinica Universidad de Navarra (CUN), Spain, where an oncologist from FHS recently completed a 4-week rotation. We compare the institutions according to symptom assessment and management, psychological and spiritual care, caregiver support and impact on the rest of the hospital. Initially, the differences between the two teams, such as culture and practice, were more noticeable, but by the end of the rotation the shared values were what stood out. FHS is a private non-profit foundation in Italy composed of three hospices that care for advanced and terminal patients, each with a …
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- 2017
- Full Text
- View/download PDF
4. Problemi vezani s krajem života u zajednici: povezivanje profesionalnoga i javnog obrazovanja
- Author
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Ana Štambuk and Joanne E. Coury
- Subjects
kognitivna praksa ,socijalna interakcija ,smrt i umiranje ,problemi vezani uz kraj života ,obrazovanje zajednice ,profesionalci u zdravstvu ,obrazovanje za hospicij ,hospicijski tim ,interdisciplinarni obrazovni plan ,socijalne mreže ,cognitive praxis ,social interaction ,death and dying ,end-of-life issues ,community education ,health professions ,hospice training ,hospice team ,interdisciplinary curricula ,social networks - Abstract
U ovom članku želimo povezati osobnu svijest o smrtnosti, umiranju i smrti s društvenom brigom, osposobljenošću i ljubavlju društva za umiruće, koje bi trebale pomoći umirućima u procesu “otpuštanja” života. Hospicij i palijativna skrb (HPS) program je koji se razvio iz ove međusobne povezanosti, ovisnosti. HPS-program preuzima aktivnu ulogu u oblikovanju zajedničkih i osobnih vrednota vezanih uz smrt i umiranje. Upotrebljavajući referentni okvir kognitivne prakse, pokazat ćemo da su ove vrednote oblikovane u društvenom životu preko stvarnih situacija i događaja, izraslih kroz hospicijski timski rad s pacijentima, obiteljima i društvenim službama. Hospicijski program se razvija kroz iskustveno učenje koje se događa u socijalnoj interakciji koja uključuje ne samo profesionalce, pacijente i obitelji već i širu zajednicu. Tko može bolje nego hospicijski tim brinuti o zaštiti društvene svijesti o specifičnim potrebama smrtnobolesnih i umirućih osoba, ili prepoznati potrebu za podrškom obitelji i prijateljima umirućih? Neki od zaista predanih liječnika imaju bogatstvo praktičnog znanja i primijenjenog istraživanja te su spremni dijeliti to s drugima. Odgovorni za profesionalno obrazovanje trebaju inicirati promjene u srednjoškolskom, dodiplomskom i permanentnom obrazovanju, kako bi prenijeli ovu mudrost u sustavno javno obrazovanje, kao i uključili ne samo profesionalni tretman i principe timskog rada nego i vještine koje izgrađuju zajednicu., In our paper, we link the private realm of awareness of one's own mortality, dying and death and the public sphere of competent and compassionate end-of-life care that helps individuals manage the process of letting go of life. Hospice and palliative care (HPC) programs have evolved through this linkage. HPC has taken an active role in shaping communal and personal values about death and dying. Using a cognitive praxis framework, we show that these values are shaped in the public arena through the “actual things and events” produced by HPC teams working with patients, family, and social networks. We expand on the idea of experiential learning through social interaction to include not just professionals, patients and families but also the community at large. Who better to secure the wider community recognition of special care needs of terminally ill and dying persons and support needs of the circle of family and friends than the hospice team? Some dedicated practitioners have a wealth of practical knowledge and applied research and they share this readily. But, to translate this wisdom into advocacy grounded in sustained public education, providers of professional education need to initiate changes in undergraduate, graduate and continuing education to include not only treatment competencies and teamwork principles but also community-building skills.
- Published
- 2002
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