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1.
J Gerontol Nurs ; 26(10): 16-26, 2000 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-11883495

RESUMO

The purpose of this study was to explore and describe the educational needs and concerns of licensed nursing staff and certified nursing assistants (CNAs) regarding end-of-life (EOL) care. Focus group interviews were conducted at two nursing homes in the Pacific Northwest. Separate interviews were conducted for licensed staff (RNs and LPN/LVNs) and CNAs. A total of 15 licensed staff and 39 CNAs participated in the study. Interviews were transcribed and themes were extracted through consensus reached by three investigators. The major concerns of these nursing home staff focused on symptom management, communication and interactions, goals of care, role delineation, time constraints, self-care needs, and emotional attachment to residents. Although both groups described similar themes, specific issues within each topic often were different for licensed staff and CNAs. These findings can be used to guide the design of educational programs aimed at assisting nursing home staff in providing high level end-of-life care.


Assuntos
Atitude do Pessoal de Saúde , Competência Clínica/normas , Enfermagem Geriátrica/educação , Conhecimentos, Atitudes e Prática em Saúde , Avaliação das Necessidades/organização & administração , Assistentes de Enfermagem/educação , Assistentes de Enfermagem/psicologia , Casas de Saúde , Recursos Humanos de Enfermagem/educação , Recursos Humanos de Enfermagem/psicologia , Assistência Terminal , Idoso , Grupos Focais , Enfermagem Geriátrica/métodos , Enfermagem Geriátrica/normas , Humanos , Papel do Profissional de Enfermagem , Relações Enfermeiro-Paciente , Pesquisa em Educação em Enfermagem , Pesquisa Metodológica em Enfermagem , Planejamento de Assistência ao Paciente , Autocuidado/métodos , Autocuidado/psicologia , Inquéritos e Questionários , Assistência Terminal/métodos , Assistência Terminal/normas , Gerenciamento do Tempo
2.
J Clin Oncol ; 17(1): 361-70, 1999 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-10458255

RESUMO

PURPOSE: Pain and symptom management is an integral part of the clinical practice of oncology. A number of guidelines have been developed to assist the clinician in optimizing comfort care. We implemented clinical guidelines for cancer pain management in the community setting and evaluated whether these guidelines improved care. PATIENTS AND METHODS: Eighty-one cancer patients, aged 37 to 76 years, were enrolled onto a prospective, longitudinal, randomized controlled study from the outpatient clinic settings of 26 western Washington-area medical oncologists. A multilevel treatment algorithm based on the Agency for Health Care Policy and Research Guidelines for Cancer Pain Management was compared with standard-practice (control) pain and symptom management therapies used by community oncologists. The primary outcome of interest was pain (Brief Pain Inventory); secondary outcomes of interest were all other symptoms (Memorial Symptom Assessment Scale) and quality of life (Functional Assessment of Cancer Therapy Scale). RESULTS: Patients randomized to the pain algorithm group achieved a statistically significant reduction in usual pain intensity, measured as slope scores, when compared with standard community practice (P < .02). Concurrent chemotherapy and patient adherence to treatment were significant mediators of worst pain. There were no significant differences in other symptoms or quality of life between the two treatment groups. CONCLUSION: This guideline implementation study supports the use of algorithmic decision making in the management of cancer pain. These findings suggest that comprehensive pain assessment and evidence-based analgesic decision-making processes do enhance usual pain outcomes.


Assuntos
Neoplasias/complicações , Dor/tratamento farmacológico , Guias de Prática Clínica como Assunto , Adulto , Idoso , Algoritmos , Assistência Ambulatorial , Analgésicos Opioides/uso terapêutico , Antineoplásicos/efeitos adversos , Antineoplásicos/uso terapêutico , Feminino , Humanos , Estudos Longitudinais , Masculino , Pessoa de Meia-Idade , Neoplasias/tratamento farmacológico , Dor/etiologia , Medição da Dor , Cooperação do Paciente , Estudos Prospectivos , Qualidade de Vida
3.
Cancer Pract ; 7(5): 226-32, 1999.
Artigo em Inglês | MEDLINE | ID: mdl-10687591

RESUMO

OBJECTIVES: The purpose of this study was to explore the reasons that cancer patients with pain find it difficult to adhere to analgesic therapy. MATERIALS AND METHODS: Twenty-one patients with advanced cancer with pain were interviewed using a semistructured schedule of questions. Participants were asked to describe their decision making regarding analgesics and the factors that made it difficult for them to take analgesics prescribed for their pain. They also were asked to describe their relationships with their healthcare providers. Themes were identified and refined using qualitative analytic techniques. Two investigators independently coded all data to ensure that findings accurately reflected participants' experiences. RESULTS: Findings reveal several factors that hindered analgesic use and the specific ways in which patients evaluated these factors in making decisions about taking pain medication. The provider-patient factors that impeded analgesic use also were described. Finally, the common use of nonpharmacologic methods of pain control offers insight into the role of these therapeutic strategies in achieving pain relief and decreasing analgesic use. CONCLUSIONS: The findings underscore the importance of early intervention to address barriers to analgesic use. Some barriers may be overcome through educational efforts. The findings suggest, however, that consistent, repeated patient education often may not be sufficient to subdue patients' negative thoughts about taking the medication. Other approaches, such as changing medications or assisting the patient to use nonpharmacologic pain strategies, may prove more successful.


Assuntos
Analgésicos/uso terapêutico , Conhecimentos, Atitudes e Prática em Saúde , Neoplasias/complicações , Dor/tratamento farmacológico , Dor/psicologia , Cooperação do Paciente/psicologia , Autoadministração/psicologia , Adaptação Psicológica , Adulto , Idoso , Tomada de Decisões , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Pesquisa Metodológica em Enfermagem , Dor/etiologia , Educação de Pacientes como Assunto , Relações Profissional-Paciente , Autoadministração/métodos , Inquéritos e Questionários
4.
Am J Hosp Palliat Care ; 16(4): 573-82, 1999.
Artigo em Inglês | MEDLINE | ID: mdl-10661065

RESUMO

Nursing homes care for people at the end of life (EOL). There is evidence to suggest, however, that nursing staff in these settings is often unprepared to provide a high level of EOL care. This article reports the findings from three preliminary studies that investigated the needs of licensed staff and certified nursing assistants in nursing homes regarding EOL care. The studies involved needs assessment surveys, focus group interviews with staff members, and telephone interviews with nursing home administrators. Data show that the major needs included a lack of knowledge and skills in symptom management; communication difficulties; conflicts with families and physicians; and emotional distress in dealing with time constraints and attachment to residents. Implications for nursing home staff education are described.


Assuntos
Avaliação das Necessidades/organização & administração , Assistentes de Enfermagem/educação , Casas de Saúde , Recursos Humanos de Enfermagem/educação , Assistência Terminal , Atitude do Pessoal de Saúde , Grupos Focais , Humanos , Descrição de Cargo , Assistentes de Enfermagem/psicologia , Recursos Humanos de Enfermagem/psicologia , Desenvolvimento de Pessoal , Inquéritos e Questionários
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