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1.
Wien Klin Wochenschr ; 122(13-14): 384-9, 2010 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-20602281

RESUMO

BACKGROUND: Care aspects of outpatient palliative-care teams involve the medical, psychological, and spiritual needs of patients and their caregivers. The objective of our study was to examine the post-mortal bereavement of family caregivers. METHODS: The investigation was based on interviews with 50 family caregivers of 50 palliative-care patients assessed by a palliative-care team. Each caregiver was interviewed using interview sheets (mixed method designs) in accordance with three groups of validated criteria for complicated grief: Prigerson, Horowitz, and ICD-10. RESULTS: Forty-six family caregivers of terminally ill patients participated in the study. Complicated grief existed in up to 30% of the caregivers, based on the three sets of criteria. There was no significant difference (P > 0.05) among the three groups and no significant differences were found (P > 0.05) in relation to age, sex, psychosocial distress, primary cancer disease, and duration of illness or quality of care. Overall, 97% of the care-giving relatives were satisfied with the help given by the palliative-care team. CONCLUSION: The results of the study suggest that care from a specialized palliative-care team providing psychological and social support may reduce the risk of complicated grief. Careful exploration of possible risk factors for complicated grief is important for optimal care. Our study shows that healthcare providers play an important role in helping family caregivers to manage the multiple burdens and the grieving reaction. Family-focused grief therapy may prevent complicated grieving reactions.


Assuntos
Luto , Cuidadores/psicologia , Entrevista Psicológica , Cuidados Paliativos/psicologia , Assistência Terminal/psicologia , Adaptação Psicológica , Adulto , Idoso , Idoso de 80 Anos ou mais , Comportamento do Consumidor , Terapia Familiar , Feminino , Alemanha , Pesar , Serviços de Assistência Domiciliar , Humanos , Masculino , Pessoa de Meia-Idade , Equipe de Assistência ao Paciente , Estudos Prospectivos , Apoio Social , Adulto Jovem
2.
Pflege Z ; 62(2): 92-6, 2009 Feb.
Artigo em Alemão | MEDLINE | ID: mdl-19263721

RESUMO

BACKGROUND: Palliative home care gains in importance in Germany. In addition to administering pain and symptom control for patients a "Palliative Care Team" (PCT) tries to address the patients' psychosocial and spiritual needs. METHODS: Retrospective analysis of caregiving relatives' expectations of the support by a PCT. RESULTS: Most relatives expected a sufficient pain therapy and support of the PCT. Additionally they wished for further outreach afterthe death of the patient. CONCLUSION: Palliative homecare is perceived as a helpful supporting factor by the care-giving relatives of palliative patients.


Assuntos
Cuidadores/psicologia , Necessidades e Demandas de Serviços de Saúde , Serviços de Assistência Domiciliar , Cuidados Paliativos , Equipe de Assistência ao Paciente , Adulto , Idoso , Idoso de 80 Anos ou mais , Luto , Comportamento do Consumidor , Feminino , Alemanha , Humanos , Masculino , Pessoa de Meia-Idade , Dor/enfermagem , Adulto Jovem
3.
BMC Palliat Care ; 7: 11, 2008 Aug 12.
Artigo em Inglês | MEDLINE | ID: mdl-18694527

RESUMO

BACKGROUND: During the last stage of life, palliative care patients often experience episodes of respiratory distress, bleeding, pain or seizures. In such situations, caregivers may call emergency medical services leading to unwanted hospital admissions. The study aims to show the influence of our palliative care team to reducing emergency calls by cancer patients or their relatives during the last six month of life. METHODS: Fifty relatives of deceased patients who had been attended by our palliative care team were randomly selected. Data was obtained retrospectively during a structured interview. In addition to demographic data, the number of emergency calls made during the final six months of the patient's life, the reason for the call and the mental compound score (MCS-12) of the caregivers was registered. RESULTS: Forty-six relatives agreed to the interview. Emergency calls were placed for 18 patients (39%) during the final six months of their lives. There were a total of 23 emergency calls. In 16 cases (70%) the patient was admitted to the hospital. Twenty-one (91%) of the calls were made before patients had been enrolled to receive palliative care from the team, and two (9%) were made afterwards. The mean mental compound score of the caregivers at the time of the interview was 41 (range 28-57). There was a lack of correlation between MCS-12 and number of emergency calls. CONCLUSION: Emergency calls were more likely to occur if the patients were not being attended by our palliative care team. Because of the lack of correlation between MCS-12 and the number of emergency calls, the MCS-12 cannot indicate that acutely stressful situations triggered the calls. However, we conclude that special palliative care programs can reduce psychosocial strain in family caregivers. Therefore, the number of emergency calls may be reduced and this fact allows more palliative patients to die at home.

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