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1.
Pain Manag Nurs ; 23(5): 663-671, 2022 10.
Artigo em Inglês | MEDLINE | ID: mdl-35431113

RESUMO

OBJECTIVES: An understanding of nurse characteristics that influence pain management, which are potentially amenable to change, can help to refine and improve nurse education and practice, resulting in better patient outcomes. The purpose of this review was to identify nurse characteristics that influence their assessment of and intention to treat postoperative pain. DESIGN: Integrative literature review. DATA SOURCES: A systematic search of electronic databases (CINAHL, Scopus, PsycINFO, Medline, and Embase), using these constructs "pain assessment", "pain management", "postoperative pain", "nurses", "cultural beliefs" and "nurses' perceptions" was conducted for the period 2000 to October 2020. REVIEW/ANALYSIS METHODS: Following a systematic screening process, the included articles were analyzed and synthesized to identify themes and subthemes. RESULTS: A total of 40 articles were included with three main themes identified: nurse knowledge; nurse sociocultural factors, personal beliefs and attitudes, and other characteristics; and believing or doubting the patient. There was evidence that targeted education interventions can improve nurse knowledge and nurses' clinical practice in relation to pain management. What was less clear was which nurse attitudes and biases influenced their pain management practice or how these could be changed. CONCLUSIONS: More studies are needed to investigate the influence of cultural characteristics on pain assessment and management. There is a need for further quantitative studies that explore the relationship between nurse characteristics and their pain management practice. Intervention studies using innovative educational approaches that change attitudes and biases, and improve practice are needed.


Assuntos
Competência Clínica , Enfermeiras e Enfermeiros , Humanos , Análise de Intenção de Tratamento , Dor , Manejo da Dor
2.
Dement Neuropsychol ; 13(2): 180-186, 2019.
Artigo em Inglês | MEDLINE | ID: mdl-31285792

RESUMO

Individuals with low health literacy have less knowledge of their own health condition. Carers play a key role in older people's activities of daily living. OBJECTIVE: to evaluate the performance of carers of older people using the S-TOFHLA (Short Test of Functional Health Literacy in Adults) and to identify caregiver characteristics associated with low functional health literacy. METHODS: a cross-sectional study was conducted. The S-TOFHLA, a sociodemographic instrument, the Mini-Mental State Exam and the Patient Health Questionnaire-2 were applied to 80 carers of older patients routinely followed by doctors from the Primary Health Care Sector of the City of Botucatu, São Paulo. The multivariate analysis used an ordinal logistic regression model with test (S-TOFHLA) scores as the dependent variable. The level of statistical significance adopted was 0.05. RESULTS: the individuals had a mean age of 54.6 (± 11.7); 27% of the carers evaluated had inadequate levels of health literacy (S-TOFHLA ≥54). A higher proportion of individuals with low education had inadequate or marginal health literacy (p<0.001). CONCLUSION: nearly 1/3 of the carers had marginal or inadequate levels of health literacy. These results highlight the difficulties of many carers in understanding health information.


Indivíduos com baixo alfabetismo em saúde têm menos conhecimento sobre sua própria condição de saúde. Cuidadores desempenham um papel fundamental nas atividades de vida diária dos idosos. OBJETIVO: avaliar o desempenho de cuidadores de pessoas idosas usando o "S-TOFHLA (Short Test of Functional Health Literacy in Adults)" e identificar características do cuidador associadas ao baixa alfabetismo em saúde. MÉTODOS: um estudo transversal foi conduzido. O S-TOFHLA, um instrumento sociodemográfico, o Miniexame do Estado Mental e o "Patient Health Questionnaire - 2" foram aplicados a 80 cuidadores de pacientes idosos rotineiramente acompanhados por médicos do Setor de Atenção Primária à Saúde da cidade de Botucatu, São Paulo. A análise multivariada utilizou um modelo de regressão logística ordinal com os escores do S-TOFHLA como variável dependente. O nível de significância estatística adotado foi de 0,05. RESULTADOS: os indivíduos tiveram idade média de 54,6 (± 11,7) anos; 27% dos cuidadores avaliados apresentavam níveis inadequados de alfabetização em saúde. Uma proporção maior de indivíduos com baixa escolaridade apresentou alfabetização em saúde inadequada e limítrofe (p<0,001). CONCLUSÃO: aproximadamente 1/3 dos cuidadores apresentaram níveis limítrofes e inadequados de alfabetização em saúde. Esses resultados destacam as dificuldades de muitos cuidadores em compreender informações sobre saúde.

3.
Dement. neuropsychol ; 13(2): 180-186, Apr.-June 2019. tab
Artigo em Inglês | LILACS | ID: biblio-1011954

RESUMO

ABSTRACT. Individuals with low health literacy have less knowledge of their own health condition. Carers play a key role in older people's activities of daily living. Objective: to evaluate the performance of carers of older people using the S-TOFHLA (Short Test of Functional Health Literacy in Adults) and to identify caregiver characteristics associated with low functional health literacy. Methods: a cross-sectional study was conducted. The S-TOFHLA, a sociodemographic instrument, the Mini-Mental State Exam and the Patient Health Questionnaire-2 were applied to 80 carers of older patients routinely followed by doctors from the Primary Health Care Sector of the City of Botucatu, São Paulo. The multivariate analysis used an ordinal logistic regression model with test (S-TOFHLA) scores as the dependent variable. The level of statistical significance adopted was 0.05. Results: the individuals had a mean age of 54.6 (± 11.7); 27% of the carers evaluated had inadequate levels of health literacy (S-TOFHLA ≥54). A higher proportion of individuals with low education had inadequate or marginal health literacy (p<0.001). Conclusion: nearly 1/3 of the carers had marginal or inadequate levels of health literacy. These results highlight the difficulties of many carers in understanding health information.


RESUMO. Indivíduos com baixo alfabetismo em saúde têm menos conhecimento sobre sua própria condição de saúde. Cuidadores desempenham um papel fundamental nas atividades de vida diária dos idosos. Objetivo: avaliar o desempenho de cuidadores de pessoas idosas usando o "S-TOFHLA (Short Test of Functional Health Literacy in Adults)" e identificar características do cuidador associadas ao baixa alfabetismo em saúde. Métodos: um estudo transversal foi conduzido. O S-TOFHLA, um instrumento sociodemográfico, o Miniexame do Estado Mental e o "Patient Health Questionnaire - 2" foram aplicados a 80 cuidadores de pacientes idosos rotineiramente acompanhados por médicos do Setor de Atenção Primária à Saúde da cidade de Botucatu, São Paulo. A análise multivariada utilizou um modelo de regressão logística ordinal com os escores do S-TOFHLA como variável dependente. O nível de significância estatística adotado foi de 0,05. Resultados: os indivíduos tiveram idade média de 54,6 (± 11,7) anos; 27% dos cuidadores avaliados apresentavam níveis inadequados de alfabetização em saúde. Uma proporção maior de indivíduos com baixa escolaridade apresentou alfabetização em saúde inadequada e limítrofe (p<0,001). Conclusão: aproximadamente 1/3 dos cuidadores apresentaram níveis limítrofes e inadequados de alfabetização em saúde. Esses resultados destacam as dificuldades de muitos cuidadores em compreender informações sobre saúde.


Assuntos
Humanos , Idoso , Educação em Saúde , Cuidadores , Escolaridade , Letramento em Saúde
4.
BMC Geriatr ; 19(1): 68, 2019 03 04.
Artigo em Inglês | MEDLINE | ID: mdl-30832575

RESUMO

BACKGROUND: A telephone intervention for caregivers of older people discharged from hospital was shown to improve preparedness to care, reduce caregiver strain and caregiver distress. No cost-effectiveness analysis has been published on this, or similar interventions. The study aims addressed here were to examine whether positive outcomes for caregivers resulting from the Further Enabling Care at Home (FECH) program changed the use and costs of health services by patients; and to assess cost-effectiveness. METHODS: A single-blind randomised controlled trial compared FECH to usual care. FECH involved a specially trained nurse addressing support needs of caregivers of older patients discharged from hospital. A minimum clinically important difference in preparedness to care was defined as an increase in Preparedness for Caregiving scale score of ≥ two points from baseline. Designated data collection was at: Time 1, within four days of discharge; Time 2, 15-21 days post-discharge; and Time 3, six weeks post-discharge. A last observation carried forward approach to loss to follow-up was used, with a sensitivity analysis including only those who completed all time points. Patient use of hospital, emergency department (ED) and ambulance services were captured for 12 weeks post-discharge using administrative data. Costs included nurse time supporting caregivers, resources used by the nurse, and time taken training the nurse to deliver FECH. Cost-effectiveness was assessed using decision trees for preparedness for caregiving. RESULTS: Sixty-two intervention dyads and 79 controls provided complete data. A significantly greater proportion of intervention group caregivers reported improved preparedness to care to Time 2 (36.4% v 20.9%, p = 0.029), though this was not sustained to Time 3. The intervention cost $AUD268.28 above usual care per caregiver. No significant differences were observed in health service use between groups. The incremental cost-effectiveness ratio for each additional caregiver reporting improved preparedness to care at Time 2 was $AUD1,730.84. CONCLUSIONS: To our knowledge this is the first work to calculate the cost-effectiveness of a telephone-delivered intervention designed to support caregivers of older people post-discharge, and will support decision-making regarding implementation. Further research should examine different settings, and assess impacts on health service use with larger samples and a longer follow-up. TRIAL REGISTRATION: Australian and New Zealand Clinical Trial Registry: ACTRN12614001174673 . Registered 07/11/2014.


Assuntos
Adaptação Psicológica , Cuidadores/psicologia , Idoso Fragilizado/psicologia , Alta do Paciente/economia , Telefone/economia , Idoso , Idoso de 80 Anos ou mais , Austrália , Análise Custo-Benefício , Feminino , Seguimentos , Humanos , Masculino , Pessoa de Meia-Idade , Método Simples-Cego
5.
Clin Interv Aging ; 14: 2223-2237, 2019.
Artigo em Inglês | MEDLINE | ID: mdl-31908433

RESUMO

BACKGROUND: Falls remain an important problem for older people in hospital, particularly those with high falls risk. This mixed methods study investigated the association between multiple bed moves and falls during hospitalisation of older patients identified as a fall risk, as well as safety of ward environments, and staff person-centredness and level of inter-professional collaboration. METHODS: Patients aged ≥70 years, admitted through the Emergency Department (ED) and identified at high fall risk, who were admitted to four target medical wards, were followed until discharge or transfer to a non-study ward. Hospital administrative data (falls, length of stay [LoS], and bed moves) were collected. Ward environmental safety audits were conducted on the four wards, and staff completed person-centredness of care, and interprofessional collaboration surveys. Staff focus groups and patient interviews provided additional qualitative data about bed moves. RESULTS: From 486 ED tracked admissions, 397 patient records were included in comparisons between those who fell and those who did not [27 fallers/370 non-fallers (mean 84.8 years, SD 7.2; 57.4% female)]. During hospitalisation, patients experienced one to eight bed moves (mean 2.0, SD 1.2). After adjusting for LoS, the number of bed moves after the move to the initial admitting ward was significantly associated with experiencing a fall (OR 1.56, 95% CI 1.11-2.18). Ward environments had relatively few falls hazards identified, and staff surveys indicated components of person-centredness of care and interprofessional collaboration were rated as good overall, and comparable to other reported hospital data. Staff focus groups identified poor communication between discharging and admitting wards, and staff time pressures around bed moves as factors potentially increasing falls risk for involved patients. Patients reported bed moves increased their stress during an already challenging time. CONCLUSION: Patients who are at high risk for falls admitted to hospital have an increased risk of falling associated with every additional bed move. Strategies are needed to minimise bed moves for patients who are at high risk for falls.


Assuntos
Acidentes por Quedas/prevenção & controle , Serviço Hospitalar de Emergência/estatística & dados numéricos , Hospitalização/estatística & dados numéricos , Hospitais/estatística & dados numéricos , Movimentação e Reposicionamento de Pacientes/efeitos adversos , Segurança do Paciente/normas , Gestão de Riscos/métodos , Acidentes por Quedas/estatística & dados numéricos , Idoso , Idoso de 80 Anos ou mais , Feminino , Humanos , Incidência , Masculino , Fatores de Risco , Austrália Ocidental/epidemiologia
6.
Worldviews Evid Based Nurs ; 15(5): 368-376, 2018 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-30160011

RESUMO

BACKGROUND: Effective pain management is unlikely to occur without consistent and timely assessments. To improve assessment and management of pain, ward-based pain resource nurses were introduced in 2007 to facilitate hospital-wide evidence-based practice changes using three key targets. One-year post implementation of this quality improvement project, promising results were revealed. AIMS: The purpose of this study, 8 years post implementation, was to (a) evaluate sustained practice improvements in pain assessment and management, (b) assess current pain resource nurse knowledge and attitudes to pain, (c) explore characteristics of the pain resource nurse role, as well as (d) any perceived contextual changes regarding study findings. METHODS: A mixed-methods approach was used to address study aims. Quantitative data were collected from documentation audits and a "Knowledge and Attitudes Survey Regarding Pain." Qualitative interviews explored the characteristics of the pain resource nurse role, and a focus group discussion explored the context of change. RESULTS: Significant improvements were observed for the documentation of pain scores on admission and for each nursing shift. Survey results highlighted potential knowledge deficits in key practice areas, even though interview findings suggested that pain resource nurses provided a resource for peers, raised awareness of best practice, and imparted knowledge to other ward staff. An important facilitator for the pain resource nurse role was the ongoing collaboration and support from specific pain teams, and barriers to engage in the role were competing workload priorities, and limited awareness among other ward staff. LINKING EVIDENCE TO ACTION: Implementing and sustaining evidence-based practice change in clinical practice is challenging. Ongoing evaluation is necessary for identifying the long-term implications of practice improvement interventions and issues that influence the adoption of evidence-based practice. Strategies to address barriers, and to increase awareness and engagement of the pain resource nurse role with wider collaboration require further investigation.


Assuntos
Manejo da Dor/normas , Medição da Dor/estatística & dados numéricos , Percepção , Especialidades de Enfermagem/normas , Documentação/métodos , Documentação/normas , Documentação/estatística & dados numéricos , Prática Clínica Baseada em Evidências/métodos , Prática Clínica Baseada em Evidências/normas , Prática Clínica Baseada em Evidências/tendências , Grupos Focais , Humanos , Enfermeiras e Enfermeiros/psicologia , Enfermeiras e Enfermeiros/estatística & dados numéricos , Manejo da Dor/enfermagem , Medição da Dor/enfermagem , Medição da Dor/normas , Pesquisa Qualitativa , Inquéritos e Questionários
7.
Health Soc Care Community ; 26(4): e578-e586, 2018 07.
Artigo em Inglês | MEDLINE | ID: mdl-29635883

RESUMO

This feasibility study aimed to identify and address the support needs of family carers (FCs) of people living with dementia and to assess whether the use of the Carer Support Needs Assessment Tool (CSNAT) intervention in home-based care was acceptable and relevant to FCs. The CSNAT intervention comprised two FC support needs assessment visits, 7 weeks apart, plus associated actions addressing prioritised needs by the Client Care Advisors of a community care service in Western Australia in 2015. Telephone interviews were conducted with FCs on their experience using the CSNAT at the end of the intervention. Twenty-one FCs were involved in the intervention and 15 of them completed the feedback interviews. Care recipients had moderate to severe dementia. The top five support needs reported by FCs were: having time to yourself in the day; knowing what to expect in the future; practical help in the home; looking after your own health and dealing with your feelings and worries. Three themes summarised their experience: a straightforward structured approach; awareness, acknowledgement and acceptance of their situation; and provision of support. FCs appreciated the opportunity to be heard and acknowledged, to have their practical and psychosocial support needs facilitated, to identify what is important to them and to receive a response in a timely manner. The CSNAT approach offered a structured carer-led, person-centred, supportive intervention that facilitated discussion between the family carer and the service provider about support needs and strategies to address them.


Assuntos
Cuidadores/psicologia , Demência/psicologia , Avaliação das Necessidades , Cuidados Paliativos/psicologia , Apoio Social , Adaptação Psicológica , Idoso , Ansiedade/prevenção & controle , Demência/terapia , Estudos de Viabilidade , Feminino , Serviços de Assistência Domiciliar , Humanos , Masculino , Austrália Ocidental
8.
Nurse Educ Today ; 42: 17-22, 2016 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-27237347

RESUMO

BACKGROUND: Nursing education appropriate to the learning needs of Aboriginal and Torres Strait Islander students is essential to prepare them for registration as nurses. Despite incentives to encourage the recruitment and retention of such students, a disproportionate number commence but do not finish their nursing studies. OBJECTIVES: To describe the barriers and enablers to the retention of Aboriginal students in a Diploma of Nursing course (Enrolled/Division 2) in Western Australia. DESIGN: An exploratory descriptive design was used. SETTINGS: One metropolitan educational facility catering for Aboriginal people offering an 18-month course in a block release format. PARTICIPANTS: A convenience sample of 16 students aged 18+years. METHODS: Newly enrolled students (n=10) participated in an investigator-developed survey to explore their motivation for entering the course. Nine of these students and a further seven students who were nearing the end of their course participated in focus groups to explore their experiences of nursing education. RESULTS: Survey respondents had a mean age of 32.7years; most were female, had nominated family as influential in the decision to enroll, and commenced with a friend. Regarding recruitment and retention, the qualitative data highlighted the importance of students': perceptions of the training organisation, characteristics, experiences of nursing education, and sources of support. CONCLUSIONS: Strategies that develop individual's resilience and engage supportive networks can assist Aboriginal students to negotiate tertiary nursing study. Academic skills assessments supplemented with tailored educational support at entry can resource students to navigate increasingly complex course content. Flexibility throughout the course enables students to negotiate study in a context of ongoing family and financial obligations.


Assuntos
Bacharelado em Enfermagem , Havaiano Nativo ou Outro Ilhéu do Pacífico/psicologia , Resiliência Psicológica , Apoio Social , Estudantes de Enfermagem/psicologia , Adulto , Escolha da Profissão , Competência Cultural , Tomada de Decisões , Bacharelado em Enfermagem/economia , Feminino , Grupos Focais , Humanos , Masculino , Motivação , Grupo Associado , Resolução de Problemas , Austrália Ocidental
9.
BMC Geriatr ; 15: 70, 2015 Jun 25.
Artigo em Inglês | MEDLINE | ID: mdl-26108207

RESUMO

BACKGROUND: Presentations to hospital of older people receiving family care at home incur substantial costs for patients, families, and the health care system, yet there can be positive carer outcomes when systematically assessing/addressing their support needs, and reductions in older people's returns to hospital attributed to appropriate discharge planning. This study will trial the Further Enabling Care at Home program, a 2-week telephone outreach initiative for family carers of older people returning home from hospital. Hypotheses are that the program will (a) better prepare families to sustain their caregiving role and (b) reduce patients' re-presentations/readmissions to hospital, and/or their length of stay; also that reduced health system costs attributable to the program will outweigh costs of its implementation. METHODS/DESIGN: In this randomised controlled trial, family carers of older patients aged 70+ discharged from a Medical Assessment Unit in a Western Australian tertiary hospital, plus the patients themselves, will be recruited at discharge (N = 180 dyads). Carers will be randomly assigned (block allocation, assessors blinded) to receive usual care (control) or the new program (intervention). The primary outcome is the carer's self-reported preparedness for caregiving (Preparedness for Caregiving Scale administered within 4 days of discharge, 2-3 weeks post-discharge, 6 weeks post-discharge). To detect a clinically meaningful change of two points with 80 % power, 126 carers need to complete the study. Patients' returns to hospital and subsequent length of stay will be ascertained for a minimum of 3 months after the index admission. Regression analyses will be used to determine differences in carer and patient outcomes over time associated with the group (intervention or control). Data will be analysed using an Intention to Treat approach. A qualitative exploration will examine patients' and their family carers' experiences of the new program (interviews) and explore the hospital staff's perceptions (focus groups). Process evaluation will identify barriers to, and facilitators of, program implementation. A comprehensive economic evaluation will determine cost consequences. DISCUSSION: This study investigates a novel approach to identifying and addressing family carers' needs following discharge from hospital of the older person receiving care. If successful, the program has potential to be incorporated into routine post-discharge support. TRIAL REGISTRATION: Australian and New Zealand Clinical Trial Registry: ACTRN12614001174673 .


Assuntos
Cuidadores , Relações Comunidade-Instituição , Alta do Paciente , Centros de Atenção Terciária , Idoso , Idoso de 80 Anos ou mais , Austrália/epidemiologia , Cuidadores/economia , Relações Comunidade-Instituição/economia , Redução de Custos/métodos , Feminino , Hospitalização/economia , Humanos , Masculino , Nova Zelândia/epidemiologia , Alta do Paciente/economia , Centros de Atenção Terciária/economia
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