Avaliação da carga de trabalho de enfermagem na unidade de cuidados intensivos Dr. Emílio Moreira em Portalegre

No âmbito do 4º Mestrado em Enfermagem com Especialização em Gestão de Unidades de Saúde, da Escola Superior de Saúde do Instituto Politécnico de Portalegre, o presente relatório pretende apresentar um documento reflexivo sobre a aquisição e o desenvolvimento de competências na área da gestão de unidades de saúde, em âmbito de estágio. O estágio decorreu na Unidade de Cuidados Intensivos Dr. Emílio Moreira da Unidade Local do Norte Alentejano, no período de Outubro de 2015 a Fevereiro de 2016. Foi aplicada a metodologia de projeto, tendo desenvolvido no decorrer do estágio o Trabalho de Projeto Avaliação da Carga de Trabalho de Enfermagem na Unidade de Cuidados Intensivos Dr. Emílio Moreira em Portalegre Os enfermeiros desempenham funções muito importantes na área da gestão dos recursos e dos cuidados, em unidades de cuidados intensivos. Uma dessas funções consiste em avaliar o índice de gravidade dos doentes internados e a carga de trabalho de enfermagem através do Therapeutic Intervention Scoring System-28. Neste sentido tornou-se pertinente o estudo retrospetivo da carga de trabalho na UCIDEM, por forma a otimizar a utilização do instrumento de gestão implementado e propor melhorias no âmbito da dotação dos enfermeiros. Concluiu-se, principalmente, que: em relação ao Índice de Enfermeiros e Score TISS, verificaram-se variações acentuadas, quer na necessidade de trabalho de enfermagem quer na gravidade dos doentes, durante 365 dias; comparando a média anual de TISS obtida com o diagnóstico atual da situação na UCIDEM, existe uma dotação desfasada de acordo com o que foi medido pelo TISS; e que a carga de trabalho dos enfermeiros não é distribuída equitativamente pelos turnos

Efetividade da rede de atenção à saúde e à assistência social à pessoa idosa na expressão de usuários e gestores : o caso de Boa Vista/RR

Este artigo trata do paradigma e da efetivação da rede de proteção à pessoa idosa nas áreas de Assistência Social e Saúde, numa perspectiva crítica, tendo como referência a cidade de Boa Vista, capital do Estado de Roraima. A rede de proteção é definida como uma mediação de forças e de poder que se pactua, atuando formal ou informalmente. Salienta-se que os direitos sociais previstos na legislação devem ser efetivados numa rede de proteção. A metodologia da pesquisa consistiu de entrevistas semiestruturadas com duas gestoras da área da Saúde e uma da área de Assistência Social e de quatro grupos focais (dois de cada área) com pessoas idosas, além de um mapa de serviços e de seus vínculos no território. Os resultados mostram que a mediação da proteção em redes se faz com pouca interatividade institucional pactuada e apenas informalmente, por meio de contatos, embora se reconheça um paradigma de ação integrada. __________________________________________________________________________________________________ ABSTRACT

Relatório de estágio de intervenção comunitária

O Mestrado em Enfermagem, com Especialização em Enfermagem Comunitária, visa a aquisição e desenvolvimento de competências para o exercício autónomo, auto refletido e com poder de avaliação critica sobre os cuidados prestados e a sua qualidade no que diz respeito aos vários níveis de prevenção do cliente comunidade. O presente relatório, realizado no âmbito da unidade curricular de Estágio, pretende descrever, analisar e refletir sobre o percurso da construção de competências específicas para a intervenção especializada em Enfermagem Comunitária e de Saúde Pública. Ele propõe-se sintetizar as etapas de crescimento pessoal e profissional que permitem uma melhoria da qualidade dos cuidados prestados, um maior desenvolvimento profissional e a melhoria da satisfação dos grupos e comunidades onde decorreram as intervenções. Nele se demonstram as competências desenvolvidas e que convergem nos objetivos académicos definidos por este Mestrado, bem como no perfil de competências preconizado pela Ordem dos Enfermeiros para o desempenho autónomo de cuidados especializados de Enfermagem a grupos e comunidades. O módulo de estágio consistiu no desenvolvimento de um Projeto de Intervenção Comunitária, baseado na metodologia do Planeamento em Saúde, com o objetivo geral de Promover a capacitação e o empoderamento dos adolescentes da E.S.S.L. no âmbito de uma sexualidade saudável e responsável. Na intervenção em enfermagem avançada na comunidade e dando resposta aos problemas/necessidades identificados, foram realizadas sessões de Educação para a Saúde como estratégia de promoção e proteção da saúde e de prevenção da doença, com a finalidade de se atingir o grau de excelência na qualidade de vida e obter ganhos em saúde. A Educação para a Saúde numa ação essencialmente voltada para a Promoção da Saúde desempenha um papel fundamental na capacitação dos indivíduos para a aquisição de hábitos de vida saudáveis e consequentemente na obtenção de ganhos em saúde. A possibilidade de ocorrerem transformações sobre as condições de vida e de saúde nas comunidades depende do acesso a determinadas formas de conhecimento, e a Educação para a Saúde tem um papel significativo face à melhoria das condições de vida e de saúde das populações. Após a intervenção, e ainda que não seja possível avaliar o impacto deste projeto, podemos constatar que as metas estabelecidas foram todas superadas e até ultrapassadas, assim como os objetivos que tinham sido delineados. Observa-se um grau de satisfação em geral com as sessões de Educação para a Saúde desenvolvidas de 98,1%. Esperamos que com a nossa intervenção, as competências pessoais e sociais adquiridas possam ser desenvolvidas e utilizadas para melhorar a vivência da Sexualidade na Adolescência. No entanto, temos consciência de que a intervenção na área da promoção e prevenção, deve ser um trabalho contínuo e dinâmico para se conseguir ganhos em saúde, com resultados a médio/longo prazo

Critical energy deficit and mortality in critically ill patients

Objective: We investigate the influence of caloric and protein deficit on mortality and length of hospital stay of critically ill patients. Methods: A cohort prospective study including 100 consecutive patients in a tertiary intensive care unit (ICU) receiving enteral or parenteral nutrition. The daily caloric and protein deficit were collected each day for a maximum of 30 days. Energy deficits were divided into critical caloric deficit (≥ 480 kcal/day) and non-critical caloric deficit (≤ 480 kcal/day); and in critical protein deficit (≥ 20 g/day) and non-critical protein deficit (≤ 20 g/day). The findings were correlated with hospital stay and mortality. Results: The mortality rate was 33%. Overall, the patients received 65.4% and 67.7% of the caloric and protein needs. Critical caloric deficit was found in 72% of cases and critical protein deficit in 70% of them. There was a significant correlation between length of stay and accumulated caloric deficit (R = 0.37; p < 0.001) and protein deficit (R = 0.28; p < 0.001). The survival analysis showed that mortality was greater in patients with both critical caloric (p < 0.001) and critical protein deficits (p < 0.01). The Cox regression analysis showed that critical protein deficit was associated with higher mortality (HR 0.25, 95% CI 0.07-0.93, p = 0.03). Conclusions: The incidence of caloric and protein deficit in the ICU is high. Both caloric and protein deficits increase the length of hospital stay, and protein deficit greater than 20 g/day is an independent factor for mortality in critical care unit.

"I’ll call you when we are ready" (One family’s experience of critical care and end of life decision making)

The purpose of this paper is to explore through narrative accounts one family's expérience of critical care, after the admission of a family member to an Intensive Care Unit (ICU) and their subséquent death five weeks later. Numerous studies support the need for effective communication and clear information to be given to the family. In this instance it was évident from their stories that there were numerous barriers to communication, including language and a lack of insight into the needs of the family. Many families do not understand the complexities of nursing care in an ICU so lack of communication by nursing staff was identified as uncaring behavior and encounters. Facilitating a family's proximity to a dying patient and encouraging them to participate in care helps to maintain some sensé of personal control. Despite a commitment to involving family members in care, which was enshrined in the Unit Philosophy, relatives were banished to the waiting room for hours. They experienced feelings of powerlessness and helplessness as they waited with other relatives for news following investigations or until 'the doctor had completed his rounds'. Explanations of "we must make 'the patient' comfortable" was no consolation for those who wished to be involved in care. The words "I'il call you when we are ready" became a mantra to the forgotten families who waited patiently for those with power to admit them to the ICU. Implications are this family felt they were left alone to cope with the traumatic expériences leading up to and surrounding the death. They felt mainly supported by the priest, who not only administered the last rites but provided spiritual support to the family and dealt sensitively with many issues. Paternalism in décision making when there is a moral obligation to ensure that discussions on end of life dilemmas are an inclusive process with families, doctors, nurses was not understood, therefore it caused conflict within the family over EOL décision making. The family felt that the opportunity to share expériences through telling and retelling their stories would enable them to reconfigure the past and create purpose in the future.

Is change in global self-rated health associated with change in affiliation with a primary care provider? Findings from a longitudinal study from New Zealand

To investigate the association of self-rated health and affiliation with a primary care provider (PCP) in New Zealand.
Methods

We used data from a New Zealand panel study of 22,000 adults. The main exposure was self-rated health, and the main outcome measure was affiliation with a PCP. Fixed effects conditional logistic models were used to control for observed time-varying and unobserved time-invariant confounding.
Results

In any given wave, the odds of being affiliated with a PCP were higher for those in good and fair/poor health relative to those in excellent health. While affiliation for Europeans increased as reported health declined, the odds of being affiliated were lower for Māori respondents reporting very good or good health relative to those in excellent health. No significant differences in the association by age or gender were observed.
Conclusions

Our data support the hypothesis that those in poorer health are more likely to be affiliated with a PCP. Variations in affiliation for Māori could arise for several reasons, including differences in care-seeking behaviour and perceived need of care. It may also mean that the message about the benefits of primary health care is not getting through equally to all population groups.

Palliative care for the person with a serious mental illness: the need for a partnership approach to care in Australia

When a person with a co-morbid mental illness requires palliative care, a balance in expert mental health and palliative care is critical to a dignified ending. The patient with a co-morbid mental illness requiring end-of-life care in Australia is currently under-recognized, and urgent consideration of the specific needs of this often discriminated against and stigmatized population is essential to provide appropriate care. This discussion paper explores the issues that arise when palliative care is necessary for a person living and dying with a mental illness, in the context of the Australian health care system and end-of-life care. A case for collaborative interprofessional clinical partnerships exists between the patient, family carers, and palliative care and specialist mental health clinicians, so that optimal care can be facilitated for the person living with a chronic or severe mental illness at the end of life.

Receiving care for intimate partner violence in primary care: barriers and enablers for women participating in the weave randomised controlled trial

BACKGROUND: Interventions in health settings for intimate partner violence (IPV) are being increasingly recognised as part of a response to addressing this global public health problem. However, interventions targeting this sensitive social phenomenon are complex and highly susceptible to context. This study aimed to elucidate factors involved in women's uptake of a counselling intervention delivered by family doctors in the weave primary care trial (Victoria, Australia).

METHODS: We analysed associations between women's and doctors' baseline characteristics and uptake of the intervention. We interviewed a random selection of 20 women from an intervention group women to explore cognitions relating to intervention uptake. Interviews were audio-recorded, transcribed, coded in NVivo 10 and analysed using the theory of planned behaviour (TPB).

RESULTS: Abuse severity and socio-demographic characteristics (apart from current relationship status) were unrelated to uptake of counselling (67/137 attended sessions). Favourable doctor communication was strongly associated with attendance. Eight themes emerged, including four sets of beliefs that influenced attitudes to uptake: (i) awareness of the abuse and readiness for help; (ii) weave as an avenue to help; (iii) doctor's communication; and (iv) role in providing care for IPV; and four sets of beliefs regarding women's control over uptake: (v) emotional health, (vi) doctors' time, (vii) managing the disclosure process and (viii) viewing primary care as a safe option.

CONCLUSIONS: This study has identified factors that can promote the implementation and evaluation of primary care-based IPV interventions, which are relevant across health research settings, for example, ensuring fit between implementation strategies and characteristics of the target group (such as range in readiness for intervention). On practice implications, providers' communication remains a key issue for engaging women. A key message arising from this work concerns the critical role of primary care and health services more broadly in reaching victims of domestic violence, and providing immediate and ongoing support (depending on the healthcare context).

Approaches to population health care : the emerging context!

This paper provides a review of recent developments in population-based approaches to community health and explores the origins of the population health concept and its implications for the operation of health service management. There is a growing perception among health professionals that the key to improving health outcomes will be the implementation of integrated and preventive population-based resource management rather than investment in systems that respond to crises and health problems at the acute end of the service provision spectrum only. That is, we will need increasingly to skew our community health and welfare investments towards preventive care, education, lifestyle change, self-management and environmental improvement if we are to reduce the rate of growth in the incidence of chronic disease and mitigate the impact of these diseases upon the acute health care system. While resources will still need to be devoted to the treatment and management of physical trauma, infectious diseases, inherited illness and chronic conditions, it is suggested we could reduce the rate at which demand for these services is increasing at present by managing our environment and communities better, and through the implementation of more effective early intervention programs across particular population groups. Such approaches are known generally as population health management, as opposed to individual or illness - based health management' or even public health - and suggest that health systems might productively focus in the future on population level causation and not just upon disease-specific problems or illness management after the fact. Population health approaches attempt to broaden our understanding of causation and manage health through an emphasis on the health of whole populations and by building healthy communities rather than seeing "health care" as predominantly about illness management or responses to health crises. The concept also presupposes the existence of cleaner and healthier environments, clean water and food, and the existence of vibrant social contexts in which individuals are able to work for the overall good of communities and, ultimately, of each other.

Managing health care in Australia : steps on the health care roundabout?

This paper explores some of the lessons of the coordinated care trials in Australia in the context of managed care in America and asks how do we best manage our finite health care dollars for the most equitable and effective outcomes for whole populations? The COAG trial in Australia tested a more structured process for managing the care of patients with chronic illness and postulated that currently fragmented health system funding could be pooled around individual patient need, and managed for improved economic outcomes and patient wellbeing. There is little doubt, following this initiative and much work in other countries, that as health care costs rise, for a range of reasons, improvements are needed in the management of our resources if we are to control rising health care costs. We also know that chronic illness, much of which is preventable and avoidable, is the major component in the rising health care cost equation and a factor likely to consume around 75% of our health dollars in the future. Much chronic illness can be prevented through social and population health strategies and we know that even if chronic illness can?t be prevented, it can be managed better through community-based chronic illness management programs. These programs rely on information, education, patient lifestyle and behaviour change, and on patients developing improved self-management skills. But, what is the best way to manage population health in Australia and ensure equity and fairness in the health care market as we evolve new approaches, especially to the management of chronic illness?

Lateral positioning for critically ill adult patients

BACKGROUND: Critically ill patients require regular body position changes to minimize the adverse effects of bed rest, inactivity and immobilization. However, uncertainty surrounds the effectiveness of lateral positioning for improving pulmonary gas exchange, aiding drainage of tracheobronchial secretions and preventing morbidity. In addition, it is unclear whether the perceived risk levied by respiratory and haemodynamic instability upon turning critically ill patients outweighs the respiratory benefits of side-to-side rotation. Thus, lack of certainty may contribute to variation in positioning practice and equivocal patient outcomes. OBJECTIVES: To evaluate effects of the lateral position compared with other body positions on patient outcomes (mortality, morbidity and clinical adverse events) in critically ill adult patients. (Clinical adverse events include hypoxaemia, hypotension, low oxygen delivery and global indicators of impaired tissue oxygenation.) We examined single use of the lateral position (i.e. on the right or left side) and repeat use of the lateral position (i.e. lateral positioning) within a positioning schedule. SEARCH METHODS: We searched the Cochrane Central Register of Controlled Trials (CENTRAL; 2015, Issue 5), MEDLINE (1950 to 23 May 2015), the Cumulative Index to Nursing and Allied Health Literature (CINAHL) (1937 to 23 May 2015), the Allied and Complementary Medicine Database (AMED) (1984 to 23 May 2015), Latin American Caribbean Health Sciences Literature (LILACS) (1901 to 23 May 2015), Web of Science (1945 to 23 May 2015), Index to Theses in Great Britain and Ireland (1950 to 23 May 2015), Trove (2009 to 23 May 2015; previously Australasian Digital Theses Program (1997 to December 2008)) and Proquest Dissertations and Theses (2009 to 23 May 2015; previously Proquest Digital Dissertations (1980 to 23 May 2015)). We handsearched the reference lists of potentially relevant reports and two nursing journals. SELECTION CRITERIA: We included randomized and quasi-randomized trials examining effects of lateral positioning in critically ill adults. We included manual or automated turns but limited eligibility to studies that included duration of body position of 10 minutes or longer. We examined each lateral position versus at least one comparator (opposite lateral position and/or another body position) for single therapy effects, and the lateral positioning schedule (repeated lateral turning) versus other positioning schedules for repetitive therapy effects. DATA COLLECTION AND ANALYSIS: We pre-specified methods to be used for data collection, risk of bias assessment and analysis. Two independent review authors carried out each stage of selection and data extraction and settled differences in opinion by consensus, or by third party adjudication when disagreements remained unresolved. We planned analysis of pair-wise comparisons under composite time intervals with the aim of considering recommendations based on meta-analyses of studies with low risk of bias. MAIN RESULTS: We included 24 studies of critically ill adults. No study reported mortality as an outcome of interest. Two randomized controlled trials (RCTs) examined lateral positioning for pulmonary morbidity outcomes but provided insufficient information for meta-analysis. A total of 22 randomized trials examined effects of lateral positioning (four parallel-group and 18 cross-over designs) by measuring various continuous data outcomes commonly used to detect adverse cardiopulmonary events within critical care areas. However, parallel-group studies were not comparable, and cross-over studies provided limited data as the result of unit of analysis errors. Eight studies provided some data; most of these were single studies with small effects that were imprecise. We pooled partial pressure of arterial oxygen (PaO2) as a measure to detect hypoxaemia from two small studies of participants with unilateral lung disease (n = 19). The mean difference (MD) between lateral positions (bad lung down versus good lung down) was approximately 50 mmHg (MD -49.26 mmHg, 95% confidence interval (CI) -67.33 to -31.18; P value < 0.00001). Despite a lower mean PaO2 for bad lung down, hypoxaemia (mean PaO2 < 60 mmHg) was not consistently reported. Furthermore, pooled data had methodological shortcomings with unclear risk of bias. We had similar doubts regarding internal validity for other studies included in the review. AUTHORS' CONCLUSIONS: Review authors could provide no clinical practice recommendations based on the findings of included studies. Available research could not eliminate the uncertainty surrounding benefits and/or risks associated with lateral positioning of critically ill adult patients. Research gaps include the effectiveness of lateral positioning compared with semi recumbent positioning for mechanically ventilated patients, lateral positioning compared with prone positioning for acute respiratory distress syndrome (ARDS) and less frequent changes in body position. We recommend that future research be undertaken to address whether the routine practice of repositioning patients on their side benefits all, some or few critically ill patients.

Perceptions et croyances relatives à l’hygiène des mains chez les infirmières de deux hôpitaux de la République démocratique du Congo

Cette étude visait à documenter les perceptions et les croyances sur l’hygiène des mains chez des infirmières de deux hôpitaux de la République démocratique du Congo (RDC). Le modèle PRECEDE-PROCEED a guidé les travaux et permis de centrer l’analyse sur les facteurs prédisposants et les facteurs facilitants, éléments favorisant l’adoption des comportements de santé. Le devis utilisé est de type descriptif corrélationnel. Un échantillon de convenance incluant 74 infirmières recrutées dans les deux hôpitaux a été assemblé. Les données ont été recueillies au moyen d’un questionnaire auto-administré composé de 34 questions, tirées d’outils repérés dans la recension des écrits. Les questions portaient sur les connaissances, les perceptions au regard de l’hygiène des mains et l’accès aux infrastructures facilitant l’adoption de ce comportement. La collecte des données s’est déroulée à Kinshasa, capitale de la RDC. Les résultats révèlent d’importantes lacunes dans les connaissances. Les perceptions relatives aux normes sociales sont ressorties comme davantage favorables. Les résultats révèlent également des lacunes en ce qui a trait aux facteurs facilitants, notamment dans l’utilisation de la friction hydro-alcoolique. Par ailleurs, les infirmières les plus instruites et les plus expérimentées étaient plus nombreuses à percevoir l'importance de la pratique d’hygiène des mains. La discussion aborde quelques pistes en termes d’actions à entreprendre pour améliorer les comportements d’hygiène chez les infirmières dans les pays en développement telle la RDC.

Perceptions et croyances relatives à l’hygiène des mains chez les infirmières de deux hôpitaux de la République démocratique du Congo

Cette étude visait à documenter les perceptions et les croyances sur l’hygiène des mains chez des infirmières de deux hôpitaux de la République démocratique du Congo (RDC). Le modèle PRECEDE-PROCEED a guidé les travaux et permis de centrer l’analyse sur les facteurs prédisposants et les facteurs facilitants, éléments favorisant l’adoption des comportements de santé. Le devis utilisé est de type descriptif corrélationnel. Un échantillon de convenance incluant 74 infirmières recrutées dans les deux hôpitaux a été assemblé. Les données ont été recueillies au moyen d’un questionnaire auto-administré composé de 34 questions, tirées d’outils repérés dans la recension des écrits. Les questions portaient sur les connaissances, les perceptions au regard de l’hygiène des mains et l’accès aux infrastructures facilitant l’adoption de ce comportement. La collecte des données s’est déroulée à Kinshasa, capitale de la RDC. Les résultats révèlent d’importantes lacunes dans les connaissances. Les perceptions relatives aux normes sociales sont ressorties comme davantage favorables. Les résultats révèlent également des lacunes en ce qui a trait aux facteurs facilitants, notamment dans l’utilisation de la friction hydro-alcoolique. Par ailleurs, les infirmières les plus instruites et les plus expérimentées étaient plus nombreuses à percevoir l'importance de la pratique d’hygiène des mains. La discussion aborde quelques pistes en termes d’actions à entreprendre pour améliorer les comportements d’hygiène chez les infirmières dans les pays en développement telle la RDC.