763 research outputs found

    Predicting parental sensitivity: contextual stress exposure across preconception to parenthood

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    This thesis investigated the influence of concurrent and historical stress on parental sensitivity to infants. Parental sensitivity was found to be mostly resilient to a history of stress but when living with stress, parents were often less responsive to infant needs. Findings support the relevance of interventions and support for enhancing parental sensitivity in contexts of pressure

    End of life care in chronic obstructive pulmonary disease: in search of a good death

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    Chronic obstructive pulmonary disease (COPD) is an incurable, progressive illness that is the fourth commonest cause of death worldwide. Death tends to occur after a prolonged functional decline associated with uncontrolled symptoms, emotional distress and social isolation. There is increasing evidence that the end of life needs of those with advanced COPD are not being met by existing services. Many barriers hinder the provision of good end of life care in COPD, including the inherent difficulties in determining prognosis. This review provides an evidence-based approach to overcoming these barriers, summarising current evidence and highlighting areas for future research. Topics include end of life needs, symptom control, advance care planning, and service development to improve the quality of end of life care

    Supporting Child and Family Wellbeing through Nature during the Pandemic

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    The global pandemic of COVID-19 poses many unprecedented challenges on our way of life. Since the introduction of social distancing measures as one of our biggest weapons in slowing the spread of disease and mitigating the effects on the health services, other challenges have been introduced. One of these is the challenge of supporting and maintaining wellbeing in children and families. A way to achieve this is through maintaining our contact and connection with the non-human natural world. Regular contact with the natural world has been found to have benefits for our mental and physical health. The aim of this paper is to identify how families can gain the benefits of nature engagement, in the instances where the access might be limited or non-existent  Whilst we are able to identify a number of opportunities and mechanisms for nature contact and connection to promoting family wellbeing there are some methodological challenges remaining, given that a significant number of research papers exploring the affective influence of nature contact and connection focuses on adults. We also identify a number of areas where research would be beneficial to better understand the mediating influences on wellbeing from nature contact and connection

    Teenage and Young Adult Cancer-Related Fatigue Is Prevalent, Distressing, and Neglected: It Is Time to Intervene. A Systematic Literature Review and Narrative Synthesis.

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    PURPOSE: Cancer-related fatigue in adults has been the subject of considerable recent research, confirming its importance as a common and debilitating symptom, and establishing a number of evidence-based interventions. There has, however, been limited focus on the fatigue suffered by teenagers and young adults with cancer, a group recognized as having unique experiences and developmental needs. We have undertaken a systematic review of the literature to provide a comprehensive overview of studies evaluating fatigue in this younger patient group in order to guide clinical practice and future research. METHOD: We searched MEDLINE, EMBASE, PsycINFO, and CINAHL databases for literature containing data relating to any aspect of fatigue in patients aged 13-24 at cancer diagnosis or treatment. RESULTS: Sixty articles were identified, of which five described interventional clinical trials. Cancer-related fatigue was consistently one of the most prevalent, severe, and distressing symptoms, and it persisted long-term in survivors. It was associated with a number of factors, including poor sleep, depression, and chemotherapy. There was little evidence for the effectiveness of any intervention, although exercise appears to be the most promising. Importantly, fatigue was itself a significant barrier to physical and social activities. CONCLUSION: Cancer-related fatigue is a major and disabling problem in young cancer patients. Effective management strategies are needed to avoid compounding the dependence and social isolation of this vulnerable patient group. Future research should focus on providing evidence for the effectiveness of interventions, of which activity promotion and management of concurrent symptoms are the most promising.SB and AS were funded by the National Institute for Health Research (NIHR) Collaboration for Leadership in Applied Health Research and Care East of England at Cambridgeshire and Peterborough NHS Foundation Trust.This is the author accepted manuscript. The final version is available via Mary Ann Liebert at http://online.liebertpub.com/doi/abs/10.1089/jayao.2014.0023#/doi/abs/10.1089/jayao.2014.0023

    Breathlessness services as a new model of support for patients with respiratory disease

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    The complexity of breathlessness in advanced disease requires a diversity of measures ideally tailored to the individual patient needs. Breathlessness services' have been systematically developed and tested to provide specific interventions and support for patients and their carers. The aim of this article is (1) to identify and describe components of breathlessness services and (2) to describe the clinical model of one specific service in more detail. This article is based on a systematic review evaluating randomized controlled trials (RCTs) and quasi-RCTs which examine the effectiveness of services aiming to improve breathlessness of patients with advanced disease. The Munich Breathlessness Service (MBS) is described in detail as an example of a recently set-up specialist service. Five service models were identified which were tested in six RCTs. Services varied regarding structure and composition with face-to-face meetings, some with additional telephone contacts. Service duration was median 6 weeks (range 2-12 weeks). Involved professions were nurses, various therapists and, in two models, also physicians. The breathing-thinking-functioning model was targeted by various service components. The MBS is run by a multi-professional team mainly with physicians and physiotherapists. Patients are seen weekly over 5-6 weeks with an individualized management plan. Breathlessness services are a new model for patients with advanced disease integrating symptom management and early access to palliative care
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