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The Mediterranean diet has emerged as a promising dietary pattern for preventing non-alcoholic fatty liver disease (NAFLD). This study aimed to examine the role of the Mediterranean diet on the risk of NAFLD in Turkish adults. A total of 252 individuals (126 NAFLD and 126 age- and sex-matched controls) participated in this case-control study. Dietary intake was assessed with a 24-h recall, and adherence to the Mediterranean diet was evaluated using the Mediterranean Diet Adherence Screener (MEDAS). Logistic regression models were applied to estimate odds ratios (ORs). The prevalence of NAFLD was higher in the lowest tertile (64.6%) and lower in the highest tertile (30.5%; p<0.001). Moderate adherence to the Mediterranean diet was associated with a 57.0% lower risk of NAFLD after adjusting for age, sex, BMI, and energy intake. High adherence conferred an 86.0% reduction after adjusting for age, sex, BMI, energy intake, and comorbidities. Frequent consumption of butter, margarine, cream, (OR=2.75; 95% CI: 1.72–6.43) and sugar-sweetened beverages (OR=2.87; 95% CI: 1.20–6.87) significantly increased the risk. However, consuming nuts three or more servings per week was protective (OR=0.46; 95% CI: 0.21–0.99). In individuals who did not consume ≥3 servings of fruit daily, the risk of NAFLD was significantly reduced (OR=0.28; 95% CI: 0.16–0.69). Adherence to the Mediterranean diet was strongly associated with a reduced risk of NAFLD, highlighting the importance of limiting saturated fats and sugar-sweetened beverages while promoting nuts as practical strategies for prevention.
Plant-based diets are favourable for both climate and health. However, not much is known about different barriers to adopting more plant-based diets across sociodemographic groups. This study examined the proportions of the population reporting a shift towards more plant-based diets and identified perceived barriers to these changes across different sociodemographic groups. The study was based on the Healthy Finland Survey 2022–2023, including 5390 participants aged 20–74 years. Participants responded to questions on plant-based diets using pre-defined response options. Results were presented as prevalences and 95% CIs. Women reported that they had changed their diets to more plant-based more often than men did (46% vs. 31%). Urban residents, higher educated participants, and those with higher income were more likely to have adopted more plant-based diets than others. Concerns about nutritional adequacy (women 20%; men 24%) and lacking skills to prepare tasty vegetarian foods (women 30%; men 28%) were common perceived barriers. In men, barriers included a dislike of vegetarian foods (23%) and a lack of interest (28%). In women, 17% cited the preferences of their close ones as a barrier. Barriers also differed between groups. Older participants were more concerned about the nutritional adequacy (29%), while younger participants struggled with cooking skills (35%). One third of men living in rural areas or with basic education reported a lack of interest in the topic. Tailored health promotion and food education strategies are critical to overcoming barriers to adopting plant-based diets in diverse sociodemographic groups.
Effective leadership is critical to ensuring safety, efficiency and maximum productivity in the operating room (OR). This practical, evidence-based third edition focuses on the dynamics of a successful OR environment to underline the key techniques for management of policies, systems, staff members and teams. Fully updated to include recent clinical guidelines, the book provides the 'A-Z' of OR management, including sections on metrics, scheduling, human resource management, leadership principles, economics, quality assurance, recovery, ambulatory practice and topics specific to anesthesia and pain service providers. Featuring new chapters on the role of artificial intelligence in transforming operating room perform, training, certification and career development, instrumentation management, and safety of operating room personnel. With contributions from authors with unrivalled experience in the field, this new edition continues to be an essential guide for anyone working in the OR including anaesthesiologists, surgeons, nurses, and administrators.
Standard Community Assessment for Public Health Emergency Response (CASPER) methods, a type of rapid needs assessment (RNA) for collecting data on household needs and impacts following emergencies, are not always suitable for rural, destroyed, or severely damaged communities, or disasters affecting small geographical areas. The objectives of this modified RNA were to: (1) identify the strengths, limitations, and operational challenges for utilization of modified RNAs for post-disaster, quick response research; and (2) capture the acute mental and physical health impacts and lived experiences of communities affected by the 2024 Arbor Day tornado in Nebraska (USA). This field study tested modifications of the CASPER methodology in rural and inaccessible communities in Washington and Douglas County, Nebraska following the 2024 Arbor Day tornado. A 60-item survey was developed using validated questions, including on mental and physical health impacts. Survey completion rates for Washington and Douglas Counties were 57.3% and 89.3%, respectively. Exacerbation of existing conditions, worsening allergies, and stress were commonly reported following the tornado. Modified RNAs were useful and feasible approaches for capturing perishable data following the 2024 Arbor Day tornado outbreak. These findings can be used to inform not only public health response but also future planning and policy.
Over the last fifty years, British patients have been made into consumers. This book considers how and why the figure of the patient-consumer was brought into being, paying particular attention to the role played by patient organisations. Making the Patient-Consumer explores the development of patient-consumerism from the 1960s to 2010 in relation to seven key areas. Patient autonomy, representation, complaint, rights, information, voice and choice were all central to the making of the patient-consumer. These concepts were used initially by patient organisations to construct the figure of the patient-consumer, but by the 1990s the government had taken over as the main actor shaping ideas about patient consumerism. Making the Patient-Consumer is the first empirical, historical account of a fundamental shift in modern British health policy and practice. The book will be of use to historians, public policy analysts and all those attempting to better understand the nature of contemporary healthcare.
This chapter examines attempts to represent the patient-consumer during the 1970s, focusing particularly on the part played by the Community Health Councils (CHCs). It suggests that a lack of clarity about what patient-consumer representation was, who was being represented, how this could best be achieved, and its ability to have any impact on health services, beset the CHCs from the outset. Uncertainty about the meaning and purpose of patient representation manifested itself in conflicting views about the CHCs’ role and effectiveness that impinged upon their ability to represent patients’ interests. Moreover, the CHCs had to contend with better established and more powerful interest groups within health care such as health professionals and health service administrators. Beginning with the origins of the CHCs, moving on to consider the meanings of representation, and then assessing the effectiveness of the councils, this chapter will demonstrate that having a voice and being heard were not the same thing.
The aim of this chapter is to explore the broader meaning and application of rights talk in connection with health from the 1970s to the early 1990s. It begins by considering the various ways in which the language of rights was used in the context of health. The chapter then moves on to consider the application of such language, through attempts to introduce a Rights of Patients Bill. A selection of patient’s rights guides and charters are also analysed, and the chapter suggests that it was unclear whether these were addressed to the individual patient, or all patients. A more collective understanding of patients’ rights was exhibited by organisations such as the Community Rights Project, which aimed to enhance democracy and accountability within the NHS through the language of rights. The establishment of Department of Health’s The Patient’s Charter in 1991, however, undermined such collective conceptualisations of rights. Addressed to the individual patient rather than all patients, The Patient’s Charter was indicative not only of an individualised approach to patients’ rights, but of a wider shift in the conceptualisation of the patient as consumer and who could speak for this figure.
This chapter will explore how it was that patient choice came to occupy a central position within health policy from the late 1990s onwards. Beginning with an exploration of the notion of choice in health prior to this period, the chapter will then go on to chart the rise of choice as a central objective of health policy under the New Labour government. The chapter suggests that although the notion of choice was present in earlier formulations of patient consumerism, the meaning and relative importance ascribed to choice changed in the late 1990s and early 2000s. A crucial shift took place that involved a move away from choice as something that was of importance to patients collectively and towards a focus on choice as an individual matter. Such a focus on the patient rather than patients undermined the position of patient-consumer organisations that aimed to represent patients as a group. Speaking for patients was more difficult when the individual was thought to be best at determining his or her own needs.
Mathematical modeling projects consequences of disasters based on algorithms and parameters, with explicit assumptions that can be varied to explore potential variation in outcomes. Modeling of mechanical trauma, thermal burn, and ionizing radiation injuries due to nuclear detonations has been used at the Department of Health and Human Services, Administration for Strategic Preparedness and Response (HHS/ASPR) to inform needs assessments for medical countermeasures. Physiological modeling for the Defense Threat Reduction Agency (DTRA) projects outcomes of injury from ionizing radiation combined with mechanical trauma and/or thermal burns including effects on physical capabilities, which are used to evaluate the population consequences of nuclear detonations. Public health response modeling explores the effects of variation in operational practices such as triage and allocation of resources for treatment, which informs decisions and practices toward improvement in planning for response to nuclear detonations. Research can inform assumptions and algorithms of modeling, and strategic use of modeling can further inform planning for such topics as shielding, survival, and survivor behavior like sheltering and evacuation.
We present the case of a 14-year-old male patient referred to paediatric cardiology for the incidental finding of a cardiac murmur and initially diagnosed with asymmetric septal hypertrophic cardiomyopathy. Due to deterioration in his functional class (NYHA II/IV), he was admitted to our institution for further evaluation. A hyperechoic mass measuring 35.7 mm × 39.4 mm was identified in the interventricular septum, with central vascularisation and a significant obstructive gradient in the right ventricular outflow tract (112 mmHg). Cardiac magnetic resonance imaging confirmed a highly vascularised lesion, hyperintense on HASTE, T1, and T2 sequences, with an extracellular volume of 67%, consistent with a cardiac haemangioma. Coronary CT angiography demonstrated perfusion by a septal branch of the left anterior descending artery. Given the anatomical involvement and the low feasibility of surgical management, cardiac catheterisation with embolisation of the septal branch using an Interlock Coil occlusion device was performed. Post-procedure angiography confirmed complete occlusion. Cardiac tumours in paediatrics are rare and generally benign, with haemangiomas being one of the least common neoplasms. Diagnosis relies on non-invasive imaging techniques, with echocardiography and magnetic resonance imaging playing crucial roles. In this case, the combination of echocardiography, coronary CT angiography, and catheterisation allowed for a comprehensive characterisation of the lesion and the development of a therapeutic strategy while minimising risks. The patient remains stable under follow-up. This multidisciplinary approach optimises the management of paediatric cardiac tumours, enabling individualised therapeutic options.
This chapter explains the rise of patient ‘voice’ in the late 1990s, explores its multiple meanings and the implications that these had for organisations claiming to speak for the patient-consumer. The abolition of the CHCs in 2003 was indicative of a change in ideas not only about who was best placed to speak for patient-consumers, but also in the kinds of things that they were expected to say. More attention was to be paid to the voice of the individual patient rather than patients’ voices as a whole. Such a view fitted with the broader reform of the NHS that was directed towards a more marketised model with a tendency to see patients as individuals rather than as a group. Examining the ‘alphabet soup’ of organisations that replaced the CHCs suggests that despite growing attention, collective mechanisms for representing the patient-consumer were weakened. Individual voice began to be equated with greater individual choice, leaving less space for collective patient representation.
Long-term pharmacological augmentation is central to care for treatment-resistant depression, yet until recently no adequately powered trials have examined it. With three such studies now published, we highlight the hope they offer for improving outcomes in this underserved population while highlighting caution in interpreting their collective findings without careful consideration of methodology and clinical context. We consider these issues and their implications for guiding more personalised treatment decisions aimed at sustained benefit in routine practice.