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This study aimed to describe medical students’ perceptions and experiences with health policy and advocacy training and practice and define motivations and barriers for engagement.
Methods:
This was a mixed-methods study of medical students from May to October 2022. Students were invited to participate in a web-based survey and optional follow-up phone interview. Surveys were analyzed using descriptive statistics. Phone interviews were audio-recorded, transcribed, and de-identified. Interviews were coded inductively using a coding dictionary. Themes were identified using thematic analysis.
Results:
35/580 survey responses (6% response rate) and 15 interviews were completed. 100% rated social factors as related to overall health. 65.7% of participants felt “very confident” or “extremely confident” in identifying social needs but only 11.4% felt “very confident” in addressing these needs. From interviews, six themes were identified: (1) participants recognized that involvement in health policy and/or advocacy is a duty of physicians; (2) participants acknowledged physicians’ voices as well respected; (3) participants were comfortable identifying social determinants of health but felt unprepared to address needs; (4) barriers to future involvement included intimidation, self-doubt, and skepticism of impact; (5) past exposures and awareness of advocacy topics motivated participants to engage in health policy and/or advocacy during medical school; and (6) participants identified areas where the training on these topics excelled and offered recommendations for improvement, including simulation, earlier integration, and teaching on health-related laws and policies.
Conclusions:
This study highlights the importance of involvement in health policy and advocacy among medical students and the need for enhanced education and exposure.
The depression, obstructive sleep apnea and cognitive impairment (DOC) screen assesses three post-stroke comorbidities, but additional information may be gained from the time to complete the screen. Cognitive screening completion time is rarely used as an outcome measure.
Objective:
To assess DOC screen completion time as a predictor of cognitive impairment in stroke/transient ischemic attack clinics.
Methods:
Consecutive English-speaking stroke prevention clinic patients consented to undergo screening and neuropsychological testing (n = 437). DOC screen scores and times were compared to scores on the NINDS-CSC battery using multiple linear regression (controlling for age, sex, education and stroke severity) and receiver operating characteristic (ROC) curve analysis.
Results:
Completion time for the DOC screen was 3.8 ± 1.3 minutes. After accounting for covariates, the completion time was a significant predictor of the speed of processing (p = 0.002, 95% CI: −0.016 to −0.004), verbal fluency (p < 0.001, CI: −0.012 to −0.006) and executive function (p = 0.004, CI: −0.006 to −0.001), but not memory. Completion time above 5.5 minutes was associated with a high likelihood of impairment on executive and speed of processing tasks (likelihood ratios 3.9–5.2).
Conclusions:
DOC screen completion time is easy to collect in routine care. People needing over 5.5 minutes to be screened likely have deficits in executive functioning and speed of processing – areas commonly impaired, but challenging to screen for, after stroke. DOC screen time provides a simple, feasible approach to assess these under-identified cognitive impairments.
This scoping review addresses gaps in the existing literature on dietary guidelines for pregnant and lactating women globally. The study delves into adherence levels, identifies influencing factors and examines outcomes associated with these guidelines. Analysing food-based dietary guidelines (FBDG) from around the world, the review reveals that half of the countries lack FBDG, with only 15% providing tailored advice for pregnant and lactating women. Utilising data extracted from forty-seven articles across MEDLINE and EMBASE, the study highlights a scarcity of adherence studies, particularly in low- or middle-income countries (LMIC), and emphasises the lack of research during lactation. Overall adherence to dietary guidelines is low, with disparities in fruit, vegetable, whole grain and fish consumption. Positive correlations with adherence include age, education, employment, social class and certain medical histories, while negative correlations involve smoking, alcohol consumption, metropolitan residence and elevated BMI. The study documented significant associations between adherence and reduced risks of gestational complications but calls for further exploration of intermediate nutritional outcomes such as micronutrient deficiencies and child growth. Emphasising the urgency for globally standardised guidelines, especially in LMIC, this review provides a foundational call for prioritised studies and strategies to enhance dietary practices for pregnant and lactating women worldwide.
This chapter offers an account of the key events shaping modern forensic psychiatry since the 1950s, including legal reforms, political initiatives and key reports which have influenced practice. These are summarised in a narrative beginning with the 1959 Mental Health Act and concluding with the most recent Wessely proposals for reform. The critical clinical events including the cases of Graham Young, Peter Sutcliffe, Christopher Clunis and Michael Stone, the Carstairs escapes and the Butler, Reed, Blom-Cooper, Fallon and Tilt reports are discussed. The chapter includes a commentary on the development of medium-secure services and the refocussing of high-secure care since 2000.
This chapter is a guide to taking on a first consultant post in forensic psychiatry, a guide to supervising trainee doctors in forensic psychiatry and an overview of advice from a group of senior clinical directors in forensic psychiatry across multiple jurisdictions. It is designed to offer informal advice to consultant forensic psychiatrists on a wide range of issues that pertain to clinical practice and management that is rarely contained in textbooks.
This article aims to provide psychiatrists with an overview of early release of serving prisoners and parole, using the example of the Parole Board for England and Wales. The centrality of risk assessment and management and its clinical implications for release are reviewed. Offenders who come before a parole board and require a psychiatrist to be a member of the panel and who need evidence from psychiatrists on their disorder are often characterised by the complexity of their mental disorder. Offenders with complex mental disorder have difficulty assessing effective treatment and aftercare pathways, which can result in not being released. Offenders remitted back to prison following hospital transfer for treatment experience particular problems in being released. Three roles for psychiatrists in parole hearings are identified and guidance for effective participation in hearings is discussed. Commissioning implications of the difficulty assessing the need for community aftercare are noted.
This article examines how mythology and fictional narratives in medieval Irish literature were used to communicate important societal ideas and to encode political messages. It is a commonplace that stories about the past were re-used, re-cycled and re-interpreted in order to justify the present. These sources were utilized by the ruling classes in medieval Ireland to help explain the status quo on the one hand and to justify emerging change on the other. As the preference of the medieval Irish was ‘to take their history in the form of fiction’, many stories like Orgain Denna Rig (The Destruction of Dinn Rig) are extant from this period, stories which provide us with an important perspective on the growth and articulation of a significant facet of medieval Irish historiography.
Keywords: Early Laigin history; Labraid Loingsech; Cycles of the Kings; medieval Irish narrative texts; pseudo-history.
In her analysis of the medieval Irish pseudo-historical prophetic text Baile in Scáil ‘The Phantom's Vision’, Máire Herbert makes the case that ‘for the Uí Néill propagandists of the early eleventh century the mythic past provided a defensive strategy in a threatening present’. What she is referencing here is the use made by literati associated with Uí Néill – and particularly with the northern branch known as Cenél nEógain – of the motif of the sovereignty goddess bestowing a drink on the rightful ruler in order to re-assert their long-established rights to the kingship of Tara, reckoned as the pre-eminent kingship in early medieval Ireland. This use of myth to back up contemporary political concerns occurred at a period in their history when Uí Néill hegemony was under serious threat from powerful political rivals; the compilation of this particular narrative has been described as ‘a recourse by Cenél nEógain to the cornerstone of tradition at a time when they “were isolated from the currents of social, political, and ecclesiastical change”’. Baile in Scáil was not the only attempt made by Uí Néill propagandists to utilize the image of the sovereignty goddess in re-affirming their rights to the kingship of Tara.
Secure forensic mental health services treat patients with high rates of treatment-resistant psychoses. High rates of obesity and medical comorbidities are common. Population-based studies have identified high-risk groups in the event of SARS-CoV-2 infection, including those with problems such as obesity, lung disease and immune-compromising conditions. Structured assessment tools exist to ascertain the risk of adverse outcome in the event of SARS-CoV-2 infection.
Aims
To assess risk of adverse outcome in the event of SARS-CoV-2 infection in a complete population of forensic psychiatry patients using structured assessment tools.
Method
All patients of a national forensic mental health service (n = 141) were rated for risk of adverse outcome in the event of SARS-CoV-2 infection, using two structured tools, the COVID-Age tool and the COVID-Risk tool.
Results
We found high rates of relevant physical comorbidities. Mean chronological age was 45.5 years (s.d. = 11.4, median 44.1), mean score on the COVID-Age tool was 59.1 years (s.d. = 19.4, median 58.0), mean difference was 13.6 years (s.d. = 15.6), paired t = 10.9, d.f. = 140, P < 0.001. Three patients (2.1%) were chronologically over 70 years of age, compared with 43 (30.5%) with a COVID-Age over 70 (χ2 = 6.99, d.f. = 1, P = 0.008, Fisher's exact test P = 0.027).
Conclusions
Patients in secure forensic psychiatric services represent a high-risk group for adverse outcomes in the event of SARS-COV-2 infection. Population-based guidance on self-isolation and other precautions based on chronological age may not be sufficient. There is an urgent need for better physical health research and treatment in this group.
The concluding chapter seeks to develop a model of how human talk and action can be simultaneously expressive and repressive, and for understanding how a collective and ideological unsaid may be produced by human action. We draw together the contributions to this book, showing how these identify “signs of silence” and develop an analysis of the unsaid from qualitative studies of social interaction. We use ideas from ethnomethodology, conversation analysis, and discourse analysis to explain how the said and unsaid provide the ground for normative and accountable conduct, which, in turn, provides the foundation for qualitative studies of silence. We exploit the topographical metaphor of a “discursive terrain,” likening human action to paths that emerge to channel conduct along the contours of the said, and which simultaneously constitute the untrodden hinterlands of the unsaid. This “stigmergic” model of discursive action allows us to imagine how to bridge divides that are evident in the chapters of the book and elsewhere: between the conditions and outcomes of action and between discursive and psychoanalytic conceptions of the unsaid.
We open the book by showing – briefly, by a consideration of the South African Truth and Reconciliation Commission – how our social worlds are structured around silences and absences; and how even the process of unsilencing can lay down new absences. We explain why qualitative research in the social and human sciences has often neglected studying silences as it focused on the presences in talk, discourse, and interaction. We then provide a quick roadmap of the silence literature that has begun to gain momentum as part of what we cal, “a turn to silence.” Finally, we outline the perspectives and objectives of this book, arguing that qualitative studies are well suited to explore the unsaid, which we conceptualized as a slippery and multilayered form of social action. The chapter provides an overview of the collection and introduces the two broad questions answered by each of its contributors, namely: (1) “What is unsaid?” – focusing attention on methods, practices, and perspectives for identifying absence, and (2) “What is the unsaid doing (here)?” – focusing attention on the ideological significance of absence.
Qualitative Studies of Silence brings together influential qualitative researchers from across the social sciences and humanities who have sought to understand the power of what remains unsaid, both psychologically and socially. Each chapter identifies one or more signs of silence and explains how these can form the basis of a rigorous qualitative investigation. The authors also demonstrate how silences operate in our private and collective lives by fulfilling psychological, relational, institutional, and ideological functions. The book contains multiple disciplinary perspectives and presents analyses of wide-ranging topics, such as medical consultations, whistleblowers, silence in court, omission-as-propaganda, trauma survivors, the silence of war museums, racism in the Americas, gendered silences, paid domestic labour, the undocumented student movement, and the Nazi past. This collection shows how such qualitative studies can reveal and contribute to understanding the unsaid as social action.
Neuropsychological investigations can help untangle the aetiological and phenomenological heterogeneity of schizophrenia but have scarcely been employed in the context of treatment-resistant (TR) schizophrenia. No population-based study has examined neuropsychological function in the first-episode of TR psychosis.
Methods
We report baseline neuropsychological findings from a longitudinal, population-based study of first-episode psychosis, which followed up cases from index admission to 10 years. At the 10-year follow up patients were classified as treatment responsive or TR after reconstructing their entire case histories. Of 145 cases with neuropsychological data at baseline, 113 were classified as treatment responsive, and 32 as TR at the 10-year follow-up.
Results
Compared with 257 community controls, both case groups showed baseline deficits in three composite neuropsychological scores, derived from principal component analysis: verbal intelligence and fluency, visuospatial ability and executive function, and verbal memory and learning (p values⩽0.001). Compared with treatment responders, TR cases showed deficits in verbal intelligence and fluency, both in the extended psychosis sample (t = −2.32; p = 0.022) and in the schizophrenia diagnostic subgroup (t = −2.49; p = 0.017). Similar relative deficits in the TR cases emerged in sub-/sensitivity analyses excluding patients with delayed-onset treatment resistance (p values<0.01–0.001) and those born outside the UK (p values<0.05).
Conclusions
Verbal intelligence and fluency are impaired in patients with TR psychosis compared with those who respond to treatment. This differential is already detectable – at a group level – at the first illness episode, supporting the conceptualisation of TR psychosis as a severe, pathogenically distinct variant, embedded in aberrant neurodevelopmental processes.