504 research outputs found

    The future of treating atypical depression: Exploring the role of Social Identity Theory in group-CBT

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    This item is only available electronically.Atypical depression (AD) is an overlooked and under-researched form of depression, with little to no research exploring the wide range of non-medication treatment options available. The lack of research in this area is concerning as evidence indicates that symptoms associated with AD include a longer and more severe depressive episode and a greater risk of suicidal behaviour than compared with the more traditional, melancholic depression (Weinstock et al., 2011). To ensure that providers are delivering the best form of intervention, it is essential to explore every treatment option. The present study sought to explore the efficacy of group cognitive behaviour therapy (CBT) on treating AD, with a focus on whether features of social identity theory have an influence during the group-intervention process. In this mixed-method study, participants (N=18) underwent a 10-week group intervention aimed to address issues associated with AD, with data collected pre-intervention, two-week post intervention, and 3-months post intervention to assess the effectiveness of the program. Feedback forms and interviews were undertaken and evaluated to explore whether there was a presence of social identity theory. Results revealed that the intervention significantly reduced depression levels and increased self-esteem levels in participants, indicating that group-CBT is an effective form of intervention for those with AD. Qualitative responses were subjected to thematic analysis, where themes aligning with social identity theory emerged, indicating that features of this theory may have influenced participants’ experiences and signified the importance that a positive group dynamic had in the outcome. This study offers a critical insight into the effectiveness of group-CBT, and provides an alternative and successful treatment option for those who experience AD.Thesis (B.PsychSc(Hons)) -- University of Adelaide, School of Psychology, 201

    Driving improvements in emerging disease surveillance through locally-relevant capacity strengthening

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    Emerging infectious diseases (EIDs) threaten the health of people, animals, and crops globally, but our ability to predict their occurrence is limited. Current public health capacity and ability to detect and respond to EIDs is typically weakest in low- and middle-income countries (LMICs). Many known drivers of EID emergence also converge in LMICs. Strengthening capacity for surveillance of diseases of relevance to local populations can provide a mechanism for building the cross-cutting and flexible capacities needed to tackle both the burden of existing diseases and EID threats. A focus on locally relevant diseases in LMICs and the economic, social, and cultural contexts of surveillance can help address existing inequalities in health systems, improve the capacity to detect and contain EIDs, and contribute to broader global goals for development

    Renewing the momentum for leptospirosis research in Africa

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    Risks of Future Droughts and their Impacts on Scottish Private Water Supplies

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    In recent years, Scotland has been experiencing lower-than-average rainfall in the spring and summer seasons leading to water scarcity in many parts of the country, especially during the summer months. Climate change is likely to exacerbate these dry conditions even more in the future, presenting significant risks to water resources management. Businesses and households, especially those relying on Private Water Supplies (PWS) in rural areas, such as boreholes and springs, have already observed noticeable changes in the quantity and quality of water during the dry periods. Around 3.5% of the Scottish population relies on PWS which includes households, industries, agriculture, and the tourism industry. This study aims to project future drier periods from 2041-2080 across Scotland on a 1-km grid, using the Standardised Precipitation and Evapotranspiration Index and the observed meteorological data from 1981-2020 as the baseline. Results suggest low to extreme drought conditions in all 1-km cells , with increases in dry conditions likely to be highest in the eastern parts of Scotland, showing a distinct spatial variability in drought characteristics across Scotland. In future work, past and future drought occurrences will be linked with the water quality characteristics of PWS to understand the likely impact of future droughts on Scotland’s water security. The water quality dataset has been made available from the Drinking Water Quality Regulator for Scotland for the period 2006-2020 for nearly 6000 PWS locations. These PWS have been monitored twice a year on an average for their water quality. They span across 25 administrative areas in Scotland and represent roughly 27% of the total PWS in Scotland. Water quality variables such as faecal coliforms, E.coli, iron, turbidity, lead, pH, colour, nitrate and phosphate will be included in the analysis to facilitate planning for effective, resilient water resources management and ensure access to clean water to maintain health and livelihoods

    Integrating serological and genetic data to quantify cross-species transmission: brucellosis as a case study

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    Epidemiological data are often fragmented, partial, and/or ambiguous and unable to yield the desired level of understanding of infectious disease dynamics to adequately inform control measures. Here, we show how the information contained in widely available serology data can be enhanced by integration with less common type-specific data, to improve the understanding of the transmission dynamics of complex multi-species pathogens and host communities. Using brucellosis in Northern Tanzania as a case-study, we developed a latent process model based on serology data obtained from the field, to reconstruct Brucella transmission dynamics. We were able to identify sheep and goats as a more likely source of human and animal infection than cattle; however, the highly cross-reactive nature of Brucella spp. meant that it was not possible to determine which Brucella species (B. abortus or B. melitensis) is responsible for human infection. We extended our model to integrate simulated serology and typing data, and show that although serology alone can identify the host source of human infection under certain restrictive conditions, the integration of even small amounts (5%) of typing data can improve understanding of complex epidemiological dynamics. We show that data integration will often be essential when more than one pathogen is present and when the distinction between exposed and infectious individuals is not clear from serology data. With increasing epidemiological complexity, serology data become less informative. However, we show how this weakness can be mitigated by integrating such data with typing data, thereby enhancing the inference from these data and improving understanding of the underlying dynamics

    Silyl trifluoromethanesulfonate-activated para-methoxybenzyl methyl ether as an alkylating agent for thiols and aryl ketones

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    para-Methoxybenzyl methyl ether acts as an alkylating agent for thiols in the presence of trimethylsilyl trifluoromethanesulfonate and trialkylamine base in good yields (58-96%). Aryl ketones are alkylated under similar conditions, probably through an enol silane intermediate, also in high yields (67-95%). The active alkylating species is likely a p-methoxybenzyl cation

    Incidence of human brucellosis in the Kilimanjaro Region of Tanzania in the periods 2007-2008 and 2012-2014

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    Background: Brucellosis causes substantial morbidity among humans and their livestock. There are few robust estimates of the incidence of brucellosis in sub-Saharan Africa. Using cases identified through sentinel hospital surveillance and health care utilization data, we estimated the incidence of brucellosis in Moshi Urban and Moshi Rural Districts, Kilimanjaro Region, Tanzania, for the periods 2007–2008 and 2012–2014. Methods: Cases were identified among febrile patients at two sentinel hospitals and were defined as having either a 4-fold increase in Brucella microscopic agglutination test titres between acute and convalescent serum or a blood culture positive for Brucella spp. Findings from a health care utilization survey were used to estimate multipliers to account for cases not seen at sentinel hospitals. Results: Of 585 patients enrolled in the period 2007–2008, 13 (2.2%) had brucellosis. Among 1095 patients enrolled in the period 2012–2014, 32 (2.9%) had brucellosis. We estimated an incidence (range based on sensitivity analysis) of brucellosis of 35 (range 32–93) cases per 100 000 persons annually in the period 2007–2008 and 33 (range 30–89) cases per 100 000 persons annually in the period 2012–2014. Conclusions: We found a moderate incidence of brucellosis in northern Tanzania, suggesting that the disease is endemic and an important human health problem in this area

    Comparison of the estimated incidence of acute leptospirosis in the Kilimanjaro Region of Tanzania between 2007-08 and 2012-14

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    Background: The sole report of annual leptospirosis incidence in continental Africa of 75–102 cases per 100,000 population is from a study performed in August 2007 through September 2008 in the Kilimanjaro Region of Tanzania. To evaluate the stability of this estimate over time, we estimated the incidence of acute leptospirosis in Kilimanjaro Region, northern Tanzania for the time period 2012–2014. Methodology and Principal Findings: Leptospirosis cases were identified among febrile patients at two sentinel hospitals in the Kilimanjaro Region. Leptospirosis was diagnosed by serum microscopic agglutination testing using a panel of 20 Leptospira serovars belonging to 17 separate serogroups. Serum was taken at enrolment and patients were asked to return 4–6 weeks later to provide convalescent serum. Confirmed cases required a 4-fold rise in titre and probable cases required a single titre of ≥800. Findings from a healthcare utilisation survey were used to estimate multipliers to adjust for cases not seen at sentinel hospitals. We identified 19 (1.7%) confirmed or probable cases among 1,115 patients who presented with a febrile illness. Of cases, the predominant reactive serogroups were Australis 8 (42.1%), Sejroe 3 (15.8%), Grippotyphosa 2 (10.5%), Icterohaemorrhagiae 2 (10.5%), Pyrogenes 2 (10.5%), Djasiman 1 (5.3%), Tarassovi 1 (5.3%). We estimated that the annual incidence of leptospirosis was 11–18 cases per 100,000 population. This was a significantly lower incidence than 2007–08 (p<0.001). Conclusions: We estimated a much lower incidence of acute leptospirosis than previously, with a notable absence of cases due to the previously predominant serogroup Mini. Our findings indicate a dynamic epidemiology of leptospirosis in this area and highlight the value of multi-year surveillance to understand leptospirosis epidemiology
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