71 research outputs found
Sustainable drainage system site assessment method using urban ecosystem services
The United Kingdom's recently updated approach to sustainable drainage enhanced biodiversity and amenity objectives by incorporating the ecosystem approach and the
ecosystem services concept. However, cost-effective and reliable methods to appraise the biodiversity and amenity values of potential sustainable drainage system (SuDS)sites and their surrounding areas are still lacking, as is a method to enable designers to distinguish and link the amenity and biodiversity benefits that SuDS schemes can offer. In this paper, therefore, the authors propose two ecosystem services- and disservices-based methods (i.e. vegetation structure cover-abundance examination and cultural ecosystem services and disservices variables appraisal) to aid SuDS designers to distinguish and link amenity and biodiversity benefits, and allow initial site
assessments to be performed in a cost-effective and reliable fashion. Forty-nine representative sites within Greater Manchester were selected to test the two methods.
Amenity and biodiversity were successfully assessed and habitat for species, carbon sequestration, recreation and education ecosystem services scores were produced,which will support SuDS retrofit design decision-making. Large vegetated SuDS sites with permanent aquatic features were found to be most capable of enhancing biodiversity- and amenity-related ecosystem services. Habitat for species and
recreation ecosystem services were also found to be positively linked to each other. Finally, waste bins on site were found to help reduce dog faeces and litter coverage. Overall, the findings presented here enable future SuDS retrofit designs to be more wildlife friendly and socially inclusive
What are family member experiences of the resuscitation of a relative?
This study aimed to gain insight into the feelings and perceptions of family members who witness an adult family member resuscitation. Little is known about family members' experiences and their needs and priorities. Resuscitation is a complex and highly emotive situation but guidance for paramedics to support families either in the decision-making process or to remain present is limited. Policy developments around improved and shared decision making are not evident in any guidance for resuscitation for paramedics. Paramedics have always been involved in resuscitation in the family home, but as they remain on scene for longer periods, it is important that the issue of family participation is addressed and specific guidance produced to enable paramedics to offer more focused and enhanced support to them, and involve the family members in the decision-making process which is a requirement from recent policy developments
Lack of association between PKLR rs3020781 and NOS1AP rs7538490 and type 2 diabetes, overweight, obesity and related metabolic phenotypes in a Danish large-scale study: case-control studies and analyses of quantitative traits
DNA methylation at birth within the promoter of ANRIL predicts markers of cardiovascular risk at 9 years
The quest for genetic risk factors for Crohn's disease in the post-GWAS era
Multiple genome-wide association studies (GWASs) and two large scale meta-analyses have been performed for Crohn's disease and have identified 71 susceptibility loci. These findings have contributed greatly to our current understanding of the disease pathogenesis. Yet, these loci only explain approximately 23% of the disease heritability. One of the future challenges in this post-GWAS era is to identify potential sources of the remaining heritability. Such sources may include common variants with limited effect size, rare variants with higher effect sizes, structural variations, or even more complicated mechanisms such as epistatic, gene-environment and epigenetic interactions. Here, we outline potential sources of this hidden heritability, focusing on Crohn's disease and the currently available data. We also discuss future strategies to determine more about the heritability; these strategies include expanding current GWAS, fine-mapping, whole genome sequencing or exome sequencing, and using family-based approaches. Despite the current limitations, such strategies may help to transfer research achievements into clinical practice and guide the improvement of preventive and therapeutic measures
A statistical method for region-based meta-analysis of genome-wide association studies in genetically diverse populations
Genome-wide association studies (GWAS) have become the preferred experimental design in exploring the genetic etiology of complex human traits and diseases. Standard SNP-based meta-analytic approaches have been utilized to integrate the results from multiple experiments. This fundamentally assumes that the patterns of linkage disequilibrium (LD) between the underlying causal variants and the directly genotyped SNPs are similar across the populations for the same SNPs to emerge with surrogate evidence of disease association. We introduce a novel strategy for assessing regional evidence of phenotypic association that explicitly incorporates the extent of LD in the region. This provides a natural framework for combining evidence from multi-ethnic studies of both dichotomous and quantitative traits that (i) accommodates different patterns of LD, (ii) integrates different genotyping platforms and (iii) allows for the presence of allelic heterogeneity between the populations. Our method can also be generalized to perform gene-based or pathway-based analyses. Applying this method on real GWAS data in type 2 diabetes (T2D) boosted the association evidence in regions well-established for T2D etiology in three diverse South-East Asian populations, as well as identified two novel gene regions and a biologically convincing pathway that are subsequently validated with data from the Wellcome Trust Case Control Consortium
The INTERVAL trial to determine whether intervals between blood donations can be safely and acceptably decreased to optimise blood supply: study protocol for a randomised controlled trial
Outcomes from elective colorectal cancer surgery during the SARS-CoV-2 pandemic
This study aimed to describe the change in surgical practice and the impact of SARS-CoV-2 on mortality after surgical resection of colorectal cancer during the initial phases of the SARS-CoV-2 pandemic
Respite: carers’ experiences and perceptions of respite at home
Background - Informal carers play an important role in supporting people with long term conditions living at home.
However, the caring role is known to have adverse effects on carers such as poorer emotional health and
social isolation. A variety of types of respite may be offered to carers but little is known about carers’
experiences of respite and their perceptions of care workers and of the benefits of respite. This study therefore
investigated these experiences and perceptions.
Method - Recorded, semi-structured interviews were undertaken with twelve carers receiving weekly four hourly
respite. Carers were either caring for a person over sixty or were over sixty themselves. Interviews were
analysed thematically.
Results and Discussion - Respite sometimes alleviated carers’ constant sense of responsibility for their cared for. Trust, whether trust
in the service provider or individual care workers, was essential. Carers lacking this trust tended to perceive
respite as less beneficial. Low expectations were common with carers frequently unwilling to find fault. Care
workers were frequently seen as very kind with some carers valuing their company. Care workers who were
flexible, communicated well and responded to the cared for’s needs were valued. Stimulation of the cared for
during respite was very important to most carers but the perceived benefits for carers were often very
individual. Many carers used respite to catch up with routine, domestic tasks rarely using it to socialise.
Conclusions - For many carers, respite was a way of maintaining normality in often difficult, restricted lives. Respite
allowed continuation of what most people take for granted. Carers frequently viewed respite as intended to
improve their cared for’s quality of life, rather than their own. This centrality of the cared for means that
carers can only really benefit from respite if the cared for is happy and also seen to benefit. Future research
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should investigate the perspectives of carers and their cared for, focussing on different demographic groups by
features such as age, gender, ethnic and diagnostic groups. However, without greater clarity about what respite
is intended to achieve, clear evidence of a positive impact of this intervention may remain difficult to identify
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