18 research outputs found
MOUSE - Mapping OUtcomes measured in pre-clinical Studies against randomised phase 3/4 Effectiveness trials. Do core outcome sets developed for phase3/4 effectiveness trials translate to pre-clinical research?
Nutrient and light limitation of periphyton in the River Thames: implications for catchment management
Soluble reactive phosphorus (SRP) concentrations in the River Thames, south east England, have significantly
decreased from an annual maximum of 2100 μg l−1 in 1997 to 344 in 2010, primarily due to the introduction
of phosphorus (P) removal at sewage treatment works within the catchment. However, despite this improvement
in water quality, phytoplankton biomass in the River Thames has greatly increased in recent years, with
peak chlorophyll concentrations increasing from 87 μg l−1 in the period 1997 to 2002, to 328 μg l−1 in 2009.
A series of within-river flume mesocosm experiments were performed to determine the effect of changing
nutrient concentrations and light levels on periphyton biomass accrual. Nutrient enrichment experiments
showed that phosphorus, nitrogen and silicon were not limiting or co-limiting periphyton growth in the
Thames at the time of the experiment (August–September 2010). Decreasing ambient SRP concentration
from 225 μg l−1 to 173 μg l−1 had no effect on periphyton biomass accrual rate or diatom assemblage. Phosphorus
limitation became apparent at 83 μg SRP l−1, at which point a 25% reduction in periphyton biomass
was observed. Diatom assemblage significantly changed when the SRP concentration was reduced to
30 μg l−1. Such stringent phosphorus targets are costly and difficult to achieve for the River Thames, due
to the high population density and intensive agriculture within the Thames basin. Reducing light levels by
shading reduced the periphyton accrual rate by 50%. Providing shading along the River Thames by planting
riparian tree cover could be an effective measure to reduce the risk of excessive algal growth. If the ecology
of the Thames is to reach the WFD's “good ecological status”, then both SRP concentration reductions (probably
to below 100 μg l−1) and increased shading will be required
The antihypoxic action of antioxidant BHT mediated via nitric oxide: A study of EPR signals in tissues of rats of different ages
Selecting Core Outcomes for Randomised Effectiveness trials In Type 2 diabetes (SCORE- IT): A patient and healthcare professional consensus on a core outcome set for type 2 diabetes
Objectives
Heterogeneity in outcomes measured across trials of glucose-lowering
interventions for people with type 2 diabetes impacts on the ability to
compare findings and may mean that the results have little importance to
healthcare professionals and the patients that they care for. The
SCORE-IT study (Selecting Core Outcomes for Randomised Effectiveness
trials In Type 2 diabetes) has addressed this issue by establishing
consensus on the most important outcomes for non-surgical interventions
for hyperglycemia in type 2 diabetes.Research design and methods
A comprehensive list of outcomes was developed from registered clinical
trials, online patient resources, qualitative literature and long-term
studies in the field. This list was then scored in a two-round online
Delphi survey completed by healthcare professionals, people with type 2
diabetes, researchers in the field and healthcare policymakers. The
results of this online Delphi were discussed and ratified at a
face-to-face consensus meeting.Results
173 people completed both rounds of the online survey (116 people with
type 2 diabetes, 37 healthcare professionals, 14 researchers and 6
policymakers), 20 of these attended the consensus meeting (13 people
with type 2 diabetes and 7 healthcare professionals). Consensus was
reached on 18 core outcomes across five domains, which include outcomes
related to diabetes care, quality of life and long-term diabetes-related
complications.Conclusions
Implementation of the core outcome set in future trials will ensure
that outcomes of importance to all stakeholders are measured and
reported, enhancing the relevance of trial findings and facilitating the
comparison of results across trials