20 research outputs found

    Multiple Chronic Conditions and Limitations in Activities of Daily Living in a Community-Based Sample of Older Adults in New York City, 2009

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    Introduction Nationally, 60% to 75% of older adults have multiple (2 or more) chronic conditions (MCCs), and the burden is even higher among low-income, racial/ethnic minority populations. MCCs limit activities of daily living (ADLs), yet this association is not well characterized outside of clinical populations. We examined the association of MCCs with ADLs in a racially/ethnically diverse population of low-income older adults living in New York City public housing. Methods A representative sample of 1,036 New York City Housing Authority residents aged 65 or older completed a telephone survey in June 2009. We examined the association of up to 5 chronic conditions with basic ADL (BADL) limitations, adjusting for potential confounders by using logistic regression. Results Of respondents, 28.7% had at least 1 BADL limitation; 92.9% had at least 1 chronic condition, and 79.0% had MCCs. We observed a graded association between at least 1 BADL limitation and number of chronic conditions (using 0 or 1 condition as the reference group): adjusted odds ratio (AOR) for 3 conditions was 2.2 (95% confidence interval [CI], 1.3–3.9); AOR for 4 conditions, 4.3 (95% CI, 2.5–7.6); and AOR for 5 conditions, 9.2 (95% CI, 4.3–19.5). Conclusion Prevalence of BADL limitations is high among low-income older adults and increases with number of chronic conditions. Initiating prevention of additional conditions and treating disease constellations earlier to decrease BADL limitations may improve aging outcomes in this population

    Restrictive or Liberal Red-Cell Transfusion for Cardiac Surgery.

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    BACKGROUND The effect of a restrictive versus liberal red-cell transfusion strategy on clinical outcomes in patients undergoing cardiac surgery remains unclear. METHODS In this multicenter, open-label, noninferiority trial, we randomly assigned 5243 adults undergoing cardiac surgery who had a European System for Cardiac Operative Risk Evaluation (EuroSCORE) I of 6 or more (on a scale from 0 to 47, with higher scores indicating a higher risk of death after cardiac surgery) to a restrictive red-cell transfusion threshold (transfuse if hemoglobin level was <7.5 g per deciliter, starting from induction of anesthesia) or a liberal red-cell transfusion threshold (transfuse if hemoglobin level was <9.5 g per deciliter in the operating room or intensive care unit [ICU] or was <8.5 g per deciliter in the non-ICU ward). The primary composite outcome was death from any cause, myocardial infarction, stroke, or new-onset renal failure with dialysis by hospital discharge or by day 28, whichever came first. Secondary outcomes included red-cell transfusion and other clinical outcomes. RESULTS The primary outcome occurred in 11.4% of the patients in the restrictive-threshold group, as compared with 12.5% of those in the liberal-threshold group (absolute risk difference, -1.11 percentage points; 95% confidence interval [CI], -2.93 to 0.72; odds ratio, 0.90; 95% CI, 0.76 to 1.07; P<0.001 for noninferiority). Mortality was 3.0% in the restrictive-threshold group and 3.6% in the liberal-threshold group (odds ratio, 0.85; 95% CI, 0.62 to 1.16). Red-cell transfusion occurred in 52.3% of the patients in the restrictive-threshold group, as compared with 72.6% of those in the liberal-threshold group (odds ratio, 0.41; 95% CI, 0.37 to 0.47). There were no significant between-group differences with regard to the other secondary outcomes. CONCLUSIONS In patients undergoing cardiac surgery who were at moderate-to-high risk for death, a restrictive strategy regarding red-cell transfusion was noninferior to a liberal strategy with respect to the composite outcome of death from any cause, myocardial infarction, stroke, or new-onset renal failure with dialysis, with less blood transfused. (Funded by the Canadian Institutes of Health Research and others; TRICS III ClinicalTrials.gov number, NCT02042898 .)

    Adjunctive rifampicin for Staphylococcus aureus bacteraemia (ARREST): a multicentre, randomised, double-blind, placebo-controlled trial.

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    BACKGROUND: Staphylococcus aureus bacteraemia is a common cause of severe community-acquired and hospital-acquired infection worldwide. We tested the hypothesis that adjunctive rifampicin would reduce bacteriologically confirmed treatment failure or disease recurrence, or death, by enhancing early S aureus killing, sterilising infected foci and blood faster, and reducing risks of dissemination and metastatic infection. METHODS: In this multicentre, randomised, double-blind, placebo-controlled trial, adults (≥18 years) with S aureus bacteraemia who had received ≤96 h of active antibiotic therapy were recruited from 29 UK hospitals. Patients were randomly assigned (1:1) via a computer-generated sequential randomisation list to receive 2 weeks of adjunctive rifampicin (600 mg or 900 mg per day according to weight, oral or intravenous) versus identical placebo, together with standard antibiotic therapy. Randomisation was stratified by centre. Patients, investigators, and those caring for the patients were masked to group allocation. The primary outcome was time to bacteriologically confirmed treatment failure or disease recurrence, or death (all-cause), from randomisation to 12 weeks, adjudicated by an independent review committee masked to the treatment. Analysis was intention to treat. This trial was registered, number ISRCTN37666216, and is closed to new participants. FINDINGS: Between Dec 10, 2012, and Oct 25, 2016, 758 eligible participants were randomly assigned: 370 to rifampicin and 388 to placebo. 485 (64%) participants had community-acquired S aureus infections, and 132 (17%) had nosocomial S aureus infections. 47 (6%) had meticillin-resistant infections. 301 (40%) participants had an initial deep infection focus. Standard antibiotics were given for 29 (IQR 18-45) days; 619 (82%) participants received flucloxacillin. By week 12, 62 (17%) of participants who received rifampicin versus 71 (18%) who received placebo experienced treatment failure or disease recurrence, or died (absolute risk difference -1·4%, 95% CI -7·0 to 4·3; hazard ratio 0·96, 0·68-1·35, p=0·81). From randomisation to 12 weeks, no evidence of differences in serious (p=0·17) or grade 3-4 (p=0·36) adverse events were observed; however, 63 (17%) participants in the rifampicin group versus 39 (10%) in the placebo group had antibiotic or trial drug-modifying adverse events (p=0·004), and 24 (6%) versus six (2%) had drug interactions (p=0·0005). INTERPRETATION: Adjunctive rifampicin provided no overall benefit over standard antibiotic therapy in adults with S aureus bacteraemia. FUNDING: UK National Institute for Health Research Health Technology Assessment

    Prevalence, associated factors and outcomes of pressure injuries in adult intensive care unit patients: the DecubICUs study

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    Funder: European Society of Intensive Care Medicine; doi: http://dx.doi.org/10.13039/501100013347Funder: Flemish Society for Critical Care NursesAbstract: Purpose: Intensive care unit (ICU) patients are particularly susceptible to developing pressure injuries. Epidemiologic data is however unavailable. We aimed to provide an international picture of the extent of pressure injuries and factors associated with ICU-acquired pressure injuries in adult ICU patients. Methods: International 1-day point-prevalence study; follow-up for outcome assessment until hospital discharge (maximum 12 weeks). Factors associated with ICU-acquired pressure injury and hospital mortality were assessed by generalised linear mixed-effects regression analysis. Results: Data from 13,254 patients in 1117 ICUs (90 countries) revealed 6747 pressure injuries; 3997 (59.2%) were ICU-acquired. Overall prevalence was 26.6% (95% confidence interval [CI] 25.9–27.3). ICU-acquired prevalence was 16.2% (95% CI 15.6–16.8). Sacrum (37%) and heels (19.5%) were most affected. Factors independently associated with ICU-acquired pressure injuries were older age, male sex, being underweight, emergency surgery, higher Simplified Acute Physiology Score II, Braden score 3 days, comorbidities (chronic obstructive pulmonary disease, immunodeficiency), organ support (renal replacement, mechanical ventilation on ICU admission), and being in a low or lower-middle income-economy. Gradually increasing associations with mortality were identified for increasing severity of pressure injury: stage I (odds ratio [OR] 1.5; 95% CI 1.2–1.8), stage II (OR 1.6; 95% CI 1.4–1.9), and stage III or worse (OR 2.8; 95% CI 2.3–3.3). Conclusion: Pressure injuries are common in adult ICU patients. ICU-acquired pressure injuries are associated with mainly intrinsic factors and mortality. Optimal care standards, increased awareness, appropriate resource allocation, and further research into optimal prevention are pivotal to tackle this important patient safety threat

    Competitive Effects on Tree Canopies: a Spatially Explicit Analysis of Crown Structure for Three Sub-Boreal Forest Species

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    Changing forest management goals have led to increased focus on maintaining stand-level complexity. Understanding complex, mixed species stands requires the quantification of competitive interactions among individual trees. A suite of recent studies has explored the influence of neighbourhood competition on factors such as growth and mortality of adult trees and saplings. In this study, we used a neighbourhood approach to quantify the influence of local competition on the structure of individual tree crowns. We measured and mapped the locations and crown dimensions of ~2400 trees in north-central British Columbia, where forests are dominated by interior spruce (Picea glauca x engelmanii), subalpine fir (Abies lasiocarpa), and lodgepole pine (Pinus contorta). Using maximum likelihood methods, we quantified crown structure as a function of tree size, species, and competition levels, estimated by the identity and spatial arrangement of neighboring trees. In the absence of competition, we found the widest tree crowns in pine, followed by spruce and fir. Crown depth showed the opposite pattern, with the deepest crowns found in fir and the shallowest in pine. All species displayed declining crown dimensions with increasing neighborhood competition, but the pattern was most dramatic in pine, where crown dimensions decreased by 75% across the observed range of neighbourhood competition. Our results will be used to parameterize a new, distance-dependent crown model for the stand simulation model SORTIE-ND. This model will improve the accuracy of understory light predictions, and consequent sapling and sub-canopy tree dynamics, across a wide range of stand densities

    Clearcut Solutions? An Evaluation of Partial Harvesting in the Black Spruce Boreal Forest

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    Bringing together field-based empirical studies, a simulation modelling experiment, and a critical analysis of the natural disturbance emulation paradigm, this thesis evaluates partial harvesting in the black spruce boreal forest. Forest management in Ontario is required to emulate natural disturbances, but in regions of the boreal forest where fire cycles are long, regulated even-aged management by clearcutting has truncated forest age-class distributions. Partial harvesting has been proposed as a means to maintain the structural complexity and biodiversity associated with old forests while allowing continued timber production. Despite the potentially important role of partial harvesting in a strategy for sustainable boreal forest management, little research has examined post-harvest stand development, a critical determinant both of habitat and timber supplies.I used a chronosequence approach in combination with dendroecological techniques, a neighbourhood modelling framework, and maximum likelihood statistical methods to quantify stand dynamics over the first decade after partial harvest in the black spruce (Picea mariana) boreal forest of northeastern Ontario, Canada. Residual trees displayed large but time-lagged growth responses to partial harvest. The largest responses were found in young trees, while old trees were largely unable to react to improved post-harvest resource availability. Growth responses were offset by elevated rates of residual-tree mortality, which peaked in the first year after harvest at nearly 13 times the pre-harvest level. Proximity to harvest machinery trails severely escalated the risk of mortality for residual trees. Considering growth and mortality responses together in a forest simulator model, I found that stand development proceeded most rapidly where skidding intensity was reduced and retention areas were aggregated. Given appropriate prescriptions, my results indicate that partial harvesting can be a viable silvicultural option for black spruce boreal forests. However, the ability of partially harvested stands to emulate natural disturbance is questionable, particularly given the strong influence of harvest machinery impacts on post-harvest stand development. I argue that the natural disturbance emulation framework has important flaws and falls short of a justifiable approach for forest management in Ontario.Ph

    Going home from hospital: the postdischarge experience of patients and carers in rural and remote Queensland

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    Objective: This paper reports on a study of the experiences of patients and carers discharged from the Townsville General Hospital into rural and remote communities in North Queensland.\ud \ud Design: The findings presented in this paper are drawn\ud from post-discharge in-depth, qualitative interviews of\ud both patients and carers.\ud \ud Results: The findings indicate the importance of examining\ud the lived experience of both patients and carers in\ud attempting to understand the impact of current discharge\ud practices.\ud \ud Conclusion: We conclude that carers are providing the bulk of post-discharge care of patients – a difficult role in which the difficulties are exacerbated when the patient or the carer or both is a long way from the home community
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