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    Forth Valley Royal Hospital,NHS Forth Valley

    EST. 2010
    555论文总数
    1.6万引用总数

    Forth Valley Royal Hospital is a hospital located in Larbert, Scotland. With 860 inpatient beds, 25 wards, and 16 operating theatres, it was Scotland's largest ever NHS construction project at the time but has been surpassed by the New Southern General hospital amongst others. Built at a cost of £300 million on the site of the old Royal Scottish National Hospital, it opened to its first patients in 2010. It is operated by NHS Forth Valley.The hospital is the first in Scotland to have a Forestry Commission ranger on site, whose job is to encourage the use of the 70-acre (28 ha) grounds formerly belonging to the Larbert House estate. It has Scotland's first fully robotic pharmacy, in which robots dispense and label medicines. The hospital also employs robots to carry out tasks such as removing waste, delivering food to wards, and cleaning operating theatres.

    论文量&引用量时间轴

    机构学者

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    James C Spratt
    James C Spratt
    Cardiology Department, University Hospital of Geneva
    论文:23引用:0H-index:0
    Andrew B. C. Crumley
    Andrew B. C. Crumley
    University Department of Surgery, Royal Infirmary
    论文:16引用:0H-index:0
    Simon J Walsh
    Simon J Walsh
    Belfast Health and Social Care Trust
    论文:15引用:0H-index:0
    Craig Mcilhenny
    Craig Mcilhenny
    NHS Forth Valley
    论文:15引用:0H-index:0
    Adrian Stanley
    Adrian Stanley
    School of Medicine, Dentistry & Nursing, University of Glasgow
    论文:11引用:0H-index:0
    Margaret B. McEntegart
    Margaret B. McEntegart
    Seymour, Paul and Gloria Milstein Division of Cardiology, Department of Medicine, Columbia University;Columbia University Irving Medical Center
    论文:8引用:0H-index:0
    Julian W. Strange
    Julian W. Strange
    King's College London
    论文:8引用:0H-index:0
    Michael D. Wilson
    Michael D. Wilson
    Science and Technology Facilities Council
    论文:8引用:0H-index:0
    Elizabeth Cannings
    Elizabeth Cannings
    University Department of Surgery Endocrine Cancer Group, Glasgow Royal Infirmary
    论文:7引用:0H-index:0

    论文(555)

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    1Acute Upper Gastrointestinal Bleeding in the UK: 2022 Audit Update
    Gaurav B Nigam,Kathryn Oakland,Sarah Hearnshaw, John Grasnt-Casey, Paul Davies,Paula Dhiman, Shane W Goodwin,Bhaskar Kumar,Elizabeth Ratcliffe,Joanna A Leithead,Raman Uberoi,Lise Estcourt,

    BACKGROUND:Acute upper gastrointestinal bleeding (AUGIB) is a common medical emergency with evolving demographics and management strategies, particularly in medical/endoscopic therapy and transfusion strategies. OBJECTIVE:To provide key data of the most recent 2022 UK audit and compare it with the preceding audit in 2007. DESIGN:Prospective multicentre audit conducted from 3 May to 2 July 2022, including adults (≥16 years) with AUGIB across 147 UK hospitals (response rate 86% vs 84% in 2007). AUGIB was defined by clinical symptoms (haematemesis, haematochezia, coffee ground vomiting or melaena confirmed by medical personnel). Patients were followed until discharge, death or 28 days, with re-admissions during the study period counted as new episodes. RESULTS:Among 5141 patients (59% male; median age 69), 15% had cirrhosis, 19% reported excess alcohol use, 7% used non-steroidal anti-inflammatory drugs (NSAIDs) and 46% were on antithrombotics. Most (77%) were new admissions, who were younger with fewer comorbidities, while the remainder bled during hospitalisation. Peptic ulcer disease accounted for 32% of cases, varices for 10% and no abnormality was found in 33%. Pre-endoscopic risk stratification was not performed in 42%.Compared with 2007, patients in 2022 had higher comorbidity (67% vs 50%), more cirrhosis (15% vs 9%), greater anticoagulant use (31% vs 13%) and higher transfusion rates (50% vs 43%). In 2022, among early transfusions (pre-endoscopy or within first 24 hrs; 38%), 43% were given at haemoglobin (Hb)>70 g/L, with 24% classified as inappropriate due to haemodynamic stability. A signal of harm was observed: while inappropriate transfusion was not associated with rebleeding at either 70 or 80 g/L, at 80 g/L it was linked to higher adjusted mortality (adjusted OR (aOR) 1.60, 95% CI 1.00 to 2.56).Inpatient endoscopy was more common (83% vs 74%), though endotherapy use remained modest (27% vs 23%). Salvage therapy rates were unchanged (3.3% vs 3.1%) but shifted from surgery to interventional radiology. Outcomes improved, with lower rebleeding (9.7% vs 13.3%), reduced in-hospital mortality (8.8% vs 10.0%) and shorter median stay (5 vs 6 days). In multivariate analysis, mortality was independently predicted by older age (≥80 years: aOR 2.32, 95% CI 1.64 to 3.30), shock (aOR 2.22, 95% CI 1.53 to 3.17) and comorbidity, while lower Hb at presentation increased risk (≤70 g/L: aOR 1.56, 95% CI 1.15 to 2.11). Anticoagulant use was associated with increased mortality (aOR 1.43, 95% CI 1.11 to 1.85), whereas NSAID use (aOR 0.49, 95% CI 0.25 to 0.96) and antiplatelet use (aOR 0.68, 95% CI 0.54 to 0.87) were associated with lower mortality. CONCLUSIONS:Despite a higher-risk case mix and incomplete adherence to guidelines (notably in transfusion thresholds and risk stratification), outcomes in AUGIB have improved. The observation of increased mortality with liberal transfusion above 80 g/L in stable patients reinforces the importance of restrictive transfusion practice. Quality improvement initiatives focused on risk stratification, endoscopic training and multidisciplinary care could further enhance outcomes in the UK and internationally.

    2026Gut(2026)引用:3
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    2Intraoperative Hypotension and Vasoactive Treatment: an International Survey of Anaesthesiologists.
    Emilie S Bækgaard,Morten Vester-Andersen, Vera Crone,Morten Hylander Møller, Shun Yamanaka, Rakel Palmarsdottir,Panu Uusalo, Felix Haidl, Madeleine Rådestad, Koene van der Sloot, Andrea Corona, Alexander Johnström,

    BACKGROUND:Intraoperative hypotension is a common occurrence in patients undergoing anaesthesia, although there is no standardised definition of hypotension. International consensus statements provide some guidelines for the management of intraoperative hypotension, but general clinical practice is unknown. We aimed to survey anaesthesiologists' values and preferences regarding intraoperative blood pressure management, including whether they would support future research on this topic. METHODS:We conducted an international, online survey of routine practice and opinion. The target population was anaesthesiologists who regularly anaesthetise adult patients. Results are reported descriptively and in accordance with the Consensus-Based Checklist for Reporting of Survey Studies (CROSS) checklist. RESULTS:A total of 1640 anaesthesiologists from 11 European countries participated in the survey. The majority of respondents were specialists (1322 of 1640, 80.6%, 95% CI 78.7-82.6). Almost all respondents worked in public hospitals (1613 of 1640, 98.4%). The overall response rate was 22.7%. Most respondents reported using absolute mean arterial pressure as their main unit of measurement to quantify hypotension (1098 of 1640, 67.0%, 95% CI 64.6-69.2). Respondents were most likely to initiate vasoactive treatment at a mean arterial pressure below 60 or 65 mmHg. Chronic arterial hypertension, traumatic brain injury and surgical procedures involving head-up positioning of the patient were the three most common scenarios where respondents would raise their threshold for treatment. Most respondents considered the establishment of safe intraoperative blood pressure thresholds a critical research question, and almost all respondents (1509 of 1640, 92.0%) indicated a willingness to randomise patients to specific blood pressure targets. For 72.9% (1196 of 1640), the lowest acceptable mean arterial pressure for randomisation was 60 mmHg. Respondents were also interested in the comparison of efficacy and safety of vasoactive agents, and the most sought-after comparison was phenylephrine versus noradrenaline (1252 of 1640, 76.3%). The willingness of respondents to administer these agents in peripheral venous access differed according to geography. CONCLUSION:In this international survey, mean arterial pressures of 60 or 65 mmHg were the most commonly reported blood pressure thresholds leading to initiation of treatment with vasoactive agents. Almost all respondents indicated patient groups for whom they would alter their treatment threshold, namely those suffering from chronic arterial hypertension, those undergoing surgery in a head-up position, and patients with traumatic brain injury. The majority of respondents supported future trials establishing optimal mean arterial pressure threshold and choice of vasoactive agent. We noticed a geographical variation in willingness to administer vasoactive agents in peripheral venous access. EDITORIAL COMMENT:This survey of anaesthesiologists from European countries queried practitioner perceptions of blood pressure management in adults during anaesthesia with focus on hypotension. Queries and responses also concerned circumstances and blood pressure levels which clinicians report being willing to treat actively, and how they might do this practically.

    2026Acta anaesthesiologica Scandinavica(2026)引用:1
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    3A Digital Diagnostic Pathway for Heart Failure: an Economic Evaluation
    Nicola Mcmeekin, Andrew Davies,Mark C. Petrie,Ross T. Campbell,David J. Lowe, Clare L. Murphy, Leeanne Macklin,Katriona Brooksbank,Olivia Wu

    Guidelines recommend prompt diagnosis of suspected heart failure in people with elevated N-terminal pro b-type natriuretic peptide (NT-proBNP). Early diagnosis of heart failure improves patient outcomes, however diagnosis is complex and can often be delayed. Digital platforms can provide clinicians with greater access to information with which to diagnose heart failure, improving on standard diagnostic pathways. We modelled the potential cost-effectiveness of a digital pathway, adapting the UK NICE guideline (NG106) cost-effectiveness model to evaluate the impact of potentially speedier diagnosis and treatment of heart failure. Posited reductions in time to treatment were modelled to reduce short-term mortality and generate approximately 0.056 incremental quality adjusted life-years over a lifetime horizon. Additional costs arose from earlier heart failure treatment, resulting in a cost per quality adjusted life-year of £5,882 (95

    2026Cost Effectiveness and Resource Allocation(2026)
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    4Transdermal Estradiol Patches in Locally Advanced Prostate Cancer.
    Ruth E Langley, Duncan C Gilbert, Stephen Mangar, Stuart Rosen, Ellie Bourmaki, Hannah L Rush, Subramaniam Kananga Sundaram,Abdulla Alhasso,Roger Kockelbergh, Hoda Abdel-Aty, Claire L Amos, Louise Brown,

    BACKGROUND:Transdermal estradiol (tE2) is an alternative to luteinizing hormone-releasing hormone (LHRH) agonists as androgen-deprivation therapy in patients with prostate cancer. With tE2, testosterone is suppressed, and the side effects of estrogen depletion due to LHRH agonists and the thromboembolic side effects of oral estrogen are mitigated. METHODS:In this phase 3, noninferiority, randomized trial, we assigned men with locally advanced (M0 and N0 or N+) prostate cancer to receive tE2 patches (100 μg of estradiol every 24 hours) or LHRH agonists. The primary outcome was 3-year metastasis-free survival. The noninferiority margin was 4 percentage points; this corresponded to a target hazard ratio of 1.31, as derived from the observed 3-year metastasis-free survival in the LHRH agonist group. Secondary outcomes included castrate levels of testosterone (<1.7 nmol per liter), overall survival, and safety. RESULTS:Between 2007 and 2022, we recruited 1360 patients at 75 U.K. centers. The median age of the patients was 72 years (interquartile range, 68 to 77); 85% had a T3 tumor stage and 65% an N0 nodal stage. Observed 3-year metastasis-free survival was 87.1% with tE2 and 85.9% with LHRH agonists (hazard ratio for confirmed metastasis or death, 0.96; upper limit of the one-sided 95% confidence interval [CI], 1.11, which met the criterion for noninferiority). Among patients continuing the assigned treatment, castrate levels of testosterone were sustained during the first year after randomization in 85% in each group. Observed 5-year overall survival was 81.1% with tE2 and 79.2% with LHRH agonists (hazard ratio for death, 0.90; 95% CI, 0.75 to 1.07). During treatment, hot flashes occurred in 44% of the patients who received tE2 and 89% of those who received LHRH agonists (grade ≥2 events, 8% and 37%, respectively) and gynecomastia in 85% and 42% (grade ≥2 events, 37% and 9%). CONCLUSIONS:In patients with locally advanced prostate cancer, tE2 was noninferior to LHRH agonists for 3-year metastasis-free survival, with a lower incidence of hot flashes but a higher incidence of gynecomastia. (Funded by Cancer Research U.K. and the U.K. Research Institute Medical Research Council; PATCH ClinicalTrials.gov number, NCT00303784; STAMPEDE-1 ClinicalTrials.gov number, NCT00268476.).

    2026The New England journal of medicine(2026)
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    5UK Consensus on Pregnancy in Multiple Sclerosis: an Update to ‘association of British Neurologists’ Guidance
    Ger Mullan, Helen L Ford, Paula Blackall, Denisse Bongol, Nicola Bonham,Peter Brex, Natasha Hoyle,Katy Murray,Catherine Nelson-Piercy, Owen R Pearson,David Rog, Paarul Prinja,

    BACKGROUND:The first Association of British Neurologists (ABN) UK multiple sclerosis (MS) pregnancy guidelines were published in 2019. Along with new disease-modifying treatments, significant new data have since become available, resulting in label changes and recognition of class effects. Alongside this, there has been increasing recognition of the importance of family planning considerations in treatment paradigms in MS. METHODS:We set out to update the ABN UK MS Pregnancy guidance with a systematic literature search, with updated guidance informed by multidisciplinary input from across neurology, obstetric medicine, pharmacy and specialist nurses.Guidance:Key updates include consideration of disease-modifying therapy mechanism and durability of action when discussing treatment approaches around pregnancy, alongside considering the impact of treatment withdrawal on relapses during pregnancy and in the postpartum period. Monoclonal antibody transfer into breast milk is generally accepted to be low, and so treatment during lactation can be considered. Active discussion around vaccination strategies during pregnancy and of the neonate is required, with vaccines generally considered safe. With active treatment strategies that take these factors into account, women can be reassured regarding disease control during pregnancy. CONCLUSION:Data sources remain limited, and further dedicated real-world studies that capture the full range of outcomes required to inform risk-benefit discussions are needed. These require collaboration and infrastructure to support the delivery of high-quality care to all women with MS considering pregnancy.

    2026Multiple sclerosis (Houndmills, Basingstoke, England)(2026)
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