11,606 results match your criteria: "National Institute for Health Research[Affiliation]"

Misrepresentation by online study participants-a threat to data integrity.

Lancet Psychiatry

November 2024

School of Health Sciences, Institute of Mental Health, University of Nottingham, Nottingham, UK; NIHR Nottingham Biomedical Research Centre, Institute of Mental Health, University of Nottingham, Nottingham, UK.

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Corrigendum to "No evidence of difference in mortality with amoxicillin versus co-amoxiclav for hospital treatment of community-acquired pneumonia" [J Infect 88 (2024) 106161].

J Infect

December 2024

Big Data Institute, Nuffield Department of Population Health, University of Oxford, Oxford, UK; The National Institute for Health Research Oxford Biomedical Research Centre, University of Oxford, Oxford, UK; Department of Infectious Diseases and Microbiology, Oxford University Hospitals NHS Foundation Trust, John Radcliffe Hospital, Oxford, UK; The National Institute for Health Research Health Protection Research Unit in Healthcare Associated Infections and Antimicrobial Resistance at the University of Oxford, Oxford, UK. Electronic address:

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Background And Objective: Post-operative periprosthetic femoral fractures (POPFF) present a growing challenge for healthcare services, but there are limited national data on patient profiles, short-term outcomes, and post-discharge follow-up. We aimed to fill these gaps.

Methods: Using Hospital Episode Statistics (HES), we identified POPFF discharges from hospitals in England for patients aged 18 and above between April 2016 and December 2022.

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Article Synopsis
  • Anti-Ro/SS-A antibodies are common in systemic autoimmune rheumatic diseases (SARDs) and suggest specific patient profiles; this study focused on the connection between protein biomarkers, symptom burden, and health-related quality of life (HR-QoL).
  • A pilot study enrolled anti-Ro positive SARD patients over six months, using various scales to measure HR-QoL and symptom burden, while assessing protein levels in the blood through advanced immunoassays.
  • Two patient clusters emerged: a 'low expression cluster' with greater symptom severity and poor HR-QoL, and a 'high expression cluster' tied to better physician assessments, highlighting potential protein markers that could lead to new therapeutic strategies for managing these patients.
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Cardiac magnetic resonance markers of pre-clinical hypertrophic and dilated cardiomyopathy in genetic variant carriers.

medRxiv

November 2024

Department of Cardiology, Amsterdam Cardiovascular Sciences, Amsterdam University Medical Centre, University of Amsterdam, Amsterdam, The Netherlands.

Article Synopsis
  • The study focused on identifying imaging biomarkers for pre-clinical cardiomyopathy in healthy people with genetic variants linked to hypertrophic cardiomyopathy (HCM) or dilated cardiomyopathy (DCM).
  • Out of 40,169 participants, 13 cardiac magnetic resonance (CMR) measurements were found to be linked to atrial fibrillation (AF) and 15 with heart failure (HF), with specific measurements correlating differently with HCM and DCM genetic risk.
  • The findings suggest that certain CMR measurements, particularly from the right side of the heart, can indicate early changes in heart function in individuals with HCM genetic variants, while left ventricular measures relate to DCM genetic risks
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Excess burden of antibiotic-resistant bloodstream infections: evidence from a multicentre retrospective cohort study in Chile, 2018-2022.

Lancet Reg Health Am

December 2024

Multidisciplinary Initiative for Collaborative Research on Bacterial Resistance (MICROB-R), Santiago, Chile.

Article Synopsis
  • Antibiotic-resistant bloodstream infections (ARB BSI) pose significant health risks to hospitalized patients in Chile, leading to higher mortality rates, longer hospital stays, and increased ICU admissions in comparison to infections caused by non-resistant bacteria.
  • In a study involving 1,218 patients, nearly half of the bloodstream infection episodes (47.3%) were attributed to ARB, with specific pathogens like Methicillin-resistant Staphylococcus aureus (MRSA) and Carbapenem-resistant Enterobacterales (CRE) being prominent.
  • The financial burden of ARB BSI is substantial, with estimated excess costs per patient at around $12,600 and an annual impact of approximately $9.6 million, highlighting the
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Abbreviated or Standard Antiplatelet Therapy After PCI in Diabetic Patients at High Bleeding Risk.

JACC Cardiovasc Interv

November 2024

Cardiocentro Ticino Institute, Ente Ospedaliero Cantonale, Lugano, Switzerland; Faculty of Biomedical Sciences, University of Italian Switzerland, Lugano, Switzerland; University of Bern, Bern, Switzerland. Electronic address:

Background: Abbreviated antiplatelet therapy (APT) reduces bleeding without increasing ischemic events in largely unselected high bleeding risk (HBR) patients undergoing percutaneous coronary intervention (PCI). Diabetes mellitus (DM) is associated with higher ischemic risk, and its impact on the safety and effectiveness of abbreviated APT in HBR PCI patients remains unknown.

Objectives: This study sought to investigate the comparative effectiveness of abbreviated (1 month) vs standard (≥3 months) APT in HBR patients with and without DM after biodegradable polymer sirolimus-eluting coronary stent implantation.

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Objectives: To investigate healthcare utilisation and cost in individuals with long COVID (LC) at population level.

Design: Case-control cohort analysis with multiple age-, sex-, ethnicity-, deprivation-, region- and comorbidity-matched control groups: (1) COVID only, no LC; (2) pre-pandemic; (3) contemporary non-COVID; and (4) pre-LC (self-controlled, pre-COVID pandemic).

Setting: National, population-based, linked UK electronic health records (British Heart Foundation/NHS England Secure Data Environment).

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Guidance for delivering surgical procedures outside operating theatres: scoping review.

BJS Open

October 2024

National Institute for Health Research, Bristol, Biomedical Research Centre Surgical Innovation Theme, Bristol Centre for Surgical Research, Bristol Medical School: Population Health Sciences, University of Bristol, Bristol, UK.

Background: This review aimed to examine in-depth the extent and content of guidance related to the delivery of surgical procedures outside of the operating theatre.

Methods: Documents concerning the delivery of surgical procedures in non-operating theatre settings were eligible for inclusion. Guidance documents were identified from three sources: electronic databases (MEDLINE and Embase), professional organization websites and expert knowledge.

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Background: We aimed to provide insights into the effects of comorbidities on sleep health in people with HIV by assessing associations between multimorbidity patterns and sleep outcomes in the Pharmacokinetic and clinical Observations in PeoPle over fiftY (POPPY) sub-study.

Methods: Principal component analysis identified six multimorbidity patterns among participants with HIV (n = 1073) at baseline: Cardiovascular diseases (CVDs), Sexually transmitted diseases, Metabolic, Mental/Joint, Neurological and Cancer/Other. Burden z-scores were calculated for each individual/pattern.

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Clinical Features, Biochemistry, Imaging, and Treatment Response in a Single-Center Cohort With Coenzyme Q Biosynthesis Disorders.

Neurol Genet

December 2024

From the Mitochondrial Research Group (A.W., S.R.), Genetics and Genomic Medicine Department, UCL Great Ormond Street Institute of Child Health, London; Medical Sciences Division (A.W.), University of Oxford; Department of Radiology (S.S.), Great Ormond Street Hospital for Children; Neurometabolic Unit (A.L., S.H.), National Hospital for Neurology and Neurosurgery; Department of Chemical Pathology, Great Ormond Street Hospital for Children; Neuromuscular Diseases (A.L.), Queen Square, UCL Institute of Neurology; Inborn Errors of Metabolism Section (J.I.R.C., P.M., S.H.), Genetics and Genomic Medicine Programme, UCL Great Ormond Street Institute of Child Health; National Institute for Health Research Great Ormond Street Hospital Biomedical Research Centre (P.G.), University College London; Metabolic Department (P.G., S.R.), Great Ormond Street Hospital for Children; North West Thames Regional Genetic Service (A.G.), North West London Hospitals; Neonatal Intensive Care Unit (J.K.), Luton and Dunstable University Hospital; and Department of Paediatric Neurology (J.H.), Great Ormond Street Hospital for Children NHS Foundation Trust, London, United Kingdom.

Background And Objectives: Disorders of coenzyme Q (CoQ) biosynthesis comprise a group of 11 clinically and genetically heterogeneous rare primary mitochondrial diseases. We sought to delineate clinical, biochemical, and neuroimaging features of these disorders, together with outcomes after oral CoQ supplementation and the utility of peripheral blood mononuclear cell (PBMNC) CoQ levels in monitoring therapy.

Methods: This was a retrospective cohort study, registered as an audit at a specialist pediatric hospital (Registration Number: 3318) of 14 patients with genetically confirmed CoQ biosynthesis deficiency, including 13 previously unreported cases.

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Coxsackievirus A6 (CVA6) has become increasingly clinically relevant as a cause of Hand, Foot and Mouth Disease (HFMD) globally since 2008. However, most laboratories do not routinely determine the enteroviral type of positive samples. The non-pharmaceutical measures introduced to curb transmission during the COVID-19 pandemic may also have perturbed CVA6 epidemiology.

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Variants Underlie Polycystic Kidneys in Prenatal and Neonatal Cases.

Genes (Basel)

October 2024

Department of Clinical Laboratory Sciences, College of Applied Medical Sciences, King Saud University, Riyadh 11433, Saudi Arabia.

Background: Nephronophthisis (NPHP) is an autosomal recessive genetic disorder that can cause early-onset kidney failure. plays an important role in early kidney development and encodes a protein that interacts with other proteins within the primary cilium. mutations are known to cause nephronophthisis 16 (NPHP-16).

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Objectives: This study evaluated the psychometric properties of the ceroid lipofuscinosis type 2 Quality of Life (CLN2 QoL) questionnaire.

Methods: Data from children with CLN2 disease aged 3-16 years receiving cerliponase alfa in the BMN 190-201 and BMN 190-202 clinical studies, collected via purposive sampling, were used to assess convergent and divergent validity, internal consistency and reliability. The clinically important difference (CID) was estimated with distribution- and anchor-based methods.

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Background: Atrial fibrillation (AF) imposes a substantial economic and clinical burden, particularly in developing countries like Iran. This study aimed to evaluate the cost-effectiveness of anticoagulation options for non-valvular atrial fibrillation (NVAF) in Iran.

Methods: We conducted a cost-effectiveness analysis comparing warfarin, apixaban, dabigatran 110 mg, dabigatran 150 mg, and rivaroxaban for NVAF patients from the Iranian payer's perspective.

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Article Synopsis
  • - The WHO Roadmap for Neglected Tropical Diseases (NTDs) emphasizes the need to integrate NTD interventions into national health systems, but there is a lack of effective implementation evidence.
  • - In Ethiopia, workshops with stakeholders, including government leaders and healthcare workers, identified 73 challenges to mainstreaming NTDs, with issues in service delivery, systems, and inputs being the most prevalent.
  • - Among the 185 strategies proposed to tackle these challenges, the top recommendations included improving supervision and monitoring, providing continuous training, and implementing performance-based motivation for healthcare workers.
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Aims: To design a regional clinical service for people with early-onset type 2 diabetes (EOT2D) in Leicester, Leicestershire and Rutland (England).

Methods: A literature search was undertaken to identify important considerations. A working group of key stakeholders was formed to design a triage system and service pathway.

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Article Synopsis
  • Carriers of BRCA1/2 pathogenic variants were studied to determine their risk of developing cancers during childhood, adolescence, and young adulthood (CAYA).
  • Analysis of data from over 47,000 individuals revealed that while young women with BRCA1/2 mutations had a significantly increased risk of breast cancer in their 20s, no increased risk was found for other types of CAYA cancers.
  • The study concluded that there's little evidence to support routine genetic testing for children of BRCA1/2 carriers or for young cancer patients, as the overall cancer risk appears low aside from breast cancer in young women.
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Article Synopsis
  • This study examines the relationship between mitochondrial diseases and hearing impairments, focusing on how specific genetic mutations affect auditory functions.
  • An observational study was conducted with 72 adults, utilizing various tests to assess both cochlear and central auditory capabilities, revealing significant hearing deficits linked to the m.3243A>G/T genetic variants.
  • The findings highlight the complexity of hearing impairment in mitochondrial diseases, suggesting that tailored auditory evaluations and management approaches may improve outcomes based on individual genetic profiles.
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Article Synopsis
  • The ellipsoid zone (EZ) on macular optical coherence tomography (OCT) scans shows high intensity due to dense mitochondria, potentially indicating mitochondrial function and offering insights into eye diseases.
  • A new analysis tool was developed to measure EZ reflectivity in patients with optic neuritis and other optic neuropathies compared to healthy individuals, revealing reliable ratios that indicate differences in reflectivity.
  • Results suggest that EZ reflectivity is lower in certain neuroinflammatory and mitochondrial disorders, indicating its potential as a non-invasive biomarker for mitochondrial health, but further research is needed.
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Article Synopsis
  • The study explores the assessment of coronary microvascular dysfunction (CMD) using a new hybrid index derived from pressure-wire measurements and angiography, promoting its potential use in clinical settings.
  • Researchers compared this hybrid index, known as IMR, with a traditional bolus thermodilution-based index in a cohort of patients with acute coronary syndrome and stable coronary artery disease.
  • Results indicate that both the new hybrid IMR and the traditional index showed strong correlations and diagnostic accuracy for CMD, suggesting IMR is a simpler and effective alternative for routine clinical use.
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Real-world impact of Elexacaftor-Tezacaftor-Ivacaftor treatment in young people with Cystic Fibrosis: A longitudinal study.

Respir Med

January 2025

National Institute for Health Research, Southampton Respiratory Biomedical Research Centre, University Hospitals Southampton NHS Foundation Trust, Southampton, UK; Southampton Children's Hospital, University Hospitals Southampton NHS Foundation Trust, Southampton, UK.

Background: Elexacaftor, Tezacaftor, Ivacaftor (ETI) became available in the UK in August 2020 to treat people with Cystic Fibrosis (CF) aged >12 years. We report a real-world study of clinical outcomes in young people treated with ETI at our CF centre within the first two years of its availability.

Methods: Participants aged 12-17 were identified within our clinic, with demographic data supplemented by the UK CF registry.

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Background: Physical activity is essential for long-term health, yet data from before the COVID-19 pandemic showed only 41% of 10- to 11-year-olds met the UK government's physical activity recommendations. Children's physical activity was limited during the national COVID-19 lockdowns. It is important to measure children's physical activity in the recovery period to assess the short- and medium-term impact of the lockdowns.

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Background: Stroke is a pressing public health issue worldwide. This study aimed to forecast the future temporal trends and distribution characteristics of the global stroke burden.

Methods And Results: Global data on stroke incidence, prevalence, deaths, and disability-adjusted life years between 1990 and 2021 were obtained from the GBD (Global Burden of Disease) Study 2021.

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