565 results match your criteria: "Thomas' Hospital NHS Foundation Trust[Affiliation]"

Introduction: Stigma adversely affects people with chronic pain. The qualities within self-compassion may be particularly useful for buffering the impact of stigma on people with pain. In the context of an Acceptance and Commitment Therapy-based (ACT) treatment for chronic pain, this study investigated the association between changes in stigma and self-compassion and pain outcomes, and the potential moderating role of self-compassion on the association between stigma and pain outcomes.

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Asthma, which affects some 300 million people worldwide and caused 455,000 deaths in 2019, is a significant burden to suffers and to society. It is the most common chronic disease in children and represents one of the major causes for years lived with disability. Significant efforts are made by organizations such as WHO in improving the diagnosis, treatment and monitoring of asthma.

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Article Synopsis
  • - Cytological specimens are crucial for diagnosing head and neck nodules, especially with the rise of personalized medicine and the use of molecular markers in diagnostics.
  • - The Updates in Head and Neck Cytopathology Short Course at the 35th European Congress of Pathology in Dublin, 2023, featured experts discussing advancements in cytopathology.
  • - Key topics covered included the Milan System for Salivary Gland Cytopathology, one-stop clinics, next-generation sequencing, and HPV detection in head and neck cases.
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The experience of clinical study and trial participation in rare diseases: A scoping review of centronuclear myopathy and other neuromuscular disorders.

Neuromuscul Disord

May 2024

Department of Neurology, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, P.O. Box 9101, 6500 HB, Nijmegen, the Netherlands. Electronic address:

The design of a clinical trial for a rare disease can be challenging. An optimal study design is required to effectively study the clinical outcomes for possible therapies for these types of disorders. Understanding the study participants' experiences as well as barriers and facilitators of participation are important to optimize future research and to inform clinical trial management.

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Artificial Intelligence in Ultrasound Diagnoses of Ovarian Cancer: A Systematic Review and Meta-Analysis.

Cancers (Basel)

January 2024

Department of Gynaecological Oncology, Surgical Oncology Directorate, Cancer Centre, Guy's Hospital, Great Maze Pond, London SE1 9RT, UK.

Ovarian cancer is the sixth most common malignancy, with a 35% survival rate across all stages at 10 years. Ultrasound is widely used for ovarian tumour diagnosis, and accurate pre-operative diagnosis is essential for appropriate patient management. Artificial intelligence is an emerging field within gynaecology and has been shown to aid in the ultrasound diagnosis of ovarian cancers.

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Objective: Social determinants of health (SDH) are important determinants of long-term conditions and multimorbidity in the general population. The intersecting relationship between SDH and multimorbidity in people with HIV remains poorly studied.

Design: A cross-sectional study investigating the relationships between eight socio-economic parameters and prevalent comorbidities of clinical significance and multimorbidity in adults of African ancestry with HIV aged 18-65 years in South London, UK.

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Objective: The aim of this narrative review is to evaluate existing questionnaires on predictive models for endometriosis. These symptom-based models have the potential to serve as screening tools for adult women to detect endometriosis.

Data Sources: A comprehensive search of PubMed and Embase databases was conducted to identify studies on endometriosis screening.

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The gut microbiome and its associated metabolites are integral to the maintenance of gut integrity and function. There is increasing evidence that its alteration, referred to as dysbiosis, is involved in the development of a systemic conditions such as cardiovascular disease (e.g.

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Background: Nintedanib slows progression of lung function decline in patients with progressive fibrosing (PF) interstitial lung disease (ILD) and was recommended for this indication within the United Kingdom (UK) National Health Service in Scotland in June 2021 and in England, Wales and Northern Ireland in November 2021. To date, there has been no national evaluation of the use of nintedanib for PF-ILD in a real-world setting.

Methods: 26 UK centres were invited to take part in a national service evaluation between 17 November 2021 and 30 September 2022.

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Knowing What We Are Talking About: The Case of Pain Catastrophizing.

J Pain

March 2024

Department of Experimental - Clinical and Health Psychology, Faculty of Psychology and Educational Sciences, Ghent University, Ghent, Belgium.

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The last two decades have seen increasing use of long-term ventilation (LTV) as an intervention in childhood. Children who use LTV have many risk factors for feeding and swallowing difficulties, including their underlying respiratory and/or neurological etiology, long hospitalizations, medical interventions, and limited exposure to oral feeding experiences. This review aimed to answer two questions: 1) 'What specific swallowing and feeding characteristics do these children experience?'; and 2) 'What impacts do these swallowing and feeding characteristics have on health status and quality of life?'.

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Purpose: The interim analysis of the phase IIIb LUCY trial demonstrated the clinical effectiveness of olaparib in patients with germline BRCA-mutated (gBRCAm), human epidermal growth factor receptor 2 (HER2)-negative metastatic breast cancer (mBC), with median progression-free survival (PFS) of 8.11 months, which was similar to that in the olaparib arm of the phase III OlympiAD trial (7.03 months).

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Improved prognostication using the inferior vena cava collapsibility index: A tool validated for adults with congenital heart disease.

Int J Cardiol

March 2024

Adult Congenital Heart Centre and National Centre for Pulmonary Hypertension, RoyalBrompton Hospital, Guy's and St Thomas' Hospital NHS Foundation Trust, London, UK; National Heart and Lung Institute, Imperial College London, London, UK.

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The effect of psychological factors on pain outcomes: lessons learned for the next generation of research.

Pain Rep

December 2023

Department of Experimental-Clinical and Health Psychology, Faculty of Psychology and Educational Sciences, Ghent University, Ghent, Belgium.

Article Synopsis
  • Big data and machine learning can help us understand how psychological factors affect pain, but we need really good data to do this correctly.
  • There are challenges with current evidence about how these factors influence chronic pain, so improvements are needed.
  • Researchers should be clearer about how they think causes and effects work, which can help design better studies and lead to more useful results.
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Impact of thoracic duct resection during radical esophagectomy on oncological and survival outcomes: Systematic review.

Eur J Surg Oncol

January 2024

Department of General Surgery, Queen Alexandra Hospital, University Hospital Portsmouth NHS Trust, Portsmouth, UK; Division of Surgery, Imperial College London, London, UK; Department of Pharmacology and Biosciences, University of Portsmouth, Portsmouth, UK. Electronic address:

Practice is variable in the inclusion or exclusion of the thoracic duct (TD) as part of the resected specimen and associated lymphadenectomy in radical esophagectomy for esophageal cancer. While some surgeons believe that the removal of TD-associated nodes may improve radicality and survival, others suggest this represents systemic disease and resection may increase morbidity without survival benefit. A systematic review was performed up to March 2023 using the search terms 'esoph∗' AND 'thoracic duct' for relevant articles which compared thoracic duct preservation (TDP) to resection (TDR) in esophagectomy for esophageal cancer.

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This study aimed to evaluate the impact of developing and implementing a care bundle intervention to improve care for patients with acute heart failure admitted to a large London hospital. The intervention comprised three elements, targeted within 24 hours of admission: N-terminal pro-B-type natriuretic peptide (NT-proBNP) test, transthoracic Doppler two-dimensional echocardiography and specialist review by cardiology team. The SHIFT-Evidence approach to quality improvement was used.

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Background: Percutaneous coronary intervention (PCI) is frequently undertaken in patients with ischemic left ventricular systolic dysfunction. The REVIVED (Revascularization for Ischemic Ventricular Dysfunction)-BCIS2 (British Cardiovascular Society-2) trial concluded that PCI did not reduce the incidence of all-cause death or heart failure hospitalization; however, patients assigned to PCI reported better initial health-related quality of life than those assigned to optimal medical therapy (OMT) alone. The aim of this study was to assess the cost-effectiveness of PCI+OMT compared with OMT alone.

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Recurrent atraumatic compartment syndrome as a manifestation of genetic neuromuscular disease.

Neuromuscul Disord

November 2023

Department of Paediatric Neurology, Neuromuscular Service, Evelina's Children Hospital, Guy's & St. Thomas' Hospital NHS Foundation Trust, London, United Kingdom; Randall Centre for Cell and Molecular Biophysics, Muscle Signalling Section, Faculty of Life Sciences and Medicine (FoLSM), King's College London, London, United Kingdom. Electronic address:

Article Synopsis
  • Compartment syndrome (CS) is a serious medical condition caused by high pressures in body compartments that can lead to reduced blood flow and tissue damage; it has acute types often linked to trauma and chronic types seen in athletes with exercise-induced pain.
  • This text discusses three patients with recurrent CS connected to genetic disorders: one with a RYR1-related condition and two with McArdle disease, highlighting that some presented symptoms years before any genetic diagnosis was made.
  • The article reviews existing literature on CS cases related to genetic neuromuscular disorders and suggests that understanding calcium signaling changes in RYR1 disorders and metabolic issues in McArdle disease is important for recognizing the broader implications of CS in these contexts.
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Novel Genetic and Phenotypic Expansion in -Related Progressive Myoclonus Epilepsy.

Genes (Basel)

September 2023

Department of Pediatrics, Faculty of Medicine and University Hospital Cologne, University of Cologne, 50937 Cologne, Germany.

Biallelic variants in the Golgi SNAP receptor complex member 2 gene () have been reported in progressive myoclonus epilepsy with neurodegeneration. Typical clinical features include ataxia and areflexia during early childhood, followed by seizures, scoliosis, dysarthria, and myoclonus. Here, we report two novel patients from unrelated families with a -related disorder and novel genetic and clinical findings.

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Purpose: While there are several prognostic classifiers, to date, there are no validated predictive models that inform treatment selection for oropharyngeal squamous cell carcinoma (OPSCC).Our aim was to develop clinical and/or biomarker predictive models for patient outcome and treatment escalation for OPSCC.

Experimental Design: We retrospectively collated clinical data and samples from a consecutive cohort of OPSCC cases treated with curative intent at ten secondary care centers in United Kingdom and Poland between 1999 and 2012.

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Pancreatitis in RYR1-related disorders.

Neuromuscul Disord

October 2023

Department of Paediatric Neurology, Neuromuscular Service, Evelina's Children Hospital, Guy's & St. Thomas' Hospital NHS Foundation Trust, London, United Kingdom; Randall Centre for Cell and Molecular Biophysics, Muscle Signalling Section, Faculty of Life Sciences and Medicine (FoLSM), King's College London, London, United Kingdom. Electronic address:

Article Synopsis
  • - Mutations in the RYR1 gene, which is responsible for the ryanodine receptor in skeletal muscle, are linked to several inherited neuromuscular disorders, but non-skeletal muscle symptoms are rarely reported.
  • - This study presents three patients with Central Core Disease, King-Denborough Syndrome, and Malignant Hyperthermia Susceptibility, who also experienced acute pancreatitis, indicating a potential connection between RYR1 mutations and pancreatic issues.
  • - The findings suggest that individuals with specific RYR1 mutations may be more prone to acute pancreatitis; hence, monitoring for this condition should be part of their medical care strategy.
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