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1.
Br J Hosp Med (Lond) ; 82(7): 1-6, 2021 Jul 02.
Article in English | MEDLINE | ID: mdl-34338010

ABSTRACT

Pulmonary embolism remains a common and potentially deadly disease, despite advances in diagnostic imaging, treatment and prevention. Managing pulmonary embolism requires a multifactorial approach involving risk stratification, determining appropriate diagnostics and selecting individualised therapy. The first part of this article reviewed the pathophysiology, risk factors, clinical presentation, diagnostic evaluation and therapeutic management and early outpatient management of pulmonary embolism. This second part summarises pulmonary embolism in the setting of pregnancy, COVID-19, recurrent disease and chronic thromboembolic pulmonary hypertension.


Subject(s)
COVID-19/epidemiology , Pulmonary Embolism/epidemiology , Pulmonary Embolism/pathology , COVID-19/pathology , Chronic Disease , Female , Humans , Hypertension, Pulmonary/epidemiology , Hypertension, Pulmonary/pathology , Male , Pregnancy , Pulmonary Embolism/diagnostic imaging , Radiography, Thoracic , Recurrence , Risk Factors , SARS-CoV-2 , Ultrasonography, Doppler , Venous Thromboembolism/epidemiology , Venous Thromboembolism/pathology
2.
Br J Hosp Med (Lond) ; 82(7): 1-16, 2021 Jul 02.
Article in English | MEDLINE | ID: mdl-34338014

ABSTRACT

Pulmonary embolism remains a common and potentially deadly disease, despite advances in diagnostic imaging, treatment and prevention. Managing pulmonary embolism requires a multifactorial approach involving risk stratification, determining appropriate diagnostics and selecting individualised therapy. This article reviews the pathophysiology, risk factors, clinical presentation, diagnostic evaluation and therapeutic management and early outpatient management of pulmonary embolism. The second part summarises pulmonary embolism in the setting of pregnancy, COVID-19, recurrent disease and chronic thromboembolic pulmonary hypertension.


Subject(s)
COVID-19/epidemiology , Pulmonary Embolism/epidemiology , Pulmonary Embolism/pathology , Biomarkers , COVID-19/pathology , Chronic Disease , Female , Humans , Hypertension, Pulmonary/epidemiology , Hypertension, Pulmonary/pathology , Male , Pregnancy , Pulmonary Embolism/diagnostic imaging , Recurrence , Risk Factors , SARS-CoV-2 , Venous Thromboembolism/epidemiology , Venous Thromboembolism/pathology
3.
J Am Coll Nutr ; 39(6): 495-500, 2020 08.
Article in English | MEDLINE | ID: mdl-31770081

ABSTRACT

Objective: Few interventions have tested the effects of different alcohol types on cardiovascular risk biomarkers. The aim of this study was to investigate the effects of red wine versus vodka on inflammatory and vascular health-related biomarkers.Methods: In a crossover study, participants were randomized to receive either red wine or vodka (3 units/day) for 2 weeks. Following a 2-week washout period, participants then consumed the alternate alcoholic drink for 2 weeks. Fasting blood samples were collected just prior to and at the end of each 2-week period. A total of 13 inflammatory and vascular health biomarkers were assessed.Results: A total of 77 of 85 recruited healthy men completed the study. Leptin levels were significantly raised after each intervention (p ≤ 0.01). APO A1 significantly increased following vodka, but not red wine, intervention (p ≤ 0.01). A significant difference between the interventions was noted for adiponectin only (p ≤ 0.01), although neither of the within-group changes were statistically significant (p > 0.01).Conclusions: The current study found significantly increased levels of leptin following both red wine and vodka consumption, increased levels of APO A1 following vodka consumption, and significant difference between both interventions for adiponectin only. Further studies are needed to investigate the effects of longer-term alcohol consumption on inflammatory and vascular health biomarkers.


Subject(s)
Cardiovascular Diseases , Wine , Alcohol Drinking , Biomarkers , Cross-Over Studies , Ethanol , Humans , Male
4.
BioDrugs ; 31(5): 393-408, 2017 Oct.
Article in English | MEDLINE | ID: mdl-28879503

ABSTRACT

Asthma is increasingly recognised as a heterogeneous group of diseases with similar clinical presentations rather than a singular disease entity. Asthma was historically categorised by clinical symptoms; however, newer methods of subgrouping, describing and categorising the disease have sub-defined asthma. These sub-definitions are intermittently called phenotypes or endotypes, but the real meanings of these words are poorly understood. Novel treatments are currently and increasingly available, partly in the monoclonal antibody environment, and also some physical therapies (bronchial thermoplasty), but additionally small molecules are not far away from clinical practice. Understanding the disease pathogenesis and the mechanism of action more completely may enable identification of treatable traits, biomarkers, mediators and modifiable therapeutic targets. However, there remains a danger that clinicians become preoccupied with the concept of endotypes and biomarkers, ignoring therapies that are hugely effective but have no companion biomarker. This review discusses our understanding of the concept of phenotypes and endotypes in appreciating and managing the heterogeneous condition that is asthma. We consider the role of functional imaging, physiology, blood-, sputum- and breath-based biomarkers and clinical manifestations that could be used to produce a personalised asthma profile, with implications on prognosis, pathophysiology and most importantly specific therapeutic responses. With the advent of increasing numbers of biological therapies and other interventional options such as bronchial thermoplasty, the importance of targeting expensive therapies to patients with the best chance of clinical response has huge health economic importance.


Subject(s)
Anti-Asthmatic Agents/therapeutic use , Asthma/drug therapy , Precision Medicine/methods , Animals , Antibodies, Monoclonal/therapeutic use , Asthma/physiopathology , Biological Therapy/methods , Biomarkers/metabolism , Humans , Phenotype , Prognosis
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