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1.
Pract Neurol ; 21(4): 336-337, 2021 Aug.
Article in English | MEDLINE | ID: mdl-33785563

Subject(s)
Stroke , Humans
2.
Int J Stroke ; 13(4): 374-378, 2018 06.
Article in English | MEDLINE | ID: mdl-29192873

ABSTRACT

Background Information on ethnic disparities in stroke between White and Pakistani population in Europe is scarce. Bradford District has the largest proportion of Pakistani people in England; this provides a unique opportunity to study the difference in stroke between the two major ethnic groups. Aim To determine the first-ever-stroke incidence and examine the disparities in stroke patterns between Whites and Pakistanis in Bradford. Methods Prospective 12 months study consisting of 273,327 adults (≥18 years) residents. Stroke cases were identified by multiple overlapping approaches. Results In the study period, 541 first-ever-strokes were recorded. The crude incidence rate was 198 per 100,000 person-years. Age adjusted-standardized rate to the World Health Organization world population of first-ever-stroke is 155 and 101 per 100,000 person-years in Pakistanis and Whites respectively. Four hundred and thirty-eight patients (81%) were Whites, 83 (15.3%) were Pakistanis, 11 (2%) were Indian and Bangladeshis, and 9 (1.7%) were of other ethnic origin. Pakistanis were significantly younger and had more obesity ( p = 0.049), and diabetes mellitus (DM) ( p = <0.001). They were less likely to suffer from atrial fibrillation ( p = <0.001), be ex- or current smokers ( p = <0.001), and drink alcohol above the recommended level ( p = 0.007) compared with Whites. In comparison with Whites, higher rates of age-adjusted stroke (1.5-fold), lacunar infarction (threefold), and ischemic infarction due to large artery disease (twofold) were found in the Pakistanis. Conclusions The incidence of first-ever-stroke is higher in the Pakistanis compared with the Whites in Bradford, UK. Etiology and vascular risk factors vary between the ethnic groups. This information should be considered when investigating stroke etiology, and when planning prevention and care provision to improve outcomes after stroke.


Subject(s)
Stroke/ethnology , Adolescent , Adult , Age Distribution , Aged , Aged, 80 and over , England/epidemiology , Female , Humans , Incidence , Male , Middle Aged , Pakistan/ethnology , Prospective Studies , White People/ethnology , Young Adult
3.
Trials ; 18(1): 162, 2017 04 05.
Article in English | MEDLINE | ID: mdl-28381307

ABSTRACT

BACKGROUND: Recruitment to randomised prevention trials is challenging, not least for intracerebral haemorrhage (ICH) associated with antithrombotic drug use. We investigated reasons for not recruiting apparently eligible patients at hospital sites that keep screening logs in the ongoing REstart or STop Antithrombotics Randomised Trial (RESTART), which seeks to determine whether to start antiplatelet drugs after ICH. METHOD: By the end of May 2015, 158 participants had been recruited at 108 active sites in RESTART. The trial coordinating centre invited all sites that kept screening logs to submit screening log data, followed by one reminder. We checked the integrity of data, focused on the completeness of data about potentially eligible patients and categorised the reasons they were not randomised. RESULTS: Of 108 active sites, 39 (36%) provided usable screening log data over a median of ten (interquartile range = 5-13) months of recruitment per site. During this time, sites screened 633 potentially eligible patients and randomised 53 (8%) of them. The main reasons why 580 patients were not randomised were: 43 (7%) patients started anticoagulation, 51 (9%) patients declined, 148 (26%) patients' stroke physicians were not uncertain about using antiplatelet drugs, 162 (28%) patients were too unwell and 176 (30%) patients were not randomised due to other reasons. CONCLUSION: RESTART recruited ~8% of eligible patients. If more physicians were uncertain about the therapeutic dilemma that RESTART is addressing, RESTART could have recruited up to four times as many participants. The trial coordinating centre continues to engage with physicians about their uncertainty. TRIAL REGISTRATION: EU Clinical Trials, EudraCT 2012-003190-26 . Registered on 3 July 2012.


Subject(s)
Cerebral Hemorrhage/prevention & control , Eligibility Determination , Fibrinolytic Agents/adverse effects , Patient Selection , Platelet Aggregation Inhibitors/adverse effects , Research Personnel , Sample Size , Secondary Prevention/methods , Attitude of Health Personnel , Cerebral Hemorrhage/chemically induced , Cerebral Hemorrhage/diagnosis , Health Knowledge, Attitudes, Practice , Humans , Physician's Role , United Kingdom
6.
Clin Med (Lond) ; 14(3): 255-9, 2014 Jun.
Article in English | MEDLINE | ID: mdl-24889568

ABSTRACT

Cerebral amyloid angiopathy is a commonly occurring condition that is not familiar to most clinicians. A common presenting feature may be transient focal neurological symptoms leading to the potential for clinical misdiagnosis as transient ischaemic attack. This may result in the inappropriate use of anti-platelets and anticoagulants or radiological misdiagnosis. It is also being increasingly recognised as an important cause of spontaneous intracerebral haemorrhage and cognitive impairment in the elderly. Cerebral amyloid angiopathy can be diagnosed based on clinical and radiological findings, but clinicians need a high index of suspicion to ensure appropriate investigations are requested. In this article we aim to cover the pathophysiology, clinical findings, radiological appearances and approach to management of cerebral amyloid angiopathy.


Subject(s)
Cerebral Amyloid Angiopathy/diagnosis , Cerebral Amyloid Angiopathy/therapy , Aged , Cerebral Amyloid Angiopathy/pathology , Diagnosis, Differential , Humans , Ischemic Attack, Transient/diagnosis , Magnetic Resonance Imaging , Male , Subarachnoid Hemorrhage/diagnosis
8.
Mult Scler ; 20(1): 120-2, 2014 Jan.
Article in English | MEDLINE | ID: mdl-23846353

ABSTRACT

We present a case report of newly diagnosed neuromyelitis optica spectrum disorder (NMOSD) with associated myocarditis and diffuse oedema of the pelvic and anterior compartment thigh muscles on magnetic resonance imaging. Aquaporin 4 antibodies are expressed in skeletal myofibres but involvement of skeletal muscle is rarely reported in NMOSD and myocarditis has not previously been described in this context. This case highlights the need for further research into the involvement of cardiac and skeletal muscle in NMOSD.


Subject(s)
Muscle, Skeletal/pathology , Myocarditis/complications , Neuromyelitis Optica/complications , Adult , Aquaporin 4/immunology , Autoantibodies/analysis , Autoantibodies/immunology , Autoantigens/immunology , Edema/etiology , Female , Humans , Myocarditis/pathology , Neuromyelitis Optica/pathology , Neuromyelitis Optica/physiopathology
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