Christine Morrell
Leeds General Infirmary
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Featured researches published by Christine Morrell.
Heart | 2001
M F Dorsch; R A Lawrance; Robert J. Sapsford; N Durham; J Oldham; Darren C. Greenwood; Beryl M. Jackson; Christine Morrell; Mike Robinson; Alistair S. Hall
OBJECTIVE To describe the clinical features, prognosis, and treatment of patients presenting with atypical forms of acute myocardial infarction. DESIGN Consecutive cases of possible acute myocardial infarction were sought from coronary care registers, biochemistry records, and hospital management systems. Case notes were reviewed and predefined epidemiological and clinical variables were abstracted. SETTING 20 adjacent hospitals in the former Yorkshire region. PATIENTS 3684 consecutive cases of possible acute myocardial infarction admitted in a three month period were identified, of whom 2096 had a first episode of confirmed acute myocardial infarction. RESULTS 20.2% of all patients admitted with an eventual diagnosis of acute myocardial infarction presented with symptoms other than chest pain. Compared with the group presenting with chest pain, these patients were older (76.6v 69.1 years, p < 0.001), were more often women (54.6% v 35.3%, p < 0.001), and were more likely to have a history of heart failure (18.6%v 6.9%, p < 0.001). They had a higher 30 and 365 day mortality (49.2% and 61.0%, respectively) compared with patients presenting with chest pain (17.9% and 26.2%). In a Cox regression analysis the hazard ratio for presentation without chest pain was 1.60 (95% confidence interval 1.30 to 1.97) (p < 0.001) adjusted for age, heart rate, blood pressure, left ventricular impairment, and infarction with ST segment elevation as covariates. Importantly, they were also less likely to receive treatments with a proven ability to improve prognosis. CONCLUSIONS Atypical presentation of myocardial infarction without chest pain is common and associated with increased mortality. This may result in part from a failure to use beneficial treatment strategies.
Heart | 2001
M F Dorsch; R A Lawrance; Robert J. Sapsford; J Oldham; Darren C. Greenwood; Beryl M. Jackson; Christine Morrell; Stephen G. Ball; Mike Robinson; Alistair S. Hall
OBJECTIVE To develop a simple risk model as a basis for evaluating care of patients admitted with acute myocardial infarction. METHODS From coronary care registers, biochemistry records and hospital management systems, 2153 consecutive patients with confirmed acute myocardial infarction were identified. With 30 day all cause mortality as the end point, a multivariable logistic regression model of risk was constructed and validated in independent patient cohorts. The areas under receiver operating characteristic curves were calculated as an assessment of sensitivity and specificity. The model was reapplied to a number of commonly studied subgroups for further assessment of robustness. RESULTS A three variable model was developed based on age, heart rate, and systolic blood pressure on admission. This produced an individual probability of death by 30 days (P30) where P30 = 1/(1 + exp(−L30)) and L30 = −5.624 + (0.085 × age) + (0.014 × heart rate) − (0.022 × systolic blood pressure). The areas under the receiver operating characteristic curves for the reference and test cohorts were 0.79 (95% CI 0.76 to 0.82) and 0.76 (95% CI 0.72 to 0.79), respectively. To aid application of the model to routine clinical audit, a normogram relating observed mortality and sample size to the likelihood of a significant deviation from the expected 30 day mortality rate was constructed. CONCLUSIONS This risk model is simple, reproducible, and permits quality of care of acute myocardial infarction patients to be reliably evaluated both within and between centres.
Heart | 2006
Rajiv Das; Niamh Kilcullen; Christine Morrell; Mike Robinson; Julian H. Barth; Alistair S. Hall
Objective: To assess the impact on observed mortality of the British Cardiac Society (BCS) definition of myocardial infarction (MI) in 11 UK hospitals. Design: Prospective observational registry. Setting: 11 adjacent hospitals in the West Yorkshire region. Patients: 2484 patients with the acute coronary syndrome (ACS) were identified during a six month period (28 April to 28 October 2003). Demographic, clinical, and treatment variables were collected on all patients. Deaths were monitored through the Office of National Statistics. Patients were categorised into three groups according to the BCS definition of MI: ACS with unstable angina (UA), ACS with myocyte necrosis, and ACS with clinical MI. Results: 30 day mortality was 4.5%, 10.4%, and 12.9% (p < 0.001) in the ACS with UA, ACS with myocyte necrosis, and ACS with clinical MI groups, respectively. At six months the mortality for patients in the groups ACS with clinical MI and ACS with myocyte necrosis was similar (19.2% v 18.7%), being higher than for ACS with UA (8.6%). Same admission percutaneous coronary intervention was similar in groups with clinical MI and myocyte necrosis (11.1% v 10.7%, respectively) as was coronary artery bypass grafting (2.6% v 2.7%, respectively). However, these two groups differed significantly in the prescribing of secondary prevention (aspirin, 79% v 69%; statins, 80% v 68%; β blockers, 66% v 53%; and angiotensin converting enzyme inhibitors, 65% v 53%; p < 0.001). Conclusions: At 30 days the new BCS categories for MI predict three distinct outcomes. However, within a contemporary UK population this was no longer apparent at six months, as mortality for patients with ACS with myocyte necrosis had risen to the same level as those for patients with ACS with clinical MI. One possible explanation for this is the apparent under use of drugs known to improve prognosis after traditionally defined MI.
PLOS ONE | 2008
Richard M. Cubbon; Afroze Abbas; Stephen B. Wheatcroft; Niamh Kilcullen; Raj Das; Christine Morrell; Julian H. Barth; Mark T. Kearney; Alistair S. Hall
Background Diabetes Mellitus (DM) is associated with adverse cardiovascular prognosis. However, the risk associated with DM may vary between individuals according to their overall cardiovascular risk burden. Therefore, we aimed to determine whether DM is associated with poor outcome in patients presenting with Acute Coronary Syndrome (ACS) according to the index episode being a first or recurrent cardiovascular event. Methods and Findings We conducted a retrospective analysis of a prospective cohort study involving 2499 consecutively admitted patients with confirmed ACS in 11 UK hospitals during 2003. Usual care was provided for all participants. Demographic factors, co-morbidity and treatment (during admission and at discharge) factors were recorded. The primary outcome was all cause mortality (median 2 year follow up), compared for cohorts with and without DM according to their prior cardiovascular disease (CVD) disease status. Adjusted analyses were performed with Cox proportional hazards regression analysis. Within the entire cohort, DM was associated with an unadjusted 45% increase in mortality. However, in patients free of a history of CVD, mortality of those with and without DM was similar (18.8% and 19.7% respectively; p = 0.74). In the group with CVD, mortality of patients with DM was significantly higher than those without DM (46.7% and 33.2% respectively; p<0.001). The age and sex adjusted interaction between DM and CVD in predicting mortality was highly significant (p = 0.002) and persisted after accounting for comorbidities and treatment factors (p = 0.006). Of patients free of CVD, DM was associated with smaller elevation of Troponin I (p<0.001). However in patients with pre-existing CVD Troponin I was similar (p = 0.992). Conclusions DM is only associated with worse outcome after ACS in patients with a pre-existing history of CVD. Differences in the severity of myocyte necrosis may account for this. Further investigation is required, though our findings suggest that aggressive primary prevention of CVD in patients with DM may have beneficially modified their first presentation with (and mortality after) ACS.
Journal of the American College of Cardiology | 2007
Niamh Kilcullen; Karthik Viswanathan; Rajiv Das; Christine Morrell; Amanda Farrin; Julian H. Barth; Alistair S. Hall; Emmace Investigators
BMJ | 2001
Richard A. Lawrance; Micha F. Dorsch; Robert J. Sapsford; Alan F Mackintosh; Darren C. Greenwood; Beryl M. Jackson; Christine Morrell; Mike Robinson; Alistair S. Hall
Diabetes Care | 2008
Richard M. Cubbon; Chris Gale; Adil Rajwani; Afroze Abbas; Christine Morrell; Raj Das; Julian H. Barth; Peter J. Grant; Mark T. Kearney; Alistair S. Hall
International Journal of Cardiology | 2004
M.F. Dorsch; R.A. Lawrance; Robert J. Sapsford; Np Durham; R. Das; Beryl M. Jackson; Christine Morrell; Stephen G. Ball; Mb Robinson; Alistair S. Hall
/data/revues/00029149/unassign/S0002914914007073/ | 2014
Olivia Manfrini; Christine Morrell; Rajiv Das; Julian H. Barth; Alistair S. Hall; Chris Gale; Edina Cenko; Raffaele Bugiardini
Heart | 2010
Mark T. Lown; Chris P Gale; Theresa Munyombwe; C Hall; Christine Morrell; Beryl M. Jackson; Robert J. Sapsford; R Das; Niamh Kilcullen; Julian H. Barth; C B Pepper; Alistair S. Hall