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Dive into the research topics where S B Wheatcroft is active.

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Featured researches published by S B Wheatcroft.


Catheterization and Cardiovascular Interventions | 2018

Transcoronary pacing to assess myocardial viability prior to percutaneous coronary intervention: Pilot study to assess feasibility

James O'Neill; Andrew J. Hogarth; Ian R Pearson; Hannah Law; Robert Bowes; Ananth Kidambi; S B Wheatcroft; U. Mohanaraj Sivananthan; Muzahir H. Tayebjee

The assessment of myocardial viability is crucial before percutaneous coronary intervention (PCI) is carried out to ensure that the patient will gain benefit. Trans‐coronary pacing (TCP) has previously been used to pace myocardium but may also provide information on myocardial viability.


Heart | 2016

26 Effect of Age and Gender on Outcomes Following Primary Percutaneous Coronary Intervention for ST-elevation Myocardial Infarction in a UK Tertiary Centre

Arvindra Krishnamurthy; Kathryn Somers; Natalie Burton-Wood; Michelle Anderson; Charlotte Harland; Claire Keeble; James McLenachan; Jonathan M Blaxill; Christopher J Malkin; Daniel J. Blackman; S B Wheatcroft; John P. Greenwood

Introduction Techniques and pharmacotherapy for Primary Percutaneous Coronary Intervention (PPCI) continue to evolve rapidly. The West Yorkshire PPCI outcome study was established to identify important clinical and procedural variables that may impact on patient outcomes following PPCI for ST-Elevation Myocardial Infarction (STEMI). We sought to clarify the influence of age and gender on major adverse cardiovascular events (MACE), which have been variably reported, in a large consecutive patient series. Methods Retrospective analysis of 3049 consecutive patients who underwent PPCI for STEMI between 1-1-2009 and 31-12-2011 at Leeds General Infirmary. Minimum 12m clinical follow-up data were collected for all; MACE was defined as total mortality, myocardial infarction and unplanned revascularisation. Unadjusted and adjusted analyses for total mortality and MACE were performed with Cox proportional hazards models for male (n = 2223) and female (n = 826) patients and for three age tertiles - under 60yrs (Group 1, n = 1276), 60 to 79yrs (Group 2, n = 1391) and 80yrs and above (Group 3, n = 382). Results Females (mean 68 ± 13yrs) had significantly higher rates of total mortality and MACE compared to males (mean 61 ± 13yrs) (Table 1, Figure 1). However, when adjusted for age, there was no statistically significant difference in total mortality or MACE between genders (Table 2, Figure 2). Age directly correlated with total mortality and MACE. Comparison between the three age tertiles showed Group 2 was associated with a higher rate of death (HR 4.17, 95% CI 2.86–6.09) and MACE (HR 2.03, 95% CI 1.60–2.57) at 12m compared to Group 1. The highest rate of death (HR 10.53, 95% CI 7.07–15.67) and MACE (HR 3.93, 95% CI 2.99–5.17) was seen in Group 3.Abstract 26 Table 1 Total mortality and MACE rates in females and males Gender Number n Death n (%) MACE n (%) Male 2223 175 (7.9) 276 (12.4) Female 826 94 (11.4) 140 (16.9) p < 0.01HR 1.48 (1.15–1.90) p < 0.01HR 1.40 (1.14–1.72)Abstract 26 Figure 1 Kaplan-Meier survival curves for total mortality and MACE in females and males Conclusion This large retrospective study has shown that whilst women appear to have significantly higher rates of death and MACE compared to men, when adjusted for age, gender was not associated with a statistically significant difference in outcomes. The difference in unadjusted outcomes may be due to the fact that women tend to present with STEMI at an older age than men. Therefore, the difference in outcomes is likely to be age-related rather than gender-related.Abstract 26 Table 2 Age-adjusted mortality and MACE rates in females and males Gender and Age Number n MACE n (%) Death n (%) Male <60 1060 78 (7.4) 26 (2.5) Female <60 216 22 (10.2) 7 (3.2) p = 0.16HR 1.40 (0.87–2.25) p = 0.51HR 1.32 (0.58–3.06) Male 60–79 976 146 (15.0) 103 (10.6) Female 60–79 415 65 (15.7) 41 (9.9) p = 0.99HR 1.00 (0.75–1.35) p = 0.53HR 0.89 (0.62–1.28) Male ≥80 187 52 (27.8) 46 (24.6) Female ≥80 195 53 (27.2) 46 (23.6) p = 0.90HR 0.98 (0.67–1.43) p = 0.83HR 0.96 (0.64–1.44)Abstract 26 Figure 2 Kaplan-Meier survival curves comparing age-adjusted mortality and MACE in females and males


Diabetes | 2005

Inducible nitric oxide synthase has divergent effects on vascular and metabolic function in obesity.

Brian T. Noronha; Jian-Mei Li; S B Wheatcroft; Ajay M. Shah; Mark T. Kearney


Diabetes | 2004

Preserved Glucoregulation but Attenuation of the Vascular Actions of Insulin in Mice Heterozygous for Knockout of the Insulin Receptor

S B Wheatcroft; Ajay M. Shah; Jian-Mei Li; Edward R. Duncan; Brian T. Noronha; Paul A. Crossey; Mark T. Kearney


77th Scientific Meeting of the American-Heart-Association | 2004

Overexpression of insulin-like growth factor binding protein-2 in mice protects against the development of insulin resistance and obesity

S B Wheatcroft; Paul A. Crossey; Ezzat; Mike Modo; Steven Williams; John P. Miell; Ajay M. Shah; Mark T. Kearney


Heart | 2005

Protection against the development of obesity, insulin resistance, and hypertension in mice by overexpression of insulin-like growth factor binding protein-2 (IGFBP-2)

S B Wheatcroft; Paul A. Crossey; Ezzat; John P. Miell; Ajay M. Shah; Mark T. Kearney


Atherosclerosis | 2005

Overexpression of insulin-like growth factor binding protein-2 in mice protects against the development of obesity, insulin resistance and hypertension

S B Wheatcroft; Paul A. Crossey; Ezzat; Steven Williams; Mike Modo; John P. Miell; Ajay M. Shah; Mark T. Kearney


Heart | 2004

Relative contributions of p40phox and p47phox subunits for basal and PMA stimulated NADPH oxidase activity in murine microvascular endothelial cells

Jian-Mei Li; Lampson M. Fan; Simon Walker; S B Wheatcroft; Mark T. Kearney; Ajay M. Shah


Heart | 2004

Mice heterozygous for knockout of the insulin receptor are glucocompetent but are hypertensive and have impaired insulin stimulated vascular nitric oxide (NO) production

S B Wheatcroft; Jian-Mei Li; Paul A. Crossey; Brian T. Noronha; Ajay M. Shah; Mark T. Kearney


Heart | 2004

Mice with a knockout for inducible nitric oxide synthase on an obesogenic diet are protected from metabolic but not vascular dysfunction

Brian T. Noronha; S B Wheatcroft; Jian-Mei Li; Ajay M. Shah; Mark T. Kearney

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Mike Modo

King's College London

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Ananth Kidambi

Leeds Teaching Hospitals NHS Trust

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Andrew J. Hogarth

Leeds Teaching Hospitals NHS Trust

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Arvindra Krishnamurthy

Leeds Teaching Hospitals NHS Trust

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