Stuart J. Pocock

ORCID: 0000-0003-2212-4007
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About
Contact & Profiles
Research Areas
  • Antiplatelet Therapy and Cardiovascular Diseases
  • Acute Myocardial Infarction Research
  • Health Systems, Economic Evaluations, Quality of Life
  • Heart Failure Treatment and Management
  • Coronary Interventions and Diagnostics
  • Statistical Methods in Clinical Trials
  • Diabetes Treatment and Management
  • Meta-analysis and systematic reviews
  • Cardiac Imaging and Diagnostics
  • Atrial Fibrillation Management and Outcomes
  • Cardiovascular Function and Risk Factors
  • Blood Pressure and Hypertension Studies
  • Lipoproteins and Cardiovascular Health
  • Pancreatic function and diabetes
  • Advanced Causal Inference Techniques
  • Venous Thromboembolism Diagnosis and Management
  • Metabolism, Diabetes, and Cancer
  • Hormonal Regulation and Hypertension
  • Acute Ischemic Stroke Management
  • Cardiac Valve Diseases and Treatments
  • Statistical Methods and Bayesian Inference
  • Cardiac, Anesthesia and Surgical Outcomes
  • Diabetes Management and Research
  • Statistical Methods and Inference
  • Cardiac Health and Mental Health

London School of Hygiene & Tropical Medicine
2016-2025

University of London
2015-2025

Spanish National Centre for Cardiovascular Research
2014-2025

NewYork–Presbyterian Hospital
2012-2024

Columbia University Irving Medical Center
2005-2024

Freeman Hospital
2024

Newcastle University
2024

Newcastle upon Tyne Hospitals NHS Foundation Trust
2024

United Lincolnshire Hospitals NHS Trust
2024

Northumbria Healthcare NHS Foundation Trust
2024

Much biomedical research is observational. The reporting of such often inadequate, which hampers the assessment its strengths and weaknesses a study's generalisability. Strengthening Reporting Observational Studies in Epidemiology (STROBE) Initiative developed recommendations on what should be included an accurate complete report observational study. We defined scope to cover three main study designs: cohort, case-control, cross-sectional studies. convened 2-day workshop September 2004, with...

10.1371/journal.pmed.0040296 article EN cc-by PLoS Medicine 2007-10-10

Much biomedical research is observational. The reporting of such often inadequate, which hampers the assessment its strengths and weaknesses a study's generalizability. Strengthening Reporting Observational Studies in Epidemiology (STROBE) Initiative developed recommendations on what should be included an accurate complete report observational study. We defined scope to cover 3 main study designs: cohort, case–control, cross-sectional studies. convened 2-day workshop September 2004, with...

10.7326/0003-4819-147-8-200710160-00010 article EN cc-by Annals of Internal Medicine 2007-10-16

Much biomedical research is observational. The reporting of such often inadequate, which hampers the assessment its strengths and weaknesses a study's generalisability. Strengthening Reporting Observational Studies in Epidemiology (STROBE) Initiative developed recommendations on what should be included an accurate complete report observational study. We defined scope to cover three main study designs: cohort, case–control, cross-sectional studies. convened 2-day workshop September 2004, with...

10.1016/j.ijsu.2014.07.013 article EN cc-by International Journal of Surgery 2014-07-18

Poor reporting of research hampers assessment and makes it less useful. An international group methodologists, researchers, journal editors sets out guidelines to improve reports observational studies

10.1136/bmj.39335.541782.ad article EN BMJ 2007-10-18

Many patients with severe aortic stenosis and coexisting conditions are not candidates for surgical replacement of the valve. Recently, transcatheter aortic-valve implantation (TAVI) has been suggested as a less invasive treatment high-risk stenosis.

10.1056/nejmoa1008232 article EN New England Journal of Medicine 2010-10-20

The cardiovascular effect of liraglutide, a glucagon-like peptide 1 analogue, when added to standard care in patients with type 2 diabetes, remains unknown.In this double-blind trial, we randomly assigned diabetes and high risk receive liraglutide or placebo. primary composite outcome the time-to-event analysis was first occurrence death from causes, nonfatal myocardial infarction, stroke. hypothesis that would be noninferior placebo regard outcome, margin 1.30 for upper boundary 95%...

10.1056/nejmoa1603827 article EN New England Journal of Medicine 2016-06-13

The use of transcatheter aortic-valve replacement has been shown to reduce mortality among high-risk patients with aortic stenosis who are not candidates for surgical replacement. However, the two procedures have compared in a randomized trial involving still

10.1056/nejmoa1103510 article EN New England Journal of Medicine 2011-06-05

Much medical research is observational. The reporting of observational studies often insufficient quality. Poor hampers the assessment strengths and weaknesses a study generalisability its results. Taking into account empirical evidence theoretical considerations, group methodologists, researchers, editors developed Strengthening Reporting Observational Studies in Epidemiology (STROBE) recommendations to improve quality studies. STROBE Statement consists checklist 22 items, which relate...

10.1016/j.ijsu.2014.07.014 article EN cc-by International Journal of Surgery 2014-12-01

Much medical research is observational. The reporting of observational studies often insufficient quality. Poor hampers the assessment strengths and weaknesses a study generalisability its results. Taking into account empirical evidence theoretical considerations, group methodologists, researchers, editors developed Strengthening Reporting Observational Studies in Epidemiology (STROBE) recommendations to improve quality studies. STROBE Statement consists checklist 22 items, which relate...

10.1371/journal.pmed.0040297 article EN cc-by PLoS Medicine 2007-10-10

Among patients with aortic stenosis who are at intermediate or high risk for death surgery, major outcomes similar transcatheter aortic-valve replacement (TAVR) and surgical replacement. There is insufficient evidence regarding the comparison of two procedures in low risk.

10.1056/nejmoa1814052 article EN New England Journal of Medicine 2019-03-16

Introduction: The Rationale of Clinical Trials. Historical Development Organization and Planning. Justificaton for Randomized Controlled Methods Randomization. Blinding Placebos. Ethical Issues. Crossover Size a Trial. Monitoring Trial Progress. Forms Data Management. Protocol Deviations. Basic Principles Statistical Analysis. Further Aspects Publication Interpretation Findings. References. Index.

10.2307/2531186 article EN Biometrics 1984-12-01

Mineralocorticoid antagonists improve survival among patients with chronic, severe systolic heart failure and after myocardial infarction. We evaluated the effects of eplerenone in chronic mild symptoms.

10.1056/nejmoa1009492 article EN New England Journal of Medicine 2010-11-14

Much biomedical research is observational. The reporting of such often inadequate, which hampers the assessment its strengths and weaknesses a study's generalisability. Strengthening Reporting Observational Studies in Epidemiology (STROBE) Initiative developed recommendations on what should be included an accurate complete report observational study. We defined scope to cover three main study designs: cohort, case-control, cross-sectional studies. convened 2-day workshop September 2004, with...

10.1371/journal.pmed.0040296 article EN DOAJ (DOAJ: Directory of Open Access Journals) 2007-10-01

In controlled clinical trials there are usually several prognostic factors known or thought to influence the patient's ability respond treatment. Therefore, method of sequential treatment assignment needs be designed so that balance is simultaneously achieved across all such patients factor. Traditional methods restricted randomization as "permuted blocks within strata" prove inadequate once number strata, combinations factor levels, approaches sample size. A new general procedure for...

10.2307/2529712 article EN Biometrics 1975-03-01

The CONSORT (Consolidated Standards of Reporting Trials) Statement, which includes a checklist and flow diagram, is guideline developed to help authors improve the reporting findings from randomized controlled trials. It was updated most recently in 2010. Its primary focus on individually trials with 2 parallel groups that assess possible superiority one treatment compared another. Statement has been extended other trial designs such as cluster randomization, recommendations for...

10.1001/jama.2012.87802 article EN JAMA 2012-12-26

Much medical research is observational. The reporting of observational studies often insufficient quality. Poor hampers the assessment strengths and weaknesses a study generalizability its results. Taking into account empirical evidence theoretical considerations, group methodologists, researchers, editors developed Strengthening Reporting Observational Studies in Epidemiology (STROBE) recommendations to improve quality studies. STROBE Statement consists checklist 22 items, which relate...

10.1097/ede.0b013e3181577511 article EN Epidemiology 2007-11-01

Iron deficiency may impair aerobic performance. This study aimed to determine whether treatment with intravenous iron (ferric carboxymaltose) would improve symptoms in patients who had heart failure, reduced left ventricular ejection fraction, and deficiency, either or without anemia.

10.1056/nejmoa0908355 article EN New England Journal of Medicine 2009-11-18

Treatment with the direct thrombin inhibitor bivalirudin, as compared heparin plus glycoprotein IIb/IIIa inhibitors, results in similar suppression of ischemia while reducing hemorrhagic complications patients stable angina and non-ST-segment elevation acute coronary syndromes who are undergoing percutaneous intervention (PCI). The safety efficacy bivalirudin high-risk unknown.We randomly assigned 3602 ST-segment myocardial infarction presented within 12 hours after onset symptoms were...

10.1056/nejmoa0708191 article EN New England Journal of Medicine 2008-05-21

Antithrombotic drugs are used after coronary-artery stenting to prevent stent thrombosis. We compared the efficacy and safety of three antithrombotic-drug regimens — aspirin alone, warfarin, ticlopidine coronary stenting.

10.1056/nejm199812033392303 article EN New England Journal of Medicine 1998-12-03

In clinical trials with sequential patient entry, fixed sample size designs are unjustified on ethical grounds and often impracticable. One solution is a group design dividing entry into number of equal-sized groups so that the decision to stop trial or continue based repeated significance tests accumulated data after each evaluated. Exact results obtained for two treatments normal response known variance. The problem determining required also considered. Simulation shows these may be...

10.1093/biomet/64.2.191 article EN Biometrika 1977-08-01
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