J
John J.V. McMurray
Researcher at University of Glasgow
Publications - 12
Citations - 1498
John J.V. McMurray is an academic researcher from University of Glasgow. The author has contributed to research in topics: Valsartan & Heart failure. The author has an hindex of 10, co-authored 12 publications receiving 967 citations. Previous affiliations of John J.V. McMurray include British Heart Foundation.
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Journal ArticleDOI
Sacubitril/Valsartan Across the Spectrum of Ejection Fraction in Heart Failure
Scott D. Solomon,Muthiah Vaduganathan,Brian Claggett,Milton Packer,Milton Packer,Michael R. Zile,Michael R. Zile,Karl Swedberg,Karl Swedberg,Jean L. Rouleau,Marc A. Pfeffer,Akshay S. Desai,Lars Lund,Lars Køber,Inder S. Anand,Nancy K. Sweitzer,Gerard C.M. Linssen,Béla Merkely,Juan Luis Arango,Dragos Vinereanu,Chen Huan Chen,Michele Senni,Antonio S. Sibulo,Sergey Boytsov,Victor Shi,Adel R. Rizkala,Martin Lefkowitz,John J.V. McMurray +27 more
TL;DR: The therapeutic effects of sacubitril/valsartan, compared with a renin-angiotensin-aldosterone–system inhibitor alone, vary by LVEF with treatment benefits, particularly for heart failure hospitalization, that appear to extend to patients with heart failure and mildly reduced ejection fraction.
Journal ArticleDOI
Effect of dapagliflozin on worsening heart failure and cardiovascular death in patients with heart failure with and without diabetes
Mark C. Petrie,Subodh Verma,Kieran F. Docherty,Silvio E. Inzucchi,Inder S. Anand,Jan Belohlavek,Michael Böhm,Chern-En Chiang,Chern-En Chiang,Vijay K. Chopra,Rudolf A. de Boer,Akshay S. Desai,Mirta Diez,Jarosław Drożdż,Andre Dukát,Junbo Ge,Jonathan G. Howlett,Tzvetana Katova,Masafumi Kitakaze,Charlotta Ljungman,Béla Merkely,Jose C. Nicolau,Eileen O'Meara,Pham Nguyen Vinh,Morten Schou,Tereshchenko Sn,Lars Køber,Mikhail Kosiborod,Anna Maria Langkilde,Felipe Martinez,Piotr Ponikowski,Marc S. Sabatine,Mikaela Sjöstrand,Scott D. Solomon,Per Johanson,Peter J. Greasley,David W. Boulton,Olof Bengtsson,Pardeep S. Jhund,John J.V. McMurray +39 more
TL;DR: In this exploratory analysis of a randomized trial of patients with HFrEF, dapagliflozin compared with placebo, when added to recommended therapy, significantly reduced the risk of worsening heart failure or cardiovascular death independently of diabetes status.
Journal ArticleDOI
Changes in Ventricular Size and Function in Patients Treated With Valsartan, Captopril, or Both After Myocardial Infarction
Scott D. Solomon,Hicham Skali,Nagesh S. Anavekar,Mikhail Bourgoun,Ståle Barvik,Jalal K. Ghali,J. Wayne Warnica,Margarita Khrakovskaya,J. Malcolm O. Arnold,Yuri Schwartz,Eric J. Velazquez,Robert M. Califf,John J.V. McMurray,Marc A. Pfeffer +13 more
TL;DR: Baseline echocardiographic measures of ejection fraction, end-diastolic volume, and infarct segment length were highly predictive of outcomes including total mortality, death or hospitalization for heart failure, or death or any cardiovascular event (heart failure, MI, stroke, resuscitated sudden death), even after adjustment for known covariates.
Journal ArticleDOI
Effects of candesartan on the development of a new diagnosis of diabetes mellitus in patients with heart failure
Salim Yusuf,Jan Östergren,Hertzel C. Gerstein,Marc A. Pfeffer,Karl Swedberg,Christopher B. Granger,Bertil Olofsson,Jeffrey L. Probstfield,John J.V. McMurray +8 more
TL;DR: The angiotensin receptor blocker candesartan appears to prevent diabetes in heart failure patients, suggesting that the renin-angiotens in axis is implicated in glucose regulation.
Journal ArticleDOI
Effects of dapagliflozin in DAPA-HF according to background heart failure therapy
Kieran F. Docherty,Pardeep S. Jhund,Silvio E. Inzucchi,Lars Køber,Mikhail Kosiborod,Felipe Martinez,Piotr Ponikowski,David L. DeMets,Marc S. Sabatine,Olof Bengtsson,Mikaela Sjöstrand,Anna Maria Langkilde,Akshay S. Desai,Mirta Diez,Jonathan G. Howlett,Tzvetana Katova,Charlotta Ljungman,Eileen O'Meara,Mark C. Petrie,Morten Schou,Subodh Verma,Pham Nguyen Vinh,Scott D. Solomon,John J.V. McMurray +23 more
TL;DR: The benefit of dapagliflozin was consistent regardless of background therapy for HF, with no significant randomized treatment-by-subgroup interaction.