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Cause of Death and Predictors of All-Cause Mortality in Anticoagulated Patients With Nonvalvular Atrial Fibrillation : Data From ROCKET AF
- Author
- Abadier R.
- Abelson M.
- Abhyankar A.
- Abram N.
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- Publication venue
- Publication date
- 01/01/2015
- Field of study
M. Kaste on työryhmän ROCKET AF Steering Comm jäsen.Background-Atrial fibrillation is associated with higher mortality. Identification of causes of death and contemporary risk factors for all-cause mortality may guide interventions. Methods and Results-In the Rivaroxaban Once Daily Oral Direct Factor Xa Inhibition Compared with Vitamin K Antagonism for Prevention of Stroke and Embolism Trial in Atrial Fibrillation (ROCKET AF) study, patients with nonvalvular atrial fibrillation were randomized to rivaroxaban or dose-adjusted warfarin. Cox proportional hazards regression with backward elimination identified factors at randomization that were independently associated with all-cause mortality in the 14 171 participants in the intention-to-treat population. The median age was 73 years, and the mean CHADS(2) score was 3.5. Over 1.9 years of median follow-up, 1214 (8.6%) patients died. Kaplan-Meier mortality rates were 4.2% at 1 year and 8.9% at 2 years. The majority of classified deaths (1081) were cardiovascular (72%), whereas only 6% were nonhemorrhagic stroke or systemic embolism. No significant difference in all-cause mortality was observed between the rivaroxaban and warfarin arms (P=0.15). Heart failure (hazard ratio 1.51, 95% CI 1.33-1.70, P= 75 years (hazard ratio 1.69, 95% CI 1.51-1.90, P Conclusions-In a large population of patients anticoagulated for nonvalvular atrial fibrillation, approximate to 7 in 10 deaths were cardiovascular, whereasPeer reviewe
Antiinflammatory Therapy with Canakinumab for Atherosclerotic Disease
- Author
- A Abbate
- A Abhyankar
- A Adams
- A Agafina
- A Akyea-Djamson
- A Alan
- A Alfieri
- A Alfrey
- A Alvarisqueta
- A Amos
- A Anadiotis
- A Anneveldt
- A Antolick
- A Arthur
- A Aslam
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- Zineldine A.
- Zirlik A
- Zucchetti C
- Publication venue
- 'Massachusetts Medical Society'
- Publication date
- 01/01/2017
- Field of study
Background: Experimental and clinical data suggest that reducing inflammation without affecting lipid levels may reduce the risk of cardiovascular disease. Yet, the inflammatory hypothesis of atherothrombosis has remained unproved. Methods: We conducted a randomized, double-blind trial of canakinumab, a therapeutic monoclonal antibody targeting interleukin-1β, involving 10,061 patients with previous myocardial infarction and a high-sensitivity C-reactive protein level of 2 mg or more per liter. The trial compared three doses of canakinumab (50 mg, 150 mg, and 300 mg, administered subcutaneously every 3 months) with placebo. The primary efficacy end point was nonfatal myocardial infarction, nonfatal stroke, or cardiovascular death. RESULTS: At 48 months, the median reduction from baseline in the high-sensitivity C-reactive protein level was 26 percentage points greater in the group that received the 50-mg dose of canakinumab, 37 percentage points greater in the 150-mg group, and 41 percentage points greater in the 300-mg group than in the placebo group. Canakinumab did not reduce lipid levels from baseline. At a median follow-up of 3.7 years, the incidence rate for the primary end point was 4.50 events per 100 person-years in the placebo group, 4.11 events per 100 person-years in the 50-mg group, 3.86 events per 100 person-years in the 150-mg group, and 3.90 events per 100 person-years in the 300-mg group. The hazard ratios as compared with placebo were as follows: in the 50-mg group, 0.93 (95% confidence interval [CI], 0.80 to 1.07; P = 0.30); in the 150-mg group, 0.85 (95% CI, 0.74 to 0.98; P = 0.021); and in the 300-mg group, 0.86 (95% CI, 0.75 to 0.99; P = 0.031). The 150-mg dose, but not the other doses, met the prespecified multiplicity-adjusted threshold for statistical significance for the primary end point and the secondary end point that additionally included hospitalization for unstable angina that led to urgent revascularization (hazard ratio vs. placebo, 0.83; 95% CI, 0.73 to 0.95; P = 0.005). Canakinumab was associated with a higher incidence of fatal infection than was placebo. There was no significant difference in all-cause mortality (hazard ratio for all canakinumab doses vs. placebo, 0.94; 95% CI, 0.83 to 1.06; P = 0.31). Conclusions: Antiinflammatory therapy targeting the interleukin-1β innate immunity pathway with canakinumab at a dose of 150 mg every 3 months led to a significantly lower rate of recurrent cardiovascular events than placebo, independent of lipid-level lowering. (Funded by Novartis; CANTOS ClinicalTrials.gov number, NCT01327846.
Omecamtiv mecarbil in chronic heart failure with reduced ejection fraction, GALACTIC‐HF: baseline characteristics and comparison with contemporary clinical trials
- Author
- Aaronson Keith
- Abadier Rafik
- Abbasi Siddique A.
- Abdullah Shuaib
- Abelson Mark
- Abhayaratna Walter
- Ablasser Klemens
- Aboyans Victor
- Abo‐Auda Wael
- Abuannadi Mohammad
- Adams Kirkwood
- Adams Kirkwood F.
- Adhya Shaumik
- Adler Alexander
- Aggarwala Gaurav
- Agostoni Piergiuseppe
- Ahmad Saad
- Aiub Jorge Roberto
- Al Mohammad Abdallah
- Alharethi Rami
- Alieksieieva Liudmyla
- Almeida Filipa
- Almousalli Omar
- Amano Tetsuya
- Amanullah Aman
- Ambardekar Amrut
- Amerena John
- Anand Inder
- Anderson William
- Ando Kenji
- Andreka Peter
- Antalik Lubomir
- Aradi Daniel
- Araiza Raul Reyes
- Arbolishvili Georgy
- Ariani Mehrdad
- Arias‐Mendoza Alexandra
- Arora Raveen
- Arroyo Julian Alonso Coronel
- Artis Andre
- Asakura Masanori
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- Terasawa Akihiro
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- Timofeev Alexander
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- Tocchetti Carlo Gabriele
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- Tomcsanyi Janos
- Toth Kalman
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- Trebacz Jaroslaw
- Trevelyan Jasper
- Triana Miguel Urina
- Trichon Benjamin
- Trochu Jean Noel
- Tsabedze Nqoba
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- Ueno Hideki
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- Usui Makoto
- Utsu Noriaki
- Vaccari Christopher
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- Van Zyl Louis
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- Vandekerckhove Hans
- Vanhecke Thomas
- Varin Claire
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- Vasilev Ivaylo
- Vasilyeva Larysa
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- Vazquez Eduardo Salcido
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- Venegas Manuel Eduardo Rodriguez
- Videbaek Lars
- Vidotti Maria Helena
- Vijay Nampalli
- Vilamajo Oscar Alberto Gomez
- Vilchez Francisco Gonzalez
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- Villoch Mario
- Villota Julio Eduardo Nuñez
- Vinanska Daniela
- Vincenzi Antonella
- Vinereanu Dragos
- Vinereanu Dragos
- Vishnevsky Alexander
- Voevoda Mikhail
- Vogel Daniel
- Voicu Olga‐Cristina
- Volterrani Maurizio
- Voors Adriaan
- Voors Adriaan A.
- Voronkov Leonid
- Vraa Soren
- Wada Atsuyuki
- Wahid Faisal
- Wal Ruud
- Wang Yi
- Wang Zhifang
- Watanabe Naoki
- Wei Yu
- Weir Robin
- Westenfeld Ralf
- Wheeler Matthew
- Whellan David
- Wiggers Henrik
- Wilkett Matt
- Willems Frank
- Williams Celeste
- Wlodarczyk Aleksander
- Wodlin Peter
- Wong Kenneth
- Wozakowska‐Kaplon Beata
- Wu Weiheng
- Yagensky Andriy
- Yamamoto Mitsutaka
- Yan Jing
- Yang Ping
- Yang Xuming
- Yang Zhenyu
- Yeoman Gary
- Yigit Zerrin
- Yilmaz Mehmet B.
- Yoshida Takeshi
- Yoshikawa Masaki
- Yousuf Kabir
- Yuan Zuyi
- Yuge Masaru
- Zabowka Maciej
- Zaca Valerio
- Zaidman Cesar
- Zanetti Fernando Tomas Lanas
- Zannad Faiez
- Zapata Gerardo
- Zdrenghea Dumitru
- Zeman Kamil
- Zeymer Uwe
- Zhang Jinguo
- Zhang Lily
- Zhang Shouyan
- Zhang Xuelian
- Zhang Yuhui
- Zhang Yuqing
- Zheng Yang
- Zheng Zhe
- Zhou Changyong
- Zieroth Shelley
- Zilahi Zsolt
- Zimmet Hendrik
- Zolty Ronald
- Zrazhevskiy Konstantin
- Zwaan Coenraad
- Publication venue
- 'Wiley'
- Publication date
- 01/11/2020
- Field of study
Aims:
The safety and efficacy of the novel selective cardiac myosin activator, omecamtiv mecarbil, in patients with heart failure with reduced ejection fraction (HFrEF) is tested in the Global Approach to Lowering Adverse Cardiac outcomes Through Improving Contractility in Heart Failure (GALACTIC‐HF) trial. Here we describe the baseline characteristics of participants in GALACTIC‐HF and how these compare with other contemporary trials.
Methods and Results:
Adults with established HFrEF, New York Heart Association functional class (NYHA) ≥ II, EF ≤35%, elevated natriuretic peptides and either current hospitalization for HF or history of hospitalization/ emergency department visit for HF within a year were randomized to either placebo or omecamtiv mecarbil (pharmacokinetic‐guided dosing: 25, 37.5 or 50 mg bid). 8256 patients [male (79%), non‐white (22%), mean age 65 years] were enrolled with a mean EF 27%, ischemic etiology in 54%, NYHA II 53% and III/IV 47%, and median NT‐proBNP 1971 pg/mL. HF therapies at baseline were among the most effectively employed in contemporary HF trials. GALACTIC‐HF randomized patients representative of recent HF registries and trials with substantial numbers of patients also having characteristics understudied in previous trials including more from North America (n = 1386), enrolled as inpatients (n = 2084), systolic blood pressure < 100 mmHg (n = 1127), estimated glomerular filtration rate < 30 mL/min/1.73 m2 (n = 528), and treated with sacubitril‐valsartan at baseline (n = 1594).
Conclusions:
GALACTIC‐HF enrolled a well‐treated, high‐risk population from both inpatient and outpatient settings, which will provide a definitive evaluation of the efficacy and safety of this novel therapy, as well as informing its potential future implementation
Angiotensin receptor neprilysin inhibition compared with enalapril on the risk of clinical progression in surviving patients with heart failure.
- Author
- Abhyankar A
- Accini J
- Adamson P
- Adelberger V
- Agarwal D K
- Ageev F
- Aggarwal R
- Aguilera M
- Ahlström P
- Ahmad W
- Ahmed F
- Akimov A
- Akinboboye O
- Aktoz M
- Akyea-Djamson A
- Al-Zoebi A
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- Zilahi Z
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- Publication venue
- 'Ovid Technologies (Wolters Kluwer Health)'
- Publication date
- 06/01/2015
- Field of study
Cause of death and predictors of all-cause mortality in anticoagulated patients with nonvalvular atrial fibrillation: Data from ROCKET AF
- Author
- Abadier R.
- Abelson M.
- Abhyankar A.
- Abram N.
- Achimastos A.
- Agacdiken Agir A.
- Agah R.
- Agamasu J.
- Aganauskiene J.
- Ageno W.
- Agnelli G.
- Aguirre A.
- Ahuad Guerrero A.
- Aidietiene S.
- Aiub J.
- Akyea-Djamson A.
- Al-Saghir Y.
- Al-Zoebi A.
- Albina G.
- Albirini A.
- Alcocer Gamba M.
- Alekseeva N.
- Alessi S.
- Alexeeva O.
- Alfieri A.
- Almaguer E.
- Almquist A.
- Altunkeser B.
- Alvarado O.
- Alvarez Garcia P.
- Alvarez Lopez H.
- Alvariqueta A.
- Alzaghrini G.
- Amaram S.
- Amerena J.
- Amosova K.
- Amuchastegui M.
- Anderson C.
- Anderson J.
- Andrews R.
- Angelova I.
- Antonios N.
- Antonishen M.
- Anusauskiene J.
- Archibald J.
- Arkhipov M.
- Aron G.
- Aroney G.
- Arouni A.
- Artis A.
- Arzola F.
- Ashchi M.
- Ata N.
- Avezum A.
- Awan N.
- Ayala-Paredes F.
- Bacon J.
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- Wallen T.
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- Publication venue
- 'Ovid Technologies (Wolters Kluwer Health)'
- Publication date
- 01/01/2015
- Field of study
Background-Atrial fibrillation is associated with higher mortality. Identification of causes of death and contemporary risk factors for all-cause mortality may guide interventions. Methods and Results-In the Rivaroxaban Once Daily Oral Direct Factor Xa Inhibition Compared with Vitamin K Antagonism for Prevention of Stroke and Embolism Trial in Atrial Fibrillation (ROCKET AF) study, patients with nonvalvular atrial fibrillation were randomized to rivaroxaban or dose-adjusted warfarin. Cox proportional hazards regression with backward elimination identified factors at randomization that were independently associated with all-cause mortality in the 14 171 participants in the intentionto- treat population. The median age was 73 years, and the mean CHADS2 score was 3.5. Over 1.9 years of median follow-up, 1214 (8.6%) patients died. Kaplan-Meier mortality rates were 4.2% at 1 year and 8.9% at 2 years. The majority of classified deaths (1081) were cardiovascular (72%), whereas only 6% were nonhemorrhagic stroke or systemic embolism. No significant difference in all-cause mortality was observed between the rivaroxaban and warfarin arms (P=0.15). Heart failure (hazard ratio 1.51, 95% CI 1.33-1.70, P<0.0001) and age 6575 years (hazard ratio 1.69, 95% CI 1.51-1.90, P<0.0001) were associated with higher all-cause mortality. Multiple additional characteristics were independently associated with higher mortality, with decreasing creatinine clearance, chronic obstructive pulmonary disease, male sex, peripheral vascular disease, and diabetes being among the most strongly associated (model C-index 0.677). Conclusions-In a large population of patients anticoagulated for nonvalvular atrial fibrillation, 487 in 10 deaths were cardiovascular, whereas <1 in 10 deaths were caused by nonhemorrhagic stroke or systemic embolism. Optimal prevention and treatment of heart failure, renal impairment, chronic obstructive pulmonary disease, and diabetes may improve survival
Evolocumab and clinical outcomes in patients with cardiovascular disease
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- Aboufakher R.
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- Publication date
- 01/01/2017
- Field of study
peer reviewedBACKGROUND Evolocumab is a monoclonal antibody that inhibits proprotein convertase subtilisin-kexin type 9 (PCSK9) and lowers low-density lipoprotein (LDL) cholesterol levels by approximately 60%. Whether it prevents cardiovascular events is uncertain. METHODS We conducted a randomized, double-blind, placebo-controlled trial involving 27,564 patients with atherosclerotic cardiovascular disease and LDL cholesterol levels of 70 mg per deciliter (1.8 mmol per liter) or higher who were receiving statin therapy. Patients were randomly assigned to receive evolocumab (either 140 mg every 2 weeks or 420 mg monthly) or matching placebo as subcutaneous injections. The primary efficacy end point was the composite of cardiovascular death, myocardial infarction, stroke, hospitalization for unstable angina, or coronary revascularization. The key secondary efficacy end point was the composite of cardiovascular death, myocardial infarction, or stroke. The median duration of follow-up was 2.2 years. RESULTS At 48 weeks, the least-squares mean percentage reduction in LDL cholesterol levels with evolocumab, as compared with placebo, was 59%, from a median baseline value of 92 mg per deciliter (2.4 mmol per liter) to 30 mg per deciliter (0.78 mmol per liter) (P<0.001). Relative to placebo, evolocumab treatment significantly reduced the risk of the primary end point (1344 patients [9.8%] vs. 1563 patients [11.3%]; hazard ratio, 0.85; 95% confidence interval [CI], 0.79 to 0.92; P<0.001) and the key secondary end point (816 [5.9%] vs. 1013 [7.4%]; hazard ratio, 0.80; 95% CI, 0.73 to 0.88; P<0.001). The results were consistent across key subgroups, including the subgroup of patients in the lowest quartile for baseline LDL cholesterol levels (median, 74 mg per deciliter [1.9 mmol per liter]). There was no significant difference between the study groups with regard to adverse events (including new-onset diabetes and neurocognitive events), with the exception of injection-site reactions, which were more common with evolocumab (2.1% vs. 1.6%). CONCLUSIONS In our trial, inhibition of PCSK9 with evolocumab on a background of statin therapy lowered LDL cholesterol levels to a median of 30 mg per deciliter (0.78 mmol per liter) and reduced the risk of cardiovascular events. These findings show that patients with atherosclerotic cardiovascular disease benefit from lowering of LDL cholesterol levels below current targets. © 2017 Massachusetts Medical Society
Apixaban versus warfarin in patients with atrial fibrillation
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- Sherri Hinton
- Shinya Goto
- Steen Husted
- Stefan H Hohnloser
- Stuart Pocock
- Sumeet Subherwal
- Sunil Nepal
- Susan Mullin
- T Akihiko
- T Andersson
- T Ayres
- T Czerski
- T H Rho
- T Hayek
- T Hisaoka
- T Hoch
- T Horacek
- T Hruczkowski
- T Hu
- T Iwao
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- T Sasaki
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- T Yamada
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- Tony Dremsizov
- U Thadani
- Uri Flato
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- V Netiazhenko
- V Nguyen
- V Oleynikov
- V Orlov
- V P Harjola
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- V Srikanthan
- V Sulimov
- V Tashchuk
- V Terekhov
- V Tseluyko
- V Vizir
- V Volkov
- V Yakusevich
- V Zadionchenko
- Veli Pekka Harjola
- Verheugt F. W. A.
- W Bowden
- W Cabrera
- W Haught
- W Haverkamp
- W Heddle
- W Henry 3rd
- W Herzog
- W Jaffrani
- W Kufs
- W Li
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- W Piotrowski
- W Ridsdill Smith
- W Rieker
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- W Smith
- W Tracz
- W Wilson
- W Zonggui
- Wallentin L. Collaborators ARISTOTLE Committees and Investigators: Christopher B Granger
- Witold Ruzyllo
- X Albert
- X Chen
- X Jiang
- X Wang
- X Yang
- Y Atsushi
- Y Burmak
- Y Chandrashekhar
- Y Chen
- Y Cohen
- Y Higashi
- Y K Chan
- Y K Wong
- Y Karpov
- Y Kawase
- Y Kobayashi
- Y Koretsune
- Y Mostovoy
- Y N Kim
- Y Nakamura
- Y Pozdnyakov
- Y Sato
- Y Shubik
- Y Tsubokou
- Y Turgeman
- Y Yin
- Y Zhang
- Z Kiedrowicz
- Z László
- Z Meneghelo
- Z Q Li
- Z Sizova
- Z Telyatnikova
- Z Yousef
- Z Yousef
- Z Yusof
- Zhu J.
- Zubin Eapen
- Á Illés
- Publication venue
- 'Massachusetts Medical Society'
- Publication date
- 01/01/2011
- Field of study
BACKGROUND: Vitamin K antagonists are highly effective in preventing stroke in patients with atrial fibrillation but have several limitations. Apixaban is a novel oral direct factor Xa inhibitor that has been shown to reduce the risk of stroke in a similar population in comparison with aspirin. METHODS: In this randomized, double-blind trial, we compared apixaban (at a dose of 5 mg twice daily) with warfarin (target international normalized ratio, 2.0 to 3.0) in 18,201 patients with atrial fibrillation and at least one additional risk factor for stroke. The primary outcome was ischemic or hemorrhagic stroke or systemic embolism. The trial was designed to test for noninferiority, with key secondary objectives of testing for superiority with respect to the primary outcome and to the rates of major bleeding and death from any cause. RESULTS: The median duration of follow-up was 1.8 years. The rate of the primary outcome was 1.27% per year in the apixaban group, as compared with 1.60% per year in the warfarin group (hazard ratio with apixaban, 0.79; 95% confidence interval [CI], 0.66 to 0.95; P<0.001 for noninferiority; P = 0.01 for superiority). The rate of major bleeding was 2.13% per year in the apixaban group, as compared with 3.09% per year in the warfarin group (hazard ratio, 0.69; 95% CI, 0.60 to 0.80; P<0.001), and the rates of death from any cause were 3.52% and 3.94%, respectively (hazard ratio, 0.89; 95% CI, 0.80 to 0.99; P = 0.047). The rate of hemorrhagic stroke was 0.24% per year in the apixaban group, as compared with 0.47% per year in the warfarin group (hazard ratio, 0.51; 95% CI, 0.35 to 0.75; P<0.001), and the rate of ischemic or uncertain type of stroke was 0.97% per year in the apixaban group and 1.05% per year in the warfarin group (hazard ratio, 0.92; 95% CI, 0.74 to 1.13; P = 0.42). CONCLUSIONS: In patients with atrial fibrillation, apixaban was superior to warfarin in preventing stroke or systemic embolism, caused less bleeding, and resulted in lower mortality. Copyright © 2011 Massachusetts Medical Society. All rights reserved
Apixaban compared with warfarin in patients with atrial fibrillation and previous stroke or transient ischaemic attack: A subgroup analysis of the ARISTOTLE trial
- Author
- A Agarwal
- A Ahsan
- A Ajala
- A Al-Mudamgha
- A Alexander
- A Alfieri
- A Alings
- A Alwail
- A Bakhai
- A Barsotti
- A Bartkowiak
- A Bauer
- A Bazylevych
- A Bazzi
- A Bethencourt González
- A Bharani
- A Bittersohl
- A Boruczkowska-Kaszkowiak
- A Boyle
- A Bragina
- A Bredero
- A Brockmyre
- A Budaj
- A Buxton
- A Caccavo
- A Cassettari
- A Chhabra
- A Chmielinski
- A Cohen
- A Cooke
- A Cziraki
- A D'Angelo
- A De Paola
- A Dharmadhikari
- A Dowell
- A Francis
- A Gabito
- A Galicia
- A Ghirarduzzi
- A Golovach
- A Gordienko
- A Govorin
- A Hamad
- A Hershson
- A Hetzel
- A Hrabar
- A Ivleva
- A Jacob
- A Jones
- A Kabour
- A Kastanayan
- A Katona
- A Kelly
- A Koniakhin
- A Kovács
- A Lebowitz
- A Levin
- A Liu
- A Lorga Filho
- A Lowy
- A MacKinnon
- A Magnano
- A Marmor
- A Matsushima
- A Meholick
- A Mirode
- A Mohácsi
- A Moriarty
- A Muniz
- A Mügge
- A Mügge
- A Naik
- A Nambiar
- A Obrezan
- A Ocicka-Kozakiewicz
- A Pandey
- A Papp
- A Parkhomenko
- A Patel
- A Peeters
- A Pálinkás
- A Quick
- A Rabelo Alves Jr
- A Reyes
- A Rodriguez
- A Roman
- A Rubin
- A Salacata
- A Salajan
- A Samal
- A Sanchez
- A Schaap
- A Sinopalnikov
- A Skolnick
- A Solomon
- A Svistov
- A Ugarriza
- A Utech
- A Vértes
- A Wade
- A Warner
- A Weiss
- A Wellford
- A Yagensky
- Aldo Maggione
- Alexander J. H.
- Alexander Parkhomenko
- Ali Zomorodi
- Alings M.
- Alvaro Albrecht
- Alvaro Avezum
- Andreas Terent
- Anna Stenborg
- Antonio Carlos Lopes
- Antonio G Hermosillo
- Antonio M W Alings
- Axel Akerblom
- B Bachhuber
- B Beanblossom
- B Blue
- B Bruneel
- B Bryhni
- B Coutu
- B Garbelini Jr
- B Gervais
- B Gorenek
- B Griewing
- B H Oh
- B Hattler
- B Iteld
- B Jackson
- B Kowalski
- B Lachterman
- B Lasko
- B Lewis
- B Malipeddi
- B McClements
- B Peart
- B Pieske
- B Platt
- B Podogrodzka
- B Ramagiri
- B Ramjattan
- B Schifferdecker
- B Sidorenko
- B Srinivasasastry
- B Stockins
- B Winkelmann
- B Wollaert
- B Yu
- B Øie
- Bahit M. C.
- Basil S Lewis
- Bernard J Gersh
- Bradley Kolls
- Byung-Hee Oh
- C Arean Martinez
- C Arsenescu Georgescu
- C Beneitez
- C Bredlau
- C Calvo Vargas
- C Chavez
- C Christersson
- C Corder
- C Cuneo
- C D Tseng
- C Dézsi
- C East
- C Erol
- C Fortin
- C G Fierbinteanu-Braticevici
- C Gonzalez Juanatey
- C Hassel
- C Höglund
- C J Lindholm
- C JerJes-Sanchez
- C Kaoru Indio do Brasil
- C Levin
- C Lovell
- C Massey
- C McPherson
- C Mihaela Tanaseanu
- C Muratore
- C Olivieri
- C Pincetti
- C Pop
- C Powers
- C Poy
- C Raffo
- C Riojas
- C Rios Vasquez
- C Rodriguez-Fierro
- C Russo
- C Sofley
- C Sotolongo
- C Toftager Larsen
- C Torp-Pedersen
- C Tuxen
- C Van der Zwaan
- C W Lee
- C Weimar
- C Y Rhim
- C Yu
- C Zaidman
- Carlo Lombardi
- Cetin Erol
- Cheryl Bushnell
- Christoph Varenhorst
- Claes Held
- D Agarwal
- D Albuquerque
- D Ashby
- D Belenky
- D Borts
- D Brieger
- D Chiu
- D Clark
- D Colan
- D Cross
- D De Jong
- D Dohan
- D Donovan
- D Duplyakov
- D Dutka
- D El Allaf
- D Fell
- D Fischer
- D G Shin
- D Gaita
- D Garcia
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- D Gottlieb
- D Gupta
- D Hassman
- D Humiston
- D Isaza
- D J Choi
- D Jiang
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- D Lok
- D Mercado
- D Mishkel
- D Morales
- D Moreira
- D Murdoch
- D O'Keefe
- D Perloff
- D Piskorz
- D Precoma
- D Rhodes
- D Riff
- D Rupka
- D Santos
- D Spence
- D Stapleton
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- D Vinereanu
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- Dan Atar
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- David Garcia
- Denis Xavier
- Diener H. -C. ARISTOTLE Committees and Investigators: Christopher B Granger
- Dipen Parikh
- Dragos Vinereanu
- E Ball
- E Blumberg
- E Carasca
- E Engeron
- E Flores
- E Galve
- E Gomez
- E Hasbani
- E Haskel
- E Julian Chuquiure-Valenzuela
- E Klainman
- E Kosinski
- E Lopez Rosas
- E Manenti
- E Mazur
- E Morales-Palomares
- E Mouhayar
- E Panchenko
- E Pelloso
- E Privalova
- E Ramos
- E Retyk
- E Richiardi
- E Rivera
- E Sabbah
- E Schwarz
- E Sivkova
- E Suprun.
- E van Nieuwenhuizen
- E von Hodenberg
- E Zemtsovsky
- E Zidkova
- Easton J. D.
- Elaine M Hylek
- Elaine M Hylek
- Emil Hagstrom
- Erik Lundstrom
- F Agnone
- F Al-Khalili
- F Al-Khalili
- F Albrecht
- F Bai
- F Collado
- F Collado
- F De Leon
- F de Looze
- F de Looze
- F de Looze
- F de Looze
- F Dunn
- F Grondin
- F Kouichi
- F Lakatos
- F Maislos
- F Medina
- F Olías de la Cruz
- F Provenier
- F Rolandi
- F Schlachetzki
- F St Maurice
- F Stockenhuber
- F Stögbauer
- F Verheugt
- F Villaça Guimaraes Filho
- F Zhang
- Fernando Lanas
- Freek W A Verheugt
- G Andrei Dan
- G Arutyunov
- G Aycock
- G Boxho
- G Brooks
- G Bustamante
- G Casolo
- G Dzyak
- G Feldman
- G Filonenko
- G Ford
- G Gojanur
- G Hanovich
- G Ignatenko
- G Jensen
- G Kahrmann
- G Kamalov
- G Kania
- G Lavabre
- G Lip
- G Lu
- G Lupkovics
- G Lysenko
- G Mairesse
- G McInnes
- G Noble
- G Oliveira
- G Popik
- G Rasmanis
- G Reis
- G Rogelio
- G Sabe-Affaki
- G Sosa-Suarez
- G Stenzel
- G Syan
- George Wyse
- Goto S.
- Granger C. B.
- Greg Flaker
- Greg Stashenko
- H B Gowdappa
- H Colombo
- H F Vöhringer
- H Hamer
- H Ikeda
- H Jure
- H Kadr
- H Karunaratne
- H Kihara
- H Kultursay
- H Lastiri
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- H Li
- H Luciardi
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- H Parikka
- H Po
- H Poppert
- H Punatar
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- H Reis
- H Salem
- H Striekwold
- H Takagi
- H Tan
- H Weich
- H Yoshii
- Hanna M.
- Hans-Christoph Diener
- Helio Guimaraes
- I Aisiku
- I Benedek
- I Bereznyakov
- I Chernichka
- I Chopey
- I Findlay
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- W Piotrowski
- W Ridsdill Smith
- W Rieker
- W Ruzyllo
- W Smith
- W Tracz
- W Wilson
- W Zonggui
- Wallentin L.
- Witold Ruzyllo
- Wojdyla D. M.
- X Albert
- X Chen
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- X Wang
- X Yang
- Y Atsushi
- Y Burmak
- Y Chandrashekhar
- Y Chen
- Y Cohen
- Y Higashi
- Y K Chan
- Y K Wong
- Y Karpov
- Y Kawase
- Y Kobayashi
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- Y Mostovoy
- Y N Kim
- Y Nakamura
- Y Pozdnyakov
- Y Sato
- Y Shubik
- Y Tsubokou
- Y Turgeman
- Y Yin
- Y Zhang
- Z Kiedrowicz
- Z László
- Z Meneghelo
- Z Q Li
- Z Sizova
- Z Telyatnikova
- Z Yousef
- Z Yousef
- Z Yusof
- Zubin Eapen
- Á Illés
- Publication venue
- 'Elsevier BV'
- Publication date
- 01/01/2012
- Field of study
Background: In the ARISTOTLE trial, the rate of stroke or systemic embolism was reduced by apixaban compared with warfarin in patients with atrial fibrillation (AF). Patients with AF and previous stroke or transient ischaemic attack (TIA) have a high risk of stroke. We therefore aimed to assess the efficacy and safety of apixaban compared with warfarin in prespecified subgroups of patients with and without previous stroke or TIA. Methods: Between Dec 19, 2006, and April 2, 2010, patients were enrolled in the ARISTOTLE trial at 1034 clinical sites in 39 countries. 18 201 patients with AF or atrial flutter were randomly assigned to receive apixaban 5 mg twice daily or warfarin (target international normalised ratio 2·0-3·0). The median duration of follow-up was 1·8 years (IQR 1·4-2·3). The primary efficacy outcome was stroke or systemic embolism, analysed by intention to treat. The primary safety outcome was major bleeding in the on-treatment population. All participants, investigators, and sponsors were masked to treatment assignments. In this subgroup analysis, we estimated event rates and used Cox models to compare outcomes in patients with and without previous stroke or TIA. The ARISTOTLE trial is registered with ClinicalTrials.gov, number NTC00412984. Findings: Of the trial population, 3436 (19%) had a previous stroke or TIA. In the subgroup of patients with previous stroke or TIA, the rate of stroke or systemic embolism was 2·46 per 100 patient-years of follow-up in the apixaban group and 3·24 in the warfarin group (hazard ratio [HR] 0·76, 95% CI 0·56 to 1·03); in the subgroup of patients without previous stroke or TIA, the rate of stroke or systemic embolism was 1·01 per 100 patient-years of follow-up with apixaban and 1·23 with warfarin (HR 0·82, 95% CI 0·65 to 1·03; p for interaction=0·71). The absolute reduction in the rate of stroke and systemic embolism with apixaban versus warfarin was 0·77 per 100 patient-years of follow-up (95% CI -0·08 to 1·63) in patients with and 0·22 (-0·03 to 0·47) in those without previous stroke or TIA. The difference in major bleeding with apixaban compared with warfarin was 1·07 per 100 patient-years (95% CI 0·09-2·04) in patients with and 0·93 (0·54-1·32) in those without previous stroke or TIA. Interpretation: The effects of apixaban versus warfarin were consistent in patients with AF with and without previous stroke or TIA. Owing to the higher risk of these outcomes in patients with previous stroke or TIA, the absolute benefits of apixaban might be greater in this population. Funding: Bristol-Myers Squibb and Pfizer. © 2012 Elsevier Ltd
Evolocumab and clinical outcomes in patients with cardiovascular disease
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- Aboufakher R
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- Accini Mendoza Jl
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- Publication venue
- 'Massachusetts Medical Society'
- Publication date
- 01/01/2017
- Field of study
BACKGROUND Evolocumab is a monoclonal antibody that inhibits proprotein convertase subtilisin-kexin type 9 (PCSK9) and lowers low-density lipoprotein (LDL) cholesterol levels by approximately 60%. Whether it prevents cardiovascular events is uncertain. METHODS We conducted a randomized, double-blind, placebo-controlled trial involving 27,564 patients with atherosclerotic cardiovascular disease and LDL cholesterol levels of 70 mg per deciliter (1.8 mmol per liter) or higher who were receiving statin therapy. Patients were randomly assigned to receive evolocumab (either 140 mg every 2 weeks or 420 mg monthly) or matching placebo as subcutaneous injections. The primary efficacy end point was the composite of cardiovascular death, myocardial infarction, stroke, hospitalization for unstable angina, or coronary revascularization. The key secondary efficacy end point was the composite of cardiovascular death, myocardial infarction, or stroke. The median duration of follow-up was 2.2 years. RESULTS At 48 weeks, the least-squares mean percentage reduction in LDL cholesterol levels with evolocumab, as compared with placebo, was 59%, from a median baseline value of 92 mg per deciliter (2.4 mmol per liter) to 30 mg per deciliter (0.78 mmol per liter) (P<0.001). Relative to placebo, evolocumab treatment significantly reduced the risk of the primary end point (1344 patients [9.8%] vs. 1563 patients [11.3%]; hazard ratio, 0.85; 95% confidence interval [CI], 0.79 to 0.92; P<0.001) and the key secondary end point (816 [5.9%] vs. 1013 [7.4%]; hazard ratio, 0.80; 95% CI, 0.73 to 0.88; P<0.001). The results were consistent across key subgroups, including the subgroup of patients in the lowest quartile for baseline LDL cholesterol levels (median, 74 mg per deciliter [1.9 mmol per liter]). There was no significant difference between the study groups with regard to adverse events (including new-onset diabetes and neurocognitive events), with the exception of injection-site reactions, which were more common with evolocumab (2.1% vs. 1.6%). CONCLUSIONS In our trial, inhibition of PCSK9 with evolocumab on a background of statin therapy lowered LDL cholesterol levels to a median of 30 mg per deciliter (0.78 mmol per liter) and reduced the risk of cardiovascular events. These findings show that patients with atherosclerotic cardiovascular disease benefit from lowering of LDL cholesterol levels below current targets
Edoxaban versus warfarin in patients with atrial fibrillation
- Author
- Abdullakutty J
- Abi-Mansour P
- Abril SB
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- Zajac E
- Zakhary B
- Zamlynskyy M
- Zamorano JL
- Zanotti A
- Zanwar I
- Zapanta M
- Zarandon RS
- Zarebinski M
- Zareczky P
- Zarpentin C
- Zateyshchikov D
- Zateyshchikova A
- Zeig S
- Zellner C
- Zeltser D
- Zenin S
- Zhang HQ
- Zhang P
- Zhang X
- Zhang YL
- Zhang Z
- Zhao RP
- Zhao XL
- Zharinov O
- Zheng X
- Zheng Y
- Zheng ZQ
- Zhou SX
- Zhukova N
- Zhurba S
- Zidkova E
- Zidkova E
- Ziegler K
- Zielinski M
- Zienciuk-Krajka A
- Zimmermann EB
- Zimmermann S
- Zoghi M
- Zoghi M
- Zondag M
- Zotova I
- Zubeeva G
- Zyatenkova E
- Åkerberg A
- Östberg S
- Ŝpinar J
- Publication venue
- 'Massachusetts Medical Society'
- Publication date
- 01/01/2013
- Field of study
Contains fulltext :
125374.pdf (publisher's version ) (Open Access)BACKGROUND: Edoxaban is a direct oral factor Xa inhibitor with proven antithrombotic effects. The long-term efficacy and safety of edoxaban as compared with warfarin in patients with atrial fibrillation is not known. METHODS: We conducted a randomized, double-blind, double-dummy trial comparing two once-daily regimens of edoxaban with warfarin in 21,105 patients with moderate-to-high-risk atrial fibrillation (median follow-up, 2.8 years). The primary efficacy end point was stroke or systemic embolism. Each edoxaban regimen was tested for noninferiority to warfarin during the treatment period. The principal safety end point was major bleeding. RESULTS: The annualized rate of the primary end point during treatment was 1.50% with warfarin (median time in the therapeutic range, 68.4%), as compared with 1.18% with high-dose edoxaban (hazard ratio, 0.79; 97.5% confidence interval [CI], 0.63 to 0.99; P<0.001 for noninferiority) and 1.61% with low-dose edoxaban (hazard ratio, 1.07; 97.5% CI, 0.87 to 1.31; P=0.005 for noninferiority). In the intention-to-treat analysis, there was a trend favoring high-dose edoxaban versus warfarin (hazard ratio, 0.87; 97.5% CI, 0.73 to 1.04; P=0.08) and an unfavorable trend with low-dose edoxaban versus warfarin (hazard ratio, 1.13; 97.5% CI, 0.96 to 1.34; P=0.10). The annualized rate of major bleeding was 3.43% with warfarin versus 2.75% with high-dose edoxaban (hazard ratio, 0.80; 95% CI, 0.71 to 0.91; P<0.001) and 1.61% with low-dose edoxaban (hazard ratio, 0.47; 95% CI, 0.41 to 0.55; P<0.001). The corresponding annualized rates of death from cardiovascular causes were 3.17% versus 2.74% (hazard ratio, 0.86; 95% CI, 0.77 to 0.97; P=0.01), and 2.71% (hazard ratio, 0.85; 95% CI, 0.76 to 0.96; P=0.008), and the corresponding rates of the key secondary end point (a composite of stroke, systemic embolism, or death from cardiovascular causes) were 4.43% versus 3.85% (hazard ratio, 0.87; 95% CI, 0.78 to 0.96; P=0.005), and 4.23% (hazard ratio, 0.95; 95% CI, 0.86 to 1.05; P=0.32). CONCLUSIONS: Both once-daily regimens of edoxaban were noninferior to warfarin with respect to the prevention of stroke or systemic embolism and were associated with significantly lower rates of bleeding and death from cardiovascular causes. (Funded by Daiichi Sankyo Pharma Development; ENGAGE AF-TIMI 48 ClinicalTrials.gov number, NCT00781391.)