4 research outputs found
Apixaban versus Enoxaparin for Thromboprophylaxis in Medically Ill Patients
- Author
- Abdool Gaffar M
- Abola T
- Abrahamovych O
- Abrosimov V
- Achkar A
- Ahuad Guerrero R
- Akkal Z
- Alabi F
- Alarcon MA
- Alcocer M
- Aleksandrov O
- Alvarez Sala L
- Alves M
- Andreev D
- Ansell J
- Ardolic B
- Baek S
- Ballard M
- Ballek L
- Baratta S
- Bareford D
- Barney J
- Basson M
- Bates J
- Batushkin V
- Bauersachs R
- Becker F
- Becker F
- Belenkov Y
- Bello F
- Beyer J
- Bhadade R
- Bharani A
- Bisbal Malig C
- Blacher C
- Boldueva S
- Borris LC
- Botnick W
- Boulet H
- Boyarkin M
- Brachmann J
- Brossoit R
- Campos E
- Capitán F
- Cepeda J
- Ceresetto J
- Ceresetto JM
- Ceska R
- Chen D
- Cheng G
- Chernichka I
- Chlumsky J
- Chlumsky J
- Choi D
- Chopey I
- Chung H
- Cohen A
- Collado F
- Conrad S
- Conri C
- Constantino M
- Cools F
- Cools F
- Coppere B
- Cotrina R
- Coughlin P
- Cunha C
- D'Souza G
- Dabbagh O
- Das S
- de Sagastizabal D
- Denesyuk V
- Dhar A
- Dishman K
- Doan C
- Doran J
- Douketis J
- Dran R
- Duck L
- Dziublyk O
- Edmilao M
- Efrati S
- El Allaf D
- Elf J
- Elias M
- Elliott CG
- Emmerich J
- Emmerich J
- Erten N
- Eyster E
- Faber J
- Fajardo L
- Faucher J
- Faucher JP
- Feldman G
- Feldman J
- Felt J
- Ferrer M
- Fine J
- Fischer D
- Flota L
- Fraiz J
- Freire A
- Frost L
- Fu M
- Fu M
- Fulmer J
- Futo L
- Gallus A
- Gallus A
- Garcia Morillo J
- Gavrysiuk V
- Ghiraduzzi A
- Ghirarduzzi A
- Gibbs H
- Ginsberg R
- Giumelli C
- Goldhaber SZ
- Goloshchekin B
- Gomez Cerezo J
- Gonzalez Garrido F
- Gordeev I
- Goyal A
- Goytia Leos D
- Gray T
- Grossman E
- Guijarro C
- Guimaraes H
- Gutierrez Valenzuela F
- Haas SK
- Habaluyas R
- Hahn B
- Hahn U
- Hamad A
- Hammerstingl C
- Harenberg J
- Haught H
- Hayek T
- Hazelrigg M
- Hecker U
- Hernandez I
- Hess T
- Hiczkiewicz J
- Horacek T
- Horna M
- Huang T
- Hussein O
- Husted S
- Husted S
- Ignatenko G
- Ikerd T
- Imberti D
- In K
- Ingerslev J
- Jacobson B
- Jacobson B
- Jagadesan R
- Jaganmani S
- Jaramillo N
- Jastrzebski D
- Jimenez D
- Jobbagy L
- Jog S
- Jorge JM
- Joslin S
- Jure H
- Kahn S
- Kakkar A
- Kakkar A
- Karan A
- Karpenko A
- Karrasch J
- Kasprzak J
- Kassis J
- Kesteven P
- Kharchenko N
- Kim S
- Klausner H
- Klepzig H
- Klochkov O
- Knabb RM
- Knudsen T
- Kobalava Z
- Kobalava Z
- Kolman P
- Kostenko V
- Kovarova K
- Kraiz I
- Krishnamurthy S
- Kuc K
- Kumar S
- Kyrle P
- Lahav M
- Landis JR
- Lawall H
- Layden M
- Leader R
- Leduc J
- Leiva J
- Leiva J
- Leizorovicz A
- Leizorovicz A
- Levenstein S
- Leães P
- Liaw D
- Ling P
- Lobo S
- Londono D
- Lopez Rosas E
- Loppinet A
- Lorcerie B
- Lugassy G
- Mahesh A
- Maignan M
- Mallibovsky L
- Marechal P
- Margolis B
- Matheis E
- McCollum P
- McLaren G
- Meade A
- Mehta M
- Mehta P
- Merah A
- Mercado DA
- Merli G
- Merli G
- Merli G
- Minar E
- Miron M
- Mismetti P
- Mitchell G
- Mkrtchian V
- Moncada Z
- Motte S
- Mottier D
- Nanez Terreros H
- Nathan R
- Nathanson A
- Nicol C
- Nielsen H
- Nony P
- O'Connell C
- Oestergaard L
- Ohanessian L
- Okoshi M
- Oliveira M
- Oliver M.
- Omar A
- Paleiron N
- Pamo O
- Parkhomenko A
- Parkhomenko A
- Patek F
- Pearl R
- Pedersen C
- Penchasky D
- Pendleton R
- Pernod G
- Peters M
- Phillips D
- Piegas L
- Piepiorka M
- Pierfranceschi G
- Pilger E
- Pinede L
- Podpera I
- Porath A
- Porreca E
- Prandoni P
- PRANDONI PAOLO
- Privalov D
- Proust A
- Psuja P
- Pulkowski G
- Pullman J
- Rajkumar J
- Rasmussen SL
- Reiterer P
- Reshetko O
- Richart C
- Risso Patron F
- Rodoman G
- Roncato C
- Rosa DD
- Rosenberg D
- Rossi L
- Rubinfeld A
- Saaibi D
- Salas M
- Salazar O
- Samama MM
- Samiuddin M
- Saraiva J
- Saraiva J
- Sathe P
- Savas I
- Savas I
- Saxena A
- Scannapieco G
- Schnabel R
- Schuller D
- Sethuraman S
- Sevilla R
- Shadan F
- Shin J
- Shvarts Y
- Siebert R
- Siegel M
- Simoneau G
- Singh P
- Sinha S
- Smith K
- Soltesz P
- Soucek M
- Spacek R
- Sparby J
- Sparby JA
- Spencer F
- Stevens S
- Streiff M
- Suarez C
- Suarez C
- Suh G
- Sundaram P
- Sushko V
- Tahirkheli N
- Talwar D
- Tarabain O
- Tay J
- Testa S
- Tillinghast A
- Toce L
- Toniolo J
- Torbicki A
- Torbiki A
- Torp Pedersen C
- Tosetto A
- Tracz W
- Tsarova O
- Tseluyko V
- Tuxen C
- Tvedegaard M
- Tyszkiewicz I
- Ueng K
- Ulloa V
- Vaince U
- Vejar M
- Vejby Christensen H
- Verhamme P
- Viergever P
- Viljoen J
- Villalta J
- Vishnevsky A
- Vita N
- Vitovec M
- Volkov V
- Ward Ch
- Weil J
- Weinstein G
- Weitz JI
- Welch M
- Welker J
- Wollaert B
- Yagensky A
- Yusof Z
- Yusoff K
- Zadionchenko V
- Zangroniz P
- Zeltser D
- Zeltser D
- Publication venue
- 'Massachusetts Medical Society'
- Publication date
- 01/01/2011
- Field of study
BACKGROUND:
The efficacy and safety of prolonging prophylaxis for venous thromboembolism in medically ill patients beyond hospital discharge remain uncertain. We hypothesized that extended prophylaxis with apixaban would be safe and more effective than short-term prophylaxis with enoxaparin.
METHODS:
In this double-blind, double-dummy, placebo-controlled trial, we randomly assigned acutely ill patients who had congestive heart failure or respiratory failure or other medical disorders and at least one additional risk factor for venous thromboembolism and who were hospitalized with an expected stay of at least 3 days to receive apixaban, administered orally at a dose of 2.5 mg twice daily for 30 days, or enoxaparin, administered subcutaneously at a dose of 40 mg once daily for 6 to 14 days. The primary efficacy outcome was the 30-day composite of death related to venous thromboembolism, pulmonary embolism, symptomatic deep-vein thrombosis, or asymptomatic proximal-leg deep-vein thrombosis, as detected with the use of systematic bilateral compression ultrasonography on day 30. The primary safety outcome was bleeding. All efficacy and safety outcomes were independently adjudicated.
RESULTS:
A total of 6528 subjects underwent randomization, 4495 of whom could be evaluated for the primary efficacy outcome--2211 in the apixaban group and 2284 in the enoxaparin group. Among the patients who could be evaluated, 2.71% in the apixaban group (60 patients) and 3.06% in the enoxaparin group (70 patients) met the criteria for the primary efficacy outcome (relative risk with apixaban, 0.87; 95% confidence interval [CI], 0.62 to 1.23; P=0.44). By day 30, major bleeding had occurred in 0.47% of the patients in the apixaban group (15 of 3184 patients) and in 0.19% of the patients in the enoxaparin group (6 of 3217 patients) (relative risk, 2.58; 95% CI, 1.02 to 7.24; P=0.04).
CONCLUSIONS:
In medically ill patients, an extended course of thromboprophylaxis with apixaban was not superior to a shorter course with enoxaparin. Apixaban was associated with significantly more major bleeding events than was enoxaparin. (Funded by Bristol-Myers Squibb and Pfizer; ClinicalTrials.gov number, NCT00457002.)
Ezetimibe added to statin therapy after acute coronary syndromes
- Author
- Aagnes I
- Aambakk MB
- Aase O
- Aaser E
- Abdel-Latief A
- Abell T
- Aboufakher R
- Abramson B
- Abrantes J
- Achilli A
- Adams A
- Adams K
- Adamus J
- Addington J
- Adgey A
- Adjei A
- Agarwal J
- Aggarwal A
- Aggarwal K
- Aggarwal R
- Agocha A
- Agraou B
- Aguirre O
- Ahmed A
- Ahmed O
- Ahsan A
- Airaksinen J
- Airoldi F
- Aji J
- Akkad H
- Akubzanova E
- Al-Ani R
- Al-Jumaily J
- Alameda J
- Albirini A
- Albuquerque A
- Albuquerque D
- Alcasena S
- Alexander J
- Alfonso F
- Ali MI
- Alings MA
- Allall O
- Allen J
- Allen RP
- Allred S
- Almeira AS
- Alonso L
- Alsagheer S
- Alshaher M
- Altschuller A
- Alvarez J
- Alvarez J
- Alvarez Y
- Alves A
- Amidon T
- Amos M
- Anaszewicz M
- Andersen M
- Andersen O
- Andersson E
- Andersson G
- Andrade G
- Andrade M
- Andrea B
- Andreou C
- Antonangelo A
- Antorrena I
- Appel K
- Arana C
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- Araujo J
- Arce R
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- Artaecheverria J
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- Baraona F
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- Zuppiroli A
- Zwart PA
- Zweiker R
- Ångman K
- Édes I
- Östberg S
- Publication venue
- 'Massachusetts Medical Society'
- Publication date
- 01/01/2015
- Field of study
BACKGROUND: Statin therapy reduces low-density lipoprotein (LDL) cholesterol levels and the risk of cardiovascular events, but whether the addition of ezetimibe, a nonstatin drug that reduces intestinal cholesterol absorption, can reduce the rate of cardiovascular events further is not known. METHODS: We conducted a double-blind, randomized trial involving 18,144 patients who had been hospitalized for an acute coronary syndrome within the preceding 10 days and had LDL cholesterol levels of 50 to 100 mg per deciliter (1.3 to 2.6 mmol per liter) if they were receiving lipid-lowering therapy or 50 to 125 mg per deciliter (1.3 to 3.2 mmol per liter) if they were not receiving lipid-lowering therapy. The combination of simvastatin (40 mg) and ezetimibe (10 mg) (simvastatin-ezetimibe) was compared with simvastatin (40 mg) and placebo (simvastatin monotherapy). The primary end point was a composite of cardiovascular death, nonfatal myocardial infarction, unstable angina requiring rehospitalization, coronary revascularization ( 6530 days after randomization), or nonfatal stroke. The median follow-up was 6 years. RESULTS: The median time-weighted average LDL cholesterol level during the study was 53.7 mg per deciliter (1.4 mmol per liter) in the simvastatin-ezetimibe group, as compared with 69.5 mg per deciliter (1.8 mmol per liter) in the simvastatin-monotherapy group (P<0.001). The Kaplan-Meier event rate for the primary end point at 7 years was 32.7% in the simvastatin-ezetimibe group, as compared with 34.7% in the simvastatin-monotherapy group (absolute risk difference, 2.0 percentage points; hazard ratio, 0.936; 95% confidence interval, 0.89 to 0.99; P = 0.016). Rates of pre-specified muscle, gallbladder, and hepatic adverse effects and cancer were similar in the two groups. CONCLUSIONS: When added to statin therapy, ezetimibe resulted in incremental lowering of LDL cholesterol levels and improved cardiovascular outcomes. Moreover, lowering LDL cholesterol to levels below previous targets provided additional benefit
Vorapaxar in the secondary prevention of atherothrombotic events
- Author
- A. Ahsan
- A. Albirini
- A. Altschuller
- A. Antolick
- A. Arthur
- A. Bank
- A. Belemer
- A. Berni
- A. Betriu
- A. Biton
- A. Brady
- A. Brito
- A. Brock
- A. Bura-Riviere
- A. Caceres
- A. Cale
- A. Camp
- A. Campolongo
- A. Carvalho
- A. Centurion
- A. Cerny
- A. Claxton
- A. Cohen
- A. Comerota
- A. Csanyi
- A. Czlonkowska
- A. Da Silva
- A. DaCosta
- A. Dahlmans
- A. Del Rio Ligorit
- A. Desai
- A. Dijkshoorn
- A. Doerr
- A. Domzal-Stryga
- A. Don
- A. Elgasen
- A. Elis
- A. Engstrom
- A. Fallden-Gunnnarsson
- A. Fernandez
- A. Findik
- A. Fiscella
- A. Ford
- A. Frey
- A. Galla
- A. Gallino
- A. Garcia Pastor
- A. Gatkova
- A. Gavazzi
- A. Gil Nunez
- A. Giordano
- A. Glanz
- A. Goldhaber
- A. Gottsater
- A. Gruszka
- A. Guenther
- A. Guimaraes
- A. Gupta
- A. Habermeier
- A. Hakansson
- A. Hallmann
- A. Hamer
- A. Hellberg
- A. Hill
- A. Horak
- A. Howard
- A. Jakal
- A. Jaltier
- A. Joergensen
- A. Kaakkomaki
- A. Katz
- A. Kilian
- A. Kofmel
- A. Koralewska
- A. Korsnack
- A. Kubiak
- A. Kuhn
- A. Kuijper
- A. Labroo
- A. Lamy
- A. Lau-Sieckman
- A. Lazzari
- A. Ledda
- A. Ledger
- A. Lewis
- A. Linhart
- A. Linor
- A. Long
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- A. Loxton
- A. Lozada
- A. Manoj
- A. Martignoni
- A. Matoltsy
- A. McCann
- A. Milnerowicz
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- A. Moore
- A. Morissette
- A. Mukherjee
- A. Munoz
- A. Murally
- A. Niederman
- A. Norden
- A. Odero
- A. Odhav
- A. Opdal
- A. Orozco
- A. Orpen
- A. Pande
- A. Pawlak
- A. Pedersen
- A. Peeters
- A. Pell
- A. Piti
- A. Podczeck-Schweighofer
- A. Prado
- A. Ramachandran
- A. Rees
- A. Rek
- A. Remes
- A. Renouf
- A. Revilla
- A. Rizzo
- A. Roach
- A. Roodt
- A. Rynkiewicz
- A. Salvador
- A. Sasaki
- A. Schaffranka
- A. Schlesinger
- A. Schmidt
- A. Scholtze
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- A. Shepler
- A. Shirwany
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- A.J. Bradley
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- D. Chiezzo
- D. Cianflone
- D. Cleveland
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- D. Connolly
- D. Crimmins
- D. Das
- D. Dion
- D. Domingo
- D. Drenning
- D. Dureau
- D. Dutka
- D. Elian
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- D. Gagne
- D. Galley
- D. Gavish
- D. Genne
- D. Gorog
- D. Gupta
- D. Hainzer
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- D. Hischier
- D. Holly
- D. Huertas
- D. Hughes
- D. Isaza
- D. Jacobson
- D. Jacoby
- D. Jefferson
- D. Jenkinson
- D. Jeter
- D. Kissos
- D. Leeman
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- D. Logwood
- D. Lopez
- D. Manns
- D. McDuffie
- D. Moliterno
- D. Nilsen
- D. Otto
- D. Overbeck
- D. Pales
- D. Peek
- D. Riou
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- D. Rodrigues
- D. Rowlands
- D. Rueda
- D. Schmid
- D. Schneider
- D. Scott
- D. Scrutinio
- D. Seaton
- D. Seraphin
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- D. Solomons
- D. Southam
- D. Sprigings
- D. Strootman
- D. Tanne
- D. Tarsi
- D. Tatum
- D. Tsalihin
- D. Wexler
- D. Winterrowd
- D. Wohns
- D. Wroblewski
- D. Zaniol
- D.A. Hinchman
- D.A. Morrow
- D.C. de Albuquerque
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- D.O. Mauro
- D.P. Suresh
- D.S. Scott
- D.W. Dietrich
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- E. Arbenser
- E. Awtry
- E. Barbieri
- E. Bjurling
- E. Blank
- E. Blessing
- E. Braunwald
- E. Butkus
- E. Cardozo
- E. Carter
- E. Casares
- E. Coetsee
- E. Collings
- E. Corrada
- E. Dagher
- E. de Mingo
- E. deGrande
- E. Dhondt
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- E. Escobar
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- E. Gershman
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- E. Marin Araez
- E. Marshall
- E. Martinez
- E. Mirek-Bryniarska
- E. Molina Aguirre
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- S. Afanasiev
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- S. Brock
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- S. Cardenas
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- S. Logvinenko
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- W. French
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- W. He
- W. Holt
- W. Horne
- W. Johnson
- W. Leimbach
- W. Palasik
- W. Penny
- W. Pluta
- W. Rogers
- W. Sobiczewski
- W. Staszkiewicz
- W. Stueflotten
- W. Sturm
- W. Szybka
- W. Van Landegem
- W. Zwinnen
- W.B. Campbell
- W.D. Doty
- W.G. Carlini
- W.P. Klinke
- W.P. McGuinn
- W.R. Ardito
- W.R. Cashion
- W.W. Wilson
- X. Garcia-Moll
- X. Liu
- Y. Aladro Benito
- Y. Chandrashekhar
- Y. Cottin
- Y. Feldman
- Y. Hirano
- Y. Hiraoka
- Y. Honda
- Y. Lampl
- Y. Manabe
- Y. Niinuma
- Y. Okada
- Y. Oono
- Y. Pesant
- Y. Rozenman
- Y. Samson
- Y. Shinohara
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- Z. Gasior
- Z. Kalita
- Z. Klimsa
- Z. Kornacewicz-Jach
- Z. Lorenc
- Z. Mohamed
- Z. Monhart
- Publication venue
- 'Massachusetts Medical Society'
- Publication date
- 01/01/2012
- Field of study
Item does not contain fulltextBACKGROUND: Thrombin potently activates platelets through the protease-activated receptor PAR-1. Vorapaxar is a novel antiplatelet agent that selectively inhibits the cellular actions of thrombin through antagonism of PAR-1. METHODS: We randomly assigned 26,449 patients who had a history of myocardial infarction, ischemic stroke, or peripheral arterial disease to receive vorapaxar (2.5 mg daily) or matching placebo and followed them for a median of 30 months. The primary efficacy end point was the composite of death from cardiovascular causes, myocardial infarction, or stroke. After 2 years, the data and safety monitoring board recommended discontinuation of the study treatment in patients with a history of stroke owing to the risk of intracranial hemorrhage. RESULTS: At 3 years, the primary end point had occurred in 1028 patients (9.3%) in the vorapaxar group and in 1176 patients (10.5%) in the placebo group (hazard ratio for the vorapaxar group, 0.87; 95% confidence interval [CI], 0.80 to 0.94; P<0.001). Cardiovascular death, myocardial infarction, stroke, or recurrent ischemia leading to revascularization occurred in 1259 patients (11.2%) in the vorapaxar group and 1417 patients (12.4%) in the placebo group (hazard ratio, 0.88; 95% CI, 0.82 to 0.95; P=0.001). Moderate or severe bleeding occurred in 4.2% of patients who received vorapaxar and 2.5% of those who received placebo (hazard ratio, 1.66; 95% CI, 1.43 to 1.93; P<0.001). There was an increase in the rate of intracranial hemorrhage in the vorapaxar group (1.0%, vs. 0.5% in the placebo group; P<0.001). CONCLUSIONS: Inhibition of PAR-1 with vorapaxar reduced the risk of cardiovascular death or ischemic events in patients with stable atherosclerosis who were receiving standard therapy. However, it increased the risk of moderate or severe bleeding, including intracranial hemorrhage. (Funded by Merck; TRA 2P-TIMI 50 ClinicalTrials.gov number, NCT00526474.)