4 research outputs found
Atmospheric particle dry deposition of major ions to the South Atlantic coastal area observed at Baía de Todos os Santos, Brazil
- Author
- Allen AG
- Bourotte C
- Brewer PG
- Cadle SH
- Campos VP
- Chakraborty A
- Chu CC
- CONAMA - Conselho Nacional de Meio Ambiente
- Da Rocha GO
- Da Rocha GO
- Da Rocha GO
- Da Rocha GO
- DENATRAN - Departamento Nacional de Trânsito
- Dockery D
- Fang GC
- Gao Y
- GISELE O. DA ROCHA
- Grosjean D
- He J
- Herut B
- Hsieh LY
- IPCC - Intergovernmental Panel on Climate Change
- Jacobson MC
- JAILSON B. DE ANDRADE
- JOSÉ S.S. DOMINGOS
- JOÃO V.S. SANTOS
- Kappos AD et al
- Karthikeyan S
- Kawamura K
- Kawamura K
- Kawamura K
- Kerminen VM
- Kerminen VM
- Khare P
- Koçak M
- Kubátová A
- Kumar A
- Kundu S
- Lee BK
- Limbeck A
- Limbeck A
- Limon-Sanchez MT
- Machado MCS
- MANUELA P. CARDOSO
- Mariani RL
- Millero FJ
- Mkoma SL
- Mkoma SL
- Mochida M
- Narukawa M
- Nicolas JF
- Peng C
- Pereira PAP
- ROGERIO L. DA SILVA
- Salma I
- STELYUS L. MKOMA
- Talbot RW
- Vasconcellos PC
- Verma SK
- Warneck P
- Witt MLI
- Yao X
- Yu J
- Zhang T
- Publication venue
- 'FapUNIFESP (SciELO)'
- Publication date
- Field of study
Challenge of Chronically Infected Mice with Homologous Trypanosoma cruzi Parasites Enhances the Immune Response but Does Not Modify Cardiopathy: Implications for the Design of a Therapeutic Vaccine
- Author
- Albareda MC
- Cazorla SI
- Cohen IR
- Dias JC
- DosReis GA
- Duan XF
- Elias RM
- Fischer E
- Fontanella GH
- Kipnis TL
- Leavey JK
- Lescure FX
- Limon-Flores AY
- Luhrs KA
- Marin-Neto JA
- Marinho CR
- Marinho CR
- Marinho CRF
- Marinho CRF
- Martin DL
- Matzinger P
- Nogueira N
- Palomino SAP
- Pereira-Chioccola VL
- Postan M
- Rodrigues MM
- Sanchez-Burgos G
- Sardinha LR
- Schofield CJ
- Scott MT
- Snapper CM
- Tarleton RL
- Vago AR
- Vasconcelos JR
- Vitetta ES
- Zapata-Estrella H
- Publication venue
- 'American Society for Microbiology'
- Publication date
- Field of study
Cardiovascular Activity
- Author
- A Baartscheer
- A Baartscheer
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- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/01/2007
- Field of study
Edoxaban versus warfarin in patients with atrial fibrillation
- Author
- Abdullakutty J
- Abi-Mansour P
- Abril SB
- Accini J
- Accini M
- Acikel M
- Acikel M
- Adachi C
- Adams K
- Adams K
- Adamus J
- Adler J
- Adler P
- Agarwal D
- Aggarwal R
- Aggarwal R
- Agirov M
- Agraou B
- Ahmad A
- Ahmadpour H
- Ahuad Guerrero R
- Ajioka M
- Akhter F
- Akihisa U
- Akilli H
- Al-Maliky T
- Al-Zoebi A
- Albert L. Waldo
- Albisu J
- Albulescu P
- Alexander J
- Alexandrova L
- Alexopoulos D
- Alexopoulos D
- Alhakim M
- Aliyar P
- Allall O
- Allison J
- Allman J
- Almaraz SP
- Almeida A
- Almeida M
- Almquist A
- Aloni I
- Alsheikh T
- Altonen D
- Alvarez C
- Alvarez M
- Alvarez RF
- Amarenco P
- Amato Vincenzo de Paola A
- Ambrovic I
- Ambrovicova V
- Ameriso P
- Ameriso S
- Amin K
- Amin M
- Amuchastegui M
- Anciu M
- Anderson C
- Anderson J
- Anderson J
- Andersson R
- Andor M
- Andrade Lotufo P
- Andresen T
- Andrews A
- Angel J
- Anscombe R
- Anthony A
- Antle S
- Antman EM
- Antman EM
- Antonino M
- Anzai T
- Apetrei E
- Apostolovic S
- Appelros P
- Aquino M
- Arakawa S
- Araújo E
- Archibald J
- Arcocha Torres M
- Ardelean A
- Arfaoui M
- Arias J
- Armas BH
- Arneja J
- Arnold T
- Arora T
- Arora V
- Arouni A
- Arrieta M
- Arroyave C
- Arstall M
- Arutyunov G
- Asakura H
- Asensio A
- Astier L
- Ata N
- Ata N
- Atar D
- Atar D
- Atar S
- Atie J
- Atkinson C
- Attanti S
- Aude Y
- Augusto Alves da Costa F
- Aull L
- Ault S
- Ausperger KM
- Avellar K
- Averett P
- Avery D
- Avila H
- Avvaru G
- Awasty V
- Awtry E
- Ayasse D
- Ayau Milla O
- Ayesu K
- Aylward P
- Azhdari M
- Azua MG
- Babbar A
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- 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.)