2 research outputs found
Clinical presentation, aetiology and outcome of infective endocarditis. Results of the ESC-EORP EURO-ENDO (European infective endocarditis) registry: a prospective cohort study
- Author
- 6zt\ufcrk C
- Abboud Cs
- Abd El-Nasser M
- Abdel-Hay M
- Abdelnaby M
- Abe K
- Abid L
- Aboal Vinas J
- Aboulenein J
- Aboyans V
- Abreu J
- Abreu J
- Actis Dato Gm
- Afonso T
- Aggeli C
- Agnoletto V
- Agricola E
- Aguero Balbin J
- Ahmed A
- Ahmed B
- Ahmed M
- Ainine K
- Al Habash O
- Al Kholy A
- Al-Mallah M
- Alarcon C
- Albert Bertran X
- Alcantara M
- Alfieri O
- Alhashmi J
- Ali Tatar-Chentir Nn
- Ali M
- Alizadehasl A
- Alla F
- Almaghraby A
- Almela M
- Alrahimi J
- Alterini B
- Alvaro M
- Alyavi B
- Amano M
- Ambrosioni J
- Amsel B
- Andarala M
- Andor M
- Andrade Jl
- Anguita M
- Ansard S
- Antit S
- Anzules N
- Aonuma K
- Arai K
- Armenis I
- Arminanzas C
- Arnaiz de Las Revillas F
- Arnaiz Garcia A
- Arnau Ma
- Arnoni R
- Arregle F
- Asch Fm
- Ashihara K
- Ashikaga K
- Assayag P
- Assef Je
- Asseray-Madani N
- Astrom Aneq M
- Atas H
- Athanasiou D
- Athanassopoulos G
- Atkocaityte J
- Attia N
- Avegliano G
- Axler O
- Axler Olivier
- Azevedo J
- B\uf6rgermann J
- Badano Lp
- Bajana Carpio A
- Balan G
- Baldenhofer G
- Bangher M
- Bansal M
- Baratta P
- Barbetseas J
- Bardaji Ruiz A
- Barsic B
- Bartykowszki A
- Baslib F
- Baumann F
- Baumard S
- Bayes-Genis A
- Beaudoin J
- Beauloye C
- Bechlioulis A
- Becker M
- Beeharry A
- Beitnes Jo
- Bekkers Sc
- Bel A
- Beleslin B
- Bellino M
- Bellio de Mattos Barretto R
- Ben Hlima M
- Benesco I
- Benvenga Rm
- Benyoussef S
- Berastegui E
- Berle C
- Bettayeb B
- Beyer R
- Bhan A
- Binder C
- Biron C
- Blanco-Gonzalez E
- Blanes M
- Blechova K
- Bohbot Y
- Bonou M
- Bordejevic A
- Borg D
- Bosch Portell D
- Botelho-Nevers E
- Bouchart F
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- Brasselet C
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- Cardaniuc I
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- Chambers J
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- Chandrasekaran B
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- Chioncel O
- Chirouze C
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- Citro R
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- Corcea V
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- Fernandez-Golfin C
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- Ferrara D
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- Fife A
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- Fiorucci E
- Fischer C
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- Floros G
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- Fraiture B
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- Gulel O
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- Gutierrez-Diez Jf
- Habib G
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- Habib Gilbert
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- Hagiwara N
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- Hancock J
- Haralambidis G
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- Izumi C
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- Lancellotti Patrizio
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- Tolosana Jm
- Tomescu Mc
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- van Dongen E
- Van Heusden H
- Van Melle Jp
- Vancata R
- Vancraeynest D
- Vanoverschelde Jl
- Varga A
- Vargovic M
- Varlamos C
- Vasallo Vidal F
- Vaskelyte J
- Vaskelyte Jolanta-Justina
- Velazco P
- Velcean La
- Velicki L
- Vella C
- Venieri E
- Vidal B
- Vieira M
- Vilacosta I
- Vilela F
- Villaca Filho F
- Villares Jimenez A
- Vincelj J
- Vriend J
- Vulin A
- Wahadat A
- Wahid A
- Wakami K
- Wallentin L
- Walther T
- Wanounou M
- Watanabe N
- Weidinger F
- Wejner-Mik P
- Weytjens C
- Widimsky J
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- Yamada H
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- Yasar Us
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- Yiannikourides V
- Yuda S
- Yuichiro O
- Zachwyc J
- Zahn R
- Zahran H
- Zakhama L
- Zaky H
- Zamorano Jl
- Zarauza J
- Zarger P
- Zayed Y
- Zeid A
- Zemedkun M
- Zerva K
- Zeymer U
- Zvirblyte R
- Publication venue
- 'Oxford University Press (OUP)'
- Publication date
- 01/01/2019
- Field of study
The EURO-ENDO registry aimed to study the management and outcomes of patients with infective endocarditis (IE).
AIMS:
The EURO-ENDO registry aimed to study the management and outcomes of patients with infective endocarditis (IE).
METHODS AND RESULTS:
Prospective cohort of 3116 adult patients (2470 from Europe, 646 from non-ESC countries), admitted to 156 hospitals in 40 countries between January 2016 and March 2018 with a diagnosis of IE based on ESC 2015 diagnostic criteria. Clinical, biological, microbiological, and imaging [echocardiography, computed tomography (CT) scan, 18F-fluorodeoxyglucose positron emission tomography/computed tomography (18F-FDG PET/CT)] data were collected. Infective endocarditis was native (NVE) in 1764 (56.6%) patients, prosthetic (PVIE) in 939 (30.1%), and device-related (CDRIE) in 308 (9.9%). Infective endocarditis was community-acquired in 2046 (65.66%) patients. Microorganisms involved were staphylococci in 1085 (44.1%) patients, oral streptococci in 304 (12.3%), enterococci in 390 (15.8%), and Streptococcus gallolyticus in 162 (6.6%). 18F-fluorodeoxyglucose positron emission tomography/computed tomography was performed in 518 (16.6%) patients and presented with cardiac uptake (major criterion) in 222 (42.9%) patients, with a better sensitivity in PVIE (66.8%) than in NVE (28.0%) and CDRIE (16.3%). Embolic events occurred in 20.6% of patients, and were significantly associated with tricuspid or pulmonary IE, presence of a vegetation and Staphylococcus aureus IE. According to ESC guidelines, cardiac surgery was indicated in 2160 (69.3%) patients, but finally performed in only 1596 (73.9%) of them. In-hospital death occurred in 532 (17.1%) patients and was more frequent in PVIE. Independent predictors of mortality were Charlson index, creatinine > 2\u2009mg/dL, congestive heart failure, vegetation length > 10 mm, cerebral complications, abscess, and failure to undertake surgery when indicated.
CONCLUSION:
Infective endocarditis is still a life-threatening disease with frequent lethal outcome despite profound changes in its clinical, microbiological, imaging, and therapeutic profiles
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
- AraĂşjo 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
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- Ĺśpinar 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.)