5 research outputs found
Association of prenatal pesticide exposures with adverse pregnancy outcomes and stunting in rural Bangladesh
- Author
- Abdel-Rahman
- Alam
- Antonia M. Calafat
- Arifeen
- Barkoski
- Barr
- Berkowitz
- Berkowitz
- Bhattacharjee
- Bill & Melinda Gates Foundation
- Budreau
- Casas
- Chanda
- Cheikh Ismail
- Cheikh Ismail
- Chevrier
- Chiu
- Chowdhury
- Chowdhury
- Danaei
- David C. Christiani
- Davis
- Dey
- Eskenazi
- Fortenberry
- Grandjean
- Haque
- Harley
- Harley
- Hioki
- Hoppin
- Hornung
- Hossain
- Institoris
- Islam
- Islam
- Jung
- Karsan
- Kartini
- Kile
- Kinniburgh
- Krishna
- Levario-Carrillo
- Lin
- Lindsay M. Jaacks
- Ling
- Maitreyi Mazumdar
- Maria Ospina
- Md Omar Sharif Ibne Hasan
- Muto
- Naksen
- Nancy Diao
- Nolan
- Paudel
- Perera
- Quazi Quamruzzaman
- Rahman
- Rahman
- Robert Wright
- Sanjose
- Sarma
- Schreinemachers
- Schwartz
- Shammi
- Shapiro
- Shirangi
- Song
- Spiegelman
- Spyker
- Textor
- VanderWeele
- Whyatt
- Whyatt
- Winchester
- Wohlfahrt-Veje
- Wylie
- Xiang
- Publication venue
- 'Elsevier BV'
- Publication date
- 01/12/2019
- Field of study
May-Thurner syndrome and iliac arteriovenous fistula in an elderly woman
- Author
- Publication venue
- 'Elsevier BV'
- Publication date
- 01/06/2016
- Field of study
May-Thurner syndrome most commonly involves compression of the left common iliac vein by the right common iliac artery and can result in leg pain and swelling as well as potentially precipitate deep venous thrombosis. These symptoms can be exacerbated by additional vascular abnormalities. This is a case report of a 91-year-old woman with intractable massive left lower extremity edema that interfered with walking. She was diagnosed with concurrent May-Thurner syndrome and pelvic arteriovenous fistula. Treatment with embolization of the fistula and stenting of the left common iliac vein relieved her symptoms and allowed her to walk again
Edoxaban versus warfarin in patients with atrial fibrillation
- Author
- Abdullakutty J
- Abi-Mansour P
- Abril SB
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- Ahuad Guerrero R
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- Akhter F
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- Akilli H
- Al-Maliky T
- Al-Zoebi A
- Albert L. Waldo
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- Albulescu P
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- 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.)
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