65 research outputs found
A Multi-Center Randomized Trial to Assess the Efficacy of Gatifloxacin versus Ciprofloxacin for the Treatment of Shigellosis in Vietnamese Children
- Author
- A Agresti
- A Arjyal
- A Pandit
- BS Traa
- Bui Li Mong
- C Dolecek
- Cao Thu Thuy
- Christian Johnson
- Christiane Dolecek
- CM Parry
- CY Kuo
- DB Bethell
- DM Grasela
- DN Fish
- DW Acheson
- DW Isenbarger
- DW Isenbarger
- H Vinh
- H Vinh
- Ha Thi Loan
- Ha Vinh
- HL DuPont
- I Kabir
- J Dubois
- James I. Campbell
- Jeremy J. Farrar
- Jeremy N. Day
- JM Sansone
- KL Kotloff
- KP Ittner
- L von Seidlein
- Le Thi Phuong
- LY Park-Wyllie
- M Rahman
- MA Salam
- Mai Thu Chinh
- Marcel Wolbers
- ME Pichichero
- Nguyen Duc Anh
- Nguyen Phu Huong Lan
- Nguyen Thi Hong Tham
- Nguyen Thi Khanh Nhu
- Nguyen Thi Thu Thao
- Nguyen Van Minh Hoang
- Nguyen Van Vinh Chau
- NT Nguyen
- P Shears
- Pham Thanh Duy
- Pham Van Minh
- Phan Van Be Bay
- PJ Sansonetti
- PK Ram
- PR Christopher
- RS Rodriguez
- Stephen Baker
- To Song Diep
- Tran Vu Thieu Nga
- TT Chau
- V Yadav
- Vo Thi Cuc Anh
- WA Khan
- Publication venue
- Public Library of Science
- Publication date
- 01/01/2011
- Field of study
The bacterial genus Shigella is the most common cause of dysentery (diarrhea containing blood and/or mucus) and the disease is common in developing countries with limitations in sanitation. Children are most at risk of infection and frequently require hospitalization and antimicrobial therapy. The WHO currently recommends the fluoroquinolone, ciprofloxacin, for the treatment of childhood Shigella infections. In recent years there has been a sharp increase in the number of organisms that exhibit resistance to nalidixic acid (an antimicrobial related to ciprofloxacin), corresponding with reduced susceptibility to ciprofloxacin. We hypothesized that infections with Shigella strains that demonstrate resistance to nalidixic acid may prevent effective treatment with ciprofloxacin. We performed a randomized controlled trial to compare 3 day ciprofloxacin therapy with 3 days of gatifloxacin, a newer generation fluoroquinolone with greater activity than ciprofloxacin. We measured treatment failure and time to the cessation of individual disease symptoms in 249 children with dysentery treated with gatifloxacin and 245 treated with ciprofloxacin. We could identify no significant differences in treatment failure between the two groups or in time to the cessation of individual symptoms. We conclude that, in Vietnam, ciprofloxacin and gatifloxacin are similarly effective for the treatment of acute dysentery
Use of anticoagulants and antiplatelet agents in stable outpatients with coronary artery disease and atrial fibrillation. International CLARIFY registry
- Author
- A. L. R. Ng
- Abardia Oliva F. J.
- Abdel Malak S.
- Abdel Wahab H.
- Abdul Kareem B. B.
- Abdul Manap H.
- Abdul Rahim A. A.
- Abdulkader F.
- Abdulla A. H. K.
- AbdulWahab M. Z.
- Abduvalieva V.
- Abele S.
- Aboyans V.
- Abreu P. E.
- Adam-Blanpain M.
- Adamaszek K.
- Adamczyk-Kot D.
- Adamkiewicz-Piejko A.
- Adda M.
- Aftab A.
- Agrawal A.
- Aguiar C.
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- Ai F.
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- Akbar M.
- Aksyutina N.
- Al Dhanki M.
- Al Ghool S.
- Al Kandari F.
- Al Lawati A.
- Al Mahmeed W.
- Al Radaideh G.
- Al Rashdan I.
- Al Sousi A.
- Al Suwaidi J.
- Al Tamimi F.
- Al Wahshi Y.
- Al Yazeedi J.
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- Al-Baker H.
- Al-Faleh H.
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- Publication venue
- 'Public Library of Science (PLoS)'
- Publication date
- 01/01/2015
- Field of study
Pan-cancer analysis of whole genomes
- Author
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- The ICGC/TCGA Pan-Cancer Analysis of Whole Genomes Consortium View Correspondence (jump link)
- Thiessen
- Thomas
- Thomas
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- wz Hupp
- x Eils
- x Yung
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- xb Felau
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- xh Fulton
- Xi
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- Xiong
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- xp Benz
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- xr Ghori
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- Xue
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- Y. -J. xn
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- Y. dy
- Y. ef
- Y. ep
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- Y. ff
- Y. fr
- Y. fv
- Y. fv
- Y. gl
- Y. hl
- Y. hq
- Y. hq
- Y. ia
- Y. kq
- Y. lw
- Y. nh
- Y. nk
- Y. nz
- Y. rg
- Y. rj
- Y. rm
- Y. S. jf
- Y. uz
- Y. vr
- Y. wt
- Y. yc
- ya Al-Ahmadie
- Yachida
- Yamaguchi
- Yamaguchi T. N. k
- Yamamoto
- Yamaue
- Yang
- Yang
- Yang
- Yang
- Yang
- Yao
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- yb Ally
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- ye Auman
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- Yellapantula
- Yellapantula
- yh Bathe
- yj Baylin
- Yoon
- Yu
- Yu
- Yu
- Yuan
- Yugawa
- z ah
- Z. ej
- Z. ep
- Z. fr
- Z. hv
- Z. hy
- Z. jq
- Z. kt
- Z. oe
- Zaikova
- Zapatka
- zd Gershenwald
- Zenklusen
- Zeps
- zf Ghossein
- Zhang
- Zhang
- Zhang
- Zhang
- Zhang
- Zhang
- Zhang H. b
- Zhao
- Zheng
- Zhou
- Zhou
- Zhu
- Zhu
- zi zj
- zm Jayaseelan
- Zou
- Zou
- zt Kim
- zw Lewis
- Ă. A. th
- Ă. sk
- Publication venue
- Publication date
- 11/12/2019
- Field of study
Cancer is driven by genetic change, and the advent of massively parallel sequencing has enabled systematic documentation of this variation at the whole-genome scale(1-3). Here we report the integrative analysis of 2,658 whole-cancer genomes and their matching normal tissues across 38 tumour types from the Pan-Cancer Analysis of Whole Genomes (PCAWG) Consortium of the International Cancer Genome Consortium (ICGC) and The Cancer Genome Atlas (TCGA). We describe the generation of the PCAWG resource, facilitated by international data sharing using compute clouds. On average, cancer genomes contained 4-5 driver mutations when combining coding and non-coding genomic elements; however, in around 5% of cases no drivers were identified, suggesting that cancer driver discovery is not yet complete. Chromothripsis, in which many clustered structural variants arise in a single catastrophic event, is frequently an early event in tumour evolution; in acral melanoma, for example, these events precede most somatic point mutations and affect several cancer-associated genes simultaneously. Cancers with abnormal telomere maintenance often originate from tissues with low replicative activity and show several mechanisms of preventing telomere attrition to critical levels. Common and rare germline variants affect patterns of somatic mutation, including point mutations, structural variants and somatic retrotransposition. A collection of papers from the PCAWG Consortium describes non-coding mutations that drive cancer beyond those in the TERT promoter(4); identifies new signatures of mutational processes that cause base substitutions, small insertions and deletions and structural variation(5,6); analyses timings and patterns of tumour evolution(7); describes the diverse transcriptional consequences of somatic mutation on splicing, expression levels, fusion genes and promoter activity(8,9); and evaluates a range of more-specialized features of cancer genomes(8,10-18).Peer reviewe
The global burden of cancer attributable to risk factors, 2010-19: a systematic analysis for the Global Burden of Disease Study 2019
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- Aali A
- Ab Khan M
- Abbas Q
- Abbasi B
- Abbasi-Kangevari M
- Abbasi-Kangevari Z
- Abbastabar H
- Abd-Elsalam S
- Abdelmasseh M
- Abdelwahab AA
- Abdoli G
- Abdulkader RS
- Abdulkadir HA
- AbdulmuhsinMohammad K
- Abedi A
- Abegaz KH
- Abidi H
- Aboagye RG
- Abolhassani H
- Absalan A
- Abtew YD
- Abu-Gharbieh E
- Achappa B
- Acheson AR
- Acuna JM
- Addison D
- Addo IY
- Adegboye OA
- Adesina MA
- Adnan M
- Adnani QES
- Advani SM
- Afrin S
- Afzal MS
- Aggarwal M
- Ahinkorah BO
- Ahmad AR
- Ahmad R
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- Ahmed H
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- Ahmed MB
- Aiman W
- Ajami M
- Akalu GT
- Akbarzadeh-Khiavi M
- Aklilu A
- Akonde M
- Akunna CJ
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- Biondi A
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- Jang S-I
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- Khaneghah AM
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- Sinha DN
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- Sitas F
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- Skryabin VY
- Skryabina AA
- Socea B
- Soeberg MJ
- Sofi-Mahmudi A
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- Soodejani MT
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- Publication venue
- Publication date
- 20/08/2022
- Field of study
Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)1.
- Author
- Abdel-Aziz AK
- Abdelfatah S
- Abdellatif M
- Abdoli A
- Abel S
- Abeliovich H
- Abildgaard MH
- Abudu YP
- Acevedo-Arozena A
- Adamopoulos IE
- Adeli K
- Adolph TE
- Adornetto A
- Aflaki E
- Agam G
- Agarwal A
- Aggarwal BB
- Agnello M
- Agostinis P
- Agrewala JN
- Agrotis A
- Aguilar PV
- Ahmad ST
- Ahmed ZM
- Ahumada-Castro U
- Aits S
- Aizawa S
- Akkoc Y
- Akoumianaki T
- Akpinar HA
- Al-Abd AM
- Al-Akra L
- Al-Gharaibeh A
- Alaoui-Jamali MA
- Alberti S
- Alcocer-GĂłmez E
- Alessandri C
- Ali M
- Alim Al-Bari MA
- Aliwaini S
- Alizadeh J
- Almacellas E
- Almasan A
- Alonso A
- Alonso GD
- Altan-Bonnet N
- Altieri DC
- Alves da Costa C
- Alves S
- Alzaharna MM
- Amadio M
- Amantini C
- Amaral C
- Ambrosio S
- Amer AO
- Ammanathan V
- An Z
- Andersen SU
- Andrabi SA
- Andrade-Silva M
- Andres AM
- Angelini S
- Ann D
- Anozie UC
- Ansari MY
- Antas P
- Antebi A
- AntĂłn Z
- Anwar T
- Apetoh L
- Apostolova N
- Araki T
- Araki Y
- Arasaki K
- Araya J
- AraĂșjo WL
- Arden C
- Arguelles S
- Arias E
- Arikkath J
- Arimoto H
- Ariosa AR
- Armstrong-James D
- Arnauné-Pelloquin L
- Aroca A
- Arroyo DS
- Arsov I
- Artero R
- Arévalo M-A
- Asaro DML
- Aschner M
- Ashrafizadeh M
- Ashur-Fabian O
- Atanasov AG
- Au AK
- Auberger P
- Auner HW
- Aurelian L
- Autelli R
- Avagliano L
- Aveic S
- Aveleira CA
- Avin-Wittenberg T
- Aydin Y
- Ayton S
- Ayyadevara S
- Azzopardi M
- Baba M
- Backer JM
- Backues SK
- Bae D-H
- Bae O-N
- Bae SH
- Baehrecke EH
- Baek A
- Baek S-H
- Baek SH
- Bagetta G
- Bagniewska-Zadworna A
- Bai H
- Bai J
- Bai X
- Bai Y
- Bairagi N
- Baksi S
- Balazadeh S
- Balbi T
- Baldari CT
- Balduini W
- Ballabio A
- Ballester M
- Balzan R
- Bandopadhyay R
- Banerjee S
- Banerjee S
- Bao Y
- Baptista MS
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- Barbati C
- Bargiela A
- BarilĂ D
- Barlow PG
- Barmada SJ
- Barreiro E
- Barreto GE
- Bartek J
- Bartel B
- Bartolome A
- Barve GR
- Basagoudanavar SH
- Bassham DC
- Bast RC
- Basu A
- Batoko H
- Batten I
- Baulieu EE
- Baumgarner BL
- Bayry J
- Beale R
- Beau I
- Beaumatin F
- Bechara LRG
- Beck GR
- Beers MF
- Begun J
- Behl C
- Behrends C
- Behrens GMN
- Bei R
- Bejarano E
- Bel S
- Belaid A
- Belgareh-Touzé N
- Bellarosa C
- Belleudi F
- Bello-Morales R
- BellĂł PĂ©rez M
- Beltran JSDO
- Beltran S
- Benbrook DM
- Bendorius M
- Benitez BA
- Benito-Cuesta I
- Bensalem J
- Berchtold MW
- Berezowska S
- Bergamaschi D
- Bergami M
- Bergmann A
- Berliocchi L
- Berlioz-Torrent C
- Bernard A
- Berthoux L
- Besirli CG
- Besteiro S
- Betin VM
- Beyaert R
- Bezbradica JS
- Bhaskar K
- Bhatia-Kissova I
- Bhattacharya R
- Bhattacharya S
- Bhattacharyya S
- Bhuiyan MS
- Bhutia SK
- Bi L
- Bi X
- Biden TJ
- Bijian K
- Billes VA
- Binart N
- Bincoletto C
- Birgisdottir AB
- Bjorkoy G
- Blanco G
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- Bornhauser BC
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- Bourdenx M
- Bourgeois B
- Bourke NM
- Bousquet G
- Boya P
- Bozhkov PV
- Bozi LHM
- Bozkurt TO
- Brackney DE
- Brand-Saberi B
- Brandts CH
- Braun RJ
- Braus GH
- Bravo-Sagua R
- Bravo-San Pedro JM
- Brest P
- Bringer M-A
- Briones-Herrera A
- Broaddus VC
- Brodersen P
- Brodsky JL
- Brody SL
- Bronson PG
- Bronstein JM
- Brown CN
- Brown RE
- Brum PC
- Brumell JH
- Brunetti-Pierri N
- Bruno D
- Bryson-Richardson RJ
- Bucci C
- Buch S
- Buchan JR
- Buchrieser C
- Buckingham EM
- Budak H
- Budini M
- Bueno M
- Buitrago-Molina LE
- Bultynck G
- Burada F
- Buraschi S
- Burgoyne JR
- BurĂłn MI
- Bustos V
- Butturini E
- Byrd A
- BĂĄnrĂ©ti Ă
- BĂŒttner S
- Cabas I
- Cabrera-Benitez S
- Cadwell K
- Cai J
- Cai L
- Cai Q
- CairĂł M
- Calbet JA
- Caldwell GA
- Caldwell KA
- Call JA
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- Xiao H-T
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- Xue Y
- Yakhine-Diop SMS
- Yamaguchi M
- Yamaguchi O
- Yamamoto A
- Yamashina S
- Yan S
- Yan S-J
- Yan Z
- Yanagi Y
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- Yi-Ren Hong C-WH
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- Yip CK
- Yiu SPT
- Yoo YH
- Yoshida K
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- Yoshimori T
- Yousefi B
- Yu B
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- Yu M-L
- Yu S-W
- Yu VC
- Yu WH
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- Yu Z
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- Yuan S-SF
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- Yun J
- Yung RL
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- Zaffagnini G
- Zambelli VO
- Zanella I
- Zang QS
- Zanivan S
- Zappavigna S
- Zaragoza P
- Zarbalis KS
- Zarebkohan A
- Zarrouk A
- Zeitlin SO
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- Zeng J-D
- Zhan L
- Zhang B
- Zhang DD
- Zhang H
- Zhang H
- Zhang H
- Zhang H
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- Zhang H
- Zhang H
- Zhang H-L
- Zhang J
- Zhang J
- Zhang J-P
- Zhang KYB
- Zhang L
- Zhang L
- Zhang L
- Zhang L
- Zhang LW
- Zhang M
- Zhang P
- Zhang S
- Zhang W
- Zhang X
- Zhang X
- Zhang X
- Zhang X
- Zhang X
- Zhang X-W
- Zhang XD
- Zhang Y
- Zhang Y
- Zhang Y
- Zhang Y
- Zhang Y
- Zhang Y-D
- Zhang Y-Y
- Zhang Z
- Zhang Z
- Zhang Z
- Zhang Z
- Zhang Z
- Zhang Z
- Zhao H
- Zhao L
- Zhao S
- Zhao T
- Zhao X-F
- Zhao Y
- Zhao Y
- Zhao Y
- Zhao Y
- Zheng G
- Zheng K
- Zheng L
- Zheng S
- Zheng X-L
- Zheng Y
- Zheng Z-G
- Zhivotovsky B
- Zhong Q
- Zhou A
- Zhou B
- Zhou C
- Zhou G
- Zhou H
- Zhou H
- Zhou H
- Zhou J
- Zhou J
- Zhou J
- Zhou J
- Zhou K
- Zhou R
- Zhou X-J
- Zhou Y
- Zhou Y
- Zhou Y
- Zhou Z
- Zhou Z-Y
- Zhu B
- Zhu C
- Zhu G-Q
- Zhu H
- Zhu H
- Zhu H
- Zhu W-G
- Zhu Y
- Zhu Y
- Zhuang H
- Zhuang X
- Zientara-Rytter K
- Zimmermann CM
- Ziviani E
- Zoladek T
- Zong W-X
- Zorov DB
- Zorzano A
- Zou W
- Zou Z
- Zou Z
- Zuryn S
- Zwerschke W
- Ălvarez ĂMC
- Ăvalos Y
- Ănal G
- ĂstĂŒn S
- ÄoliÄ M
- ÄokiÄ J
- Ćœerovnik E
- Publication venue
- 'Informa UK Limited'
- Publication date
- 01/01/2021
- Field of study
In 2008, we published the first set of guidelines for standardizing research in autophagy. Since then, this topic has received increasing attention, and many scientists have entered the field. Our knowledge base and relevant new technologies have also been expanding. Thus, it is important to formulate on a regular basis updated guidelines for monitoring autophagy in different organisms. Despite numerous reviews, there continues to be confusion regarding acceptable methods to evaluate autophagy, especially in multicellular eukaryotes. Here, we present a set of guidelines for investigators to select and interpret methods to examine autophagy and related processes, and for reviewers to provide realistic and reasonable critiques of reports that are focused on these processes. These guidelines are not meant to be a dogmatic set of rules, because the appropriateness of any assay largely depends on the question being asked and the system being used. Moreover, no individual assay is perfect for every situation, calling for the use of multiple techniques to properly monitor autophagy in each experimental setting. Finally, several core components of the autophagy machinery have been implicated in distinct autophagic processes (canonical and noncanonical autophagy), implying that genetic approaches to block autophagy should rely on targeting two or more autophagy-related genes that ideally participate in distinct steps of the pathway. Along similar lines, because multiple proteins involved in autophagy also regulate other cellular pathways including apoptosis, not all of them can be used as a specific marker for bona fide autophagic responses. Here, we critically discuss current methods of assessing autophagy and the information they can, or cannot, provide. Our ultimate goal is to encourage intellectual and technical innovation in the field
Complete genome characterization of two wild-type measles viruses from Vietnamese infants during the 2014 outbreak
- Author
- Baker S
- Berto A
- Bogaardt C
- Boni MF
- Bryant JE
- Bui DP
- Campbell J
- Carrique-Mas J
- Chase-Topping M
- Cotten M
- Cotten M
- Dang MH
- Dang TH
- Dang TO
- Day JN
- Deijs M
- Dinh VT
- Dung N
- Duong AH
- Farrar JJ
- Farsani SMJ
- Hau TTT
- Ho DTN
- Hoang BL
- Hoang VD
- Huynh TKT
- Ivens A
- Jebbink MF
- Kellam P
- Kellam P
- Kiet BT
- Lam CC
- Le MH
- Le TP
- Le TP
- Le TP
- Le XL
- Lu L
- Luu TTH
- Ly VC
- Mai TPL
- Munnink BBO
- Munnink BBO
- My VTP
- My VTP
- Nadjm B
- Ngo TB
- Ngo TH
- Ngo TT
- Nguyen CT
- Nguyen D
- Nguyen DT
- Nguyen KC
- Nguyen NA
- Nguyen NV
- Nguyen QH
- Nguyen TB
- Nguyen TD
- Nguyen THT
- Nguyen THT
- Nguyen TKC
- Nguyen TLH
- Nguyen TLN
- Nguyen TM
- Nguyen TN
- Nguyen TND
- Nguyen TNL
- Nguyen TSC
- Nguyen TT
- Nguyen TV
- Nguyen TYC
- Nguyen VC
- Nguyen VH
- Nguyen VK
- Nguyen VM
- Nguyen VMH
- Nguyen VT
- Nguyen VT
- Nguyen VVC
- Nguyen VX
- Pham HA
- Pham HM
- Pham TMK
- Pham TTT
- Pham VL
- Pham VM
- Phan VBB
- Rabaa MA
- Rahman M
- Rambaut A
- Saylors K
- Simmonds P
- Ta TDN
- Thompson C
- Thwaites G
- Tran DHN
- Tran HMC
- Tran KT
- Tran MP
- Tran TH
- Tran TKH
- Tran TN
- Tran TND
- Tran TTM
- Tran TTT
- Trinh QT
- Van der Hoek L
- Van Doorn HR
- Vo BH
- Vo NT
- Vo QC
- Voong VP
- Vu TLH
- Vu TTH
- Wertheim H
- Wolfe N
- Woolhouse M
- Publication venue
- 'American Society for Microbiology'
- Publication date
- 01/01/2016
- Field of study
A large measles virus outbreak occurred across Vietnam in 2014. We identified and obtained complete measles virus genomes in stool samples collected from two diarrheal pediatric patients in Dong Thap Province. These are the first complete genome sequences of circulating measles viruses in Vietnam during the 2014 measles outbreak
Genome sequences of a novel Vietnamese bat bunyavirus
- Author
- Bach TK
- Baker S
- Berto A
- Bogaardt C
- Boni MF
- Bryant JE
- Bui DP
- Campbell JI
- Carrique-Mas J
- Chase-Topping M
- Cotten M
- Cotten M
- Dang MH
- Dang TH
- Dang TO
- Day JN
- Deijs M
- Dinh VT
- Dodd K
- Dung N
- Duong AH
- Euren J
- Farrar JJ
- Farsani SMJ
- Hau TTT
- Ho DTN
- Hoang BL
- Hoang VD
- Huong VUTL
- Huynh TKT
- Ivens AL
- Jebbink MF
- Kellam P
- Kellam P
- Lam CC
- Le MH
- Le TP
- Le TP
- Le TP
- Le XL
- Lu L
- Lucas A
- Luu TTH
- Ly VC
- Mai TPL
- Munnink BBO
- Munnink BO
- My VTP
- Nadjm B
- Ngo TB
- Ngo TH
- Ngo TT
- Nguyen CT
- Nguyen D
- Nguyen DT
- Nguyen KC
- Nguyen NA
- Nguyen NV
- Nguyen QH
- Nguyen TB
- Nguyen TD
- Nguyen THT
- Nguyen THT
- Nguyen TKC
- Nguyen TLH
- Nguyen TLN
- Nguyen TM
- Nguyen TN
- Nguyen TND
- Nguyen TNL
- Nguyen TSC
- Nguyen TT
- Nguyen TV
- Nguyen TYC
- Nguyen VC
- Nguyen VH
- Nguyen VK
- Nguyen VM
- Nguyen VMH
- Nguyen VT
- Nguyen VT
- Nguyen VVC
- Nguyen VX
- Ortiz N
- Pennacchio L
- Pham HA
- Pham HM
- Pham TMK
- Pham TTT
- Pham VL
- Pham VM
- Phan MVT
- Phan VBB
- Phan VTM
- Rabaa MA
- Rahman M
- Rambaut A
- Rubin E
- Saylors KE
- Simmonds P
- Ta TDN
- Thompson C
- Thwaites G
- Tran DHN
- Tran HMC
- Tran KT
- Tran MH
- Tran MP
- Tran TH
- Tran TKH
- Tran TN
- Tran TND
- Tran TTM
- Tran TTT
- Trinh QT
- Van der Hoek L
- Van der Hoek L
- Van Doorn HR
- Vo BH
- Vo NT
- Vo QC
- Voong VP
- Vu TTH
- Wertheim H
- Wolfe ND
- Woolhouse M
- Publication venue
- 'American Society for Microbiology'
- Publication date
- 01/01/2016
- Field of study
To document the viral zoonotic risks in Vietnam, fecal samples were systematically collected from a number of mammals in southern Vietnam and subjected to agnostic deep sequencing. We describe here novel Vietnamese bunyavirus sequences detected in bat feces. The complete L and S segments from 14 viruses were determined
Estimating the burden of selected non-communicable diseases in Africa: a systematic review of the evidence
- Author
- A Awoke
- A Damasceno
- A de-Graft Aikins
- A Giday
- A Malaza
- A Niakara
- A Omorogiuwa
- A Tran
- AP Kengne
- AP N'Gouin-Claih
- AV Chobanian
- BA Burket
- BC Ozumba
- BH Latifa
- BO Mbah
- C Agyemang
- C Laouani Kechrid
- C Nejjari
- CA Alikor
- Catriona Basquill
- CH Bunker
- CMM Lawes
- CO Amira
- D Maher
- Davies Adeloye
- DP Capingana
- DS Houinato
- E Macia
- EA Williams
- EC Ejim
- EK Oghagbon
- EO Asekun-Olarinmoye
- F Hamida
- F Mauny
- F Tesfaye
- FM Goma
- FP Cappuccio
- G Danaei
- G Musinguzi
- GH Anderson
- GI Ahaneku
- H Balshem
- H Ben Romdhane
- H Ben Romdhane
- H Ghannem
- I Hajar
- IA Suleiman
- II Ulasi
- II Ulasi
- IO Amole
- J Addo
- J Addo
- J Kayima
- J Mufunda
- J Negin
- JA Whitworth
- JE Pires
- JF Wamala
- JJE Koopman
- JK Cruickshank
- JR M'Buyamba-Kabangu
- K Mezue
- K Peltzer
- K Steyn
- K Steyn
- K Steyn
- K Yayehd
- KA Abegunde
- KP Msyamboza
- L Fezeu
- LD Nshisso
- LH Opie
- LH Opie
- M Alberts
- M Allal-Elasmi
- M Cook-Huynh
- M Dionadji
- M Suhrcke
- M Temmar
- M Thorogood
- M Twagirumukiza
- MA Tazi
- MA van der Sande
- MA van der Sande
- MD Balde
- ME Ahmed
- ME Hendriks
- MJ Dewhurst
- MM Ibrahim
- MR Mohamed
- NR Poulter
- OI Ekwunife
- OO Oladapo
- OS Ogah
- P Astagneau
- P Bovet
- P Bovet
- PB Katchunga
- PM Kearney
- R Beaglehole
- R Cooper
- R Edwards
- RA Adedoyin
- RA Adedoyin
- Renate B. Schnabel
- RM Kamadjeu
- RW Mayega
- S Baragou
- S Hammami
- S MacMahon
- SA Isezuo
- SJM Van De Vijver
- SS de Ramirez
- TA Gaziano
- TO Odugbemi
- US Ekanem
- V Mohan
- V Perkovic
- VO Omuemu
- W Mathenge
- WH Giles
- WO Erhun
- YK Seedat
- Publication venue
- 'Public Library of Science (PLoS)'
- Publication date
- 01/01/2012
- Field of study
Background
The burden of non-communicable diseases (NCDs) is rapidly increasing globally, and
particularly in Africa, where the health focus, until recently, has been on infectious diseases. The
response to this growing burden of NCDs in Africa has been affected owing to a poor
understanding of the burden of NCDs, and the relative lack of data and low level of research on
NCDs in the continent. Recent estimates on the burden of NCDs in Africa have been mostly
derived from modelling based on data from other countries imputed into African countries, and
not usually based on data originating from Africa itself. In instances where few data were
available, estimates have been characterized by extrapolation and over-modelling of the scarce
data. It is therefore believed that underestimation of NCDs burden in many parts of Africa cannot
be unexpected. With a gradual increase in average life expectancy across Africa, the region now
experiencing the fastest rate of urbanization globally, and an increase adoption of unhealthy
lifestyles, the burden of NCDs is expected to rise. This thesis will, therefore, be focussing on
understanding the prevalence, and/or where there are available data, the incidence, of four major
NCDs in Africa, which have contributed highly to the burden of NCDs, not only in Africa, but
also globally.
Methods
I conducted a systematic search of the literature on three main databases (Medline, EMBASE and
Global Health) for epidemiological studies on NCDs conducted in Africa. I retained and
extracted data from original population-based (cohort or cross sectional), and/or health service
records (hospital or registry-based studies) on prevalence and/or incidence rates of four major
NCDs in Africa. These include: cardiovascular diseases (hypertension and stroke), diabetes,
major cancer types (cervical, breast, prostate, ovary, oesophagus, bladder, Kaposi, liver, stomach,
colorectal, lung and non-Hodgkin lymphoma), and chronic respiratory diseases (chronic
obstructive pulmonary disease (COPD) and asthma). From extracted crude prevalence and
incidence rates, a random effect meta-analysis was conducted and reported for each NCD. An
epidemiological model was applied on all extracted data points. The fitted curve explaining the
largest proportion of variance (best fit) from the model was further applied. The equation
generated from the fitted curve was used to determine the prevalence and cases of the specific
NCD in Africa at midpoints of the United Nations (UN) population 5-year age-group population
estimates for Africa.
Results
From the literature search, studies on hypertension had the highest publication output at 7680, 92
of which were selected, spreading across 31 African countries. Cancer had 9762 publications and
39 were selected across 20 countries; diabetes had 3701 publications and 48 were selected across
28 countries; stroke had 1227 publications and 19 were selected across 10 countries; asthma had
790 publications and 45 were selected across 24 countries; and COPD had the lowest output with
243 publications and 13 were selected across 8 countries. From studies reporting prevalence
rates, hypertension, with a total sample size of 197734, accounted for 130.2 million cases and a
prevalence of 25.9% (23.5, 34.0) in Africa in 2010. This is followed by asthma, with a sample
size of 187904, accounting for 58.2 million cases and a prevalence of 6.6% (2.4, 7.9); COPD,
with a sample size of 24747, accounting for 26.3 million cases and a prevalence of 13.4% (9.4,
22.1); diabetes, with a sample size of 102517, accounting for 24.5 million cases and a prevalence
of 4.0% (2.7, 6.4); and stroke, with a sample size of about 6.3 million, accounting for 1.94
million cases and a prevalence of 317.3 per 100000 population (314.0, 748.2). From studies
reporting incidence rates, stroke accounted for 496 thousand new cases in Africa in 2010, with a
prevalence of 81.3 per 100000 person years (13.2, 94.9). For the 12 cancer types reviewed, a total
of 775 thousand new cases were estimated in Africa in 2010 from registry-based data covering a
total population of about 33 million. Among women, cervical cancer and breast cancer had 129
thousand and 81 thousand new cases, with incidence rates of 28.2 (22.1, 34.3) and 17.7 (13.0,
22.4) per 100000 person years, respectively. Among men, prostate cancer and Kaposi sarcoma
closely follows with 75 thousand and 74 thousand new cases, with incidence rates of 14.5 (10.9,
18.0) and 14.3 (11.9, 16.7) per 100000 person years, respectively.
Conclusion
This study suggests the prevalence rates of the four major NCDs reviewed (cardiovascular
diseases (hypertension and stroke), diabetes, major cancer types, and chronic respiratory diseases
(COPD and asthma) in Africa are high relative to global estimates. Due to the lack of data on
many NCDs across the continent, there are still doubts on the true prevalence of these diseases
relative to the current African population. There is need for improvement in health information
system and overall data management, especially at country level in Africa. Governments of
African nations, international organizations, experts and other stakeholders need to invest more
on NCDs research, particularly mortality, risk factors, and health determinants to have
evidenced-based facts on the drivers of this epidemic in the continent, and prompt better,
effective and overall public health response to NCDs in Africa
International Consensus Statement on Rhinology and Allergy: Rhinosinusitis
- Author
- Aanaes K
- Abadie WM
- Abi Najm S
- Abigail P
- Abrahams JJ
- Abrass LJ
- Abreu CB
- Abreu NA
- Abshirini H
- Abuzeid WM
- Abuzeid WM
- Achar P
- Ackerhans M
- Adam P
- Adappa ND
- Adappa ND
- Adappa ND
- Adappa ND
- Adriaensen G
- Agache I
- Aghamohammadi A
- Agius AM
- Agyeman AA
- Ahn CN
- Ahn HJ
- Ahn JC
- Ahn SH
- AhovuoâSaloranta A
- Aitken M
- Ajaiyeoba A
- Akbari E
- Akdis CA
- Akira S
- Akiyama K
- Akiyama K
- Akiyama K
- Al Komser MK
- Alam ES
- Alandejani T
- Alanin MC
- Albritton FDT
- Albu S
- Albu S
- Albu S
- Aldini G
- Alexander NS
- Aljebab F
- Alkire BC
- Allen EK
- Alobid I
- Alobid I
- Alobid I
- Aloulah M
- Alqudah M
- Alromaih S
- Alsaleh S
- Alsharif S
- Alt JA
- Alt JA
- Alt JA
- Alt JA
- Alt JA
- Alves MP
- AlâQudah M
- AlâQudah M.
- AlâQudah M.
- AlâRawi MM
- AlâShaikh S
- AlâShemari H
- AlâSwiahb JN
- Amali A
- Amar YG
- Amble FR
- American Academy of Pediatrics Steering Committee on Quality Improvement and Management (AAP SCQIM)
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- Amine M
- Amodu EJ
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- Anderson DE
- Anderson WC
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- Ankichetty SP
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- Anon JB
- AnselmoâLima WT
- Antisdel JL
- Antisdel JL
- Antunes MB
- Antunes MB
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- Anzai Y
- AnziÄ SA
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- Baba S
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- Bachert C
- Bachert C
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- Bednarski KA
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- ZielinskaâBlizniewska H
- Zou L
- Zuckerman JD
- Zurlo JJ
- Zuskin E
- Äulig J
- Publication venue
- 'Wiley'
- Publication date
- 01/01/2021
- Field of study
Background: The 5 years since the publication of the first International Consensus Statement on Allergy and Rhinology: Rhinosinusitis (ICARâRS) has witnessed foundational progress in our understanding and treatment of rhinologic disease. These advances are reflected within the more than 40 new topics covered within the ICARâRSâ2021 as well as updates to the original 140 topics. This executive summary consolidates the evidenceâbased findings of the document. Methods: ICARâRS presents over 180 topics in the forms of evidenceâbased reviews with recommendations (EBRRs), evidenceâbased reviews, and literature reviews. The highest grade structured recommendations of the EBRR sections are summarized in this executive summary. Results: ICARâRSâ2021 covers 22 topics regarding the medical management of RS, which are grade A/B and are presented in the executive summary. Additionally, 4 topics regarding the surgical management of RS are grade A/B and are presented in the executive summary. Finally, a comprehensive evidenceâbased management algorithm is provided. Conclusion: This ICARâRSâ2021 executive summary provides a compilation of the evidenceâbased recommendations for medical and surgical treatment of the most common forms of RS
Safety and efficacy of fluoxetine on functional outcome after acute stroke (AFFINITY): a randomised, double-blind, placebo-controlled trial
- Author
- -Thi Binh Nguyen
- Abul Mamun
- Ai Ling Tan
- Aicuratiya Withanage
- Aileen Wu
- Alan J. McDougall
- Alanah Bailey
- Alejandra Malavera
- Alessandro Zagami
- Alexis Brown
- Altman
- Amanda Boudville
- Amanda Masterson
- Amy Kunchok
- Amy McDonald
- An-Gia Pham
- Andrew Evans
- Andrew Granger
- Andrew H. Ford
- Andrew Lee
- Andrew Moey
- Andrew Murray
- Angela Abraham
- Anh-Hai Dam
- Anh-Ngoc Nguyen
- Anne Claxton
- Annie Winker
- Benjamin Nham
- Benjamin Trewin
- Beverley Macdonald
- Bhavesh Lallu
- Bich-Thi Doan
- Binh-Nguyen Pham
- Binh-Thanh Nguyen
- Binh-Thanh Nguyen
- Binh-Thi Thanh Nguyen
- Binh-Van Le
- Boon L. Tan
- Brett Jones
- Bronwen Pepperell
- Bruno
- BrÀnnström
- Camelia Burdusel
- Cameron Redpath
- Candice Delcourt
- Caroline Roberts
- Casey Hair
- Cassandra McLennan
- Cecilia Cappelen-Smith
- Chantal Baldwin
- Chermaine Chua
- Cheryl Carcel
- Chi-Minh Do
- Chi-Van Nguyen
- Chinh-Dinh Duong
- Chollet
- Christie Drummond
- Christopher Etherton-Beer
- Christopher Taylor
- Chun Phua
- Chung-Quang Do
- Cipriani
- Clare Williams
- Colette Sanctuary
- Colette Sanctuary
- Colette Sanctuary
- Colette Sanctuary
- Counsell
- Coupland
- Craig Davenport
- Craig S. Anderson
- Cuong-Van Pham
- Cynthia Chen
- Dai-Quoc Khuong
- Danielle Wheelwright
- Darshan Ghia
- David Blacker
- David Jackson
- David Shivlal
- de Jager
- Deborah Field
- Dennis
- Dennis Cordato
- Dev Nathani
- Diana Ramirez
- Diana Schmid
- Duncan
- Dung Do Nguyen
- Dung-Tien Nguyen
- Duong-Huu Luong
- Duong-Van Kieu
- Ehsan E. Shandiz
- Elizabeth Pepper
- Elizabeth Ray
- Emily Duckett
- Emma Siracusa
- Erik Lundström
- Essie Low
- Fintan O'Rourke
- Fix Sangvatanakul
- Gab Silver
- Gary Cheuk
- Geoffrey A. Donnan
- Giang-Truong Nguyen
- Giau-Thi Kim Tran
- Gillian E. Mead
- Gillian Edmonds
- Graeme J. Hankey
- Graham
- Gregory Carter
- Ha-Thi Hai Dinh
- Ha-Thi Thu Nguyen
- Ha-Van Mai
- Hai-Thanh Ngo
- Hanh-Cao Dang
- Hanh-Hong Dang
- Hanh-Thi Truc Phan
- Hankey
- Hannah Coyle
- Hannah Coyle
- Harry McNaughton
- Heike Burnet
- Helen Baines
- Hien-Thi Bich Nguyen
- Hillary Hayes
- Ho Choong
- Hoa-Ngoc Nguyen
- Hoa-Van Hoang
- Hoai-Thi Le
- Hong-Thi Tran
- Hop-Quang Huynh
- Howard
- Huong-Huynh To Dinh
- Huong-Thi Bich Nguyen
- Huong-Thi Nguyen
- Huy Thai
- Huy-Quoc Huynh
- Huy-Thang Nguyen
- Huyen-Ngoc Lu
- Huyen-Thanh Han
- Jenni White
- Jenni White
- Jenni White
- Jennifer Bergqvist
- Jennifer Massey
- Jeremy Christley
- Jeremy Lanford
- Jess Tsoleridis
- John Chalissery
- John Gommans
- Judith Dunne
- Julia O'Dea
- Kapila Abeysuriya
- Karen Knight
- Karen Ruddell
- Karim Mahawish
- Kate Hickey
- Katherine Mohr
- Kerri-Ann Whittaker
- Kerry Boyle
- Kerry Boyle
- Khanh-Kim Le
- Khanh-Thi Ngoc Thach
- Khoa-Duy Dao
- Kim Oakley
- Kimberley Veitch
- Kimberley Veitch
- Kimberley Veitch
- Kimberley Veitch
- Kirsty Page
- Koushik Nagesh
- Kraglund
- Lai-Kin Wong
- Lan-Tuong Vu
- Lap-Van Dinh
- Latitia Kernaghan
- Lauren Tarrant
- Laurent Billot
- Lay Kho
- Legg
- Leon Flicker
- Lim
- Lina Lee
- Lindsey Bunce
- Linh-Hai Nguyen
- Linh-Thi Cam Dam
- Linh-Thi Cam Le
- Linh-Thi My Le
- Loan-Thi Ngoc Vo
- Loan-Thi Nguyen
- Loan-Tran Truc Mai Le
- Long-Thanh Nguyen
- Long-Van Nguyen
- Lorralee Deane
- Louise Rigney
- Luisa Hewitt
- Luisa Hewitt
- Luisa Hewitt
- Luyen-Van Truong
- Ly-Thi Khanh Tran
- Lynda Southwell
- Mai-Hue Nguyen
- Maree Duroux
- Maree L. Hackett
- Maria Lopez
- Marjan Tabesh
- Mark Rollason
- Martin Jude
- Martin Krause
- Martin S. Dennis
- Mead
- Mead
- Mead
- Mead
- Megan Ewing
- Megan O'Neill
- Megan O'Neill
- Megan Ratcliffe
- Melissa Daines
- Melissa Spooner
- Merridie Rees
- Michael Pollack
- Michael Pollack
- Michelle Carr
- Michelle Tang
- Minh-Thao Nguyen
- Miriam Priglinger
- Monique Hourn
- Monique Hourn
- Monique Hourn
- Monique Hourn
- Mudassar Latif
- Na Le
- Nga-Thuy Lam
- Ngan-Thi Le
- Ngoc-Duc Ngo
- Ngoc-Hoang Nguyen
- Ngoc-Thuy Nhu Dinh
- Ngoc-Xuan Huynh
- Nha-Thi Thanh Dao
- Nhu-Quynh Truong
- Nicole O'Loughlin
- Ninh-Hong Le
- Noreen Mughal
- Norman
- Oanh-Thi Kieu Ha
- Oanh-Thi Le
- Osvaldo P. Almeida
- Patricia Morgan
- Paul Stockle
- Paula Broughton
- Pesi Katrak
- Peter New
- Phuong-Doan Nguyen
- Phuong-Hoai Tran
- Phuong-Hong Tran
- Phuong-Thai Truong
- Phuong-Thanh Trinh
- Phuong-Thi Do
- Phuong-Viet Dao
- Qi Cheng
- Qi Cheng
- Qiang Li
- Qilong Yi
- Queenie Leung
- Quoc-Nguyen Bao Pham
- Quyen-Thi Ngoc Pham
- Quynh-Nhu Le
- Rachael McCoy
- Rachael McQueen
- Ramesh Sahathevan
- Raymond Kumar
- Richard Geraghty
- Richard I. Lindley
- Robert Herbert
- Romesh Markus
- Rosanna Robertson
- Sally Ormond
- Sam Akbari
- Sam Akbari
- Sam Bolitho
- Sam-Hoanh Nguyen
- Samantha Shone
- Sandercock
- Sang-Van Nguyen
- Sara Laubscher
- Sarah Barrett
- Sarah Mccormack
- Severine Bompoint
- Shabeel Askar
- Shenae Peterson
- Sherisse Celestino
- Si-Tri Le
- Stanley Levy
- Steel
- Stephen Davis
- Stephen Jan
- Steven Faux
- Sumana Gopinath
- Sung-Phuoc Pham
- Susan Day
- Susan DeCaigney
- Susan Walker
- Tabitha Hartwell
- Tai-Anh Nguyen
- Tai-Ngoc Tran
- Tam-Nhat Dang
- Tan-Van Vo
- Thai-Nguyen Thanh Pham
- Tham-Hong Pham
- Thang-Ba Nguyen
- Thanh-Trung Tran
- Thao-Thi Thu Nguyen
- Thomas Lung
- Thuc-Van Tran
- Thuong-Thi Huyen Dang
- Thuy-Anh Diem Nguyen
- Thuy-Le Vu Kieu
- Thuy-Thi Vu
- Timothy Kleinig
- Timothy R. Bates
- Tissa Wijeratne
- Toan-Dinh Le
- Ton-Duy Mai
- Toni Withiel
- Tram-Ngoc Bui
- Tram-Thi Bich Ngo
- Trang-Le Huyen Nguyen
- Trang-Mai Tong
- Trang-Thi Huyen Le
- Trinh-Thi Kim Ngo
- Trung-Xuan Vuong
- Tuan-Quoc Dinh
- Tuan-Van Le
- Tue-Chau Bui
- Tuyen-Van Nguyen
- Uyen-Ha Hong
- Uyen-Thi To Hoang
- van der Vliet
- Vanessa Maxwell
- Vathani Surendran
- Veronica Duque
- Veronica Murray
- Vien-Chi Le
- Vinh-Phuong Do
- Vishal Patel
- Vivian Fu
- Vy-Tuong Nguyen
- Wang
- Ware
- Williams
- Wilson Vallat
- Yash Gawarikar
- Ye Min Kuang
- Yen-Bao Mai
- Yen-Hai Nguyen
- Yvonne Liu
- Zeljka Calic
- Publication venue
- 'Elsevier BV'
- Publication date
- 01/01/2020
- Field of study
Background
Trials of fluoxetine for recovery after stroke report conflicting results. The Assessment oF FluoxetINe In sTroke recoverY (AFFINITY) trial aimed to show if daily oral fluoxetine for 6 months after stroke improves functional outcome in an ethnically diverse population.
Methods
AFFINITY was a randomised, parallel-group, double-blind, placebo-controlled trial done in 43 hospital stroke units in Australia (n=29), New Zealand (four), and Vietnam (ten). Eligible patients were adults (aged â„18 years) with a clinical diagnosis of acute stroke in the previous 2â15 days, brain imaging consistent with ischaemic or haemorrhagic stroke, and a persisting neurological deficit that produced a modified Rankin Scale (mRS) score of 1 or more. Patients were randomly assigned 1:1 via a web-based system using a minimisation algorithm to once daily, oral fluoxetine 20 mg capsules or matching placebo for 6 months. Patients, carers, investigators, and outcome assessors were masked to the treatment allocation. The primary outcome was functional status, measured by the mRS, at 6 months. The primary analysis was an ordinal logistic regression of the mRS at 6 months, adjusted for minimisation variables. Primary and safety analyses were done according to the patient's treatment allocation. The trial is registered with the Australian New Zealand Clinical Trials Registry, ACTRN12611000774921.
Findings
Between Jan 11, 2013, and June 30, 2019, 1280 patients were recruited in Australia (n=532), New Zealand (n=42), and Vietnam (n=706), of whom 642 were randomly assigned to fluoxetine and 638 were randomly assigned to placebo. Mean duration of trial treatment was 167 days (SD 48·1). At 6 months, mRS data were available in 624 (97%) patients in the fluoxetine group and 632 (99%) in the placebo group. The distribution of mRS categories was similar in the fluoxetine and placebo groups (adjusted common odds ratio 0·94, 95% CI 0·76â1·15; p=0·53). Compared with patients in the placebo group, patients in the fluoxetine group had more falls (20 [3%] vs seven [1%]; p=0·018), bone fractures (19 [3%] vs six [1%]; p=0·014), and epileptic seizures (ten [2%] vs two [<1%]; p=0·038) at 6 months.
Interpretation
Oral fluoxetine 20 mg daily for 6 months after acute stroke did not improve functional outcome and increased the risk of falls, bone fractures, and epileptic seizures. These results do not support the use of fluoxetine to improve functional outcome after stroke
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