274 research outputs found
Mapping inequalities in exclusive breastfeeding in low- and middle-income countries, 2000â2018
- Author
- Abady GG
- Abd-Allah F
- Abdelalim A
- Abebo ZH
- Abejie AN
- Abosetugn AE
- Abreu LG
- Abrigo MRM
- Abu-Gharbieh E
- Abushouk AI
- Adamu AL
- Adedeji IA
- Adegbosin AE
- Adekanmbi V
- Adetokunboh OO
- Agudelo-Botero M
- Aji B
- Akinyemi OO
- Alamneh AA
- Alanezi FM
- Alanzi TM
- Albright J
- Alcalde-Rabanal JE
- Alemu BW
- Alhassan RK
- Ali BA
- Ali S
- Alinia C
- Alipour V
- Amit AML
- Amugsi DA
- Anbesu EW
- Ancuceanu R
- Anjomshoa M
- Ansari F
- Antonio CAT
- Anvari D
- Arabloo J
- Arora A
- Artanti KD
- Asemahagn MA
- Asmare WN
- Atout MMW
- Ausloos M
- Awoke N
- Ayanore MA
- Aynalem YA
- Ayza MA
- Azene ZN
- Badiye AD
- Baig AA
- Bakkannavar SM
- Banach M
- Banik PC
- Basaleem H
- Bayati M
- Baye BA
- Bedi N
- Belay SA
- Bhagavathula AS
- Bhandari D
- Bhardwaj N
- Bhardwaj P
- Bhattacharjee NV
- Bhutta ZA
- Bijani A
- Birhan TA
- Birihane BM
- Bitew ZW
- Bohlouli S
- Bohluli M
- Bojia HA
- Boloor A
- Brady OJ
- Bragazzi NL
- Brunoni AR
- Budhathoki SS
- Butt ZA
- BĂ€rnighausen TW
- Castaldelli-Maia JM
- Castro F
- Cernigliaro A
- Charan J
- Chatterjee P
- Chatterjee S
- Chattu VK
- Chaturvedi S
- Chowdhury MAK
- Chu D-T
- Collison ML
- Cook AJ
- Cork MA
- Couto RAS
- CĂĄrdenas R
- Dagnew B
- Dai H
- Dandona L
- Dandona R
- Daneshpajouhnejad P
- Darshan BB
- Darwesh AM
- Darwish AH
- Daryani A
- Das JK
- Davis AC
- de Hidru, HD
- Denova-Gutiérrez E
- Deribe K
- Desalew A
- Deshpande A
- Dessie A
- Deuba K
- Dharmaratne SD
- Dhimal M
- Dhungana GP
- Diaz D
- Didarloo A
- Dipeolu IO
- Doan LP
- Donkers KM
- Duko B
- Duraes AR
- Dwyer-Lindgren L
- DĂĄvila-Cervantes CA
- Earl L
- El-Jaafary SI
- Elema TB
- Elhabashy HR
- Faris PS
- Faro A
- Farzadfar F
- Feigin VL
- Feleke BE
- Ferede TY
- Fischer F
- Foigt NA
- Folayan MO
- Franklin RC
- Gad MM
- Gaidhane S
- Gardner WM
- Geberemariyam BS
- Gebregiorgis BG
- Gebremedhin KB
- Gebremichael B
- Ghaffarpasand F
- Gilani SA
- Ginindza TG
- Glagn M
- Golechha M
- Gonfa KB
- Goulart BNG
- Gudi N
- Guido D
- Guled RA
- Guo Y
- Gupta RD
- Hamidi S
- Handiso DW
- Hasaballah AI
- Hassan A
- Hay SI
- Hay SI
- Hayat K
- Hegazy MI
- Heidari B
- Henry NJ
- Herteliu C
- Ho HC
- Hoang CL
- Holla R
- Hon J
- Hosseini M
- Hosseinzadeh M
- Househ M
- Hsairi M
- Hu G
- Huda TM
- Hwang B-F
- Ibitoye SE
- Ilesanmi OS
- Ilic IM
- Ilic MD
- Inbaraj LR
- Iqbal U
- Irvani SSN
- Islam MM
- Iwu CCD
- Iwu CJ
- Jain A
- Janodia MD
- Javaheri T
- John-Akinola YO
- Johnson KB
- Joukar F
- Jozwiak JJ
- Jr
- Kabir A
- Kalankesh LR
- Kalhor R
- Kamath A
- Kamyari N
- Kanchan OT
- Kapoor N
- Karimi SE
- Karyani AK
- Kasaye HK
- Kassahun G
- Kassebaum NJ
- Kayode GA
- Keiyoro PN
- Kelkay B
- Khalid N
- Khan MN
- Khaneghah AM
- Khatab K
- Khater AM
- Khater MM
- Khatib MN
- Kim YJ
- Kimokoti RW
- Kinyoki DK
- Kisa A
- Kisa S
- Kosen S
- Krishan K
- Kulkarni V
- Kumar GA
- Kumar M
- Kumar N
- Kumar P
- Kurmi OP
- Kusuma D
- Lad SD
- Lami FH
- Landires I
- Lansingh VC
- Lasrado S
- Lazzar-Atwood A
- Lee PH
- LeGrand KE
- Letourneau ID
- Lewycka S
- Li B
- Li M-C
- Li S
- Liu X
- Local Burden of Disease Exclusive Breastfeeding Collaborators
- Lodha R
- Lopez JCF
- Louie C
- Lu D
- Machado DB
- Mahesh PA
- Maled V
- Maleki S
- Malta DC
- Mamun AA
- Manafi N
- Mansournia MA
- Mapoma CC
- Marczak LB
- Martins-Melo FR
- Matin BK
- Mehndiratta MM
- Mejia-Rodriguez F
- Mekonnen TC
- Mendoza W
- Menezes RG
- Mengesha EW
- Mersha AM
- Miller TR
- Mini GK
- Mirrakhimov EM
- Misra S
- Moghadaszadeh M
- Mohammad DK
- Mohammadian-Hafshejani A
- Mohammed JA
- Mohammed S
- Mokdad AH
- Montero-Zamora PA
- Moradi M
- Moradzadeh R
- Moraga P
- Mosser JF
- Mousavi SM
- Munro SB
- Muriithi MK
- Mustafa G
- Muthupandian S
- Nagaraja SB
- Nagarajan AJ
- Naik G
- Naimzada MD
- Nangia V
- Nascimento BR
- Nayak VC
- Ndejjo R
- Ndwandwe DE
- Negoi I
- Nguefack-Tsague G
- Ngunjiri JW
- Nguyen CT
- Nguyen DN
- Nguyen HLT
- Nigussie SN
- Nigussie TTN
- Nikbakhsh R
- Nnaji CA
- Nunez-Samudio V
- Oancea B
- Oghenetega OB
- Olagunju AT
- Olusanya BO
- Olusanya JO
- Omer MO
- Onwujekwe OE
- Ortega-Altamirano DV
- Osgood-Zimmerman AE
- Otstavnov N
- Otstavnov SS
- Owolabi MO
- Padubidri JR
- Pana A
- Pandey A
- Pandi-Perumal SR
- Pangaribuan HU
- Parsekar SS
- Pasupula DK
- Patel UK
- Pathak A
- Pathak M
- Pattanshetty SM
- Patton GC
- Paulos K
- Pepito VCF
- Pickering BV
- Pinheiro M
- Piwoz EG
- Pokhrel KN
- Pourjafar H
- Prada SI
- Pribadi DRA
- Quintanilla BPA
- Rabiee M
- Rabiee N
- Rahim F
- Rahimzadeh S
- Rahman A
- Rahman MHU
- Rahmani AM
- Rai RK
- Ranabhat CL
- Rao SJ
- Rastogi P
- Rathi P
- Rawaf DL
- Rawaf S
- Rawassizadeh R
- Rawat R
- Rawat R
- Regassa LD
- Rego MAS
- Reiner RC
- Reshmi B
- Rezapour A
- Ribeiro AI
- Rickard J
- Roever L
- Rumisha SF
- Rwegerera GM
- Sagar R
- Sajadi SM
- Salem MR
- Samy AM
- Santric-Milicevic MM
- Saraswathy SYI
- Sarker AR
- Sartorius B
- Sathian B
- Saxena D
- Sbarra AN
- Schaeffer LE
- Schipp MF
- Sengupta D
- Senthilkumaran S
- Sha F
- Shafaat O
- Shaheen AA
- Shaikh MA
- Shalash AS
- Shannawaz M
- Sheikh A
- Shetty BSK
- Shetty RS
- Shibuya K
- Shiferaw WS
- Shin JI
- Silva DAS
- Singh NP
- Singh P
- Singh S
- Sintayehu Y
- Skryabin VY
- Skryabina AA
- Soheili A
- Soltani S
- Sorrie MB
- Spurlock EE
- Steuben KM
- Sudaryanto A
- Sufiyan MB
- Swartz SJ
- Syed ZQ
- Tadesse EG
- Tamiru AT
- Tantawi ME
- Tapak L
- Tareque MI
- Tarigan IU
- Tesema GA
- Tesfay FH
- Teshome A
- Tessema ZT
- Thankappan KR
- Thapar R
- Thomas N
- Topor-Madry R
- Tovani-Palone MR
- Traini E
- Tran BX
- Truong PN
- Tsegaye BTBT
- Ullah I
- Umeokonkwo CD
- Unnikrishnan B
- Upadhyay E
- Uzochukwu BSC
- VanderHeide JD
- Vecchia CL
- Violante FS
- Vo B
- Wado YD
- Waheed Y
- Wamai RG
- Wang F
- Wang Y
- Wang Y-P
- Weaver ND
- Wickramasinghe ND
- Wiens KE
- Wiysonge CS
- Woyczynski L
- Wu A-M
- Wu C
- Yamada T
- Yaya S
- Yeshaneh A
- Yeshaw Y
- Yeshitila YG
- Yilma MT
- Yip P
- Yonemoto N
- Yosef T
- Younis MZ
- Yousuf AY
- Yu C
- Yu Y
- Yuce D
- Zafar S
- Zaidi SS
- Zaki L
- Zaki MES
- Zakzuk J
- Zamanian M
- Zar HJ
- Zastrozhin MS
- Zastrozhina A
- Zelellw DA
- Zhang Y
- Zhang Z-J
- Zhao X-JG
- Zodpey S
- Zuniga YMH
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/01/2021
- Field of study
Exclusive breastfeeding (EBF)-giving infants only breast-milk for the first 6 months of life-is a component of optimal breastfeeding practices effective in preventing child morbidity and mortality. EBF practices are known to vary by population and comparable subnational estimates of prevalence and progress across low- and middle-income countries (LMICs) are required for planning policy and interventions. Here we present a geospatial analysis of EBF prevalence estimates from 2000 to 2018 across 94 LMICs mapped to policy-relevant administrative units (for example, districts), quantify subnational inequalities and their changes over time, and estimate probabilities of meeting the World Health Organization's Global Nutrition Target (WHO GNT) of â„70% EBF prevalence by 2030. While six LMICs are projected to meet the WHO GNT of â„70% EBF prevalence at a national scale, only three are predicted to meet the target in all their district-level units by 2030.This work was primarily supported by grant no. OPP1132415 from the Bill & Melinda Gates Foundation. Co-authors used by the Bill & Melinda Gates Foundation (E.G.P. and R.R.3) provided feedback on initial maps and drafts of this manuscript. L.G.A. has received support from Coordenação de Aperfeiçoamento de Pessoal de NĂvel Superior, Brasil (CAPES), CĂłdigo de Financiamento 001 and Conselho Nacional de Desenvolvimento CientĂfico e TecnolĂłgico (CNPq) (grant nos. 404710/2018-2 and 310797/2019-5). O.O.Adetokunboh acknowledges the National Research Foundation, Department of Science and Innovation and South African Centre for Epidemiological Modelling and Analysis. M.Ausloos, A.Pana and C.H. are partially supported by a grant from the Romanian National Authority for Scientific Research and Innovation, CNDS-UEFISCDI, project no. PN-III-P4-ID-PCCF-2016-0084. P.C.B. would like to acknowledge the support of F. Alam and A. Hussain. T.W.B. was supported by the Alexander von Humboldt Foundation through the Alexander von Humboldt Professor award, funded by the German Federal Ministry of Education and Research. K.Deribe is supported by the Wellcome Trust (grant no. 201900/Z/16/Z) as part of his international intermediate fellowship. C.H. and A.Pana are partially supported by a grant of the Romanian National Authority for Scientific Research and Innovation, CNDS-UEFISCDI, project no. PN-III-P2-2.1-SOL-2020-2-0351. B.Hwang is partially supported by China Medical University (CMU109-MF-63), Taichung, Taiwan. M.Khan acknowledges Jatiya Kabi Kazi Nazrul Islam University for their support. A.M.K. acknowledges the other collaborators and the corresponding author. Y.K. was supported by the Research Management Centre, Xiamen University Malaysia (grant no. XMUMRF/2020-C6/ITM/0004). K.Krishan is supported by a DST PURSE grant and UGC Centre of Advanced Study (CAS II) awarded to the Department of Anthropology, Panjab University, Chandigarh, India. M.Kumar would like to acknowledge FIC/NIH K43 TW010716-03. I.L. is a member of the Sistema Nacional de InvestigaciĂłn (SNI), which is supported by the SecretarĂa Nacional de Ciencia, TecnologĂa e InnovaciĂłn (SENACYT), PanamĂĄ. M.L. was supported by China Medical University, Taiwan (CMU109-N-22 and CMU109-MF-118). W.M. is currently a programme analyst in Population and Development at the United Nations Population Fund (UNFPA) Country Office in Peru, which does not necessarily endorses this study. D.E.N. acknowledges Cochrane South Africa, South African Medical Research Council. G.C.P. is supported by an NHMRC research fellowship. P.Rathi acknowledges support from Kasturba Medical College, Mangalore, Manipal Academy of Higher Education, Manipal, India. Ramu Rawat acknowledges the support of the GBD Secretariat for supporting the reviewing and collaboration of this paper. B.R. acknowledges support from Manipal College of Health Professions, Manipal Academy of Higher Education, Manipal. A.Ribeiro was supported by National Funds through FCT, under the programme of âStimulus of Scientific EmploymentâIndividual Supportâ within the contract no. info:eu-repo/grantAgreement/FCT/CEEC IND 2018/CEECIND/02386/2018/CP1538/CT0001/PT. S.Sajadi acknowledges colleagues at Global Burden of Diseases and Local Burden of Disease. A.M.S. acknowledges the support from the Egyptian Fulbright Mission Program. F.S. was supported by the Shenzhen Science and Technology Program (grant no. KQTD20190929172835662). A.Sheikh is supported by Health Data Research UK. B.K.S. acknowledges Kasturba Medical College, Mangalore, Manipal Academy of Higher Education, Manipal for all the academic support. B.U. acknowledges support from Manipal Academy of Higher Education, Manipal. C.S.W. is supported by the South African Medical Research Council. Y.Z. was supported by Science and Technology Research Project of Hubei Provincial Department of Education (grant no. Q20201104) and Outstanding Young and Middle-aged Technology Innovation Team Project of Hubei Provincial Department of Education (grant no. T2020003). The funders of the study had no role in study design, data collection and analysis, decision to publish or preparation of the manuscript. The corresponding author had full access to all the data in the study and had final responsibility for the decision to submit for publication. All maps presented in this study are generated by the authors and no permissions are required to publish them
Mapping geographical inequalities in access to drinking water and sanitation facilities in low-income and middle-income countries, 2000-17
- Author
- Abbastabar H
- Abd-Allah F
- Abdelalim A
- Abdollahpour I
- Abegaz KH
- Abejie AN
- Abreu LG
- Abrigo MRM
- Abualhasan A
- Accrombessi MMK
- Adamu AA
- Adebayo OM
- Adedeji IA
- Adedoyin RA
- Adekanmbi V
- Adetokunboh OO
- Adhikari TB
- Afarideh M
- Agudelo-Botero M
- Ahmadi K
- Ahmadi M
- Ahmed AE
- Ahmed MB
- Akalu TY
- Akanda AS
- Al-Aly Z
- Al-Mekhlafi HM
- Alahdab F
- Alam N
- Alam S
- Alamene GM
- Alanzi TM
- Albright J
- Albujeer A
- Alcalde-Rabanal JE
- Alebel A
- Alemu ZA
- Ali M
- Alijanzadeh M
- Alipour V
- Aljunid SM
- Almasi A
- Almasi-Hashiani A
- Altirkawi KA
- Alvis-Guzman N
- Alvis-Zakzuk NJ
- Amini S
- Amit AML
- Amul GGH
- Andrei CL
- Anjomshoa M
- Ansariadi A
- Antonio CAT
- Antony B
- Antriyandarti E
- Arabloo J
- Aref HMA
- Aremu O
- Armoon B
- Arora A
- Aryal KK
- Arzani A
- Asadi-Aliabadi M
- Asmelash D
- Atalay HT
- Athari SM
- Athari SS
- Atre SR
- Ausloos M
- Awasthi S
- Awoke N
- Ayala Quintanilla BP
- Ayano G
- Ayanore MA
- Aynalem YA
- Azari S
- Azman AS
- Babaee E
- Badawi A
- Bagherzadeh M
- Bakkannavar SM
- Balakrishnan S
- Banach M
- Banoub JAM
- Barac A
- Barboza MA
- Basu S
- Baumann MM
- Bay VD
- Bayati M
- Bedi N
- Beheshti M
- Behzadifar M
- Behzadifar M
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- Berbada DA
- Bernstein RS
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- Bhattacharyya K
- Bhaumik S
- Bhutta ZA
- Bijani A
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- Bin Sayeed MS
- Biswas RK
- Blacker BF
- Bohlouli S
- Boufous S
- Brady OJ
- Briko AN
- Briko NI
- Britton GB
- Brown A
- Burugina Nagaraja S
- Butt ZA
- BĂ€rnighausen TW
- Campos-Nonato IR
- Campuzano Rincon JC
- Cano J
- Car J
- Carvalho F
- Castañeda-Orjuela CA
- Castro F
- Cerin E
- Chalise B
- Chattu VK
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- Christopher DJ
- Chu D-T
- Cormier NM
- Costa VM
- Cromwell EA
- CĂĄmera LA
- CĂĄrdenas R
- Dadi AFF
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- Dahlawi SMA
- Dandona L
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- Darwesh AM
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- Das Gupta R
- Das JK
- Dash AP
- Davis Weaver N
- De la Hoz FP
- De Neve J-W
- Demissie DB
- Demoz GT
- Denova-Gutiérrez E
- Deribe K
- Desalew A
- Deshpande A
- Dharmaratne SD
- Dhillon P
- Dhimal M
- Dhungana GP
- Diaz D
- Dipeolu IO
- Do HT
- Dolecek C
- Doyle KE
- Dubljanin E
- Duraes AR
- DĂĄvila-Cervantes CA
- Edinur HA
- Effiong A
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- Elkout H
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- Enany S
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- Etemadi A
- Ezekannagha O
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- Fareed M
- Faro A
- Farzadfar F
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- Fazlzadeh M
- Feigin VL
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- Fentahun N
- Fereshtehnejad S-M
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- Filip I
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- Foigt NA
- Folayan MO
- Foroutan M
- Franklin RC
- Frostad JJ
- Fukumoto T
- Gad MM
- Garcia GM
- Gatotoh AM
- Gayesa RT
- Gebremedhin KB
- Geramo YCD
- Gesesew HA
- Gezae KE
- Ghashghaee A
- Ghazi Sherbaf F
- Gill PS
- Gill TK
- Ginindza TG
- Girmay A
- Gizaw Z
- Goodridge A
- Gopalani SV
- Goulart AC
- Goulart BNG
- Grada A
- Green MS
- Gubari MIM
- Gugnani HC
- Guido D
- GuimarĂŁes RA
- Guo Y
- Gupta R
- Gupta R
- Ha GH
- Haagsma JA
- Hafezi-Nejad N
- Haile DH
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- Handiso DW
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- Hasaballah AI
- Hasan MM
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- Hassen HY
- Hay SI
- Hayelom DH
- Hegazy MI
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- Herteliu C
- Heydarpour F
- Hidru HDD
- Hird TR
- Hoang CL
- Hollerich GI
- Hoogar P
- Hossain N
- Hosseinzadeh M
- Househ M
- Hu G
- Humayun A
- Hussain SA
- Hussen MAA
- Ibitoye SE
- Ilesanmi OS
- Ilic MD
- Imani-Nasab MH
- Iqbal U
- Irvani SSN
- Islam SMS
- Ivers RQ
- Iwu CJ
- Jahanmehr N
- Jakovljevic M
- Jalali A
- Jayatilleke AU
- Jenabi E
- Jha RP
- Jha V
- Ji JS
- Johnson KB
- Jonas JB
- Jozwiak JJ
- Kabir A
- Kabir Z
- Kanchan T
- Karch A
- Karki S
- Kasaeian A
- Kasahun GG
- Kasaye HK
- Kassa GG
- Kassa GM
- Kayode GA
- Kebede MM
- Keiyoro PN
- Ketema DB
- Khader YS
- Khafaie MA
- Khalid N
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- Khan EA
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- Khatab K
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- Khosravi MH
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- Kiadaliri A
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- Komaki H
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- Koyanagi A
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- Lansingh VC
- Lasrado S
- Lebedev G
- Lee PH
- LeGrand KE
- Leili M
- Lenjebo TL
- Leshargie CT
- Levine AJ
- Lewycka S
- Li S
- Lindstedt PA
- Linn S
- Liu S
- Lopez JCF
- Lopukhov PD
- Magdy Abd El Razek M
- Mahadeshwara Prasad DR
- Mahasha PW
- Mahotra NB
- Majeed A
- Malekzadeh R
- Malta DC
- Mamun AA
- Manafi N
- Mansournia MA
- Mapoma CC
- Martinez G
- Martini S
- Martins-Melo FR
- Mathur MR
- Mayala BK
- Mazidi M
- McAlinden C
- Meharie BG
- Mehndiratta MM
- Mehrabi Nasab E
- Mehta KM
- Mekonnen T
- Mekonnen TC
- Meles GG
- Meles HG
- Memiah PTN
- Memish ZA
- Mendoza W
- Menezes RG
- Mereta ST
- Meretoja TJ
- Mestrovic T
- Metekiya WM
- Metekiya WM
- Miazgowski B
- Miller TR
- Miller-Petrie MK
- Mini GK
- Mirrakhimov EM
- Moazen B
- Mohajer B
- Mohammad Gholi Mezerji N
- Mohammad DK
- Mohammad Y
- Mohammadibakhsh R
- Mohammed H
- Mohammed JA
- Mohammed S
- Mohebi F
- Mokdad AH
- Moodley Y
- Moradi G
- Moradi M
- Moradi-Joo M
- Moraga P
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- Mosapour A
- Mosser JF
- Mouodi S
- Mousavi SM
- Mozaffor M
- Munro SB
- Muriithi MK
- Murray CJL
- Musa KI
- Mustafa G
- Muthupandian S
- Naderi M
- Nagarajan AJ
- Naghavi M
- Naik G
- Nangia V
- Nascimento BR
- Nazari J
- Ndwandwe DE
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- Netsere HB
- Ngunjiri JW
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- Nigatu SG
- Ningrum DNA
- Nnaji CA
- Nojomi M
- Norheim OF
- Noubiap JJ
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- Oh I-H
- Olagunju AT
- Olusanya BO
- Olusanya JO
- Onwujekwe OE
- Ortega-Altamirano DV
- Osarenotor O
- Osei FB
- Owolabi MO
- P A M
- Padubidri JR
- Pakhale S
- Pana A
- Park E-K
- Patel SK
- Pathak A
- Patle A
- Paulos K
- Pepito VCF
- Perico N
- Pervaiz A
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- Ziapour A
- Zodpey S
- Zuniga YMH
- Publication venue
- Publication date
- 01/01/2020
- Field of study
Background Universal access to safe drinking water and sanitation facilities is an essential human right, recognised in the Sustainable Development Goals as crucial for preventing disease and improving human wellbeing. Comprehensive, high-resolution estimates are important to inform progress towards achieving this goal. We aimed to produce high-resolution geospatial estimates of access to drinking water and sanitation facilities. Methods We used a Bayesian geostatistical model and data from 600 sources across more than 88 low-income and middle-income countries (LMICs) to estimate access to drinking water and sanitation facilities on continuous continent-wide surfaces from 2000 to 2017, and aggregated results to policy-relevant administrative units. We estimated mutually exclusive and collectively exhaustive subcategories of facilities for drinking water (piped water on or off premises, other improved facilities, unimproved, and surface water) and sanitation facilities (septic or sewer sanitation, other improved, unimproved, and open defecation) with use of ordinal regression. We also estimated the number of diarrhoeal deaths in children younger than 5 years attributed to unsafe facilities and estimated deaths that were averted by increased access to safe facilities in 2017, and analysed geographical inequality in access within LMICs. Findings Across LMICs, access to both piped water and improved water overall increased between 2000 and 2017, with progress varying spatially. For piped water, the safest water facility type, access increased from 40.0% (95% uncertainty interval [UI] 39.4-40.7) to 50.3% (50.0-50.5), but was lowest in sub-Saharan Africa, where access to piped water was mostly concentrated in urban centres. Access to both sewer or septic sanitation and improved sanitation overall also increased across all LMICs during the study period. For sewer or septic sanitation, access was 46.3% (95% UI 46.1-46.5) in 2017, compared with 28.7% (28.5-29.0) in 2000. Although some units improved access to the safest drinking water or sanitation facilities since 2000, a large absolute number of people continued to not have access in several units with high access to such facilities (>80%) in 2017. More than 253 000 people did not have access to sewer or septic sanitation facilities in the city of Harare, Zimbabwe, despite 88.6% (95% UI 87.2-89.7) access overall. Many units were able to transition from the least safe facilities in 2000 to safe facilities by 2017; for units in which populations primarily practised open defecation in 2000, 686 (95% UI 664-711) of the 1830 (1797-1863) units transitioned to the use of improved sanitation. Geographical disparities in access to improved water across units decreased in 76.1% (95% UI 71.6-80.7) of countries from 2000 to 2017, and in 53.9% (50.6-59.6) of countries for access to improved sanitation, but remained evident subnationally in most countries in 2017. Interpretation Our estimates, combined with geospatial trends in diarrhoeal burden, identify where efforts to increase access to safe drinking water and sanitation facilities are most needed. By highlighting areas with successful approaches or in need of targeted interventions, our estimates can enable precision public health to effectively progress towards universal access to safe water and sanitation. Copyright (C) 2020 The Author(s). Published by Elsevier Ltd.Peer reviewe
Global age-sex-specific fertility, mortality, healthy life expectancy (HALE), and population estimates in 204 countries and territories, 1950-2019 : a comprehensive demographic analysis for the Global Burden of Disease Study 2019
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- Abbasi-Kangevari M
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- Abd El Razek HM
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- Publication venue
- Publication date
- 01/01/2020
- Field of study
Background Accurate and up-to-date assessment of demographic metrics is crucial for understanding a wide range of social, economic, and public health issues that affect populations worldwide. The Global Burden of Diseases, Injuries, and Risk Factors Study (GBD) 2019 produced updated and comprehensive demographic assessments of the key indicators of fertility, mortality, migration, and population for 204 countries and territories and selected subnational locations from 1950 to 2019. Methods 8078 country-years of vital registration and sample registration data, 938 surveys, 349 censuses, and 238 other sources were identified and used to estimate age-specific fertility. Spatiotemporal Gaussian process regression (ST-GPR) was used to generate age-specific fertility rates for 5-year age groups between ages 15 and 49 years. With extensions to age groups 10-14 and 50-54 years, the total fertility rate (TFR) was then aggregated using the estimated age-specific fertility between ages 10 and 54 years. 7417 sources were used for under-5 mortality estimation and 7355 for adult mortality. ST-GPR was used to synthesise data sources after correction for known biases. Adult mortality was measured as the probability of death between ages 15 and 60 years based on vital registration, sample registration, and sibling histories, and was also estimated using ST-GPR. HIV-free life tables were then estimated using estimates of under-5 and adult mortality rates using a relational model life table system created for GBD, which closely tracks observed age-specific mortality rates from complete vital registration when available. Independent estimates of HIV-specific mortality generated by an epidemiological analysis of HIV prevalence surveys and antenatal clinic serosurveillance and other sources were incorporated into the estimates in countries with large epidemics. Annual and single-year age estimates of net migration and population for each country and territory were generated using a Bayesian hierarchical cohort component model that analysed estimated age-specific fertility and mortality rates along with 1250 censuses and 747 population registry years. We classified location-years into seven categories on the basis of the natural rate of increase in population (calculated by subtracting the crude death rate from the crude birth rate) and the net migration rate. We computed healthy life expectancy (HALE) using years lived with disability (YLDs) per capita, life tables, and standard demographic methods. Uncertainty was propagated throughout the demographic estimation process, including fertility, mortality, and population, with 1000 draw-level estimates produced for each metric. Findings The global TFR decreased from 2.72 (95% uncertainty interval [UI] 2.66-2.79) in 2000 to 2.31 (2.17-2.46) in 2019. Global annual livebirths increased from 134.5 million (131.5-137.8) in 2000 to a peak of 139.6 million (133.0-146.9) in 2016. Global livebirths then declined to 135.3 million (127.2-144.1) in 2019. Of the 204 countries and territories included in this study, in 2019, 102 had a TFR lower than 2.1, which is considered a good approximation of replacement-level fertility. All countries in sub-Saharan Africa had TFRs above replacement level in 2019 and accounted for 27.1% (95% UI 26.4-27.8) of global livebirths. Global life expectancy at birth increased from 67.2 years (95% UI 66.8-67.6) in 2000 to 73.5 years (72.8-74.3) in 2019. The total number of deaths increased from 50.7 million (49.5-51.9) in 2000 to 56.5 million (53.7-59.2) in 2019. Under-5 deaths declined from 9.6 million (9.1-10.3) in 2000 to 5.0 million (4.3-6.0) in 2019. Global population increased by 25.7%, from 6.2 billion (6.0-6.3) in 2000 to 7.7 billion (7.5-8.0) in 2019. In 2019, 34 countries had negative natural rates of increase; in 17 of these, the population declined because immigration was not sufficient to counteract the negative rate of decline. Globally, HALE increased from 58.6 years (56.1-60.8) in 2000 to 63.5 years (60.8-66.1) in 2019. HALE increased in 202 of 204 countries and territories between 2000 and 2019. Interpretation Over the past 20 years, fertility rates have been dropping steadily and life expectancy has been increasing, with few exceptions. Much of this change follows historical patterns linking social and economic determinants, such as those captured by the GBD Socio-demographic Index, with demographic outcomes. More recently, several countries have experienced a combination of low fertility and stagnating improvement in mortality rates, pushing more populations into the late stages of the demographic transition. Tracking demographic change and the emergence of new patterns will be essential for global health monitoring. Copyright (C) 2020 The Author(s). Published by Elsevier Ltd.Peer reviewe
Mapping geographical inequalities in oral rehydration therapy coverage in low-income and middle-income countries, 2000-17
- Author
- Abbastabar H
- Abd-Allah F
- Abdelalim A
- Abdollahpour I
- Abegaz KH
- Abejie AN
- Abreu LG
- Abrigo MRM
- Abualhasan A
- Accrombessi MMK
- Acharya D
- Adabi M
- Adamu AA
- Adebayo OM
- Adedoyin RA
- Adekanmbi V
- Adetokunboh OO
- Adhena BM
- Afarideh M
- Ahmad S
- Ahmadi K
- Ahmed AE
- Ahmed MB
- Ahmed R
- Akalu TY
- Al-Aly Z
- Al-Mekhlafi HM
- Alahdab F
- Alam N
- Alam S
- Alamene GM
- Alanzi TM
- Alcalde-Rabanal JE
- Ali BA
- Alijanzadeh M
- Alipour V
- Aljunid SM
- Almasi A
- Almasi-Hashiani A
- Altirkawi KA
- Alvis-Guzman N
- Alvis-Zakzuk NJ
- Amini S
- Amit AML
- Andrei CL
- Anjomshoa M
- Anoushiravani A
- Ansari F
- Antonio CAT
- Antony B
- Antriyandarti E
- Arabloo J
- Aref HMA
- Aremu O
- Armoon B
- Arora A
- Aryal KK
- Arzani A
- Asadi-Aliabadi M
- Atalay HT
- Athari SM
- Athari SS
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- Ausloos M
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- Ayala Quintanilla BP
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- Zerfu TA
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- Zhao X-JG
- Ziapour A
- Zodpey S
- Zuniga YMH
- Publication venue
- Publication date
- 01/01/2020
- Field of study
Background Oral rehydration solution (ORS) is a form of oral rehydration therapy (ORT) for diarrhoea that has the potential to drastically reduce child mortality; yet, according to UNICEF estimates, less than half of children younger than 5 years with diarrhoea in low-income and middle-income countries (LMICs) received ORS in 2016. A variety of recommended home fluids (RHF) exist as alternative forms of ORT; however, it is unclear whether RHF prevent child mortality. Previous studies have shown considerable variation between countries in ORS and RHF use, but subnational variation is unknown. This study aims to produce high-resolution geospatial estimates of relative and absolute coverage of ORS, RHF, and ORT (use of either ORS or RHF) in LMICs. Methods We used a Bayesian geostatistical model including 15 spatial covariates and data from 385 household surveys across 94 LMICs to estimate annual proportions of children younger than 5 years of age with diarrhoea who received ORS or RHF (or both) on continuous continent-wide surfaces in 2000-17, and aggregated results to policy-relevant administrative units. Additionally, we analysed geographical inequality in coverage across administrative units and estimated the number of diarrhoeal deaths averted by increased coverage over the study period. Uncertainty in the mean coverage estimates was calculated by taking 250 draws from the posterior joint distribution of the model and creating uncertainty intervals (UIs) with the 2 center dot 5th and 97 center dot 5th percentiles of those 250 draws. Findings While ORS use among children with diarrhoea increased in some countries from 2000 to 2017, coverage remained below 50% in the majority (62 center dot 6%; 12 417 of 19 823) of second administrative-level units and an estimated 6 519 000 children (95% UI 5 254 000-7 733 000) with diarrhoea were not treated with any form of ORT in 2017. Increases in ORS use corresponded with declines in RHF in many locations, resulting in relatively constant overall ORT coverage from 2000 to 2017. Although ORS was uniformly distributed subnationally in some countries, within-country geographical inequalities persisted in others; 11 countries had at least a 50% difference in one of their units compared with the country mean. Increases in ORS use over time were correlated with declines in RHF use and in diarrhoeal mortality in many locations, and an estimated 52 230 diarrhoeal deaths (36 910-68 860) were averted by scaling up of ORS coverage between 2000 and 2017. Finally, we identified key subnational areas in Colombia, Nigeria, and Sudan as examples of where diarrhoeal mortality remains higher than average, while ORS coverage remains lower than average. Interpretation To our knowledge, this study is the first to produce and map subnational estimates of ORS, RHF, and ORT coverage and attributable child diarrhoeal deaths across LMICs from 2000 to 2017, allowing for tracking progress over time. Our novel results, combined with detailed subnational estimates of diarrhoeal morbidity and mortality, can support subnational needs assessments aimed at furthering policy makers' understanding of within-country disparities. Over 50 years after the discovery that led to this simple, cheap, and life-saving therapy, large gains in reducing mortality could still be made by reducing geographical inequalities in ORS coverage. Copyright (c) 2020 The Author(s). Published by Elsevier Ltd. This is an Open Access article under the CC BY 4.0 license.Peer reviewe
Global burden of 369 diseases and injuries in 204 countries and territories, 1990-2019: a systematic analysis for the Global Burden of Disease Study 2019
- Author
- Abbafati C
- Abbas KM
- Abbasi M
- Abbasi-Kangevari M
- Abbasifard M
- Abbastabar H
- Abd El Razek HM
- Abd El Razek MM
- Abd-Allah F
- Abdelalim A
- Abdollahi M
- Abdollahpour I
- Abdulkader RS
- Abdullah KH
- Abedi A
- Abedi P
- Abegaz KH
- Abolhassani H
- Abosetugn AE
- Aboyans V
- Abrams EM
- Abreu LG
- Abrigo MRM
- Abu Haimed AK
- Abu-Gharbieh E
- Abu-Raddad LJ
- Abualhasan A
- Abushouk AI
- Acebedo A
- Ackerman IN
- Adabi M
- Adair T
- Adamu AA
- Adebayo OM
- Adedeji IA
- Adekanmbi V
- Adelson JD
- Adeoye AM
- Adetokunboh OO
- Adham D
- Advani SM
- Afarideh M
- Afshari M
- Afshin A
- Agardh EE
- Agarwal G
- Agasthi P
- Agesa KM
- Aghaali M
- Aghamir SMK
- Agrawal A
- Ahmad T
- Ahmadi A
- Ahmadi K
- Ahmadi M
- Ahmadieh H
- Ahmadpour E
- Ahmed MB
- Aji B
- Akalu TY
- Akinyemi RO
- Akinyemiju T
- Akombi B
- Akunna CJ
- Al-Aly Z
- Al-Mekhlafi HM
- Al-Raddadi RM
- Alahdab F
- Alam K
- Alam N
- Alam S
- Alam T
- Alanezi FM
- Alanzi TM
- Albertson SB
- Alcalde-Rabanal JE
- Alema NM
- Alemu BW
- Alemu YM
- Alhabib KF
- Alhassan RK
- Ali M
- Ali S
- Alicandro G
- Alijanzadeh M
- Alinia C
- Alipour V
- Alizade H
- Aljunid SM
- Alla F
- Allebeck P
- Almadi MAH
- Almasi A
- Almasi-Hashiani A
- Almasri NA
- Almulhim AM
- Alonso J
- Altirkawi KA
- Alumran AK
- Alvis-Guzman N
- Alvis-Zakzuk NJ
- Amare AT
- Amare B
- Amini S
- Amini-Rarani M
- Aminorroaya A
- Amiri F
- Amit AML
- Amugsi DA
- Amul GGH
- Anbesu EW
- Ancuceanu R
- Anderlini D
- Anderson JA
- Andrei CL
- Andrei T
- Androudi S
- Angus C
- Anjomshoa M
- Ansari F
- Ansari I
- Ansari-Moghaddam A
- Antonazzo IC
- Antonio CAT
- Antony CM
- Antriyandarti E
- Anvari D
- Anwer R
- Appiah SCY
- Arab-Zozani M
- Arabloo J
- Aravkin AY
- Arba AAK
- Aremu O
- Ariani F
- Aripov T
- Armoon B
- Arnlov J
- Arowosegbe OO
- Aryal KK
- Arzani A
- Asaad M
- Asadi-Aliabadi M
- Asadi-Pooya AA
- Asgari S
- Asghari B
- Ashbaugh C
- Assmus M
- Atafar Z
- Athari SS
- Atnafu DD
- Atout MMW
- Atre SR
- Atteraya MS
- Ausloos F
- Ausloos M
- Avila-Burgos L
- Avokpaho EFGA
- Ayano G
- Ayanore MA
- Aynalem GL
- Aynalem YA
- Ayza MA
- Azari S
- Azarian G
- Azene ZN
- Azhar G
- Azzopardi PS
- Babaee E
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- Skou ST
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- Smith EUR
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- Stein DJ
- Steiner C
- Steiner TJ
- Steuben KM
- Stockfelt L
- Stokes MA
- Stovner LJ
- Straif K
- Stranges S
- Stubbs JL
- Suchdev PS
- Sudaryanto A
- Sufiyan MB
- Suleria HAR
- Sulo G
- Sultan I
- Swope CB
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- Sylte DO
- Szocska M
- Szumowski L
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- Tabb KM
- Tabuchi T
- Tadakamadla SK
- Taddele BW
- Tadesse DB
- Taherkhani A
- Tahir Z
- Tajdini M
- Takahashi K
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- Tareque MI
- Tarigan IU
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- Taylor HJ
- Teagle WL
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- Tediosi F
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- Tehrani-Banihashemi A
- Teklehaimanot BF
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- Terrason S
- Tesema GA
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- Thurston GD
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- Toroudi HP
- Torre AE
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- Trias-Llimos S
- Troeger CE
- Truelsen TC
- Tsai AC
- Tsatsakis A
- Tyrovolas S
- Uddin R
- Ullah I
- Ullah S
- Umeokonkwo CD
- Undurraga EA
- Unnikrishnan B
- Upadhyay E
- Uthman OA
- Vacante M
- Vaicekonyte R
- Vakilian A
- Valdez PR
- Valli A
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- Vardavas C
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- Vasankari TJ
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- Vasseghian Y
- Veisani Y
- Velasquez IM
- Venketasubramanian N
- Vidale S
- Violante FS
- Vlassov V
- Vollset SE
- Vongpradith A
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- Wickramasinghe ND
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- Wojtyniak B
- Woldu G
- Wolfe CDA
- Wondmeneh TG
- Wondmieneh AB
- Wool EE
- Wozniak SS
- Wu A-M
- Wu C
- Wu J
- Wunrow HY
- Xie Y
- Xu G
- Xu R
- Yadgir S
- Yamada T
- Yamagishi K
- Yaminfirooz M
- Yano Y
- Yaya S
- Yazdi-Feyzabadi V
- Yearwood JA
- Yeheyis TY
- Yeshitila YG
- Yilgwan CS
- Yilma MT
- Yip P
- Yonemoto N
- Yoon S-J
- York HW
- Younis MZ
- Younker TP
- Yousefi B
- Yousefi Z
- Yousefifard M
- Yousefinezhadi T
- Yousuf AY
- Yu C
- Yu Y
- Yuan C-W
- Yuce D
- Yusefzadeh H
- Zadey S
- Zahabi SS
- Zaidi SS
- Zaki L
- Zaki MES
- Zakzuk J
- Zamani M
- Zamanian M
- Zandian H
- Zangeneh A
- Zarafshan H
- Zastrozhin MS
- Zewdie KA
- Zhang J
- Zhang Y
- Zhang Z-J
- Zhao JT
- Zhao X-JG
- Zhao Y
- Zheleva B
- Zheng P
- Zhou M
- Zhu C
- Ziapour A
- Zimsen SRM
- Zlavog BS
- Zodpey S
- Publication venue
- 'Elsevier BV'
- Publication date
- 17/10/2020
- Field of study
Five insights from the Global Burden of Disease Study 2019
- Author
- Abbafati C
- Abbas KM
- Abbasi M
- Abbasi-Kangevari M
- Abbasifard M
- Abbastabar H
- Abd El Razek HM
- Abd El Razek MM
- Abd-Allah F
- Abdelalim A
- Abdollahi M
- Abdollahpour I
- Abdulkader RS
- Abdullah KH
- Abedi A
- Abedi P
- Abegaz KH
- Abolhassani H
- Abosetugn AE
- Aboyans V
- Abrams EM
- Abreu LG
- Abrigo MRM
- Abu Haimed AK
- Abu-Gharbieh E
- Abu-Raddad LJ
- Abualhasan A
- Abushouk AI
- Acebedo A
- Ackerman IN
- Adabi M
- Adair T
- Adamu AA
- Adebayo OM
- Adedeji IA
- Adekanmbi V
- Adelson JD
- Adeoye AM
- Adetokunboh OO
- Adham D
- Advani SM
- Afarideh M
- Afshari M
- Afshin A
- Agardh EE
- Agarwal G
- Agasthi P
- Agesa KM
- Aghaali M
- Aghamir SMK
- Agrawal A
- Ahmad T
- Ahmadi A
- Ahmadi K
- Ahmadi M
- Ahmadieh H
- Ahmadpour E
- Ahmed MB
- Aji B
- Akalu TY
- Akinyemi RO
- Akinyemiju T
- Akombi B
- Akunna CJ
- Al-Aly Z
- Al-Mekhlafi HM
- Al-Raddadi RM
- Alahdab F
- Alam K
- Alam N
- Alam S
- Alam T
- Alanezi FM
- Alanzi TM
- Albertson SB
- Alcalde-Rabanal JE
- Alema NM
- Alemu BW
- Alemu YM
- Alhabib KF
- Alhassan RK
- Ali M
- Ali S
- Alicandro G
- Alijanzadeh M
- Alinia C
- Alipour V
- Alizade H
- Aljunid SM
- Alla F
- Allebeck P
- Almadi MAH
- Almasi A
- Almasi-Hashiani A
- Almasri NA
- Almulhim AM
- Alonso J
- Altirkawi KA
- Alumran AK
- Alvis-Guzman N
- Alvis-Zakzuk NJ
- Amare AT
- Amare B
- Amini S
- Amini-Rarani M
- Aminorroaya A
- Amiri F
- Amit AML
- Amugsi DA
- Amul GGH
- Anbesu EW
- Ancuceanu R
- Anderlini D
- Anderson JA
- Andrei CL
- Andrei T
- Androudi S
- Angus C
- Anjomshoa M
- Ansari F
- Ansari I
- Ansari-Moghaddam A
- Antonazzo IC
- Antonio CAT
- Antony CM
- Antriyandarti E
- Anvari D
- Anwer R
- Appiah SCY
- Arab-Zozani M
- Arabloo J
- Aravkin AY
- Arba AAK
- Aremu O
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- Armoon B
- Arnlov J
- Arowosegbe OO
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- Asadi-Pooya AA
- Asgari S
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- Ashbaugh C
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- Atafar Z
- Athari SS
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- Atout MMW
- Atre SR
- Atteraya MS
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- Avokpaho EFGA
- Ayano G
- Ayanore MA
- Aynalem GL
- Aynalem YA
- Ayza MA
- Azari S
- Azarian G
- Azene ZN
- Azhar G
- Azzopardi PS
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- Badawi A
- Badiye AD
- Bagherzadeh M
- Bagli E
- Bahrami MA
- Baig AA
- Bairwa M
- Bakhshaei MH
- Bakhtiari A
- Bakkannavar SM
- Balachandran A
- Balakrishnan S
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- Balassyano S
- Baldasseroni A
- Bali AO
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- Ballew SH
- Balzi D
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- Bandpei MAM
- Banerjee SK
- Banik PC
- Bannick MS
- Bante AB
- Bante SA
- Baraki AG
- Barboza MA
- Barker-Collo SL
- Barnighausen TW
- Barrero LH
- Barthelemy CM
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- Bibi S
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- Bilano V
- Bin Sayeed MS
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- Birihane BM
- Bisanzio D
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- Biswas RK
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- Breusov AV
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- Britton GB
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- Bryazka D
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- Burkart K
- Burnett RT
- Busse R
- Butt ZA
- Caetano dos Santos FL
- Cahill LE
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- Camera LA
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- Castaneda-Orjuela CA
- Castelpietra G
- Castle CD
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- Cercy KM
- Cerin E
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- Chandan JS
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- Cherbuin N
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- Chin KL
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- Chu D-T
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- Cowie BC
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- da Silva DD
- Dahlawi SMA
- Dai H
- Dai H
- Damasceno AAM
- Damiani G
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- Dangel WJ
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- Dean FE
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- Deen A
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- Demeke FM
- Demoz GT
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- Dereje ND
- Deribe K
- Dervenis N
- Desai R
- Desalew A
- Dessie GA
- Deuba K
- Dharmaratne SD
- Dhungana GP
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- Diaz D
- Dichgans M
- Didarloo A
- Dingels ZV
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- Dirac MA
- Djalalinia S
- Do HT
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- Doku DT
- Dolecek C
- Dolgert AJ
- Dorostkar F
- Doshi CP
- Doshi PP
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- Douiri A
- Doxey MC
- Doyle KE
- Driscoll TR
- Dubljanin E
- Dunachie SJ
- Duncan BB
- Duraes AR
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- Ebrahimi H
- Edvardsson D
- Effiong A
- Ehrlich JR
- El Nahas N
- El Sayed I
- El Tantawi M
- El-Jaafary SI
- Elbarazi I
- Elgendy IY
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- Elyazar IRF
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- Erskine HE
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- Farahmand M
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- Faro A
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- Fazaeli AA
- Fazlzadeh M
- Feigin VL
- Feldman R
- Fereshtehnejad S-M
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- Ferreira ML
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- Filip I
- Fischer F
- Fisher JL
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- Folayan MO
- Fomenkov AA
- Force LM
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- Forooshani ZSD
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- Fox JT
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- Fukutaki K
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- Fullman N
- Furtado JM
- Gad MM
- Gaidhane AM
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- Galles NC
- Gallus S
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- Gardner WM
- Geberemariyam BS
- Gebrehiwot AM
- Gebremedhin KB
- Gebremeskel GG
- Gebremeskel LG
- Gebresillassie BM
- Gebreslassie AAAA
- Gela JD
- Geramo YCD
- Geremew A
- Gesesew HA
- Gething PW
- Gezae KE
- Ghadimi M
- Ghadiri K
- Ghaffarifar F
- Ghafourifard M
- Ghajar A
- Ghamari F
- Ghashghaee A
- Ghiasvand H
- Ghith N
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- Gilani SA
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- Guled RA
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- Jayatilleke AU
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- Publication venue
- Publication date
- 01/01/2020
- Field of study
The Global Burden of Diseases, Injuries, and Risk Factors Study (GBD) 2019 provides a rules-based synthesis of the available evidence on levels and trends in health outcomes, a diverse set of risk factors, and health system responses. GBD 2019 covered 204 countries and territories, as well as first administrative level disaggregations for 22 countries, from 1990 to 2019. Because GBD is highly standardised and comprehensive, spanning both fatal and non-fatal outcomes, and uses a mutually exclusive and collectively exhaustive list of hierarchical disease and injury causes, the study provides a powerful basis for detailed and broad insights on global health trends and emerging challenges. GBD 2019 incorporates data from 281 586 sources and provides more than 3.5 billion estimates of health outcome and health system measures of interest for global, national, and subnational policy dialogue. All GBD estimates are publicly available and adhere to the Guidelines on Accurate and Transparent Health Estimate Reporting. From this vast amount of information, five key insights that are important for health, social, and economic development strategies have been distilled. These insights are subject to the many limitations outlined in each of the component GBD capstone papers.Peer reviewe
Measurement and interpretation of same-sign W boson pair production in association with two jets in pp collisions at s = 13 TeV with the ATLAS detector
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- Zhemchugov A
- Zheng J
- Zheng K
- Zheng X
- Zheng Z
- Zhong D
- Zhou B
- Zhou H
- Zhou N
- Zhou Y
- Zhu CG
- Zhu J
- Zhu Y
- Zhu Y
- Zhuang X
- Zhukov K
- Zhulanov V
- Zimine NI
- Zinsser J
- Ziolkowski M
- Zoccoli A
- Zoch K
- Zorbas TG
- Zormpa O
- Zou W
- Zwalinski L
- Ă kesson TPA
- Ăncel ĂO
- ĆœeniĆĄ T
- ĆœivkoviÄ L
- Publication venue
- Springer Nature
- Publication date
- 01/04/2024
- Field of study
This paper presents the measurement of fducial and diferential cross sections for both the inclusive and electroweak production of a same-sign W-boson pair in association with two jets (W±W±jj) using 139 fbâ1 of proton-proton collision data recorded at a centre-of-mass energy of âs = 13 TeV by the ATLAS detector at the Large Hadron Collider. The analysis is performed by selecting two same-charge leptons, electron or muon, and at least two jets with large invariant mass and a large rapidity diference. The measured fducial cross sections for electroweak and inclusive W±W±jj production are 2.92 ± 0.22 (stat.) ± 0.19 (syst.)fb and 3.38±0.22 (stat.)±0.19 (syst.)fb, respectively, in agreement with Standard Model predictions. The measurements are used to constrain anomalous quartic gauge couplings by extracting 95% confdence level intervals on dimension-8 operators. A search for doubly charged Higgs bosons H±± that are produced in vector-boson fusion processes and decay into a same-sign W boson pair is performed. The largest deviation from the Standard Model occurs for an H±± mass near 450 GeV, with a global signifcance of 2.5 standard deviations
Combination of searches for heavy spin-1 resonances using 139 fbâ1 of proton-proton collision data at s = 13 TeV with the ATLAS detector
- Author
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- Aakvaag E
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- Abicht NJ
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- Zhemchugov A
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- Ă kesson TPA
- Ăncel ĂO
- ĆœeniĆĄ T
- ĆœivkoviÄ L
- Publication venue
- Springer Nature
- Publication date
- 19/04/2024
- Field of study
A combination of searches for new heavy spin-1 resonances decaying into different pairings of W, Z, or Higgs bosons, as well as directly into leptons or quarks, is presented. The data sample used corresponds to 139 fbâ1 of proton-proton collisions at
= 13 TeV collected during 2015â2018 with the ATLAS detector at the CERN Large Hadron Collider. Analyses selecting quark pairs (qq, bb,
, and tb) or third-generation leptons (ÏÎœ and ÏÏ) are included in this kind of combination for the first time. A simplified model predicting a spin-1 heavy vector-boson triplet is used. Cross-section limits are set at the 95% confidence level and are compared with predictions for the benchmark model. These limits are also expressed in terms of constraints on couplings of the heavy vector-boson triplet to quarks, leptons, and the Higgs boson. The complementarity of the various analyses increases the sensitivity to new physics, and the resulting constraints are stronger than those from any individual analysis considered. The data exclude a heavy vector-boson triplet with mass below 5.8 TeV in a weakly coupled scenario, below 4.4 TeV in a strongly coupled scenario, and up to 1.5 TeV in the case of production via vector-boson fusion
Measurement of the ttÂŻttÂŻ production cross section in pp collisions at âs=13 TeV with the ATLAS detector
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- Zemaityte G
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- Zhemchugov A
- Zheng Z
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- Zhulanov V
- Zieminska D
- Zimine NI
- Zimmermann S
- Ziolkowski M
- Zoccoli A
- Zoch K
- Zorbas TG
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- Ă kesson TPA
- Ăncel ĂO
- ĆœeniĆĄ T
- ĆœivkoviÄ L
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 16/11/2021
- Field of study
A measurement of four-top-quark production using proton-proton collision data at a centre-of-mass energy of 13 TeV collected by the ATLAS detector at the Large Hadron Collider corresponding to an integrated luminosity of 139 fbâ1 is presented. Events are selected if they contain a single lepton (electron or muon) or an opposite-sign lepton pair, in association with multiple jets. The events are categorised according to the number of jets and how likely these are to contain b-hadrons. A multivariate technique is then used to discriminate between signal and background events. The measured four-top-quark production cross section is found to be 26+17â15 fb, with a corresponding observed (expected) significance of 1.9 (1.0) standard deviations over the background-only hypothesis. The result is combined with the previous measurement performed by the ATLAS Collaboration in the multilepton final state. The combined four-top-quark production cross section is measured to be 24+7â6 fb, with a corresponding observed (expected) signal significance of 4.7 (2.6) standard deviations over the background-only predictions. It is consistent within 2.0 standard deviations with the Standard Model expectation of 12.0 ± 2.4 fb
Measurements of W+Wâ+ â„ 1 jet production cross-sections in pp collisions at sâ = 13 TeV with the ATLAS detector
- Author
- Aad G
- Abbott B
- Abbott DC
- Abed Abud A
- Abeling K
- Abhayasinghe DK
- Abidi SH
- AbouZeid OS
- Abraham NL
- Abramowicz H
- Abreu H
- Abulaiti Y
- Abusleme Hoffman AC
- Acharya BS
- Achkar B
- Adam Bourdarios C
- Adam L
- Adamczyk L
- Adamek L
- Adelman J
- Adiguzel A
- Adorni S
- Adye T
- Affolder AA
- Afik Y
- Agapopoulou C
- Agaras MN
- Aggarwal A
- Agheorghiesei C
- Aguilar-Saavedra JA
- Ahmad A
- Ahmadov F
- Ahmed WS
- Ai X
- Aielli G
- Akatsuka S
- Akbiyik M
- Akilli E
- Akimov AV
- Al Khoury K
- Alberghi GL
- Albert J
- Alconada Verzini MJ
- Alderweireldt S
- Aleksa M
- Aleksandrov IN
- Alexa C
- Alexopoulos T
- Alfonsi A
- Alfonsi F
- Alhroob M
- Ali B
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- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/06/2021
- Field of study
Fiducial and differential cross-section measurements of W+Wâ production in
association with at least one hadronic jet are presented. These measurements are sensitive
to the properties of electroweak-boson self-interactions and provide a test of perturbative
quantum chromodynamics and the electroweak theory. The analysis is performed using
proton-proton collision data collected at p
s = 13TeV with the ATLAS experiment, corresponding
to an integrated luminosity of 139 fbâ1. Events are selected with exactly one oppositely
charged electron-muon pair and at least one hadronic jet with a transverse momentum
of pT > 30 GeV and a pseudorapidity of |ïżœ| < 4.5. After subtracting the background
contributions and correcting for detector effects, the jet-inclusive W+Wâ+ ïżœ 1 jet fiducial
cross-section and W+Wâ+ jets differential cross-sections with respect to several kinematic
variables are measured. These measurements include leptonic quantities, such as the lepton
transverse momenta and the transverse mass of the W+Wâ system, as well as jet-related
observables such as the leading jet transverse momentum and the jet multiplicity. Limits on
anomalous triple-gauge-boson couplings are obtained in a phase space where interference
between the Standard Model amplitude and the anomalous amplitude is enhanced
- âŠ