Abstract
Original language | English (US) |
---|---|
Pages (from-to) | 1084-1150 |
Number of pages | 67 |
Journal | The Lancet |
Volume | 390 |
Issue number | 10100 |
DOIs | |
State | Published - Sep 16 2017 |
Bibliographical note
Generated from Scopus record by KAUST IRTS on 2021-03-16ASJC Scopus subject areas
- General Medicine
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In: The Lancet, Vol. 390, No. 10100, 16.09.2017, p. 1084-1150.
Research output: Contribution to journal › Article › peer-review
TY - JOUR
T1 - Global, regional, and national under-5 mortality, adult mortality, age-specific mortality, and life expectancy, 1970-2016: A systematic analysis for the Global Burden of Disease Study 2016
AU - Wang, Haidong
AU - Abajobir, Amanuel Alemu
AU - Abate, Kalkidan Hassen
AU - Abbafati, Cristiana
AU - Abbas, Kaja M.
AU - Abd-Allah, Foad
AU - Abera, Semaw Ferede
AU - Abraha, Haftom Niguse
AU - Abu-Raddad, Laith J.
AU - Abu-Rmeileh, Niveen M.E.
AU - Adedeji, Isaac Akinkunmi
AU - Adedoyin, Rufus Adesoji
AU - Adetifa, Ifedayo Morayo O.
AU - Adetokunboh, Olatunji
AU - Afshin, Ashkan
AU - Aggarwal, Rakesh
AU - Agrawal, Anurag
AU - Agrawal, Sutapa
AU - Ahmad Kiadaliri, Aliasghar
AU - Ahmed, Muktar Beshir
AU - Aichour, Amani Nidhal
AU - Aichour, Ibthiel
AU - Aichour, Miloud Taki Eddine
AU - Aiyar, Sneha
AU - Akanda, Ali Shafqat
AU - Akinyemiju, Tomi F.
AU - Akseer, Nadia
AU - Al-Eyadhy, Ayman
AU - Al Lami, Faris Hasan
AU - Alabed, Samer
AU - Alahdab, Fares
AU - Al-Aly, Ziyad
AU - Alam, Khurshid
AU - Alam, Noore
AU - Alasfoor, Deena
AU - Aldridge, Robert William
AU - Alene, Kefyalew Addis
AU - Alhabib, Samia
AU - Ali, Raghib
AU - Alizadeh-Navaei, Reza
AU - Aljunid, Syed M.
AU - Alkaabi, Juma M.
AU - Alkerwi, Ala'a
AU - Alla, François
AU - Allam, Shalini D.
AU - Allebeck, Peter
AU - Al-Raddadi, Rajaa
AU - Alsharif, Ubai
AU - Altirkawi, Khalid A.
AU - Martin, Elena Alvarez
AU - Alvis-Guzman, Nelson
AU - Amare, Azmeraw T.
AU - Ameh, Emmanuel A.
AU - Amini, Erfan
AU - Ammar, Walid
AU - Amoako, Yaw Ampem
AU - Anber, Nahla
AU - Andrei, Catalina Liliana
AU - Androudi, Sofia
AU - Ansari, Hossein
AU - Ansha, Mustafa Geleto
AU - Antonio, Carl Abelardo T.
AU - Anwari, Palwasha
AU - Ärnlöv, Johan
AU - Arora, Megha
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AU - Awasthi, Ashish
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AU - Topor-Madry, Roman
AU - Topouzis, Fotis
AU - Tortajada, Miguel
AU - Tran, Bach Xuan
AU - Truelsen, Thomas
AU - Trujillo, Ulises
AU - Tsilimparis, Nikolaos
AU - Tuem, Kald Beshir
AU - Tuzcu, Emin Murat
AU - Tyrovolas, Stefanos
AU - Ukwaja, Kingsley Nnanna
AU - Undurraga, Eduardo A.
AU - Uthman, Olalekan A.
AU - Uzochukwu, Benjamin S.Chudi
AU - Van Boven, Job F.M.
AU - Varakin, Yuri Y.
AU - Varughese, Santosh
AU - Vasankari, Tommi
AU - Vasconcelos, Ana Maria Nogales
AU - Venketasubramanian, Narayanaswamy
AU - Vidavalur, Ramesh
AU - Violante, Francesco S.
AU - Vishnu, Abhishek
AU - Vladimirov, Sergey K.
AU - Vlassov, Vasiliy Victorovich
AU - Vollset, Stein Emil
AU - Vos, Theo
AU - Waid, Jillian L.
AU - Wakayo, Tolassa
AU - Wang, Yuan Pang
AU - Weichenthal, Scott
AU - Weiderpass, Elisabete
AU - Weintraub, Robert G.
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AU - Wesana, Joshua
AU - Wijeratne, Tissa
AU - Wilkinson, James D.
AU - Wiysonge, Charles Shey
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AU - Wolfe, Charles D.A.
AU - Workicho, Abdulhalik
AU - Workie, Shimelash Bitew
AU - Xavier, Denis
AU - Xu, Gelin
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AU - Yalew, Ayalnesh Zemene
AU - Yan, Lijing L.
AU - Yano, Yuichiro
AU - Yaseri, Mehdi
AU - Ye, Pengpeng
AU - Yimam, Hassen Hamid
AU - Yip, Paul
AU - Yirsaw, Biruck Desalegn
AU - Yonemoto, Naohiro
AU - Yoon, Seok Jun
AU - Yotebieng, Marcel
AU - Younis, Mustafa Z.
AU - Zaidi, Zoubida
AU - El Sayed Zaki, Maysaa
AU - Zeeb, Hajo
AU - Zenebe, Zerihun Menlkalew
AU - Zerfu, Taddese Alemu
AU - Zhang, Anthony Lin
AU - Zhang, Xueying
AU - Zodpey, Sanjay
AU - Zuhlke, Liesl Joanna
AU - Lopez, Alan D.
AU - Murray, Christopher J.L.
N1 - Generated from Scopus record by KAUST IRTS on 2021-03-16
PY - 2017/9/16
Y1 - 2017/9/16
N2 - Background: Detailed assessments of mortality patterns, particularly age-specific mortality, represent a crucial input that enables health systems to target interventions to specific populations. Understanding how all-cause mortality has changed with respect to development status can identify exemplars for best practice. To accomplish this, the Global Burden of Diseases, Injuries, and Risk Factors Study 2016 (GBD 2016) estimated age-specific and sex-specific all-cause mortality between 1970 and 2016 for 195 countries and territories and at the subnational level for the five countries with a population greater than 200 million in 2016. Methods: We have evaluated how well civil registration systems captured deaths using a set of demographic methods called death distribution methods for adults and from consideration of survey and census data for children younger than 5 years. We generated an overall assessment of completeness of registration of deaths by dividing registered deaths in each location-year by our estimate of all-age deaths generated from our overall estimation process. For 163 locations, including subnational units in countries with a population greater than 200 million with complete vital registration (VR) systems, our estimates were largely driven by the observed data, with corrections for small fluctuations in numbers and estimation for recent years where there were lags in data reporting (lags were variable by location, generally between 1 year and 6 years). For other locations, we took advantage of different data sources available to measure under-5 mortality rates (U5MR) using complete birth histories, summary birth histories, and incomplete VR with adjustments; we measured adult mortality rate (the probability of death in individuals aged 15-60 years) using adjusted incomplete VR, sibling histories, and household death recall. We used the U5MR and adult mortality rate, together with crude death rate due to HIV in the GBD model life table system, to estimate age-specific and sex-specific death rates for each location-year. Using various international databases, we identified fatal discontinuities, which we defined as increases in the death rate of more than one death per million, resulting from conflict and terrorism, natural disasters, major transport or technological accidents, and a subset of epidemic infectious diseases; these were added to estimates in the relevant years. In 47 countries with an identified peak adult prevalence for HIV/AIDS of more than 0.5% and where VR systems were less than 65% complete, we informed our estimates of age-sex-specific mortality using the Estimation and Projection Package (EPP)-Spectrum model fitted to national HIV/AIDS prevalence surveys and antenatal clinic serosurveillance systems. We estimated stillbirths, early neonatal, late neonatal, and childhood mortality using both survey and VR data in spatiotemporal Gaussian process regression models. We estimated abridged life tables for all location-years using age-specific death rates. We grouped locations into development quintiles based on the Socio-demographic Index (SDI) and analysed mortality trends by quintile. Using spline regression, we estimated the expected mortality rate for each age-sex group as a function of SDI. We identified countries with higher life expectancy than expected by comparing observed life expectancy to anticipated life expectancy on the basis of development status alone. Findings: Completeness in the registration of deaths increased from 28% in 1970 to a peak of 45% in 2013; completeness was lower after 2013 because of lags in reporting. Total deaths in children younger than 5 years decreased from 1970 to 2016, and slower decreases occurred at ages 5-24 years. By contrast, numbers of adult deaths increased in each 5-year age bracket above the age of 25 years. The distribution of annualised rates of change in age-specific mortality rate differed over the period 2000 to 2016 compared with earlier decades: increasing annualised rates of change were less frequent, although rising annualised rates of change still occurred in some locations, particularly for adolescent and younger adult age groups. Rates of stillbirths and under-5 mortality both decreased globally from 1970. Evidence for global convergence of death rates was mixed; although the absolute difference between age-standardised death rates narrowed between countries at the lowest and highest levels of SDI, the ratio of these death rates - a measure of relative inequality - increased slightly. There was a strong shift between 1970 and 2016 toward higher life expectancy, most noticeably at higher levels of SDI. Among countries with populations greater than 1 million in 2016, life expectancy at birth was highest for women in Japan, at 86.9 years (95% UI 86.7-87.2), and for men in Singapore, at 81.3 years (78.8-83.7) in 2016. Male life expectancy was generally lower than female life expectancy between 1970 and 2016, and the gap between male and female life expectancy increased with progression to higher levels of SDI. Some countries with exceptional health performance in 1990 in terms of the difference in observed to expected life expectancy at birth had slower progress on the same measure in 2016. Interpretation Globally, mortality rates have decreased across all age groups over the past five decades, with the largest improvements occurring among children younger than 5 years. However, at the national level, considerable heterogeneity remains in terms of both level and rate of changes in age-specific mortality; increases in mortality for certain age groups occurred in some locations. We found evidence that the absolute gap between countries in age-specific death rates has declined, although the relative gap for some age-sex groups increased. Countries that now lead in terms of having higher observed life expectancy than that expected on the basis of development alone, or locations that have either increased this advantage or rapidly decreased the deficit from expected levels, could provide insight into the means to accelerate progress in nations where progress has stalled.
AB - Background: Detailed assessments of mortality patterns, particularly age-specific mortality, represent a crucial input that enables health systems to target interventions to specific populations. Understanding how all-cause mortality has changed with respect to development status can identify exemplars for best practice. To accomplish this, the Global Burden of Diseases, Injuries, and Risk Factors Study 2016 (GBD 2016) estimated age-specific and sex-specific all-cause mortality between 1970 and 2016 for 195 countries and territories and at the subnational level for the five countries with a population greater than 200 million in 2016. Methods: We have evaluated how well civil registration systems captured deaths using a set of demographic methods called death distribution methods for adults and from consideration of survey and census data for children younger than 5 years. We generated an overall assessment of completeness of registration of deaths by dividing registered deaths in each location-year by our estimate of all-age deaths generated from our overall estimation process. For 163 locations, including subnational units in countries with a population greater than 200 million with complete vital registration (VR) systems, our estimates were largely driven by the observed data, with corrections for small fluctuations in numbers and estimation for recent years where there were lags in data reporting (lags were variable by location, generally between 1 year and 6 years). For other locations, we took advantage of different data sources available to measure under-5 mortality rates (U5MR) using complete birth histories, summary birth histories, and incomplete VR with adjustments; we measured adult mortality rate (the probability of death in individuals aged 15-60 years) using adjusted incomplete VR, sibling histories, and household death recall. We used the U5MR and adult mortality rate, together with crude death rate due to HIV in the GBD model life table system, to estimate age-specific and sex-specific death rates for each location-year. Using various international databases, we identified fatal discontinuities, which we defined as increases in the death rate of more than one death per million, resulting from conflict and terrorism, natural disasters, major transport or technological accidents, and a subset of epidemic infectious diseases; these were added to estimates in the relevant years. In 47 countries with an identified peak adult prevalence for HIV/AIDS of more than 0.5% and where VR systems were less than 65% complete, we informed our estimates of age-sex-specific mortality using the Estimation and Projection Package (EPP)-Spectrum model fitted to national HIV/AIDS prevalence surveys and antenatal clinic serosurveillance systems. We estimated stillbirths, early neonatal, late neonatal, and childhood mortality using both survey and VR data in spatiotemporal Gaussian process regression models. We estimated abridged life tables for all location-years using age-specific death rates. We grouped locations into development quintiles based on the Socio-demographic Index (SDI) and analysed mortality trends by quintile. Using spline regression, we estimated the expected mortality rate for each age-sex group as a function of SDI. We identified countries with higher life expectancy than expected by comparing observed life expectancy to anticipated life expectancy on the basis of development status alone. Findings: Completeness in the registration of deaths increased from 28% in 1970 to a peak of 45% in 2013; completeness was lower after 2013 because of lags in reporting. Total deaths in children younger than 5 years decreased from 1970 to 2016, and slower decreases occurred at ages 5-24 years. By contrast, numbers of adult deaths increased in each 5-year age bracket above the age of 25 years. The distribution of annualised rates of change in age-specific mortality rate differed over the period 2000 to 2016 compared with earlier decades: increasing annualised rates of change were less frequent, although rising annualised rates of change still occurred in some locations, particularly for adolescent and younger adult age groups. Rates of stillbirths and under-5 mortality both decreased globally from 1970. Evidence for global convergence of death rates was mixed; although the absolute difference between age-standardised death rates narrowed between countries at the lowest and highest levels of SDI, the ratio of these death rates - a measure of relative inequality - increased slightly. There was a strong shift between 1970 and 2016 toward higher life expectancy, most noticeably at higher levels of SDI. Among countries with populations greater than 1 million in 2016, life expectancy at birth was highest for women in Japan, at 86.9 years (95% UI 86.7-87.2), and for men in Singapore, at 81.3 years (78.8-83.7) in 2016. Male life expectancy was generally lower than female life expectancy between 1970 and 2016, and the gap between male and female life expectancy increased with progression to higher levels of SDI. Some countries with exceptional health performance in 1990 in terms of the difference in observed to expected life expectancy at birth had slower progress on the same measure in 2016. Interpretation Globally, mortality rates have decreased across all age groups over the past five decades, with the largest improvements occurring among children younger than 5 years. However, at the national level, considerable heterogeneity remains in terms of both level and rate of changes in age-specific mortality; increases in mortality for certain age groups occurred in some locations. We found evidence that the absolute gap between countries in age-specific death rates has declined, although the relative gap for some age-sex groups increased. Countries that now lead in terms of having higher observed life expectancy than that expected on the basis of development alone, or locations that have either increased this advantage or rapidly decreased the deficit from expected levels, could provide insight into the means to accelerate progress in nations where progress has stalled.
UR - https://linkinghub.elsevier.com/retrieve/pii/S0140673617318330
UR - http://www.scopus.com/inward/record.url?scp=85031719180&partnerID=8YFLogxK
U2 - 10.1016/S0140-6736(17)31833-0
DO - 10.1016/S0140-6736(17)31833-0
M3 - Article
SN - 1474-547X
VL - 390
SP - 1084
EP - 1150
JO - The Lancet
JF - The Lancet
IS - 10100
ER -