Dhiraj Motilal Agarwal
54398213500
Publications - 2
Global, regional, and national trends in routine childhood vaccination coverage from 1980 to 2023 with forecasts to 2030: a systematic analysis for the Global Burden of Disease Study 2023
Simeon Okechukwu Ajakwe
Mushood Ahmed
Naveed Ahmed
Rana Kamal Abu Farha
Eman Abu-Gharbieh
Aanuoluwapo Adeyimika Afolabi
Giuseppina Affinito
Kamoru Ademola Adedokun
Nurudeen A. Adegoke
Dolapo Emmanuel Ajala
Armita Abedi
Usha Adiga
Mitra Abbasifard
Mohammad Amin Aalipour
Aqeel Ahmad
Dariush Abtahi
Ripon Kumar Adhikary
Mohd Adnan
Williams Agyemang-Duah
Danish Ahmad
Hana J. Abukhadijah
Rotimi Felix Afolabi
Saira Afzal
Emad M. Abdallah
Meqdad Saleh Ahmed
Muktar Beshir Ahmed
Syed Anees Ahmed
Suneth Buddhika Agampodi
Ayman Ahmed
Khurshid Ahmad
Tauseef Ahmad
Sepehr Aghajanian
Meriem Abdoun
Salahdein Aburuz
Lucas Guimarães Abreu
Qorinah Estiningtyas Sakilah Adnani
Olivia D. Nesbit
Taylor Noyes
Noga Shalev
Latera Tesfaye Olana
Catherine Bisignano
Emily Haeuser
Sam Byrne
Jason Nguyen
Catalina Raggi
Susan A. McLaughlin
Ashley A. Harris
Amanda E. Smith
Paulina A. Lindstedt
Georgia Smith
Samuel James Herold
Rana Kamal Abu Farha
Dmitry Abramov
Sherief Abd-Elsalam
Hedayat Abbastabar
Faezeh Abbaspour
Reda Abdel-Hameed
Samar Abd ElHafeez
Atef Abdelkader
Adam Abdullahi
Kulmira Abdykerimova
Deldar Morad Abdulah
Abdu A. Adamu
Haroon Ahmed
Rahim Abo Kasem
Lisa C. Adams
Toufik Abdul-Rahman
Constanza Elizabeth Aguilera Arriagada
Mahsa Ahadi
Rabbiya Ahmad
Shoaib Ahmad
Asrat Agalu Abejew
Juliana Bunmi Adetunji
Bilyaminu Abubakar
Ousman Adal
Meshack Achore
Nagah M. Abourashed
Mohamed Abouzid
David Adedia
Oyelola A. Adegboye
Habeeb Abiodun Afolabi
Roberto Ariel Abeldaño Zuñiga
Anirudh Balakrishna Acharya
Juan Manuel Acuna
Arman Abdous
Auwal Abdullahi
Hasan Aalruz
Dhiraj Motilal Agarwal
Syed Hani Abidi
Abdullahi Tunde Aborode
Olumide Abiodun
Richard Gyan Aboagye
Hassan Abolhassani
Ulric Sena Abonie
Wakgari Mosisa Abdisa
Prince Owusu Adoma
Leticia Akua Adzigbli
Tajudeen Adesanmi Adebisi
Oluwatobi E. Adegbile
Olumide Thomas Adeleke
Mache Tsadik Adhana
Publication Name: Lancet
Publication Date: 2025-07-19
Volume: 406
Issue: 10500
Page Range: 235-260
Description:
Background: Since its inception in 1974, the Essential Programme on Immunization (EPI) has achieved remarkable success, averting the deaths of an estimated 154 million children worldwide through routine childhood vaccination. However, more recent decades have seen persistent coverage inequities and stagnating progress, which have been further amplified by the COVID-19 pandemic. In 2019, WHO set ambitious goals for improving vaccine coverage globally through the Immunization Agenda 2030 (IA2030). Now halfway through the decade, understanding past and recent coverage trends can help inform and reorient strategies for approaching these aims in the next 5 years. Methods: Based on the Global Burden of Diseases, Injuries, and Risk Factors Study 2023, this study provides updated global, regional, and national estimates of routine childhood vaccine coverage from 1980 to 2023 for 204 countries and territories for 11 vaccine-dose combinations recommended by WHO for all children globally. Employing advanced modelling techniques, this analysis accounts for data biases and heterogeneity and integrates new methodologies to model vaccine scale-up and COVID-19 pandemic-related disruptions. To contextualise historic coverage trends and gains still needed to achieve the IA2030 coverage targets, we supplement these results with several secondary analyses: (1) we assess the effect of the COVID-19 pandemic on vaccine coverage; (2) we forecast coverage of select life-course vaccines up to 2030; and (3) we analyse progress needed to reduce the number of zero-dose children by half between 2023 and 2030. Findings: Overall, global coverage for the original EPI vaccines against diphtheria, tetanus, and pertussis (first dose [DTP1] and third dose [DTP3]), measles (MCV1), polio (Pol3), and tuberculosis (BCG) nearly doubled from 1980 to 2023. However, this long-term trend masks recent challenges. Coverage gains slowed between 2010 and 2019 in many countries and territories, including declines in 21 of 36 high-income countries and territories for at least one of these vaccine doses (excluding BCG, which has been removed from routine immunisation schedules in some countries and territories). The COVID-19 pandemic exacerbated these challenges, with global rates for these vaccines declining sharply since 2020, and still not returning to pre-COVID-19 pandemic levels as of 2023. Coverage for newer vaccines developed and introduced in more recent years, such as immunisations against pneumococcal disease (PCV3) and rotavirus (complete series; RotaC) and a second dose of the measles vaccine (MCV2), saw continued increases globally during the COVID-19 pandemic due to ongoing introductions and scale-ups, but at slower rates than expected in the absence of the pandemic. Forecasts to 2030 for DTP3, PCV3, and MCV2 suggest that only DTP3 would reach the IA2030 target of 90% global coverage, and only under an optimistic scenario. The number of zero-dose children, proxied as children younger than 1 year who do not receive DTP1, decreased by 74·9% (95% uncertainty interval 72·1–77·3) globally between 1980 and 2019, with most of those declines reached during the 1980s and the 2000s. After 2019, counts of zero-dose children rose to a COVID 19-era peak of 18·6 million (17·6–20·0) in 2021. Most zero-dose children remain concentrated in conflict-affected regions and those with various constraints on resources available to put towards vaccination services, particularly sub-Saharan Africa. As of 2023, more than 50% of the 15·7 million (14·6–17·0) global zero-dose children resided in just eight countries (Nigeria, India, Democratic Republic of the Congo, Ethiopia, Somalia, Sudan, Indonesia, and Brazil), emphasising persistent inequities. Interpretation: Our estimates of current vaccine coverage and forecasts to 2030 suggest that achieving IA2030 targets, such as halving zero-dose children compared with 2019 levels and reaching 90% global coverage for life-course vaccines DTP3, PCV3, and MCV2, will require accelerated progress. Substantial increases in coverage are necessary in many countries and territories, with those in sub-Saharan Africa and south Asia facing the greatest challenges. Recent declines will need to be reversed to restore previous coverage levels in Latin America and the Caribbean, especially for DTP1, DTP3, and Pol3. These findings underscore the crucial need for targeted, equitable immunisation strategies. Strengthening primary health-care systems, addressing vaccine misinformation and hesitancy, and adapting to local contexts are essential to advancing coverage. COVID-19 pandemic recovery efforts, such as WHO's Big Catch-Up, as well as efforts to bolster routine services must prioritise reaching marginalised populations and target subnational geographies to regain lost ground and achieve global immunisation goals. Funding: The Bill & Melinda Gates Foundation and Gavi, the Vaccine Alliance.
Open Access: Yes
Global, Regional, and National Burden of Cardiovascular Diseases and Risk Factors in 204 Countries and Territories, 1990-2023
Nermeen Abu-Elala
Rana Kamal Abu Farha
Madineh Abbasi
Abdallah H.A. Abd Al Magied
Eman Abu-Gharbieh
Kamoru Ademola Adedokun
Nurudeen A. Adegoke
Lisa C. Adams
Armita Abedi
Mesfin Abebe
A. Bhoomadevi
Mohammad Amin Aalipour
Bedru J. Abafita
Ukachukwu O. Abaraogu
Dariush Abtahi
Ripon Kumar Adhikary
Mohd Adnan
E. S. Abhilash
Hasan Aalruz
Muhammad Sohail Afzal
Hana J. Abukhadijah
Bedru J. Abafita
Nasir Abbas
Tanin Adl Parvar
César Agostinis Sobrinho
Saira Afzal
Samar Abd ElHafeez
Olorunsola Israel Adeyomoye
Navidha Aggarwal
Johnathan M. Hsu
Catherine O. Johnson
Laura Lara-Castor
Nermeen Abu-Elala
Kate E. LeGrand
Prof Bhoomadevi A
Benjamin A. Stark
Nicole K. DeCleene
Emily C. Desai
Mohammad Abavisani
Mohammadreza Abbasian
Prerna Agarwal
Temesgen Anjulo Ageru
Oladimeji Muritala Adebayo
Suneth Buddhika Agampodi
Sepehr Aghajanian
Salahdein Aburuz
Prof Ahmed Abdelalim
Omar M. Abdelfattah
Prof Reda Abdel-Hameed
Prof Wael M Abdel-Rahman
Daba Abdissa
Mahmoud Abdelnabi
Prof Olumide Abiodun
Lucas Guimarães Abreu
Rui Adão
Aminu Kende Kende Abubakar
Apurba Acharya
Mujahid Abdullah
Ibrahim Jatau Abubakar
Swetha Acharya
Charles Oluwaseun Adetunji
Rishan Adha
Wirawan Adikusuma
Lawan Hassan Adamu
Qorinah Estiningtyas Sakilah Adnani
Gina Agarwal
Ahmed M. Afifi
Fatemeh Afrashteh
Hedayat Abbastabar
Samar Abd ElHafeez
Kulmira Abdykerimova
Rahim Abo Kasem
Asrat Agalu Abejew
Dmitry Abramov
Ousman Adal
Meshack Achore
Aidin Abedi
Olugbenga Olusola Abiodun
Shady Abohashem
Nagah M. Abourashed
David Adedia
Oyelola A. Adegboye
Habeeb Abiodun Afolabi
Anirudh Balakrishna Acharya
Isaac Yeboah Addo
Arman Abdous
Auwal Abdullahi
David Adzrago
Hasan Aalruz
Kishor Adhikari
Dhiraj Motilal Agarwal
Abdullahi Tunde Aborode
Richard Gyan Aboagye
Hassan Abolhassani
Ulric Sena Abonie
Wakgari Mosisa Abdisa
Parsa Abdi
Prince Owusu Adoma
Leticia Akua Adzigbli
Victor Adekanmbi
Arya Afrooghe
Dina Abushanab
Tajudeen Adesanmi Adebisi
Oluwatobi E. Adegbile
Olumide Thomas Adeleke
Nasir Abbas
Salahdein Aburuz
Publication Name: Journal of the American College of Cardiology
Publication Date: 2025-12-02
Volume: 86
Issue: 22
Page Range: 2167-2243
Description:
Background: Cardiovascular diseases (CVDs) are the leading cause of mortality and are among the foremost causes of disability globally. CVD burden has continued to increase in most countries since 1990, with trends driven by changing exposures to harmful risk factors, population growth, and population aging. Objectives: We report estimates of global, national, and subnational CVD burden, including 18 subdiseases and 12 associated modifiable risk factors. We analyzed change in CVD burden from 1990 to 2023 and identified drivers of change including population growth, population aging, and risk factor exposure. Methods: The Global Burden of Disease (GBD) 2023 study, a multinational collaborative research study, quantified burden due to 375 diseases including CVD burden and identified drivers of change from 1990 to 2023 using all available data and statistical models. GBD 2023 estimated the population-level burden of diseases in 204 countries and territories from 1990 to 2023. Results: CVDs were the leading cause of disability-adjusted life years (DALYs) and deaths estimated in the GBD. As of 2023, there were 437 million (95% UI: 401 to 465 million) CVD DALYs globally, a 1.4-fold increase from the number in 1990 of 320 million (292 to 344 million). Ischemic heart disease, intracerebral hemorrhage, ischemic stroke, and hypertensive heart disease were the leading cardiovascular causes of DALYs in 2023 globally. As of 2023, age-standardized CVD DALY rates were highest in low and low-middle Socio-demographic Index (SDI) settings and lowest in high SDI settings. The number of CVD deaths increased globally from 13.1 million (95% UI: 12.2 to 14.0 million) in 1990 to 19.2 million (95% UI: 17.4 to 20.4 million) in 2023. The number of prevalent cases of CVD more than doubled since 1990, with 311 million (95% UI: 294 to 333 million) prevalent cases of CVD in 1990 and 626 million (95% UI: 591 to 672 million) prevalent cases in 2023 globally. A total of 79.6% (95% UI: 75.7% to 82.5%) of CVD burden is attributable to modifiable risk factors 347 million [95% UI: 318 to 373 million] DALYs in 2023). Globally, high systolic blood pressure, dietary risks, high low-density lipoprotein cholesterol, and air pollution were the modifiable risks responsible for most attributable CVD burden in 2023. Since 1990, changes in exposure to modifiable risk factors have had mixed effects on CVD burden, with increases in high body mass index, high fasting plasma glucose, and low physical activity leading to higher burden, while reductions in tobacco usage have mitigated some of these increases. Population growth and population aging were the main drivers of the increasing burden since 1990, adding 128 million (95% UI: 115 to 139 million) and 139 million (95% UI: 126 to 151 million) CVD DALYs to the increase in CVD burden since 1990. Conclusions: CVD remains the leading cause of disease burden and death worldwide with the greatest burden in low, low-middle, and middle SDI regions. Large variation exists in CVD burden even for countries at similar levels of development, a gap explained substantially by known, modifiable risk factors that are inadequately controlled. The decades-long increase in CVD burden was the result of population growth, population aging, and increased exposure to a subset of risk factors led by metabolic risks. Countries will need to adopt effective health system and public health strategies if they are to progress in achieving global goals to reduce the burden of CVD.
Open Access: Yes