Global, regional, and national time trends in mortality for congenital heart disease, 1990-2019: An age-period-cohort analysis for the Global Burden of Disease 2019 study.

age-period-cohort congenital heart disease health disparities mortality

Journal

EClinicalMedicine
ISSN: 2589-5370
Titre abrégé: EClinicalMedicine
Pays: England
ID NLM: 101733727

Informations de publication

Date de publication:
Jan 2022
Historique:
received: 16 09 2021
revised: 27 11 2021
accepted: 07 12 2021
entrez: 21 1 2022
pubmed: 22 1 2022
medline: 22 1 2022
Statut: epublish

Résumé

Congenital heart disease (CHD) is the leading cause of morbidity and mortality from birth defects worldwide. We report an overview of trends in CHD mortality in 204 countries and territories over the past 30 years and associations with age, period, and birth cohort. Cause-specific CHD mortality estimates were derived from the Global Burden of Disease 2019 study. We utilised an age-period-cohort model to estimate overall annual percentage changes in mortality (net drifts), annual percentage changes from 0 to 4 to 65-69 years (local drifts), period and cohort relative risks (period/cohort effects) between 1990 and 2019. This approach allows for the examination and differentiation of age, period, and cohort effects in the mortality trends, with the potential to identify disparities and treatment gaps in cardiac care. CHD is the leading cause of deaths from non-communicable diseases (NCDs) in those under 20 years. Global CHD deaths in 2019 were 217,000 (95% uncertainty interval 177,000-262,000). There were 129 countries with at least 50 deaths. India, China, Pakistan, and Nigeria had the highest mortality, accounting for 39.7% of deaths globally. Between 1990 and 2019, the net drift of CHD mortality ranged from -2.41% per year (95% confidence interval [CI] -2.55, -2.67) in high Socio-demographic Index (SDI) countries to -0.62% per year (95% CI: -0.82, -0.42) in low-SDI countries. Globally, there was an emerging transition in the age distribution of deaths from paediatric to adult populations, except for an increasing trend of mortality in those aged 10-34 years in Mexico and Pakistan. During the past 30 years, favourable mortality reductions were generally found in most high-SDI countries like South Korea (net drift = -4.0% [95% CI -4.8 to -3.1] per year) and the United States (-2.3% [-2.5 to -2.0]), and also in many middle-SDI countries like Brazil (-2.7% [-3.1 to 2.4]) and South Africa (-2.5% [-3.2 to -1.8]). However, 52 of 129 countries had either increasing trends (net drifts ≥0.0%) or stagnated reductions (≥-0.5%) in mortality. The relative risk of mortality generally showed improving trends over time and in successively younger birth cohorts amongst high- and high-middle-SDI countries, with the exceptions of Saudi Arabia and Kazakhstan. 14 middle-SDI countries such as Ecuador and Mexico, and 16 low-middle-SDI countries including India and 20 low-SDI countries including Pakistan, had unfavourable or worsening risks for recent periods and birth cohorts. CHD mortality is a useful and accessible indicator of trends in the provision of congenital cardiac care both in early childhood and across later life. Improvements in the treatment of CHD should reduce the risk for successively younger cohorts and shift the risk for all age groups over time. Although there were gains in CHD mortality globally over the past three decades, unfavourable period and cohort effects were found in many countries, raising questions about adequacy of their health care for CHD patients across all age groups. These failings carry significant implications for the likelihood of achieving the Sustainable Development Goal targets for under-5 years and NCD mortality. Supported by the National Natural Science Foundation of China (81525002, 31971048, 82073573 to ZZ and HZ), Shanghai Outstanding Medical Academic Leader program (2019LJ22 to HZ), and Collaborative Innovation Program of Shanghai Municipal Health Commission (2020CXJQ01 to HZ), the Bill & Melinda Gates Foundation for the Global Burden of Disease Project (to NJK) and NHMRC fellowship administered through the University of Melbourne (to GCP).

Sections du résumé

BACKGROUND BACKGROUND
Congenital heart disease (CHD) is the leading cause of morbidity and mortality from birth defects worldwide. We report an overview of trends in CHD mortality in 204 countries and territories over the past 30 years and associations with age, period, and birth cohort.
METHODS METHODS
Cause-specific CHD mortality estimates were derived from the Global Burden of Disease 2019 study. We utilised an age-period-cohort model to estimate overall annual percentage changes in mortality (net drifts), annual percentage changes from 0 to 4 to 65-69 years (local drifts), period and cohort relative risks (period/cohort effects) between 1990 and 2019. This approach allows for the examination and differentiation of age, period, and cohort effects in the mortality trends, with the potential to identify disparities and treatment gaps in cardiac care.
FINDINGS RESULTS
CHD is the leading cause of deaths from non-communicable diseases (NCDs) in those under 20 years. Global CHD deaths in 2019 were 217,000 (95% uncertainty interval 177,000-262,000). There were 129 countries with at least 50 deaths. India, China, Pakistan, and Nigeria had the highest mortality, accounting for 39.7% of deaths globally. Between 1990 and 2019, the net drift of CHD mortality ranged from -2.41% per year (95% confidence interval [CI] -2.55, -2.67) in high Socio-demographic Index (SDI) countries to -0.62% per year (95% CI: -0.82, -0.42) in low-SDI countries. Globally, there was an emerging transition in the age distribution of deaths from paediatric to adult populations, except for an increasing trend of mortality in those aged 10-34 years in Mexico and Pakistan. During the past 30 years, favourable mortality reductions were generally found in most high-SDI countries like South Korea (net drift = -4.0% [95% CI -4.8 to -3.1] per year) and the United States (-2.3% [-2.5 to -2.0]), and also in many middle-SDI countries like Brazil (-2.7% [-3.1 to 2.4]) and South Africa (-2.5% [-3.2 to -1.8]). However, 52 of 129 countries had either increasing trends (net drifts ≥0.0%) or stagnated reductions (≥-0.5%) in mortality. The relative risk of mortality generally showed improving trends over time and in successively younger birth cohorts amongst high- and high-middle-SDI countries, with the exceptions of Saudi Arabia and Kazakhstan. 14 middle-SDI countries such as Ecuador and Mexico, and 16 low-middle-SDI countries including India and 20 low-SDI countries including Pakistan, had unfavourable or worsening risks for recent periods and birth cohorts.
INTERPRETATION CONCLUSIONS
CHD mortality is a useful and accessible indicator of trends in the provision of congenital cardiac care both in early childhood and across later life. Improvements in the treatment of CHD should reduce the risk for successively younger cohorts and shift the risk for all age groups over time. Although there were gains in CHD mortality globally over the past three decades, unfavourable period and cohort effects were found in many countries, raising questions about adequacy of their health care for CHD patients across all age groups. These failings carry significant implications for the likelihood of achieving the Sustainable Development Goal targets for under-5 years and NCD mortality.
FUNDING BACKGROUND
Supported by the National Natural Science Foundation of China (81525002, 31971048, 82073573 to ZZ and HZ), Shanghai Outstanding Medical Academic Leader program (2019LJ22 to HZ), and Collaborative Innovation Program of Shanghai Municipal Health Commission (2020CXJQ01 to HZ), the Bill & Melinda Gates Foundation for the Global Burden of Disease Project (to NJK) and NHMRC fellowship administered through the University of Melbourne (to GCP).

Identifiants

pubmed: 35059612
doi: 10.1016/j.eclinm.2021.101249
pii: S2589-5370(21)00530-7
pmc: PMC8760503
doi:

Types de publication

Journal Article

Langues

eng

Pagination

101249

Informations de copyright

© 2022 Published by Elsevier Ltd.

Déclaration de conflit d'intérêts

NJK reports consulting fees from Merck as a one-day consultation on a potential public visualization tool. All the other authors declare no competing interests.

Références

J Am Coll Cardiol. 2018 May 29;71(21):2434-2446
pubmed: 29793633
Lancet. 2014 Aug 30;384(9945):747-54
pubmed: 24768155
JAMA Netw Open. 2018 Nov 2;1(7):e184707
pubmed: 30646368
JAMA Netw Open. 2021 Apr 1;4(4):e215237
pubmed: 33830227
Can J Cardiol. 2019 Dec;35(12):1609-1619
pubmed: 31813496
Circulation. 2015 May 26;131(21):1884-931
pubmed: 25896865
Braz J Cardiovasc Surg. 2020 Apr 01;35(2):IV-VI
pubmed: 32369288
JAMA Intern Med. 2017 Feb 1;177(2):224-230
pubmed: 27992621
Int J Cardiol. 2012 May 17;157(1):70-4
pubmed: 21190745
Lancet Child Adolesc Health. 2020 Mar;4(3):185-200
pubmed: 31978374
Future Cardiol. 2018 Jan;14(1):1-4
pubmed: 29168647
Cancer Epidemiol Biomarkers Prev. 2011 Jul;20(7):1263-8
pubmed: 21610223
Cancer Epidemiol Biomarkers Prev. 2014 Nov;23(11):2296-302
pubmed: 25146089
Lancet Child Adolesc Health. 2018 Jun;2(6):430-439
pubmed: 30169284
Lancet. 2018 Sep 22;392(10152):1072-1088
pubmed: 30264707
Lancet. 2020 Oct 17;396(10258):1160-1203
pubmed: 33069325
Cardiovasc J Afr. 2017 Jan/Feb 23;28(1):54-59
pubmed: 27701490
Arch Dis Child. 2012 Oct;97(10):861-5
pubmed: 22753769
Nat Rev Cardiol. 2011 Jan;8(1):50-60
pubmed: 21045784
Circ Res. 2017 Mar 17;120(6):908-922
pubmed: 28302739
Ann Hum Biol. 2020 Mar;47(2):208-217
pubmed: 32429768
World J Pediatr Congenit Heart Surg. 2019 Mar;10(2):206-213
pubmed: 30841824
Circulation. 2020 Sep 22;142(12):1132-1147
pubmed: 32795094
Stat Med. 2010 May 20;29(11):1228-38
pubmed: 20209480
World J Pediatr Congenit Heart Surg. 2011 Apr;2(2):301-7
pubmed: 23804988
Ann Thorac Surg. 2017 Jul;104(1):361-366
pubmed: 28633226
Congenit Heart Dis. 2018 Sep;13(5):690-699
pubmed: 30178578
World J Pediatr Congenit Heart Surg. 2014 Apr;5(2):248-55
pubmed: 24668973
BMJ Open. 2019 Jun 22;9(6):e028307
pubmed: 31230022
Circulation. 2020 Mar 10;141(10):790-799
pubmed: 31941371
Front Pediatr. 2019 Jun 13;7:214
pubmed: 31263686
Circulation. 2019 Apr 16;139(16):1889-1899
pubmed: 30813762
Am J Prev Med. 2016 May;50(5):663-671
pubmed: 26895742
J Thorac Cardiovasc Surg. 2020 Mar;159(3):987-996.e6
pubmed: 31128897
Int J Cardiol. 2019 Oct 1;292:100-105
pubmed: 31085084
JAMA Netw Open. 2019 Jul 3;2(7):e196762
pubmed: 31276179
Cardiol Young. 2017 Dec;27(S6):S22-S30
pubmed: 29198259
Braz J Cardiovasc Surg. 2016 May-Jun;31(3):3-4
pubmed: 27737413
Glob Heart. 2018 Dec;13(4):293-303
pubmed: 30245177
Int J Cardiol. 2013 Oct 15;168(6):5182-9
pubmed: 23972963
Cureus. 2019 Aug 7;11(8):e5339
pubmed: 31598445
Medicine (Baltimore). 2020 Jun 5;99(23):e20593
pubmed: 32502030
Lancet. 2020 Oct 17;396(10258):1204-1222
pubmed: 33069326
J Am Coll Cardiol. 2020 Dec 22;76(25):2982-3021
pubmed: 33309175
Lancet Child Adolesc Health. 2020 Apr;4(4):e7
pubmed: 32197102
Lancet. 2017 Jan 7;389(10064):16-18
pubmed: 27989557

Auteurs

Zhanhao Su (Z)

State Key Laboratory of Cardiovascular Disease, Fuwai Hospital, National Center for Cardiovascular Diseases, Pediatric Cardiac Surgery Center, Fuwai Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.

Zhiyong Zou (Z)

Institute of Child and Adolescent Health, National Health Commission Key Laboratory of Reproductive Health, Peking University School of Public Health, No.38 Xueyuan Rd, Haidian District, Beijing 100191, China.

Simon I Hay (SI)

Institute for Health Metrics and Evaluation, University of Washington, Seattle, WA, United States.
Department of Health Metrics Sciences, School of Medicine, University of Washington, Seattle, WA, United States.

Yiwei Liu (Y)

Heart Center and Shanghai Institute of Pediatric Congenital Heart Disease, Shanghai Children's Medical Center, National Children's Medical Center, Shanghai Jiaotong University School of Medicine, Room 7016, Heart centre, Shanghai Children's Medical centre, No. 1678, Dongfang Rd, Pudong District, Shanghai, China.

Shoujun Li (S)

State Key Laboratory of Cardiovascular Disease, Fuwai Hospital, National Center for Cardiovascular Diseases, Pediatric Cardiac Surgery Center, Fuwai Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.

Huiwen Chen (H)

Heart Center and Shanghai Institute of Pediatric Congenital Heart Disease, Shanghai Children's Medical Center, National Children's Medical Center, Shanghai Jiaotong University School of Medicine, Room 7016, Heart centre, Shanghai Children's Medical centre, No. 1678, Dongfang Rd, Pudong District, Shanghai, China.

Mohsen Naghavi (M)

Institute for Health Metrics and Evaluation, University of Washington, Seattle, WA, United States.
Department of Health Metrics Sciences, School of Medicine, University of Washington, Seattle, WA, United States.

Meghan S Zimmerman (MS)

Division of Pediatric Cardiology, Dartmouth-Hitchcock Medical Center, Lebanon, NH, United States.
Milken Institute School of Public Health, George Washington University, Washington, DC, United States.
Department of Cardiology, Children's National Health System, Washington, DC, United States.

Gerard R Martin (GR)

Department of Cardiology, Children's National Health System, Washington, DC, United States.

Lauren B Wilner (LB)

Institute for Health Metrics and Evaluation, University of Washington, Seattle, WA, United States.
Department of Health Metrics Sciences, School of Medicine, University of Washington, Seattle, WA, United States.

Craig A Sable (CA)

Department of Cardiology, Children's National Health System, Washington, DC, United States.

Christopher J L Murray (CJL)

Institute for Health Metrics and Evaluation, University of Washington, Seattle, WA, United States.
Department of Health Metrics Sciences, School of Medicine, University of Washington, Seattle, WA, United States.

Nicholas J Kassebaum (NJ)

Institute for Health Metrics and Evaluation, University of Washington, Seattle, WA, United States.
Department of Anesthesiology and Pain Medicine, Harborview Medical Center, University of Washington, Seattle, WA, United States.

George C Patton (GC)

Institute of Child and Adolescent Health, National Health Commission Key Laboratory of Reproductive Health, Peking University School of Public Health, No.38 Xueyuan Rd, Haidian District, Beijing 100191, China.
Department of Pediatrics, The University of Melbourne, Parkville, Victoria, Australia.
Centre for Adolescent Health, Royal Children's Hospital, Parkville, Victoria, Australia.
Murdoch Children's Research Institute, Melbourne, Victoria, Australia.

Hao Zhang (H)

Heart Center and Shanghai Institute of Pediatric Congenital Heart Disease, Shanghai Children's Medical Center, National Children's Medical Center, Shanghai Jiaotong University School of Medicine, Room 7016, Heart centre, Shanghai Children's Medical centre, No. 1678, Dongfang Rd, Pudong District, Shanghai, China.

Classifications MeSH