The burden of bacterial antimicrobial resistance in the WHO African region in 2019: a cross-country systematic analysis
Open accessAbstract
BACKGROUND: A critical and persistent challenge to global health and modern health care is the threat of antimicrobial resistance (AMR). Previous studies have reported a disproportionate burden of AMR in low-income and middle-income countries, but there remains an urgent need for more in-depth analyses across Africa. This study presents one of the most comprehensive sets of regional and country-level estimates of bacterial AMR burden in the WHO African region to date. METHODS: We estimated deaths and disability-adjusted life-years (DALYs) attributable to and associated with AMR for 23 bacterial pathogens and 88 pathogen-drug combinations for countries in the WHO African region in 2019. Our methodological approach consisted of five broad components: the number of deaths in which infection had a role, the proportion of infectious deaths attributable to a given infectious syndrome, the proportion of infectious syndrome deaths attributable to a given pathogen, the percentage of a given pathogen resistant to an antimicrobial drug of interest, and the excess risk of mortality (or duration of an infection) associated with this resistance. These components were then used to estimate the disease burden by using two counterfactual scenarios: deaths attributable to AMR (considering an alternative scenario where infections with resistant pathogens are replaced with susceptible ones) and deaths associated with AMR (considering an alternative scenario where drug-resistant infections would not occur at all). We obtained data from research hospitals, surveillance networks, and infection databases maintained by private laboratories and medical technology companies. We generated 95% uncertainty intervals (UIs) for final estimates as the 25th and 975th ordered values across 1000 posterior draws, and models were cross-validated for out-of-sample predictive validity. FINDINGS: In the WHO African region in 2019, there were an estimated 1·05 million deaths (95% UI 829 000-1 316 000) associated with bacterial AMR and 250 000 deaths (192 000-325 000) attributable to bacterial AMR. The largest fatal AMR burden was attributed to lower respiratory and thorax infections (119 000 deaths [92 000-151 000], or 48% of all estimated bacterial pathogen AMR deaths), bloodstream infections (56 000 deaths [37 000-82 000], or 22%), intra-abdominal infections (26 000 deaths [17 000-39 000], or 10%), and tuberculosis (18 000 deaths [3850-39 000], or 7%). Seven leading pathogens were collectively responsible for 821 000 deaths (636 000-1 051 000) associated with resistance in this region, with four pathogens exceeding 100 000 deaths each: Streptococcus pneumoniae, Klebsiella pneumoniae, Escherichia coli, and Staphylococcus aureus. Third-generation cephalosporin-resistant K pneumoniae and meticillin-resistant S aureus were shown to be the leading pathogen-drug combinations in 25 and 16 countries, respectively (53% and 34% of the whole region, comprising 47 countries) for deaths attributable to AMR. INTERPRETATION: This study reveals a high level of AMR burden for several bacterial pathogens and pathogen-drug combinations in the WHO African region. The high mortality rates associated with these pathogens demonstrate an urgent need to address the burden of AMR in Africa. These estimates also show that quality and access to health care and safe water and sanitation are correlated with AMR mortality, with a higher fatal burden found in lower resource settings. Our cross-country analyses within this region can help local governments to leverage domestic and global funding to create stewardship policies that target the leading pathogen-drug combinations. FUNDING: Bill & Melinda Gates Foundation, Wellcome Trust, and Department of Health and Social Care using UK aid funding managed by the Fleming Fund.
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The reduction in AMR mortality in sub-Saharan Africa is due to a substantial decline in AMR deaths in children younger than 5 years, and is consistent with the principles that AMR deaths can be averted with infection prevention and control measures, vaccination, and access to antibiotics.
“This reduction in mortality is due to a substantial decline in AMR deaths in children younger than 5 years, and is consistent with the principles described in the recent Lancet series, that AMR deaths can be averted with infection prevention and control measures, vaccination, and access to antibiotics.60”
From Global burden of bacterial antimicrobial resistance 1990–2021: a systematic analysis with forecasts to 2050 (2024) · cites this paper as [60]
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Experimental — accuracy not yet measuredThe scarcity of data is mainly due to insufficient laboratory infrastructure and capacity, scarce or absent microbiological facilities, weak health systems and governance and information systems, and scarce resources.
“Such sparsity is mainly due to insufficient laboratory infrastructure and capacity, scarce or absent microbiological facilities, weak health systems and governance and information systems, and scarce resources.60, 72, 73”
From Global burden of bacterial antimicrobial resistance 1990–2021: a systematic analysis with forecasts to 2050 (2024) · cites this paper as [60]
The scarce data in some countries substantially affected the prevalence of resistance and relative risk modelling components.
“The scarce data in some countries substantially affected our prevalence of resistance and relative risk modelling components, akin to the situation in our previous publications.6, 50, 51, 60”
From Global burden of bacterial antimicrobial resistance 1990–2021: a systematic analysis with forecasts to 2050 (2024) · cites this paper as [60]
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Naghavi, M., Vollset, S. E., Ikuta, K. S., Swetschinski, L. R., Gray, A. P., Wool, E. E., Robles Aguilar, G., Mestrovic, T., Smith, G., Han, C., et al. (2024) · The Lancet · doi:10.1016/s0140-6736(24)01867-1 · Cited by 3,791 · see citing works
Self-citation
- Authors
- Sartorius, B., Gray, A. P., Davis Weaver, N., Robles Aguilar, G., Swetschinski, L. R., Ikuta, K. S., Mestrovic, T., Chung, E., Wool, E. E., Han, C., Gershberg Hayoon, A., Araki, D. T., Abd-Elsalam, S., Aboagye, R. G., Adamu, L. H., Adepoju, A. V., Ahmed, A., Akalu, G. T., Akande-Sholabi, W., Amuasi, J. H., Amusa, G. A., Argaw, A. M., Aruleba, R. T., Awoke, T., Ayalew, M. K., Azzam, A. Y., Babin, F.-X., Banerjee, I., Basiru, A., Bayileyegn, N. S., Belete, M. A., Berkley, J. A., Bielicki, J. A., Dekker, D., Demeke, D., Demsie, D. G., Dessie, A. M., Dunachie, S. J., Ed-Dra, A., Ekholuenetale, M., Ekundayo, T. C., El Sayed, I., Elhadi, M., Elsohaby, I., Eyre, D., Fagbamigbe, A. F., Feasey, N. A., Fekadu, G., Fell, F., Forrest, K. M., Gebrehiwot, M., Gezae, K. E., Ghazy, R. M., Hailegiyorgis, T. T., Haines-Woodhouse, G., Hasaballah, A. I., Haselbeck, A. H., Hsia, Y., Iradukunda, A., Iregbu, K. C., Iwu, C. C. D., Iwu-Jaja, C. J., Iyasu, A. N., Jaiteh, F., Jeon, H., Joshua, C. E., Kassa, G. G., Katoto, P. D., Krumkamp, R., Kumaran, E. A. P., Kyu, H. H., Manilal, A., Marks, F., May, J., McLaughlin, S. A., McManigal, B., Melese, A., Misgina, K. H., Mohamed, N. S., Mohammed, M., Mohammed, S., Mohammed, S., Mokdad, A. H., Moore, C. E., Mougin, V., Mturi, N., Mulugeta, T., Musaigwa, F., Musicha, P., Musila, L. A., Muthupandian, S., Naghavi, P., Negash, H., Nuckchady, D. C., Obiero, C. W., Odetokun, I. A., Ogundijo, O. A., Okidi, L., Okonji, O. C., Olagunju, A. T., Olufadewa, I. I., Pak, G. D., Perovic, O., Pollard, A., Raad, M., Rafaï, C., Ramadan, H., Redwan, E. M. M., Roca, A., Rosenthal, V. D., Saleh, M. A., Samy, A. M., Sharland, M., Shittu, A., Siddig, E. E., Sisay, E. A., Stergachis, A., Tesfamariam, W. B., Tigoi, C., Tincho, M. B., Tiruye, T. Y., Umeokonkwo, C. D., Walsh, T., Walson, J. L., Yusuf, H., Zeru, N. G., Hay, S. I., Dolecek, C., Murray, C. J. L., & Naghavi, M.
- Affiliations
- University of Washington (US)
- University of Ibadan (NG)
- The University of Queensland (AU)
- Corresponding author
- Naghavi, Mohsen
- ORCID
- Sartorius, Benn
- Ikuta, Kevin S
- Chung, Erin
- Wool, Eve E
- Abd-Elsalam, Sherief
- Aboagye, Richard Gyan
- Ahmed, Ayman
- Akalu, Gizachew Taddesse
- Amuasi, John H
- Aruleba, Raphael Taiwo
- Ayalew, Melese Kitu
- Azzam, Ahmed Y
- Banerjee, Indrajit
- Basiru, Afisu
- Bayileyegn, Nebiyou Simegnew
- Belete, Melaku Ashagrie
- Berkley, James A
- Bielicki, Julia A
- Dekker, Denise
- Demeke, Dessalegn
- Demsie, Desalegn Getnet
- Dessie, Anteneh Mengist
- Dunachie, Susanna J
- Ekholuenetale, Michael
- Ekundayo, Temitope Cyrus
- Elhadi, Muhammed
- Elsohaby, Ibrahim
- Eyre, David
- Fagbamigbe, Adeniyi Francis
- Feasey, Nicholas A
- Fekadu, Ginenus
- Gebrehiwot, Mesfin
- Gezae, Kebede Embaye
- Ghazy, Ramy Mohamed
- Hasaballah, Ahmed I
- Haselbeck, Andrea Haekyung
- Hsia, Yingfen
- Iradukunda, Arnaud
- Iregbu, Kenneth Chukwuemeka
- Iyasu, Assefa N
- Kassa, Gebrehiwot G
- Katoto, Patrick DMC
- Krumkamp, Ralf
- Kumaran, Emmanuelle A P
- Kyu, Hmwe Hmwe
- Manilal, Aseer
- Marks, Florian
- May, Jürgen
- Melese, Addisu
- Misgina, Kebede Haile
- Mohamed, Nouh Saad
- Mohammed, Mustapha
- Mohammed, Shafiu
- Mohammed, Shikur
- Mokdad, Ali H
- Moore, Catrin E
- Mougin, Vincent
- Mturi, Neema
- Mulugeta, Temesgen
- Musaigwa, Fungai
- Musicha, Patrick
- Musila, Lillian A
- Naghavi, Pirouz
- Nuckchady, Dooshanveer C
- Obiero, Christina W
- Odetokun, Ismail A
- Ogundijo, Oluwaseun Adeolu
- Okidi, Lawrence
- Okonji, Osaretin Christabel
- Olagunju, Andrew T
- Olufadewa, Isaac Iyinoluwa
- Pak, Gi Deok
- Perovic, Olga
- Pollard, Andrew
- Roca, Anna
- Saleh, Mohamed A
- Samy, Abdallah M
- Sharland, M
- Shittu, Aminu
- Siddig, Emmanuel Edwar
- Sisay, Eskinder Ayalew
- Stergachis, Andy
- Tesfamariam, Wegen Beyene
- Tigoi, Caroline
- Tincho, Marius Belmondo
- Tiruye, Tenaw Yimer
- Umeokonkwo, Chukwuma David
- Walson, Judd L
- Yusuf, Hadiza
- Hay, Simon I
- Dolecek, Christiane
- Murray, Christopher J L
- Naghavi, Mohsen
- Venue
- The Lancet Global Health
- Publisher
- Elsevier BV
- Published
- 2024-02
- Volume
- 12
- Issue
- 2
- Pages
- e201-e216
- ISSN
- 2214-109X (ISSN-L)
- PMC
- PMC10805005
- OpenAlex
- W4389932972
- Cited by
- 354
- References
- 5
- Citations by year
- 2026: 123 · 2025: 168 · 2024: 61 · 2023: 2
- FWCI
- 67.57
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- Locations
- The Lancet Global Health (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- St George's Online Research Archive (St George's University of London) (acceptedVersion)
- LSTM Online Archive (Liverpool School of Tropical Medicine) (acceptedVersion)
- LSHTM Research Online (London School of Hygiene and Tropical Medicine) (acceptedVersion)
- CityU Scholars (submittedVersion, cc-by)
- UniSA Research Outputs Repository (University of South Australia) (submittedVersion, other-oa)
- Funders
- Wellcome Trust (A126042)
- Bill and Melinda Gates Foundation (OPP1176062)
- Topics
- Life Sciences › Immunology and Microbiology › Applied Microbiology and Biotechnology › Antibiotic Use and Resistance
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Medicine › Antibiotic Resistance in Bacteria
- Health Sciences › Medicine › Infectious Diseases › Antimicrobial Resistance in Staphylococcus
- Keywords
- antimicrobial resistance, bacterial infection, disease burden, mortality, disability-adjusted life years, WHO African Region, lower respiratory tract infection, bloodstream infection, intra-abdominal infection, drug-resistant pathogens, counterfactual scenarios, infection duration, economic burden, antimicrobial resistance policy, infection control, antimicrobial stewardship, low- and middle-income countries
- MeSH terms
- Anti-Bacterial Agents, Bacterial Infections, Drug Combinations, Humans, Global Health, World Health Organization, Drug Resistance, Bacterial, Methicillin-Resistant Staphylococcus aureus
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