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      Global, regional, and national disease burden estimates of acute lower respiratory infections due to respiratory syncytial virus in children younger than 5 years in 2019: a systematic analysis

      research-article
      , PhD, , PhD, , PhD, , MD, , MD, , MD, , PhD, , MBBS, , MD, , MD, , MSc, , MD, , MD, , , PhD, , PhD, , PhD, , , PhD, , MD, , PhD, , MD, , PhD, , , MD, , MD, , MD, , PhD, , PhD, , MD, , MD, , PhD, , PhD, , PhD, , PhD, , MD, , PhD, , MD, , MD, , MD, , MD, , BSc, , PhD, , , PhD, , PhD, , MBChB, , PhD Respiratory Virus Global Epidemiology Network investigators
      RESCEU investigators
      Lancet (London, England)

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          Summary

          Background

          Respiratory syncytial virus (RSV) is the most common cause of acute lower respiratory infection in young children. We previously estimated that in 2015, 33·1 million episodes of RSV-associated acute lower respiratory infection occurred in children aged 0–60 months, resulting in a total of 118 200 deaths worldwide. Since then, several community surveillance studies have been done to obtain a more precise estimation of RSV associated community deaths. We aimed to update RSV-associated acute lower respiratory infection morbidity and mortality at global, regional, and national levels in children aged 0–60 months for 2019, with focus on overall mortality and narrower infant age groups that are targeted by RSV prophylactics in development.

          Methods

          In this systematic analysis, we expanded our global RSV disease burden dataset by obtaining new data from an updated search for papers published between Jan 1, 2017, and Dec 31, 2020, from MEDLINE, Embase, Global Health, CINAHL, Web of Science, LILACS, OpenGrey, CNKI, Wanfang, and ChongqingVIP. We also included unpublished data from RSV GEN collaborators. Eligible studies reported data for children aged 0–60 months with RSV as primary infection with acute lower respiratory infection in community settings, or acute lower respiratory infection necessitating hospital admission; reported data for at least 12 consecutive months, except for in-hospital case fatality ratio (CFR) or for where RSV seasonality is well-defined; and reported incidence rate, hospital admission rate, RSV positive proportion in acute lower respiratory infection hospital admission, or in-hospital CFR. Studies were excluded if case definition was not clearly defined or not consistently applied, RSV infection was not laboratory confirmed or based on serology alone, or if the report included fewer than 50 cases of acute lower respiratory infection. We applied a generalised linear mixed-effects model (GLMM) to estimate RSV-associated acute lower respiratory infection incidence, hospital admission, and in-hospital mortality both globally and regionally (by country development status and by World Bank Income Classification) in 2019. We estimated country-level RSV-associated acute lower respiratory infection incidence through a risk-factor based model. We developed new models (through GLMM) that incorporated the latest RSV community mortality data for estimating overall RSV mortality. This review was registered in PROSPERO (CRD42021252400).

          Findings

          In addition to 317 studies included in our previous review, we identified and included 113 new eligible studies and unpublished data from 51 studies, for a total of 481 studies. We estimated that globally in 2019, there were 33·0 million RSV-associated acute lower respiratory infection episodes (uncertainty range [UR] 25·4–44·6 million), 3·6 million RSV-associated acute lower respiratory infection hospital admissions (2·9–4·6 million), 26 300 RSV-associated acute lower respiratory infection in-hospital deaths (15 100–49 100), and 101 400 RSV-attributable overall deaths (84 500–125 200) in children aged 0–60 months. In infants aged 0–6 months, we estimated that there were 6·6 million RSV-associated acute lower respiratory infection episodes (4·6–9·7 million), 1·4 million RSV-associated acute lower respiratory infection hospital admissions (1·0–2·0 million), 13 300 RSV-associated acute lower respiratory infection inhospital deaths (6800–28 100), and 45700 RSV-attributable overall deaths (38 400–55 900). 2·0% of deaths in children aged 0–60 months (UR 1·6–2·4) and 3·6% of deaths in children aged 28 days to 6 months (3·0–4·4) were attributable to RSV. More than 95% of RSV-associated acute lower respiratory infection episodes and more than 97% of RSV-attributable deaths across all age bands were in low-income and middle-income countries (LMICs).

          Interpretation

          RSV contributes substantially to morbidity and mortality burden globally in children aged 0–60 months, especially during the first 6 months of life and in LMICs. We highlight the striking overall mortality burden of RSV disease worldwide, with one in every 50 deaths in children aged 0–60 months and one in every 28 deaths in children aged 28 days to 6 months attributable to RSV. For every RSV-associated acute lower respiratory infection in-hospital death, we estimate approximately three more deaths attributable to RSV in the community. RSV passive immunisation programmes targeting protection during the first 6 months of life could have a substantial effect on reducing RSV disease burden, although more data are needed to understand the implications of the potential age-shifts in peak RSV burden to older age when these are implemented.

          Funding

          EU Innovative Medicines Initiative Respiratory Syncytial Virus Consortium in Europe (RESCEU).

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          Most cited references33

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          Global, regional, and national disease burden estimates of acute lower respiratory infections due to respiratory syncytial virus in young children in 2015: a systematic review and modelling study

          Summary Background We have previously estimated that respiratory syncytial virus (RSV) was associated with 22% of all episodes of (severe) acute lower respiratory infection (ALRI) resulting in 55 000 to 199 000 deaths in children younger than 5 years in 2005. In the past 5 years, major research activity on RSV has yielded substantial new data from developing countries. With a considerably expanded dataset from a large international collaboration, we aimed to estimate the global incidence, hospital admission rate, and mortality from RSV-ALRI episodes in young children in 2015. Methods We estimated the incidence and hospital admission rate of RSV-associated ALRI (RSV-ALRI) in children younger than 5 years stratified by age and World Bank income regions from a systematic review of studies published between Jan 1, 1995, and Dec 31, 2016, and unpublished data from 76 high quality population-based studies. We estimated the RSV-ALRI incidence for 132 developing countries using a risk factor-based model and 2015 population estimates. We estimated the in-hospital RSV-ALRI mortality by combining in-hospital case fatality ratios with hospital admission estimates from hospital-based (published and unpublished) studies. We also estimated overall RSV-ALRI mortality by identifying studies reporting monthly data for ALRI mortality in the community and RSV activity. Findings We estimated that globally in 2015, 33·1 million (uncertainty range [UR] 21·6–50·3) episodes of RSV-ALRI, resulted in about 3·2 million (2·7–3·8) hospital admissions, and 59 600 (48 000–74 500) in-hospital deaths in children younger than 5 years. In children younger than 6 months, 1·4 million (UR 1·2–1·7) hospital admissions, and 27 300 (UR 20 700–36 200) in-hospital deaths were due to RSV-ALRI. We also estimated that the overall RSV-ALRI mortality could be as high as 118 200 (UR 94 600–149 400). Incidence and mortality varied substantially from year to year in any given population. Interpretation Globally, RSV is a common cause of childhood ALRI and a major cause of hospital admissions in young children, resulting in a substantial burden on health-care services. About 45% of hospital admissions and in-hospital deaths due to RSV-ALRI occur in children younger than 6 months. An effective maternal RSV vaccine or monoclonal antibody could have a substantial effect on disease burden in this age group. Funding The Bill & Melinda Gates Foundation.
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            Estimates of the global, regional, and national morbidity, mortality, and aetiologies of lower respiratory infections in 195 countries, 1990–2016: a systematic analysis for the Global Burden of Disease Study 2016

            Summary Background Lower respiratory infections are a leading cause of morbidity and mortality around the world. The Global Burden of Diseases, Injuries, and Risk Factors (GBD) Study 2016, provides an up-to-date analysis of the burden of lower respiratory infections in 195 countries. This study assesses cases, deaths, and aetiologies spanning the past 26 years and shows how the burden of lower respiratory infection has changed in people of all ages. Methods We used three separate modelling strategies for lower respiratory infections in GBD 2016: a Bayesian hierarchical ensemble modelling platform (Cause of Death Ensemble model), which uses vital registration, verbal autopsy data, and surveillance system data to predict mortality due to lower respiratory infections; a compartmental meta-regression tool (DisMod-MR), which uses scientific literature, population representative surveys, and health-care data to predict incidence, prevalence, and mortality; and modelling of counterfactual estimates of the population attributable fraction of lower respiratory infection episodes due to Streptococcus pneumoniae, Haemophilus influenzae type b, influenza, and respiratory syncytial virus. We calculated each modelled estimate for each age, sex, year, and location. We modelled the exposure level in a population for a given risk factor using DisMod-MR and a spatio-temporal Gaussian process regression, and assessed the effectiveness of targeted interventions for each risk factor in children younger than 5 years. We also did a decomposition analysis of the change in LRI deaths from 2000–16 using the risk factors associated with LRI in GBD 2016. Findings In 2016, lower respiratory infections caused 652 572 deaths (95% uncertainty interval [UI] 586 475–720 612) in children younger than 5 years (under-5s), 1 080 958 deaths (943 749–1 170 638) in adults older than 70 years, and 2 377 697 deaths (2 145 584–2 512 809) in people of all ages, worldwide. Streptococcus pneumoniae was the leading cause of lower respiratory infection morbidity and mortality globally, contributing to more deaths than all other aetiologies combined in 2016 (1 189 937 deaths, 95% UI 690 445–1 770 660). Childhood wasting remains the leading risk factor for lower respiratory infection mortality among children younger than 5 years, responsible for 61·4% of lower respiratory infection deaths in 2016 (95% UI 45·7–69·6). Interventions to improve wasting, household air pollution, ambient particulate matter pollution, and expanded antibiotic use could avert one under-5 death due to lower respiratory infection for every 4000 children treated in the countries with the highest lower respiratory infection burden. Interpretation Our findings show substantial progress in the reduction of lower respiratory infection burden, but this progress has not been equal across locations, has been driven by decreases in several primary risk factors, and might require more effort among elderly adults. By highlighting regions and populations with the highest burden, and the risk factors that could have the greatest effect, funders, policy makers, and programme implementers can more effectively reduce lower respiratory infections among the world's most susceptible populations. Funding Bill & Melinda Gates Foundation.
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              Causes of severe pneumonia requiring hospital admission in children without HIV infection from Africa and Asia: the PERCH multi-country case-control study

              Summary Background Pneumonia is the leading cause of death among children younger than 5 years. In this study, we estimated causes of pneumonia in young African and Asian children, using novel analytical methods applied to clinical and microbiological findings. Methods We did a multi-site, international case-control study in nine study sites in seven countries: Bangladesh, The Gambia, Kenya, Mali, South Africa, Thailand, and Zambia. All sites enrolled in the study for 24 months. Cases were children aged 1–59 months admitted to hospital with severe pneumonia. Controls were age-group-matched children randomly selected from communities surrounding study sites. Nasopharyngeal and oropharyngeal (NP-OP), urine, blood, induced sputum, lung aspirate, pleural fluid, and gastric aspirates were tested with cultures, multiplex PCR, or both. Primary analyses were restricted to cases without HIV infection and with abnormal chest x-rays and to controls without HIV infection. We applied a Bayesian, partial latent class analysis to estimate probabilities of aetiological agents at the individual and population level, incorporating case and control data. Findings Between Aug 15, 2011, and Jan 30, 2014, we enrolled 4232 cases and 5119 community controls. The primary analysis group was comprised of 1769 (41·8% of 4232) cases without HIV infection and with positive chest x-rays and 5102 (99·7% of 5119) community controls without HIV infection. Wheezing was present in 555 (31·7%) of 1752 cases (range by site 10·6–97·3%). 30-day case-fatality ratio was 6·4% (114 of 1769 cases). Blood cultures were positive in 56 (3·2%) of 1749 cases, and Streptococcus pneumoniae was the most common bacteria isolated (19 [33·9%] of 56). Almost all cases (98·9%) and controls (98·0%) had at least one pathogen detected by PCR in the NP-OP specimen. The detection of respiratory syncytial virus (RSV), parainfluenza virus, human metapneumovirus, influenza virus, S pneumoniae, Haemophilus influenzae type b (Hib), H influenzae non-type b, and Pneumocystis jirovecii in NP-OP specimens was associated with case status. The aetiology analysis estimated that viruses accounted for 61·4% (95% credible interval [CrI] 57·3–65·6) of causes, whereas bacteria accounted for 27·3% (23·3–31·6) and Mycobacterium tuberculosis for 5·9% (3·9–8·3). Viruses were less common (54·5%, 95% CrI 47·4–61·5 vs 68·0%, 62·7–72·7) and bacteria more common (33·7%, 27·2–40·8 vs 22·8%, 18·3–27·6) in very severe pneumonia cases than in severe cases. RSV had the greatest aetiological fraction (31·1%, 95% CrI 28·4–34·2) of all pathogens. Human rhinovirus, human metapneumovirus A or B, human parainfluenza virus, S pneumoniae, M tuberculosis, and H influenzae each accounted for 5% or more of the aetiological distribution. We observed differences in aetiological fraction by age for Bordetella pertussis, parainfluenza types 1 and 3, parechovirus–enterovirus, P jirovecii, RSV, rhinovirus, Staphylococcus aureus, and S pneumoniae, and differences by severity for RSV, S aureus, S pneumoniae, and parainfluenza type 3. The leading ten pathogens of each site accounted for 79% or more of the site's aetiological fraction. Interpretation In our study, a small set of pathogens accounted for most cases of pneumonia requiring hospital admission. Preventing and treating a subset of pathogens could substantially affect childhood pneumonia outcomes. Funding Bill & Melinda Gates Foundation.
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                Author and article information

                Contributors
                Journal
                2985213R
                Lancet
                Lancet
                Lancet (London, England)
                0140-6736
                1474-547X
                31 August 2022
                28 May 2022
                19 May 2022
                08 September 2022
                : 399
                : 10340
                : 2047-2064
                Affiliations
                School of Public Health, Nanjing Medical University, Nanjing, China
                School of Public Health, Nanjing Medical University, Nanjing, China
                Center for Global Health, Centers for Disease Control and Prevention, Atlanta, GA, USA
                Fundacion INFANT, Buenos Aires, Argentina
                Department of Immunizations, Vaccines, and Biologicals, WHO, Geneva, Switzerland
                Boston University School of Public Health, Department of Global Health, Boston, Massachusetts, USA
                South African Medical Research Council Vaccines and Infectious Diseases Analytics Research Unit
                University of the Witwatersrand, Faculty of Health Sciences, Johannesburg, South Africa; Yale Institute for Global Health, New Haven, CT, USA
                Department of Pediatrics, Section of Infectious Diseases, University of Colorado, School of Medicine, Aurora, CO, USA
                Centre for Global Health, Usher Institute, University of Edinburgh, Edinburgh, UK
                Centre for Global Health, Usher Institute, University of Edinburgh, Edinburgh, UK
                National Center for Communicable Diseases (Mongolia), Ulaanbaatar, Mongolia
                ISGlobal, Hospital Clínic – Universitat de Barcelona, Barcelona, Spain
                National Center for Disease Control and Public Health, Tbilisi, Georgia
                The Royal Children’s Hospital, Melbourne, Australia
                The University of Melbourne, Melbourne, Australia; Smorodintsev Research Institute of Influenza, Saint Petersburg, Russia
                Department of Paediatrics
                Clinical Virology Unit, Centro de Educación Médica e Investigaciones Clínicas, Buenos Aires, Argentina
                Ricardo Gutiérrez Children Hospital, Buenos Aires, Argentina
                Department of Epidemiology, University of Michigan, Ann Arbor, MI, USA
                Pediatrics, University of Turku and Turku University Hospital, Turku, Finland
                WHO National Influenza Centre, Institute of Environmental Science and Research, Wellington, New Zealand
                Jigme Dorji Wangchuck National Referral Hospital, Gongphel Lam, Thimphu, Bhutan
                Centre for Community Medicine, All India Institute of Medical Sciences, New Delhi, India
                Hospital de Niños Dr. Ricardo Gutiérrez, Department of Medicine, Pediatric Infectious Diseases Program, Universidad de Buenos Aires, Buenos Aires, Argentina
                Department of Pediatrics, University Hospital Split, Split, Croatia
                Área de Investigación en Vacunas, Fundación para el Fomento de la Investigación Sanitaria y Biomédica de la Comunitat Valenciana, Salud Pública, Valencia, Spain
                Wesfarmers Centre for Vaccines and Infectious Diseases, Telethon Kids Institute, University of Western Australia, Perth, Australia
                National Institute for Communicable Diseases of the National Health Laboratory Service, Johannesburg, South Africa
                Boston University School of Public Health, Department of Global Health, Boston, Massachusetts, USA
                Kenya Medical Research Institute–Wellcome Trust Research Programme, Kilifi, Kenya
                Department of Microbiology, Faculty of Medicine, University of Peradeniya, Peradeniya, Sri Lanka
                Virology Department, Noguchi Memorial Institute for Medical Research, University of Ghana, Legon, Accra, Ghana
                Department of Microbiology, Jawaharlal Institute of Postgraduate Medical Education & Research, Puducherry, India
                Vysnova Partners, Lima, Perú
                Department of Virology, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran
                MAHAN Trust Mahatma Gandhi Tribal Hospital, Karmgram, Utavali, Tahsil, Dharni, India
                Department of Pediatrics, Dongguk University Ilsan Hospital, Dongguk University College of Medicine, Goyang, South Korea
                Department of Pediatrics, Hospital Santa Maria, Centro Hospitalar Universitário Lisboa Norte, Lisbon, Portugal
                Alaska Native Tribal Health Consortium, Anchorage, AK, USA
                The University of Melbourne, Melbourne, Australia; Smorodintsev Research Institute of Influenza, Saint Petersburg, Russia
                Glaxo Smith Kline, Rockville, Maryland, USA
                Department of Pathology, Faculty of Health Sciences, University of Cape Town, Cape Town, South Africa
                Murdoch Children’s Research Institute, Melbourne, Australia
                Department of Pediatric Infectious Diseases, Institute of Tropical Medicine, Nagasaki University, Nagasaki, Japan
                Infectious Diseases Service, Department of Paediatrics, KK Women’s and Children’s Hospital, Singapore
                Department of Paediatrics and Child Health, and South African Medical Research Council Unit on Child & Adolescent Health, University of Cape Town and Red Cross War Memorial Children’s Hospital, Cape Town, South Africa
                Nanjing Medical University Nanjing, China
                University of Edinburgh
                Centers for Disease Control and Prevention, Atlanta, GA, USA
                Fundacion INFANT, Buenos Aires, Argentina
                WHO, Geneva, Switzerland
                Boston University, Boston, MA, USA
                University of the Witwatersrand, Johannesburg, South Africa
                Yale University, New Haven, CT, USA
                University of Colorado, Aurora, CO, USA
                National Center for Communicable Diseases, Ulaanbaatar, Mongolia
                Universitat de Barcelona, Barcelona, Spain
                Hôpital de la Croix-Rousse, Lyon, France
                National Center for Disease Control Public Health, Tbilisi, Georgia
                The Royal Children’s Hospital, Melbourne, Australia
                Smorodintsev Research Institute of Influenza, St. Petersburg, Russian Federation
                Murdoch Children’s Research Institute, Melbourne, Australia
                Centro de Educación Médica e Investigaciones Clínicas, Argentina
                Ricardo Gutiérrez Children Hospital, Buenos Aires, Argentina
                University of Michigan, Ann Arbor, MI, USA
                University of Turku Turku University Hospital, Turku, Finland
                Institute of Environmental Science Research, Wellington, New Zealand
                All India Institute of Medical Sciences, New Delhi, India
                Hospital de Niños Dr. Ricardo Gutiérrez, Buenos Aires, Argentina
                University Hospital Split, Split, Croatia
                Fundación para el Fomento de la Investigación Sanitaria y Biomédica de la Comunitat Valenciana, Salud Pública, Valencia, Spain
                University of Western Australia, Australia
                National Institute for Communicable Diseases of the National Health Laboratory Service, Johannesburg, South Africa
                Kenya Medical Research Institute-WellcomeTrust Research Programme, Kilifi, Kenya
                University of Peradeniya, Peradeniya, Sri Lanka
                University of Ghana, Legon, Accra, Ghana
                Jawaharlal Institute of Postgraduate Medical Education & Research, Puducherry, India
                Vysnova Partners Inc., Lima, Perú
                Tehran University of Medical Sciences, Tehran, Iran
                MAHAN Trust Mahatma Gandhi Tribal Hospital, Karmgram, Utavali, Tahsil, Dharni, India
                Dongguk University, Goyang, Republic of Korea
                Hospital Santa Maria, Centro Hospitalar Universitário Lisboa Norte, Lisbon, Portugal
                Alaska Native Tribal Health Consortium, Anchorage, AK, USA
                Glaxo Smith Kline, Rockville, MD, USA
                Nagasaki University, Nagasaki, Japan
                KK Women’s Children’s Hospital, Singapore
                University of Cape Town Red Cross War Memorial Children’s Hospital, Cape Town, South Africa
                Ministry of Health, Managua, Nicaragua
                World Health Organization Collaborating Centre for Reference Research on Influenza, Melbourne, Australia
                Centers for Disease Control Prevention, Anchorage, AK, USA)
                National Institute of Hygiene and Epidemiology, Hanoi, Vietnam
                Yukon Kuskokwim Health Corporation, Bethel, AK, USA
                Cayetano Heredia National Hospital, Lima, Perú
                US Naval Medical Research Unit No6, Lima, Perú
                General Hospital, Kegalle, Sri Lanka
                Robert Koch Institute, Berlin, Germany
                Nanjing Medical University, Nanjing, China
                University of Edinburgh, Edinburgh, UK
                University of Antwerp, Antwerpen, Belgium
                University Medical Centre Utrecht, the Netherlands
                University of Oxford, Oxford, UK
                Imperial College London, London, UK
                Servicio Galego de Saude, Santiago de Compostela, Spain
                University of Turku and Turku University Hospital, Turku, Finland
                Institute for Public Health and the Environment, Bilthoven, the Netherlands
                Statens Serum Institut, Copenhagen, Denmark
                University of Groningen, Groningen, the Netherlands
                PENTA Foundation, Padua, Italy
                AstraZeneca, Gaithersburg, MD, USA
                GlaxoSmithKline, Wavre, Belgium
                Sanofi Pasteur, Lyon, France
                Janssen, Beerse, Belgium
                Author notes
                Correspondence to: Prof Harish Nair, Centre for Global Health, Usher Institute, University of Edinburgh, Edinburgh EH8 9AG, UK harish.nair@ 123456ed.ac.uk
                [‡]

                On behalf of the VRS study group in Lyon

                [§]

                Members listed at the end of the Article

                Article
                EMS153575
                10.1016/S0140-6736(22)00478-0
                7613574
                35598608
                9dfc89d2-e3d3-4c27-b69c-edde1c978d9f

                This work is licensed under a CC BY 4.0 International license.

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