11
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Global respiratory syncytial virus-associated mortality in young children (RSV GOLD): a retrospective case series

      research-article
      , MD a , , MD c , , MD c , , PhD d , e , , PhD d , f , , PhD g , , PhD g , , PhD h , i , , MD i , , FCPaed j , , MD k , , MD l , , MD m , , PhD n , , MD o , , MD p , PERCH Study Group, , MD q , , MD r , , PhD s , t , , MD s , t , , MD u , , MD v , , PhD w , x , , MD y , , FRCPC z , , MD aa , , MD ab , , PhD ac , ac , , PhD ad , ae , af , ag , ah , , MD ai , aj , ak , , MD al , , PhD am , , MBBS an , , PhD m , , BSc ao , , MD ap , , PhD aq , ar , , MD as , , MD at , , MD au , , MD av , , PhD aw , , PhD ax , ay , , PhD az , , , Dr, MD a , b , , *
      The Lancet. Global Health
      Elsevier Ltd

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Summary

          Background

          Respiratory syncytial virus (RSV) infection is an important cause of pneumonia mortality in young children. However, clinical data for fatal RSV infection are scarce. We aimed to identify clinical and socioeconomic characteristics of children aged younger than 5 years with RSV-related mortality using individual patient data.

          Methods

          In this retrospective case series, we developed an online questionnaire to obtain individual patient data for clinical and socioeconomic characteristics of children aged younger than 5 years who died with community-acquired RSV infection between Jan 1, 1995, and Oct 31, 2015, through leading research groups for child pneumonia identified through a comprehensive literature search and existing research networks. For the literature search, we searched PubMed for articles published up to Feb 3, 2015, using the key terms “RSV”, “respiratory syncytial virus”, or “respiratory syncytial viral” combined with “mortality”, “fatality”, “death”, “died”, “deaths”, or “CFR” for articles published in English. We invited researchers and clinicians identified to participate between Nov 1, 2014, and Oct 31, 2015. We calculated descriptive statistics for all variables.

          Findings

          We studied 358 children with RSV-related in-hospital death from 23 countries across the world, with data contributed from 31 research groups. 117 (33%) children were from low-income or lower middle-income countries, 77 (22%) were from upper middle-income countries, and 164 (46%) were from high-income countries. 190 (53%) were male. Data for comorbidities were missing for some children in low-income and middle-income countries. Available data showed that comorbidities were present in at least 33 (28%) children from low-income or lower middle-income countries, 36 (47%) from upper middle-income countries, and 114 (70%) from high-income countries. Median age for RSV-related deaths was 5·0 months (IQR 2·3–11·0) in low-income or lower middle-income countries, 4·0 years (2·0–10·0) in upper middle-income countries, and 7·0 years (3·6–16·8) in high-income countries.

          Interpretation

          This study is the first large case series of children who died with community-acquired RSV infection. A substantial proportion of children with RSV-related death had comorbidities. Our results show that perinatal immunisation strategies for children aged younger than 6 months could have a substantial impact on RSV-related child mortality in low-income and middle-income countries.

          Funding

          Bill & Melinda Gates Foundation.

          Related collections

          Most cited references23

          • Record: found
          • Abstract: found
          • Article: not found

          Global and regional burden of hospital admissions for severe acute lower respiratory infections in young children in 2010: a systematic analysis

          Summary Background The annual number of hospital admissions and in-hospital deaths due to severe acute lower respiratory infections (ALRI) in young children worldwide is unknown. We aimed to estimate the incidence of admissions and deaths for such infections in children younger than 5 years in 2010. Methods We estimated the incidence of admissions for severe and very severe ALRI in children younger than 5 years, stratified by age and region, with data from a systematic review of studies published between Jan 1, 1990, and March 31, 2012, and from 28 unpublished population-based studies. We applied these incidence estimates to population estimates for 2010, to calculate the global and regional burden in children admitted with severe ALRI in that year. We estimated in-hospital mortality due to severe and very severe ALRI by combining incidence estimates with case fatality ratios from hospital-based studies. Findings We identified 89 eligible studies and estimated that in 2010, 11·9 million (95% CI 10·3–13·9 million) episodes of severe and 3·0 million (2·1–4·2 million) episodes of very severe ALRI resulted in hospital admissions in young children worldwide. Incidence was higher in boys than in girls, the sex disparity being greatest in South Asian studies. On the basis of data from 37 hospital studies reporting case fatality ratios for severe ALRI, we estimated that roughly 265 000 (95% CI 160 000–450 000) in-hospital deaths took place in young children, with 99% of these deaths in developing countries. Therefore, the data suggest that although 62% of children with severe ALRI are treated in hospitals, 81% of deaths happen outside hospitals. Interpretation Severe ALRI is a substantial burden on health services worldwide and a major cause of hospital referral and admission in young children. Improved hospital access and reduced inequities, such as those related to sex and rural status, could substantially decrease mortality related to such infection. Community-based management of severe disease could be an important complementary strategy to reduce pneumonia mortality and health inequities. Funding WHO.
            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            Respiratory syncytial virus-associated hospitalizations among children less than 24 months of age.

            Respiratory syncytial virus (RSV) infection is a leading cause of hospitalization among infants. However, estimates of the RSV hospitalization burden have varied, and precision has been limited by the use of age strata grouped in blocks of 6 to ≥ 12 months. We analyzed data from a 5-year, prospective, population-based surveillance for young children who were hospitalized with laboratory-confirmed (reverse-transcriptase polymerase chain reaction) RSV acute respiratory illness (ARI) during October through March 2000-2005. The total population at risk was stratified by month of age by birth certificate information to yield hospitalization rates. There were 559 (26%) RSV-infected children among the 2149 enrolled children hospitalized with ARI (85% of all eligible children with ARI). The average RSV hospitalization rate was 5.2 per 1000 children <24 months old. The highest age-specific rate was in infants 1 month old (25.9 per 1000 children). Infants ≤ 2 months of age, who comprised 44% of RSV-hospitalized children, had a hospitalization rate of 17.9 per 1000 children. Most children (79%) were previously healthy. Very preterm infants (<30 weeks' gestation) accounted for only 3% of RSV cases but had RSV hospitalization rates 3 times that of term infants. Young infants, especially those who were 1 month old, were at greatest risk of RSV hospitalization. Four-fifths of RSV-hospitalized infants were previously healthy. To substantially reduce the burden of RSV hospitalizations, effective general preventive strategies will be required for all young infants, not just those with risk factors.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              Viral etiology of severe pneumonia among Kenyan infants and children.

              Pneumonia is the leading cause of childhood death in sub-Saharan Africa. Comparative estimates of the contribution of causative pathogens to the burden of disease are essential for targeted vaccine development. To determine the viral etiology of severe pneumonia among infants and children at a rural Kenyan hospital using comprehensive and sensitive molecular diagnostic techniques. Prospective observational and case-control study during 2007 in a rural Kenyan district hospital. Participants were children aged 1 day to 12 years, residing in a systematically enumerated catchment area, and who either were admitted to Kilifi District Hospital meeting World Health Organization clinical criteria for severe pneumonia or very severe pneumonia; (2) presented with mild upper respiratory tract infection but were not admitted; or (3) were well infants and children attending for immunization. The presence of respiratory viruses and the odds ratio for admission with severe disease. Of 922 eligible admitted patients, 759 were sampled (82% [median age, 9 months]). One or more respiratory viruses were detected in 425 of the 759 sampled (56% [95% confidence interval {CI}, 52%-60%]). Respiratory syncytial virus (RSV) was detected in 260 participants (34% [95% CI, 31%-38%]) and other respiratory viruses were detected in 219 participants (29%; 95% CI, 26%-32%), the most common being Human coronavirus 229E (n = 51 [6.7%]), influenza type A (n = 44 [5.8%]), Parainfluenza type 3 (n = 29 [3.8%]), Human adenovirus (n = 29 [3.8%]), and Human metapneumovirus (n = 23 [3.0%]). Compared with well control participants, detection of RSV was associated with severe disease (5% [corrected] in control participants; adjusted odds ratio, 6.11 [95% CI, 1.65-22.6]) while collectively, other respiratory viruses were not associated with severe disease (23% in control participants; adjusted odds ratio, 1.27 [95% CI, 0.64-2.52]). In a sample of Kenyan infants and children admitted with severe pneumonia to a rural hospital, RSV was the predominant viral pathogen.
                Bookmark

                Author and article information

                Contributors
                Journal
                Lancet Glob Health
                Lancet Glob Health
                The Lancet. Global Health
                Elsevier Ltd
                2214-109X
                11 September 2017
                October 2017
                11 September 2017
                : 5
                : 10
                : e984-e991
                Affiliations
                [a ]Department of Paediatric Infectious Diseases and Immunology, Wilhelmina Children's Hospital, University Medical Centre Utrecht, Utrecht, Netherlands
                [b ]ReSViNET Respiratory Syncytial Virus Network, Utrecht, Netherlands
                [c ]Department of Epidemiology, Ricardo Gutiérrez Children's Hospital, Buenos Aires, Argentina
                [d ]Kenya Medical Research Institute, Wellcome Trust Research Programme, Centre for Geographic Medicine Research—Coast, Kilifi, Kenya
                [e ]School of Life Sciences, University of Warwick, Coventry, UK
                [f ]Department of Nursing Sciences, Pwani University, Kilifi, Kenya
                [g ]Medical Research Council: Respiratory and Meningeal Pathogens Research Unit and Department of Science and Technology/National Research Foundation: Vaccine Preventable Diseases, University of the Witwatersrand, Johannesburg, South Africa
                [h ]School of Public Health, University of the Witwatersrand, Johannesburg, South Africa
                [i ]Centre for Respiratory Disease and Meningitis, National Institute for Communicable Diseases, Johannesburg, South Africa
                [j ]Department of Paediatric Intensive Care, Alder Hey Children's Hospital, Liverpool, UK
                [k ]Division of Global Health Protection, Thailand Ministry of Public Health—US Centers for Disease Control and Prevention Collaboration, Nonthaburi, Thailand
                [l ]Department of Virology, Tohoku University Graduate School of Medicine, Aoba-ku, Sendai, Miyagi, Japan
                [m ]Research Institute for Tropical Medicine, Alabang Muntinlupa City, Metro Manila Philippines
                [n ]Department of Epidemiology, School of Public Health, University of Michigan, MI, USA
                [o ]Department of Medicine, Hospital Infantil Manuel de Jesus Rivera, Managua, Nicaragua
                [p ]International Vaccine Access Center, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, USA
                [q ]Agence de Medecine Preventive, Paris, France
                [r ]West Nusa Tenggara Provincial Government, Lombok, Indonesia
                [s ]Department of Pediatrics, Division of Infectious Diseases, Ohio State University, Columbus, OH, USA
                [t ]Center for Vaccines and Immunity at Nationwide Children's Hospital, Ohio State University, Columbus, OH, USA
                [u ]Department of Pediatrics, University of Jordan, Aljubeiha, Amman, Jordan
                [v ]Vanderbilt University Medical Center, Nashville, TN, USA
                [w ]Molecular Biology Laboratory, Hospital de Clínicas de Porto Alegre, Bairro Santa Cecília, Porto Alegre, Brazil
                [x ]Infection Control Commission, Hospital de Clínicas de Porto Alegre, Bairro Santa Cecília, Porto Alegre, Brazil
                [y ]Division of Pediatric Critical Care, University of Virginia School of Medicine, Charlottesville, VA, USA
                [z ]Neonatal Division, Department of Pediatrics, McMaster University, Hamilton, ON, Canada
                [aa ]Department of Pediatrics and Center for Global Health, University of Colorado, Aurora, CO, USA
                [ab ]Department of Paediatrics, Faculty of Medicine and Chinese University of Hong Kong-University Medical Center Utrecht Joint Research Laboratory of Respiratory Virus and Immunobiology, Chinese University of Hong Kong, Shatin, New Territories, Hong Kong Special Administrative Region, China
                [ac ]Health Secretariat of the City of Belo Horizonte, Belo Horizonte, Brazil
                [ad ]ISGlobal, Barcelona Centre for International Health Research, Hospital Clínic-Universitat de Barcelona, Barcelona, Spain
                [ae ]ICREA, Catalan Institution for Research and Advanced Studies, Barcelona, Spain
                [af ]Department of Pediatrics, Hospital Sant Joan de Déu, Barcelona, Spain
                [ag ]Centro de Investigação em Saúde de Manhiça, Maputo, Mozambique
                [ah ]Faculty of Medicine, Universidad Europea de Madrid, Madrid, Spain
                [ai ]Department of Intensive Care, Royal Children's Hospital, Melbourne, VIC, Australia
                [aj ]Department of Paediatrics, University of Melbourne, Melbourne, VIC, Australia
                [ak ]Murdoch Children's Research Institute, Parkville, VIC, Australia
                [al ]Department of Pediatric Infectious Disease, MacKay Children's Hospital, Taipei, Taiwan
                [am ]Department of Virology, National Institute of Health, Islamabad, Pakistan
                [an ]Department of Paediatrics and Child Health, Aga Khan University, Karachi, Pakistan
                [ao ]Public Health Institute, Ñuñoa, Santiago, Chile
                [ap ]Hospital Dr. Ernesto Torres Galdames, Iquique, Chile
                [aq ]Vienna Vaccine Safety Initiative, Berlin, Germany
                [ar ]University of Nottingham School of Medicine, Nottingham, UK
                [as ]Fundacion Infant, Buenos Aires, Argentina
                [at ]Department of Microbiology, Division of Pediatric Infectious Diseases, McGill University Health Centre, Montreal, QC, Canada
                [au ]Department of Paediatric Infectious Diseases, University Hospital for Infectious Diseases, Zagreb, Croatia
                [av ]Department of Pediatrics, Nantan General Hospital, Ueno, Yagichoyagi, Nantan-shi, Kyoto, Japan
                [aw ]School of Health and Related Research, University of Sheffield, Sheffield, UK
                [ax ]Julius Global Health, Julius Center for Health Sciences and Primary Care, University Medical Center Utrecht, Utrecht, Netherlands
                [ay ]Julius Clinical Science, Zeist, Netherlands
                [az ]Centre for Global Health Research, Usher Institute of Population Health Sciences and Informatics, University of Edinburgh, Edinburgh, UK
                Author notes
                [* ]Correspondence to: Dr Louis J Bont, Department of Paediatric Infectious Diseases and Immunology, Wilhelmina Children's Hospital, University Medical Centre Utrecht, 3508 AB Utrecht, NetherlandsCorrespondence to: Dr Louis J Bont, Department of Paediatric Infectious Diseases and ImmunologyWilhelmina Children's HospitalUniversity Medical Centre UtrechtUtrechtAB3508Netherlands l.bont@ 123456umcutrecht.nl
                [†]

                Contributed equally

                Article
                S2214-109X(17)30344-3
                10.1016/S2214-109X(17)30344-3
                5599304
                28911764
                d811ec26-9a7a-488d-afe1-c69a5fcc6e7e
                © 2017 The Author(s). Published by Elsevier Ltd. This is an Open Access article under the CC BY 4.0 license

                This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).

                History
                Categories
                Articles

                Comments

                Comment on this article