TY - JOUR
T1 - Global burden of acute lower respiratory infection associated with human parainfluenza virus in children younger than 5 years for 2018
T2 - a systematic review and meta-analysis
AU - Respiratory Virus Global Epidemiology Network
AU - Wang, Xin
AU - Li, You
AU - Deloria-Knoll, Maria
AU - Madhi, Shabir A.
AU - Cohen, Cheryl
AU - Arguelles, Vina Lea
AU - Basnet, Sudha
AU - Bassat, Quique
AU - Brooks, W. Abdullah
AU - Echavarria, Marcela
AU - Fasce, Rodrigo A.
AU - Gentile, Angela
AU - Goswami, Doli
AU - Homaira, Nusrat
AU - Howie, Stephen R.C.
AU - Kotloff, Karen L.
AU - Khuri-Bulos, Najwa
AU - Krishnan, Anand
AU - Lucero, Marilla G.
AU - Lupisan, Socorro
AU - Mathisen, Maria
AU - McLean, Kenneth A.
AU - Mira-Iglesias, Ainara
AU - Moraleda, Cinta
AU - Okamoto, Michiko
AU - Oshitani, Histoshi
AU - O'Brien, Katherine L.
AU - Owor, Betty E.
AU - Rasmussen, Zeba A.
AU - Rath, Barbara A.
AU - Salimi, Vahid
AU - Sawatwong, Pongpun
AU - Scott, J. Anthony G.
AU - Simões, Eric A.F.
AU - Sotomayor, Viviana
AU - Thea, Donald M.
AU - Treurnicht, Florette K.
AU - Yoshida, Lay Myint
AU - Zar, Heather J.
AU - Campbell, Harry
AU - Nair, Harish
N1 - Funding Information:
This study was funded by the Bill & Melinda Gates Foundation (OPP 1172551). HN and HC are members of the Respiratory Syncytial Virus Consortium in Europe, which has received funding from the Innovative Medicines Initiative 2 Joint Undertaking (116019) that receives support from the EU Horizon 2020 research and innovation programme and the European Federation of Pharmaceutical Industries and Associations. Nagasaki University Vietnam study site data were supported by the Agency for Medical Research and Development (grant no JP19fm0108001; Japan Initiative for Global Research Network on Infectious Diseases). XW and YL were supported by scholarships from the China Scholarship Council during the conduct of this study. The findings and conclusions in this manuscript are those of the authors and do not necessarily represent the official position of the National Institutes of Health, the US Department of Health and Human Services, the Centers for Disease Control and Prevention, Department of Health and Human Services, the Centers for Disease Control and Prevention, or the US Government.
Funding Information:
This study was funded by the Bill & Melinda Gates Foundation (OPP 1172551). HN and HC are members of the Respiratory Syncytial Virus Consortium in Europe, which has received funding from the Innovative Medicines Initiative 2 Joint Undertaking (116019) that receives support from the EU Horizon 2020 research and innovation programme and the European Federation of Pharmaceutical Industries and Associations. Nagasaki University Vietnam study site data were supported by the Agency for Medical Research and Development (grant no JP19fm0108001; Japan Initiative for Global Research Network on Infectious Diseases). XW and YL were supported by scholarships from the China Scholarship Council during the conduct of this study. The findings and conclusions in this manuscript are those of the authors and do not necessarily represent the official position of the National Institutes of Health, the US Department of Health and Human Services, the Centers for Disease Control and Prevention, Department of Health and Human Services, the Centers for Disease Control and Prevention, or the US Government.
Publisher Copyright:
© 2021 The Author(s). Published by Elsevier Ltd. This is an Open Access article under the CC BY 4.0 license
PY - 2021/8
Y1 - 2021/8
N2 - Background: Human parainfluenza virus (hPIV) is a common virus in childhood acute lower respiratory infections (ALRI). However, no estimates have been made to quantify the global burden of hPIV in childhood ALRI. We aimed to estimate the global and regional hPIV-associated and hPIV-attributable ALRI incidence, hospital admissions, and mortality for children younger than 5 years and stratified by 0–5 months, 6–11 months, and 12–59 months of age. Methods: We did a systematic review of hPIV-associated ALRI burden studies published between Jan 1, 1995, and Dec 31, 2020, found in MEDLINE, Embase, Global Health, Cumulative Index to Nursing and Allied Health Literature, Web of Science, Global Health Library, three Chinese databases, and Google search, and also identified a further 41 high-quality unpublished studies through an international research network. We included studies reporting community incidence of ALRI with laboratory-confirmed hPIV; hospital admission rates of ALRI or ALRI with hypoxaemia in children with laboratory-confirmed hPIV; proportions of patients with ALRI admitted to hospital with laboratory-confirmed hPIV; or in-hospital case–fatality ratios (hCFRs) of ALRI with laboratory-confirmed hPIV. We used a modified Newcastle-Ottawa Scale to assess risk of bias. We analysed incidence, hospital admission rates, and hCFRs of hPIV-associated ALRI using a generalised linear mixed model. Adjustment was made to account for the non-detection of hPIV-4. We estimated hPIV-associated ALRI cases, hospital admissions, and in-hospital deaths using adjusted incidence, hospital admission rates, and hCFRs. We estimated the overall hPIV-associated ALRI mortality (both in-hospital and out-hospital mortality) on the basis of the number of in-hospital deaths and care-seeking for child pneumonia. We estimated hPIV-attributable ALRI burden by accounting for attributable fractions for hPIV in laboratory-confirmed hPIV cases and deaths. Sensitivity analyses were done to validate the estimates of overall hPIV-associated ALRI mortality and hPIV-attributable ALRI mortality. The systematic review protocol was registered on PROSPERO (CRD42019148570). Findings: 203 studies were identified, including 162 hPIV-associated ALRI burden studies and a further 41 high-quality unpublished studies. Globally in 2018, an estimated 18·8 million (uncertainty range 12·8–28·9) ALRI cases, 725 000 (433 000–1 260 000) ALRI hospital admissions, and 34 400 (16 400–73 800) ALRI deaths were attributable to hPIVs among children younger than 5 years. The age-stratified and region-stratified analyses suggested that about 61% (35% for infants aged 0–5 months and 26% for 6–11 months) of the hospital admissions and 66% (42% for infants aged 0–5 months and 24% for 6–11 months) of the in-hospital deaths were in infants, and 70% of the in-hospital deaths were in low-income and lower-middle-income countries. Between 73% and 100% (varying by outcome) of the data had a low risk in study design; the proportion was 46–65% for the adjustment for health-care use, 59–77% for patient groups excluded, 54–93% for case definition, 42–93% for sampling strategy, and 67–77% for test methods. Heterogeneity in estimates was found between studies for each outcome. Interpretation: We report the first global burden estimates of hPIV-associated and hPIV-attributable ALRI in young children. Globally, approximately 13% of ALRI cases, 4–14% of ALRI hospital admissions, and 4% of childhood ALRI mortality were attributable to hPIV. These numbers indicate a potentially notable burden of hPIV in ALRI morbidity and mortality in young children. These estimates should encourage and inform investment to accelerate the development of targeted interventions. Funding: Bill & Melinda Gates Foundation.
AB - Background: Human parainfluenza virus (hPIV) is a common virus in childhood acute lower respiratory infections (ALRI). However, no estimates have been made to quantify the global burden of hPIV in childhood ALRI. We aimed to estimate the global and regional hPIV-associated and hPIV-attributable ALRI incidence, hospital admissions, and mortality for children younger than 5 years and stratified by 0–5 months, 6–11 months, and 12–59 months of age. Methods: We did a systematic review of hPIV-associated ALRI burden studies published between Jan 1, 1995, and Dec 31, 2020, found in MEDLINE, Embase, Global Health, Cumulative Index to Nursing and Allied Health Literature, Web of Science, Global Health Library, three Chinese databases, and Google search, and also identified a further 41 high-quality unpublished studies through an international research network. We included studies reporting community incidence of ALRI with laboratory-confirmed hPIV; hospital admission rates of ALRI or ALRI with hypoxaemia in children with laboratory-confirmed hPIV; proportions of patients with ALRI admitted to hospital with laboratory-confirmed hPIV; or in-hospital case–fatality ratios (hCFRs) of ALRI with laboratory-confirmed hPIV. We used a modified Newcastle-Ottawa Scale to assess risk of bias. We analysed incidence, hospital admission rates, and hCFRs of hPIV-associated ALRI using a generalised linear mixed model. Adjustment was made to account for the non-detection of hPIV-4. We estimated hPIV-associated ALRI cases, hospital admissions, and in-hospital deaths using adjusted incidence, hospital admission rates, and hCFRs. We estimated the overall hPIV-associated ALRI mortality (both in-hospital and out-hospital mortality) on the basis of the number of in-hospital deaths and care-seeking for child pneumonia. We estimated hPIV-attributable ALRI burden by accounting for attributable fractions for hPIV in laboratory-confirmed hPIV cases and deaths. Sensitivity analyses were done to validate the estimates of overall hPIV-associated ALRI mortality and hPIV-attributable ALRI mortality. The systematic review protocol was registered on PROSPERO (CRD42019148570). Findings: 203 studies were identified, including 162 hPIV-associated ALRI burden studies and a further 41 high-quality unpublished studies. Globally in 2018, an estimated 18·8 million (uncertainty range 12·8–28·9) ALRI cases, 725 000 (433 000–1 260 000) ALRI hospital admissions, and 34 400 (16 400–73 800) ALRI deaths were attributable to hPIVs among children younger than 5 years. The age-stratified and region-stratified analyses suggested that about 61% (35% for infants aged 0–5 months and 26% for 6–11 months) of the hospital admissions and 66% (42% for infants aged 0–5 months and 24% for 6–11 months) of the in-hospital deaths were in infants, and 70% of the in-hospital deaths were in low-income and lower-middle-income countries. Between 73% and 100% (varying by outcome) of the data had a low risk in study design; the proportion was 46–65% for the adjustment for health-care use, 59–77% for patient groups excluded, 54–93% for case definition, 42–93% for sampling strategy, and 67–77% for test methods. Heterogeneity in estimates was found between studies for each outcome. Interpretation: We report the first global burden estimates of hPIV-associated and hPIV-attributable ALRI in young children. Globally, approximately 13% of ALRI cases, 4–14% of ALRI hospital admissions, and 4% of childhood ALRI mortality were attributable to hPIV. These numbers indicate a potentially notable burden of hPIV in ALRI morbidity and mortality in young children. These estimates should encourage and inform investment to accelerate the development of targeted interventions. Funding: Bill & Melinda Gates Foundation.
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U2 - 10.1016/S2214-109X(21)00218-7
DO - 10.1016/S2214-109X(21)00218-7
M3 - Article
C2 - 34166626
AN - SCOPUS:85110681931
SN - 2214-109X
VL - 9
SP - e1077-e1087
JO - The Lancet Global Health
JF - The Lancet Global Health
IS - 8
ER -