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. 2022 Aug:12:100272.
doi: 10.1016/j.lana.2022.100272. Epub 2022 May 17.

Paediatric critical COVID-19 and mortality in a multinational prospective cohort

Collaborators, Affiliations

Paediatric critical COVID-19 and mortality in a multinational prospective cohort

Sebastian Gonzalez-Dambrauskas et al. Lancet Reg Health Am. 2022 Aug.

Abstract

Background: To understand critical paediatric coronavirus disease 2019 (COVID-19) and evaluate factors associated with mortality in children from high and low-middle income countries.

Methods: Prospective, observational study of critically ill children hospitalised for COVID-19 in 18 countries throughout North America, Latin America, and Europe between April 1 and December 31, 2020. Associations with mortality were evaluated using logistic regression.

Findings: 557 patients (median age, 8 years; 24% <2 years) were enrolled from 55 sites (63% Latin American). Half had comorbidities. Invasive (41%) or non-invasive (20%) ventilation and vasopressors (56%) were the most common support modalities. Hospital mortality was 10% and higher in children <2 years old (15%; odds ratio 1·94, 95%CI 1·08-3·49). Most who died had pulmonary disease. When adjusted for age, sex, region, and illness severity, mortality-associated factors included cardiac (aOR 2·89; 95%CI 1·2-6·94) or pulmonary comorbidities (aOR 4·43; 95%CI 1·70-11·5), admission hypoxemia (aOR 2·44; 95%CI 1·30-4·57), and lower respiratory symptoms (aOR 2·96; 95%CI 1·57-5·59). MIS-C (aOR 0·25; 95%CI 0·1-0·61) and receiving methylprednisolone (aOR 0·5; 95%CI 0·25-0·99), IVIG (aOR 0·32; 95%CI 0·16-0·62), or anticoagulation (aOR 0·49; 95%CI 0·25-0·95) were associated with lower mortality although these associations might be limited to children >2 years old.

Interpretation: We identified factors associated with COVID-19 mortality in critically ill children from both high and low-middle income countries, including higher mortality with younger age and COVID-related pulmonary disease but lower mortality in MIS-C. Further research is needed on optimal treatments for younger children and respiratory failure in paediatric COVID-19.

Funding: None.

Keywords: COVID-19; Epidemiology; Mortality; Outcomes; Paediatric intensive care unit.

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Conflict of interest statement

No authors have any conflicts of interest to disclose

Figures

Figure 1:
Figure 1
Multivariable Associations with Mortality. Odds ratio for each variable adjusted for sex, age<2, region, and admission PRISM III. Abbreviations: PRISM III= Pediatric Risk of Mortality III; HFNC = high flow nasal cannula; NIV = noninvasive ventilation; IMV = invasive mechanical ventilation; RRT = renal replacement therapy; IVIG = intravenous immune globulin; HCQ/CQ = hydroxychloroquine or chloroquine; ARDS = acute respiratory distress syndrome; MIS-C = multisystem inflammatory syndrome in children.
Figure 2:
Figure 2
Multivariable Associations with Mortality in the subset of children without MIS-C. Odds ratio for each variable adjusted for sex, age<2, region, and admission PRISM III. Abbreviations: PRISM III= Pediatric Risk of Mortality III; HFNC = high flow nasal cannula; NIV = noninvasive ventilation; IMV = invasive mechanical ventilation; RRT = renal replacement therapy; IVIG = intravenous immune globulin; HCQ/CQ = hydroxychloroquine or chloroquine; ARDS = acute respiratory distress syndrome; MIS-C = multisystem inflammatory syndrome in children.

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