Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection is rarely fatal in children and young people (CYP, <18 years old), but quantifying the risk of death is challenging because CYP are often infected with SARS-CoV-2 exhibiting no or minimal symptoms. To distinguish between CYP who died as a result of SARS-CoV-2 infection and those who died of another cause but were coincidentally infected with the virus, we undertook a clinical review of all CYP deaths with a positive SARS-CoV-2 test from March 2020 to February 2021. The predominant SARS-CoV-2 variants were wild-type and Alpha. Here we show that, of 12,023,568 CYP living in England, 3,105 died, including 61 who were positive for SARS-CoV-2. Of these deaths, 25 were due to SARS-CoV-2 infection (mortality rate, two per million), including 22 due to coronavirus disease 2019—the clinical disease associated with SARS-CoV-2 infection—and 3 were due to pediatric inflammatory multisystem syndrome temporally associated with SARS-CoV-2. In total, 99.995% of CYP with a positive SARS-CoV-2 test survived. CYP older than 10 years, Asian and Black ethnic backgrounds and comorbidities were over-represented in SARS-CoV-2-related deaths compared with other CYP deaths. These results are important for guiding decisions on shielding and vaccinating children. New variants might have different mortality risks and should be evaluated in a similar way.
Identifying CYP at risk of severe illness and death after SARS-CoV-2 infection is essential to guide families, clinicians and policymakers about future shielding policies, school attendance, novel therapeutic agents and vaccine prioritization.
SARS-CoV-2 infection is usually mild and asymptomatic in CYP1,2,3. Therefore, CYP have comprised a very low proportion of all hospitalizations and deaths from coronavirus disease 2019 (COVID-19) globally4. The clinical manifestations of COVID-19 in CYP are different than those in adults1. Although many CYP present with the typical fever, cough and shortness of breath, they also present with broader non-specific symptoms, including abdominal pain, nausea, headache and sore throat1,3. This, in combination with a mild or asymptomatic phenotype2, provides a challenge for describing how SARS-CoV-2 directly affects CYP.
Severe illness and death associated with SARS-CoV-2 in CYP is rare and can be due to either acute COVID-19 or pediatric inflammatory multisystem syndrome temporally associated with SARS-CoV-2 (PIMS-TS)2,5. PIMS-TS, also called multisystem inflammatory syndrome in children, is a rare syndrome characterized by persistent fever, inflammation (neutrophilia, lymphopenia and raised C-reactive protein) and evidence of single- or multi-organ dysfunction that might occur concurrently or after infection6. As death from acute COVID-19 or PIMS-TS in CYP is extremely rare4,7,8, those who have died have been poorly characterized9. Furthermore, it remains unclear to what extent these rare deaths relate directly to the pathological processes of COVID-19 or whether CYP who died from alternative causes were coincidentally positive for SARS-CoV-2 around the time of death. This issue is made more difficult by the very high prevalence of asymptomatic infection at times of high prevalence, with reported prevalence up to 4–6% of United Kingdom CYP during December 2020 (ref. 10). The distinction between those who died of SARS-CoV-2 infection and those who died of an alternative cause with a coincidental positive SARS-CoV-2 test is important for understanding which CYP are truly at higher risk for severe disease or death.
Answering this important question required detailed examination of all deaths in a large population, going beyond simple cause of death registration, to review the contribution of SARS-CoV-2 to death. We used detailed clinical data in the National Child Mortality Database (NCMD)11, which is a comprehensive and unique mandatory national dataset of deaths of individuals younger than 18 years of age, to review the contribution of SARS-CoV-2 to death.
If higher-risk groups are identified, they might benefit from vaccination and/or protective ‘shielding’ at times of high prevalence, whereas ‘shielding’ based upon erroneous assumptions of vulnerability is likely to cause significant secondary harms—for example, the effects of not attending school and restrictive or reduced socializing, affecting both development and mental health. Similarly, risks from the disease need to be weighed against potential risks of vaccination in informing vaccination policy. Therefore, this study aimed to:
Quantify the number of CYP who died of SARS-CoV-2 by differentiating between CYP who died of SARS-CoV-2 and those who died of an alternative cause with a coincidental positive SARS-CoV-2 test.
Assess the clinical and demographic characteristics of the CYP who died of SARS-CoV-2 compared to CYP deaths from all other causes during the first pandemic year.
Between March 2020 and February 2021, 3,105 CYP in England died of all causes. Of these, 61 CYP had a positive SARS-CoV-2 test, and 3,044 died of all other causes.
Clinical records of the 61 CYP who died with a positive SARS-CoV-2 test were reviewed to identify if SARS-CoV-2 contributed to death. This process initially included identifying whether SARS-CoV-2 was listed as 1a (the direct cause of death) on the Certificate of Cause of Death and whether the clinical course described was typical of SARS-CoV-2 infection. In these circumstances, the classification ‘SARS-CoV-2 clearly contributed to death’ was applied. In England, the Certificate of Cause of Death is set out in two parts12. Part 1a is the immediate, direct cause of death. The sequence of events or conditions that led to the death are then listed as 1b and 1c (if necessary)12.
If the role of SARS-CoV-2 in contributing to death was not clearly apparent, each case underwent review by three independent senior clinical experts in relevant fields (General Pediatrics, Neonatology and Pediatric Intensive Care) who were asked to classify each case. Definitions for each category and the details behind the process are outlined in the Supplementary Information and in Fig. 1.
In total, 25 (41%) of the 61 CYP died of SARS-CoV-2, including 22 with acute COVID-19 and three with PIMS-TS. In the other 36 (59%) of the 61 test-positive CYP, SARS-CoV-2 did not contribute to death (Table 1 and Figs. 1 and 2).
An estimated 469,982 CYP were infected with SARS-CoV-2 in England from March 2020 to February 2021, giving an infection fatality rate of five per 100,000 CYP (0.005%) and, based on a population of 12,023,568, a mortality rate of two per million CYP (0.0002%)13.
There were small amounts of missing demographic data for the reference population (2.3% sex, 10.6% ethnicity and 0.6% deprivation (Table 1), but there were no missing demographic data for the 25 CYP who died of SARS-CoV-2.
CYP who died of SARS-CoV-2 (n = 25) were older than those who died from all other causes (n = 3,080) in the same time period. Eighteen of 25 (72%) young people who died of SARS-CoV-2 were aged 10 years or older compared to 19% in the deaths from all other causes (chi-squared 59.7, P < 0.001). All three deaths in CYP who died of PIMS-TS were aged 10–14 years. Of interest, specific to vaccination policy in the United Kingdom, there were eight deaths in young people aged 12–15 years. The sex distribution was equally split between males and females (12 (48%) and 13 (52%), respectively) and did not differ from the deaths from all other causes (chi-squared 0.64, P = 0.28). A greater proportion of CYP from Asian (36% compared to 16%) and Black (20% compared to 8%) ethnicity died of SARS-CoV-2 compared to deaths from all other causes (chi-squared 17.9, P < 0.001). The three CYP who died of PIMS-TS were from different ethnic groups. No significant difference was observed in the deprivation categories between CYP who died of SARS-CoV-2 and deaths from all other causes (chi-squared 0.35, P = 0.99), although more CYP from more deprived areas died in both groups.
The mortality rate in CYP who died of SARS-CoV-2 was 0.2 per 100,000 (95% confidence interval (CI), 0.1–0.3) compared to 25.5 per 100,000 (95% CI, 24.7–26.5) for all other causes of death. Although the proportion of CYP from Asian and Black ethnic groups who died of SARS-CoV-2 was higher, their absolute risk of death from SARS-CoV-2 was still extremely low at 0.6 per 100,000 (95% CI, 0.3–1.1) and 0.8 per 100,000 (95% CI, 0.3–1.8), respectively. Similarly, the proportion of CYP aged 10–14 years and 15–17 years who died of SARS-CoV-2 was higher than the proportion of CYP in the same age categories who died of all other causes. However, their absolute risk of death from SARS-CoV-2 was still extremely low at 0.3 per 100,000 (95% CI, 0.1–0.5) and 0.5 (95% CI, 0.2–0.9) per 100,000, respectively.
A similar proportion of the 25 CYP who died of SARS-CoV-2 (n = 19, 76%) and the 3,080 deaths from all other causes (n = 2,267, 74%) (chi-squared 0.004, P = 0.60) had a chronic underlying health condition (Tables 2 and 3). Significantly more CYP who died of SARS-CoV-2 had a life-limiting condition (n = 15, 60%) compared to deaths from all other causes (n = 988, 32%) (chi-squared 8.5, P = 0.005). Of the 25 CYP who died of SARS-CoV-2, 64% (n = 16) had comorbidities in two or more body systems compared to 45% (n = 1,373) of the CYP who died from all other causes (chi-squared 5.5, P = 0.14).
Six (24%) of the 25 CYP who died of SARS-CoV-2 appeared to have no underlying health conditions, similar to 24% (729 of the 3,080 CYP) who died of all other causes. These six deaths included two CYP who died of PIMS-TS.
Neurological conditions were the most common comorbidity in both the CYP who died of SARS-CoV-2 (n = 13/25, 52%) and the CYP who died of all other causes (n = 1,218/3,080, 40%) (chi-squared 1.6, P = 0.29). The chronic disease coding list used to identify neurological conditions included mental-health-related and learning-disability-related codes. All 13 CYP who died of SARS-COV-2 with a neurological comorbidity had a complex neurodisability due to a combination of an underlying genetic or metabolic condition, hypoxic ischemic events or prematurity. Eight (32%) of the 13 CYP who had a neurological comorbidity also had a respiratory comorbidity, including five who required home respiratory support, four with non-invasive ventilation or high-flow oxygen and one with low-flow oxygen. There were zero CYP who died of SARS-CoV-2 who were invasively home ventilated. There was one death in a young person with a tracheostomy required for airway patency.
Of the 25 CYP who died of SARS-CoV-2, there was one child with each of the following comorbidities: congenital cardiac, oncological, obesity (under endocrinology) and complications of prematurity. There were two CYP who died with a hematological comorbidity.
There were no deaths in CYP with the following conditions:
An isolated respiratory condition—for example, cystic fibrosis or asthma (three of the CYP with a complex neurodisability had a historic diagnosis of asthma; however, the asthma diagnosis was not considered to contribute to death).
Type 1 diabetes
Isolated diagnosis of epilepsy
A mental health disorder that caused or contributed to death
There were CYP with asthma and epilepsy who died of SARS-CoV-2 infection. However, all of these deaths occurred in CYP with other underlying health conditions, rather than as a single diagnosis (Fig. 3).
The estimated mortality rate for CYP who died of SARS-CoV-2 with a life-limiting condition was 11.5 per 100,000 (95% CI, 5.6–21.2) compared to 1,124 per 100,000 (95% CI, 1,054–1,197) for all other causes of death. Although the proportion of CYP with a life-limiting neurodisability who died of SARS-CoV-2 was higher, their absolute risk of death was 88.9 per 100,000 (95% CI, 47.3–152) compared to 2,441 per 100,000 (95% CI, 2,194–2,707) in CYP with a life-limiting neurodisability who died of all other causes.
Place of death
Nine (36%) of the 25 CYP who died of SARS-CoV-2 died in a pediatric intensive care unit, and four died in a hospital ward. The remaining 12 CYP died either at home (unexpected (n = 6) or expected (n = 2)) or in an emergency department (n = 4). There were five deaths in CYP with advance care plans in place to provide hospital-ward-level care rather than escalation to intensive care.
Time interval between positive SARS-CoV-2 test and death
Twenty-three CYP died of SARS-CoV-2 within 28 d of a positive SARS-CoV-2 test; of these deaths, 21 occurred within 7 d of a positive test. The maximum time between death and a positive SARS-CoV-2 test was 45 d.
The 3,044 CYP who died and did not have a positive SARS-CoV-2 test would have only had a SARS-CoV-2 test in the following circumstances: asymptomatic lateral flow tests performed for education or social activities (note that this is highly variable); symptoms consistent with acute SARS-CoV-2 infection; hospital admission; and unexpected death or postmortem examination. Therefore, not all of the 3,044 CYP who died from other causes would have been tested for SARS-CoV-2. However, none of them had a positive SARS-CoV-2 test, because we included all CYP who tested positive at any time point during the pandemic (n = 61), and zero positive tests were excluded from the study.
We used a high-quality, unique national mortality dataset linked to national hospital and SARS-CoV-2 Public Health England testing data, in conjunction with clinical review, to identify 25 CYP who died of SARS-CoV-2 infection during the first pandemic year. This corresponds to two deaths per million across the CYP population in England. We estimated the infection fatality rate to be five per 100,000, indicating that more than 99.995% of CYP recover from SARS-CoV-2 infection. SARS-CoV-2 contributed to 0.8% of the 3,105 deaths from all causes. During the same time period studied, there were 124 deaths from suicide and 268 deaths from trauma, emphasizing that COVID-19 is rarely fatal in CYP.
To our knowledge, this is the first study to differentiate between CYP who died of SARS-CoV-2 infection and CYP who died with a positive SARS-CoV-2 test as a coincidental finding. Our result is 60% lower than the figures derived from positive tests, thereby markedly reducing the estimated number of CYP who are potentially at risk of death during this pandemic14.
The CYP who died of SARS-CoV-2 were more likely to be teenagers than younger children, suggesting a continuum of risk increasing through the life course from infancy to older adult life15. Higher proportions of Asian and Black CYP died of SARS-CoV-2 compared to all other causes of death, although deaths were still extremely rare. The three CYP who died of PIMS-TS were all aged 10–14 years, two were male, all were from different ethnic groups and two did not have evidence of an underlying health condition.
The reason for ethnic differences might be due to biological predisposition and/or access to care. Of note, the differences persist when controlling for deprivation16. These findings support those found in adult studies15,17.
Our findings emphasize the importance of underlying comorbidities as the main risk factor for death, as 76% had chronic conditions, 64% had multiple comorbidities and 60% had life-limiting conditions. The comorbidity group at highest risk included CYP with complex neurodisability, which comprised 52% of all deaths in CYP who died of SARS-CoV-2. CYP with combined neurodisability and respiratory conditions (eight of the 13 deaths with neurodisability) might be at particularly high risk. CYP with a life-limiting neurodisability have a higher background mortality rate than the general population18. There are approximately 500 deaths annually in this group, and, therefore, SARS-CoV-2 contributed to only 3% during the pandemic. Similarly, for all other comorbidity groups, those who died of SARS-CoV-2 represented a very small proportion of all deaths during the pandemic year. It is important to note that we observed no deaths in groups that have been considered at higher risk of respiratory infections, such as CYP with asthma, cystic fibrosis, type 1 diabetes or trisomy 21.
The inclusion of trauma as a chronic condition relates to the broad definition of chronic conditions used in this work to ensure optimal capture. The chronic condition definition (Supplementary Information) includes any health problem requiring follow-up services in more than 50% of cases, and follow-up includes use of support services such as physiotherapy. There is a subcategory of skeletal injuries/amputations that accounts for these trauma codes that are historic but chronic in nature. The high number of CYP with ear, nose and throat (ENT) conditions is due to a high proportion of CYP with neurological and/or respiratory conditions having ENT conditions and does not relate to CYP with isolated ENT conditions. It also includes CYP with a tracheostomy.
Six CYP who died of SARS-CoV-2 had no evidence of an underlying health condition. This contrasts with other studies that have only reported deaths in CYP who have comorbidity7,19. It is possible, due to the hospital data being available only for the last 5 years, that some CYP might have had a comorbidity that was not identified in this linkage. It is also possible that CYP in our study had an undiagnosed genetic predisposition to severe disease with SARS-CoV-2 infection20.
Our findings extend previous more limited reports on deaths due to SARS-CoV-2 in the United Kingdom7,8,19. The International Severe Acute Respiratory and Emerging Infection Consortium study reported six deaths from 651 admissions across 138 hospitals up to July 2020 (ref. 19). All six CYP had ‘profound comorbidity’, which included neurodisability, extreme prematurity, malignancy and sepsis; three were infants under 28 d of age; and three were aged 15–18 years19. The methodology in our study enabled demonstration that zero neonates died of SARS-CoV-2, highlighting the value of having real-time, complete mortality surveillance for CYP, with linkage to virology data and the detailed clinical review that we undertook to determine the role of SARS-CoV-2 in death.
The current United Kingdom advice on those defined as ‘clinically extremely vulnerable’ was initially extrapolated from adult risk, and it remains very cautious14. Even taking into consideration the effect of shielding (as both adults and CYP shielded at times during this period), the risk of serious outcomes from SARS-CoV-2 for individuals under 18 years of age remains extremely low. The risk of removal of CYP from their normal activities across education and social events might prove a greater risk than that of SARS-CoV-2 itself21.
The SARS-CoV-2 virus strains circulating at the time of this review were wild-type and the Alpha variant from November 2020. These data are specific to the time period studied and before the advent of the Delta variant.
The data analyzed in this study largely relied upon the quality of the data entered through the NCMD death reporting process. Data completeness was variable, depending on stage of the child death review process. Where possible, we overcame this through discussion with reporting clinicians and data linkage. Rapid data linkage methods were undertaken using NHS number alone, so this might have resulted in some CYP not being matched to their hospital data.
Eight of the CYP who died of SARS-CoV-2 had a non-congenital cardiac condition recorded, despite our attempts to modify the International Classification of Diseases (ICD)-10 coding lists to account for this. Owing to the complexity of these cases, some of these conditions might have been as a result of COVID-19 rather than pre-existing chronic conditions.
Even though we undertook rigorous clinical review, there might still have been a potential for misclassification of deaths in this study. All sudden and unexpected deaths were tested for SARS-CoV-2 as part of the amended Joint Agency Response policy from March 2020 (ref. 22). However, not all community deaths will have been routinely tested.
As there is no diagnostic test for PIMS-TS, and coding was a challenge, it is possible that there might be omissions due to the methods of diagnosis and reporting.
The mortality rate calculations used data from the Office for National Statistics for the estimated number of children by age in England during mid-2019 (ref. 13). There is a paucity of accurate data on the number of children who have had SARS-CoV-2 testing, affecting the accuracy of the infection fatality rate calculation.
Going forward, linkage of the NCMD to other national datasets will enable complete capture of comorbidities in CYP. These findings are representative of the wild-type and Alpha SARS-CoV-2 variants that were prevalent at the time of the study. It would be beneficial to repeat this for the subsequent 12 months (March 2021–February 2022) to identify the effect of other variants (including Delta) and vaccination.
The cohort investigated in this study is all CYP under 18 years of age who died in England between 1 March 2020 and 28 February 2021 (ref. 11). The aim of this study was to identify CYP in which SARS-CoV-2 contributed to death—that is, they died of SARS-CoV-2 infection.
Ethics approval was granted by the Central Bristol NHS Research and Ethics Committee. Informed consent was not obtained for use of these data. The NCMD has a legal basis to collect data without consent (Supplementary Information)27. Current Control Of Patient Information regulations provide a legal basis for linking NCMD data with Secondary Uses Service data without consent28. Additional details are provided in the Supplementary Information.
A statistical risk assessment for this study determined that, although data are anonymized, identification of individuals might be possible. However, the risk of attribute details being disclosed was low, and the public benefit of reporting these small numbers outweighed this risk. We minimized this risk by providing data that are two dimensional rather than three dimensional—for example, we provided the number of CYP in each age or ethnicity category rather than providing linked comorbidity and demographic details for each CYP. Given the sensitive nature of these data and our awareness that clinicians and families might recognize personal experience, we met with a clinician or professional involved in the care of each child or young person who died of SARS-CoV-2 infection. We asked the respective clinician or professional to communicate this work directly to the families.
The NCMD is a mandatory system that records all deaths in CYP under 18 years of age in England since it began in April 2019 (ref. 11) and includes demographic and clinical data of the events leading up to death.
In this analysis, demographic details included age (coded as 0–27 d, 28–364 d, 1–4 years, 5–9 years, 10–14 years and 15–17 years), sex, ethnicity (coded as Asian or Asian British, Black or African or Caribbean or Black British, mixed, multiple, other (includes Arab and other ethnic groups) and white)29 and deprivation (Supplementary Information)30,31.
To ensure comprehensive identification of comorbidities, NCMD data were linked to the preceding 5 years (March 2015 onwards) of national admitted patient care Secondary Uses Service data for England32 and to the national Paediatric Intensive Care Audit Network data. A validated list of ICD-10 codes was used to identify CYP with chronic comorbidities33 and life-limiting conditions34 (Supplementary Information). Of note, the chronic disease list for cardiac conditions was modified to remove ‘I46-Cardiac Arrest’ and ‘I51-Complications and ill-defined descriptions of heart disease, as these are acute presentations of cardiac disease and likely to represent PIMS-TS rather than pre-existing comorbidity. We also identified CYP with chronic comorbidities in two or more body systems and with the following single diagnoses: asthma, diabetes, epilepsy, sickle cell disease and trisomy 21. These single diagnoses were identified as common long-term conditions in CYP and speculated to be risk factors for severe disease based on adult data (refs. 15,17).
During the pandemic, the NCMD was linked by NHS number to Public Health England Pillar 1 and Pillar 2 testing data35 to identify all CYP who died with a positive SARS-CoV-2 test. Pillar 1 testing occurs in health and care settings, whereas Pillar 2 testing occurs in the community35, both of which started in March 2020. The NCMD contributed to modification of the protocol for sudden, unexpected deaths in CYP to include postmortem testing for SARS-CoV-2 (ref. 22). All CYP who died with a positive SARS-CoV-2 test were included, regardless of the time interval between positive test and death. This is different than the definition used for reporting adult deaths, to ensure that all potential cases were identified for review and to optimize capture of possible PIMS-TS cases. In addition, the NCMD coding team identified potential cases of PIMS-TS (Supplementary Information).
Identifying CYP who died of SARS-CoV-2
Clinical records of all CYP who died with a positive SARS-CoV-2 test were reviewed to identify if SARS-CoV-2 clearly, probably, possibly or unlikely contributed to death. This process initially included identifying whether SARS-CoV-2 was listed as 1a (the direct cause of death) on the Certificate of Cause of Death and whether the clinical course described was typical of SARS-CoV-2 infection. In these circumstances, the classification ‘SARS-CoV-2 clearly contributed to death’ was applied. In England, the Certificate of Cause of Death is set out in two parts12. Part 1a is the immediate, direct cause of death. The sequence of events or conditions that led to the death are then listed as 1b and 1c (if necessary). Other disease, injuries, conditions or events that contributed to death but were not part of the direct sequence are then documented in Part 2 (ref. 12).
If it was not clearly apparent, each case underwent review by three independent senior clinical experts in relevant fields (General Pediatrics, Neonatology and Pediatric Intensive Care) who were asked to classify each case. Each senior clinical expert was blinded to the opinion of the other reviewers. Definitions for each category and the details behind the process are outlined in the Supplementary Information and Fig. 1.
The CYP who died of SARS-CoV-2 were compared to CYP who died from all other causes using summary statistics, and differences between groups were compared using the two-sided chi-squared test or Fisher’s exact test if small numbers. The comparator cohort, death from all other causes, included CYP who tested positive for SARS-CoV-2 but died of another cause. Owing to a small amount of missing data, multiple imputation was not undertaken.
The absolute risk of death was calculated for the whole population and for demographic groups in which denominator data were available. The quality of available data on the number of CYP in the population with comorbidities was variable. We used estimates for comorbidity groups, where we have enough confidence in the data, to derive estimated absolute risk. These data came from a range of sources and are referenced in Table 3.
The infection fatality rate was calculated using the number of CYP infected with SARS-CoV-2 during the same time period (March 2020–February 2021) estimated through Public Health England modeling data36. This was chosen rather than the absolute number of positive SARS-CoV-2 tests as CYP might test positive more than once, and many CYP were not tested in the first wave of the pandemic. Mortality rate was calculated using a population of 12,023,568 CYP living in England13 during the study year.
This study was reported according to the ‘Strengthening the Reporting of Observational Studies in Epidemiology Statement: guideline for reporting observational studies’37.
Further information on research design is available in the Nature Research Reporting Summary linked to this article.
Data used for this study are not publicly available because the information is highly sensitive, owing to it being available at the identifiable patient level because of small numbers. The analysis was performed in Microsoft Excel using basic count functions to identify CYP within each category. Statistical analyses were performed in Stata using the data in Tables 1 and 2.
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We would like to thank the three senior clinical expert reviewers who independently reviewed clinical case notes of the CYP who died with a positive SARS-CoV-2 test: P. Fleming, Professor of Infant Health and Developmental Physiology, University of Bristol; G. Rossouw, General Paediatrics and Neonates, Research Fellow, National Child Mortality Database (NCMD); and D. Alison Perry, Paediatric Intensive Care, Bristol Royal Hospital for Children. We are grateful to members of the Child Death Overview Panels for their support and expertise and all child death review professionals for submitting data and providing additional information when requested. The entire NCMD team (particularly N. Cook, S. Stoianova, V. Sleap and T. Williams) have been very helpful in providing data for linkage and supporting analysis. We thank the NHS Digital and the NHS England and NHS Improvement Children and Young People teams (particularly R. Owen, S. Solti and T. Watson-Koszel) for their contributions and support. We thank Public Health England’s Field Service and National Child and Maternal Health Intelligence Network teams for their collaboration in establishing the real-time surveillance system on child deaths potentially related to COVID-19 and their ongoing support in the daily linkage with SARS-CoV-2 test results. We would like to acknowledge support from the National Institute of Health Research (NIHR) through the National School for Public Health Research Programme and the Applied Research Collaboration North West London. We would like to thank the Royal College of Paediatrics and Child Health for their contributions and support. Parent and public involvement is at the heart of the NCMD program. We are indebted to C. Bevan (Stillbirth and Neonatal Death Charity), T. McAlorum (Child Bereavement UK) and J. Ward (Lullaby Trust), who represent bereaved families on the NCMD program steering group, for their advice and support with setting up the real-time child mortality surveillance system at the beginning of the COVID-19 pandemic. The authors received no specific funding for this work. Three of the authors are in receipt of research funding for their broader employment. R.H. is in receipt of a funded fellowship from Kidney Research UK (grant no. TF_010_20171124). J.W. is in receipt of a Medical Research Council Fellowship (grant reference MR/R00160X/1). L.K.F. is in receipt of funding from Martin House Childrens Hospice (there is no specific grant number for this funding). R.V. is in receipt of a grant from the NIHR (grant no. NIHR202322, ‘Understanding the disruption of children and young people’s health and healthcare use during and after COVID-19 to inform healthcare and policy responses’). These funders had no role in study design, data collection and analysis, decision to publish or preparation of the manuscript. The NCMD program, including this work, is funded by NHS England and commissioned by the Healthcare Quality Improvement Partnership as part of the National Clinical Audit and Patient Outcomes Programme.
The authors declare no competing financial interests.
Peer review information Nature Medicine thanks Olivia Swann and the other, anonymous, reviewer(s) for their contribution to the peer review of this work. Alison Farrell and João Monteiro are the primary editors on this article and managed its editorial process and peer review in collaboration with the rest of the editorial team.
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is a bar chart demonstrating the age group of Children and Young People (CYP) who died of SARS-CoV-2 (n = 25) compared to the age group of CYP deaths from all other causes (n = 3080).
is a bar chat demonstrating the ethnic group of Children and Young People (CYP) who died of SARS-CoV-2 (n = 25) compared to the ethnic group of CYP deaths from all other causes (n = 3080).
Supplementary Information contains: (1) markers of deprivation; (2) development of the chronic disease and life-limiting coding lists; (3) identification of potential PIMS-TS cases; (4) process to identify if SARS-CoV-2 contributed to death (Fig. 1); (5) summary table of review categories and level of agreement among the senior clinical experts; and (6) small number reporting, information governance and legal basis
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Smith, C., Odd, D., Harwood, R. et al. Deaths in children and young people in England after SARS-CoV-2 infection during the first pandemic year. Nat Med 28, 185–192 (2022). https://doi.org/10.1038/s41591-021-01578-1
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