Article Text

Post-COVID-19 condition at 6 months and COVID-19 vaccination in non-hospitalised children and young people
  1. Snehal M Pinto Pereira1,
  2. Manjula D Nugawela1,
  3. Natalia K Rojas1,
  4. Roz Shafran1,
  5. Kelsey McOwat2,
  6. Ruth Simmons2,
  7. Tamsin Ford3,
  8. Isobel Heyman1,
  9. Shamez N Ladhani2,4,
  10. Emily Y Cheung1,
  11. Lana Fox-Smith1,
  12. Emma Dalrymple1,
  13. Terence Stephenson1
  1. 1UCL Great Ormond Street Institute of Child Health, London, UK
  2. 2Immunisation Department, Public Health England, London, UK
  3. 3Department of Psychiatry, University of Cambridge, Cambridge, UK
  4. 4Paediatric Infectious Diseases Research Group, St George's University, London, UK
  1. Correspondence to Dr Snehal M Pinto Pereira, Division of Surgery & Interventional Science, Faculty of Medical Sciences, University College London, London, WC1E 6BT, UK; snehal.pereira{at}ucl.ac.uk

Abstract

Objectives To describe the physical and mental health of children and young people (CYP) 6 months after infection with SARS-CoV-2 and explore whether this varies by COVID-19 vaccination.

Design A non-hospitalised, national cohort of people aged 11–17 years old with PCR-confirmed SARS-CoV-2 infection and PCR negatives matched at study invitation, by age, sex, region and date of testing who completed questionnaires 6 months after PCR testing. The questionnaire included 21 symptoms and standardised scales (eg, EQ-5D-Y and Chalder Fatigue Scale).

Results 6407 test-positive and 6542 test-negative CYP completed the 6-month questionnaire: 60.9% of test-positive vs 43.2% of test-negative CYP reported at least one symptom 6 months post-test; 27.6% of test-positive vs 15.9% of test-negative CYP reported 3+ symptoms. Common symptoms at 6 months were tiredness and shortness of breath among both test-positive and test-negative CYP; however, the prevalence of both was higher in test-positive (38.4% and 22.8%, respectively) compared with test-negative CYP (26.7% and 10.9%, respectively). 24.5% test-positive vs 17.8% test-negative CYP met the Delphi research definition of long COVID. Mental health, well-being, fatigue and health-related quality of life scores were similar among test-positive and test-negative CYP 6 months post-test. Similarly, symptomatology was similar among COVID-19-vaccinated and COVID-19-unvaccinated test-positive and test-negative CYP.

Conclusions Six-months post-PCR testing, CYP who tested positive for SARS-CoV-2 had similar symptoms to those who tested negative, but test-positive CYP had higher symptom prevalence. Mental health, well-being, fatigue and health-related quality of life were similar among test-positive and test-negative CYP, and symptoms at 6 months were similar in COVID-19 vaccinated and unvaccinated.

Trial registration number ISRCTN 34804192.

  • adolescent health
  • child health
  • COVID-19
  • paediatrics
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WHAT IS ALREADY KNOWN ON THIS TOPIC

  • Few studies of long COVID in children and young people include a suitable comparison group.

  • To our knowledge, no study has described self-reported overall health of children and young people 6 months after confirmed SARS-CoV-2 infection.

  • No study has described post-COVID-19 symptoms in children and young people by vaccination status after proven SARS-CoV-2 infection.

WHAT THIS STUDY ADDS

  • Six-months post-PCR testing, adolescents who tested positive for SARS-CoV-2 had similar symptoms to those who tested negative, but test-positives had a higher prevalence of symptoms.

  • Applying a Delphi-derived research definition of long COVID, 24.5% of test-positive and 17.8% of test-negative children and young people would be classified as having long COVID at 6 months.

  • Physical, mental health, fatigue and health-related quality of life were similar among COVID-19-vaccinated and COVID-19-unvaccinated test-positive and test-negative children and young people.

HOW THIS STUDY MIGHT AFFECT RESEARCH, PRACTICE OR POLICY

  • Six months post-test, there was little difference in mental health between test-positive and test-negative adolescents, suggesting the impact on mental health of SARS-CoV-2 infection is small.

  • A symptom-based definition of ‘long COVID’ may not be ideal, and more detailed phenotyping looking for changes in biomarkers, immunotype and imaging is needed.

  • Data from this subsample suggest that a COVID-19 vaccination policy based on reducing long-term symptoms in adolescents might not be efficacious.

Introduction

Research on the long-term physical and mental health of SARS-CoV-2 infection in children and young people (CYP), who have also suffered from the indirect effects of the pandemic, including school closures, education disruption and social isolation, is key.1

Our systematic review on persistent symptoms following SARS-CoV-2 in CYP found only 8 studies with an appropriate control group and 15 with an adequate follow-up period, mostly less than 4 months.2 Published reports on the natural history of long COVID and persistence of both physical and mental symptoms over time vary widely.3–9

The effect of COVID-19 vaccination on persistent symptoms in CYP is not known. In the UK, vaccination was recommended in August 2021 for healthy adolescents aged 16–17 years old and September 2021 for those 12–15 years old. By January 2022, 52.5% of adolescents aged 12–15 years old and 69.7% of those 16–17 years old in state-funded schools in England had received at least one dose of a COVID-19 vaccine, while 5.8% and 46.0%, respectively, received two doses.10

COVID-19 vaccination may reduce the risk of long COVID in adults who are subsequently infected with SARS-CoV-2.11 Furthermore, for pre-existing long COVID in adults, vaccination was associated with a 12.8% decrease in self-reported prevalence of long COVID; a second dose was associated with an 8.8% decrease.12

We describe the physical and mental health of adolescents aged 11–17 years old, 6 months after PCR testing for SARS-CoV-2 infection in those who tested positive and tested negative and explore variation by COVID-19 vaccination status using data from the CLoCk Study,13 the largest, prospective, matched cohort study of test-positive and test-negative CYP.

Methods

The CLoCk Study13 is a national cohort study of SARS-CoV-2 PCR-positive (‘exposed’) CYP aged 11–17 years, matched at study invitation, by month of test, age, sex and geographical area to SARS-CoV-2 test-negative (‘unexposed’) CYP using the national SARS-CoV-2 testing dataset held by the UK Health Security Agency (UKHSA). UKHSA received results of all SARS-CoV-2 PCR tests in England irrespective of reason (school attendance, contact of positive case, symptomatic). Only UK National Health Service number, name, age, sex and postcode were recorded. UKHSA can access the electronic Patient Demographic Service allowing us to approach CYP by post for them to consent online and undertake our questionnaire. The CLoCk Study involves follow-up for 2 years after a SARS-CoV-2 PCR test taken September 2020–March 2021. Depending on month of test, for some participants this is at 3, 6, 12 and 24 months post-test; for others 6, 12 and 24 months post-test; and for some 12 and 24 months post-test. This paper reports on all 6-month data post-test. Approximately 25% of these participants had reported follow-up data at 3 months post-test (see the Results section for details).

Measures

The questionnaire included demographics, elements of the International Severe Acute Respiratory and emerging Infection Consortium questionnaire,14 21 symptoms, the EQ-Visual Analogue Scale15 and EQ-5D-Y16 scale, Strengths and Difficulties Questionnaire (SDQ),17 Short Warwick-Edinburgh Mental Wellbeing Scale (SWEMWBS)18 and Chalder Fatigue Scale19 (online supplemental text 1). Those who consented completed the online questionnaire describing their health at the time of PCR testing (baseline) and 6 months post-test. Hence, baseline data relating to health at PCR testing were collected retrospectively; data 6 months later were collected prospectively.

CYP who were originally PCR negative but received a positive SARS-CoV-2 test by 6 months were excluded (determined by PCR test results held by UKHSA and self-report). Similarly, those who tested positive originally and were reinfected were also excluded. In addition, both test-positive and test-negative CYP were excluded if they responded to the 6-month questionnaire more than 34 weeks after their baseline PCR test.

Statistical methods

The representativeness of our study population was assessed by comparing their demographics (sex, age, region of residence and Index of Multiple Deprivation (IMD)) with those of the target population (all invited participants). Baseline characteristics of study participants, symptoms reported at PCR testing and symptoms reported 6 months post-test were further assessed according to SARS-CoV-2 status. As the prevalence of long COVID might vary by age,5 20 we also stratified analyses into two age groups, reflecting key educational stages (11–14 and 15–17 years).21

We operationalised our Delphi research definition of long COVID22 as having at least 1 of 21 symptoms and experiencing more than minimal problems on any one of the five EQ-5D-Y questions23 (see footnote of online supplemental table 4). The Delphi definition requires laboratory confirmation of SARS-CoV-2 infection but of course that was not required when assessing how many test-negative CYP would also have met this definition. Participants’ characteristics at baseline and 6 months post-test were stratified by SARS-CoV-2 test status and then further stratified by their long COVID status. Similarly, we produced tables stratified by SARS-CoV-2 infection and COVID-19 vaccination status. There were missing data only for information on vaccination (an optional question at the time of questionnaire completion), where 20 (15 PCR-negative and 5 PCR-positive) CYP did not answer. These CYP were omitted from tables stratifying by vaccination status.

To assess the effect of potential response bias, we reweighted all symptom frequencies according to the age, sex, region, IMD and SARS-CoV-2 status of the respondents so that analyses align with the characteristics of the target population.

This is a descriptive study and, in line with guidance, significance tests were avoided.24 Therefore, our study does not assess causality nor report measures of association, and instead aims to describe distributions with the purpose of identifying areas for future formal investigation. This study is registered with the ISRCTN registry (ISRCTN 34804192).

Results

A total of 14 377 participants completed a follow-up questionnaire 6 months after their SARS-CoV-2 PCR test between September 2020 and March 2021 (figure 1).13 Of these, 317 of 7499 CYP who were originally PCR negative received a positive SARS-CoV-2 test by 6 months and were excluded. Similarly, 48 of 6878 who tested positive originally were reinfected and excluded. An additional 1063 CYP (423 test positive and 640 test negative) were excluded because they responded to the 6-month questionnaire more than 34 weeks after their PCR test. The final study sample comprised 12 949 CYP (6407 tested positive, 6542 tested negative) and included 576 PCR-positive and 695 PCR-negative CYP who self-reported receiving a COVID-19 vaccine by their 6-month questionnaire . Although the study recruited non-hospitalised CYP at time of testing, 104 PCR-positive CYP did subsequently attend hospital appointments in relation to their COVID-19 infection of whom 50 were hospitalised overnight. A total of 1658 test-positive and 1737 test-negative participants who completed the questionnaire at 6 months had also completed the questionnaire at 3 months (when they reported on their baseline symptoms).21

Figure 1

Participant flow. *Determined by PCR test results held by the UK Health Security Agency and self-report of whether (or not) the participant ever had a positive COVID-19 test.

The 6-month follow-up questionnaire was returned at a median of 27.8 (IQR: 26.3–29.7) weeks after testing. Overall, 6542 of 72 449 (9.0%) test-negative and 6407 of 55 447 (11.6%) test-positive CYP completing the 6-month questionnaire formed part of the analytical sample (see online supplemental table 1). Compared with the target population, both test-positive and test-negative respondents were more likely to be female and older teenagers (table 1). Study participants were also more likely to be from the East Midlands and the South West and less likely to be from London or the North West; they were also more likely to be from the least deprived areas. Test-negative and test-positive respondents in both the target population and analytical sample were broadly similar in terms of demographics, reflecting the matched cohort design.

Table 1

Demographics of target population and participants included in the 6-month sample

At testing

At testing, test-positive CYP reported more symptoms than test-negative CYP (table 2). The most common symptoms among test-positive CYP were headaches, loss of smell and tiredness; among test-negative CYP they were sore throat, headaches and cough (table 2 and figure 2). The prevalence of symptoms varied by SARS-CoV-2 status (eg, headaches were reported by 29.0% of test-positive compared with 5.4% of test-negative CYP). The burden of symptoms was slightly higher at older ages (online supplemental table 2).

Figure 2

Proportion of participants experiencing symptoms at time of testing and 6 months post-testing by SARS-CoV-2 status: (A) test-positive children and young people (CYP) and (B) test-negative CYP.

Table 2

Reported symptoms, and self-rated physical and mental health*, by SARS-CoV-2 status, at time of testing and 6 months post-test

Six months post-testing

Six months post-testing, the most common symptoms in test-positive CYP were tiredness, shortness of breath, headaches, loss of smell and dizziness in that order (table 2 and figure 2); all other symptoms affected less than 10% of test-positive CYP. The most common symptoms in test-negative CYP were tiredness, headaches and shortness of breath in that order; all other symptoms affected less than 10% of test-negative CYP. The prevalence of individual symptoms was higher in the test-positive CYP (table 2) and in the older age group (online supplemental table 3). Notably, 6 months post-test, despite the higher prevalence of symptoms in test-positive CYP compared with test-negative CYP, self-rated health was similar in both groups, overall and when stratified by age (online supplemental table 3).

Six months post-test, mental health and well-being were similar between test-positive and test-negative CYP. Among those aged 11–14 years old, the SDQ (total difficulties) median was 9 (IQR 5–14) for test-positive and 10 (IQR 6–15) for test-negative CYP (higher SDQ scores indicate more problems). Among those aged 15–17 years old, the SDQ median was 11 (IQR 7–16) for test-positive and 12 (IQR 7–17) for test-negative CYP. The distribution of SWEMWBS scores (higher scores indicate better mental well-being) was similar between the test-positive (mean=21.7; SD 4.3) and the test-negative CYP (mean=21.4; SD 4.3). Mean fatigue scores (higher scores indicate more severe fatigue) were also similar between the test-positive (13.4; SD 5.1) and test-negative CYP (13.0; SD 5.1). EQ-5D-Y scores, representing health-related quality of life, showed that test-positive and test-negative CYP were equally likely to report problems with mobility, self-care, doing usual activities, pain/discomfort and feeling worried/sad, for example, 45.5% of test-positive CYP aged 15–17 years old, and 46.5% of test-negative CYP felt worried, sad or unhappy, as indicated on a single item of the EQ-5D-Y (figure 3).

Figure 3

Proportion of participants reporting experiencing some or a lot of problems* 6 months post-test by SARS-CoV-2 status, by age. *Assessed using the five items from the EQ-5D-Y scale, each of which has a three-level response (no problems, some problems, a lot of problems). The graph shows the proportion who experiences some/a lot of problems with mobility, self-care, doing usual activities, having pain/discomfort, or feeling a bit/very worried/sad.

Six months post-test, 24.5% of test-positive and 17.8% of test-negative CYP met our Delphi research definition of long COVID22 (online supplemental table 4). Regardless of SARS-CoV-2 status, those meeting the research definition of long COVID at 6 months also reported worse mental health, well-being and fatigue (online supplemental table 5).

Between testing and 6 months post-test, 10.7% of test-negative and 9.0% of test-positive CYP received a COVID-19 vaccine (online supplemental table 6). When assessed by SARS-CoV-2 PCR test status at baseline, there was little difference between vaccinated and unvaccinated CYP in terms of symptoms, mental health or well-being at 6 months post-test (online supplemental table 7).

When we reweighted the percentage of reported symptoms at baseline and at 6 months post-test according to the age, sex, region, IMD and SARS-CoV-2 test status of the respondents, so that analyses align with the characteristics of the target population, broadly similar patterns were observed to those reported above (online supplemental table 8).

Discussion

At time of testing for SARS-CoV-2 infection, test-positive CYP reported more symptoms than test-negative CYP. Six months post-testing, the overall prevalence of symptoms had increased in both groups and the prevalence of symptoms remained higher in test-positive compared with test-negative CYP. As in our previous analysis at 3 months post-test,21 prevalence of tiredness and shortness of breath increased at 6 months post-test compared with baseline in both test-positive and test-negative CYP. It is these two large increases which underlie the overall increase in symptom prevalence in both groups. This may be partly due to self-selection by participants with symptoms to report. Study participants were more likely to be female, older, from certain geographical areas and from less deprived areas.

Employing our Delphi consensus definition of long COVID in CYP,22 those without long COVID are more likely to be male, younger, and have good/very good physical and mental health before PCR testing (online supplemental table 4).

With respect to mental health, well-being and fatigue 6 months post-test, there was little difference in scores between test-positive and test-negative CYP. Moreover, the scores were very similar to those we described at 3-month follow-up.21 For example, at both 3 and 6 months post-test, median SDQ was 9–12 depending on age.

It might appear incongruent that 6 months post-test, while test-positive CYP had a higher prevalence of symptoms than test-negative CYP, their mental health, self-rated health, well-being and fatigue levels were similar. These observations suggest that by 6 months post-test, while test-positive CYP do experience more symptoms than test-negative CYP, these symptoms are mostly mild with little effect on overall well-being.

Acknowledging only 10% of CYP were vaccinated by 6 months post-test, we found little difference in symptoms, mental health or well-being at 6 months in vaccinated and unvaccinated PCR-positive and PCR-negative CYP. Indeed, EQ-5D-Y scores were somewhat worse and self-rated health lower, for the vaccinated group, which could represent self-selection of more severely affected CYP undergoing vaccination or self-selection of respondents.

The very few studies with follow-up of CYP for at least 6 months after SARS-COV-2 infection4 6 7 show conflicting findings. However, all findings, including ours, need to be considered within the context of bias (selection and recall), low response rates and recognising that a temporal association with infection does not prove causality as indirect effects of the pandemic need to be considered.25 Therefore, our findings are important because we have a test-negative group of CYP who have lived through the ‘long pandemic’ and who never tested positive for SARS-CoV-2 before or during the study period, although we acknowledge that (re)infections may have gone undetected. However, PCR and lateral flow tests were widely and freely available in the UK before and during the 6 months post-test period (April–September 2021). Hence, our data provide a unique perspective on long COVID in CYP.

Our study has limitations.21 First, the questionnaire response rate was low (9.0% (test-negative CYP); 11.6% (test-positive CYP)). However, this is similar to the Office for National Statistics random household survey (response rate 12% October 2021, Daniel Ayoubkhani: personal communication). Second, the study design may risk selection biases of those with internet access; symptoms to report (perhaps explaining why relative frequencies of many symptoms were higher 6 months post-test compared with baseline); recall bias for symptoms at time of testing; returning to school from March 2021, following national lockdown from January 2021, with exposure to other infections. Furthermore, some symptoms might have predated SARS-CoV-2 infection. Participants did not report on symptom severity. Third, although the number of symptoms is a proxy of illness severity, a single severe symptom might be more disabling than several mild symptoms. EQ-5D-Y served as a severity indicator because it assesses the effect on daily living. Fourth, it is possible that some participants might have been misdiagnosed as SARS-CoV-2 negative and vice-versa. False negatives can arise from PCR timing, swab technique and assay sensitivity but false-positive PCR results are rare. Fifth, we could not recruit or match on ethnicity, medical history or testing location but subsequent self-reported ethnicity was very similar in both test groups and geographical address served as a proxy for socioeconomic status. We used established scales to measure mental health, well-being and fatigue but acknowledge the limitations of self-reporting and floor and ceiling effects.

All self-reported symptoms are subjective. Researchers want to ask as much as possible to allow analysis of as many research questions as possible. In our pilot, the researchers’ initial draft questionnaire took over an hour to complete and teenagers said they would be willing to spend 20 minutes maximum completing the survey, despite a financial reward. This compromise means our wide-ranging and unique data have limitations in terms of information available.

Conclusions

Tiredness and shortness of breath were two dominant symptoms 6 months after SARS-CoV-2 PCR testing, irrespective of test result. Secondly, 27.6% of test-positive and 15.9% of test-negative CYP had three or more physical symptoms 6 months post-test, which was similar to the 30.3% and 16.2%, respectively, we reported at 3 months post-test.21 Thirdly, at 6 months post-test, there was little difference in well-being and mental health between test-positive and test-negative CYP. Fourth, 24.5% of test-positive CYP met our Delphi definition of long COVID22 at 6 months compared with 17.8% of test-negative CYP. Finally, the profile of symptoms, well-being and mental health in test-positive and test-negative CYP by COVID-19 vaccination status was similar.

Ethics statements

Patient consent for publication

Ethics approval

This study involves human participants and ethical approval was provided by the Yorkshire and the Humber-South Yorkshire Research Ethics Committee (REC reference: 21/YH/0060; IRAS project ID:293495). Participants gave informed consent to participate in the study before taking part.

Acknowledgments

Michael Lattimore, UKHSA, as Project Officer for the CLoCk Study. Olivia Swann and Elizabeth Whittaker designed the elements of the ISARIC Paediatric COVID-19 follow-up questionnaire which were incorporated into the online questionnaire used in this study to which all the CLoCk Consortium members contributed. Bianca De Stavola, for advice on addressing reviewer comments. Jake Dudley for supporting with editing the manuscript.

References

Supplementary materials

  • Supplementary Data

    This web only file has been produced by the BMJ Publishing Group from an electronic file supplied by the author(s) and has not been edited for content.

Footnotes

  • Twitter @SPintoPereira, @shamezladhani

  • Collaborators Additional co-applicants on the grant application and CLoCk Consortium members (alphabetical): Marta Buszewicz; Trudie Chalder; Esther Crawley; Bianca De Stavola; Shruti Garg, University of Manchester; Dougal Hargreaves, Imperial College London; Anthony Harnden, University of Oxford; Michael Levin, Imperial College London; Vanessa Poustie, University of Liverpool; Terry Segal, University College London Hospitals NHS Foundation Trust; Malcolm Semple, University of Liverpool; Kishan Sharma (deceased), Manchester University NHS Foundation Trust; Olivia Swann, University of Edinburgh; Elizabeth Whittaker.

  • Contributors TS conceived the idea for the study, submitted the successful grant application and drafted the manuscript. SPP designed and conducted the statistical analyses for the manuscript, accessed and verified the data and drafted the manuscript. SPP acts as guarantor for the manuscript. RS contributed to the design of the study, submitted the ethics and R&D applications and drafted the manuscript. MDN conducted the statistical analysis for the manuscript, accessed and verified the data and drafted the manuscript. NKR assisted with the statistical analysis for the manuscript, accessed the data and reviewed the manuscript. KM adapted the questionnaire for the online SNAP survey platform. RS accessed and verified the data, designed the participant sampling and data flow. TF contributed to the design of the study and reviewed the manuscript. IH contributed to the design of the study and reviewed the manuscript. SNL developed the study methodology, operationalised the regulatory and recruitment ideas for the study and revised the manuscript. EYC assisted with the references for the literature review and contributed to the manuscript. LF-S assisted with the drafting, formatting of the manuscript and references. ED conducted the PPI meetings, contributed to and reviewed the manuscript. All members of the CLoCk Consortium made contributions to the conception or design of the work and were involved in the funding application and this manuscript.

  • Funding Funded by the Department of Health and Social Care, in their capacity as the National Institute for Health Research (NIHR), and by UK Research & Innovation (UKRI) who has awarded funding (grant number COVLT0022). All research at Great Ormond Street Hospital NHS Foundation Trust and UCL Great Ormond Street Institute of Child Health is made possible by the NIHR Great Ormond Street Hospital Biomedical Research Centre. SPP is supported by a UK Medical Research Council Career Development Award (ref: MR/P020372/1).

  • Disclaimer The views expressed are those of the authors and not necessarily those of the NHS, the NIHR, UKRI or the Department of Health.

  • Competing interests TS is Chair of the Health Research Authority and therefore recused himself from the Research Ethics Application. Trudie Chalder is a member of the National Institute for Health and Care Excellence committee for long COVID. She has written self-help books on chronic fatigue and has done workshops on chronic fatigue and post-infectious syndromes.

  • Provenance and peer review Not commissioned; externally peer reviewed.

  • Supplemental material This content has been supplied by the author(s). It has not been vetted by BMJ Publishing Group Limited (BMJ) and may not have been peer-reviewed. Any opinions or recommendations discussed are solely those of the author(s) and are not endorsed by BMJ. BMJ disclaims all liability and responsibility arising from any reliance placed on the content. Where the content includes any translated material, BMJ does not warrant the accuracy and reliability of the translations (including but not limited to local regulations, clinical guidelines, terminology, drug names and drug dosages), and is not responsible for any error and/or omissions arising from translation and adaptation or otherwise.