Evidence map›Paper›PMID 36995712›Full record

ArticleJAMA network open2023

Prevalence and Characteristics Associated With Post-COVID-19 Condition Among Nonhospitalized Adolescents and Young Adults.

Joel Selvakumar, Lise Beier Havdal, Martin Drevvatne, Elias Myrstad Brodwall, Lise Lund Berven, Tonje Stiansen-Sonerud, Gunnar Einvik, Truls Michael Leegaard, Trygve Tjade, Annika E Michelsen and 9 more

Open access · goldAbstract read
In one paragraph

Article in JAMA network open, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 66 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
66citing papers in PubMed, 2 pooled it
23.9field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

66 citing papers in PubMed, 2 syntheses or guidelines pooled it, 116 citations in OpenAlex.

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6 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

19 authors at 8 institutions in 4 countries.

Joel SelvakumarDepartment of Paediatrics and Adolescent Health, Akershus University Hospital, Lørenskog, Norway.
Lise Beier HavdalDepartment of Paediatrics and Adolescent Health, Akershus University Hospital, Lørenskog, Norway.
Martin DrevvatneDepartment of Paediatrics and Adolescent Health, Akershus University Hospital, Lørenskog, Norway.
Elias Myrstad BrodwallDepartment of Paediatrics and Adolescent Health, Akershus University Hospital, Lørenskog, Norway.
Lise Lund BervenDepartment of Paediatrics and Adolescent Health, Akershus University Hospital, Lørenskog, Norway.
Tonje Stiansen-SonerudDepartment of Paediatrics and Adolescent Health, Akershus University Hospital, Lørenskog, Norway.
Gunnar EinvikInstitute of Clinical Medicine, University of Oslo, Oslo, Norway.
Truls Michael LeegaardInstitute of Clinical Medicine, University of Oslo, Oslo, Norway.
Trygve TjadeFürst Medical Laboratory, Oslo, Norway.
Annika E MichelsenInstitute of Clinical Medicine, University of Oslo, Oslo, Norway.
Tom Eirik MollnesDepartment of Immunology, University of Oslo and Oslo University Hospital, Oslo, Norway.
Fridtjof Lund-JohansenDepartment of Immunology, University of Oslo and Oslo University Hospital, Oslo, Norway.
Trygve HolmøyInstitute of Clinical Medicine, University of Oslo, Oslo, Norway.
Henrik ZetterbergInstitute of Neuroscience and Physiology, Department of Psychiatry and Neurochemistry, Sahlgrenska Academy, University of Gothenburg, Mölndal, Sweden.
Kaj BlennowInstitute of Neuroscience and Physiology, Department of Psychiatry and Neurochemistry, Sahlgrenska Academy, University of Gothenburg, Mölndal, Sweden.
Carolina X SandlerSchool of Health Sciences, Western Sydney University, Penrith, Australia.
Erin CvejicSchool of Public Health, Faculty of Medicine and Health, University of Sydney, Sydney Australia.
Andrew R LloydThe Kirby Institute, University of New South Wales, Sydney, Australia.
Vegard Bruun Bratholm WyllerDepartment of Paediatrics and Adolescent Health, Akershus University Hospital, Lørenskog, Norway.
University of Oslo · NOAkershus University Hospital · NOOslo University Hospital · NOSahlgrenska University Hospital · SEThe University of Sydney · AUUniversity of Gothenburg · SEUNSW Sydney · AUWestern Sydney University · AU

Funding

The effects of iron on oxidative stress and Alzheimer's biomarkers in amyloid-positive and negative elderly normalR01AG068398 · NIA · WEILL MEDICAL COLL OF CORNELL UNIV · PI CHIANG, GLORIA CHIA-YI · 2020 to 2024
$2.8M
NIA NIH HHS R01 AG068398
6 · The paper itself

Abstract

Importance: The prevalence and baseline risk factors of post-COVID-19 condition (PCC) remain unresolved among the large number of young people who experienced mild COVID-19. Objectives: To determine the point prevalence of PCC 6 months after the acute infection, to determine the risk of development of PCC adjusted for possible confounders, and to explore a broad range of potential risk factors. Design, Setting, and Participants: This cohort study included nonhospitalized individuals from 2 counties in Norway between ages 12 and 25 years who underwent reverse transcription-polymerase chain reaction (RT-PCR) testing. At the early convalescent stage and at 6-month follow-up, participants underwent a clinical examination; pulmonary, cardiac, and cognitive functional testing; immunological and organ injury biomarker analyses; and completion of a questionnaire. Participants were classified according to the World Health Organization case definition of PCC at follow-up. Association analyses of 78 potential risk factors were performed. Exposures: SARS-CoV-2 infection. Main Outcomes and Measures: The point prevalence of PCC 6 months after RT-PCR testing in the SARS-CoV-2-positive and SARS-CoV-2-negative groups, and the risk difference with corresponding 95% CIs. Results: A total of 404 individuals testing positive for SARS-CoV-2 and 105 individuals testing negative were enrolled (194 male [38.1%]; 102 non-European [20.0%] ethnicity). A total of 22 of the SARS-CoV-2-positive and 4 of the SARS-CoV-2-negative individuals were lost to follow-up, and 16 SARS-CoV-2-negative individuals were excluded due to SARS-CoV-2 infection in the observational period. Hence, 382 SARS-CoV-2-positive participants (mean [SD] age, 18.0 [3.7] years; 152 male [39.8%]) and 85 SARS-CoV-2-negative participants (mean [SD] age, 17.7 [3.2] years; 31 male [36.5%]) could be evaluated. The point prevalence of PCC at 6 months was 48.5% in the SARS-CoV-2-positive group and 47.1% in the control group (risk difference, 1.5%; 95% CI, -10.2% to 13.1%). SARS-CoV-2 positivity was not associated with the development of PCC (relative risk [RR], 1.06; 95% CI, 0.83 to 1.37; final multivariable model utilizing modified Poisson regression). The main risk factor for PCC was symptom severity at baseline (RR, 1.41; 95% CI, 1.27-1.56). Low physical activity (RR, 0.96; 95% CI, 0.92-1.00) and loneliness (RR, 1.01; 95% CI, 1.00-1.02) were also associated, while biological markers were not. Symptom severity correlated with personality traits. Conclusions and Relevance: The persistent symptoms and disability that characterize PCC are associated with factors other than SARS-CoV-2 infection, including psychosocial factors. This finding raises questions about the utility of the World Health Organization case definition and has implications for the planning of health care services as well as for further research on PCC.

Indexed as

COVID-19AdolescentAdultChildCohort StudiesHumansMalePrevalenceRisk FactorsSARS-CoV-2Young Adult

Identifiers

PMID36995712
PMCPMC10064252
OpenAlexW4361270388

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.