Evidence map›Paper›PMID 39046739›Full record

ArticleJAMA network open2024

Myalgic Encephalomyelitis/Chronic Fatigue Syndrome After SARS-CoV-2 Infection.

Elizabeth R Unger, Jin-Mann S Lin, Lauren E Wisk, Huihui Yu, Michelle L'Hommedieu, Helen Lavretsky, Juan Carlos C Montoy, Michael A Gottlieb, Kristin L Rising, Nicole L Gentile and 17 more

Abstract readMulticenter Study
In one paragraph

Article in JAMA network open, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
–field-weighted citation impact
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

14 citing papers in PubMed.

  1. Review
  2. Article
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  4. Observational
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  7. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

27 authors.

Elizabeth R UngerDivision of High-Consequence Pathogens and Pathology, National Center for Emerging and Zoonotic Infectious Diseases, Centers for Disease Control and Prevention, Atlanta, Georgia.
Jin-Mann S LinDivision of High-Consequence Pathogens and Pathology, National Center for Emerging and Zoonotic Infectious Diseases, Centers for Disease Control and Prevention, Atlanta, Georgia.
Lauren E WiskDivision of General Internal Medicine & Health Services Research, David Geffen School of Medicine at the University of California, Los Angeles.
Huihui YuCenter for Outcomes Research & Evaluation (CORE), Section of Cardiovascular Medicine, Department of Internal Medicine, Yale School of Medicine, New Haven, Connecticut.
Michelle L'HommedieuDivision of General Internal Medicine & Health Services Research, David Geffen School of Medicine at the University of California, Los Angeles.
Helen LavretskyDepartment of Psychiatry and Biobehavioral Sciences, David Geffen School of Medicine at the University of California, Los Angeles.
Juan Carlos C MontoyDepartment of Emergency Medicine, University of California, San Francisco.
Michael A GottliebDepartment of Emergency Medicine, Rush University Medical Center, Chicago, Illinois.
Kristin L RisingDepartment of Emergency Medicine, Thomas Jefferson University, Philadelphia, Pennsylvania.
Nicole L GentilePost-COVID Rehabilitation and Recovery Clinic, University of Washington, Seattle.
Michelle SantangeloDivision of Infectious Diseases, Department of Internal Medicine, Rush University Medical Center, Chicago, Illinois.
Arjun K VenkateshCenter for Outcomes Research & Evaluation (CORE), Section of Cardiovascular Medicine, Department of Internal Medicine, Yale School of Medicine, New Haven, Connecticut.
Robert M RodriguezDepartment of Emergency Medicine, University of California, San Francisco.
Mandy J HillDepartment of Emergency Medicine, UTHealth Houston, Houston, Texas.
Rachel E GeyerDepartment of Family Medicine, University of Washington, Seattle.
Efrat R KeanDepartment of Emergency Medicine, Thomas Jefferson University, Philadelphia, Pennsylvania.
Sharon SaydahNational Center for Immunizations and Respiratory Diseases, Centers for Disease Control and Prevention, Atlanta, Georgia.
Samuel A McDonaldDepartment of Emergency Medicine, University of Texas Southwestern Medical Center, Dallas.
Ryan HuebingerDepartment of Emergency Medicine, UTHealth Houston, Houston, Texas.
Ahamed H IdrisDepartment of Emergency Medicine, University of Texas Southwestern Medical Center, Dallas.
Jocelyn DorneyCenter for Outcomes Research & Evaluation (CORE), Section of Cardiovascular Medicine, Department of Internal Medicine, Yale School of Medicine, New Haven, Connecticut.
Bala HotaTendo Systems, Inc, Philadelphia, Pennsylvania.
Erica S SpatzCenter for Outcomes Research & Evaluation (CORE), Section of Cardiovascular Medicine, Department of Internal Medicine, Yale School of Medicine, New Haven, Connecticut.
Kari A StephensDepartment of Family Medicine, University of Washington, Seattle.
Robert A WeinsteinDivision of Infectious Diseases, Department of Internal Medicine, Rush University Medical Center, Chicago, Illinois.
Joann G ElmoreDivision of General Internal Medicine & Health Services Research, David Geffen School of Medicine at the University of California, Los Angeles.
Innovative Support for Patients with SARS-CoV-2 Infections Registry (INSPIRE) Group

Funding

Yale Clinical and Translational Science Award (U Component)UL1TR001863 · NCATS · YALE UNIVERSITY · PI John H. Krystal, LUCILA OHNO-MACHADO · 2016 to 2026
$102.9M
NCATS NIH HHS UL1 TR001863
6 · The paper itself

Abstract

Importance: Chronic symptoms reported following an infection with SARS-CoV-2, such as cognitive problems, overlap with symptoms included in the definition of myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS). Objective: To evaluate the prevalence of ME/CFS-like illness subsequent to acute SARS-CoV-2 infection, changes in ME/CFS symptoms through 12 months of follow-up, and the association of ME/CFS symptoms with SARS-CoV-2 test results at the acute infection-like index illness. Design, Setting, and Participants: This prospective, multisite, longitudinal cohort study (Innovative Support for Patients with SARS-CoV-2 Infections Registry [INSPIRE]) enrolled participants from December 11, 2020, to August 29, 2022. Participants were adults aged 18 to 64 years with acute symptoms suggestive of SARS-CoV-2 infection who received a US Food and Drug Administration-approved SARS-CoV-2 test at the time of illness and did not die or withdraw from the study by 3 months. Follow-up surveys were collected through February 28, 2023. Exposure: COVID-19 status (positive vs negative) at enrollment. Main Outcome and Measures: The main outcome was the weighted proportion of participants with ME/CFS-like illness based on the 2015 Institute of Medicine clinical case definition using self-reported symptoms. Results: A total of 4378 participants were included in the study. Most were female (3226 [68.1%]). Mean (SD) age was 37.8 (11.8) years. The survey completion rates ranged from 38.7% (3613 of 4738 participants) to 76.3% (1835 of 4738) and decreased over time. The weighted proportion of participants identified with ME/CFS-like illness did not change significantly at 3 through 12 months of follow-up and was similar in the COVID-19-positive (range, 2.8%-3.7%) and COVID-19-negative (range, 3.1%-4.5%) groups. Adjusted analyses revealed no significant difference in the odds of ME/CFS-like illness at any time point between COVID-19-positive and COVID-19-negative individuals (marginal odds ratio range, 0.84 [95% CI, 0.42-1.67] to 1.18 [95% CI, 0.55-2.51]). Conclusions and Relevance: In this prospective cohort study, there was no evidence that the proportion of participants with ME/CFS-like illness differed between those infected with SARS-CoV-2 vs those without SARS-CoV-2 infection up to 12 months after infection. A 3% to 4% prevalence of ME/CFS-like illness after an acute infection-like index illness would impose a high societal burden given the millions of persons infected with SARS-CoV-2.

Indexed as

COVID-19Fatigue Syndrome, ChronicSARS-CoV-2AdolescentAdultFemaleHumansLongitudinal StudiesMaleMiddle AgedPrevalenceProspective StudiesUnited StatesYoung Adult

Identifiers

PMID39046739
PMCPMC11270135

What Socratic holds

Textmetadata
LicenceCC BY
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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 Socratic graph.