Evidence map›Paper›PMID 36174032›Full record

Observational studyPloS one2022

Post-acute sequelae of COVID-19 symptom phenotypes and therapeutic strategies: A prospective, observational study.

Jennifer A Frontera, Lorna E Thorpe, Naomi M Simon, Adam de Havenon, Shadi Yaghi, Sakinah B Sabadia, Dixon Yang, Ariane Lewis, Kara Melmed, Laura J Balcer and 2 more

Open access · goldAbstract readObservational Study
In one paragraph

Observational study in PloS one, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed, 1 pooled it
6.1field-weighted citation impact, top 3% 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

28 citing papers in PubMed, 1 synthesis or guideline pooled it, 51 citations in OpenAlex.

  1. Pooled it
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  10. Long COVID as an Infection-Associated Chronic Condition: Implications.American journal of health promotion : AJHP · 2025
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  19. Musculoskeletal and Neuropathic Pain in COVID-19.Diagnostics (Basel, Switzerland) · 2024
    Review
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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

12 authors at 4 institutions in 1 country.

Jennifer A FronteraDepartment of Neurology, New York University Grossman School of Medicine, New York, New York, United States of America.ORCID 0000-0002-0719-2522
Lorna E ThorpeDepartment of Population Health, New York University, New York, New York, United States of America.
Naomi M SimonDepartment of Psychiatry, New York University Grossman School of Medicine, New York, New York, United States of America.
Adam de HavenonDepartment of Neurology, Yale University School of Medicine, New Haven, Connecticut, United States of America.
Shadi YaghiDepartment of Neurology, Brown University School of Medicine, Providence, Rhode Island, United States of America.
Sakinah B SabadiaDepartment of Neurology, New York University Grossman School of Medicine, New York, New York, United States of America.
Dixon YangDepartment of Neurology, New York Presbyterian, Columbia Medical Center, New York, New York, United States of America.ORCID 0000-0002-7155-8904
Ariane LewisDepartment of Neurology, New York University Grossman School of Medicine, New York, New York, United States of America.
Kara MelmedDepartment of Neurology, New York University Grossman School of Medicine, New York, New York, United States of America.
Laura J BalcerDepartment of Neurology, New York University Grossman School of Medicine, New York, New York, United States of America.
Thomas WisniewskiDepartment of Neurology, New York University Grossman School of Medicine, New York, New York, United States of America.
Steven L GalettaDepartment of Neurology, New York University Grossman School of Medicine, New York, New York, United States of America.
New York University · USBrown University · USNewYork–Presbyterian Hospital · USYale University · US

Funding

Research Education ComponentP30AG066512 · NIA · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI Mary Sherman Mittelman · 2020 to 2026
$28.4M
Transgenic/Behavior CoreP01AG060882 · NIA · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI SHAO, YONGZHAO · 2020 to 2024
$12.0M
NIA NIH HHS P01 AG060882NIA NIH HHS P30 AG066512
6 · The paper itself

Abstract

backgroundPost-acute sequelae of COVID-19 (PASC) includes a heterogeneous group of patients with variable symptomatology, who may respond to different therapeutic interventions. Identifying phenotypes of PASC and therapeutic strategies for different subgroups would be a major step forward in management.

methodsIn a prospective cohort study of patients hospitalized with COVID-19, 12-month symptoms and quantitative outcome metrics were collected. Unsupervised hierarchical cluster analyses were performed to identify patients with: (1) similar symptoms lasting ≥4 weeks after acute SARS-CoV-2 infection, and (2) similar therapeutic interventions. Logistic regression analyses were used to evaluate the association of these symptom and therapy clusters with quantitative 12-month outcome metrics (modified Rankin Scale, Barthel Index, NIH NeuroQoL).

resultsAmong 242 patients, 122 (50%) reported ≥1 PASC symptom (median 3, IQR 1-5) lasting a median of 12-months (range 1-15) post-COVID diagnosis. Cluster analysis generated three symptom groups: Cluster1 had few symptoms (most commonly headache); Cluster2 had many symptoms including high levels of anxiety and depression; and Cluster3 primarily included shortness of breath, headache and cognitive symptoms. Cluster1 received few therapeutic interventions (OR 2.6, 95% CI 1.1-5.9), Cluster2 received several interventions, including antidepressants, anti-anxiety medications and psychological therapy (OR 15.7, 95% CI 4.1-59.7) and Cluster3 primarily received physical and occupational therapy (OR 3.1, 95%CI 1.3-7.1). The most severely affected patients (Symptom Cluster 2) had higher rates of disability (worse modified Rankin scores), worse NeuroQoL measures of anxiety, depression, fatigue and sleep disorder, and a higher number of stressors (all P<0.05). 100% of those who received a treatment strategy that included psychiatric therapies reported symptom improvement, compared to 97% who received primarily physical/occupational therapy, and 83% who received few interventions (P = 0.042).

conclusionsWe identified three clinically relevant PASC symptom-based phenotypes, which received different therapeutic interventions with varying response rates. These data may be helpful in tailoring individual treatment programs.

Indexed as

COVID-19Disease ProgressionHumansPhenotypeProspective StudiesSARS-CoV-2

Identifiers

PMID36174032
PMCPMC9521913
OpenAlexW4297984273

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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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.