Evidence map›Paper›PMID 39907931›Full record

ArticleClinical autonomic research : official journal of the Clinical Autonomic Research Society2025

Chronic autonomic symptom burden in long-COVID: a follow-up cohort study.

Ella F Eastin, Jannika V Machnik, Lauren E Stiles, Nicholas W Larsen, Jordan Seliger, Linda N Geng, Hector Bonilla, Phillip C Yang, Mitchell G Miglis

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Article in Clinical autonomic research : official journal of the Clinical Autonomic Research Society, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors.

Ella F EastinDepartment of Neurology and Neurological Sciences, Stanford University, 213 Quarry Road, Stanford, CA, 94304, USA.
Jannika V MachnikDepartment of Neurology and Neurological Sciences, Stanford University, 213 Quarry Road, Stanford, CA, 94304, USA.
Lauren E StilesDepartment of Neurology and Neurological Sciences, Stanford University, 213 Quarry Road, Stanford, CA, 94304, USA.
Nicholas W LarsenDepartment of Neurology and Neurological Sciences, Stanford University, 213 Quarry Road, Stanford, CA, 94304, USA.
Jordan SeligerDepartment of Neurology and Neurological Sciences, Stanford University, 213 Quarry Road, Stanford, CA, 94304, USA.
Linda N GengDepartment of Medicine, Stanford University, Stanford, CA, USA.
Hector BonillaDepartment of Medicine, Stanford University, Stanford, CA, USA.
Phillip C YangDepartment of Medicine, Stanford University, Stanford, CA, USA.
Mitchell G MiglisDepartment of Neurology and Neurological Sciences, Stanford University, 213 Quarry Road, Stanford, CA, 94304, USA. mmiglis@stanford.edu.ORCID http://orcid.org/0000-0001-8488-0313

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeAutonomic dysfunction is a common and often debilitating feature of long-COVID (LC), however, studies evaluating frequency and severity of chronic autonomic dysfunction in LC are limited. We utilized an established online cohort of participants with LC to assess duration and severity of autonomic dysfunction, impact on quality of life, risk factors of autonomic diagnoses including postural tachycardia syndrome (POTS), and efficacy of common treatments.

methodsOur international cohort included 526 adults with LC aged 20-65 years who previously completed baseline evaluations of LC symptoms, autonomic symptom burden, and quality of life. Participants repeated survey instruments and completed new instruments assessing risk factors and symptom mitigation strategies. A subset of individuals completed a 10-min active stand test. Multivariable logistic regression identified predictors of autonomic symptom burden and incident autonomic diagnoses including POTS.

resultsA total of 71.9% of participants with LC had a Composite Autonomic Symptom Score-31 (COMPASS-31) score ≥ 20, suggestive of moderate-to-severe autonomic dysfunction. The median symptom duration was 36 [30-40] months, and 37.5% of participants could no longer work or had to drop out of school due to their illness. In addition, 40.5% of individuals with autonomic dysfunction were newly diagnosed with POTS, representing 33% of the total LC cohort. Female sex and joint hypermobility were associated with an increased risk of autonomic dysfunction.

conclusionsEvidence of chronic moderate-to-severe autonomic dysfunction was seen in most participants with LC in our cohort and was significantly associated with reduced quality of life and functional disability. POTS was the most common post-COVID autonomic diagnosis.

Indexed as

Autonomic Nervous System DiseasesCOVID-19AdultAgedChronic DiseaseCohort StudiesFemaleFollow-Up StudiesHumansMaleMiddle AgedPost-Acute COVID-19 SyndromeQuality of LifeRisk FactorsSymptom BurdenYoung AdultAutonomic dysfunctionDysautonomiaLong-COVIDPost-acute sequalae of COVID-19 (PASC)Postural orthostatic tachycardia syndrome (POTS)

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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.