Evidence map›Paper›PMID 39412208›Full record

Observational studyCritical care explorations2024

Persistent Fatigue, Weakness, and Aberrant Muscle Mitochondria in Survivors of Critical COVID-19.

Kirby P Mayer, Ahmed Ismaeel, Anna G Kalema, Ashley A Montgomery-Yates, Melissa K Soper, Philip A Kern, Jonathan D Starck, Stacey A Slone, Peter E Morris, Esther E Dupont-Versteegden and 1 more

Abstract readObservational Study
In one paragraph

Observational study in Critical care explorations, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

  1. Trial
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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

11 authors.

Kirby P MayerDepartment of Physical Therapy, College of Health Sciences, University of Kentucky, Lexington, KY.ORCID 0000-0003-3844-3846
Ahmed IsmaeelCenter for Muscle Biology, University of Kentucky, University of Kentucky, Lexington, KY.
Anna G KalemaKentucky Research Alliance for Lung Disease, University of Kentucky, Lexington, KY.
Ashley A Montgomery-YatesKentucky Research Alliance for Lung Disease, University of Kentucky, Lexington, KY.
Melissa K SoperKentucky Research Alliance for Lung Disease, University of Kentucky, Lexington, KY.
Philip A KernDivision of Endocrinology, College of Medicine, University of Kentucky, University of Kentucky, Lexington, KY.
Jonathan D StarckDepartment of Physical Therapy, College of Health Sciences, University of Kentucky, Lexington, KY.
Stacey A SloneDepartment of Statistics, University of Kentucky, University of Kentucky, Lexington, KY.
Peter E MorrisDivision of Pulmonary, Critical Care and Sleep Medicine, Internal Medicine, College of Medicine, University of Kentucky, University of Kentucky, Lexington, KY.
Esther E Dupont-VersteegdenDepartment of Physical Therapy, College of Health Sciences, University of Kentucky, Lexington, KY.
Kate KosmacDepartment of Physical Therapy, College of Health Sciences, University of Kentucky, Lexington, KY.

Funding

Kentucky Center for Clinical and Translational ScienceUL1TR001998 · NCATS · UNIVERSITY OF KENTUCKY · PI HARTMANN, KATHERINE E, KERN, PHILIP A · 2016 to 2025
$34.2M
Muscle and physical function recovery after acute critical illnessR01AR081002 · NIAMS · UNIVERSITY OF KENTUCKY · PI Esther E Dupont-Versteegden · 2023 to 2026
$1.7M
Cellular and Physical Function Outcomes Leading to Failed Muscle Recovery After Critical IllnessK23AR079583 · NIAMS · UNIVERSITY OF KENTUCKY · PI Kirby P Mayer · 2022 to 2026
$744k
College of Health Sciences, University of Kentucky Pilot AwardNCATS NIH HHS L32 TR005558NCATS NIH HHS UL1 TR001998NIAMS NIH HHS K23 AR079583NIAMS NIH HHS R01 AR081002NIMHD NIH HHS L32 MD017732
6 · The paper itself

Abstract

objectivesPersistent skeletal muscle dysfunction in survivors of critical illness due to acute respiratory failure is common, but biological data elucidating underlying mechanisms are limited. The objective of this study was to elucidate the prevalence of skeletal muscle weakness and fatigue in survivors of critical illness due to COVID-19 and determine if cellular changes associate with persistent skeletal muscle dysfunction.

designA prospective observational study in two phases: 1) survivors of critical COVID-19 participating in physical outcome measures while attending an ICU Recovery Clinic at short-term follow-up and 2) a nested cohort of patients performed comprehensive muscle and physical function assessments with a muscle biopsy; data were compared with non-COVID controls.

settingICU Recovery Clinic and clinical laboratory. PATIENTS/SUBJECTS: Survivors of critical COVID-19 and non-COVID controls.

interventionsNone. MEASUREMENTS AND MAIN

resultsOne hundred twenty patients with a median of 56 years old (interquartile range [IQR], 42-65 yr old), 43% female, and 33% individuals of underrepresented race attended follow-up 44 ± 17 days after discharge. Patients had a median Acute Physiology and Chronic Health Evaluation-II score of 24.0 (IQR, 16-29) and 98 patients (82%) required mechanical ventilation with a median duration of 14 days (IQR, 9-21 d). At short-term follow-up significant physical dysfunction was observed with 93% of patients reporting generalized fatigue and performing mean 218 ± 151 meters on 6-minute walk test (45% ± 30% of predicted). Eleven patients from this group agreed to participate in long-term assessment and muscle biopsy occurring a mean 267 ± 98 days after discharge. Muscle tissue from COVID exhibited a greater abundance of M2-like macrophages and satellite cells and lower activity of mitochondrial complex II and complex IV compared with controls.

conclusionsOur findings suggest that aberrant repair and altered mitochondrial activity in skeletal muscle associates with long-term impairments in patients surviving an ICU admission for COVID-19.

Indexed as

COVID-19Critical IllnessFatigueMitochondria, MuscleMuscle WeaknessSurvivorsAdultAgedFemaleHumansMaleMiddle AgedMuscle, SkeletalProspective StudiesSARS-CoV-2

Identifiers

PMID39412208
PMCPMC11487221

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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 OpenQuestion graph.