Evidence map›Paper›PMID 36303290›Full record

ArticleEuropean journal of neurology2023

Factors associated with the severity of COVID-19 outcomes in people with neuromuscular diseases: Data from the International Neuromuscular COVID-19 Registry.

Chiara Pizzamiglio, Robert D S Pitceathly, Michael P Lunn, Stefen Brady, Fabiola De Marchi, Lucia Galan, Jeannine M Heckmann, Alejandro Horga, Maria J Molnar, Acary S B Oliveira and 11 more

Abstract read
In one paragraph

Article in European journal of neurology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Article
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

21 authors.

Chiara PizzamiglioDepartment of Neuromuscular Diseases, UCL Queen Square Institute of Neurology, London, UK.ORCID 0000-0001-5519-0313
Robert D S PitceathlyDepartment of Neuromuscular Diseases, UCL Queen Square Institute of Neurology, London, UK.ORCID 0000-0002-6123-4551
Michael P LunnDepartment of Neuromuscular Diseases, UCL Queen Square Institute of Neurology, London, UK.
Stefen BradyDepartment of Neurology, John Radcliffe Hospital, Oxford, UK.
Fabiola De MarchiDepartment of Neurology and ALS Centre, Translational Medicine, University of Piemonte Orientale, Maggiore Della Carità Hospital, Novara, Italy.
Lucia GalanNeuromuscular Diseases Unit, Department of Neurology, Hospital Clínico San Carlos and Instituto de Investigación Sanitaria San Carlos (IdISSC), Madrid, Spain.
Jeannine M HeckmannDivision of Neurology, Department of Medicine, University of Cape Town, Cape Town, South Africa.
Alejandro HorgaNeuromuscular Diseases Unit, Department of Neurology, Hospital Clínico San Carlos and Instituto de Investigación Sanitaria San Carlos (IdISSC), Madrid, Spain.
Maria J MolnarInstitute of Genomic Medicine and Rare Disorders, Semmelweis University, Budapest, Hungary.
Acary S B OliveiraDivision of Neuromuscular Diseases, Department of Neurology and Neurosurgery, Federal University of São Paulo (UNIFESP), São Paulo, Brazil.
Wladimir B V R PintoDivision of Neuromuscular Diseases, Department of Neurology and Neurosurgery, Federal University of São Paulo (UNIFESP), São Paulo, Brazil.
Guido PrimianoNeurophysiopathology Unit, Fondazione Policlinico Universitario A. Gemelli, IRCCS, Rome, Italy.
Ernestina SantosDepartment of Neurology, Centro Hospitalar Universitario do Porto, Hospital de Santo Antonio, Oporto, Portugal.
Benedikt SchoserDepartment of Neurology, LMU Klinikum, Friedrich-Baur-Institute, Ludwig-Maximilians-University Munich, Munich, Germany.
Serenella ServideiNeurophysiopathology Unit, Fondazione Policlinico Universitario A. Gemelli, IRCCS, Rome, Italy.
Paulo V Sgobbi SouzaDivision of Neuromuscular Diseases, Department of Neurology and Neurosurgery, Federal University of São Paulo (UNIFESP), São Paulo, Brazil.
Vishnu VenugopalanDepartment of Neurology, All India Institute of Medical Sciences, New Delhi, India.ORCID 0000-0002-3654-8137
Michael G HannaDepartment of Neuromuscular Diseases, UCL Queen Square Institute of Neurology, London, UK.
Mazen M DimachkieDepartment of Neurology, University of Kansas Medical Centre, Kansas City, Kansas, USA.
Pedro M MachadoDepartment of Neuromuscular Diseases, UCL Queen Square Institute of Neurology, London, UK.ORCID 0000-0002-8411-7972
Neuromuscular Diseases and COVID-19 Study Group

Funding

Department of HealthMedical Research Council MC_PC_21046Medical Research Council MR/K000608/1Medical Research Council MR/S002065/1Medical Research Council MR/S005021/1
6 · The paper itself

Abstract

background and purposeClinical outcome information on patients with neuromuscular diseases (NMDs) who have been infected with SARS-CoV-2 is limited. The aim of this study was to determine factors associated with the severity of COVID-19 outcomes in people with NMDs.

methodsCases of NMD, of any age, and confirmed/presumptive COVID-19, submitted to the International Neuromuscular COVID-19 Registry up to 31 December 2021, were included. A mutually exclusive ordinal COVID-19 severity scale was defined as follows: (1) no hospitalization; (2) hospitalization without oxygenation; (3) hospitalization with ventilation/oxygenation; and (4) death. Multivariable ordinal logistic regression analyses were used to estimate odds ratios (ORs) for severe outcome, adjusting for age, sex, race/ethnicity, NMD, comorbidities, baseline functional status (modified Rankin scale [mRS]), use of immunosuppressive/immunomodulatory medication, and pandemic calendar period.

resultsOf 315 patients from 13 countries (mean age 50.3 [±17.7] years, 154 [48.9%] female), 175 (55.5%) were not hospitalized, 27 (8.6%) were hospitalized without supplemental oxygen, 91 (28.9%) were hospitalized with ventilation/supplemental oxygen, and 22 (7%) died. Higher odds of severe COVID-19 outcomes were observed for: age ≥50 years (50-64 years: OR 2.4, 95% confidence interval [CI] 1.33-4.31; >64 years: OR 4.16, 95% CI 2.12-8.15; both vs. <50 years); non-White race/ethnicity (OR 1.81, 95% CI 1.07-3.06; vs. White); mRS moderately severe/severe disability (OR 3.02, 95% CI 1.6-5.69; vs. no/slight/moderate disability); history of respiratory dysfunction (OR 3.16, 95% CI 1.79-5.58); obesity (OR 2.24, 95% CI 1.18-4.25); ≥3 comorbidities (OR 3.2, 95% CI 1.76-5.83; vs. ≤2; if comorbidity count used instead of specific comorbidities); glucocorticoid treatment (OR 2.33, 95% CI 1.14-4.78); and Guillain-Barré syndrome (OR 3.1, 95% CI 1.35-7.13; vs. mitochondrial disease).

conclusionsAmong people with NMDs, there is a differential risk of COVID-19 outcomes according to demographic and clinical characteristics. These findings could be used to develop tailored management strategies and evidence-based recommendations for NMD patients.

Indexed as

COVID-19Neuromuscular DiseasesFemaleHumansMaleMiddle AgedOxygenRegistriesSARS-CoV-2OxygenCOVID-19Guillain-Barré syndromemitochondrial diseaseneuromuscular diseasesoutcome

Identifiers

PMID36303290
PMCPMC9874570

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.