Evidence map›Paper›PMID 36551891›Full record

ArticleBiomedicines2022

Monoclonal Antibodies and Antivirals against SARS-CoV-2 Reduce the Risk of Long COVID: A Retrospective Propensity Score-Matched Case-Control Study.

Antonio Cimellaro, Desirée Addesi, Michela Cavallo, Francesco Spagnolo, Edoardo Suraci, Raffaella Cordaro, Ines Spinelli, Francesco Passafaro, Manuela Colosimo, Medea Pintaudi and 2 more

Open access · goldAbstract read
In one paragraph

Article in Biomedicines, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 1 pooled it
1.0field-weighted citation impact, top 22% 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

5 citing papers in PubMed, 1 synthesis or guideline pooled it, 8 citations in OpenAlex.

  1. Pooled it
  2. Bridging Gaps in Long COVID Therapy: A Review.Current medicinal chemistry · 2026
    Review
  3. Review
  4. Article
  5. 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

12 authors at 2 institutions in 1 country.

Antonio CimellaroInternal Medicine Unit, Department of Medicine, "Pugliese-Ciaccio" Hospital of Catanzaro, Via Pio X n.83, 88100 Catanzaro, Italy.ORCID 0000-0002-5223-4402
Desirée AddesiInternal Medicine Unit, Department of Medicine, "Pugliese-Ciaccio" Hospital of Catanzaro, Via Pio X n.83, 88100 Catanzaro, Italy.
Michela CavalloInternal Medicine Unit, Department of Medicine, "Pugliese-Ciaccio" Hospital of Catanzaro, Via Pio X n.83, 88100 Catanzaro, Italy.
Francesco SpagnoloInternal Medicine Unit, Department of Medicine, "Pugliese-Ciaccio" Hospital of Catanzaro, Via Pio X n.83, 88100 Catanzaro, Italy.
Edoardo SuraciInternal Medicine Unit, Department of Medicine, "Pugliese-Ciaccio" Hospital of Catanzaro, Via Pio X n.83, 88100 Catanzaro, Italy.
Raffaella CordaroInternal Medicine Unit, Department of Medicine, "Pugliese-Ciaccio" Hospital of Catanzaro, Via Pio X n.83, 88100 Catanzaro, Italy.
Ines SpinelliInternal Medicine Unit, Department of Medicine, "Pugliese-Ciaccio" Hospital of Catanzaro, Via Pio X n.83, 88100 Catanzaro, Italy.
Francesco PassafaroCoordination of Special Unit of Continuity Care for Local Health Authority, Via Vinicio Cortese n.25, 88100 Catanzaro, Italy.
Manuela ColosimoMicrobiology and Virology Unit, Service Department, "Pugliese-Ciaccio" Hospital of Catanzaro, Via Pio X n.83, 88100 Catanzaro, Italy.
Medea PintaudiNeurophysiology and Neurobiology Unit, Department of Medicine, Fondazione Policlinico Universitario Campus Bio-Medico, Via Alvaro del Portillo n.200, 00128 Rome, Italy.
Carmelo PintaudiInternal Medicine Unit, Department of Medicine, "Pugliese-Ciaccio" Hospital of Catanzaro, Via Pio X n.83, 88100 Catanzaro, Italy.
On Behalf Of The CATAnzaro LOng Covid Cataloco Study Group
Azienda Ospedaliera Pugliese Ciaccio · ITCampus Bio Medico University Hospital · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Long COVID is a complex condition affecting quality of life, with limited therapeutic options. We investigated the occurrence of long COVID in subjects receiving early therapy with monoclonal antibodies (mAbs) or antivirals to reduce the risk of COVID-19 progression. In this retrospective study we enrolled 737 adult patients (aged 65.16 ± 13.46; 361F), who experienced COVID-19 between January 2021 and March 2022. Antiviral or mAbs were administered to symptomatic patients who did not require oxygen therapy or hospital admission for SARS-CoV-2 infection, and who were at high risk of progression to severe disease, as identified by age > 65 years or the presence of comorbidities. Long COVID, defined as newly or persistent long-term symptoms 4 weeks after the onset of the acute illness, was reported in 204 cases (28%). Age (OR 1.03; p < 0.001), gender (OR 1.88; p < 0.001) and at least three comorbidities (OR 3.49; p = 0.049) were directly associated with long COVID; conversely, vaccination (OR 0.59; p = 0.005) and mAbs/antivirals (OR 0.44; p = 0.002) were independently associated with a reduced risk of long COVID. At a propensity-score-matched analysis, the mAbs/antivirals group had a significantly lower occurrence of long COVID in comparison with untreated controls (11% vs. 34%; p = 0.001). In conclusion, mAbs and antivirals administered against the progression of COVID-19 were associated with a reduced risk of long COVID.

Indexed as

antiviralsCOVID-19long COVIDmonoclonal antibodiespost-COVID syndromeSARS-CoV-2

Identifiers

PMID36551891
PMCPMC9775930
OpenAlexW4311625844

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.