Evidence map›Paper›PMID 33615209›Full record

ReviewJournal of translational autoimmunity2021

Benefits of early aggressive immunomodulatory therapy (tocilizumab and methylprednisolone) in COVID-19: Single center cohort study of 685 patients.

Buzon-Martín Luis, Montero-Baladía Miguel, Delgado-López Pedro, Iglesias-Posadilla David, Astigarraga Itziar, Galacho-Harriero Ana, Iglesias-Julián Enrique, López-Veloso María, De La Torre-Ferrera Noelia, Barraza-Bengoechea Julio César and 18 more

Abstract readReview
In one paragraph

Review in Journal of translational autoimmunity, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 3 pooled it
–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

10 citing papers in PubMed, 3 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Article
  5. Article
  6. Review
  7. Analysis of the factors predicting clinical response to tocilizumab therapy in patients with severe COVID-19.International journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases · 2022
    Article
  8. Review
  9. OM-85 Broncho-VaxomBiomedicines · 2021
    Article
  10. Review
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

28 authors.

Buzon-Martín LuisInfectious Diseases Unit, Internal Medicine, Hospital de Burgos, Spain.
Montero-Baladía MiguelIntensive Care, Hospital de Burgos, Spain.
Delgado-López PedroNeurosurgery, Hospital de Burgos, Spain.
Iglesias-Posadilla DavidIntensive Care, Hospital de Burgos, Spain.
Astigarraga ItziarPediatrics, Biocruces Bizkaia Health Research Institute, Hospital Universitario de Cruces, University of the Basque Country UPV/EHU, Baracaldo, Spain.
Galacho-Harriero AnaInfectious Diseases Unit, Internal Medicine, Hospital de Burgos, Spain.
Iglesias-Julián EnriqueSystemic Autoimmune Diseases, Internal Medicine Department, Hospital de Burgos, Spain.
López-Veloso MaríaSystemic Autoimmune Diseases, Internal Medicine Department, Hospital de Burgos, Spain.
De La Torre-Ferrera NoeliaSystemic Autoimmune Diseases, Internal Medicine Department, Hospital de Burgos, Spain.
Barraza-Bengoechea Julio CésarSystemic Autoimmune Diseases, Internal Medicine Department, Hospital de Burgos, Spain.
Ubeira-Iglesias MartaPharmacy Department, Hospital de Burgos, Spain.
San Llorente-Sebastián RodrigoAnesthesiology Department, Hospital de Burgos, Spain.
Colazo-Burlato MaríaReumatology Department, Hospital de Burgos, Spain.
Lorenzo-Martín AndrésReumatology Department, Hospital de Burgos, Spain.
Minguito de la Iglesia JavierPneumology Department, Hospital de Burgos, Spain.
García-Muñoz Juan PabloPneumology Department, Hospital de Burgos, Spain.
Hermida-Fernández GerardoHematology Department, Hospital de Burgos, Spain.
Navarro-San Francisco CarolinaInfectious Diseases Unit, Internal Medicine, Hospital de Burgos, Spain.
Boado-Lama JorgeInternal Medicine, Hospital de Burgos, Spain.
Fernández-Regueras MaríaInfectious Diseases Unit, Internal Medicine, Hospital de Burgos, Spain.
Callejo-Torre FernandoIntensive Care, Hospital de Burgos, Spain.
Ossa-Echeverri SergioIntensive Care, Hospital de Burgos, Spain.
Fisac-Cuadrado LourdesIntensive Care, Hospital de Burgos, Spain.
Gero-Escapa MaríaIntensive Care, Hospital de Burgos, Spain.
Megías-Lobón GregoriaMicrobiology Department, Hospital de Burgos, Spain.
Simón-Rodríguez AdolfoPneumology Department, Hospital de Burgos, Spain.
Fernández-Ratero José AntonioIntensive Care, Hospital de Burgos, Spain.
HUBU-COVID-19 group

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionA growing evidence suggests that immune dysregulation and thrombotic phenomena are key features in the pathophysiology of COVID-19. Apart from antivirals and respiratory support, anticoagulants, corticoids and immunomodulators are increasingly being prescribed, especially for more severe cases. We describe the clinical outcome of a large cohort of patients preferentially treated with glucocorticoids and interleukin inhibitors.

methodsSingle center and retrospective case series. Adult patients admitted with COVID-19 related respiratory insufficiency were included. Patients who died within 2 days after admission and those testing positive but asymptomatic were excluded. We defined two study periods: from March 3rd to March 31 st, 2020 (beginning of epidemic until peak of incidence) and April 1 st to May 7 th, 2020 (second half of epidemic). The majority of patients received respiratory support, combinations of antimicrobials, anticoagulants, corticoids and interleukin inhibitors. Antivirals were preferentially given in the first period. The clinical outcome (death and ventilator dependency) of both periods was compared.

resultsFrom March 3 rd to May 7 th, 685 patients were included for analysis (58.4% males, mean age 68.9 years). Patients in the first period (n ​= ​408) were younger (66.6 vs 71.1 years, p ​= ​0.003), presented lower mean P a O 2/F i O2 ratio at admission (256.5 vs 270.4 ​mm Hg,p ​= ​0.0563), higher ferritin (1520 vs 1221 ​ng/ml, p ​= ​0.01), higher IL-6 (679 vs 194 ​pg/ml, p ​< ​0.0001) and similar D-dimer levels (3.59 vs 3.39 ​μg/mL, p ​= ​0.65) compared to the second period (n ​= ​277). Lopinavir/ritonavir and interferon were preferentially given in the first period (23.8% and 32% vs 1.8% and 11.9%, p ​< ​0.0001). Use of corticoids (88.2% vs 87.4%, p ​= ​0,74) and tocilizumab (26.29 vs 20.22% p ​= ​0.06) were similarly administered in both periods. Patients in the second period needed less mechanical ventilation (4.9% vs 16.9%, p ​< ​0.0001), fewer ICU admission (6.1% vs 20.1%,p ​< ​0.0001) and showed similar mortality (17.7% vs 15.4%, p ​= ​0.43). Infectious and thrombotic complications were comparable in both periods (both around 8%, with no statistical difference). Patients treated with tocilizumab (n ​= ​163) had lower mortality rate compared to those untreated under the same indication (7.9% vs 24.2%, p ​< ​0.0001).

conclusionsIn this large retrospective COVID-19 in-hospital cohort, lopinavir/ritonavir and interferon showed no significant impact on survival. Extensive use of corticosteroids and tocilizumab resulted in good overall outcome and showed acceptable complication rates.

Indexed as

CoronavirusCOVID-19DiagnosisEpidemiologyImmunomodulationSARS-CoV-2Treatment

Identifiers

PMID33615209
PMCPMC7879932

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.