Evidence map›Paper›PMID 36328291›Full record

ArticleInternational journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases2022

Baricitinib vs tocilizumab treatment for hospitalized adult patients with severe COVID-19 and associated cytokine storm: a prospective, investigational, real-world study.

Botond Lakatos, Bálint Gergely Szabó, Ilona Bobek, Noémi Kiss-Dala, Zsófia Gáspár, Alexandra Riczu, Borisz Petrik, Balázs Ferenc Farkas, Gabriella Sebestyén, László Gopcsa and 6 more

Open access · goldAbstract read
In one paragraph

Article in International journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases, 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
0.5field-weighted citation impact, top 35% 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, 6 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  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

16 authors at 1 institution in 1 country.

Botond LakatosSouth Pest Central Hospital, National Institute of Hematology and Infectious Diseases, Budapest, Hungary; Semmelweis University, Department of Internal Medicine and Hematology, Division of Infectology, Budapest, Hungary. Electronic address: lakatos.botond_tibor@med.semmelweis-univ.hu.
Bálint Gergely SzabóSouth Pest Central Hospital, National Institute of Hematology and Infectious Diseases, Budapest, Hungary; Semmelweis University, Department of Internal Medicine and Hematology, Division of Infectology, Budapest, Hungary.
Ilona BobekSouth Pest Central Hospital, National Institute of Hematology and Infectious Diseases, Budapest, Hungary.
Noémi Kiss-DalaSouth Pest Central Hospital, National Institute of Hematology and Infectious Diseases, Budapest, Hungary; Semmelweis University, Doctoral School of Clinical Medicine, Budapest, Hungary.
Zsófia GáspárSouth Pest Central Hospital, National Institute of Hematology and Infectious Diseases, Budapest, Hungary; Semmelweis University, Doctoral School of Clinical Medicine, Budapest, Hungary.
Alexandra RiczuSouth Pest Central Hospital, National Institute of Hematology and Infectious Diseases, Budapest, Hungary.
Borisz PetrikSouth Pest Central Hospital, National Institute of Hematology and Infectious Diseases, Budapest, Hungary.
Balázs Ferenc FarkasSemmelweis University, 1st Department of Paediatrics, Budapest, Hungary.
Gabriella SebestyénSouth Pest Central Hospital, National Institute of Hematology and Infectious Diseases, Budapest, Hungary.
László GopcsaSouth Pest Central Hospital, National Institute of Hematology and Infectious Diseases, Budapest, Hungary.
Gabriella BekőSouth Pest Central Hospital, National Institute of Hematology and Infectious Diseases, Budapest, Hungary.
János SinkóSouth Pest Central Hospital, National Institute of Hematology and Infectious Diseases, Budapest, Hungary.
Péter ReményiSouth Pest Central Hospital, National Institute of Hematology and Infectious Diseases, Budapest, Hungary.
János SzlávikSouth Pest Central Hospital, National Institute of Hematology and Infectious Diseases, Budapest, Hungary.
Dóra MathiászSouth Pest Central Hospital, National Institute of Hematology and Infectious Diseases, Budapest, Hungary.
István Vályi-NagySouth Pest Central Hospital, National Institute of Hematology and Infectious Diseases, Budapest, Hungary.
Semmelweis University · HU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesOur aim was to compare outcomes of hospitalized adults with severe COVID-19 and cytokine storm treated with tocilizumab or baricitinib.

methodsA prospective, investigational, real-world study was performed from April 2020 to April 2021 at our center. COVID-19 severity was classified by World Health Organization criteria, and cytokine storm was documented along predefined criteria. Eligible patients were enrolled at diagnosis if they fulfilled a priori inclusion criteria and received standard-of-care plus tocilizumab or baricitinib for >48 hours. Patients were followed per protocol for 28 days post-diagnosis. The primary outcome was all-cause mortality; secondary outcomes were invasive mechanical ventilation and major infectious complications.

resultsOf 463 patients, 102/463 (22.1%) received tocilizumab, and 361/463 (77.9%) baricitinib. Baseline characteristics were balanced. At 28 days, there was no difference in all-cause mortality (22/102, 21.6% vs 64/361, 17.7%; P-value = 0.38). Requirement for invasive mechanical ventilation was more frequent after tocilizumab (52/102, 50.9% vs 96/361, 26.6%; P <0.01), rate of major infectious complications was similar (32/102, 31.4% vs 96/361, 26.6%; P-value = 0.34). In logistic regression, the immunomodulatory drug was not retained as a predictor of all-cause mortality. Kaplan-Meier analysis revealed statistically similar survival distributions.

conclusionAll-cause mortality was similar between adults treated with baricitinib or tocilizumab for severe COVID-19 with cytokine storm.

Indexed as

COVID-19Cytokine Release SyndromeAdultAntibodies, Monoclonal, HumanizedAzetidinesHumansProspective StudiesPurinesPyrazolesSARS-CoV-2SulfonamidesTreatment OutcomeAntibodies, Monoclonal, HumanizedAzetidinesbaricitinibPurinesPyrazolesSulfonamidestocilizumabBaricitinibCOVID-19Cytokine stormSARS-CoV-2Tocilizumab

Identifiers

PMID36328291
PMCPMC9621622
OpenAlexW4307734713

What OpenQuestion holds

Textmetadata
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.