Evidence map›Paper›PMID 33621264›Full record

ArticlePloS one2021

Development and validation of a prediction model for tocilizumab failure in hospitalized patients with SARS-CoV-2 infection.

Cristina Mussini, Alessandro Cozzi-Lepri, Marianna Menozzi, Marianna Meschiari, Erica Franceschini, Jovana Milic, Lucio Brugioni, Antonello Pietrangelo, Massimo Girardis, Andrea Cossarizza and 15 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
0.7field-weighted citation impact, top 29% 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

9 citing papers in PubMed, 1 synthesis or guideline pooled it, 12 citations in OpenAlex.

  1. Pooled it
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  5. Observational
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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

25 authors at 9 institutions in 2 countries.

Cristina MussiniDepartment of Infectious Diseases, Azienda Ospedaliero-Universitaria, Policlinico of Modena, Modena, Italy.ORCID 0000-0002-6615-4198
Alessandro Cozzi-LepriCentre for Clinical Research, Epidemiology, Modelling and Evaluation (CREME), Institute for Global Health, UCL Population Health Sciences, University College London, London, United Kingdom.
Marianna MenozziDepartment of Infectious Diseases, Azienda Ospedaliero-Universitaria, Policlinico of Modena, Modena, Italy.
Marianna MeschiariDepartment of Infectious Diseases, Azienda Ospedaliero-Universitaria, Policlinico of Modena, Modena, Italy.
Erica FranceschiniDepartment of Infectious Diseases, Azienda Ospedaliero-Universitaria, Policlinico of Modena, Modena, Italy.
Jovana MilicDepartment of Surgical, Medical, Dental and Morphological Sciences, University of Modena and Reggio Emilia, Modena, Italy.
Lucio BrugioniInternal Medicine Department, Azienda Ospedaliero-Universitaria, Policlinico of Modena, Modena, Italy.
Antonello PietrangeloDepartment of Medical and Surgical Sciences for Children and Adults, University of Modena and Reggio Emilia, Modena, Italy.ORCID 0000-0002-7411-935X
Massimo GirardisDepartment of Surgical, Medical, Dental and Morphological Sciences, University of Modena and Reggio Emilia, Modena, Italy.
Andrea CossarizzaDepartment of Medical and Surgical Sciences for Children and Adults, University of Modena and Reggio Emilia, Modena, Italy.
Roberto TonelliRespiratory Diseases Unit, Azienda Ospedaliero-Universitaria, Policlinico of Modena, Modena, Italy.
Enrico CliniDepartment of Medical and Surgical Sciences for Children and Adults, University of Modena and Reggio Emilia, Modena, Italy.
Marco MassariInfectious Disease Unit, Azienda USL-IRCCS di Reggio Emilia, Reggio Emilia, Italy.
Michele BartolettiDepartment of Medical and Surgical Sciences, University of Bologna, Bologna, Italy.
Anna FerrariInfectious Disease Unit, Azienda Ospedale, University of Padua, Padua, Italy.
Anna Maria CattelanInfectious Disease Unit, Azienda Ospedale, University of Padua, Padua, Italy.
Paola ZuccalàDepartment of Public Health and Infectious Disease, Sapienza University of Rome, Polo Pontino, Italy.
Miriam LichtnerDepartment of Public Health and Infectious Disease, Sapienza University of Rome, Polo Pontino, Italy.
Roberto RossottiNiguarda Hospital Milan, Milano, Italy.ORCID 0000-0003-4965-8789
Enrico GirardiNational Institute for Infectious Diseases L. Spallanzani (INMI), Rome, Italy.
Emanuele NicastriNational Institute for Infectious Diseases L. Spallanzani (INMI), Rome, Italy.
Massimo PuotiNational Institute for Infectious Diseases L. Spallanzani (INMI), Rome, Italy.
Andrea AntinoriNational Institute for Infectious Diseases L. Spallanzani (INMI), Rome, Italy.
Pierluigi VialeDepartment of Medical and Surgical Sciences, University of Bologna, Bologna, Italy.
Giovanni GuaraldiDepartment of Infectious Diseases, Azienda Ospedaliero-Universitaria, Policlinico of Modena, Modena, Italy.
University of Modena and Reggio Emilia · ITAzienda Ospedaliero-Universitaria di Modena · ITIstituto Nazionale per le Malattie Infettive Lazzaro Spallanzani · ITSapienza University of Rome · ITUniversity of Bologna · ITUniversity of Padua · ITAzienda Sanitaria Unità Locale di Reggio Emilia · ITAzienda Socio Sanitaria Territoriale Grande Ospedale Metropolitano Niguarda · ITNational Institute for Health Research · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe aim of this secondary analysis of the TESEO cohort is to identify, early in the course of treatment with tocilizumab, factors associated with the risk of progressing to mechanical ventilation and death and develop a risk score to estimate the risk of this outcome according to patients' profile.

methodsPatients with COVID-19 severe pneumonia receiving standard of care + tocilizumab who were alive and free from mechanical ventilation at day 6 after treatment initiation were included in this retrospective, multicenter cohort study. Multivariable logistic regression models were built to identify predictors of mechanical ventilation or death by day-28 from treatment initiation and β-coefficients were used to develop a risk score. Secondary outcome was mortality. Patients with the same inclusion criteria as the derivation cohort from 3 independent hospitals were used as validation cohort.

results266 patients treated with tocilizumab were included. By day 28 of hospital follow-up post treatment initiation, 40 (15%) underwent mechanical ventilation or died [26 (10%)]. At multivariable analysis, sex, day-4 PaO2/FiO2 ratio, platelets and CRP were independently associated with the risk of developing the study outcomes and were used to generate the proposed risk score. The accuracy of the score in AUC was 0.80 and 0.70 in internal validation and test for the composite endpoint and 0.92 and 0.69 for death, respectively.

conclusionsOur score could assist clinicians in identifying, early after tocilizumab administration, patients who are likely to progress to mechanical ventilation or death, so that they could be selected for eventual rescue therapies.

Indexed as

COVID-19 Drug TreatmentAgedAntibodies, Monoclonal, HumanizedCohort StudiesFemaleHospitalizationHumansMaleMiddle AgedMulticenter Studies as TopicRetrospective StudiesSARS-CoV-2Treatment OutcomeAntibodies, Monoclonal, Humanizedtocilizumab

Identifiers

PMID33621264
PMCPMC7901750
OpenAlexW3130646206

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Registered trials

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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.