Evidence map›Paper›PMID 36983304›Full record

ArticleJournal of clinical medicine2023

Tocilizumab Outcomes in Critically Ill COVID-19 Patients Admitted to the ICU and the Role of Non-Tocilizumab COVID-19-Specific Medical Therapeutics.

Alyaa Elhazmi, Ahmed A Rabie, Awad Al-Omari, Hani N Mufti, Hend Sallam, Mohammed S Alshahrani, Ahmed Mady, Adnan Alghamdi, Ali Altalaq, Mohamed H Azzam and 11 more

Open access · goldAbstract read
In one paragraph

Article in Journal of clinical medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.6field-weighted citation impact, top 36% 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

0 citing papers in PubMed, 3 citations in OpenAlex.

No citing paper in PubMed yet.

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 at 12 institutions in 3 countries.

Alyaa ElhazmiDepartment of Critical Care, Dr. Sulaiman Al-Habib Medical Group, Riyadh 11643, Saudi Arabia.ORCID 0000-0001-8315-7393
Ahmed A RabieCritical Care Department, King Saud Medical City, Riyadh 11196, Saudi Arabia.ORCID 0000-0002-0438-1977
Awad Al-OmariResearch Center, Dr. Sulaiman Alhabib Medical Group, Riyadh 11643, Saudi Arabia.
Hani N MuftiSection of Cardiac Surgery, Department of Cardiac Sciences, King Faisal Cardiac Center, King Abdulaziz Medical City, MNGHA-WR, Jeddah 21423, Saudi Arabia.
Hend SallamDepartment of Adult Critical Care Medicine, King Faisal Specialist Hospital & Research Centre, Jeddah 23431, Saudi Arabia.
Mohammed S AlshahraniDepartment of Emergency and Critical Care, King Fahad Hospital of the University, Dammam University, Al Khobar 31952, Saudi Arabia.
Ahmed MadyCritical Care Department, King Saud Medical City, Riyadh 11196, Saudi Arabia.
Adnan AlghamdiPrince Sultan Military Medical City, Military Medical Services, Ministry of Defense, Riyadh 12233, Saudi Arabia.
Ali AltalaqPrince Sultan Military Medical City, Military Medical Services, Ministry of Defense, Riyadh 12233, Saudi Arabia.
Mohamed H AzzamIntensive Care Department, King Abdullah Medical Complex, Jeddah 23816, Saudi Arabia.
Anees SindiDepartment of Medicine, Intensive Care, King Abdulaziz University, Jeddah 21589, Saudi Arabia.
Ayman KharabaDepartment of Critical Care, King Fahad Hospital, Al Medina Al Munawara 41477, Saudi Arabia.
Zohair A Al-AseriDepartments of Emergency Medicine and Critical Care, College of Medicine, King Saud University, Riyadh 11451, Saudi Arabia.
Ghaleb A AlmekhlafiPrince Sultan Military Medical City, Military Medical Services, Ministry of Defense, Riyadh 12233, Saudi Arabia.
Wail TashkandiDepartment of Adult Critical Care, Fakeeh Care Group, Jeddah 23323, Saudi Arabia.
Saud A AlajmiPrince Sultan Military Medical City, Military Medical Services, Ministry of Defense, Riyadh 12233, Saudi Arabia.
Fahad FaqihiDepartment of Critical Care, Dr. Sulaiman Al-Habib Medical Group, Riyadh 11643, Saudi Arabia.
Abdulrahman AlharthyCritical Care Department, King Saud Medical City, Riyadh 11196, Saudi Arabia.
Jaffar A Al-TawfiqInfectious Disease Unit, Specialty Internal Medicine, Johns Hopkins Aramco Healthcare, Dhahran 34464, Saudi Arabia.
Rami Ghazi MelibariDepartment of Critical Care, King Abdullah Medical City, Makah 24246, Saudi Arabia.
Yaseen M ArabiIntensive Care Department, King Abdullah International Medical Research Center, College of Medicine, King Saud Bin Abdulaziz University for Health Sciences, Ministry of National Guard Health Affairs, Riyadh 11426, Saudi Arabia.
Riyadh Armed Forces Hospital · SAKing Saud Medical City · SAKing Abdulaziz University · SAKing Saud bin Abdulaziz University for Health Sciences · SASulaiman Al Rajhi Colleges · SAAlfaisal University · SAKing Abdullah Medical City · SAKing Fahad Hospital Jeddah · SAKing Fahd Hospital of the University · SAKing Faisal Specialist Hospital & Research Centre · SAKing Saud University · SASaudi Aramco Medical Services Organization · SA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTocilizumab is a monoclonal antibody proposed to manage cytokine release syndrome (CRS) associated with severe COVID-19. Previously published reports have shown that tocilizumab may improve the clinical outcomes of critically ill patients admitted to the ICU. However, no precise data about the role of other medical therapeutics concurrently used for COVID-19 on this outcome have been published.

objectivesWe aimed to compare the overall outcome of critically ill COVID-19 patients admitted to the ICU who received tocilizumab with the outcome of matched patients who did not receive tocilizumab while controlling for other confounders, including medical therapeutics for critically ill patients admitted to ICUs.

methodsA prospective, observational, multicenter cohort study was conducted among critically ill COVID-19 patients admitted to the ICU of 14 hospitals in Saudi Arabia between 1 March 2020, and October 31, 2020. Propensity-score matching was utilized to compare patients who received tocilizumab to patients who did not. In addition, the log-rank test was used to compare the 28 day hospital survival of patients who received tocilizumab with those who did not. Then, a multivariate logistic regression analysis of the matched groups was performed to evaluate the impact of the remaining concurrent medical therapeutics that could not be excluded via matching 28 day hospital survival rates. The primary outcome measure was patients' overall 28 day hospital survival, and the secondary outcomes were ICU length of stay and ICU survival to hospital discharge.

resultsA total of 1470 unmatched patients were included, of whom 426 received tocilizumab. The total number of propensity-matched patients was 1278. Overall, 28 day hospital survival revealed a significant difference between the unmatched non-tocilizumab group (586; 56.1%) and the tocilizumab group (269; 63.1%) (

conclusionThe tocilizumab treatment in critically ill COVID-19 patients admitted to the ICU improved the overall 28 day hospital survival, which might not be influenced by the concurrent use of other COVID-19 medical therapeutics, although further research is needed to confirm this.

Indexed as

COVID-19outcomepropensity-matchingtocilizumab

Identifiers

PMID36983304
PMCPMC10053430
OpenAlexW4327621582

What Socratic 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 Socratic graph.