Evidence map›Paper›PMID 38350878›Full record

ArticleBMC infectious diseases2024

Dexamethasone versus methylprednisolone for multiple organ dysfunction in COVID-19 critically ill patients: a multicenter propensity score matching study.

Ohoud Aljuhani, Ghazwa B Korayem, Ali F Altebainawi, Daniah AlMohammady, Amjaad Alfahed, Elaf F Altebainawi, Mohammed Aldhaeefi, Hisham A Badreldin, Ramesh Vishwakarma, Faisal E Almutairi and 10 more

Abstract readMulticenter Study
In one paragraph

Article in BMC infectious diseases, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–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

2 citing papers in PubMed.

  1. Article
  2. 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

20 authors.

Ohoud AljuhaniDepartment of Pharmacy Practice, Faculty of Pharmacy, King Abdulaziz University, Jeddah, Saudi Arabia.
Ghazwa B KorayemDepartment of Pharmacy Practice, College of Pharmacy, Princess Nourah bint Abdulrahman University, Riyadh, Saudi Arabia.
Ali F AltebainawiPharmaceutical Care Services, King Salman Specialist Hospital, Hail Health Cluster, Ministry of Health, Hail, Saudi Arabia.
Daniah AlMohammadyDepartment of Pharmacy Practice, Faculty of Pharmacy, King Abdulaziz University, Jeddah, Saudi Arabia.
Amjaad AlfahedDepartment of Pharmacy Practice, College of Pharmacy, Princess Nourah bint Abdulrahman University, Riyadh, Saudi Arabia.
Elaf F AltebainawiDepartment of Medicine, King Khalid Hospital, Hail Health Cluster, Hail, Saudi Arabia.
Mohammed AldhaeefiClinical and Administrative Pharmacy Sciences, College of Pharmacy, Howard University, Washington, DC, 20059, USA.
Hisham A BadreldinPharmaceutical Care Department, King Abdulaziz Medical City, Riyadh, Saudi Arabia.
Ramesh VishwakarmaNorwich clinical trial unit, Norwich medical school, University of east Anglia, Norwich, UK.
Faisal E AlmutairiClinical Pharmacy Department, Pharmacy Services Administration, King Fahad Medical City, Riyadh, Saudi Arabia.
Abeer A AlenaziPharmaceutical Care Department, Prince Sultan Military Medical City, Riyadh, Saudi Arabia.
Thamer AlsulaimanFamily Medicine Department, King Faisal Specialist Hospital & Research Center, Riyadh, Saudi Arabia.
Rahaf Ali AlqahtaniPharmaceutical Care Department, King Abdulaziz Medical City, Riyadh, Saudi Arabia.
Fahad Al DhahriPharmaceutical Care Department, King Abdulaziz Medical City, Riyadh, Saudi Arabia.
Namareq AldardeerPharmaceutical Care Services, King Faisal Specialist Hospital and Research Center, Jeddah, Saudi Arabia.
Ahmed O AlenaziPharmaceutical Care Department, King Abdulaziz Medical City, Dammam, Saudi Arabia.
Shmeylan Al HarbiPharmaceutical Care Department, King Abdulaziz Medical City, Riyadh, Saudi Arabia.
Raed KensaraKing Abdullah International Medical Research Center-King Saud Bin Abdulaziz University for Health Sciences, Ministry of National Guard - Health Affairs, Riyadh, Saudi Arabia.
Mai AlalawiPharmaceutical Care Services, King Abdulaziz Medical City, Jeddah, Saudi Arabia.
Khalid Al SulaimanPharmaceutical Care Department, King Abdulaziz Medical City, Riyadh, Saudi Arabia. alsulaimankh@hotmail.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDexamethasone usually recommended for patients with severe coronavirus disease 2019 (COVID-19) to reduce short-term mortality. However, it is uncertain if another corticosteroid, such as methylprednisolone, may be utilized to obtain better clinical outcome. This study assessed dexamethasone's clinical and safety outcomes compared to methylprednisolone.

methodsA multicenter, retrospective cohort study was conducted between March 01, 2020, and July 31, 2021. It included adult COVID-19 patients who were initiated on either dexamethasone or methylprednisolone therapy within 24 h of intensive care unit (ICU) admission. The primary outcome was the progression of multiple organ dysfunction score (MODS) on day three of ICU admission. Propensity score (PS) matching was used (1:3 ratio) based on the patient's age and MODS within 24 h of ICU admission.

resultsAfter Propensity Score (PS) matching, 264 patients were included; 198 received dexamethasone, while 66 patients received methylprednisolone within 24 h of ICU admission. In regression analysis, patients who received methylprednisolone had a higher MODS on day three of ICU admission than those who received dexamethasone (beta coefficient: 0.17 (95% CI 0.02, 0.32), P = 0.03). Moreover, hospital-acquired infection was higher in the methylprednisolone group (OR 2.17, 95% CI 1.01, 4.66; p = 0.04). On the other hand, the 30-day and the in-hospital mortality were not statistically significant different between the two groups.

conclusionDexamethasone showed a lower MODS on day three of ICU admission compared to methylprednisolone, with no statistically significant difference in mortality.

Indexed as

COVID-19AdultCOVID-19 Drug TreatmentCritical IllnessDexamethasoneHumansMethylprednisoloneMultiple Organ FailurePropensity ScoreRetrospective StudiesDexamethasoneMethylprednisolone30-day mortalityCOVID-19Critically illDexamethasoneICUsIn-hospital mortalityMethylprednisoloneSARS-Cov-2Ventilation free days (VFDs)

Identifiers

PMID38350878
PMCPMC10863167

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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.