Evidence map›Paper›PMID 41545952›Full record

ArticleBMC infectious diseases2026

Evaluation of the clinical impact of de-escalated versus non-de-escalated antibiotics for the treatment of methicillin-susceptible staphylococcus aureus pneumonia in critically ill patients admitted to intensive care units: a multicenter cohort study.

Khalid Al Sulaiman, Sufyan Mohammed Alomair, Aisha Alharbi, Rahaf Alqahtani, Asma A Alshehri, Atheer O Aldairem, Nada Alsuhebany, Khalid Bin Saleh, Abdulaali R Almutairi, Abdulmajeed A Alzahrani and 13 more

Abstract readMulticenter Study
In one paragraph

Article in BMC infectious diseases, 2026. 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
–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

0 citing papers in PubMed.

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

23 authors.

Khalid Al SulaimanPharmaceutical Care Department, King Abdulaziz Medical City, Riyadh, Saudi Arabia. alsulaimankh@hotmail.com.
Sufyan Mohammed Alomair *Department of Pharmacy Practice, College of Clinical Pharmacy, King Faisal University, Al-Ahsa, Saudi Arabia.
Aisha AlharbiPharmaceutical Care Department, King Abdulaziz Medical City, PO Box 9515, Jeddah, 21423, Saudi Arabia.
Rahaf AlqahtaniPharmaceutical Care Department, King Abdulaziz Medical City, Riyadh, Saudi Arabia.
Asma A AlshehriPharmaceutical Care Department, Prince Sultan Military Medical City, Riyadh, Saudi Arabia.
Atheer O AldairemPharmaceutical Care Department, King Abdulaziz Medical City, Riyadh, Saudi Arabia.
Nada AlsuhebanyPharmaceutical Care Department, King Abdulaziz Medical City, Riyadh, Saudi Arabia.
Khalid Bin SalehPharmaceutical Care Department, King Abdulaziz Medical City, Riyadh, Saudi Arabia.
Abdulaali R AlmutairiAlfaisal University, Riyadh, Saudi Arabia.
Abdulmajeed A AlzahraniPharmaceutical Care Department, King Fahad Hospital, Jeddah, Saudi Arabia.
Manea F Al MunjemNajran Health Cluster, Najran, Saudi Arabia.
Noura H AlotaibiCollege of Pharmacy, Princess Nourah Bint Abdulrahman University, Riyadh, Saudi Arabia.
Rahaf A AlnemaryPharmaceutical Practices Department, College of Pharmacy, Umm Al-Qura University, Makkah, Saudi Arabia.
Abdullah MusallyPharmaceutical Care Department, King Abdulaziz Hospital, Jeddah, Saudi Arabia.
Ahmed M AlnefaiePharmaceutical Care Department, King Abdulaziz Medical City, PO Box 9515, Jeddah, 21423, Saudi Arabia.
Saja AlasmariCollege of Pharmacy, King Khalid University, Abha, Saudi Arabia.
Ibrahim MahdiPharmaceutical Care Department, East Jeddah Hospital (EJH), 2277 King Abdullah Rd, Jeddah, Saudi Arabia.
Nadin AlanaziPharmaceutical Care Department, King Abdulaziz Medical City, Riyadh, Saudi Arabia.
Ahlam H AlmutairiCollege of Pharmacy, King Saud bin Abdulaziz University for Health Sciences, Riyadh, Saudi Arabia.
Abdullah N AlkhuraifCollege of Pharmacy, King Saud bin Abdulaziz University for Health Sciences, Riyadh, Saudi Arabia.
Abdulaziz F AlanaziCollege of Pharmacy, King Saud bin Abdulaziz University for Health Sciences, Riyadh, Saudi Arabia.
Wafa Al HarbiPharmaceutical Care Department, Dr. Sulaiman Al Habib Medical Group, Riyadh, Saudi Arabia.
Ohoud AljuhaniPharmacy Practice Department, Faculty of Pharmacy, King Abdulaziz University, Jeddah, Saudi Arabia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCritically ill patients are at a higher risk of developing infections and related complications, which can lead to death. Each additional day of antipseudomonal β-lactam use increases the risk of resistance; therefore, de-escalation is highly recommended to improve antibiotic use. To our knowledge, there are limited studies that have evaluated the clinical impact of de-escalation in critically ill patients with proven Methicillin-Susceptible Staphylococcus aureus (MSSA) pneumonia alone. Therefore, our study aimed to assess the clinical impact of the de-escalation strategy compared with the non-de-escalation strategy in critically ill patients with proven MSSA pneumonia.

methodsThis multicenter retrospective cohort study was conducted in three tertiary hospitals from January 2016 to July 2021. Adult critically ill patients admitted to the intensive care unit with proven MSSA respiratory culture who received antibiotics with anti-MSSA activity were screened for eligibility. Eligible patients were categorized into two groups according to their de-escalation status: De-escalated and Non-de-escalated. The De-escalation was defined as the reduction of the antimicrobial activity spectrum of antibiotics by switching to a narrower-spectrum agent that targets MSSA. The primary outcome was treatment failure rate, while other outcomes were considered secondary. Propensity score (PS) matching was applied at a 1:1 ratio, and multivariate regression analyses were utilized as appropriate.

resultsAfter PS matching (1:1), 58 patients were included in the study (29 patients in non-deescalated vs 29 patients in de-escalated). The treatment failure rate was significantly higher in the de-escalated group compared to the non-de-escalated (OR 16.98; 95% CI (3.304–87.225), p = 0.0007). In contrast, no significant differences were found in 30-day mortality, hospital and ICU length of stays, ventilator-free days, ICU readmission rate, or MSSA infection recurrence rate.

conclusionOur results showed that de-escalation of antibiotics in critically ill patients with confirmed MSSA pneumonia was associated with significantly higher rate of treatment failure while no significant differences were observed in the other clinical outcomes. These findings highlight the need for prospective studies to better inform safe and effective de-escalation strategies in this population.

Indexed as

Anti-Bacterial AgentsPneumonia, StaphylococcalStaphylococcus aureusAgedCritical IllnessFemaleHumansIntensive Care UnitsMaleMiddle AgedRetrospective StudiesTreatment OutcomeAnti-Bacterial AgentsAntibioticsDe-escalationMicrobiological sterilizationMSSAPneumoniaTreatment failure

Identifiers

PMID41545952
PMCPMC12892537

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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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 Socratic graph.