Evidence map›Paper›PMID 41322101›Full record

ArticleInfection and drug resistance2025

Effectiveness of Carbapenem-Sparing Antibiotics Versus Carbapenems for Treating Non-Bacteremic Extended-Spectrum Beta-Lactamase-Producing Enterobacterales Infections.

Bashayer Mohammed Alshehail, Marwan Jabr Alwezzeh, Zainab Al Jamea, Fatimah Alsalem, Fatimah Alabkari, Mohammed AlAtayah, Mahdi Alamrani, Mohammad Alsameen, Husain Aljanoubi, Wareef Belal Tersin and 12 more

Abstract read
In one paragraph

Article in Infection and drug resistance, 2025. 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. 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

22 authors.

Bashayer Mohammed AlshehailPharmacy Practice Department, College of Clinical Pharmacy, Imam Abdulrahman bin Faisal University, Dammam, 31441, Kingdom of Saudi Arabia.
Marwan Jabr AlwezzehInternal Medicine Department, King Fahd University Hospital, Imam Abdulrahman bin Faisal University, Dammam, 31441, Kingdom of Saudi Arabia.
Zainab Al JameaPharmaceutical Care Department, King Fahd University Hospital, Imam Abdulrahman bin Faisal University, Dammam, 31441, Kingdom of Saudi Arabia.ORCID 0000-0003-4549-2638
Fatimah AlsalemInternal Medicine Department, King Fahd University Hospital, Imam Abdulrahman bin Faisal University, Dammam, 31441, Kingdom of Saudi Arabia.
Fatimah AlabkariInternal Medicine Department, King Fahd University Hospital, Imam Abdulrahman bin Faisal University, Dammam, 31441, Kingdom of Saudi Arabia.
Mohammed AlAtayahCollege of Clinical Pharmacy, Imam Abdulrahman bin Faisal University, Dammam, 31441, Kingdom of Saudi Arabia.
Mahdi AlamraniCollege of Clinical Pharmacy, Imam Abdulrahman bin Faisal University, Dammam, 31441, Kingdom of Saudi Arabia.
Mohammad AlsameenCollege of Clinical Pharmacy, Imam Abdulrahman bin Faisal University, Dammam, 31441, Kingdom of Saudi Arabia.
Husain AljanoubiCollege of Clinical Pharmacy, Imam Abdulrahman bin Faisal University, Dammam, 31441, Kingdom of Saudi Arabia.
Wareef Belal TersinPharmaceutical Care Department, King Fahd University Hospital, Imam Abdulrahman bin Faisal University, Dammam, 31441, Kingdom of Saudi Arabia.
Haytham WaliPharmacy Practice Department, College of Clinical Pharmacy, King Faisal University, Alahsa'a, 31982, Kingdom of Saudi Arabia.ORCID 0000-0001-6279-3809
Yazed S AlsowaidaDepartment of Clinical Pharmacy, College of Clinical Pharmacy, Hail University, Hail, 81442, Saudi Arabia.
Abdulatif S Al RashedDepartment of Microbiology, College of Medicine, Imam Abdulrahman bin Faisal University, Dammam, 31441, Saudi Arabia.ORCID 0000-0003-3174-9287
Khalid AlamerPharmacy Practice Department, College of Clinical Pharmacy, Imam Abdulrahman bin Faisal University, Dammam, 31441, Kingdom of Saudi Arabia.
Yousef AlqarniPharmacy Practice Department, College of Clinical Pharmacy, Imam Abdulrahman bin Faisal University, Dammam, 31441, Kingdom of Saudi Arabia.ORCID 0000-0002-4195-3110
Faten AlhomoudPharmacy Practice Department, College of Clinical Pharmacy, Imam Abdulrahman bin Faisal University, Dammam, 31441, Kingdom of Saudi Arabia.ORCID 0000-0002-6638-1390
Farah Kais AlhomoudPharmacy Practice Department, College of Clinical Pharmacy, Imam Abdulrahman bin Faisal University, Dammam, 31441, Kingdom of Saudi Arabia.
Mohammed IslamPharmacy Practice Department, College of Clinical Pharmacy, Imam Abdulrahman bin Faisal University, Dammam, 31441, Kingdom of Saudi Arabia.
Fawaz AlotaibiPharmacy Practice Department, College of Clinical Pharmacy, Imam Abdulrahman bin Faisal University, Dammam, 31441, Kingdom of Saudi Arabia.
Dhafer AlshaybanPharmacy Practice Department, College of Clinical Pharmacy, Imam Abdulrahman bin Faisal University, Dammam, 31441, Kingdom of Saudi Arabia.
Shams AlshehailInternal Medicine Department, King Abdulaziz University (Medical Services), Jeddah, 21487, Saudi Arabia.
Khalid EljaalyPharmacy 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

Introduction: Extended-spectrum β-lactamase-producing Enterobacterales (ESBL-E) pose a significant public health threat. While carbapenems are known to be superior in treating bacteremic infections, the evidence is unclear for non-bacteremic infections. Objective: To assess the effectiveness of carbapenem-sparing therapies compared to carbapenems for non-bacteremic ESBL-E infections. Methodology: This is a retrospective observational cohort study involving patients aged 18 years or older with confirmed diagnoses of ESBL-E non-bacteremic infections who received either carbapenems or carbapenem-sparing targeted therapy during the study period. The primary outcomes were clinical cure and 30-day all-cause mortality. Secondary outcomes included microbiological eradication, recurrence of ESBL-E infection within 6 months, and the 30-day incidence of new multidrug-resistant infections. Results: The study included 216 patients: 117 in the carbapenem group and 99 in the carbapenem-sparing group. Both groups showed no significant differences in 30-day all-cause mortality and clinical resolution. However, notable statistical differences were observed in three secondary outcomes: the carbapenem group had a higher recurrence rate of ESBL infections (RR 1.65, 95% CI: 1.05-2.59, P = 0.025) and more secondary multidrug-resistant infections (RR 1.92, 95% CI: 1.11-3.31, P = 0.015), including carbapenem-resistant Enterobacterales infections (RR 2.26, 95% CI: 1.10-4.63, P = 0.020). Conclusion: The study demonstrates that carbapenem-sparing therapies for ESBL-E nonbacteremic infections are non-inferior to carbapenems, with comparable 30-day all-cause mortality, clinical cure, and bacteriological resolution rates. Additionally, carbapenem-sparing options showed lower recurrence rates of ESBL-E infections and reduced development of secondary multidrug-resistant infections, including CRE infections.

Indexed as

carbapenemcarbapenem-sparing antibioticsenterobacteralesESBL-Enon-bacteremic infection

Identifiers

PMID41322101
PMCPMC12664316

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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.