Evidence map›Paper›PMID 42129697›Full record

ArticleBMC infectious diseases2026

Epidemiology and clinical outcomes of carbapenamase-producing organism (CPO) colonization: a tertiary care center experience in Saudi Arabia.

Nawaf M Alzahrani, Reem Abanamy, Abdulrahman Alsaedy, Sameera Aljohani, Bassam Alalwan, Faisal N Alqahtani, Mohammed Altamimi, Ziyad M Alhajeri, Ahmad H Alsahhaf, Ahmad Alharbi

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Article in BMC infectious diseases, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

10 authors.

Nawaf M AlzahraniDepartment of Medicine, King Abdulaziz Medical City, Ministry of National Guard Health Affairs, Riyadh, Saudi Arabia. AlZahraniNa9@mngha.med.sa.ORCID http://orcid.org/0000-0002-1821-9145
Reem AbanamyDepartment of Medicine, King Abdulaziz Medical City, Ministry of National Guard Health Affairs, Riyadh, Saudi Arabia.
Abdulrahman AlsaedyDepartment of Medicine, King Abdulaziz Medical City, Ministry of National Guard Health Affairs, Riyadh, Saudi Arabia.
Sameera AljohaniKing Abdullah International Medical Research Center, Riyadh, Saudi Arabia.
Bassam AlalwanKing Abdullah International Medical Research Center, Riyadh, Saudi Arabia.
Faisal N AlqahtaniDepartment of Medicine, King Abdulaziz Medical City, Ministry of National Guard Health Affairs, Riyadh, Saudi Arabia.
Mohammed AltamimiDepartment of Medicine, King Abdulaziz Medical City, Ministry of National Guard Health Affairs, Riyadh, Saudi Arabia.
Ziyad M AlhajeriDepartment of Medicine, King Abdulaziz Medical City, Ministry of National Guard Health Affairs, Riyadh, Saudi Arabia.
Ahmad H AlsahhafDepartment of Pediatrics, Prince Sultan Military Medical City, Ministry of Defense, Riyadh, Saudi Arabia.
Ahmad AlharbiDepartment of Medicine, King Abdulaziz Medical City, Ministry of National Guard Health Affairs, Riyadh, Saudi Arabia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe global emergence of carbapenem-resistant Enterobacterales (CRE) infections has critically reduced therapeutic options and are associated with high mortality. While CRE epidemiology has been extensively studied worldwide, data on intestinal CRE colonization in Saudi Arabia remain limited. This study aims to determine the prevalence of intestinal Carbapenem Producing Organisms (CPO) carriage, characterize carbapenemase genes, and evaluate associated clinical outcomes among hospitalized patients.

methodsA retrospective cohort study was conducted at King Abdulaziz Medical City (KAMC), Riyadh, Saudi Arabia. Hospitalized adult patients (≥ 18 years) in critical care and hematology/oncology areas were screened for CPO colonization via rectal swab and tested utilizing Cepheid Xpert

resultsAmong 6405 screened patients, 778 carbapenemase-producing isolates were detected (12.1%), OXA-48 was most prevalent (49.7%), followed by NDM (23.6%), OXA-48 + NDM co-producers (15.2%), KPC (4.8%), VIM (5.0%), and IMP-1 (1.7%). Most patients were ≥ 65 years (52.3%), and 84.3% were ICU inpatients. Common comorbidities included hypertension (57.5%) and diabetes mellitus (57.5%). Recent antibiotic exposure occurred in 73.3% of patients. The 30-day mortality rate was 24.6%, with no significant difference among carbapenemase types (p = 0.44). Subsequent infection within 90 days occurred in 29%, significantly associated with enzyme type (p = 0.001), highest among KPC (48.6%) and OXA-48 + NDM (38.1%) producers. Persistent colonization occurred in 29.3% of cases (p = 0.006), particularly among VIM (46.2%) and KPC (40.5%) producers.

conclusionOXA-48 and NDM were the dominant carbapenemase genes among intestinal CPO carriers in this tertiary care hospital. High rates of subsequent infection and mortality highlight the clinical importance of CPO colonization, especially in the ICU and elderly populations. Strengthened infection control practices and active surveillance are essential to limit CPO spread and improve patient outcomes. CLINICAL TRIAL NUMBER: Not applicable.

Indexed as

Bacterial Proteinsbeta-LactamasesCarbapenem-Resistant EnterobacteriaceaeEnterobacteriaceae InfectionsAdultAgedAnti-Bacterial AgentsFemaleHumansMaleMiddle AgedPrevalenceRetrospective StudiesSaudi ArabiaTertiary Care CentersTreatment OutcomeAnti-Bacterial AgentsBacterial Proteinsbeta-LactamasescarbapenemaseAntimicrobial resistanceCarbapenemase genesCarbapenem-resistant Enterobacterales (CRE)Intestinal colonizationSaudi Arabia

Identifiers

PMID42129697
PMCPMC13343699

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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.