Symbolic illustration of CPE detection in a hospital setting

Is Your Hospital Safe? Comparing the Best Methods for Detecting Antibiotic-Resistant Superbugs

"A New Study Shows How to Quickly Identify Carbapenemase-Producing Bacteria to Prevent Deadly Infections"


In today’s healthcare landscape, the rise of antibiotic-resistant bacteria, often called “superbugs,” poses a significant threat. Carbapenemase-producing Enterobacteriaceae (CPE) are particularly concerning. These bacteria have developed resistance to carbapenems, which are often the last line of defense against severe infections. The spread of CPE can lead to increased morbidity, mortality, and considerable strain on healthcare resources.

The ability to rapidly detect CPE is crucial for implementing effective infection control measures. Early identification allows hospitals to isolate affected patients, prevent further transmission, and administer appropriate treatment. Traditional detection methods can be slow, prompting the need for faster, more reliable screening techniques.

A recent study published in the Revista Chilena de Infectología evaluated three different screening methods for detecting CPE in rectal swabs. This research offers valuable insights for hospitals seeking to improve their detection strategies and safeguard patient health.

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The Global CRE Threat

Transmissible carbapenem resistance in Enterobacteriaceae has been recognized for two decades, while global dissemination of carbapenemase-producing Enterobacteriaceae has accelerated more recently. CRE resistance can arise through carbapenemases, porin changes, efflux pumps, penicillin-binding protein alterations, and biofilm production. The CDC reports that carbapenemase-gene detection varies by organism and is influenced by antibiotic use, environmental persistence, infection-control practices, and regional spread.

From Resistance to Clinical Threat

CRE refers to Enterobacteriaceae resistant to carbapenem antibiotics, often through carbapenemase-producing genes identified in environmental reservoirs including water, animals, food, and soil. CRE emerged as a major threat to modern medicine because commonly used antibiotics are generally inactive against these organisms. Carbapenemase-producing Enterobacteriaceae are especially important because timely laboratory detection is essential, while rapid geographic spread and resistance to many alternative antibiotics intensify the danger.

Decoding the Study: Comparing CPE Screening Methods

Symbolic illustration of CPE detection in a hospital setting

The study, conducted at Fundación Clínica Shaio in Colombia, prospectively compared three methodologies for CPE detection using 73 rectal swabs from patients admitted to various hospital units, including the emergency department, intensive care unit (ICU), and cardiovascular care unit (CCU). Each method was assessed for its ability to accurately and rapidly identify CPE-producing bacteria.

Here's a breakdown of the three methods:

  • Method 1: ChromID CARBA® Agar: A chromogenic agar that allows for the direct recovery of carbapenem-resistant organisms from rectal swabs. This method uses antimicrobials to inhibit accompanying microbiota and contains chromogens that facilitate the presumptive identification of microorganisms. Results are typically available within 24 to 48 hours.
  • Method 2: HB&L Carbapenemase Kit®: This kit uses vials with a nutritive broth, carbapenemics, and antifungals. It employs laser nephelometry in the HB&L® equipment to provide a bacterial count of resistant bacteria. This method detects carbapenemase-producing microorganisms in rectal swab samples in a maximum of 6 hours.
  • Method 3: Xpert CARBA-R®: A rapid, real-time polymerase chain reaction (PCR) technique that detects carbapenemase-producing microorganisms in about 1 hour directly from rectal swab samples. The GeneXpert® equipment uses specific probes to reveal the presence of genes encoding carbapenemases, such as KPC, VIM, IMP-1, NDM, and OXA-48.
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Current Research Directions

A 2025 systematic review examined oral antibiotics as a decolonization strategy for intestinal CRE carriage. The review describes CRE infections as associated with increased mortality and higher healthcare costs in hospitalized patients, supporting interest in decolonization approaches. In a retrospective study from a tertiary hospital in Havana, Cuba, metallo-beta-lactamase was detected in all 124 CRE isolates, with NDM-type carbapenemase dominant; three isolates coproduced KPC-type enzyme and showed high resistance to all antibiotics except colistin.

The study used the "Protocol for detection of Escherichia coli and Klebsiella spp producing carbapenemases in rectal swabs" from the Centers for Disease Control and Prevention (CDC) as the reference standard. The performance of each method was evaluated based on sensitivity, specificity, concordance, positive predictive value (PPV), and negative predictive value (NPV).

Choosing the Right Method for Your Hospital

The study’s findings highlight the strengths and weaknesses of each screening method. While the ChromID CARBA® agar offers high sensitivity and ease of use, it requires a longer incubation period. The HB&L Carbapenemase Kit® provides rapid results but may have lower sensitivity. The Xpert CARBA-R® offers excellent specificity and rapid detection but comes at a higher cost. Ultimately, the choice of screening method will depend on the specific needs and resources of each healthcare facility. Factors to consider include the prevalence of CPE in the region, the availability of laboratory equipment and expertise, and the budget for infection control.

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The Hospital-Level Reality

A 2026 study describes carbapenem-resistant Enterobacterales as a major global public-health concern and carbapenemase-producing Enterobacterales as a severe clinical threat. It focuses on infections in secondary hospitals, where epidemiological data remain scarce. The study aims to characterize carbapenemase phenotypes and antimicrobial patterns, highlighting the need for better real-world surveillance outside major tertiary centers.

What a rectal-swab comparison can establish

Observational study (level 4 of 8)

The evidence comes from a defined set of samples, so the results describe method performance in that study rather than performance across all hospitals or patient groups.[1]

Agreement against the study reference

  • 95.9% concordance indexHB&L Carbapenemase had a concordance index of 95.9%; its reported sensitivity was 85% and specificity 100%.[1]

Where this comparison is most limited

  • The abstract reports false-positive results for ChromID, so a positive screen was not always confirmed by the reference approach.[1]
Study at a glance
Study designObservational study[1]
Populationrectal swabs[1]
Sample sizeSeventy three[1]
Comparisonthree screening methods[1]
Main outcomedetection of CPE in rectal swabs[1]
Effect sizeMethod 1: sensitivity 100%, specificity 90%, concordance index 93.2%; Method 2: sensitivity 85%, specificity 100%, concordance index 95.9%; Method 3: sensitivity 95%, specificity 100%, concordance index 97%.[1]
Times cited9[1]

What a follow-up comparison could clarify

  • Would the relative performance remain similar in other patient groups or settings beyond the rectal-swab samples evaluated here?[1]
  • How often do screening results align with the confirmatory tests used to establish carbapenemase production?[1]
  • How do the methods compare when cost-effectiveness is assessed alongside sensitivity and specificity?[1]

Terms behind the comparison

Modified Hodge test
A test used to confirm carbapenemase production.[1]

About this Article -

Written with AI assistance from published research, and reviewed by the Mystum team. See our About page for more information.

This article is based on research published under:

DOI-LINK: 10.4067/s0716-10182018000300253, Alternate LINK

Title: Evaluación De Tres Métodos De Tamizaje Para Detección De Enterobacteriaceae Productoras De Carbapenemasas En Hisopados Rectales

Subject: Infectious Diseases

Journal: Revista chilena de infectología

Publisher: SciELO Agencia Nacional de Investigacion y Desarrollo (ANID)

Authors: Diego Fernando Josa, Gisell Bustos, Isabel Cristina Torres, Germán Esparza S.

Published: 2018-01-01

Everything You Need To Know

1

What are Carbapenemase-producing Enterobacteriaceae (CPE) and why are they a concern?

Carbapenemase-producing Enterobacteriaceae (CPE) are a family of bacteria that have become resistant to carbapenems, a powerful class of antibiotics often used as a last resort for treating severe infections. This resistance makes CPE infections very difficult to treat, leading to increased risks of complications and even death. The rise of CPE is a serious concern in healthcare settings because these infections can spread rapidly and are often resistant to multiple antibiotics, leaving few treatment options.

2

Why is it so important to detect CPE quickly in hospitals?

Rapid detection of CPE is critical because it allows hospitals to quickly implement infection control measures, such as isolating infected patients. This helps prevent the spread of CPE to other patients and healthcare workers. Early detection also enables doctors to administer appropriate treatments sooner, improving the chances of successful outcomes and reducing the reliance on more toxic or less effective antibiotics. Without rapid detection, CPE can spread unchecked, leading to outbreaks and increased healthcare costs.

3

Can you explain how the ChromID CARBA® agar method works for detecting CPE?

The ChromID CARBA® agar is a screening method that involves growing bacteria from rectal swabs on a special type of agar (a gel-like substance) that contains antimicrobials to inhibit the growth of non-resistant bacteria. The agar also includes chromogens, which produce different colors depending on the type of bacteria present, allowing for presumptive identification of carbapenem-resistant organisms. While it is easy to use and has high sensitivity, it typically takes 24 to 48 hours to get results.

4

What is the HB&L Carbapenemase Kit® and how does it detect CPE?

The HB&L Carbapenemase Kit® is a method to detect carbapenemase-producing microorganisms. This kit uses vials with a nutritive broth, carbapenemics, and antifungals. It employs laser nephelometry in the HB&L® equipment to provide a bacterial count of resistant bacteria. This method detects carbapenemase-producing microorganisms in rectal swab samples in a maximum of 6 hours.

5

How does the Xpert CARBA-R® test work, and what are its advantages and disadvantages?

The Xpert CARBA-R® is a rapid, real-time polymerase chain reaction (PCR) technique used to detect carbapenemase-producing microorganisms directly from rectal swab samples in about 1 hour. It uses specific probes to identify the presence of genes, such as KPC, VIM, IMP-1, NDM, and OXA-48, that encode carbapenemases. While the Xpert CARBA-R® offers excellent specificity and rapid results, it is more expensive than other methods.

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