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Liver TransplantationNCT05594901

Impact of a Risk Stratification Tool on the Outcome of Liver Transplant Recipients Colonized With Carbapenem Resistant Enterobacteriaceae: an Observational Study

An observational study of Liver Transplantation and Carbapenem-Resistant Enterobacteriaceae Colonization, run by University of Bologna at 6 sites in 3 countries.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

Although CRE infection after OLT have a dramatic impact on patient survival and several implementations have been proposed (i.e. preventive strategies or targeted surgical prophylaxis), a standardized approach in colonized patients is still missing. Read more about this study

Who is it for?
Ages 18 years and older
What is being tested?
Application of a prognostic score
How many people
240 participants
Where
6 sitesin 3 countries
Study dates
1 Nov 2022to 30 Jun 2025
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: OLT recipients colonized by CRE

Who may be able to join

  • Signature of the informed consent
  • Age ≥ 18 years
  • CRE colonization within 60 days prior to or after transplantation

Who cannot join

  • Patients receiving targeted antibiotic prophylaxis (against CRE) for a period longer than 48 hours
  • Patients receiving graft from a donor with cultures yielding a carbapenem-resistant Gram negative bacteria

Trial locations and contacts

6 sites in 3 countries.

6 sites in 3 countries

Italy4 sites
  • Università degli Studi di Padova - Unit Multivisceral Transplant Unit

    Padova

  • Irccs Ismett

    Palermo

  • ASST-Sette Laghi Università degli Studi dell'Insubria

    Varese

  • Università degli Studi di Verona - Gastroenterologia

    Verona

Other trials in Italy

Brazil1 site
  • Hospital das Clinicas da Faculdade de Medicina da Universidade de São Paulo

    São Paulo

Other trials in Brazil

Spain1 site
  • Hospital General Universitario Gregorio Maranon

    Madrid

Other trials in Spain

About this study

Although CRE infection after OLT have a dramatic impact on patient survival and several implementations have been proposed (i.e. preventive strategies or targeted surgical prophylaxis), a standardized approach in colonized patients is still missing. The investigators recently developed and internally validated a bed-side score to stratify the risk of CRE infection in OLT recipients colonized by CRE. The goal of this pre/post observational study is to investigate the impact on all-cause 90-day mortality in OLT recipients colonized with CRE using such score (CRECOOLT score) for the systematic evaluation of CRE infection risk.

The secondary objectives are:

  • To analyse days of therapy with anti-CRE antibiotic regimens in patients with and without systematic evaluation of CRE infection risk, according to clinical practices.
  • To evaluate rates of documented CRE infections and their relapses with selection of further resistance in patients with and without systematic evaluation of CRE infection risk.
  • To evaluate the length of hospital, ICU stay and rates of hospital readmission in patients with and without systematic evaluation of CRE infection risk.
Read the detailed description

Patients undergoing orthotopic liver transplantation (OLT) are more susceptible to acquire colonization with multidrug resistant Gram-negative bacteria, in particular with carbapenem resistant Enterobacterales (CRE), than non-solid organ transplant (SOT) recipients or patients with other types of SOT. CRE colonization, either acquired before either emerged after OLT, has been associated with highest risk of developing CRE infection after OLT with a dramatic impact on patient survival. For these reasons, along with the improvement of infection control and antimicrobial stewardship policies, preventive strategies targeted to patients colonized with CRE have been suggested. However, several uncertainties have to be considered concerning the optimal timing for intervention, the correct patient stratification, and the choice of drugs. Regarding the timing for intervention, surgical prophylaxis is regarded as an option. However, it should be considered that of the overall burden of CRE carriage in OLT recipients, pre-transplant acquisition accounted for lower than one third of isolations in a large multicenter retrospective study. Furthermore, even when CRE carriage is present at transplantation, the colonization status is frequently recognized in the immediate post-operative period by results of rectal swabs done at surgery. Finally, current data about the efficacy of targeted prophylaxis in patients colonized with CRE are very limited and showed controversial results. Thus, in the majority of cases the unique window for preventive strategies is represented by the post-transplant course. This requires an active screening policy as well as the possibility of stratifying colonized patients according to their risk of developing CRE infection, and eventually to die, in order to target specific interventions in those patients who could most benefit, and to optimize essential resources as the new drugs. Indeed, since the availability of new drugs such as ceftazidime/avibactam, meropenem/vaborbactam and cefiderocol, the therapeutic management and outcome of patients colonized and/or infected with CRE has changed in both general population and SOT recipients. New drugs are associated with higher rates of clinical cure and patient survival, as well as with lower toxicity, compared with old regimens. However, rates of microbiological failure around 10%, consisting in persistent positive cultures or relapsing infections associated with development of further resistance, have been reported raising concerns about the need of optimizing the use of new drugs to avoid the loss of their efficacy.

To this end, the investigators have recently carried out a large multicenter observational study aimed at building a prediction model to stratify patients according to their risk of developing CRE infection after OLT. The study cohort consisted of 800 OLT recipients colonized with CRE, 25% were colonized at OLT, and 75% acquired colonization within two weeks after OLT. Infection rate was of 30% and was similar between the two groups as well as the infection severity. All-cause 6-month mortality rate among patients who developed CRE infection was 58% vs. 20% among carries who did not develop infection (p<0.001). Almost all infections occurred within 60 days after transplant. Thus, the investigators derived, and internally validated, a prediction tool able to stratify the risk of CRE infection at 30 and 60 days after OLT (CRECOOLT score) based on six variables easily to monitor such as CRE colonization detected in the 60 days prior to transplant, CRE colonization detected post-transplant, multisite colonization, need of prolonged (≥48 hours) mechanical ventilation, acute renal failure, and reintervention. The calculated cumulative incidence of CRE infection and nomogram-derived prediction for a low-risk and a high-risk patient were made available as app to be used bed-side. The investigators explored the potential clinical utility of our model using a decision-curve analysis to examine the "net benefit" of applying the prediction model across a range of CRE infection threshold probabilities. A theoretical risk-model guided strategy (i.e. empiric administration of CRE-active antibiotics) was compared against two default strategies- "treat all" and "treat none" suggesting that the model-directed intervention would show net benefit over default strategies when the overall CRE infection risk exceeded 10%.

Finally, the investigators have explored the risk of death using the same variables included in the CRECOOLT score by a multi-state model obtaining three risk groups: low, intermedium and high. The investigators have then estimated the potential impact of using ceftazidime-avibactam in each of such groups finding a significant protective role (HR 0.32) only in patients with intermedium or high risk of dying.

Being tested
Application of a prognostic score

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Application of a prognostic scoreOther

    The CRECOOLT score, for the prospective cohort, will be systematically calculated once week, or at the occurrence of complications, until 60 days after OLT. The therapeutic management of all patients, during both retrospective and prospective periods, will be established by the attending physicians according with routine practice and not dictated by study protocol.

Study groups in NCT05594901
Study groupRoleWhat they receive
Retrospective CohortNot described
Prospective CohortNot described
Receives: Other: Application of a prognostic score

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. The primary objective is to investigate the impact on all-cause 90-day mortality in OLT recipients colonized with CRE using the CRECOOLT score for the systematic evaluation of CRE infection risk.

    Measured: 24 months

Secondary outcomes (5)
  1. To analyse days of therapy with anti-CRE antibiotic regimens in patients with and without systematic evaluation of CRE infection risk, according to clinical practices.

    Measured: 24 months

  2. To evaluate rates of documented CRE infections and their relapses.

    Measured: 24 months

  3. To evaluate the length of hospital and ICU stay (days) in patients with and without systematic evaluation of CRE infection risk.

    Measured: 24 months

  4. To evaluate selection of further resistance in patients with documented CRE infection relapse with and without systematic evaluation of CRE infection risk.

    Measured: 24 months

  5. To evaluate rates of hospital readmission in patients with and without systematic evaluation of CRE infection risk.

    Measured: 24 months

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted26 Oct 2022
  2. Study start1 Nov 2022
  3. Primary completion31 Oct 2024
  4. Study completion30 Jun 2025

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Other
Enrolment
240 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05594901
Sponsor's protocol ID
CRECOOLT 3.0
Status last verified
Oct 2026
First submitted
12 Oct 2022
Last updated
26 Oct 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Undecided

Questions about this trial

What is this clinical trial studying?

An observational study of Liver Transplantation and Carbapenem-Resistant Enterobacteriaceae Colonization, run by University of Bologna at 6 sites in 3 countries.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 26 Oct 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 6 sites in Italy, Brazil, Spain. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

The primary objective is to investigate the impact on all-cause 90-day mortality in OLT recipients colonized with CRE using the CRECOOLT score for the systematic evaluation of CRE infection risk. (time frame: 24 months). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 26 Oct 2026.

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