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Diagnosis of ECMO Cannula Infection: Prospective Comparison of Sampling Methods (ECMO-CSI-DIAG)

4. november 2026 oppdatert av: Assistance Publique - Hôpitaux de Paris

Diagnosis of ECMO Cannula Infection: a Prospective Comparison of Sampling Methods

Extracorporeal membrane oxygenation (ECMO) is increasingly used as rescue support in patients with refractory respiratory and/or circulatory failure. ECMO cannula site infection (ECMO-CSI) complicates approximately 10% of ECMO runs and is associated with septic shock, prolonged intensive care unit (ICU) stay and increased mortality. To date, there is neither a standardized definition nor consensus diagnostic criteria for ECMO-CSI, and the optimal microbiological sampling strategy, as well as the diagnostic accuracy of the available methods, remains undetermined.

This single-center, prospective, non-interventional study aims to compare the diagnostic accuracy of three microbiological sampling methods (superficial swab of the cannula insertion site, needle aspiration along the cannula tract, and cannula tip culture) for the diagnosis of ECMO-CSI in adult patients receiving veno-venous or veno-arterial ECMO.

A superficial swab and a needle aspirate will be obtained at each cannulation site on the day ECMO-CSI is clinically suspected and on the day of decannulation. In addition, the tip of each cannula will be cultured at decannulation. The results of these index tests will be compared with a reference diagnosis of ECMO-CSI established by an adjudication committee of expert clinicians blinded to the index test results.

A total of 500 patients will be enrolled in order to obtain at least 50 patients with adjudicated ECMO-CSI.

Studieoversikt

Detaljert beskrivelse

BACKGROUND ECMO is a life-support technique widely used in refractory respiratory and/or circulatory failure. It is associated with infectious complications, notably cannula infections, whose incidence is estimated at about 10%. These infections are associated with an increased risk of septic shock and contribute to longer ICU stay and higher mortality. There is to date neither a standardized definition nor consensus diagnostic criteria, particularly regarding the nature and diagnostic performance of the microbiological samples to be collected. Superficial swabbing of the insertion site is simple and minimally invasive but frequently yields contaminated results or results reflecting colonizing flora. More invasive methods (needle aspiration, culture of the cannula tip at decannulation) may be more specific but are less commonly performed and have not been comparatively validated. A recent international Delphi consensus identified cannula aspiration and cannula swab as the two preferred microbiological methods. The lack of an established diagnostic algorithm leads to heterogeneous management, with potential consequences for antibiotic stewardship and patient outcomes.

DESIGN Single-center, prospective, non-interventional study conducted in the medical ICU of Pitié-Salpêtrière Hospital (AP-HP, Paris, France), which manages about 300 ECMO patients per year. All adult patients on veno-venous or veno-arterial ECMO are eligible. The patient (or trusted person, relative or legal representative) is informed and the patient is included unless an objection is expressed. Inclusion period: 24 months. Participation: duration of ICU stay (maximum 2 months). Total study duration: 26 months.

SAMPLING

  • Swab (performed for the research): a sterile single-use swab is applied to the cannula insertion orifice.
  • Needle aspiration (standard of care): 1 mL of sterile saline is injected along the cannula through a syringe and a plastic catheter, re-aspirated and transferred to a sterile container.
  • Cannula tip (standard of care): at decannulation, the distal 5 cm of the cannula is cut with a sterile blade and placed in a sterile container.

On the day the clinician in charge suspects a cannulation site infection, a swab and a needle aspiration are performed at each cannulation site. On the day of decannulation, a swab and a needle aspiration are performed at each cannulation site and the tip of each cannula is sent for culture.

MICROBIOLOGY Samples are cultured in the microbiology laboratory using the Brun-Buisson technique: suspension in 1 mL of sterile saline and vortexing for about 1 minute, then 100 microliters are plated on fresh blood agar, chocolate agar and Sabouraud agar, incubated for 48 hours to 10 days under aerobic and anaerobic conditions and read daily. In case of positive culture, identification is performed by mass spectrometry (MALDI-TOF). Each sample is recorded as culture positive or culture negative.

REFERENCE STANDARD The reference diagnosis of ECMO cannula infection is the clinical diagnosis established by an adjudication committee of three clinician experts, ruling retrospectively and blinded to the results of the index tests, on the basis of the available clinical, biological, microbiological and outcome data.

DATA Data are collected prospectively from the electronic medical record into a REDCap electronic case report form hosted by AP-HP. At each sampling: local appearance of the insertion site (photograph), general and hemodynamic status, biological inflammatory markers, nosocomial infection during the stay, antibiotic therapy within the previous 7 days, rectal colonization with a multidrug-resistant organism, positive blood culture within the previous 48 to 72 hours, duration of ECMO support.

STATISTICS The sample size was set to obtain at least 50 cases of cannula infection; with an expected incidence of 10%, 500 patients will be included. Sensitivity, specificity and predictive values of each sampling strategy are computed against the reference diagnosis. Paired comparisons use the McNemar test. Agreement between methods is assessed with the kappa coefficient. Exploratory logistic regression analyses will identify factors associated with microbiological positivity. Analyses are performed on complete cases; a failed sampling technique is considered negative.

Studietype

Observasjonsmessig

Registrering (Antatt)

500

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiekontakt

Studer Kontakt Backup

Studiesteder

      • Paris, Frankrike
        • Hôpital Pitié Salpêtrière, Service de médecine intensive et réanimation
        • Ta kontakt med:
        • Ta kontakt med:
        • Hovedetterforsker:
          • Charles Edouard LUYT, MD, PhD

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

18 år og eldre (Voksen, Eldre voksen)

Tar imot friske frivillige

Nei

Kjønn som er kvalifisert for studier

Alle

Prøvetakingsmetode

Ikke-sannsynlighetsprøve

Studiepopulasjon

Adult patients managed in the medical intensive care unit of Pitié-Salpêtrière Hospital (Paris, France) on veno-venous or veno-arterial ECMO during the inclusion period.

Beskrivelse

Inclusion Criteria:

  • Age >= 18 years
  • Patient admitted to the intensive care unit with veno-venous or veno-arterial ECMO

Exclusion Criteria:

  • Pregnant women
  • Persons deprived of liberty
  • Sample collection impossible for technical reasons
  • Patients on central ECMO

Studieplan

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

  • Observasjonsmodeller: COHORT
  • Tidsperspektiver: PROSPECTIVE

Kohorter og intervensjoner

Gruppe / Kohort
Adult patients on ECMO

Adult patients on veno-venous or veno-arterial ECMO in the ICU. Swab and needle aspiration of each cannulation site on the day of clinical suspicion of cannula infection and on the day of decannulation; culture of each cannula tip at decannulation.

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Diagnostic performance of each sampling strategy (superficial swab, needle aspiration, cannula tip culture) for the diagnosis of ECMO cannula infection
Tidsramme: On the day of clinical suspicion of cannula infection and on the day of decannulation, up to ICU discharge (maximum 2 months)

Sensitivity, specificity, positive and negative predictive values of each sampling strategy, and its agreement with the reference diagnosis of cannula infection established by the adjudication committee.

On the day of clinical suspicion of cannula infection and on the day of decannulation, up to ICU discharge (maximum 2 months)

Sekundære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Factors associated with positivity of the microbiological samples
Tidsramme: On the day of clinical suspicion of cannula infection and on the day of decannulation, up to ICU discharge (maximum 2 months)

Variables assessed at each sampling: weight (kg); height (meters), BMI (kg/m2), local appearance of the cannula insertion site on a photograph (purulence, inflammatory signs), fever (temperature (°C), systolic blood pressure (mmHg), diastolic blood pressure (mmHg), heart rate (bpm), noradrenaline (µg/kg/min), dobutamine (µg/kg/min)), biological criteria: hemoglobin (g/dL), white blood cell count (G/L), CRP (mg/L), PCT (ng/l), pH, bicarbonates (mmol/L), arterial lactate (mmol/L), nosocomial infection during the stay, antibiotic therapy within 7 days before sampling, rectal colonization with a multidrug-resistant organism, positive blood culture within 48 to 72 hours before sampling, positive culture of the ECMO cannula tip, duration of ECMO support.

On the day of clinical suspicion of cannula infection and on the day of decannulation, up to ICU discharge (maximum 2 months)
Agreement between the sampling methods
Tidsramme: On the day of clinical suspicion of cannula infection and on the day of decannulation, up to ICU discharge (maximum 2 months)

Agreement on culture positivity and on microbiological identification between swab, needle aspiration and cannula tip culture (kappa coefficient).

On the day of clinical suspicion of cannula infection and on the day of decannulation, up to ICU discharge (maximum 2 months)

Samarbeidspartnere og etterforskere

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Etterforskere

  • Hovedetterforsker: Charles Edouard LUYT, MD, PhD, Assistance Publique - Hôpitaux de Paris

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart (Antatt)

1. november 2026

Primær fullføring (Antatt)

1. januar 2029

Studiet fullført (Antatt)

1. januar 2029

Datoer for studieregistrering

Først innsendt

19. oktober 2026

Først innsendt som oppfylte QC-kriteriene

19. oktober 2026

Først lagt ut (Faktiske)

26. oktober 2026

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

6. november 2026

Siste oppdatering sendt inn som oppfylte QC-kriteriene

4. november 2026

Sist bekreftet

1. november 2026

Mer informasjon

Begreper knyttet til denne studien

Legemiddel- og utstyrsinformasjon, studiedokumenter

Studerer et amerikansk FDA-regulert medikamentprodukt

Nei

Studerer et amerikansk FDA-regulert enhetsprodukt

Nei

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