Lower Limb Surveillance During VA-ECLS

Sponsor
Central Hospital, Nancy, France (Other)
Overall Status
Completed
CT.gov ID
NCT03910062
Collaborator
(none)
40
1
14
2.9

Study Details

Study Description

Brief Summary

Temporary cardiac support by VA-ECLS can lead to lower limb ischemia. The aim of this study is to evaluate a multi-modal strategy (physical examination, NIRS monitoring and angiography through the reperfusion canula) of lower limb surveillance.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Lower limb angiography via the reperfusion cannula and NIRS monitoring

Detailed Description

VA ECLS is used as a temporary circulatory support during cardiogenic shock and refractory cardiac arrest. Complications of VA ECLS include hemorrhagic, infectious and ischemic events. VA ECLS requires arterial and venous canules which are frequently positioned in the femoral artery and vein, which carries the risk of lower limb ischemia due to retrograde flow and obstruction of the femoral artery lumen. VA ischemia during VA ECLS is frequent (11-52%) and requires the use of reperfusion canula in the femoral common artery on VA ECLS implantation in a primary prevention strategy, before lower limb ischemia occurs. Even with this strategy, lower limb ischemia can occur due to arterial thrombosis, arterial spasm or insufficient blood flow through the reperfusion canula. Lower limb complications are prevented by monitoring of regional oxygen saturation, control of the reperfusion canula position (ultrasound, angiography) and rapid management when lower limb ischemia is suspected. There are no clear recommendations regarding prevention of lower limb complications during VA ECLS and arterial angiography has been described to diagnose ischemic events and evaluate the effectiveness of an intervention such as injection of vasodilators. This study is a prospective evaluation of a strategy to prevent lower limb complications during VA ECLS with a systematic arterial angiography on VA ECLS implantation and when lower limb ischemia is suspected (regional oxygen tissue saturation <50% or a differential >15% between both lower limbs) in addition to continuous NIRS monitoring of lower limbs during VA ECLS.

Study Design

Study Type:
Observational
Actual Enrollment :
40 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Lower Limb Surveillance During VA-ECLS: Evaluation of Angiography Through the Reperfusion Cannula at VA-ECMO Implantation and of Near Infrared Spectroscopy (NIRS) Monitoring
Actual Study Start Date :
Apr 1, 2019
Actual Primary Completion Date :
Apr 1, 2020
Actual Study Completion Date :
Jun 1, 2020

Arms and Interventions

Arm Intervention/Treatment
VA ECMO

Patients under VA-ECMO with a femoral reperfusion cannula.

Procedure: Lower limb angiography via the reperfusion cannula and NIRS monitoring
Data collection only (lower limb angiography, lower limbs NIRS values).

Outcome Measures

Primary Outcome Measures

  1. Severe limb ischemia [60 days]

    Ischemia leading to surgical intervention, functional sequelae, necrosis of the extremities or compartment syndrome

Secondary Outcome Measures

  1. Mortality [28 days and 60 days]

    Mortality rate

  2. Incidence of ischemia of the lower limb during ICU stay [2 months]

    StO2 < 50% during 4 consecutive minutes AND/OR StO2 differential > 15% during ICU stay

  3. Incidence of renal replacement therapy during ICU stay [2 months]

    Number of patients who underwent renal replacement therapy

  4. Duration of ICU stay [60 days]

    Number of days in the ICU

  5. Duration of hospital stay [60 days]

    Number of days in the hospital

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Temporary circulatory support with VA ECLS

  • Age > 18 years

Exclusion Criteria:
  • Pregnancy

  • History of iodinated contrast allergy

  • History of lower limb amputation above the ankle

  • Lower limb ischemia before starting of VA-ECLS

  • Femoro-axillary VA-ECLS

  • Absence of the lower limb reperfusion canula

Contacts and Locations

Locations

Site City State Country Postal Code
1 CHU de Nancy Nancy France

Sponsors and Collaborators

  • Central Hospital, Nancy, France

Investigators

  • Principal Investigator: Matthieu Koszutski, Dr, CHU de Nancy

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Central Hospital, Nancy, France
ClinicalTrials.gov Identifier:
NCT03910062
Other Study ID Numbers:
  • PSS2018/MIRECMO-KOSZUTSKI/YB
First Posted:
Apr 10, 2019
Last Update Posted:
May 24, 2021
Last Verified:
Mar 1, 2020
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Central Hospital, Nancy, France
Additional relevant MeSH terms:

Study Results

No Results Posted as of May 24, 2021