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Extracorporeal CO2 Removal in Acute Exacerbation of COPD Not Responding to Non-Invasive Ventilation

C

Centre Hospitalier de Saint-Denis

Status

Completed

Conditions

COPD Exacerbation Acute

Study type

Observational

Funder types

Other

Identifiers

NCT04882410
0004_CohorteECCO2R

Details and patient eligibility

About

Background: Acute exacerbation of chronic obstructive pulmonary disease (ae-COPD) has a gold standard treatment: non-invasive ventilation (NIV). However, this treatment sometime fails, and an invasive mechanical ventilation (IMV) is required. The extracorporeal CO₂ removal (ECCO₂R) device can be an alternative to intubation. The aim of the study is to evaluate ECCO₂R efficiency and safety and enlighten ECCO₂R benefit/risk compared to IMV.

Methods: Successive ae-COPD patients for whom NIV failed were retrospectively analyzed during two periods: before and after the ECCO₂R device implementation in our ICU in 2015. We considered the before period as standard of care and patients were treated with IMV. The ECCO₂R device was a pump-driven veno-venous system (Xenios AG).

Full description

The study compare 2 strategies for COPD patients not responding to non invasive ventilation: the gold standard which is mechanical ventilation and a new technique which is extracorporeal CO2 removal. This technique have been implemented in februrary 2015 in our intensive care unit so we choose to compare patients' outcome before and after the arriving of this device.

Enrollment

56 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • age > 18 years old
  • no improvement or worsening of respiratory acidosis after more than one hour of non invasive ventilation treatment
  • and non improvement of respiratory distress signs
  • and pH < 7,35 and PaCO2 > 45 mmHg

Exclusion criteria

  • patients not eligible for endotracheal intubation because of ethical limitations

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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