ECCO2R Therapy
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Why ECCO2R therapy?
Acute hypercapnia can be a barrier to the use of guideline recommended lung-protective ventilation (LPV) and non-invasive ventilation (NIV) strategies. Extracorporeal carbon dioxide removal (ECCO2R) therapy removes CO2 from a patient’s blood with an extracorporeal circuit to effectively manage acute hypercapnia and respiratory acidosis that can result from lung-protective mechanical ventilation strategies.
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Acute Hypercapnia
ECCO2R therapy can effectively manage acute hypercapnia to help bring the clinical and economic benefits of LPV and NIV to more patients.
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ARDS
ECCO2R therapy can effectively manage hypercapnia to facilitate the use of LPV or ultra lung-protective ventilation (ULPV) in patients with mild-to-moderate ARDS.1 - 4
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aeCOPD
ECCO2R therapy can effectively manage acute hypercapnia to enable the use of NIV strategies which reduce the need for intubation in patients with aeCOPD.
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Multiple Organ Failure
ECCO2R therapy can be integrated with other organ support therapies for more efficient management of patients with multiple organ dysfunction.
“….respiratory diseases are a leading cause of death and disability in the world….” “prevention, control, and cure of these diseases and….promotion of respiratory health must be a top priority for health-care systems and decision makers.”
Forum of International Respiratory Societies. The Global Impact of Respiratory Disease – Second Edition. Sheffield, European Respiratory Society, 2017. (Ref 5)
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Addressing barriers in caring for your patients
Acute hypercapnia can be a barrier to the use of guideline recommended LPV and NIV strategies:
- Invasive mechanical ventilation (IMV) with higher plateau pressures, tidal volumes or driving pressures can lead to ventilator-induced lung injury (VILI) and may contribute to multiorgan dysfunction.6 - 10
- Consequently, clinical guidelines recommend using mechanical ventilation strategies to decrease the risk of lung injury in patients with acute respiratory failure, including lung-protective ventilation (LPV),11 - 13 ultra lung-protective ventilation (ULPV),14 or non-invasive ventilation (NIV).15
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Facilitating use of ventilation strategies for patients with ARDS
- ECCO2R therapy can effectively manage hypercapnia to facilitate the use of LPV or ultra lung-protective ventilation (ULPV) in patients with ARDS.1 - 4
- ECCO2R therapy may help manage hypercapnia in patients with ARDS secondary to COVID-19.16
- ECCO2R therapy–enabled LPV and ULPV strategies may provide a cost-effective survival benefit in patients with moderate ARDS.17
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Enabling use of NIV strategies for patients with aeCOPD
- ECCO2R therapy, at blood flow ≤ 450 mL/min, may help reduce the need for invasive mechanical ventilation in patients with aeCOPD.23
- ECCO2R therapy can help to prevent intubation and IMV in patients with aeCOPD at risk of NIV failure.16, 19 - 21
- Data from a matched cohort study using historic controls indicate that patients with aeCOPD receiving NIV and ECCO2R therapy had a 73% decreased risk of intubation (HR 0.27; 95% CI 0.07–0.98; P = 0.047) compared with patients receiving NIV alone.19
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Integrating with other organ support therapies
- Patients with acute respiratory failure often experience other forms of organ dysfunction, including renal failure.20, 23 - 25
- ECCO2R therapy can be used at blood flow rates of ≤450 mL/min,23 enabling integration with other organ support therapies, such as CRRT or blood purification using the same platform.23,24
- Clinicians can provide multiple organ support therapies using a single vascular access, helping to minimize the invasiveness of treatment20,23,24 and reduce the risk of infection for patients with multiple organ dysfunction.26 - 28
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Understanding COVID-19 and ECCO2R therapy
ECCO2R therapy can support the use of LPV by managing elevated CO2 levels:
1. Respiratory cells can become infected with the SARS-CoV-2 virus.29
2. Viral infection and a dysregulated inflammatory immune response can both contribute to lung injury.30,31
3. Lung injury can present as type L pneumonia, which can progress to severe “ARDS-like” type H, characterized by edema, tissue damage, and severe hypoxemia.32,33
4. The complications of severe lung injury and its treatment can lead to multiorgan dysfunction, including acute kidney injury.31,34