Around 20% of the patients requiring hospitalization for Acute Exacerbation of Chronic Obstructive Pulmonary Disease (AECOPD) develop hypercapnia, which is associated with an increased risk of death. Once Non Invasive Ventilation (NIV) has been initiated, a reduction in Respiratory Rate (RR) and improvement in pH within 4 h predicts NIV success. If pH \<7.25 and RR \>35 breath per minutes persist, NIV failure is likely. Worsening acidosis, after initial improvement with NIV, is also associated with a worse prognosis. In addition, it has been shown that delaying intubation in patients at high risk for NIV failure has a negative impact on patient survival. Hence, assessing the risk of NIV failure is extremely important. NIV has some limitations: a) intolerance, discomfort and claustrophobia requiring frequent interruptions; b) poor patient-ventilator synchrony, especially in presence of air leaks or high ventilatory requirements. Since removing carbon dioxide by means of an artificial lung reduces the minute ventilation required to maintain an acceptable arterial partial pressure of carbon dioxide (PaCO2), the investigators hypothesize that applying Extra-Corporeal CO2 Removal (ECCO2R) in high-risk AECOPD patients may reduce the incidence of NIV failure and improve patient-ventilator interaction. After the beginning of ECCO2R, NIV could be gradually replaced by High Flow Nasal Cannula Oxygen Therapy (HFNCOT), potentially reducing the risk of ventilator induced lung injury, improving patient's comfort and probably allowing the adoption of a more physiologically "noisy" pattern of spontaneous breathing.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
40
NIV will be discontinued, the ECCO2R setting will be unchanged (both sweep gas flow and blood flow through the artificial lung) and HFNCOT will be started, titrating the fraction of inspired Oxygen (FiO2) to obtain an oxygen saturation at periphery (SpO2) 88-92%; HFNCOT start temperature will be 31°C, the initial flow rate will be 60 L/min.
Ospedale Maggiore Policlinico
Milan, Italy
RECRUITINGNumber of partecipants failing HFNCOT+ECCO2R treatment with need of restoring NIV or need of invasive mechanical ventilation
ECCO2R+HFNCOT failure criteria are defined by at least two of the following after at least 1 hour of treatment 1. Respiratory acidosis (pH \<7.35) 2. RR ≥ 30 bpm 3. Development of progressive hypoxemia (PaO2/FiO2 \< 150) 4. Paradoxical breathing
Time frame: Through study completion, an average of 2 years
Number of partecipants failing NIV+ECCO2R treatment with need of invasive mechanical ventilation
NIV+ECCO2R failure is defined by two of the following occurring for at least 2 hours: 1. No improvement or worsening of respiratory acidosis (pH \<7.35) 2. RR ≥30 bpm 3. Development of progressive hypoxemia (PaO2/FiO2 ≤150)
Time frame: Through study completion, an average of 2 years
Number of patients treated with ECCO2R reporting one or more side effects due to ECCO2R
1. Bleeding (any bleeding event requiring the administration of 1 U of packed red cells) 2. Vein perforation at cannula insertion 3. Hemodynamic instability (80-90 mmHg increase or 30-40 mmHg decrease systolic arterial pressure compared to baseline value or need of vasopressors to maintain systolic blood pressure higher than 85 mmHg or electrocardiogram evidence of ischemia/arrhythmias) 4. Pneumothorax 5. Ischemic bowel 6. Acute kidney failure 7. Neurological complications (occurrence, after initiation of ECCO2R, of ischemic/hemorrhagic ictus or clinical seizure or cerebral oedema) 8. Metabolic complications (occurrence, after initiation of ECCO2R of hyperbilirubinemia or glucose≥240 mg/dL) 9. Thromboembolic complications (occurrence, after initiation of ECCO2R, of deep venous thrombosis, pulmonary embolism)
Time frame: Through study completion, an average of 2 years
Variation of pulmonary arterial pressure before and after ECCO2R treatment either in association with NIV or HNFCOT
Echocardiographic measurement
Time frame: Through study completion, an average of 2 years
Variation of tricuspid annluar plane systolic excursion before and after ECCO2R treatment either in association with NIV or HNFCOT
Echocardiographic measurement
Time frame: Through study completion, an average of 2 years
Variation of respiratory mechanic during ECCO2R+NIV
Measurement of Respiratory Rate (breaths per minute)
Time frame: Through study completion, an average of 2 years
Variation of dyspnea during ECCO2R+NIV
Measurement of dyspnea through Borg dyspnea scale. (ranging from a minimum of 0 point, indicating no shortness of breath, to a maximum of 10 points, indicating maximum shortness of breath)
Time frame: Through study completion, an average of 2 years
Variation of comfort during ECCO2R+NIV
Measurement of comfort through Visual Analogic Scale for comfort, ranging from a minimum of 0 point, indicating no comfort, to a maximun of 10 point, indicating maximum comfort
Time frame: Through study completion, an average of 2 years
Variation of respiratory mechanic during ECCO2R+HFNCOT
Measurement of Respiratory Rate (breaths per minute)
Time frame: Through study completion, an average of 2 years
Variation of dyspnea during ECCO2R+HFNCOT
Measurement of dyspnea through Borg dyspnea scale, ranging from a minimum of 0 point, indicating no shortness of breath, to a maximum of 10 points, indicating maximum shortness of breath
Time frame: Through study completion, an average of 2 years
Variation of comfort during ECCO2R+HFNCOT
Measurement of comfort through Visual Analogic Scale for comfort, ranging from a minimum of 0 point, indicating no comfort, to a maximun of 10 point, indicating maximum comfort
Time frame: Through study completion, an average of 2 years
Variation of breathing pattern during ECCO2R+NIV
Measurement of expiratory tidal volume, expressed in mL
Time frame: Through study completion, an average of 2 years
Variation of breathing pattern during ECCO2R+NIV
Measurement of minute ventilation, expressed in liters/minute
Time frame: Through study completion, an average of 2 years
Variation of acid-base balance during ECCO2R+NIV
emogasanalysis
Time frame: Through study completion, an average of 2 years
Variation of acid-base balance during ECCO2R+HFNCOT
emogasanalysis
Time frame: Through study completion, an average of 2 years
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