A novel extracorporeal CO2 removal system: results of a pilot study of hypercapnic respiratory failure in patients with COPD

Background - Hypercapnic respiratory failure in patients with COPD frequently requires mechanical ventilatory support. Extracorporeal CO2 removal (ECCO2R) techniques have not been systematically evaluated in these patients. - Methods - This is a pilot study of a novel ECCO2R device that utilizes a s...

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Hauptverfasser: Burki, Nausherwan K. (VerfasserIn) , Mani, Raj Kumar (VerfasserIn) , Herth, Felix (VerfasserIn) , Schmidt, Werner (VerfasserIn) , Teschler, Helmut (VerfasserIn) , Bonin, Frank (VerfasserIn) , Becker, Heinrich (VerfasserIn) , Randerath, Winfried J. (VerfasserIn) , Stieglitz, Sven (VerfasserIn) , Hagmeyer, Lars (VerfasserIn) , Priegnitz, Christina (VerfasserIn) , Pfeifer, Michael (VerfasserIn) , Blaas, Stefan H. (VerfasserIn) , Putensen, Christian (VerfasserIn) , Theuerkauf, Nils (VerfasserIn) , Quintel, Michael (VerfasserIn) , Moerer, Onnen (VerfasserIn)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: 2013
In: Chest
Year: 2015, Jahrgang: 143, Heft: 3, Pages: 678-686
ISSN:1931-3543
DOI:10.1378/chest.12-0228
Online-Zugang:Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1378/chest.12-0228
Verlag, lizenzpflichtig, Volltext: http://www.sciencedirect.com/science/article/pii/S0012369213601476
Volltext
Verfasserangaben:Nausherwan K. Burki, MD, PhD, FCCP; Raj Kumar Mani, MD, FCCP; Felix J.F. Herth, MD, FCCP; Werner Schmidt, MD; Helmut Teschler, MD; Frank Bonin, MD; Heinrich Becker, MD; Winfried J. Randerath, MD, FCCP; Sven Stieglitz, MD; Lars Hagmeyer, MD; Christina Priegnitz, MD; Michael Pfeifer, MD; Stefan H. Blaas, MD; Christian Putensen, MD, PhD; Nils Theuerkauf, MD; Michael Quintel, MD, PhD; and Onnen Moerer, MD

MARC

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520 |a Background - Hypercapnic respiratory failure in patients with COPD frequently requires mechanical ventilatory support. Extracorporeal CO2 removal (ECCO2R) techniques have not been systematically evaluated in these patients. - Methods - This is a pilot study of a novel ECCO2R device that utilizes a single venous catheter with high CO2 removal rates at low blood flows. Twenty hypercapnic patients with COPD received ECCO2R. Group 1 (n = 7) consisted of patients receiving noninvasive ventilation with a high likelihood of requiring invasive ventilation, group 2 (n = 2) consisted of patients who could not be weaned from noninvasive ventilation, and group 3 (n = 11) consisted of patients on invasive ventilation who had failed attempts to wean. - Results - The device was well tolerated, with complications and rates similar to those seen with central venous catheterization. Blood flow through the system was 430.5 ± 73.7 mL/min, and ECCO2R was 82.5 ± 15.6 mL/min and did not change significantly with time. Invasive ventilation was avoided in all patients in group 1 and both patients in group 2 were weaned; PaCO2 decreased significantly (P < .003) with application of the device from 78.9 ± 16.8 mm Hg to 65.9 ± 11.5 mm Hg. In group 3, three patients were weaned, while the level of invasive ventilatory support was reduced in three patients. One patient in group 3 died due to a retroperitoneal bleed following catheterization. - Conclusions - This single-catheter, low-flow ECCO2R system provided clinically useful levels of CO2 removal in these patients with COPD. The system appears to be a potentially valuable additional modality for the treatment of hypercapnic respiratory failure. - Trial registry - ClinicalTrials.gov; No.: NCT00987740 and 01021605; URL: www.clinicaltrials.gov 
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